Method and apparatus for purifying aqueous solutions by shielding or subjecting chemical substances to low frequency electromagnetic radiation

Technical Field

The present invention relates to the fields of influencing chemical elements and molecules in water, and more specific to a method to prevent said chemical elements and molecules from absorbing electromagnetic energy and according to the preamble of claim 1.

Background and Prior Art

It is known that the rotation of the earth creates currents with 24-hour period in the magnetosphere, known as the Birkeland currents.

It is known that Maxwell's equations postulate that this current generates plane transverse electromagnetic waves.

The global electric circuit is known since the 1920ies and it supplies the earth crust and the air with charge; electrons, negative and positive ions. The 200 kV potential between the ionosphere and earth creates vertical current density of approximately 3 pA/m ³ as well as an electron density of approximately 500 pC/m ³ and positive ion density of approximately 200 pC/m ³ in the air.

It is known that Maxwell ^' s equations postulate that the plane transverse electromagnetic waves exhibit a force on said electrons thereby generating alternating currents in the air and in the earth crust.

The above alternating current as well as the resonance phenomena created in the air as well as measurement methods have been described by Giertz (2010a). These currents have the period 24/(m-2 ⁿ ) hours.

It is known that H ₂ 0 forms molecule structures (e.g. tetrahedral structure), that water is polar in nature and dissolves salts (e.g. NaCI) into ions where Na ⁺ is attracted to ^δ Ό and CI ^" to ^δ+ Η and H ₂ 0 molecules are bonded by the extremely weak hydrogen bond.

It is known that water that contains salts (e.g. H ₂ 0 + Na ⁺ + CI ^" ) is a dielectric medium. It is also known that a dielectric medium is a forced damped oscillator.

It is known that low frequency electromagnetic energy creates resonance in water, described by Giertz (2010b).

It is known that many chemical elements and compounds, (e.g. Ag, Al, As, Au, C, Ca, Cd, CI, Co, Cr, Cu, F, Fe, Ga, Hg, I, K, Li, Mg, Mn, N, Na, Nd, Ni, O, P, Pb, S, Se, Sn, Ti, Zn, V, W, C0 ₂ , N0 ₂₍ N0 ₃ , NH ₄ , S0 ₂ and S0 ₄ ), dissolve in water (e.g. as ions) and that an ion forms a specific water molecule structure in the solvation shells.

It is known that aluminium (Al) accumulates in the human body and which causes health effects, primarily in the brain. It is also known that tap water, food and beverages can contain traces of aluminium. It is known that arsenic (As) and many of its compounds are extremely potent poisons, both for the environment and for humans. Water supplies close to mines are sometimes contaminated by arsenic. Arsenic in drinking water is known to cause arsenicosis.

It is known that cadmium (Cd) accumulates in the human body and which causes health effects, primarily in the brain. It is also known that tobacco contains cadmium and that smokers accumulate cadmium.

It is also known that cadmium is a toxic waste and which occurs in industrial waste and in sewage.

It is known that cobalt (Co) is an essential element of life in minute amounts. Cobalt is considered carcinogenic.

It is known that copper (Cu) accumulates in the human body and which can cause health effects. Specific examples of this include Wilson's disease, Alzheimer's disease and symptoms like vomiting, jaundice and cirrhosis.

It is known that fluoride (F) containing compounds can be toxic and that some reports claim that fluoride can cause brain disorders.

It is known that mercury (Hg) and most of its compounds are extremely toxic. Mercury can cause both chronic and acute poisoning. Research on the treatment of mercury poisoning is limited.

It is known that lead (Pb) accumulates in the human body and which causes health effects, primarily in the brain. It is also known that tap water, food and beverages can contain traces of lead.

Tin (Sn) plays no known natural biological role in humans.

Most tin salts are toxic. It is known that tin accumulates in the human body and which can cause health effects.

It is known that the corrosion of tin plated food cans by acidic food and beverages has caused several intoxications with soluble compounds.

It is known that organotin compounds are very toxic.

It is known that many molecules dissolve in water.

It is known that sulfur dioxide (S0 ₂ ) is used in increasing amounts as a food preservative or enhancer. Sulfur dioxide is counted among the top nine food allergens. It is known that sulfur dioxide deteriorate the taste of wine and that it contributes to headache.

It is known that sulfur dioxide (S0 ₂ ) is a major air pollutant and has significant impact on human health.

It is known that sulfur dioxide (S0 ₂ ) is a major water pollutant and has significant impact on sea, lake and ground water.

It is known that sulfur dioxide (S0 ₂ ) is removed from oil in refineries; however some S0 ₂ is left in, oil, petrol and petroleum distillates. Burning coal, gas oil and petrol releases S0 ₂ and that is a major air pollutant.

It is known that removal of sulfur dioxide (S0 ₂ ) in coal, gas, oil and petrol is a major environmental issue. Removal of sulfur dioxide from outlets when burning coal, gas and oil is a major environmental issue. It is known that carbon dioxide (C0 ₂ ) produced when burning coal, gas and oil as well as exhaust from cars is a major environmental issue.

It is known that fertilizers contain nitrates (N0 ₃ ), ammonium (NH ₄ ) and phosphates (e.g. P0 ₄ ) which dissolve in water and resulting in pollution of rivers, lakes and seawater and which is a major environmental issue.

It is known that the herbicide glyphosate dissolves in water and that creates a specific water molecule structure close to the glyphosate molecule.

It is known that glyphosate is used as one of the most common herbicides and is therefore found on vegetables such as tomatoes, cucumbers, salads, zucchini, onions and apples.

It is known that the pesticide dioctyl sodium sulfosuccinate (abbreviated DSS) dissolve in water and that creates a specific water molecule structure close to the DSS molecule.

It is known that DSS is used as one of the most common pesticides when growing grapes, olives, caper, oranges, bananas, corn and almonds.

It is known that DSS is used when producing sugar.

It is known that DSS is used as a laxative to make stools softer and as an excipient in the production of tablets (as a lubricant) and as suspensions (as an emulsifier).

It is known that imidacloprid is one of the most used insecticides used on vegetables, wheat, potatoes, beets, hops, corn, sunflowers, grapes, olives and fruit.

It is known that imidacloprid is readily taken up by plant roots and translocate up into the plant leaves, pollen and fruits.

It is known that phoxim has been a widely used insecticide. Phoxim is banned for use on crops in the European Union since 2007.

It is known that bitertanol (sibutol) is one of the most used fungicides used preventively or curatively for the control of certain diseases in fruits, vegetables and seed.

Summary of the Invention: Enabier Novel measurement technique described by Giertz (2010a, b) enables measurement of current in the air, resonance phenomena in water in vitro, in situ and in vivo. It enables a novel way to measure and describe the low frequency electromagnetic characteristics of water in vitro, in situ and in vivo.

Summary of the Invention: object of the invention

The object of this invention is to influence and/or change a chemical element, compound or molecule dissolved in water. The method is to prevent said chemical element, compound or molecule from absorbing electromagnetic energy, present in the air and in water, with the natural period or natural periods of the chemical element, compound or molecule dissolved in water. It facilitates removal and/or separation of chemical elements, compounds and molecules from water in vitro, in situ and in vivo. Summary of the Invention: short description The invention builds on the observation that the air, the earth crust and water contain extremely low amplitude and low frequency electromagnetic energy consisting of conduction current. This electromagnetic energy has periods equal to the harmonics of the period 24 - hours, i.e. the periods 24/(m-2 ⁿ ) hour. A chemical element ion has charge whereby coulomb forces attract water molecules. These water molecules form solvation shells that are specific to the chemical element, and which depend on the ion's charge and size. The charged ion, the mass of the ion + H ₂ 0 molecules and the elasticity of the hydrogen bond constitute a dielectric media and a forced damped oscillator. Thus, each ion and the H ₂ 0 molecule specific solvation shells constitute a forced damped oscillator that creates resonance and absorbs electromagnetic energy at chemical element specific natural periods. A chemical element dissolves in water when one or many of these natural periods coincide with electromagnetic energy present in the air and in water, whereby the ion and the solvation shells create resonance and absorb electromagnetic energy at one or many of the periods 24/(m-2 ⁿ ) hour. The natural period(s) depend on the type of chemical element (ion), i.e. its charge and its radius. Some compounds (e.g. HC0 ₃ ^" , S0 ₄ ^2" , NH ₄ ⁺ , N0 ₂ ^" , N0 ₃ ^" ) have charge (is an ion) and form solvation shells similar to a chemical element ion. This constitutes forced damped oscillators and the compound has unique natural periods 24/(m-2 ⁿ ) hour. Chemical elements and compounds can lack charge (e.g. 0 ₂ ). However, the compound has charge displacement(s), i.e. one dipole or many dipoles, and the dipole creates solvation shells. Thus, many compounds create resonance and absorb electromagnetic energy at one or many of the periods 24/(m-2 ⁿ ) hour. Many molecules dissolve in water (e.g. imidacloprid, C ₉ Hi ₀ CIN ₅ O ₂ ). The molecule has charge displacements, i.e. one dipole or many dipoles, and the dipole creates solvation shells. Thus, many molecules create resonance and absorb electromagnetic energy at one or many of the periods 24/(m-2 ⁿ ) hour. This is valid for all types of chemical elements, compounds and molecules that dissolve in water and the present invention encompasses all chemical elements, compounds and molecules that dissolve in water. The present invention describes the chemical elements Ag, Al, As, Au, C, Ca, Cd, CI, Co, Cr, Cu, F, Fe, Ga, Hg, I, K, Li, Mg, Mn, Na, Nd, Ni, O, P, Pb, S, Se, Sn, Ti, Zn, V and W. The present invention describes the molecules glyphosate (C ₃ H ₈ N0 ₅ P), imidacloprid (C ₉ H ₁₀ CIN ₅ O ₂ ), phoxim (C ₁₂ H ₁₅ N ₂ 0 ₃ PS), dioctyl sodium sulfosuccinate (C ₂ oH ₃₇ N0 ₇ S), bitertanol (C ₂₀ H ₂₃ N ₃ O ₂ ), drugs containing the six membered carbon ring (e.g. C ₆ H ₆ , C ₆ H ₅ OH, C ₆ Hi ₂ ), carbon dioxide (C0 ₂ ), nitrogen compounds (including N0 ₂ , N0 ₃ and NH ₄ ), ammonium chloride (NH ₄ CI), phosphates (including P0 ₄ and Ca(H ₂ P0 ₄ ), sulfites (e.g. H ₂ S and S0 ₂ ) and sodium chloride (NaCl).

The invention builds on the observation that the solvation shells are destroyed when the chemical element, compound or molecule is stopped from absorbing electromagnetic energy with periods equal to the natural periods of the chemical element, compound or molecule. This results in a reaction where the chemical element, compound or molecule ceases to dissolve and where it is changed into an atom, ion, metal and/or one or many compounds, including one or many compounds without charge.

The invention describes a method that makes it possible to influence and/or change a chemical element, compound or molecule and/or to remove a chemical element, compound or molecule from water.

Detailed Theory: introduction

The air, the earth crust and water contains low frequency and extremely low amplitude

electromagnetic energy of conduction current (i.e. current). This electromagnetic energy contains large amounts of harmonics with periods 24/(m-2 ⁿ ) hour. This is described in the first part; Air. Water creates resonance in the same frequency range and that is explained in the second part: Water. The behaviour of chemical elements, compounds and molecules dissolved in water is explained in the third part: Chemical Elements and Molecules. The fourth and fifth part describes the theory of passive forced damped oscillators as well as methods and apparatus based on these oscillators. These apparatus can be used to extinct electromagnetic energy whereby a chemical element dissolved in water is influenced.

Detailed Theory: Air

This part has been published in Journal of Atmospheric and Solar-Terrestrial Physics 72 (2010) 767- 773. http://dx.doi.Org/10.1016/i.iastp.2010.03.022 That paper describes the presence of low frequency electromagnetic energy in the air, in water and in the earth crust. It originates from the rotation of the earth and thus its period is 24 hours.

However, it contains a large amount of harmonics with periods 24/(m-2 ⁿ ) hour, including harmonics in the period range 0.1-1 s. The electromagnetic energy consists of slowly propagating electrons creating alternating currents. That paper describes detailed measurement methods, and which are used in the present invention.

Detailed Theory: Water

Water creates electromagnetic resonance in the 1-10 Hz frequency range (0.1 - I s period range), i.e. the same frequency/period range as harmonics of electromagnetic energy in air, in water and in the earth crust. Water contains angular molecules (H ₂ 0) in which hydrogen and oxygen is joined by single covalent bonds where electron pairs making up the covalent bond create a small residual or partial positive charge (δ+) on the hydrogen atom, and a partial negative charge (δ-) on the oxygen atom. Water can dissolve a large number of ionic substances because of the interaction between the appropriate polarized end of the water molecule and ions. For example sodium chloride (Na ⁺ CI ) solve in water with Na ⁺ attracted to ^δ Ό and CI ^" to ^δ+ Η. The polarized ends of H ₂ 0 create an extremely small force that bonds H ₂ 0 molecules called the hydrogen bond and this bond is elastic. Thus water can be described as a dielectric media having charge, mass and elasticity and the classical model based on a damped oscillator can be used, as described by Melrose and McPhedran (1991). Consider a classical oscillator that corresponds to a mass m with charge q at a displacement X(t) from its mean position. Let the frequency of the oscillator be ω ₀ , and let it be damped with the decay constant y. The oscillator is assumed to be forced by an electric field E(i). The equation of motion is

Χ"(Γ)+|/Χ'(Γ)+ω ² ₀ Χ(Γ) = qE(t)/m (1)

When the decay constant y is small the mass (and charge) oscillates at its natural frequency (Jonsson, 1991):

The absorbed current amplitude Ι(ω) of the forced damped oscillator as a function of the frequency ω of the electric field E(t) (Ω is a constant) is (Jonsson, 1991):

Ι(ω) = Ω|//((ω ₀ . ω) ² + 74) (3) k is the elasticity (spring constant) which in this case corresponds to the elasticity of the hydrogen bond. It is the electromagnetic energy E(f) acting on the charge q that supplies the oscillator with energy and the oscillator resonance frequency (natural frequency) ω ₀ is determined by its mechanical properties m and k. The oscillator is in resonance with the applied energy when the energy E(r) has a frequency ω = ω ₀ and then absorbed energy and oscillator amplitude is maximized. An adaptive media, like water, can change its molecule structure and consequently, its natural frequency u) ₀ . The normal state is where the absorbed energy is maximized, i.e. ω ₀ = ω and the media is then in resonance with the applied energy. The number of possible resonance frequencies (modes) in water containing ions is very large. Consider an overall tetrahedral water molecule structure as reported by Chaplin and Head-Gordon et al. (1999). Positive ions (e.g. Na ⁺ ) and negative ions (e.g. CI ^" ) can form molecule structures together with H ₂ 0 molecules (solvation shells) where the structures creating resonance have small mass m and short distances (few hydrogen bonds equal to high spring constant k) giving high resonance frequency according to Eq. (2) or the opposite giving low resonance frequency. The hydrogen bond and its corresponding spring constant k depend on the force F between two residual charges following Coulombs law and it has a certain size in the longitudinal direction (Bleaney, 1965):

F = q^r/ ne^ ³ (4)

Ion-water molecule structures can be enforced to create resonance with electromagnetic energy in the 1-10 Hz range (i.e. 0.1-1 sec period range).

Detailed Theory: Chemical Elements and Molecules The present invention builds on empirical observations of the dynamic electromagnetic behavior of chemical elements, compounds and molecules dissolved in water or in contact with water.

Influencing the absorbed electromagnetic energy can result in changed characteristics of the chemical element or compound or molecule. This section offers a theoretical description that may turn out to be correct. It may also turn out to be incorrect. However, the exact theory is irrelevant as long as the context of the claims is correct.

This part of the description is based on the properties of chemical element ions, e.g. metal ions. However, the invention encompasses chemical elements in general, and not only their ions. In general a metal ion and its isotopes, dissolved in water, have positive charge, i.e. a cation, of chemical formula [M(H ₂ 0) _n ] ^z+ . n is the solvation number and z is the electric charge. This forms a first and second solvation shell of H ₂ 0 molecules around the ion. The solvation shell molecule structure depends on the ion's charge z and its radius. The ion and the H ₂ 0 solvation shells molecule structures constitutes forced damped oscillators and which create resonance at absorb electromagnetic energy as described in the section Water and by Eq. (1).

In the following this mechanism is described based on the tin ion (Sn ⁴⁺ ). However, the description is general for all types of chemical elements dissolved in water. Dissolved tin creates solvation shells where the ion-water molecule structure creates resonance and absorbs electromagnetic energy; i.e. the natural periods are 24/(1·2 ¹⁸ ) hour and 24/(9·2 ¹⁶ ) hour and 24/(17·2 ¹⁵ ) hour. This creates resonance in water in vitro, in situ as well as in vivo, i.e. in organism water, including humans. This resonance and the absorbed electromagnetic energy may have positive health effects (e.g. trace metals) as well as negative health effects (e.g. As, Al, Cd, Cr, Hg, Pb). Similar processes have been described in detail, Giertz (2010b). Negative health effects have been described, Giertz (2010b). Chemical elements, including Al, As, Au, C, Cd, CI, Co, Cr, Cu, F, Fe, Ga, Hg, I, K, Li, Mg, Mn, Na, Nd, Ni, 0, P, Pb, S, Se, Ti, Zn, V and W form solvation shells and resonance in similar way. However, each type of chemical element forms its specific solvation shells and which have chemical element specific natural periods as described in the section Achieved results.

The air contains electromagnetic energy with period 24/(m-2 ⁿ ) hour. Water in vitro, in situ and in vivo normally create resonance and absorbs electromagnetic energy with the period 24/(3·2 ¹⁷ ) hour, enforced by resonance created by Na ions and also 0 ₂ . Thus, the normal state of water is to have resonance and to absorb low frequency electromagnetic energy with the period 24/(3·2 ¹⁷ ) hour.

In absence of electromagnetic energy water containing dissolved chemical elements (e.g. ions) is static. Coulomb forces maintain the bonds between the chemical element and water molecules in the solvation shells.

In presence of electromagnetic energy the ion-water molecule structure (solvation shells) creates resonance (and the ion absorbs energy) at the natural period(s) of the chemical element (e.g. for tin; 24/(1·2 ¹⁸ ) hour and 24/(9·2 ¹⁶ ) hour and 24/(17·2 ¹⁵ ) hour). A major part of the rest of the water creates resonance (its ions, e.g. Na, absorb electromagnetic energy) at the period 24/(3-2 ¹⁷ ) hour (and at other periods created by the presence of other chemical elements, compounds and/or molecules). Resonance at the natural period(s) (e.g. for tin; 24/(1·2 ¹⁸ ) hour and 24/(9·2 ¹⁵ ) hour and 24/(17·2 ¹⁵ ) hour) probably strengthens the bonds in the tin solvation shells (i.e. resonance enhanced bond).

Stopping water from absorbing electromagnetic energy with the natural period(s) of the chemical element (e.g. for tin; 24/(1·2 ¹⁸ ) hour and 24/(9·2 ¹⁶ ) hour and 24/(17·2 ¹⁵ ) hour) stops the ion-water molecule structure (solvation shells) from creating resonance at the natural period(s). However, adjacent ion-water molecule structures have resonance at the period 24/(3·2 ¹⁷ ) hour (or other periods). This resonance disturbs the molecule structure close to the chemical element (i.e. the solvation shells), alternatively it enforces resonance and alters the molecule structure close to the ion. This destroys or weakens the bonds between the ion and water molecules and which releases the ion and it is no longer locked in the water; it can move as a free ion in the water. It also implies that the solvation shells do not neutralize its charge. However, the ion is exposed to energy from adjacent oscillating H ₂ 0 molecules (i.e. that oscillate at a period deviating from the natural period(s) of the chemical element). The ion has charge and therefore it causes a reaction. The product of this reaction can be a tin atom (four electrons are added to the Sn ⁴⁺ ion) and/or a (tin) metal and/or a compound caused by bonding to ions with opposite charge. The atom and/or metal and/or compound do not dissolve or has low solubility and its weight makes it drift downwards (i.e. by gravity) in the water, while some compounds may have high solubility. Some chemical elements drift upwards and evaporate.

Chemical elements can also be removed by exposing the water to electromagnetic energy with one or many of the natural periods of the chemical element; however, the amplitude must be significantly higher (approximately 10 times) than the amplitude of the corresponding

electromagnetic energy present in the air and in water. This creates resonance in the ion-water molecule structure (solvation shells); however, the amplitude of this resonance is so high that the solvation shells are destroyed and the ion is released, whereby it can react and create an atom, metal or new compounds. This enables influence on and/or separation of chemical elements, including Ag, Al, As, Au, C, Cd, CI, Co, Cr, Cu, F, Fe, Ga, Hg, I, K, Li, Mg, Mn, Na, Nd, Ni, 0, P, Pb, S, Se Sn, Ti, Zn, V and W from water using different methods.

Thus chemical elements are influenced and/or separated and/or removed from water in vitro, in situ and in vivo by preventing the chemical element from absorbing electromagnetic energy present in the air and in water with the natural period or natural periods of the chemical element (e.g. for tin; 24/(1·2 ¹⁸ ) hour and 24/(9·2 ¹⁶ ) hour and 24/(17·2 ¹⁵ ) hour) and this is achieved using apparatus which cancel this energy. Observe that influence and/or release of Ag, As, C, Cd, CI, Co, Cr, Cu, F, Fe, Ga, Hg, I, K, Li, Mg, Mn, Na, Nd, Ni, O, P, Pb, S, Se, Sn, Zn, V and W is only achieved when the chemical element and water is prevented from absorbing electromagnetic energy simultaneously with all two or all three or all four of the natural periods of the chemical element being influenced.

Some compounds (e.g. HC0 ₃ ^" , S0 ₄ ^2" , NH ₄ ⁺ , N0 ₂ ^~ , N0 ₃ ^" ) have charge (i.e. an ion) and form solvation shells similar to a chemical element ion. This constitutes forced damped oscillators and the compound has unique natural periods 24/(m-2 ⁿ ) hour. The compound is influenced and/or separated and/or removed from water in vitro, in situ and in vivo by preventing the compound from absorbing electromagnetic energy present in the air and in water with the natural period or natural periods of the compound.

Some compounds (e.g. 0 ₂ , NaCI) and molecules that dissolve in water have charge displacement, i.e. they are polarized and contain one or many dipoles. These dipoles create solvation shells of H ₂ 0 molecules and therefore they constitute one or many forced damped oscillators and which create resonance and absorb electromagnetic energy at one or many periods 24/(m-2 ⁿ ) hour. Stopping a compound or a molecule from absorbing electromagnetic energy at the natural period or natural periods of the compound or molecule destroys the solvation shells. The compound or molecule is then exposed to energy from adjacent oscillating H ₂ 0 molecules and which result in that the compound ceases to dissolve (e.g. 0 ₂ ) or is split by H ₂ 0 molecules (e.g. NaCI) or exposed to other (charged) ions or compounds and which split the compound or molecule into new compounds and/or chemical elements. This enables influence on and/or separation of compounds and molecules from water using different methods.

Detailed Theory; Resonance in conductors

Current normally propagates in a conductor with almost the speed of light. There are two mechanisms involved in this process. Electrons in a conductor drift with their drift velocity, in copper the drift velocity is 1.517 mm/s. Injected electrons create a charge gradient and coulomb forces, according to:

This creates a force gradient, which acts on nearby electrons and this creates a chain reaction that propagates with almost the same speed as the coulomb forces, i.e. the current propagates with almost the speed of the light. Electrons on the conductor surface, called surface charge, always conduct the current transport. When the injected energy is extremely small, < lpA, the gradient is also extremely small. The surface charge attracts positive ions present in the air and the number of positive ions is sufficient to neutralize the gradient of the surface charge, i.e. the coulomb forces are neutralized. Thus the current propagates with the drift velocity of the electrons, i.e. 1.517 mm/s. A conductor submerged in water behaves in the same way since positive ions in the water neutralize the surface charge. The inventor has measured the current speed in copper to 1.517 mm/s. The wave propagation in a conductor at current < 1 pA is described by the classical wave propagation in one dimension (Jonsson, 1999). One solution is a harmonic wave that satisfies ξ = a-sin(iot + δ), where a is the amplitude, δ is the phase constant and ω is the angular frequency. The phase speed is equal to the velocity v of the current, i.e. the drift velocity of the electrons: v - 1.517 mm/s in copper.

Resonance and a standing wave inside the conductor occurs when its length is equal to one half wavelength (λ/2) or a multiple, i.e. (λ/2)· 2 ^q . A conductor with length L creates a standing wave and resonance at

L = (λ/2)·2 «= (T/2)-2 ^q -v , q = 0, 1, 2, 3, 4.... (5)

T is the period. This constitutes a resonance circuit or a forced damped oscillator having the natural period T. The forced damped oscillator has low impedance at its natural period T.

Detailed Theory: Extinction of energy

Extinction of electromagnetic energy in the air and in water can be made in many ways, e.g. by shielding and by different forms of electromagnetic interference. The invention uses a method where two or more forced damped oscillators create electromagnetic interference in the air and/or in water and this stops electromagnetic energy from propagating to the water containing the dissolved chemical element. These forced damped oscillators can consist of copper conductors as described in the section Detailed Theory; Resonance in conductors. Each forced damped oscillator natural period T is equal to one of the natural periods of the chemical element, compound or molecule dissolved in water.

In the following tin (Sn) is used as an example. Tin has the natural period 24/(1-2 ) hour and 24/(9-2 ¹⁶ ) hour and 24/(17·2 ¹⁵ ) hour.

Stopping electromagnetic energy and/or current in the air and in water, with the period 24/(1·2 ¹⁸ ) hour and 24/(9·2 ¹⁶ ) hour and 24/(17·2 ¹⁵ ) hour, from propagating to dissolved tin (Sn) is made by an apparatus consisting of three passive oscillators with natural period 24/(1·2 ¹⁸ ) hour, 24/(9·2 ¹⁶ ) hour and 24/(17·2 ¹⁵ ) hour. The oscillators are positioned with an angle a (45° < a < 90°) and at a distance of 0.1-10 mm. The copper conductor lengths according to Eq. (5) are preferably 3.56 mm, 3.76 mm and 4.00 mm or 7.11 mm, 7.53 mm and 8.00 mm. They create electromagnetic interference and this disturbs the resonance mechanism in air and which stops resonance at these periods. This cancels electromagnetic energy and/or current close to the oscillators, typically within a radius of 5-10 meters; however, depending on the quality factor of the oscillators and the internal position of the oscillators, i.e. distance and angle.

The oscillators can also be positioned in (submerged into) water whereby they stop the ion-water molecule structures from creating resonance and from absorbing electromagnetic energy (at the period 24/(1·2 ¹⁸ ) hour and 24/(9·2 ¹⁶ ) hour and 24/(17·2 ¹⁵ ) hour) in this example). This converts soluble Sn ions into insoluble Sn whereby the water has lost its capability to create resonance at the period 24/(1·2 ¹⁸ ) hour and 24/(9·2 ¹⁶ ) hour and 24/(17·2 ¹⁵ ) hour). This results in that adjacent Sn ions are influenced and cease to create resonance whereby they are converted into insoluble Sn. This creates a chain reaction, resulting in that an increasing volume of water ceases to create resonance (at the natural periods of Sn). Eventually every Sn ion is converted into insoluble Sn. It is possible to remove all Sn in a large volume of water by positioning three copper conductors with length 3.56 mm, 3.76 mm and 4.00 mm in the water during few hours. The method is applicable on all chemical elements, compounds and molecules that dissolve in water.

The section Description of the invention describes oscillators and apparatus applicable on chemical elements, compounds and molecules.

Detailed Theory: Conclusions

Chemical elements, compounds and molecules dissolve in water by means of the bonds between the chemical element, compound or molecule and H ₂ 0 molecules forming one or many solvation shells. This creates chemical element, compound or molecule specific solvation shells consisting of specific H ₂ 0 molecule structures. This constitutes one or many forced damped oscillators that absorb electromagnetic energy present in the air and in water with the natural period or natural periods of the chemical element, compound or molecule. Electromagnetic energy, present in the air, normally also creates resonance in water at the period 24/(3·2 ¹⁷ ) hour (caused by Na and 0 ₂ ). Preventing water, containing a dissolved chemical element, compound or molecule, from absorbing

electromagnetic energy with the natural period(s) of the dissolved chemical element, compound or molecule stops resonance at its natural period(s). Adjacent ion-water molecule structures, having resonance at the period 24/(3·2 ¹⁷ ) hour, disturbs or destroys the molecule structure in the solvation shells. This creates a reaction. The reaction results in change into atom, ion, metal and/or one or any compounds. The atom, metal or compounds normally create sediment and form precipitate on the bottom of the water solution. The precipitate can then be removed and/or separated from the water using different methods, e.g. decantation, filtering and/or centrifugation. Some chemical elements and compounds float and evaporate (e.g. 0 ₂ , N ₂ ).

Detailed Theory: References

1. Bleaney, B.I. Electricity and Magnetism. Oxford at the Clerendon Press (1965).

2. Chaplin M. A proposal for structuring of water. Biophysical Chemistry. 83, 211-221 (1999).

3. Head-Gordon T, Johnsson M. E. Tetrahedral structure or chains for liquid water. Available online http://www.pnas.org/cgi/doi/10.1073/pnas.0510593103 (2006).

4. Giertz, H.W. Journal of Atmospheric and Solar-Terrestrial Physics 72 (2010a) 767-773.

http://dx.doi.Org/10.1016/i.iastp.2010.03.022

5. Giertz, H.W. IT Medicine, a Novel Approach to Management of Infectious Diseases. Katarina Tryck. ISBN 978-91-976841-4-9. (2010b).

6. Jonsson G. Vaglara och optik (Wave theory and optics). Teach Support, Lund. (1999).

7. Melrose D. B, McPhedran R. C. Electromagnetic processes in dispersive media. Cambridge University Press, Cambridge, pp 106-110 (1991).

Achieved results; Chemical elements

The chemical elements Ag, Al, As, Au, C, Cd, CI, Co, Cr, Cu, F, Fe, Ga, Hg, I, K, Li, Mg, Mn, Na, Nd, Ni, O, P, Pb, S, Se, Sn, Ti, Zn, V and W, dissolved in water, were measured in vitro and in vivo using the method described by Giertz (2010a, b). The absorbed current was measured as function of the frequency using an analogue generator as well as current present in the air. Aluminum (Al)

Aluminum in combination with water created resonance and absorbed electromagnetic energy with the frequency 5.69 Hz; that was the natural frequency of aluminum contained in water. This was verified on water contained in an aluminum can, a piece of pure aluminum positioned in a glass of water, Coca Cola, Pepsi Cola and beer previously contained in aluminum cans, tap water polluted by aluminum and many different types of wine (containing aluminum). Thus, aluminium molecule structures (compounds) in contact with water as well as aluminum ions dissolved in water created resonance at 5.69 Hz.

The natural frequency 5.69 Hz coincided with electromagnetic energy (current), present in the air and in water, with the period 24/(15·2 ¹⁵ ) hour (5.69 Hz), whereby the water absorbed this current, present in the air and in water. The current amplitude was proportional to the solution volume or the surface area of aluminum in contact with water. Thus, the natural period of aluminum is 24/(15-2 ¹⁵ ) hour.

The absorbed current was also measured in vivo, and which displayed that the brain primarily absorbed the current. This indicates a concentration of aluminum to the brain.

Experiments performed on one liter of water containing dissolved aluminum displayed that aluminum atoms (or metal or compound) were positioned as sediment at the bottom of the container within 1 minute, when the water was prevented from absorbing electromagnetic energy with the period 24/(15·2 ¹⁵ ) hour during one minute, using the apparatus according to claim 55. The above process was also achieved by preventing the water from absorbing electromagnetic energy with the period 24/(15·2 ¹⁵ ) hour and at the same time the water was exposed to electromagnetic energy with period 0.1-1 s and deviating from the period 24/(15·2 ¹⁵ ) hour, whereby the water created resonance. The above results were also achieved by exposing the water to high amplitude electromagnetic energy with the period 24/(15·2 ¹⁵ ) hour.

The above experiments were also performed on bottles containing wine, displaying that it was possible to separate aluminum from wine and which improved its taste. Separating aluminum from Coca Cola displayed a change in taste, and which may be explained by the high content of aluminum in Coca Cola sold in aluminum cans.

The above experiments were repeated using extinction of all energy, i.e. the water was prevented from creating any type of low frequency resonance. In that case the aluminum was not influenced and remained dissolved in the water. Consequently, the aluminum-water solution was only influenced when prevented from creating resonance at the period 24/(15·2 ¹⁵ ) hour and at the same time allowed or enforced to create resonance at a deviating period in the range 0.1-1 s.

Experiments in vivo displayed that aluminum was removed from the brain and the rest of the body, transported by the lymph to the urine bladder, and subsequently removed with the urine, when the human was prevented from absorbing electromagnetic energy with the period 24/(15·2 ¹⁵ ) hour during one minute and repeated every 20 minutes, using the apparatus according to claim 55. This process took approximately 10 hours. This process was repeated after one week, whereby a large part of the remaining aluminum was released or separated from the human body. It was possible to monitor the process by measuring the current absorbed by the brain prior to the experiment and then as function of the time. Aluminum contained in the urine was also measured. The results are displayed in Figure 6. Aluminum cans containing beer and Coca Cola were prevented from absorbing electromagnetic energy with the period 24/(15·2 ¹⁵ ) hour during one minute, using the apparatus according to claim 55. This resulted in that the aluminum surface was influenced so that beer and Coca Cola ceased to dissolve aluminum from the surface. Thus, it is possible to treat aluminum in order to prevent aluminum (e.g. ions) from dissolving from its surface.

Silver (Ag ⁺ )

Pure silver was positioned in water and in moist atmosphere and then measured. Silver was polished and the residue was dissolved in water and measured. Silver contained in humans was measured. Silver displayed the natural periods 24/(5·2 ¹⁶ ) hour (3.79 Hz), 24/(31·2 ¹⁴ ) hour (5.88 Hz) and

24/(139·2 ^η ) hour (3.30 Hz). It was possible to remove silver from water in vitro and in vivo.

Experiments were also performed on silver contained in pathogens in vivo, as well as silver in bacteria/pathogens in chicken and silver in lactobacillus bacteria.

Arsenic (As ³ )

Arsenic contained in stuffed birds was measured. Arsenic dissolved in water was measured. Arsenic contained in humans was measured. Arsenic displayed the natural periods 24/(9·2 ¹⁶ ) hour (6.83 Hz), 24/(15·2 ¹⁵ ) hour (5.69 Hz) and 24/(99·2 ¹² ) hour (4.69 Hz). It was possible to remove arsenic from water in vitro and in vivo. Experiments were performed on arsenic contained in pathogens in vivo, as well as arsenic in bacteria/pathogens in chicken and arsenic in bacteria in hen eggs and in lactobacillus bacteria.

Gold (Au)

Gold (Au) in combination with water created resonance and absorbed electromagnetic energy with the frequency 6.54 Hz; that was the natural frequency of gold contained in water. This was verified on a piece of pure gold (18 and 24 K) positioned in a glass of water, a piece of gold in air (containing moisture) and on water from a deep drilled well where the water contained traces of gold as well as lake water containing gold. Thus, gold molecule structures in contact with water as well as gold dissolved in water created resonance at 6.54 Hz.

The natural frequency 6.54 Hz coincided with current, present in the air and in water, with the period 24/(69·2 ¹³ ) hour (6.54 Hz), whereby the water absorbed current, present in the air and in water. The current amplitude was proportional to the solution volume or the surface area of gold in contact with water. Thus, the natural period of gold is 24/(69·2 ¹³ ) hour.

Experiments performed on one liter water containing dissolved gold displayed that the gold was positioned as sediment at the bottom of the container within 1 minute, when the water was prevented from absorbing electromagnetic energy with the period 24/(69·2 ¹³ ) hour, using the apparatus according to claim 57. The above process was also achieved by preventing the water from absorbing electromagnetic energy with the period 24/(69·2 ¹³ ) hour and at the same time the water was exposed to electromagnetic energy with period 0.1-1 s, whereby the water created resonance. Exposing the water to high amplitude electromagnetic energy with the period 24/(69·2 ¹³ ) hour displayed similar result.

The above procedure was also performed on water from a deep drilled well (80 m deep) outside Gnesta, Sweden as well as on lake water (Sjundasjon). Water from the well was pumped into a container (see Figure 5) and allowed to flow out from the top of the container. Electromagnetic energy with the period 24/(69-2 ) hour was prevented from propagating to the container, using the apparatus according to claim 57. After 24 hours the bottom sediment (precipitate containing gold) was filtered. Drying the filter displayed small flakes, assumingly containing gold (diameter 0.1 - 0.5 mm).

Calcium (Ca ^z+ )

Calcium has the natural periods 24/(7-2 ¹⁶ ) hour, 24/(9-2 ¹⁶ ) hour and 24/(35-2 ¹⁴ ) hour.

Electromagnetic energy with the periods 24/(7-2 ¹⁶ ) hour and 24/(9-2 ¹⁶ ) hour creates electromagnetic interference with electromagnetic energy with one of the natural periods of phosphates ((e.g. P0 ₄ , Ca(H ₂ P0 ₄ )), 24/(73-2 ¹³ ) hour (see section Phosphates below). In the following experiment a bottle of water with dissolved calcium was positioned close to a bottle of water containing dissolved phosphate (P0 ₄ ). This resulted in that the phosphate was prevented from absorbing electromagnetic energy with one of its natural periods and the phosphate was changed into a phosphorus compound (see section Phosphorus) with the natural periods 24/(9-2 ¹⁶ ) hour and 24/(33-2 ¹⁴ ) hour and 0 ₂ . Electromagnetic energy with the periods 24/(7-2 ¹⁶ ) hour, 24/(9-2 ¹⁶ ) hour create electromagnetic interference with electromagnetic energy with the period 24/(17-2 ¹⁴ ) hour, i.e. one of the natural periods of sulfites (e.g. H ₂ S, S0 ₂ ) and sulfate (S0 ₄ ). In the following experiment a bottle of water with dissolved calcium was positioned close to a bottle of water containing dissolved sulfite (S0 ₂ ). This resulted in that the sulfite was prevented from absorbing electromagnetic energy with one of its natural periods and the sulfite was changed into sulfur (S) and 0 ₂ . Please observe that the calcium was not in physical contact with P or S0 ₂ , thus the caused reaction was purely electromagnetic. In Sweden calcium is used in farming in order to reduce leakage of phosphates into rivers, lakes and the Baltic Sea. Calcium is also used in order to reduce sulfites, sulfate and acidity in lakes. However, large-scale use of calcium has a number of negative effects. The present invention displays that use of calcium can be substituted with the methods described in the section Phosphates and the section Sulfites and Sulfate. Sodium (Na ⁺ ) dissolved in water has the natural periods 24/(3-2 ¹⁷ ) hour, 24/(43-2 ¹⁴ ) hour and 24/(129-2 ¹² ) hour and this energy creates electromagnetic interference with electromagnetic energy with the natural periods of calcium, 24/(7-2 ¹⁶ ) hour (5.31 Hz), 24/(9-2 ¹⁶ ) hour (6.83 Hz) and 24/(35-2 ¹⁴ ) hour 6.64 Hz). Dissolved Na prevents calcium from absorbing

electromagnetic energy with its natural periods and this changes the calcium solvation shells somewhat whereby they create resonance at 5.35 Hz, 6.86 Hz and 6.67 Hz and which does not coincide with the period 24/(m-2 ⁿ ) hour (i.e. similar to the shift in natural frequency which occurs in NaCI). The human skeleton does not absorb electromagnetic energy with the natural periods of calcium due to the presence of dissolved Na and its electromagnetic influence on Ca.

Cadmium (Cd)

Cadmium (Cd) in combination with water created resonance and absorbed electromagnetic energy with the frequency 3.89 Hz and 3.98 Hz, i.e. those were the natural frequencies of cadmium contained in water. This was verified on a piece of PVC (containing cadmium) positioned in a glass of water (H ₂ 0 + 150 mM NaCI), a piece of pure cadmium positioned in a glass of water, the content of a battery containing cadmium dissolved in water, PVC (containing cadmium) positioned in alcohol (35 %) whereby cadmium dissolved in the alcohol (i.e. water), several types of non-rechargeable batteries (> 5 years old), several different types of rechargeable Ni-Cd batteries. Thus, cadmium molecule structures in contact with water as well as cadmium dissolved in water created resonance at 3.89 Hz and 3.98 Hz. The natural frequency 3.89 Hz coincided with current, present in the air and in water, with the period 24/(41·2 ¹³ ) hour (3.89 Hz) whereby the water absorbed this current, present in the air. The natural frequency 3.98 Hz coincided with current, present in the air, with the period 24/(21·2 ¹⁴ ) hour (3.98 Hz), whereby the water absorbed current, present in the air and in water. The current amplitude was proportional to the solution volume. Thus, the natural periods of cadmium are 24/(21·2 ¹⁴ ) hour and 24/(41-2 ¹³ ) hour.

The absorbed current was also measured in vivo, and which displayed that the brain and also the kidneys absorbed current with the period 24/(21·2 ¹⁴ ) hour and 24/(41·2 ¹³ ) hour. This was observed only on smokers, non-smokers displayed cadmium levels below measurement accuracy.

Experiments on water containing cadmium were performed as follows. PVC was positioned in alcohol (35 % C ₂ H ₅ OH, 65 % H ₂ 0 + ions) during 5 hours. This created dissolved cadmium. The PVC was subsequently removed. The solution was measured, displaying that the dissolved cadmium was evenly distributed (dissolved in the solution). This alcohol water solution containing dissolved cadmium displayed that cadmium atoms (or compound) were positioned as sediment at the bottom of the container within 1 minute, when the solution was prevented from absorbing electromagnetic energy simultaneously with the period 24/(21·2 ¹⁴ ) hour and 24/(41·2 ¹³ ) hour, using the apparatus according to claim 59. The experiment was repeated on cadmium contained in a battery and dissolved in water, displaying similar result. The above process was also achieved by preventing the water or solution from absorbing electromagnetic energy simultaneously with the period 24/(21·2 ¹⁴ ) hour and 24/(41·2 ¹³ ) hour and at the same time the water or solution was exposed to

electromagnetic energy with period 0.1-1 s, whereby it created resonance. Exposing the water or solution to high amplitude electromagnetic energy with the period 24/(21·2 ¹⁴ ) hour and/or

24/(41·2 ¹³ ) hour displayed similar result.

Cadmium dissolved in water was exposed to extinction of all electromagnetic energy present in the air and in water, i.e. the water was prevented from creating any type of low frequency resonance. In that case the cadmium was not influenced and remained dissolved in the water. Consequently, cadmium dissolved in water was only influenced when prevented from creating resonance simultaneously at the period 24/(21·2 ¹⁴ ) hour and 24/(41-2 ¹³ ) hour and at the same time allowed or enforced to create resonance at a deviating period.

Experiments in vivo displayed that cadmium was removed from the brain and the rest of the body, transported by the lymph to the urine, and subsequently removed with the urine, when the human was prevented from absorbing electromagnetic energy simultaneously with the period 24/(21·2 ¹⁴ ) hour and 24/(41·2 ¹³ ) hour during one minute and repeated every 20 minutes, using apparatus according to claim 59. This process took approximately 6 hours. It was possible to monitor the process by measuring the current absorbed by the brain prior to the experiment and then as function of the time, see Figure 7.

Cobalt (Co ³⁺ )

Cobalt contained in cobalt blue color was dissolved in water and measured. Water contained in cups containing cobalt paint was measured. Hot coffee positioned in cups containing cobalt paint was subsequently transferred to a glass container and the dissolved cobalt was measured. Cobalt contained in humans was measured. Cobalt displayed the natural periods 24/(17·2 ¹⁴ ) hour (3.22 Hz) and 24/(23·2 ¹⁵ ) hour (8.72 Hz). It was possible to remove cobalt from water in vitro and in vivo. Chloride and sodium, CI ^" , Na ⁺ and NaCI

Chloride (CI ) dissolved in water created resonance and absorbed electromagnetic energy with the natural periods 24/(73-2 ¹³ ) hour (6.92Hz) and 24/(89·2 ¹² ) hour (4.22 Hz). Sodium (Na ⁺ ) dissolved in water created resonance and absorbed electromagnetic energy with the natural periods 24/(3·2 ¹⁷ ) hour (4.55 Hz), 24/(43·2 ¹⁴ ) hour (8.15 Hz) and 24/(129·2 ¹² ) hour (6.12 Hz). Crystalline salt (NaCI) and NaCI dissolved in water created resonance and absorbed electromagnetic energy with the natural periods 24/(167·2 ¹² ) hour (7.92Hz) and 24/(173-2 ¹² ) hour (8.20 Hz).

In the following experiments NaCI was dissolved in water, resulting in dissolved Na and dissolved CI. The solution containing dissolved Na (ion) and dissolved CI (ion) created resonance at the natural periods of Na; 24/(3·2 ¹⁷ ) hour, 24/(43·2 ¹⁴ ) hour and 24/(129·2 ¹² ) hour, and at the natural periods of CI; 24/(73·2 ¹³ ) hour and 24/(89·2 ¹² ) hour

1) The solution containing dissolved Na and dissolved CI was prevented from absorbing

electromagnetic energy with the natural periods of CI, 24/(73-2 ¹³ ) hour and 24/(89-2 ¹² ) hour, during 1 minute, using the apparatus according to claim 60. This resulted in that CI ceased to dissolve and it created a NaCI compound (whereby Na also ceased to dissolve). The solution created resonance and absorbed electromagnetic energy with (only) the natural periods of NaCI; 24/(167·2 ¹² ) hour and 24/(173·2 ¹² ) hour. Then this solution very slowly (after many hours) changed into dissolved Na and dissolved CI. The experiment was repeated; however, this time one drop of water containing dissolved Na and dissolved CI was added to the solution. This resulted in that all NaCI changed quickly (within a minute) into dissolved Na and dissolved CI.

2) The solution containing dissolved Na and dissolved CI was prevented from absorbing

electromagnetic energy with the natural periods of Na, 24/(3·2 ¹⁷ ) hour, 24/(43·2 ¹⁴ ) hour and 24/(129·2 ¹² ) hour, during 1 minute, using the apparatus according to claim 71. This resulted in that Na ceased to dissolve and it created a NaCI compound (whereby also CI ceased to dissolve). The solution created resonance and absorbed electromagnetic energy with (only) the natural periods of NaCI; 24/(167·2 ¹² ) hour and 24/(173·2 ¹² ) hour. Then this solution very slowly (after many hours) changed into dissolved Na and dissolved CI. The experiment was repeated; however, this time one drop of water containing dissolved Na and dissolved CI was added to the solution. This resulted in that all NaCI changed quickly (within a minute) into dissolved Na and dissolved CI.

3) The solution 1) as well as the solution 2) consisting of dissolved NaCI was prevented from absorbing electromagnetic energy with the natural periods of NaCI, 24/(167·2 ¹² ) hour and 24/(173·2 ¹² ) hour, during 1 minute, using the apparatus according to claim 89. This resulted in that the solution permanently ceased to create resonance and ceased to absorb electromagnetic energy with the natural periods of NaCI, Na and CI. The NaCI compound created a liquid precipitate at the bottom of the solution. This precipitate created resonance at 7.94 Hz (compared to previously 7.92 Hz) and 8.22 Hz compared to previously 8.20 Hz). It is proposed that the solvation shell molecule structure had changed somewhat whereby it did not create resonance at the period 24/(m-2") hour. It was possible to separate this precipitate using decanting and the supernate displayed little content of NaCI. Consequently, it is possible to influence Na, CI and NaCI and to reduce (or remove completely) the salinity of salt water. It was also possible to change this precipitate into soluble NaCI by adding a few grains of salt. The dissolved NaCI created resonance at the period 24/(167·2 ¹² ) hour and 24/(173·2 ¹² ) hour. It was also possible to change the precipitate into dissolved Na and dissolved CI by enforcing resonance (in the 2-10 Hz range) in the water, e.g. at 3.0 Hz.

4) Crystalline salt (NaCI) was prevented from absorbing electromagnetic energy at the natural periods of NaCI, 24/(167·2 ¹² ) hour and 24/(173·2 ¹² ) hour, during 1 minute, using the apparatus according to claim 89. This resulted in a NaCI compound that ceased permanently to create resonance at the periods 24/(167·2 ¹² ) hour and 24/(173·2 ¹² ) hour. The new compound created resonance at 7.94 Hz and 8.22 Hz. This NaCI compound dissolved poorly in water and the NaCI compound created a precipitate and it was possible to remove the precipitate using decanting. The supernate displayed little content of NaCI.

The experiments 1), 2), 3) and 4) illustrate the present invention. Experiment 1) and 2) show that when the solvation shells are destroyed the free ion causes a reaction. Experiment 1) displays that the free CI ion reacts with the dissolved Na and which creates the (dissolved) compound NaCI.

Experiment 2) displays that the free Na ion reacts with the dissolved CI and which creates the (dissolved) compound NaCI. This supports the theory of the present invention.

The solutions contain no dissolved Na and no dissolved CI, when prevented from absorbing electromagnetic energy with the natural periods of CI and/or Na, during one minute. Hence, the absorbed energy at the natural periods of Na and CI is zero. Therefore the solvation shells of the dissolved NaCI are undisturbed, resulting in that the NaCI molecule remains dissolved during long time (hours). It absorbs electromagnetic energy at its natural periods and which maintains the solvation shells. Adding one drop water containing dissolved Na and dissolved CI changes the electromagnetic energy in the solution, resulting in that this energy destroys the NaCI solvation shells, whereby the compound is changed into dissolved Na and dissolved CI. Enforcing resonance by injecting energy (e.g. at 3.0 Hz) also results in destroyed solvation shells and change into dissolved Na and dissolved CI. This experiment illustrates that solvation of NaCI in water is not primarily a static process but a dynamic process created by low frequency electromagnetic energy.

Experiment 3) and 4) display that the natural frequencies of the NaCI molecule changed from 7.92 Hz and 8.20 Hz into 7.94 Hz and 8.22 Hz, when prevented from absorbing electromagnetic energy with the periods 24/(167-2 ¹² ) hour (7.92 Hz) and 24/(173·2 ¹² ) hour (8.20 Hz). In absence of

electromagnetic energy the solvation shells are static and their natural frequencies are 7.94 Hz and 8.22 Hz. These natural frequencies did not coincide with the period 24/(m-2 ⁿ ) hour, hence the NaCI did not absorb electromagnetic energy present in the air and in water (whereby the solvation shells were static). Resonance at the periods 24/(167·2 ¹² ) hour (7.92 Hz) and 24/(173·2 ¹² ) hour (8.20 Hz) changed the molecule structure in the solvation shells somewhat (i.e. the water molecule structure is adaptive). Thus, the exact structure of NaCI and its solvation shells depend on its static respectively dynamic electromagnetic state, i.e. the static respectively dynamic electromagnetic process in the solvation shells. These two experiments prove that the NaCI molecule and its solvation shells have one (static) structure in absence of electromagnetic energy and a slightly different (dynamic) structure in presence of electromagnetic energy with its natural periods. Consequently, the present invention does include change of a molecule into the same type of molecule; however, with (slight) change in characteristics, i.e. the solvation shells. The present invention does also include change of an ion into the same type of ion; however, with (slight) change in the solvation shells. It was possible to repeat the experiments 1), 2) and 3) any number of times and thereby changing the same solution from dissolved Na and dissolved CI into dissolved NaCI and then back to dissolved Na and dissolved CI etc. as well as NaCI with static or dynamic solvation shells.

Preventing sodium (Na) dissolved in water from absorbing electromagnetic energy with its natural periods can also be achieved using electromagnetic interference. For instance electromagnetic energy with the period 24/(67-2 ¹³ ) hour extinct electromagnetic energy with the natural periods of Na, i.e. the period 24/(3·2 ¹⁷ ) hour, 24/(43·2 ¹⁴ ) hour and 24/(129·2 ¹² ) hour. The natural period of potassium (K) is 24/(67·2 ¹³ ) hour. Hence, potassium extinct the natural periods of sodium and which results in that sodium ceases to dissolve in water and dissolved Na and CI is changed into dissolved NaCI. This was verified in the following experiments. In the first experiment a bottle containing dissolved Na and dissolved CI was positioned close to a bottle containing water with dissolved K. The dissolved Na and CI were changed into dissolved NaCI within a minute. The bottles were not in physical contact; hence, the process was purely electromagnetic. In the second experiment potassium was added to a water solution containing dissolved Na and CI. This resulted in that Na and CI changed into NaCI.

The amount of dissolved Na and CI respectively amount of dissolved NaCI is balanced in the human organism. This balance is carefully regulated so that a healthy organism always absorbs the same energy amplitude at the period 24/(3·2 ¹⁷ ) hour. This balance is probably a prerequisite for proper function of many biological processes. In the following experiment potassium was positioned close to (but not in contact with) a human. This resulted in rapid drop of absorbed electromagnetic energy at the natural periods of Na and CI and rapid increase in absorbed electromagnetic energy at the natural periods of NaCI. Removing the potassium resulted in a slow (within a minute) return to the original balance. It is proposed that one important feature of potassium and the potassium ion pump is to regulate the concentration of dissolved Na and dissolved CI in the human organism. The present invention describes this mechanism in order to illustrate the importance of chemical elements and their dynamic electromagnetic processes in organisms, and the consequence of disturbing these processes.

Copper (Cu)

Copper (Cu) in combination with water created resonance and absorbed electromagnetic energy with the frequency 6.92Hz and 7.87Hz, i.e. those were the natural frequencies of the copper contained in water. This was verified on warm tap water from a house with copper pipes, a piece of pure copper positioned in a glass of hot water and coffee from coffee brewers containing copper parts. Thus, copper dissolved in water created resonance at 7.87Hz and 6.92Hz.

Copper in absence of water did not absorb low frequency electromagnetic energy.

The natural frequency 6.92Hz coincided with current, present in the air, with the period 24/(73-2 ¹³ ) hour (6.92Hz), whereby the water absorbed current, present in the air and in water. The natural frequency 7.87Hz coincided with current, present in the air, with the period 24/(83·2 ¹³ ) hour (7.87Hz) whereby the water absorbed current, present in the air and in water. The current amplitude was proportional to the solution volume. Thus, the natural periods of copper are 24/(73·2 ¹³ ) hour and 24/(83·2 ¹³ ) hour. The absorbed current was also measured in vivo, and which displayed that the brain and the rest of the body absorbed current with period 24/(73·2 ¹³ ) hour and 24/(83-2 ¹³ ) hour. This current indicated an even distribution of copper.

Experiments performed on one liter of water containing dissolved copper displayed that copper atoms (or metal or compound) were positioned as sediment at the bottom of the container within 1 minute, when the water was prevented from absorbing electromagnetic energy simultaneously with the period 24/(73·2 ¹³ ) hour and 24/(83·2 ¹³ ) hour, using the apparatus according to claim 63. The above process was also achieved by preventing the water from absorbing electromagnetic energy simultaneously with the period 24/(73·2 ¹³ ) hour and 24/(83·2 ¹³ ) hour and at the same time the water was exposed to electromagnetic energy with period 0.1-1 s, whereby the water created resonance. Exposing the water to high amplitude electromagnetic energy with the period 24/(73·2 ¹³ ) hour and/or 24/(83·2 ¹³ ) hour displayed similar result.

The above procedure was also performed on coffee containing copper, displaying that it was possible to separate the copper from the coffee and at the same time improving the experienced taste.

The above processes were repeated using extinction of all energy, i.e. the water was prevented from creating any type of low frequency resonance. In that case the copper was not influenced and remained dissolved in the water. Consequently, water, containing dissolved copper, was only influenced when prevented from creating resonance simultaneously at the period 24/(73·2 ¹³ ) hour and 24/(83·2 ¹³ ) hour and at the same time allowed or enforced to create resonance at a deviating period.

Experiments in vivo displayed that copper was removed from the brain and the rest of the body, transported by the lymph to the urine, and subsequently removed with the urine, when the human was prevented from absorbing electromagnetic energy simultaneously with the period 24/(73·2 ¹³ ) hour and 24/(83-2 ¹³ ) hour during one minute and repeated every 20 minutes, using the apparatus according to claim 63. This process took approximately 8 hours. This process was interrupted before all copper was removed since copper in small amount is an important trace metal used in some biological processes (normal density is approximately 2 mg/Kg of body mass). It was possible to monitor the process by measuring the current with period 24/(83·2 ¹³ ) hour absorbed by the brain prior to the experiment and then as function of the time, see Figure 8. The experiment was performed on a person exhibiting very large amount of copper.

Fluoride (F )

Fluoride contained in different forms of toothpaste (e.g. Colgate, Pepsodent, Vademecum and NaF contained in water (e.g. Flux/Actavis, Sensodyne/GlaxoSmithKline). Fluoride contained in humans was measured. Fluoride displayed the natural periods 24/(3·2 ¹⁷ ) hour (4.55 Hz) and 24/(5·2 ¹⁷ ) hour (7.59 Hz). It was possible to remove fluoride from water in vitro and in vivo. Mercury (Hg ²⁺ ) contained in batteries was measured. The content of batteries containing mercury was dissolved in water and measured. Pure mercury in water was measured. Pure mercury in moist atmosphere was measured. Mercury contained in dental amalgams was measured. Mercury contained in a thermometer was measured. Mercury contained in humans was measured. Mercury displayed the natural periods 24/(1·2 ¹⁸ ) hour (3.03 Hz) and 24/(9·2 ¹⁵ ) hour (3.41 Hz), 24/(45·2 ¹⁴ ) hour (8.53 Hz) and 24/(71·2 ¹³ ) hour (6.73 Hz). It was possible to remove mercury from water in vitro and in vivo.

Oxygen (0 ₂ ) Oxygen (0 ₂ ) dissolved in water has the natural periods 24/(3·2 ¹⁷ ) hour (4.55 Hz) and 24/(47·2 ¹³ ) hour (4.46 Hz). Oxygen ceased to dissolve whereby it evaporated when the oxygen dissolved in water was prevented from absorbing electromagnetic energy with the period 24/(3·2 ¹⁷ ) hour and/or 24/(47·2 ¹³ ) hour.

Preventing oxygen and water from absorbing electromagnetic energy with one or both natural periods can also be achieved using electromagnetic interference. For instance electromagnetic energy with the period 24/(63·2 ¹³ ) hour extinct electromagnetic energy with the period 24/(3·2 ¹⁷ ) hour. Electromagnetic energy with the period 24/(17 -2 ¹⁴ ) hour extinct electromagnetic energy with the period 24/(47·2 ¹³ ) hour. Hence, sulfites and sulfate, which have the natural periods 24/(17·2 ¹⁴ ) hour and 24/(63-2 ¹³ ) hour, extinct the natural periods of oxygen and this results in that oxygen (0 ₂ ) ceased to dissolve in water. This explains why lakes containing high content of sulfites and sulfate (acid lakes) contain little or no oxygen. This was verified in the following experiments. In the first experiment a bottle containing oxygen (0 ₂ ) dissolved in water was positioned close to a bottle containing water from an acid lake (Stora Alsjon, Sodermanland, Sweden). The dissolved oxygen evaporated within a minute. The two bottles were not in physical contact; hence, the process was purely electromagnetic. In the second experiment a bottle containing oxygen (0 ₂ ) dissolved in water was positioned close to a bottle of wine containing sulfites. The dissolved oxygen evaporated within a minute. The bottles were not in physical contact; hence, the process was purely electromagnetic. This explains one of the reasons why bacteria do not grow in wine containing sulfites; there is no oxygen present. It also explains one aspect why acid lakes are "dead".

The above experiments were repeated with using aluminum (Al), arsenic (As), carbon (C), cadmium (Cd), chromium (Cr), mercury (Hg), lead (Pb), vanadium (V), wolfram (W) and Zinc (Zn). These chemical elements displayed similar results, i.e. these chemical elements created interference with one or both natural periods of 0 ₂ whereby 0 ₂ ceased to dissolve. This may explain one aspect of the toxicity of many of these chemical elements. They disturb a vital biological process, i.e. the presence of 0 ₂ . The disturbance is caused by a dynamic electromagnetic process and not by a chemical processes.

Oxygen is included in the present invention because of its large impact on many organisms and because of its relation to many molecular substances dissolved in water, and which is explained in the section Achieved results; Summary.

Phosphorus (P)

Phosphorus is highly reactive and can only exist as compounds. Many phosphorus compounds dissolved in water (except phosphates) created resonance and absorbed electromagnetic energy at the period 24/(9·2 ¹⁶ ) hour (6.83 Hz) and 24/(33·2 ¹⁴ ) hour (6.26Hz). This was verified on water solutions containing dissolved match striking surface, on the PI phosphorus compound found in an oscilloscope tube, on red phosphorus in a color TV CRT, on P4 phosphorus contained in a black and white CRT and in phosphoric acid (H ₃ P0 ) in Coca Cola and Pepsi Cola. It was also verified on phosphorus found in every organism that was investigated, including humans, mammals, insects, plants and microbes. All types of beverages, tap water, lake water, Baltic seawater, water in wells and drilled wells contained phosphorus and which created resonance at the period 24/(9·2 ¹⁶ ) hour and 24/(33-2 ¹⁴ ) hour.

Phosphorus is a key chemical element in all forms of life. The following experiment explains one aspect. Experiments were performed on water containing dissolved phosphorus and a large number of dissolved chemical elements (e.g. Al, As, Cd, Cr, Pb, Sn, Zn, V and W). The water was prevented from absorbing electromagnetic energy with the period 24/(9·2 ¹⁶ ) hour and 24/(33·2 ¹⁴ ) hour during 1 minute, using the apparatus according to claim 73. This changed the dissolved phosphorus compounds into insoluble phosphorus compound(s) (which created sediment). Then something interesting occurred. Gradually every dissolved chemical element (e.g. Al, As, Cd, Cr, Pb, Sn, Zn, V and W) ceased to dissolve and where converted into insoluble atoms and/or compounds. These atoms/compounds formed sediment. Decanting removed the sediment. The experiment was repeated on tap water, lake water, water from a drilled well and seawater, and always displaying the same result. The experiment was repeated on bacteria, whereby dissolved chemical elements in the bacteria ceased to create resonance and ceased to absorb electromagnetic energy. This destroyed the bacteria, i.e. the bacteria died within a week.

The speed of the process depended on the chemical element, wherein Pb dissolved in water ceased to dissolve in approximately 15 minutes, while As ceased to dissolve in 1 hour and Cr in 2 hours.

Dissolved chemical elements are a prerequisite for many organisms. Chemical elements can cease to dissolve without a reactive agent and where phosphorus plays a key role. Therefore it is possible to kill microbes (e.g. in sewage and in food) by simply changing soluble phosphorus compounds into insoluble phosphorus compounds. It is possible to remove dissolved chemical elements from water solutions (e.g. sewage, oil) by simply converting soluble phosphorus into insoluble phosphorus.

Lead (Pb)

Lead (Pb) in combination with water created resonance and absorbed electromagnetic energy with the frequency 2.99 Hz and 3.79 Hz, i.e. those were the natural frequencies of lead contained in water. This was verified on water contained in a crystal (lead) glass, a piece of pure lead positioned in a glass of water, a piece of solder (tin-lead alloy) positioned in a glass of water, a piece of brass (alloy containing lead ¹ ') positioned in a glass of water, tap water polluted by brass, water polluted by paint containing lead, many different types of wine (containing lead) and olives (containing lead) and olive oil. Thus, lead molecule structures in contact with water as well as lead dissolved in water created resonance at 2.99 Hz and 3.79 Hz.

The natural frequency 2.99 Hz coincided with current, present in the air, with the period 24/(63·2 ¹² ) hour (2.99 Hz) whereby the water absorbed current, present in the air. The natural frequency 3.79 Hz coincided with current, present in the air, with the period 24/(5·2 ¹⁶ ) hour (3.79 Hz), whereby the water absorbed current, present in the air. The current amplitude was proportional to the solution volume. Thus, the natural periods of lead are 24/(5·2 ¹⁶ ) hour and 24/(63·2 ¹² ) hour.

Experiments performed on one liter water containing dissolved lead displayed that the lead atoms (or metal or compound) were positioned as sediment at the bottom of the container within 1 minute, when the water was prevented from absorbing electromagnetic energy simultaneously with the period 24/(5·2 ¹⁶ ) hour and 24/(63·2 ¹² ) hour, using the apparatus according to claim 74. The above process was also achieved by preventing the water from absorbing electromagnetic energy simultaneously with the period 24/(5·2 ¹⁶ ) hour and 24/(63·2 ¹² ) hour and at the same time the water was exposed to electromagnetic energy with period 0.1-1 s, whereby the water created resonance. The above process was also achieved by exposing the water to high amplitude electromagnetic energy with the period 24/(5·2 ¹⁶ ) hour and/or 24/(63·2 ¹² ) hour. The above process was also performed on wine, displaying that it was possible to separate lead from wine and this changed the taste of wine.

The above processes were repeated using extinction of all energy, i.e. the water was prevented from creating any type of low frequency resonance. In that case the lead was not influenced and remained dissolved in the water. Consequently, water, containing dissolved lead, was only influenced when prevented from creating resonance simultaneously at the period 24/(5-2 ¹⁶ ) hour and 24/(63·2 ¹² ) hour and at the same time allowed or enforced to create resonance at a deviating period in the range 0.1- l s.

Experiments in vivo displayed that lead was removed from the brain and the rest of the body, transported by the lymph to the urine, and subsequently removed with the urine, when the human was prevented from absorbing electromagnetic energy with the period 24/(5·2 ¹⁶ ) hour and

24/(63·2 ¹² ) hour during one minute and repeated every 20 minutes, using the apparatus according to claim 74. This process took approximately 12 hours. This process was repeated after one week, whereby a large part of the remaining lead was released or removed from the human body. It was possible to monitor the process by measuring the current absorbed by the brain prior to the experiment and then as function of the time, see Figure 9. The brain and the spine absorbed the current, indicating concentration of lead to the brain and the spine.

¹¹ Brass sometimes contains some lead (» 2- 4 %) to ease/improve machining of brass. Selenium (Se)

Selenium has the natural periods 24/(5·2 ¹⁶ ) hour, 24/(9·2 ¹⁶ ) hour and 24/(29·2 ¹⁴ ) hour.

Electromagnetic energy with the periods 24/(5-2 ¹⁶ ) hour, 24/(9·2 ¹⁶ ) hour and 24/(29·2 ¹⁴ ) hour create electromagnetic interference with electromagnetic energy with the natural period of potassium (K), 24/(67·2 ¹³ ) hour. In the following experiment a bottle of water with dissolved selenium was positioned close to a bottle of water containing dissolved potassium. This resulted in that the potassium ceased to absorb electromagnetic energy at its natural periods, ceased to dissolve and it created sediment.

Electromagnetic energy with the periods 24/(5·2 ¹⁶ ) hour, 24/(9·2 ¹⁶ ) hour and 24/(29·2 ¹⁴ ) hour create electromagnetic interference with electromagnetic energy with the natural period of vanadium (V), 24/(9·2 ¹⁵ ) hour, 24/(33-2 ¹⁴ ) hour and 24/(43·2 ¹³ ) hour. In the following experiment a bottle of water with dissolved selenium was positioned close to a bottle of water containing dissolved vanadium. This resulted in that the vanadium ceased to absorb electromagnetic energy at its natural periods, ceased to dissolve and it created sediment.

Electromagnetic energy with the periods 24/(5·2 ¹⁶ ) hour, 24/(9-2 ¹⁶ ) hour and 24/(29·2 ¹⁴ ) hour create electromagnetic interference with electromagnetic energy with the natural period of tungsten (W), 24/(7·2 ¹⁵ ) hour and 24/(73·2 ¹³ ) hour. In the following experiment a bottle of water with dissolved selenium was positioned close to a bottle of water containing dissolved tungsten. This resulted in that the tungsten ceased to absorb electromagnetic energy at its natural periods, ceased to dissolve and it created sediment.

Tin (Sn)

Tin (Sn) in combination with water always created resonance and absorbed electromagnetic energy with the frequency 3.03 Hz, 6.45 Hz and 6.83 Hz, i.e. those were the natural frequencies of tin contained in water. This was verified on water contained in a tin can, on water contained in a tin plated food can, a piece of pure tin positioned in a glass of water, a piece of pure tin in moist atmosphere, solder (tin-lead alloy) positioned in a glass of water, acidic water previously contained in a tin plated food can, food and beverages contained in tin plated food cans. Thus, tin molecule structures in contact with water as well as tin dissolved in water created resonance at 3.03 Hz, 6.45 Hz and 6.83 Hz.

The natural frequency 3.03 Hz coincided with current, present in the air, with the period 24/(1·2 ¹⁸ ) hour (3.03 Hz) whereby the water absorbed current, present in the air and in water. The natural frequency 6.45 Hz coincided with current, present in the air, with the period 24/(17·2 ¹⁵ ) hour (6.45 Hz) whereby the water absorbed current, present in the air and in water. The natural frequency 6.83 Hz coincided with current, present in the air, with the period 24/(9·2 ¹⁶ ) hour (6.83 Hz), whereby the water absorbed current, present in the air and in water. The current amplitude was proportional to the solution volume and the surface area of the tin object. Thus, the natural periods of tin are 24/(1·2 ¹⁸ ) hour and 24/(9·2 ¹⁶ ) hour and 24/(17·2 ¹⁵ ) hour.

The absorbed current was also measured in vivo, and which displayed that the current was evenly distributed to the whole body, including the brain.

Experiments performed on one liter water containing dissolved tin displayed that tin atoms (or metal or compound) were positioned as sediment at the bottom of the container within 1 minute, when the water was prevented from absorbing electromagnetic energy simultaneously with the period 24/(1·2 ¹⁸ ) hour and 24/(9·2 ¹⁶ ) hour and 24/(17-2 ¹⁵ ) hour, using the apparatus according to claim 75. The above process was also achieved by preventing the water from absorbing electromagnetic energy simultaneously with the period 24/(1·2 ¹⁸ ) hour and 24/(9-2 ¹⁶ ) hour and 24/(17·2 ¹⁵ ) hour and at the same time the water was exposed to electromagnetic energy with period 0.1-1 s, whereby the water created resonance. The above process was also achieved by exposing the water to high amplitude electromagnetic energy with the period 24/(1·2 ¹⁸ ) hour and/or 24/(9·2 ¹⁶ ) hour and/or 24/(17·2 ¹⁵ ) hour.

The above process was repeated using extinction of all energy, i.e. the water was prevented from creating any type of low frequency resonance. In that case the tin was not influenced and remained dissolved in the water. Consequently, water, containing tin, was only influenced when prevented from creating resonance simultaneously at the period 24/(1·2 ¹⁸ ) hour and 24/(9·2 ¹⁶ ) hour and 24/(17·2 ¹⁵ ) hour and at the same time allowed or enforced to create resonance at a deviating period.

Experiments in vivo displayed that tin was removed from the brain and the rest of the body, transported by the lymph to the urine bladder, and subsequently removed with the urine, when the human was prevented from absorbing electromagnetic energy simultaneously with the period 24/(l-2 ¹⁸ ) hour and 24/(9·2 ¹⁶ ) hour and 24/(17·2 ¹⁵ ) hour during one minute and repeated every 20 minutes, using the apparatus according to claim 75. This process took approximately 16 hours. It was possible to monitor the process by measuring the current absorbed by the body prior to the experiment and then as function of the time, see Figure 10.

Carbon (C), Chromium (Cr), Iron (Fe), Gallium (Ga), Mercury (Hg), Iodine (I), Potassium (K), Lithium (Li), Magnesium (Mg), Manganese (Mn), Neodymium (Nd), Nickel (Ni), Sulphur (S), Titanium (Ti), Vanadium (V), Tungsten (W) and Zinc (Zn), Carbon (C ⁴⁺ ), chromium (Cr ³⁺ ), iron (Fe), gallium (Ga ³⁺ ), mercury (Hg ²⁺ ), iodine (I), potassium (K ⁺ ), lithium (Li), magnesium (Mg ²⁺ ), manganese (Mn ²⁺ ), neodymium (Nd), nickel (Ni ²⁺ ), sulfur (S), titanium (Ti), vanadium (V ³⁺ ), tungsten (W ⁶⁺ ) and zinc (Zn ²⁺ ) were also included in the study. Experiments were also performed on a large number of other chemical elements dissolved in water and which displayed similar type of resonance and absorbed electromagnetic energy with one or many periods 24/(m-2") hour.

Carbon (C) displayed the natural periods 24/(71·2 ¹³ ) hour and 24/(73·2 ¹³ ) hour. Chromium (Cr) displayed the natural periods 24/(3·2 ¹⁷ ) hour, 24/(11·2 ¹⁵ ) hour and 24/(71·2 ¹³ ) hour. Iron (Fe) displayed the natural periods 24/(5·2 ¹⁶ ) hour, 24/(7·2 ¹⁵ ) hour and 24/(9·2 ¹⁵ ) hour. Iron oxide (FeO) displayed the natural period 24/(3-2 ¹⁷ ) hour. Gallium (Ga) displayed the natural periods 24/(1·2 ¹⁹ ) hour and 24/(7·2 ¹⁶ ) hour. Iodine (I) displayed the natural periods 24/(7·2 ¹⁶ ) hour, 24/(19·2 ¹⁵ ) hour and 24/(33·2 ¹⁴ ) hour. Potassium (K) displayed the natural period 24/(67-2 ¹³ ) hour. Lithium (Li) displayed the natural periods 24/(5·2 ¹⁷ ) hour and 24/(29·2 ¹⁴ ) hour. Magnesium (Mg) displayed the natural periods 24/(1·2 ¹⁷ ) hour and 24/(5·2 ¹⁶ ) hour. Manganese (Mn) displayed the natural periods 24/(7·2 ¹⁶ ) hour and 24/(35·2 ¹⁴ ) hour. Neodymium (Nd) displayed the natural periods 24/(25·2 ¹⁴ ) hour and 24/(39·2 ¹³ ) hour. Nickel (Ni) displayed the natural periods 24/(21·2 ¹⁵ ) hour and 24/(121·2 ¹² ) hour. Sulfur (S) displayed the natural periods 24/(ll-2 ¹⁵ ) hour and 24/(21·2 ¹⁵ ) hour. Titanium (Ti) displayed the natural period 24/(79·2 ¹³ ) hour. Titanium dioxide (Ti0 ₂ ) displayed the natural period 24/(37·2 ¹⁴ ) hour. Vanadium (V) displayed the natural periods 24/(9·2 ¹⁵ ) hour, 24/(33·2 ¹⁴ ) hour and 24/(43·2 ¹³ ) hour. Tungsten (W) displayed the natural periods 24/(7·2 ¹⁶ ) hour and 24/(73·2 ¹³ ) hour. Zinc (Zn) displayed the natural periods 24/(15·2 ¹⁵ ) hour and 24/(87·2 ¹² ) hour).

Ag, Al, As, Au, Co, Cd, Cu, F, Hg, Ni, Pb and Zn was dissolved in water and exposed to electrolysis. In the case of Ag, Al, Au, Co, Cd, Cu, Hg, Ni, Pb, Sn, Zn the chemical element accumulated on the cathode, conforming that the dissolved chemical element had positive charge. In the case of As and F the chemical element accumulated on the anode, conforming that the dissolved element had negative charge. This experiment was repeated on each chemical element (i.e. the supernate and the precipitate or sediment) after prevented from absorbing electromagnetic energy at the natural periods according to the claims 1-77. The electrolysis gave no result, conforming that the chemical and/or compound element (i.e. precipitate) had been changed from a chemical element with charge into atoms (or metals or compounds) without charge. Ag, As, C, Ca, Cr, Fe, Ga, Hg, I, Mg, Mn, Pb, Se, Sn, V and W (as chemical element or in compound or in molecule) was found in microbes, including pathogenic bacteria, virus and autoimmune diseases. Each type of microbe and/or disease contained at least one of these chemical elements, and which created resonance and absorbed electromagnetic energy at the natural periods of the chemical element(s). Examples are the bacteria lactobacillus reuteri which contains Pb, lactobacillus rhamnosus which contains W, pathogenic legionella bacteria which contains I, anaerobic bacteria metano sarsino which contain Se, the DMD (Duchene Muscular Dystrophy) which contains Sn, virus in some warts which contains Fe and cold (flu) virus where V was found in some types of flu and W in other types of flu. All of these microbes contained also carbon (C) and which is described below. Preventing the microbe from absorbing electromagnetic energy with the natural periods of the chemical element (i.e. for Sn the period 24/(1·2 ¹⁸ ) hour and 24/(9·2 ¹⁶ ) hour and 24/(17-2 ¹⁵ ) hour resulted in that the chemical element was removed from the microbe and the microbe ceased to absorb electromagnetic energy at these periods. Exposing the microbe to high amplitude electromagnetic energy with the natural periods (e.g. 24/(l-2 ¹⁸ ) hour and/or 24/(9·2 ¹⁶ ) hour and/or 24/(17·2 ¹⁵ ) hour) resulted in that the chemical element was removed from the microbe and the microbe ceased to absorb electromagnetic energy at these periods. However, the microbes always absorbed the same type(s) of chemical element(s) within approximately 24 hours. Consequently, the chemical element(s) must be removed many times; alternatively the microbe is prevented from absorbing electromagnetic energy continuously during approximately 7-14 days. Thus, it is possible to influence a chemical element contained in microbes in vitro and in situ as well as in pathogens and many autoimmune diseases in vivo, and thereby killing microbes and/or curing diseases caused by pathogens and autoimmune diseases.

Cold (flu) is one interesting example. The cold virus often contains vanadium (V). Vanadium was influenced when prevented from absorbing electromagnetic energy with its natural periods

24/(9·2 ¹⁵ ) hour, 24/(33·2 ¹⁴ ) hour and 24/(43-2 ¹³ ) hour, using the apparatus according to claim 76. This removed vanadium from the virus, whereby the virus died and the persons were cured within 2-3 days. The experiment was repeated on another type of flu virus that contained tungsten (W), using the apparatus according to claim 77. This removed vanadium from the virus, whereby the virus died and the persons were cured within 2-3 days. However, preventing vanadium from absorbing electromagnetic energy with the periods 24/(9·2 ¹⁵ ) hour, 24/(33·2 ¹⁴ ) hour and 24/(43-2 ¹³ ) hour or tungsten with the periods 24/(7·2 ¹⁶ ) hour and 24/(73·2 ¹³ ) hour can also be achieved by means of electromagnetic interference; e.g. caused by electromagnetic energy with the periods 24/(5·2 ¹⁶ ) hour and 24/(29·2 ¹⁴ ) hour, i.e. the natural periods of selenium (Se). Positioning selenium close to vanadium or tungsten extinct energy with the natural periods of vanadium and tungsten.

Another example is the pulp and paper industry where growth of legionella bacteria in process water is a large problem. At Domsjo paper mill sewage water is treated with bio cleaning using anaerobic bacteria; however, the sewage also contains legionella. Experiments were performed on this sewage. The legionella bacteria created resonance at the periods 24/(7·2 ¹⁶ ) hour, 24/(19·2 ¹⁵ ) hour and 24/(33·2 ¹⁴ ) hour, caused by iodine (I). The anaerobic bacteria, metano sarsino, created resonance at the periods 24/(5·2 ¹⁶ ) hour, 24/(9·2 ¹⁶ ) hour and 24/(29·2 ¹⁴ ) hour, caused by selenium (Se). The sewage was prevented from absorbing electromagnetic energy with the periods 24/(7·2 ¹⁶ ) hour and 24/(19-2 ¹⁵ ) hour and 24/(33·2 ¹⁴ ) hour during 5 minutes, using the apparatus according to claim 68. This resulted in rapid decline of legionella bacteria and rapid growth of anaerobic bacteria. It is proposed that resonance and absorption of electromagnetic energy is an important feature of microbes and an important defense mechanism towards other microbes and the animal/human immune system. It is also proposed that the legionella bacteria were negatively influenced when the iodine was removed from the legionella bacteria and when the legionella bacteria ceased to absorb electromagnetic energy. The legionella bacteria were then open to assault from the anaerobic bacteria. Thus, it was possible to remove (i.e. kill) legionella bacteria using a combination of electrodynamics and other types of bacteria. In order to demonstrate this mechanism once more the bacteria lactobacillus rhamnosus was added to the solution and the absorbed electromagnetic energy amplitude was measured during 24 hours, displaying constant absorbed amplitude at the natural periods of the anaerobic bacteria and lactobacillus rhamnosus. This indicated that the number of respective bacteria were constant. The sewage was subsequently prevented from absorbing electromagnetic energy with the period 24/(5·2 ¹⁶ ) hour and 24/(9·2 ¹⁵ ) hour and 24/(29-2 ¹⁴ ) hour (i.e. Se) during 5 minutes. This resulted in rapid decline of anaerobic bacteria metano sarsino and rapid growth of lactobacillus rhamnosus. The above anaerobic bacteria metano sarsino (and metano strix) contains selenium (Se). The section Carbon dioxide describes that selenium changes carbon dioxide (C0 ₂ ) into C and 0 ₂ . Thus, the bacteria metano sarsino changes C0 ₂ into 0 ₂ , thereby producing its own oxygen in an anaerobic environment.

In the following experiment yeast (Kronjast, Jastbolaget AB), dissolved in water, was positioned in two identical containers. Yeast displayed resonance and absorbed electromagnetic energy at the periods 24/(9·2 ¹⁵ ) hour, 24/(33·2 ¹⁴ ) hour and 24/(43·2 ¹³ ), caused by vanadium (V). Bacteria lactobacillus rhamnosus were added to both containers and the absorbed amplitude at the natural periods of the yeast and lactobacillus rhamnosus was measured during 24 hours, displaying constant absorbed amplitude at the natural periods of yeast and lactobacillus rhamnosus. One container was prevented from absorbing electromagnetic energy with the period 24/(9·2 ¹⁵ ) hour and 24/(33-2 ¹⁴ ) hour and 24/(43·2 ¹³ ) hour (i.e. V) during 5 minutes, using the apparatus according to claim 76. This resulted in rapid decline of yeast and rapid growth of lactobacillus rhamnosus.

Every pathogen and most microbes investigated contained carbon (C) or a carbon compound or a molecule containing carbon and which created resonance and absorbed electromagnetic energy at the natural periods of carbon, 24/(71·2 ¹³ ) hour and 24/(73·2 ¹³ ) hour. One exception is bacteria that live in symbioses with the human host, e.g. human gut bacteria. It is proposed that carbon and resonance at the period 24/(71·2 ¹³ ) hour plays a very important role in pathogens and most microbes. Resonance and absorbed electromagnetic energy with the period 24/(71·2 ¹³ ) hour creates electromagnetic interference with electromagnetic energy with the period 24/(3·2 ¹⁷ ) hour.

24/(73·2 ¹³ ) hour creates electromagnetic interference with electromagnetic energy with the period 24/(1·2 ¹⁹ ) hour. 24/(3·2 ¹⁷ ) hour is the natural period of water in most organisms, including humans as well as one of the natural periods of 0 ₂ and one of the natural periods of Na. Hence, the pathogen or microbe is prevented from being influenced by electromagnetic energy with the period 24/(3-2 ¹⁷ ) hour. This prevents disturbance of the solvation shells of the carbon (chemical element, compound or molecule) as well as disturbance of the solvation shells of other contained chemical elements, compounds or molecules (e.g. Ag, As, Ca, Cr, Fe, Ga, Hg, I, Mg, Mn, Pb, Se, Sn, V or W). Preventing microbes, including pathogens, from absorbing electromagnetic energy with the period 24/(71·2 ¹³ ) hour or the periods 24/(71·2 ¹³ ) hour and 24/(73·2 ¹³ ) hour during one minute, resulted in that the microbes, including pathogens, released carbon and they ceased to absorb electromagnetic energy with the natural periods 24/(71·2 ¹³ ) hour and 24/(73·2 ¹³ ) hour. This carbon created sediment (valid for microbes in water) or was transported to the urine bladder and dispelled with the urine (valid for pathogens in vivo). In most cases it also resulted in that the other contained chemical element (or compound), (e.g. Ag, As, Ca, Cr, Fe, Ga, Hg, I, Mg, Mn, Pb, Se, Sn, V or W) was influenced and released and it created sediment (valid for microbes in water) or was transported to the urine bladder and dispelled with the urine (valid for pathogens in vivo). Repeating this method once or twice daily during 7-14 days, depending on type of microbe or pathogen, resulted in its death. Alternatively microbes, including pathogens, were prevented from absorbing electromagnetic energy with the period 24/(71-2 ¹³ ) hour or the periods 24/(71·2 ¹³ ) hour and 24/(73-2 ¹³ ) hour continuously during 7-14 days, depending on type of microbe or pathogen. This resulted in microbe and pathogen death and effective disease management. This method can be used on a broad range of microbes and pathogens and has been successfully tested on pathogenic bacteria, virus and some autoimmune diseases. The advantage with this method is that exact analyze of the microbe or pathogen type (i.e. disease) is not necessary. This method was successfully combined with the method described above, e.g. flu was successfully treated with a device that contained one apparatus according to claim 58 (C) and one apparatus according to claim 76 (V).

Most organisms create resonance at the period 24/(3·2 ¹⁷ ) hour. One exception is birds that create resonance at the period 24/(1·2 ¹⁹ ) hour. Hence, disease management of birds (e.g. hen, duck) encompasses the period 24/(73-2 ¹³ ) hour or the periods 24/(71·2 ¹³ ) hour and 24/(73-2 ¹³ ) hour. The method has been successfully deployed on 25 hen exhibiting salmonella.

Hence, microbes, including pathogens, contain chemical elements which create electromagnetic processes and which also influences other chemical elements or compounds to their benefit. Many microbes, including pathogens, contain carbon (C) and which prevents the microbe from being disturbed by electromagnetic energy with the periods 24/(1·2 ¹⁹ ) hour and 24/(3·2 ¹⁷ ) hour. Pathogenic bacteria and virus often contain arsenic (As), cadmium (Cd), chromium (Cr), mercury (Hg), lead (Pb), vanadium (V) or wolfram (W), and where one feature is that oxygen (0 ₂ ) ceases to dissolve in the pathogenic area (se section Oxygen) and which may harm the host and his immune defense system. The anaerobic bacteria metano sarsino and metano strix may live in an anaerobic environment; however, they produce their own oxygen using selenium (Se). The inventor claims that microbes have developed a number of advanced mechanisms based on electromagnetic processes created by chemical elements and/or compounds. The present invention facilitates selective and no invasive influence on these mechanisms, based on electromagnetic theory.

Consequently, the present invention can be used to selectively influence and/or to kill a specific type or specific types of microbes, and at the same time not influencing other types of microbes. It is possible to influence and/or to kill microbes with or without assistance from other types of microbes and/or the immune system.

It is important to note that the actual natural frequency (i.e. the peak resonance = ω ₀ in Eq (2)) of a chemical element sometimes deviated slightly from the above-described frequencies/periods (i.e. ω in Eq (3)). However, paramount in this context is that the chemical element created resonance with electromagnetic energy present in the air and in water with the period 24/(m-2 ⁿ ) hour, although this period/frequency (i.e. ω) deviated slightly from the peak resonance (i.e. ω ₀ ). This was enabled by the limited quality factor (i.e. Q ~ 500) of the oscillator (in the ion-solvation shell structure) and which allowed resonance at minor frequency offset, according to Eq. (3).

The present invention describes, among others, how the electromagnetic process of one chemical element influences other chemical elements and compounds. The present invention describes that K influences Na. Na and Sn influences Ca. Se influences K, V and W. Zn influences C. Al, C, Cd, Hg, Pb, V W and Zn influences 0 ₂ . Pb and Se influences and changes C0 ₂ into C and 0 ₂ . Zn influences and changes C and 0 ₂ into C0 ₂ . Chemistry and organisms, including humans, contain a number of processes that cannot be described or understood with state of the art chemistry. The present invention offers an explanation and the invention describes how these processes can be influenced and also how (negative) influence can be avoided.

Achieved results; Molecules

Molecules dissolved in water were measured in vitro and in vivo using the method described by Giertz (2010a, b). The absorbed current was measured as function of the frequency using an analogue generator as well as current present in the air. Herbicides (e.g. glyphosate)

Water solutions that contained glyphosate (C ₃ H ₈ N0 ₅ P, Roundup/Monsanto and Rambo/Weibulls) created resonance at 5.88 Hz, 6.87 Hz, 3.14 Hz and 3.86 Hz. Roundup and Rambo absorbed electromagnetic energy present in the air and water with the period 24/(31·2 ¹⁴ ) hour (5.88 Hz) and 24/(145·2 ¹² ) hour (6.87 Hz). The natural frequencies 3.14 Hz and 3.86 Hz did not coincide with the period 24/(m-2 ⁿ ) implying that electromagnetic energy present in the air and in water was not absorbed at these frequencies. Resonance at 5.88 Hz and 6.87 Hz was also found in many foods, e.g. tomatoes, cucumbers, zucchini, salads, onions, paprika and apples. It was also found in most wines, in whiskey, vodka and gin. These beverages and vegetables absorbed electromagnetic energy present in the air with the period 24/(31·2 ¹⁴ ) hour (5.88 Hz) and 24/(145·2 ¹² ) hour (6.87 Hz).

Resonance at 5.88 Hz and 6.87 Hz was also found in the human brain of all investigated persons (22 persons), in lake water (Malaren, Hjalmaren, Vanern, Vattern and Sjundasjon), in Stockholm tap water and in the Baltic seawater as well as in the North Sea close to the Swedish West-coast. The human brain, lake water, tap water and seawater absorbed electromagnetic energy, present in the air and in water, with the period 24/(31·2 ¹⁴ ) hour (5.88 Hz) and 24/(145·2 ¹² ) hour (6.87 Hz). Using a signal generator displayed resonance at 3.14 Hz and 3.86 Hz.

Experiments on one liter water containing dissolved glyphosate from Roundup and Rambo were performed. The water was prevented from absorbing electromagnetic energy with the period 24/(31·2 ¹⁴ ) hour and 24/(145-2 ¹² ) hour during 1 minute, using apparatus according to claim 78. This displayed that the glyphosate molecule was split, forming new compounds. One compound drifted to the bottom as sediment (precipitate), this sediment displayed resonance and absorbed

electromagnetic energy with the period 24/(145·2 ¹² ) hour (6.87 Hz) and at 3.14 Hz during the transition phase. The other compound drifted upwards and floated (as precipitate) on top of the water. This floating compound displayed resonance and absorbed electromagnetic energy with the period 24/(31-2 ¹⁴ ) hour and at 3.86 Hz during the transition phase. This compound evaporated. The sediment (precipitate) was removed using decanting. The remaining (95%) water (i.e. the supernate) displayed no resonance nor absorbed electromagnetic energy at 3.14 Hz, 3.86 Hz, 5.88 Hz or 6.87 Hz. The above results were also achieved by exposing the water to high amplitude electromagnetic energy with the period 24/(31·2 ¹⁴ ) hour and/or 24/(145·2 ¹² ) hour and/or 3.14 Hz and/or 3.86 Hz.

The above experiment was repeated on wine, gin, whiskey and vinegar, displaying that it was possible to change the contained molecule into two compounds; one sediment (6.87 Hz and 3.14 Hz) and one floating and evaporating compound (5.88 Hz and 3.86 Hz). These compounds were removed using evaporation and decanting.

Investigating matured (stored) wine (Haut-Bages Liberal 2006 and Haut-Bages 2007) displayed that these wines created resonance at the period 24/(31·2 ¹⁴ ) hour and 24/(145·2 ¹² ) hour; however at low amplitude. Young wine created, without exception, resonance at period 24/(31·2 ¹⁴ ) hour and

24/(145·2 ¹² ) hour and at relatively high amplitude. It is proposed that the molecule that creates this resonance changed into two compounds in matured wine, whereby they ceased to dissolve. It is also proposed that this molecule consisted of glyphosate and/or similar molecules, i.e. herbicides.

Tomatoes, cucumbers, zucchini, ruccola salad, paprika, bananas and apples were investigated and the absorbed current amplitude at the period 24/(31·2 ¹⁴ ) hour and 24/(145·2 ¹² ) hour was measured. Subsequently, vegetables and apples were washed in cold water as well as hot tap water during 2 minutes. The absorbed current amplitude at the period 24/(31-2 ¹⁴ ) hour was measured, displaying no change in absorbed energy amplitude, indicating that it was impossible to remove the molecules by washing. Pealing bananas, cucumbers, zucchini and apples displayed that the molecule was primarily located within the vegetable and not on the surface. Electromagnetic energy, with the period 24/(31·2 ¹⁴ ) hour and 24/(145·2 ¹² ) hour was prevented from propagating to the vegetables and apples during 1 minute, using the apparatus according to claim 78. After this treatment the vegetables and apples displayed no measurable absorbed electromagnetic energy at these periods, neither at the frequency 3.14 Hz nor at 3.86 Hz (measured using signal generator as source). This indicated that it was possible to remove or destroy the molecule, i.e. change the molecule into new compounds. The above results were also achieved by exposing the vegetables to high amplitude electromagnetic energy with the period 24/(31·2 ¹⁴ ) hour and/or 24/(145·2 ¹² ) hour and/or 3.14 Hz and/or 3.86 Hz. Tomatoes and apples were compared before and after removing the molecule. The change in taste was distinct, displaying improved taste. It is proposed that these vegetables contained glyphosate and/or similar molecules, i.e. herbicides.

Experiments in vivo displayed that all persons investigated (22) created resonance and absorbed electromagnetic energy at the period 24/(31·2 ¹⁴ ) hour and 24/(145-2 ¹² ) hour, primarily concentrated to the brain. Three humans were prevented from absorbing electromagnetic energy with the period 24/(31·2 ¹⁴ ) hour and 24/(145-2 ¹² ) hour during one minute, repeated every 20 minutes, using the apparatus according to claim 78. The persons urinated approximately every 20 minutes, enforced by large consumption of water. The electromagnetic energy absorbed by the person's brain was measured, this amplitude decreased almost linearly with time. The urine displayed high amplitude resonance at the period 24/(31-2 ¹⁴ ) hour and 24/(145·2 ¹² ) hour. It is proposed that herbicides, or a part of the herbicide molecule, accumulate in the human brain and that it is possible to remove this molecule.

The above processes were repeated on water containing Roundup and Rambo, using extinction of all energy, i.e. the water was prevented from creating any type of low frequency resonance. In that case the glyphosate was not influenced and remained dissolved in the water. Consequently, glyphosate dissolved in water was only influenced when prevented from creating resonance at the period 24/(31-2 ¹⁴ ) hour and/or 24/(145·2 ¹² ) hour and at the same time allowed or enforced to create resonance at a deviating period.

Experiments performed on one liter of lake water (Malaren, Hjalmaren, Vanern, Vattern and Sjundasjon), one liter of Stockholm tap water and one liter of Baltic seawater and one liter of North seawater displayed that all contained molecules that created resonance and absorbed

electromagnetic energy at the period 24/(31·2 ¹⁴ ) hour and 24/(145-2 ¹² ) hour. Electromagnetic energy, with the period 24/(31·2 ¹⁴ ) hour and 24/(145-2 ¹² ) hour was prevented from propagating to these water samples during 1 minute, using the apparatus according to claim 78. This resulted in that these water samples ceased permanently to create resonance at the period 24/(31·2 ¹⁴ ) hour and 24/(145-2 ¹² ) hour. The apparatus according to claim 78 was submerged into the water (close to the shore) of lake Sjundasjon during four days. This resulted in that all measured water in the lake ceased permanently to create resonance at the period 24/(31·2 ¹⁴ ) hour and 24/(145·2 ¹² ) hour.

One purpose with the present invention is to influence and/or to remove molecules with natural period 24/(31·2 ¹⁴ ) hour and 24/(145·2 ¹² ) hour. These molecules can be identical to glyphosate or slightly deviating and which is irrelevant as long as their natural period is 24/(31-2 ¹⁴ ) hour and 24/(145·2 ¹² ) hour. In order to avoid confusion molecules with natural period 24/(31·2 ¹⁴ ) hour and 24/(145·2 ¹² ) hour are called Herbicides in the present invention. In order to illustrate this, measurements were made on a number of different herbicides. The following herbicides displayed resonance and absorbed electromagnetic energy at the period 24/(31·2 ¹⁴ ) hour and 24/(145·2 ¹² ) hour; Hedonal (2,4-diklorfenoxipropionacid (diklorprop), Bayer Agro, Prefix, diklobenil, Rhone- Poulenc Agro, Paraquat (dichloride), ICI Limited and Gesatop 50, simazin (2-klor-4,6-bis-(etylamin)-s- triazin), J.R. Geigy AG. All of these herbicides ceased to dissolve and to absorb (permanently) electromagnetic energy when electromagnetic energy, with the period 24/(31-2 ¹⁴ ) hour and 24/(145·2 ¹² ) hour, was prevented from propagating to these herbicides during 1 minute, using the apparatus according to claim 78.

Insecticides A (e.g. imidacloprid)

Water that contained imidacloprid (CgHioCINsOa, Provado/Bayer Garden) created resonance at 3.84 Hz, 3.23 Hz and 4.81 Hz. This water absorbed electromagnetic energy present in the air with the period 24/(81-2 ¹² ) hour (3.84 Hz). Resonance at 3.84 Hz, 3.23 Hz and 4.81 Hz was also found in a large variety of food such as bread, flour, vegetables, grapes, olives, caper, canned corn, oranges, orange juice, lemons, bananas, pineapples, olive oil, vinegar, wine, whiskey, vodka and gin. These beverages and foods absorbed electromagnetic energy present in the air with the period 24/(81·2 ¹² ) hour (3.84 Hz). Resonance at 3.84 Hz, 3.23 Hz and 4.81 Hz was also found in the human brain and body of all investigated persons (22 persons). The human brain in all investigated persons (22) absorbed high amplitude electromagnetic energy present in the air with the period 24/(81·2 ¹² ) hour, and measured using a signal generator also at 3.23 Hz and 4.81 Hz. Thus, humans normally contain relatively large amount of molecules identical to or similar to imidacloprid and located to the brain, and in some cases estimated to 50 mg/kg bodymass. Lake water ( alaren, Hjalmaren, Vanem, Vattern and Sjundasjon), Stockholm tap water and the Baltic seawater absorbed electromagnetic energy present in the air with the period 24/(81·2 ¹² ) hour and measured using a signal generator also at 3.23 Hz and 4.81 Hz.

Experiments on one liter of water containing dissolved imidacloprid from Provado/Bayer Garden were performed by preventing the water from absorbing electromagnetic energy with the period 24/(81·2 ¹² ) hour during 1 minute, using the apparatus according to claim 79. This displayed that the imidacloprid molecule was split, forming new compounds. One compound drifted to the bottom as sediment (precipitate), this sediment displayed resonance and absorbed electromagnetic energy with the frequency 3.84 Hz and 3.23 Hz during a short transition phase; afterwards it ceased to create resonance. The other compound drifted upwards and floated (as precipitate) on top of the water. This floating compound displayed resonance and absorbed electromagnetic energy at 4.81 Hz during a short transition phase. This compound evaporated. The sediment was removed using decanting. The remaining (95%) water (i.e. the supernate) displayed no resonance or absorbed electromagnetic energy at 3.84 Hz, 3.23 Hz or 4.81 Hz. The above results were also achieved by exposing the water to high amplitude electromagnetic energy with the period 24/(81·2 ¹² ) hour and/or 3.23 Hz and/or 4.81 Hz. This resulted in that the imidacloprid ceased to dissolve.

The above experiment was repeated on one liter orange juice, lake water, tap water, seawater and 15 different red and white wines from France, Italy, South Africa and Spain, as well as three different types of vinegar and two different types of olive oil, whiskey, vodka and gin, using the apparatus according to claim 79. This displayed that the molecules that created resonance at 24/(81-2 ¹² ) hour, 3.23 Hz and 4.81 Hz were split, forming new compounds. One compound drifted to the bottom as sediment (precipitate), this sediment displayed resonance and absorbed electromagnetic energy with the frequency 3.84 Hz and 3.23 Hz during a short transition phase and afterwards it ceased to create resonance. The other compound drifted upwards and floated (as precipitate) on top of the water. This floating compound displayed resonance and absorbed electromagnetic energy at 4.81 Hz, during a short transition phase. This compound evaporated. The sediment was removed using decanting. The remaining (95%) water (i.e. the supernate) displayed no resonance or absorbed electromagnetic energy at 3.84 Hz, 3.23 Hz and 4.81 Hz. The processed wines were stored. They displayed no change over time.

Tomatoes, cucumbers, onions, zucchini, apples, potatoes, grapes, olives, oranges, lemons, bananas and pineapples were investigated and the absorbed current amplitude at the period 24/(81·2 ¹² ) hour was measured. Then the vegetables and fruits were washed in cold as well as in hot tap water during 2 minutes. Then the absorbed current amplitude at the period 24/(81·2 ¹² ) hour was measured; the amplitude was identical to the previous amplitude, indicating that it was impossible to remove molecule(s) that created resonance at 24/(81·2 ¹² ) hour by washing. Pealing oranges and bananas displayed that the molecule(s) that created resonance were evenly positioned within the fruits. The vegetables and fruits were prevented from absorbing electromagnetic energy, with the period 24/(81·2 ¹² ) hour, during 1 minute, using the apparatus according to claim 79. The vegetables and fruits displayed no measurable absorbed electromagnetic energy at the period 24/(81·2 ¹² ) hour. The above results were also achieved by exposing vegetables and fruits to high amplitude

electromagnetic energy with the period 24/(81·2 ¹² ) hour and/or 3.23 Hz and/or 4.81 Hz. Vegetables, grapes and orange juice were compared before and after, displaying that a chemical scent disappeared.

Experiments in vivo displayed that all persons investigated (22) created resonance and absorbed electromagnetic energy at the period 24/(81·2 ¹² ) hour. Three humans were prevented from absorbing electromagnetic energy with the period 24/81-2 ¹² hour during one minute and repeated every 20 minutes, using the apparatus according to claim 79. The persons urinated approximately every 20 minutes, enforced by large consumption of water. The electromagnetic energy absorbed by the person was measured, this amplitude decreased almost linearly with time. The urine displayed resonance at the period 24/(81-2 ¹² ) hour, 3.23 Hz and 4.81 Hz. It was concluded that it was possible to remove molecule(s) that create resonance at the period 24/(81·2 ¹² ) hour, 3.23 Hz and 4.81 Hz from humans. It was also concluded the dissolved molecule accumulated in the human brain and the body.

The above processes were repeated on water containing Provado/Bayer Garden, using extinction of all energy, i.e. the water was prevented from creating any type of low frequency resonance. In that case the imidacloprid was not influenced and remained dissolved in the water. Consequently, water that contains imidacloprid was only influenced when prevented from creating resonance at the period 24/(81·2 ¹² ) hour and at the same time allowed or enforced to create resonance at a deviating period (e.g. the period 24/(3-2 ¹⁷ ) hour).

Experiments performed on one liter of lake water (Malaren, Hjalmaren, Vanern, Vattern and Sjundasjon), one liter of Stockholm tap water and one liter of Baltic seawater displayed that all contained molecule(s) that created resonance and absorbed electromagnetic energy at the period 24/(81·2 ¹² ) hour, 3.23 Hz and 4.81 Hz. Electromagnetic energy, with the period 24/(81·2 ¹² ) hour was prevented from propagating to these water samples during 1 minute, using the apparatus according to claim 79. This resulted in that these water samples ceased permanently to create resonance at the period 24/(81·2 ¹² ) hour, 3.23 Hz and 4.81 Hz. The apparatus according to claim 79 was submerged into the water (close to the shore) of lake Sjundasjon during four days. This resulted in that all measured water ceased permanently to create resonance at the period 24/(81·2 ¹² ) hour, 3.23 Hz and 4.81 Hz.

One purpose with the present invention is to influence and/or to remove molecules with natural period 24/(81·2 ¹² ) hour. These molecules can be identical to imidacloprid or slightly deviating and which is irrelevant as long as their natural period is 24/(81·2 ¹² ) hour. In order to avoid confusion molecules with natural period 24/(81·2 ¹² ) hour are called Insecticides A in the present invention.

Insecticides B (e.g. phoxim)

Water that contained phoxim (C12H15 2O3PS Baythion/Bayer AG) created resonance at 3.60 Hz, 3.98 Hz 5.50 Hz, 5.93 Hz and 6.54 Hz. This water absorbed electromagnetic energy present in the air with the period 24/(19·2 ¹⁴ ) hour (3.60 Hz), 24/(21·2 ¹⁴ ) hour (3.98 Hz), 24/(29·2 ¹⁴ ) hour (6.54 Hz),

24/(69·2 ¹³ ) hour (6.54 Hz) and 24/(125·2 ¹² ) hour (5.93 Hz). Resonance at the period 24/(19-2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29·2 ¹⁴ ) hour, 24/(69·2 ¹³ ) hour and 24/(125-2 ¹² ) hour was also found in a large variety of food such as bread, flour (also in flour marked ecological), vegetables, olives, caper, oranges, orange juice, lemons, bananas (also on bananas marked ecological), pineapples, olive oil, vinegar, wine (also on wine marked ecological), whiskey, vodka, gin, beer, milk, and cheese.

Resonance at the period 24/(19-2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29·2 ¹⁴ ) hour, 24/(69-2 ¹³ ) hour and 24/(125·2 ¹² ) hour was also found in the human brain and body of all investigated persons (22 persons). The human brain and body in all investigated persons (22) absorbed high amplitude electromagnetic energy present in the air with these periods. Thus, humans normally contain relatively large amount of molecules identical to or similar to phoxim located to the brain and the body. Lake water (Malaren, Hjalmaren, Va ^' nern and Vattern), Stockholm tap water, the Baltic seawater and the North seawater absorbed electromagnetic energy present in the air with the period 24/(19·2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29·2 ¹⁴ ) hour, 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour.

Experiments on one liter of water containing dissolved phoxim contained in Baythion/Bayer AG were performed by preventing the water from absorbing electromagnetic energy with the period

24/(19-2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour and 24/(29-2 ¹⁴ ) hour and 24/(69·2 ¹³ ) hour and 24/(125-2 ¹² ) hour during 1 minute, using the apparatus according to claim 77. This displayed that the phoxim molecule was split, forming new compounds that ceased to dissolve. The above results were also achieved by exposing the water to high amplitude electromagnetic energy with the period

24/(19·2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29·2 ¹⁴ ) hour, 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour. It resulted in that phoxim ceased to dissolve.

The above experiment was repeated on one liter orange juice, lake water, tap water, seawater and 15 different red and white wines from France, Italy, South Africa and Spain, as well as vinegar, olive oil, whiskey, vodka and gin, using the apparatus according to claim 80. This displayed that the molecule(s) that created resonance at the period 24/(19·2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29·2 ¹⁴ ) hour, 24/(69-2 ¹³ ) hour and 24/(125·2 ¹² ) hour were split, forming new compounds that ceased to dissolve. The sediment was removed using decanting. The processed wines were stored. They displayed no change over time.

Tomatoes, cucumbers, zucchini, apples, oranges, lemons and bananas were investigated and the absorbed current amplitude at the period 24/(19·2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29·2 ¹⁴ ) hour, 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour was measured. Then the vegetables and fruits were washed in cold tap water during 2 minutes. Then the absorbed current amplitude at the period 24/(19-2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29-2 ¹⁴ ) hour, 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour was measured; the amplitude was zero, indicating that it was possible to remove molecule(s) that created resonance at the period 24/(19-2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29-2 ¹⁴ ) hour, 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour by washing. Pealing oranges and bananas displayed that the molecule(s) that created resonance were positioned primarily on the surface. The vegetables and fruits were prevented from absorbing electromagnetic energy, with the period 24/(19·2 ¹⁴ ) hour and 24/(21-2 ¹⁴ ) hour and 24/(29·2 ¹⁴ ) hour and 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour, during 1 minute, using the apparatus according to claim 80. The vegetables and fruits displayed no measurable absorbed electromagnetic energy at these periods. The above results were also achieved by exposing vegetables and fruits to high amplitude electromagnetic energy with the period 24/(19·2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29-2 ¹⁴ ) hour, 24/(69-2 ¹³ ) hour and 24/(125-2 ¹² ) hour. Vegetables, grapes and orange juice were compared before and after, displaying that a chemical taste disappeared.

Experiments in vivo displayed that all persons investigated (22) created resonance and absorbed electromagnetic energy at the period 24/(19·2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29·2 ¹⁴ ) hour, 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour. One human was prevented from absorbing electromagnetic energy with the period 24/(19·2 ¹⁴ ) hour and 24/(21-2 ¹⁴ ) hour and 24/(29·2 ¹⁴ ) hour and 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour during one minute and repeated every 20 minutes, using the apparatus according to claim 80. The persons urinated approximately every 20 minutes, enforced by large consumption of water. The electromagnetic energy absorbed by the person was measured, this amplitude decreased almost linearly with time. The urine displayed resonance at the period 24/(19-2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29·2 ¹⁴ ) hour, 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour. It was concluded that it was possible to remove molecule(s) that create resonance at the period 24/(19-2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29·2 ¹⁴ ) hour, 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour from humans. It was also concluded these dissolved molecule(s) accumulated in the human brain and the body.

The above processes were repeated on water containing phoxim (Baythion/Bayer Garden), using extinction of all energy, i.e. the water was prevented from creating any type of low frequency resonance. In that case the phoxim was not influenced and remained dissolved in the water.

Consequently, water that contains phoxim was influenced when prevented from absorbing electromagnetic energy at the period 24/(19·2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour and 24/(29·2 ¹⁴ ) hour and 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour and at the same time allowed or enforced to create resonance at a deviating period (e.g. 24/(3-2 ¹⁷ ) hour).

Experiments performed on one liter of lake water ( alaren, Hjalmaren, Vanern and Vattern), one liter of Stockholm tap water, one liter of Baltic seawater and one liter of North seawater displayed that all contained molecules that created resonance and absorbed electromagnetic energy at the period 24/(19·2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29·2 ¹⁴ ) hour, 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour. Electromagnetic energy, with the period 24/(19·2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29·2 ¹⁴ ) hour, 24/(69-2 ¹³ ) hour and 24/(125·2 ¹² ) hour was prevented from propagating to these water samples during 1 minute, using the apparatus according to claim 80. This resulted in that these water samples ceased permanently to create resonance at the period 24/(19-2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29·2 ¹⁴ ) hour, 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour. The purpose with the present invention is to influence and/or to remove molecules with natural period 24/(19·2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29·2 ¹⁴ ) hour, 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour. These molecules can be identical to phoxim or slightly deviating and which is irrelevant as long as their natural period is 24/(19·2 ¹⁴ ) hour, 24/(21·2 ¹⁴ ) hour, 24/(29·2 ¹⁴ ) hour, 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour. In order to avoid confusion molecules with natural period 24/(19-2 ¹⁴ ) hour, 24/(21-2 ¹⁴ ) hour, 24/(29·2 ¹⁴ ) hour, 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour are called Insecticides B in the present invention.

Pesticides (e.g. dioctyl sodium sulfosuccinate)

Water that contained docusate sodium sulfosuccinate, DSS, (C ₂ oH3 ₇ a0 ₇ S, DulcoEase/Boerhinger Ingelheim, KLYX/Ferringer and Resulax BioPhausia AB) created resonance at 6.07 Hz, 6.92 Hz, 7.49 Hz, 3.20 Hz and 3.52 Hz. These three water solutions absorbed electromagnetic energy present in the air with the period 24/1-2 ¹⁹ hour (6.07 Hz), 24/73-2 ¹³ hour (6.92 Hz) and 24/(79-2 ¹³ ) hour (7.49 Hz). Resonance at 6.07 Hz, 6.92 Hz, 7.49 Hz, 3.20 Hz and 3.52 Hz was also found in a large variety of food such as grapes, olives, caper, canned corn, oranges, orange juice, lemons, bananas, pineapples, olive oil, vinegar, wine, whiskey, vodka, gin and sugar. These beverages and foods absorbed electromagnetic energy present in the air with the period 24/(1·2 ¹⁹ ) hour, 24/(73·2 ¹³ ) hour and 24/(79·2 ¹³ ) hour. Resonance at 6.07 Hz, 6.92 Hz, 7.49 Hz, 3.20 Hz and 3.52 was also found in the human brain of all investigated persons (22 persons) as well as in lake water (Malaren, Hjalmaren, Vanern Vattern and Sjundasjon), in Stockholm tap water and in the Baltic seawater and in North seawater. The human brain in all investigated persons (22), lake water, tap water and seawater absorbed electromagnetic energy present in the air and in water with the period 24/(l-2 ¹⁹ ) hour, 24/(73·2 ¹³ ) hour and 24/(79·2 ¹³ ) hour. Thus lake water and tap water in Sweden, and the Baltic seawater and North seawater as well as humans normally contain relatively large amount of molecules identical to or similar to DSS.

Experiments (1) made on one liter of water containing dissolved DSS from DulcoEase/Boerhinger Ingelheim, KLYX/Ferringer and Resulax BioPhausia AB, were performed by preventing the water solution from absorbing electromagnetic energy with the period 24/(73·2 ¹³ ) hour during 1 minute. This displayed that the DSS molecule was split, forming new compounds. The first compound drifted to the bottom as sediment (precipitate), this sediment displayed resonance and absorbed electromagnetic energy with the frequency 3.52 Hz during the transition phase. The other compound drifted upwards and floated (as precipitate) on top of the water. This floating compound displayed resonance and absorbed electromagnetic energy with the period 24/(73·2 ¹³ ) hour (6.92 Hz) and at 3.20 Hz during the transition phase. This compound evaporated. The third compound remained dissolved and displayed resonance and absorbed electromagnetic energy with the period 24/(1·2 ¹⁹ ) hour and 24/(79-2 ¹³ ) hour. The sediment was removed using decanting. The remaining (95%) water (i.e. the supernate) displayed resonance and absorbed electromagnetic energy at 24/(1·2 ¹⁹ ) hour and 24/(79·2 ¹³ ) hour. The above results were also achieved by exposing the water to high amplitude electromagnetic energy with the period 24/(73·2 ¹³ ) hour. It was concluded that the DSS molecule was split into one compound that remained dissolved and two compounds and/or chemical elements that did not dissolve.

Experiments (2) made on one liter of water containing dissolved DSS from DulcoEase/Boerhinger Ingelheim, KLYX/Ferringer and Resulax BioPhausia AB, were performed by preventing the water solution from absorbing electromagnetic energy with the period 24/(1·2 ¹⁹ ) hour and 24/(79·2 ¹³ ) hour during 1 minute. This displayed that the DSS molecule was split, forming new compounds. One compound remained dissolved and displayed resonance and absorbed electromagnetic energy with the period 24/(73·2 ¹³ ) hour (6.92 Hz) and at 3.20 Hz. The above results were also achieved by exposing the water to high amplitude electromagnetic energy with the period 24/(1·2 ¹⁹ ) hour and 24/(79·2 ¹³ ) hour. It was concluded that the DSS molecule was split and one compound remained dissolved.

Experiments (3) made on one liter of water containing dissolved DSS from DulcoEase/Boerhinger Ingelheim, KLYX/Ferringer and Resulax BioPhausia AB were performed by preventing the water solution from absorbing electromagnetic energy with the period 24/(1·2 ¹⁹ ) hour and 24/73-2 ¹³ hour and 24/(79·2 ¹³ ) hour during 1 minute, using the apparatus according to claim 81. This displayed that the DSS molecule was split, forming new compounds that did not dissolve and did not create resonance and did not absorb electromagnetic energy.

The above three experiments (1), (2) and (3) display the importance of analyzing a molecule correctly and the importance of influencing the solvation shells correctly, otherwise a part of the molecule can remain dissolved (as illustrated in the experiments (1) and (2)).

Experiment were performed on one liter orange juice and 15 different red and white wines from France, Italy, South Africa and Spain as well as three different types of vinegar and two different types of olive oil. These beverages were prevented from prevented from absorbing electromagnetic energy with the period 24/(1·2 ¹⁹ ) hour and 24/(73·2 ¹³ ) hour and 24/(79·2 ¹³ ) hour during 1 minute, using the apparatus according to claim 81. This displayed that the molecule(s) ceased to create resonance, ceased to absorb electromagnetic energy and ceased to dissolve. These processed wines were stored, displaying no change over time.

Investigating old wine (Brane Cantenac 1983, Vieux Telegraph 1985, Haut-Bages 2007) displayed that every bottle contained molecule(s) that created resonance at period 24/(1·2 ¹⁹ ) hour, 24/(73·2 ¹³ ) hour and 24/(79·2 ¹³ ) hour; however at low amplitude. Young wine, almost without exception and including some wines labeled Ecological, contained a similar or identical molecule. The absorbed current amplitude was relatively high in young wine. It is proposed that the molecule(s) were gradually changed into insoluble compounds/chemical elements in matured wine.

Grapes, olives, oranges, lemons, bananas and pineapples were investigated and the absorbed current amplitude at the period 24/(l-2 ¹⁹ ) hour, 24/(73·2 ¹³ ) hour and 24/(79-2 ¹³ ) hour was measured. Then the fruits were washed in cold as well as in hot tap water during 2 minutes. Then the absorbed current amplitude at the period 24/(1·2 ¹⁹ ) hour, 24/(73·2 ¹³ ) hour and 24/(79·2 ¹³ ) hour was measured; the amplitude was identical to the previous amplitude, indicating that it was impossible to remove the molecule(s) by washing. Pealing oranges, lemons and bananas displayed little change in absorbed energy, indicating that the molecule(s) was located within the fruits. The fruits were prevented from absorbing electromagnetic energy, with the period 24/(1·2 ¹⁹ ) hour and 24/(73·2 ¹³ ) hour and

24/(79·2 ¹³ ) hour, during 1 minute, using the apparatus according to claim 81. Afterwards the fruits displayed no measurable absorbed electromagnetic energy at the period 24/(1·2 ¹⁹ ) hour or

24/(73·2 ¹³ ) hour or 24/(79·2 ¹³ ) hour, or at the frequency 3.20 Hz or at 3.52 Hz (measured using signal generator as source). This indicated that it was possible to change (almost) the molecule into new insoluble compounds/chemical elements. The above results were also achieved by exposing fruits to high amplitude electromagnetic energy with the period 24/(1·2 ¹⁹ ) hour and 24/(73·2 ¹³ ) hour and 24/(79·2 ¹³ ) hour and/or 3.20 Hz and/or 3.52 Hz. Grapes and orange juice were compared before and after removing the molecules. It displayed that a bitter taste disappeared. KLYX/Ferringer displayed the same bitter taste.

Experiments in vivo displayed that all persons investigated (22) contained this type of molecule, concentrated to the brain. Three humans were prevented from absorbing electromagnetic energy with the period 24/(1·2 ¹⁹ ) hour and 24/(73-2 ¹³ ) hour and 24/(79·2 ¹³ ) hour during one minute and repeated every 20 minutes, using the apparatus according to claim 81. The persons urinated approximately every 20 minutes, enforced by large consumption of water. The electromagnetic energy absorbed by the person was measured, this amplitude decreased almost linearly with time. The urine absorbed high amplitude electromagnetic at the period 24/(1·2 ¹⁹ ) hour, 24/(73·2 ¹³ ) hour and 24/(79·2 ¹³ ) hour. It was concluded that this type of molecule (or molecules) accumulated in the brain and that it was possible to remove the molecule (or molecules) from humans.

Experiments were performed on water containing DulcoEase/Boerhinger Ingelheim, KLYX/Ferringer and Resulax/BioPhausia AB, using extinction of all energy, i.e. the water was prevented from creating any type of low frequency resonance. In that case the DSS was not influenced and remained dissolved in the water. Consequently, water that contained DSS was influenced when prevented from creating resonance at the period 24/(1·2 ¹⁹ ) hour and/or 24/(73·2 ¹³ ) hour and/or 24/(79·2 ¹³ ) hour and at the same time allowed or enforced to create resonance at a deviating period (e.g. the period 24/(3·2 ¹⁷ ) hour).

Experiments performed on one liter lake water (Malaren, Hjalmaren, Vanern, Vattern and

Sjundasjon), one liter Stockholm tap water and one liter Baltic seawater displayed that all contained a molecule or molecules that created resonance and absorbed electromagnetic energy at the period 24/(1·2 ¹⁹ ) hour, 24/(73·2 ¹³ ) hour and 24/(79-2 ¹³ ) hour. Electromagnetic energy, with the period 24/(l-2 ¹⁹ ) hour and 24/(73·2 ¹³ ) hour and 24/(79·2 ¹³ ) hour was prevented from propagating to these water samples during 1 minute, using the apparatus according to claim 81. This resulted in that these water samples ceased permanently to create resonance at the period 24/(1·2 ¹⁹ ) hour, 24/(73·2 ¹³ ) hour and 24/(79·2 ¹³ ) hour. The apparatus according to claim 81 was submerged into the water (close to the shore) of lake Sjundasjon during four days. This resulted in that all measured water in the lake ceased permanently to create resonance at the period 24/(1·2 ¹⁹ ) hour, 24/(73·2 ¹³ ) hour and 24/(79·2 ¹³ ) hour.

One purpose with the present invention is to influence and/or to remove molecules with natural period 24/(1·2 ¹⁹ ) hour, 24/(73·2 ¹³ ) hour and 24/(79·2 ¹³ ) hour. These molecules can be identical to dioctyl sodium sulfosuccinate or slightly deviating and which is irrelevant as long as their natural periods are 24/(1·2 ¹⁹ ) hour and 24/(73·2 ¹³ ) hour and 24/(79-2 ¹³ ) hour. In order to avoid confusion molecules with natural period 24/(1·2 ¹⁹ ) hour and 24/(73·2 ¹³ ) hour and 24/(79·2 ¹³ ) hour are called Pesticides in the present invention.

Fungicides (e.g. bitertanol)

Water that contained bitertanol/sibutol (C20H23 3O2, Bitertanol/Bayer AG) created resonance at 3.60 Hz, 3.98 Hz and 4.17 Hz Hz. This water absorbed electromagnetic energy present in the air with the period 24/(11·2 ¹⁵ ) hour (4.17 Hz), 24/(19·2 ¹⁴ ) hour (3.60 Hz) and 24/(21·2 ¹⁴ ) hour (3.98 Hz).

Resonance at 3.60 Hz, 3.98 Hz and 4.17 Hz was also found in bread, flour, muesli, grapes, olives, oranges, orange juice, lemons, tomatoes, olive oil, vinegar, wine, whiskey, vodka and gin. Some of these products were marked Ecological. These beverages and foods absorbed electromagnetic energy present in the air with the period 24/(11·2 ¹⁵ ) hour, 24/(19·2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour. Resonance and absorbed electromagnetic energy at the period 24/(11·2 ¹⁵ ) hour, 24/(19·2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour was also found in the human brain of all investigated persons (22 persons) as well as in lake water (Malaren, Hjalmaren, Vanern, Vattern), in Stockholm tap water and in the Baltic seawater and North seawater.

Washing oranges, lemons and tomatoes displayed that this type of molecule disappeared. The molecules were positioned on the surface.

The above food, beverages and water were prevented from absorbing electromagnetic energy with the period 24/(11·2 ¹⁵ ) hour and 24/(19-2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour during 1 minute, using the apparatus according to claim 82. This displayed that the molecule ceased permanently to create resonance and to absorb electromagnetic energy and to dissolve.

Three humans were prevented from absorbing electromagnetic energy with the period 24/(11·2 ¹⁵ ) hour, 24/(19·2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour during one minute and repeated every 20 minutes, using the apparatus according to claim 82. The persons urinated approximately every 20 minutes, enforced by large consumption of water. The electromagnetic energy absorbed by the person was measured, this amplitude decreased almost linearly with time. The urine absorbed high amplitude

electromagnetic at the period 24/(11·2 ¹⁵ ) hour, 24/(19·2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour. It was concluded that this molecule (or molecules) accumulates in the brain and that it was possible to remove this molecule (or molecules) from humans.

The purpose with the present invention is to influence and/or to remove molecules with natural period 24/(11·2 ¹⁵ ) hour and 24/(19·2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour. These molecules can be identical to bitertanol or slightly deviating and which is irrelevant as long as their natural periods are

24/(11·2 ¹⁵ ) hour and 24/(19·2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour. In order to avoid confusion molecules with natural periods 24/(11·2 ¹⁵ ) hour and 24/(19·2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour are called Fungicides in the present invention.

Drugs

Benzene (C ₆ H ₆ ), phenol (C ₆ H ₅ OH) and cyclohexhane (C ₆ H ₁₂ ) are six membered carbon ring molecules. They serve as important solvents and precursors in the production of drugs. These molecules create resonance and absorb electromagnetic energy at the period 24/(19·2 ¹⁴ ) hour (3.60Hz) and 24/(21·2 ¹⁴ ) hour (3.98 Hz). Drug molecular substances that contain one or many six membered carbon ring(s) have one thing in common; they create resonance and have the natural period 24/(19·2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour. In addition each type of drug create resonance at frequencies specific to the rest of the molecule, e.g. ebastin (3.22 Hz), xylometazoline (4.16 Hz, 4.27 Hz and 4.61 Hz). It can also be noted that the fungicide bitertanol contains two benzene groups and the insecticide phoxim contains one benzene group and that is the reason why bitertanol and phoxim create resonance at the period 24/(19-2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour.

Almost every investigated drug displayed the natural periods 24/(19·2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour, including imitinib (Novartis), everolimus (Novartis), sunitinib (Pfizer), acetylsalicylate acid Meda AB), paraceamol (GlaxoSmithKline), naproxen (Orion Pharma), ibuprofen (McNeil), diklofenak (Novartis), ebastin (Almiral), xylometazoline hydrochloride (Novartis), oximetazoline hydrochlorine

(GlaxoSmithKline), budesonide (AstraZeneca), salbutamol/albuterol (GlaxoSmithKline), mirtazapine (Mirtazapin Krka), sertraline (Sertraline Krka), Zolpidem (Zolpidemtartrat ratiopharm Gmbh) and roxithromycin (Chinese generica). Each of these 16 drugs was dissolved in water and was prevented from absorbing electromagnetic energy with the period 24/(19·2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour during 1 minute, using the apparatus according to claim 83. This displayed that the each drug was split into insoluble compounds (i.e. sediment); however, sometimes into soluble compounds.

The purpose with the present invention is to influence and/or to remove drugs with the natural period 24/(19·2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour. In order to avoid confusion molecules with natural periods 24/(19·2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour (but not 24/(11·2 ¹⁵ hour and not 24/(29·2 ¹⁴ ) hour, 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour) are called Drugs in the present invention. The inventor is aware that this may include molecules not classed as drugs; however, containing the six membered carbon ring. The implication is that such molecules can be influenced when influencing and/or removing drugs.

Nitrogen compounds (e.g. N0 ₂ , N0 ₃ , NH ₄ )

Nitrogen compounds (e.g. N0 ₂ , N0 ₃ , NH ₄ ) dissolved in water created resonance and absorbed electromagnetic energy at the period 24/(65·2 ¹³ ) hour (6.16 Hz). This was verified on nitrates found in fertilizers (NPK), on ammonia (NH ₄ , Nitor), on nitrates in mineral water and on nitrites, nitrates and ammonia in lake water (Malaren, Hjalmaren, Vanern, Vattern, Sjundasjon), Stockholm tap water, Baltic seawater and North seawater. Nitrites (N0 ₂ ) and nitrates (N0 ₃ ) ceased to dissolve whereby they evaporated (and some oxygen (0 ₂ ) dissolved in the water) when the water was prevented from absorbing electromagnetic energy with the period 24/(65·2 ¹³ ), using the apparatus according to claim 84.

Ammonium (NH ₄ ) was changed into a compound which created resonance and absorbed electromagnetic energy at the period 24/(11·2 ¹⁵ ) hour and 24/(63·2 ¹³ ) hour, when the water was prevented from absorbing electromagnetic energy with the period 24/(65·2 ¹³ ) hour, using the apparatus according to claim 84. This coincided with the natural periods of ammonium chloride (NH ₄ CI) and it is proposed that NH ₄ was changed into NH ₄ CI.

The apparatus according to claim 84 was submerged into the water (close to the shore) of lake

Sjundasjon during four days. This resulted in that all measured water ceased to create resonance at the period 24/(65·2 ¹³ ) hour. A slight increase in absorbed energy at the period 24/(11·2 ¹⁵ ) hour and 24/(63·2 ¹³ ) hour was observed. This experiment displays that it is possible to remove nitrites, nitrates and ammonium from a lake; however, with some increase in ammonium chloride. The ammonium chloride can be removed as described below.

Phosphates (e.g. P0 ₄ )

Phosphates as found in fertilizers (e.g. P0 ₄ , Ca(H ₂ P0 ₄ )) created resonance and absorbed

electromagnetic energy at the period 24/(35-2 ¹⁴ ) hour (6.64 Hz) and 24/(73-2 ¹³ ) hour (6.92 Hz). This was verified on fertilizers (NPK fertilizers), lake water (Malaren, Hjalmaren, Vanern, Vattern, Sjundasjon), Stockholm tap water, Baltic seawater and North seawater. Water samples were prevented from absorbing electromagnetic energy with the period 24/(35-2 ¹⁴ ) hour and 24/(73·2 ¹³ ) hour during 1 minute, using the apparatus according to claim 85. This resulted in that the phosphates were changed into other phosphorus compounds (described in Chemical element P) which created resonance at the period 24/(9·2 ¹⁶ ) hour and 24/(33·2 ¹⁴ ) hour and perhaps also changed into insoluble phosphorus compounds. It also resulted in an increase of dissolved oxygen (0 ₂ ). Carbon dioxide (C0 ₂ )

C0 ₂ (AGA, E290, gascode 4301) dissolved in water, liquid C0 ₂ contained in a bottle (AGA, E290, gascode 4301) and C0 ₂ exhaust from cars as well as C0 ₂ in human breath created resonance and absorbed electromagnetic energy at the period 24/(131·2 ¹² ) hour (6.21 Hz). Note that liquid C0 ₂ contained some water that created solvation shells and that C0 ₂ in exhaust also contained some water that created solvation shells. C0 ₂ was also found in lake water, Stockholm tap water, Baltic seawater and North seawater; however not in very acid lake water.

Experiments were performed on one liter of water that contained dissolved carbon dioxide (C0 ₂ ). The water solution was prevented from absorbing electromagnetic energy with the period

24/(131·2 ¹² ) hour during 1 minute, using the apparatus according to claim 86. This resulted in that the C0 ₂ molecule was split. One part formed sediment that consisted of carbon (or a carbon compound), and created resonance and absorbed electromagnetic energy the period 24/(71·2 ¹³ ) hour and 24/(73·2 ¹³ ) hour. This coincided with the natural periods of carbon (C). The other part evaporated and created resonance and absorbed electromagnetic energy with the period 24/(3·2 ¹⁷ ) hour and 24/(43·2 ¹³ ) hour. This coincided with the natural periods of oxygen (0 ₂ ) and it was assumed that this part consisted of oxygen (0 ₂ ). Some 0 ₂ dissolved in the water. The water solution ceased permanently to create resonance at the period 24/(131·2 ¹² ) hour.

Experiments were performed on a gas tube that contained approximately 10 % of the initial 0.66 kg C0 ₂ (AGA, E290, gascode 4301). The gas tube was prevented from absorbing electromagnetic energy with the period 24/(131·2 ¹² ) hour during 1 minute, using the apparatus according to claim 86. This displayed that the C0 ₂ molecule was split. One part formed sediment and consisted of carbon (or a carbon compound) and created resonance and absorbed electromagnetic energy with the period 24/(71-2 ¹³ ) hour and 24/(73·2 ¹³ ) hour. The other part remained evenly distributed in the bottle and created resonance and absorbed electromagnetic energy with the period 24/(3·2 ¹⁷ ) hour and 24/(43·2 ¹³ ) hour. This coincided with the natural periods of oxygen (0 ₂ ) and it was assumed that this part consisted of oxygen (0 ₂ ). The content of the bottle ceased permanently to create resonance at the period 24/(131·2 ¹² ) hour.

Experiments were performed on exhaust from cars. The exhaust was prevented from absorbing electromagnetic energy with the period 24/(131·2 ¹² ) hour, using the apparatus according to claim 86. This displayed that the C0 ₂ molecule was split. The exhaust created resonance and absorbed electromagnetic energy at the period 24/(3-2 ¹⁷ ) hour and 24/(43·2 ¹³ ) hour, assumingly created by oxygen (0 ₂ ). The exhaust ceased to create resonance with the period 24/(131·2 ¹² ) hour. However; measures must be taken which collects the carbon.

The apparatus according to claim 86 was submerged into the water (close to the shore) of lake Sjundasjon during 12 hours. This resulted in that all measured water in the lake ceased to create resonance at the period 24/(131·2 ¹² ) hour. A significant increase (approximately 3 times) in absorbed electromagnetic energy at the period 24/(3·2 ¹⁷ ) hour and 24/(43·2 ¹³ ) hour was observed, indicating increase in dissolved oxygen (0 ₂ ). This experiment displays that it is possible to remove carbon dioxide from a lake. Then the lake slowly absorbed carbon dioxide from the air (the surface water contained approximately 5 % of the initial C0 ₂ concentration after 24 hours). The process was repeated, resulting in renewed change of C0 ₂ into oxygen and carbon.

The apparatus according to claim 86 was submerged into the water (close to the shore) of an approximately 20 km ² large bay in the Baltic Sea during 24 hours. This resulted in that all measured water in the bay ceased to create resonance at the period 24/(131·2 ¹² ) hour. A significant increase (approximately 4 times) in absorbed energy at the period 24/(3·2 ¹⁷ ) hour and 24/(43·2 ¹³ ) hour was observed in surface water, indicating increase in dissolved oxygen (0 ₂ ). This experiment displays that it was possible to remove carbon dioxide from seawater. Then the bay slowly absorbed carbon dioxide from the air and from organisms (the surface water contained approximately 5 % of the initial C0 ₂ concentration after 48 hours).

Thus, it is possible to change carbon dioxide, present in the air, into oxygen and carbon, using water, lake water, seawater and oceans. The method can be used to reduce carbon dioxide in the atmosphere. The method can also be used to reduce carbon dioxide outlet from power plant exhaust, in one or two steps. The first step includes removal of C0 ₂ directly from the exhaust. In the second step the exhaust is fed, in a continuous process, through water whereby the C0 ₂ is changed into oxygen and carbon.

The mechanism behind photosynthesis and change of C0 ₂ into 0 ₂ in plants is not understood by science, probably because science expects to find a chemical process. However, the process is a dynamic electromagnetic process. Chlorophyll contains lead (Pb). One of the natural periods of lead is 24/(63·2 ¹² ) hour. Electromagnetic energy with the period 24/(63·2 ¹² ) hour creates electromagnetic interference and extinct electromagnetic energy with the period 24/(131·2 ¹² ) hour, i.e. the natural period of C0 ₂ . Thus, the electromagnetic process caused by lead contained in plant chlorophyll changes C0 ₂ into C and 0 ₂ . This was verified in the following experiments. A bottle containing C0 ₂ dissolved in water was positioned close to a pot plant. This changed the C0 ₂ into C and 0 ₂ . Note that the C0 ₂ was not in physical contact with the plant. Hence, the process was purely electromagnetic. In the second experiment a piece of lead was positioned in a bottle containing C0 ₂ dissolved in water; this changed the C0 ₂ into C and 0 ₂ . In the third experiment ammonium chloride (NH ₄ CI) was added to a bottle containing C0 ₂ dissolved in water. This resulted in that the C0 ₂ disappeared. One of the natural periods of NH ₄ CL is 24/(63·2 ¹² ) hour. In the fourth experiment sulfite (S0 ₂ ) was added to a bottle containing water and dissolved C0 ₂ . This resulted in that the C0 ₂ disappeared. One of the natural periods of S0 ₂ is 24/(63·2 ¹² ) hour. Selenium (Se) dissolved in water created similar electromagnetic interference and resulted in that dissolved C0 ₂ was changed into S and 0 ₂ .

In the following experiment a bottle containing C0 ₂ dissolved in water was prevented from absorbing electromagnetic energy with the period 24/(131·2 ¹² ) hour during one minute, using the apparatus according to claim 86. This resulted in that the C0 ₂ changed into dissolved C that absorbed electromagnetic energy with the periods 24/(71·2 ¹³ ) hour and 24/(73·2 ¹³ ) hour (i.e. the natural periods of C) and dissolved 0 ₂ that absorbed electromagnetic energy with the periods 24/(3·2 ¹⁷ ) hour and/or 24/(47·2 ¹³ ) hour (i.e. the natural periods of 0 ₂ ). A piece of zinc (Zn) was submerged into the solution. The zinc absorbed electromagnetic energy with its natural periods 24/(15·2 ¹⁵ ) hour and 24/(87·2 ¹² ) hour. Electromagnetic energy with the period 24/(15-2 ¹⁵ ) hour created electromagnetic interference with the period 24/(131·2 ¹² ) hour (i.e. natural period of 0 ₂ ) and with the period 24/(73·2 ¹³ ) hour (i.e. one natural period of C). Electromagnetic energy with the period 24/(87·2 ¹² ) hour created electromagnetic interference with the period 24/(71·2 ¹³ ) hour (i.e. the other natural period of C). This resulted in that C and 0 ₂ ceased to dissolve and whereby they formed the compound C0 ₂ . Then this C0 ₂ was changed into C and 0 ₂ using the apparatus according to claim 86. Then back to C and 0 ₂ by submerging the piece of zinc into the solution. This procedure was repeated 10 times, displaying that it was possible to change C and 0 ₂ into C0 ₂ and back to C and 0 ₂ probably any number of times. It is well known that the human organism contain zinc and measurements display that the body absorbs electromagnetic energy with the natural periods of zinc, and where the absorbed energy is distributed over the complete body. It is proposed that zinc serves as a catalyst when 0 ₂ is converted into C0 ₂ .

Sulfites (e.g. H ₂ S, S0 ₂ ) and sulfate (SO„)

Alcohol-water solutions that contained sulfites and sulfate created resonance and absorbed electromagnetic energy with the period 24/(17 ·2 ¹⁴ ) hour (3.22 Hz) and 24/(63·2 ¹³ ) hour (5.97 Hz). This type of resonance was found in cheap and medium prized red and white wine, labelled

"Contains sulfites". However, resonance at the period 24/(17·2 ¹⁴ ) hour and 24/(63·2 ¹³ ) hour was also found in expensive wines as well as in beer, cognac, whiskey, olive oil and vinegar.

Experiments performed on one liter of water containing dissolved sulfur dioxide (S0 ₂ ) were performed by preventing the water from absorbing electromagnetic energy with the period

24/(17·2 ¹⁴ ) hour and/or 24/(63·2 ¹³ ) hour during 1 minute, using the apparatus according to claim 87. This displayed that the S0 ₂ molecule was split, forming new compounds. One compound (or atom) drifted to the bottom as sediment (precipitate). This part consisted of sulfur (or a sulfur compound), and which created resonance and absorbed electromagnetic energy at the period 24/(11·2 ¹⁵ ) hour and 24/(21·2 ¹⁵ ) hour. This coincided with the natural periods of sulfur (S). The other compound drifted upwards. This part exhibited the natural periods of oxygen (0 ₂ ) dissolved in water with the period 24/(3·2 ¹⁷ ) hour (4.55 Hz) and 24/(43·2 ¹³ ) hour (4.08 Hz). Then this compound evaporated (and some remained dissolved). This procedure was repeated on a number of different wines, olive oils, vinegars, whiskeys, vodka and gin displaying that the S0 ₂ ceased to dissolve. It was concluded that the S0 ₂ had lost its ability to dissolve in the water, caused by a reaction. The experiment was repeated using wine with large content of H ₂ S, resulting in that the H ₂ S molecule was split and the sulfur (S) created sediment.

Experiments performed on one liter water that contained dissolved sulfate (S0 ) were performed by preventing the water from absorbing electromagnetic energy with the period 24/(17·2 ¹⁴ ) hour and/or 24/(63·2 ¹³ ) hour during 1 minute, using the apparatus according to claim 87. This displayed that the S0 ₄ molecule was split, forming new compounds. One compound (or atom) drifted to the bottom as sediment (precipitate). This part exhibited the natural periods of sulfur, and created resonance and absorbed electromagnetic energy at the period 24/(11·2 ¹⁵ ) hour and 24/(21·2 ¹⁵ ) hour. The other compound drifted upwards. This part exhibited the natural periods of oxygen (0 ₂ ) dissolved in water with the period 24/(3-2 ¹⁷ hour (4.55 Hz) and 24/(43·2 ¹³ ) hour (4.08 Hz). Then this compound evaporated (and some remained dissolved).

The above results were also achieved by exposing the water to high amplitude electromagnetic energy with the period 24/(17·2 ¹⁴ ) hour and/or 24/(63·2 ¹³ ) hour.

Removing sulfites from wine, olive oil, vinegar and whiskey significantly improved their taste. This was tested and confirmed by a number of persons as well as the founder and owner of a company importing Italian wine in Sweden as well as the founder and co-owner of one of Sweden's larger (private) wine importing companies as well as four wine producers in Italy and the professor in oneology at the University Polytechnica, Milano.

Storing the above processed wine bottles displayed that precipitate (S) remained on the bottom of the bottle. Investigating old wine (Brane Cantenac 1983, Vieux Telegraph 1985, Haut Bages 2007,

Schlossbokelheimer 2007 and Schloss Johannishof 2007) displayed that every bottle contained some dissolved sulfites. Young wines contained, without exception, higher sulfites content. Obviously, sulfite molecules in matured wine gradually changed into new insoluble compounds/chemical elements.

Mineral oil (Statoil), petrol (e.g. 95 octane Statoil) and petroleum products/distillates labeled (in Sweden) as Avfettning (Petrolia AB), Lack Nafta (Petrolia AB), Lampoil (AIIKemi) and Tandvatska (ICA AB) created resonance and absorbed electromagnetic energy with the period 24/(17-2 ¹⁴ ) hour and 24/(63·2 ¹³ ) hour. Adding 1 % water increased the amplitude of the absorbed current by a magnitude. It was concluded that these petroleum products contained low concentration of water and which in combination with S0 ₂ and/or S0 ₄ created resonance. Experiments were performed on 1 liter each of oil, petrol and petroleum distillates positioned in 10 liter containers and where the remaining 9 liters consisted of air. Subsequently each container was prevented from absorbing electromagnetic energy with the period 24/(17·2 ¹⁴ ) hour and/or 24/(63·2 ¹³ ) hour during 1 minute, using the apparatus according to claim 87, and positioned within the container. This displayed that the S0 ₂ and/or S0 ₄ was changed into probably S that created sediment and 0 ₂ that evaporated. The above results were also achieved by exposing the oil, petrol and petroleum distillates to high amplitude electromagnetic energy with the period 24/(17·2 ¹⁴ ) hour and/or 24/(63-2 ¹³ ). Consequently, it was possible to remove sulfites and/or sulfate from oil, petrol and petroleum distillates.

Gas (propane C ₃ H _8< AGA) created resonance and absorbed electromagnetic energy with the period the period 24/(17·2 ¹⁴ ) hour and 24/(63·2 ¹³ ) hour. This gas was prevented from absorbing electromagnetic energy with the period 24/(17·2 ¹⁴ ) hour and/or 24/(63-2 ¹³ ) hour during 1 minute, using the apparatus according to claim 87. This resulted in that sulfur (S) formed a sediment and the oxygen (0 ₂ ) floated. The above results were also achieved by exposing the gas to high amplitude electromagnetic energy with the period 24/(17-2 ¹⁴ ) hour and/or 24/(63·2 ¹³ ) hour. Consequently, it was possible to remove sulfites and/or sulfate from gas.

The above procedures and/or experiments were repeated using extinction of all energy, i.e. the water was prevented from creating any type of low frequency resonance. In that case the sulfites and S0 ₄ was not influenced and remained dissolved in the water. Consequently, sulfites and S0 ₄ was influenced when prevented from creating resonance at the period 24/(17-2 ¹⁴ ) hour and/or

24/(63·2 ¹³ ) hour and at the same time allowed or enforced to create resonance at a deviating period (e.g. the period 24/(13·2 ¹⁷ ) hour.

The above experiments were repeated on lake water, Stockholm tap water and Baltic seawater exhibiting presence of S0 ₂ and S0 ₄ and displaying that it was possible to permanently remove S0 ₂ and S0 ₄ .

The theory behind the environmental impact of sulfites and sulfate is explained in the present invention. C0 ₂ is changed into C and 0 ₂ and oxygen (0 ₂ ) ceases to dissolve in water in presence of sulfites and sulfate. Thus, the basis for life on earth (C0 ₂ and 0 ₂ ) is destroyed in presence of high concentration of sulfites and sulfate. That is the reason why acid lakes die, that is the reason why sulfites stop fermentation and preserve wine.

Ammonium chloride (NH ₄ CI)

Ammonium chloride (NH ₄ CI) dissolved in water created resonance and absorbed electromagnetic energy at the period 24/(11·2 ¹⁵ ) hour (4.17 Hz) and 24/(63·2 ¹³ ) hour (5.97 Hz). Ammonium chloride ceased to create resonance and ceased to absorb electromagnetic energy when the water solution was prevented from absorbing electromagnetic energy with the period 24/(11·2 ¹⁵ ) hourand

24/(63-2 ¹³ ) hour, using the apparatus according to claim 88.

Achieved results; summary

Chemistry has been successful in creating molecules that dissolve in water. This facilitates herbicides, insecticides, pesticides and fungicides that penetrate vegetables, fruits etc. It allows effective invasion of the target, i.e. plants, insects, bacteria, fungus, mold etc. It facilitates drugs that dissolve in human fluids and that effectively invade the target, i.e. pathogens, inflammations, cancer cells etc.

The backside is that these molecules and/or parts of these molecules remain dissolved in water, i.e. in food, in beverages, in ground water, in lakes and in seawater. When consumed the majority is dispelled with the urine; however, some is dissolved and transported by the blood to the brain and stopped by the brain-blood-barrier (BBB), whereby they accumulate in the brain. This causes an increasing chemical and electromagnetic interference in the brain. The present invention describes methods to remove these molecules from organisms, including animals and humans.

The natural state of ground water, lake water, seawater and water in advanced organisms is to have resonance at the period 24/(3·2 ¹⁷ ) hour (4.55Hz). One reason is that one natural period of sodium (Na) and oxygen (0 ₂ ) is 24/(3·2 ¹⁷ ) hour. The amount of oxygen (0 ₂ ) that can dissolve in water is proportional to the ability of water to create resonance and absorb electromagnetic energy at the period 24/(3·2 ¹⁷ ) hour.

Ground water, lakes and seawater exhibit increasing pollution from accumulated herbicides, insecticides, pesticides, fungicides, drugs, nitrates, ammonium, sulfites, sulfate and phosphates. These molecules create resonance at periods deviating from 24/(3·2 ¹⁷ ) hour, and which decreases the ability of water to create resonance at the period 24/(3·2 ¹⁷ ) hour. This results in that little oxygen can be dissolved. It increases the ability of algae to survive. It decreases the ability of other organisms, including many bacteria to survive.

Changing one parameter, e.g. removing herbicides, results in practically nothing. Changing many parameters provides dramatic results. Removing herbicides and insecticides and pesticides and fungicides and drugs and nitrates and ammonium and phosphates from lake water or seawater results in dramatic change in electromagnetic resonance and absorbed energy and where resonance at the period 24/(3·2 ¹⁷ ) hour increases dramatically (typically 5-20 times). 0 ₂ released from nitrates and phosphates can now dissolve resulting in large increase in dissolved 0 ₂ . This results in growth of bacteria and which dispel algae within weeks. The combination of chemical and electromagnetic processes can create a chain reaction that can restore vast amounts of water in months. Removing carbon dioxide (C0 ₂ ) from lakes and seawater results in an increase of dissolved oxygen (0 ₂ ).

However, it also results in that lakes and oceans can dissolve carbon dioxide present in the air and which will reduce carbon dioxide in the atmosphere. The present invention describes methods to clean drinking water, water reservoirs, sewage, industrial processes, rivers, lakes, the Baltic Sea and in principle oceans.

The present invention describes methods to remove sulfites and sulfate from acid lakes.

Food and beverages, including orange juice, olive oil, vinegar, wine and liquor contain a variety of herbicides, insecticides, pesticides, fungicides, antibiotics (in beef, pork, chicken) and sulfites. This is illustrated with wine and where most wines are polluted with herbicides, insecticides, pesticides, fungicides and sulfites. Changing one of these parameters (e.g. removing herbicides) results in insignificant change in taste. Removing all 5 results in dramatic change in taste. Removing these molecular substances from food, beverages and tap water results in improved taste and decreased brain pollution. The present invention describes methods to clean food and beverages at the source (at production) and/or during distribution and/or by the end customer.

The invention describes methods to remove dissolved phosphorus compounds resulting in that dissolved chemical elements can be removed from e.g. sewage or industrial processes.

The invention describes methods to influence dissolved phosphorus compounds in microbes resulting in that chemical elements are influenced which harms and/or kills microbes (e.g. bacteria, virus, fungal microbes).

The invention describes methods to remove sulfites and carbon dioxide at the source. It will be possible to produce energy from coal, oil and gas with only minor release of sulfur and carbon dioxide. It will have major environmental impact.

The invention describes methods to remove poisonous chemical elements from water and from humans and animals.

The invention describes methods to influence and remove chemical elements from microbes, including bacteria and pathogens, resulting in their death and diseases management.

The invention describes methods to influence chemical elements, compounds and molecules, resulting in fundamentally new ways of controlling chemical processes.

The invention describes methods to influence the outer molecular layers of metals and molecular substances resulting in novel ways to treat matter.

Brief Description of the Drawings

The invention will be described in more detail in the following, with reference to the appended drawings, in which:

Figure 1 describes an apparatus to remove chemical element.

Figure 2 describes an apparatus to remove chemical element.

Figure 3 describes the enclosure of the apparatus described in Figure 1 and Figure 2.

Figure 4 describes a method to remove chemical element,

Figure 5 describes a method to remove chemical element.

Figure 6 describes absorbed current by Al in the body as function of the time,

Figure 7 describes absorbed current by Cd in the body as function of the time,

Figure 8 describes absorbed current by Cu in the body as function of the time.

Figure 9 describes absorbed current by Pb in the body as function of the time.

Figure 10 describes absorbed current by Sn in the body as function of the time.

Description of the Invention

The object of this invention is to influence and/or remove a chemical element, compound molecule contained and/or dissolved in water. Said chemical element and said compound include all chemical elements and compounds that dissolve in water, including Ag, Al, As, Au, C, Ca, Cd, CI, Co, Cr, Cu, F, Fe, Ga, Hg, I, K, Li, Mg, Mn, Na, Nd, Ni, O, P, Pb, S, Se, Sn, Ti, Zn, V and W and their compounds.

Said molecule includes all types of molecules that dissolve in water. However, the invention describes in detail molecules that have environmental and health impact.

Said molecule includes herbicides (e.g. glyphosate, C ₃ H ₈ N0 ₅ P, N-(phosphonomethyl)glycine, 2- [(phosphonomethyl)amino]acetic acid and the CAS number 1071-83-6), and where the natural periods of said molecule are 24/(31·2 ¹⁴ ) hour and 24/(145·2 ¹² ) hour.

Said molecule includes insecticides A (e.g. imidacloprid, CgHxoCINsC , N-[l-[(6-Chloro-3- pyridyl)methyl]-4,5-dihydroimidazol-2-yl]nitramide and the CAS number 138261-41-3), and where the natural period of said molecule is 24/(81·2 ¹² ) hour.

Said molecule includes insecticides B (e.g. phoxim, C ₁₂ H ₁₅ N ₂ 0 ₃ PS, N-[(Diethoxyphosphorothioyl)oxy] benzenecarboximidoyl cyanide, and the CAS number 14816-18-3), and where the natural periods of said molecule are 24/(19-2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour and 24/(29·2 ¹⁴ ) hour and 24/(69·2 ¹³ ) hour and 24/(125·2 ¹² ) hour.

Said molecule includes pesticides (e.g. dioctyl sodium sulfosuccinate, C ₂ oH37Na0 ₇ S, sodium l,4-bis(2- ethylhexoxy)-l,4-dioxobutane-2-sulfonate, Aerosol OT, AOT, sodium bis(2-ethylhexyl) sulfosuccinate; docusate sodium, and the CAS number 577-11-7), and where the natural periods of said molecule are 24/(1·2 ¹⁹ ) hour and 24/(73-2 ¹³ ) hour and 24/(79·2 ¹³ ) hour.

Said molecule includes fungicides (e.g. bitertanol, sibutol, C ₂ oH ₂ 3N ₃ 0 ₂ , l-(biphenyll-4-yloxy)-3,3- dimethyl-l-(lH-l,2,4-triazol-l-yl)butan-2-ol, and the CAS number 55179-31-2), and where the natural periods of said molecule are 24/(11·2 ¹⁵ ) hour and 24/(19·2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour.

Said molecule includes drugs, antibiotics and hormones that use the six membered carbon ring and/or benzene (C ₆ H ₆ ) and/or phenol (C ₆ H ₅ 0H) and/or cyclohehane (C ₆ H ₁₂ ) as solvents and/or precursors (e.g. imitinib (Novartis), everolimus (Novartis), sunitinib (Pfizer), acetylsalicylate acid Meda AB), paraceamol (GlaxoSmithKline), naproxen (Orion Pharma, ibuprofen (McNeil), diklofenak (Novartis), ebastin Almiral), xylometazoline hydrochloride (Novartis), oximetazoline hydrochlorine (GlaxoSmithKline), budesonide (AstraZeneca), salbutamol/albuterol (GlaxoSmithKline), mirtazapine ( irtazapin Krka), sertraline (sertraline Krka), Zolpidem (Zolpidemtartrat ratiopharm Gmbh) and roxithromycin, and where the natural periods of said molecule are 24/(19·2 ¹⁴ ) hour and 24/(21·2 ¹⁴ ) hour.

Said molecule includes nitrogen compounds (e.g. N0 ₂ , N0 ₃ , NH ₄ ), and where the natural period of said molecule is 24/(65·2 ¹³ ) hour.

Said molecule includes phosphates (e.g. P0 ₄ , Ca(H ₂ P0 ₄ )), and where the natural periods of said molecule are 24/(35·2 ¹⁴ ) hour and 24/(73·2 ¹³ ) hour.

Said molecule includes carbon dioxide (C0 ₂ ), and where the natural period of said molecule is 24/(131·2 ¹² ) hour.

Said molecule includes sulfites (e.g. H ₂ S, S0 ₂ ) and sulfate (S0 ₄ ), and where the natural periods of said molecule are 24/(17·2 ¹⁴ ) hour and 24/(63·2 ¹³ ) hour. Said molecule includes ammonium chloride (NH ₄ CI), and where the natural periods of said molecule are 24/(11·2 ¹⁵ ) hour and 24/(63·2 ¹³ ) hour.

Said molecule includes sodium chloride (NaCI), and where the natural periods of said molecule are 24/(167·2 ¹² ) hourand 24/(173·2 ¹² ) hour.

The method is to stop and/or prevent said chemical element, compound or molecule from absorbing electromagnetic energy present in the air and in water, with the natural period or natural periods of said chemical element, compound or molecule. This is achieved by stopping electromagnetic energy with said natural period or said natural periods, +/- 1 %°, from propagating to and/or reaching said chemical element, compound or molecule. Said chemical element, compound or molecule can have one or many natural periods. Electromagnetic energy with all said natural periods must be stopped simultaneously from propagating to and/or reaching said chemical element. Stopping

electromagnetic energy with only one or two natural period(s) can sometimes influence said compound or molecule; however the preferred method is to simultaneously stop electromagnetic energy with all of said natural periods from propagating to and/or reaching said compound or molecule.

Said chemical element, compound or molecule can be dissolved as an ion and the present invention describes a method which causes a reaction where the product of the reaction is that the solute, i.e. said chemical element, compound or molecule, is insoluble in the solvent, i.e. said water, or the solubility of said solute is decreased. This type of reaction is sometimes called precipitation and the result is settling or sedimentation of said chemical element, compound or molecule. The precipitate or sediment can consist of atom or ion and/or metal and/or one or many compounds and/or salts. It facilitates removal and/or separation of said chemical element, compound or molecule from said water. Said product of the reaction can also be change of an ion into atom and/or metal and/or one or many compounds or into the same type of ion; however with change in characteristics (e.g. solvation shells). Said product of the reaction can also be that a compound or molecule is changed into one or many compounds and/or chemical elements or the same type of compound; however with change in characteristics (e.g. solvation shells). Said product of the reaction can also be that said chemical element, compound or molecule in humans and animals are released from their positions and transported by lymph and/or blood and removed with urine and/or excrements. Said product of the reaction can also be that said chemical element or compound is influenced and/or removed from microbes, including pathogens.

Said water include all types of water, all types of water solutions, all types of aqueous solutions, all types of water in industrial processes, all types of sewage, all types of water reservoirs, sea and lake water, all types of beverages and food. Said water include all types of water contained in all types of organisms and/or simpler life forms, including humans, animals, plants, insects, microbes, bacteria, fungal microbes, mold, virus, prions and all types of pathogens. Said water include H ₂ 0 molecules contained in coal, oil, petrol, all types of petroleum products and all types of petroleum distillates. Said water includes all types of H ₂ 0 + ion or molecule structures including the presence of all other types of atoms, compounds and molecules.

Coal, gas (e.g. in liquid form), oil, petrol and petroleum distillates and products contain chemical elements (e.g. lead) and molecules (e.g. S0 ₂ ) dissolved in H ₂ 0 molecules. Said method results in a reaction which changes the chemical element (e.g. ion) into insoluble atom and/or metal and/or compound and the S0 ₂ molecule into e.g. S and 0 ₂ . Thus part of said coal, gas, oil, petrol and petroleum distillates and products are an aqueous solution and are thus included in the present invention.

Air contains chemical elements, compounds and molecules dissolved in or surrounded by H ₂ 0 molecules. Said method results in a reaction which forms said chemical element, compound or molecule into insoluble atom, ion and/or metal and/or compound. Thus part of said air is an aqueous solution and is thus included in the present invention.

Preventing said chemical element, compound or molecule from absorbing said electromagnetic energy present in the air and in water, normally results in that said product of the reaction is achieved within one minute. However, the method can also be used during a longer time or continuously. Said product of the reaction (e.g. precipitate) normally drifts downward in said water and can preferably be removed and/or separated as sediment at the bottom of a container using different methods.

Said product of the reaction (chemical element and/or compound) can be removed and/or separated using decanting.

Said product of the reaction (chemical element and/or compound) can be removed and/or separated using filtering.

Said product of the reaction (chemical element and/or compound) can be removed and/or separated using centrifugation.

Said product of the reaction (chemical element and/or compound) can sometimes be removed and/or separated using evaporation.

Said chemical element, compound or molecule is removed in vivo with urine and excrements.

The method can be used or performed where only one selected chemical element or compound or molecule is selectively influenced and where other types of chemical elements, molecules, compounds, atoms, ions and/or metals are not influenced. This is achieved by simultaneously selecting all natural period(s) of the selected chemical element or compound or molecule. Thus, the method is non-invasive, except for its controlled and selective influence on the selected chemical element or compound or molecule.

The method can be used or performed in sequence by addressing any one of many types of chemical elements, compounds and/or molecules in sequence. This is achieved by selecting simultaneously all natural periods of the first chemical element or compound or molecule, then selecting

simultaneously all natural periods of the second chemical element or compound or molecule, etc. This is performed in sequence.

The method can be used or performed in parallel by simultaneously addressing any combination of many types of chemical elements, compounds and/or molecules in parallel. This is achieved by selecting simultaneously all natural periods of all addressed chemical elements, compounds and/or molecules in parallel.

The method can also be used simultaneously in sequence and in parallel.

One method to stop electromagnetic energy and/or current in the air and in water from propagating to said chemical element, compound or molecule is to disturb and/or cancel and/or to change the resonance in the air and/or in water using electromagnetic interference. This can be achieved using two, three or four passive forced damped oscillators, and which have natural periods equal to the natural period or natural periods of said chemical element, compound or molecule. The invention encompasses apparatus consisting of two, three, four or five passive forced damped oscillators (1), (2), (3) and (4) positioned with an angle (5) a (45° < a < 90°) and at a distance (6) of 0.1- 10 mm, and where said oscillators have the natural periods of said chemical element, compound or molecule. This is illustrated in Figure 1. Alternatively said oscillators can be positioned as illustrated in Figure 2. The copper conductor lengths according to Eq. (5) are listed below. Said oscillators can be positioned in the air whereby they create electromagnetic interference and this disturbs the resonance mechanism in air (i.e. the 3D matrix) and which stops resonance in the air (i.e. the 3D matrix) at said natural period or said natural periods. Thus, electromagnetic energy is prevented from propagating to said chemical element, compound or molecule and prevented from creating resonance in said water. This cancels electromagnetic energy and/or current close to the oscillators, typically within a radius of 5-10 meters; however, depending on the quality factor of the oscillators and the internal position of the oscillators, i.e. angle and distance.

The oscillators can also be submerged into said water containing said chemical element, compound or molecule or a solution or substance (e.g. oil, gas) containing said water and said chemical element, compound or molecule. This prevents said chemical element, compound or molecule from absorbing said electromagnetic energy present in the air and in water. This prevents said chemical element, compound or molecule and H ₂ 0 molecules in the solvation shells from creating resonance at said natural period or said natural periods. This results in that said chemical element, compound or molecule ceases to dissolve and/or to create resonance. This results in that water in this region looses its ability to create resonance at said natural period or said natural periods and which results in a chain reaction where adjacent chemical element, compound or molecule is influenced and which then results in a chain reaction covering a very large water volume or area. Experiments display that it was possible to remove one specific chemical element, compound or molecule from all water in a lake by submerging the below described oscillators (apparatus) at only one location during one week.

An alternative method is to inject electromagnetic energy with a frequency or period that creates electromagnetic interference with said natural period or said natural periods. A passive forced damped oscillator can produce the injected electromagnetic energy. This method is used in claim 90.

The forced damped oscillator can consist of a conductor. Resonance and a standing wave in the conductor occurs when its length is equal to one half wavelength, λ/2, or a multiple, i.e. (λ/2)· 2 ^q . A conductor with length L and current speed v (1.517 mm/s in copper) creates a standing wave and resonance at the natural period T:

L = (λ/2)·2 ^q = (T/2)-2 ^q -i/ , q = 0, 1, 2, 3, 4....10 (11)

Apparatus for Silver (Ag)

The apparatus for silver (Ag) consists of three oscillators (1), (2) and (3) with natural period T ₅ = 24/(5·2 ¹⁶ ) hour, T ₃₁ = 24/(31·2 ¹⁴ ) hour and T ₁₃₉ = 24/(139·2 ^η ) hour.

The invention encompasses oscillators with the natural period T ₅ = 24/(5·2 ¹⁶ ) hour. This is achieved using a copper conductor with the length L ₅ :

T ₅ = 24/(5·2 ¹⁶ ) hour (3.79 Hz), L ₅ = 24-60-60-i -2 ^q /(5-2-2 ¹⁶ ) -= 200 μηι (q = 0) or e.g. L ₅ = 3.20 mm (q = 4) or L ₅ = 6.40 mm (q = 5). The invention encompasses oscillators with the natural period T ₃₁ = 24/(31-2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L ₃₁ :

T ₃₁ = 24/(31-2 ¹⁴ ) hour (5.88 Hz), L ₃₁ = 24-60-60-v-2 ^q /(31-2-2 ¹⁴ ) = 129 μπ) (q = 0) or e.g. L ₃₁ = 4.13 mm (q = 5) or L ₃ i = 8.26 mm (q = 6).

The invention encompasses oscillators with the natural period Ti ₃₉ = 24/(139·2 ¹³ ) hour. This is achieved using a copper conductor with the length L ₁₃₉ :

Tug = 24/(139·2 ^η ) hour (3.29Hz), L ₁₃₉ = 24-60-60· i -2 ^q /(139-2-2 ⁿ ) = 230 μη\ (q = 0) or e.g. L ₁₃₉ = 3.68 mm (q = 4) or l_i ₃₉ = 7.37 mm (q = 5).

Apparatus for Aluminum (Al)

The apparatus for aluminum (Al) consists of two oscillators (1) and (2) with natural period T ₁₅ = 24/(15-2 ¹⁵ ) hour.

The invention encompasses oscillators with the natural period T ₁₅ = 24/(15-2 ¹⁵ ) hour. This is achieved using a copper conductor with the length Li ₅ :

Ti5 = 24/(15-2 ¹⁵ ) hour (5.69 Hz), L ₁₅ = 24-60-60-v-2 ^q /(15-2-2 ¹⁵ ) = 133 μηι (q = 0) or e.g. L ₁₅ = 4.27 mm (q = 5) or Us = 8.53 mm (q - 6).

Apparatus for Arsenic (As)

The apparatus for arsenic (As) consists of three oscillators (1), (2) and (3) with natural period T ₉ = 24/(9-2 ¹⁶ ) hour, T ₁₅ = 24/(15-2 ¹⁵ ) hour and T ₉₉ = 24/(99-2 ¹² ) hour.

The invention encompasses oscillators with the natural period T ₉ = 24/(9-2 ¹⁵ ) hour. This is achieved using a copper conductor with the length L ₉ :

T ₉ = 24/(9-2 ¹⁶ ) hour (6.83 Hz), L ₉ = 24-60-60-v-2 ^q /(9-2-2 ¹⁶ ) = 111 μηι (q = 0) or e.g. Lg = 3.56 mm (q = 5) or L ₉ = 7.11 mm (q = 6).

The invention encompasses oscillators with the natural period T ₁₅ = 24/(15-2 ¹⁵ ) hour. This is achieved using a copper conductor with the length L ₁₅ :

T ₁₅ = 24/(15-2 ¹⁵ ) hour (5.69 Hz), L ₁₅ = 24-60-60- v-2 ^q /(15-2-2 ¹⁵ ) = 133 μιη (q = 0) or e.g. L ₁₅ = 4.27 mm (q = 5) or Us = 8.53 mm (q = 6).

The invention encompasses oscillators with the natural period T ₉₉ = 24/(99-2 ¹² ) hour. This is achieved using a copper conductor with the length L ₉₉ :

T ₉₉ = 24/(99-2 ¹² ) hour (4.69 Hz), L ₉₉ = 24-60-60-v-2 ^q /(99-2-2 ¹² ) = 162 μηι (q = 0) or e.g. L ₉₉ = 5.17 mm (q = 5) or L ₉₉ = 10.34 mm (q = 6).

Apparatus for Gold (Au)

The apparatus for gold (Au) consists of two oscillators (1) and (2) with natural period T ₆₉ = 24/(69-2 ¹³ ) hour.

The invention encompasses oscillators with the natural period T ₆₉ = 24/(69-2 ¹³ ) hour. This is achieved using a copper conductor with the length L ₆₉ :

T ₅₉ = 24/(69-2 ¹³ ) hour (6.54 Hz), L ₆₉ = 24-60-60-i/-2 ^q /(69-2-2 ¹³ ) = 116 μπι (q = 0) or e.g. L ₆₉ = 3.71 mm (q = 5) or L ₆₉ = 7.42mm (q = 6). Apparatus for Carbon (C)

The apparatus for carbon (C) consists of two oscillators (1) and (2) with natural period T ₇₁ =

24/(71·2 ¹⁵ ) hour and T ₇₃ = 24/(73-2 ¹³ ) hour.

The invention encompasses oscillators with the natural period T ₇₁ = 24/(71·2 ¹⁵ ) hour. This is achieved using a copper conductor with the length L ₇₁ :

TTI = 24/(71·2 ¹³ ) hour (6.73 Hz), L ₇₁ = 24·60·60·ι/·2 ^ς /(71·2·2 ¹³ ) = 113μπι (q = 0) or e.g. L ₇₁ = 3.61 mm (q = 5) or L ₇ i = 7.21 mm (q = 6).

The invention encompasses oscillators with the natural period T ₇₃ = 24/(73-2 ¹³ ) hour. This is achieved using a copper conductor with the length L ₇₃ :

T ₇₃ = 24/(73·2 ¹³ ) hour (6.92 Hz), L ₇₃ = 24·60·60·ν·27(73·2·2 ¹³ ) = 110 μm (q = 0) or e.g. L ₇₃ = 3.51 mm (q = 5) or L ₇₃ = 7.01 mm (q = 6).

Apparatus for Cadmium (Cd)

The apparatus for cadmium (Cd) consists of two oscillators (1) and (2) with natural period T ₂ i = 24/(21·2 ¹⁴ ) hour and T ₄₁ = 24/(41·2 ¹³ ) hour.

The invention encompasses oscillators with the natural period T ₂₁ = 24/(21·2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L ₂ i:

T ₂₁ = 24/(21-2 ¹⁴ ) hour (3.98 Hz), L ₂₁ = 24·60·60·ι/·27(21·2·2 ¹⁴ ) = 190 μπι (q = 0) or e.g. L ₂₁ = 3.05 mm (q = 4) or L ₂₁ = 6.10 mm (q = 5).

The invention encompasses oscillators with the natural period T ₄₁ = 24/(41·2 ¹³ ) hour. This is achieved using a copper conductor with the length L _4i :

(q = 0) or e.g. L ₄ i = 3.12 mm (q

Apparatus for Chloride (CI)

The apparatus for chloride (CI) consists of two oscillators (1) and (2) with natural period T ₇₃ = 24/(73·2 ¹³ ) hour and T ₈₉ = 24/(89·2 ¹² ) hour.

The invention encompasses oscillators with the natural period T ₇₃ = 24/(73·2 ¹³ ) hour. This is achieved using a copper conductor with the length L ₇₃ :

T ₇₃ = 24/(73·2 ¹³ ) hour (6.92 Hz), L ₇₃ = 24·60·60·ν·27(73·2·2 ¹³ ) = 110 μηη (q = 0) or e.g. L ₇₃ = 3.51 mm (q = 5) or L ₇₃ = 7.01 mm (q = 6).

The invention encompasses oscillators with the natural period T ₈₉ = 24/(89·2 ¹² ) hour. This is achieved using a copper conductor with the length L ₈₉ :

T ₈₉ = 24/(89-2 ¹² ) hour (4.22 Hz), L ₈₉ = 24·60·60·ι/·27(89·2·2 ¹² ) = 180 μηι (q = 0) or e.g. L ₈₉ = 2.88 mm (q = 5) or L ₈₉ = 5.75 mm (q = 5).

Apparatus for Cobalt (Co)

The apparatus for cobalt (Co) consists of two oscillators (1) and (2) with natural period T ₁₇ = 24/(17·2 ¹⁴ ) hour and T ₂₃ = 24/(23·2 ¹⁵ ) hour. The invention encompasses oscillators with the natural period T ₁₇ = 24/(17·2 ¹⁴ ) hour. This is achieved using a copper conductor with the length l ₁₇ :

T ₁₇ = 24/(17·2 ¹⁴ ) hour (3.22 Hz), L ₁₇ = 24·60·60·ι/·27(17·2·2 ¹⁴ ) = 235 μπι (q = 0) or e.g. l ₁₇ = 3.76 mm (q = 4) or I_i7 = 7.54 mm (q = 5).

The invention encompasses oscillators with the natural period T ₂₃ = 24/(23·2 ¹⁵ ) hour. This is achieved using a copper conductor with the length L ₂₃ :

T ₂₃ = 24/(23·2 ¹⁵ ) hour (8.72 Hz), L ₂₃ = 24·60·60·ι/·2Υ(23·2·2 ¹⁵ ) = 87 μηι (q = 0) or e.g. L ₂₃ = 5.57 mm (q = 6) or L ₂₃ = 11.13 mm (q = 7).

Apparatus for Chromium (Cr)

The apparatus for chromium (Cr) consists of three oscillators (1), (2) and (3) with natural period T ₃ = 24/(3-2 ¹⁷ ) hour, T _n = 24/(11·2 ¹⁵ ) hour and T ₇₁ = 24/(71·2 ¹³ ) hour.

The invention encompasses oscillators with the natural period T ₃ = 24/(3·2 ¹⁷ ) hour. This is achieved using a copper conductor with the length L ₃ :

T ₃ = 24/(3·2 ¹⁷ ) hour (4.55Hz), L ₃ = 24-60-60 i -2 ^q /(3-2-2 ¹⁷ ) = 167 μη (q = 0) or e.g. L ₃ = 5.33 mm (q = 5) or L ₃ = 10.67 mm (q = 6).

The invention encompasses oscillators with the natural period T = 24/(11·2 ¹⁵ ) hour. This is achieved using a copper conductor with the length L _u :

Tu = 24/(ll-2 ¹⁵ ) hour (4.17 Hz), L _n = 24·60·60·ι/·27(11·2·2 ¹⁵ ) = 181 μηι (q = 0) or e.g. L _u = 2.91 mm (q = 4) or Lai = 5.82 mm (q = 5).

The invention encompasses oscillators with the natural period T ₇₁ = 24/(11·2 ¹⁵ ) hour. This is achieved using a copper conductor with the length L :

T ₇₁ = 24/(71·2 ¹³ ) hour (6.73 Hz), L _7i = 24·60·60·ι/·27(71·2·2 ¹³ ) = 113μηι (q = 0) or e.g. L ₇₁ = 3.61 mm (q = 5) or L ₇ i = 7.21 mm (q = 6).

Apparatus for Copper (Cu)

The apparatus for copper (Cu) consists of two oscillators (1) and (2) with natural period T ₇₃ = 24/(73·2 ¹³ ) hour and T ₈₃ = 24/(83·2 ¹³ ) hour.

The invention encompasses oscillators with the natural period T ₇₃ = 24/(73·2 ¹³ ) hour. This is achieved using a copper conductor with the length L ₇₃ :

T ₇₃ = 24/(73-2 ¹³ ) hour (6.92 Hz), L ₇₃ = 24·60·60·ν·27(73·2·2 ¹³ ) = 110 μηη (q = 0) or e.g. L ₇₃ = 3.51 mm (q = 5) or L ₇₃ = 7.01 mm (q = 6).

The invention encompasses oscillators with the natural period T ₈₃ = 24/(83·2 ¹³ ) hour. This is achieved using a copper conductor with the length L ₈₃ :

T ₈₃ = 24/(83·2 ¹³ ) hour (7.87Hz), L ₈₃ = 24·60·60-ι ·27(83·2·2 ¹³ ) = 96 μιτι (q = 0) or e.g. L ₈₃ = 3.08 mm (q = 5) or L ₈₃ = 6.17 mm (q = 6).

Apparatus for Fluoride (F)

The apparatus for fluoride (F) consists of two oscillators (1) and (2) with natural period T ₃ = 24/(3·2 ¹⁷ ) hour and T ₅ = 24/(5·2 ¹⁷ ) hour. The invention encompasses oscillators with the natural period T ₃ = 24/(3·2 ¹⁷ ) hour. This is achieved using a copper conductor with the length L ₃ :

T ₃ = 24/(3·2 ¹⁷ ) hour (4.55Hz), L ₃ = 24-60-60 v-2 ^q /(3-2-2 ¹⁷ ) = 167 μπι (q = 0) or e.g. L ₃ = 5.33 mm (q = 5) or L ₃ = 10.67 mm (q = 6).

The invention encompasses oscillators with the natural period T ₅ = 24/(5·2 ¹⁷ ) hour. This is achieved using a copper conductor with the length L ₅ :

T ₅ = 24/(5-2 ¹⁷ ) hour (7.59 Hz), L ₅ = 24·60·60·ι ·27(5·2·2 ¹⁷ ) = 100 urn (q = 0) or e.g. L ₅ = 3.20 mm (q = 5) or L ₅ = 6.40 mm (q = 6).

Apparatus for Iron (Fe)

The apparatus for iron (Fe) consists of three oscillators (1), (2) and (3) with natural period T ₅ = 24/(5·2 ¹⁶ ) hour, T ₇ = 24/(7·2 ¹⁶ ) hour and T ₉ = 24/(9·2 ¹⁵ ) hour.

The invention encompasses oscillators with the natural period T ₅ = 24/(5·2 ¹⁷ ) hour. This is achieved using a copper conductor with the length L ₅ :

T ₅ = 24/(5-2 ¹⁵ ) hour (3.79 Hz), L ₅ = 24·60·60·ν·27(5·2·2 ¹⁷ ) = 200 urn (q = 0) or e.g. L ₅ = 3.20 mm (q = 4) or L ₅ = 6.40 mm (q = 5).

The invention encompasses oscillators with the natural period T ₇ = 24/(7·2 ¹⁶ ) hour. This is achieved using a copper conductor with the length L ₇ :

T ₇ = 24/(7-2 ¹⁶ ) hour (5.31 Hz), L ₇ = 24·60·60·ν·27(7·2·2 ¹⁶ ) = 143 μηι (q = 0) or e.g. L ₇ = 4.57 mm (q = 5) or L ₇ = 9.14 mm (q = 6).

The invention encompasses oscillators with the natural period T ₉ = 24/(9·2 ¹⁵ ) hour. This is achieved using a copper conductor with the length L ₉ :

T ₉ = 24/(9·2 ¹⁵ ) hour (3.41 Hz), L ₉ = 24·60·60·ν·27(9·2·2 ¹⁵ ) = 222 μιτι (q = 0) or e.g. L ₉ = 3.56 mm (q = 4) or Lg = 7.11 mm (q = 5).

Apparatus for Gallium (Ga)

The apparatus for gallium (Ga) consists of two oscillators (1) and (2) with natural period Ti =

24/(1·2 ¹⁹ ) hour and T ₇ = 24/(7·2 ¹⁶ ) hour.

The invention encompasses oscillators with the natural period T _x = 24/(1·2 ¹⁹ ) hour. This is achieved using a copper conductor with the length U:

Ti = 24/(l-2 ¹⁹ ) hour (6.07 Hz), L _{1 =} 24·60·60·ι ·27(1·2·2 ¹⁹ ) = 125 μνη (q = 0) or e.g. U = 4.00 mm (q = 5)

The invention encompasses oscillators with the natural period T ₇ = 24/(7·2 ¹⁶ ) hour. This is achieved using a copper conductor with the length L ₇ :

T ₇ - 24/(7·2 ¹⁶ ) hour (5.31 Hz), L ₇ = 24·60·60·ν·27(7-2·2 ¹⁶ ) = 143 μπι (q = 0) or e.g. L ₇ = 4.57 mm (q = 5) or L ₇ = 9.14 mm (q = 6).

Apparatus for Mercury (Hg)

The apparatus for mercury (Hg) consists of four oscillators (1), (2), (3) and (4) with natural period T ₁ = 24/(l-2 ¹⁸ ) hour, T ₉ = 24/(9-2 ¹⁵ ) hour, T ₄₅ = 24/(45·2 ¹⁴ ) hour and T ₇₁ = 24/(71·2 ¹³ ) hour. The invention encompasses oscillators with the natural period Ti = 24/(1·2 ¹⁸ ) hour. This is achieved using a copper conductor with the length U:

T _j = 24/(1·2 ¹⁸ ) hour (3.03 Hz), U= 24·60·60 ν·27(1·2·2 ¹⁸ ) = 250 μm (q = 0) or e.g. U = 4.00 mm (q = 4) or U = 8.00 mm (q = 5).

The invention encompasses oscillators with the natural period T ₉ = 24/(9·2 ¹⁵ ) hour. This is achieved using a copper conductor with the length L ₉ :

T ₉ = 24/(9·2 ¹⁵ ) hour (3.41 Hz), L ₉ = 24·60·60 ι ·27(9·2·2 ¹⁵ ) = 222 μηι (q = 0) or e.g. L, = 3.56 mm (q = 4) or L ₉ = 7.11 mm (q = 5).

The invention encompasses oscillators with the natural period T ₄₅ = 24/(45·2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L45:

T ₄₅ = 24/(45·2 ¹⁴ ) hour (8.53 Hz), U ₅ = 2.84 mm (q = 5) or U ₅ = 5.69 mm (q = 6).

The invention encompasses oscillators with the natural period T _7i = 24/(11·2 ¹⁵ ) hour. This is achieved using a copper conductor with the length L ₇ i:

T ₇₁ = 24/(71·2 ¹³ ) hour (6.73 Hz), L ₇₁ = 24·60·60·ν·27(71·2·2 ¹³ ) = 113μιτι (q = 0) or e.g. l ₇₁ = 3.61 mm (q = 5) or L ₇₁ = 7.21 mm (q = 6).

Apparatus for Iodine (I)

The apparatus for iodine (I) consists of three oscillators (1), (2) and (3) (with natural period T ₇ = 24/(7·2 ¹⁶ ) hour, T ₁₉ = 24/(19·2 ¹⁵ ) hour and T ₃₃ = 24/(33-2 ¹⁴ ) hour.

The invention encompasses oscillators with the natural period T ₇ = 24/(7·2 ¹⁶ ) hour. This is achieved using a copper conductor with the length L ₇ :

T ₇ = 24/(7·2 ¹⁶ ) hour (5.31 Hz), L ₇ = 24·60·60·ι ·27(7·2·2 ¹⁶ ) = 143 m (q = 0) or e.g. L ₇ = 4.57 mm (q = 5) or L ₇ = 9.14 mm (q = 6).

The invention encompasses oscillators with the natural period T ₁₉ = 24/(19·2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L ₁₉ :

T ₁₉ 0) or e.g. L ₁₉ = 3.37 mm (q = 4) or Li ₉ = 6.74 mm (q = 5).

The invention encompasses oscillators with the natural period T ₃₃ = 24/(33·2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L ₃₃ :

T ₃₃ = 24/(33·2 ¹⁴ ) hour (6.26 Hz), L ₃₃ = 24·60·60·ι ·27(33·2·2 ¹⁴ ) = 121 μπι (q = 0) or e.g. L ₃₃ = 3.88 mm (q = 5) or L ₃₃ = 7.76 mm (q = 6)

Apparatus for Magnesium (Mg)

The apparatus for magnesium (Mg) consists of two oscillators (1) and (2) with natural period T! = 24/(1·2 ¹⁹ ) hour and T ₅ = 24/(5-2 ¹⁶ ) hour.

The invention encompasses oscillators with the natural period T _x = 24/(1·2 ¹⁹ ) hour. This is achieved using a copper conductor with the length U:

Ti = 24/(1·2 ¹⁹ ) hour (6.07 Hz), L _{1 =} 24·60·60·ι/·27(1·2·2 ¹⁹ ) = 125 μηη (q = 0) or e.g. U = 4.00 mm (q = 5) or Li = 8.00 mm (q = 6). The invention encompasses oscillators with the natural period T ₅ = 24/(5·2 ¹⁶ ) hour. This is achieved using a copper conductor with the length L ₅ :

T ₅ = 24/(5·2 ¹⁵ ) hour (3.79 Hz), L ₅ = 24·60·60·ι/·2Υ(5·2·2 ¹⁶ ) = 200 pm (q = 0) or e.g. L ₅ = 3.20 mm (q = 4) or L ₅ = 6.40 mm (q = 5).

Apparatus for Manganese (Mn)

The apparatus for manganese (Mn) consists of two oscillators (1) and (2) with natural period T ₇ = 24/(7·2 ¹⁶ ) hour and T _3S = 24/(35·2 ¹⁴ ) hour.

The invention encompasses oscillators with the natural period T ₇ = 24/(7·2 ¹⁶ ) hour. This is achieved using a copper conductor with the length L ₇ :

T ₇ = 24/(7·2 ¹⁶ ) hour (5.31 Hz), L ₇ = 24·60·60·ι/·2 ^ς /(7-2·2 ¹⁶ ) = 143 μηη (q = 0) or e.g. L ₇ = 4.57 mm (q = 5) or L ₇ = 9.14 mm (q = 6).

The invention encompasses oscillators with the natural period T ₃₅ = 24/(35·2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L ₃₅ :

T ₃₅ = 24/(35·2 ¹⁴ ) hour (6.64 Hz), L ₃₅ = 24·60·60·ι/·2Υ(35·2·2 ¹⁴ ) = H4 μπι (q = 0) or e.g. L ₃₅ = 3.66 mm (q = 5) or L ₃₅ = 7.31 mm (q = 6).

Apparatus for Sodium (Na)

The apparatus for sodium (Na) consists of three oscillators (1), (2) and (3) with natural period T ₃ = 24/(3-2 ¹⁷ ) hour, T ₄₃ = 24/(43·2 ¹³ ) hour and T ₁₂₉ = 24/(129·2 ¹² ) hour.

The invention encompasses oscillators with the natural period T ₃ = 24/(3·2 ¹⁷ ) hour. This is achieved using a copper conductor with the length L ₃ :

T ₃ = 24/(3-2 ¹⁷ ) hour (4.55Hz), L ₃ = 24-60-60-v2 ^q /(3-2-2 ¹⁷ ) = 167 pm (q = 0) or e.g. L ₃ = 5.33 mm (q = 5) or L ₃ = 10.67 mm (q = 6).

The invention encompasses oscillators with the natural period T ₄₃ = 24/(43-2 ¹³ ) hour. This is achieved using a copper conductor with the length U ₃ :

T ₄₃ = 24/(43·2 ¹³ ) hour (4.08 Hz), U ₃ = 24-60-60-i/-2 ^q /(43-2-2 ¹³ ) = 186 μηι (q = 0) or e.g. Us = 2.98 mm (q = 4) or L43 = 5.95 mm (q = 5).

The invention encompasses oscillators with the natural period T ₁₂₉ = 24/(129·2 ¹² ) hour. This is achieved using a copper conductor with the length L ₁₂₉ :

T ₁₂₉ = 24/(129·2 ¹² ) hour (6.12 Hz), L ₁₂₉ = 24-60-60-v2 ^q /(129-2-2 ¹² ) = 124 μηι (q = 0) or e.g. L ₁₂₉ = 3.97 mm (q = 5) or L ₁₂₉ = 7.94 mm (q = 6).

Apparatus for Nickel (Ni)

The apparatus for nickel (Ni) consists of two oscillators (1) and (2) with natural period T ₂₁ =

24/(21-2 ¹⁵ ) hour and T ₁₂₁ = 24/(121·2 ¹² ) hour.

The invention encompasses oscillators with the natural period T ₂₁ = 24/(21·2 ¹⁵ ) hour. This is achieved using a copper conductor with the length L ₂₁ :

T ₂ i = 24/(21·2 ¹⁵ ) hour (7.96 Hz), L ₂₁ = 24·60·60·ι/·2Υ(21·2·2 ¹⁵ ) = 95 μιη (q = 0) or e.g. L ₂₁ = 3.05 mm (q = 5) or L ₂₁ = 6.10 mm (q = 6). The invention encompasses oscillators with the natural period T _m = 24/(121·2 ¹² ) hour. This is achieved using a copper conductor with the length Li ₂ i:

Ti2i = 24/(121·2 ¹² ) hour (5.74 Hz), L ₁₂₁ = 24·60·60·ι/·27(121·2·2 ¹² ) = 132 μm (q = 0) or e.g. L ₁₂₁ = 4.23 mm (q = 5) or i _m = 8.46 mm (q = 6).

Apparatus for Phosphorus (P)

This apparatus consists of two oscillators (1) and (2) with natural period T ₉ = 24/(9·2 ¹⁶ ) hour and T ₃₃ = 24/(33-2 ¹⁴ ) hour. It influences phosphorus compounds (e.g. PI, P4, H ₃ P0 ₄ )

The invention encompasses oscillators with the natural period T ₉ = 24/(9·2 ¹⁶ ) hour. This is achieved using a copper conductor with the length L ₉ :

T ₉ = 24/(9·2 ¹⁶ ) hour (6.83 Hz), L ₉ = 24·60·60·ι ·2 ^ς /(9·2·2 ^1θ ) = 111 μηι (q = 0) or e.g. L ₉ = 3.56 mm (q = 5) or L ₉ = 7.11 mm (q = 6).

The invention encompasses oscillators with the natural period T ₃₃ = 24/(33·2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L ₃₃ :

T ₃₃ = 24/(33·2 ¹⁴ ) hour (6.26 Hz), L ₃₃ = 24-60-60-i -2 ^q /(33-2-2 ¹⁴ ) = 121 μπι (q = 0) or e.g. L ₃₃ = 3.88 mm (q = 5) or L ₃₃ = 7.76 mm (q = 6)

Apparatus for Lead (Pb)

The apparatus for lead (Pb) consists of two oscillators (1) and (2) with natural period T ₅ = 24/(5·2 ¹⁶ ) hour and T ₆₃ = 24/(63·2 ¹² ) hour.

The invention encompasses oscillators with the natural period T ₅ = 24/(5·2 ¹⁶ ) hour. This is achieved using a copper conductor with the length L ₅ :

T ₅ = 24/(5·2 ¹⁶ ) hour (3.79 Hz), L ₅ = 24-60-60-v2 ^q /(5-2-2 ¹⁶ ) = 200 μπι (q = 0) or e.g. L ₅ = 3.20 mm (q = 4) or L ₅ = 6.40 mm (q = 5).

The invention encompasses oscillators with the natural period T ₆₃ = 24/(63·2 ¹² ) hour. This is achieved using a copper conductor with the length L ₅₃ :

T ₆₃ = 24/(63·2 ¹² ) hour (2.99 Hz), L ₆₃ = 24-60-60 v -2 ^q /(63-2-2 ¹² ) = 254 μιη (q = 0) or e.g. L ₆₃ = 4.06 mm (q = 4) or L ₆₃ = 8.13 mm (q = 5).

Apparatus for Tin (Sn)

The apparatus for tin (Sn) consists of three oscillators (1), (2) and (3) with natural period T _x = 24/(1·2 ¹⁸ ) hour, T ₉ = 24/(9·2 ¹⁶ ) hour and T ₁₇ = 24/(17-2 ¹⁵ ) hour.

The invention encompasses oscillators with the natural period T _! = 24/(1·2 ¹⁸ ) hour. This is achieved using a copper conductor with the length U:

Tj = 24/(1·2 ¹⁸ ) hour (3.03 Hz), L _{1 =} 24-60-60-v2 ^q /(l-2-2 ¹⁸ ) = 250 μηι (q = 0) or e.g. U = 4.00 mm (q = 4) or Li = 8.00 mm (q = 5).

The invention encompasses oscillators with the natural period T ₉ = 24/(9·2 ¹⁶ ) hour. This is achieved using a copper conductor with the length L ₉ :

T ₉ = 24/(9·2 ¹⁶ ) hour (6.83 Hz), L ₉ = 24·60·60·ι ·2Υ(9·2·2 ¹⁶ ) = 111 μηι (q = 0) or e.g. L ₉ = 3.56 mm (q = 5) or L ₉ = 7.11 mm (q = 6). The invention encompasses oscillators with the natural period T ₁₇ = 24/(17·2 ¹⁵ ) hour. This is achieved using a copper conductor with the length L ₁₇ :

Ti7 = 24/(17-2 ¹⁵ ) hour (6.45 Hz), L ₁₇ = 24-60-60· v2 ^q /(17-2-2 ¹⁵ ) = 118 im (q = 0) or e.g. L ₁₇ = 3.76 mm (q = 5) or L _i7 = 7.53 mm (q = 6).

Apparatus for Vanadium (V)

The apparatus for vanadium (V) consists of three oscillators (1), (2) and (3) with natural period T ₉ = 24/(9·2 ¹⁶ ) hour T ₃₃ = 24/(33·2 ¹⁴ ) hour and T ₄₃ = 24/(43·2 ¹³ ) hour.

The invention encompasses oscillators with the natural period T ₉ = 24/(9-2 ¹⁶ ) hour. This is achieved using a copper conductor with the length L ₉ :

T ₉ = 24/(9-2 ¹⁶ ) hour {6.83 Hz), L ₉ = 24-60-60-v-2 ^q /(9-2-2 ¹⁶ ) = ill _μΓ η (q = 0) or e.g. L ₉ = 3.56 mm (q = 5) or L ₉ = 7.11 mm (q = 6).

The invention encompasses oscillators with the natural period T ₃₃ = 24/(33·2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L ₃₃ :

= 121 μηι (q = 0) or e.g. L ₃₃ = 3.88 mm (q = 5) or L ₃₃ = 7.76 mm (q = 6)

The invention encompasses oscillators with the natural period T ₄₃ = 24/(43·2 ¹³ ) hour. This is achieved using a copper conductor with the length U ₃ :

T ₄₃ = 24/(43·2 ¹³ ) hour (4.08 Hz), L, ₃ = 24-60-60-i -2 ^q /(43-2-2 ¹³ ) = 186 μπι (q = 0) or e.g. U ₃ = 2.98 mm (q = 5) or L43 = 5.95 mm (q = 6).

Apparatus for Tungsten (W)

The apparatus for tungsten (W) consists of two oscillators (1) and (2) with natural period T ₇ = 24/(7·2 ¹⁶ ) hour and T ₇₃ = 24/(73·2 ¹³ ) hour.

The invention encompasses oscillators with the natural period T ₇ = 24/(7-2 ¹⁶ ) hour. This is achieved using a copper conductor with the length L ₇ :

T ₇ = 24/{7·2 ¹⁶ ) hour (5.31 Hz), L ₇ = 24·60·60·ν·2 ^ς /(7·2·2 ¹⁶ ) = 143 \xm (q = 0) or e.g. L ₇ = 4.57 mm (q = 5) or L ₇ = 9.14 mm (q = 6).

The invention encompasses oscillators with the natural period T ₇₃ = 24/(73·2 ¹³ ) hour. This is achieved using a copper conductor with the length L ₇₃ :

T ₇₃ = 24/(73·2 ¹³ ) hour (6.92 Hz), L ₇₃ = 24-60-60-v2 ^q /(73-2-2 ¹³ ) = no μηι (q = 0) or e.g. L ₇₃ = 3.51 mm (q = 5) or L ₇₃ = 7.01 mm (q = 6).

Apparatus for e.g. Herbicides

This apparatus consists of two oscillators (1) and (2) with natural period T _3i = 24/(31-2 ¹⁴ ) and Τ _Μ5 = 24/(145-2 ¹² ) hour. It includes herbicides (e.g. glyphosate, C ₃ H ₈ N0 ₅ P).

The invention encompasses oscillators with the natural period T ₃₁ = 24/(31·2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L ₃₁ :

T ₃ i = 24/(31·2 ¹⁴ ) hour (5.88 Hz), L ₃₁ = 24-60-60-i -2 ^q /(31-2-2 ¹⁴ ) = 129 μηι (q = 0) or e.g. L ₃₁ = 4.13 mm (q = 5) or L ₃₁ = 8.26 mm (q = 6). The invention encompasses oscillators with the natural period T ₁₄₅ = 24/(145·2 ¹² ) hour. This is achieved using a copper conductor with the length L ₁₄₅ :

T ₁₄₅ = 24/(145·2 ¹² ) hour (6.87 Hz), L ₁₄₅ = 24-60-60-v-2 ^q /(145-2-2 ¹² ) = 110 pm (q = 0) or e.g. L ₁₄₅ = 3.53 mm (q = 5) or L _M5 = 7.06 mm (q = 6).

Apparatus for e.g. Insecticides A

This apparatus consists of two oscillators (1) and (2) with natural period T ₈ i = 24/(81-2 ¹² ) hour. It includes insecticides A (e.g. imidacloprid, C ₉ H ₁₀ CIN ₅ O ₂ ).

The invention encompasses oscillators with the natural period T ₈₁ = 24/(81-2 ¹² ) hour. This is achieved using a copper conductor with the length L ₈ i:

T ₈₁ = 24/(81·2 ¹² ) hour (3.84 Hz), L ₈ i= 24·60·60·ι/·27(81·2-2 ¹² ) = 196 pm (q = 0) or e.g. L ₈ i = 3.16 mm (q = 4) or L ₈₁ = 6.32 mm (q = 5).

Apparatus for e.g. Insecticides B

This apparatus consists of five oscillators (1), (2) (3), (4) and (5) with natural period T ₁₉ = 24/(19·2 ¹⁴ ) hour, T ₂₁ = 24/(21·2 ¹⁴ ) hour, T ₂₉ = 24/(29·2 ¹⁴ ) hour, T ₆₉ = 24/(69·2 ¹³ ) hour and T ₁₂₅ = 24/(125·2 ¹² ) hour. It includes insecticides B (e.g. phoxim Ci ₂ H ₁₅ N ₂ 0 ₃ PS).

The invention encompasses oscillators with the natural period T ₁₉ = 24/(19-2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L ₁₉ :

T ₁₉ = 24/(19·2 ¹⁴ ) hour (3.60 Hz), L ₁₉ = 211 pm (q - 0) or e.g. L ₁₉ = 3.37 mm (q = 4) or Li ₉ = 6.74 mm (q = 5).

The invention encompasses oscillators with the natural period T ₂₁ = 24/(21·2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L _2i :

T ₂₁ = 24/(21·2 ¹⁴ ) hour (3.98 Hz), L ₂₁ = 24-60-60 i -2 ^q /(21-2-2 ¹⁴ ) = 190 pm (q = 0) or e.g. L ₂₁ = 3.05 mm (q = 4) or L ₂ i = 6.10 mm (q = 5).

The invention encompasses oscillators with the natural period T ₂₉ = 24/(29·2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L ₂₉ :

T ₂₉ = 24/(29·2 ¹⁴ ) hour (5.50 Hz), L ₂₉ = 24-60-60-v2 ^q /(29-2-2 ¹⁴ ) = 138 pm (q - 0) or e.g. L ₂₉ = 4.41 mm (q = 5) or L ₂₉ = 8.83 mm (q = 6).

The invention encompasses oscillators with the natural period T ₆₉ = 24/(69·2 ^1Β ) hour. This is achieved using a copper conductor with the length L ₆₉ :

T ₆₉ = 24/(69-2 ¹³ ) hour (6.54 Hz), L ₇₃ = 24-60·60·ι ·2 ^ς /(69·2·2 ¹³ ) = 116 μπι (q = 0) or e.g. L ₆₉ = 3.71 mm (q = 5) or L ₆₉ = 7.42 mm (q = 6).

The invention encompasses oscillators with the natural period T ₁₂₅ = 24/(125·2 ¹² ) hour. This is achieved using a copper conductor with the length L ₁₂₅ :

T ₁₂₅ = 24/(125·2 ¹² ) hour (5.93 Hz), L ₁₂₅ = 24·60·60·ν·2"/(125·2·2 ¹² ) = 128 pm (q = 0) or e.g. L ₁₂₅ = 4.10 mm (q = 5) or L ₁₂₅ = 8.20 mm (q = 6).

Apparatus for e.g. Pesticides This apparatus consists of three oscillators (1), (2) and (3) with natural period. Ti = 24/(1·2 ¹⁹ ) hour, T ₇₃ = 24/(73·2 ¹³ ) hour and T ₇₉ = 24/(79·2 ¹³ ) hour. It influences pesticides (e.g. dioctyl sodium

sulfosuccinate, C20H37NO7S).

The invention encompasses oscillators with the natural period T _! = 24/(l-2 ¹⁹ ) hour. This is achieved using a copper conductor with the length U:

Ti = 24/(1·2 ¹⁹ ) hour (6.07 Hz), = 24-60-60-v-2 ^q /(l-2-2 ¹⁹ ) = 125 pm (q - 0) or e.g. = 4.00 mm (q = 5) or U = 8.00 mm (q = 6).

The invention encompasses oscillators with the natural period T ₇₃ = 24/(73-2 ¹³ ) hour. This is achieved using a copper conductor with the length L ₇₃ :

T ₇₃ = 24/(73-2 ¹³ ) hour (6.92 Hz), L ₇₃ = 24-60-60-v-2 ^q /(73-2-2 ¹³ ) = 110 μηι (q = 0) or e.g. L ₇₃ = 3.51 mm (q = 5) or L ₇₃ = 7.01 mm (q = 6).

The invention encompasses oscillators with the natural period T ₇₉ = 24/(79-2 ¹³ ) hour. This is achieved using a copper conductor with the length L ₇₉ :

T ₇₉ = 24/(79-2 ¹³ ) hour (7.49 Hz), L ₇₉ = 24-60-60-v2 ^q /(79-2-2 ¹³ ) = 101 pm (q = 0) or e.g. L ₇₉ = 3.24 mm (q = 5) or L ₇₉ = 6.48 mm (q = 6).

Apparatus for e.g. Fungicides

This apparatus consists of three oscillators (1), (2) and (3) with natural period. T _n = 24/(ll-2 ¹⁵ ) hour, T ₁₉ = 24/(19-2 ¹⁴ ) hour and T ₂₁ = 24/(21-2 ¹⁴ ) hour. It influences fungicides (e.g. bitertanol, C ₂ oH2 ₃ N ₃ 02).

The invention encompasses oscillators with the natural period T _n = 24/(ll-2 ¹⁵ ) hour. This is achieved using a copper conductor with the length Ln:

Tn = 24/(ll-2 ¹⁵ ) hour (4.17 Hz), L _n = 24-60-60-v2 ^q /(ll-2-2 ¹⁵ ) = 182 μπι (q = 0) or e.g. l _n = 2.91 mm (q= 4) or L _n = 5.82 mm (q = 5).

The invention encompasses oscillators with the natural period T ₁₉ = 24/(19-2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L ₁₉ :

T ₁₉ = 24/(19-2 ¹⁴ ) hour (3.60 Hz), L ₁₉ = 24-60-60-v-2 ^q /(19-2-2 ¹⁴ ) = 211 pm (q = 0) or e.g. L _M = 3.37 mm (q = 4) or L ₁₉ = 6.74 mm (q = 5).

The invention encompasses oscillators with the natural period T ₂₁ = 24/(21-2 ¹⁴ ) hour. This is achieved using a copper conductor with the length l ₂ i.

T ₂₁ = 24/(21-2 ¹⁴ ) hour (3.98 Hz), L ₂₁ = 24-60-60-i -2 ^q /(21-2-2 ¹⁴ ) = 190 pm (q = 0) or e.g. l ₂₁ = 3.05 mm (q = 4) or L _2X = 6.10 mm (q = 5).

Apparatus for Drugs, antibiotics and hormones

This apparatus consists of two oscillators (1) and (2) with natural period T _i9 = 24/(19-2 ¹⁴ ) hour and T ₂ i = 24/(21-2 ¹⁴ ) hour. It influences drug, antibiotic and hormone molecular substances that contain the six membered carbon ring structure.

The invention encompasses oscillators with the natural period T ₁₉ = 24/(19-2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L ₁₉ :

Tig = 24/(19-2 ¹⁴ ) hour (3.60 Hz), L ₁₉ = 24-60-60-v-2 ^q /(19-2-2 ¹⁴ ) = 211 pm (q = 0) or e.g. L ₁₉ = 3.37 mm (q = 4) or L ₁₉ = 6.74 mm (q = 5). The invention encompasses oscillators with the natural period T ₂ i = 24/(21·2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L ₂ i:

T ₂₁ = 24/(21·2 ¹⁴ ) hour (3.98 Hz), L ₂₁ = 24-60-60 v2 ^q /(21-2-2 ¹⁴ ) = 190 μηι (q = 0) or e.g. L ₂₁ = 3.05 mm (q = 4) or L79 = 6.10 mm (q = 5).

Apparatus for Nitrogen compounds

This apparatus consists of two oscillators (1) and (2) with natural period T ₆₅ = 24/(65·2 ¹³ ) hour. It influences nitrogen compounds (e.g. N0 ₂ , N0 ₃ , NH ₄ ).

The invention encompasses oscillators with the natural period T ₆₅ = 24/(65·2 ¹³ ) hour. This is achieved using a copper conductor with the length L ₆₅ :

T ₆₅ = 24/(65·2 ¹³ ) hour (6.16 Hz), L ₆₅ = 24-60-60 v2 ^q /(65-2-2 ¹³ ) = 123 pm (q = 0) or e.g. L ₆₅ = 3.94 mm (q = 5) or L ₆₅ = 7.88 mm (q = 6).

Apparatus for Phosphates

This apparatus consists of two oscillators (1) and (2) with natural period T ₃₅ = 24/(35·2 ¹⁴ ) hour and T ₇₃ = 24/(73-2 ¹³ ) hour. It influences phosphates (e.g. P0 ₄ , Ca(H ₂ P0 ₄ ).

The invention encompasses oscillators with the natural period T ₃₅ = 24/(35·2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L ₃₅ :

T ₃₅ = 24/(35·2 ¹⁴ ) hour (6.64 Hz), L ₃₅ = 24-60-60-v2 ^q /(35-2-2 ¹⁴ ) = 114 pm (q = 0) or e.g. L ₃₅ = 3.66 mm (q = 5) or L ₃₅ = 7.31 mm (q = 6).

The invention encompasses oscillators with the natural period T ₇₃ = 24/(73-2 ¹³ ) hour. This is achieved using a copper conductor with the length L ₇₃ :

T ₇₃ = 24/(73·2 ¹³ ) hour (6.92 Hz), L ₇₃ = 24-60-60 t -2 ^q /(73-2-2 ¹³ ) = 110 μηι (q = 0) or e.g. L ₇₃ = 3.51 mm (q = 5) or L ₇₃ = 7.01 mm (q = 6).

Apparatus for Carbon Dioxide

This apparatus consists of two oscillators (1) and (2) with natural period T _m = 24/(131-2 ¹² ) hour. It influences carbon dioxide (C0 ₂ ).

The invention encompasses oscillators with the natural period T ₁₃₁ = 24/(131·2 ¹² ) hour. This is achieved using a copper conductor with the length L ₁₃₁ :

½ = 24/(131-2 ¹² ) hour (6.21 Hz), L ₁₃₁ = 24-60-60-v-2 ^q /(131-2-2 ¹² ) = 122 im (q = 0) or e.g. L ₁₃₁ = 3.91 mm (q = 5) or L _m = 7.82 mm (q = 6).

Apparatus for Sulfites and Sulfate

This apparatus consists of two oscillators (1) and (2) with natural period T _i7 = 24/(17·2 ¹⁴ ) hour and T ₆₃ = 24/(63·2 ¹³ ) hour. It influences sulfites (e.g. H ₂ S, S0 ₂ ) and sulfate (S0 ₄ ).

The invention encompasses oscillators with the natural period T ₁₇ = 24/(17·2 ¹⁴ ) hour. This is achieved using a copper conductor with the length L _i7 :

T ₁₇ = 24/(17·2 ¹⁴ ) hour (3.22 Hz), L ₁₇ = 24-60-60-v2 ^q /(17-2-2 ¹⁴ ) = 235 μιη (q = 0) or e.g. L ₁₇ = 3.76 mm (q = 4) or L ₁₇ = 7.53 mm (q = 5). The invention encompasses oscillators with the natural period T ₆₃ = 24/(63·2 ¹³ ) hour. This is achieved using a copper conductor with the length L ₅₃ :

T ₆₃ = 24/(63·2 ¹³ ) hour (5.97 Hz), L ₆₃ = 24-60-60 i -2 ^q /(63-2-2 ¹³ ) = 127 μπι (q = 0) or e.g. L ₆₃ = 4.06 mm (q = 5) or L ₆₃ = 8.13 mm (q = 6).

Apparatus for Ammonium Chloride (NH ₄ CI)

This apparatus consists of two oscillators (1) and (2) with natural period Tn = 24/(ll-2 ¹⁵ ) hour and T ₆₃ = 24/(63·2 ¹³ ) hour. It influences ammonium chloride (NH ₄ CI).

The invention encompasses oscillators with the natural period T _n = 24/(11·2 ¹⁵ ) hour. This is achieved using a copper conductor with the length L :

Tu = 24/(ll-2 ¹⁵ ) hour (4.17 Hz), L _n = 24·60·60·ν·27(11·2·2 ¹⁵ ) = 182 μη\ (q = 0) or e.g. L _n = 2.91 mm (q = 4) or Lu = 5.82 mm (q = 5).

The invention encompasses oscillators with the natural period T ₆₃ = 24/(63·2 ¹³ ) hour. This is achieved using a copper conductor with the length L ₆₃ :

T ₆₃ = 24/(63·2 ¹³ ) hour (5.97 Hz), L ₆₃ = 24·60·60·ι/·27(63·2·2 ¹³ ) = 127 μηη (q = 0) or e.g. L ₆₃ = 4.06 mm (q = 5) or L ₆₃ = 8.13 mm (q = 6).

Apparatus for Sodium Chloride (NaCI)

This apparatus consists of two oscillators (1) and (2) with natural period T ₁₆₇ = 24/(167-2 ¹² ) hour and Ti73 = 24/(173·2 ¹² ) hour. It influences sodium chloride (NaCI).

The invention encompasses oscillators with the natural period T ₁₆₇ = 24/(167 ·2 ¹² ) hour. This is achieved using a copper conductor with the length L ₁₆₇ :

T ₁₆₇ = 24/(167·2 ¹² ) hour (7.92 Hz), L ₁₆₇ = 24-60-60 v2 ^q /(167-2-2 ¹² ) = 96 μηι (q = 0) or e.g. L ₁₆₇ = 3.07 mm (q = 5) or Li ₆ = 6.13 mm (q = 6).

The invention encompasses oscillators with the natural period T _i73 = 24/(173-2 ¹² ) hour. This is achieved using a copper conductor with the length L ₁₇₃ :

Ti73 = 24/(173·2 ¹² ) hour (8.20 Hz), L ₁₇₃ = 24·60·60·ν·27(173·2·2 ¹² ) = 92 xm (q = 0) or e.g. L ₁₇₃ = 2.96 mm (q = 5) or L _i73 = 5.92 mm (q = 6).

Apparatus for Sulfites, Herbicides, Insecticides A, Insecticides B, Pesticides, Fungicides and Drugs

Extinction of electromagnetic energy can also be achieved by electromagnetic interference where electromagnetic energy at one period interferes with electromagnetic energy at a large number of other periods. Thus, extinction of electromagnetic energy at a large number of periods is achieved with only one oscillator. This apparatus consists of one oscillator (1) with natural period Ti ₈₉ =

24/(189·2 ¹² ) hour. This oscillator extinct electromagnetic energy with the natural periods of sulfites and herbicides and insecticides A and insecticides B and pesticides and fungicides and drugs, and it influences any one of these molecular substances.

The invention encompasses oscillators with the natural period T _:89 = 24/(189·2 ¹² ) hour. This is achieved using a copper conductor with the length L ₁₈₉ :

T ₁₈₉ = 24/(189·2 ¹² ) hour (8.96 Hz), L ₁₈₉ = 24·60·60·ι/·27(189·2·2 ¹² ) = 85 μιη (q = 0) or e.g. L ₁₈₉ = 5.42 mm (q = 6) or L ₁₈₉ = 10.84 mm (q = 7). The accuracy in all conductor lengths is preferably +/- 1%-

The invention encompasses apparatus where the oscillators are preferably manufactured using printed circuit board (PCB) technique. The oscillators can be mounted in an enclosure (7), illustrated in Figure 3. The enclosure contains 1-10 holes (8), with approximately 1-4 mm diameter, which allows air or water (or oil or gas) and its positive ions to enter the enclosure. Positive ions are a prerequisite for proper function of said oscillators. As an option the enclosure can be supplied with different types of fastening devices. Said fastening devices include any device which fastens the enclosure to objects, humans, animals or clothes including screws, leash, strap, harness, band and/or belt.

Said enclosure (7) can consist of e.g. plastic and in which case the oscillators are always "active", i.e. they influence resonance in air and in water and can be used in air and in water.

A multiple of apparatus can be used in large industrial processes or when covering large areas or volumes. The methods and apparatus can be employed continuously (e.g. in continuous industrial processes, cleaning of sewage, water reservoirs and lakes) or during a limited time, e.g. < 1 minute in order to remove chemical elements, compounds and molecules from food, beverages and humans. The apparatus can be positioned in the air close (< 5 m) to said water including industrial processes, food, beverages, humans, animals and microbes. The apparatus can be positioned in the pocket, in the purse, fastened or positioned on an object, a table etc. Any position within 5 m from the human, animal, microbes or water is possible.

The apparatus can be positioned in said water and where said oscillators are in direct contact with said water, including industrial processes, sea water, lake water, wells, aqueous solutions, oil and gas (containing H ₂ 0 molecules).

One example is removing e.g. cadmium, lead, herbicides, insecticides, pesticides, fungicides and sulfites during olive oil production. This can be performed in the steal container (e.g. 10-50 hi) during the production phase, i.e. the oscillators (apparatus) are submerged into the olive oil inside the container (during a few minutes).

A second example is removing e.g. herbicides, insecticides, pesticides and fungicides during wine production. This can be performed in the steal container (e.g. 10-50 hi) during the fermentation phase, i.e. the oscillators (apparatus) are submerged into the wine inside the container (during a few minutes).

A third example is removing e.g. lead and/or S0 ₂ from crude oil in which case one or many oscillators (apparatus) are submerged into the oil tank, e.g. on a ship or a storage tank.

A fourth example is removing chemical elements, herbicides, insecticides, pesticides, fungicides, sulfites, carbon dioxide, nitrates and/or phosphates from sewage, water reservoirs, wells, rivers, lakes and seawater and in which case the oscillators (apparatus) are submerged into the water. This creates a chain reaction and which removes the addressed chemical elements, compounds and molecules in all water, e.g. in a lake.

An alternative is to position said apparatus (7) in a metal container (9) (e.g. steel, iron, aluminum, copper) containing air and where said water (10) is positioned in the container and in the air inside the container as illustrated in Figure 4. This often yields a better result, i.e. the extinction of electromagnetic energy at said natural period(s) is more effective. In addition it has the advantage that no extinction of electromagnetic energy occurs outside the container, i.e. the environment outside the container is not influenced. This container can have any size and a multitude of said apparatus (7) or other means to extinct said energy.

One example is removing herbicides, insecticides, pesticides, fungicides, antibiotics and sulfites from wine, beverages, drink water and food in domestic (home) use. In this case the size of the container is preferably 1-5 liters, and the oscillators (apparatus) are positioned in the air within the container. The wine bottle, beverages/water contained in a bottle or a glass or food is positioned in the container during < 1 minute. Instead of using many apparatus according to claims 78-83 and claim 87 only one apparatus according to claim 90 can be used. The apparatus according to claim 90 includes drugs, resulting in that antibiotic in meat, pork and chicken is influenced as well.

Said water can also be processed in a continuous process where said water (11) is continuously transported through a container (9), as illustrated in Figure 5. This container can have any size and a multitude of apparatus (7) or other means to extinct electromagnetic energy. One example is removing lead and S0 ₂ from gas, oil and petrol in which case the container size can be e.g. 1000 m ³ .

The method is non-invasive, i.e. nothing is added to water, aqueous solutions, food, beverages, humans and animals.

Said chemical element, compound or molecule can also be influenced and/or removed by exposing said water to electromagnetic energy with one or many of the natural periods of said chemical element, compound or molecule, preferably +/- 1 · However, the amplitude must be significantly higher (approximately 10 times) than the amplitude of the corresponding electromagnetic energy present in the air or in water. This creates resonance in the solvation shells; however, the amplitude of this resonance is so high that the solvation shells are destroyed, resulting in a reaction that creates atom(s), ion(s) and/or metal and/or one or many compounds. The correct amplitude is adjusted empirically and depends on the type of water solution and its volume as well as the type of chemical element, compound or molecule. Too high amplitude destroys resonance in all of said water, whereby said chemical element, compound or molecule is not influenced. Said chemical element, compound or molecule and the solvation shells can also create resonance at a natural frequency (i.e. natural period) deviating from the period 24/(m-2 ⁿ ) hour. Said chemical element, compound or molecule creates resonance when exposed to electromagnetic energy with said natural frequency, resulting in that they form insoluble atom(s), ion(s) and/or metal and/or one or many compounds. Thus, the invention encompasses said natural frequencies, referred to as "one or many of the natural frequencies of said chemical element, compound or molecule" in claim 1 and claim 48. Exposing a chemical element, compounds or molecule to electromagnetic energy, according to this method, normally results in a reaction within one minute. However, the method can also be used during a longer time or continuously. This method is invasive and should therefore, preferably, not be used in vivo. It is among others suitable for large volume application, e.g. removing said chemical element, compound or molecule from crude oil or sewage.

This method can be illustrated with the following experiment where a container (9) with 1.5 liter volume was used, see Figure 4. A coaxial cable was connected to the container; the shield to the container and 5 cm of the inner conductor was exposed inside the container (i.e. as an electrode). The coaxial cable was connected to a signal generator. A bottle (10) containing a chemical element, dissolved in 1 liter water (containing 150 mM NaCI), was positioned inside the container. This experiment revealed that the chemical element was influenced and created precipitate when the signal generator voltage U was typically 0.1 mV < U < 5 mV (RMS); however, depending somewhat on the type of chemical element and the natural period or natural frequency used. Voltage below 0.1 mV resulted in no reaction, probably because the amplitude was too low to cause disturbance in the solvation shells. Voltage above 5 mV resulted in no reaction occurred, probably because resonance was enforced in all water.

Figure 6 displays results obtained on a human containing aluminum (Al) when electromagnetic energy with said natural period was prevented from propagating to the human using the apparatus according to claim 55. Graph (12) displays the absorbed current in the brain at the period 24/(15·2 ¹⁵ ) hour, as function of the time when electromagnetic energy with the period 24/(15·2 ¹⁵ ) hour was prevented from propagating to the human. Graph (12) shows that approximately 80 % of the aluminum was located to the brain, while the remaining aluminum was located to the rest of the body.

Figure 7 displays results obtained on a human containing cadmium (Cd) when electromagnetic energy with said natural periods were prevented from propagating to the human using the apparatus according to claim 59. Graph (13) displays the absorbed current in the brain at the period 24/(21·2 ¹⁴ ) hour, as function of the time when electromagnetic energy with the period 24/(21-2 ¹⁴⁾ hour and 24/(41-2 ¹³ ) hour were prevented from propagating to the human. Graph (13) shows that

approximately 80 % of the cadmium was located to the brain, while the remaining cadmium was located to the rest of the body.

Figure 8 displays results obtained on a human containing copper (Cu) when electromagnetic energy with said natural periods were prevented from propagating to the human using the apparatus according to claim 63. Graph (14) displays the absorbed current in the brain at the period 24/(73-2 ¹³ ) hour, as function of the time when electromagnetic energy with the period 24/(73·2 ¹³ ) hour and 24/(83·2 ¹³ ) hour were prevented from propagating to the human. Graph (14) shows that

approximately 40 % of the copper was located to the brain, while the remaining copper was located to the rest of the body.

Figure 9 displays results obtained on a human containing lead (Pb) when electromagnetic energy with said natural periods were cancelled or prevented from propagating to the human using the apparatus according to claim 74. Graph (15) displays the absorbed current in the brain at the period 24/(5·2 ¹⁶ ) hour, as function of the time when electromagnetic energy with the period 24/(5·2 ¹⁶ ) hour and 24/(63·2 ¹² ) hour were prevented from propagating to the human. Graph (15) shows that approximately 60 % of the lead was located to the brain, while the remaining lead was located to the rest of the body and primarily to the spine.

Figure 10 displays results obtained on a human containing tin (Sn) when electromagnetic energy with said natural periods were cancelled or prevented from propagating to the human using the apparatus according to claim 75. Graph (16) displays the absorbed current in the body at the period 24/(1·2 ¹⁸ ) hour, as function of the time when electromagnetic energy with the period 24/(1·2 ¹⁸ ) hour and 24/(9-2 ¹⁶ ) hour and 24/(17·2 ¹⁵ ) hour were prevented from propagating to the human. Tin was distributed to the whole body.

The present invention displays that some chemical elements, which are considered toxic, create resonance and absorb electromagnetic energy in vitro, in situ and in vivo. In vivo these toxic elements accumulate in the human body. The reason may be that this resonance enhances their bonds to water. The present invention describes a method to remove these toxic elements from the human body, from industrial processes, from sewage, from drinking water, from food and beverages. It also facilitates effective control of chemical elements in sensitive industrial and medical processes. The following chemical elements are considered toxic; Ag, Al, As, Cd, Co (in large concentration), Cr, Cu (in large concentration), F, Hg, Pb and Sn. The present invention facilitates removal of extremely low concentration (i.e. down to one ion) of said chemical element in humans, in industrial processes, in tap water and in sewage.

The invention describes silver because humans sometimes contain relatively large amount of silver, one reason may be that silver is used as a food additive in Europe (e.g. E174) and in some dental filling compounds. Safety aspects of silver are disputed. The method also allows extraction or production of silver from water. Cobalt and copper are important trace metals in miniscule amounts; however, toxic in large concentration. Some humans display very high concentration of cobalt (probably from cobalt in pottery) and copper (probably from coffee brewers and copper piping).

The invention allows extraction or production of gold and rare chemical elements from water.

The invention facilitates influence of the outer layers of a metal or a chemical element structure or a compound or a molecular structure, wherein the outer layers change and cease to create resonance and to absorb electromagnetic energy at said natural period or said natural periods. The invention can be used to treat and/or to change the outer layers or surface of metals and molecular structures in numerous ways. The invention can among others be used to prevent leakage of a chemical element from a metal surface. One example is to treat the surface of aluminum cans containing beverages (beer, soda, Coca Cola), wherein the can ceases to leak aluminum. This treatment can be performed using the apparatus according to claim 55 during 1 minute. Another example is vinyl chloride. Vinyl chloride creates resonance and absorbs electromagnetic energy at the period 24/(71·2 ¹³ ) hour and 24/(73·2 ¹³ ) hour, probably caused by carbon. Thus, clothes that contain vinyl chloride absorb electromagnetic energy and which can have health effects. Preventing vinyl chloride from absorbing electromagnetic energy with the period 24/(71·2 ¹³ ) hour and 24/(73-2 ¹³ ) hour (e.g. during one minute), using the apparatus according to claim 58, changes the outer molecular layers of the vinyl chloride, whereby it permanently ceases to absorb electromagnetic energy at the period 24/(71-2 ¹³ ) hour and 24/(73·2 ¹³ ) hour.

Olive oil, olives, grapes and vinegar often contain chemical elements (e.g. aluminum, lead, nickel, zinc and copper). Thus, the producer or the distributor or the consumer can remove dissolved chemical elements from food and beverages or convert soluble chemical elements into insoluble chemical elements and/or compounds. This improves the taste and contributes to health effects.

Wine and alcoholic beverages contain, almost without exception, metals such as Al, Cd, Cu, Ni, Pb and Zn in small concentration (i.e. less than 10 μg/l). This may seem harmless; however, it creates electromagnetic resonance and absorbs electromagnetic energy and which disturbs the human taste receptors. Removing these chemical elements, using the present invention, can improve the taste. However, chemical elements often contribute to taste, i.e. the terroire of wine.

The theory presented in the present invention was confirmed by measurements made on wine. Young wine always displayed presence of one or many dissolved chemical elements, primarily lead and aluminum, but also copper, nickel and zinc, verified by XRF made in Sweden and in Italy. These dissolved chemical elements absorbed electromagnetic energy at their natural periods. Mature wine displayed few dissolved metals; however, they exhibited lead, aluminum, copper, nickel and/or zinc as atoms and/or compounds positioned as precipitate or sediment. This was valid for the following wine; Brunello di Montalcino, Argano, 1981, Brane Cantenac 1983, Vieux Telegraph 1985, Haut Bages 2007, Schlossbokelheimer 2007 and Schloss Johannishof 2007). Obviously the aging process in mature wine influenced dissolved chemical elements. In matured wine they ceased to dissolve. It is proposed that the present invention creates similar type of aging within minutes.

Mineral oil (Classicway, Statoil), petrol (95 octane, Statoil), gas (propane/C ₃ H ₈ , AGA) and petroleum distillates (Avfettning, Petrolia AB, Lacknafta, Petrolia AB and Tandvatska, ICA) contained traces of lead (approximately 1 Lead in these products was removed using the present invention and apparatus according to claim 74. Thus, the present invention includes removal of lead and other chemical elements from oil, gas and petroleum products.

Microbes and pathogens (e.g. bacteria, virus, fungal microbes and mold) contain chemical elements, among others Ag, As, C, Ca, Cd, Cr, F, Fe, Ga, Hg, I, Mg, Mn, P, Pb, Se, Sn, V and W. Examples are the bacteria lactobacillus reuteri which contains C and Pb, lactobacillus rhamnosus which contains C and W, pathogenic legionella bacteria which contains C and I, anaerobic bacteria metano sarsino which contain C and Se, DMD (Duchene Muscular Dystrophy) which contains C and Sn, some flu virus which contains C and V and some flu virus which contains C and W and virus in some warts which contains C and Fe. The microbe absorbs electromagnetic energy with the natural periods of these chemical elements, e.g. flu virus with the natural periods of carbon (C) and vanadium (V). The present invention allows selective influence of said chemical element and influence on selected types of microbes and pathogens. This can be performed in a wide area (e.g. in sewage) or within in a limited area (e.g. in humans), and where the chemical element is influenced and/or removed from the microbe, resulting in that the microbe ceases to absorb electromagnetic energy at the natural periods of the chemical element. This can be achieved by applying the methods and apparatus according to claims 1- 77 during approximately five minutes repeated every 12 hour during less than two weeks. However, it is also possible to apply these methods and apparatus during a longer time as well as continuously. This has negative influence on said microbes and pathogens, and which results in microbe and pathogen destruction. It can also result in that the selected microbe is exposed to assault from other microbes, leading to microbe extinction. It also prevents pathogens in vivo from absorbing electromagnetic energy whereby this energy ceases to disturb human biological processes (e.g. the immune defense). Influencing and removing only carbon (C) results in death of microbes and pathogens in most cases. This facilitates a broad-spectrum use and effective disease management without the need of exact analyzes of pathogen type. The invention includes the method to influence any one of the two chemical elements contained in many microbes (e.g. for flu C or V) or both (e.g. for flu C and V).

Many organisms including microbes need oxygen to survive. Removing oxygen kills microbes.

Experiments were performed on legionella bacteria (in water) displaying that legionella bacteria died within one minute when oxygen (0 ₂ ) was removed from water using the method according to claim 25. Some anaerobic bacteria need carbon dioxide to survive. Experiments were performed on anaerobic bacteria metano sarsino (in water) displaying that they died within 5 minutes when carbon dioxide (C0 ₂ ) was removed from water using the method according to claim 42. Hence, the invention includes killing organisms (which live on oxygen) including microbes by influencing oxygen. The invention also includes killing organisms (which live on carbon dioxide) including microbes by influencing carbon dioxide. Herbicides, insecticides, pesticides and fungicides dissolve in water and are therefore present almost everywhere in the environment; in ground water, lakes, seawater, vegetables, fruits, flour, bread, pasta, corn flakes muesli, olives, different oils, mineral water, orange juice, wine, liquor and the human brain.

The invention enables removal of herbicides, insecticides, pesticides and fungicides from water, food and beverages at the source, during production, during distribution and by the end customer.

The invention enables removal of herbicides, insecticides, pesticides and fungicides from the human brain and body and from animals.

Drugs, antibiotics and hormones, including antibiotics used in beef, pork and chicken production dissolve in water and are therefore present in the environment; in ground water, tap water, lakes, seawater and in food (e.g. beef, pork, salami, chicken) and in the human brain.

The invention enables removal of drugs, antibiotics and hormones from industrial processes, sewage, water reservoirs, drinking water, lakes, seawater, food, animals and the human brain and body.

Rivers, lakes, water reservoirs, seawater and sometimes ground water is polluted by fertilizers, i.e. nitrogen compounds and phosphorus compounds.

The invention enables removal of nitrogen compounds (e.g. N0 ₂ , N0 ₃ , NH ₄ , NH ₄ CI) and phosphorus compounds (e.g. PI, P4, P0 ₄ , H ₃ P0 ₄ ) from rivers, lakes, water reservoirs and seawater.

C0 ₂ is a major environmental threat. The invention enables removal of C0 ₂ from e.g. power plant exhaust and car exhaust. The invention can be applied on C0 ₂ exhaust in air, or by feeding C0 ₂ exhaust through water and removing the C0 ₂ in the water, whereby carbon remains in the water and 0 ₂ evaporates.

The invention enables removal of C0 ₂ from lake and seawater, whereby lakes and oceans afterwards can dissolve and accumulate C0 ₂ contained in the air, thereby reducing C0 ₂ in the atmosphere. Thus, the invention facilitates continuous conversion of C0 ₂ in the atmosphere into carbon and oxygen.

Sulfur compounds are a major environmental threat. The invention enables removal of sulfites (e.g. S0 ₂ ) and S0 ₄ from crude oil, oil, petrol, petroleum products, gas and coal.

The invention enables removal of sulfur compounds from power plant exhaust.

Many lakes are almost "dead" because of high sulfur content (e.g. S0 ₂ and S0 ₄ ). The invention enables removal of sulfites (e.g. H ₂ S, S0 ₂ ) and sulfate (S0 ₄ ) from wells, water reservoirs, rivers, lakes and seawater.

Sulfites degrade the taste of wine and many beverages (e.g. whiskey). The invention enables removal of sulfites from wine and all types of food and beverages.

The invention enables removal of dissolved phosphorus compounds. This results in that dissolved chemical elements cease to dissolve whereby they sediment. Thus, the invention enables removal of phosphorus and chemical elements from water, e.g. in sewage and industrial processes.

The invention enables influence on phosphorus compounds in organisms, including microbes (e.g. bacteria, virus). This results in that chemical elements in these organisms are influenced and whereby these organisms are influenced and/or killed. Thus, the invention enables influence on and/or killing microbes by influencing phosphorus. The invention enables change of dissolved Na and dissolved CI into NaCI. The NaCI is separated using e.g. centrifugation. Thus, the invention includes reduction of Na and CI and/or NaCI in water, including seawater.

The present invention includes the influence on chemical processes by influencing chemical elements, compounds and/or molecules dissolved in water or by preventing chemical elements and/or compounds from becoming dissolved. Thus, the present invention facilitates fundamentally new ways of controlling, creating and/or preventing chemical processes.

Agriculture and food production use a large variety of molecular substances classed as herbicides, insecticides, pesticides and fungicides. The present invention encompasses the empiric observation that a majority of these molecular substances are influenced when the methods according to claims 34-38 are used and the apparatus according to claims 78-82 and claim 90 are used. Different producers and brands may utilize slightly different molecular substances; however, they often have the same natural periods or a subset of these natural periods. Thus, the invention encompasses all molecular substances that are influenced when methods according to claims 34-38 are used and apparatus according to claims 72-82 and claim 90 are used.

Some compounds and molecules have many natural periods. One example is S0 ₂ that has the natural period 24/(17·2 ¹⁴ ) hour and 24/(63·2 ¹³ ) hour. The S0 ₂ molecule is split when prevented from absorbing electromagnetic energy with the period 24/(17·2 ¹⁴ ) hour. The S0 ₂ molecule is also split when prevented from absorbing electromagnetic energy with the period 24/(63·2 ¹³ ) hour. The S0 ₂ molecule is also split when prevented from absorbing electromagnetic energy with the period 24/(17·2 ¹⁴ ) hour and 24/(63·2 ¹³ ) hour. Another example is glyphosate where the molecule is split when prevented from absorbing electromagnetic energy with the period 24/(31·2 ¹⁴ ) hour or with the period 24/(145·2 ¹² ) hour or with the periods 24/(31·2 ¹⁴ ) hour and 24/(145-2 ¹² ) hour. Some molecules are only influenced when prevented from absorbing electromagnetic energy simultaneously with all of its natural periods. Consequently, the present invention encompasses the method to influence some compounds and molecules, which have e.g. the natural periods Tl, T2 and T3, by preventing the compound or molecule from absorbing electromagnetic energy with the period Tl and/or T2 and/or T3. However, the preferred method is to prevent said compound or molecule from absorbing electromagnetic energy with the periods Tl and T2 and T3.

In summary the present invention encompasses all chemical elements, compounds and molecules in water and/or dissolved in water. However, the invention describes in detail chemical elements, compounds and molecules that have environmental impact and impact on humans, including disease management. Fertilizers based on phosphorus and nitrogen pollutes rivers, lakes, sea and drinking water. The present invention facilitates removal of e.g. phosphates, nitrates and ammonia from water and which will allow continued use of fertilizers in agriculture while minimizing the environmental impact. Effective agriculture is almost impossible without use of herbicides, insecticides, pesticides and fungicides. However, they have major environmental impact. The present invention facilitates removal of these molecular substances from rivers, lakes, seawater, tap water, food, beverages and the human body. It allows the use of herbicides, insecticides, pesticides and fungicides in agriculture and food production, and at the same time minimizing the environmental impact. S0 ₂ and C0 ₂ outlets from cars and power plants are a major environmental hazard. The present invention facilitates removal of S0 ₂ and S0 ₄ at the source, e.g. in crude oil, and removal of S0 ₂ , S0 ₄ and C0 ₂ at the outlet. This may turn oil, gas and coal into environmentally safe energy. Drugs, antibiotics and hormones are necessary in diseases management and food production. The present invention facilitates removal of many of these molecular substances at the source

(pharmaceutical manufacturer, hospital, food producer) or in rivers, lakes and seawater or by the end customer. Fresh water is a rare resource in many parts of the word, while salt water is plentiful. The present invention describes methods to reduce the salinity of water. State of the art diseases management is enormously complex resulting in that state of the art medicine is loosing ground against multi resistant bacteria and new types of virus. The present invention describes that microbes contain chemical elements that create electromagnetic processes that are essential for the microbe's survival. Thus, the vital kernel of microbes is one or two chemical elements. The present invention describes a fundamentally new way of killing microbes and disease management, facilitated by influencing chemical elements and/or compounds contained in microbes.