FIELD OF INVENTION

This inventiΩn relates tΩ the enhancement Ωf biΩcidal efficacy cf ccmmΩnly used halΩgens in the disinfecticn cf fluids, and tΩ their use tΩ disinfect SΩlids in CΩntact with these fluids such as the inner walls cf pipes.

BACKGROUND OF THE INVENTION

Drinking, waste, ΩΓ industrial water is currently treated with halcgens whΩse Ωxidizing biccidal and disinfecting acticn is well kncwn. With regard tc drinking water, the most ccmmΩn disinfecticn treatment is with chlcrine and by-products therecf.

ChlΩrine has a strcng biccidal acticn and residual free chlcrine is usually maintained in water supplied tc consumers to ensure that harmful bacteria are destroyed before the water reaches its estination.

Unfortunate /, during the complex reactions which occur between the chlorine and organisms and organic pollutants various chloramines and other noxious products are formed whose biocidal action is weaker than chlorine or not biocidal at all, and these tend to leave a disagreeable smell and taste in the water. In addition the production of chloramines and other chlorinated prcducts results in the requirement that additicnal chlorine must be added to the water in order to maintain the desired residual free chlcrine required to destroy bacteria.

Presently within the art there are a few methods which have proposed a combination of two disinfecting species wherein one is used as a chemical reagent (not a disinfectant) whose sole purpose is to regenerate biocidal forms of the second ε ecies from spent forms of the second species. Examples of these where the two halogens chlorine and iodine are used, are U.S. Patent No. 2,443,429 issued June 15, 1948 in the name of H.C. Markes et al and U.S. Patent NΩ. 3,975,271 issued August 17, 1976 in the name Ωf B. Saumier. In the case of these two prior patents the halogen chlorine or its partially reacted forms such as HOCl and NHC1 are introduced to

Ωxidize iodide to biocidal iodine (I ₂ ) which reacts with bacteria and is so reduced to I~ at which time more chlorine is introduced to re-oxidize the iodide back to biocidal iodine in order to allow the process to be repeated.

In each of these systems the stated purpose of the invention is to lower the cost of biocidal iodine (I-) by re- oxidation and re-use: both cases use the biocidal properties of iodine, not of the oxidizer. HΩwever, these methods require levels of iΩdine to be present in the water well above those generally considered physiologically acceptable for continuous human consumption, as only these high levels Ωf iodine are sufficiently biocidal for use as disinfectants. (Minimum levels of biocidal iodine normally deemed acceptable for water treatment purposes in Canada and the United States are 0.5 mg/1 to 10 mg/1 depending on the condition of the water and also the volume to be consumed daily by humans over a period of time).

Also it has been found that in systems using chlorine to regenerate or reoxidize iΩdine to biocidal forms, significant bacterial growth takes place that would not normally be found in this amount of chlorine or iodine used along (see Favero et al. Survival Ωf Pseudomonas in an Iodinated Swimming Pool Applied MicrobiΩlogy, Vol. 14, p. 627, 1966).

The present invention overcomes these disadvantages by employing a BZ reaction in which a minor bistable iodine system at levels below those found physiologically unacceptable for human consumption is coupled with a major bistable chlorine system by the presence of microbial life or their metabolic by- prcducts into an active disinfecting BZ reaction which enhances chlorine's biocidal ability.

In recent years the phenomenΩn of oscillating chemical reactions, more commonly known as BZ (for Belousov- ZhabΩtinsky) reacticns, has been recognized. The BZ reaction has been recently described by Epstein et al in an article in the publication Scientific American, March 1983, p. 112, in which three basic conditions were laid out as requirement for designing a chemical oscillatcr. The first condition is that

the chemical system must be far from equilibrium. The second condition is feedback; in other words some product of a step in the reaction sequence must exert an influence on its own rate of formation. The third conditiΩn is that the chemical system must exhibit bistability, meaning that under the same set of external ccnditions the system must be able to exist in two different stable steady states. These reactions to date have not found any type of useful applicaticn.

The present inventiΩn overcomes the aforesaid disadvantages in the prior art by maintaining a physiological acceptable concentration level of iodine to persons consuming the water who have an iodine deficiency, or who have adequate dietary iodine. The present invention also reduces the presence, in water treated with chlorine, of combined chlorines such as chlorΩfΩrm and chloramines which cause bad taste and an odour. Furthermore the present invention enhances the biocidal strength of chlorine by allowing low levels of chlorine to kill bacteria that would otherwise be immune.

When the organic content of water is particularly high at some point in the system, for example due to bacterial colonizatiΩn on the inner walls of the pipe carrying the water, it may be impossible in present practice to disinfect the water so that is suitable to drink. Chlorine at levels acceptable for potable water is not always capable of killing all forms of microbial life although it is generally capable of killing organisms of public health concern. Chlcrine resistant organisms such as autochemotrophic or hetrotrophic organisms colonize on pipe walls and form organic slimes which remove chlorine from the system, rendering the arriΩunt of chlorine which is generally considered acceptable to introduce during treatment, insufficient to make the water supply contain residual free chlorine.

To meet this problem of the buildup of bacteria and their by-products on the inner walls of pipes, the present methΩd of removing bacterial colonization debris is through the physical method of pigging and/or swabbing.

It is an object of the present invention to provide a BZ reaction using chlorine and iodine to disinfect the inner walls of pipe or to disinfect other solids using a continuously flowing fluid containing this BZ reaction.

SUMMARY OF THE INVENTION

In its broadest aspect the invention consists of a process of producing a disinfecting BZ reaction comprising adding, continuously to a fluid in a continuΩusly flΩwing system, halΩgens or halogen containing compounds to create two bistable systems at equilibrium. The first bistable system consist of HOCl, 0C1~, and chloramines in the fluid and the second bistable system consists of IO_, I_ and HIO in the fluid. The bistable systems when perturbed by a reductant consisting of microbial life forms or their metabolic by¬ products will initiate an oscillating reaction certain of whose intermediate products are microbiocidal.

DESCRIPTION OF THE DRAWINGS

Example embodiments of the invention are shown in the accompanying drawings in which:

FIGURE 1 is a schematic diagram showing apparatus to carry out experimental testing of the invention.

DESCRIPTION OF THE INVENTION

A preferred embodiment Ωf the present inventiΩn consists of adding iodine or an iodine releasing compound to continuously flowing water containing a concentration range of chlorine of about 0.15 - 5.0 mg/1 of water, the concentration range of iodine being about 0.025 - 0.15 mg/1 of water. The addition of the iodine or iodine releasing compound should be done at a point in the continuously flowing water where the chlorine is 35%-65%, (the preferred being 50%) of unhydrolysized, unreacted Cl ₂ and the remainder of the chlorine is reacted to form HOCl, OC1 and, where nitrogenous matter is present, chloramines, the concentration of chloramines being less than 25% of the concentration of HOCl.

In some cases it r / be necessary to pretreat the water by breakpoint chlorination whereby Cl ₂ is added to oxidize the chloramines, or by other procedures to reduce the concentration of chloramines to the above specified amount.

The presence of HOCl, chloramines, and 0C1 will establish the first bistable system near the injection point of iodine or iodine releasing compΩund.

At r abΩut the injecticn point of iodine or the iodine releasing compound, a portion of iodine will be over- oxidized by the chlorine present in the system to produce iodate (10^), a portion will remain as I« and a portiΩn will hydrolyse to hypoiΩdus acid (HIO). This establishes the seccnd bistable system required f r the oscillating reaction.

All of the chemical species are at very low concentration levels with chlorine being the major bistable system and iodine the minor bistable system. The two bistable systems are far from equilibrium but temporarily at steady state. The Cl ₂ compΩunds are at biΩcidal levels whereas the iodine compounds are not at levels generally recognized as biocidal.

The reductant or perturbing force is the presence of organic material already in situ on the pipe wall or present in the flowing water. This reductant initiates the oscillating reaction by creating an hysteresis IOΩP in the bistable chemical systems. This reaction increases the cidal efficiency of the chemicals and their intermediaries.

The range of chlorine concentration as stated in the preferred embodiment is based solely on government standards and industry practice in maintaining potable water. The chlorine concentration level is not proportional to the iodine concentraticn level. Chlorine concentrations higher than that specified can be used for non-potable water provided that Cl ₂ concentration does not exceed 5.0 mg/1 at the iodine injection point.

It is well known that bacteria in a water system can adhere to the inner wall of a pipe and produce a build-up of by-products, which allow these organisms to be extremely

resistant tΩ the disinfecting abilities Ωf very high concentration levels of biocidal halogens. Colonies of the above-mentioned resistant bacteria and their by-products form on the inner walls of pipes and provide protective cover f r additional bacterial to harbour. This build-up of bacteria and by-products are an engineering concern as they impede the flow of water, may damage the pipes, and are a public health concern as they provide sheltered harbourage for potentially pathenogenic additional bacteria in the system which can occasionally shed from the wall and contaminate potable water. It is known that concentration levels of chlorine as high as 20 mg/1 of water or concentration levels of iodine as high as 5 mg/1 of water have virtually no effect on this type of bacteria. The current method of controlling this bacterial build-up is through the physical means of pigging and swabbing of the lines. Such means are costly and inefficient compared to the use of the present invention for keeping piping systems free of bacterial build-up on inner pipe walls. The oscillating chemical reaction as described above allows iodine and chlorine mclecules to slowly penetrate the protective overburden, exposing the organism. As the bacteria are exposed they are killed by chlorination. The dead Ωrganism no longer adheres to the inner wall of the pipe and the organism and its protective overburden are then swept down stream by the current.

Separately, high levels of iodine or high levels of chlorine acceptable for water treatment, are unable effectively to penetrate the protective overburden of the organism because of the high probability of reaction at the surface. In accordance with this invention as the halogen molecules in their proportiΩnal relatiΩnship come into contact with bacteria or the protective overburden of the bacteria, the molecules begin to accumulate on the surface and in the marginal interior of this matter. This bioaccumulation allows the BZ reaction to take place within the matter, allowing penetration of the halogens deeper into the overburden to contact the active organism whereby the chlorine compounds are able to kill them.

The iodine can be intrcduced into the system in a saturated solution by an iodine dispensing system such as that disclosed in U.S. Patent No. 4,555,347 issued November 26, 1985 to Iomech Limited assignee of Dennis O'Dowd and John Barry. Alternatively, the iodine can be introduced into the system as thermodynamically free iodine in the manner disclosed in my co- pending U.S. Patent Application Serial No. 296,371 filed January 10, 1989.

The preferred method Ωf intrΩducing chlorine into the system is in a form resulting in the production or by the introduction of Cl ₂ .

Experimental testing of the invention was carried out using apparatus shown schematically in Figure 1 of the drawings.

Experimentation was conducting using pipe sections extracted from a working distribution system where bacterial colonization debris had accumulated on the inner wall of the pipes. The pipe sections were capped and filled with the water found in them at situ. The capped pipe sections were then transported to the laboratΩry where the apparatus shown in FIG. 1 was constructed. Two identical apparati were constructed and experimentation was conducted using one as a control and one as a test. In the apparatus of Figure 1 four 20 imperial gallon tanks 10 were connected with pipes 12 (the pipe sections mentioned above) to form a test system 13 simulating a water distribution system. Centrifugal pumps 14 located one in each section 12a, 12b, 12c and 12d of pipe 12 and were used to pump the water (clockwise as seen in the drawing) through distribution system 13. Connected to system 13, in one section 12c pipe 12, was an activated carbcn and string polished/filter 16 which allowed for dehalogenation of the water after a specified number of cycles. A bypass 18 around filter 16 was opened when dehalogenation by filter 16 was not wanted. A valve 20 controlled the release of chlorine from a chlorine bottle 21 through a line 22 to section 12d of pipe 12 and into the flow of water that was being pumped through the system. An iodine dispenser 24 of the type shown in U.S. Patent No.

4,555,347 mentioned above was connected by a pair of lines 26,28 to section 12d of pipe 12 and control valves 30,32, one in each of lines 26,28 regulated the release of iodine from dispenser 24. The iodine was injected through line 30 at a tee 34 and the chlorine was injected at a tee 36 upstream frcm tee 34.

The control system (not shown, but identical to. Figure 1 except for the presence of iodine dispenser 24) was chlorinated with 5 mg/1 of chlorine to duplicate conditiΩns in the working distribution system from which it was removed. Bypass 18 remained open so that dechlorination by the active carbon filter did not take place. In the test system iodine was also added at a concentration level of 2 mg/1 of water to simulate the conditions of U.S. Patent No. 2,443,429 mentioned above.

Both the contrΩl system and the test system 13 were allΩwed to run for 12 hours and at the end of 12 hours both systems were shut down for testing the water in tanks 10. In the control tank the chlorine residual was found to be 0.05 mg/1 of water. In the test tank the chlorine residual was less than 0.05 mg/1 of water and the iodine concentration was less than 0.1 mg/1 water. Bacteria identified as coliforms were found in the following amounts:

Test ContrΩl

Tank 10a >10 coli/100 ml 20 coli/100 ml

Tank 10b 9 coli/100 ml >10 ccli/100 ml

Tank 10C >10 coli/100 ml 9 coli/100 ml

Tank lOd >10 coli/100 ml >10 ccli/100 ml

The results cf the experiment shΩw that bacteria levels were not reduced by the introduction of I ₂ at concentration levels of 2 mg/1 of water contrary to the results stated in U.S. Patent No. 2,443,429.

Both the control system and the test system were dehalogenated by being driven through activated carbon filter 16 for 10 passes in preparation for the next experiment, in which a chlorine concentration of 5 mg/1 of water was again

added to the control system and bypass 18 remain open. Test system 13 was also chlorinated to a concentration level of 5 mg/1 of water but iodine was alsΩ added to the system at a concentration level less than 0.1 mg/1 of water. Over the next two hours, test system 13 began to shed particular matter from the inner walls of the sections of pipe 12. The control system, on the Ωther hand, continued to operate normally.

Test system 13 was shut down and the inner walls of pipe 12 were examined. First section 12a of pipe 12 in the test system had essentially all of the bacterial colΩnizatiΩn on the inner wall of the pipe removed. Second section 12b of pipe 12 in the system had its biofilm reduced by apprcximately 1/2 at the inlet end of the pipe section and 1/10 at the outlet end of the pipe section. The third and fourth pipe sections 12c and 12d appeared unaffected.

Both the contrΩl system and test system 13 were dehalΩgenated by active carbon filter 16 and particulate matter was removed from the test system by placing course spun glass mats in tank 10c of the test apparatus.

A final experiment was conducted in which a chlorine concentration of 5 mg/1 of water was added to the control system and to test system 13. A concentration level of I ₂ was introduced to test system 13 at around 0.15 ± 0.05 rag/1 of water and concentration readings of I ₂ were taken at points around the test system. It was found that particulate matter began to shed from the inner walls of the sections of pipe 12 when traces of I ₂ (measurable only at levels of 0.025 or greater) were present and the particulate matter stopped shedding from the inner walls of the pipe sections once the concentration level of I ₂ reached 0.15 mg/1 of water. From th s it was determined that the maximum concentration range of I ₂ allowed to initiate the BZ reaction was 0.15 mg/1 of water. Both systems were then disassembled and on examination it was found that the inner walls of the sections of pipe 12 of the test system were cleaned of all organic matter and no organic or inorganic debris was found adhering to the inner walls. An examination of the contrΩl system showed that it had

essentially the same amount of organic and inorganic debris adhering to the inner walls of the pipe sections as when the piping was removed from the working distribution system.