Background of the Invention This invention relates to an improved all-purpose liquid cleaning composition designed in particular for cleaning hard surfaces and which is effective in removing grease soil and/or bath soil and in leaving unrinsed surfaces with a shiny appearance and the compositions exhibits improved foam collapse properties.

In recent years all-purpose liquid detergents have become widely accepte for cleaning hard surfaces, e. g., painted woodwork and panels, tiled walls, wash bowls, bathtubs, linoleum or tile floors, washable wall paper, etc. Such all-purpose liquids comprise clear and opaque aqueous mixtures of water-soluble synthetic organic detergents and water-soluble detergent builder salts. In order to achieve comparable cleaning efficiency with granular or powdered all-purpose cleaning compositions, use of water-soluble inorganic phosphate builder salts was favored in the prior art all-purpose liquids. For example, such early phosphate-containing compositions are described in U. S. Patent Nos. 2,560,839; 3,234,138; 3,350,319; and British Patent No. 1,223,739.

In view of the environmentalist's efforts to reduce phosphate levels in ground water, improved all-purpose liquids containing reduced concentrations of inorganic phosphate builder salts or non-phosphate builder salts have appeared. A particularly useful seif-opacified liquid of the latter type is described in U. S. Patent No. 4,244,840.

However, these prior art all-purpose liquid detergents containing detergent builder salts or other equivalent tend to leave films, spots or streaks on cleaned unrinsed surfaces, particularly shiny surfaces. Thus, such liquids require thorough rinsing of the cleaned surfaces which is a time-consuming chore for the user.

In order to overcome the foregoing disadvantage of the prior art all-purpose liquid, U. S. Patent No. 4,017,409 teaches that a mixture of paraffin sulfonate and a reduced concentration of inorganic phosphate builder salt should be employed.

However, such compositions are not completely acceptable from an environmental point of view based upon the phosphate content. On the other hand, another alternative to achieving phosphate-free all-purpose liquids has been to use a major proportion of a mixture of anionic and nonionic detergents with minor amounts of glycol ether solvent and organic amine as shown in U. S. Patent NO. 3,935,130. Again, this approach has not been completely satisfactory and the high levels of organic detergents necessary to achieve cleaning cause foaming which, in turn, leads to the need for thorough rinsing which has been found to be undesirable to today's consumers.

Another approach to formulating hard surface or all-purpose liquid detergent composition where product homogeneity and clarity are important considerations involves the formation of oil-in-water (o/w) microemulsions which contain one or more surface-active detergent compound, a water-immiscible solvent (typically a hydrocarbon solvent), water and a"cosurfactant"compound which provides product stability. By definition, an o/w microemulsion is a spontaneously forming colloidal dispersion of"oil"phase particles having a particle size in the range of 25 to 800 A in a continuous aqueous phase.

In view of the extremely fine particle size of the disperse oil phase particles, microemulsions are transparent to light and are clear and usually highly stable against phase separation.

Patent disclosures relating to use of grease-removal solvents in o/w microemulsions inclue, for example, European Patent Applications EP 0137615 and EP 0137616-Herbots et al; European Patent Application EP 0160762-Johnston et al; and U. S. Patent No. 4,561,991-Herbots et al. Each of these patent disclosures also teaches using at least 5% by weight of grease-removal solvent.

It also is known from British Patent Application GB 2144763A to Herbots et al, published March 13,1985, that magnesium salts enhance grease-removal performance of organic grease-removal solvents, such as the terpenes, in o/w microemulsion liquid detergent compositions. The compositions of this invention described by Herbots et al. require at least 5% of the mixture of grease-removal solvent and magnesium salt and preferably at least 5% of solvent (which may be a mixture of water-immiscible non-polar solvent with a sparingly soluble slightly polar solvent) and at least 0.1 % magnesium salt.

However, since the amount of water immiscible and sparingly soluble components which can be present in an o/w microemulsion, with low total active ingredients without impairing the stability of the microemulsion is rather limited (for example, up to 18% by weight of the aqueous phase), the presence of such high quantities of grease-removal solvent tend to reduce the total amount of greasy or oily soils which can be taken up by and into the microemulsion without causing phase separation.

The following representative prior art patents also relate to liquid detergent cleaning compositions in the form of o/w microemulsions: U. S. Patents No. 4,472,291- Rosario; U. S. Patent No. 4,540,448-Gauteer et al; U. S. Patent No. 3,723,330- Sheflin; etc.

Liquid detergent compositions which include terpenes, such as d-limonene, or other grease-removal solvent, although not disclosed to be in the form of o/w microemulsions, are the subject matter of the following representative patent documents: European Patent Application 0080749; British Patent Specification 1,603,047; and U. S. Patent Nos. 4,414,128 and 4,540,505. For example, U. S. Patent No. 4,414,128 broadly discloses an aqueous liquid detergent composition characterized by, by weight: (a) from 1 % to 20% of a synthetic anionic, nonionic, amphoteric or zwitterionic surfactant or mixture thereof;

(b) from 0.5% to 10% of a mono-or sesquiterpene or mixture thereof, at a weight ratio of (a): (b) being in the range of 5: 1 to 1: 3; and (c) from 0.5% 10% of a polar solvent having a solubility in water at 15°C in the range of from 0.2% to 10%. Other ingredients present in the formulations disclosed in this patent include from 0.05% to 2% by weight of an alkali metal, ammonium or alkanolammonium soap of a C 1 3-C24 fatty acid; a calcium sequestrant from 0.5% to 13% by weight; non-aqueous solvent, e. g., alcools and glycol ethers, up to 10% by weight; and hydrotropes, e. g., urea, ethanolamines, salts of lower alkylaryl sulfonates, up to 10% by weight. All of the formulations shown in the Examples of this patent include relatively large amounts of detergent builder salts which are detrimental to surface shine.

U. S. Patent 5,082,584 discloses a microemulsion composition having an anionic surfactant, a cosurfactant, nonionic surfactant, perfume and water; however, these compositions do not possess the ecotoxicity and the improved interfacial tension properties as exhibited by the compositions of the instant invention.

Summary of the Invention The present invention provides an improved, clear, liquid cleaning compositior ; having improved interfacial tension which improves cleaning hard surface and is suitable for cleaning hard surfaces such as plastic, vitreous and metal surfaces having a shiny finish, oil stained floors, automotive engines and other engines. The instant compositions exhibit improved foam collapse properties. More particularly, the improved cleaning compositions exhibit good grease soil removal properties due to the improved interfacial tensions, when used in undiluted (neat) form and leave the cleaned surfaces shiny without the need of or requiring only minimal additional rinsing or wiping.

The latter characteristic is evidenced by little or no visible residues on the unrinsed cleaned surfaces and, accordingly, overcomes one of the disadvantages of prior art products.

Surprisingly, these desirable results are accomplished even in the absence of polyphosphate or other inorganic or organic detergent builder salts and also in the complete absence or substantially complete absence of grease-removal solvent.

In one aspect, the invention generally provides a stable, optically clear hard surface cleaning composition especially effective in the removal of oily and greasy oil which composition inclues, on a weight basis: 0.1 % to 8% of an anionic surfactant; 0.1 % to 10% of an ethoxylated nonionic surfactant; 0 to 8% of a compound which is a mixture of a partially esterified ethoxylated polyhydric alcool, a fully esterified ethoxylated polyhydric alcohol and a nonesterified ethoxylated polyhydric alcohol (said mixture being herein after referred to as an ethoxylated polyhydric alcohol type compound such as an ethoxylated glycerol type compound); 0 to 10% of magnesium sulfate heptahydrate; 0 to 2% of a fatty acid; 0.4 to 10.0% of a perfume, essential oil, or water insoluble hydrocarbon having 6 to 18 carbon atoms; 0.1 % to 10% of an ethoxylated/butoxylated nonionic surfactant; and the balance being water.

In a second aspect, the invention comprises an all purpose hard surface cleaning composition in the form of a microemulsion and comprising approximately by weight: 0.1 % to 8% of an anionic surfactant; 0.1 % to 10% of an ethoxylated nonionic surfactant; 0 to 8% of said ethoxylated polyhydric alcohol type compound; 0 to 10% of magnesium sulfate heptahydrate; 0 to 2 % fatty acid; 0 to 10%, more preferably 0.1 % to 10% of a perfume, essential oil or water insoluble hydrocarbon having 6 to 18 carbon atoms;

0.1 % to 10% of an ethoxylated/butoxylated nonionic surfactant; and the balance being water.

Detailed Description of the Invention The present invention relates to a stable optically clear cleaning composition comprising approximately by weight: 0.1 % to 8% of an anionic surfactant, 0.1 % to 10.0% of an ethoxylated nonionic surfactant, 0 to 10% of an ethoxylated polyhydric alcohol type compound, 0 to 10%, more preferably 0.4% to 10% of a water insoluble hydrocarbon, essential oil or a perfume, 0 to 2% of a fatty acid; 0.1 % to 10% of an ethoxylated/butoxylated nonionic surfactant and the balance being water, wherein the composition does not contain aliphatic organic acids or glycol ether type cosurfactants.

According to the present invention, the role of the water insoluble hydrocarbon can be provided by a non-water-soluble perfume. Typically, in aqueous based compositions the presence of a solubilizers, such as alkali metal lower alkyl aryl sulfonate hydrotrope, triethanolamine, urea, etc., is required for perfume dissolution, especially at perfume levels of 1 % and higher, since perfumes are generally a mixture of fragrant essential oils and aromatic compound which are generally not water- soluble.

As used herein and in the appende claims the term"perfume"is used in its ordinary sense to refer to and include any non-water soluble fragrant substance or mixture of substances including natural (i. e., obtained by extraction of flower, herb, blossom or plant), artificial (i. e., mixture of natural oils or oil constituents) and synthetically produced substance) odoriferous substances. Typically, perfumes are complex mixtures of blends of various organic compound such as alcools, aldehydes, ethers, aromatic compound and varying amounts of essential oils (e. g., terpenes) such as from 0% to 80%, usually from 10% to 70% by weight, the essential oils themselves being volatile odoriferous compound and also serving to dissolve the other components of the perfume.

In the present invention the precise composition of the perfume is of no particular consequence to cleaning performance so long as it meets the criteria of

water immiscibility and having a leasing odor. Naturally, of course, especially for cleaning compositions intended for use in the home, the perfume, as well as all other ingredients, should be cosmetically acceptable, i. e., non-toxic, hypoallergenic, etc.

The hydrocarbon such as a perfume is present in the composition in an amount of from 0 to 10%, more preferably 0.4% to 10% by weight, preferably from 0.4% to 3.0% by weight, especially preferably from 0.5% to 2.0% by weight, such as weight percent. Although superior grease removal performance will be achieved for perfume compositions not containing any terpene solvents, it is apparently difficult for perfumers to formulate sufficiently inexpensive perfume compositions for products of this type (i. e., very cost sensitive consumer-type products) which inclues less than 20%, usually less than 30%, of such terpene solvents.

Thus, merely as a practical matter, based on economic consideration, the detergent cleaning compositions of the present invention may often include as much as 0.2% to 7% by weight, based on the total composition, of terpene solvents introduced thereunto via the perfume component. However, even when the amount of terpene solvent in the cleaning formulation is less than 1.5% by weight, such as up to 0.6% by weight or 0.4% by weight or less, satisfactory grease removal and oil removal capacity is provided by the inventive compositions.

In place of the perfume in the hard surface cleaning composition at the same previously defined concentrations that the perfume was used in the hard surface cleaning composition one can employ an essential oil or a water insoluble hydrocarbon having 6 to 18 carbon such as a paraffin or isoparaffin.

Suitable essential oils are selected from the group consisting of: Anethole 20/21 natural, Aniseed oil china star, Aniseed oil globe brand, Balsam (Peru), Basil oil (India), Black pepper oil, Black pepper oleoresin 40/20, Bois de Rose (Brazil) FOB, Borneol Flakes (China), Camphor oil, White, Camphor powder synthetic technical, Cananga oil (Java), Cardamom oil, Cassia oil (China), Cedarwood oil (China) BP, Cinnamon bark oil, Cinnamon leaf oil, Citronella oil, Clove bud oil, Clove leaf, Coriander (Russia), Coumarin 69°C (China), Cyclamen Aldehyde, Diphenyl oxide, Ethyl

vanilin, Eucalyptol, Eucalyptus oil, Eucalyptus citriodora, Fennel oil, Geranium oil, Ginger oil, Ginger oleoresin (India), White grapefruit oil, Guaiacwood oil, Gurjun balsam, Heliotropin, Isobornyl acetate, Isolongifolene, Juniper berry oil, L-methyl acetate, Lavender oil, Lemon oil, Lemongrass oil, Lime oil distille, Litsea Cubeba oil, Longifolene, Menthol crystals, Methyl cedryl ketone, Methyl chavicol, Methyl salicylate, Musk ambrette, Musk ketone, Musk xylol, Nutmeg oil, Orange oil, Patchouli oil, Peppermint oil, Phenyl ethyl alcool, Pimento berry oil, Pimento leaf oil, Rosalin, Sandalwood oil, Sandenol, Sage oil, Clary sage, Sassafras oil, Spearmint oil, Spike lavender, Tagetes, Tea tree oil, Vanilin, Vetyver oil (Java), Wintergreen Regarding the anionic surfactant present in the instant compositions any of the conventionally used water-soluble anionic surfactants or mixtures of said anionic surfactants and anionic surfactants can be used in this invention. As used herein the term"anionic surfactant"is intended to refer to the class of anionic and mixed anionic- nonionic detergents providing detersive action.

Suitable water-soluble non-soap, anionic surfactants include those surface- active or detergent compound which contain an organic hydrophobic group containing generally 8 to 26 carbon atoms and preferably 10 to 18 carbon atoms in their molecular structure and at least one water-solubilizing group selected from the group of sulfonate, sulfate and carboxylate so as to form a water-soluble detergent. Usually, the hydrophobic group will include or comprise a Cg-C22 alkyl, alkyl or acyl group. Such surfactants are employed in the form of water-soluble salts and the salt-forming cation usually is selected from the group consisting of sodium, potassium, ammonium, magnesium and mono-, di-or tri-C2-C3 alkanolammonium, with the sodium, magnesium and ammonium cations again being preferred.

Examples of suitable sulfonated anionic surfactants are the well known higher alkyl mononuclear aromatic sulfonates such as the higher alkyl benzene sulfonates containing from 10 to 16 carbon atoms in the higher alkyl group in a straight or branche chain, C8-Cl5 alkyl toluene sulfonates and C8-Cl5 alkyl phenol sulfonates.

One sulfonate useful in the instant invention is linear alkyl benzene sulfonate having a

high content of 3- (or higher) phenyl isomers and a correspondingly low content (well below 50%) of 2- (or lower) phenyl isomers, that is, wherein the benzene ring is preferably attache in large part at the 3 or higher (for example, 4,5,6 or 7) position of the alkyl group and the content of the isomers in which the benzene ring is attache in the 2 or 1 position is correspondingly low. Particularly preferred materials are set forth in U. S. Patent 3,320,174.

Other suitable anionic surfactants are the olefin sulfonates, including long-chain alkene sulfonates, long-chain hydroxyalkane sulfonates or mixtures of alkene sulfonates and hydroxyalkane sulfonates. These olefin sulfonate detergents may be prepared in a known manner by the rection of sulfur trioxide (S03) with long-chain olefins containing 8 to 25, preferably 12 to 21 carbon atoms and having the formula RCH=CHR1 where R is a higher alkyl group of 6 to 23 carbons and RI is an alkyl group of 1 to 17 carbons or hydrogen to form a mixture of sultones and alkene sulfonic acids which is then treated to convert the sultones to sulfonates. Preferred olefin sulfonates contain from 14 to 16 carbon atoms in the R alkyl group and are obtained by sulfonating an a-olefin.

Preferred anionic sulfonate surfactants are the paraffin sulfonates containing 10 to 20, preferably 13 to 17, carbon atoms. Primary paraffin sulfonates are made by reacting long-chai alpha olefins and bisulfites and paraffin sulfonates having the sulfonate group distributed along the paraffin chain are shown in U. S. Patents Nos..

2,503,280; 2,507,088; 3,260,744; 3,372,188; and German Patent 735,096.

Examples of satisfactory anionic sulfate surfactants are the Cg C1 g alkyl sulfate salts and the Cg-C1 g alkyl sulfate salts and the Cg-C1 g alkyl ether polyethenoxy sulfate salts having the formula R (OC2H4) n OS03M wherein n is 1 to 12, preferably 1 to 5, and M is a solubilizing cation selected from the group consisting of sodium, potassium, ammonium, magnesium and mono-, di-and triethanol ammonium ions.

The alkyl sulfates may be obtained by sulfating the alcools obtained by reducing glycerides of coconut oil or tallow or mixtures thereof and neutralizing the resultant product.

On the other hand, the alkyl ether polyethenoxy sulfates are obtained by sulfating the condensation product of ethylene oxide with a Cg-C1g alkanol and neutralizing the resultant product. The alkyl sulfates may be obtained by sulfating the alcools obtained by reducing glycerides of coconut oil or tallow or mixtures thereof and neutralizing the resultant product. On the other hand, the alkyl ether polyethenoxy sulfates are obtained by sulfating the condensation product of ethylene oxide with a Cg-C1g alkanol and neutralizing the resultant product. The alkyl ether polyethenoxy sulfates differ from one another in the number of moles of ethylene oxide reacted with one mole of alkanol. Preferred alkyl sulfates and preferred alkyl ether polyethenoxy sulfates contain 10 to 16 carbon atoms in the alkyl group.

The Cg-C12 alkylphenyl ether polyethenoxy sulfates containing from 2 to 6 moles of ethylene oxide in the molecule also are suitable for use in the inventive compositions. These surfactants can be prepared by reacting an alkyl phenol with 2 to 6 moles of ethylene oxide and sulfating and neutralizing the resultant ethoxylated alkylphenol.

Other suitable anionic detergents are the Cg-C1 s alkyl ether polyethenoxyl carboxylates having the structural formula R (OC2H4) nOX COOH wherein n is a number from 4 to 12, preferably 5 to 10 and X is selected from the group consisting of CH2. C (O) R1 and wherein R1 is a Cl-C3 alkylene group. Preferred compound include Cg-Cl 1 alkyl ether polyethenoxy (7-9) C (O) CH2CH2COOH, C13-C15 alkyl ether polyethenoxy (7-9) and C10-C12 alkyl ether polyethenoxy (5-7) CH2COOH. These compound may be prepared by condensing ethylene oxide with appropriate alkanol and reacting this rection product with chloracetic acid to make the ether carboxylic acids as shown in US Pat. No. 3,741,911 or with succinic anhydride or phtalic anhydride.

Obviously, these anionic detergents will be present either in acid form or salt form depending upon the pH of the final composition, with the salt forming cation being the same as for the other anionic detergents.

Of the foregoing non-soap anionic surfactants, the preferred surfactants are the Cg-C1 s linear alkylbenzene sulfonates and the Cl 3-Cl 7 paraffin or alkane sulfonates.

Particularly, preferred compound are sodium C10-C13 alkylbenzene sulfonate and sodium C13-C17 alkane sulfonate.

Generally, the proportion of the nonsoap-anionic surfactant will be in the range of 0.1 % to 8%, preferably from 0.5% to 7%, by weight of the composition.

The ethoxylated nonionic surfactant is present in amounts of about 0.1% to 10%, preferably 0.5% to 8% by weight of the composition and provides superior performance in the removal of oily soil and mildness to human skin.

The water soluble nonionic surfactants utilized in this invention are commercially well known and include the primary aliphatic alcohol ethoxylates, secondary aliphatic alcohol ethoxylates, alkylphenol ethoxylates and condensates of ethylene oxide with sorbitan fatty acid esters such as the Tweens (ICI). The nonionic synthetic organic detergents generally are the condensation products of an organic aliphatic or alkyl aromatic hydrophobic compound and hydrophilic ethylene oxide groups. Practically any hydrophobic compound having a carboxy, hydroxy, amido, or amino group with a free hydrogen attache to the nitrogen can be condense with ethylene oxide or with the polyhydration product thereof, polyethylene glycol, to form a water-soluble nonionic detergent. Further, the length of the polyethenoxy chain can be adjusted to achieve the desired balance between the hydrophobic and hydrophilic elements.

The nonionic detergent class inclues the condensation products of a higher alcohol (e. g., an alkanol containing about 8 to 18 carbon atoms in a straight or branche chain configuration) condense with about 5 to 30 moles of ethylene oxide, for example, lauryl or myristyl alcohol condense with about 16 moles of ethylene oxide (EO), tridecanol condense with about 6 to moles of EO, myristyl alcohol condense with about 10 moles of EO per mole of myristyl alcool, the condensation product of

EO with a cut of coconut fatty alcohol containing a mixture of fatty alcools with alkyl chains varying from 10 to about 14 carbon atoms in length and wherein the condensate contains either about 6 moles of EO per mole of total alcohol or about 9 moles of EO per mole of alcohol and tallow alcohol ethoxylates containing 6 EO to 11 EO per mole of alcool.

A preferred group of the foregoing nonionic surfactants are the Neodol ethoxylates (Shell Co.), which are higher aliphatic, primary alcohol containing about 9- 15 carbon atoms, such as C11 alkanol condense with 9 moles of ethylene oxide (Neodol 1-9), C12 13 alkanol condense with 6.5 moles ethylene oxide (Neodol 23- 6.5), C12 15 alkanol condense with 7 or 3 moles ethylene oxide (Neodol 25-7 or Neodol 25-3), C14 15 alkanol condense with 13 moles ethylene oxide (Neodol 45-13), and the like. Such ethoxamers have an HLB (hydrophobic lipophilic balance) value of about 8 to 15 and give good O/W emulsification, whereas ethoxamers with HLB values below 8 contain less than 5 ethyleneoxide groups and tend to be poor emulsifiers and poor detergents.

Additional satisfactory water soluble alcohol ethylene oxide condensates are the condensation products of a secondary aliphatic alcohol containing 8 to 18 carbon atoms in a straight or branche chain configuration condense with 5 to 30 moles of ethylene oxide. Examples of commercially available nonionic detergents of the foregoing type are C11-C1 s secondary alkanol condense with either 9 EO (Tergitol 15-S-9) or 12 EO (Tergitol 15-S-12) marketed by Union Carbide.

Other suitable nonionic detergents include the polyethylene oxide condensates of one mole of alkyl phenol containing from about 8 to 18 carbon atoms in a straight-or branche chain alkyl group with about 5 to 30 moles of ethylene oxide. Specific examples of alkyl phenol ethoxylates include nonyl condense with about 9.5 moles of EO per mole of nonyl phenol, dinonyl phenol condense with about 12 moles of EO per mole of phenol, dinonyl phenol condense with about 15 moles of EO per mole of phenol and di-isoctylphenol condense with about 15 moles of EO per mole of phenol.

Commercially available nonionic surfactants of this type include Igepal CO-630 (nonyl phenol ethoxylate) marketed by GAF Corporation.

Other suitable water-soluble nonionic detergents which are less preferred are marketed under the trade name"Pluronics."The compound are formed by condensing ethylene oxide with a hydrophobic base formed by the condensation of propylene oxide with propylene glycol. The molecular weight of the hydrophobic portion of the molecule is of the order of 950 to 4000 and preferably 200 to 2,500. The addition of polyoxyethylene radicals to the hydrophobic portion tends to increase the solubility of the molecule as a whole so as to make the surfactant water-soluble. The molecular weight of the block polymers varies from 1,000 to 15,000 and the polyethylene oxide content may comprise 20% to 80% by weight. Preferably, these surfactants will be in liquid form and satisfactory surfactants are available as grades L 62 and L 64.

The ethoxylated/butoxylated nonionic surfactants are used in the instant compositions at a concentration of about 0.1 wt. % to 10 wt. %, more preferably 0.5 wt.

% to 8 wt. % and are the condensation product of ethylene oxide, butylene oxide and a C6-Cl6 fatty alcool. A preferred ethoxylated/butoxylated nonionic surfactant is EB96- 0779 manufactured by Dow Chemical Co. from a Cg alcool, 8 moles of ethylene oxide and 2 moles of butylene oxide.

The instant composition can optionally contain a composition (herein after referred to as an ethoxylated polyhydric alcohol type compound such as an ethoxylated glycerol type compound) which is a mixture of a fully esterified ethoxylated polyhydric alcool, a partially esterified ethoxylated polyhydric alcohol and a nonesterified ethoxylated polyhydric alcool, wherein the preferred polyhydric alcohol is glycerol, and the compound is

Formula (I) Formula (II) wherein w quais one to four, most preferably one, and B is selected from the group consisting of hydrogen or a group represented by: wherein R is selected from the group consisting of alkyl group having 6 to 22 carbon atoms, more preferably 11 to 15 carbon atoms and alkenyl groups having 6 to 22 carbon atoms, more preferably 11 to 15 carbon atoms, wherein a hydrogenated tallow alkyl chain or a coco alkyl chain is most preferred, wherein at least one of the B groups is represented by said and R'is selected from the group consisting of hydrogen and methyl groups; x, y and z have a value between 0 and 60, more preferably 0 to 40, provided that (x+y+z) equals 2 to 100, preferably 4 to 24 and most preferably 4 to 19, wherein in Formula (I) the weight ratio of monoester/diester/triester is 40 to 90/5 to 35/1 to 20, more preferably 50 to 90/9 to 32/1 to 12, wherein the weight ratio of Formula (I) to Formula

(I I) is a value between 3 to 0.02, preferably 3 to 0.1, most preferably 1.5 to 0.2, wherein it is most preferred that there is more of Formula (II) than Formula (I) in the mixture that forms the compound.

The ethoxylated glycerol type compound used in the instant composition is manufactured by the Kao Corporation and sold under the trade name Levenol such as Levenol F-200 which has an average EO of 6 and a molar ratio of coco fatty acid to glycerol of 0.55 or Levenol V501/2 which has an average EO of 17 and a molar ratio of tallow fatty acid to glycerol of 1.0. It is preferred that the molar ratio of the fatty acid to glycerol is less than 1.7, more preferably less than 1.5 and most preferably less than 1.0. The ethoxylated glycerol type compound has a molecular weight of 400 to 1600, and a pH (50 grams/liter of water) of 5-7. The Levenol compound are substantially non irritant to human skin and have a primary biodegradabillity higher than 90% as measured by the Wickbold method Bias-7d.

Two examples of the Levenol compound are Levenol V-501/2 which has 17 ethoxylated groups and is derived from tallow fatty acid with a fatty acid to glycerol ratio of 1.0 and a molecular weight of 1465 and Levenol F-200 has 6 ethoxylated groups and is derived from coco fatty acid with a fatty acid to glycerol ratio of 0.55. Both Levenol F- 200 and Levenol V-501/2 are compose of a mixture of Formula (I) and Formula (il).

The Levenol compound has ecoxicity values of algae growth inhibition > 100 mg/liter; acute toxicity for Daphnie > 100 mg/liter and acute fish toxicity > 100 mg/liter. The Levenol compound have a ready biodegradability higher than 60% which is the minimum required value according to OECD 301 B measurement to be acceptably biodegradable.

Polyesterified nonionic compound also useful in the instant compositions are Crovol PK-40 and Crovol PK-70 manufactured by Croda GMBH of the Netherlands.

Crovol PK-40 is a polyoxyethylene (12) Palm Kernel Glyceride which has 12 EO groups. Crovol PK-70 which is prefered is a polyoxyethylene (45) Palm Kernel Glyceride have 45 EO groups.

In the hard surface cleaning compositions the ethoxylated polyhydric alcohol compound or the polyesterified nonionic compound will be present in admixture with the anionic surfactant. The proportion of the ethoxylated polyhydric alcohol compound based upon the weight of the all purpose hard surface cleaning composition will be 0 to 8%, more preferably 0.5% to 6% by weight.

The final essential ingredient in the inventive compositions having improved interfacial tension properties is water. The proportion of water in the cleaning composition compositions generally is in the range of 20% to 97%, preferably 70% to 97% by weight.

In addition to the above-described essential ingredients required for the formation of the composition, the compositions of this invention may often and preferably do contain one or more additional ingredients which serve to improve overall product performance.

One such ingredient is an inorganic or organic salt of oxide of a multivalent metal cation, particularly Mg++. The metal salt or oxide provides several benefits including improved cleaning performance in dilute usage, particularly in soft water areas.

Magnesium sulfate, either anhydrous or hydrate (e. g., heptahydrate), is especially preferred as the magnesium salt. Good results also have been obtained with magnesium oxide, magnesium chloride, magnesium acetate, magnesium propionate and magnesium hydroxide. These magnesium salts can be used with formulations at neutral or acidic pH since magnesium hydroxide will not precipitate at these pH levels.

Although magnesium is the preferred multivalent metal from which the salts (inclusive of the oxide and hydroxide) are formed, other polyvalent metal ions also can be used.

Thus, depending on such factors as the pH of the system, the nature of the primary surfactants and cosurfactant, and so on, as well as the availability and cost factors, other suitable polyvalent metal ions include aluminum, copper, nickel, iron, calcium, etc. can be used. It should be noted, for example, that with the preferred paraffin sulfonate anionic detergent calcium salts will precipitate and should not be

used. It has also been found that the aluminum salts work best at pH below 5 or when a low level, for example 1 weight percent, of citric acid is added to the composition which is designed to have a neutral pH. Alternatively, the aluminum salt can be directly added as the citrate in such case. As the salt, the same general classes of anions as mentioned for the magnesium salts can be used, such as halide (e. g., bromide, chloride), sulfate, nitrate, hydroxide, oxide, acetate, propionate, etc.

Preferably, in the compositions the metal compound is added to the composition in an amount sufficient to provide at least a stoichiometric equivalent between the anionic surfactant and the multivalent metal cation. For example, for each gram-ion of Mg++ there will be 2 gram moles of paraffin sulfonate, alkylbenzene sulfonate, etc., while for each gram-ion of Au 3+ there will be 3 gram moles of anionic surfactant. Thus, the proportion of the multivalent salt generally will be selected so that one equivalent of compound will neutralize from 0.1 to 1.5 equivalents, preferably 0.9 to 1.4 equivalents, of the acid form of the anionic surfactant. At higher concentrations of anionic surfactant, the amount of multivalent salt will be in range of 0.5 to 1 equivalents per equivalent of anionic surfactant.

The instant compositions can include from 0 to 2%, preferably from 0.1 % to 2.0% by weight of the composition of a Cg-C22 fatty acid or fatty acid soap as a foam suppressant.

The addition of fatty acid or fatty acid soap provides an improvement in the rinseability of the composition whether applied in neat or diluted form. Generally, however, it is necessary to increase the level of cosurfactant to maintain product stability when the fatty acid or soap is present. If more than 2.5 wt. % of a fatty acid is used in the instant compositions, the composition will become unstable at low temperatures as well as having an objectionable smell.

As example of the fatty acids which can be used as such or in the form of soap, mention can be made of distille coconut oil fatty acids,"mixed vegetable"type fatty acids (e. g. high percent of saturated, mono-and/or polyunsaturated Cl 8 chains); oleic

acid, stearic acid, palmitic acid, eiocosanoic acid, and the like, generally those fatty acids having from 8 to 22 carbon atoms being acceptable.

The all-purpose liquid cleaning composition of this invention may, if desired, also contain other components either to provide additional effect or to make the product more attractive to the consumer. The following are mentioned by way of example: Colors or dyes in amounts up to 0.5% by weight; bactericides in amounts up to 1 % by weight; preservatives or antioxidizing agents, such as formalin, 5-bromo-5-nitro-dioxan- 1,3; 5-chloro-2-methyl-4-isothaliazolin-3-one, 2,6-di-tert. butyl-p-cresol, etc., in amounts up to 2% by weight; and pH adjusting agents, such as sulfuric acid or sodium hydroxide, as needed. Furthermore, if opaque compositions are desired, up to 4% by weight of an opacifier may be added.

In final form, the all-purpose hard surface liquid cleaning compositions exhibit stability at reduced and increased temperatures. More specifically, such compositions remain clear and stable in the range of 5 C to 50 C, especially 1 00C to 43 C. Such compositions exhibit a pH in the acid or neutral range depending on intended end use.

The liquids are readily pourable and exhibit a viscosity in the range of 6 to 60 milliPascal. second (mPas.) as measured at 25 C. with a Brookfield RVT Viscometer using a #1 spindle rotating at 20 RPM. Preferably, the viscosity is maintained in the range of 10 to 40 muas.

The compositions are directly ready for use or can be diluted as desired and in either case no or only minimal rinsing is required and substantially no residue or streaks are left behind. Furthermore, because the compositions are free of detergent builders such as alkali metal polyphosphates they are environmentally acceptable and provide a better"shine"on cleaned hard surfaces.

Because the compositions as prepared are aqueous liquid formulations and since no particular mixing is required to form the compositions, the compositions are easily prepared simply by combining all the ingredients in a suitable vessel or container. The order of mixing the ingredients is not particularly important and generally the various ingredients can be added sequentially or all at once or in the form

of aqueous solutions of each or all of the primary detergents and cosurfactants can be separately prepared and combine with each other and with the perfume. The magnesium salt, or other multivalent metal compound, when present, can be added as an aqueous solution thereof or can be added directly. It is not necessary to use elevated temperatures in the formation step and room temperature is sufficient.

The instant compositions explicitly exclude alkali metal silicates and alkali metal builders such as alkali metal polyphosphates, alkali metal carbonates, alkali metal phosphonates and alkali metal citrates because these materials, if used in the instant composition, would cause the composition to have a high pH as well as leaving residue on the surface being cleaned.

The following examples illustrate liquid cleaning compositions of the described invention. Unless otherwise specified, all percentages are by weight. The exemplified compositions are illustrative only and do not limit the scope of the invention. Unless otherwise specified, the proportions in the examples and elsewhere in the specification are by weight.

Example 1 The following compositions in wt. % were prepared by simple mixing at 25°C: A B C D Mr Proper St. Marc Lemon Sodium C13-C17 Paraffin sulfonate 4.7 2 2 2 2. 9 -- EO/BO nonionic EB 96-0779 0 4 4 3 -- -- Levenol F-200 2.3 0 0 0 Dobanol91-5 0 2 0 0---- Dobanol 91-2. 5 0 0 2 3 0 0 C13-15 EO14 nonionic 0 0 0 0 3.3 0 Coco fatty acid 0.75 0.5 0.5 0.5 0.65 0.3 Dieth tene I col monometh I ether 4 0 0 0 4.4 3 Tripropylene glycol n-butyl ether 0 0 0 0 0 0 MgSO4 7 H20 2.2 0.5 1.0 1.0---- Perfume (a) 0.8 0.8 0.8 0.8 resent resent Water + Minors Bal. Bal. Bai. Bal. Bal. Bai. pH 6.5 6.5 6.5 6.5 9.5 7 Foam control STD Better Better Better Better N/A Degreasingneat Dynamic test STD Equal Equal Equal Worse Worse Autoactivit STD Worse Equal Equal Worse Worse Dilute degreasing STD Better Better Better Worse Worse Residue test on PMMA STD Equal Worse Worse Worse E ual Stability STD E ual E ual E ual E ual E ual