EP0292910A2 - Hard surface cleaning composition - Google Patents

Hard surface cleaning composition Download PDF

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Publication number
EP0292910A2
EP0292910A2 EP88108207A EP88108207A EP0292910A2 EP 0292910 A2 EP0292910 A2 EP 0292910A2 EP 88108207 A EP88108207 A EP 88108207A EP 88108207 A EP88108207 A EP 88108207A EP 0292910 A2 EP0292910 A2 EP 0292910A2
Authority
EP
European Patent Office
Prior art keywords
composition
soap
amount
fatty acid
ranges
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP88108207A
Other languages
German (de)
French (fr)
Other versions
EP0292910A3 (en
EP0292910B1 (en
Inventor
Pierre Fonsny
Nicole Andries
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Colgate Palmolive Co
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Colgate Palmolive Co
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Publication of EP0292910A2 publication Critical patent/EP0292910A2/en
Publication of EP0292910A3 publication Critical patent/EP0292910A3/en
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Publication of EP0292910B1 publication Critical patent/EP0292910B1/en
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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2075Carboxylic acids-salts thereof
    • C11D3/2079Monocarboxylic acids-salts thereof
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D10/00Compositions of detergents, not provided for by one single preceding group
    • C11D10/04Compositions of detergents, not provided for by one single preceding group based on mixtures of surface-active non-soap compounds and soap
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0008Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
    • C11D17/0013Liquid compositions with insoluble particles in suspension
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/14Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/72Ethers of polyoxyalkylene glycols

Definitions

  • This invention relates to liquid, aqueous, stable, effective, safe, non-scratching hard surface cleaning compositions commonly referred to as scouring cleansers.
  • the compositions are physically stable, do not separate, whereby the user is assured of the optimum performance to be expected from the various components and their amounts and ratios with respect to one another, are safe and do not scratch the usual surfaces to be cleaned, such as glass, porcelain, ceramic, plastic, metal, wood, painted wood (enamelled and lacquered).
  • U.S. Patent 4,005,027 describes compositions which include clay and insoluble abrasive. Only inorganic abrasives are shown. The compositions include surfactants which are bleach stable. Nonionics are not used. It is alleged that the products are physically stable and also do not "appreciably run along vertical surfaces" (column 10, lines 45-47). Such stability is a manifestation of a false body fluid formed when using the smectite and attapulgite clays necessary in such composi­tions. In U.S. Patent 4,116,849 the compositions are very similar to those in U.S. Patent 4,005,027. In addition, U.S.
  • Patent 4,116,849 discloses thickening agents instead of the preferred smectite and attapulgite clays, such as colloidal silica, polystyrenes, sulfonated polystyrenes, polyethylene, oxidized polyethylenes, polypropylene, copolymers of styrene with methacrylic acid, methyl or ethyl acrylate, vinyl acetate, among others; patentee states that "...ethoxylated nonionic surfactants are to be avoided.” Neither of these two patents disclose soaps or fatty acids as suitable materials as well.
  • U.S. Patent 4,240,919 describes compositions of multivalent stearate soap, water and water-insoluble abrasive.
  • abrasives are disclosed and among the “organic” types are “melamine, urea formaldehyde resins, ground rigid polymeric materials, such as polyurethane foam." (column 3, lines 10-12).
  • substantially any surfactant materials which are compatible with the other components in the composition of the present invention. These include water-soluble anionic, nonionic, amphoteric, cationic and zwitterionic surfactants.” (column 3, lines 57-62). Further reference is made to U.S.
  • Patents 4,051,056 (expanded perlite as abrasive), 4,457,856 (polyacrylate abrasive), German 1,956,616 (polyvinyl chloride as abrasive), 3,645,904 (skin cleanser containing polymer abrasive material) and 4,302,347.
  • a composition manifesting the optimum desiderata for a non-scratching, stable, effective and safe aqueous scouring cleanser has eluded the art.
  • the ability to remove most stains from all normally encountered hard surfaces and particularly plastic surfaces without damaging such delicate plastic materials as one might find as, for example, kitchen counter tops, anti-­stick coatings on metal pots, polystyrene, polymethyl methacrylate, polyvinyl chloride, nylon, polyester (e.g. fiberglass) and the like articles is the major thrust of this invention.
  • the composition should have good degreasing characteristics as well. Physical stability as demonstrated by the prior art cited above is a major problem and for good consumer acceptability is a must.
  • liquid non-scratching, aqueous, scouring cleansing composition comprises a fatty acid and/or fatty acid soap, non-soap anionic surfactant, nonionic surfactant, electrolyte and particulate abrasive.
  • the fatty acid component may be any fatty acid having a carbon chain of from about C6-C30 with C8-C20 preferred. Most preferred are C10-C18 and typically, naturally occuring materials, such as coconut oil, palm kernel oil, and animal tallow, serve admirably as sources for the fatty acids. A particularly preferred range of fatty acids is C12-C18 as one would find in coconut oil. A typical coconut oil fatty acid composition contains about 50% C12: 20% C14; 8.5% C16; and 10% C18 the balance other acid and even perhaps some neutral material, and is a liquid at 40°C.
  • the soaps used are the alkali metal and ammonium salts with sodium and potassium preferred.
  • the fatty acid may comprise from about 0.5 to 15% by weight and preferably 1 to 10% and, more preferably 1 to 7% of the compo­sition.
  • the non-stop anionic may be chosen from any of the conventional anionics, such as the alkyl benzene sulfonates, the alkyl sulfates, alcohol sulfates, the alcohol ether sulfates, olefin sulfonates, paraffin sulfonates, fatty acid monoglyceride sulfates, sarcosides, taurides and the like and their salts, such as alkali, alkaline, earth and ammonium salts. Of these, the sulfates and sulfonates are preferred.
  • the preferred non-soap anionic surfactants are the paraffin sulfonates (C10-C20); the linear alkyl benzene sulfonates, the alcohol and the alcohol ether sulfates.
  • the most preferred anionics are the C12-C18 paraffin sulfonates in the form of their alkali metal or ammonium salts; C8-C20 alkyl benzene sulfonates with C12-C16 being most highly preferred; the alkyl (i.e. alcohol) sulfates of C12-C18 and the corresponding ether sulfates with 3 to 50 (e.g. 3, 5, 10, 20, 30 or 50) moles of condensed ethylene oxide.
  • the most preferred salt forming cation is sodium.
  • the amount of the non-soap anionic may range from 1 to 15% by weight, preferably 1 to 10% and more preferably 1 to 5% by weight.
  • anionics are sodium lauryl sulfate, sodium paraffin (C14-C17) sulfonate, sodium decyl sulfate, sodium tridecyl sulfonate, sodium tallow alkyl sulfate, sodium coconut alkyl sulfate, sodium oxotridecyl-­(triethoxyl) [sulfate (sulfated - 3 E.O.
  • the nonionic surfactants which are usable herein are generally characterized by a long chain hydrophobe and a poly­(ethylene oxide) hydrophilic chain.
  • the hydrophobe may and preferably is from an alcohol (C6-C30, preferably C8-C18; most preferably C10-C16, typically a C13 alcohol, such as linear tridecyl alcohol), or a polypropylene backbone.
  • Other hydrophobes such as thioalcohols, acids, amines and the like, may also be used.
  • the preferred alcohol is a C10-C16 alcohol with 1 to less than 5 moles of ethylene oxide and most preferably 2 to 4 moles of ethylene oxide, typically 3 moles of ethylene oxide.
  • the level of nonionic in the formulation may vary from about 0.5% to about 15% by weight with preferred levels ranging from 1 to 10% and most preferred from about 3.5 to 6.5% typically and most highly preferred is 5%.
  • the electrolyte used herein is typically an alkaline, builder-type inorganic or organic salt.
  • the usual salts comprise the alkali metal bicarbonates, borates, carbonates, phosphates, polyphosphates and silicates among the inorganics and the polycarboxylates, such as polyacetates, tartrates, citrates, maleates, oxydiacetates, alkenyl succinates, carboxymethyloxy succinates, oxydisuccinates and the like, among the organics.
  • Polymeric builder salts such as the water-soluble salts of polymers of maleic acid, itaconic acid and the like, may be used as well as copolymers and interpolymers thereof with polymerizable ⁇ , ⁇ -ethylenically unsaturated compounds, such as vinyl ethers, esters, alkyl alcohol, acrylic and methacrylic acid and esters thereof, etc.
  • the electrolyte may vary over a considerable range from as little as 0.5% to 25% or more.
  • a preferred range is from about 2% to 15%; typically a mixture of carbonate and phosphate may total 5 to 10%; other convenient and preferred mixtures may comprise carbonate, polyphosphate and optionally some silicate in amounts of from 5 to 10% as well.
  • Specific electrolytes include sodium and potassium carbonate, sodium and potassium bicarbonate, sodium and potassium sesquicarbonate, sodium and potassium orthophosphates, pyro­phosphates, tripolyphosphate and hexametaphosphates, sodium and potassium tetraborate anhydrous, pentahydrate, decahydrate, sodium silicate (e.g. sodium metasilicate or other silicates with the Na2O to SiO2 ratio ranging from 3.5 to 1 to 1:1) as illustrative of the inorganics and ethylenediamine tetraacetic acid tetrasodium or potassium salt, trisodium nitrilotriacetate, disodium polymaleate, and the like, as merely illustrative of the organics.
  • sodium silicate e.g. sodium metasilicate or other silicates with the Na2O to SiO2 ratio ranging from 3.5 to 1 to 1:1
  • the abrasive may be any material derived from a polymeri­zable composition, such as polyethylene, polypropylene, poly­styrene, polyester, polyvinyl chloride, polyvinyl acetate, polymethyl methacrylate and various copolymers and interpolymers of the foregoing.
  • the criteria for suitability are that the material does not scratch polymethyl methacrylate and that the average particle size ranges from about 10 to 150 microns and preferably from 25 to 100 microns and most preferably from 30 to 75 microns, e.g. 60 microns.
  • a polyvinyl chloride abrasive powder whose average particle size is about 60 microns, with a major amount being within the range of 30 to 75 microns.
  • the molecular weight ranges of the polymeric abrasives may vary widely just so long as the physical properties set out above are met. Generally, milecular weights will range from several thousand (e.g. 2,000; 5,000; 20,000) to several hundred thousand (e.g. 125,000; 250,000; 400,000) and upwards of several million (e.g. 1,000,000; 2,000,000; 4,000,000; 6,000,000).
  • the amount of abrasive may range from about 2% to 30% or more (e.g. 40%; 50%).
  • a preferred range in the preferred formulations is from 5 to 25% and more preferred is a range of 5 to 15%, such as 7%; 10%; or 12%.
  • a large variety of optional ingredients may be included in the formulations of this invention. Some are even preferred, such as inorganic viscosity modifiers (e.g. montmorillonite clays, such as bentonite; attapulgites, etc.); organic ones, such as methylcellulose, carboxyl methylcellulose, hydroxy propylmethylcellulose. Such materials are particularly advan­tageous for a "cream” scouring cleanser where a "thickened” type of material is desired by the consumer. For such products it may be desirable to have viscosities ranging from several hundred (250 cps; 400 cps; 500 cps) to several thousand (e.g. 1,100 cps; 1,500 cps; 2,000 cps, etc.).
  • inorganic viscosity modifiers e.g. montmorillonite clays, such as bentonite; attapulgites, etc.
  • organic ones such as methylcellulose, carboxyl methylcellulose, hydroxy propy
  • the formulations of this invention exhibit unusual stability (i.e. lack of or minimum phase separation) in the absence of the viscosity "elevators," their major function as mentioned above to merely thicken.
  • the amount of the viscosity modifier may range from about 0.1 to 5 to 10%; usually 0.5 to 3%.
  • Other optional but, again, preferred additives include a hydrocarbon material, particularly a terpene, such as d-limonene. Such terpenes are readily available in many perfume materials which are generally added to most consumer cleaning products.
  • the amount of the hydrocarbon may vary from 0.05 to 5% and preferably from 0.1 to 2 to 3%.
  • Other additives which may be used include bleaches (liquid and solid hypochlorites, available, e.g.
  • auxiliary materials as NaOCl solution or calcium hypochlorite powder; chloramines, chlorinated di- and trisodium phosphates, sodium and potassium dichlorisocyanurate, trichlorocyanuric acid, and so forth); buffers, caustic soda; caustic potash; suds boosters; enzymes; preservatives; disinfectants; colorants; fragrances and the like, may be used where desired and compatible. Generally, minor amounts of such auxiliary materials are employed, e.g. 0.01 to 10% and often 0.1% to 5%.
  • compositions of this invention are alkaline and generally have a pH from about 10 to 12. It is generally preferred to add in the formulations the fatty acid in free acid form and neutralize in situ with caustic soda (NaOH) or caustic potash (KOH), at the same time adjusting the pH to the desired level.
  • CaOH caustic soda
  • KOH caustic potash
  • compositions of this invention are generally prepared by adding to the formula weight of hot water with stirring in a suitable mixer and homogenizer (at a temperature of about 50 to 80°C, e.g. 60°C) the following composition in the order given: fatty acid, nonionic, viscosity modifier (if used), abrasive polymer particles, and alkali for neutralization of fatty acid; at this point the temperature of the mixture is lowered to about room temperature and then the electrolyte (e.g.
  • composition is prepared in the manner described previously as preferred. To the formula weight of water at 60°C are added the fatty acid, nonionic, clay, abrasive and caustic potash with vigorous stirring. After a uniform mixture is obtained, it is cooled to room temperature (20°C) and the remaining components (in the order listed) are added with stirring. A creamy, stable product results; the pH is about 11 and the viscosity is about 1,100 cps.
  • Example I is repeated except that the following fatty acids are used in place of 2% distilled coconut fatty acid:
  • Example I is repeated using 5% sodium lauryl sulfate in place of the sodium paraffin sulfonate.
  • Examples I and III are repeated separately replacing the TKPP and K2CO3 with 4% soda ash (anhydrous Na2CO3).
  • Example I The product of Example I is used in a standarized test procedure to determine the degree of scratching against a plastic surface. This is compared with two commercial products.
  • the procedure involves the use of a reciprocating moving sponge (spontex) containing 1 g of test product which is applied to a plastic tile and after 200 strokes the plastic tile is washed and the gloss is compared with that of the original.
  • the tile used has an initial gloss reading of 79 and this is unchanged after the test with the product of Example I.
  • the two commercial products gave readings of 72 and 73 demonstrating thereby some damage to the tile by the commercial materials and none by the composition of this invention.

Abstract

Physically stable, liquid, aqueous non-scratching hard surface cleaning compositions are provided and include a fatty acid or fatty acid soap, a non-soap anionic surfactant, a nonionic surfactant, electrolyte, and, as an abrasive, polymer particles having a hardness not greater than homopolymeric methyl methacrylate, and a particle size ranging from about 10 to 150 microns. These compositions can be safely used to clean, without scratching or damaging, all types of hard surfaces, including glass, plastics, enamels, and the like.

Description

    Background of the Invention (1) Field of Invention
  • This invention relates to liquid, aqueous, stable, effective, safe, non-scratching hard surface cleaning compositions commonly referred to as scouring cleansers. The compositions are physically stable, do not separate, whereby the user is assured of the optimum performance to be expected from the various components and their amounts and ratios with respect to one another, are safe and do not scratch the usual surfaces to be cleaned, such as glass, porcelain, ceramic, plastic, metal, wood, painted wood (enamelled and lacquered).
  • (2) Prior Art Discussion
  • The art is, of course, replete with liquid scouring compositions alleged to perform in a safe and effective manner, others stated to be physically and chemically stable and so on.
  • Some examples of prior art scouring compositions include U.S. Patent 4,005,027 which describes compositions which include clay and insoluble abrasive. Only inorganic abrasives are shown. The compositions include surfactants which are bleach stable. Nonionics are not used. It is alleged that the products are physically stable and also do not "appreciably run along vertical surfaces" (column 10, lines 45-47). Such stability is a manifestation of a false body fluid formed when using the smectite and attapulgite clays necessary in such composi­tions. In U.S. Patent 4,116,849 the compositions are very similar to those in U.S. Patent 4,005,027. In addition, U.S. Patent 4,116,849 discloses thickening agents instead of the preferred smectite and attapulgite clays, such as colloidal silica, polystyrenes, sulfonated polystyrenes, polyethylene, oxidized polyethylenes, polypropylene, copolymers of styrene with methacrylic acid, methyl or ethyl acrylate, vinyl acetate, among others; patentee states that "...ethoxylated nonionic surfactants are to be avoided." Neither of these two patents disclose soaps or fatty acids as suitable materials as well. U.S. Patent 4,240,919 describes compositions of multivalent stearate soap, water and water-insoluble abrasive. Various abrasives are disclosed and among the "organic" types are "melamine, urea formaldehyde resins, ground rigid polymeric materials, such as polyurethane foam..." (column 3, lines 10-12). Optionally, there may be present "substantially any surfactant materials which are compatible with the other components in the composition of the present invention..." These include water-soluble anionic, nonionic, amphoteric, cationic and zwitterionic surfactants." (column 3, lines 57-62). Further reference is made to U.S. Patents 4,051,056 (expanded perlite as abrasive), 4,457,856 (polyacrylate abrasive), German 1,956,616 (polyvinyl chloride as abrasive), 3,645,904 (skin cleanser containing polymer abrasive material) and 4,302,347.
  • A composition manifesting the optimum desiderata for a non-scratching, stable, effective and safe aqueous scouring cleanser has eluded the art. The ability to remove most stains from all normally encountered hard surfaces and particularly plastic surfaces without damaging such delicate plastic materials as one might find as, for example, kitchen counter tops, anti-­stick coatings on metal pots, polystyrene, polymethyl methacrylate, polyvinyl chloride, nylon, polyester (e.g. fiberglass) and the like articles is the major thrust of this invention. In addition to removing stains, the composition should have good degreasing characteristics as well. Physical stability as demonstrated by the prior art cited above is a major problem and for good consumer acceptability is a must.
  • Accordingly, it is an object of the present invention to provide liquid, aqueous, stable, abrasive-containing cleaning composition.
  • It is another object of this invention to provide a liquid, aqueous abrasive-containing cleaning composition which is safe and also substantially non-scratching on most encountered surfaces, including plastic surfaces.
  • It is still another object of our invention to provide stable, liquid, aqueous polymer abrasive-containing cleaning compositions which are safe, effective and non-scratching.
  • It is a further object of the invention to provide method for making the compositions of the invention.
  • Other objects will appear hereinafter as the description proceeds.
  • Description of the Invention
  • The objects of this invention are obtained in accordance with the following description wherein the liquid non-scratching, aqueous, scouring cleansing composition comprises a fatty acid and/or fatty acid soap, non-soap anionic surfactant, nonionic surfactant, electrolyte and particulate abrasive.
  • The fatty acid component may be any fatty acid having a carbon chain of from about C₆-C₃₀ with C₈-C₂₀ preferred. Most preferred are C₁₀-C₁₈ and typically, naturally occuring materials, such as coconut oil, palm kernel oil, and animal tallow, serve admirably as sources for the fatty acids. A particularly preferred range of fatty acids is C₁₂-C₁₈ as one would find in coconut oil. A typical coconut oil fatty acid composition contains about 50% C₁₂: 20% C₁₄; 8.5% C₁₆; and 10% C₁₈ the balance other acid and even perhaps some neutral material, and is a liquid at 40°C. While the most convenient sources are natural oils or fats yielded, mixed acids, of course, the individual specific acids, and indeed any mixture of any number and chain length of acids within the parameter of C₆-C₃₀ may be used. The soaps used are the alkali metal and ammonium salts with sodium and potassium preferred. The fatty acid may comprise from about 0.5 to 15% by weight and preferably 1 to 10% and, more preferably 1 to 7% of the compo­sition.
  • The non-stop anionic may be chosen from any of the conventional anionics, such as the alkyl benzene sulfonates, the alkyl sulfates, alcohol sulfates, the alcohol ether sulfates, olefin sulfonates, paraffin sulfonates, fatty acid monoglyceride sulfates, sarcosides, taurides and the like and their salts, such as alkali, alkaline, earth and ammonium salts. Of these, the sulfates and sulfonates are preferred.
  • The preferred non-soap anionic surfactants are the paraffin sulfonates (C₁₀-C₂₀); the linear alkyl benzene sulfonates, the alcohol and the alcohol ether sulfates.
  • The most preferred anionics (non-soap) are the C₁₂-C₁₈ paraffin sulfonates in the form of their alkali metal or ammonium salts; C₈-C₂₀ alkyl benzene sulfonates with C₁₂-C₁₆ being most highly preferred; the alkyl (i.e. alcohol) sulfates of C₁₂-C₁₈ and the corresponding ether sulfates with 3 to 50 (e.g. 3, 5, 10, 20, 30 or 50) moles of condensed ethylene oxide. The most preferred salt forming cation is sodium. The amount of the non-soap anionic may range from 1 to 15% by weight, preferably 1 to 10% and more preferably 1 to 5% by weight.
  • Some specific examples of suitable anionics are sodium lauryl sulfate, sodium paraffin (C₁₄-C₁₇) sulfonate, sodium decyl sulfate, sodium tridecyl sulfonate, sodium tallow alkyl sulfate, sodium coconut alkyl sulfate, sodium oxotridecyl-­(triethoxyl) [sulfate (sulfated - 3 E.O. condensate with oxotri­decyl alcohol], sodium dodecyl benzene sulfonate, sodium tri­decyl benzene sulfonate, sodium tetradecyl benzene sulfonate and sodium (C₁₅) olefin sulfonate.
  • The nonionic surfactants which are usable herein are generally characterized by a long chain hydrophobe and a poly­(ethylene oxide) hydrophilic chain. The hydrophobe may and preferably is from an alcohol (C₆-C₃₀, preferably C₈-C₁₈; most preferably C₁₀-C₁₆, typically a C₁₃ alcohol, such as linear tridecyl alcohol), or a polypropylene backbone. Other hydrophobes, such as thioalcohols, acids, amines and the like, may also be used. The preferred alcohol is a C₁₀-C₁₆ alcohol with 1 to less than 5 moles of ethylene oxide and most preferably 2 to 4 moles of ethylene oxide, typically 3 moles of ethylene oxide. The level of nonionic in the formulation may vary from about 0.5% to about 15% by weight with preferred levels ranging from 1 to 10% and most preferred from about 3.5 to 6.5% typically and most highly preferred is 5%.
  • The electrolyte used herein is typically an alkaline, builder-type inorganic or organic salt. The usual salts comprise the alkali metal bicarbonates, borates, carbonates, phosphates, polyphosphates and silicates among the inorganics and the polycarboxylates, such as polyacetates, tartrates, citrates, maleates, oxydiacetates, alkenyl succinates, carboxymethyloxy succinates, oxydisuccinates and the like, among the organics. Polymeric builder salts, such as the water-soluble salts of polymers of maleic acid, itaconic acid and the like, may be used as well as copolymers and interpolymers thereof with polymerizable α,β-ethylenically unsaturated compounds, such as vinyl ethers, esters, alkyl alcohol, acrylic and methacrylic acid and esters thereof, etc.
  • The electrolyte may vary over a considerable range from as little as 0.5% to 25% or more. A preferred range is from about 2% to 15%; typically a mixture of carbonate and phosphate may total 5 to 10%; other convenient and preferred mixtures may comprise carbonate, polyphosphate and optionally some silicate in amounts of from 5 to 10% as well.
  • Specific electrolytes include sodium and potassium carbonate, sodium and potassium bicarbonate, sodium and potassium sesquicarbonate, sodium and potassium orthophosphates, pyro­phosphates, tripolyphosphate and hexametaphosphates, sodium and potassium tetraborate anhydrous, pentahydrate, decahydrate, sodium silicate (e.g. sodium metasilicate or other silicates with the Na₂O to SiO₂ ratio ranging from 3.5 to 1 to 1:1) as illustrative of the inorganics and ethylenediamine tetraacetic acid tetrasodium or potassium salt, trisodium nitrilotriacetate, disodium polymaleate, and the like, as merely illustrative of the organics.
  • The abrasive may be any material derived from a polymeri­zable composition, such as polyethylene, polypropylene, poly­styrene, polyester, polyvinyl chloride, polyvinyl acetate, polymethyl methacrylate and various copolymers and interpolymers of the foregoing. The criteria for suitability are that the material does not scratch polymethyl methacrylate and that the average particle size ranges from about 10 to 150 microns and preferably from 25 to 100 microns and most preferably from 30 to 75 microns, e.g. 60 microns. For optimum performance it is most desirable to utilize a polyvinyl chloride abrasive powder whose average particle size is about 60 microns, with a major amount being within the range of 30 to 75 microns. The molecular weight ranges of the polymeric abrasives may vary widely just so long as the physical properties set out above are met. Generally, milecular weights will range from several thousand (e.g. 2,000; 5,000; 20,000) to several hundred thousand (e.g. 125,000; 250,000; 400,000) and upwards of several million (e.g. 1,000,000; 2,000,000; 4,000,000; 6,000,000). The amount of abrasive may range from about 2% to 30% or more (e.g. 40%; 50%). A preferred range in the preferred formulations is from 5 to 25% and more preferred is a range of 5 to 15%, such as 7%; 10%; or 12%.
  • A large variety of optional ingredients may be included in the formulations of this invention. Some are even preferred, such as inorganic viscosity modifiers (e.g. montmorillonite clays, such as bentonite; attapulgites, etc.); organic ones, such as methylcellulose, carboxyl methylcellulose, hydroxy propylmethylcellulose. Such materials are particularly advan­tageous for a "cream" scouring cleanser where a "thickened" type of material is desired by the consumer. For such products it may be desirable to have viscosities ranging from several hundred (250 cps; 400 cps; 500 cps) to several thousand (e.g. 1,100 cps; 1,500 cps; 2,000 cps, etc.).
  • It is extremely significant that the formulations of this invention exhibit unusual stability (i.e. lack of or minimum phase separation) in the absence of the viscosity "elevators," their major function as mentioned above to merely thicken. The amount of the viscosity modifier may range from about 0.1 to 5 to 10%; usually 0.5 to 3%. Other optional but, again, preferred additives include a hydrocarbon material, particularly a terpene, such as d-limonene. Such terpenes are readily available in many perfume materials which are generally added to most consumer cleaning products. The amount of the hydrocarbon may vary from 0.05 to 5% and preferably from 0.1 to 2 to 3%. Other additives which may be used include bleaches (liquid and solid hypochlorites, available, e.g. as NaOCl solution or calcium hypochlorite powder; chloramines, chlorinated di- and trisodium phosphates, sodium and potassium dichlorisocyanurate, trichlorocyanuric acid, and so forth); buffers, caustic soda; caustic potash; suds boosters; enzymes; preservatives; disinfectants; colorants; fragrances and the like, may be used where desired and compatible. Generally, minor amounts of such auxiliary materials are employed, e.g. 0.01 to 10% and often 0.1% to 5%.
  • The compositions of this invention are alkaline and generally have a pH from about 10 to 12. It is generally preferred to add in the formulations the fatty acid in free acid form and neutralize in situ with caustic soda (NaOH) or caustic potash (KOH), at the same time adjusting the pH to the desired level. A typical, preferred pH 11±0.5.
  • The compositions of this invention are generally prepared by adding to the formula weight of hot water with stirring in a suitable mixer and homogenizer (at a temperature of about 50 to 80°C, e.g. 60°C) the following composition in the order given: fatty acid, nonionic, viscosity modifier (if used), abrasive polymer particles, and alkali for neutralization of fatty acid; at this point the temperature of the mixture is lowered to about room temperature and then the electrolyte (e.g. builder salts) is added followed by the non-stop anionic and finally the perfume (also as a source of hydrocarbon where desired), where no hydrocarbon is to be used one may, obviously, use a non-hydrocarbon containing fragrance the use, however, of a hydrocarbon material has proven desirable for increased grease removal characteristics.
  • The following examples will serve to illustrate the present invention without being deemed limitative thereof. Parts and percents are by weight unless otherwise indicated.
  • Example I
  • A formulation of the following ingredients is prepared:
    Figure imgb0001
  • The composition is prepared in the manner described previously as preferred. To the formula weight of water at 60°C are added the fatty acid, nonionic, clay, abrasive and caustic potash with vigorous stirring. After a uniform mixture is obtained, it is cooled to room temperature (20°C) and the remaining components (in the order listed) are added with stirring. A creamy, stable product results; the pH is about 11 and the viscosity is about 1,100 cps.
  • Example II
  • Example I is repeated except that the following fatty acids are used in place of 2% distilled coconut fatty acid:
    • (a) lauric acid      2.0%
    • (b) palmitic acid      2.0%
    • (c) coconut oil fatty acids      3.0%
    • (d) coconut oil fatty acids      4.0%
    • (e) lauric-stearic (3:1)      3.5%
    Example III
  • Example I is repeated using 5% sodium lauryl sulfate in place of the sodium paraffin sulfonate.
  • Example IV
  • Examples I and III are repeated separately replacing the TKPP and K₂CO₃ with 4% soda ash (anhydrous Na₂CO₃).
  • Example V
  • Each of the previous examples is separately repeated but in place of 5% nonionic there is used
    • (a) 3% nonionic
    • (b) 6% nonionic.
  • The product of Example I is used in a standarized test procedure to determine the degree of scratching against a plastic surface. This is compared with two commercial products. The procedure involves the use of a reciprocating moving sponge (spontex) containing 1 g of test product which is applied to a plastic tile and after 200 strokes the plastic tile is washed and the gloss is compared with that of the original. The tile used has an initial gloss reading of 79 and this is unchanged after the test with the product of Example I. The two commercial products gave readings of 72 and 73 demonstrating thereby some damage to the tile by the commercial materials and none by the composition of this invention.

Claims (12)

1. A stable, liquid, aqueous, non-scratching scouring cleaning composition comprising a fatty acid or fatty acid soap, a non-soap anionic surfactant, a nonionic surfactant, electrolyte, and particulate abrasive, said anionic surfactant being selected from the group consisting of sulfonate and sulfate surfactants, said nonionic surfactant having the molecular configuration of an hydrophobe condensed with ethylene oxide, said electrolyte comprising a water-soluble inorganic or organic builder salt and said abrasive being a solid polymerizate derived from a polymerizable, α,β-ethylenically unsaturated monomer having a hardness not greater than homopolymeric methyl methacrylate and having an average particle size ranging from about 10 to 150 microns.
2. A composition as defined in claim 1 wherein the fatty acid or soap is a C₆-C₃₀, the non-soap anionic and the nonionic surfactants contain a C₁₀-C₂₀ linear aliphatic hydrocarbon chain, the number of oxyethyl groups in the nonionic surfactant ranges from 1 to 8 and the electrolyte is an alkaline builder salt or precursor thereof.
3. A composition as defined in claim 2 wherein the fatty acid or soap is a C₈-C₂₀ acid, the non-soap anionic contains a C₁₂-C₁₈ linear aliphatic hydrocarbon and the nonionic surfactant contains C₁₀-C₁₆ linear aliphatic hydrocarbon.
4. A composition as defined in claim 2 wherein the amount of fatty acid or soap ranges from 0.5 to 15%, the amount of non-soap anionic ranges from 1 to 15%, the amount of nonionic from 0.5 to 15%, the amount of electrolyte from 1 to 25% and the amount of abrasive from 2 to 30%.
5. A composition as defined in claim 4 including a hydrocarbon in an amount ranging from 0.05% to 5%.
6. A composition as defined in claim 4 wherein the fatty acid or soap is derived from coconut oil, the non-soap anionic is a paraffin sulfonate, the nonionic is a C₁₀-C₁₆ alcohol containing from 1 to less than 5 oxyethyl groups and the electrolyte comprises a polyphosphate.
7. A composition as defined in claim 6 wherein the abrasive is polyvinyl chloride.
8. A composition as defined in claim 7 including up to 5% hydrocarbon.
9. A composition as defined in claim 8 wherein the hydrocarbon is a terpene.
10. A composition as defined in claim 8 including from 0.05 to 5% of the hydrocarbon.
11. A composition as defined in claim 10 wherein the hydrocarbon is d-limonene.
12. A composition as defined in claim 7 wherein the amount of fatty acid or soap ranges from 1 to 5% by weight, the amount of non-soap anionic ranges from 1 to 5% by weight, the weight of nonionic ranges from 1 to 10% by weight, the amount of electrolyte ranges from 5 to 10% by weight; and the amount of abrasive ranges from 5 to 15% by weight.
EP88108207A 1987-05-28 1988-05-21 Hard surface cleaning composition Expired - Lifetime EP0292910B1 (en)

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EP0346994A2 (en) * 1988-06-13 1989-12-20 Unilever N.V. Liquid detergent compositions
EP0372427A2 (en) * 1988-12-02 1990-06-13 Kao Corporation Detergent composition
EP0415395A2 (en) * 1989-08-30 1991-03-06 Dow Corning Corporation Aqueous cleaning dispersions using adsorptive polymeric powder and method of using
WO1991010718A1 (en) * 1990-01-20 1991-07-25 Henkel Kommanditgesellschaft Auf Aktien Anti-froth cleaning agents and use thereof
WO1992020776A1 (en) * 1991-05-15 1992-11-26 Eftichios Van Vlahakis Liquid hand soap composition
WO1997039099A1 (en) * 1996-04-12 1997-10-23 Reckitt & Colman Inc. Stable bleach-containing cleansing compositions with soft abrasives
WO2003018737A1 (en) * 2001-08-31 2003-03-06 Hydro Particles As Use of spherical and monodisperse polymer particles in cleaning agents, and such cleaning agents
EP1321514A1 (en) * 2001-12-21 2003-06-25 Maclean S.A. Liquid scouring composition containing polyethylene particles
WO2004035720A1 (en) 2002-10-16 2004-04-29 Henkel Kommanditgesellschaft Auf Aktien Transparent abrasive cleaning product, especially washing up liquid
GB2398571A (en) * 2003-02-22 2004-08-25 Reckitt Benckiser Inc Acidic hard surface cleaning and/or disinfecting composition
US7119055B2 (en) 2001-08-31 2006-10-10 Reckitt Benckiser Inc. Hard surface cleaners comprising a thickening gum mixture
US7196046B2 (en) 2001-08-31 2007-03-27 Reckitt Benckiser Inc. Hard surface cleaner comprising a suspension of alginate beads
US7256167B2 (en) * 2001-08-31 2007-08-14 Reckitt Benckiser Inc. Hard surface cleaner comprising suspended particles and oxidizing agent
US7288512B2 (en) 2003-02-22 2007-10-30 Reckitt Benckiser Inc. Hard surface cleaning compositions comprising suspended alginate inclusions
US7291586B2 (en) 2003-02-22 2007-11-06 Reckitt Benckiser Inc. Hard surface cleaning compositions comprising suspended alginate inclusions
EP1965930A2 (en) * 2005-12-30 2008-09-10 Lam Research Corporation Method and system for using a two-phases substrate cleaning compound
EP2035537A4 (en) * 2006-05-26 2010-07-14 Gs Dev Ab Dishwashing unit for granule dishawhing machine
EP3040408A1 (en) * 2014-12-31 2016-07-06 Hayata Kimya Sanayi Anonim Sirketi Aqueous liquid cleaning compositions comprising bleaching agent and abrasive particles
FR3046061A1 (en) * 2015-12-23 2017-06-30 Oreal COMPOSITION COMPRISING TWO NEUTRALIZED FATTY ACIDS, DIFFERENT FROM ONE ANOTHER, AND A PARTICULAR CLAY

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US4678596A (en) * 1986-05-01 1987-07-07 Rohm And Haas Company Rinse aid formulation
US20050176614A1 (en) 2002-10-16 2005-08-11 Heinz-Dieter Soldanski Transparent abrasive cleaning product, especially manual dishwashing liquid

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US4655957A (en) * 1984-06-25 1987-04-07 Bausch & Lomb Incorporated Contact lens cleaning composition with polymeric beads
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EP0063472A2 (en) * 1981-04-20 1982-10-27 Alcon Laboratories, Inc. Cleansing composition for optical surfaces and method of cleansing a contact lens
US4655957A (en) * 1984-06-25 1987-04-07 Bausch & Lomb Incorporated Contact lens cleaning composition with polymeric beads
GB2181738A (en) * 1985-10-16 1987-04-29 Kao Corp Liquid abrasive detergent composition

Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0346994A2 (en) * 1988-06-13 1989-12-20 Unilever N.V. Liquid detergent compositions
EP0346994B1 (en) * 1988-06-13 1996-03-06 Unilever N.V. Liquid detergent compositions
EP0372427A2 (en) * 1988-12-02 1990-06-13 Kao Corporation Detergent composition
EP0372427A3 (en) * 1988-12-02 1991-07-03 Kao Corporation Detergent composition
EP0415395A2 (en) * 1989-08-30 1991-03-06 Dow Corning Corporation Aqueous cleaning dispersions using adsorptive polymeric powder and method of using
EP0415395A3 (en) * 1989-08-30 1991-07-17 Dow Corning Corporation Aqueous cleaning dispersions using adsorptive polymeric powder and method of using
WO1991010718A1 (en) * 1990-01-20 1991-07-25 Henkel Kommanditgesellschaft Auf Aktien Anti-froth cleaning agents and use thereof
WO1992020776A1 (en) * 1991-05-15 1992-11-26 Eftichios Van Vlahakis Liquid hand soap composition
WO1997039099A1 (en) * 1996-04-12 1997-10-23 Reckitt & Colman Inc. Stable bleach-containing cleansing compositions with soft abrasives
US5821214A (en) * 1996-04-12 1998-10-13 Reckitt & Colman Inc. Stable bleach-containing cleansing compositions with soft abrasives
AU718606B2 (en) * 1996-04-12 2000-04-20 Reckitt Benckiser Inc. Stable bleach-containing cleansing compositions with soft abrasives
US7256167B2 (en) * 2001-08-31 2007-08-14 Reckitt Benckiser Inc. Hard surface cleaner comprising suspended particles and oxidizing agent
WO2003018737A1 (en) * 2001-08-31 2003-03-06 Hydro Particles As Use of spherical and monodisperse polymer particles in cleaning agents, and such cleaning agents
US7196046B2 (en) 2001-08-31 2007-03-27 Reckitt Benckiser Inc. Hard surface cleaner comprising a suspension of alginate beads
US7119055B2 (en) 2001-08-31 2006-10-10 Reckitt Benckiser Inc. Hard surface cleaners comprising a thickening gum mixture
EP1321514A1 (en) * 2001-12-21 2003-06-25 Maclean S.A. Liquid scouring composition containing polyethylene particles
WO2004035720A1 (en) 2002-10-16 2004-04-29 Henkel Kommanditgesellschaft Auf Aktien Transparent abrasive cleaning product, especially washing up liquid
GB2398571A (en) * 2003-02-22 2004-08-25 Reckitt Benckiser Inc Acidic hard surface cleaning and/or disinfecting composition
US7186676B2 (en) 2003-02-22 2007-03-06 Reckitt Benckiser Inc. Hard surface cleaning compositions comprising alginate materials and xanthan gum
US7288512B2 (en) 2003-02-22 2007-10-30 Reckitt Benckiser Inc. Hard surface cleaning compositions comprising suspended alginate inclusions
US7291586B2 (en) 2003-02-22 2007-11-06 Reckitt Benckiser Inc. Hard surface cleaning compositions comprising suspended alginate inclusions
EP1965930A2 (en) * 2005-12-30 2008-09-10 Lam Research Corporation Method and system for using a two-phases substrate cleaning compound
EP1965930A4 (en) * 2005-12-30 2012-09-26 Lam Res Corp Method and system for using a two-phases substrate cleaning compound
EP2035537A4 (en) * 2006-05-26 2010-07-14 Gs Dev Ab Dishwashing unit for granule dishawhing machine
EP3040408A1 (en) * 2014-12-31 2016-07-06 Hayata Kimya Sanayi Anonim Sirketi Aqueous liquid cleaning compositions comprising bleaching agent and abrasive particles
WO2016118096A1 (en) * 2014-12-31 2016-07-28 Hayat Kimya Sanayi Anonim Sirketi Aqueous liquid cleaning compositions comprising bleaching agent and abrasive particles
FR3046061A1 (en) * 2015-12-23 2017-06-30 Oreal COMPOSITION COMPRISING TWO NEUTRALIZED FATTY ACIDS, DIFFERENT FROM ONE ANOTHER, AND A PARTICULAR CLAY

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EP0292910A3 (en) 1990-03-28
CA1315636C (en) 1993-04-06
NO172592B (en) 1993-05-03
EP0292910B1 (en) 1994-12-28
NO882339L (en) 1988-11-29
DE3852571D1 (en) 1995-02-09
DK293188A (en) 1988-11-29
NO882339D0 (en) 1988-05-27
AU1666788A (en) 1988-12-01
NO172592C (en) 1993-08-11
AU609482B2 (en) 1991-05-02
DE3852571T2 (en) 1995-08-17
DK293188D0 (en) 1988-05-27

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