EP0261718A2 - Creamy scouring compositions - Google Patents

Creamy scouring compositions Download PDF

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Publication number
EP0261718A2
EP0261718A2 EP87201698A EP87201698A EP0261718A2 EP 0261718 A2 EP0261718 A2 EP 0261718A2 EP 87201698 A EP87201698 A EP 87201698A EP 87201698 A EP87201698 A EP 87201698A EP 0261718 A2 EP0261718 A2 EP 0261718A2
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EP
European Patent Office
Prior art keywords
composition
weight
compositions
accordance
organic solvent
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Application number
EP87201698A
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German (de)
French (fr)
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EP0261718B1 (en
EP0261718A3 (en
Inventor
Stephen Culshaw
Patrick Goethals
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Procter and Gamble European Technical Center
Procter and Gamble Co
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Procter and Gamble European Technical Center
Procter and Gamble Co
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Priority claimed from GB868624156A external-priority patent/GB8624156D0/en
Application filed by Procter and Gamble European Technical Center, Procter and Gamble Co filed Critical Procter and Gamble European Technical Center
Priority to AT87201698T priority Critical patent/ATE61401T1/en
Publication of EP0261718A2 publication Critical patent/EP0261718A2/en
Publication of EP0261718A3 publication Critical patent/EP0261718A3/en
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Publication of EP0261718B1 publication Critical patent/EP0261718B1/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
    • 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
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2068Ethers

Definitions

  • the present invention relates to stable, viscous abrasive-containing scouring compositions, which show excellent cleaning, ease-of-rinsing, and shine performance, and are not aggressive to surfaces to be cleansed therewith and packaging materials.
  • compositions are substantially free of terpene solvents, and contain a narrowly-defined solvent derived from propylene glycol.
  • creamy scouring compositions containing an abrasive and binary solvent system constituted of terpenes and polar solvents have been disclosed in European Patent Application 0,126,545, published on November 28, 1984.
  • the terpenes show both cleaning and desirable emulsification properties, which enhance product viscosity.
  • viscous terpene solvent free creamy scouring cleanser compositions showing remarkable cleaning efficiency, ease-of-rinsing and surface-compatibility, can be formulated which contain a narrowly-defined solvent derived from propylene glycol.
  • the present invention relates to a viscous creamy scouring cleanser being substantially free of terpene solvents, containing a surface-active agent, an abrasive, and an organic solvent and if desired conventional additives, characterized in that said cleanser is substantially free of terpene solvents and that the organic solvent is represented by the formula: wherein R is a C1 to C8 alkyl, alkenyl or alkyl aryl group, preferably a C1 to C4 alkyl group, and n is an integer from 1 to 4, preferably 1 or 2.
  • Water-soluble detersive surfactants useful herein include well-known synthetic anionic, nonionic, amphoteric and zwitterionic surfactants and mixtures thereof. Typical of these are the alkyl benzene sulfates and sulfonates, paraffin sulfonates, olefin sulfonates, alkoxylated (especially ethoxylated) alcohols and alkyl phenols, amine oxides, sulfonates of fatty acids and of fatty acid esters, and the like, which are well-known in the detergency art.
  • such detersive surfactants contain an alkyl group in the C10-C18 range; the anionic detersive surfactants are most commonly used in the form of their sodium, potassium or triethanolammonium salts.
  • the nonionics generally contain from 3 to 17 ethylene oxide groups per mole of hydrophobic moeity.
  • Particular preferred in the compositions of the present invention are: C12-C16 alkyl benzene sulfonates, C12-C18 paraffin-sulfonates and the ethoxylated alcohols of the formula RO(CH2CH2O) n , with R being a C12-C15 alkyl chain and n being a number from 6 to 10.
  • Anionic sufactants are frequently present at levels from 0.3 to 8%, preferably 2 to 4%, of the composition.
  • Nonionic surfactants are used at levels between 0.1% to 6% by weight of the composition. Mixtures of the like surfactants can also be used.
  • the total level of surface-active agent is preferably from 3% to 5%.
  • Abrasive - The abrasive types employed herein are selected from water-insoluble, non-gritty materials well-known in the literature for their relatively mild abrasive properties. It is highly preferred that the abrasives used herein not be undesirably "scratchy". Abrasive materials having a Mohs hardness in the range of about 7, or below, are typically used; abrasives having a Mohs hardness of 3, or below, can be used to avoid scratches on aluminum or stainless steel finishes.
  • Suitable abrasives herein include inorganic materials, especially such materials as calcium carbonate and diatomaceous earth, as well as materials such as Fuller's earth, magnesium carbonate, China clay, attapulgite, calcium hydroxyapatite, calcium orthophosphate, dolomite and the like.
  • the aforesaid inorganic materials can be qualified as "strong abrasives”.
  • Synthetic organic abrasives such as urea-formaldehyde, methyl methacrylate melamine-formaldehyde resins, polyethylene spheres and polyvinylchloride can be advantageously used in order to avoid scratching on certain surfaces, especially plastic surfaces. When such "soft abrasives” are used, strong builders can be incorporated in the composition.
  • abrasives typically have a particle size range of 10-1000 microns and are used at concentrations of 5% to 30% in the compositions. Thickeners are frequently added to suspend the abrasives.
  • the organic solvent - The organic solvent to be used in the present composition has the general formula wherein R is an alkyl, alkenyl, or alkyl-aryl group having from 1 to 8 carbon atoms, and n is an integer from 1 to 4.
  • R is a alkyl group containing 1 to 4 carbon atoms, and n is 1 or 2.
  • Especially preferred R groups are n-butyl or isobutyl.
  • 1-n-butoxypropane-2-ol is especially preferred.
  • the organic solvent herein is used at levels of from 2 to 10% by weight of the composition, preferably 4 to 6%.
  • the solvent system can optionally contain, in combination with the solvent described hereinabove, water-soluble CARBITOL® solvents or water-soluble CELLOSOLVE® solvents.
  • Water-soluble CARBITOL® solvents are compounds of the 2-(2-alkoxyethyoxy)ethanol class wherein the alkoxy group is derived from ethyl, propyl or butyl; a preferred water-soluble carbitol is 2-(2-butoxyethoxy)ethanol also known as butyl carbitol.
  • Water-soluble CELLOSOLVE® solvents are compound of the 2-alkoxy ethanol class, with 2-butyl ethanol being preferred.
  • Suitable solvents to be used with the solvents of the invention are also benzyl alcohol, and diols such as 2-ethyl-2,3-hexanediol and 2,2,4-trimethyl-1,3-pentanediol.
  • co-solvents can be used in levels ranging from 0.1 to 5% of the composition.
  • compositions herein are substantially free of terpene-solvents.
  • solvents are generally used at levels exceeding about 2%, terpenes cannot be incorporated in the claimed compositions in such proportions.
  • relatively minor sub-additive levels of terpenes e.g., below about 0.6% (calculated on the total cleanser composition), can be present originating from conventional ingredients such as perfumes.
  • the present composition can contain additional components, which can be highly desirable.
  • compositions contain a detergent builder and/or metal ion sequestrant.
  • detergent builders include the nitrilotriacetates, (NTA), ethylene diamine tetracetate (EDTA), amino-polyphosphonates (DEQUEST), water-soluble phosphates such as tri-polyphosphate and sodium ortho- and pryo-phosphates, silicates, and mixtures thereof. These builders are preferably not used in combination with strong abrasives like calcium carbonate, but are recommended in combination with soft organic abrasives like polyvinylchloride.
  • Metal ion sequestrants of lower metal sequestration constant can advantageously be used in combination with strong or soft abrasives.
  • Those metal ion sequestrants include polycarboxylates, citrates.
  • Preferred builders/sequestrants for use in the present invention are NTA, EDTA, citrates and mixtures thereof.
  • the builders/sequestrant will be present at levels of from 1% to 15%, preferably from 2% to 7%.
  • soaps in the compositions of the invention. Soaps prepared from coconut oil fatty acids are preferred.
  • Soaps are used in amounts ranging from 0.2% to 3% by weight of the composition, preferably in an amount in excess of 1%, typically from 1% to 2% by weight.
  • Thickeners should preferably be included in the compositions of the invention, in order to suspend the abrasive. However, the level will be kept under 2%, preferably from 0.2% to 1.5%. Common thickeners such as the polyacrylates, xanthan gums, carboxymethyl celluloses, swellable smectite clays, and the like, can be used herein.
  • Optional components also represented by ingredients typically used in commercial products to provide aesthetic or additional product performance benefits.
  • Typical ingredients include pH regulants, perfumes, dyes, optical brighteners, soil suspending agents, detersive enzymes, gel-control agents, freeze thaw stabilizers, bactericides, preservatives, and the like.
  • Another optional ingredient for use herein is represented by conventional detergent hydrotropes.
  • suitable hydrotropes are urea, monoethanolamine, diethanolamine, triethanolamine and the sodium potassium, ammonium and alkanol ammonium salts of xylene-, toluene-, ethylbenzene- and isopropyl-benzene sulfonates. It is a particular feature of the present invention, however, that stable formulations can be prepared without the need for hydrotropic materials of this kind.
  • compositions herein typically contain up to about 90% water as a carrier.
  • water-level can vary in the range from e.g. 50% to 80%.
  • Water-alchol e.g., ethanol, isopropanol, butanol, etc.
  • Alkylated polysaccharides can be used to increase the stability and performance characteristics of the compositions.
  • compositions herein are preferbly formulated in the alkaline pH range, generally in the range of pH 8-11, preferably about 10-10.8.
  • Caustics such as sodium hydroxide and sodium carbonate can be used to adjust and buffer the pH as desired.
  • Creamy cleansers were prepared by mixing the listed ingredients in the stated proportions (% by weight).
  • test-soils were prepared as follows.
  • the plates are placed in the oven at 115°C ("soft soil”) or 170°C (“hard soil”) for 2 hours and then allowed to age at least 1 day.
  • the testing conditions were as follows:
  • compositions are prepared:

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Detergent Compositions (AREA)

Abstract

Stable, viscous creamy scouring compositions are disclosed, which are substantially free of terpene solvents, and contain a narrowly-defined solvent derived from propylene glycol.
The compositions of the invention show excellent cleaning ease-of-rinsing, shine performance, and are not aggressive to cleansed surfaces and packaging materials.

Description

    Technical Field
  • The present invention relates to stable, viscous abrasive-containing scouring compositions, which show excellent cleaning, ease-of-rinsing, and shine performance, and are not aggressive to surfaces to be cleansed therewith and packaging materials.
  • These compositions are substantially free of terpene solvents, and contain a narrowly-defined solvent derived from propylene glycol.
  • Background
  • It is well-known to formulate scouring compositions, in liquid or creamy form, containing solvents.
  • In particular, creamy scouring compositions containing an abrasive and binary solvent system constituted of terpenes and polar solvents have been disclosed in European Patent Application 0,126,545, published on November 28, 1984. In these compositions, the terpenes show both cleaning and desirable emulsification properties, which enhance product viscosity.
  • It has become desirable, however, to replace terpenes by solvents which are fully compatible with all types of surfaces to be cleansed therewith, and packaging materials, and at the same time exhibit good cleaning and emulsification properties.
  • It now been found that viscous terpene solvent free creamy scouring cleanser compositions showing remarkable cleaning efficiency, ease-of-rinsing and surface-compatibility, can be formulated which contain a narrowly-defined solvent derived from propylene glycol.
  • US-3,591,510 discloses the use of solvents of this type in liquid hard surface cleaning compositions free of abrasive. EP-A-O 040 882 mentions the use of propylene glycol-derived solvents, in combination with terpenes and benzyl alcohols, in liquid hard surface cleanser free of abrasive.
  • It is an object of the present invention to provide viscous creamy cleanser compositions which are fully compatible with surfaces to be cleansed therewith and packaging materials. It is a further object of the present invention to provide a cleanser composition with excellent cleaning, ease-off-reasing and shine performance.
  • Summary of the Invention
  • The present invention relates to a viscous creamy scouring cleanser being substantially free of terpene solvents, containing a surface-active agent, an abrasive, and an organic solvent and if desired conventional additives, characterized in that said cleanser is substantially free of terpene solvents and that the organic solvent is represented by the formula:
    Figure imgb0001
    wherein R is a C₁ to C₈ alkyl, alkenyl or alkyl aryl group, preferably a C₁ to C₄ alkyl group, and n is an integer from 1 to 4, preferably 1 or 2.
  • Detailed Description of the Invention
  • The surface-active agents, the abrasives, the solvent and the optional ingredients are described in more detail hereinafter.
  • Unless indicated to the contrary, the %-indications stand for "% by weight".
  • Surface-active Agents
  • Water-soluble detersive surfactants useful herein include well-known synthetic anionic, nonionic, amphoteric and zwitterionic surfactants and mixtures thereof. Typical of these are the alkyl benzene sulfates and sulfonates, paraffin sulfonates, olefin sulfonates, alkoxylated (especially ethoxylated) alcohols and alkyl phenols, amine oxides, sulfonates of fatty acids and of fatty acid esters, and the like, which are well-known in the detergency art. In general, such detersive surfactants contain an alkyl group in the C₁₀-C₁₈ range; the anionic detersive surfactants are most commonly used in the form of their sodium, potassium or triethanolammonium salts. The nonionics generally contain from 3 to 17 ethylene oxide groups per mole of hydrophobic moeity. Especially preferred in the compositions of the present invention are: C₁₂-C₁₆ alkyl benzene sulfonates, C₁₂-C₁₈ paraffin-sulfonates and the ethoxylated alcohols of the formula RO(CH₂CH₂O)n, with R being a C₁₂-C₁₅ alkyl chain and n being a number from 6 to 10.
  • Anionic sufactants are frequently present at levels from 0.3 to 8%, preferably 2 to 4%, of the composition. Nonionic surfactants, are used at levels between 0.1% to 6% by weight of the composition. Mixtures of the like surfactants can also be used. The total level of surface-active agent is preferably from 3% to 5%.
  • Abrasive - The abrasive types employed herein are selected from water-insoluble, non-gritty materials well-known in the literature for their relatively mild abrasive properties. It is highly preferred that the abrasives used herein not be undesirably "scratchy". Abrasive materials having a Mohs hardness in the range of about 7, or below, are typically used; abrasives having a Mohs hardness of 3, or below, can be used to avoid scratches on aluminum or stainless steel finishes. Suitable abrasives herein include inorganic materials, especially such materials as calcium carbonate and diatomaceous earth, as well as materials such as Fuller's earth, magnesium carbonate, China clay, attapulgite, calcium hydroxyapatite, calcium orthophosphate, dolomite and the like. The aforesaid inorganic materials can be qualified as "strong abrasives". Synthetic organic abrasives such as urea-formaldehyde, methyl methacrylate melamine-formaldehyde resins, polyethylene spheres and polyvinylchloride can be advantageously used in order to avoid scratching on certain surfaces, especially plastic surfaces. When such "soft abrasives" are used, strong builders can be incorporated in the composition.
  • Typically, abrasives have a particle size range of 10-1000 microns and are used at concentrations of 5% to 30% in the compositions. Thickeners are frequently added to suspend the abrasives.
  • The organic solvent - The organic solvent to be used in the present composition has the general formula
    Figure imgb0002
    wherein R is an alkyl, alkenyl, or alkyl-aryl group having from 1 to 8 carbon atoms, and n is an integer from 1 to 4. Preferably, R is a alkyl group containing 1 to 4 carbon atoms, and n is 1 or 2. Especially preferred R groups are n-butyl or isobutyl. Most preferred species are 1-n-butoxypropane-2-ol (n=1); and 1(2-n-butoxy-1methylethoxy)propane-2-ol (n=2), and mixtures thereof. 1-n-butoxypropane-2-ol is especially preferred.
  • The organic solvent herein is used at levels of from 2 to 10% by weight of the composition, preferably 4 to 6%.
  • The solvent system can optionally contain, in combination with the solvent described hereinabove, water-soluble CARBITOL® solvents or water-soluble CELLOSOLVE® solvents. Water-soluble CARBITOL® solvents are compounds of the 2-(2-alkoxyethyoxy)ethanol class wherein the alkoxy group is derived from ethyl, propyl or butyl; a preferred water-soluble carbitol is 2-(2-butoxyethoxy)ethanol also known as butyl carbitol. Water-soluble CELLOSOLVE® solvents are compound of the 2-alkoxy ethanol class, with 2-butyl ethanol being preferred.
  • Suitable solvents to be used with the solvents of the invention are also benzyl alcohol, and diols such as 2-ethyl-2,3-hexanediol and 2,2,4-trimethyl-1,3-pentanediol.
  • The above-described co-solvents can be used in levels ranging from 0.1 to 5% of the composition.
  • The compositions herein are substantially free of terpene-solvents. Inasmuch as solvents are generally used at levels exceeding about 2%, terpenes cannot be incorporated in the claimed compositions in such proportions. It is understood, however, that relatively minor sub-additive levels of terpenes, e.g., below about 0.6% (calculated on the total cleanser composition), can be present originating from conventional ingredients such as perfumes.
  • Optional Ingredients - In addition to the essential ingredients listed hereinbefore, the present composition can contain additional components, which can be highly desirable.
  • For example, it is highly preferred that the compositions contain a detergent builder and/or metal ion sequestrant. Compounds classifiable and well-known in the art as detergent builders include the nitrilotriacetates, (NTA), ethylene diamine tetracetate (EDTA), amino-polyphosphonates (DEQUEST), water-soluble phosphates such as tri-polyphosphate and sodium ortho- and pryo-phosphates, silicates, and mixtures thereof. These builders are preferably not used in combination with strong abrasives like calcium carbonate, but are recommended in combination with soft organic abrasives like polyvinylchloride.
  • Metal ion sequestrants of lower metal sequestration constant can advantageously be used in combination with strong or soft abrasives. Those metal ion sequestrants include polycarboxylates, citrates. Preferred builders/sequestrants for use in the present invention are NTA, EDTA, citrates and mixtures thereof. The builders/sequestrant will be present at levels of from 1% to 15%, preferably from 2% to 7%.
  • It is highly preferred, as well, to include soaps in the compositions of the invention. Soaps prepared from coconut oil fatty acids are preferred.
  • Soaps are used in amounts ranging from 0.2% to 3% by weight of the composition, preferably in an amount in excess of 1%, typically from 1% to 2% by weight.
  • This level is clearly above levels currently used in similar compositions, since it has surprisingly been discovered that the presence of soaps at these higher levels not only provides suds control, but also has a thickening effect on the compositions containing the specific organic solvent of the invention. This finding allows to keep the amount of thickener at a very low level, thus substantially reducing certain drawbacks of thickeners, such as rinsing difficulties resulting from their use at substantial levels.
  • Thickeners should preferably be included in the compositions of the invention, in order to suspend the abrasive. However, the level will be kept under 2%, preferably from 0.2% to 1.5%. Common thickeners such as the polyacrylates, xanthan gums, carboxymethyl celluloses, swellable smectite clays, and the like, can be used herein.
  • Optional components also represented by ingredients typically used in commercial products to provide aesthetic or additional product performance benefits. Typical ingredients include pH regulants, perfumes, dyes, optical brighteners, soil suspending agents, detersive enzymes, gel-control agents, freeze thaw stabilizers, bactericides, preservatives, and the like.
  • Another optional ingredient for use herein is represented by conventional detergent hydrotropes. Examples of suitable hydrotropes are urea, monoethanolamine, diethanolamine, triethanolamine and the sodium potassium, ammonium and alkanol ammonium salts of xylene-, toluene-, ethylbenzene- and isopropyl-benzene sulfonates. It is a particular feature of the present invention, however, that stable formulations can be prepared without the need for hydrotropic materials of this kind.
  • The compositions herein typically contain up to about 90% water as a carrier. By way of example the water-level can vary in the range from e.g. 50% to 80%. Water-alchol (e.g., ethanol, isopropanol, butanol, etc.) mixtures can also be used. Alkylated polysaccharides can be used to increase the stability and performance characteristics of the compositions.
  • The compositions herein are preferbly formulated in the alkaline pH range, generally in the range of pH 8-11, preferably about 10-10.8. Caustics such as sodium hydroxide and sodium carbonate can be used to adjust and buffer the pH as desired.
  • The following examples are given by way of illustrating the compositions herein, but are not intended to be limiting of the scope of the invention.
    Figure imgb0003
  • Creamy cleansers were prepared by mixing the listed ingredients in the stated proportions (% by weight).
    Figure imgb0004
  • The above compositions were comparatively tested on synthetic soils representative of typical hard surface household soils. The test-soils were prepared as follows.
    • a) HBTS soil: is composed of 250 ml isopropyl alcohol, 75g calcium stearate powder and 0.5g carbon black. It is applied on an enamel-coated metal plate (cleaned with a detergent and then with alcohol) with a paint roller, and the plates are baked at 180°C for 20 minutes.
    • b) KD soil: is composed of 25% HSW® soil with carbon black (2), 37.5% Crisco® (1) oil, 37.5% Puritan® (1) oil. This soil is rolled onto stainless steel plates (beforehand cleaned with a detergent and then with alcohol) using a paint roller. A very thin uniform layer is needed since the soil is difficult to cure.
  • The plates are placed in the oven at 115°C ("soft soil") or 170°C ("hard soil") for 2 hours and then allowed to age at least 1 day.
    • (1) commercial cooking oil sold by The Procter & Gamble Company
    • (2) commercial soil sold by Chem Pack Inc., U.S.A.
  • The testing conditions were as follows:
  • The test was run with the aid of an Erichsen washability machine. A sponge of approximately 0.5 x 5 x 4 cm was used after being carefully washed under hot running water and squeezed through drying rolls. 5g of the undiluted cleanser to be tested was spread over one side of the sponge. The number of strokes of the cleaning machine varied with the type of soil. Performance readings were done as soon as visible cleaning diffrences became noticeable. The gradings were done visually by three judges working independently. The performance benefits were established via paired comparison with duplicates as follows. A 0-4 scale was used whereby: 0 means no difference; 1 = probable difference; 2 = consistent difference; 3 = clear difference; 4 = big difference.
  • The testing results were as listed below. Prior art composition A was the reference against which the composition of example I was compared.
    Figure imgb0005
  • The above test clearly confirms the significant performance benefits derivable from the inventive compositions vs. related art composition.
  • In addition, the following compositions are prepared:
    Figure imgb0006

Claims (8)

1. A viscous, creamy scouring cleanser containing a surface-active agent, an organic solvent, an abrasive, and if desired conventional additives, characterized in, that said cleanser is substantially free of terpene-solvents; and that the organic solvent is represented by the formula:
Figure imgb0007
wherein R is a C₁ to C₈ alkyl, alkenyl or alkyl aryl group, preferably a C₁ to C₄ alkyl group, and n is an integer from 1 to 4.
2. A composition in accordance with Claim 1 wherein R is C₁ to C₄ alkyl group, and n is 1 or 2.
3. A composition in accordance with Claims 1 and 2 wherein the organic solvent is 1-n-butoxypropane-2-ol or is 1(2-n-butoxy-1-methyl ethoxy)propane-2-ol, or is a mixture thereof.
4. A composition in accordance with Claims 1-3 wherein the organic solvent is present at levels of from 2% to 10% by weight.
5. A composition in accordance with Claims 1-4 which contains from 1 to 15% by weight of a detergent builder and/or metal ion sequestrant.
6. A composition in accordance with Claim 5 wherein said detergent builder and/or metal ion sequestrant material is selected from nitrilotriacetate, ethylene diamine tetraacetate, citrate, and mixtures thereof.
7. A composition in accordance with Claims 1-5 which contains from 0.2% to 3% of a fatty acid soap.
8. A viscous creamy scouring cleanser containing
- from 3% to 5% by weight of organic surface-active agent;
- from 1% to 2% by weight of fatty acid soap;
- 4% to 6% by weight of an organic solvent selected from 1-n-butoxypropane-2-ol, 1(2-n-butoxy-1-methyl ethoxy)propane-2-ol, and mixtures thereof;
- from 2% to 7% by weight of a detergent builder and/or metal ion sequestrant material selected from nitrilotriacetate, ethylene diamine tetraacetate, citrate, and mixtures thereof.
EP19870201698 1986-09-22 1987-09-08 Creamy scouring compositions Expired EP0261718B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT87201698T ATE61401T1 (en) 1986-09-22 1987-09-08 PASTE DETERGENTS.

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US91056186A 1986-09-22 1986-09-22
US910561 1986-09-22
GB868624156A GB8624156D0 (en) 1986-10-08 1986-10-08 Creamy scouring compositions
GB8624156 1986-10-08

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EP0261718A2 true EP0261718A2 (en) 1988-03-30
EP0261718A3 EP0261718A3 (en) 1989-01-25
EP0261718B1 EP0261718B1 (en) 1991-03-06

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Cited By (20)

* Cited by examiner, † Cited by third party
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EP0329209A2 (en) * 1988-01-30 1989-08-23 The Procter & Gamble Company Creamy scouring compositions
EP0426943A2 (en) * 1989-11-08 1991-05-15 Arakawa Chemical Industries, Ltd. Agent and method for removing rosinbase solder flux
US5330582A (en) * 1989-11-08 1994-07-19 Arakawa Chemical Industries, Ltd. Method for cleaning rosin-base solder flux
US5547476A (en) * 1995-03-30 1996-08-20 The Procter & Gamble Company Dry cleaning process
US5591236A (en) * 1995-03-30 1997-01-07 The Procter & Gamble Company Polyacrylate emulsified water/solvent fabric cleaning compositions and methods of using same
US5630847A (en) * 1995-03-30 1997-05-20 The Procter & Gamble Company Perfumable dry cleaning and spot removal process
US5630848A (en) * 1995-05-25 1997-05-20 The Procter & Gamble Company Dry cleaning process with hydroentangled carrier substrate
US5632780A (en) * 1995-03-30 1997-05-27 The Procter & Gamble Company Dry cleaning and spot removal proces
US5681355A (en) * 1995-08-11 1997-10-28 The Procter & Gamble Company Heat resistant dry cleaning bag
US5687591A (en) * 1995-06-20 1997-11-18 The Procter & Gamble Company Spherical or polyhedral dry cleaning articles
US5762648A (en) * 1997-01-17 1998-06-09 The Procter & Gamble Company Fabric treatment in venting bag
US5789368A (en) * 1996-01-26 1998-08-04 The Procter & Gamble Company Fabric care bag
US5804548A (en) * 1995-03-30 1998-09-08 The Procter & Gamble Company Dry cleaning process and kit
US5840675A (en) * 1996-02-28 1998-11-24 The Procter And Gamble Company Controlled released fabric care article
US5849039A (en) * 1997-01-17 1998-12-15 The Procter & Gamble Company Spot removal process
US5872090A (en) * 1996-10-25 1999-02-16 The Procter & Gamble Company Stain removal with bleach
US5891197A (en) * 1996-08-02 1999-04-06 The Proctor & Gamble Company Stain receiver for dry cleaning process
US5912408A (en) * 1995-06-20 1999-06-15 The Procter & Gamble Company Dry cleaning with enzymes
US5942484A (en) * 1995-03-30 1999-08-24 The Procter & Gamble Company Phase-stable liquid fabric refreshment composition
US6233771B1 (en) 1996-01-26 2001-05-22 The Procter & Gamble Company Stain removal device

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US3591509A (en) * 1968-09-30 1971-07-06 Procter & Gamble Liquid hard surface cleaning compositions
GB1533390A (en) * 1976-04-08 1978-11-22 Shell Int Research Detergent compositions
EP0040882A1 (en) * 1980-05-27 1981-12-02 THE PROCTER & GAMBLE COMPANY Liquid detergent compositions
EP0126545A1 (en) * 1983-04-19 1984-11-28 The Procter & Gamble Company Liquid scouring cleansers containing solvent system

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US3591509A (en) * 1968-09-30 1971-07-06 Procter & Gamble Liquid hard surface cleaning compositions
GB1533390A (en) * 1976-04-08 1978-11-22 Shell Int Research Detergent compositions
EP0040882A1 (en) * 1980-05-27 1981-12-02 THE PROCTER & GAMBLE COMPANY Liquid detergent compositions
EP0126545A1 (en) * 1983-04-19 1984-11-28 The Procter & Gamble Company Liquid scouring cleansers containing solvent system

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0329209A2 (en) * 1988-01-30 1989-08-23 The Procter & Gamble Company Creamy scouring compositions
EP0329209A3 (en) * 1988-01-30 1990-05-23 The Procter & Gamble Company Creamy scouring compositions
EP0426943A2 (en) * 1989-11-08 1991-05-15 Arakawa Chemical Industries, Ltd. Agent and method for removing rosinbase solder flux
EP0426943A3 (en) * 1989-11-08 1991-09-04 Arakawa Chemical Industries, Ltd. Agent and method for removing rosinbase solder flux
US5330582A (en) * 1989-11-08 1994-07-19 Arakawa Chemical Industries, Ltd. Method for cleaning rosin-base solder flux
US5591236A (en) * 1995-03-30 1997-01-07 The Procter & Gamble Company Polyacrylate emulsified water/solvent fabric cleaning compositions and methods of using same
US5804548A (en) * 1995-03-30 1998-09-08 The Procter & Gamble Company Dry cleaning process and kit
US5630847A (en) * 1995-03-30 1997-05-20 The Procter & Gamble Company Perfumable dry cleaning and spot removal process
US5632780A (en) * 1995-03-30 1997-05-27 The Procter & Gamble Company Dry cleaning and spot removal proces
US5547476A (en) * 1995-03-30 1996-08-20 The Procter & Gamble Company Dry cleaning process
US5942484A (en) * 1995-03-30 1999-08-24 The Procter & Gamble Company Phase-stable liquid fabric refreshment composition
US5630848A (en) * 1995-05-25 1997-05-20 The Procter & Gamble Company Dry cleaning process with hydroentangled carrier substrate
US5687591A (en) * 1995-06-20 1997-11-18 The Procter & Gamble Company Spherical or polyhedral dry cleaning articles
US5912408A (en) * 1995-06-20 1999-06-15 The Procter & Gamble Company Dry cleaning with enzymes
US5681355A (en) * 1995-08-11 1997-10-28 The Procter & Gamble Company Heat resistant dry cleaning bag
US5789368A (en) * 1996-01-26 1998-08-04 The Procter & Gamble Company Fabric care bag
US6233771B1 (en) 1996-01-26 2001-05-22 The Procter & Gamble Company Stain removal device
US5840675A (en) * 1996-02-28 1998-11-24 The Procter And Gamble Company Controlled released fabric care article
US5891197A (en) * 1996-08-02 1999-04-06 The Proctor & Gamble Company Stain receiver for dry cleaning process
US5872090A (en) * 1996-10-25 1999-02-16 The Procter & Gamble Company Stain removal with bleach
US5849039A (en) * 1997-01-17 1998-12-15 The Procter & Gamble Company Spot removal process
US5762648A (en) * 1997-01-17 1998-06-09 The Procter & Gamble Company Fabric treatment in venting bag

Also Published As

Publication number Publication date
EP0261718B1 (en) 1991-03-06
IE60580B1 (en) 1994-07-27
EP0261718A3 (en) 1989-01-25
DE3768398D1 (en) 1991-04-11
IE872538L (en) 1988-03-22

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