EP0030986A1 - Composition détergente liquide contenant un adjuvant et un abrasif - Google Patents

Composition détergente liquide contenant un adjuvant et un abrasif Download PDF

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Publication number
EP0030986A1
EP0030986A1 EP79200802A EP79200802A EP0030986A1 EP 0030986 A1 EP0030986 A1 EP 0030986A1 EP 79200802 A EP79200802 A EP 79200802A EP 79200802 A EP79200802 A EP 79200802A EP 0030986 A1 EP0030986 A1 EP 0030986A1
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EP
European Patent Office
Prior art keywords
water
compositions
abrasive
sodium
alkyl
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.)
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Application number
EP79200802A
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German (de)
English (en)
Inventor
Sharon Janosik Mitchell
Jonathan Spinner
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Procter and Gamble Co
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Procter and Gamble Co
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Filing date
Publication date
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Priority to EP79200802A priority Critical patent/EP0030986A1/fr
Publication of EP0030986A1 publication Critical patent/EP0030986A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005—Other compounding ingredients characterised by their effect
    • C11D3/0094—High foaming compositions
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
    • C11D17/0013—Liquid compositions with insoluble particles in suspension

Definitions

  • the invention relates to liquid detergent compositions containing specified amounts and types of insoluble abrasives which are especially useful in the washing of dishes.
  • the compositions also contain high-sudsing surfactants and detergency builders which complement the action of the abrasive.
  • Scouring cleansers generally contain a relatively high level of abrasive. When used in the dishwashing process such products provide abrading power to make the removal of cooked, burnt or dried-on foods on kitchenware easier and more convenient. More recently, liquid scouring cleansers containing water-insoluble abrasives have become available. Such liquid compositions are disclosed in U.S. Patents 3,149,078; 3,210,285; 3,210,286; 3,214,380; 3,579,456; 3,623,990; 3,677,954; 3,813,349 and 3,966,432. The use of scouring cleansers, however, is normally in addition to a specific dishwashing product one product being required for removal of non-sticking soils, especially fats and oils, and a second product being required for scouring purposes.
  • the present invention provides a liquid detergent composition containing by weight
  • the detergent compositions of the present invention contain four essential components:
  • compositions of this invention contain from about 15% to about 50% of a surfactant selected from the group consisting of anionic, nonionic, ampholytic, zwitterionic surface active agents and mixtures thereof.
  • a surfactant selected from the group consisting of anionic, nonionic, ampholytic, zwitterionic surface active agents and mixtures thereof.
  • Preferred compositions contain from about 25% to about 35% of surfactant by weight of the composition.
  • anionic surfactants and mixtures of anionic and nonionic surfactants are especially preferred.
  • anionic detergents can be broadly described as the water-soluble salts, particularly the alkali metal, ammonium and amine salts, of organic sulfuric reaction products having in their molecular structure an alkyl radical containing from about 8 to about 22 carbon atoms and a radical selected from the group consisting of sulfonic acid and sulfuric acid ester radicals. Included in the term alkyl is the alkyl portion of high acyl radicals.
  • anionic synthetic detergents which can form the surfactant component of the compositions of the present invention are the sodium or potassium alkyl sulfates, especially those obtained by sulfating the higher alcohols (C 8 -C 1 g carbon atoms) produced by reducing the glycerides of tallow or coconut oil; sodium or potassium alkyl benzene or toluene sulfonates, in which the alkyl group contains from about 9 to about 15 carbon atoms, (the alkyl radical can be a straight or branched aliphatic chain); sodium or potassium paraffin sulfonates and olefin sulfonates in which the alkyl or alkenyl group contains from about 10 to about 20 carbon atoms; sodium alkyl glyceryl ether sulfonates, especially those ethers of the higher alcohols derived from tallow and coconut oil; sodium coconut oil fatty acid monoglyceride sulfates and sulfonates;
  • alkyl sulfate salts which can be employed in the instant detergent compositions include sodium lauryl alkyl sulfate, sodium stearyl alkyl sulfate sodium palmityl alkyl sulfate, sodium decyl sulfate, sodium myristyl alkyl sulfate, potassium lauryl alkyl sulfate, potassium stearyl alkyl sulfate, potassium decyl sulfate, potassium palmityl alkyl sulfate, potassium myristyl alkyl sulfate, sodium dodecyl sulfate, potassium dodecyl sulfate, potassium tallow alkyl sulfate, sodium tallow alkyl sulfate, sodium coconut alkyl sulfate,.potassium coconut alkyl sulfate and mixtures of these surfactants.
  • Highly preferred alkyl sulfates are sodium coconut alkyl
  • Suitable alkylbenzene or alkyltoluene sulfonates include the alkali metal (lithium, sodium, potassium) and alkanolamine salts of straight-or branched-chain alkylbenzene or alkyltoluene sulfonic acids.
  • Alkyl- benzene sulfonic acids useful as precursors for these surfactants include decyl benzene sulfonic acid, undecyl benzene sulfonic acid, dodecyl benzene sulfonic acid, tridecyl benzene sulfonic acid, tetrapropylene benzene sulfonic acid.
  • Preferred sulfonic acids as precursors of the alkyl-benzene sulfonates useful for compositions herein are those in which the alkyl chain is linear and averages about 12 carbon atoms in length.
  • Examples of commercially available alkyl benzene sulfonic acids useful in the present invention include Conoco SA 515, SA 597 all marketed by the Continental Oil Company and Calsoft LAS 99 marketed by the Pilot Chemical Company.
  • alkyl ether sulfates having the formula RO(C 2 H 4 O) x SO 3 M wherein R is alkyl or alkenyl of about 10 to about 20 carbon atoms, x is 1 to 30, and M is a water-soluble cation.
  • the alkyl ether sulfates useful in the present invention are condensation products of ethylene oxide and monohydric alcohols having about 10 to about 20 carbon atoms. Preferably, R has 12 to 18 carton atoms.
  • the alcohols can be derived from natural fats, e.g., coconut oil or tallow, or can be synthetic. Such alcohols are reacted with 1 to 30, and especially 1 to 12, molar proportions of ethylene oxide and the resulting mixture of molecular species is sulfated and neutralized.
  • alkyl ether sulfates of the present invention are sodium coconut alkyl triethylene glycol ether sulfate, lithium tallow alkyl triethylene glycol ether sulfate, and sodium tallow alkyl hexaoxy- ethylene sulfate.
  • Preferred alkyl ether sulfates are those comprising a mixture of individual compounds, said mixture having an average alkyl chain length of from about 12 to 16 carbon atoms and an average degree of ethoxylation of from about 1 to 12 moles of ethylene oxide.
  • anionic surfactants useful herein are the compounds which contain two anionic functional groups. These are referred to as di-anionic surfactants.
  • Suitable dianionic surfactants are the disulfonates, disulfates, or mixtures thereof which may be represented by the following formula: R(SO 3 ) 2 M 2 ,R(SO 4 ) 2 M 2 ,R(SO 3 )(SO 4 )M 2 where R is an acyclic aliphatic hydrocarbyl group having 15 to 20 carbon atoms and M is a water-solubilizing cation, for example, the C 15 to C 20 disodium 1,2-alkyldisulfates, C 15 to C 20 dipotassium-l,2-alkyldisulfonates or disulfates, disodium 1,9-hexadecyl disulfates, C 15 to C 20 disodium 1,2-alkyldisulfonates, disodium 1,9-stearyldisulfates and 6,10-oc
  • Nonionic surface active agents operable in the instant compositions can be any of three basic types -the alkylene oxide condensates, the amides and the semi-polar nonionics.
  • alkylene oxide condensates are broadly defined as compounds produced by the condensation of alkylene oxide groups (hydrophilic in nature) with an organic hydrophobic compound, which can be aliphatic or alkyl aromatic in nature.
  • the length of the hydrophilic or polyoxyalkylene radical which is condensed with any particular hydrophobic group can be readily adjusted to yield a water-soluble compound having the desired degree of balance between hydrophilic and hydrophobic elements.
  • alkylene oxide condensates examples include:
  • amide type of nonionic surface active agent examples include the ammonia, monoethanol and diethanol amides of fatty acids having an acyl moiety of from about 8 to about 18 carbon atoms.
  • acyl moieties are normally derived from naturally occurring glycerides, e.g., coconut oil, palm oil, soybean oil and tallow, but can be derived synthetically, e.g., by the oxidation of petroleum, or by hydrogenation of carbon monoxide by the Fischer-Tropsch process.
  • amine oxides examples include the amine oxides, phosphine oxides and sulfoxides. These materials are described more fully in Berry, U.S. Patent 3,819,528, issued June 25, 1974, incorporated herein by reference. Particularly preferred are amine oxides of the formula: wherein R 1 is a C 10-18 alkyl and R2and R 3 are methyl or ethyl.
  • Ampholytic synthetic detergents can be broadly described as derivatives of aliphatic amines which contain a long chain of about 8 to 18 carbon atoms and an anionic water-solubilizing group, e.g. carboxy, sulfo or sulfato. Examples of compounds falling within this definition are sodium 3-dodecylamino-propionate, sodium-3-dodecylamino propane sulfonate, and dodecyl dimethylammonium hexanoate.
  • Zwitterionic surface active agents operable in the instant composition are broadly described as internally- neutralized derivatives of aliphatic quaternary ammonium and phosphonium and tertiary sulfonium compounds in which the aliphatic radical can be straight chain or branched, and wherein one of the aliphatic substituents contains from about 8 to 18 carbon atoms and one contains an anionic water solubilizing group, e.g., carboxy, sulfo, sulfato, phosphato, or phosphono.
  • the level and type of surfactant used in the compositions of this invention provide an initial suds cover to a dishwashing solution and a suds cover after the washing of 8 plates when used at a concentration of 0.07% in 2 gallons of 115°F. water containing 7 grains/ gallon water hardness measured as CaC03, each plate carrying 4.0 ml of a triglyceride containing soil. Suds are generated by mechanical agitation and the suds cover and height measured. A dinner plate carrying the soil is washed successively with the introduction of 4.0 ml of soil each time. An essentially complete suds cover of the washing solution is more important than suds height, but, preferably, the suds cover after the washing of-8 plates is at least about 1/2 inch in height.
  • the required sudsing characteristic of the compositions of the invention is that necessary to provide the user of the product with an indication of cleaning potential in a dishwashing solution. Soils encountered in dishwashing act as suds depressants and the presence or absence of suds from the surface of a dishwashing solution is a convenient guide to product usage.
  • Mixtures of anionic surfactants and nonionic surfactants, especially amides and amine oxide nonionic surfactants, are particularly preferred in the- compositions of the invention because of their high sudsing characteristics, their suds stability in the presence of food soils and their ability to indicate accurately an adequate level of product usage in the presence of soil.
  • a preferred ratio of anionic surfactants to nonionic surfactants is from about 2:1 to about 10:1 by weight.
  • Cationic surfactants such as quaternary ammonium compounds can find optional use in the practice of the invention, particularly in compositions containing nonionic surfactants.
  • the abrasive agent can be any of the water-insoluble abrasive materials known in the art which have a particle diameter of from about 1 to about 150, preferably from about 20 to about 100, microns and a hardness on the Mohs scale of from about 2 to about 7.
  • materials such as agate, mica, calcite, garnet, quartz, kieselguhr, silica, marble, tripoli, flint, feldspar, emery, pumice, alumina, perlite, expanded perlite, volcanic ash, diatomaceous earth, bentonite, amorphous silica from dehydrated silica gels, precipitated silica, plastics such as polystyrene and polyacrylates, and natural and synthetic aluminosilicates and mixtures thereof.
  • the amount of abrasive included in the compositions is in the range of from about 3% to about 20% of the total composition by weight.
  • Preferred compositions contain from about 5% to about 10% by weight of abrasive.
  • compositions of this invention contain from about 3% to about 20%, preferably from about 5% to about 15%, by weight of detergency builders either of the organic or inorganic types.
  • detergency builders either of the organic or inorganic types.
  • water-soluble inorganic builders which can be used, alone or in admixture with themselves and organic alkaline sequestrant builder salts, are alkali metal carbonates, polyphosphates, and silicates.
  • specific examples of such salts are sodium tripolyphosphate, sodium carbonate, potassium carbonate, sodium pyrophosphate, potassium pyrophosphate, potassium tripolyphosphate, and sodium hexametaphosphate.
  • organic builder salts which can be used alone, or in admixture with each other or with the preceding inorganic alkaline builder salts, are alkali metal polycarboxylates, e.g., water-soluble citrates such as sodium and potassium citrate, sodium and potassium tartrate, sodium and potassium ethylenediaminetetraacetate, sodium and potassium N-(2-hydroxyethyl)-ethylene diamine triacetates, sodium and potassium nitrilo triacetates (NTA) and sodium and potassium N-(2-hydroxyethyl)-nitrilo diacetates.
  • alkali metal polycarboxylates e.g., water-soluble citrates such as sodium and potassium citrate, sodium and potassium tartrate, sodium and potassium ethylenediaminetetraacetate, sodium and potassium N-(2-hydroxyethyl)-ethylene diamine triacetates, sodium and potassium nitrilo triacetates (NTA) and sodium and potassium N-(2-hydroxyeth
  • compositions of this invention can contain insoluble builder salts selected from certain zeolites or aluminosilicates.
  • aluminosilicate which is useful in the compositions of the invention is water-insoluble crystalline aluminosilicate ion exchange material of the formula: wherein Z and y are at least 6, the molar ratio of Z to y is from 1.0 to 0.5 and x is from 10 to 264, said material having a particle size diameter of from about 0.1 micron to about 10 microns, a calcium ion exchange capacity of at least about 200 mg. CaCO 3 eq./gram and a calcium ion exchange rate of at least about 2 grains Ca ++ /gallon/ minute/gram.
  • This ion exchange builder is more fully described in Gedge et al's French patent 2,237,839 published February 14, 1975, herein incorporated by reference.
  • a preferred aluminosilicate of this type is Zeolite A.
  • a second water-insoluble aluminosilicate ion exchange material useful herein is water-insoluble amorphous hydrated aluminosilicate material of the emperical formula: wherein M is sodium, potassium, ammonium, or substituted ammonium, Z is from about 0.5 to about 2, y is 1 and said material having a particle size diameter of less than 100 microns, a magnesium ion exchange capacity of at least about 50 milligrams equivalent of CaC0 3 hardness per gram of anhydrous aluminosilicate and a Mg ++ exchange rate of at least about 1 grain/gallon/minute/gram/gallon; and mixtures thereof.
  • This ion exchange builder is more fully described in Belgian patent 814,874 issued on November 12, 1974 to Corkill et al, herein incorporated by reference.
  • compositions of this invention contain water, preferably in an amount of from about 40% to about 79% by weight.
  • Alcohols such as ethyl alcohol, and hydrotropes, such as sodium and potassium toluene sulfonate, sodium and potassium xylene sulfonate trisodium sulfosuccinate and related compounds (as disclosed in U.S. Patent 3,915,903, incorporated herein by reference) and urea, can be utilized in the interests of achieving a desired product phase stability and viscosity.
  • suspending or thickening agents such as those disclosed in U.S.
  • Patent 3,393,153 incorporated herein by reference including colloidal silica having a mean particle diameter ranging from about 0.01 micron to about 0.05 micron and particulate polymers such as polystyrene, oxidized polystyrene having an acid number of from 20 to about 40, sulfonate polystyrene having an acid number of from about 10 to about 30, polyethylene, oxidized polyethylene having an acid number of from about 10 to about 30; sulfonated polyethylene having an acid number of from about 5 to about 25; polypropylene, oxidized polypropylene having an acid number of from about 10 to about 30 and sulfonated polypropylene having an acid number of from about 5 to about 25, all of said particulate polymers having mean particle diameters ranging from about 0.01 micron to about 30 microns.
  • particulate polymers such as polystyrene, oxidized polystyrene having an acid number of from 20 to about 40, sulfonate polysty
  • suspending and thickening agents include copolymers of styrene with monomers such as maleic anhydride, nitrilonitrile, methacrylic acid and lower alkyl esters of methacrylic acid, copolymers of styrene with methyl or ethyl acrylate, methyl or ethyl maleate, vinyl acetate, acrylic, maleic or fumaric acids and mixtures thereof.
  • the mole ratio of ester and/or acid to styrene is preferably in the range from about 4 to about 40 styrene units per ester and/or acid unit.
  • Such materials preferably have a mean particle diameter range of from about 0.05 micron to about 1 micron and molecular weights ranging from about 500,000 to about 2,000,000.
  • Cellulosic polymers such as carboxymethyl cellulose and hydroxypropyl cellulose and gums such as guar gum and gum tragacanth are also suitable suspending and thickening agents.
  • the detergent compositions of this invention can contain, if desired, any of the usual adjuvants, diluents and additives, for example, perfumes, enzymes, dyes, antitarnishing agents, antimicrobial agents, and the like, without detracting from the advantageous properties of the compositions.
  • Alkalinity sources and pH buffering agents such as alkali metal carbonates and bicarbonates, monoethanolamine, triethanolamine, alkali metal hydroxides, etc., can also be utilized.
  • a preferred pH range for a l% solution in water is from about 6 to about 11.
  • Liquid detergent compositions were prepared containing the ingredients listed below:
  • composition B within the scope of the invention containing both an abrasive and a detergency builder was compared to comparable compositions containing neither an abrasive nor a detergency builder (A), only detergency builders (C) and only an abrasive (D).
  • Aluminum strips were treated with oatmeal and egg food soils and baked to create typical, hard-to-remove soils.
  • the relative effort required to remove the soils after direct application or direct application plus a soak (0.2% product in water) using the compositions of the example was obtained by using a "Gardner Abrasion Machine" using a series of progressively heavier weights. The first ten strokes by the machine were made with a one-pound weight mounted over a holder with a sponge saturated with 0.2% product in water. The next ten strokes were made with a three-pound weight over the sponge and the final ten strokes were made with a six- pound weight. The percentage of soil removed after each ten stroke cycle was recorded.
  • composition B within the scope of the invention which contains both a detergency builder and an abrasive.
  • Potassium pyrophosphate is substituted for the sodium aluminosilicate. Comparable cleaning results are obtained.

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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)
  • Detergent Compositions (AREA)
EP79200802A 1979-12-24 1979-12-24 Composition détergente liquide contenant un adjuvant et un abrasif Withdrawn EP0030986A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP79200802A EP0030986A1 (fr) 1979-12-24 1979-12-24 Composition détergente liquide contenant un adjuvant et un abrasif

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EP79200802A EP0030986A1 (fr) 1979-12-24 1979-12-24 Composition détergente liquide contenant un adjuvant et un abrasif

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3439872A1 (de) * 1983-11-22 1985-07-18 Lion Corp., Tokio/Tokyo Klare fluessige detergenzzusammensetzung
EP0079646B1 (fr) * 1981-11-16 1986-05-21 Unilever N.V. Composition détergente liquide
EP0368559A3 (en) * 1988-11-10 1990-12-05 Trico-Folberth Limited Glass cleaning preparation
US6759377B2 (en) * 1999-07-29 2004-07-06 Reckitt Benckiser N.V. Detergent for vitroceramic surfaces

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3623990A (en) * 1967-06-26 1971-11-30 Procter & Gamble Liquid detergent composition
US3813349A (en) * 1969-12-29 1974-05-28 Procter & Gamble Liquid detergent composition
DE2516003A1 (de) * 1974-04-17 1975-11-06 Procter & Gamble Waessriges halbfluessiges reinigungsmittel fuer harte oberflaechen
GB1481685A (en) * 1973-08-15 1977-08-03 Unilever Ltd Detergent ingredient
GB1534680A (en) * 1977-10-14 1978-12-06 Colgate Palmolive Co Cleaning compositions

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3623990A (en) * 1967-06-26 1971-11-30 Procter & Gamble Liquid detergent composition
US3813349A (en) * 1969-12-29 1974-05-28 Procter & Gamble Liquid detergent composition
GB1481685A (en) * 1973-08-15 1977-08-03 Unilever Ltd Detergent ingredient
DE2516003A1 (de) * 1974-04-17 1975-11-06 Procter & Gamble Waessriges halbfluessiges reinigungsmittel fuer harte oberflaechen
GB1534680A (en) * 1977-10-14 1978-12-06 Colgate Palmolive Co Cleaning compositions

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0079646B1 (fr) * 1981-11-16 1986-05-21 Unilever N.V. Composition détergente liquide
DE3439872A1 (de) * 1983-11-22 1985-07-18 Lion Corp., Tokio/Tokyo Klare fluessige detergenzzusammensetzung
EP0368559A3 (en) * 1988-11-10 1990-12-05 Trico-Folberth Limited Glass cleaning preparation
US6759377B2 (en) * 1999-07-29 2004-07-06 Reckitt Benckiser N.V. Detergent for vitroceramic surfaces

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