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EP0295590A2 - Agent de nettoyage liquide pour les surfaces dures - Google Patents

Agent de nettoyage liquide pour les surfaces dures Download PDF

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Publication number
EP0295590A2
EP0295590A2 EP88109326A EP88109326A EP0295590A2 EP 0295590 A2 EP0295590 A2 EP 0295590A2 EP 88109326 A EP88109326 A EP 88109326A EP 88109326 A EP88109326 A EP 88109326A EP 0295590 A2 EP0295590 A2 EP 0295590A2
Authority
EP
European Patent Office
Prior art keywords
cleaning
weight
agents
highly
acid
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.)
Withdrawn
Application number
EP88109326A
Other languages
German (de)
English (en)
Other versions
EP0295590A3 (fr
Inventor
Frantisek Dr. Jost
Klaus-Dieter Dr. Wisotzki
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.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP0295590A2 publication Critical patent/EP0295590A2/fr
Publication of EP0295590A3 publication Critical patent/EP0295590A3/fr
Withdrawn legal-status Critical Current

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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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/76Synthetic resins containing no nitrogen
    • 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
    • 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
    • C11D3/3769(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
    • C11D3/3773(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines in liquid compositions

Definitions

  • DE-AS 10 51 440 discloses liquid cleaning agents which are used for all purposes, but especially for washing textiles, and which, in addition to anionic and nonionic surfactants to increase the dirt-carrying capacity, include small amounts of water-soluble cellulose or starch derivatives or else of water-soluble or colloidally soluble polymers, such as polyvinylpyrrolidone.
  • AT-PS 278 216 discloses liquid cleaning agents which can also contain water-soluble high-molecular substances as dirt carriers.
  • examples include water-soluble salts of polyacrylic acid and also water-soluble derivatives of cellulose such as carboxymethyl cellulose. Mixtures of anionic and nonionic surfactants are also preferably used here.
  • liquid builder-containing cleaning agents for hard surfaces with small amounts of preferably anionic surfactants in combination with small amounts of a mixture of polyvinyl alcohol and / or polyvinyl pyrrolidone and polysaccharide salt are known, which should also have an improved dirt removal capacity.
  • German patent specification 27 09 690 describes liquid detergents for hard surfaces which essentially consist of a mixture of anionic and nonionic surfactants and, if appropriate, other conventional constituents of such agents, such as, for example, framework substances, adducts of ethylene oxide with aliphatic vicinal diols being used as nonionic surfactants or partially etherified diols with a linear alkyl chain of 10 to 20 carbon atoms. They can also contain cleaning-enhancing additives to water-soluble high-molecular substances, such as polyvinyl alcohol, polyvinyl pyrrolidone and carboxymethyl cellulose.
  • German Offenlegungsschrift 29 13 049 shows that one can even dispense with the proportion of anionic surfactants and still achieve comparable good cleaning results if instead of them water-soluble nonionic, weakly anionic or cationic polymers from the group of polyethylene glycols, polyvinyl alcohols , Polyvinylpyrrolidones, cellulose ethers, polysaccharides, proteins and polyacrylamides with average molecular weights of 5,000 to 10,000,000, preferably 20,000 to 2,000,000, or mixtures of these polymers.
  • the liquid detergents contain approximately 0.5 to 40, preferably 5 to 20 percent by weight of surfactants or surfactant mixtures, 0 to 6, preferably 1.0 to 6 percent by weight of organic or inorganic builders, 0.01 to 1, preferably 0.05 to 0.5 percent by weight of cleaning boosters, as well as up to a total of 100% by weight of water, solvents, hydrotropes, preservatives, antimicrobial agents, viscosity regulators, pH regulators, perfume and dyes.
  • surfactants and mixtures of surfactants that are commonly used in the claimed cleaning agent type can be used. These are generally those which contain at least one hydrophobic organic radical and one water-solubilizing anionic, nonionic or cationic radical in the molecule.
  • the hydrophobic radical is usually an aliphatic hydrocarbon radical with 8 to 26, preferably 10 to 22 and in particular 12 to 18 carbon atoms or an alkyl aromatic radical with 6 to 18, preferably 8 to 16 aliphatic carbon atoms.
  • the surfactant mixtures the known incompatibility of many anionic and cationic surfactants would have to be taken into account.
  • Surfactants from the group of nonionic and synthetic anionic surfactants, soaps and mixtures thereof are preferably used.
  • Surfactant combinations of the nonionic surfactants of the ethoxylated alkanediols, alkanols, alkenols and alkylphenols type and the synthetic anionic surfactants from the group of the sulfonate and sulfate surfactants are particularly preferred.
  • a soap can be included as a further component.
  • Addition products of 4 to 40, preferably 4 to 20 moles of ethylene oxide or ethylene oxide and propylene oxide with 1 mole of fatty alcohols, preferably terminal or vicinal internal alkanediols, alkylphenols, fatty acids, fatty amines, fatty acid amides or alkanesulfonamides, can be used as nonionic surfactants.
  • fatty alcohols preferably terminal or vicinal internal alkanediols, alkylphenols, fatty acids, fatty amines, fatty acid amides or alkanesulfonamides
  • nonionic surfactants include the adducts of 5 to 16 moles of ethylene oxide or ethylene and propylene oxide with coconut or tallow fatty alcohols, with oleyl alcohol or with secondary alcohols with 8 to 18, preferably 12 to 18 carbons as well as with mono- or dialkylphenols with 6 to 14 carbon atoms in the Alkyl residues.
  • non-ionic surfactants that can be used are the water-soluble adducts of ethylene oxide with polypropylene oxide, alkylene diamine polypropylene glycol and alkyl polypropylene glycols with 1 to 10 carbon atoms in the alkyl chain, in which the polypropylene glycol chain acts as a hydrophobic residue, containing polypropylene oxide, alkylene diamine polypropylene glycol and 10 to 100 propylene glycol ether groups.
  • Nonionic surfactants of the amine oxide type can also be used. Typical representatives are, for example, the compounds N-dodecyl-N, N-dimethylamine oxide, N-tetradecyl-N, N-dihydroxyethylamine oxide and N-hexadecyl-N, N-bis- (2,3-dihydroxypropyl) amine oxide. Alkyl glucosides with 10 to 18, preferably 12 to 14 carbon atoms in the alkyl radical and 1 to 10, preferably 1 to 2, glucose units in the molecule are also suitable as nonionic surfactants.
  • Synthetic anionic surfactants of the sulfonate type include alkylbenzenesulfonates (C 9-15 -alkyl), mixtures of alkene and hydroxyalkanesulfonates and disulfonates, such as those obtained from monoolefins with terminal or internal double bonds by sulfonation with gaseous sulfur trioxide and subsequent alkaline or acid hydrolysis Sulfonating group. Also suitable are alkanesulfonates which are obtained from alkanes by sulfochlorination or sulfoxidation and subsequent hydrolysis or neutralization or by bisulfite addition to olefins receives.
  • esters of alpha-sulfo fatty acids for example the alpha-sulfonic acids from hydrogenated methyl or ethyl esters of coconut, palm kernel or tallow fatty acid.
  • Suitable synthetic anionic surfactants of the sulfate type are the sulfuric acid monoesters of primary alcohols (e.g. from coconut fatty alcohols, tallow fatty alcohols or oleyl alcohol) and those of secondary alcohols. Sulfated fatty acid alkanolamides, fatty acid monoglycerides or reaction products of 1 to 4 moles of ethylene oxide with primary or secondary fatty alcohols or alkylphenols are also suitable.
  • Suitable synthetic anionic surfactants are the fatty acid esters or amides of hydroxy or aminocarboxylic acids or sulfonic acids, e.g. the fatty acid sarcosides, glycolates, lactates, taurides or isethionates.
  • anionic surfactants can be present in the form of their alkali, alkaline earth and ammonium salts and as soluble salts of organic bases, such as mono-, di- or triethanolamine.
  • the sodium salts are preferred for cost reasons.
  • cationic surfactants they contain at least one hydrophobic and at least one basic group, which may be in the form of a salt and make water soluble.
  • the hydrophobic group is an aliphatic or cycloaliphatic hydrocarbon group with preferably 10 to 22 carbon atoms or an alkyl or cycloalkyl aromatic group with preferably 8 to 16 aliphatic carbon atoms.
  • basic groups come primarily basic nitrogen atoms in question, which can also be present more than once in a surfactant molecule; it is preferably quaternary ammonium compounds such as N-dodecyl-N, N, N-trimethylammonium methosulfate, N-hexadecyl or N-octadecyl-N, N, N-trimethylammonium chloride, N, N-dicocosalkyl-N, N-dimethylammonium chloride, N-cocoalkyl-N, N-dimethyl-N-benzylammonium chloride, N-dodecyl-N, N-dimethyl-N-benzylammonium bromide, the reaction product of 1 mol of tallow alkylamine with 10 mol of ethylene oxide, N-dodecyl-N, N ′, N ′ -trimethyl-1,3-diaminopropane, N-hexadecy
  • the nitrogen compounds mentioned can be replaced by corresponding compounds with a quaternary phosphorus atom or with a tertiary sulfur atom.
  • liquid cleaning agents for the liquid cleaning agents according to the invention, 0 to 6, preferably 1.0 to 6, percent by weight of inorganic or organic compounds which are alkaline in their entirety, in particular inorganic or organic complexing agents, preferably in the form of their alkali metal or amine salts, in particular the Potassium salts are present.
  • the alkaline polyphosphates are particularly suitable as inorganic complex-forming framework substances. They can be replaced in whole or in part by organic complexing agents.
  • Further inorganic builder substances which can be used according to the invention are, for example, dicarbonates, carbonates, borates, silicates or orthophosphates of the alkalis.
  • the inorganic builders also include the alkali hydroxides, of which the potassium hydroxide is preferably used.
  • Organic complexing agents of the aminopolycarboxylic acid type include nitrilotriacetic acid, ethylenediaminetetraacetic acid, N-hydroxyethyl ethylene diamine triacetic acid and polyalkylene polyamine N polycarboxylic acids.
  • di- and polyphosphonic acids examples include: methylenediphosphonic acid, 1-hydroxy-ethane-1,1-diphosphonic acid, propane-1,2,3-triphosphonic acid, butane-1,2,3,4-tetraphosphonic acid, polyvinylphosphonic acid, copolymers Vinylphosphonic acid and acrylic acid, ethane-1,2-dicarboxy-1,2-diphosphonic acid, ethane-1,2-dicarboxy-1,2-dihydroxy-diphosphonic acid, phosphonosuccinic acid, 1-aminoethane-1,1-diphosphonic acid, aminotri- (methylenephosphonic acid ), Methyl-amino- or ethylamino-di- (methylenephosphonic acid) and ethylenediamine-tetra- (methylenephosphonic acid).
  • N- or P-free polycarboxylic acids can also be used as builders, many, if not exclusively, of polymers containing carboxyl groups.
  • a large number of these polycarboxylic acids have a complexing ability for calcium. These include e.g. Citric acid, tartaric acid, gluconic acid, benzene hexacarboxylic acid, tetrahydrofuran tetracarboxylic acid etc. and their mixtures.
  • the cleaning booster mixture consists of polyacrylamides and highly polyethoxylated mono- or polyhydric alkanols. Their weight ratio is 1: 3 to 3: 1, preferably 1: 2 to 2: 1.
  • the polyacrylamides are polymers and copolymers of acrylamide of the general formula (-CH2-CH (CONH2) -) n with molecular weights of 300,000 to 15,000,000, preferably 2,000,000 to 12,000,000 the companies Dow (Separan® MG 205; Separan® NP 10), Stockhausen (Praestol® 2850; Praestol® 2935/73; Praestol® 114/73) BASF (Sedipur® AF 200; Sedipur® AF 400, Sedipur® NF 100) and Henkel (P3-ferrocryl® 8720; P3-ferrocryl® 8721®; P3-ferrocryl® 8723; P3-ferrocryl® 8740).
  • the highly polyethoxylated mono- or poly-, preferably mono- or dihydric alkanols are addition products of 30 to 150, preferably 40 to 90 mol ethylene oxide onto terminal or internal hydroxyalkanols with 12 to 22, preferably 14 to 20 carbon atoms in the molecule, such as stearyl or 12-hydroxystearyl alcohol.
  • Suitable acidic substances are customary inorganic or organic acids or acidic salts, such as, for example, hydrochloric acid, sulfuric acid, bisulfates of alkalis, aminosulfonic acid, phosphoric acid or other acids of phosphorus, in particular the anhydrous acids of phosphorus or their acidic salts or their acid-reacting solid compounds Urea or other lower carboxylic acid amides, partial amides of phosphoric acids or anhydrous phosphoric acid, adipic acid, glutaric acid, succinic acid, citric acid, tartaric acid, lactic acid and the like, some of which additionally have complex-forming properties.
  • hydrochloric acid such as, for example, hydrochloric acid, sulfuric acid, bisulfates of alkalis, aminosulfonic acid, phosphoric acid or other acids of phosphorus
  • anhydrous acids of phosphorus or their acidic salts or their acid-reacting solid compounds Urea or other lower carboxylic acid amides, partial amide
  • alkaline builders If the content of alkaline builders is not sufficient to regulate the pH, organic or inorganic compounds such as alkanolamines, namely mono-, di- or triethanolamine or ammonia, which have an alkaline action, can also be added.
  • alkanolamines namely mono-, di- or triethanolamine or ammonia, which have an alkaline action
  • solubilizers can be incorporated, which in addition to the water-soluble organic solvents such as, in particular, low-molecular aliphatic alcohols having 1 to 4 carbon atoms, also include the so-called hydrotropic substances of the lower alkylarylsulfonate type, for example toluene, xylene or cumene sulfonate. They can also be in the form of their sodium and / or potassium and / or alkylamino salts.
  • Water-soluble organic solvents can also be used as solubilizers, in particular those with boiling points above 75 ° C., for example the ethers from the same or different polyhydric alcohols or the partial ethers from polyhydric alcohols.
  • These include, for example, di or triethylene glycol polyglycerols and the partial ethers of ethylene glycol, propylene glycol, butylene glycol or glycerol with aliphatic monohydric alcohols containing 1 to 4 carbon atoms in the molecule.
  • Suitable water-soluble or water-emulsifiable organic solvents are also ketones, such as acetone, methyl ethyl ketone and aliphatic, cycloaliphatic, aromatic and chlorinated hydrocarbons, and also various terpene alcohols as individual substances or in a mixture. Terpene alcohols also have a fragrance effect.
  • the claimed agents can contain additives of colorants and fragrances, preservatives and, if desired, antimicrobial agents of any kind.
  • Suitable antimicrobial agents to be used are those compounds which are those in the invention liquid funds are stable and effective.
  • phenolic compounds of the halogenated phenol type with 1 to 5 halogen substituents in particular chlorinated phenols, alkyl, cycloalkyl, aralkyl and phenylphenols with 1 to 12 carbon atoms in the alkyl radicals and with 1 to 4 halogen substituents, in particular chlorine and Bromine in the molecule
  • Particularly preferred antimicrobial agents of the phenyl type are, for example, O-phenylphenol, 2-phenylphenol, 2-hydroxy-2 ', 4,4'-trichlorodiphenyl ether, 3,4', 5-tribromosalicylanilide and 3.3 ', 5.5', 6 , 6'-Hexachloro-2,2'-dihydroxy-diphenylmethane.
  • Other useful antimicrobial agents are the lower alcohols or diols with 3 to 5 carbon atoms substituted by both bromine and by the nitro group, such as e.g. the compounds 2-bromo-2-nitropropanediol-1,3, 1-bromo-1-nitro-3,3,3-trichloropropanol, 2,2-bromo-2-nitro-butanol-1.
  • bis-diguanides such as 1,6-bis (p-chlorophenyldiguanido) hexane in the form of the hydrochloride, acetate or gluconate and also N, N'-disubstituted 2-thiontetrahydro-1,3,5-thiadiazines such as 3,5-dimethyl-, 3,5-diallyl-, 3-benzyl-5-methyl- and especially 3-benzyl-5-carboxymethyl-tetrahydro-1,3,5-thiadiazine as additional antimicrobial agents.
  • bis-diguanides such as 1,6-bis (p-chlorophenyldiguanido) hexane in the form of the hydrochloride, acetate or gluconate and also N, N'-disubstituted 2-thiontetrahydro-1,3,5-thiadiazines such as 3,5-dimethyl-, 3,5-diallyl-, 3-benzyl-5-methyl- and especially 3-benzyl-5-carbox
  • the formulation to be tested for its cleaning ability was applied to an artificially soiled white PVC plastic surface.
  • a mixture of carbon black, machine oil, a trigylceride of saturated fatty acids and low-boiling aliphatic hydrocarbons was used as artificial soiling.
  • test area of 26 x 4.0 cm was coated evenly with 0.3 or 0.6 g (diluted or undiluted product application) of the artificial soiling and stored for one hour at room temperature before the start of the test. Subsequently, a plastic sponge with 10 ml (6 ml in the undiluted application) of the cleaning agent solution to be tested was soaked and mechanically moved back and forth on the test surface, the sponge covering both the soiled central area and the non-soiled edge zones. After 10 wiping movements under precisely defined contact pressure conditions of 2 kp, the cleaned test area was rinsed with 400 ml tap water and the loosened dirt was thereby removed.
  • the cleaning ability ie the degree of whiteness of the plastic surface cleaned in this way, was measured with a photoelectric reflection measuring device LF 90 (from Dr. B. Lange), the whiteness of the part of the test surface which was originally soiled used to determine the cleaning ability.
  • the clean, white PVC plastic surface was used as the white standard.
  • the deflection of the measuring device was set to 100 percent and for the soiled area to 0 percent, the readings on the cleaned plastic surfaces could be regarded as "percent cleaning ability" (% RV).
  • the specified delta RV values are average values from a quadruple determination.

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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)
EP19880109326 1987-06-19 1988-06-11 Agent de nettoyage liquide pour les surfaces dures Withdrawn EP0295590A3 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19873720262 DE3720262A1 (de) 1987-06-19 1987-06-19 Fluessiges reinigungsmittel fuer harte oberflaechen
DE3720262 1987-06-19

Publications (2)

Publication Number Publication Date
EP0295590A2 true EP0295590A2 (fr) 1988-12-21
EP0295590A3 EP0295590A3 (fr) 1990-09-12

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ID=6329888

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19880109326 Withdrawn EP0295590A3 (fr) 1987-06-19 1988-06-11 Agent de nettoyage liquide pour les surfaces dures

Country Status (4)

Country Link
US (1) US4880558A (fr)
EP (1) EP0295590A3 (fr)
JP (1) JPS6420296A (fr)
DE (1) DE3720262A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0467472A2 (fr) * 1990-07-16 1992-01-22 Colgate-Palmolive Company Composition liquide de nettoyage pour surfaces dures avec polymères antisalissantes
WO2007073801A1 (fr) * 2005-12-15 2007-07-05 Henkel Kommanditgesellschaft Auf Aktien Détergent pour lave-vaisselle

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5326492A (en) * 1991-11-18 1994-07-05 Medical Polymers, Inc. Disinfectant mixture containing water soluble lubricating and cleaning agents and method
WO1993014181A1 (fr) * 1992-01-06 1993-07-22 Olin Corporation Composition nettoyante, aqueuse et biodegradable pour filtres contenant un agent tensioactif ethoxyle/propoxyle, de l'acide carboxylique et un solvant
DE4209923A1 (de) * 1992-03-27 1993-09-30 Henkel Kgaa Flüssige Reinigungsmittel für harte Oberflächen
CA2225016A1 (fr) * 1995-06-21 1997-01-09 Virginia L. Lazarowitz Procede pour augmenter l'efficacite d'un agent deodorant
JPH11508618A (ja) * 1995-06-27 1999-07-27 ザ、プロクター、エンド、ギャンブル、カンパニー 非食品無生物表面用のクリーニング/消毒法、組成物および/または物品
US5837665A (en) * 1996-05-02 1998-11-17 Young; Robert Spot cleaner for carpets
US6159924A (en) * 1998-07-24 2000-12-12 Reckitt Benckiser Inc. Low residue aqueous hard surface cleaning and disinfecting compositions
WO2000043318A2 (fr) * 1999-01-22 2000-07-27 The Procter & Gamble Company Produit adjuvant de rinçage acide colore contenu dans un flacon resistant aux ultraviolets
US6559116B1 (en) * 1999-09-27 2003-05-06 The Procter & Gamble Company Antimicrobial compositions for hard surfaces
US7799751B2 (en) * 2000-12-14 2010-09-21 The Clorox Company Cleaning composition
WO2003042413A1 (fr) * 2001-10-23 2003-05-22 Steen Research, Llc Procede et compositions permettant de traiter des plumes de volaille
US7255750B2 (en) 2003-03-24 2007-08-14 The Clorox Company Cleaner with soil flocculant
US6762162B1 (en) 2003-06-18 2004-07-13 S. C. Johnson & Son, Inc. Disinfecting cationic polymer cleaner comprising an acrylate cationic polymer
US7049281B2 (en) * 2003-11-06 2006-05-23 Colgate-Palmolive Company Liquid cleaning composition containing an anionic polyacrylamide copolymer
US7048806B2 (en) * 2003-12-16 2006-05-23 The Clorox Company Cleaning substrates having low soil redeposition
AR072859A1 (es) 2008-05-23 2010-09-29 Colgate Palmolive Co Metodos y composiciones liquidas de limpieza

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1139229B (de) * 1961-04-08 1962-11-08 Boehme Fettchemie Gmbh Spuel- und Reinigungsmittel
US3989633A (en) * 1974-11-27 1976-11-02 Nalco Chemical Company Windshield washer fluids containing from 10-1000 ppm of acrylamide polymer to reduce wear of wiper blades and reduce windage losses of fluid
EP0017149A1 (fr) * 1979-03-31 1980-10-15 Henkel Kommanditgesellschaft auf Aktien Utilisation d'une composition liquide pour le nettoyage de surfaces dures

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2709690B1 (de) * 1977-03-05 1978-05-11 Henkel Kgaa Fluessiges Reinigungsmittel

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1139229B (de) * 1961-04-08 1962-11-08 Boehme Fettchemie Gmbh Spuel- und Reinigungsmittel
US3989633A (en) * 1974-11-27 1976-11-02 Nalco Chemical Company Windshield washer fluids containing from 10-1000 ppm of acrylamide polymer to reduce wear of wiper blades and reduce windage losses of fluid
EP0017149A1 (fr) * 1979-03-31 1980-10-15 Henkel Kommanditgesellschaft auf Aktien Utilisation d'une composition liquide pour le nettoyage de surfaces dures

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0467472A2 (fr) * 1990-07-16 1992-01-22 Colgate-Palmolive Company Composition liquide de nettoyage pour surfaces dures avec polymères antisalissantes
GR910100312A (en) * 1990-07-16 1992-08-26 Colgate Palmolive Co Liquid cleaning composition for rough surfaces
EP0467472A3 (en) * 1990-07-16 1993-06-02 Colgate-Palmolive Company Hard surface liquid cleaning composition with anti-soiling polymer
WO2007073801A1 (fr) * 2005-12-15 2007-07-05 Henkel Kommanditgesellschaft Auf Aktien Détergent pour lave-vaisselle

Also Published As

Publication number Publication date
JPS6420296A (en) 1989-01-24
DE3720262A1 (de) 1988-12-29
US4880558A (en) 1989-11-14
EP0295590A3 (fr) 1990-09-12

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