EP0269169A2 - Detergent compositions containing cellulase - Google Patents
Detergent compositions containing cellulase Download PDFInfo
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- EP0269169A2 EP0269169A2 EP87202190A EP87202190A EP0269169A2 EP 0269169 A2 EP0269169 A2 EP 0269169A2 EP 87202190 A EP87202190 A EP 87202190A EP 87202190 A EP87202190 A EP 87202190A EP 0269169 A2 EP0269169 A2 EP 0269169A2
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- Prior art keywords
- composition according
- cellulase
- composition
- detergent
- compositions
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Classifications
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- 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
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
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- 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
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38645—Preparations containing enzymes, e.g. protease or amylase containing cellulase
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- 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
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3723—Polyamines or polyalkyleneimines
Definitions
- the present invention relates to detergent compostions which comprise a detergent cellulase and a low level of a narrowly defined polymer.
- Preferred compositions further contain a fabric-softening clay.
- the present invention relates to detergent compositions comprising a detergent cellulase.
- the compositions are formulated to provide a near-neutral or mildly alkaline wash liquor pH. They contain a low level of a narrowly defined soil release polymer.
- cellulolytic enzymes i.e. cellulase
- a harshness reducing agent in fabric softening compositions is taught in British Patent 1.368.599.
- EP-A 0 120 528 teaches alkaline softening detergent compositions comprising a synergistic mixture of a water-insoluble C10-C26 tertiary amine and cellulase.
- EP-A 0 177 165 discloses alkaline softening detergent compositions containing a mixture of smectite clay and cellulase.
- the present invention answers the above need, and provides efficient near neutral or mildly alkaline detergent compositions, which exhibit good cleaning properties, especially on cotton fabrics.
- EP-A 0 112 593 describes alkoxylated amines having clay-soil removal/anti-redeposition properties when used in detergent compositions.
- EP-A 0 137 615 describes solvent-based liquid detergent compositions containing alkoxylated polyamines.
- the present invention relates to detergent compositions comprising a surface-active agent and a detergent cellulase.
- the detergent compositions of this invention are characterized in that they contain from 0.1% to 1% of an alkoxylated polyamine as defined herein below, and in that the pH of a 1% solution of the detergent compositions in distilled water is from 6.5 to 9.5.
- Preferred are detergent compositions which further comprise from 1% to 10% of a fabric softening clay material, preferably a bentonite clay.
- Preferred are also compositions that are essentially free of water-insoluble, long-chain alkyl amines, or derivatives thereof.
- the detergent cellulase is preferably a bacterial or fungal cellulase having an optimum pH in the range of from 5 to 11.5, more preferably from 6.5 to 9.5.
- the amount of cellulase in the composition is preferably such that the cellulase activity of the composition ranges from 5 to 100 CMCase units per gram.
- compositions that comprise from 0.5% to 5% of a water-soluble quaternary ammonium compound.
- detergent compositions having a pH in 1% aqueous solution in the range of from 6.5 to 9.5.
- the clay soil removal performance of such compositions is relatively poor as compared to compositions formulated to provide a wash liquor pH of 10 or above.
- Certain water-soluble quaternary ammonium compounds are highly desirable as cationic co-surfactants in detergent compositions, as these compounds provide important greasy soil removal benefits. Due to their positive charge, however, these cationics tend to negatively interact with the clay soil removal performance of a detergent composition. This effect is more pronounced at relatively low pH, at which clay particles are less able to peptize viz negative charge repulsion effects than at pH>10.
- the surface-active agent is the surface-active agent
- the surface-active agent useful herein preferably contains at least 50% by weight, more preferably from 60% to 100% by weight of the surface active agent of a non-soap anionic surface-active agent (salt form).
- anionic surfactants can be used in the compositions of the present invention.
- Suitable anionic surfactants are water-soluble salts of alkyl benzene sulphonates, alkyl sulphates, alkyl polyethoxy ether sulphates, paraffin sulphonates, alpha-olefin sulphonates, alpha-sulphocarboxylates and their esters, alkyl glyceryl ether sulphonates, fatty acid monoglyceride sulphates and sulphonates, alkyl phenol polyethoxy ether sulphates, 2-acyloxy-alkane-1-sulphonates, and beta-alkyloxy alkane sulphonates.
- Paraticularly preferred alkyl benzene sulphonates have from 9 to 15 carbon atoms in a linear or branched alkyl chain, especially from 11 to 13 carbon atoms.
- Suitable alkyl sulphates have from 10 to 22 carbon atoms in the alkyl chain, more especially from 12 to 18 carbon atoms.
- Suitable alkyl polyethoxy ether sulphates have from 10 to 18 carbon atoms in the alkyl chain and have an average of from 1 to 12 - CH2CH2O- groups per molecule, especially from 10 to 16 carbon atoms in the alkyl chain and an average of from 1 to 6 -CH2CH2O-groups per molecule.
- Suitable paraffin sulphonates are essentially linear and contain from 8 to 24 carbon atoms, more particularly rom 14 to 18 carbon atoms.
- Suitable alpha-olefin sulphonates have from 10 to 24 carbon atoms, more particularly from 14 to 16 carbon atoms; alpha-olefin sulphonates can be made by reaction with sulphur trioxide, followed by neutralization under conditions such that any sultones present are hydrolyzed to the corresponding hydroxy alkane sulphonates.
- Suitable alpha-sulphocarboxylates contain from 6 to 20 carbon atoms; included herein are not only the salts of alpha-sulphonated fatty acids but also their esters made from alcohols containing 1 to 14 carbon atoms.
- Suitable alkyl glyceryl ether sulphates are ethers of alcohols having from 10 to 18 carbon atoms, more particularly those derived from coconut oil and tallow.
- Suitable alkyl phenol polyethoxy ether sulphates have from 8 to 12 carbon atoms in the alkyl chain and an average of from 1 to 6 - CH2CH2O-groups per molecule.
- Suitable 2-acyloxyalkane-1-sulphonates contain from 2 to 9 carbon atoms in the acyl group and from 9 to 23 carbon atoms in the alkane moiety.
- Suitable beta-alkyloxy alkane sulphonates contain from 1 to 3 carbon atoms in the alkyl group and from 8 to 20 carbon atoms in the alkane moiety.
- the alkyl chains of the foregoing anionic surfactants can be derived from natural sources such as coconut oil or tallow, or can be made synthetically as for example by using the Ziegler or Oxo processes. Water-solubility can be achieved by using alkali metal, ammonium, or alkanol-ammonium cations; sodium is preferred. Mixtures of anionic surfactants are contemplated by this invention; a satisfactory mixture contains alkyl benzene sulphonate having 11-13 carbon atoms in the alkyl group and alkyl sulphate having 12 to 18 carbon atoms in the alkyl goup.
- Nonionic surfactants may be incorporated in the compositions herein, in limited amounts (less than 50%).
- Suitable nonionics are water-soluble ethoxylated materials of HLB 11.5-17.0 and include (but are not limited to) C10-C20 primary and secondary alcohol ethoxylates and C5-C10 alkylphenol ethoxylates.
- C14-C18 linear primary alcohols condensed with from seven to thirty moles of ethylene oxide per mole of alcohol are preferred, examples being C14-C15 (EO)7, C16-C18 (EO)25 and especially C16-C18 (EO)11.
- surfactants can be used in limited amounts, in combination with the anionic surface-active agent. They include zwitterionic amphoteric, as well as cationic surfactants.
- Cationic co-surfactants which can be used herein, include water-soluble quaternary ammonium compounds of the form R4R5R6R7N+X ⁇ , wherein R4 is alkyl having from 10 to 20, preferably from 12-18 carbon atoms, R5, R6 and R7 are independently, C1-C4 alkyl, and X ⁇ is an anion, e.g. chloride.
- R4 is alkyl having from 10 to 20, preferably from 12-18 carbon atoms
- R5, R6 and R7 are independently, C1-C4 alkyl
- X ⁇ is an anion, e.g. chloride.
- Examples are the trimethyl ammonium compounds, including C12-C14 alkyl trimethyl ammonium chloride and cocoalkyl trimethyl ammonium methosulfate.
- Alkoxylated polyamines suitable as clay-soil removal/anti-redeposition agents, as well as their preparation, are disclosed in EP-PA 0 112 593, the disclosures of which are incorporated herein by reference.
- polyamines as used herein represents generically the alkoxylated polyamines, both in their amine form and in their quaternarized form.
- Such materials can conventiently be represented as molecules of the empirical structures with repeating units : wherein R is a hydrocarbyl group, usually of 2-6 carbon atoms; R1 may be a C1-C20 hydrocarbon; the alkoxy groups are ethoxy, propoxy, and the like, and y is 2-30, most preferably 10-20; n is an integer of at least 2, preferably from 2-20, most preferably 3-5; and X ⁇ is an anion such as halide or methylsulfate, resulting from the quaternization reaction.
- polyamines for use herein are the so-called ethoxylated polyethylene imines, i.e., the polymerized reaction product of ethylene oxide with ethylene-imine, having the general formula : wherein n is an integer of 3 to 5 and y is an integer of 10 to 20.
- the cellulase usable in the present invention may be any bacterial or fungal cellulase having a pH optimum of between 5 and 9.5.
- Suitable cellulases are disclosed in GB-A-2.075.028; GB-A-2.095.275 and DE-OS-2.247.832.
- cellulases examples include cellulases produced by a strain of Humicola insolens (Humicola grisea var. thermoidea), particularly the Humicola strain DSM 1800, and cellulases produced by a fungus of Bacillus N or a cellulase 212-producing fungus belonging to the genus Aeromonas, and cellulase extracted from the hepatopancreas of a marine mullosc (Dolabella Auricula Solander).
- the cellulase added to the composition of the invention may be in the form of a non-dusting granulate, e.g. "marumes” or “prills”, or in the form of a liquid in which the cellulase is provided as a cellulase concentrate suspended in e.g. a nonionic surfactant or dissolved in an aqueous medium.
- a non-dusting granulate e.g. "marumes” or "prills”
- a liquid in which the cellulase is provided as a cellulase concentrate suspended in e.g. a nonionic surfactant or dissolved in an aqueous medium.
- Activity determination for the cellulase herein is based on the hydrolysis of carboxymethyl cellulose. Generated low molecular reducing carbohydrates are colorimetrically determined by the ferrocyanide reaction as descirbed by W.S. Hoffman "J. Biol. Chem.” 120,51 (1973). Key conditions of incubation are pH-7.0, temperature of 40°C and incubation time of 20 minutes.
- One CMCase unit is defined as the amount of enzyme which forms per minute an amount of reducing carbohydrate equivalent to 10 ⁇ 6 mole of glucose, in the above-described conditions.
- a highly preferred range of cellulase activity in the present context is from 5 to 100 CMCase activity units/gram of composition.
- compositions herein are essentially free of water-insoluble long-chain alkyl amine softening agents, and derivatives thereof, since it has surprisingly been discovered that such compounds negatively interact with cellulase under the pH conditions as used herein.
- the cellulase-incompatible amines generally have the formula R8R9R10N, wherein R8 and R9 are, independently, C10-C22 alkyl, and R10 is hydrogen or C1-C3 alkyl. Derivatives of these amines like, e.g., the corresponding amides, also negatively interact with cellulase.
- compositions herein are formulated at a pH in the range of from 6.5 to 9.5, measured as a 1% solution of the composition in distilled water. At this pH-range, the cellulase for use herein have their optimum performance.
- compositions herein may contain, in addition to the essential ingredients, optional ingredients, which can be highly desirable.
- the compositions herein contain a clay softening agent, in combination with the cellulase.
- clay softening agents are well-known in the detergency patent literature and are in broad commercial use, both in Europe and in the United States. Included among such clay softeners are various heat-treated kaolins and various multi-layer smectites.
- Preferred clay softeners are smectite softener clays that are described in German patent document 23 34 899 and in U.K. patent 1,400,898, which can be referred to for details.
- the most preferred clay fabric softening materials include those materials of bentonitic origin, bentonites being primarily montmorillonite type clays together with various impurities, the level and nature of which depends on the source of the clay material.
- Softener clays are used in the preferred compositions at levels of at least 1%, generally 1-20°, preferably 2-10%.
- the alkoxy polyamine does not negatively interact with the deposition of softener clays.
- the detergent compositions contain a detergent builder and/or metal ion sequestrant.
- detergent builders include the nitrilotriacetates, polycarboxylates, citrates, water-soluble phosphates such as tri-polyphosphate and sodium ortho- and pyro-phosphates, and mixtures thereof.
- Metal ion sequestrants include all of the above, plus materials like ethylenediaminetetraacetate, the amino-polyphosphonates and a wide variety of other poly-functional organic acids and salts too numerous to mention in detail here. See U.S. Patent 3.579.454 for typical examples of the use of such materials in various cleaning compositions.
- Preferred polyfunctional organic acids species for use herein are citric acid, ethylene diamine tetramethylenephosphonic acid, and diethylene triaminepentamethylenephosphonic acid.
- a further class of detergency builder materials useful in the present invention are insoluble sodium aluminosilicates.
- the 1-10 micron size zeolite (e.g., zeolite A) builders disclosed in German Parent 24.22.655 are especially preferred for use in low-phsophate or non-phosphate compositions.
- the builder/sequestrant will comprise from 0.5% to 45% of the composition.
- compositions herein can also contain fatty acids, saturated or unsaturated, and the corresponding soaps.
- Suitable fatty acids, saturated or unsaturated have from 10 to 18 carbon atoms in the alkyl chain.
- Preferred are unsaturated species having from 14 to 18 carbon atoms in the alkyl chain, most preferably oleic acid.
- the corresponding soaps can also be used.
- the optional fatty acid/soaps are used in levels up to 20%.
- compositions herein can also contain compounds of the general formula R-CH(COOH)CH2(COOH) i.e. derivatives of succinic acid, wherein R is C10-C20 alkyl or alkenyl, preferably C12-C16, wherein R may be substituted with hydroxyl, sulfo, sulfoxy or sulfone substituents.
- the succinate builders are preferably used in the form of their water-soluble salts, including the sodium, potassium, ammonium and alkanoammonium salts.
- succinate builders include : lauryl succinate, myristyl succinate, palmityl succinate, 2-dodecenyl succinate (preferred), 2-pentadecenyl succinate, and the like.
- Also useful as builders in the present context are the compounds described in US patent 4.663.071, i.e. mixtures of tartrate monosuccinic acid and tartrate disuccinic acid in a weight ratio of monosuccinic to disuccinic of from 97:3 to 20:80, preferably 95:5 to 40:60.
- bleaching agent Another optional ingredient is a bleaching agent.
- peroxygen bleaching agents such as sodium perborate, commercially available in the form of mono- and tetra-hydrates, sodium carbonate peroxyhydrate, sodium pyrophosphate peroxyhydrate and urea peroxyhydrate.
- Bleach activators may be used in combination with the above peroxygen bleaching agents.
- Classes of bleach activators include esters, imides, imidazoles, oximes, and carbonates.
- preferred materials include methyl o-acetoxy benzoates; sodium-p-acetoxy benzene sulfonates such as sodium 4-octanoyloxybenzene sulfonate; sodium-4-octanoyloxybenzene sulfonate, and sodium-4-decanoyloxybenzenesulfonate : biophenol diacetate; tetra acetyl ethylene diamine; tetra acetyl hexamethylene diamine; tetra acetyl methylene diamine.
- alpho-substituted alkyl or alkenyl esters such as sodium-4(2-chlorooctanoyloxy) benzene sulfonate, sodium 4-(3,5,5-trimethyl hexanoyloxy)benzene sulfonate.
- Suitable peroxyacids are also peroxygen bleach activators such as described in published European Patent Application 0 166 571, i.e., compounds of the general type RXAOOH and RXAL, wherein R is a hydroxcarbyl group, X is a hetero-atom, A is a carbonyl bridging group and L is a leaving group, especially oxybenzenesulfonate.
- Enzymes other than cellulases can be used in combination with the cellulase herein.
- All generally known enzyme stabilizing systems can be used in the liquid executions of the compositions herein at the art established levels. Examples of suitable stabilizing systems include short C 1-4 chain carboxylic acid, particularly formic acid in combination with a low level of calcium, boric acid and the water-soluble salts thereof possibly in combination with polyols.
- compositions herein can contain, in addtion to ingredients already mentioned, various other optioal 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, hydrotropes and gel-control agents, freeze-thaw stabilizers, bactericides, preservatives, suds control agents, bleach stabilizing agents.
- the detergent compositions of this invention can be present in any suitable physical state inclusive of granular, liquid, pasty, or sheet-like form. They may be prepared in any way, as appropriate to their physical form, by mixing the components, co-agglomerating them, micro-encapsulating them, dispersing them in a liquid carrier, and releasably adsorbing or coating them onto a non-particulate substrate, such as a non-woven or paper sheet.
- Granular detergents were prepared, having the following compositions :
- liquid detergent composition was also prepared :
Abstract
Description
- The present invention relates to detergent compostions which comprise a detergent cellulase and a low level of a narrowly defined polymer. Preferred compositions further contain a fabric-softening clay.
- The present invention relates to detergent compositions comprising a detergent cellulase. The compositions are formulated to provide a near-neutral or mildly alkaline wash liquor pH. They contain a low level of a narrowly defined soil release polymer.
- the use of cellulolytic enzymes, i.e. cellulase, as a harshness reducing agent in fabric softening compositions, is taught in British Patent 1.368.599.
- The use of cellulase in detergent compositions has been further disclosed in GB-A-2,075,028; GB-A-2,095,275; GB-A-2,094,826 and Jap. Patent 57108-199.
- EP-A 0 120 528 teaches alkaline softening detergent compositions comprising a synergistic mixture of a water-insoluble C₁₀-C₂₆ tertiary amine and cellulase.
- EP-A 0 177 165 discloses alkaline softening detergent compositions containing a mixture of smectite clay and cellulase.
- To date however detergent cellulases have not found wide acceptance in the detergent industry. One reason is that the interaction of cellulase and other, more conventional detergent ingredients is poorly understood. Another reason is that compositions formulated according to art-disclosed recipes do not use cellulase at their optimum pH-range.
- To date as well, the tendency in the formulation of detergent compositions has been to increase the pH of the compositions (clearly above 10) in order to boost cleaning performance, especially on clay soil stains. However, at such alkaline pH ranges commercially available detergent cellulases do not provide optimum performance ; there is, consequently, a standing need for compositions formulated at pH below 10, which show optimum cellulase performance, while having good clay soil cleaning properties.
- The present invention answers the above need, and provides efficient near neutral or mildly alkaline detergent compositions, which exhibit good cleaning properties, especially on cotton fabrics.
- EP-A 0 112 593 describes alkoxylated amines having clay-soil removal/anti-redeposition properties when used in detergent compositions. EP-A 0 137 615 describes solvent-based liquid detergent compositions containing alkoxylated polyamines.
- The present invention relates to detergent compositions comprising a surface-active agent and a detergent cellulase. The detergent compositions of this invention are characterized in that they contain from 0.1% to 1% of an alkoxylated polyamine as defined herein below, and in that the pH of a 1% solution of the detergent compositions in distilled water is from 6.5 to 9.5. Preferred are detergent compositions which further comprise from 1% to 10% of a fabric softening clay material, preferably a bentonite clay. Preferred are also compositions that are essentially free of water-insoluble, long-chain alkyl amines, or derivatives thereof.
The detergent cellulase is preferably a bacterial or fungal cellulase having an optimum pH in the range of from 5 to 11.5, more preferably from 6.5 to 9.5. The amount of cellulase in the composition is preferably such that the cellulase activity of the composition ranges from 5 to 100 CMCase units per gram. - Preferred are further compositions that comprise from 0.5% to 5% of a water-soluble quaternary ammonium compound.
- For optimum performance of detergent cellulases it is desirable to formulate detergent compositions having a pH in 1% aqueous solution in the range of from 6.5 to 9.5. As may be expected, the clay soil removal performance of such compositions is relatively poor as compared to compositions formulated to provide a wash liquor pH of 10 or above.
- Certain water-soluble quaternary ammonium compounds are highly desirable as cationic co-surfactants in detergent compositions, as these compounds provide important greasy soil removal benefits. Due to their positive charge, however, these cationics tend to negatively interact with the clay soil removal performance of a detergent composition. This effect is more pronounced at relatively low pH, at which clay particles are less able to peptize viz negative charge repulsion effects than at pH>10.
- It has now been found that relatively small amounts of a narrowly defined alkoxylated polyamine clay soil removal polymer off-set the negative effects on clay soil removal performance as result from a pH of 9.5 or below, and from the negative interaction of water-soluble quaternary ammonium compounds. It has further been found that the presence of this clay soil release polymer at the pH specified does not affect the deposition of such clays as may be used to provide fabric softening benefits (e.g., bentonite clays).
Hence, the preferred compositions of this invention address the conflicting needs of removing clay soil, while leaving the deposition of desirable softening clays inimpaired. This highly surprising result may be due to the relatively low level of clay soil release polymer that is sufficient to obtain satisfactory clay soil removal with the compositions of the present invention. - The surface-active agent useful herein preferably contains at least 50% by weight, more preferably from 60% to 100% by weight of the surface active agent of a non-soap anionic surface-active agent (salt form). A wide range of anionic surfactants can be used in the compositions of the present invention.
- Suitable anionic surfactants are water-soluble salts of alkyl benzene sulphonates, alkyl sulphates, alkyl polyethoxy ether sulphates, paraffin sulphonates, alpha-olefin sulphonates, alpha-sulphocarboxylates and their esters, alkyl glyceryl ether sulphonates, fatty acid monoglyceride sulphates and sulphonates, alkyl phenol polyethoxy ether sulphates, 2-acyloxy-alkane-1-sulphonates, and beta-alkyloxy alkane sulphonates.
- Paraticularly preferred alkyl benzene sulphonates have from 9 to 15 carbon atoms in a linear or branched alkyl chain, especially from 11 to 13 carbon atoms. Suitable alkyl sulphates have from 10 to 22 carbon atoms in the alkyl chain, more especially from 12 to 18 carbon atoms. Suitable alkyl polyethoxy ether sulphates have from 10 to 18 carbon atoms in the alkyl chain and have an average of from 1 to 12 - CH₂CH₂O- groups per molecule, especially from 10 to 16 carbon atoms in the alkyl chain and an average of from 1 to 6 -CH₂CH₂O-groups per molecule.
- Suitable paraffin sulphonates are essentially linear and contain from 8 to 24 carbon atoms, more particularly rom 14 to 18 carbon atoms. Suitable alpha-olefin sulphonates have from 10 to 24 carbon atoms, more particularly from 14 to 16 carbon atoms; alpha-olefin sulphonates can be made by reaction with sulphur trioxide, followed by neutralization under conditions such that any sultones present are hydrolyzed to the corresponding hydroxy alkane sulphonates. Suitable alpha-sulphocarboxylates contain from 6 to 20 carbon atoms; included herein are not only the salts of alpha-sulphonated fatty acids but also their esters made from alcohols containing 1 to 14 carbon atoms.
- Suitable alkyl glyceryl ether sulphates are ethers of alcohols having from 10 to 18 carbon atoms, more particularly those derived from coconut oil and tallow. Suitable alkyl phenol polyethoxy ether sulphates have from 8 to 12 carbon atoms in the alkyl chain and an average of from 1 to 6 - CH₂CH₂O-groups per molecule. Suitable 2-acyloxyalkane-1-sulphonates contain from 2 to 9 carbon atoms in the acyl group and from 9 to 23 carbon atoms in the alkane moiety. Suitable beta-alkyloxy alkane sulphonates contain from 1 to 3 carbon atoms in the alkyl group and from 8 to 20 carbon atoms in the alkane moiety.
- The alkyl chains of the foregoing anionic surfactants can be derived from natural sources such as coconut oil or tallow, or can be made synthetically as for example by using the Ziegler or Oxo processes. Water-solubility can be achieved by using alkali metal, ammonium, or alkanol-ammonium cations; sodium is preferred. Mixtures of anionic surfactants are contemplated by this invention; a satisfactory mixture contains alkyl benzene sulphonate having 11-13 carbon atoms in the alkyl group and alkyl sulphate having 12 to 18 carbon atoms in the alkyl goup.
- Nonionic surfactants may be incorporated in the compositions herein, in limited amounts (less than 50%). Suitable nonionics are water-soluble ethoxylated materials of HLB 11.5-17.0 and include (but are not limited to) C₁₀-C₂₀ primary and secondary alcohol ethoxylates and C₅-C₁₀ alkylphenol ethoxylates. C₁₄-C₁₈ linear primary alcohols condensed with from seven to thirty moles of ethylene oxide per mole of alcohol are preferred, examples being C₁₄-C₁₅ (EO)₇, C₁₆-C₁₈ (EO)₂₅ and especially C₁₆-C₁₈ (EO)₁₁.
- Other types of surfactants can be used in limited amounts, in combination with the anionic surface-active agent. They include zwitterionic amphoteric, as well as cationic surfactants.
- Cationic co-surfactants which can be used herein, include water-soluble quaternary ammonium compounds of the form R₄R₅R₆R₇N⁺X⁻, wherein R₄ is alkyl having from 10 to 20, preferably from 12-18 carbon atoms, R₅, R₆ and R₇ are independently, C₁-C₄ alkyl, and X⁻ is an anion, e.g. chloride. Examples are the trimethyl ammonium compounds, including C₁₂-C₁₄ alkyl trimethyl ammonium chloride and cocoalkyl trimethyl ammonium methosulfate.
- Alkoxylated polyamines suitable as clay-soil removal/anti-redeposition agents, as well as their preparation, are disclosed in EP-PA 0 112 593, the disclosures of which are incorporated herein by reference.
- It is to be understood that the term "polyamines" as used herein represents generically the alkoxylated polyamines, both in their amine form and in their quaternarized form. Such materials can conventiently be represented as molecules of the empirical structures with repeating units :
-
- The cellulase usable in the present invention may be any bacterial or fungal cellulase having a pH optimum of between 5 and 9.5.
- Suitable cellulases are disclosed in GB-A-2.075.028; GB-A-2.095.275 and DE-OS-2.247.832.
- Examples of such cellulases are cellulases produced by a strain of Humicola insolens (Humicola grisea var. thermoidea), particularly the Humicola strain DSM 1800, and cellulases produced by a fungus of Bacillus N or a cellulase 212-producing fungus belonging to the genus Aeromonas, and cellulase extracted from the hepatopancreas of a marine mullosc (Dolabella Auricula Solander).
- The cellulase added to the composition of the invention may be in the form of a non-dusting granulate, e.g. "marumes" or "prills", or in the form of a liquid in which the cellulase is provided as a cellulase concentrate suspended in e.g. a nonionic surfactant or dissolved in an aqueous medium.
- Activity determination for the cellulase herein is based on the hydrolysis of carboxymethyl cellulose. Generated low molecular reducing carbohydrates are colorimetrically determined by the ferrocyanide reaction as descirbed by W.S. Hoffman "J. Biol. Chem." 120,51 (1973). Key conditions of incubation are pH-7.0, temperature of 40°C and incubation time of 20 minutes.
- One CMCase unit is defined as the amount of enzyme which forms per minute an amount of reducing carbohydrate equivalent to 10⁻⁶ mole of glucose, in the above-described conditions.
- A highly preferred range of cellulase activity in the present context is from 5 to 100 CMCase activity units/gram of composition.
- Preferred compositions herein are essentially free of water-insoluble long-chain alkyl amine softening agents, and derivatives thereof, since it has surprisingly been discovered that such compounds negatively interact with cellulase under the pH conditions as used herein. The cellulase-incompatible amines generally have the formula R₈R₉R₁₀N, wherein R₈ and R₉ are, independently, C₁₀-C₂₂ alkyl, and R₁₀ is hydrogen or C₁-C₃ alkyl. Derivatives of these amines like, e.g., the corresponding amides, also negatively interact with cellulase.
- The compositions herein are formulated at a pH in the range of from 6.5 to 9.5, measured as a 1% solution of the composition in distilled water.
At this pH-range, the cellulase for use herein have their optimum performance. - The compositions herein may contain, in addition to the essential ingredients, optional ingredients, which can be highly desirable.
- For example, it is preferred that the compositions herein contain a clay softening agent, in combination with the cellulase. Such clay softening agents are well-known in the detergency patent literature and are in broad commercial use, both in Europe and in the United States. Included among such clay softeners are various heat-treated kaolins and various multi-layer smectites. Preferred clay softeners are smectite softener clays that are described in German patent document 23 34 899 and in U.K. patent 1,400,898, which can be referred to for details.
- The most preferred clay fabric softening materials include those materials of bentonitic origin, bentonites being primarily montmorillonite type clays together with various impurities, the level and nature of which depends on the source of the clay material. Softener clays are used in the preferred compositions at levels of at least 1%, generally 1-20°, preferably 2-10%. Surprisingly, the alkoxy polyamine does not negatively interact with the deposition of softener clays.
- It is preferred as well that the detergent compositions contain a detergent builder and/or metal ion sequestrant. Compounds classifiable and well-known in the art as detergent builders include the nitrilotriacetates, polycarboxylates, citrates, water-soluble phosphates such as tri-polyphosphate and sodium ortho- and pyro-phosphates, and mixtures thereof. Metal ion sequestrants include all of the above, plus materials like ethylenediaminetetraacetate, the amino-polyphosphonates and a wide variety of other poly-functional organic acids and salts too numerous to mention in detail here. See U.S. Patent 3.579.454 for typical examples of the use of such materials in various cleaning compositions. Preferred polyfunctional organic acids species for use herein are citric acid, ethylene diamine tetramethylenephosphonic acid, and diethylene triaminepentamethylenephosphonic acid.
- A further class of detergency builder materials useful in the present invention are insoluble sodium aluminosilicates. The 1-10 micron size zeolite (e.g., zeolite A) builders disclosed in German Parent 24.22.655 are especially preferred for use in low-phsophate or non-phosphate compositions. In general, the builder/sequestrant will comprise from 0.5% to 45% of the composition.
- The compositions herein can also contain fatty acids, saturated or unsaturated, and the corresponding soaps. Suitable fatty acids, saturated or unsaturated, have from 10 to 18 carbon atoms in the alkyl chain. Preferred are unsaturated species having from 14 to 18 carbon atoms in the alkyl chain, most preferably oleic acid. The corresponding soaps can also be used. The optional fatty acid/soaps are used in levels up to 20%.
- The compositions herein can also contain compounds of the general formula R-CH(COOH)CH₂(COOH) i.e. derivatives of succinic acid, wherein R is C₁₀-C₂₀ alkyl or alkenyl, preferably C₁₂-C₁₆, wherein R may be substituted with hydroxyl, sulfo, sulfoxy or sulfone substituents.
- The succinate builders are preferably used in the form of their water-soluble salts, including the sodium, potassium, ammonium and alkanoammonium salts.
- Specific examples of succinate builders include : lauryl succinate, myristyl succinate, palmityl succinate, 2-dodecenyl succinate (preferred), 2-pentadecenyl succinate, and the like.
- Also useful as builders in the present context are the compounds described in US patent 4.663.071, i.e. mixtures of tartrate monosuccinic acid and tartrate disuccinic acid in a weight ratio of monosuccinic to disuccinic of from 97:3 to 20:80, preferably 95:5 to 40:60.
- Another optional ingredient is a bleaching agent. Preferred are peroxygen bleaching agents such as sodium perborate, commercially available in the form of mono- and tetra-hydrates, sodium carbonate peroxyhydrate, sodium pyrophosphate peroxyhydrate and urea peroxyhydrate.
- Bleach activators may be used in combination with the above peroxygen bleaching agents. Classes of bleach activators include esters, imides, imidazoles, oximes, and carbonates. In those classes, preferred materials include methyl o-acetoxy benzoates; sodium-p-acetoxy benzene sulfonates such as sodium 4-octanoyloxybenzene sulfonate; sodium-4-octanoyloxybenzene sulfonate, and sodium-4-decanoyloxybenzenesulfonate : biophenol diacetate; tetra acetyl ethylene diamine; tetra acetyl hexamethylene diamine; tetra acetyl methylene diamine.
- Other highly preferred peroxygen bleach activators which are disclosed in U.S. Patents 4,483,778 and 4,539,130, are alpho-substituted alkyl or alkenyl esters, such as sodium-4(2-chlorooctanoyloxy) benzene sulfonate, sodium 4-(3,5,5-trimethyl hexanoyloxy)benzene sulfonate. Suitable peroxyacids are also peroxygen bleach activators such as described in published European Patent Application 0 166 571, i.e., compounds of the general type RXAOOH and RXAL, wherein R is a hydroxcarbyl group, X is a hetero-atom, A is a carbonyl bridging group and L is a leaving group, especially oxybenzenesulfonate.
- Enzymes other than cellulases, such as proteolytic, amylolytic, or lipolytic enzymes can be used in combination with the cellulase herein. All generally known enzyme stabilizing systems can be used in the liquid executions of the compositions herein at the art established levels. Examples of suitable stabilizing systems include short C1-4 chain carboxylic acid, particularly formic acid in combination with a low level of calcium, boric acid and the water-soluble salts thereof possibly in combination with polyols.
- Moreover, the compositions herein can contain, in addtion to ingredients already mentioned, various other optioal 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, hydrotropes and gel-control agents, freeze-thaw stabilizers, bactericides, preservatives, suds control agents, bleach stabilizing agents.
- The detergent compositions of this invention can be present in any suitable physical state inclusive of granular, liquid, pasty, or sheet-like form. They may be prepared in any way, as appropriate to their physical form, by mixing the components, co-agglomerating them, micro-encapsulating them, dispersing them in a liquid carrier, and releasably adsorbing or coating them onto a non-particulate substrate, such as a non-woven or paper sheet.
- The following examples illustrate the present invention, but are not intended to limit its scope.
-
-
-
Claims (10)
- the composition contains from 0.1% to 1% of a clay-soil release polymer of the formula :
- the pH of a 1% solution of the detergent composition in distilled water is from 6.5 to 9.5.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT87202190T ATE79398T1 (en) | 1986-11-21 | 1987-11-11 | CLEANING PRODUCTS CONTAINING CELLULASE. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB868627915A GB8627915D0 (en) | 1986-11-21 | 1986-11-21 | Detergent compositions |
GB8627915 | 1986-11-21 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0269169A2 true EP0269169A2 (en) | 1988-06-01 |
EP0269169A3 EP0269169A3 (en) | 1989-06-07 |
EP0269169B1 EP0269169B1 (en) | 1992-08-12 |
Family
ID=10607739
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP87202190A Expired - Lifetime EP0269169B1 (en) | 1986-11-21 | 1987-11-11 | Detergent compositions containing cellulase |
Country Status (14)
Country | Link |
---|---|
EP (1) | EP0269169B1 (en) |
JP (1) | JPS63213598A (en) |
KR (1) | KR880006355A (en) |
CN (1) | CN87107307A (en) |
AT (1) | ATE79398T1 (en) |
AU (1) | AU8143287A (en) |
DE (1) | DE3781101T2 (en) |
DK (1) | DK611587A (en) |
EG (1) | EG18326A (en) |
FI (1) | FI86884C (en) |
GB (1) | GB8627915D0 (en) |
GR (1) | GR3006203T3 (en) |
IE (1) | IE60696B1 (en) |
TR (1) | TR23328A (en) |
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0365103A2 (en) * | 1988-10-21 | 1990-04-25 | Colgate-Palmolive Company | Heavy duty particulate synthetic organic nonionic detergent compositions of improved cleaning action on laundry containing hard-to-remove soils |
US5120463A (en) * | 1989-10-19 | 1992-06-09 | Genencor International, Inc. | Degradation resistant detergent compositions based on cellulase enzymes |
WO1992013057A1 (en) * | 1991-01-16 | 1992-08-06 | The Procter & Gamble Company | Compact detergent compositions with high activity cellulase |
WO1994003577A1 (en) * | 1992-07-29 | 1994-02-17 | Henkel Kommanditgesellschaft Auf Aktien | Enzyme-containing washing agent |
US5443750A (en) * | 1991-01-16 | 1995-08-22 | The Procter & Gamble Company | Detergent compositions with high activity cellulase and softening clays |
US5520838A (en) * | 1991-01-16 | 1996-05-28 | The Procter & Gamble Company | Compact detergent compositions with high activity cellulase |
WO1997000936A1 (en) * | 1995-06-20 | 1997-01-09 | The Procter & Gamble Company | Nonaqueous detergent compositions comprising clay soil removal polymers |
EP0794245A1 (en) * | 1996-03-04 | 1997-09-10 | The Procter & Gamble Company | Laundry pretreatment process and bleaching compositions |
WO1997042283A1 (en) * | 1996-05-03 | 1997-11-13 | The Procter & Gamble Company | Laundry bar compositions |
WO1997042284A1 (en) * | 1996-05-03 | 1997-11-13 | The Procter & Gamble Company | Detergent compositions comprising polyamine scavenger agents and enzymes |
WO1997042294A1 (en) * | 1996-05-03 | 1997-11-13 | The Procter & Gamble Company | Detergent compositions comprising modified polyamine polymers and cellulase enzymes |
WO1997042292A1 (en) * | 1996-05-03 | 1997-11-13 | The Procter & Gamble Company | Laundry detergent compositions comprising cationic surfactants and modified polyamine soil dispersents |
WO1997042293A1 (en) * | 1996-05-03 | 1997-11-13 | The Procter & Gamble Company | Liquid laundry detergent compositions comprising cotton soil release polymers and protease enzymes |
WO1998004233A1 (en) * | 1996-07-31 | 1998-02-05 | The Procter & Gamble Company | Conditioning shampoo compositions comprising polyalkoxylated polyalkyleneamine |
WO1998012295A1 (en) * | 1996-09-19 | 1998-03-26 | The Procter & Gamble Company | Color care compositions |
WO1998015608A2 (en) * | 1996-10-07 | 1998-04-16 | The Procter & Gamble Company | Alkoxylated, quaternized polyamine detergent ingredients |
US5747440A (en) * | 1996-01-30 | 1998-05-05 | Procter & Gamble Company | Laundry detergents comprising heavy metal ion chelants |
EP0893489A1 (en) * | 1997-07-22 | 1999-01-27 | Calgon Corporation | Composition and method for cleaning surfaces |
US6020302A (en) * | 1997-09-18 | 2000-02-01 | The Procter & Gamble Company | Color care compositions |
US6143713A (en) * | 1996-05-03 | 2000-11-07 | The Procter & Gamble Company | Polyamines having fabric appearance enhancement benefits |
WO2000066696A1 (en) * | 1999-04-29 | 2000-11-09 | Genencor International, Inc. | Cellulase detergent matrix |
US6677289B1 (en) | 1999-07-16 | 2004-01-13 | The Procter & Gamble Company | Laundry detergent compositions comprising polyamines and mid-chain branched surfactants |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8627914D0 (en) * | 1986-11-21 | 1986-12-31 | Procter & Gamble | Softening detergent compositions |
BR0012517B1 (en) | 1999-07-16 | 2010-12-28 | laundry detergent compositions comprising zwitterionic polyamines and branched intermediate chain surfactants. | |
US6696401B1 (en) | 1999-11-09 | 2004-02-24 | The Procter & Gamble Company | Laundry detergent compositions comprising zwitterionic polyamines |
ATE393813T1 (en) | 2002-09-12 | 2008-05-15 | Procter & Gamble | POLYMER SYSTEMS AND CLEANING OR DETERGENT COMPOSITIONS CONTAINING SAME |
JP6235144B2 (en) | 2013-08-26 | 2017-11-22 | ザ プロクター アンド ギャンブル カンパニー | Composition comprising an alkoxylated polyamine having a low melting point |
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GB2075028A (en) * | 1980-04-30 | 1981-11-11 | Novo Industri As | Enzymatic additive |
EP0112593A2 (en) * | 1982-12-23 | 1984-07-04 | THE PROCTER & GAMBLE COMPANY | Detergent compositions containing ethoxylated amines having clay soil removal/anti-redeposition properties |
EP0120528A1 (en) * | 1983-03-10 | 1984-10-03 | Unilever N.V. | Detergent compositions |
EP0206513A1 (en) * | 1985-05-18 | 1986-12-30 | The Procter & Gamble Company | Laundry detergent compositions |
-
1986
- 1986-11-21 GB GB868627915A patent/GB8627915D0/en active Pending
-
1987
- 1987-11-11 DE DE8787202190T patent/DE3781101T2/en not_active Expired - Fee Related
- 1987-11-11 AT AT87202190T patent/ATE79398T1/en not_active IP Right Cessation
- 1987-11-11 EP EP87202190A patent/EP0269169B1/en not_active Expired - Lifetime
- 1987-11-19 EG EG673/87A patent/EG18326A/en active
- 1987-11-20 IE IE315187A patent/IE60696B1/en not_active IP Right Cessation
- 1987-11-20 DK DK611587A patent/DK611587A/en unknown
- 1987-11-20 TR TR815/87A patent/TR23328A/en unknown
- 1987-11-20 AU AU81432/87A patent/AU8143287A/en not_active Abandoned
- 1987-11-20 FI FI875138A patent/FI86884C/en not_active IP Right Cessation
- 1987-11-21 JP JP62295003A patent/JPS63213598A/en active Pending
- 1987-11-21 KR KR870013127A patent/KR880006355A/en not_active Application Discontinuation
- 1987-11-21 CN CN198787107307A patent/CN87107307A/en active Pending
-
1992
- 1992-11-11 GR GR920402532T patent/GR3006203T3/el unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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GB2075028A (en) * | 1980-04-30 | 1981-11-11 | Novo Industri As | Enzymatic additive |
EP0112593A2 (en) * | 1982-12-23 | 1984-07-04 | THE PROCTER & GAMBLE COMPANY | Detergent compositions containing ethoxylated amines having clay soil removal/anti-redeposition properties |
EP0120528A1 (en) * | 1983-03-10 | 1984-10-03 | Unilever N.V. | Detergent compositions |
EP0206513A1 (en) * | 1985-05-18 | 1986-12-30 | The Procter & Gamble Company | Laundry detergent compositions |
Cited By (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0365103A2 (en) * | 1988-10-21 | 1990-04-25 | Colgate-Palmolive Company | Heavy duty particulate synthetic organic nonionic detergent compositions of improved cleaning action on laundry containing hard-to-remove soils |
GR890100672A (en) * | 1988-10-21 | 1990-11-29 | Colgate Palmolive Co | Heavy duty particulate synthetic organic nonionic detergent compositions of improved cleaning action on laundry containing hard-to-remove soils |
EP0365103A3 (en) * | 1988-10-21 | 1991-04-03 | Colgate-Palmolive Company | Heavy duty particulate synthetic organic nonionic detergent compositions of improved cleaning action on laundry containing hard-to-remove soils |
US5120463A (en) * | 1989-10-19 | 1992-06-09 | Genencor International, Inc. | Degradation resistant detergent compositions based on cellulase enzymes |
WO1992013057A1 (en) * | 1991-01-16 | 1992-08-06 | The Procter & Gamble Company | Compact detergent compositions with high activity cellulase |
US5443750A (en) * | 1991-01-16 | 1995-08-22 | The Procter & Gamble Company | Detergent compositions with high activity cellulase and softening clays |
US5520838A (en) * | 1991-01-16 | 1996-05-28 | The Procter & Gamble Company | Compact detergent compositions with high activity cellulase |
WO1994003577A1 (en) * | 1992-07-29 | 1994-02-17 | Henkel Kommanditgesellschaft Auf Aktien | Enzyme-containing washing agent |
WO1997000936A1 (en) * | 1995-06-20 | 1997-01-09 | The Procter & Gamble Company | Nonaqueous detergent compositions comprising clay soil removal polymers |
US5929010A (en) * | 1996-01-30 | 1999-07-27 | Procter & Gamble Company | Laundry detergents comprising heavy metal ion chelants |
US5747440A (en) * | 1996-01-30 | 1998-05-05 | Procter & Gamble Company | Laundry detergents comprising heavy metal ion chelants |
EP0794245A1 (en) * | 1996-03-04 | 1997-09-10 | The Procter & Gamble Company | Laundry pretreatment process and bleaching compositions |
WO1997042293A1 (en) * | 1996-05-03 | 1997-11-13 | The Procter & Gamble Company | Liquid laundry detergent compositions comprising cotton soil release polymers and protease enzymes |
WO1997042283A1 (en) * | 1996-05-03 | 1997-11-13 | The Procter & Gamble Company | Laundry bar compositions |
WO1997042294A1 (en) * | 1996-05-03 | 1997-11-13 | The Procter & Gamble Company | Detergent compositions comprising modified polyamine polymers and cellulase enzymes |
US6143713A (en) * | 1996-05-03 | 2000-11-07 | The Procter & Gamble Company | Polyamines having fabric appearance enhancement benefits |
WO1997042292A1 (en) * | 1996-05-03 | 1997-11-13 | The Procter & Gamble Company | Laundry detergent compositions comprising cationic surfactants and modified polyamine soil dispersents |
US6004922A (en) * | 1996-05-03 | 1999-12-21 | The Procter & Gamble Company | Laundry detergent compositions comprising cationic surfactants and modified polyamine soil dispersents |
WO1997042284A1 (en) * | 1996-05-03 | 1997-11-13 | The Procter & Gamble Company | Detergent compositions comprising polyamine scavenger agents and enzymes |
WO1998004233A1 (en) * | 1996-07-31 | 1998-02-05 | The Procter & Gamble Company | Conditioning shampoo compositions comprising polyalkoxylated polyalkyleneamine |
WO1998012296A1 (en) * | 1996-09-19 | 1998-03-26 | The Procter & Gamble Company | Color care compositions |
WO1998012295A1 (en) * | 1996-09-19 | 1998-03-26 | The Procter & Gamble Company | Color care compositions |
KR100336148B1 (en) * | 1996-09-19 | 2002-05-09 | 데이비드 엠 모이어 | Color care compositions |
WO1998015608A3 (en) * | 1996-10-07 | 1998-05-22 | Procter & Gamble | Alkoxylated, quaternized polyamine detergent ingredients |
WO1998015608A2 (en) * | 1996-10-07 | 1998-04-16 | The Procter & Gamble Company | Alkoxylated, quaternized polyamine detergent ingredients |
EP0893489A1 (en) * | 1997-07-22 | 1999-01-27 | Calgon Corporation | Composition and method for cleaning surfaces |
US6020302A (en) * | 1997-09-18 | 2000-02-01 | The Procter & Gamble Company | Color care compositions |
WO2000066696A1 (en) * | 1999-04-29 | 2000-11-09 | Genencor International, Inc. | Cellulase detergent matrix |
US6565613B1 (en) | 1999-04-29 | 2003-05-20 | Genencor International, Inc. | Cellulase detergent matrix |
US6677289B1 (en) | 1999-07-16 | 2004-01-13 | The Procter & Gamble Company | Laundry detergent compositions comprising polyamines and mid-chain branched surfactants |
Also Published As
Publication number | Publication date |
---|---|
EP0269169A3 (en) | 1989-06-07 |
DK611587D0 (en) | 1987-11-20 |
DE3781101T2 (en) | 1992-12-17 |
EG18326A (en) | 1992-09-30 |
FI875138A0 (en) | 1987-11-20 |
AU8143287A (en) | 1988-05-26 |
JPS63213598A (en) | 1988-09-06 |
FI875138A (en) | 1988-05-22 |
GB8627915D0 (en) | 1986-12-31 |
FI86884C (en) | 1992-10-26 |
KR880006355A (en) | 1988-07-22 |
IE60696B1 (en) | 1994-08-10 |
GR3006203T3 (en) | 1993-06-21 |
FI86884B (en) | 1992-07-15 |
TR23328A (en) | 1989-11-08 |
ATE79398T1 (en) | 1992-08-15 |
DE3781101D1 (en) | 1992-09-17 |
DK611587A (en) | 1988-05-22 |
EP0269169B1 (en) | 1992-08-12 |
IE873151L (en) | 1988-05-21 |
CN87107307A (en) | 1988-06-01 |
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