IE60696B1 - Detergent compositions containing cellulase - Google Patents

Detergent compositions containing cellulase

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Publication number
IE60696B1
IE60696B1 IE315187A IE315187A IE60696B1 IE 60696 B1 IE60696 B1 IE 60696B1 IE 315187 A IE315187 A IE 315187A IE 315187 A IE315187 A IE 315187A IE 60696 B1 IE60696 B1 IE 60696B1
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Ireland
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composition according
composition
cellulase
detergent
compositions
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IE315187A
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IE873151L (en
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Procter & Gamble
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Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • 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
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/386Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38645Preparations containing enzymes, e.g. protease or amylase containing cellulase
    • 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
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3723Polyamines or polyalkyleneimines

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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)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

Detergent compositions comprising detergent cellulases are disclosed. The compositions are formulated to provide a near-neutral or mildly-alkaline wash liquor pH. The compositions comprise a clay soil removal polymer and, optionally, a fabric-softening clay.

Description

The present invention relates to detergent compostions which comprise a detergent cellules® and a low level of a narrowly defined polymer. Preferred compositions further contain a fabric-softening clay.
V - 2 — 8a e k ground The present invention relates to detergent compositions comprising a detergent cellulase. The compositions are formulated to prouide a near-neutral or mildly alkaline wash liquor pH. They contain a low leuel of a narrowly defined soil release polymer.
The use of cellulolytic enzymes, i.e. cellulase. es 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 C,_-C„, tertiary amine and cellulase. 1Q 20 EP-A 0 177 165 discloses alkaline softening detergent compositions containing a mixture of smectite clay and cellulase.
To date however detergent cellulases haue not found 20 wide acceptance in the detergent industry. On© reason is that the interaction of cellulase and other, mor® 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 abvove 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.
Summary of the Invention The present invention relates to detergent compositions comprising a surface-active agent and a detergent cellulase. The detergent compositions of this 2o 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 20% of a fabric softening elay material, preferably a bentonite clay. Preferred are also compositions that are essentially fre® of water-Insoluble. long-chain alkyl amines, or derivatives thereof.
The detergent cellules® 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 cellules© 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.
Detailed Description of the Invention for optimum performance of detergent cellulases it is desirable to formulate detergent compositions having © pH in 1% agueous 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 positiue 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 via negative charge repulsion effects than at pH>10.
Xt 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 ihe pH specified does not affect the deposition of such clays as may be used to prouide 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 unimpaired. This highly surprising result may be due to the relatively low leuel 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 The surface-active agent useful herein preferably contains at least 50% by weight, mor© 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 inuention.
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 • 25 their esters, alkyl glyceryl ether sulphonates, fatty acid monoglyceride sulphates and sulphonates, alkyl phenol polyethoxy ether sulphates, 2-acyloxy-alkane-l-sulphonates, and beta-alkyloxy alkane sulphonates.
I Particularly preferred alkyl benzene sulphonates haue from 9 to 15 carbon atoms in a linear or branched alkyl chain, especially from ll 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 l to 12 - CH CH 0- groups per molecule, especially from 10 to 16 carbon (atoms in the alkyl chain and an auerage of from X to 6 "CH^CH?O-groups per molecule.
Suitable paraffin sulphonates are essentially linear and contain from 8 to 24 carbon atoms, more particularly from 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 to 20 carbon salts of their esters made atoms . alpha-sulphocarboxylates contain from 6 atoms; included herein are not only the alpha-sulphonated fatty acids but also from alcohols containing 1 to 14 carbon Suitable alkyl glyceryl of alcohols having from 10 to ether sulphates are ethers 18 carbon atoms, more particularly those derived from coconut oil and tallow. Suitable alkyl phenol polyethoxy ether sulphates have rrom 8 to 12 carbon atoms in the alkyl chain and an average of from 1 to 6 -CH7CH7O-groups per molecule. Suitable 2-acyloxyalkane-l-sulphonates contain from 2 to 9 carbon atoms in the acyl group and from 9 to 23 carbon atoms in Suitable beta-alkyloxy alkane from 1 to 3 carbon atoms in the alkyl carbon atoms in the alkane moiety. the alkane moiety, sulphonates contain group and from 8 to - 7 The alkvl 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 b® 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 carbon atoms in the alkyl group.
Nonionic surfactants may be incorporated in the compositions herein, in limited amounts (less than 50¾). Suitable nonionics are water-soluble ethoxylated materials of HLB 11.5-17.0 and include (but are not limited to) CIO"C9O and secondary alcohol ethoxylates and C.-C alkylphenol ethoxylates. C -C1fl linear primary alcohols condensed with from seven to thirty moles of ethylene oxide per mole of alcohol are preferred, examples being (EO)„, C1g-Clg (£0)^^ and especially Cl6~Clg (EO)1V Other types of surfactants can b® used in limited amounts, in combination with th® 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 R„ R. fi.. , wherein is alkyl «•50/ ** having from 10 to 20. preferably from 12-18 carbon atoms, fiP, R. and R„ are independently, C -C, alkyl, o 7 1 * and X is an anion, e.g. chloride. Examples ar® the - 8 trimethvl ammonium compounds, including C,_-Cia alkyl * Ids.** trimethyl ammonium chloride and cocoalkyl trimethyl ammonium methosulfate.
Pol Vamines Alkoxylated polyamines suitable as clay-soil remoual/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 guaternarized form. Such materials can conuentiently be represented as molecules of the empirical structures with repeating units : —£n 9 - r]~ - n Amine form and (alkoxy)^ ‘1 R rC _iM - iU R? -8 n Quaternized form (Alkoxy) V .s Wherein R is a hydrocarbyl group, usually of 2-6- carbon 1 atoms; R may be a ^V^rocarbon; the alkoxy groups are ethoxy, propoxy, butoxy 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 am anion such as halide or methylsulfate, resulting from the quaternization reaction.
The most highly preferred polysmines for use herein are th© so-called ethoxylated polyethylene imines, i.e., the polymerized reaction product of ethylene oxide with ethylene-imine, hawing the general formula : (EtO)——-[n-CH2_CH2 3---N_(EtO)y (EtO)^ (Efe°)y wherein n is ©n integer of 3 to 5 and y is an integer of 10 to 20.
The Cellulase The cellulase usable in the present invention may be ©ny bacterial or fungal cellulase having a pH optimum of between S and 9.5.
Suitable cellulases arte 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 1000, i. and cellulases produced by a fungus of Bacillus N or a cellulase 212-producing fungus belonging te 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 described by W.-S. Hoffman J. Biol. Chem. 120,51 (1973) . Key conditions of incubation are pHsT.Q. 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~δ mole of glucose, in the above-described conditions. ft 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 ,θΝ. wherein ί?θ and RQ are. independently, alkyl, and R1Q is hydrogen or C -C. alkvl. Derivatives of these amines like, e.g., 13' 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 IX solution of the composition in distilled water.
At this pH-range, the cellulase for us® herein haue their optimum performance.
Optional ingredients 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 15 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.ft. 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 ©f 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 ethylenediaminetetraaeetate, the amino-polyphosphonates and a wide variety of other poly-functional organic acids and salts too numerous to mention in detail her®. 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 nm size zeolite (e.g., zeolite ft) builders disclosed in German Parent 24.22.655 are especially preferred for us© in low-phosphate 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 ι acids, saturated or unsaturated, and the corresponding soaps. Suitable fatty acids, saturated or unsaturated, haue from 10 to 18 carbon atoms in the alkyl chain. Preferred are unsaturated species hauing from 14 to 18 carbon atoms in the alkyl chain, most preferably oleic acid. Th® corresponding soaps can also be used. The optional fatty acid/soaps are used in levels up to 20¾.
The compositions herein can also contain compounds of the general formula R-CH(C00H)CH7(COOH) i.e. derivatives of succinic acid, wherein R is alkyl or alkenyl, preferably C^-C^. or 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 th© present context are the compounds described in US patent 4.663.071, i.e. mixtures of tartrate monosuccinie acid and tartrate disuccinic acid in a weight ratio of monosuccinie 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 th© 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 A-octanoyloxybenzene sulfonate; <9 Λ — A a* — 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 actiuators which are disclosed in U.S. Patents 4,483,778 and 4,539,130, are alpho-substituted alkyl or alkenyl esters, such as $odium-4(2-ehlorooctanoyloxy) benzene sulfonate, sodium 4~(3,5,S-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 C, Λ chain carboxylic acid.
* X ** ®«· 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 optional 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.
Form and Preparation of the compositions - The detergent compositions of this invention can b® 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-sgglomerating 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.
Example I Granular detergents were prepared, having the following compositions : ingredients weicsht Sodium linear C^7 alkyl sulfonate Sodium tallow alkyl sulfate Tallow alcohol ethoxylate Sodium tripolyphosphate Bentonite clay Coconuttrimethyl ammonium chloride Boric acid Cellulase (1350 CMCase units/g) Proteolytic enzyme Clay soil release polymer* Sodium sulfate, minors, water A 11.0 .0 0.3 . o 8.5 3.0 0.9 0.5 7.0 balance to 100 pH (XX solution in distilled water) a.? 9.0 - 2 6 *an ethoxylated polyamine of fche formula (Eto)--fw -CH2 - Ch23tt- N (eto)s (Eto>y wherein n=4 and y»25 The following granular compositions were also prepared : ingredient X by weight Example II Exampl Sodium Linear ali Sodium sulfate Sodium tripolyphosphate Zeolite fi Sodium nitrilotriacetate Bentonite clay Cellulase Proteolytic enzyme Sodium Perborate tetrahydrate TfiED* Boric acid Optical brightener Clay soil remoual polymer*** minors and water pH (iX solution in distilled water) 2.0 .0 .0 6.5 3.5** 0.5 .0 1.2 4.0 0.3 0.4 ---balance 26.0 5.0 6 . S 3 . 5 0.5 .0 3.0 4.0 0.5 0.6 9.0 9.0 per example I ••Represents 47CMCase units per g of composition *t®tra acetyl ethylene diamine a 7 — Example IU The following liquid detergent composition was also prepared : ingredient % by weight Linear c ~ alkyl benzene sulphonic acid 11.0 A Coconut alkyl sulphate (TEA salt) 4.0 Tallow C,_ ,, alcohol ethoxylate (E07) 10.0 12—15 Coconut fatty acid 10.0 Oleic acid 5.0 Citric acid 1 0 Trethanolamine 4.o Ethanol 6.
Propanediol 1·5 Sodium hydroxide 3.
Sodium formate 1· Cellulase 2.5* Protease 0.6 Clay soil removal polymer** 0.3 minors, water balance ♦Represents 34CMCase units per g composition **As per example I

Claims (8)

1. A deterge softening agent and that : nt composition (for the of fabrics) comprising a detergent cellulase, cleaning and a surface-active characterized in - the composition contains from 0.1% to 1% of a clay-soil release polymer having the repeated units -’ 3-TT or —i N — 3-n- X (Alkoxy)^ (Alkoxy)^ wherein R is hydrocarbyl having from 2 to 6 carbon atoms, R 1 is C, to 0 9 θ hydrocarbon, alkoxy is selected from ethoxy, propoxy, butoxy, or mixtures thereof, y is 2-30, n is an integer of at least 2, and X~ is an anion; and - the pH of a composition 1% solution of the in distilled water detergent is from 6 5 to 9.5
2. A composition according to Claim 1 wherein the alkoxylated polyamine is the polymerized reaction product of ethylene oxide with ethylene imine, having che general formula · (EtO) y _β—— N -(EtO) ( (EtO) y (EtO) y wherein n is an i nteger from 3 to 5 and y is an integer f rom 10 to 20.
3. A composition according to claim 2 wherein the cellulase has an optimum pH in tne range from 6.5 to 9.5. I
4. A composition according to any one of the preceding claims hauing a cellulase activity of from 5 to 100 CMCase units per gram of composition. 5 e A composition according to any one of the preceding claims, wherein the surface active agent contains from 60% to 100% by weight of ©nionic surface-active agent.
5.A composition according to any on® of the preceding claims which further comprises from 1% to 20% of a fabric-softening clay material.
6. 7. A compositor» according to any on© of the preceding claims which further comprises from 0.5% to 5% of a water-soluble quaternary ammonium compound of the formula ft, R_R.R-W^X , wherein R„ is alkvl hawing from 10 to 20 carbon atoms, R„ . ft. and ft„ are. independently, C -C 4 alkyl, and X” is an anion. g a A composition according to any on® of the preceding claims, further characterized in that it is essentially free of water-insoluble long chain alkyl amines or derivatives thereof.
7. 9 ω A composition according to any one of the preceding claims characterized in that the pH of a 1% solution of the composition in distilled water is from 8.5 to 9.5.
8. 10. A detergent composition according to Claim 1, substantially as hereinbefore described with particular reference to the accompanying Examples.
IE315187A 1986-11-21 1987-11-20 Detergent compositions containing cellulase IE60696B1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB868627915A GB8627915D0 (en) 1986-11-21 1986-11-21 Detergent compositions

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IE873151L IE873151L (en) 1988-05-21
IE60696B1 true IE60696B1 (en) 1994-08-10

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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)

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GR3006203T3 (en) 1993-06-21
DK611587D0 (en) 1987-11-20
EP0269169A2 (en) 1988-06-01
EP0269169A3 (en) 1989-06-07
DK611587A (en) 1988-05-22
ATE79398T1 (en) 1992-08-15
CN87107307A (en) 1988-06-01
IE873151L (en) 1988-05-21
GB8627915D0 (en) 1986-12-31
JPS63213598A (en) 1988-09-06
DE3781101T2 (en) 1992-12-17
AU8143287A (en) 1988-05-26
DE3781101D1 (en) 1992-09-17
FI86884C (en) 1992-10-26
FI875138A (en) 1988-05-22
FI875138A0 (en) 1987-11-20
TR23328A (en) 1989-11-08
FI86884B (en) 1992-07-15
EG18326A (en) 1992-09-30
EP0269169B1 (en) 1992-08-12
KR880006355A (en) 1988-07-22

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