WO1997043378A1 - COMPOSITIONS DETERGENTES COMPRENANT UNE COMBINAISON D'α-AMYLASES POUR ELIMINER LES MAUVAISES ODEURS - Google Patents
COMPOSITIONS DETERGENTES COMPRENANT UNE COMBINAISON D'α-AMYLASES POUR ELIMINER LES MAUVAISES ODEURS Download PDFInfo
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- WO1997043378A1 WO1997043378A1 PCT/US1996/007090 US9607090W WO9743378A1 WO 1997043378 A1 WO1997043378 A1 WO 1997043378A1 US 9607090 W US9607090 W US 9607090W WO 9743378 A1 WO9743378 A1 WO 9743378A1
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- amylase
- detergent composition
- alkyl
- amylases
- cellulase
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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
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38627—Preparations containing enzymes, e.g. protease or amylase containing lipase
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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
Definitions
- the present invention relates to detergent compositions comprising a combination of different ⁇ -amylases delivering improved malodor stripping from soiled items in hard surface cleaning, dishwashing and laundry applications.
- amylase enzymes have been used for a variety of different purposes, the most important of which are starch liquefaction, textile desizing, starch modification in the paper and pulp industry, and for brewing and baking.
- amylase enzymes have long been recognised in dishwashing, hard surface cleaning and laundry compositions to provide the removal of starchy food residues or starchy films from dishware, flatware, glasses and hard surfaces or to provide cleaning performance on starchy soils as well as other soils typically encountered in laundry applications.
- WO/94/02597 Novo Nordisk A/S published February 03, 1994, describes cleaning compositions which incorporate mutant amylases. See also WO/94/18314, Genencor, published August 18, 1994 and WO/95/10603, Novo Nordisk A/S, published April 20,1995.
- Other amylases known for use in cleaning compositions include both ⁇ - and ⁇ -amylases.
- ⁇ -Amylases are known in the art and include those disclosed in US Pat. no. 5,003,257; EP 252,666; WO/91 /00353; FR 2,676,456; EP 285,123; EP 525,610; EP 368,341 ; and British Patent specification no. 1 ,296,839 (Novo).
- ⁇ -amylases products are Termamyl ® Ban* and Fungamyl ® , all available from Novo Nordisk A/S Denmark.
- the present invention relates to detergent compositions comprising a combination of different ⁇ -amylases delivering improved malodor stripping from soiled items in hard surface cleaning, dishwashing and laundry applications.
- Essential components of the detergent compositions of the present invention are ⁇ -amylase enzymes.
- ⁇ -amylases provides a more effective activity in solution and/or a broader hydrolytic cleavage pattern than a single amylase type as different amylases show different hydrolytic activity on various substrates. Odorous materials are entrapped into these substrates and a rapid and effective hydrolysis achieved on several different cleavage points allows a more effective suspension and dissolution of the odorous materials therein entrapped.
- Suitable ⁇ -amylases include those disclosed in US Pat. no. 5,003,257; EP 252,666; WO/91 /00353; FR 2,676,456; EP 285,123; EP 525,610; EP 368,341 ; and British Patent specification no. 1 ,296,839 (Novo).
- Examples of commercial ⁇ -amylases products are Termamyl* Ban* and Fungamyl*, all available from Novo Nordisk A/S Denmark.
- Other suitable ⁇ -amylases are derived from B. Subtilis or B. stearothermophilus.
- ⁇ -amylases herein have the commonality of being derived using site-directed mutagenesis from one or more of the Bacillus ⁇ - amyiases, regardless of whether one, two or multiple amylases strains are the immediate precursors.
- ⁇ -Amylases of this invention include those amylases having improved stability in detergents, especially improved oxidative stability.
- the stability-enhanced amylases can be obtained from Novo Nordisk A/S or from Genencor International :
- corresponding ⁇ -amylases will therefore include : (i) a variant ⁇ -amylase that is the expression product of a mutated
- DNA sequence encoding an ⁇ -amylase the mutated DNA sequence being derived from a precursor ⁇ -amylase by the deletion or substitution of one or more oxidisable acids selected from the group consiting of Met, Trp, Cys and Tyr amino acid residues, in the precursor ⁇ -amylase,
- amylase variants having additional modification in the immediate parent available from Novo Nordisk A/S. These amylases are disclosed in WO95/10603, published April 1995 :
- WO95/26397 Novo Nordisk, published October 05, 1995 describes other suitable amylases : ⁇ -amylases characterised by having a specific activity at least 25% higher than the specific activity of Termamyl* at a temperature range of 25°C to 55°C and at a pH value in the range of 8 to 10, measured by the Phadebas* ⁇ -amylase activity assay.
- Phadebas* ⁇ -amylase activity assay is described at pages 9-10, WO95/26397;
- Amylolytic enzymes with improved properties with respect to the activity level and the combination of thermostability and a higher activity level are described in WO95/35382.
- Said ⁇ -amylase is derived from an ⁇ -amylase of Bacillus licheniformis or an enzyme having at least 70% amino acid identity therewith which comprises one or more amino acid changes at positions selected from the group consisting of positions 104, 128, 187 and 188 of the amino acid sequence of the ⁇ -amylase of Bacillus licheniformis,
- Preferred combinations of ⁇ -amylases are combinations of a non- modified ⁇ -amylase derived from B. licheniformis,
- a more preferred combination is the combination of the ⁇ - amylase derived from B. licheniformis, known as Termamyl® and an ⁇ - amylase as described in WO95/10603, known as Duramyl®.
- the detergent compositions of the present invention can comprise a combination of more than two ⁇ -amylases.
- a cellulase can be added to such combinations.
- These enzymes are incorporated into detergent compositions at a level from 0.0001 % to 0.1 % total pure ⁇ -enzymes by weight of the total composition, preferably from 0.0002% to 0.06%, more preferably from 0.0003% to 0.05% total pure ⁇ -am ⁇ lase enzymes by weight of total composition.
- the ⁇ -amylases are preferably incorporated into the detergent compositions of the present invention in the range of from 1 :3 to 3:1 , more preferred ratios are 1 :1 , 3:7 or 7:3.
- the cellulases usable in the present invention include both bacterial or fungal cellulase. Preferably, they will have a pH optimum of between 5 and 9.5. Suitable cellulases are disclosed in U.S. Patent 4,435,307, Barbesgoard et al, which discloses fungal cellulase produced from Humicola insolens. Suitable cellulases are also disclosed in GB-A- 2.075.028; GB-A-2.095.275 and DE-OS-2.247.832.
- cellulase components which may be usable in the present invention are :
- WO91/17244 or an endoglucanase component which is immunoreactive with an antibody raised against a highly purified 50kD (apparent molecular weight, the amino acid composition corresponds to 45kD with 2n glycosylation sites) endoglucanase derived from Fusarium oxysporum, DSM 2672, or which is a homologue or derivative of the 50kD endoglucanase exhibiting cellulase activity; a preferred endoglucanase component has the amino acid sequence disclosed in PCT Patent Application No. WO91/17244, or any of the cellulases disclosed in the published European Patent Application No.
- the cellulases having a non-degrading index (NDI) of not less than 500 and being alkalophiiic cellulases having an optimum pH not less than 7 or whose relative activity at a pH of not less than 8 is 50% or over of the activity under optimum conditions when carboxy methyl cellulose (CMC) is used as a substrate, or an endoglucanase component which is immunoreactive with an antibody raised against a highly purified 43kD endoglucanase derived from Humicola insolens, DSM 1800, or which is a homologue or derivative of the 43kD endoglucanase exhibiting cellulase activity; a preferred endoglucanase component has the amino acid sequence disclosed in PCT Patent Application No.
- WO 91/17243 or an endoglucanase component which is immunoreactive with an antibody raised against a highly purified 60kD endoglucanase derived from Bacillus lautus, NCIMB 40250, or which is a homologue or derivative of the 60kD endoglucanase exhibiting cellulase activity; a preferred endoglucanase component has the amino acid sequence disclosed in PCT Patent Application No. WO 91/10732.
- Especially suitable cellulases are the cellulases having color care benefits.
- Examples of such cellulases are cellulases described in European patent application No. 91202879.2, filed November 6, 1991 (Novo).
- preferred cellulases are those as described in Danish Patent Application 1159/90 or PCT patent application WO91/17243 which is also known as CarezyiWTM' available from Novo Nordisk A/S in Bagsvaerd, in Denmark.
- the cellulase preparation described in these publications and the Carezyme'TM) consistent with this description can consist essentially of a homogeneous endoglucanase component, which is immunoreactive with an anti-body raised against a highly purified 43 kD cellulase derived from Humicola Insulens, DSM 1800, or which is homologous to said 43 kD endoglucanase.
- An alternative screening for appropriate cellulases for use in the laundry detergent composition according to the present invention is the method specified in EP-A-495 258 or more specifically in EP-A-350 098.
- Preferred cellulases to be used in the present invention are 50 kD endoglucanase and 43kD endoglucanase.
- Detergent components 50 kD endoglucanase and 43kD endoglucanase.
- the detergent compositions of the invention may also contain additional detergent components.
- additional detergent components and levels of incorporation thereof will depend on the physical form of the composition, and the nature of the cleaning operation for which it is to be used.
- the cleaning compositions according to the invention can be liquid, paste, gels, bars, tablets, powder or granular forms.
- Granular compositions can also be in "compact” form, the liquid compositions can also be in a "concentrated” form.
- compositions of the invention may for example, be formulated as hard surface cleaner, hand and machine dishwashing compositions, hand and machine laundry detergent compositions including laundry additive compositions and compositions suitable for use in the soaking and/or pretreatment of stained fabrics, rinse added fabric softener compositions.
- compositions of the invention When formulated as compositions for use in manual dishwashing methods the compositions of the invention preferably contain a surfactant and preferably other detergent compounds selected from organic polymeric compounds, suds enhancing agents, group II metal ions, solvents, hydrotropes and additional enzymes.
- a surfactant preferably other detergent compounds selected from organic polymeric compounds, suds enhancing agents, group II metal ions, solvents, hydrotropes and additional enzymes.
- compositions of the invention When formulated as compositions suitable for use in a laundry machine washing method, the compositions of the invention preferably contain both a surfactant and a builder compound and additionally one or more detergent components preferably selected from organic polymeric compounds, bleaching agents, additional enzymes, suds suppressors, dispersants, lime-soap dispersants, soil suspension and anti-redeposition agents and corrosion inhibitors. Laundry compositions can also contain softening agents, as additional detergent components.
- the compositions of the invention can also be used as detergent additive products. Such additive products are intended to supplement or boost the performance of conventional detergent compositions.
- the density of the granular laundry detergent compositions herein ranges from 400 to 1200 g/litre, preferably 600 to 950 g/litre of composition measured at 20°C.
- the "compact" form of the granular laundry detergent compositions herein is best reflected by density and, in terms of composition, by the amount of inorganic filler salt; inorganic filler salts are conventional ingredients of detergent compositions in powder form; in conventional detergent compositions, the filler salts are present in substantial amounts, typically 17-35% by weight of the total composition. In the compact compositions, the filler salt is present in amounts not exceeding 15% of the total composition, preferably not exceeding 10%, most preferably not exceeding 5% by weight of the composition.
- the inorganic filler salts are selected from the alkali and alkaline-earth-metal salts of sulphates and chlorides.
- a preferred filler salt is sodium sulphate.
- Liquid detergent compositions according to the present invention can also be in a "concentrated form", in such case, the liquid detergent compositions according the present invention will contain a lower amount of water, compared to conventional liquid detergents.
- the water content of the concentrated liquid detergent is preferably less than 40%, more preferably less than 30%, most preferably less than 20% by weight of the detergent composition.
- the detergent compositions according to the present invention comprise a surfactant system wherein the surfactant can be selected from nonionic and/or anionic and/or cationic and/or ampholytic and/or zwitterionic and/or semi-polar surfactants.
- the surfactant is typically present at a level of from 0.1 % to 60% by weight. More preferred levels of incorporation are 1 % to 35% by weight, most preferably from 1 % to 20% by weight of detergent compositions in accord with the invention.
- the surfactant is preferably formulated to be compatible with enzyme components present in the composition.
- the surfactant is most preferably formulated such that it promotes, or at least does not degrade, the stability of any enzyme in these compositions.
- Preferred surfactant systems to be used according to the present invention comprise as a surfactant one or more of the nonionic and/or anionic surfactants described herein.
- Polyethylene, polypropylene, and polybytylene oxide condensates of alkyl phenols are suitable for use as the nonionic surfactant of the surfactant systems of the present invention, with the polyethylene oxide condensates being preferred.
- These compounds include the condensation products of alkyl phenols having an alkyl group containing from about 6 to about 14 carbon atoms, preferably from about 8 to about 14 carbon atoms, in either a straight-chain or branched-chain configuration with the alkylene oxide.
- the ethylene oxide is present in an amount equal to from about 2 to about 25 moles, more preferably from about 3 to about 15 moles, of ethylene oxide per mole of alkyl phenol.
- nonionic surfactants of this type include IgepalTM CO-630, marketed by the GAF Corporation; and TritonTM X-45, X-114, X- 100 and X-102, all marketed by the Rohm & Haas Company. These surfactants are commonly referred to as alkylphenol alkoxylates (e.g., alkyl phenol ethoxylates).
- the condensation products of primary and secondary aliphatic alcohols with from about 1 to about 25 moles of ethylene oxide are suitable for use as the nonionic surfactant of the nonionic surfactant systems of the present invention.
- the alkyl chain of the aliphatic alcohol can either be straight or branched, primary or secondary, and generally contains from about 8 to about 22 carbon atoms.
- About 2 to about 7 moles of ethylene oxide and most preferably from 2 to 5 moles of ethylene oxide per mole of alcohol are present in said condensation products.
- nonionic surfactants of this type include TergitolTM 15-S-9 (the condensation product of C11 -C15 linear alcohol with 9 moles ethylene oxide), TergitolTM 24-L-6 NMW (the condensation product of C12-C14 primary alcohol with 6 moles ethylene oxide with a narrow molecular weight distribytion), both marketed by Union Carbide Corporation; NeodolTM 45-9 (the condensation product of C14-C15 linear alcohol with 9 moles of ethylene oxide), NeodolTM 23-3 (the condensation product of c 12" c 13 linear alcohol with 3.0 moles of ethylene oxide), NeodolTM 45-7 (the condensation product of C14-C15 linear alcohol with 7 moles of ethylene oxide), NeodolTM 45-5 (the condensation product of C14-C15 linear alcohol with 5 moles of ethylene oxide) marketed by Shell Chemical Company, KyroTM EOB (the condensation product of C13-C15 alcohol with 9 moles ethylene oxide), marketed by The Procter & Gamble
- nonionic surfactant of the surfactant systems of the present invention are the alkylpolysaccharides disclosed in U.S. Patent 4,565,647, Llenado, issued January 21 , 1986, having a hydrophobic group containing from about 6 to about 30 carbon atoms, preferably from about 10 to about 16 carbon atoms and a polysaccharide, e.g. a polyglycoside, hydrophilic group containing from about 1.3 to about 10, preferably from about 1.3 to about 3, most preferably from about 1.3 to about 2.7 saccharide units.
- a hydrophobic group containing from about 6 to about 30 carbon atoms, preferably from about 10 to about 16 carbon atoms and a polysaccharide, e.g. a polyglycoside, hydrophilic group containing from about 1.3 to about 10, preferably from about 1.3 to about 3, most preferably from about 1.3 to about 2.7 saccharide units.
- Any reducing saccharide containing 5 or 6 carbon atoms can be used, e.g., glucose, galactose and galactosyl moieties can be substituted for the glucosyl moieties (optionally the hydrophobic group is attached at the 2-, 3-, 4-, etc. positions thus giving a glucose or galactose as opposed to a glucoside or galactoside).
- the intersaccharide bonds can be, e.g., between the one position of the additional saccharide units and the 2-, 3-, 4-, and/or 6- positions on the preceding saccharide units.
- the preferred alkylpolyglycosides have the formula
- R 2 is selected from the group consisting of alkyl, alkylphenyl, hydroxyalkyl, hydroxyalkylphenyl, and mixtures thereof in which the alkyl groups contain from about 10 to about 18, preferably from about 12 to about 14, carbon atoms; n is 2 or 3, preferably 2; t is from 0 to about 10, preferably 0; and x is from about 1.3 to about 10, preferably from about 1.3 to about 3, most preferably from about 1.3 to about 2.7.
- the glycosyl is preferably derived from glucose. To prepare these compounds, the alcohol or alkylpolyethoxy alcohol is formed first and then reacted with glucose, or a source of glucose, to form the glucoside (attachment at the 1-position). The additional glycosyl units can then be attached between their 1-position and the preceding glycosyl units 2-, 3-, 4- and/or 6- position, preferably predominately the 2-position.
- the condensation products of ethylene oxide with a hydrophobic base formed by the condensation of propylene oxide with propylene glycol are also suitable for use as the additional nonionic surfactant systems of the present invention.
- the hydrophobic portion of these compounds will preferably have a molecular weight of from about 1500 to about 1800 and will exhibit water insolubility.
- the addition of polyoxyethylene moieties to this hydrophobic portion tends to increase the water solubility of the molecule as a whole, and the liquid character of the product is retained up to the point where the polyoxyethylene content is about 50% of the total weight of the condensation product, which corresponds to condensation with up to about 40 moles of ethylene oxide.
- Examples of compounds of this type include certain of the commercially-available PluronicTM surfactants, marketed by BASF.
- nonionic surfactant of the nonionic surfactant system of the present invention are the condensation products of ethylene oxide with the product resulting from the reaction of propylene oxide and ethylenediamine.
- the hydrophobic moiety of these products consists of the reaction product of ethylenediamine and excess propylene oxide, and generally has a molecular weight of from about 2500 to about 3000.
- This hydrophobic moiety is condensed with ethylene oxide to the extent that the condensation product contains from about 40% to about 80% by weight of polyoxyethylene and has a molecular weight of from about 5,000 to about 1 1 ,000.
- Examples of this type of nonionic surfactant include certain of the commercially available TetronicTM compounds, marketed by BASF.
- Preferred for use as the nonionic surfactant of the surfactant systems of the present invention are polyethylene oxide condensates of alkyl phenols, condensation products of primary and secondary aliphatic alcohols with from about 1 to about 25 moles of ethylene oxide, alk ⁇ lpolysaccharides, and mixtures thereof. Most preferred are C8-C14 alkyl phenol ethoxylates having from 3 to 15 ethoxy groups and Cg-C-i ⁇ alcohol ethoxylates (preferably C10 avg.) having from 2 to 10 ethoxy groups, and mixtures thereof.
- Highly preferred nonionic surfactants are polyhydroxy fatty acid amide surfactants of the formula.
- R ⁇ is H, or R 1 is C1.4 hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl or a mixture thereof, R 2 is C5.31 hydrocarbyl, and Z is a polyhydroxyhydrocarbyl having a linear hydrocarbyl chain with at least 3 hydroxyls directly connected to the chain, or an alkoxylated derivative thereof.
- R 1 is methyl
- R 2 is a straight Cn-15 alkyl or C-
- Z is derived from a reducing sugar such as glucose, fructose, maltose, lactose, in a reductive amination reaction.
- Suitable anionic surfactants to be used are linear alkyl benzene sulfonate, alkyl ester sulfonate surfactants including linear esters of C ⁇ C20 carboxylic acids (i.e., fatty acids) which are sulfonated with gaseous SO3 according to "The Journal of the American Oil Chemists Society", 52 (1975), pp. 323-329.
- Suitable starting materials would include natural fatty substances as derived from tallow, palm oil, etc.
- alkyl ester sulfonate surfactant especially for laundry applications, comprise alkyl ester sulfonate surfactants of the structural formula :
- R ⁇ is a Cg-C20 hydrocarbyl, preferably an alkyl, or combination thereof
- R 4 is a C-
- M is a cation which forms a water soluble salt with the alkyl ester sulfonate.
- Suitable salt-forming cations include metals such as sodium, potassium, and lithium, and substituted or unsubstituted ammonium cations, such as monoethanolamine, diethanolamine, and triethanolamine.
- R ⁇ is C10-C16 alkyl
- R 4 is methyl, ethyl or isopropyl.
- R 3 is Cio-Ci ⁇ alkyl.
- Suitable anionic surfactants include the linear alkyl benzene sulfonate, alkyl sulfate surfactants which are water soluble salts or acids of the formula ROSO3M wherein R preferably is a C10-C24 hydrocarbyl, preferably an alkyl or hydroxyalkyl having a C-J0-C20 a ' kvl component, more preferably a C12-C18 alkyl or hydroxyalkyl, and M is H or a cation, e.g., an alkali metal cation (e.g. sodium, potassium, lithium), or ammonium or substituted ammonium (e.g.
- R preferably is a C10-C24 hydrocarbyl, preferably an alkyl or hydroxyalkyl having a C-J0-C20 a ' kvl component, more preferably a C12-C18 alkyl or hydroxyalkyl
- M is H or a cation, e.
- alkylamines such as ethylamine, diethylamine, triethylamine, and mixtures thereof, and the like.
- alkyl chains of C12-C16 are preferred for lower wash temperatures (e.g. below about 50°C) and C15.
- alkyl chains are preferred for higher wash temperatures (e.g. above about 50°C).
- anionic surfactants useful for detersive purposes can also be included in the detergent compositions of the present invention. These can include salts (including, for example, sodium, potassium, ammonium, and substituted ammonium salts such as mono-, di- and triethanolamine salts) of soap, C8-C22 primary of secondary alkanesulfonates, C8-C24 olefinsulfonates, sulfonated polycarboxylic acids prepared by sulfonation of the pyrolyzed product of alkaline earth metal citrates, e.g., as described in British patent specification No.
- alkylpolyglycolethersulfates (containing up to 10 moles of ethylene oxide); alkyl glycerol sulfonates, fatty acyl glycerol sulfonates, fatty oleyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, paraffin sulfonates, alkyl phosphates, isethionates such as the acyl isethionates, N-acyi taurates, alkyl succinamates and sulfosuccinates, monoesters of sulfosuccinates (especially saturated and unsaturated C12-C18 monoesters) and diesters of sulfosuccinates (especially saturated and unsaturated C6-C12 diesters), acyl sarcosinates, sulfates of alkylpoiysaccharides such as the s
- the laundry detergent compositions of the present invention typically comprise from about 1 % to about 40%, preferably from about 3% to about 20% by weight of such anionic surfactants.
- alkyl alkoxylated sulfate surfactants hereof are water soluble salts or acids of the formula RO(A) m SO3M wherein R is an unsubstituted C10-C24 a,k Y' or hydroxyalkyl group having a C10-C24 alkyl component, preferably a C12-C20 a,k Y' or hydroxyalkyl, more preferably C12-C18 a'M or hydroxyalkyl, A is an ethoxy or propoxy unit, m is greater than zero, typically between about 0.5 and about 6, more preferably between about 0.5 and about 3, and M is H or a cation which can be, for example, a metal cation (e.g., sodium, potassium, lithium, calcium, magnesium, etc.), ammonium or substituted- ammonium cation.
- R is an unsubstituted C10-C24 a,k Y' or hydroxyalkyl group having a C10-C24
- Alkyl ethoxylated sulfates as well as alkyl propoxylated sulfates are contemplated herein.
- Specific examples of substituted ammonium cations include methyl-, dimethyl, trimethyl-ammonium cations and quaternary ammonium cations such as tetramethyl-ammonium and dimethyl piperdinium cations and those derived from alkylamines such as ethylamine, diethylamine, triethylamine, mixtures thereof, and the like.
- Exemplary surfactants are C12-C18 alkyl polyethoxylate (1.0) sulfate (C12- C ⁇ E(1.0)M), C-
- the detergent compositions of the present invention may also contain cationic, ampholytic, zwitterionic, and semi-polar surfactants, as well as the nonionic and/or anionic surfactants other than those already described herein.
- Cationic detersive surfactants suitable for use in the detergent compositions of the present invention are those having one long-chain hydrocarbyl group.
- cationic surfactants include the ammonium surfactants such as alkyltrimethylammonium halogenides, and those surfactants having the formula :
- R 2 is an alkyl or alkyl benzyl group having from about 8 to about 18 carbon atoms in the alkyl chain
- each R 3 is selected from the group consisting of -CH2CH2-, -CH 2 CH(CH 3 )-, -CH 2 CH(CH 2 OH)-, -CH 2 CH 2 CH 2 - , and mixtures thereof
- each R 4 is selected from the group consisting of C1-C4 alkyl, C1-C4 hydroxyalkyl, benzyl ring structures formed by joining the two R 4 groups, -CH2CHOH-CHOHCOR 6 CHOHCH2OH wherein R 6 is any hexose or hexose polymer having a molecular weight less than about 1000, and hydrogen when y is not 0
- R is the same as R 4 or is an alkyl chain wherein the total number of carbon atoms of R 2 plus R ⁇ is not more than about 18
- each y is from 0 to about 10 and the sum
- Quaternary ammonium surfactant suitable for the present invention has the formula (I):
- R1 is a short chainlength alkyl (C6-C10) or alkylamidoalkyl of the formula (II) :
- y is 2-4, preferably 3. whereby R2 is H or a C1-C3 alkyl, whereby x is 0-4, preferably 0-2, most preferably 0, whereby R3, R4 and R5 are either the same or different and can be either a short chain alkyl (C1-C3) or alkoxylated alkyl of the formula III,
- X" is a counterion, preferably a halide, e.g. chloride or methylsulfate.
- R6 is C1-C4 and z is 1 or 2.
- Preferred quat ammonium surfactants are those as defined in formula I whereby Rf is C ⁇ . C-
- Highly preferred cationic surfactants are the water-soluble quaternary ammonium compounds useful in the present composition having the formula :
- is C ⁇ -Ci ⁇ alkyl
- each of R2, R3 and R4 is independently C1 -C4 alkyl, C1 -C4 hydroxy alkyl, benzyl, and -(C2H4 0 ) X H where x has a value from 2 to 5, and X is an anion.
- R2, R3 or R4 should be benzyl.
- is C12-C15 particularly where the alkyl group is a mixture of chain lengths derived from coconut or palm kernel fat or is derived synthetically by olefin byild up or OXO alcohols synthesis.
- Preferred groups for R2R3 and R4 are methyl and hydroxyethyl groups and the anion X may be selected from halide, methosulphate, acetate and phosphate ions.
- Suitable quaternary ammonium compounds of formulae (i) for use herein are : coconut trimethyl ammonium chloride or bromide; coconut methyl dihydroxyethyl ammonium chloride or bromide; decyl triethyl ammonium chloride; decyl dimethyl hydroxyethyl ammonium chloride or bromide; C-
- CH2-CH2-O-C-C12-14 alkyl and R2R3R4 are methyl ) .
- I I 0 di-alkyl imidazolines [compounds of formula (i)].
- Other cationic surfactants useful herein are also described in U.S. Patent 4,228,044, Cambre, issued October 14, 1980 and in European Patent Application EP 000,224.
- the detergent compositions of the present invention typically comprise from 0.2% to about 25%, preferably from about 1 % to about 8% by weight of such cationic surfactants.
- Ampholytic surfactants are also suitable for use in the detergent compositions of the present invention. These surfactants can be broadly described as aliphatic derivatives of secondary or tertiary amines, or aliphatic derivatives of heterocyclic secondary and tertiary amines in which the aliphatic radical can be straight- or branched-chain.
- One of the aliphatic substituents contains at least about 8 carbon atoms, typically from about 8 to about 18 carbon atoms, and at least one contains an anionic water- solubilizing group, e.g. carboxy, sulfonate, sulfate. See U.S. Patent No. 3,929,678 to Laughlin et al., issued December 30, 1975 at column 19, lines 18-35, for examples of ampholytic surfactants.
- the detergent compositions of the present invention typically comprise from 0.2% to about 15%, preferably from about 1 % to about 10% by weight of such ampholytic surfactants.
- Zwitterionic surfactants are also suitable for use in detergent compositions. These surfactants can be broadly described as derivatives of secondary and tertiary amines, derivatives of heterocyclic secondary and tertiary amines, or derivatives of quaternary ammonium, quaternary phosphonium or tertiary sulfonium compounds. See U.S. Patent No. 3,929,678 to Laughlin et al., issued December 30, 1975 at column 19, line 38 through column 22, line 48, for examples of zwitterionic surfactants.
- the detergent compositions of the present invention typically comprise from 0.2% to about 15%, preferably from about 1 % to about 10% by weight of such zwitterionic surfactants.
- Semi-polar nonionic surfactants are a special category of nonionic surfactants which include water-soluble amine oxides containing one alkyl moiety of from about 10 to about 18 carbon atoms and 2 moieties selected from the group consisting of alkyl groups and hydroxyalkyl groups containing from about 1 to about 3 carbon atoms; water-soluble phosphine oxides containing one alkyl moiety of from about 10 to about 18 carbon atoms and 2 moieties selected from the group consisting of alkyl groups and hydroxyalkyl groups containing from about 1 to about 3 carbon atoms; and water-soluble sulfoxides containing one alkyl moiety of from about 10 to about 18 carbon atoms and a moiety selected from the group consisting of alkyl and hydroxyalkyl moieties of from about 1 to about 3 carbon atoms.
- Semi-polar nonionic detergent surfactants include the amine oxide surfactants having the formula
- R 3 is an alkyl, hydroxyalkyl, or alkyl phenyl group or mixtures therof containing from about 8 to about 22 carbon atoms
- R 4 is an alkylene or hydroxyalkylene group containing from about 2 to about 3 carbon atoms or mixtures thereof
- x is from 0 to about 3
- each R ⁇ is an alkyl or hydroxyalkyl group containing from about 1 to about 3 carbon atoms or a polyethylene oxide group containing from about 1 to about 3 ethylene oxide groups.
- the R 5 groups can be attached to each other, e.g., through an oxygen or nitrogen atom, to form a ring structure.
- amine oxide surfactants in particular include C10-C18 alkvl dimethyl amine oxides and CQ-C-
- the detergent compositions of the present invention typically comprise from 0.2% to about 15%, preferably from about 1 % to about 10% by weight of such semi-polar nonionic surfactants.
- the detergent composition of the present invention may further comprise a cosurfactant selected from the group of primary or tertiary amines.
- Suitable primary amines for use herein include amines according to the formula R1 NH2 wherein R-j is a C ⁇ -Ci 2, preferably C ⁇ -C-io alkyl chain or R4X(CH2)rv x is -O-,-C(O)NH- or -NH- # R4 is a C ⁇ -Ci 2 alkyl chain n is between 1 to 5, preferably 3.
- alkyl chains may be straight or branched and may be interrupted with up to 12, preferably less than 5 ethylene oxide moieties.
- Preferred amines according to the formula herein above are n-alkyl amines.
- Suitable amines for use herein may be selected from 1-hexylamine, 1- octylamine, 1-decylamine and laurylamine.
- Other preferred primary amines include C8-C10 oxypropylamine, octyloxypropylamine, 2-ethylhexyl- oxypropylamine, lauryl amido propylamine and amido propylamine.
- Suitable tertiary amines for use herein include tertiary amines having the formula R1 R2R3N wherein R1 and R2 are C-j-C ⁇ alkylchains or
- R3 is either a C ⁇ -C-j 2, preferably Cg-C-io a,k y' chain, or R3 is R4X(CH2)n» whereby X is -O-, -C(O)NH- or -NH- R4 is a C4-C12, n is between 1 to 5, preferably 2-3.
- R5 is H or C1-C2 alkyl and x is between 1 to 6 .
- R3 and R4 may be linear or branched ; R3 alkyl chains may be interrupted with up to 12, preferably less than 5, ethylene oxide moieties.
- Preferred tertiary amines are R1 R2R3N where R1 is a C6-C12 alkyl chain, R2 and R3 are C1-C3 alkyl or
- R-j is C ⁇ -Ci2 alk Y
- : n is 2-4, preferably n is 3; R2 and R3 is C1 -C4
- Most preferred amines of the present invention include 1-octylamine, 1-hexylamine, 1-decylamine, 1-dodecylamine,C8-10oxypropylamine, N coco 1-3diaminopropane, coconutalkyldimethylamine, lauryldimethylamine, lauryl bis(hydroxyethyl)amine, coco bis(hydroxyehtyl)amine, lauryl amine 2 moles propoxylated, octyl amine 2 moles propoxylated, lauryl amidopropyldimethylamine, C8-10 amidopropyldimethylamine and C10 amidopropyldimethylamine.
- the most preferred amines for use in the compositions herein are 1- hexylamine, 1-octylamine, 1-decylamine, 1-dodecylamine. Especially desirable are n-dodecyldimethylamine and bishydroxyethylcoconutalkylamine and oleylamine 7 times ethoxylated, lauryl amido propylamine and cocoamido propylamine.
- the detergent compositions can in addition to the combination of ⁇ - amylase enzymes and eventually cellulases further comprise one or more enzymes which provide cleaning performance and/or fabric care benefits.
- Said enzymes include enzymes selected from hemicellulases, peroxidases, proteases, gluco-amylases, other amylases, xylanases, lipases, esterases, cutinases, pectinases, reductases, oxidases, phenoloxidases, lipoxygenases, ligninases, pullulanases, tannases, pentosanases, malanases, ⁇ -glucanases, arabinosidases chondroitinase, laccase or mixtures thereof.
- a preferred combination is a cleaning composition having a cocktail of conventional applicable enzymes like protease, amylase, lipase, cutinase and/or cellulase in conjunction with one or more plant cell wall degrading enzymes.
- Peroxidase enzymes are used in combination with oxygen sources, e.g. percarbonate, perborate, persulfate, hydrogen peroxide, etc. They are used for "solution bleaching", i.e. to prevent transfer of dyes or pigments removed from substrates during wash operations to other substrates in the wash solution.
- Peroxidase enzymes are known in the art, and include, for example, horseradish peroxidase, ligninase, and haioperoxidase such as chloro- and bromo-peroxidase.
- Peroxidase-containing detergent compositions are disclosed, for example, in PCT International Application WO 89/099813 and in European Patent application EP No. 91202882.6, filed on November 6, 1991.
- Said peroxidases are normally incorporated in the detergent composition at levels from 0.0001 % to 2% of active enzyme by weight of the detergent composition.
- protease enzymes include those sold under the tradenames Alcalase, Savinase, Primase, Durazym, and Esperase by Novo Nordisk A/S (Denmark), those sold under the tradename Maxatase, Maxacal, Maxapem and Properase by Gist-Brocades, those sold by Genencor International, and those sold under the tradename Opticlean and Optimase by Solvay Enzymes.
- proteases described in patent applications EP 251 446, WO91/06637, WO94/10591 and US serial number 08/322676 can be included in the detergent composition of the invention.
- Protease enzyme may be incorporated into the compositions in accordance with the invention at a level of from 0.0001 % to 2% active enzyme by weight of the composition.
- Suitable lipase enzymes for detergent usage include those produced by microorganisms of the Pseudomonas group, such as Pseudomonas stutzeri ATCC 19.154, as disclosed in British Patent 1 ,372,034.
- Suitable lipases include those which show a positive immunological cross-reaction with the antibody of the lipase, produced by the microorganism Pseudomonas fluorescent IAM 1057. This lipase is available from Amano Pharmaceutical Co. Ltd., Nagoya, Japan, under the trade name Lipase P "Amano,” hereinafter referred to as "Amano-P".
- lipases such as M1 Lipase R and Lipomax R (Gist-Brocades) and Lipolase R and Lipolase Ultra R (Novo) which have found to be very effective when used in combination with the compositions of the present invention.
- cutinases [EC 3.1.1.50] which can be considered as a special kind of lipase, namely lipases which do not require interfacial activation.
- Suitable cutinases are described in WO 94/14963 and WO 94/14964. Addition of cutinases to detergent compositions have been described in e.g. WO-A-88/09367 (Genencor).
- the lipases and/or cutinases are normally incorporated in the detergent composition at levels from 0.0001 % to 2% of active enzyme by weight of the detergent composition.
- the above-mentioned enzymes may be of any suitable origin, such as vegetable, animal, bacterial, fungal and yeast origin. Said enzymes are normally incorporated in the detergent composition at levels from 0.0001 % to 2% of active enzyme by weight of the detergent composition. They can be added as separate ingredients ( prills, granulates,...) or as cogranulate of two or more enzymes.
- enzyme oxidation scavengers which are described in the copending European patent application 92870018.6 filed on January 31 , 1992.
- enzyme oxidation scavengers are ethoxylated tetraethylene polyamines.
- Bleach systems that can be included in the detergent compositions of the present invention include bleaching agents such as PB1 , PB4 and percarbonate with a particle size of 400-800 microns. These bleaching agent components can include one or more oxygen bleaching agents and, depending upon the bleaching agent chosen, one or more bleach activators. When present oxygen bleaching compounds will typically be present at levels of from about 1 % to about 25%.
- the bleaching agent component for use herein can be any of the bleaching agents useful for detergent compositions including oxygen bleaches as well as others known in the art.
- the bleaching agent suitable for the present invention can be an activated or non-activated bleaching agent.
- oxygen bleaching agent that can be used encompasses percarboxylic acid bleaching agents and salts thereof. Suitable examples of this class of agents include magnesium monoperoxyphthalate hexahydrate, the magnesium salt of meta-chloro perbenzoic acid, 4-nonylamino-4-oxoperoxybytyric acid and diperoxydodecanedioic acid.
- Such bleaching agents are disclosed in U.S. Patent 4,483,781 , U.S. Patent Application 740,446, European Patent Application 0,133,354 and U.S. Patent 4,412,934.
- Highly preferred bleaching agents also include 6-nonylamino-6-oxoperoxycaproic acid as described in U.S. Patent 4,634,551.
- bleaching agents that can be used encompasses the halogen bleaching agents.
- hypohalite bleaching agents include trichloro isocyanuric acid and the sodium and potassium dichloroisocyanurates and N-chloro and N-bromo alkane sulphonamides. Such materials are normally added at 0.5-10% by weight of the finished product, preferably 1-5% by weight.
- the hydrogen peroxide releasing agents can be used in combination with bleach activators such as tetraacetylethylenediamine (TAED), nonanoyloxybenzene-sulfonate (NOBS, described in US 4,412,934), 3,5,- trimethylhexanoloxybenzenesulfonate (ISONOBS, described in EP 120,591 ), Phenolsulfonate ester of N-nonanoyl-6-aminocaproic acid (NACA-OBS, described in WO94/28106) or pentaacetylglucose (PAG), which are perhydrolyzed to form a peracid as the active bleaching species, leading to improved bleaching effect.
- bleach activators such as tetraacetylethylenediamine (TAED), nonanoyloxybenzene-sulfonate (NOBS, described in US 4,412,934), 3,5,- trimethylhexanoloxybenzenesulf
- bleaching agents including peroxyacids and bleaching systems comprising bleach activators and peroxygen bleaching compounds for use in detergent compositions according to the invention are described in our co-pending applications USSN 08/136,626, PCT/US95/07823,
- the hydrogen peroxide may also be present by adding an enzymatic system (i.e. an enzyme and a substrate therefore) which is capable of generating hydrogen peroxide at the beginning or during the washing and/or rinsing process.
- an enzymatic system i.e. an enzyme and a substrate therefore
- Such enzymatic systems are disclosed in EP Patent
- Bleaching agents other than oxygen bleaching agents are also known in the art and can be utilized herein.
- One type of non-oxygen bleaching agent of particular interest includes photoactivated bleaching agents such as the sulfonated zinc and/or aluminum phthalocyanines.
- These materials can be deposited upon the substrate during the washing process.
- the sulfonated zinc phthalocyanine Upon irradiation with light, in the presence of oxygen, such as by hanging clothes out to dry in the daylight, the sulfonated zinc phthalocyanine is activated and, consequently, the substrate is bleached.
- detergent compositions will contain about 0.025% to about 1.25%, by weight, of sulfonated zinc phthalocyanine.
- compositions according to the present invention may further comprise a builder system.
- Any conventional builder system is suitable for use herein including aiuminosilicate materials, silicates, polycarboxylates and fatty acids, materials such as ethylenediamine tetraacetate, diethylene triamine pentamethyieneacetate, metal ion sequestrants such as aminopolyphosphonates, particularly ethylenediamine tetramethylene phosphonic acid and diethylene triamine pentamethylenephosphonic acid.
- Phosphate builders as sodium tripolyphosphate can also be used herein.
- Suitable builders can be an inorganic ion exchange material, commonly an inorganic hydrated aiuminosilicate material, more particularly a hydrated synthetic zeolite such as hydrated zeolite A, X, B, HS or MAP.
- an inorganic builder material is layered silicate, e.g. SKS-6 (Hoechst).
- SKS-6 is a crystalline layered silicate consisting of sodium silicate (Na2Si2 ⁇ 5).
- Suitable polycarboxylates containing one carboxy group include lactic acid, glycolic acid and ether derivatives thereof as disclosed in Belgian Patent Nos. 831 ,368, 821 ,369 and 821 ,370.
- Polycarboxylates containing two carboxy groups include the water-soluble salts of succinic acid, malonic acid, (ethylenedioxy) diacetic acid, maleic acid, diglycollic acid, tartaric acid, tartronic acid and fumaric acid, as well as the ether carboxylates described in German Offenlegenschrift 2,446,686, and 2,446,687 and U.S. Patent No. 3,935,257 and the sulfinyl carboxylates described in Belgian Patent No. 840,623.
- Polycarboxylates containing three carboxy groups include, in particular, water-soluble citrates, aconitrates and citraconates as well as succinate derivatives such as the carboxymethyloxysuccinates described in British Patent No. 1 ,379,241 , lactoxysuccinates described in Netherlands Application 7205873, and the oxypolycarboxylate materials such as 2-oxa-1 , 1 ,3-propane tricarboxylates described in British Patent No. 1 ,387,447.
- Polycarboxylates containing four carboxy groups include oxydisuccinates disclosed in British Patent No. 1 ,261 ,829, 1 ,1 ,2,2-ethane tetracarboxylates, 1 , 1 ,3,3-propane tetracarboxylates and 1 , 1 ,2,3-propane tetracarboxylates.
- Polycarboxylates containing sulfo substituents include the sulfosuccinate derivatives disclosed in British Patent Nos. 1 ,398,421 and 1 ,398,422 and in U.S. Patent No. 3,936,448, and the sulfonated pyrolysed citrates described in British Patent No. 1 ,082,179, while polycarboxylates containing phosphone substituents are disclosed in British Patent No. 1 ,439,000.
- Alicyclic and heterocyclic polycarboxylates include cyclopentane- cis,cis,cis-tetracarboxylates, cyclopentadienide pentacarboxylates, 2,3,4,5- tetrahydro-furan - cis, cis, cis-tetracarboxylates, 2,5-tetrahydro-furan -cis - dicarboxylates, 2,2,5,5-tetrahydrofuran - tetracarboxylates, 1 ,2,3,4,5,6- hexane -hexacar-boxylates and and carboxymethyl derivatives of polyhydric alcohols such as sorbitol, mannitol and xylitol.
- Aromatic poly ⁇ carboxylates include mellitic acid, pyromellitic acid and the phthalic acid derivatives disclosed in British Patent No. 1 ,425,343.
- the preferred polycarboxylates are hydroxycarboxylates containing up to three carboxy groups per molecule, more particularly citrates.
- Preferred builder systems for use in the present compositions include a mixture of a water-insoluble aiuminosilicate builder such as zeolite A, zeolite MAP or of a layered silicate (SKS-6), and a water-soluble carboxylate chelating agent such as citric acid.
- a water-insoluble aiuminosilicate builder such as zeolite A, zeolite MAP or of a layered silicate (SKS-6)
- a water-soluble carboxylate chelating agent such as citric acid.
- a suitable chelant for inclusion in the detergent compositions in accordance with the invention is ethylenediamine-N,N'-disuccinic acid (EDDS) or the alkali metal, alkaline earth metal, ammonium, or substituted ammonium salts thereof, or mixtures thereof.
- EDDS compounds are the free acid form and the sodium or magnesium salt thereof. Examples of such preferred sodium salts of EDDS include Na2EDDS and Na4EDDS. Examples of such preferred magnesium salts of EDDS include MgEDDS and Mg2EDDS. The magnesium salts are the most preferred for inclusion in compositions in accordance with the invention.
- Preferred builder systems include a mixture of a water-insoluble aiuminosilicate builder such as zeolite MAP, zeolite A, and a watersoluble carboxylate chelating agent such as citric acid.
- a water-insoluble aiuminosilicate builder such as zeolite MAP, zeolite A
- a watersoluble carboxylate chelating agent such as citric acid.
- Other builder materials that can form part of the builder system for use in granular compositions include inorganic materials such as alkali metal carbonates, bicarbonates, silicates, and organic materials such as the organic phosphonates, amino polyalkylene phosphonates and amino polycarboxylates.
- Suitable water-soluble organic salts are the homo- or co- polymeric acids or their salts, in which the polycarboxylic acid comprises at least two carboxyl radicals separated from each other by not more than two carbon atoms.
- Polymers of this type are disclosed in GB-A-1 , 596,756.
- Examples of such salts are polyacrylates of MW 2000-5000 and their copolymers with maleic anhydride, such copolymers having a molecular weight of from 20,000 to 70,000, especially about 40,000.
- Detergency builder salts are normally included in amounts of from 10% to 80% by weight of the composition preferably from 20% to 70% and most usually from 30% to 60% by weight.
- a suds suppressor exemplified by silicones, and silica-silicone mixtures.
- Silicones can be generally represented by alkylated polysiloxane materials while silica is normally used in finely divided forms exemplified by silica aerogels and xerogels and hydrophobic silicas of various types. These materials can be incorporated as particulates in which the suds suppressor is advantageously releasably incorporated in a water-soluble or water-dispersible, substantially non- surface-active detergent impermeable carrier.
- the suds suppressor can be dissolved or dispersed in a liquid carrier and applied by spraying on to one or more of the other components.
- a preferred silicone suds controlling agent is disclosed in Bartollota et al. U.S. Patent 3 933 672.
- Other particularly useful suds suppressors are the self-emulsifying silicone suds suppressors, described in German Patent Application DTOS 2 646 126 published April 28, 1977.
- An example of such a compound is DC- 544, commercially available from Dow Corning, which is a siloxane-glycol copolymer.
- Especially preferred suds controlling agent are the suds suppressor system comprising a mixture of silicone oils and 2-alkyl-alcanols. Suitable 2-alkyl-alkanols are 2-bytyl-octanol which are commercially available under the trade name Isofol 12 R.
- Such suds suppressor system are described in Copending European Patent application N 92870174.7 filed 10 November, 1992.
- compositions can comprise a silicone/silica mixture in combination with fumed nonporous silica such as Aerosil R .
- the suds suppressors described above are normally employed at levels of from 0.001 % to 2% by weight of the composition, preferably from 0.01 % to 1 % by weight.
- detergent compositions may be employed, such as soil-suspending agents, soil-release agents, optical brighteners, abrasives, bactericides, tarnish inhibitors, coloring agents, and/or encapsulated or non-encapsulated perfumes.
- encapsulating materials are water soluble capsules which consist of a matrix of polysaccharide and polyhydroxy compounds such as described in GB 1 ,464,616.
- Suitable water soluble encapsulating materials comprise dextrins derived from ungelatinized starch acid-esters of substituted dicarboxylic acids such as described in US 3,455,838. These acid-ester dextrins are, preferably, prepared from such starches as waxy maize, waxy sorghum, sago, tapioca and potato. Suitable examples of said encapsulating materials include N-Lok manufactured by National Starch. The N-Lok encapsulating material consists of a modified maize starch and glucose. The starch is modified by adding monofunctional substituted groups such as octenyl succinic acid anhydride.
- Antiredeposition and soil suspension agents suitable herein include cellulose derivatives such as methylcellulose, carboxymethylcellulose and hydroxyethylcellulose, and homo- or co-polymeric polycarboxylic acids or their salts.
- Polymers of this type include the polyacrylates and maleic anhydride-acrylic acid copolymers previously mentioned as builders, as well as copolymers of maleic anhydride with ethylene, methylvinyl ether or methacrylic acid, the maleic anhydride constituting at least 20 mole percent of the copolymer. These materials are normally used at levels of from 0.5% to 10% by weight, more preferably from 0.75% to 8%, most preferably from 1 % to 6% by weight of the composition.
- Preferred optical brighteners are anionic in character, examples of which are disodium 4,4'-bis-(2-diethanolamino-4-anilino -s- triazin-6- ylamino)stilbene-2:2' disulphonate, disodium 4, - 4'-bis-(2-morpholino-4- anilino-s-triazin-6-ylamino-stilbene-2:2' - disulphonate, disodium 4,4' - bis- (2,4-dianilino-s-triazin-6-ylamino)stilbene-2:2' - disulphonate, monosodium 4', 4" -bis-(2,4-dianilino-s-tri-azin-6 ylamino)stilbene-2-sulphonate, disodium 4,4' -bis-(2-anilino-4-(N-methyl-N-2-hydroxyethylamino)-s-triazin-6- ylamino)stilbene-2,2
- polyethylene glycols particularly those of molecular weight 1000-10000, more particularly 2000 to 8000 and most preferably about 4000. These are used at levels of from 0.20% to 5% more preferably from 0.25% to 2.5% by weight. These polymers and the previously mentioned homo- or co-polymeric polycarboxylate salts are valuable for improving whiteness maintenance, fabric ash deposition, and cleaning performance on clay, proteinaceous and oxidizable soils in the presence of transition metal impurities.
- Soil release agents useful in compositions of the present invention are conventionally copolymers or terpolymers of terephthalic acid with ethylene glycol and/or propylene glycol units in various arrangements. Examples of such polymers are disclosed in the commonly assigned US Patent Nos. 4116885 and 4711730 and European Published Patent Application No. 0 272 033. A particular preferred polymer in accordance with EP-A-0 272 033 has the formula
- PEG is -(OC2H4)O-,PO is (OC3H6O) and T is (pcOC6H 4 CO).
- modified polyesters as random copolymers of dimethyl terephthalate, dimethyl sulfoisophthalate, ethylene glycol and 1-2 propane diol, the end groups consisting primarily of sulphobenzoate and secondarily of mono esters of ethylene glycol and/or propane-diol.
- the target is to obtain a polymer capped at both end by sulphobenzoate groups, "primarily", in the present context most of said copolymers herein will be end-capped by sulphobenzoate groups.
- some copolymers will be less than fully capped, and therefore their end groups may consist of monoester of ethylene glycol and/or propane 1-2 diol, thereof consist “secondarily” of such species.
- the selected polyesters herein contain about 46% by weight of dimethyl terephthalic acid, about 16% by weight of propane -1.2 diol, about 10% by weight ethylene glycol about 13% by weight of dimethyl sulfobenzoic acid and about 15% by weight of sulfoisophthalic acid, and have a molecular weight of about 3.000.
- the polyesters and their method of preparation are described in detail in EPA 311 342.
- Fabric softening agents can also be incorporated into laundry detergent compositions in accordance with the present invention. These agents may be inorganic or organic in type. Inorganic softening agents are exemplified by the smectite clays disclosed in GB-A-1 400 898 and in USP 5,019,292. Organic fabric softening agents include the water insoluble tertiary amines as disclosed in GB-A1 514 276 and EP-BO 01 1 340 and their combination with mono C12-C14 quaternary ammonium salts are disclosed in EP-B-0 026 527 and EP-B-0 026 528 and di-long-chain amides as disclosed in EP-B-0 242 919. Other useful organic ingredients of fabric softening systems include high molecular weight polyethylene oxide materials as disclosed in EP-A-0 299 575 and 0 313 146.
- Levels of smectite clay are normally in the range from 2% to 20%, more preferably from 5% to 15% by weight, with the material being added as a dry mixed component to the remainder of the formulation.
- Organic fabric softening agents such as the water-insoluble tertiary amines or dilong chain amide materials are incorporated at levels of from 0.5% to 5% by weight, normally from 1 % to 3% by weight whilst the high molecular weight polyethylene oxide materials and the water soluble cationic materials are added at levels of from 0.1 % to 2%, normally from 0.15% to 1.5% by weight.
- These materials are normally added to the spray dried portion of the composition, although in some instances it may be more convenient to add them as a dry mixed particulate, or spray them as molten liquid on to other solid components of the composition.
- the detergent composition of the present invention can also include compounds for inhibiting dye transfer from one fabric to another of solubilized and suspended dyes encountered during fabric laundering operations involving colored fabrics.
- Polymeric dye transfer inhibiting agents The detergent compositions according to the present invention also comprise from 0.001 % to 10 %, preferably from 0.01 % to 2%, more preferably from 0.05% to 1 % by weight of polymeric dye transfer inhibiting agents.
- Said polymeric dye transfer inhibiting agents are normally incorporated into detergent compositions in order to inhibit the transfer of dyes from colored fabrics onto fabrics washed therewith. These polymers have the ability to complex or adsorb the fugitive dyes washed out of dyed fabrics before the dyes have the opportunity to become attached to other articles in the wash.
- polymeric dye transfer inhibiting agents are polyamine N-oxide polymers, copolymers of N-vinylpyrrolidone and N-vinylimidazole, polyvinylpyrrolidone polymers, polyvinyloxazolidones and polyvinylimidazoles or mixtures thereof.
- polyamine N-oxide polymers suitable for use contain units having the following structure formula :
- P is a polymerisable unit, whereto the R-N-O group can be attached to or wherein the R-N-O group forms part of the polymerisable unit or a combination of both.
- A is NC, CO, C, -0- , -S- , -N- ; x is 0 or 1 ;
- R are aliphatic, ethoxylated aliphatics, aromatic, heterocyclic or alicyclic groups or any combination thereof whereto the nitrogen of the N-O group can be attached or wherein the nitrogen of the N-O group is part of these groups.
- the N-O group can be represented by the following general structures :
- R1 , R2, and R3 are aliphatic groups, aromatic, heterocyclic or alicyclic groups or combinations thereof, x or/and y or/and z is 0 or 1 and wherein the nitrogen of the N-O group can be attached or wherein the nitrogen of the N-O group forms part of these groups.
- the N-O group can be part of the polymerisable unit (P) or can be attached to the polymeric backbone or a combination of both.
- Suitable polyamine N-oxides wherein the N-O group forms part of the polymerisable unit comprise polyamine N-oxides wherein R is selected from aliphatic, aromatic, alicyclic or heterocyclic groups.
- R is selected from aliphatic, aromatic, alicyclic or heterocyclic groups.
- One class of said polyamine N-oxides comprises the group of polyamine N- oxides wherein the nitrogen of the N-O group forms part of the R-group.
- Preferred polyamine N-oxides are those wherein R is a heterocyclic group such as pyrridine, pyrrole, imidazole, pyrrolidine, piperidine, quinoline, acridine and derivatives thereof.
- Another class of said polyamine N-oxides comprises the group of polyamine N-oxides wherein the nitrogen of the N-O group is attached to the R-group.
- polyamine N-oxides are the polyamine oxides whereto the N-O group is attached to the polymerisable unit.
- Preferred class of these polyamine N-oxides are the polyamine N-oxides having the general formula (I) wherein R is an aromatic, heterocyclic or alicyclic groups wherein the nitrogen of the N-O functional group is part of said R group.
- polyamine oxides wherein R is a heterocyclic compound such as pyrridine, pyrrole, imidazole and derivatives thereof.
- R is a heterocyclic compound such as pyrridine, pyrrole, imidazole and derivatives thereof.
- Another preferred class of polyamine N-oxides are the polyamine oxides having the general formula (I) wherein R are aromatic, heterocyclic or alicyclic groups wherein the nitrogen of the N-O functional group is attached to said R groups.
- polyamine oxides wherein R groups can be aromatic such as phenyl.
- Any polymer backbone can be used as long as the amine oxide polymer formed is water-soluble and has dye transfer inhibiting properties.
- polymeric backbones examples include polyvinyls, polyalkylenes, polyesters, polyethers, polyamide, polyimides, polyacrylates and mixtures thereof.
- the amine N-oxide polymers of the present invention typically have a ratio of amine to the amine N-oxide of 10:1 to 1 :1000000.
- the amount of amine oxide groups present in the polyamine oxide polymer can be varied by appropriate copolymerization or by appropriate degree of N- oxidation.
- the ratio of amine to amine N-oxide is from 2:3 to 1 :1000000. More preferably from 1 :4 to 1 :1000000, most preferably from 1 :7 to 1 :1000000.
- the polymers of the present invention actually encompass random or block copolymers where one monomer type is an amine N-oxide and the other monomer type is either an amine N-oxide or not.
- the amine oxide unit of the polyamine N-oxides has a PKa ⁇ 10, preferably PKa ⁇ 7, more preferred PKa ⁇ 6.
- the polyamine oxides can be obtained in almost any degree of polymerisation. The degree of polymerisation is not critical provided the material has the desired water-solubility and dye-suspending power.
- the average molecular weight is within the range of 500 to 1000,000; preferably from 1 ,000 to 50,000, more preferably from 2,000 to 30,000, most preferably from 3,000 to 20,000.
- N-vinylimidazole N-vinylpyrrolidone polymers used in the present invention have an average molecular weight range from 5,000-1 ,000,000, preferably from 5,000-200,000.
- Highly preferred polymers for use in detergent compositions according to the present invention comprise a polymer selected from N- vinylimidazole N-vinylpyrrolidone copolymers wherein said polymer has an average molecular weight range from 5,000 to 50,000 more preferably from 8,000 to 30,000, most preferably from 10,000 to 20,000.
- the average molecular weight range was determined by light scattering as described in Barth H.G. and Mays J.W. Chemical Analysis Vol 1 13, "Modern Methods of Polymer Characterization".
- N-vinylimidazole N-vinylpyrrolidone copolymers have an average molecular weight range from 5,000 to 50,000; more preferably from 8,000 to 30,000; most preferably from 10,000 to 20,000.
- the N-vinylimidazole N-vinylpyrrolidone copolymers characterized by having said average molecular weight range provide excellent dye transfer inhibiting properties while not adversely affecting the cleaning performance of detergent compositions formulated therewith.
- the N-vinylimidazole N-vinylpyrrolidone copolymer of the present invention has a molar ratio of N-vinylimidazole to N-vinylpyrrolidone from 1 to 0.2, more preferably from 0.8 to 0.3, most preferably from 0.6 to 0.4 .
- the detergent compositions of the present invention may also utilize polyvinylpyrrolidone ("PVP") having an average molecular weight of from about 2,500 to about 400,000, preferably from about 5,000 to about 200,000, more preferably from about 5,000 to about 50,000, and most preferably from about 5,000 to about 15,000.
- PVP polyvinylpyrrolidone
- Suitable polyvinylpyrrolidones are commercially vailable from ISP Corporation, New York, NY and Montreal, Canada under the product names PVP K-15 (viscosity molecular weight of 10,000), PVP K-30 (average molecular weight of 40,000), PVP K-60 (average molecular weight of 160,000), and PVP K-90 (average molecular weight of 360,000).
- polyvinylpyrrolidones which are commercially available from BASF Cooperation include Sokalan HP 165 and Sokalan HP 12; polyvinylpyrrolidones known to persons skilled in the detergent field (see for example EP-A-262,897 and EP-A-256,696).
- the detergent compositions of the present invention may also utilize polyvinyloxazolidone as a polymeric dye transfer inhibiting agent.
- Said polyvinyloxazolidones have an average molecular weight of from about 2,500 to about 400,000, preferably from about 5,000 to about 200,000, more preferably from about 5,000 to about 50,000, and most preferably from about 5,000 to about 15,000.
- Cross-linked polymers are polymers whose backbone are interconnected to a certain degree; these links can be of chemical or physical nature, possibly with active groups n the backbone or on branches; cross-linked polymers have been described in the Journal of Polymer Science, volume 22, pages 1035-1039.
- the cross-linked polymers are made in such a way that they form a three-dimensional rigid structure, which can entrap dyes in the pores formed by the three-dimensional structure.
- the cross-linked polymers entrap the dyes by swelling.
- compositions of the invention may be used in essentially any washing or cleaning methods, including soaking methods, pretreatment methods and methods with rinsing steps for which a separate rinse aid composition may be added.
- the process described herein comprises contacting fabrics with a laundering solution in the usual manner and exemplified hereunder.
- the process of the invention is conveniently carried out in the course of the cleaning process.
- the method of cleaning is preferably carried out at 5 °C to 95 °C, especially between 10°C and 60°C.
- specific amylase enzymes within the specified enzymatic concentration have demonstrated superior starch cleaning even for wash cycles occuring at very low temperatures (between 10°C and 25°C).
- the pH of the treatment solution is preferably from 7 to 1 1.
- a preferred machine dishwashing method comprises treating soiled articles with an aqueous solution of the machine diswashing or rinsing composition.
- a conventional effective amount of the machine dishwashing composition means from 8-60 g of product dissolved or dispersed in a wash volume from 3-10 litres.
- soiled dishes are contacted with an effective amount of the diswashing composition, typically from 0.5-20g (per 25 dishes being treated).
- Preferred manual dishwashing methods include the application of a concentrated solution to the surfaces of the dishes or the soaking in large volume of dilute solution of the detergent composition.
- compositions of the invention may also be formulated as hard surface cleaner compositions.
- compositions of the present invention are not necessarily meant to limit or otherwise define the scope of the invention.
- the enzymes levels are expressed in pure enzyme by weight of the total composition and the abbreviated component identifications have the following meanings:
- SAS C12-C14 secondary (2,3) alkyl sulfate in the form of the sodium salt
- PA30 Polyacrylic acid of average molecular weight of approximately 8,000.
- Paraffin Paraffin oil sold under the tradename Winog 70 by Wintershall.
- Pectinase Pectolytic enzyme sold under the tradename Pectinex AR by Novo Nordisk A/S.
- Xylanase Xylanolytic enzyme sold under the tradenames Pulpzyme HB or SP431 by Novo Nordisk A/S or Lyxasan (Gist-Brocades) or Optipulp or Xylanase (Solvay).
- Protease Proteolytic enzyme sold under the tradename Savinase, Alcalase, Durazym by Novo Nordisk A/S, Maxapem and Maxacal sold by Gist- Brocades and proteases described in patent applications WO91/06637 and/or WO95/10591 and/or EP 251 446.
- Lipase Lipolytic enzyme sold under the tradename Lipolase and Lipolase Ultra by Novo Nordisk A/S. Peroxidase Peroxidase enzyme.
- DETPMP Diethylene triamine penta (methylene phosphonic acid), marketed by Monsanto under the Trade name Dequest 2060.
- PAAC pentaamine acetate cobalt (III) sal PAAC pentaamine acetate cobalt (III) sal.
- PVP Polyvinyl pyrrolidone polymer
- Granular fabric cleaning compositions in accord with the invention were prepared as follows:
- Amylase I 0.0035 0.01 0.005 0.003 0.014
- Amylase II 0.0025 0.01 0.005 0.007 0.006
- Granular fabric cleaning compositions in accord with the invention were prepared as follows:
- Zeolite A 26.0 26.0 26.0 26.0 26.0 26.0 26.0
- Amylase I 0.01 0.0045 0.05 0.014 0.005
- Amylase II 0.01 0.0105 0.05 0.006 0.005
- Granular fabric cleaning compositions in accord with the invention which are especially useful in the laundering of coloured fabrics were prepared as follows :
- Amylase I 0.015 0.02 0.0025
- Amylase II 0.015 0.01 0.0035
- Granular fabric cleaning compositions in accord with the invention were prepared as follows:
- a compact granular fabric cleaning composition in accord with the invention was prepared as follows:
- Granular suds suppressor 3.5 water/minors Up to 100%
- a granular fabric cleaning composition in accord with the invention which provide "softening through the wash” capability were prepared as follows:
- Amylase 1 0.015 0.0035
- Amylase II 0.015 0.0025
- Liquid fabric cleaning compositions in accord with the invention were prepared as follows:
- Amylase I 0.006 0.007 0.008 0.009 0.006 0.006
- Amylase II 0.006 0.003 0.005 0.004 0.009 0.007
- Borax-Ca Format 2.0 3.0 2.0 1.5 2.0 2.0
- Brightener 36 0.1 0.1 0.1 0.1 0.1 0.1 0.1 0.1 0.1 0.1 0.1 0.1
- Liquid fabric cleaning compositions in accord with the invention were prepared as follows:
- Amylase I 0.006 0.007 0.008 0.009 0.006
- Amylase II 0.006 0.003 0.005 0.004 0.009
- Borax-Ca Format 2.0 3.0 2.0 1.5 2.0 Brightener 36 0.1 0.1 0.1 0.1 0.1 0.1 0.1
- Liquid fabric cleaning compositions in accord with the invention were prepared as follows:
- Amido propyl amine 1.0 1.0 1.0 1.5 1.0
- Amylase I 0.015 0.006 0.007 0.008 0.009
- Amylase II 0.014 0.006 0.003 0.005 0.004
- Brightener 36 0.1 0.1 0.1 0.1 0.1 0.1 0.1 0.1
- Heavy duty liquid fabric cleaning compositions suitable for use in the pretreatment of stained fabrics, and for use in a machine laundering method, in accord with the invention were prepared as follows:
- Amylase I 0.005 0.005 0.001 0.01 0.002
- Amylase II 0.0025 0.002 0.001 0.007 0.002
- Heavy duty liquid fabric cleaning compositions in accord with the invention were prepared as follows:
- Oleic acid 1.8 - 1.0 -
- Amylase 1 0.002 0.007 0.003 0.005
- Amylase II 0.002 0.003 0.002 0.005
- the following rinse added fabric softener composition in accord with the invention, was prepared (parts by weight).
- Syndet bar fabric cleaning compositions in accord with the invention were prepared as follows:
- Amylase II 0.005 0.014 0.003 0.005
- Filler* balance to 100% *Can be selected from convenient materials such as CaCO3, talc, clay (Kaolinite, Smectite), silicates, and the like.
- Amylase I 0.005 0.003 0.005 0.01 0.005 0.0007
- Amylase II 0.005 0.002 0.01 0.005 0.005 0.0018
- Amylase I 0.002 0.001 0.005 0.006 0.007 0.01
- Amylase II 0.001 0.001 0.005 0.014 0.003 0.005
- detergent composition tablets of 25g weight were prepared in accord with the present invention by compression of a granular dishwashing detergent composition at a pressure of 13KN/cm 2 using a standard 12 head rotary press:
- Amylase I 0.005 0.002 0.001
- Amylase II 0.005 0.003 0.001 cellulase I - 0.01 0.01
- liquid dishwashing detergent compositions in accord with the present invention I to II, of density 1.40Kg/L were prepared:
- Amylase I 0.0025 0.0018
- Amylase II 0.00025 0.0007
- liquid hard surface cleaning compositions were prepared in accord with the present invention :
- Amylase I 0.01 0.002 0.005 0.006 0.0007 0.003
- Amylase II 0.01 0.003 0.005 0.014 0.0003 0.002
Landscapes
- 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)
Abstract
Priority Applications (18)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US1996/007090 WO1997043378A1 (fr) | 1996-05-15 | 1996-05-15 | COMPOSITIONS DETERGENTES COMPRENANT UNE COMBINAISON D'α-AMYLASES POUR ELIMINER LES MAUVAISES ODEURS |
AU58619/96A AU5861996A (en) | 1996-05-15 | 1996-05-15 | Detergent compositions comprising a combination of alpha-amylases for malodor stripping |
MX9809587A MX9809587A (en) | 1996-05-15 | 1996-05-15 | Detergent compositions comprising a combination of alpha-amylases for malodor stripping |
EP97925549A EP0912687A1 (fr) | 1996-05-15 | 1997-05-13 | COMPOSITIONS DETERGENTES COMPRENANT UNE COMBINAISON D'$g(a)-AMYLASES POUR SUPPRIMER LES MAUVAISES ODEURS |
BR9709004A BR9709004A (pt) | 1996-05-15 | 1997-05-13 | Composições detergentes comprendendo uma combinação de alfa-amilases para remoção do mau cheiro |
CA002254069A CA2254069A1 (fr) | 1996-05-15 | 1997-05-13 | Compositions detergentes comprenant une combinaison d'.alpha.-amylases pour supprimer les mauvaises odeurs |
US09/180,679 US6197070B1 (en) | 1996-05-15 | 1997-05-13 | Detergent compositions comprising alpha combination of α-amylases for malodor stripping |
JP09541069A JP3095786B2 (ja) | 1996-05-15 | 1997-05-13 | 悪臭除去のためのα―アミラーゼ類の組み合わせを含む洗剤組成物 |
CN97196488A CN1225674A (zh) | 1996-05-15 | 1997-05-13 | 含有用于去除臭气的α-淀粉酶组合的洗涤剂组合物 |
AU30656/97A AU3065697A (en) | 1996-05-15 | 1997-05-13 | Detergent compositions comprising improved amylases, cellulase and cationic surfactant |
PCT/US1997/008103 WO1997043385A1 (fr) | 1996-05-15 | 1997-05-13 | COMPOSITIONS DETERGENTES COMPRENANT UNE COMBINAISON D'α-AMYLASES POUR SUPPRIMER LES MAUVAISES ODEURS |
PCT/US1997/008104 WO1997043386A1 (fr) | 1996-05-15 | 1997-05-13 | Compositions detergentes comportant des amylases ameliorees, de la cellulase et un tensioactif cationique |
JP9541070A JPH11511785A (ja) | 1996-05-15 | 1997-05-13 | 改良アミラーゼ、セルラーゼおよびカチオン性界面活性剤を含んでなる洗剤組成物 |
CZ983649A CZ364998A3 (cs) | 1996-05-15 | 1997-05-13 | Čisticí prostředky obsahující směs alfa-amylas pro odstraňování zápachu |
BR9710440A BR9710440A (pt) | 1996-05-15 | 1997-05-13 | Composi-{es de detergente compreendendo amilases aperfei-oadas celulase e tensoativo catiÄnico |
EP97925550A EP0912688A1 (fr) | 1996-05-15 | 1997-05-13 | Compositions detergentes comportant des amylases ameliorees, de la cellulase et un tensioactif cationique |
CA002254067A CA2254067A1 (fr) | 1996-05-15 | 1997-05-13 | Compositions detergentes comportant des amylases ameliorees, de la cellulase et un tensioactif cationique |
MA24608A MA24180A1 (fr) | 1996-05-15 | 1997-05-14 | Compositions detergentes comprenant des amylases ameliorees, une cellulase et un agent tensio-actif cationique |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US1996/007090 WO1997043378A1 (fr) | 1996-05-15 | 1996-05-15 | COMPOSITIONS DETERGENTES COMPRENANT UNE COMBINAISON D'α-AMYLASES POUR ELIMINER LES MAUVAISES ODEURS |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1997043378A1 true WO1997043378A1 (fr) | 1997-11-20 |
Family
ID=22255112
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1996/007090 WO1997043378A1 (fr) | 1996-05-15 | 1996-05-15 | COMPOSITIONS DETERGENTES COMPRENANT UNE COMBINAISON D'α-AMYLASES POUR ELIMINER LES MAUVAISES ODEURS |
PCT/US1997/008103 WO1997043385A1 (fr) | 1996-05-15 | 1997-05-13 | COMPOSITIONS DETERGENTES COMPRENANT UNE COMBINAISON D'α-AMYLASES POUR SUPPRIMER LES MAUVAISES ODEURS |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1997/008103 WO1997043385A1 (fr) | 1996-05-15 | 1997-05-13 | COMPOSITIONS DETERGENTES COMPRENANT UNE COMBINAISON D'α-AMYLASES POUR SUPPRIMER LES MAUVAISES ODEURS |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP0912687A1 (fr) |
JP (1) | JP3095786B2 (fr) |
CN (1) | CN1225674A (fr) |
AU (1) | AU5861996A (fr) |
BR (1) | BR9709004A (fr) |
CA (1) | CA2254069A1 (fr) |
CZ (1) | CZ364998A3 (fr) |
MX (1) | MX9809587A (fr) |
WO (2) | WO1997043378A1 (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002066591A1 (fr) * | 2001-02-17 | 2002-08-29 | Novozymes A/S | Reduction des mauvaises odeurs d'une buanderie |
US6794350B2 (en) | 2001-02-17 | 2004-09-21 | Novozymes A/S | Reduction of malodor from laundry |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2243011C (fr) * | 1998-07-13 | 2007-02-13 | Life Science Technology Group, Inc. | Agent de suppression d'odeurs pour tapis, moquettes, etc., et son mode d'emploi |
US8383097B2 (en) * | 2006-08-11 | 2013-02-26 | Novozymes Biologicals, Inc | Bacteria cultures and compositions comprising bacteria cultures |
JP5890193B2 (ja) * | 2012-02-15 | 2016-03-22 | 花王株式会社 | 自動洗浄機用粉末洗浄剤組成物 |
EP2856896A1 (fr) | 2013-09-23 | 2015-04-08 | Life Science TGO, SRL | Produits de lutte contre les mauvaises odeurs imprégnées et leurs procédés de fabrication |
WO2017202887A1 (fr) * | 2016-05-26 | 2017-11-30 | Novozymes A/S | Utilisation d'enzymes, composition de nettoyage et procédé de lavage |
US20220315866A1 (en) * | 2019-09-19 | 2022-10-06 | Novozymes A/S | Detergent Composition |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2036477A1 (de) * | 1970-07-23 | 1972-01-27 | Rohm Gmbh, 6100 Darmstadt | Enzymhaltiges flussiges Geschirrspul mittel |
EP0252730A2 (fr) * | 1986-07-09 | 1988-01-13 | Novo Nordisk A/S | Mélanges d'alpha-amylase pour la liquéfaction d'amidon |
EP0368341A2 (fr) * | 1988-11-11 | 1990-05-16 | Kao Corporation | Composition détergente contenant des enzymes |
WO1991019807A1 (fr) * | 1990-06-14 | 1991-12-26 | Novo Nordisk A/S | Activation d'hydrolase de polysaccharide |
JPH06299196A (ja) * | 1993-04-09 | 1994-10-25 | T Paul Kk | 粉末漂白洗浄剤組成物 |
WO1995010603A1 (fr) * | 1993-10-08 | 1995-04-20 | Novo Nordisk A/S | Variants d'amylase |
-
1996
- 1996-05-15 WO PCT/US1996/007090 patent/WO1997043378A1/fr active Application Filing
- 1996-05-15 AU AU58619/96A patent/AU5861996A/en not_active Abandoned
- 1996-05-15 MX MX9809587A patent/MX9809587A/es unknown
-
1997
- 1997-05-13 BR BR9709004A patent/BR9709004A/pt unknown
- 1997-05-13 CN CN97196488A patent/CN1225674A/zh active Pending
- 1997-05-13 JP JP09541069A patent/JP3095786B2/ja not_active Expired - Fee Related
- 1997-05-13 CZ CZ983649A patent/CZ364998A3/cs unknown
- 1997-05-13 CA CA002254069A patent/CA2254069A1/fr not_active Abandoned
- 1997-05-13 EP EP97925549A patent/EP0912687A1/fr not_active Withdrawn
- 1997-05-13 WO PCT/US1997/008103 patent/WO1997043385A1/fr not_active Application Discontinuation
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2036477A1 (de) * | 1970-07-23 | 1972-01-27 | Rohm Gmbh, 6100 Darmstadt | Enzymhaltiges flussiges Geschirrspul mittel |
EP0252730A2 (fr) * | 1986-07-09 | 1988-01-13 | Novo Nordisk A/S | Mélanges d'alpha-amylase pour la liquéfaction d'amidon |
EP0368341A2 (fr) * | 1988-11-11 | 1990-05-16 | Kao Corporation | Composition détergente contenant des enzymes |
WO1991019807A1 (fr) * | 1990-06-14 | 1991-12-26 | Novo Nordisk A/S | Activation d'hydrolase de polysaccharide |
JPH06299196A (ja) * | 1993-04-09 | 1994-10-25 | T Paul Kk | 粉末漂白洗浄剤組成物 |
WO1995010603A1 (fr) * | 1993-10-08 | 1995-04-20 | Novo Nordisk A/S | Variants d'amylase |
Non-Patent Citations (3)
Title |
---|
DATABASE WPI Section Ch Week 8625, Derwent World Patents Index; Class D22, AN 86-160663, XP002023287, ANONYMOUS: "Odour-free proteolytic enzyme compsn. - contg. other enzymes such as amylolytic, lipolytic and cellulolytic enzymes to enhance smell removal" * |
DATABASE WPI Section Ch Week 9502, Derwent World Patents Index; Class A97, AN 95-012126, XP002023286 * |
RESEARCH DISCLOSURE, vol. 265, no. 054, 10 May 1986 (1986-05-10), EMSWORTH, GB * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002066591A1 (fr) * | 2001-02-17 | 2002-08-29 | Novozymes A/S | Reduction des mauvaises odeurs d'une buanderie |
US6794350B2 (en) | 2001-02-17 | 2004-09-21 | Novozymes A/S | Reduction of malodor from laundry |
AU2002231607B2 (en) * | 2001-02-17 | 2008-02-28 | Novozymes A/S | Reduction of malodour from laundry |
Also Published As
Publication number | Publication date |
---|---|
AU5861996A (en) | 1997-12-05 |
CZ364998A3 (cs) | 1999-04-14 |
CN1225674A (zh) | 1999-08-11 |
EP0912687A1 (fr) | 1999-05-06 |
BR9709004A (pt) | 1999-08-03 |
WO1997043385A8 (fr) | 1999-04-29 |
MX9809587A (en) | 1999-03-01 |
JP3095786B2 (ja) | 2000-10-10 |
WO1997043385A1 (fr) | 1997-11-20 |
JPH11511784A (ja) | 1999-10-12 |
CA2254069A1 (fr) | 1997-11-20 |
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