Classifications

• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/66—Non-ionic compounds
  • C11D1/825—Mixtures of compounds all of which are non-ionic
• • 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
  • C11D3/39—Organic or inorganic per-compounds
  • C11D3/3942—Inorganic per-compounds
• • 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
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/66—Non-ionic compounds
  • C11D1/667—Neutral esters, e.g. sorbitan esters
• • 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
  • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
  • C11D1/66—Non-ionic compounds
  • C11D1/72—Ethers of polyoxyalkylene glycols

Definitions

• the present invention relates to the cleaning of fabrics in soaking conditions, i.e., in conditions where the fabrics are left to soak in a soaking liquor comprising water and detergent ingredients, typically without undergoing any mechanical agitation, either as a first step before a typical washing operation, or as a single step.
• Fabric soaking operations have been described in the art.
• fabrics are left in contact with a soaking liquor for a prolonged period of time, typically ranging from a few minutes to overnight or even 24 hours.
• This laundering process has the advantage that it maximises the contact time between the fabrics and the key active ingredients of the soaking liquor. It also has the advantage that it reduces or eliminates the need for a typical laundering operation involving the need for mechanical agitation, or that it improves the efficiency of the subsequent typical laundering operation.
• Such soaking operations are typically desirable to remove tough outdoor dirt from fabrics, such as particulate soil like mud, silt and/or clays.
• clays usually have a microcrystalline mineral structure (e.g., hydrous aluminum silicate like illite, montmorillonite, kaolinite and the like) with the presence of an organic fraction.
• the organic fraction can contain a variety of compounds (e.g., humic acid, fulvic acid, plant/animal biomass and the like).
• Clays can also contain several kinds of metals (e.g., magnesium, calcium, potassium, iron and the like).
• metals e.g., magnesium, calcium, potassium, iron and the like.
• this object can be met by soaking fabrics in an aqueous soaking liquor comprising an effective amount of a soaking detergent composition comprising an oxygen bleach and a highly alkoxylated nonionic surfactant, as defined herein after.
• a highly alkoxylated nonionic surfactant and oxygen bleach in a soaking composition, delivers improved stain removal performance on tough outdoor dirt like particulate soil, enzymatic stains and/or bleachable stains under soaking conditions (i.e., when left in contact for prolonged period of time typically more than 1 hour up to 24 hours), as compared to the stain removal performance delivered with the same composition being free of such a highly alkoxylated nonionic surfactant.
• the present invention encompasses a process of soaking fabrics, wherein said fabrics are immersed for more than one hour in a soaking liquor comprising water and an effective amount of a composition comprising a highly alkoxylated nonionic surfactant and an oxygen bleach, as defined herein, then removed from said soaking liquor.
• An advantage of the present invention is that the stain removal performance, when soaking a fabric in presence of a soaking composition comprising an oxygen bleach and such a highly alkoxylated nonionic surfactant as defined herein, is improved even in the presence of relatively high levels of hardness ions.
• hardness ions calcium or magnesium ions
• the soaking detergent manufacturer may make use of builders which are not the more performing at sequestering free hardness ions, and thus may use less expensive builders in such a soaking composition.
• the stain removal performance on particulate soil, enzymatic stains and/or bleachable stains is further improved by combining said highly alkoxylated nonionic surfactant and oxygen bleach with a sorbitan ester, as defined hereinafter, in a soaking detergent composition.
• a soaking detergent composition comprising a sorbitan ester as defined herein, a highly alkoxylated nonionic surfactant as defined herein, and an oxygen bleach, as well as a process of soaking fabrics in a soaking liquor formed with said soaking detergent composition.
• An advantage of the present invention is that not only improved particulate soil removal performance is delivered, but also that the soil redeposition on fabrics in prolonged soaking condition is prevented. Furthermore, the soaking compositions of the present invention comprising sorbitan ester, such a highly alkoxylated nonionic surfactant and oxygen bleach also provide effective stain removal performance on other types of stains like greasy stains, e.g., dirty motor oil, spaghetti sauce.
• EP-A-736 594 discloses soaking compositions comprising a sorbitan ester in combination with a high amount of a building and soil suspending system comprising a compound selected from citric acid or citrates, silicates, zeolites, polycarboxylates phosphates and mixtures thereof.
• Oxygen bleach are include amongst the optional ingredients.
• No alkoxylated nonionic surfactants are disclosed, nor exemplified.
• the present invention encompasses a granular soaking composition comprising:
• the present invention further encompasses a process of soaking fabrics, wherein said fabrics are immersed in a soaking liquor comprising water and an effective amount of a composition as described herein above, for an effective period of time, then removed from said soaking liquor.
• the present invention encompasses a process of soaking fabrics, wherein said fabrics are immersed for more than one hour in a soaking liquor comprising water and an effective amount of a composition comprising an oxygen bleach and an alkoxylated nonionic surfactant as defined herein, then removed from said soaking liquor.
• the present invention encompasses a composition and a process of soaking fabrics.
• the composition hereinafter referred to as the soaking composition, is used in the soaking process.
• the granular compositions herein comprise at least a sorbitan ester, a particular alkoxylated nonionic surfactant as defined herein and an oxygen bleach.
• the first essential ingredient of the compositions of the present invention is a sorbitan ester according to the formula C 6 H 9 O 2 (C 2 H 4 O) x R 1 R 2 R 3 , wherein x is an integer of from 0 to 40, R 1 , R 2 are independently OH or (C n H 2n+1)COO, and R 3 is (C n H 2n+1 )COO group, where n is an integer of from 11 to 17.
• x is 0 or 20
• the most preferred compositions herein comprise polyethoxylated (20) sorbitan tristearate, i.e. C 6 H 9 O 2 (C 2 H 4 O) 20 (C 17 H 35 COO) 3 , or polyethoxylated (20) sorbitan monostearate, i.e. C 6 H 9 O 2 (C 2 H 4 O) 20 (OH) 2 (C 17 H 35 COO), or sorbitan monostearate, i.e. C 6 H 9 O 2 (OH) 2 (C 17 H 35 COO), or sorbitan monopalmitate, i.e. C 6 H 9 O 2 (OH) 2 (C 15 H 31 COO), or mixtures thereof.
• Glycosperse TS 20 from Lonza (polyethoxylated sorbitan tristearate)
• Glycosperse S 20 from Lonza (polyethoxylated sorbitan monostearate)
• Radiasurf 7145 from Fina from sorbitan monostearate
• Radiasurf 7135 from Fina (sorbitan monopalmitate)
• Armotan MP from Akzo (sorbitan monopalmitate).
• the soaking compositions herein comprise from 0.001% to 15% by weight of the total composition of said sorbitan ester or mixtures thereof, preferably from 0.01% to 10%, more preferably from 0.1% to 5% and most preferably from 0.5% to 4%.
• the nonionic surfactant is a nonionic surfactant:
• the second essential ingredient of the compositions of the present invention is an alkoxylated nonionic surfactant according to the formula RO-(A) n H, wherein R is a substituted or unsubstituted, saturated or unsaturated, linear or branched hydrocarbon chain having from 6 to 40 carbon atoms, A is an alkoxy group having from 2 to 10 carbon atoms, and wherein n is an integer from 9 to 100, or a mixture thereof.
• R is a substituted or unsubstituted, saturated or unsaturated, linear or branched alkyl group or aryl group having from 6 to 40 carbon atoms, preferably from 8 to 25, more preferably from 12 to 20.
• Typical aryl groups include the C12 -C18 alkyl benzene groups.
• n is an integer from 9 to 100, more preferably from 10 to 80 and most preferably from 10 to 30.
• A preferably is an alkoxy group having from 2 to 8 carbon atoms, preferably from 2 to 5 and more preferably is propoxy and/or ethoxy.
• alkoxylated nonionic surfactants for use herein are Dobanol® 91-10 (R is a mixture of C 9 to C 11 alkyl chains, A is ethoxy, n is 10) Luthensol AT® or AO® surfactants (where R is a mixture of linear C16 to C18 alkyl chain or unbranched C13-C15, A is ethoxy, and n can be 11, 18, 25, 50 or 80), or mixtures thereof.
• Dobanol® surfactants are commercially available from SHELL, while the Luthensol® surfactants are available from BASF.
• Suitable chemical processes for preparing the alkoxylated nonionic surfactants for use herein include condensation of corresponding alcohols with alkylene oxide, in the desired proportions. Such processes are well known to the man skilled in the art and have been extensively described in the art.
• Such highly alkoxylated nonionic surfactants are particularly suitable to be used herein as they deliver improved particulate stains removal performance. Indeed, it is speculated that they act as a soil suspending agent, i.e. they allow suspension of particulate soils and prevent/avoid the redeposition of said soils.
• the soaking compositions herein comprise from 0.001% to 20% by weight of the total composition of said alkoxylated nonionic surfactant, as defined herein, or a mixture thereof, preferably from 0.01% to 15%, more preferably from 0.1% to 10% and most preferably from 0.5% to 5%.
• the oxygen bleach is a mixture of the oxygen bleach:
• the compositions according to the present invention comprise an oxygen bleach or a mixture thereof.
• oxygen bleaches provide a multitude of benefits such as bleaching of stains, deodorization, as well as disinfectancy.
• the sorbitan esters and alkoxylated nonionic surfactants as defined herein have a further particular advantage that they are resistant to oxydation by oxygen bleaches.
• the oxygen bleach in the composition may come from a variety of sources, such as hydrogen peroxide or any of the addition compounds of hydrogen peroxide, or organic peroxyacid, or mixtures thereof.
• addition compounds of hydrogen peroxide it is meant compounds which are formed by the addition of hydrogen peroxide to a second chemical compound, which may be for example an inorganic salt, urea or organic carboxylate, to provide the addition compound.
• a second chemical compound which may be for example an inorganic salt, urea or organic carboxylate
• the addition compounds of hydrogen peroxide include inorganic perhydrate salts, the compounds hydrogen peroxide forms with organic carboxylates, urea, and compounds in which hydrogen peroxide is clathrated.
• inorganic perhydrate salts include perborate, percarbonate, perphosphate and persilicate salts.
• the inorganic perhydrate salts are normally the alkali metal salts.
• the alkali metal salt of percarbonate, perborate or mixtures thereof, are the preferred inorganic perhydrate salts for use herein.
• Preferred alkali metal salt of percarbonate is sodium percarbonate.
• oxygen beaches include persulphates, particularly potassium persulphate K 2 S 2 O 8 and sodium persulphate Na 2 S 2 O 8 .
• inorganic perhydrate salts include perborate, percarbonate, perphosphate and persilicate salts.
• the inorganic perhydrate salts are normally the alkali metal salts.
• the soaking compositions in the present invention comprise from 0.01% to 80% by weight of the total composition of an oxygen bleach or mixtures thereof, preferably from 5% to 45% and more preferably from 10% to 40%.
• the soaking compositions of the present invention are granular compositions.
• This compositions can be made by a variety of methods well known in the art, including dry-mixing, spray drying, agglomeration and granulation and combinations thereof.
• the compositions herein can be prepared with different bulk densities, from conventional granular products to so called “concentrated” products (i.e., with a bulk density above 600g/l).
• the soaking compositions of the present invention may further comprise a variety of other ingredients.
• compositions herein further comprise a bleach activator or a mixture thereof up to 30% by weight of the total composition.
• suitable compounds of this type are disclosed in British Patent GB 1 586 769 and GB 2 143 231.
• Preferred examples of such compounds are tetracetyl ethylene diamine, (TAED), sodium 3, 5, 5 trimethyl hexanoyloxybenzene sulphonate, diperoxy dodecanoic acid as described for instance in US 4 818 425 and nonylamide of peroxyadipic acid as described for instance in US 4 259 201 and n-nonanoyloxybenzenesulphonate (NOBS), and acetyl triethyl citrate (ATC) such as described in European patent application 91870207.7.
• N-acyl caprolactam selected from the group consisting of substituted or unsubstituted benzoyl caprolactam, octanyl caprolactam, nonanoyl caprolactam, hexanoyl caprolactam, decanoyl caprolactam, undecenoyl caprolactam, formyl caprolactam, acetyl caprolactam, propanoyl caprolactam, butanoyl caprolactam pentanoyl caprolactam.
• the soaking compositions herein may comprise mixtures of said bleach activators.
• Preferred mixtures of bleach activators herein comprise n-nonanoyloxybenzenesulphonate (NOBS) together with a second bleach activator having a low tendency to generate diacyl peroxide, but which delivers mainly peracid.
• Said second bleach activators may include tetracetyl ethylene diamine (TAED), acetyl triethyl citrate (ATC), acetyl caprolactam, benzoyl caprolactam and the like, or mixtures thereof.
• mixtures of bleach activators comprising n-nonanoyloxybenzenesulphonate and said second bleach activators, contribute to further boost particulate soil removal performance while exhibiting at the same time good performance on diacyl peroxide sensitive soil (e.g., beta-carotene) and on peracid sensitive soil (e.g., body soils).
• diacyl peroxide sensitive soil e.g., beta-carotene
• peracid sensitive soil e.g., body soils
• the soaking compositions herein may comprise from 0% to 15% by weight of the total composition of n-nonanoyloxybenzenesulphonate, preferably from 1% to 10% and more preferably from 3% to 7% and from 0% to 15% by weight of the total composition of said second bleach activator preferably from 1% to 10% and more preferably from 3% to 7%.
• compositions herein may comprise an acidifying system amongst the preferred optional ingredients.
• the purpose of said acidifying system is to control the alkalinity generated by the source of available oxygen and any alkaline compounds present in the wash solution.
• Said system comprises anhydrous acidifying agent, or mixtures thereof, which needs to be incorporated in the product in an anhydrous form, and to have a good stability in oxidizing environment.
• Suitable anhydrous acidifying agents for use herein are carboxylic acids such as citric acid, adipic acid, glutaric acid, 3 chetoglutaric acid, citramalic acid, tartaric acid and maleic acid or their salts or mixtures thereof.
• Other suitable acidifying agents include sodium bicarbonate, sodium sesquicarbonate and silicic acid.
• citric acid can be used in its acidic form or in the form of its salts (mono-, di-, tri- salts) and in all its anhydrous and hydrated forms, or mixtures thereof. It may additionally act as a builder and a chelant, and it is biodegradable.
• the compositions according to the present invention comprise from up to 20% by weight of the total composition of anhydrous citric acid, preferably from 5% to 15%, most preferably about 10%.
• compositions herein may comprise an alkali metal salt of silicate, or mixtures thereof, amongst the preferred optional ingredients.
• Preferred alkali metal salt of silicate to be used herein is sodium silicate.
• the soaking compositions comprise an oxygen bleach, it has been found that the decomposition of available oxygen produced in the soaking liquors upon dissolution of the soaking compositions is reduced by the presence of at least 40 parts per million of sodium silicate in said soaking liquors.
• alkali metal salt of silicate can be used herein, including the crystalline forms as well as the amorphous forms of said alkali metal salt of silicate or mixtures thereof.
• Suitable crystalline forms of sodium silicate to be used are the crystalline layered silicates of the granular formula: NaMSi x O 2x+1 .yH 2 O wherein M is sodium or hydrogen, x is a number from 1.9 to 4 and y is a number from 0 to 20, or mixtures thereof.
• Crystalline layered sodium silicates of this type are disclosed in EP-A-164 514 and methods for their preparation are disclosed in DE-A-34 17 649 and DE-A-37 42 043.
• x in the general formula above has a value of 2, 3 or 4 and is preferably 2.
• M is sodium and y is 0 and preferred examples of this formula comprise the a , b , g and d forms of Na 2 Si 2 O 5 .
• These materials are available from Hoechst AG FRG as respectively NaSKS-5, NaSKS-7, NaSKS-11 and NaSKS-6. The most preferred material is d - Na 2 Si 2 O 5, NaSKS-6.
• Crystalline layered silicates are incorporated in soaking compositions herein, either as dry mixed solids, or as solid components of agglomerates with other components.
• Suitable amorphous forms of sodium silicate to be used herein have the following general formula: NaMSi x O 2x+1 wherein M is sodium or hydrogen and x is a number from 1.9 to 4, or mixtures thereof.
• M is sodium or hydrogen and x is a number from 1.9 to 4, or mixtures thereof.
• Preferred to be used herein are the amorphous forms of Si 2 O 5 Na 2 O.
• Suitable Zeolites for use herein are aluminosilicates including those having the empirical formula: Mz(zAlO2.ySiO2) wherein M is sodium, potassium, ammonium or substituted ammonium, z is from about 0.5 to about 2; and y is 1; this material having a magnesium ion exchange capacity of at least about 50 milligram equivalents of CaCO3 hardness per gram of anhydrous aluminosilicate.
• Preferred zeolites which have the formula: Naz ⁇ (AlO2)z(SiO2)yù.xH2O wherein z and y are integers of at least 6, the molar ratio of z to y is in the range from 1.0 to about 0.5, and x is an integer from about 15 to about 264.
• aluminosilicates can be crystalline or amorphous in structure and can be naturally-occurring aluminosilicates or synthetically derived.
• a method for producing aluminosilicate ion exchange materials is disclosed in U.S. Patent 3,985,669, Krummel, et al, issued October 12, 1976.
• Preferred synthetic crystalline aluminosilicate ion exchange materials useful herein are available under the designations Zeolite A, Zeolite P (B), and Zeolite X.
• the crystalline aluminosilicate ion exchange material has the formula: Na12 ⁇ (AlO2)12(SiO2)12ù.xH2O wherein x is from 20 to 30, especially about 27.
• This material is known as Zeolite A.
• the aluminosilicate has a particle size of about 0.1-10 microns in diameter.
• compositions herein may comprise from 0.5% to 15% by weight of the total composition of an alkali metal salt of silicate or mixtures thereof, preferably from 1% to 10% and more preferably from 2% to 7%.
• composition herein may also comprise a builder amongst the preferred optional ingredients.
• All builders known to those skilled in the art may be used herein.
• Suitable phosphate builders for use herein include sodium and potassium tripolyphosphate, pyrophosphate, polymeric metaphosphate having a degree of polymerization of from about 6 to 21, and orthophosphate.
• Other phosphorus builder compounds are disclosed in U.S. Pat. Nos. 3,159,581; 3,213,030; 3,422,021; 3,422,137; 3,400,176 and 3,400,148, incorporated herein by reference.
• Suitable polycarboxylate builders for use herein include ether polycarboxylates, including oxydisuccinate, as disclosed in Berg, U.S. Patent 3,128,287, issued April 7, 1964, and Lamberti et al, U.S. Patent 3,635,830, issued January 18, 1972. See also "TMS/TDS" builders of U.S. Patent 4,663,071, issued to Bush et al, on May 5, 1987.
• Suitable ether polycarboxylates also include cyclic compounds, particularly alicyclic compounds, such as those described in U.S. Patents 3,923,679; 3,835,163; 4,120,874 and 4,102,903.
• Other useful detergency builders include the ether hydroxypolycarboxylates, 1,3,5-trihydroxy benzene-2,4,6-trisulphonic acid, and carboxymethyloxysuccinic acid, the various alkali metal, ammonium and substituted ammonium salts of polyacetic acids such as ethylenediamine tetraacetic acid and nitrilotriacetic acid, as well as polycarboxylates such as mellitic acid, succinic acid, oxydisuccinic acid, polymaleic acid, benzene 1,3,5-tricarboxylic acid, carboxymethyloxysuccinic acid, and soluble salts thereof.
• polyacetic acids such as ethylenediamine tetraacetic acid and nitrilotriacetic acid
• polycarboxylates such as mellitic acid, succinic acid, oxydisuccinic acid, polymaleic acid, benzene 1,3,5-tricarboxylic acid, carboxymethyl
• succinic acid builders include the C 5 -C 20 alkyl and alkenyl succinic acids and salts thereof.
• a particularly preferred compound of this type is dodecenylsuccinic acid.
• succinate builders include: laurylsuccinate, myristylsuccinate, palmitylsuccinate, 2-dodecenylsuccinate (preferred), 2-pentadecenylsuccinate, and the like. Laurylsuccinates are the preferred builders of this group, and are described in European Patent Application 86200690.5/0,200,263, published November 5, 1986.
• Suitable polycarboxylate builders for use herein include builders according to formula I wherein Y is a comonomer or comonomer mixture; R 1 and R 2 are bleach- and alkali-stable polymer-end groups; R 3 is H, OH or C 1-4 alkyl; M is H, alkali metal, alkaline earth metal, ammonium or substituted ammonium; p is from 0 to 2; and n is at least 10, or mixtures thereof.
• the first category belongs to the class of copolymeric polymers which are formed from an unsaturated polycarboxylic acid such as maleic acid, citraconic acid, itaconic acid, mesaconic acid and salts thereof as first monomer, and an unsaturated monocarboxylic acid such as acrylic acid or an alpha -C 1-4 alkyl acrylic acid as second monomer.
• the polymers belonging to said first class are those where p is not 0 and Y is selected from the acids listed hereinabove.
• Preferred polymers of this class are those according to formula I hereinabove, where Y is maleic acid.
• R 3 and M are H
• n is such that the polymers have a molecular weight of from 1000 to 400 000 atomic mass units.
• the second category of preferred polymers for use herein belongs to the class of polymers in which, referring to formula I hereinabove, p is 0 and R 3 is H or C 1-4 alkyl.
• n is such that the polymers have a molecular weight of from 1000 to 400 000 atomic mass units.
• R 3 and M are H.
• alkali-stable polymer end groups R 1 and R 2 in formula I hereinabove suitably include alkyl groups, oxyalkyl groups and alkyl carboxylic acid groups and salts and esters thereof.
• n the degree of polymerization of the polymer can be determined from the weight average polymer molecular weight by dividing the latter by the average monomer molecular weight.
• n 182 (i.e. 15,500 / (116 x 0.3 + 72 x 0.7)).
• highly preferred polymers for use herein are those of the first category in which n averages from 100 to 800, preferably from 120 to 400.
• Preferred builders for use herein are polymers of maleic or acrylic acid, or copolymers of maleic and acrylic acid.
• compositions of the present invention comprise up to 50% by weight of the total composition of a builder or mixtures thereof, preferably from 0.1% to 20% and more preferably from 0.5 to 11%.
• the soaking compositions herein further comprise a cheating agent or mixtures thereof.
• Chelating agents are desired herein as they help to control the level of free heavy metal ions in the soaking liquors, thus avoiding rapid decomposition of the oxygen released by oxygen bleach.
• Suitable amino carboxylate cheating agents which may be used herein include diethylene triamino pentacetic acid, ethylenediamine tetraacetates (EDTA), N-hydroxyethylethylenediamine triacetates, nitrilotriacetates, ethylenediamine tetraproprionates, triethylenetetraamine hexaacetates, and ethanoldiglycines, alkali metal ammonium and substituted ammonium salts thereof or mixtures thereof.
• chelating agents include ethylenediamine-N,N'-disuccinic acids (EDDS) or alkali metal, alkaline earth metal, ammonium, or substituted ammonium salts thereof.
• EDDS compounds are the free acid form and the sodium or magnesium salt or complex thereof.
• suitable chelating agents may be the organic phosphonates, including amino alkylene poly(alkylene phosphonate), alkali metal ethane 1-hydroxy diphosphonates, nitrilo trimethylene phosphonates, ethylene diamine tetra methylene phosphonates and diethylene triamine penta methylene phosphonates.
• the phosphonate compounds may be present either in their acid form or in the form of their metal alkali salt.
• the organic phosphonate compounds where present are in the form of their magnesium salt.
• the soaking compositions in the present invention may accordingly comprise from 0% to 5% by weight of the total compositions of said chelating agents, preferably from 0% to 3%, more preferably from 0.05% to 2%.
• compositions herein may also comprise other surfactants on top of the sorbitan ester and alkoxylated nonionic surtactant as described herein before.
• surfactants may be desirable as they may further contribute to the benefit of the compositions herein: i.e., improved stain removal on particulate soils as well as other types of soils like enzymatic and/or grease.
• Such surfactants may be present in the soaking compositions according to the present invention, on top of sorbitan ester and the alkoxylated nonionic surfactant as described herein before, in amounts of from 0.1% to 50% by weight of the total composition, preferably of from 0.1% to 20% and more preferably of from 1% to 10%.
• Surfactants to be used herein include nonionic surfactants, anionic surfactants, cationic surfactants, amphoteric surfactants, zwitterionic surfactants, and mixtures thereof.
• Suitable anionic surfactant for use herein include water soluble salts or acids of the formula ROSO 3 M wherein R preferably is a C 10 -C 24 hydrocarbyl, preferably an alkyl or hydroxyalkyl having a C 10 -C 20 alkyl component, more preferably a C 12 -C 18 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., methyl-, dimethyl-, and trimethyl ammonium cations and quaternary ammonium cations, such as tetramethyl-ammonium and dimethyl piperdinium cations and quarternary ammonium cations derived from alkylamines such as ethylamine, diethylamine, triethylamine, and mixtures thereof, and the like).
• alkyl chains of C 12
• Suitable anionic surfactants for use herein are water soluble salts or acids of the formula RO(A) m SO 3 M wherein R is an unsubstituted C 10 -C 24 alkyl or hydroxyalkyl group having a C 10 -C 24 alkyl component, preferably a C 12 -C 20 alkyl or hydroxyalkyl, more preferably C 12 -C 18 alkyl 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 C 10 -C 24 alkyl or hydroxyalkyl group having a C 10 -C 24 alkyl component, preferably a C 12 -C
• Alkyl ethoxylated sulfates as well as alkyl propoxylated sulfates are contemplated herein.
• Specific examples of substituted ammonium cations include methyl-, dimethyl-, trimethyl-ammonium and quaternary ammonium cations, such as tetramethyl-ammonium, dimethyl piperdinium and cations derived from alkanolamines such as ethylamine, diethylamine, triethylamine, mixtures thereof, and the like.
• Exemplary surfactants are C 12 -C 18 alkyl polyethoxylate (1.0) sulfate, C 12 -C 18 E(1.0)M), C 12 -C 18 alkyl polyethoxylate (2.25) sulfate, C 12 -C 18 E(2.25)M), C 12 -C 18 alkyl polyethoxylate (3.0) sulfate C 12 -C 18 E(3.0), and C 12 -C 18 alkyl polyethoxylate (4.0) sulfate C 12 -C 18 E(4.0)M), wherein M is conveniently selected from sodium and potassium.
• anionic surfactants useful for detersive purposes can also be used herein. These can include salts (including, for example, sodium, potassium, ammonium, and substituted ammonium salts such as mono-, di- and triethanolamine salts) of soap, C 9 -C 20 linear alkylbenzenesulfonates, C 8 -C 24 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.
• salts including, for example, sodium, potassium, ammonium, and substituted ammonium salts such as mono-, di- and triethanolamine salts
• C 9 -C 20 linear alkylbenzenesulfonates C 8 -C 24 olefinsulfonates
• sulfonated polycarboxylic acids prepared by sulfonation of the pyrolyzed product of al
• alkylpolyglycolethersulfates (containing up to 10 moles of ethylene oxide); alkyl ester sulfonates such as C 14-16 methyl ester sulfonates; acyl glycerol sulfonates, fatty oleyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, alkyl phosphates, isethionates such as the acyl isethionates, N-acyl taurates, alkyl succinamates and sulfosuccinates, monoesters of sulfosuccinate (especially saturated and unsaturated C 12 -C 18 monoesters) diesters of sulfosuccinate (especially saturated and unsaturated C 6 -C 14 diesters), acyl sarcosinates, sulfates of alkylpolysaccharides such as the sulfates
• Resin acids and hydrogenated resin acids are also suitable, such as rosin, hydrogenated rosin, and resin acids and hydrogenated resin acids present in or derived from tall oil. Further examples are given in "Surface Active Agents and Detergents" (Vol. I and II by Schwartz, Perry and Berch). A variety of such surfactants are also generally disclosed in U.S. Patent 3,929,678, issued December 30, 1975 to Laughlin, et al. at Column 23, line 58 through Column 29, line 23 (herein incorporated by reference).
• anionic surfactants suitable to be used herein may also include those according to the formula R-SO3M, wherein R is a substituted or unsubstituted, saturated or unsaturated, linear or branched hydrocarbon chain having from 6 to 40 carbon atoms and M is H or a cation.
• R is a substituted or unsubstituted, saturated or unsaturated, linear or branched alkyl group having from 6 to 40 carbon atoms, preferably from 8 to 30, more preferably from 10 to 25 and most preferably from 12 to 18.
• M is a cation which can be for example a metal cation (e.g., sodium, potassium.
• ammonium or substituted-ammonium e.g., methyl-, dimethyl- , and trimethyl ammonium cations and quaternary ammonium cations, such as tetramethyl-ammonium and dimethyl piperdinium cations and quaternary ammonium cations derived from alkylamines such as ethylamine, diethylamine, triethylamine and mixtures thereof and the like).
• Suitable anionic sulphonates to used herein are sodium paraffin sulphonate. They may be commercially available from Hoescht under the name of Hostapur® or Hostatat®.
• compositions herein may further comprise a filler like inorganic filler salts such as alkali metal carbonates, bicarbonates and sulphates.
• a filler like inorganic filler salts such as alkali metal carbonates, bicarbonates and sulphates.
• Such fillers for instance sodium bicarbonate, may also act as acidifying agent as described herein after. Accordingly, sodium bicarbonate and sodium sulphate are the preferred filler materials for use herein.
• compositions of the present invention comprise up to 50% by weight of the total composition of a filler or mixtures thereof, preferably from 0.1% to 20% and more preferably from 0.5 % to 10%.
• compositions herein typically also comprise an enzyme or a mixture thereof.
• the compositions herein comprise a protease or mixtures thereof.
• Protease enzymes are usually present in preferred embodiments of the invention at levels sufficient to provide from 0.005 to 0.2 Anson units (AU) of activity per gram of composition.
• the proteolytic enzyme can be of animal, vegetable or, preferably microorganism preferred origin. More preferred is serine proteolytic enzyme of bacterial origin. Purified or nonpurified forms of enzyme may be used. Proteolytic enzymes produced by chemically or genetically modified mutants are included by definition, as are close structural enzyme variants.
• proteolytic enzyme is bacterial serine proteolytic enzyme obtained from Bacillus , Bacillus subtilis and/or Bacillus licheniformis .
• Suitable commercial proteolytic enzymes include Alcalase ®, Esperase ®, Durazym ®, Savinase ®, Maxatase ®, Maxacal ®, and Maxapem ® 15 (protein engineered Maxacal); Purafect ® and subtilisin BPN and BPN' are also commercially available.
• Preferred proteolytic enzymes also encompass modified bacterial serine proteases, such as those described in European Patent Application Serial Number 87303761.8, filed April 28, 1987 (particularly pages 17, 24 and 98), and which is called herein "Protease B", and in European Patent Application 199,404, Venegas, published October 29, 1986, which refers to a modified bacterial serine proteolytic enzyme, which is called “Protease A” herein. More preferred is what is called herein “Protease C”, which is a triple variant of an alkaline serine protease from Bacillus in which tyrosine replaced valine at position 104, serine replaced asparagine at position 123, and alanine replaced threonine at position 274. Protease C is described in EP 90915958.4, corresponding to WO 91/06637, Published May 16, 1991, which is incorporated herein by reference. Genetically modified variants, particularly of Protease C, are also included herein.
• protease herein referred to as "Protease D” which is a carbonyl hydrolase variant having an amino acid sequence not found in nature, which is derived from a percursor carbonyl hydrolase by substituting a different amino acid for a plurality of amino acid residues at a position in said carbonyl hydrolase equivalent to position +76 in combination with one or more amino acid residue positions equivalent to those selected from the gorup consisting of +99, +101, +103, +107 and +123 in Bacillus amyloliquefaciens subtilisin as described in the concurrently filed patent applications of A. Baeck, C.K. Ghosh, P.P. Greycar, R.R. Bott and L.J.
• proteolytic enzymes are selected from the group consisting of Savinase ®, Esperase ®, Maxacal ®, Purafect ®, BPN', Protease A and Protease B, and mixtures thereof.
• Bacterial serine protease enzymes obtained from Bacillus subtilis and/or Bacillus licheniformis are preferred. Particularly preferred are Savinase ®, Alcalase ®, Protease A and Protease B.
• compositions herein also comprise an amylase or a mixtures thereof.
• an amylase or a mixtures thereof.
• Engineering of enzymes for improved stability, e.g. oxidative stability is known. See, for example J. Biological Chem., vol. 260, No. 11, June 1985, pp 6518-6521.
• Reference amylase hereinafter refers to an amylase outside the scope of the amylase component of this invention and against which stability of any amylase within the invention can be measured.
• the present invention thus makes use of amylases having improved stability in detergents, especially improved oxidative stability.
• a convenient absolute stability reference-point against which amylases used in the instant invention represent a measurable improvement is the stability of TERMAMYL (R) in commercial use in 1993 and available from Novo Nordisk A/S.
• This TERMAMYL (R) amylase is a "reference amylase”.
• Amylases within the spirit and scope of the present invention share the characteristic of being "stability-enhanced" amylases, characterized, at a minimum, by a measurable improvement in one or more of: oxidative stability, e.g.
• amylases herein can demonstrate further improvement versus more challenging reference amylases, the latter reference amylases being illustrated by any of the precursor amylases of which the amylases within the invention are variants. Such precursor amylases may themselves be natural or be the product of genetic engineering. Stability can be measured using any of the art-disclosed technical tests. See references disclosed in WO 94/02597, itself and documents therein referred to being incorporated by reference.
• stability-enhanced amylases respecting the invention can be obtained from Novo Nordisk A/S, or from Genencor International.
• Preferred amylases herein have the common ability of being derived using site-directed mutagenesis from one or more of the Bacillus amylases, especially the Bacillus alpha-amylases, regardless of whether one, two or multiple amylase strains are the immediate precursors.
• amylases are preferred for use herein. Such amylases are non-limitingly illustrated by the following:
• Any other oxidative stability-enhanced amylase can be used, for example as derived by site-directed mutagenesis from known chimeric, hybrid or simple mutant parent forms of available amylases.
• the soaking compositions herein may also comprise a soil suspending agent or a mixture thereof, typically at a level up to 20% by weight, preferably from 0.1% to 10%, more preferably from 0.5% to 2%.
• Suitable soil suspending agents include ethoxylated diamines, ethoxylated polyamines, ethoxylated amine polymers as described in EP-A-112 593, incorporated herein by reference.
• Preferred soil suspending agents to be used herein include ethoxylated polyethyleneamine having a molecular weight of from 140 to 310 prior ethoxylation, ethoxylated 15-18 tetraethylenepentamine, ethoxylated 15-18 polyethylenamine, ethoxylated 15-18 ethylenediamine, ethoxylated polyethyleneimine having a molecular weight of from 600 to 1800 prior ethoxylation, and mixtures thereof.
• Soaking compositions of the present invention may further comprise other optional ingredients such optical brighteners, other enzymes, other chelants, dispersants, soil release agents, photoactivated bleaches such as Zn phthalocyanine sulphonate, dyes, dye transfer inhibitors, pigments, perfumes and the like. Said optional ingredients can be added in varying amounts as desired.
• the present invention encompasses processes of soaking fabrics. Indeed, the present invention encompasses a process of soaking fabrics, wherein said fabrics are immersed in a soaking liquor comprising water and an effective amount of a composition as described herein before, for an effective period of time, then removed from said soaking liquor.
• the expression "process of soaking fabrics” refers to the action of leaving fabrics to soak in a soaking liquor comprising water and a composition as described herein above, for a period of time sufficient to clean said fabrics.
• the soaking process herein allows prolonged contact time between the fabrics and the soaking liquor, typically up to 24 hours.
• the soaking process can be performed independently from any other process, such as a typical laundering operation, or a first step before a second, typical laundering step.
• fabrics are left to soak for a period of time ranging from 10 minutes to 24 hours, preferably from 30 min to 24 hours, more preferably more than 1 hour to 24 hours, even more preferably 2 hours to 24 hours, and most preferably 4 hours to 24 hours.
• fabrics After the fabrics have been immersed in said soaking liquor for a sufficient period of time, they can be removed and rinsed with water.
• the fabrics can also be washed in a normal laundering operation after they have been soaked, with or without having been rinsed in-between the soaking operation and the subsequent laundering operation.
• a soaking composition described hereinabove is diluted in an appropriate amount of water to produce a soaking liquor.
• Suitable doses may range from 40 to 55 grams of soaking composition in 3.5 to 5 liters of water, down to 90 to 100 grams of soaking composition in 20 to 45 liters of water.
• one dose is 40-55 grams in 3.5 to 5 liters for a concentrated soak (bucket/sink).
• the dose is 90-100 grams in about 20 (Europe) to 45 (US) liters of water.
• the fabrics to be soaked are then immersed in the soaking liquor for an appropriate period of time. There are factors which may influence overall performance of the process on particulate dirt/soils. Such factors include prolonged soaking time.
• soaking time is overnight, i.e., 8 hours up to 24 hours, preferably 12 hours to 24 hours.
• Another factor is the initial warm or warmluke temperature. Indeed, higher initial temperatures of the soaking liquors ensure large benefits in performance.
• the process herein is suitable for cleaning a variety of fabrics, but finds a preferred application in the soaking of socks, which are particularly exposed to silt and clay pick-up.
• the present invention encompasses a process of soaking fabrics, wherein said fabrics are immersed in a soaking liquor comprising water and an effective amount of a composition comprising an oxygen bleach and an alkoxylated nonionic surfactant according to the formula RO-(A) n H, wherein R is a substituted or unsubstituted, saturated or unsaturated, linear or branched hydrocarbon chain having from 6 to 40 carbon atoms, A is an alkoxy group having from 2 to 10 carbon atoms, and wherein n is an integer from 9 to 100, for more than 1 hour, preferably 2 hours to 24 hours and more preferably 4 hours to 24 hours, then removed from said soaking liquor.
• RO-(A) n H wherein R is a substituted or unsubstituted, saturated or unsaturated, linear or branched hydrocarbon chain having from 6 to 40 carbon atoms
• A is an alkoxy group having from 2 to 10 carbon atoms
• n is an integer from 9 to 100, for more than 1 hour
• the stain removal performance of a given composition on a soiled fabric under soaking conditions may be evaluated by the following test method. Soaking liquors are formed by diluting for instance 45 g of the soaking compositions herein in 3.78 liter of water or 90g of the soaking composition in 45 liters of water. Fabrics are then immersed in the resulting soaking liquor for a time ranging from more than 1 hour to 18 hours. Finally, the fabrics are removed from the soaking liquors, rinsed with water and washed with a regular washing process, handwash or washing machine wash, with a regular detergent, with or without re-using the soaking liquor, then said fabrics are left to dry.
• typical soiled fabrics to be used in this stain removal performance test may be commercially available from EMC (Empirical Manufacturing Company) Cincinnati, Ohio, USA, such as clay, grass, spaghetti sauce, gravy, dirty motor oil, make-up, barbecue sauce, tea, blood on two different substrates: cotton (CW120) and polycotton (PCW28).
• EMC Electronic Manufacturing Company
• CW120 cotton
• PCW28 polycotton
• the stain removal performance may be evaluated by comparing side by side the soiled fabrics treated with the soaking composition according to the present invention with those treated with the reference, e.g., the same composition without such highly alkoxylated nonionic surfactant according to the present invention.
• a visual grading scale may be used to assign differences in panel score units (psu), in a range from 0 to 4.
• compositions are prepared by mixing the listed ingredients in the listed proportions.
• Soaking liquors are formed by diluting each time 45 g of the above compositions in between 3.5 lit. to 5.0 lit. of water. 0.5 to 2 Kg of fabrics are then each time immersed in said soaking liquor.
• the soaking periods for the soaking liquors comprising any of the above soaking compositions 1 to 6 or 9 are typically from 10 minutes to 24 hours.
• the soaking time according to the process of soaking of the present invention is of more than 1 hour and preferably 4 to 24 hours.
• the fabrics are removed from the soaking liquors, rinsed with water and washed with a regular washing process, handwash or washing machine wash, with a regular detergent, with or without re-using the soaking liquor, then said fabrics are left to dry.
• Excellent stain removal performance is obtained with these compositions on various stains including mud/clay stains as well as enzymatic stains and/or bleachable stains and the like.

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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)
• Inorganic Chemistry (AREA)
• Detergent Compositions (AREA)
• Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
• Lubricants (AREA)
• Silicates, Zeolites, And Molecular Sieves (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Control Of Eletrric Generators (AREA)
• Percussion Or Vibration Massage (AREA)
• Compositions Of Macromolecular Compounds (AREA)

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• 1997
  • 1997-02-27 ES ES97870028T patent/ES2221683T3/es not_active Expired - Lifetime
  • 1997-02-27 AT AT97870028T patent/ATE271595T1/de not_active IP Right Cessation
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  • 1997-02-27 EP EP97870028A patent/EP0861884B1/fr not_active Expired - Lifetime
• 1998
  • 1998-02-13 AU AU62772/98A patent/AU6277298A/en not_active Abandoned
  • 1998-02-13 CN CN98804568.0A patent/CN1253580A/zh active Pending
  • 1998-02-13 WO PCT/US1998/002720 patent/WO1998038272A1/fr not_active Application Discontinuation
  • 1998-02-13 JP JP53768898A patent/JP2001513136A/ja not_active Withdrawn
  • 1998-02-13 PL PL98335507A patent/PL335507A1/xx unknown
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• 1999
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