EP0794245B1 - Procédé de prétraitement pour le lavage du ligne et compositions de blanchiment - Google Patents

Procédé de prétraitement pour le lavage du ligne et compositions de blanchiment Download PDF

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Publication number
EP0794245B1
EP0794245B1 EP96870116A EP96870116A EP0794245B1 EP 0794245 B1 EP0794245 B1 EP 0794245B1 EP 96870116 A EP96870116 A EP 96870116A EP 96870116 A EP96870116 A EP 96870116A EP 0794245 B1 EP0794245 B1 EP 0794245B1
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EP
European Patent Office
Prior art keywords
ethoxylated
composition
moiety
mixtures
alkyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
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EP96870116A
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German (de)
English (en)
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EP0794245A1 (fr
Inventor
Valerio Del Duca (Nmn)
Valentina Masotti (Nmn)
Stefano Scialla (Nmn)
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Procter and Gamble Co
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Procter and Gamble Co
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Filing date
Publication date
Priority claimed from EP96870023A external-priority patent/EP0735131A3/fr
Priority claimed from EP96202104A external-priority patent/EP0823474A1/fr
Priority claimed from EP96202168A external-priority patent/EP0822183A3/fr
Application filed by Procter and Gamble Co filed Critical Procter and Gamble Co
Priority to EP96870116A priority Critical patent/EP0794245B1/fr
Priority to AT96870116T priority patent/ATE244752T1/de
Priority to DE69629006T priority patent/DE69629006T2/de
Priority to ES96870116T priority patent/ES2202424T3/es
Priority to IL12603997A priority patent/IL126039A0/xx
Priority to US09/142,395 priority patent/US6310025B1/en
Priority to RU98118379/04A priority patent/RU2168578C2/ru
Priority to AU19831/97A priority patent/AU1983197A/en
Priority to KR1019980706966A priority patent/KR19990087531A/ko
Priority to JP09531855A priority patent/JP2000514846A/ja
Priority to PCT/US1997/003238 priority patent/WO1997032962A1/fr
Priority to CA002247969A priority patent/CA2247969A1/fr
Priority to TR1998/01744T priority patent/TR199801744T2/xx
Priority to PL97330913A priority patent/PL330913A1/xx
Priority to CZ982793A priority patent/CZ279398A3/cs
Priority to CN97194234A priority patent/CN1265135A/zh
Priority to SK1225-98A priority patent/SK122598A3/sk
Priority to BR9708168A priority patent/BR9708168A/pt
Priority to IDP970672A priority patent/ID16124A/id
Priority to ARP970100858A priority patent/AR006096A1/es
Publication of EP0794245A1 publication Critical patent/EP0794245A1/fr
Priority to NO984060A priority patent/NO984060L/no
Publication of EP0794245B1 publication Critical patent/EP0794245B1/fr
Application granted granted Critical
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/34—Organic compounds containing sulfur
    • C11D3/3418—Toluene -, xylene -, cumene -, benzene - or naphthalene sulfonates or sulfates
    • 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
    • C11D1/38—Cationic compounds
    • C11D1/42—Amino alcohols or amino ethers
    • C11D1/44—Ethers of polyoxyalkylenes with amino alcohols; Condensation products of epoxyalkanes with amines
    • 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
    • C11D1/75—Amino oxides
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/37—Polymers
    • C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3723—Polyamines or polyalkyleneimines
    • 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
    • C11D3/3902—Organic or inorganic per-compounds combined with specific additives
    • C11D3/3905—Bleach activators or bleach catalysts
    • C11D3/3907—Organic 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
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/39—Organic or inorganic per-compounds
    • C11D3/3947—Liquid compositions

Definitions

  • the present invention relates to bleaching compositions particularly suitable to be used as a pretreater and to a process of pretreating fabrics.
  • EP-A-598170 discloses a particular type of cleaning compositions which are aqueous emulsions of a nonionic surfactant system further comprising hydrogen peroxide or water-soluble source thereof and a liquid bleach activator, or any other hydrophobic ingredient which needs to be separated from said hydrogen peroxide.
  • EP-A-0 735 133 discloses a particular type of cleaning compositions which are aqueous microemulsions of a bleach activator in a matrix comprising water, hydrogen peroxide and a hydrophilic surfactant system.
  • a drawback associated with such emulsions or microemulsions comprising a peroxygen bleach and a bleach activator is that they do not deliver effective performance which satisfactorily meet consumer's needs on all types of stains including greasy stains, enzymatic stains, mud/clay stains as well as bleachable stains. Indeed, there is still some room to further improve the stain removal performance as well as the bleaching performance of such bleach-containing compositions when pretreating a fabric therewith.
  • a liquid composition comprising a peroxygen bleach and a soil dispersing agent selected from the group consisting of an ethoxylated monoamine, an ethoxylated diamine, an ethoxylated polyamine, an ethoxylated amine polymer and mixture thereof, as described hereinafter, to pretreat soiled fabrics.
  • a soil dispersing agent selected from the group consisting of an ethoxylated monoamine, an ethoxylated diamine, an ethoxylated polyamine, an ethoxylated amine polymer and mixture thereof, as described hereinafter, to pretreat soiled fabrics.
  • a soil dispersing agent in a liquid composition comprising a peroxygen bleach, and optionally a bleach activator, delivers improved stain removal performance on various types of stains including greasy stains, enzymatic stains, clay/mud stains, and the like, under pretreatment conditions, as compared to the stain removal performance delivered by the same composition without said soil dispersing agent.
  • the liquid compositions comprising both the peroxygen bleach and said soil dispersing agent when used to pretreat fabrics, provide improved bleaching efficacy, as compared to the same compositions without said soil dispersing agent.
  • the present invention encompasses a process for bleaching a fabric with a liquid composition comprising from 0.01% to 15% by weight of the total composition of a peroxygen bleach, and a soil dispersing agent, said process comprising the steps of applying said liquid composition in its neat form onto at least one portion of said fabric, optionally allowing said composition to remain in contact with said fabric and then washing said fabric.
  • a soil dispersing agent selected from the group consisting of an ethoxylated monoamine, an ethoxylated diamine, an ethoxylated polyamine, an ethoxylated amine polymer and mixture thereof, in a liquid composition formulated either as an emulsion or microemulsion, comprising a peroxygen bleach and a surfactant, reduces the viscosity of said composition, whatever the viscosity was before the addition of said soil dispersing agent.
  • an advantage of the liquid compositions of the present invention formulated either as an emulsion or a microemulsion is that they deliver improved stain removal performance and improved bleaching performance while delivering acceptable viscosity, without the need to add viscosity control agents.
  • the present invention allows to formulate emulsions or microemulsions with improved overall stain removal/bleaching performance and desirable physical characteristics at reduced costs, i.e., without adding any viscosity control agent that would raise the cost formula and bulk to the compositions without contributing to the bleaching/cleaning performance of said compositions.
  • Another advantage of the present invention is that stable liquid emulsions or microemulsions are provided that are suitable to be used in the most efficient manner by the consumer over prolonged period of time.
  • compositions according to the present invention which are formulated as emulsions or microemulsions is that they provide also excellent cleaning and/or bleaching performance when used in applications other than laundry pretreaters, such as in other laundry applications, as laundry detergents or laundry additives.
  • EP-A-0 754 214 discloses laundry compositions suitable for pretreating fabrics comprising polyamines and peroxygen bleach. No ethoxylated amines, ethoxylated polyamines or ethoxylated amine polymers are disclosed.
  • EP-A-271 312 discloses laundry compositions comprising a peroxyacid bleach and a soil release agent like particular alkyl and hydroxyalkyl ethers of cellulose, polymers comprising ethylene terephthalate and polyethylene oxide terephthalate. No ethoxylated amines, ethoxylated polyamines or ethoxylated amine polymers are disclosed.
  • WO96/12004 discloses laundry compositions comprising a lipophilic enzyme and a primary and/or tertiary amine. These compositions provide enhanced cleaning of greasy/oily soils and stains, particularly when used in pretreatment laundering process for cleaning fabrics stained with greasy soils.
  • the compositions exemplified comprise tetraethylenepentamine ethoxylated (15-18) but no bleach.
  • the present invention encompasses a process of bleaching a fabric with a liquid composition comprising from 2% to 15% by weight of the total composition of a peroxygen bleach, and a soil dispersing agent selected from the group consisting of
  • the present invention encompasses a liquid composition suitable for pretreating fabrics, comprising from 2% to 15% by weight of the total composition of a peroxygen bleach, a surfactant and a soil dispersing agent selected from the group consisting of an ethoxylated monoamine, an ethoxylated diamine, an ethoxylated polyamine, an ethoxylated amine polymers and mixture thereof as previously defined, said composition being formulated either as an emulsion or a microemulsion.
  • the present invention relates to a process of pretreating a fabric with a liquid composition comprising a soil dispersing agent, as defined herein, and from 2% to 15% by weight of the total composition of a peroxygen bleach.
  • pretreating a fabric it is to be understood that the liquid composition herein is applied in its neat form onto at least a portion of a soiled fabric, optionally left to act onto said fabric typically for a period of time of 1 minute to several hours, before said fabric is washed, as described hereinafter, in the process of bleaching fabrics according to the present invention.
  • the present invention is based on the finding that by adding a soil dispersing agent, as described herein, in a liquid composition comprising a peroxygen bleach, improved stain removal performance is obtained with said composition when used to pretreat a soiled fabric before said fabric is washed, as compared to the stain removal performance delivered with the same composition without said soil dispersing agent.
  • stain removal performance it is meant herein stain removal performance on a variety of stains/soils such as greasyloily stains, and/or enzymatic stains and/or mud/clay stains as well as bleachable stains.
  • greasy/oily stains any soil and stain of greasy nature that can be found on a fabric like dirty motor oil, mineral oil, make-up, lipstick vegetal oil, spaghetti sauce, mayonnaise and the like.
  • bleachable stains examples include tea, coffee, wine and the like.
  • enzymatic stains examples include grass, chocolate and blood.
  • the stain removal performance of a given composition on a soiled fabric under pretreatment conditions may be evaluated by the following test method.
  • a composition according to the present invention is first applied to the stained portion of said fabric, left to act from about 1 to about 10 minutes, typically 5 minutes, and said pretreated fabric is then washed according to common washing conditions with a conventional detergent composition, at a temperature of from 30°C to 70°C for a period of time sufficient to bleach said fabric.
  • typical soiled fabrics to be used in this stain removal performance test method may be commercially available from EMC (Empirical Manufacturing Company) Cincinnati, Ohio, USA such as clay, chocolate, spaghetti sauce, dirty motor oil, make-up, tea, coffee, blood on two different substrate/fabric, e.g., cotton (CW120) and polycotton (PCW28).
  • EMC Electronic Manufacturing Company
  • Cincinnati, Ohio, USA such as clay, chocolate, spaghetti sauce, dirty motor oil, make-up, tea, coffee, blood on two different substrate/fabric, e.g., cotton (CW120) and polycotton (PCW28).
  • the stain removal performance may then be evaluated by comparing side by side the soiled fabric pretreated with the composition according to the present invention with those pretreated with the reference, e.g., the same composition without such a soil dispersing agent 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.
  • the present invention encompasses a process of bleaching a fabric with a liquid composition comprising from 2% to 15% by weight of the total composition of a peroxygen bleach and a soil dispersing agent, as defined herein, said process comprises the steps of applying said composition in its neat form onto at least a portion of said fabric, optionally allowing said composition to remain in contact with said fabric preferably without leaving said composition to dry onto said fabric, before said fabric is washed.
  • Said composition may remain in contact with said fabric, typically for a period of 1 minute to several hours, preferably 1 minute to 1 hour, more preferably 1 minute to 30 minutes, and most preferably 2 to 10 minutes.
  • said composition may be rubbed and/or brushed more or less intensively, for example, by means of a sponge or a brush or simply by rubbing two pieces of fabric each against the other.
  • washing it is to be understood herein to simply rinse the fabric with water, or the fabric may be washed with a conventional composition comprising at least one surface active agent, this by the means of a washing machine or simply by hand.
  • liquid compositions are applied directly onto the fabrics to be pre-treated without undergoing any dilution, e.g., the liquid compositions according to the present invention are applied as described herein.
  • the liquid compositions used in said process should preferably not be left to dry onto the fabrics. Indeed, it has been found that water evaporation contributes to increase the concentration of free radicals onto the surface of the fabrics and, consequently, the rate of chain reaction. It is also speculated that an auto-oxidation reaction occurs upon evaporation of water when the liquid compositions are left to dry onto the fabrics. Said reaction of auto-oxidation contributes to generate peroxy-radicals which may cause color damage and/or fabric damage. Thus, not leaving the liquid bleaching compositions used according to the present invention to dry onto the fabrics, in the process of bleaching fabrics according to the present invention would result in a safer pretreating operation with liquid bleaching compositions.
  • compositions to be used according to the present invention comprise a peroxygen bleach or mixtures thereof.
  • the peroxygen bleach to be used herein is any peroxygen bleach, known to those skilled in the art.
  • Such peroxygen bleach includes hydrogen peroxide, or a water-soluble source thereof, or mixtures thereof. Indeed, the presence of the peroxygen bleach contributes to the excellent cleaning and bleaching benefits of the compositions used according to the present invention.
  • a hydrogen peroxide source refers to any compound which produces perhydroxyl ions when said compound is in contact with water.
  • Suitable water-soluble sources of hydrogen peroxide for use herein include percarbonates, persilicate, persulphate such as monopersulfate, perborates, peroxyacids such as diperoxydodecandioic acid (DPDA), magnesium perphtalic acid, perlauric acid, perbenzoic and alkylperbenzoic acids, hydroperoxides, diacyl peroxides and mixtures thereof.
  • Preferred peroxygen bleaches used herein are hydrogen peroxide, hydroperoxide and/or aliphatic diacyl peroxide.
  • Suitable hydroperoxides for use herein are tert-butyl hydroperoxide, cumyl hydroperoxide, 2,4,4-trimethylpentyl-2-hydroperoxide, di-isopropylbenzene-monohydroperoxide, tert-amyl hydroperoxide and 2,5-dimethyl-hexane-2,5-dihydroperoxide.
  • Such hydroperoxides have the advantage to be particularly safe to fabrics and color while delivering excellent bleaching performance.
  • Suitable aliphatic diacyl peroxides for use herein are dilauroyl peroxide, didecanoyl peroxide, dimyristoyl peroxide or mixtures thereof. Such aliphatic diacyl peroxides have the advantage to be particularly safe to fabrics and color while delivering excellent bleaching performance.
  • compositions used according to the present invention comprise from 2% to 15% by weight of the total composition of such a peroxygen bleach or mixtures thereof, preferably from 2% to 12%, more preferably from 2% to 10% and most preferably from 2% to 8%.
  • compositions to be used according to the present invention comprise a soil dispersing agent selected from the group consisting of ethoxylated monoamines, ethoxylated diamines, ethoxylated polyamines, ethoxylated amine polymers, as previously defined and mixtures thereof.
  • R 1 can be branched or most preferably linear alkylene, hydroxyalkylene, alkenylene, alkarylene or oxyalkylene.
  • R 1 is preferably C 2 -C 6 alkylene for the ethoxylated diamines and amine polymers.
  • the minimum degree of ethoxylation required for suitable soil removal/anti-redeposition properties decreases on going from C 2 -C 3 alkylene (ethylene, propylene) to hexamethylene.
  • ethoxylated amine polymers in particular the ethoxylated polyalkyleneamines and polyalkyleneimines, especially at higher molecular weights, C 2 -C 3 alkylene (ethylene, propylene) are preferred for R 1 with ethylene being most preferred.
  • R 2 is preferably the moiety ⁇ L ⁇ X.
  • hydrophilic chain L usually consists entirely of the polyoxyalkylene moiety ⁇ [(R 5 O) m (CH 2 CH 2- O) n ] ⁇ .
  • the moieties ⁇ (R 5 O) m ⁇ and ⁇ (CH 2 CH 2 O) n ⁇ of the polyoxyalkylene moiety can be mixed together or preferably form blocks of ⁇ (R 5 O) m ⁇ and ⁇ (CH 2 CH 2 O) n ⁇ moieties.
  • R 5 is preferably C 3 H 6 (propylene).
  • m is preferably from 0 to 5.
  • m is most preferably 0, i.e. the polyoxyalkylene moiety consists entirely of the moiety ⁇ (CH 2 CH 2 O) n ⁇ .
  • the moiety ⁇ (CH 2 CH 2 O) n ⁇ preferably comprises at least 85% by weight of the polyoxyalkylene moiety and most preferably 100% by weight (m is O).
  • X can be any compatible nonionic group, anionic group or mixture thereof.
  • Suitable nonionic groups include C 1 -C 4 alkyl or hydroxyalkyl ester or ether groups, preferably acetate or methyl ether, respectively; hydrogen (H); or mixtures thereof.
  • the particularly preferred nonionic group is H.
  • anionic groups PO 3 -2 and SO 3 - are suitable.
  • the particularly preferred anionic group is SO 3 - . It has been found that the percentage of anionic groups relative to nonionic groups can be important to the soil removal/anti-redeposition properties provided by the ethoxylated amine.
  • a mixture of from 0 to 30% anionic groups and from 70 to 100% nonionic groups provides preferred properties.
  • a mixture of from 5 to 10% anionic groups and from 90 to 95% nonionic groups provides the most preferred properties.
  • a mixture of from 0 to 80% anionic groups and from 20 to 100% nonionic groups provides suitable soil removal/anti-redeposition properties.
  • Preferred ethoxylated mono- and diamines have the formula: wherein X and n are defined as before, a is 0 or 1 and b is from 0 to 4.
  • n is at least 15, with a typical range of from 15 to 35.
  • n is at least 12 with a typical range of from 12 to 42.
  • R 3 (linear, branched, or cyclic) is preferably a substituted C 3 -C 6 alkyl, hydroxyalkyl or aryl group;
  • a 1 is preferably n is preferably at least 12, with a typical range of from 12 to 42;
  • p is preferably from 3 to 6.
  • q is preferably 1 and R 4 is preferably C 2 -C 3 alkylene.
  • R 3 is an alkyl, hydroxyalkyl, or alkenyl group, and when q is 0, R 1 is preferably a C 2 -C 3 oxyalkylene moiety; when q is 1, R 4 is preferably C 2 -C 3 alkylene.
  • ethoxylated polyamines can be derived from polyamino amides such as:
  • ethoxylated polyamines can also be derived from polyaminopropylene-oxide derivatives such as: wherein each c is a number from 2 to 20.
  • Preferred ethoxylated amine polymers are the ethoxylated C 2 -C 3 polyalkyleneamines and polyalkyleneimines Particularly preferred ethoxylated polyalkyleneamines and polyalkyleneimines are the ethoxylated polyethyleneamines (PEA's) and polyethyleneimines (PEI's). These preferred compounds comprise units having the general formula: wherein X, w, x, y, z and n are defined as before.
  • the PEAs used in preparing compounds of the present invention have the following general formula: wherein x + y + z is from 2 to 9, y + z is from 2 to 9 and w is 0 or 1 (molecular weight of from 100 to 400). Each hydrogen atom attached to each nitrogen atom represents an active site for subsequent ethoxylation.
  • y + z is from 3 to 7 (molecular weight of from 140 to 310) and most prefarably from 3 to 4 (molecular weight of from 140 to 200).
  • These PEA's can be obtained by reactions involving ammonia and ethylene dichloride, followed by fractional distillation.
  • the common PEA's obtained are triethylenetetramine (TETA) and tetraethylenepentamine (TEPA).
  • TETA triethylenetetramine
  • TEPA tetraethylenepentamine
  • the cogenerically derived mixture does not appear to separate by distillation and can include other materials such as cyclic amines and particularly piperazines.
  • cyclic amines with side chains in which nitrogen atoms appear. See US Patent 2,792,372 to Dickson, issued May 14, 1957, which describes the preparation of PEAs.
  • n is preferably at least about 6.
  • y + z is from 4 to 9, suitable benefits are achieved when n is at least 3.
  • n is at least 12, with a typical range of from 12 to 42.
  • the PEIs used in preparing the compounds of the present invention have a molecular weight of at least 440 prior to ethoxylation, which represents at least 10 units.
  • Preferred PEls used in preparing these compounds have a molecular weight of from 600 to 1800.
  • the polymer backbone of these PEIs can be represented by the general formula: wherein the sum of x, y, and z represents a number of sufficient magnitude to yield a polymer having the molecular weights previously specified. Although linear polymer backbones are possible, branch chains can also occur.
  • the relative proportions of primary, secondary and tertiary amine groups present in the polymer can vary, depending on the manner of preparation. The distribution of amine groups is typically as follows:
  • Each hydrogen atom attached to each nitrogen atom of the PEI represents an active site for subsequent ethoxylation.
  • These PEIs can be prepared, for example, by polymerizing ethyleneimine in the presence of a catalyst such as carbon dioxide, sodium bisulfite, sulfuric acid, hydrogen peroxide, hydrochloric acid or acetic acid.
  • a catalyst such as carbon dioxide, sodium bisulfite, sulfuric acid, hydrogen peroxide, hydrochloric acid or acetic acid.
  • Specific methods for preparing PEIs are disclosed in U.S. Patent 2,182,306 to Ulrich et al., issued December 5, 1939; U.S. Patent 3,033,746 to Mayle et al., issued May 8, 1962; US Patent 2,208,095 to Esselmann et al., issued July 16, 1940; US Patent 2,806,839 to Crowther, issued Sept. 17, 1957; and US Patent. 2,553,696 to Wilson, issued May 21, 1951.
  • n is at least 3 for the ethoxylated PEIs.
  • the minimum degree of ethoxylation required for suitable soil removal/anti-redeposition performance can increase as the molecular weight of the PEI increases, especially much beyond 1800.
  • the degree of ethoxylation for preferred compounds increases as the molecular weight of the PEI increases.
  • n is preferably at least 12, with a typical range of from 12 to 42.
  • n is preferably at least 24, with a typical range of from 24 to 42.
  • compositions used according to the present invention comprise from 0.01% to 20% by weight of the total composition of such a soil dispersing agent or mixtures thereof, preferably from 0.1% to 10%, more preferably 0.2% to 4% and most preferably from 0.5% to 2%.
  • the liquid compositions used according to the process of the present invention are preferably aqueous compositions.
  • the compositions used in the process herein have a pH of from 0 to 6, preferably from 1 to 5, and more preferably from 2 to 5 and most preferably from 3 to 5. Acidic compositions are preferred herein for stability reasons.
  • compositions used according to the present invention may comprise optional ingredients like bleach activators, surfactants, perfumes, brighteners, chelating agents, radical scavengers, stabilisers, soil suspenders, dye transfer agents, solvents, dyes, other amines, or mixtures thereof.
  • optional ingredients are further described in more details hereinafter.
  • the present invention also encompasses a liquid composition suitable for pretreating fabrics, comprising from 2% to 15% by weight of the total composition of a peroxygen bleach, a soil dispersing agent selected from the group consisting of an ethoxylated monoamine, an ethoxylated diamine, an ethoxylated polyamine, an ethoxylated amine polymer and mixture thereof, as defined hereinbefore, and a surfactant, said composition being formulated either as an emulsion or a microemulsion.
  • a soil dispersing agent selected from the group consisting of an ethoxylated monoamine, an ethoxylated diamine, an ethoxylated polyamine, an ethoxylated amine polymer and mixture thereof, as defined hereinbefore
  • a surfactant said composition being formulated either as an emulsion or a microemulsion.
  • a soil dispersing agent in a liquid composition comprising a peroxygen bleach, a surfactant and being formulated either as an emulsion or a microemulsion, that not only improved stain removal performance is obtained especially under pretreatment conditions, on various stains including greasy stains, enzymatic stains, clay/mud stains as well as improved bleaching performance but also desirable viscosity is achieved.
  • the soil dispersing agents according to the present invention are easily processed in a composition being formulated either as an emulsion or a microemulsion, while providing the appropriate viscosity, i.e., the viscosity of said composition is reduced, whatever the viscosity was before the addition of said soil dispersing agents into said composition comprising a peroxygen bleach and a surfactant.
  • compositions of the present invention being formulated either as an emulsion or a microemulsion including anionic, nonionic, cationic, amphotheric, zwitternionic surfactants at a level of from 0.01% to 50% by weight of the total composition, preferably from 1% to 30%, and more preferably from 2% to 20%.
  • a surfactant system is used in the compositions according to the present invention comprising at least one hydrophilic surfactant and at least one hydrophobic surfactant.
  • Said two surfactants in order to form emulsions or microemulsions which are stable preferably have different HLB values (hydrophilic lipophilic balance) and typically the difference in value of the HLBs of said two surfactants is at least 1, preferably at least 2 and most preferably at least 3.
  • hydrophobic surfactant it is meant herein a surfactant having an HLB up to 10 or mixtures thereof, preferably below 10, more preferably below 9.
  • the hydrophobic surfactants to be used herein have excellent grease cutting properties, i.e., they have a solvent effect which contributes to hydrophobic soil removal.
  • hydrophilic surfactant it is meant herein a surfactant having an HLB above 10 or mixtures thereof, preferably above 10.5, and more preferably above 11.
  • compositions according to the present invention formulated either as an emulsion or a microemulsion comprise from 1 % to 50 % by weight of the total composition of said hydrophilic and hydrophobic surfactants, more preferably from 5 % to 40 % and most preferably from 8 % to 30 %.
  • the preferred compositions according to the present invention comprise at least from 0.01 % by weight of the total composition of said hydrophobic surfactant, or mixtures thereof, preferably at least 2 % and more preferably at least 4 % and at least from 0.01 % by weight of the total composition of said hydrophilic surfactant, or mixtures thereof, preferably at least 2%, and more preferably at least 4%.
  • nonionic surfactants particularly preferred surfactants to be used in the compositions according to the present invention are nonionic surfactants.
  • suitable nonionic surfactants for use herein include alkoxylated fatty alcohols preferably, fatty alcohol ethoxylates and/or propoxylates.
  • alkoxylated fatty alcohols preferably, fatty alcohol ethoxylates and/or propoxylates.
  • a great variety of such alkoxylated fatty alcohols are commercially available which have very different HLB values (hydrophilic / lipophilic balance).
  • HLB values of such alkoxylated nonionic surfactants depend essentially on the chain length of the fatty alcohol, the nature of the alkoxylation and the degree of alkoxylation.
  • Hydrophilic nonionic surfactants tend to have a high degree of alkoxylation and a short chain fatty alcohol, while hydrophobic surfactants tend to have a low degree of alkoxylation and a long chain fatty alcohol.
  • Surfactant catalogs are available which list a number of surfactants including nonionics, together with their respective HLB values.
  • Suitable chemical processes for preparing the 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. As an alternative, a great variety of alkoxylated alcohols suitable for use herein is commercially available from various suppliers.
  • Preferred hydrophobic nonionic surfactants to be used in the compositions according to the present invention are surfactants having an HLB up to 10 and being according to the formula RO-(C 2 H 4 O) n (C 3 H 6 O) m H, wherein R is a C 6 to C 22 alkyl chain or a C 6 to C 28 alkyl benzene chain, and wherein n+m is from 0.5 to 5 and n is from 0 to 5 and m is from 0 to 5 and preferably n+m is from 0.5 to 4.5 and, n and m are from 0 to 4.5.
  • the preferred R chains for use herein are the C 8 to C 22 alkyl chains.
  • Dobanol R 23-3 or Dobanol R 23-2, Lutensol R TO3, or mixtures thereof.
  • These Dobanol R surfactants are commercially available from SHELL.
  • These Lutensol R surfactants are commercially available from BASF and these Tergitol R surfactants are commercially available from UNION CARBIDE.
  • Other suitable hydrophobic nonionic surfactants to be used herein are non alkoxylated surfactants.
  • An example is Dobanol R 23 (HLB ⁇ 3).
  • Preferred hydrophilic nonionic surfactants to be used in the compositions according to the present invention are surfactants having an HLB above 10 and being according to the formula RO-(C 2 H 4 O) n (C 3 H 6 O) m H, wherein R is a C 6 to C 22 alkyl chain or a C 6 to C 28 alkyl benzene chain, and wherein n+m is from 5 to 11 and n is from 0 to 11 and m is from 0 to 11, preferably n+m is from 6 to 10 and, n and m are from 0 to 10.
  • n and m refer to the average degree of the ethoxylation/propoxylation.
  • the preferred R chains for use herein are the C 8 to C 22 alkyl chains.
  • R is a mixture of C 9 to C 11 alkyl chains, n is 10 and m is 0), or mixtures thereof.
  • Preferred herein are Dobanol R 91-10, or Dobanol R 45-7, Dobanol R 23-6.5, or mixtures thereof.
  • These Dobanol R surfactants are commercially available from SHELL.
  • hydrophilic surfactants may further be used in the compositions of the present invention such as polyhydroxy fatty acid amide surfactants, or mixtures thereof, according to the formula R 2 -C(O)-N(R 1 )-Z, wherein R 1 is H, or C 1- C 4 alkyl, C 1- C 4 hydrocarbyl, 2-hydroxy ethyl, 2-hydroxy propyl or a mixture thereof, R 2 is C 5- C 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 C 1- C 4 alkyl, more preferably C 1 or C 2 alkyl and most preferably methyl
  • R 2 is a straight chain C 7- C 19 alkyl or alkenyl, preferably a straight chain C 9- C 18 alkyl or alkenyl, more preferably a straight chain C 11- C 18 alkyl or alkenyl, and most preferably a straight chain C 11- C 14 alkyl or alkenyl, or mixtures thereof.
  • Z preferably will be derived from a reducing sugar in a reductive amination reaction; more preferably Z is a glycityl.
  • Suitable reducing sugars include glucose, fructose, maltose, lactose, galactose, mannose and xylose.
  • high dextrose corn syrup, high fructose corn syrup, and high maltose corn syrup can be utilised as well as the individual sugars listed above. These corn syrups may yield a mix of sugar components for Z. It should be understood that it is by no means intended to exclude other suitable raw materials.
  • Z preferably will be selected from the group consisting of -CH 2 -(CHOH) n -CH 2 OH, -CH(CH 2 OH)-(CHOH) n-1 -CH 2 OH, -CH 2 -(CHOH) 2 -(CHOR')(CHOH)-CH 2 OH, where n is an integer from 3 to 5, inclusive, and R' is H or a cyclic or aliphatic monosaccharide, and alkoxylated derivatives thereof. Most preferred are glycityls wherein n is 4, particularly CH 2 -(CHOH) 4 -CH 2 OH.
  • R 1 can be, for example, N-methyl, N-ethyl, N-propyl, N-isopropyl, N-butyl, N-2-hydroxy ethyl, or N-2-hydroxy propyl.
  • R 2 - C(O) - N ⁇ can be, for example, cocamide, stearamide, oleamide, lauramide, myristamide, capricamide, palmitamide, tallowamide and the like.
  • Z can be 1-deoxyglucityl, 2-deoxyfructityl, 1-deoxymaltityl, 1-deoxylactityl, 1-deoxygalactityl, 1-deoxymannityl, 1-deoxymaltotriotityl and the like.
  • Suitable polyhydroxy fatty acid amide surfactants to be used herein may be commercially available under the trade name HOE® from Hoechst.
  • polyhydroxy fatty acid amide surfactants are known in the art. In general, they can be made by reacting an alkyl amine with a reducing sugar in a reductive amination reaction to form a corresponding N-alkyl polyhydroxyamine, and then reacting the N-alkyl polyhydroxyamine with a fatty aliphatic ester or triglyceride in a condensation/amidation step to form the N-alkyl, N-polyhydroxy fatty acid amide product.
  • compositions containing polyhydroxy fatty acid amides are disclosed for example in GB patent specification 809,060, published February 18, 1959, by Thomas Hedley & Co., Ltd., US patent 2,965,576, issued December 20, 1960 to E.R. Wilson, US patent 2,703,798, Anthony M. Schwartz, issued March 8, 1955, US patent 1,985,424, issued December 25, 1934 to Piggott and WO92/06070, each of which is incorporated herein by reference.
  • hydrophilic surfactants to be used in the compositions herein include the anionic surfactants and mixtures thereof.
  • Suitable anionic surfactants to be used in the compositions 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 quaternary ammonium cations derived from alkylamines such as ethylamine, diethylamine, triethylamine, and mixtures thereof, and the like).
  • R
  • 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 22 primary or secondary alkanesulfonates, 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 22 primary or secondary alkanesulfonates
  • 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, paraffin sulfonates, 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), sulfates of alkylpolysaccharides such as the sulfates of alkylpolysaccharides such as
  • 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).
  • acyl sarcosinate or mixtures thereof, in its acid and/or salt form preferably long chain acyl sarcosinates having the following formula: wherein M is hydrogen or a cationic moiety and wherein R is an alkyl group of from 11 to 15 carbon atoms, preferably of from 11 to 13 carbon atoms.
  • M are hydrogen and alkali metal salts, especially sodium and potassium.
  • Said acyl sarcosinate surfactants are derived from natural fatty acids and the aminoacid sarcosine (N-methyl glycine). They are suitable to be used as aqueous solution of their salt or in their acidic form as powder. Being derivatives of natural fatty acids, said acyl sarcosinates are rapidly and completely biodegradable and have good skin compatibility.
  • particularly preferred long chain acyl sarcosinates to be used herein include C 12 acyl sarcosinate (i.e. an acyl sarcosinate according to the above formula wherein M is hydrogen and R is an alkyl group of 11 carbon atoms) and C 14 acyl sarcosinate (i.e. an acyl sarcosinate according to the above formula wherein M is hydrogen and R is an alkyl group of 13 carbon atoms).
  • C 12 acyl sarcosinate is commercially available, for example, as Hamposyl L-30® supplied by Hampshire.
  • C 14 acyl sarcosinate is commercially available, for example, as Hamposyl M-30® supplied by Hampshire.
  • a surfactant system comprising a hydrophilic nonionic surfactant and a hydrophobic nonionic surfactant as well as a further hydrophilic surfactant like a polyhydroxy fatty acid amide surfactant and/or an alkyl ethoxylated sulphate.
  • the bleaching compositions of the present invention may further comprise an amine oxide surfactant according to the formula R1R2R3NO, wherein each of R1, R2 and R3 is independently a C 1 -C 30 , preferably a C 1 -C 20 , most preferably a C 1 -C 16 hydrocarbon chain.
  • compositions are formulated as emulsions
  • said compositions are opaques.
  • centrifugation examination it was observed that said emulsions herein showed no phase separation after 15 minutes at 6000 rpm. Under microscopic examination, said emulsions appeared as a dispersion of droplets in a matrix.
  • compositions are macroscopically transparent in the absence of opacifiers and dyes.
  • said microemulsions In centrifugation examination, it was observed that said microemulsions herein showed no phase separation after 15 minutes at 6000 rpm. Under microscopic examination, said microemulsions appeared as a dispersion of droplets in a matrix. We have observed that the particles had a size which is typically around or below 3 micron diameter, preferably below 2 micron diameter.
  • an adequate surfactant system would comprise a hydrophobic nonionic surfactant with for instance an HLB of 6, such as a Dobanol R 23-2 and a hydrophilic nonionic surfactant with for instance an HLB of 15, such as a Dobanol R 91-10.
  • compositions of the present invention formulated in the form of emulsions or microemulsions are chemically stable.
  • chemically stable it is meant herein that said compositions of the present invention comprising a peroxygen bleach do not undergo more than 10% available oxygen loss at 50°C in 2 weeks.
  • concentration of available oxygen can be measured by chemical titration methods known in the art, such as the iodimetric method, the permanganometric method and the cerimetric method. Said methods and the criteria for the choice of the appropriate method are described for example in "Hydrogen Peroxide", W. C. Schumb, C. N. Satterfield and R. L. Wentworth, Reinhold Publishing Corporation, New York, 1955 and “Organic Peroxides", Daniel Swem, Editor Wiley Int. Science, 1970.
  • the stability of said compositions may also be evaluated by a bulging test method.
  • said bleaching compositions of the present invention may be packaged in a given deformable container/bottle without compromising the stability of said container/bottle comprising it upon standing, for long periods of time.
  • compositions of the present invention formulated either as an emulsion or microemulsion are typically aqueous and are formulated in the acidic pH range up to 6, preferably at a pH of from 1 to 5, more preferably of from 2 to 5 and most preferably from 3 to 5. Formulating the compositions of the present invention in the acidic pH range contributes to the stability of said compositions.
  • the pH of the compositions of the present invention can be adjusted by using organic or inorganic acids.
  • compositions of the present invention may further comprise optional ingredients like bleach activators, stabilisers, chelating agents, radical scavengers, builders, soil suspenders, dye transfer agents, solvents, brighteners, perfumes, foam suppressors or dyes or mixtures thereof.
  • the compositions of the present invention comprise a bleach activator or mixtures thereof.
  • bleach activator it is meant herein a compound which reacts with hydrogen peroxide to form a peracid.
  • the peracid thus formed constitutes the activated bleach.
  • Paticularly suitable bleach activators to be used herein are hydrophobic bleach activators, i.e., a bleach activator which is not substantially and stably miscible with water.
  • such hydrophobic bleach activators have a secondary HLB (hydrophilic lipophilic balance) below 11, preferably below 10.
  • Secondary HLB is known to those skilled in the art and is defined for example in “Emulsions theory and practice” by P. Becher, Reinhold, New York, 1957, or in “Emulsion science” by P. Sherman, Academic Press, London, 1969.
  • Suitable bleach activators to be used herein include those belonging to the class of esters, amides, imides, or anhydrides. Examples of suitable compounds of this type are disclosed in British Patent GB 1 586 769 and GB 2 143 231 and a method for their formation into a prilled form is described in European Published Patent Application EP-A-62 523.
  • Suitable examples of such compounds to be used herein 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).
  • TAED tetracetyl ethylene diamine
  • NOBS n-nonanoyloxybenzenesulphonate
  • N-acyl caprolactams selected from the group consisting of substituted or unsubstituted benzoyl caprolactam, octanoyl caprolactam, nonanoyl caprolactam, hexanoyl caprolactam, decanoyl caprolactam, undecenoyl caprolactam, formyl caprolactam, acetyl caprolactam, propanoyl caprolactam, butanoyl caprolactam pentanoyl caprolactam or mixtures thereof.
  • a particular family of bleach activators of interest was disclosed in EP 624 154, and particularly preferred in that family is acetyl triethyl citrate (ATC).
  • Acetyl triethyl citrate has the advantage that it is environmental-friendly as it eventually degrades into citric acid and alcohol. Furthermore, acetyl triethyl citrate has a good hydrolytical stability in the product upon storage and it is an efficient bleach activator. Finally, it provides good building capacity to the composition.
  • compositions according to the present invention may comprise from 0.01% to 20% by weight of the total composition of said bleach activator, or mixtures thereof, preferably from 1% to 10%, and more preferably from 3% to 7%.
  • Suitable chelating agents to be used herein include chelating agents selected from the group of phosphonate chelating agents, amino carboxylate chelating agents, polyfunctionally-substituted aromatic chelating agents, and further chelating agents like glycine, salicylic acid, aspartic acid, glutamic acid, malonic acid, or mixtures thereof. Chelating agents when used, are typically present herein in amounts ranging from 0.001% to 5% by weight of the total composition and preferably from 0.05% to 2% by weight.
  • Suitable phosphonate chelating agents to be used herein may include ethydronic acid as well as amino phosphonate compounds, 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 as salts of different cations on some or all of their acid functionalities.
  • Preferred amino phosphonate chelating agents to be used herein are diethylene triamine penta methylene phosphonates. Such phosphonate chelating agents are commercially available from Monsanto under the trade name DEQUEST® .
  • the most preferred phosphonate chelating agent to be used herein is aminotri(methylene phosphonic acid), herein referred to as ATMP. Indeed, it has been found that the addition of ATMP, i.e. the compound of formula : in a liquid composition of the present invention considerably reduces the damage otherwise associated with the pretreatment of fabrics with peroxygen bleach-containing compositions, especially those fabrics which contain metal ions, such as copper, iron, chromium, and manganese.
  • Polyfunctionally-substituted aromatic chelating agents may also be useful in the compositions herein. See U.S. patent 3,812,044, issued May 21, 1974, to Connor et al.
  • Preferred compounds of this type in acid form are dihydroxydisulfobenzenes such as 1,2-dihydroxy -3,5-disulfobenzene.
  • a preferred biodegradable chelating agent for use herein is ethylene diamine N,N'- disuccinic acid, or alkali metal, or alkaline earth, ammonium or substitutes ammonium salts thereof or mixtures thereof.
  • Ethylenediamine N,N'- disuccinic acids, especially the (S,S) isomer have been extensively described in US patent 4, 704, 233, November 3, 1987, to Hartman and Perkins.
  • Ethylenediamine N,N'-disuccinic acids is, for instance, commercially available under the tradename ssEDDS® from Palmer Research Laboratories.
  • Suitable amino carboxylates to be used herein include ethylene diamine tetra acetates, diethylene triamine pentaacetates, diethylene triamine pentaacetate (DTPA),N- hydroxyethylethylenediamine triacetates, nitrilotri-acetates, ethylenediamine tetrapropionates, triethylenetetraaminehexa-acetates, ethanol-diglycines, propylene diamine tetracetic acid (PDTA) and methyl glycine diacetic acid (MGDA), both in their acid form, or in their alkali metal, ammonium, and substituted ammonium salt forms.
  • PDTA propylene diamine tetracetic acid
  • MGDA methyl glycine diacetic acid
  • Particularly suitable amino carboxylates to be used herein are diethylene triamine penta acetic acid, propylene diamine tetracetic acid (PDTA) which is, for instance, commercially available from BASF under the trade name Trilon FS® and methyl glycine di-acetic acid (MGDA).
  • PDTA propylene diamine tetracetic acid
  • MGDA methyl glycine di-acetic acid
  • R 1 , R 2 , R 3 , and R 4 are independently selected from the group consisting of -H, alkyl, alkoxy, aryl, aryloxy, -Cl, -Br, -NO 2 , -C(O)R', and - SO 2 R''; wherein R' is selected from the group consisting of -H, -OH, alkyl, alkoxy, aryl, and aryloxy; R" is selected from the group consisting of alkyl, alkoxy, aryl, and aryloxy; and R 5 , R 6 , R 7 , and R 8 are independently selected from the group consisting of -H and alkyl.
  • Particularly preferred chelating agents to be used herein are ATMP, diethylene triamine methylene phosphonate, ethylene N,N'-disuccinic acid, diethylene triamine pantaacetate, glycine, salicylic acid, aspartic acid, glutamic acid, malonic acid or mixtures thereof and highly preferred is ATMP.
  • Suitable radical scavengers for use herein include the well-known substituted mono and dihydroxy benzenes and their analogs, alkyl and aryl carboxylates and mixtures thereof.
  • Preferred such radical scavengers for use herein include di-tert-butyl hydroxy toluene (BHT), hydroquinone, di-tert-butyl hydroquinone, mono-tert-butyl hydroquinone, tert-butyl-hydroxy anysole, benzoic acid, toluic acid, catechol, t-butyl catechol, benzylamine, 1,1,3-tris(2-methyl-4-hydroxy-5-t- butylphenyl) butane, n-propyl-gallate or mixtures thereof and highly preferred is di-tert-butyl hydroxy toluene.
  • Radical scavengers when used, are typically present herein in amounts ranging from 0.001% to 2% by weight of the total composition and
  • chelating agents especially ATMP, and/or radical scavengers allows to contribute to the safety profile of the compositions of the present invention suitable for pretreating a soiled colored fabric upon prolonged contact times before washing said fabric.
  • compositions of the present invention may further comprise up to 20%, preferably from 2% to 10% by weight of the total composition of a solvent or mixtures thereof. More particularly, it has been found that the addition of a solvent system comprising at least one hydrophobic solvent and at least one hydrophilic solvent, in a liquid composition according to the present invention, further contributes to the benefits of said composition, i.e., further improves the overall stain removal performance on various type of stains including greasy stains, enzymatic stains as well as bleachable stains.
  • Suitable-hydrophobic solvents to be used herein include terpenes like mono- and bicyclic monoterpenes, especially those of the hydrocarbon class, which include the terpinenes, terpinolenes, limonenes and pinenes and mixtures thereof. Highly preferred materials of this type are d-limonene, dipentene, alpha-pinene and/or beta-pinene.
  • Other hydrophobic solvents include all type of paraffins, both linear and not, containing from 2 to 20 carbons, preferably from 4 to 10, more preferably from 6 to 8. Preferred herein is octane.
  • Another hydrophobic solvent suitable to be used herein is benzyl alcohol. Particularly preferred hydrophobic solvents to be used herein include d-limonene, dipentene, alpha-pinene, beta-pinene, octane, benzyl alcohol, or mixtures thereof.
  • Suitable hydrophilic solvents to be used herein include alkoxylated aliphatic alcohols like methoxy propanol, ethoxy propanol, propoxy propanol, buthoxy propanol as well as alkoxylated glycols like ethoxy-ethoxy-ethanol, aliphatic or aromatic alcohols like ethanol, propanol, as well as glycols like propanediol or mixtures thereof.
  • Polymeric soil release agents are characterized by having both hydrophilic segments, to hydrophilize the surface of hydrophobic fibres, such as polyester and nylon, and hydrophobic segments, to deposit upon hydrophobic fibres and remain adhered thereto through completion of washing and rinsing cycles and, thus, serve as an anchor for the hydrophilic segments. This can enable stains occurring subsequent to treatment with the soil release agent to be more easily cleaned in later washing procedures.
  • the polymeric soil release agents useful herein especially include those soil release agents having: (a) one or more nonionic hydrophile components consisting essentially of (i) polyoxyethylene segments with a degree of polymerization of at least 2, or (ii) oxypropylene or polyoxypropylene segments with a degree of polymerization of from 2 to 10, wherein said hydrophile segment does not encompass any oxypropylene unit unless it is bonded to adjacent moieties at each end by ether linkages, or (iii) a mixture of oxyalkylene units comprising oxyethylene and from 1 to about 30 oxypropylene units wherein said mixture contains a sufficient amount of oxyethylene units such that the hydrophile component has hydrophilicity great enough to increase the hydrophilicity of conventional polyester synthetic fiber surfaces upon deposit of the soil release agent on such surface, said hydrophile segments preferably comprising at least about 25% oxyethylene units and more preferably, especially for such components having about 20 to 30 oxypropylene units, at least about 50% oxyethylene units; or
  • the polyoxyethylene segments of (a)(i) will have a degree of polymerization of from about 1 to about 200, although higher levels can be used, preferably from 3 to about 150, more preferably from 6 to about 100.
  • Suitable oxy C 4 -C 6 alkylene hydrophobe segments include, but are not limited to, end-caps of polymeric soil release agents such as MO 3 S(CH 2 ) n OCH 2 CH 2 O-, where M is sodium and n is an integer from 4-6, as disclosed in U.S. Patent 4,721,580, issued January 26, 1988 to Gosselink.
  • Polymeric soil release agents useful in the present invention also include cellulosic derivatives such as hydroxyether cellulosic polymers, copolymeric blocks of ethylene terephthalate or propylene terephthalate with polyethylene oxide or polypropylene oxide terephthalate, and the like. Such agents are commercially available and include hydroxyethers of cellulose such as METHOCEL (Dow). Cellulosic soil release agents for use herein also include those selected from the group consisting of C 1 -C 4 alkyl and C 4 hydroxyalkyl cellulose; see U.S. Patent 4,000,093, issued December 28, 1976 to Nicol, et al.
  • Soil release agents characterized by poly(vinyl ester) hydrophobe segments include graft copolymers of poly(vinyl ester), e.g., C 1 -C 6 vinyl esters, preferably poly(vinyl acetate) grafted onto polyalkylene oxide backbones, such as polyethylene oxide backbones.
  • poly(vinyl ester) e.g., C 1 -C 6 vinyl esters
  • poly(vinyl acetate) grafted onto polyalkylene oxide backbones such as polyethylene oxide backbones.
  • Commercially available soil release agents of this kind include the SOKALAN type of material, e.g., SOKALAN HP-22, available from BASF (West Germany).
  • One type of preferred soil release agent is a copolymer having random blocks of ethylene terephthalate and polyethylene oxide (PEO) terephthalate.
  • the molecular weight of this polymeric soil release agent is in the range of from about 25,000 to about 55,000. See U.S. Patent 3,959,230 to Hays, issued May 25, 1976 and U.S. Patent 3,893,929 to Basadur issued July 8, 1975.
  • Another preferred polymeric soil release agent is a polyester with repeat units of ethylene terephthalate units which contains 10-15% by weight of ethylene terephthalate units together with 90-80% by weight of polyoxyethylene terephthalate units, derived from a polyoxyethylene glycol of average molecular weight 300-5,000.
  • this polymer include the commercially available material ZELCON 5126 (from Dupont) and MILEASE T (from ICI). See also U.S. Patent 4,702,857, issued October 27, 1987 to Gosselink.
  • Another preferred polymeric soil release agent is a sulfonated product of a substantially linear ester oligomer comprised of an oligomeric ester backbone of terephthaloyl and oxyalkyleneoxy repeat units and terminal moieties covalently attached to the backbone.
  • These soil release agents are described fully in U.S. Patent 4,968,451, issued November 6, 1990 to J.J. Scheibel and E.P. Gosselink.
  • Other suitable polymeric soil release agents include the terephthalate polyesters of U.S. Patent 4,711,730, issued December 8, 1987 to Gosselink et al, the anionic end-capped oligomeric esters of U.S. Patent 4,721,580, issued January 26, 1988 to Gosselink, and the block polyester oligomeric compounds of U.S. Patent 4,702,857, issued October 27, 1987 to Gosselink.
  • Preferred polymeric soil release agents also include the soil release agents of U.S. Patent 4,877,896, issued October 31, 1989 to Maldonado et al, which discloses anionic, especially sulfoaroyl, end-capped terephthalate esters.
  • Still another preferred soil release agent is an oligomer with repeat units of terephthaloyl units, sulfoisoterephthaloyl units, oxyethyleneoxy and oxy-1,2-propylene units.
  • the repeat units form the backbone of the oligomer and are preferably terminated with modified isethionate end-caps.
  • a particularly preferred soil release agent of this type comprises about one sulfoisophthaloyl unit, 5 terephthaloyl units, oxyethyleneoxy and oxy-1,2-propyleneoxy units in a ratio of from about 1.7 to about 1.8, and two end-cap units of sodium 2-(2-hydroxyethoxy)-ethanesulfonate.
  • Said soil release agent also comprises from about 0.5% to about 20%, by weight of the oligomer, of a crystalline-reducing stabilizer, preferably selected from the group consisting of xylene sulfonate, cumene sulfonate, toluene sulfonate, and mixtures thereof.
  • a crystalline-reducing stabilizer preferably selected from the group consisting of xylene sulfonate, cumene sulfonate, toluene sulfonate, and mixtures thereof.
  • soil release agents will generally comprise from about 0.01% to about 10.0%, by weight, of the detergent compositions herein, typically from about 0.1% to about 5%, preferably from about 0.2% to about 3.0%.
  • compositions of the present invention may also include one or more materials effective for inhibiting the transfer of dyes from one dyed surface to another during the cleaning process.
  • dye transfer inhibiting agents include polyvinyl pyrrolidone polymers, polyamine N-oxide polymers, copolymers of N-vinylpyrrolidone and N-vinylimidazole, manganese phthalocyanine, peroxidases, and mixtures thereof. If used, these agents typically comprise from about 0.01% to about 10% by weight of the composition, preferably from about 0.01% to about 5%, and more preferably from about 0.05% to about 2%.
  • Preferred polyamine N-oxides are those wherein R is a heterocyclic group such as pyridine, pyrrole, imidazole, pyrrolidine, piperidine and derivatives thereof.
  • the N-O group can be represented by the following general structures: wherein R 1 , R 2 , R 3 are aliphatic, aromatic, heterocyclic or alicyclic groups or combinations thereof; x, y and z are 0 or 1; and the nitrogen of the N-O group can be attached or form part of any of the aforementioned groups.
  • the amine oxide unit of the polyamine N-oxides has a pKa ⁇ 10, preferably pKa ⁇ 7, more preferred pKa ⁇ 6.
  • Any polymer backbone can be used as long as the amine oxide polymer formed is water-soluble and has dye transfer inhibiting properties.
  • suitable polymeric backbones are polyvinyls, polyalkylenes, polyesters, polyethers, polyamide, polyimides, polyacrylates and mixtures thereof. These polymers include random or block copolymers where one monomer type is an amine N-oxide and the other monomer type is an N-oxide.
  • the amine N-oxide polymers typically have a ratio of amine to the amine N-oxide of 10:1 to 1:1,000,000. 1:1,000,000.
  • the number of amine oxide groups present in the polyamine oxide polymer can be varied by appropriate copolymerization or by an appropriate degree of N-oxidation.
  • the polyamine oxides can be obtained in almost any degree of polymerization. Typically, the average molecular weight is within the range of 500 to 1,000,000; more preferred 1,000 to 500,000; most preferred 5,000 to 100,000. This preferred class of materials can be referred to as "PVNO".
  • the most preferred polyamine N-oxide useful in the detergent compositions herein is poly(4-vinylpyridine-N-oxide) which as an average molecular weight of about 50,000 and an amine to amine N-oxide ratio of about 1:4.
  • Copolymers of N-vinylpyrrolidone and N-vinylimidazole polymers are also preferred for use herein.
  • the PVPVI has an average molecular weight range from 5,000 to 1,000,000, more preferably from 5,000 to 200,000, and most preferably from 10,000 to 20,000. (The average molecular weight range is determined by light scattering as described in Barth, et al., Chemical Analysis , Vol 113.
  • the PVPVI copolymers typically have a molar ratio of N-vinylimidazole to N-vinylpyrrolidone from 1:1 to 0.2:1, more preferably from 0.8:1 to 0.3:1, most preferably from 0.6:1 to 0.4:1. These copolymers can be either linear or branched.
  • compositions may also employ a polyvinylpyrrolidone ("PVP") having an average molecular weight of from about 5,000 to about 400,000, preferably from about 5,000 to about 200,000, and more preferably from about 5,000 to about 50,000.
  • PVP's are known to persons skilled in the detergent field; see, for example, EP-A-262,897 and EP-A-256,696, incorporated herein by reference.
  • Compositions containing PVP can also contain polyethylene glycol (“PEG”) having an average molecular weight from about 500 to about 100,000, preferably from about 1,000 to about 10,000.
  • PEG polyethylene glycol
  • the ratio of PEG to PVP on a ppm basis delivered in wash solutions is from about 2:1 to about 50:1, and more preferably from about 3:1 to about 10:1.
  • suds boosters such as C 10 -C 16 alkanolamides can be incorporated into the compositions, typically at 1%-10% levels.
  • the C 10 -C 14 monoethanol and diethanol amides illustrate a typical class of such suds boosters.
  • Use of such suds boosters with high sudsing adjunct surfactants such as the amine oxides, betaines and sultaines noted above is also advantageous.
  • soluble magnesium salts such as MgCl 2 , MgSO 4 , and the like, can be added at levels of, for example, 0.1%-2%, to provide additional suds and to enhance grease removal performance.
  • optical brighteners fluorescent whitening agents or other brightening or whitening agents known in the art can be incorporated in the instant compositions when they are designed for fabric treatment or laundering, at levels typically from about 0.05% to about 1.2%, by weight, of the detergent compositions herein.
  • Commercial optical brighteners which may be useful in the present invention can be classified into subgroups, which include, but are not necessarily limited to, derivatives of stilbene, pyrazoline, coumarin, carboxylic acids, methinecyanines, dibenzothiophene-5,5-dioxide, azoles, 5-and 6-membered-ring heterocyclic brighteners, this list being illustrative and non-limiting. Examples of such brighteners are disclosed in "The Production and Application of Fluorescent Brightening Agents", M. Zahradnik, Published by John Wiley & Sons, New York (1982).
  • optical brighteners which are useful in the present compositions are those identified in U.S. Patent 4,790,856, issued to Wixon on December 13, 1988. These brighteners include the PHORWHITE series of brighteners from Verona. Other brighteners disclosed in this reference include: Tinopal UNPA, Tinopal CBS and Tinopal 5BM; available from Ciba-Geigy; Artic White CC and Artic White CWD, available from Hilton-Davis, located in Italy; the 2-(4-styryl-phenyl)-2H-naphthol[1,2-d]triazoles; 4,4'-bis- (1,2,3-triazol-2-yl)-stil- benes; 4,4'-bis(styryl)bisphenyls; and the aminocoumarins.
  • these brighteners include 4-methyl-7-diethyl- amino coumarin; 1,2-bis(-benzimidazol-2-yl)ethylene; 2,5-bis(benzoxazol-2-yl)thiophene; 2-styrylnapth-[1,2-d]oxazole; and 2-(stilbene-4-yl)-2H-naphtho- [1,2-d]triazole. See also U.S. Patent 3,646,015, issued February 29, 1972 to Hamilton. Anionic brighteners are typically preferred herein.
  • compositions described herein may also be used as a laundry detergent or as a laundry detergent booster and as a household cleaner in the bathroom or in the kitchen.
  • compositions of the present invention suitable for pretreating fabrics can be packaged in a variety of containers including conventional bottles, bottles equipped with roll-on, sponge, brusher or sprayers.
  • compositions I II III IV V VI Dobanol® 45-7 6.4 6.4 6.4 1.5 12.0 6.0
  • Dilauroyl peroxide 0.5 - - 1.0 - 2.0 Ethoxylated 15-18 tetraethylenepentamine 0.5 0.5 0.5 0.2 1.0 0.7 Limonene D(+) - - 0.5 0.1 0.5 1.0
  • Benzoyl alcohol - - 2.0 1.0 - - 1-methoxy-2 propanol - - 5.0 - 2.0
  • Excellent stain removal performance is obtained on a variety of stains including greasy/oily stains like clay, dirty motor oil, make-up, lipstick, carotenoid-type stains like spaghetti sauce, bleachable stains like tea and enzymatic stains like grass, blood, when pretreating soiled fabrics with any of the compositions I to VI, as described above, e.g., when leaving such a composition to act onto the fabrics for a contact period of about 5 minutes, before rinsing said fabrics with water or washing with a conventional detergent composition like Tide® powder at a dilution level of, for example, 1 to 400.

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Claims (13)

  1. Un procédé de blanchiment de tissu utilisant une composition liquide comprenant de 2 % à 15 % en poids de la composition totale d'un agent de blanchiment peroxygène, et d'un agent de dispersion des salissures choisi dans le groupe constitué par
    (1) les monoamines éthoxylées de formule : (X―L)―N―(R2)2
    (2) les diamines éthoxylées de formule :
    Figure 00530001
       ou (X - L -)2- N - R1 - N - (R2)2
    (3) les polyamines éthoxylées de formule :
    Figure 00530002
    (4) les polymères d'amines éthoxylées de formule générale :
    Figure 00540001
    et (5) les mélanges de ces substances,
    où A1 représente
    Figure 00540002
    Figure 00540003
    R représente H ou un radical alkyle ou hydroxyalkyle en C1-C4 ; R1 représente un radical alkylène, hydroxyalkylène, alkénylène, arylène ou alkarylène en C2-C12, ou un fragment oxyalkylène en C2-C3 comportant de 2 à 20 unités d'oxyalkylène à condition qu'il n'y ait pas de liaisons O ― N ; chaque R2 représente un radical alkyle ou hydroxyalkyle en C1-C4, le fragment ― L ― X, ou bien deux R2 ensemble constituent le fragment ― (CH2)r ― A2 ― (CH2)s ―, où A2 représente ― O ― ou ― CH2 ―, r est 1 ou 2, s est 1 ou 2, et r+s est 3 ou 4 ; X représente un groupe non ionique, un groupe anionique ou leurs mélanges ; R3 représente un groupe alkyle, hydroxyalkyle, alkényle, aryle, ou alkaryle substitué en C3-C12 avec des sites de substitution p ; R4 représente un radical alkylène, hydroxyalkylène, alkenylène, arylène ou alkarylène en C1-C12, ou un fragment oxyalkylène en C2-C3 comportant de 2 à 20 unités d'oxyalkylène à condition qu'il n'y ait pas de liaisons O ― O ou O ― N ; L représente une chaíne hydrophile qui contient le fragment polyoxyalkylène ―[(R5O)m(CH2CH2O)n]―, où R5 représente un radical alkylène ou hydroxyalkylène en C3-C4 et m et n sont des chiffres de tels que le fragment ―(CH2CH2O)n― est constitué d'au moins 50 % en poids dudit fragment polyoxyalkylène ; pour lesdites monoamines, m est compris entre 0 et 4, et n est égal ou supérieur à 12 ; pour lesdites diamines, m est compris entre 0 et 3, et n est égal ou supérieur à 6 lorsque R1 représente un radical alkylène, hydroxyalkylène, ou alkénylène en C2-C3, et égal ou supérieur à 3 lorsque R1 n'est pas un radical alkylène, hydroxyalkylène ou alkénylène en C2-C3; pour lesdites polyamines et les polymères aminés, m est compris entre 0 et 10 et n est égal ou supérieur à 3 ; p est compris entre 3 et 8 ; q est 1 ou 0 ; t est 1 ou 0, à condition que t soit égal à 1 lorsque q est égal à 1 ; w est 1 ou 0 ; la somme x + y + z est égale ou supérieur à 2 ; et la somme y + z est égale ou supérieur à 2, ledit procédé comprenant les étapes d'application de ladite composition sous sa forme pure sur au moins une partie du tissu, avant lavage dudit tissu.
  2. Un procédé selon la revendication 1 dans lequel on laisse ladite composition en contact avec ledit tissu pendant 1 minute à 1 heure, de préférence de 1 à 30 minutes, et encore plus préférablement de 2 minutes à 10 minutes, avant lavage dudit tissu.
  3. Une composition de blanchiment liquide adaptée au prétraitement des tissus, comprenant de 2 % à 15 % en poids de la composition totale d'un agent de blanchiment peroxygéné, d'un agent tensioactif et d'un agent de dispersion des salissures choisi dans le groupe constitué par
    (1) les monoamines éthoxylées de formule : (X―L―)―N―(R2)2
    (2) les diamines éthoxylées de formule:
    Figure 00560001
       ou (X - L -)2- N - R1 - N - (R2)2
    (3) les polyamines éthoxylées de formule:
    Figure 00560002
    (4) les polymères d'amines éthoxylées de formule générale :
    Figure 00560003
    et (5) les mélanges de ces substances,
    Où A1 représente
    Figure 00570001
    R représente H ou un radical alkyle ou hydroxyalkyle en C1-C4 ; R1 représente un radical alkylène, hydroxyalkylène, alkenylène, arylène ou alkarylène en C2-C12, ou un fragment oxyalkylène en C2-C3 comprenant de 2 à 20 unités d'oxyalkylène à condition qu'il n'y ait pas de liaisons O _ N ; chaque R2 représente un radical alkyle ou hydroxyalkyle en C1-C4, le fragment ― L ― X, ou bien deux R2 ensemble forment le fragment ― (CH2)r ― A2 ― (CH2)s ―, dans lequel A2 représente ― O ― ou ― CH2 ―, r est 1 ou 2, s est 1 ou 2, et r+s est 3 ou 4 ; X représente un groupe non ionique, un groupe anionique ou leurs mélanges ; R3 représente un radical alkyle, hydroxyalkyle, alkényle, aryle substitué en C3-C12, ou un groupe alkaryle avec des sites de substitution p ; R4 représente un radical alkylène, hydroxyalkylène, alkenylène, arylène ou alkarylène en C1-C12, ou un fragment oxyalkylène en C2-C3 comportant de 2 à 20 unités d'oxyalkylène à condition qu'il n'y ait pas de liaisons O ― O ou O ― N ; L est une chaíne hydrophile contenant le fragment polyoxyalkylène ―[(R5O)m(CH2CH2O)n]― où R5 représente un radical alkylène ou hydroxyalkylène en C3-C4 et m et n sont des chiffres tels que le fragment ―(CH2CH2O)n― est constitué d'au moins 50 % en poids dudit fragment polyoxyalkylène ; pour lesdites monoamines, m est compris entre 0 et 4, et n est égal ou supérieur à 12 ; pour lesdites diamines, m est compris entre 0 et 3, et n est égal ou supérieur à 6 lorsque R1 représente un radical alkylène, hydroxyalkylène, ou alkénylène en C2-C3, et égal ou supérieur à 3 lorsque R1 n'est pas un radical alkylène, hydroxyalkylène ou alkénylène en C2-C3 ; pour lesdits polyamines et les polymères aminés, m est compris entre 0 et 10 et n est égal ou supérieur à 3 ; p est compris entre 3 et 8 ; q est 1 ou 0 ; t est 1 ou 0, à condition que t soit égal à 1 lorsque q est égal à 1 ; w est 1 ou 0 ; la somme x + y + z est égale ou supérieure à 2 ; et la somme y + z est égale ou supérieure à 2, ladite composition étant formulée sous la forme soit d'une émulsion soit d'une micro-émulsion.
  4. Une composition selon la revendication 3, dans laquelle ledit agent de blanchiment peroxygèné est du peroxyde d'hydrogène ou une source hydrosoluble de celui-ci choisie de préférence parmi un percarbonate, un persilicate, un persulphate, un perborate, des peroxyacides, des hydroperoxydes, des peroxydes de diacyle et des mélanges de ces substances et est de préférence du peroxyde d'hydrogène, de l'hydroperoxyde tert-butylique, de l'hydroperoxyde de cumyle, du 2,4,4-triméthylpentyl-2-hydroperoxyde, du di-isopropylbenzène-monohydroperoxyde, de l'hydroperoxyde de tert-amyle, du 2,5-diméthyl-hexane-2,5-dihydroperoxyde, du peroxyde de dilauroyle, du péroxyde de didécanoyle, du peroxyde de dimyristoyle, ou des mélanges de ces substances.
  5. Une composition selon les revendications 3 ou 4 dans laquelle ladite composition comprend 2 % à 15 % en poids de la composition totale dudit agent de blanchiment peroxygèné, ou des mélanges de ces substances, de préférence 2 % à 12 %, plus préférablement 2 % à 10 %, et le plus préférablement 2 % à 8 %.
  6. Une composition selon l'une quelconque des revendications 3 à 5 dans laquelle ledit agent de dispersion des salissures est un polymère d'amine éthoxylée, où R1 représente un radical alkylène en C2-C3, de préférence l'éthylène, et L est constitué en totalité du fragment -(CH2CH2O)n- et n est égal ou supérieur à 12.
  7. Une composition selon la revendication 6 dans laquelle ledit polymère d'amine éthoxylée est une polyéthylène-amine éthoxylée ayant un poids moléculaire de 140 à 310 avant éthoxylation.
  8. Une composition selon la revendication 6 dans laquelle ledit polymère d'amine éthoxylée est une polyéthylène-imine éthoxylée ayant un poids moléculaire de 600 à 1800 avant éthoxylation.
  9. Une composition selon l'une quelconque des revendications 3 à 8, dans laquelle ladite composition comprend de 0,01 % à 20 % en poids de la composition totale dudit agent de dispersion des salissures, ou des mélanges de ces substances, de préférence de 0,1 % à 10 %, plus préférablement de 0,2 % à 4 %, et le plus préférablement de 0,5 % à 2 %.
  10. Une composition selon l'une quelconque des revendications 3 à 9 dans laquelle ladite composition comprend en outre un activateur de blanchiment, de préférence à hauteur de 0,01 % à 20 % en poids de la composition totale, plus préférablement de 1 % à 10 %, et le plus préférablement de 3 % à 7 %.
  11. Une composition selon la revendication 10 dans laquelle ledit activateur de blanchiment est choisi parmi le citrate d'acétyl-triéthyle, la tétracétyl éthylène diamine, le 3,5,5 triméthyl hexanoyloxybenzène sulfonate de sodium, l'acide diperoxy-dodécanoïque, le nonylamide de l'acide peroxyadipique, le N-nonanoyloxybenzènesulfonate, le N-acyle caprolactame, le caprolactame de benzoyle substitué et non substitué, le caprolactame d'octanoyle, le caprolactame de nonanoyle, le caprolactame d'hexanoyle, le caprolactame de décanoyle, le caprolactame d'undecenoyle, le caprolactame de formyle, le caprolactame d'acétyle, le caprolactame de propanoyle, le caprolactame de butanoyle, le caprolactame de pentanoyle et des mélanges de ces substances, et est de préférence un citrate d'acétyl-triéthyle.
  12. Une composition selon l'une quelconque des revendications 3 à 11, dans laquelle ladite composition est aqueuse et a un pH allant jusqu'à 6, de préférence de 1 à 5, plus préférablement de 2 à 5, et le plus préférablement de 3 à 5.
  13. Une composition selon l'une quelconque des revendications 3 à 12 précédentes dans laquelle ladite composition comprend au moins un agent tensioactif hydrophobe ayant un rapport hydro-lipophile allant jusqu'à 10, ou des mélanges de ces substances, de préférence inférieur à 10, plus préférablement inférieur à 9, et au moins un agent tensioactif hydrophile ayant un rapport hydro-lipophile supérieur à 10, ou des mélanges de ces substances, de préférence supérieur à 10,5, plus préférablement supérieur à 11.
EP96870116A 1996-03-04 1996-09-13 Procédé de prétraitement pour le lavage du ligne et compositions de blanchiment Expired - Lifetime EP0794245B1 (fr)

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EP96870116A EP0794245B1 (fr) 1996-03-04 1996-09-13 Procédé de prétraitement pour le lavage du ligne et compositions de blanchiment
AT96870116T ATE244752T1 (de) 1996-03-04 1996-09-13 Wäsche-vorbehandlungsverfahren und bleichmittelzusammensetzungen
DE69629006T DE69629006T2 (de) 1996-03-04 1996-09-13 Wäsche-Vorbehandlungsverfahren und Bleichmittelzusammensetzungen
ES96870116T ES2202424T3 (es) 1996-03-04 1996-09-13 Proceso de tratamiento de las prendas antes del lavado y composiciones blanqueadoras.
SK1225-98A SK122598A3 (en) 1996-03-04 1997-02-26 Laundry pretreatment process and bleaching compositions
BR9708168A BR9708168A (pt) 1996-03-04 1997-02-26 Processo de pré-tratamento de lavagem de roupas e composições alvejantes
PCT/US1997/003238 WO1997032962A1 (fr) 1996-03-04 1997-02-26 Procede de pretraitement de lessive et compositions blanchissantes
CN97194234A CN1265135A (zh) 1996-03-04 1997-02-26 洗衣预处理方法和漂白组合物
RU98118379/04A RU2168578C2 (ru) 1996-03-04 1997-02-26 Процесс предварительной обработки ткани перед стиркой и отбеливающий состав
AU19831/97A AU1983197A (en) 1996-03-04 1997-02-26 Laundry pretreatment process and bleaching compositions
KR1019980706966A KR19990087531A (ko) 1996-03-04 1997-02-26 세탁 전처리 방법 및 표백 조성물
JP09531855A JP2000514846A (ja) 1996-03-04 1997-02-26 洗濯前処理法および漂白組成物
IL12603997A IL126039A0 (en) 1996-03-04 1997-02-26 Laudry pretreatment process and bleaching compositions
CA002247969A CA2247969A1 (fr) 1996-03-04 1997-02-26 Procede de pretraitement de lessive et compositions blanchissantes
TR1998/01744T TR199801744T2 (xx) 1996-03-04 1997-02-26 �ama��r �n-muamele i�lemi ve a�artma bile�imleri.
PL97330913A PL330913A1 (en) 1996-03-04 1997-02-26 Method of pretreating a laundry before washing and bleaching agents
CZ982793A CZ279398A3 (cs) 1996-03-04 1997-02-26 Způsob předpírání a bělící prostředky
US09/142,395 US6310025B1 (en) 1996-03-04 1997-02-26 Laundry pretreatment process and bleaching compositions
ARP970100858A AR006096A1 (es) 1996-03-04 1997-03-04 Proceso para blanquear una tela con una composicion liquida y una composicion blanqueadora liquida para pretratar telas mediante dicho proceso
IDP970672A ID16124A (id) 1996-03-04 1997-03-04 Proses perlakuan awal cucian dan komposisi-komposisi pemutih
NO984060A NO984060L (no) 1996-03-04 1998-09-03 FremgangsmÕte for vaskeforbehandling og sammensetning for bleking

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EP96870023 1996-03-04
EP96870023A EP0735131A3 (fr) 1995-03-27 1996-03-04 Utilisation des oxydes d'amine tensioactifs ayant une capacité améliorée pour l'enlèvement des taches
EP96202104A EP0823474A1 (fr) 1996-07-24 1996-07-24 Peracides, compositions aqueuses stables contenant ces peracides et procédé pour la formation de ces peracides
EP96202104 1996-07-24
EP96202168A EP0822183A3 (fr) 1996-07-31 1996-07-31 Procédé pour la préparation de peracides et compositions les contenant
EP96202168 1996-07-31
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CZ279398A3 (cs) 1999-02-17
RU2168578C2 (ru) 2001-06-10
PL330913A1 (en) 1999-06-07
SK122598A3 (en) 1999-05-07
DE69629006D1 (de) 2003-08-14
CA2247969A1 (fr) 1997-09-12
AU1983197A (en) 1997-09-22
DE69629006T2 (de) 2004-04-22
JP2000514846A (ja) 2000-11-07
ATE244752T1 (de) 2003-07-15
EP0794245A1 (fr) 1997-09-10
NO984060L (no) 1998-11-03
ES2202424T3 (es) 2004-04-01
ID16124A (id) 1997-09-04
WO1997032962A1 (fr) 1997-09-12
NO984060D0 (no) 1998-09-03
TR199801744T2 (xx) 2004-12-21
CN1265135A (zh) 2000-08-30
BR9708168A (pt) 1999-07-27
IL126039A0 (en) 1999-05-09

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