MXPA01009728A - Laundry detergent compositions with certain cationically charged dye maintenance polymers. - Google Patents

Laundry detergent compositions with certain cationically charged dye maintenance polymers.

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Publication number
MXPA01009728A
MXPA01009728A MXPA01009728A MXPA01009728A MXPA01009728A MX PA01009728 A MXPA01009728 A MX PA01009728A MX PA01009728 A MXPA01009728 A MX PA01009728A MX PA01009728 A MXPA01009728 A MX PA01009728A MX PA01009728 A MXPA01009728 A MX PA01009728A
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Mexico
Prior art keywords
mixtures
alkyl
polymer
hydrogen
copolymer
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Application number
MXPA01009728A
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Spanish (es)
Inventor
Eugene Paul Gosselink
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Procter & Gamble
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Publication of MXPA01009728A publication Critical patent/MXPA01009728A/en

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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0021Dye-stain or dye-transfer inhibiting compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/28Heterocyclic compounds containing nitrogen in the ring
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/26Organic compounds containing nitrogen
    • C11D3/30Amines; Substituted amines ; Quaternized amines
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3723Polyamines or polyalkyleneimines
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3769(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3746Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/3769(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines
    • C11D3/3773(Co)polymerised monomers containing nitrogen, e.g. carbonamides, nitriles or amines in liquid compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3792Amine oxide containing polymers

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The present invention relates to laundry detergent compositions providing dye protection benefits to fabric comprising: a) from about 4 % to about 70 % by weight, of a surfactant; b) from about 0.01 % by weight, of a dye maintenance polymer or oligomer, said polymer or copolymer comprising one or more linearly polymerizing monomers, cyclically polymerizing monomers, and mixtures thereof; and c) the balance carriers and adjunct ingredients.

Description

DETERGENT COMPOSITIONS FOR LAUNDRY WITH CERTAIN DOWNLOADED COLORING CONSERVATION POLYMERS CANONICALLY FIELD OF THE INVENTION The present invention relates to compositions, either in liquid form or in granule form, for use in laundry applications, in which the compositions comprise certain dye preservation polymers having a positive net charge. Compositions comprising the dye preservation polymers of this invention impart appearance and integrity benefits to fabrics and textiles washed in wash solutions formed from said compositions.
BACKGROUND OF THE INVENTION It is well known, of course, that alternating cycles of use and washing of fabrics and textiles, such as garment items and used clothing accessories, will inevitably adversely affect the appearance and integrity of the fabric and the textile materials used. and washed in this way. Fabrics and textiles simply wear out over time and with use. The washing of fabrics and textiles is necessary to remove dirt and stains that accumulate in them during ordinary use. However, the washing operation itself, after many cycles, can accentuate and contribute to the deterioration of the integrity and appearance of said fabrics and textiles. The deterioration of the appearance and integrity of the fabrics can manifest itself in several ways. The short fibers are detached from spun and woven structures of fabrics / textiles by the mechanical action of washing. These loose fibers can form lint, lint or "balls" that are visible on the fabric surfaces and diminish the appearance of new product of the fabric. In addition, repeated washing of fabrics and textiles, especially laundry products containing bleach, can remove dye from fabrics and textiles and impart a worn, worn appearance as a result of decreased color intensity, and in many cases, as a result of changes in shades or shades of color. Given the above, there is clearly a growing need to identify materials that could be added to laundry products that would associate themselves with the fibers of the fabrics and textiles that are washed using said products and thus reduce or minimize the tendency of washed fabrics / textiles to deteriorate in appearance. Any such detergent additive materials should, of course, be able to benefit the appearance and integrity of the fabrics without unduly interfering with the stability of the laundry product to perform its designed function. The present invention is directed to the use of dye preservation polymers in laundry applications that function in this desired manner.
BRIEF DESCRIPTION OF THE INVENTION The present invention satisfies the aforementioned need because it has been discovered with surprise that the fabric to be treated, and subsequently re-treated with the compositions of the present invention, will resist fading and loss of color regardless of the circumstances, inter alia, to mechanical use and abrasion. In addition, the fabric that has not been treated may exhibit attenuated loss of fabric colorant by washing the laundry with the laundry detergent compositions of the present invention. The compositions of the present invention can take any information inter alia, heavy duty liquid (HDL), heavy duty granular (HDG), bars, pastes, thixotropic compositions. The first aspect of the present invention relates to laundry detergent compositions that provide dye protection benefits to fabrics comprising: a) from 4% to 70% of a surfactant which is preferably selected from the group consisting of non-surface active agents. ionic, anionic, cationic, amphoteric, switerionic and mixtures thereof, preferably at least one of the surfactants is an anionic surfactant; b) from 0.01 to 0.1% from about 0.5%, most preferably from about 0.8%, to about 10%, preferably to 8%, most preferably to 6%, most preferably to 5% by weight of a preservative polymer or oligomer of dye comprising at least one or more units having the formula: (I) Linear polymer units having the formula: wherein each R1 is independently a) hydrogen; b) C1-C4 alkyl; c) substituted or unsubstituted phenyl; d) substituted or unsubstituted benzyl; e) carbocyclic; f) heterocyclic; g) and their mixtures; each R2 is independently a) hydrogen; b) halogen; c) C 1 -C 4 alkyl d) C 1 -C 4 alkoxy; e) substituted or unsubstituted phenyl; f) substituted or unsubstituted benzyl; g) carbocyclic; h) heterocyclic; i) and their mixtures; each Z is independently a) hydrogen; B) hydroxyl; c) halogen; d) - (CH2) mR; wherein R is: i) hydrogen; I) hydroxyl iii) halogen; iv) nitrile; v) -OR3; vi) -O (CH2) nN (R3) 2; 20 vii) -0 (CH2) nN + (R3) 3? -; vii) -OCO (CH2) nN (R3) 2; ix) -OCO (CH2) nN + (R3) 3X; x) -NHCO (CH2) nN (R3) 2; xi) -NHCO (CH2) nN + (R3) 3? -; xii) - (CH2) nN (R3) 2; xiü) - (CH2) nN + (R3) 3X '; xiv) carbocyclic; xv) heterocyclic; xvi) nitrogen quaternary ammonium heterocycle; xvii) N-nitrogen oxide heterocycle; xvii) N-heterocyclic aromatic quaternary ammonium; xix) aromatic N-heterocyclic N-oxide; xx) -NHCHO; xxi) or their mixtures; each R3 is independently hydrogen, C-i alkyl Cβ, C2-Cs hydroxyalkyl and mixtures thereof; X is a water soluble anion; the index n is from 0 to 6 e) - (CH2) mCOR 'in which R' is i) -OR3; ii) -O (CH2) nN (R3) 2; iii) -O (CH2) nN + (R3) 3? -; iv) -NR3 (CH2) nN (R3) 2; v) -NR3 (CH2) nN + (R3) 3? -; vi) - (CH2) nN (R3) 2; vii) - (CH2) nN + (R3) 3? -; viii) or their mixtures; each R3 is independently hydrogen, C8 alkyl) C2-Cd hydroxyalkyl, and mixtures thereof; X is a water soluble anion; the index n is from 0 to 6; f) and their mixtures; the index m is from 0 to 6; II) the cyclic units derived from cyclic polymerization monomers having the formula: R4 X R4- ± R5 I R5 wherein R4 is independently an olefin comprising a unit that is capable of propagating the polymerization in addition to forming a cyclic residue with an adjacent R4 unit; R5 is linear or branched alkyl of C? -C12"benzyl, substituted benzyl and mixtures thereof; X is a water soluble anion; and III) their mixtures; with the proviso that the polymer or copolymer has a net cationic charge; and wherein the dye preservation polymer is not a polyethyleneimine or its alkoxylated derivative; and b) balance vehicles other adjunct ingredients.
In addition to the surfactant and dye preservation polymer of this invention, the laundry detergent compositions herein comprise from 0.01% to 80% by weight of an organic or inorganic builder and other conventional laundry detergent products. In this aspect of the method, the present invention relates to the washing or treatment of fabrics and textile materials in aqueous solutions for washing, rinsing, or treatment formed from effective amounts of any of the detergent compositions, fabric softening compositions, or treatments of aqueous solutions as described herein, or formed from the individual components of said compositions. The washing of fabrics and textiles in said washing, rinsing and / or treatment solutions, followed by drying, imparts fabric appearance benefits to articles of fabrics and textiles treated in this manner. Such benefits may include improved overall appearance, ball / lint reduction, anti-fading, improved abrasion resistance, and / or improved softness. It has been surprisingly determined that the dye preservation polymers of this invention impart fabric appearance and integrity benefits that are larger than the benefits that are achieved by a corresponding amount of any component alone. These and other objects, features and advantages will become apparent to those skilled in the art from the reading of the following detailed description and the appended claims. All percentages, ratios and proportions herein are by weight, unless otherwise specified. All temperatures are in degrees Celsius (° C) unless otherwise specified. All the cited documents are included, a considerable part, in the present by way of reference.
DETAILED DESCRIPTION OF THE INVENTION As noted, when the fabrics or textiles are washed in solutions comprising the dye preservation polymers of the present invention the appearance and integrity of the fabrics are improved. The dye preservation polymers can be added to wash solutions by incorporating them into a detergent composition, a fabric softener, or by adding them separately to the washing solution. The dye preservation polymers are described herein primarily as liquid or granular detergent additives but the present invention does not mean that it is limited in that way. The dye preservation polymers, the detergent compositions, the optional ingredients for said compositions and methods for using said compositions are described in detail below. All percentages are by weight unless otherwise specified.
Dye preservation polymers The compositions and systems of the present invention comprise from about 0.1%, preferably about 1%, most preferably about 2%, most preferably from 3% to about 10%, preferably to 7%, most preferably at 5% by weight, of a polymer, copolymer or its mixture, in which the polymer or copolymer comprises at least one cationically charged unit, inter alia, quaternary ammonium portion or unit that can form a cationic charge in situ, inter alia, primary amine portion. Put another way, the oligomer, polymer, or copolymer resulting from the monomer units described hereunder must have a net cationic charge. The load can be distributed among any of the units described herein. The dye preservation polymers of this invention can be used in any fabric washing process and provide certain appearance benefits to fabrics washed in those processes. Said fabrics appearance benefits may include, for example, improved overall appearance of the washed fabrics, reduction of ball and lint formation, protection against color wear, improved abrasion resistance, etc. The colorant preservation polymers that are used in the compositions and methods herein can provide such fabric appearance benefits when included in washing or rinsing products.
As be apparent to those skilled in the art, an oligomer is a molecule consisting of only a few monomer units while the polymers comprise considerably more monomer units. For the present invention, the oligomers are defined as molecules having an average molecular weight below 1, 000, and the polymers are molecules having an average molecular weight greater than 1,000. The copolymers are polymers or oligomers in which two or more dissimilar monomers have been polymerized simultaneously or sequentially. The copolymers of the present invention can include, for example, acrylamide copolymerizable with polymers or oligomers with dimethyldiallylammonium chloride, vinylamine with vinyl alcohol, etc. Cationic polymers in general and their manufacturing methods are known. For example, a detailed description of cationic polymers can be found in an article by M. Fred Hoover which was published in the Journal of Macromolecular Science-Chemistry, A4 (6), pp 1327-1417 in October 1970. The full description of the Hoover's article is incorporated herein by reference. The dye preservation polymers of this invention be better understood when read in light of the Hoover article, the present disclosure and the examples herein.
I) Linear Polymer Units The polymers or copolymers of the present invention may comprise one or more linear polymer units having the formula: wherein R, R2, and Z are defined later herein. Preferably, the linear polymeric units are formed from linear polymerization monomers. Linear polymerization monomers are defined herein as monomers which under standard polymerization conditions result in a linear polymer chain or alternatively propagate the polymerization in a linear manner. The linear polymerization monomers in the present invention have the formula: however, those skilled in the art will recognize that many units of linear monomers are introduced indirectly, inter alia, vinylamine units, vinyl alcohol units and not by linear polymerization monomers. For example, the vinyl acetate monomers, once incorporated into the main trunk, are hydrolyzed to form vinyl alcohol units. For the purposes of the present invention, the linear polymer units may be introduced directly, i.e., by linear polymerization units, or indirectly, i.e. by a precursor as in the case of the vinyl alcohol mentioned herein. Each R 1 is independently hydrogen, C 1 -C 4 alkyl, substituted or unsubstituted phenyl, substituted or unsubstituted benzyl, carbocyclic, heterocyclic and mixtures thereof. Preferably R1 is hydrogen, C1-C4 alkyl, phenyl, and mixtures thereof, most preferably hydrogen and methyl. Each R 2 is independently hydrogen, halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, substituted or unsubstituted phenyl, substituted or unsubstituted benzyl, carbocyclic, heterocyclic and mixtures thereof. The preferred R 2 is hydrogen, C 1 -C 4 alkyl and mixtures thereof. Each Z is independently hydrogen; hydroxyl; halogen; - (CH2) mR, in which R is hydrogen, hydroxyl, halogen, nitrile, -OR3, -O (CH2) nN (R3) 2, -0 (CH2) nN + (R3) 3? -, -OCO (CH2) ) nN (R3) 2, -OCO (CH2) nN + (R3) 3? -, -NHCO (CH2) nN (R3) 2, -NHCO (CH2) nN + (R3) 3X ", - (CH2) nN (R3) ) 2, - (CH ^ nN ^ R3) ^ -, a non-aromatic nitrogen heterocycle comprises a quaternary ammonium ion, a non-aromatic nitrogen heterocycle comprises a portion of N-oxide, an aromatic nitrogen containing heterocyclic in which one or more of the nitrogen atoms is quaternized, an aromatic nitrogen containing heterocycle in which at least one nitrogen is an N-oxide, -NHCHO (formamide) or mixtures thereof, wherein each R3 is independently hydrogen, alkyl of Ci-Cs, C2-C8 hydroxyalkyl, and mixtures thereof, X is a water-soluble anion, the n-index is 0 to 6, carbocyclic, heterocyclic or mixtures thereof, - (CH2) mCOR \ in which R ' is -OR3, -O (CH2) nN (R3) 2, -O (CH2) nN + (R3) 3? -, -NR3 (CH2) nN (R3) 2, -NR3 (CH2) nN + (R3) 3? -, - (CH2) nN (R3) 2, - (CH2) nN + (R3) 3 X ", or mixtures thereof, in which R3, X and n are equal as defined above; a preferred Z is -O (CH2) nN + (R3) 3X ", in which the index n is from 2 to 4. The index m is from 0 to 6, preferably 0 to 2, most preferably 0. Non-limiting examples of linear polymerization monomers comprising a heterocyclic Z unit includes 1-vinyl-2-pyrrolidone, 1-vinylimidazole, 2-vinyl-1,3-dioxolane, 1,2-epoxide of 4-vinyl-1-cyclohexene and 2-vinylpyridine. The polymers and copolymers of the present invention comprise Z units that have a cationic charge or that result in a unit that forms a cationic charge in situ When the copolymers of the present invention comprise more than one Z unit, for example Z1 units, Z2, ... Zn, at least about 1% of the monomers comprising the copolymers will comprise a cationic unit.The preferred cationic units include -0 (CH2) nN + (R3) 3X "and - (CH2) nN + (R3 ) 3X. "When the copolymers of the present invention are formed of two monomers, Z1 and Z2 the ratio from Z1 to Z2 is preferably from about 9: 1 to about 1: 9.
A non-limiting example of a Z unit that can be made to form a cationic charge in situ is the unit -NHCHO, formamide. The formulator can prepare a polymer or copolymer comprising formamide units some of which are subsequently hydrolyzed to form vinylamine equivalent. For example, the formulator can prepare a copolymer having the general formula: comprising a formamide unit and then subsequently treating the copolymer so that some of the formamide units are hydrolyzed to form a copolymer comprising vinylamine units, the copolymer having the formula: wherein Z can be a cationic or non-cationic unit comprising a portion y x '+ x "= x.
Another class of linearly polymerizable monomers comprises cationically charged heteroaromatic Z units having the formula: a non-limiting example of which is 4-vinyl (N-alkyl) pyridine in which R1 and R2 are each hydrogen and R6 is methyl. Another class of linearly polymerizable monomers comprising a heterocyclic ring includes Z units comprising an N-oxide, for example, the N-oxide having the formula: a non-limiting example of which is 4-vinylpyridine N-oxide. The N-alkyl vinylpyridine monomers and N-vinylpyridine monomers can be suitably combined with other aromatic monomers, inter alia, with vinylamine. However, the preferred polymers of the present invention include derived copolymers and a combination of quaternized N-oxide and nitrogen-containing heteroaromatic monomers, non-limiting examples of which include a copolymer of N-methylvinylpyridine and vinylpyridine in a ratio of 4 to 1.; a copolymer of N-methylvinylpyridine and vinylpyridine in a ratio of 4 to 6, a copolymer of poly (N-methylvinylpyridine) and N-oxide of vinylpyridine in a polymer to monomer ratio of 4 to 1, poly (N-methylvinylpyridine) and N-vinylpyridine oxide in a polymer to monomer ratio of 4 to 6 and mixtures thereof. A preferred linear copolymer according to the present invention has the formula: in which Z1 has the formula: Z has the formula: in which X is chlorine; X has the value of approximately 10 to about 100,000; and it has the value of approximately 10 to about 100,000; the ratio of X to Y is from 9: 1 to 1: 9. Copolymers of this type are available, for example, as Sedipur® CF104 ex BASF. As described herein, some preferred polymer residues can be formed by treating the resulting polymer. For example, vinylamine residues are preferably introduced by formamide monomers which are subsequently hydrolyzed to the free amino unit. Also the vinyl alcohol units are obtained by hydrolysis of the residues formed of the vinylacetate monomers. Also, the acrylic acid residues can be esterified after the polymerization, for example, the units having the formula: they can be formed more convenient after the main stem has been formed by polymerization with acrylic acid or acrylic acid precursor monomers. II) Cyclic units derived from cyclic polymerization monomers. The polymers or copolymers of the present invention may comprise one or more cyclic polymer units which are derived from cyclically polymerizable monomers. The cyclic polymerization monomers are defined herein as monomers which, under standard polymerization conditions, result in a cyclic polymer residue as well as serve to propagate the polymerization linearly. Preferred cyclic polymerization monomers of the present invention have the formula: R4 X "R4- N + - R5 wherein each R4 is independently an olefin comprising a unit that is capable of propagating the polymerization in addition to forming a cyclic residue with an adjacent unit R4; R5 is alkyl, benzyl, substituted, linear or branched benzyl of C1-C12 and mixtures thereof; X is a water soluble anion. Non-limiting examples of R 4 units include allyl, allyl and substituted alkyl units. Preferably the resulting cyclic residue is a 6-membered ring comprising a quaternary nitrogen atom. R5 is preferably C1-C4 alkyl, preferably methyl. An example of a cyclic polymerization monomer is dimethyidiallylammonium having the formula: which results in a polymer or copolymer having units with the formula: in which preferably the Z-index is from about 10 to about 50,000. lll) Their mixtures. The polymers or copolymers of the present invention must retain a net cationic charge, whether the charge is developed in situ, or the polymer or copolymer itself has a formal positive charge. Preferably the polymer or copolymer has at least 10%, most preferably at least about 25%, most preferably at least 35%, most preferably at least 50% of the residues comprising a cationic charge. The polymers or copolymers of the present invention can comprise mixtures of linear or cyclic polymerization monomers, for example the copolymer of dimethyldiallylammonium polychloride / acrylamide having the formula: wherein Z1, Z2, x, y and z are the same as defined herein and x is chloride ion. A particularly preferred embodiment of this invention is the composition comprising a polymer based on dimethyldiallylammonium chloride and a copolymer which is based on acrylamide with a comonomer selected from the group consisting of N, N dialkylaminoalkyl (meth) acrylate, N, N dialkylaminoalkylacrylate, N, N dialkylaminoalkylacrylamide, N, N dialkylaminoalkyl (meth) acrylamide, their quaternized derivatives and mixtures thereof. Non-limiting examples of the preferred polymers according to the present invention include dye preservation copolymers comprising: i) a first monomer selected from the group consisting of N. N.dialkylaminoalkylmethacrylate, N, N dialkylaminoalkylacrylate, N, N dialkylaminoalkylacrylamide, N, N dialkylaminoalkylmethacrylamide, quaternized derivatives thereof and mixtures thereof; and ii) a second monomer selected from the group consisting of acrylic acid, methacrylic acid, C 1 -C 6 alkyl methacrylate, Ci-Cß, CI-CB hydroxyalkyl acrylate, Ci-Cs hydroxyalkyl methacrylate, acrylamide, CiC-iß alkylacrylamide, C? -C-? 6 dialkylacrylamide, 2-acrylamido-methylpropanesulfonic acid or its alkali metal salt, methacrylamide, alkyl methacrylamide ? -C- | 6, dialkylmethacrylamide of C -? - C16, vinylformamide, vinylacetamide, vinyl alcohol, vinyl alkyl ether of Ci-Cs, vinylpyridine, itaconic acid, vinylacetate, vinylpropionate, vinylbutyrate and their mixtures; wherein the copolymer comprises at least 25 mol% of the first monomer.
Other ingredients The compositions of the present invention may also optionally comprise one or more adjunct ingredients. Non-limiting examples of adjunct ingredients are selected from the group consisting of detersive surfactants, electrolytes, stabilizers, water-soluble solvents of low molecular weight, chelating agents, dispersion aids, soil release agents, non-ionic fabric softening agents. , concentration aids, perfumes, preservatives, dyes, optical brighteners, opacifiers, germicides, funjicides, anticorrosion agents, antifoaming agents and their mixtures. The following are applications that describe various detergent additives, methods for making these additives and methods for using them, all are included herein by way of reference. WO 99/07813 A1 Randall et al., "Laundry Detergent Compositions with Amino Acid Base Polymers to Provide Appearance and Integrity Benefits to Fabrics Laundered Therewith", WO 99/07814 A1 Randall et al., "Laundry Detergent Compositions with Amino Acid Based Polymers to Provide Appearance and Integrity Benefits to Fabrics Laundered Therewith ", WO 99/14299 A1 Panandiker et al. "Laundry Detergent Compositions with Anionically Modified, Cyclic Amine Based Polymers"; WO 99/14300 A1 Panandiker et al., "Laundry Detergent Compositions with Cyclic Amine-Based Polymers to Provide Appearance and Integrity Benefits to Fabrics Laundered Therewith"; WO 99/14301 A1 Panandiker et al., "Laundry Detergent Compositions and Fabric Conditioning Compositions with Oxidized Cyclic Amine-Based Polymers"; and E.U.A. 99/23146 Panandiker et al., "Laundry Detergent Compositions with A Combination of Cyclic Amine Based Polymers and Hydrophobically Modified Carboxy Methyl Cellulose" Surfactant System The laundry detergent compositions of the present invention comprise a surfactant system. The surfactant systems of the present invention can comprise any type of detersive surfactant, non-limiting examples of which include one or more branched alkyl sulfate surfactants in the middle region of its chain, one or more branched alkylalkoxysulfate surfactants in the middle region of its chain, one or more branched aryl sulfonate surfactants in the middle region of its chain, one or more branched sulfonates in the middle region of its chain, sulfates, cationic surfactants, switerionics, ampholytics and mixtures thereof. The total amount of surfactant present in the compositions of the present invention is about 4% by weight, preferably 10% by weight, most preferably from 15% by weight to about 60% by weight, preferably 30% by weight of the composition. Non-limiting examples of surfactants useful herein include: a) alkylbenzene sulfonate (LAS) of Cn-C-iß; b) arylsulfonates (BLAS) branched in the middle region of its C6-C-j8 chain; c) primary alkyl sulfates (AS) a or? branched and random C10-C20; d) branched alkyl sulphates (BAS) in the middle region of their C14-C20 chain; e) (2,3) C 10 -C 18 secondary alkyl sulfates as described in E.U.A. 3,234,258 to Morris, issued on February 8, 1966; E.U.A. 5,075,041 to Lutz, issued December 24, 1991; E.U.A. 5,349,101 to Lutz et al., Issued September 20, 1994 and E.U.A. 5,389,277 to Prieto, issued on February 14, 1995, each included hereby by way of reference; f) alkylalcoxy sulfates (AEXS) of C? o-C-? 8 wherein preferably x is from 1 to 7; g) alkylalkoxy sulfates (BAExS) branched in the middle region of its C1-C2o chain h) C-io-C-i1 alkylalkoxycarboxylates preferably comprising 1 to 5 ethoxy units; i) C12-C18 alkyl ethoxylates, C6-C12 alkylphenylalkoxylates in which the alkoxylate units are a mixture of ethyleneoxy and propyleneoxy units fused from C12-C18 alcohol and C6-C12 alkylphenol with oxide blocking polymers of ethylene-propylene oxide inter alia Pluronic® that are described in the USA 3,929,678 to Laughiin et al., Issued December 30, 1975, included herein by way of reference; j) branched BAEX alkylalkoxylates in the middle region of their C1-C22 chain; k) alkylpolysaccharides are described in E.U.A. 4,565,647 to Llenado, issued on January 26, 1986, included herein by way of reference; I) Fatty acid polyhydroxyamides having the formula: wherein R7 is C5-C3 alkyl ?; R8 is selected from the group consisting of hydrogen, C1-C4 alkyl, C1-C4 hydroxyalkyl, Q is a hydroxy alkyl portion having a linear alkyl chain with at least 3 hydroxyl directly connected to the chain, or its derivative alkoxylated; the preferred alkoxy is ethoxy or epoxy and mixtures thereof; the preferred Q is derived from a reducing sugar in a reductive amination reaction, most preferably Q is a glycityl portion; Q is most preferably selected from the group consisting of -CH2 (CHOH) mCH2OH, -CH (CH2OH) (CHOH) n-1CH2OH, CH2 (CHOH) 2 (CHOR ') (CHOH) CH2OH, and their alkoxylated derivatives, in the which n is an integer from 3 to 5, inclusive, and R 'is hydrogen or a cyclic or aliphatic monosaccharide, which is described in the US 5,489,393 to Connor et al., Issued February 6, 1996; and E.U.A. 5,45,982 to Murch et al., Issued October 3, 1995, both are included herein by way of reference. A non-limiting example of a nonionic surfactant suitable for use in the present invention has the formula: wherein R is C7-C2 linear alkyl, branched C-C2 alkyl, linear C-C2- alkyl, branched C2-C2- alkenyl? and its mixtures. R1 is ethylene; R2 is C3-C4 linear alkyl, branched C3-C4 alkyl, and mixtures thereof; preferably R2 is 1, 2-propylene. The nonionic surfactants comprising a mixture of units R1 and R2 preferably comprise from about 4 to about 12 ethylene units in combination with from about 1 to about 4 units of 1,2-propylene. The units can be alternated, or grouped in any combination appropriate to the formulator. Preferably the ratio of units R1 to units R2 is from about 4: 1 to about 8: 1. Preferably the units R2 (ie, 1, 2-propylene) are attached to the nitrogen atom followed by the remainder of the chain comprising from 4 to 8 ethylene units. R 2 is hydrogen, linear C 1 -C 4 alkyl, branched C 3 -C 4 alkyl, and mixtures thereof; preferably hydrogen or methyl, most preferably hydrogen. R 4 is hydrogen, linear C 1 -C 4 alkyl, branched C 3 -C alkyl, and mixtures thereof; preferably hydrogen. When the index m is equal to 2 the index n must be equal to 0 and the unit R4 is absent and instead replaced by a unit - [(R1O) x (R2O) and R3]. The index m is 1 or 2, the index n is 0 or 1, with the proviso that when m is equal to 1, n is equal to 1; and when m is equal to 2 n is 0; preferably, m is equal to 1 and n is equal to 1, resulting in a unit - [(R1O) x (R2O) and R3] and R4 is present in the nitrogen. The index x is 0 to about 50, preferably from 3 to about 25, most preferably from 3 to 10. The index y is from 0 to about 10, preferably 0, however when the index y is not equal to 0, and is from 1 to approximately 4.
Preferably all alkyleneoxy units are ethyleneoxy units. Those skilled in the art of ethoxylated polyoxyalkylenealkylamide surface active agents will recognize that the values for the indices x and y are average values and that the actual values can vary by several values depending on the procedure used to alkoxylate the amides.
The branched alkyl sulfate surfactants in the middle region of their chain of the present invention have the formula: R R1 R ^ I CH3CH2 (CH2) wCH (CH2)? CH (CH2) CH (CH2) zOS03M, Alkylalcoxy sulfates have the formula: R R1 R2 CH3CH2 (CH2) wCH (CH2)? H (CH2) CH (CH2) z (OR3) mOS03M, The alkylalkoxylates have the formula: wherein R, R and R2 are each independently hydrogen, C?-C3 alkyl, and mixtures thereof; with the proviso that at least one of R, R1 and R2, is not hydrogen; preferably R, R1 and R2 are methyl; preferably one of R, R and R2 is methyl and the other units are hydrogen. The total number of carbon atoms in the alkyl sulfate surfactants branched in the middle region of its chain and alkylalkoxysulfate surfactants is from 14 to 20; the index w is an integer from 0 to 13; x is an integer from 0 to 13; and is an integer from 0 to 13; z is an integer of at least 1; with the proviso that w + x + y + z is from 8 to 14 and the total number of carbon atoms in a surfactant is from 14 to 20; R 3 is branched or linear C 1 -C 4 alkylene, preferably ethylene, 1,2-propylene, 1,3-propylene, 1,2-butylene, 1,4-butylene, and mixtures thereof. However, a preferred embodiment of the present invention comprises from 1 to 3 units in which R3 is 1,2-propylene, 1,3-propylene, or mixtures thereof followed by the remaining R3 units comprising ethylene units. Another preferred embodiment comprises R3 units which are random units of ethylene and 1,2-propylene. The average value of the index m is at least approximately 0.01. When the index m has lower values, the surfactant system comprises mainly alkyl sulfates with a small amount of alkylalkoxysulfate surfactant. Some tertiary carbon atoms may be present in the alkyl chain, however, in this embodiment it is not convenient. M denotes a cation, preferably hydrogen, a soluble cation and its mixtures. Non-limiting examples of water-soluble cations include sodium, potassium, lithium, ammonium, alkylammonium, and mixtures thereof.
Detergency builder The detergent compositions herein can also comprise from 0.1% to 80% by weight of a builder. Preferably said compositions in liquid form will comprise from 1% to 10% by weight of the builder component. Preferably said compositions in granular form will comprise from 1% to 50% by weight of the builder component. Builders are well known in the art and can comprise, for example, phosphate salts as well as various non-organic and inorganic phosphorus builders. The non-phosphorus, water-soluble organic builders, useful herein include the various alkali metal, ammonium and substituted ammonium polycarboxylates, carboxylates, polycarboxylates and polyhydroxy sulphonates. Polycarboxylates suitable for use herein are the polyacetal carboxylates that are described in the U.S.A. 4,144,226, issued March 13, 1979 to Crutchfield et al, and in the U.S. patent. 4,246,495, issued March 27, 1979 to Crutchfield et al, both of which are incorporated herein by reference. Particularly preferred polycarboxylate builders are oxydisuccinates and carboxylate ether builder compositions which comprise a combination of tartrate monosucinate and tartrate disucinate which are described in the U.S.A. 4, 663,071, Bush et al, issued May 5, 1987, the description of which is incorporated herein by reference. Examples of non-phosphorus, inorganic detergency builders include silicates, aluminosilicates, borates and carbonates. Particular preference is given to carbonate, bicarbonate, sesquicarbonate, tetraborate, sodium and potassium decahydrate, and silicates having a weight ratio of SiO to alkali metal oxide of 0.5 to 4.0, preferably 1.0 to 2.4. Aluminosilicates including zeolites are also preferred. Such materials and their use as detergency builders are more fully described in Corkill et al, U.S. Pat. No. 4,605,509, the description of which is incorporated herein by reference. They are also described in the patent of E.U.A. No. 4,605,509 the layered crystalline silicates which are suitable for use in the detergent compositions of this invention.
Optional Detergent Ingredients In addition to the surfactants, builders and dye preservation polymers of the detergent compositions of the present invention, any number of optional additional ingredients may also be included. These include conventional detergent composition components such as enzymes and enzyme stabilizing agents, foaming impellers or suds suppressors, anti-oxidation and anti-corrosion agents, bleaching agents, soil suspending agents, soil release agents, germicides, surface release agents pH adjustment, alkalinity sources not detergent builders, chelating agents, organic and inorganic fillers, solvents, hydrotropes, optical brighteners, dyes and perfumes. Agents for pH adjustment may be necessary in certain applications where the pH of the wash solution is greater than 10.0 because the fabric integrity benefits of the defined compositions begin to decrease at a higher pH. Hence, if the wash solution is larger than 10.0 after the addition of the dye preservation polymers of the present invention, a pH adjuster should be used to reduce the pH of the wash solution to below 10.0, preferably at a pH below 9.5, and more preferably below 7.5. Suitable pH adjusters will be known to those skilled in the art. A preferred optional ingredient for incorporation into the detergent compositions herein comprises a bleaching agent, for example, a peroxygen bleach. Said peroxygen bleaching agents may be organic or inorganic in nature. Inorganic peroxygen bleaching agents are often used in combination with a bleach activator. Useful organic peroxygen bleaching agents include percarboxylic acid bleaching agents and salts thereof. Suitable examples of this class of agents include magnesium monoperoxyphthalate hexahydrate, the magnesium salt of metachloroperbenzoic acid, 4-nonylamino-4-oxoperoxybutyric acid and diperoxydecanedioic acid. Said bleaching agents are described in the patent of E.U.A. 4,483,781, Hartman, issued November 20, 1984; European Patent Application EP-A-133,354, Banks et al, published February 20, 1985; and the US patent. 4,412,934, Chung et al, issued November 1, 1983. Preferred bleaching agents also include 6-nonylamino-6-oxoperoxycaproic acid (NAPAA) as described in U.S. Pat. 4,634,551, issued on January 6, 1987 to Bums et al. The inorganic peroxygen bleaching agents can also be used, generally in the form of a particulate form, in the detergent compositions herein. Inorganic bleaching agents are in fact preferred. Such inorganic peroxygen compounds include alkali metal materials of perborate and percarbonate. For example, sodium perborate (for example mono- or tetrahydrate) can be used. Suitable inorganic bleaching agents may also include sodium or potassium carbonate peroxyhydrate and equivalent "percarbonate" bleaches, sodium pyrophosphate peroxyhydrate, urea peroxyhydrate, and sodium peroxide. Persulfate bleach (for example OXONE, commercially manufactured by DuPont) can also be used. Inorganic peroxygen bleaches will often be coated with silicate, borate, sulfate or water-soluble surfactants. For example, coated percarbonate particles are available from various commercial sources such as FMC, Solvay Interox, Tokai Denka and Degussa. Inorganic peroxygen bleaching agents, for example, perborates, percarbonates, etc., are preferably combined with bleach activators, which leads to in situ production in aqueous solution (i.e. while using the present compositions for washing / bleaching fabrics) of the peroxy acid corresponding to the bleach activator. Several non-limiting examples of activators are described in U.S. Patent No. 4,915,854, issued April 10, 10, 1990 to Mao et al, and the U.S. patent. 4,412,934 issued November 1, 1983 to Chung et al. The nonanoyloxybenzenesulfonates (NOBS) and tetraacetyl ethylenediamine (TAED) are typical and preferred activators. Mixtures thereof can also be used. See also the patent of E.U.A. 4,634,551 to which reference is made above for other typical bleaches and activators useful herein. Other useful amido-derived bleach activators are those of the formulas: R1N (R5) C (O) RC (O) L or R1C (0) N (R5) RC (O) L wherein R1 is an alkyl group which contains from about 6 to about 12 carbon atoms, R 2 is an alkylene containing from about 1 to about 6 carbon atoms, R 5 is H or alkyl, aryl, or alkaryl containing from about 1 to about 10 carbon atoms. carbon, and L is any suitable residual group. A residual group is any group that is displaced from the bleach activator as a consequence of the nucleophilic attack on the bleach activator by the perhydrolysis anion. A preferred residual group is phenol sulfate. Preferred examples of bleach activators of the above formulas include (6-octanamido-caproyl) oxybenzenesulfonate, (6-nonanamidocaproyl) oxybenzenesulfonate, (6-decanamido-caproxy) oxybenzenesulfonate and mixtures thereof as described in the patent of US Pat. 4,634,551 to which reference is made above.
Another class of useful bleach activators comprises the benzoxazine type activators that are described by Hodge et al in the U.S. patent. 4,966,723, issued October 30, 1990, incorporated herein by reference. See also the patent of E.U.A. 4,545,784, issued to Sanderson, October 8, 1985, incorporated herein by reference, which discloses acylcaprolactams, including benzoyl caprolactam, adsorbed to sodium perborate. If used, the peroxygen bleaching agent will generally comprise from 2% to 30% by weight of the detergent compositions herein. More preferably, the peroxygen bleaching agent will comprise from 2% to 20% by weight of the compositions. More preferably, the peroxygen bleaching agent will be present to the extent of 3% to 15% by weight of the present compositions. If used, the bleach activators may comprise from 2% to 10% by weight of the detergent compositions present. Frequently, the activators are used so that the molar ratio of bleaching agent to activator is in the range of 1: 1 to 10: 1, more preferably 1.5: 1 to 5: 1. Additional suitable bleach activators and bleach activators are described in one or more of the co-pending PCT applications listed in Table A and incorporated herein by reference. Another highly preferred optional ingredient in the detergent compositions herein is a detersive enzyme component. The enzymes can be included in the detergent compositions present for a variety of purposes, including spot removal of protein-based substrates, based on carbohydrate, or based on triglycerides, for the prevention of transfer of refugee dye in fabric washing, and for restoration of fabrics. Suitable enzymes include proteases, amylases, lipases, cellulases, peroxidases, and mixtures thereof of any suitable origin, such as plant, animal, bacterial, fungal and yeast origin. Preferred selections are influenced by factors such as pH activity and / or stability, optimal thermostability, and stability to detergent actives, builders and the like. In this regard, bacterial or fungal enzymes, such as bacterial amylases and proteases, and fungal cellulases are preferred. "Detersive enzyme", as used herein, means any enzyme that has a cleaning, dirt removal or otherwise beneficial effect in a laundry detergent composition. Preferred enzymes for laundry purposes include, but are not limited to, proteases, cellulases, lipases, amylases and peroxidases. Enzymes are normally incorporated in detergent compositions at levels sufficient to provide an "effective amount for cleaning". The term "effective amount for cleaning" refers to any amount capable of producing a cleaning, stain removal, dirt removing, bleaching, deodorizing, or freshness improving effect on substrates such as fabrics. In practical terms for current commercial preparations, typical amounts are up to 5 mg by weight, more typically from 0.01 mg to 3 mg of active enzyme per gram of detergent composition. Established otherwise, the present compositions will typically contain from 0.001% to 5%, preferably 0.01% -1% by weight of a commercial enzyme preparation. Protease enzymes are normally present in such commercial preparations at levels sufficient to provide 0.005 to 0.1 Anson units (AU) of activity per gram of composition. Higher active levels may be desirable in highly concentrated detergent formulations. Cellulases that can be used herein include those described in the U.S.A. No. 4,435,307, Barbesgoard et al, March 6, 1984, and GB-A-2,075,028; GB-A-2,095,275 and DE-OS-2,247,832. CAREZYME® and CELLUZYME® (Novo) are especially useful. See also WO 9117243 to Novo. The enzyme-containing compositions herein may also optionally comprise from about 0.001% to about 10%, preferably from about 0.005% to about 8%, more preferably from 0.01% to 6%, by weight of an enzyme stabilizing system . The enzyme stabilizing system can be any stabilizing system which is compatible with the detersive enzyme. Such a system can be provided inherently by other formulation actives, or it can be added separately, for example, by the formulator or by a manufacturer of ready-to-use detergent enzymes. Said stabilizing systems can, for example, comprise calcium ions, boric acid, propylene glycol, short chain carboxylic acids, boronic acids, and mixtures thereof, and are designed to face different stabilization problems depending on the type and physical form of the detergent composition.
Preparation of the detergent composition The detergent compositions according to the present invention may be in liquid, paste or granular form. Said compositions can be prepared by combining the essential and optional components in the required concentrations in any suitable order and by any conventional means. The aforementioned description of uses for the dye preservation polymers that are defined herein is intended to be illustrative and other uses will be apparent to those skilled in the art and are designed to be within the scope of the present invention. For example, granular compositions are generally made by combining base granule ingredients, for example, surfactants, builders, water, etc., as a suspension, and spray drying the resulting suspension at a low level of residual moisture ( 5-12%). The remaining dry ingredients, for example, granules of the essential dye preservation polymers, can be mixed in the form of granular powder with the spray-dried granules in a rotating mixing drum. Liquid ingredients, for example, solutions of the essential coloring preservative polymers, enzymes, binders and perfumes, can be sprayed onto the resulting granules to form the finished detergent composition. The granular compositions according to the present invention can also be in "compact form", that is, they can have a relatively higher density than conventional granular detergents, ie from 550 to 950 g / l. In such a case, the granular detergent compositions according to the present invention will contain a lower amount of "inorganic filler salt", in comparison to conventional granular detergents; typical filler salts are alkaline earth metal salts of sulfates and chlorides, typically sodium sulfate; "Compact" detergents typically comprise no more than 10% filler salt. Liquid detergent compositions can be prepared by mixing the essential and optional ingredients thereof in any desired order to provide compositions containing components in the required concentrations. The liquid compositions according to the present invention can be in "compact form", in such case, the liquid detergent compositions according to the present invention will contain a lower amount of water, compared to conventional liquid detergents. The addition of the dye preservation polymers to the liquid detergent or other aqueous compositions of this invention can be achieved simply by mixing the desired dye preservation polymers in the liquid solutions.
Fabric Washing Method The present invention also provides a method for washing fabrics in a manner that imparts appearance benefits of fabrics provided by the colorant preservation polymers that are used herein. Said method uses contacting said fabrics with an aqueous wash solution formed from an effective amount of the detergent compositions herein described above or formed from the individual components of said compositions. The contact of the fabrics with the washing solution will generally occur under stirring conditions although the compositions of the present invention can also be used to form aqueous solutions for soaking without stirring for fabric cleaning and treatment. As discussed above, it is preferred that the wash solution has a pH of less than 10.0, preferably has a pH of about 9.5, and more preferably has a pH of about 7.5. The agitation is preferably provided in a washing machine for good cleaning. The washing is preferably followed by drying the wet cloth in a conventional cloth dryer. An effective amount of a high density liquid or granular detergent composition in the aqueous wash solution in the washing machine is preferably from 500 to 7000 ppm, more preferably from 1000 to 3000 ppm.
EXAMPLES The following examples illustrate the compositions and methods of the present invention, but do not necessarily mean that they limit or otherwise define the scope of the invention.
EXAMPLE I Table 1 comprises numerous examples according to the present invention together with some comparative examples of the material known in the laundry detergent art. The chemical structures shown in the following examples are ideal structures. Collateral reactions that are expected to occur during condensation are not shown.
TABLE II EXAMPLE II Preparation of granular detergent test composition Various heavy duty granular detergent compositions are prepared containing one or more dye preservation polymers having a DMP according to this invention. These granular detergent compositions have the following basic formula: TABLE II Component% by weight C12 linear alkylbenzene sulfonate 9.31 C? 4-5 alkyl ether sulfate (0.35 EO) 12.74 Zeolite builder 27.79 Sodium carbonate 27.31 PEG 4000 1.60 Dispersant 2.26 C12-13 ethoxylate alcohol (9 EO) 1.5 Perborate sodium 1.03 Dirt release polymer 0.41 Enzymes 0.59 Color preservation polymer 3.0 Perfume, polish, foam suppressant, others Other ingredients, humidity, 100% sulfate EXAMPLE III Preparation of liquid detergent test composition Several heavy duty liquid compositions are prepared containing one or more dye preservation polymers having a DMP according to this invention. All of these liquid detergent compositions have the following base formula: TABLE III EXAMPLE IV Preparation of granular detergent test composition Various granular detergent compositions are prepared containing one or more dye preservation polymers having a DMP according to this invention. Said granular detergent compositions all have the following basic formula: TABLE IV Comparative Example Component% by weight% by weight Linear alkyl of C12 Na 9.40 9.40 Alkylsulfonate of C14.15 Na 11.26 11.26 Detergent builder of zeolite 27.79 27.29 Sodium carbonate 27.31 27.31 PEG 4000 1.60 1.60 Dispersant, sodium polyacrylate 2.26 2.26 C12-? 3 alkyl ethoxylate (E9) 1.5 1.5 Perborate Sodium 1.03 1.03 Dye preservation polymer 0.8 0 Other ingredients attached Rest Rest 100% 100%

Claims (11)

NOVELTY OF THE INVENTION CLAIMS
1. - A detergent composition characterized in that it comprises: a) from 4% to 70% by weight of a surfactant; b) from 0.01% to 5% by weight of a dye preservation polymer or oligomer, the polymer or copolymer comprises one or more units having the formula: I) linear polymer units having the formula: wherein each R1 is independently a) hydrogen; b) C1-C4 alkyl; c) substituted or unsubstituted phenyl; d) substituted or unsubstituted benzyl; e) carbocyclic; f) heterocyclic; g) and their mixtures; each R2 is independently a) hydrogen; b) halogen; c) C 1 -C 4 alkyl d) C 1 -C 4 alkoxy; e) substituted or unsubstituted phenyl; f) substituted or unsubstituted benzyl; g) carbocyclic; h) heterocyclic; and its mixtures; each Z is independently a) hydrogen; b) hydroxyl; c) halogen; d) - (CH2) mR; wherein R is: i) hydrogen; ii) hydroxyl ii) halogen; iv) nitrile; v) -OR3; vi) -O (CH2) nN (R3) 2; vii) -O (CH2) nN + (R3) 3? -; viii) -OCO (CH2) nN (R3) 2; ix) -OCO (CH2) nN + (R3) 3? -; x) -NHCO (CH2) nN (R3) 2; xi) -NHCO (CH2) nN + (R3) 3? -; xii) - (CH2) nN (R3) 2; xiü) - (CH2) nN + (R3) 3X "; xiv) carbocyclic; xv) heterocyclic; xvi) nitrogen quaternary ammonium heterocycle; xvü) nitrogen N-oxide heterocycle; xvii) aromatic quaternary ammonium N-heterocyclic; xix) N -N-heterocyclic aromatic oxide; xx) -NHCHO; xxi) or mixtures thereof: each R3 is independently hydrogen, C?-C8 alkyl, C2-C8 hydroxyalkyl and mixtures thereof, X is a water-soluble anion; n is from 0 to 6 e) - (CH2) mCOR 'in which R' is i) -OR3; ii) -0 (CH2) nN (R3) 2; iü) -0 (CH2) nN + (R3) 3 ? -; iv) -NR3 (CH2) nN (R3) 2; v) -NR3 (CH2) nN + (R3) 3? -; vi) - (CH2) nN (R3) 2; vii) - (CH2) nN + (R3) 3? -; viii) or mixtures thereof: each R3 is independently hydrogen, C -? - C8 alkyl, C2-C8 hydroxyalkyl and mixtures thereof, X is a water soluble anion, the n-index is 0 a 6; f) and their mixtures, the index m is from 0 to 6; ll) the cyclic units derived from cyclic polymerization monomers having the formula: R 4 I x - R 4 - N + R 5 R 5 in which each R 4 is independ an olefin comprising a unit that is capable of propagating the polymerization in addition to forming a cyclic residue with an adjacent R4 unit; R5 is linear or branched alkyl of C? -C? 2"benzyl, substituted benzyl and mixtures thereof; X is a water soluble anion; and III) their mixtures; with the proviso that the polymer or copolymer has a net cationic charge; and wherein the dye preservation polymer is not a polyethyleneimine or its alkoxylated derivative; and b) balancing vehicles and other adjunct ingredients.
2. The detergent composition according to claim 1, further characterized in that the dye preservation polymer is a copolymer comprising: i) a first monomer selected from the group consisting of N, N dialkylaminoalkyl (meth) acrylate, N, N-dialkylaminoalkylacrylate, N, N-dialkylaminoacylacrylamide, N, N-dialkylaminoa-quil (meth) acrylamide, quaternized derivatives thereof and mixtures thereof; and ii) a second monomer selected from the group consisting of acrylic acid, methacrylic acid, C-pCß alkyl methacrylate, Ci-Cß alkyl acrylate, Ci-Cs hydroxyalkylacrylate, Ci-Cs hydroxyalkyl methacrylate, acrylamide, C1-C16 alkylacrylamide, C1-C16 dialkylacrylamide, 2-acrylamido-2-methylpropanesulfonic acid or its alkali metal salt, methylacrylamide, CiC-iß aicylmethacrylamide, CiC-iß dialkyl methacrylamide, vinylformamide, vinylacetamide, vinyl alcohol, CrC8 vinyl alkyl ether, vinylpyridine, taconic acid , vinyl acetate, vinyl propionate, vinyl butyrate and their mixtures; wherein the copolymer comprises at least 25 mol% of the first monomer.
3. The composition according to claim 1 or 2 further characterized in that the adjunct ingredients are selected from the group consisting of electrolytes, stabilizers, water soluble solvents of low molecular weight, chelating agents, dispersion aids, release agents, dirt, non-ionic fabric softening agents, concentration aids, perfume, preservatives, dyes, optical brighteners, opacifiers, germicides, fungicides, anti-corrosion agents, anti-foaming agents and their mixtures.
4. A detergent composition characterized in that it comprises: a) from 4% to 70% of a surfactant; b) from 0.01% to 10% by weight of a dye preservation polymer or oligomer, said dye preservation polymer is selected from the group consisting of homopolymers, copolymers, terpolymers and mixtures thereof having the formula: wherein each R1, R2 is hydrogen or methyl; Z has the formula: - (CH2) mR in which m is equal to 0 or 1; R is -N (R3) 2 or -N + (R3) 3X-R3 is selected from the group consisting of hydrogen, C1-C4 alkyl, C2-C4 hydroxyalkyl and mixtures thereof; X is a water soluble anion; and c) equilibrium carriers and adjunct ingredients.
5. The composition according to any of claims 1 to 4 further characterized in that it comprises from 0.1% to 8% by weight of the color preservation polymer.
6. The composition according to any of claims 1 to 5, further characterized in that the color preservation polymer is a copolymer comprising linear polymerization monomers and a cyclic polymerization monomer having the formula: wherein R is C 1 -C 4 alkyl and mixtures thereof; X is a water soluble anion.
7. The composition according to any of claims 1 to 5, further characterized in that the color preservation polymer is selected from the group consisting of homopolymers, copolymers, terpolymers and mixtures thereof, diallyl dimethyl ammonium chloride, bromide or methyl sulfate. and a comonomer selected from the group consisting of acrylic acid, methacrylic acid, C 1 -C 5 alkymethacrylate, Ci-Cβ alkylacrylate, Ci-Cs hydroxyalkylacrylate, Ci-Cs hydroxyalkyl methacrylate, acrylamide, C 1 -C 16 alkylacrylamide, dialkylacrylamide of C 1 -C16, 2-acrylamido-methylpropanesulfonic acid or its alkali metal salt, methacrylamide, C1-C16 alkylmethacrylamide, C1-C16 dialkylmethacrylamide, vinylformamide, vinylacetamide, vinyl alcohol, Ci-Cd vinyl alkyl ether, vinylpyridine, itaconic acid, vinylacetate, vinylpropionate , vinylbutyrate and their mixtures.
8. The composition according to any of claims 1 to 5, further characterized in that the dye preservation polymer or copolymer comprises linear polymerization monomers and a cyclic polymerization monomer, the cyclic polymerization monomer has the formula: wherein R5 is C1-C4 alkyl and mixtures thereof; X is a water soluble anion.
9. The composition according to any of claims 1 to 5, further characterized in that it comprises a copolymer in which Z has the formula: - (CH2) mCOR in which each R is independently -O (CH2) nN (R3 )2; -O (CH2) nN + (R3) 3X '; - (CH2) nN (R3) 2; - (CR2) nN "," (R3) 3X "and their mixtures, m is 0, n is from 2 to 4.
10. The composition according to claim 1, further characterized in that the dye preservation polymer comprises a copolymer of N-methylvinylpyridine and vinylpyridine in a ratio of 4: 1, a copolymer of N-methylvinylpyridine and vinylpyridine in a ratio of 4: 6, a copolymer of poly (N-methylvinylpyridine) and N-oxide of vinylpyridine in a polymer to monomer ratio of 4: 1, a polymer comprising poly (N-methylvinylpyridine) and vinylpyridine N-oxide in a polymer to monomer ratio of 4: 6, and mixtures thereof.
11. A method for reducing the loss of fabric dye comprising the step of contacting the dyed fabric with a laundry detergent comprising: a) from 4% to 70% by weight of a surfactant; b) from 0.01% to 5% by weight of a dye preservation polymer or oligomer, the polymer or copolymer comprises one or more units having the formula: I) linear polymer units having the formula: wherein each R1 is independently a) hydrogen; b) C 1 -C 4 alkyl; c) substituted or unsubstituted phenyl; d) substituted or unsubstituted benzyl; e) carbocyclic; f) heterocyclic; g) and their mixtures; each R2 is independently a) hydrogen; b) halogen; c) C 1 -C 4 alkyl d) C 1 -C 4 alkoxy; e) substituted or unsubstituted phenyl; f) substituted or unsubstituted benzyl; g) carbocyclic; h) heterocyclic; and its mixtures; each Z is independently a) hydrogen; b) hydroxyl; c) halogen; d) - (CH2) mR; wherein R is: i) hydrogen; ii) hydroxyl iii) halogen; iv) nitrile; v) -OR3; vi) -0 (CH2) nN (R3) 2; vii) -O (CH2) nN + (R3) 3? -; vii) -OCO (CH2) nN + (R3) 3? -; ix) -OCO (CH2) nN (R3) 2; x) -NHCO (CH2) nN (R3) 2; xi) -NHCO (CH2) nN + (R3) 3? -; xii) - (CH2) nN (R3) 2; xiii) - (CH2) nN + (R3) 3X "; xiv) carbocyclic; xv) heterocyclic; xvi) nitrogen quaternary ammonium heterocycle; xvii) N-nitrogen oxide heterocycle; xviii) N-heterocyclic aromatic quaternary ammonium; xix) N N-aromatic heterocyclic oxide; xx) -NHCHO; xxi) or their mixtures; each R 3 is independently hydrogen, C 1 -C 8 alkyl, C 2 -C 16 hydroxyalkyl and mixtures thereof; X is a water soluble anion; the index n is from 0 to 6 e) - (CH2) mCOR 'in which R' is i) -OR3; ii) -O (CH2) nN (R3) 2; iii) -O (CH2) nN + (R3) 3? -; iv) -NR3 (CH2) nN (R3) 2; v) -NR3 (CH2) nN + (R3) 3? -; vi) - (CH2) nN (R3) 2; vii) - (CH2) nN + (R3) 3X "; viii) or their mixtures, each R3 is independently hydrogen, C? -C8 alkyl, C2-C8 hydroxyalkyl, and mixtures thereof; X is a water soluble anion; the index n is from 0 to 6, f) and their mixtures, the index m is from 0 to 6, II) the cyclic units derived from cyclic polymerization monomers that have the formula: R4 X R4- N + R5 Rü wherein R4 is independently an olefin comprising a unit that is capable of propagating the polymerization in addition to forming a cyclic residue with an adjacent R4 unit; R5 is linear or branched alkyl of C? -C? 2, benzyl, substituted benzyl, and mixtures thereof; X is a water soluble anion; and III) their mixtures; with the proviso that the polymer or copolymer has a net cationic charge; and wherein the dye preservation polymer is not a polyethyleneimine or its alkoxylated derivative; and b) balancing vehicles and other adjunct ingredients.
MXPA01009728A 1999-03-25 2000-03-24 Laundry detergent compositions with certain cationically charged dye maintenance polymers. MXPA01009728A (en)

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Families Citing this family (52)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6733538B1 (en) * 1999-03-25 2004-05-11 The Procter & Gamble Company Laundry detergent compositions with certain cationically charged dye maintenance polymers
DE10027634A1 (en) 2000-06-06 2001-12-13 Basf Ag Use of hydrophobic polymer particles, cationically modified by coating with cationic polymer, as additives in washing or care materials for textiles and as additives in detergents
DE10150724A1 (en) 2001-03-03 2003-04-17 Clariant Gmbh Washing agents such as detergents contain dye transfer inhibitors which are polyamine/cyanamide/amidosulfuric acid, cyanamide/aldehyde/ammonium salt or amine/epichlorhydrin reaction products
EP1239025A3 (en) * 2001-03-03 2003-09-03 Clariant GmbH Detergent composition and laundry treatment compositon comprising dye transfer inhibiting and dye fixing agent
US7799421B2 (en) 2002-02-14 2010-09-21 Akzo Nobel N.V. Controlled release materials
US6924259B2 (en) 2002-04-17 2005-08-02 National Starch And Chemical Investment Holding Corporation Amine copolymers for textile and fabric protection
KR20050090994A (en) * 2002-12-23 2005-09-14 시바 스폐셜티 케미칼스 홀딩 인코포레이티드 Hydrophobically modified polymers as laundry additives
DE102005039168A1 (en) * 2005-08-17 2007-02-22 Cognis Ip Management Gmbh Solid agents containing cationic polymers
GB0518059D0 (en) 2005-09-06 2005-10-12 Dow Corning Delivery system for releasing active ingredients
RU2011103096A (en) 2008-08-28 2012-10-10 Дзе Проктер Энд Гэмбл Компани (US) COMPOSITIONS FOR CARE OF FABRIC, METHOD OF MANUFACTURE AND METHOD OF APPLICATION
BRPI0924622A2 (en) 2009-06-30 2016-03-01 Procter & Gamble tissue treatment compositions, manufacturing process, and method of use.
US8188027B2 (en) 2009-07-20 2012-05-29 The Procter & Gamble Company Liquid fabric enhancer composition comprising a di-hydrocarbyl complex
US8309505B2 (en) 2009-07-30 2012-11-13 The Procter & Gamble Company Hand dish composition in the form of an article
US8288332B2 (en) 2009-07-30 2012-10-16 The Procter & Gamble Company Fabric care conditioning composition in the form of an article
US8367596B2 (en) 2009-07-30 2013-02-05 The Procter & Gamble Company Laundry detergent compositions in the form of an article
EP2529001B1 (en) 2010-01-29 2018-09-19 The Procter and Gamble Company Novel linear polydimethylsiloxane-polyether copolymers with amino and/or quaternary ammonium groups and use thereof
US20110201532A1 (en) 2010-02-12 2011-08-18 Jennifer Beth Ponder Benefit compositions comprising crosslinked polyglycerol esters
US20110201534A1 (en) 2010-02-12 2011-08-18 Jennifer Beth Ponder Benefit compositions comprising polyglycerol esters
US20110201537A1 (en) 2010-02-12 2011-08-18 Jennifer Beth Ponder Benefit compositions comprising crosslinked polyglycerol esters
WO2011100411A1 (en) 2010-02-12 2011-08-18 The Procter & Gamble Company Benefit compositions comprising polyglycerol esters
DE102011112778A1 (en) 2011-09-09 2013-03-14 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. The primary washing power improving polymeric agents
DE102014017962A1 (en) 2014-12-05 2016-06-09 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Detergents and cleaning agents with polymeric agent
DE102014017964A1 (en) 2014-12-05 2016-06-09 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Detergents and cleaning agents with polymeric agent
DE102015004399A1 (en) 2015-04-10 2016-10-13 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Detergents and cleaning agents with polymeric agent
DE102015004400A1 (en) 2015-04-10 2016-10-13 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Detergents and cleaning agents with polymeric agent
US20180142188A1 (en) * 2016-11-18 2018-05-24 The Procter & Gamble Company Fabric treatment compositions having polymers and fabric softening actives and methods for providing a benefit
US20190376006A1 (en) 2017-02-13 2019-12-12 Conopco, Inc., D/B/A Unilever Laundry composition
WO2019070838A1 (en) 2017-10-03 2019-04-11 Lubrizol Advanced Materials, Inc. Esterquat free liquid fabric softener compositions
WO2019084375A1 (en) 2017-10-26 2019-05-02 Lubrizol Advanced Materials, Inc. Esterquat free liquid fabric softener compositions containing unsaturated fatty acid soap
US10377966B2 (en) 2017-12-01 2019-08-13 The Procter & Gamble Company Particulate laundry softening wash additive
US10655084B2 (en) 2017-12-01 2020-05-19 The Procter & Gamble Company Particulate laundry softening and freshening wash additive
US10648115B2 (en) 2017-12-01 2020-05-12 The Procter & Gamble Company Process for treating an article of clothing utilizing water-soluble particles comprising an esterquat
US10392582B2 (en) 2017-12-01 2019-08-27 The Procter & Gamble Company Particulate laundry softening wash additive
US10487293B2 (en) 2017-12-01 2019-11-26 The Procter & Gamble Company Particulate laundry softening wash additive
EP3746534A1 (en) 2018-01-29 2020-12-09 The Procter & Gamble Company Particulate laundry softening wash additive
CA3098043C (en) 2018-05-30 2023-05-09 The Procter & Gamble Company Particulate laundry softening wash additive
WO2020106662A1 (en) 2018-11-20 2020-05-28 The Lubrizol Corporation Graphene production and composition
EP3663384A1 (en) 2018-12-04 2020-06-10 The Procter & Gamble Company Particulate laundry softening wash additive
EP3663385A1 (en) 2018-12-04 2020-06-10 The Procter & Gamble Company Particulate laundry softening wash additive
WO2020131678A1 (en) 2018-12-19 2020-06-25 Lubrizol Advanced Materials, Inc. Cleansing composition and method
EP3736320A1 (en) 2019-05-08 2020-11-11 The Procter & Gamble Company Particles for through the wash laundry softening
BR112022009597A2 (en) 2019-11-19 2022-08-16 Lubrizol Advanced Mat Inc REDEPOSITION-INHIBITING POLYMERS AND DETERGENT COMPOSITIONS CONTAINING THE SAME
BR112022011360A2 (en) 2019-12-11 2022-08-23 Unilever Ip Holdings B V SOLID DETERGENT COMPOSITION, FABRIC SOFTENING METHOD AND USE
WO2021126986A1 (en) 2019-12-19 2021-06-24 Lubrizol Advanced Materials, Inc. Redeposition inhibiting polymers and detergent compositions containing same
EP4106717A1 (en) 2020-02-20 2022-12-28 The Procter & Gamble Company Flexible, porous, dissolvable solid sheet articles containing cationic surfactant
EP4349950A3 (en) 2020-05-14 2024-06-19 The Procter & Gamble Company Fabric care composition
WO2022109208A1 (en) 2020-11-19 2022-05-27 Lubrizol Advanced Materials, Inc. Antimicrobial cleaning compositions containing polyurethane salted with bis-biguanide free base
US11560534B2 (en) 2020-12-15 2023-01-24 Henkel Ag & Co. Kgaa Surfactant compositions for improved transparency of DADMAC-acrylamide co-polymers
US11505766B2 (en) * 2020-12-15 2022-11-22 Henkel Ag & Co. Kgaa Surfactant compositions for improved transparency of DADMAC-acrylic acid co-polymers
US20240060015A1 (en) 2022-08-12 2024-02-22 The Procter & Gamble Company Solid dissolvable compositions
WO2024036125A1 (en) 2022-08-12 2024-02-15 The Procter & Gamble Company Low-water compositions
WO2024119295A1 (en) 2022-12-05 2024-06-13 The Procter & Gamble Company Laundry treatment composition including a polyalkylenecarbonate compound

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2041667A5 (en) * 1969-05-30 1971-01-29 Protex
JPS5813700A (en) * 1981-07-17 1983-01-26 花王株式会社 Detergent composition
US4418011A (en) * 1982-08-03 1983-11-29 Colgate-Palmolive Company Detergent composition providing antistatic properties
JPS6131499A (en) * 1984-07-23 1986-02-13 ライオン株式会社 Laundry aid composition
FR2732031B1 (en) * 1995-03-23 1997-04-30 Coatex Sa USE OF AMPHOTERIC AGENTS AS MODIFIERS OF LAMELLAR PHASES OF LIQUID OR PASTY DETERGENT OR COSMETIC COMPOSITIONS
ES2162893T3 (en) * 1995-07-20 2002-01-16 Procter & Gamble DETERGENT COMPOSITIONS THAT INHIBIT THE TRANSFER OF COLORS.
FR2746808B1 (en) * 1996-03-27 1998-05-07 Protex Manuf Prod Chimiq AGENT AND METHOD FOR IMPROVING THE FRICTION STRENGTH OF DYES OR PRINTS
DE69728778D1 (en) * 1996-09-19 2004-05-27 Procter & Gamble SOFTENER WITH IMPROVED PERFORMANCE
BR9711906A (en) * 1996-10-16 1999-08-24 Unilever Nv Fabric softener composition uses a cpe or rse and a sorbitan mono di or trioleate and liquid fatty acid ester or soft glucose solid
DE19649288A1 (en) * 1996-11-28 1998-06-04 Henkel Kgaa Cotton-active dirt-releasing polymers
WO1999005248A1 (en) * 1997-07-23 1999-02-04 Unilever Plc Automatic dishwashing compositions containing water soluble cationic or amphoteric polymers
CN1227345C (en) * 1998-10-13 2005-11-16 宝洁公司 Lundry detergent compositions with cationically charged dye maintenance polymer

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