CA2257201A1 - Fabric softening compositions - Google Patents
Fabric softening compositions Download PDFInfo
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- CA2257201A1 CA2257201A1 CA002257201A CA2257201A CA2257201A1 CA 2257201 A1 CA2257201 A1 CA 2257201A1 CA 002257201 A CA002257201 A CA 002257201A CA 2257201 A CA2257201 A CA 2257201A CA 2257201 A1 CA2257201 A1 CA 2257201A1
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- Prior art keywords
- fabric softening
- alkyl
- weight
- cationic
- dye fixing
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0021—Dye-stain or dye-transfer inhibiting compositions
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- Oil, Petroleum & Natural Gas (AREA)
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- Organic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
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Abstract
The present invention relates to a liquid fabric softening composition which reduces the amount of dyes released from coloured fabrics upon wet domestic treatment such as those which occur in a laundry operation. The said composition comprises a cationic fabric softener having at least two long chains, a cationic dye fixing agent in amount of 0.1 % to 10 % by weight and is free of detergent materials.
Description
CA 022~7201 1998-11-30 W O 97t466Sl PCTAUS97/08966 FABRIC SOFTENING COMPOSITIONS
Field of the invention The present invention relates to fabric softening compositions and moreparticularly to compositions which reduce the amount of dyes released from coloured fabrics upon wet treatment such as those which occur in a laundry operation.
Background of the invention The domestic treatment of coloured fabrics is a problem known in the art to the formulator of laundry compositions. More particularly, the problem of formulating laundry compositions which reduce the amount of dyes released from coloured fabrics upon wet treatment is a particular challenge to the formulator. This problem is now even more acute with the trends of consumer to move towards more colored fabrics.
Numerous solutions have been proposed in the art to solve this problem such as by treating the fabric with a dye scavenger during the washing process as described in EP 0,341,205, EP 0,033,815 and with a polyvinyl substance as described in WO g4/11482 or in the rinse cycle with a dye fixing agent as described in EP 0,462,806. However, a problem encountered with these solutions is that the dye fixing agents when used in the washing process may be destroyed or damaged by contact on storage and/or during the process, whilst when used in the rinse cycle the 8U~$TITUTE SIIEET ~ULE Zfil .. ~ .. ,.................. . , . .. . . , ~.. ..
CA 022~7201 1998-11-30 need for a detergent active and a high level of dye fixing agent is required to provide effective dye fixation performance. Furthermore, a problem related with the use of dye fixing agents in a softening composition is that of its weight efficiency. So that, although levels of dye fixing agents above 10% by weight would provide effective dye fixation, such use would result in an increase in the formulation cost. Another problem relating to the use of a high level of dye fixing agents in fabric softening compositions is that the resulting products show phase instability. On the other hand, lowering the level of dye fixing agents would not provide sufficient dye fixing properties and the need for a detergent material would be required.
Accordingly, notwithstanding the advances in the art, there is still a need for a fabric softening composition which effectively reduces the amount of dyes released from coloured fabrics upon wet treatment.
The Applicant has now found that the use of a liquid composition comprising a cationic fabric softener having at least two long chains, a cationic dye fixing agent in amount of 0.1 % to 10% by weight, said composition being free of detergent materials, fulfills such a need.
It is therefore an advantage of the invention to provide liquid fabric softening compositions which provide effective reduction of the amount of dyes released from coloured fabrics upon wet domestic tre~atments.
It is another advantage of the invention to provide liquid fabric softening compositions with effective softening properties.
It is another advantage of the invention to provide liquid fabric softening compositions with effective storage stability properties.
For the purpose of the invention, the term "detergent materials"
encompasses detergent surfactant materials selected from soaps, non-soap ~nionic, nonionic, zwitterionic and amphoteric synthetic and natural detergent surfactants which are not softeners. Not included by this definition are the fatty acids which are fabric softeners, contrary to said soaps components which do not have fabric softener properties.
SUBSllllllt 811EE~ (IIULE 261 CA 022~7201 1998-11-30 wo 97t46651 PCT/USg7/08966 Summary of the invention The present invention relates to a liquid fabric softening composition comprising a cationic fabric softener having at least two long chains and a cationic dye fixing agent in amount of 0.1 % to 10% by weight, said composition being free of detergent materials.
In accordance with another aspect of the present invention, a method for treating fabrics is provided. The method comprises contacting the fabrics during the rinse cycle of a consumer laundry process with an aqueous medium containing at least 50 ppm of a fabric softening composition of the invention.
Detailed descriDtion of the invention Cationic fabric softeners An essential component of the invention is a cationic fabric softener component having at least two long chains. By component having at least two long chains is meant a component containing at least two alkyl or alkenyl chains, each comprising from 10 to 25 carbon atoms. Such fabric softener provides effective softness benefit to the treated fabrics.
Typical levels of said fabric softener components within the liquid softener compositions are from 1% to 80% by weight of the compositions.
Depending on the composition execution which can be dilute with a preferred level of fabric softening components from 1% to 5%, or concentrated, with a preferred level of fabric softening components from 5% to 80%, more preferably 10% to 50%, most preferably 15% to 35%
by weight.
.
Typical cationic fabric softening components having at least two long chains include the water-insoluble quaternary-ammonium fabric softening 8UI~TITU~E SHEE~ ~UIE 2~) ., . .. ., . ~, . . . . . .
CA 022~7201 1998-11-30 actives, the most commonly used having been di-long alkyl chains ammonium chloride.
Preferred cationic softeners among these include the following:
1 ) ditallow dimethylammonium chloride ~DTDMAC);
Field of the invention The present invention relates to fabric softening compositions and moreparticularly to compositions which reduce the amount of dyes released from coloured fabrics upon wet treatment such as those which occur in a laundry operation.
Background of the invention The domestic treatment of coloured fabrics is a problem known in the art to the formulator of laundry compositions. More particularly, the problem of formulating laundry compositions which reduce the amount of dyes released from coloured fabrics upon wet treatment is a particular challenge to the formulator. This problem is now even more acute with the trends of consumer to move towards more colored fabrics.
Numerous solutions have been proposed in the art to solve this problem such as by treating the fabric with a dye scavenger during the washing process as described in EP 0,341,205, EP 0,033,815 and with a polyvinyl substance as described in WO g4/11482 or in the rinse cycle with a dye fixing agent as described in EP 0,462,806. However, a problem encountered with these solutions is that the dye fixing agents when used in the washing process may be destroyed or damaged by contact on storage and/or during the process, whilst when used in the rinse cycle the 8U~$TITUTE SIIEET ~ULE Zfil .. ~ .. ,.................. . , . .. . . , ~.. ..
CA 022~7201 1998-11-30 need for a detergent active and a high level of dye fixing agent is required to provide effective dye fixation performance. Furthermore, a problem related with the use of dye fixing agents in a softening composition is that of its weight efficiency. So that, although levels of dye fixing agents above 10% by weight would provide effective dye fixation, such use would result in an increase in the formulation cost. Another problem relating to the use of a high level of dye fixing agents in fabric softening compositions is that the resulting products show phase instability. On the other hand, lowering the level of dye fixing agents would not provide sufficient dye fixing properties and the need for a detergent material would be required.
Accordingly, notwithstanding the advances in the art, there is still a need for a fabric softening composition which effectively reduces the amount of dyes released from coloured fabrics upon wet treatment.
The Applicant has now found that the use of a liquid composition comprising a cationic fabric softener having at least two long chains, a cationic dye fixing agent in amount of 0.1 % to 10% by weight, said composition being free of detergent materials, fulfills such a need.
It is therefore an advantage of the invention to provide liquid fabric softening compositions which provide effective reduction of the amount of dyes released from coloured fabrics upon wet domestic tre~atments.
It is another advantage of the invention to provide liquid fabric softening compositions with effective softening properties.
It is another advantage of the invention to provide liquid fabric softening compositions with effective storage stability properties.
For the purpose of the invention, the term "detergent materials"
encompasses detergent surfactant materials selected from soaps, non-soap ~nionic, nonionic, zwitterionic and amphoteric synthetic and natural detergent surfactants which are not softeners. Not included by this definition are the fatty acids which are fabric softeners, contrary to said soaps components which do not have fabric softener properties.
SUBSllllllt 811EE~ (IIULE 261 CA 022~7201 1998-11-30 wo 97t46651 PCT/USg7/08966 Summary of the invention The present invention relates to a liquid fabric softening composition comprising a cationic fabric softener having at least two long chains and a cationic dye fixing agent in amount of 0.1 % to 10% by weight, said composition being free of detergent materials.
In accordance with another aspect of the present invention, a method for treating fabrics is provided. The method comprises contacting the fabrics during the rinse cycle of a consumer laundry process with an aqueous medium containing at least 50 ppm of a fabric softening composition of the invention.
Detailed descriDtion of the invention Cationic fabric softeners An essential component of the invention is a cationic fabric softener component having at least two long chains. By component having at least two long chains is meant a component containing at least two alkyl or alkenyl chains, each comprising from 10 to 25 carbon atoms. Such fabric softener provides effective softness benefit to the treated fabrics.
Typical levels of said fabric softener components within the liquid softener compositions are from 1% to 80% by weight of the compositions.
Depending on the composition execution which can be dilute with a preferred level of fabric softening components from 1% to 5%, or concentrated, with a preferred level of fabric softening components from 5% to 80%, more preferably 10% to 50%, most preferably 15% to 35%
by weight.
.
Typical cationic fabric softening components having at least two long chains include the water-insoluble quaternary-ammonium fabric softening 8UI~TITU~E SHEE~ ~UIE 2~) ., . .. ., . ~, . . . . . .
CA 022~7201 1998-11-30 actives, the most commonly used having been di-long alkyl chains ammonium chloride.
Preferred cationic softeners among these include the following:
1 ) ditallow dimethylammonium chloride ~DTDMAC);
2) dihydrogenated tallow dimethylammonium chloride;
3) dihydrogenated tallow dimethylammonium methylsulfate;
4) distearyl dimethylammonium chloride;
5) dioleyl dimethylammonium chloride;
6) dipalmityl hydroxyethyl methylammonium chloride;
7) stearyl benzyl dimethylammonium chloride;
8) tallow trimethylammonium chloride;
9) hydrogenated tallow trimethylammonium chloride;
10) C 1 2-14 alkyl hydroxyethyl dimethylammonium chloride;
11) C12 1g alkyl dihydroxyethyl methylammonium chloride;
12) ditallow imidazolinium methylsulfate;
13) 1-(2-tallowylamidoethyl)-2-tallowyl imidazolinium methylsulfate .
However, in recent years, the need has arisen for more environmental-friendly materials, and rapidly biodegradable quaternary ammonium compounds have been presented as alternatives to the traditionally used di-long chain ammonium chlorides. Such quaternary ammonium compounds contain long chain alk(en)yl groups interrupted by functional groups such as carboxy groups. Said materials and fabric softening compositions containing them are disclosed in numerous publications such as EP-A-0,040,562, and EP-A-0,239,910.
The quaternary ammonium compounds and amine precursors herein have the formula (I) or (Il), below: _ R3\ R3 \ / 1 + N--(CH2)n-CI H -CH2 x ~
_ + I (C~h~-Q~ X R3 Q
Rl l l T2 or _ (I) (Il) SUBSTITUTE SIIEE~ ~IUIE 2~
CA 022~7201 1998-11-30 WO 97/46651 PCTtUS97/08966 wherein Q is selected from -O-C(O)-, -C(O)-O-, -O-C(O)-O-, -NR4-C(o)-, -C(o)-NR4-;
R1 is (CH2)n-Q-T2 or T3;
R2 is (CH2)m-Q-T4 or T5 or R3;
R3 is C1-C4 alkyl or C1-C4 hydroxyalkyl or H;
R4 is H or C1-C4 alkyl or C1-C4 hydroxyalkyl;
T1, T2, T3, T4, T5 are independently C1 1-C22 alkyl or alkenyl;
n and m are integers from 1 to 4; and X~ is a softener-compatible aniom Non-limiting examples of softener-compatible anions include chloride ormethyl sulfate.
The alkyl, or alkenyl, chain T1, T2, T3, T4, T5 must contain at least 11 carbon atoms, preferably at least 16 carbon atoms. The chain may be straight or branched.
Tallow is a convenient and inexpensive source of long chain alkyl and alkenyl material. The compounds wherein T1, T2, T3, T4, T5 represents the mixture of long chain materials typical for tallow are particularly preferred .
Specific examples of quaternary ammonium compounds suitable for use in the aqueous fabric softening compositions herein include:
1 ) N,N-di(tallowoyl-oxy-ethyl)-N,N-dimethyl ammonium chloride;
2) N,N-di(tallowoyl-oxy-ethyl)-N-methyl, N-(2-hydroxyethyl) ammonium chloride;
3) N,N-di(2-tallowyl-oxy-2-oxo-ethyl)-N,N-dimethyl ammonium chloride;
4) N,N-di(2-tallowyl-oxy-ethylcarbonyl-oxy-ethyl)-N,N-dimethyl ammonium chloride;
O N-(2-tallowoyl-oxy-2-ethyl)-N-(2-tallowyl-oxy-2-oxo-ethyl)-N,N-dimethyl ammonium chloride;
6) N,N,N-tri(tallowyl-oxy-ethyl)-N-methyl ammonium chloride;
SlB81ll~lt SIET (I~U~E 2~3 CA 022~7201 1998-11-30 7) N-(2-tallowyl-oxy-2-oxo-ethyl)-N-(tallowyl-N,N-dimethyl-ammonium chloride;
8) N - methyl - N - (3 - tallowamidopropyl), N-(2-tallowoyloxyethyl) ammonium chloride;
9) 1, 2-ditallowyl-oxy-3-trimethylammoniopropane chloride;
and mixtures of any of the above materials.
Of these, compounds 1-8 are examples of compounds of Formula (I);
compound 9 is a compound of Formula (Il). Particularly preferred is N,N-di(tallowoyl-oxy-ethyl)-N,N-dimethyl ammonium chloride, where the tallow chains are at least partially unsaturated. The level of unsaturation of the tallow chain can be measured by the lodine Value (IV) of the corresponding fatty acid, which in the present case should preferably be in the range of from 5 to 100 with two categories of compounds being distinguished, having a IV below or above 25. Indeed, for compounds of Formula (I) made from tallow fatty acids having an IV of from 5 to 25, preferably 15 to 20, it has been found that a cisttrans isomer weight ratio greater than 30/70, preferably greater than 50/50 and more preferably greater than 70/30 provides optimal concentrability. For compounds of Formula (I) made from tallow fatty acids having an IV of above 25, the ratio of cis to trans isomers has been found to be less critical unless very high concentrations are needed.
Other examples of suitable quaternary ammoniums of Formula (I) and (Il) are obtained by, e.g.:
- replacing "tallow" in the above compounds with, for example, coco, palm, lauryl, oleyl, ricinoleyl, stearyl, palmityl, or the like, said fatty acylchains being either fully saturated, or preferably at least partly unsaturated;
- replacing "methyl" in the above compounds with ethyl, ethoxy, propyl, propoxy, isopropyl, butyl, isobutyl or t-butyl;
- replacing "chloride" in the above compounds with bromide, methylsulfate, formate, sulfate, nitrate, and the like.
, , .
In fact, the anion is merely present as a counterion of the positively charged quaternary ammonium compounds. The nature of the counterion is $UBS~ t SHE~ LE 2~) CA 022~7201 1998-11-30 not critical at all to the practice of the present invention. The scope of this invention is not considered limited to any particular anion.
By "amine precursors thereof" is meant the secondary or tertiary aminescorresponding to the above quaternary ammonium compounds, said amines being substantially protonated in the present compositions due to the pH
values.
For the preceding biodegradable fabric softening agents, the pH of the compositions herein is an essential parameter of the present invention.
Indeed, it influences the stability of the quaternary ammonium or amine precursors compounds, especially in prolonged storage conditions. The pH, as defined in the present context, is measured in the neat compositions at 20~C. For optimum hydrolytic stability of these compositions, the neat pH, measured in the above-mentioned conditions, must be in the range of from 2.0 to 4.5. Preferably, where the liquid fabric softening compositions of the invention are in a diluted form, the pH of the neat composition is in the range of 2.0 to 3Ø The pH of these compositions herein can be regulated by the addition of a Bronsted acid. Examples of suitable acids include the inorganic mineral acids, carboxylic acids, in particular the low molecular weight ~C1-Cs) carboxylic acids, and alkylsulfonic acids. Suitable inorganic acids include HCI, H2S04, HNO3 and H3P04. Suitable organic acids include formic, acetic, citric, methylsulfonic and ethylsulfonic acid.
Preferred acids are citric, hydrochloric, phosphoric, formic, methylsulfonic acid, and benzoic acids.
Cationic dve fixative agent The other essential component of the invention is a cationic dye fixative agent. Cationic dye fixing agents, or "fixatives", are well-known, commercially available materials which are designed to improve the appearance of dyed fabric by minimizing the loss of dye from fabrics due to ~vashing. Cationic dye fixatives are based on various quaternized or otherwise cationically charged organic nitrogen compounds. Cationic fixatives are available under various trade names from several suppliers.
Representative examples include: CROSCOLOR PMF (July 1981, Code No.
SUBSTITUTE SHEEr ~RDLE 2~) CA 022~7201 1998-ll-30 7894) and CROSCOLOR NOFF ~January 1988, Code No. 8544) from Crosfield; INDOSOL E-50 (February 27, 1984, Ref. No. 6008.35.84;
polyethyleneamine-based) from Sandoz; SANDOFIX TPS, which is also available from Sandoz and is a preferred polycationic fixative for use herein and SANDOFIX SWE (cationic resinous compound), REWIN SRF, REWIN
SRF-O and REWIN DWR from CHT-Beitlich GMBH.
Other cationic dye fixing agents are described in "Aftertreatments for improving the fastness of dyes on textile fibres" by Christopher C. Cook (REV. PROG. COLORATION Vol. 12, 1982). Dye fixing agents suitable for use in the present invention are ammonium compounds such as fatty acid -diamine condensates e.g. the hydrochloride, acetate, metosulphate and benzyl hydrochloride of oleyldiethyl aminoethylamide, oleylmethyl-diethylenediaminemethosulphate, monostearyl-ethylene diaminotrimethylammonium methosulphate and oxidized products of tertiary amines; derivatives of polymeric alkyldiamines, polyamine-cyanuric chloride condensates and aminated glycerol dichlorohydrins.
The amount of dye fixing agent to be employed in the composition of theinvention is in amount of from 0.1 % to 10% by weight of the composition, preferably from 0.5% to 8% by weight, more preferably from 0.8% to 5.5% by weight of the composition.
For optimum dye fixing benefit as well as softness benefit, the weight ratio of fabric softener to dye fixing agent is of from 60: 1 to 1.5: 1, more preferably from 20:1 to 3.5:1, most preferably from 10:1 to 3.5:1.
Detergent materials For the purpose of the invention, the term "detergent materials"
encompasses detergent surfactant materials selected from soaps, non-soap anionic, nonionic, zwitterionic and amphoteric synthetic and natural detergent surfactants which are not softeners. Not included by this definition are the fatty acids which are fabric softeners, contrary to said soaps components which do not have fabric softener properties.
SUB~TITUTE 81E~ (;IULE 2~
CA 022~7201 1998-11-30 Soaps and non-soaps anionic materials are the linear and branched primary alkyl sulfates, alkyl ethoxysulfates, fatty oleyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, the C5-C17 acyl-N-(C1-C4 alkyl) and -N-tC1-C2 hydroxyalkyl) glucamine sulfates, and sulfates of alkylpolysaccharides; anionic sulfonate surfactants such as the salts of C5-C20 linear alkylbenzene sulfonates, alkyl ester sulfonates, C6-C22 primary or secondary alkane sulfonates, C6-C24 olefin sulfonates, sulfonated polycarboxylic acids, alkyl glycerol sulfonates, fatty acyl or oleyl glycerol sulfonates, alkyl ethoxy carboxvlates, and the alkali metal sarcosinates.
Nonionic detergent materials are the polyhydroxy fatty acid amides, polyethylene, polypropylene, and polybutylene oxide condensates of alkyl phenols; alkyl ethoxylate condensation products of aliphatic alcohols with from about 1 to about 25 moles of ethylene oxide; ethoxylated C6-C1g fatty alcohols and C6-C1g mixed ethoxylated/propoxylated fatty alcohols;
alkylpolysaccharides and the fatty acid amides.
Zwiterrionic and amphoteric materials are the amine oxides, the alkyl amphocarboxylic acids, the betaines such as coconut acylamidopropyldimethyl betaine and hexadecyl dimethyl betaine.
Additional comconents The composition may also optionally contain additional components such as additional fabric softener materials, electrolyte concentration aids, stabilisers, such as well known antioxidants and reductive agents, soil release polymers, bacteriocides, colorants, perfumes, preservatives, optical brighteners, anti ionisation agents, antifoam agents and chelating agents.
Additional fabric softener materials Additiona! fabric softening materials may be used in addition to the di-long chain cationic fabric softener. When used, such additional fabric softening materials will typically be present in an amount of from 0 to 15 % by SUBSTITUTE SIIEE~ ~UIE 26~
. .
CA 022~7201 1998-ll-30 weight of the composition. Such materials are the single long chain alkyl cationic softeners and/or the fatty acids.
Single long chain alkvl cationic softeners Such mono-long-chain-alkyl cationic softeners suitable for use herein are, preferably, quaternary ammonium salts of the general formula:
[R2N + R3] X~
wherein the R2 group is C10-c22 hydrocarbon group, preferably C12-C1g alkyl group of the corresponding ester linkage interrupted group with a short alkylene (C1-C4) group between the ester linkage and the N, and having a similar hydrocarbon group, e.g., a fatty acid ester of choline, preferably C12-C14 ~coco) choline ester and/or C16-C1g tallow choline ester at from 0.1% to 20% by weight of the softener active. Each R3 is a C1-C4 alkyl or substituted (e.g., hydroxy) alkyl, or hydrogen, preferably methyl, and the counterion X~ is a softener compatible anion, for example, chloride, bromide, methyl sulfate, etc.
Other cationic materials with ring structures such as alkyl imidazoline, imidazolinium, pyridine, and pyridinium salts having a single C12-C30 alkyl chain can also be used. Very low pH is required to stabilize, e.g., imidazoline ring structures.
Some alkyl imidazolinium salts and their imidazoline precursors useful in the present invention have the general formula:
N~ ,N C2H4--Y--R X
R
wherein y2 is -C(O)-O-, -O-(O)C-, -C(o)-N(R5)-, or-N(R5)-C(O)- in which R5 is hydrogen or a C1-C4 alkyl radical; R6 is a C1-C4 alkyl radical or H (for imidazoline precursors); R7 and R8 are each independently selected from R3 and R2 as defined hereinbefore for the single-long-chain cationic surfactant with only one being R2.
SUBSTI~U~E S~ UIE 211) CA 022~7201 1998-11-30 Some alkyl pyridinium salts useful in the present invention have the general formula:
R--N\~3 X
wherein R2 and X- are as defined above. A typical material of this type is cetyl pyridinium chloride.
Fatty acids Suitable fatty acids include those containing from 10 to 25, preferably from 12 to 25 total carbon atoms, with the fatty moiety containing from 10 to 22, preferably from 16 to 22, carbon atoms. The shorter moiety contains from 1 to 4, preferably from 1 to 2 carbon atoms. The level of unsaturation of the tallow chain can be measured by the lodine Value (IV) of the corresponding fatty acid, which in the present case should preferably be in the range of from 5 to 100, more preferably in the range of from 0 to 25.
Specific examples of fatty acid compounds suitable for use in the liquid fabric softening compositions herein include compounds selected from lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid, behenicacid, oleic acid, coconut fatty acid, tallow fatty acid, partially hydrogenated tallow fatty acid and mixtures thereof. A most preferred fatty acid compound is tallow fatty acid with an lodine Value (IV) of 18.
When the above mentioned fatty acids are used, the fatty acid will be present in a weight ratio of said cationic fabric softening agents having di-long chains to said fatty acid compounds of from 25:1 to 6.5:1, more preferably from 20:1 to 10:1 and most preferably from 20:1 to 15:1.
Indeed, if used outside of these ratios, the resulting product will tend to exhibit phase instability and/or viscosity problems.
SUBSTITUTE SIIET ~ULE 20) , . .. . .. .. ..... , . ~ ..
CA 022~7201 1998-ll-30 Electrolyte Concentration Aids Inorganic viscosity control agents which can also act like or augment the effect of the surfactant concentration aids, include water-soluble, ionizable salts which can also optionally be incorporated into the compositions of the present invention. Incorporation of these components to the composition must be processed at a very slow rate.
A wide variety of ionizable salts can be used. Examples of suitable salts are the halides of the Group IA and IIA metals of the Periodic Table of the Elements, e.g., calcium chloride, magnesium chloride, sodium chloride, potassium bromide, and lithium chloride. The ionizable salts are particularly useful during the process of mixing the ingredients to make the compositions herein, and later to obtain the desired viscosity. The amount of ionizable salts used depends on the amount of active ingredients used in the compositions and can be adjusted according to the desires of the formulator. Typical levels of salts used to control the composition viscosity are from 20 to 20,000 parts per million (ppm), preferably from 20 to 11,000 ppm, by weight of the composition.
Alkylene polyammonium salts can be incorporated into the composition togive viscosity control in addition to or in place of the water-soluble, ionizable salts above. In addition, these agents can act as scavengers, forming ion pairs with anionic detergent carried over from the main wash, in the rinse, and on the fabrics, and may improve softness performance.
These agents may stabilise the viscosity over a broader range of temperature, especially at low temperatures, compared to the inorganic electrolytes. Specific examples of alkylene polyammonium salts include L-lysine monohydrochloride and 1,5-diammonium 2-methyl pentane dihydrochloride .
Another ingredient is a liquid carrier. Suitable liquid carriers are selected from water, organic solvents and mixtures thereof. The liquid carrier employed in the instant compositions is preferably at least primarily water due to its low cost relative availability, safety, and environmental compatibility. The level of water in the liquid carrier is preferably at least SU08TITUTE $1EET ~UlE 2~) CA 022~7201 1998-11-30 50%, most preferably at least 60%, by weight of the carrier. Mixtures of water and low molecular weight, e.g., <200, organic solvent, e.g., lower alcohol such as ethanol, propanol, isopropanol or butanol are useful as the carrier liquid. Low molecular weight alcohols include monohydric, dihydric - (glycol, etc.) trihydric (glycerol, etc.), and higher polyhydric (polyols) alcohols .
Form of the com~osition The fabric softening composition can take a variety of physical forms including liquid such as aqueous or non-aqueous compositions.
Such compositions may be used as a rinse added product, or as a spray or foam product. Preferably, the present composition is in a rinse added form.
The compositions of the invention can be added directly in the rinse both to provide adequate usage concentration, e.g., at least 50 ppm and more preferably from 100 to 10,000 ppm of the liquid rinse added fabric softener compositions of the present invention.
Accordingly, a method is provided for treating fabrics comprising contacting said fabrics in the rinse cycle with an aqueous medium containing at least 50 ppm, preferably from 100 to 10,000 ppm of the liquid fabric softening composition of the invention.
Process The fabric softening composition can conveniently be made according to well- known processes to the skilled person. An exemplary disclosure is given in EP-A-0,668,902.
, The invention is illustrated in the following non-limiting examples, in which all percentages are on a weight basis unless otherwise stated.
81B8TITUTE SIIEE~ ~UILE 2e) . = . ... .. . ... ... . ........ ...... . .... ... . . ... .
CA 022~7201 1998-ll-30 In the examples, the abbreviated component identifications have the following meanings:
DEQA : Di-ltallowoyl-oxy-ethyl) dimethyl ammonium chloride Fatty acid : Stearic acid of IV=18 Electrolyte : Calcium chloride PEG : Polyethylene Glycol MW 4000 Example 1 The following fabric softening composition according to the present invention was prepared:
Component A
DEQA 1 9.0 Hydrochlorid acid 0.02 Soil Release Polymer 0.2 PEG 0 . 6 Perfume 1.0 Electrolyte 1 200ppm Dye 50ppm Sandofix TPS 5 .0 Water and minors to balance to 100%
Example 2 T~he following fabric softening compositions are in accordance with theinvention:
SUISTITUTE 8HEE~ ~IUI E 211~
Component B C D
DEQA 2. 6 2.9 18 .0 Fatty acid 0.3 - 1.0 Hydrochlorid acid 0.02 0.02 0.02 Soil Release Polymer - - 0.2 PEG - - O. 6 Perfume 1.0 0.5 1.0 Electrolyte - - 600ppm Dye 1 Oppm 1 Oppm 50ppm Sandofix TPS 1.6 1.6 5.0 Water and minors ~o balance to 100%
TITUTE SIE~ ~UIE 26)
However, in recent years, the need has arisen for more environmental-friendly materials, and rapidly biodegradable quaternary ammonium compounds have been presented as alternatives to the traditionally used di-long chain ammonium chlorides. Such quaternary ammonium compounds contain long chain alk(en)yl groups interrupted by functional groups such as carboxy groups. Said materials and fabric softening compositions containing them are disclosed in numerous publications such as EP-A-0,040,562, and EP-A-0,239,910.
The quaternary ammonium compounds and amine precursors herein have the formula (I) or (Il), below: _ R3\ R3 \ / 1 + N--(CH2)n-CI H -CH2 x ~
_ + I (C~h~-Q~ X R3 Q
Rl l l T2 or _ (I) (Il) SUBSTITUTE SIIEE~ ~IUIE 2~
CA 022~7201 1998-11-30 WO 97/46651 PCTtUS97/08966 wherein Q is selected from -O-C(O)-, -C(O)-O-, -O-C(O)-O-, -NR4-C(o)-, -C(o)-NR4-;
R1 is (CH2)n-Q-T2 or T3;
R2 is (CH2)m-Q-T4 or T5 or R3;
R3 is C1-C4 alkyl or C1-C4 hydroxyalkyl or H;
R4 is H or C1-C4 alkyl or C1-C4 hydroxyalkyl;
T1, T2, T3, T4, T5 are independently C1 1-C22 alkyl or alkenyl;
n and m are integers from 1 to 4; and X~ is a softener-compatible aniom Non-limiting examples of softener-compatible anions include chloride ormethyl sulfate.
The alkyl, or alkenyl, chain T1, T2, T3, T4, T5 must contain at least 11 carbon atoms, preferably at least 16 carbon atoms. The chain may be straight or branched.
Tallow is a convenient and inexpensive source of long chain alkyl and alkenyl material. The compounds wherein T1, T2, T3, T4, T5 represents the mixture of long chain materials typical for tallow are particularly preferred .
Specific examples of quaternary ammonium compounds suitable for use in the aqueous fabric softening compositions herein include:
1 ) N,N-di(tallowoyl-oxy-ethyl)-N,N-dimethyl ammonium chloride;
2) N,N-di(tallowoyl-oxy-ethyl)-N-methyl, N-(2-hydroxyethyl) ammonium chloride;
3) N,N-di(2-tallowyl-oxy-2-oxo-ethyl)-N,N-dimethyl ammonium chloride;
4) N,N-di(2-tallowyl-oxy-ethylcarbonyl-oxy-ethyl)-N,N-dimethyl ammonium chloride;
O N-(2-tallowoyl-oxy-2-ethyl)-N-(2-tallowyl-oxy-2-oxo-ethyl)-N,N-dimethyl ammonium chloride;
6) N,N,N-tri(tallowyl-oxy-ethyl)-N-methyl ammonium chloride;
SlB81ll~lt SIET (I~U~E 2~3 CA 022~7201 1998-11-30 7) N-(2-tallowyl-oxy-2-oxo-ethyl)-N-(tallowyl-N,N-dimethyl-ammonium chloride;
8) N - methyl - N - (3 - tallowamidopropyl), N-(2-tallowoyloxyethyl) ammonium chloride;
9) 1, 2-ditallowyl-oxy-3-trimethylammoniopropane chloride;
and mixtures of any of the above materials.
Of these, compounds 1-8 are examples of compounds of Formula (I);
compound 9 is a compound of Formula (Il). Particularly preferred is N,N-di(tallowoyl-oxy-ethyl)-N,N-dimethyl ammonium chloride, where the tallow chains are at least partially unsaturated. The level of unsaturation of the tallow chain can be measured by the lodine Value (IV) of the corresponding fatty acid, which in the present case should preferably be in the range of from 5 to 100 with two categories of compounds being distinguished, having a IV below or above 25. Indeed, for compounds of Formula (I) made from tallow fatty acids having an IV of from 5 to 25, preferably 15 to 20, it has been found that a cisttrans isomer weight ratio greater than 30/70, preferably greater than 50/50 and more preferably greater than 70/30 provides optimal concentrability. For compounds of Formula (I) made from tallow fatty acids having an IV of above 25, the ratio of cis to trans isomers has been found to be less critical unless very high concentrations are needed.
Other examples of suitable quaternary ammoniums of Formula (I) and (Il) are obtained by, e.g.:
- replacing "tallow" in the above compounds with, for example, coco, palm, lauryl, oleyl, ricinoleyl, stearyl, palmityl, or the like, said fatty acylchains being either fully saturated, or preferably at least partly unsaturated;
- replacing "methyl" in the above compounds with ethyl, ethoxy, propyl, propoxy, isopropyl, butyl, isobutyl or t-butyl;
- replacing "chloride" in the above compounds with bromide, methylsulfate, formate, sulfate, nitrate, and the like.
, , .
In fact, the anion is merely present as a counterion of the positively charged quaternary ammonium compounds. The nature of the counterion is $UBS~ t SHE~ LE 2~) CA 022~7201 1998-11-30 not critical at all to the practice of the present invention. The scope of this invention is not considered limited to any particular anion.
By "amine precursors thereof" is meant the secondary or tertiary aminescorresponding to the above quaternary ammonium compounds, said amines being substantially protonated in the present compositions due to the pH
values.
For the preceding biodegradable fabric softening agents, the pH of the compositions herein is an essential parameter of the present invention.
Indeed, it influences the stability of the quaternary ammonium or amine precursors compounds, especially in prolonged storage conditions. The pH, as defined in the present context, is measured in the neat compositions at 20~C. For optimum hydrolytic stability of these compositions, the neat pH, measured in the above-mentioned conditions, must be in the range of from 2.0 to 4.5. Preferably, where the liquid fabric softening compositions of the invention are in a diluted form, the pH of the neat composition is in the range of 2.0 to 3Ø The pH of these compositions herein can be regulated by the addition of a Bronsted acid. Examples of suitable acids include the inorganic mineral acids, carboxylic acids, in particular the low molecular weight ~C1-Cs) carboxylic acids, and alkylsulfonic acids. Suitable inorganic acids include HCI, H2S04, HNO3 and H3P04. Suitable organic acids include formic, acetic, citric, methylsulfonic and ethylsulfonic acid.
Preferred acids are citric, hydrochloric, phosphoric, formic, methylsulfonic acid, and benzoic acids.
Cationic dve fixative agent The other essential component of the invention is a cationic dye fixative agent. Cationic dye fixing agents, or "fixatives", are well-known, commercially available materials which are designed to improve the appearance of dyed fabric by minimizing the loss of dye from fabrics due to ~vashing. Cationic dye fixatives are based on various quaternized or otherwise cationically charged organic nitrogen compounds. Cationic fixatives are available under various trade names from several suppliers.
Representative examples include: CROSCOLOR PMF (July 1981, Code No.
SUBSTITUTE SHEEr ~RDLE 2~) CA 022~7201 1998-ll-30 7894) and CROSCOLOR NOFF ~January 1988, Code No. 8544) from Crosfield; INDOSOL E-50 (February 27, 1984, Ref. No. 6008.35.84;
polyethyleneamine-based) from Sandoz; SANDOFIX TPS, which is also available from Sandoz and is a preferred polycationic fixative for use herein and SANDOFIX SWE (cationic resinous compound), REWIN SRF, REWIN
SRF-O and REWIN DWR from CHT-Beitlich GMBH.
Other cationic dye fixing agents are described in "Aftertreatments for improving the fastness of dyes on textile fibres" by Christopher C. Cook (REV. PROG. COLORATION Vol. 12, 1982). Dye fixing agents suitable for use in the present invention are ammonium compounds such as fatty acid -diamine condensates e.g. the hydrochloride, acetate, metosulphate and benzyl hydrochloride of oleyldiethyl aminoethylamide, oleylmethyl-diethylenediaminemethosulphate, monostearyl-ethylene diaminotrimethylammonium methosulphate and oxidized products of tertiary amines; derivatives of polymeric alkyldiamines, polyamine-cyanuric chloride condensates and aminated glycerol dichlorohydrins.
The amount of dye fixing agent to be employed in the composition of theinvention is in amount of from 0.1 % to 10% by weight of the composition, preferably from 0.5% to 8% by weight, more preferably from 0.8% to 5.5% by weight of the composition.
For optimum dye fixing benefit as well as softness benefit, the weight ratio of fabric softener to dye fixing agent is of from 60: 1 to 1.5: 1, more preferably from 20:1 to 3.5:1, most preferably from 10:1 to 3.5:1.
Detergent materials For the purpose of the invention, the term "detergent materials"
encompasses detergent surfactant materials selected from soaps, non-soap anionic, nonionic, zwitterionic and amphoteric synthetic and natural detergent surfactants which are not softeners. Not included by this definition are the fatty acids which are fabric softeners, contrary to said soaps components which do not have fabric softener properties.
SUB~TITUTE 81E~ (;IULE 2~
CA 022~7201 1998-11-30 Soaps and non-soaps anionic materials are the linear and branched primary alkyl sulfates, alkyl ethoxysulfates, fatty oleyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, the C5-C17 acyl-N-(C1-C4 alkyl) and -N-tC1-C2 hydroxyalkyl) glucamine sulfates, and sulfates of alkylpolysaccharides; anionic sulfonate surfactants such as the salts of C5-C20 linear alkylbenzene sulfonates, alkyl ester sulfonates, C6-C22 primary or secondary alkane sulfonates, C6-C24 olefin sulfonates, sulfonated polycarboxylic acids, alkyl glycerol sulfonates, fatty acyl or oleyl glycerol sulfonates, alkyl ethoxy carboxvlates, and the alkali metal sarcosinates.
Nonionic detergent materials are the polyhydroxy fatty acid amides, polyethylene, polypropylene, and polybutylene oxide condensates of alkyl phenols; alkyl ethoxylate condensation products of aliphatic alcohols with from about 1 to about 25 moles of ethylene oxide; ethoxylated C6-C1g fatty alcohols and C6-C1g mixed ethoxylated/propoxylated fatty alcohols;
alkylpolysaccharides and the fatty acid amides.
Zwiterrionic and amphoteric materials are the amine oxides, the alkyl amphocarboxylic acids, the betaines such as coconut acylamidopropyldimethyl betaine and hexadecyl dimethyl betaine.
Additional comconents The composition may also optionally contain additional components such as additional fabric softener materials, electrolyte concentration aids, stabilisers, such as well known antioxidants and reductive agents, soil release polymers, bacteriocides, colorants, perfumes, preservatives, optical brighteners, anti ionisation agents, antifoam agents and chelating agents.
Additional fabric softener materials Additiona! fabric softening materials may be used in addition to the di-long chain cationic fabric softener. When used, such additional fabric softening materials will typically be present in an amount of from 0 to 15 % by SUBSTITUTE SIIEE~ ~UIE 26~
. .
CA 022~7201 1998-ll-30 weight of the composition. Such materials are the single long chain alkyl cationic softeners and/or the fatty acids.
Single long chain alkvl cationic softeners Such mono-long-chain-alkyl cationic softeners suitable for use herein are, preferably, quaternary ammonium salts of the general formula:
[R2N + R3] X~
wherein the R2 group is C10-c22 hydrocarbon group, preferably C12-C1g alkyl group of the corresponding ester linkage interrupted group with a short alkylene (C1-C4) group between the ester linkage and the N, and having a similar hydrocarbon group, e.g., a fatty acid ester of choline, preferably C12-C14 ~coco) choline ester and/or C16-C1g tallow choline ester at from 0.1% to 20% by weight of the softener active. Each R3 is a C1-C4 alkyl or substituted (e.g., hydroxy) alkyl, or hydrogen, preferably methyl, and the counterion X~ is a softener compatible anion, for example, chloride, bromide, methyl sulfate, etc.
Other cationic materials with ring structures such as alkyl imidazoline, imidazolinium, pyridine, and pyridinium salts having a single C12-C30 alkyl chain can also be used. Very low pH is required to stabilize, e.g., imidazoline ring structures.
Some alkyl imidazolinium salts and their imidazoline precursors useful in the present invention have the general formula:
N~ ,N C2H4--Y--R X
R
wherein y2 is -C(O)-O-, -O-(O)C-, -C(o)-N(R5)-, or-N(R5)-C(O)- in which R5 is hydrogen or a C1-C4 alkyl radical; R6 is a C1-C4 alkyl radical or H (for imidazoline precursors); R7 and R8 are each independently selected from R3 and R2 as defined hereinbefore for the single-long-chain cationic surfactant with only one being R2.
SUBSTI~U~E S~ UIE 211) CA 022~7201 1998-11-30 Some alkyl pyridinium salts useful in the present invention have the general formula:
R--N\~3 X
wherein R2 and X- are as defined above. A typical material of this type is cetyl pyridinium chloride.
Fatty acids Suitable fatty acids include those containing from 10 to 25, preferably from 12 to 25 total carbon atoms, with the fatty moiety containing from 10 to 22, preferably from 16 to 22, carbon atoms. The shorter moiety contains from 1 to 4, preferably from 1 to 2 carbon atoms. The level of unsaturation of the tallow chain can be measured by the lodine Value (IV) of the corresponding fatty acid, which in the present case should preferably be in the range of from 5 to 100, more preferably in the range of from 0 to 25.
Specific examples of fatty acid compounds suitable for use in the liquid fabric softening compositions herein include compounds selected from lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid, behenicacid, oleic acid, coconut fatty acid, tallow fatty acid, partially hydrogenated tallow fatty acid and mixtures thereof. A most preferred fatty acid compound is tallow fatty acid with an lodine Value (IV) of 18.
When the above mentioned fatty acids are used, the fatty acid will be present in a weight ratio of said cationic fabric softening agents having di-long chains to said fatty acid compounds of from 25:1 to 6.5:1, more preferably from 20:1 to 10:1 and most preferably from 20:1 to 15:1.
Indeed, if used outside of these ratios, the resulting product will tend to exhibit phase instability and/or viscosity problems.
SUBSTITUTE SIIET ~ULE 20) , . .. . .. .. ..... , . ~ ..
CA 022~7201 1998-ll-30 Electrolyte Concentration Aids Inorganic viscosity control agents which can also act like or augment the effect of the surfactant concentration aids, include water-soluble, ionizable salts which can also optionally be incorporated into the compositions of the present invention. Incorporation of these components to the composition must be processed at a very slow rate.
A wide variety of ionizable salts can be used. Examples of suitable salts are the halides of the Group IA and IIA metals of the Periodic Table of the Elements, e.g., calcium chloride, magnesium chloride, sodium chloride, potassium bromide, and lithium chloride. The ionizable salts are particularly useful during the process of mixing the ingredients to make the compositions herein, and later to obtain the desired viscosity. The amount of ionizable salts used depends on the amount of active ingredients used in the compositions and can be adjusted according to the desires of the formulator. Typical levels of salts used to control the composition viscosity are from 20 to 20,000 parts per million (ppm), preferably from 20 to 11,000 ppm, by weight of the composition.
Alkylene polyammonium salts can be incorporated into the composition togive viscosity control in addition to or in place of the water-soluble, ionizable salts above. In addition, these agents can act as scavengers, forming ion pairs with anionic detergent carried over from the main wash, in the rinse, and on the fabrics, and may improve softness performance.
These agents may stabilise the viscosity over a broader range of temperature, especially at low temperatures, compared to the inorganic electrolytes. Specific examples of alkylene polyammonium salts include L-lysine monohydrochloride and 1,5-diammonium 2-methyl pentane dihydrochloride .
Another ingredient is a liquid carrier. Suitable liquid carriers are selected from water, organic solvents and mixtures thereof. The liquid carrier employed in the instant compositions is preferably at least primarily water due to its low cost relative availability, safety, and environmental compatibility. The level of water in the liquid carrier is preferably at least SU08TITUTE $1EET ~UlE 2~) CA 022~7201 1998-11-30 50%, most preferably at least 60%, by weight of the carrier. Mixtures of water and low molecular weight, e.g., <200, organic solvent, e.g., lower alcohol such as ethanol, propanol, isopropanol or butanol are useful as the carrier liquid. Low molecular weight alcohols include monohydric, dihydric - (glycol, etc.) trihydric (glycerol, etc.), and higher polyhydric (polyols) alcohols .
Form of the com~osition The fabric softening composition can take a variety of physical forms including liquid such as aqueous or non-aqueous compositions.
Such compositions may be used as a rinse added product, or as a spray or foam product. Preferably, the present composition is in a rinse added form.
The compositions of the invention can be added directly in the rinse both to provide adequate usage concentration, e.g., at least 50 ppm and more preferably from 100 to 10,000 ppm of the liquid rinse added fabric softener compositions of the present invention.
Accordingly, a method is provided for treating fabrics comprising contacting said fabrics in the rinse cycle with an aqueous medium containing at least 50 ppm, preferably from 100 to 10,000 ppm of the liquid fabric softening composition of the invention.
Process The fabric softening composition can conveniently be made according to well- known processes to the skilled person. An exemplary disclosure is given in EP-A-0,668,902.
, The invention is illustrated in the following non-limiting examples, in which all percentages are on a weight basis unless otherwise stated.
81B8TITUTE SIIEE~ ~UILE 2e) . = . ... .. . ... ... . ........ ...... . .... ... . . ... .
CA 022~7201 1998-ll-30 In the examples, the abbreviated component identifications have the following meanings:
DEQA : Di-ltallowoyl-oxy-ethyl) dimethyl ammonium chloride Fatty acid : Stearic acid of IV=18 Electrolyte : Calcium chloride PEG : Polyethylene Glycol MW 4000 Example 1 The following fabric softening composition according to the present invention was prepared:
Component A
DEQA 1 9.0 Hydrochlorid acid 0.02 Soil Release Polymer 0.2 PEG 0 . 6 Perfume 1.0 Electrolyte 1 200ppm Dye 50ppm Sandofix TPS 5 .0 Water and minors to balance to 100%
Example 2 T~he following fabric softening compositions are in accordance with theinvention:
SUISTITUTE 8HEE~ ~IUI E 211~
Component B C D
DEQA 2. 6 2.9 18 .0 Fatty acid 0.3 - 1.0 Hydrochlorid acid 0.02 0.02 0.02 Soil Release Polymer - - 0.2 PEG - - O. 6 Perfume 1.0 0.5 1.0 Electrolyte - - 600ppm Dye 1 Oppm 1 Oppm 50ppm Sandofix TPS 1.6 1.6 5.0 Water and minors ~o balance to 100%
TITUTE SIE~ ~UIE 26)
Claims (7)
1- A liquid fabric softening composition comprising a cationic fabric softener having at least two long chains and a cationic dye fixing agent in amount of 0.1% to 10% by weight, said composition being free of detergent materials.
2- A liquid fabric softening composition according to Claim 1, wherein said cationic dye fixing agent is a polycationic dye fixing agent.
3- A liquid fabric softening composition according to either one of Claims 1 or 2, wherein said cationic dye fixing agent is in amount of from 0.5% to 8% by weight, preferably from 0.8% to 5.5% by weight of the composition.
4- A liquid fabric softening composition according to any one of Claims 1-3, wherein said fabric softener is a biodegradable fabric softening material.
5- A liquid fabric softening composition according to Claim 4, wherein said biodegradable fabric softening material is selected from quaternary ammonium compounds and amine precursors having the formula (I) or (II), below:
or wherein Q is selected from -O-C(O)-, -C(O)-O-, -O-C(O)-O-, -NR4-C(O)-, -(O)-NR4-;
R1 is (CH2)n-Q-T2 or T3;
R2 is (CH2)m-Q-T4 or T5 or R3;
R3 is C1-C4 alkyl or C1-C4 hydroxyalkyl or H;
R4 is H or C1-C4 alkyl or C1-C4 hydroxyalkyl;
T1, T2, T3, T4, T5 are independently C11-C22 alkyl or alkenyl;
n and m are integers from 1 to 4; and X- is a softener-compatible anion.
or wherein Q is selected from -O-C(O)-, -C(O)-O-, -O-C(O)-O-, -NR4-C(O)-, -(O)-NR4-;
R1 is (CH2)n-Q-T2 or T3;
R2 is (CH2)m-Q-T4 or T5 or R3;
R3 is C1-C4 alkyl or C1-C4 hydroxyalkyl or H;
R4 is H or C1-C4 alkyl or C1-C4 hydroxyalkyl;
T1, T2, T3, T4, T5 are independently C11-C22 alkyl or alkenyl;
n and m are integers from 1 to 4; and X- is a softener-compatible anion.
6- A liquid fabric softening composition according to any one of Claims 1-5, wherein said fabric softener is present in amount of 1% to 80%
by weight.
by weight.
7- A method for treating fabrics comprising contacting said fabrics in the rinse cycle with an aqueous medium containing at least 50 ppm of a liquid fabric softening composition according to any one of Claims 1-6.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP96870068A EP0811679B1 (en) | 1996-06-03 | 1996-06-03 | Fabric softening compositions |
EP96870068.2 | 1996-06-03 | ||
PCT/US1997/008966 WO1997046651A1 (en) | 1996-06-03 | 1997-05-23 | Fabric softening compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2257201A1 true CA2257201A1 (en) | 1997-12-11 |
Family
ID=8226145
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002257201A Abandoned CA2257201A1 (en) | 1996-06-03 | 1997-05-23 | Fabric softening compositions |
Country Status (11)
Country | Link |
---|---|
EP (1) | EP0811679B1 (en) |
JP (1) | JP3784417B2 (en) |
CN (1) | CN1093878C (en) |
AR (1) | AR007374A1 (en) |
AU (1) | AU3287497A (en) |
BR (1) | BR9709634A (en) |
CA (1) | CA2257201A1 (en) |
CZ (1) | CZ394598A3 (en) |
DE (1) | DE69628285T2 (en) |
ES (1) | ES2200047T3 (en) |
WO (1) | WO1997046651A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0990695A1 (en) | 1998-09-30 | 2000-04-05 | Witco Surfactants GmbH | Fabric softener with dye transfer inhibiting properties |
CA2346805A1 (en) * | 1998-10-23 | 2000-05-04 | The Procter & Gamble Company | Fabric color care method |
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 |
WO2011131412A1 (en) | 2010-04-22 | 2011-10-27 | Unilever Plc | Improvements relating to fabric conditioners |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3501521A1 (en) * | 1985-01-18 | 1986-07-24 | Henkel KGaA, 4000 Düsseldorf | AQUEOUS CONCENTRATED TEXTILE SOFTENER |
JPH03199472A (en) * | 1989-12-27 | 1991-08-30 | Kao Corp | Liquid softening, finishing agent |
JPH0441776A (en) * | 1990-06-01 | 1992-02-12 | Kao Corp | Liquid soft finishing agent |
GB9013784D0 (en) * | 1990-06-20 | 1990-08-08 | Unilever Plc | Process and composition for treating fabrics |
GB9301728D0 (en) * | 1993-01-28 | 1993-03-17 | Unilever Plc | Fabric softening composition |
US5616553A (en) * | 1993-08-12 | 1997-04-01 | The Procter & Gamble Company | Fabric conditioning compositions |
US5445747A (en) * | 1994-08-05 | 1995-08-29 | The Procter & Gamble Company | Cellulase fabric-conditioning compositions |
-
1996
- 1996-06-03 DE DE69628285T patent/DE69628285T2/en not_active Expired - Lifetime
- 1996-06-03 EP EP96870068A patent/EP0811679B1/en not_active Expired - Lifetime
- 1996-06-03 ES ES96870068T patent/ES2200047T3/en not_active Expired - Lifetime
-
1997
- 1997-05-23 CN CN97197016A patent/CN1093878C/en not_active Expired - Fee Related
- 1997-05-23 WO PCT/US1997/008966 patent/WO1997046651A1/en not_active Application Discontinuation
- 1997-05-23 CZ CZ983945A patent/CZ394598A3/en unknown
- 1997-05-23 AU AU32874/97A patent/AU3287497A/en not_active Abandoned
- 1997-05-23 JP JP50065098A patent/JP3784417B2/en not_active Expired - Fee Related
- 1997-05-23 BR BR9709634A patent/BR9709634A/en not_active Application Discontinuation
- 1997-05-23 CA CA002257201A patent/CA2257201A1/en not_active Abandoned
- 1997-06-02 AR ARP970102382A patent/AR007374A1/en unknown
Also Published As
Publication number | Publication date |
---|---|
BR9709634A (en) | 1999-08-10 |
CN1093878C (en) | 2002-11-06 |
CN1227594A (en) | 1999-09-01 |
JP2000503733A (en) | 2000-03-28 |
EP0811679B1 (en) | 2003-05-21 |
AR007374A1 (en) | 1999-10-27 |
DE69628285T2 (en) | 2004-04-01 |
JP3784417B2 (en) | 2006-06-14 |
CZ394598A3 (en) | 1999-07-14 |
ES2200047T3 (en) | 2004-03-01 |
WO1997046651A1 (en) | 1997-12-11 |
DE69628285D1 (en) | 2003-06-26 |
EP0811679A1 (en) | 1997-12-10 |
AU3287497A (en) | 1998-01-05 |
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