IE920735A1 - Concentrated fabric softening compositions - Google Patents

Concentrated fabric softening compositions

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Publication number
IE920735A1
IE920735A1 IE920735A IE920735A IE920735A1 IE 920735 A1 IE920735 A1 IE 920735A1 IE 920735 A IE920735 A IE 920735A IE 920735 A IE920735 A IE 920735A IE 920735 A1 IE920735 A1 IE 920735A1
Authority
IE
Ireland
Prior art keywords
weight
fabric softening
composition
composition according
concentrated
Prior art date
Application number
IE920735A
Inventor
Bruno Albert Jean Hubesch
Original Assignee
Procter & Gamble
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Publication date
Priority claimed from EP91870105.3A external-priority patent/EP0503218A1/en
Priority claimed from EP19910870187 external-priority patent/EP0503221B1/en
Application filed by Procter & Gamble filed Critical Procter & Gamble
Publication of IE920735A1 publication Critical patent/IE920735A1/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
    • C11D3/16Organic compounds
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • C11D3/3734Cyclic silicones
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    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/835Mixtures of non-ionic with cationic compounds
    • 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
    • C11D3/001Softening compositions
    • C11D3/0015Softening compositions liquid
    • 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
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/2017Monohydric alcohols branched
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    • 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
    • C11D3/20Organic compounds containing oxygen
    • C11D3/2003Alcohols; Phenols
    • C11D3/2006Monohydric alcohols
    • C11D3/2017Monohydric alcohols branched
    • C11D3/202Monohydric alcohols branched fatty or with at least 8 carbon atoms in the alkyl chain
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    • 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
    • C11D3/3707Polyethers, e.g. polyalkyleneoxides
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/144Alcohols; Metal alcoholates
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    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/165Ethers
    • D06M13/17Polyoxyalkyleneglycol ethers
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    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/35Heterocyclic compounds
    • D06M13/352Heterocyclic compounds having five-membered heterocyclic rings
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/35Heterocyclic compounds
    • D06M13/355Heterocyclic compounds having six-membered heterocyclic rings
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    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/46Compounds containing quaternary nitrogen atoms
    • D06M13/463Compounds containing quaternary nitrogen atoms derived from monoamines
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    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/46Compounds containing quaternary nitrogen atoms
    • D06M13/47Compounds containing quaternary nitrogen atoms derived from heterocyclic compounds
    • D06M13/473Compounds containing quaternary nitrogen atoms derived from heterocyclic compounds having five-membered heterocyclic rings
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    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/227Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of hydrocarbons, or reaction products thereof, e.g. afterhalogenated or sulfochlorinated
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    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/327Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof
    • D06M15/333Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof of vinyl acetate; Polyvinylalcohol
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    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/53Polyethers
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    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/643Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
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    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/58Heterocyclic compounds
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    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/62Quaternary ammonium compounds
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    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
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    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/50Modified hand or grip properties; Softening compositions

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Textile Engineering (AREA)
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  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

Concentrated fabric softening compositions are described which retain viscosity upon dilution in water. The compositions comprise cationic fabric softening actives, as well as a specific combination of emulsifiers and polymers. The present invention also encompasses a method for the softening of fabrics.

Description

The present invention relates to fabric softeners. The compositions according to the invention are concentrated aqueous fabric softening compositions which retain viscosity upon dilution.
Background Concentrated aqueous fabric softening compositions have been extensively described in the art, and one aspect which has often been discussed is the viscosity of these concentrated compositions; indeed these concentrated compositions are typically extremely viscous and the prior art has often described means by which the viscosity of these concentrated compositions could be controlled or decreased. One aspect which has been much less dealt with is the viscosity of these concentrated compositions upon dilution; indeed it has been observed that the viscosity of such concentrated compositions dramatically drops upon dilution, and this viscosity loss is clearly undesirable, essentially in terms of consumer acceptance.
It is therefore an object of the present invention to provide a concentrated aqueous fabric softening composition which has an acceptable viscosity in the concentrated form, and which retains acceptable viscosity after it has been diluted.
This technical problem was discussed in GB 2 007 734 which proposes to use a combination of a fatty quaternary ammonium salt having two long chain alkyl groups together with an oily substance.
Concentrated aqueous fabric softeners have been described for instance in EP 56 695, EP 13 780, DE 26 31 114 and EP 60 003, and a process for the preparation of concentrated fabric softening compositions is disclosed in EP-A-316 996.
Summary of the invention It has now been found that the above object can be achieved by formulating a concentrated aqueous fabric softening composition comprising from 10% to 35% by weight of a cationic fabric softening active or mixtures thereof, said composition further comprising: from 0.3% to 3 % by weight of the total composition of a linear fatty alcohol ethoxylate of the formula RO(Etox)n, wherein R is a linear Cg-C^g alkyl chain, and n representing the weighted average ethoxylation degree is of from 3 to 35, or mixtures thereof; From 0.5% to 6% by weight of the total composition of a nonionic hydrophilic polymer, or mixtures thereof; from 0% to 2% by weight of the total composition of a highly branched fatty alcohol having from 8 to 18 carbon atoms, or mixtures thereof; from 0% to 0.5 % by weight of the total composition of a linear or cyclic polydialkylsiloxane of the formula ,R ? R—[-Si-0-] —Si-R \ \ R R wherein R is a C1-C5 alkyl chain, and m is an integer of from 1 to 500, or mixtures thereof.
The present invention also encompasses a method for the softening of fabrics, wherein the above concentrated compositions are diluted in water before they are contacted with said fabrics in the rinse water.
Detailed description of the invention The compositions according to the invention are concentrated fabric softeners; by concentrated, it is meant that the compositions comprise from 10% to 35% by weight of the total composition of a cationic fabric softening active or mixtures thereof, preferably 15% to 25%. By cationic, it is meant any softening compound which is in cationic form in the concentrated softening composition. Suitable cationic fabric softening actives include (i) acylic quaternary ammonium salts having the formula : “ I r4 wherein R2 is an acylic aliphatic Ci5~C22 hydrocarbon group which may be interrupted by ester groups, R3 is a C1-C4 saturated alkyl or hydroalkyl group, R4 is selected from R2 and R3, and A is an anion; rapidly biodegradable compounds of formula (i) where R2, and possibly R4, are interrupted by ester groups, are disclosed in EPA 239 910; (ii) diamido quaternary ammonium salts having the formula : + A 0 i5 I R-L-C-NH-R2 -N-R2 -NH-C -Rx I Rs wherein R is an acyclic aliphatic C15-C22 hydrocarbon group, R2 is a divalent alkylene group having 1 to 3 carbon atoms, R5 and R8 are C1-C4 saturated alkyl or hydroxyalkyl groups, and A“ is an anion. (iii) diamido alkoxylated quaternary ammonium salts having the formula : (CH2CH2O)nH wherein n is an integer of from about 1 to about 5, and Rx, R2, R5 and A” are as defined above. (iv) quaternary imidazolinium compounds having the formula: wherein R^ = C15-C17 saturated alkyl, R2 = C1-C4 alkyl, Z = NH or O, and A“ is an anion. saturated Examples of Component (i) are the well-known dialkyldimethylammonium salts such as ditallowdimethylammonium chloride (DTDMAC), ditallowdimethylammonium methylsulfate, di(hydrogenated tallow) dimethylammonium chloride, dibehenyldimethylammonium chloride.
Examples of Component (ii) and (iii) are methylbis(tallowamidoethyl) (2-hydroxyethyl) ammonium methylsulfate and methyIbis(hydrogenated tallowamidoethyl) (2-hydroxyethyl) ammonium methylsulfate, wherein R^ is an acyclic aliphatic C15-C17 hydrocarbon group, R2 is an ethylene group, R5 is a methyl group, R8 is a hydroxyalkyl group and A is a methylsulfate anion; these materials are available from Sherex Chemical Company under the trade names Varisoft 222 R and Varisoft 110 R, respectively.
Examples of Component (iv) are 1-methyl-l-tallowamino-ethyl2-tallowimidazolinium methylsulfate and 1-methyl-l(hydrogenated tallowamidoethyl)-methylsulfate.
Other suitable fabric softening actives include the following amines, provided they are present in the concentrated softening composition in a protonated form; such amines are of the formula : /--(CH2)n_ N - X - R2R1 wherein n is 2 or 3, preferably 2; Rj and R2 are, independently, a C3-C3Q alkyl or alkenyl, preferably Οχ2-Ο20 alkyl, more preferably Cis-Cjg alkyl, or mixtures of such alkyl radicals. Examples of such mixtures are the alkyl radicals obtained from coconut oil, ’’soft” (non-hardened) tallow, and hardened tallow. Q is CH2 or N, preferably Ν, X is R4 - T - C II 0 wherein T is O or NR5, R5 being H or Ci-C4 alkyl, preferably H, and R4 is a divalent ¢^-03 alkylene group or (C2H4O)m, wherein m is an integer of from 1 to 8; or X is R4.
Most preferred softening agents according to the above formula are imidazolines of the following formula ; O 0 r\ ll Γ\ II Ν N — (CH2) 2 — NH — C — Rx and Ν N — (CH2) 2 — O —C — Rx V V c c Ri Ri wherein Rl is a tallow group.
The softening amines described herein above are suitable for the purpose of the present invention provided they are present in the concentrated softening composition in a protonated form; a suitable means to protonate these amines is described for instance in EP 199 383.
A preferred softening active mixture for use herein is a mixture of 20% to 70% by weight of the softening active of ditallow dimethyl ammonium chloride (DTDMAC) and 30% to 80% ditallow imidazoline. Preferably, the concentrated compositions according to the invention comprise from 15% to 25% by weight of the finished product of such a mixture.
In an alternative preferred embodiment of the present invention, the softening active comprises a ditallow imidazoline ester such as described herein above (i.e. when T is O and Rj and R2 are both tallow in the formula above).
This embodiment is particularly preferred for environmental reasons.
The compositions according to the invention further comprise from 0.3% to 3% by weight of the total composition of a linear fatty alcohol ethoxylate of the formula RO(Etox)n, wherein R is a linear C3-13 alkyl chain, and n representing the weighted average ethoxylation degree is of from 3 to 35, or mixtures thereof. Preferred are linear fatty alcohol ethoxylates wherein R is a linear chain having from 10 to 13 carbon atoms, and wherein n is from 5 to 10, preferably 8. Preferably, these compounds, or mixtures thereof are present at levels of from about 1 to about 1.5% by weight of the total composition. These compounds are commercially available from BASF under the trade name LUTENSOL TO(Bi The compositions according to the present invention further comprise from 0.5% to 6% , preferably from 1.5% to 2.5% by weight of the composition of a nonionic hydrophylic polymer, or mixtures thereof. Such suitable polymers include polyethylene glycol, polypropylene glycol, polyvinylalcolhol and the like. Particularly preferred is a polyethylene glycol having a molecular weight of from 300 to 50000, preferably 2000 to 10000. In the preferred embodiment herein where the softening active is a mixture of DTDMAC and ditallow imidazoline, it is preferred to use a polyethylene glycol with a molecular weight of about 4000. In the alternative preferred embodiment where the softening active comprises ditallow imidazoline ester, it is preferred to use a polyethylene glycol with a molecular weight of about 8000.
The compositions according to the present invention further comprise from 0% to 2%, preferably from 0% to 0.1% by weight of the total composition of a highly branched fatty alcohol having from 8 to 18 carbon atoms, preferably 12 to 14, or mixtures thereof, most preferably 13. Branched compounds similar to said highly branched fatty alcohols are often present in perfumes; thus, the level of said highly branched fatty alcohol to be added to the composition must be adjusted depending on the perfume which is used, if any. Such highly branched fatty alcohols suitable for use in the compositions according to the present invention are commercially available from EXXON under the trade name EXXAL The compositions according to the invention may further comprise from 0% to 0.5% by weight of the total composition of a linear or cyclic polydialkylsiloxane of the formula: ,R R-[- Si-O-]m-Si-R, I \ R R where R is a C1-C5 alkyl group and m is an integer of 1 to 500, or mixtures thereof. Said polydialkylsiloxanes components are not essential ingredients in the compositions according to the invention, as the compositions will retain viscosity upon dilution even in the abscence of such polydialkylsiloxanes. However, several benefits can be obtained from these polydialkylsiloxane, including improved stability of the finished product, improved water absorbancy of the treated fabrics. Said polydialkylsiloxanes can also be helpful in avoiding the formation of fabric softener residues which may occur in the dispenser of the washing machine. Thus, preferred compositions according to the present invention comprise from 0.05% to 0.5%, most preferably from 0.1% to 0.3% by weight of the total composition of the above polydialkylsiloxanes, or mixtures thereof. In the compositions according to the present invention where the softening active comprises the ditallow imidazoline ester described herein above, it is preferred to use a polydialkylsiloxane where R is methyl and m is about 200. In other compositions, it is preferred to use a polydialkylsiloxane where R is methyl and m is 7. Suitable polydialkylsiloxanes are commercially available from DOW CORNING under the trade name 200 fluid, and the preferred polydialkylsiloxanes for use herein are DOW CORNING's 200 fluid 350 CS (R is methyl and m is 203) and 5 CS (R is methyl and m is 7).
The compositions according to the invention may additionally comprise such conventional ingredients as perfumes, preservatives, germicides, colorants, fungicides, stabilizers, brighteners, opacifiers and the like, at conventional levels, i.e. up to about 5% by weight of the composition.
The compositions in their concentrated form have a viscosity of from 40 to 400 cps at 60 RPM shear rate. The compositions according to the invention can be used directly in the concentrated form, or they can preferably be diluted before they are used. The compositions according to the present invention are meant to be diluted in water, preferably in 2 to 3 times their weight of water. In diluted form, the compositions have a viscosity of from 20 to 60 cps at 60 RPM shear rate, preferably 30 to 50 cps at 6o RPM shear rate.
Thus, the present invention also encompasses a method for the softening of fabrics wherein the concentrated fabric softening compositions described herein above are diluted in water before they are contacted with said fabrics. In a preferred embodiment of said method, a concentrated softening composition as described hereinabove, which has a viscosity of from 40 to 400 cps at 60 RPM shear rate, is diluted in two times its weight of water so as to obtain a diluted fabric softening composition having a viscosity of from 20 to 60, preferably 30 to 50 cps at 60 RPM shear rate, and said diluted faoric softening composition is contacted with said fabrics in the rinse water.
The compositions according to the present invention are illustrated by the following examples.
Example 1 A composition according to the present invention is made, which comprises : - Ditallow dimethyl ammonium chloride 7.60% - Ditallow dimethyl imidazoline 14.20% - HC1 0.82% - Polyethylene glycol 4000 MW 2.00%% - Silicone oil 5CS 0.19% - Lutensol T08 1.30% - Exxal 13 0.08% - CaCl2 0.20% - Perfume 0.70% - water and minors to 100% silicone oil 5 CS is a polydialkylsiloxane as defined in the description. Lutensol TO 8 is a linear fatty alcohol ethoxylate, and EXXAL® 13 is a highly branched fatty alcohol, both according to the description hereinbefore.
The above composition was made by adding the HC1 to a water seat at 6O’C-65’C. To this solution, a molten permix of ditallow dimethyl ammonium chloride, ditallowimidazoline and Lutensol TO 8 is added at about 8O'C-85°C, under agitation during about 10 minutes. An aqueous solution of CaCl2 is then injected for about 5 minutes. A mixture of perfume and the silicone oil is then added. The composition is then cooled to room temperature. Finally a 50% solution of the polyethylene glycol 4000 MW is added.
The composition thus obtained has a viscosity of about 65cps before dilution, and 50cps after dilution in 2 times its weight of water.
Example 2 A composition is made which contains: -Ditallow imidazoline ester 22.00% -HCL 1.27% -Lutensol ® TO3 0.12% -Lutensol ® TO5 0.24% -Lutensol TO8 1.00% -CaCL2 0.15% -Polyethylene Glycol i B000 MW 2.00% -Perfume 1.06% -Water & minors Example 3 Balance A composition is made which contains: -Ditallow imidazoline ester 22.00% -HCl 1.27% -Lutensol ® TO3 0.12% -Lutensol ® TO5 0.24% -Lutensol ® TO8 1.00% -Exxal ® 13 0.06% -Dow Corning 200 fluid 350 CS 0.19% -CaC12 0.15% -Polyethylene glycol 8000 MW 2.00% -Perfume 0.90% -Water & minors Balance

Claims (17)

1. A concentrated aqueous fabric softening composition comprising from 10 to 35 % by weight of a cationic fabric softening active or mixtures thereof, said composition further comprising - from 0.3% to 3% by weight of the total composition of a linear fatty alcohol ethoxylate of the formula RO(Etox) n , wherein R is a linear Cq-C^q alkyl chain, and n representing the weighted average ethoxylation degree is of from 3 to 35, or mixtures thereof; - from 0.5% to 6% by weight of the total composition of a nonionic hydrophilic polymer, or mixtures thereof; - from 0 to 2% by weight of the total composition of a highly branched fatty alcohol having from 8 to 18 carbon atoms, or mixtures thereof; - from 0 to 0.5 %by weight of the total composition of a linear or cyclic polydialkylsiloxane of the formula: R R R-[-Si-O-]-Tn—Si-R I | R R wherein R is a C1-C5 alkyl chain, and m is an integer of from 1 to 500, or mixtures thereof.
2. A composition according to claim 1 which comprises from 15 % to 25% by weight of the total composition of said cationic fabric softening active, or mixtures thereof.
3. A concentrated fabric softening composition according to the preceding claims wherein said cationic softening active is a mixture of ditallow dimethyl ammonium chloride and ditallow imidazoline.
4. A concentrated fabric softening composition according to claim 3 which consists of from 20% to 70% by weight of said softening active of ditallowdimethyl ammonium chloride and from 30% to 80% by weight of said softening active of ditallow imidazoline.
5. A concentrated fabric softening composition according to claims 3 and 4 which comprises from 1.5% to 2.5% by weight of the total composition of a polyethylene glycol having a molecular weight of 4000.
6. A concentrated fabric softening composition according to claims 3-5 which comprises from 0.05% to 0.5 %, preferably 0.1% to 0.3% by weight of the total composition of said linear or cyclic polydialkylsiloxane of the formula R R R —[—Si—O -]-th—Si—R I I R R wherein R is methyl, and m is 7.
7. A concentrated fabric softening composition according to claims 1 and 2 wherein said softening active comprises ditallow imidazoline ester.
8. A concentrated fabric softening composition according to claim 7 which comprises a polyethylene glycol having a molecular weight of 8000.
9. A concentrated fabric softening composition according to claims 7-8 which comprises from 0.05% to 0.5 %, preferably from 0.1% to 0.3% by weight of the total composition of said linear or cyclic polydialkylsiloxane of the formula: R R R-C-Si-O-J-B-S'i-R R R wherein R is a methyl, and m is 203.
10. A concentrated fabric softening composition according to the preceding claims which comprises from 1% to 1.5% by weight of the total composition of said fatty alcohol ethoxylate of the formula RO(Etox) n , wherein R is a linear C 10 -Ci3 alkyl chain, and n representing the weighted average ethoxylation degree is from 5 to 10, preferably 8.
11. A concentrated fabric softening composition according to the preceding claims which comprises from 0% to 0.1% by weight of the total composition of said highly branched fatty alcohol, said highly branched fatty alcohol having from 12 to 14 carbon atoms, preferably 13.
12. A concentrated fabric softening composition according to any of the preceeding claims, said composition having a viscosity of from 40 to 400 cps at 60 RPM shear rate before dilution, and said composition having a viscosity of from 20 to 60cps at 60 RPM shear rate after it has been diluted in 2 times its weight of water.
13. A concentrated fabric softening composition according to claim 12 which has a viscosity of from 30 to 50 cps at 60 RPM shear rate after it has been diluted in 2 times its weight of water.
14. λ method for the softening of fabrics wherein a concentrated fabric softening composition according to claims 1 to 10 and having a viscosity of from 40 to 400 cps at 60 RPM Shear rate is diluted in 2 times its weight of water so as to obtain a diluted fabric softening composition having a viscosity of 20 to 60 cps at 60 RPM shear rate, and wherein said diluted fabric softening composition is contacted with said fabrics in the rinse water.
15. A method according to claim 14 wherein the concentrated fabric softening composition having a viscosity of from 40 to 400 cps at 60 RPM shear rate is diluted in 2 times its weight of water so as to obtain a diluted fabric softening composition having a viscosity of from 30 to 50 cps at 60 RPM shear rate.
16. A composition according to claim 1, substantially as hereinbefore described and exemplified.
17. A method according to claim 14 for the softening of fabrics, substantially as hereinbefore described.
IE920735A 1991-03-08 1992-03-06 Concentrated fabric softening compositions IE920735A1 (en)

Applications Claiming Priority (3)

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EP91200507 1991-03-08
EP91870105.3A EP0503218A1 (en) 1991-03-08 1991-07-03 Concentrated fabric softening compositions
EP19910870187 EP0503221B1 (en) 1991-03-08 1991-11-22 Concentrated fabric softening compositions

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ATE229064T1 (en) * 1994-09-30 2002-12-15 Procter & Gamble BLOCK COPOLYMERS FOR IMPROVED VISCOSITY STABILITY IN CONCENTRATED FABRIC SOFTENERS
NZ286025A (en) * 1995-03-01 1997-04-24 Colgate Palmolive Co Laundry detergent concentrates; contains nonionic surfactant and water insoluble oil with a hydrophilic polar group, converts to liquid crystal phase dispersion on dilution
AU713278B2 (en) 1996-03-14 1999-11-25 Johnson & Johnson Consumer Companies, Inc. Cleansing and moisturizing surfactant compositions
DE19714044C1 (en) * 1997-04-05 1998-04-16 Henkel Kgaa Hydrophilic textile conditioners containing no polyolefin waxes
GB0001778D0 (en) * 2000-01-27 2000-03-22 A I N Manufacturing Limited Laundry detergent composition
GB0310974D0 (en) * 2003-05-13 2003-06-18 Unilever Plc Fabric conditioning compositions
CN102438583A (en) * 2008-12-18 2012-05-02 莫门蒂夫性能材料股份有限公司 Composition comprising at least two different cycloalkylmethicones and use thereof
CN103459576B (en) * 2011-03-30 2015-11-25 宝洁公司 Comprise the Fabrid care composition of front end stablizer
CN103668962A (en) * 2013-11-22 2014-03-26 南通信一服饰有限公司 Concentrated softener for dry cotton fabric

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US4025444A (en) * 1975-08-18 1977-05-24 The Procter & Gamble Company Fabric softening agents
US3962100A (en) * 1975-08-18 1976-06-08 The Procter & Gamble Company Fabric softening agents
GB1587122A (en) * 1976-10-29 1981-04-01 Procter & Gamble Ltd Fabric conditioning compositions
DE2824024C2 (en) * 1978-06-01 1987-01-29 Henkel KGaA, 4000 Düsseldorf Liquid detergent
GB8508129D0 (en) * 1985-03-28 1985-05-01 Procter & Gamble Ltd Textile treatment composition
GB8617255D0 (en) * 1986-07-15 1986-08-20 Procter & Gamble Ltd Laundry compositions

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PT100210A (en) 1993-05-31
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CZ184693A3 (en) 1994-03-16
CN1046774C (en) 1999-11-24
MX9200990A (en) 1992-09-01
CN1064717A (en) 1992-09-23
AU1444592A (en) 1992-10-06
WO1992015745A1 (en) 1992-09-17
HUT66690A (en) 1994-12-28

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