WO1996015213A1 - Agents assouplissants pour textiles - Google Patents

Agents assouplissants pour textiles Download PDF

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Publication number
WO1996015213A1
WO1996015213A1 PCT/EP1995/004349 EP9504349W WO9615213A1 WO 1996015213 A1 WO1996015213 A1 WO 1996015213A1 EP 9504349 W EP9504349 W EP 9504349W WO 9615213 A1 WO9615213 A1 WO 9615213A1
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WO
WIPO (PCT)
Prior art keywords
carbon atoms
alkyl
group
alkenyl
textile
Prior art date
Application number
PCT/EP1995/004349
Other languages
German (de)
English (en)
Inventor
Ansgar Behler
Manfred Weuthen
Günther Uphues
Almud Folge
Karlheinz Hill
Original Assignee
Henkel Kommanditgesellschaft Auf Aktien
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Application filed by Henkel Kommanditgesellschaft Auf Aktien filed Critical Henkel Kommanditgesellschaft Auf Aktien
Priority to DE59505051T priority Critical patent/DE59505051D1/de
Priority to EP95937869A priority patent/EP0792337B1/fr
Publication of WO1996015213A1 publication Critical patent/WO1996015213A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005—Other compounding ingredients characterised by their effect
    • C11D3/001—Softening compositions
    • C11D3/0015—Softening compositions liquid
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/835—Mixtures of non-ionic with cationic compounds
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10—Treating 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
    • D06M13/144—Alcohols; Metal alcoholates
    • D06M13/148—Polyalcohols, e.g. glycerol or glucose
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322—Treating 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
    • D06M13/46—Compounds containing quaternary nitrogen atoms
    • D06M13/463—Compounds containing quaternary nitrogen atoms derived from monoamines
    • 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
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/662—Carbohydrates or derivatives
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/667—Neutral esters, e.g. sorbitan esters
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/72—Ethers of polyoxyalkylene glycols
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/72—Ethers of polyoxyalkylene glycols
    • C11D1/721—End blocked ethers
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66—Non-ionic compounds
    • C11D1/74—Carboxylates or sulfonates esters of polyoxyalkylene glycols
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/50—Modified hand or grip properties; Softening compositions

Definitions

  • the invention lies in the general field of textile treatment agents for the household and in textile technology and relates to agents for textiles which give them excellent softness.
  • the textile softening agents contain sugar derivatives which carry ecologically very well tolerated alkyl, alkenyl and / or acyl residues, as well as special combinations of non-ionic and cationic emulsifiers.
  • the special combination of non-ionic emulsifiers and cationic emulsifiers has the effect that the softness of the plasticizers does not deteriorate and stable aqueous dispersions of the plasticizers are possible over a wide range of concentrations.
  • Textile softening agents are understood in the context of the invention means which can be used both in textile technology for finishing, for example, yarns, fibers, knitted fabrics, fabrics and nonwovens, and in private households for aftertreatment of washed textiles.
  • the textile softening agents contain plasticizers and an emulsifier combination which enable stable aqueous dispersions of the plasticizers.
  • Plasticizers are used in textile technology and in the home for finishing, for example to produce a pleasant, fluffy feel, to increase wearing comfort, to improve the processing properties or also to care for the textiles Quaternary ammonium compounds are used, since they are particularly easy to pull onto textiles.
  • plasticizers which contain compounds as main plasticizing components which no longer have any quaternary nitrogen groups.
  • German Offenlegungsschrift DE-A-43 01 459 describes aqueous fabric softeners which can contain sugar or polysaccharide derivatives such as saccharide difatty acid esters or fatty alkyl polyglycoside fatty acid esters as non-ionic plasticizers.
  • sugar or polysaccharide derivatives such as saccharide difatty acid esters or fatty alkyl polyglycoside fatty acid esters as non-ionic plasticizers.
  • non-ionic emulsifiers such as fatty alcohol ethoxylates
  • cationic protective colloids such as chitosan is necessary.
  • Such agents show good fabric softening effects, but if chitosan is also used as a cationic protective colloid, it is necessary to use organic acids as solubilizers.
  • chitosan is only effective as a protective colloid in acidic medium.
  • the main plasticizing components should show very good softness performances, which are comparable to those of the classic plasticizers. Since the textile softening agents are generally used as aqueous dispersions at the same time, it was necessary to find emulsifiers for the plasticizing main components, which on the one hand did not negatively influence the softness performance of the main components. On the other hand, the emulsifiers should ensure stable aqueous dispersions, especially with different contents of main plasticizing components, without being dependent on the addition of solubilizers.
  • the requirements are met if the textile softening agents contain sugar derivatives carrying alkyl, alkenyl and / or acyl residues as the main softening components, and special emulsifier combinations of nonionic emulsifiers and cationic emulsifiers.
  • the present invention therefore relates to textile softening agents containing, as plasticizers, alkyl, alkenyl and / or acyl radicals with 8 to 24 carbon atoms and sugar derivatives, as well as emulsifier combinations selected from at least one nonionic emulsifier and at least one cationic emulsifier the group of the al) quaternized alkoxylated alkylamines of the general formula (I)
  • R an aliphatic hydrocarbon residue with 6-22 carbon atoms
  • R C0 - a saturated or unsaturated acyl group with 12 to 22 C atoms
  • R3 is an alkyl group with 1 to 4 carbon atoms or a hydroxyalkyl group with 2 to 4 carbon atoms, in each case 2 or 3, u, v and w in each case a number from 1 to 4 and
  • R5 is an aliphatic hydrocarbon radical having 1 to 4 carbon atoms or the group (CH2CHR7 ⁇ ) 0 H, where R7 * H or CH3 and 0 is a number from 1 to 20 and
  • R8 H or an aliphatic hydrocarbon radical with 1 to 4 carbon atoms and
  • sucrose derivatives includes derivatives of mono- and / or disaccharides and of oligoglycosides. This also includes the derivatives of hydrogenated monosaccharides such as xylitol, sorbitol and sorbitan. Furthermore, the terms “main plasticizing component” and “plasticizer” are used synonymously in the present application.
  • the mono- and / or disaccharides and the oligoglycosides carry at least one, preferably at least two, alkyl, alkenyl and / or acyl radicals which have 8 to 24 carbon atoms.
  • the alkyl, alkenyl and / or acyl radicals having 8 to 24 carbon atoms can be glycosidically or linked to the sugars via an ester bond.
  • the sugars it is possible for the sugars to carry, in addition to the two alkyl, alkenyl and / or acyl radicals having 8 to 24 carbon atoms, further alkyl, alkenyl and / or acyl radicals, these further radicals having no restriction on C.
  • These further radicals which may also be glycosidically linked or linked to the sugars via an ester compound, preferably have 1 to 24 carbon atoms.
  • the highest possible number of alkyl, alkenyl and / or acyl residues results from the number of free OH groups of the sugar, it being preferred for the mono- and disaccharides that at least one free OH group and Preferred at least 2 free OH groups remain. For the monosaccharides and disaccharides, it is recommended that about half of the free OH groups originally present remain free, and the rest, linked, carries the alkyl, alkenyl and / or acyl radicals.
  • Suitable mono- and / or disaccharides are glucose, mannose, galactose, xylose, maltose, lactose, sucrose and Cl-C4-alkyl glycosides such as methyl glucoside.
  • suitable hydrogenated monosaccharides are xylitol, sorbitan and sorbitol. Of these, glucose, methyl glucoside and sucrose are preferred.
  • R9 stands for alkyl or alkenyl residues with 1 to 24 C atoms
  • [G] for a sugar residue with 5 or 6 C atoms
  • p stands for a number from 1 to 10
  • Alkyl and / or alkenyl oligoglycosides are known substances which can be obtained by the relevant methods of preparative organic chemistry. A process for their production is, for example, the acid-catalyzed acetalization of glucose with fatty alcohols. Representative of the extensive literature, reference is made to the European patent application EP-A-0301 298.
  • alkyl and / or alkenyl oligoglycosides are preferred which are derived from aldoses or ketoses and, because of their ready availability, in particular from glucose, so that [G] in formula (IV) preferably represents glucose.
  • the index number p in the general formula (IV) indicates the degree of oligomerization (DP degree), ie the number of aldoses or ketoses linked to one another by glycosides.
  • DP degree degree of oligomerization
  • the value p is an analytically determined arithmetic parameter, which usually represents a fractional number.
  • Alkyl and / or alkenyl oligoglycosides with an average degree of oligomerization p of 1.1 to 3.0 are preferred; those alkyl and / or alkenyl oligoglycosides whose degree of oligomerization is between 1.2 and 1.7 are particularly preferred.
  • the R 1 radical can be derived from saturated and / or unsaturated primary alcohols having 1 to 24, preferably 8 to 24, carbon atoms. Typical examples are 2-ethylhexanol, caprylic alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, linolyl alcohol, linolenyl alcohol, gaducyl alcohol, arachyl alcohol, arachyl alcohol, arachyl alcohol which these alcohols can contain in different amounts.
  • the sugars carry at least one, preferably at least two alkyl, alkenyl and / or acyl radicals which have 8 to 24 carbon atoms.
  • R ⁇ in the formula (IV) is an alkyl or alkenyl radical having 1 to 7 carbon atoms, this means that those from the group of the alkyl and / or alkenyl glycosides of the formula (IV) are particularly preferred, the two further alkyl, alkenyl and / or acyl radicals with 8 to 24 carbon atoms in order to arrive at the particularly preferred sugar derivatives with at least two alkyl, alkenyl and / or acyl radicals with 8 to 24 carbon atoms.
  • Very particularly preferred examples from the group of mono- and disaccharides are methyl glucoside difatty acid esters such as methyl glucoside distearate and sucrose tetrafatty acid esters such as sucrose tetrastearate.
  • Suitable examples from the group of alkyl and / or alkenyl oligoglycosides are fatty alkyl oligoglucoside fatty acid monoesters such as lauryl oligoglucoside lauric acid ester, lauryl oligoglucoside stearic acid ester and stearyl oligoglucoside stearyl acid ester, the degree of oligomerization being between 1.2 and 1.7.
  • Suitable examples from the group of hydrogenated monosaccharides are sorbitan ono and trifatty acid esters such as sorbitan mono and tristearate.
  • the textile plasticizers according to the invention contain emulsifier combinations of nonionic and cationic emulsifiers as plasticizers.
  • Quaternized alkoxylated alkylamines of the formula (I), quaternized fatty acid alkanolamine esters of the general formula (II) and / or quaternized alkylamines of the formula (III) are present as cationic emulsifiers.
  • the quaternized alkoxylated alkylamines of the formula (I) are known compounds which can be prepared, for example, according to DE-A-20 52 321 by ethoxylation of the corresponding alkylamines in the presence of water and subsequent neutralization.
  • the products are obtained as thin, liquid aqueous solutions.
  • Preferred are solutions of the quaternized alkoxylated alkylamines of the formula (I) which have an active substance content of 40 to 60% by weight.
  • the aqueous solutions are preferably adjusted to a pH of 6 to 8.
  • a ⁇ in formula (I) represents a corresponding equivalent proportion of the phosphate.
  • the anion is H2P04 "and / or HPO4 2 -.
  • R represents an aliphatic hydrocarbon radical having 12 to 22 carbon atoms and x, y, z independently of one another represent a number from 1 to 10, the sum of x + y + z is in the range from 3 to 10.
  • the quaternized ethoxylated alkylamines (R'-H) are particularly suitable.
  • esterquats are also known compounds which can be obtained by the relevant methods of preparative chemistry and are usually referred to as "esterquats".
  • WO 91/01295 describes a process for their preparation, according to which fatty acids are reacted with triethanolamine in the presence of reducing agents and with passage of air, and the diesters obtained are then quaternized with alkylating agents such as dimethyl sulfate, trimethyl phosphate or methyl halide. Since these are technical products, the ester quats of the general formula (II) are always mixtures of quaternized mono-, di- and tri-esters. If desired, the ester quats can be used in the form of organic solutions, for example dissolved in a branched lower alcohol such as isopropanol.
  • R ⁇ O represents an acyl group which is derived from pure fatty acids or technical mixtures of fatty acids such as lauric, myristic, palmitic, stearic, derives oleic, elaidic, petroselinic, linoleic, linolenic, arachic, behenic and / or erucic acid.
  • R C0 very particularly preferably stands for a saturated acyl group with 16 and / or 18 C atoms, R3 for a methyl group, m for the number 2, u, v and w for the number 1 and A ⁇ for a halide, methosulfate or methophosphate.
  • the quaternized alkylamines of the formula (III) are also known compounds.
  • the neutralized tertiary amines falling under this group (R8 stands for H) can be neutralized by trialkylamines (R5 and R *> standing for an aliphatic hydrocarbon residue) or alkoxyalkylamines (R-5 and / or R ⁇ standing for the group) (CH2CHR 7 0) n H).
  • Inorganic acids such as hydrochloric acid are preferably used for neutralization.
  • the neutralization is preferably carried out in situ, ie the non-neutralized amines are used and the pH of the aqueous dispersions of the plasticizer according to the invention is adjusted from neutral to acidic by adding inorganic acids, as a result of which the neutralization of the tertiary amines is achieved.
  • Non-ionic emulsifiers are contained in the textile softening agents as a further emulsifier component.
  • Non-ionic emulsifiers which can be used are those known from the prior art, especially those which have no tendency to swell when emulsified in water.
  • Particularly suitable nonionic emulsifiers are compounds selected from the group consisting of b1) ethoxylated and / or propoxylated fatty acids and / or ethoxylated and / or propoxylated fatty acid esters and b2) fatty alcohol polyglycol ethers and / or end group-capped fatty alcohol polyglycol ethers and b3) alkyl and / or alkenyl oligoglycosides.
  • Ethoxylated and / or propoxylated fatty acids or fatty acid esters are also known compounds which are obtained by ethoxy and / or propoxylation of the fatty acids or fatty acid esters in the presence of catalysts.
  • a process is known from DE-A-40 10 606, according to which ethoxylated and / or propoxylated fatty acid esters with a narrow homolog distribution are obtained, provided that the work is carried out in the presence of hydrophobized hydrotalils as catalysts.
  • the optionally end-capped fatty alcohol polyglycol ethers are also a known class of compounds which can be prepared by appropriate methods in organic chemistry, for example by reacting alkyl halides with ethoxylated and / or propoxylated fatty alcohols in the presence of a catalyst.
  • the fatty alcohol polyglycol ethers can be prepared by known ethoxylation and / or propoxylation of fatty alcohols.
  • R 12 is an aliphatic hydrocarbon radical having 12 to 22 C atoms
  • s is a number from 2 to 8
  • t is a number from 0 to 5
  • R 13 represents hydrogen or an alkyl radical having 1 to 4 carbon atoms.
  • R 12 can be derived from pure fatty alcohols or technical mixtures of fatty alcohols such as lauryl, myristyl, palmityl, stearyl, arachidyl, behenyl, oleyl, elaidyl, linoleyl and / or linolenyl alcohol.
  • alkyl and / or alkenyl oligoglycosides are also a known class of compounds which can be prepared, for example, by the acid-catalyzed acetalization of glucose with fatty alcohols.
  • EP-A-0 301 298 As a representative of the large number of literature, reference is made to the European patent application EP-A-0 301 298. Suitable alkyl and / or alkenyl oligoglycosides have been described in connection with formula (IV) of the present patent application.
  • nonionic emulsifiers are added at least in the same weight ratio, but preferably in smaller amounts in relation to the cationic emulsifiers.
  • Preferred weight ratios of nonionic emulsifiers to cationic emulsifiers are 1: 1 to 3: 1, preferably 1.5: 1 to 2: 1.
  • the textile plasticizers contain the plasticizer in amounts of 60 to 95% by weight, the emulsifier combination in amounts of 5 to 40% by weight and, if appropriate, in amounts of 0 to 20% by weight of customary auxiliaries.
  • the textile plasticizers preferably contain 70 to 90% by weight of the plasticizer, the emulsifier combination in amounts of 10 to 30% by weight and 0 to 20% by weight of customary auxiliaries.
  • the amounts given relate to the active substance salary. Active substance content is understood to mean the content of plasticizers, emulsifiers and conventional auxiliaries, but not water.
  • Typical auxiliaries are, for example, pH regulators such as organic and inorganic acids, foam inhibitors, viscosity regulators, antioxidants, colorants, fragrances and soil release active substances. If the not yet neutralized tertiary alkylamines are used as cationic emulsifiers, the addition of acids, as already described, is absolutely necessary to adjust the pH.
  • the textile softening agents are generally used in the form of their aqueous dispersions.
  • the usual concentrations of 3 to 6% by weight - based on the active substance content - are set.
  • it is also possible to prepare higher concentrates with 10 to 30% by weight of active substance and either subsequently dilute to 3 to 6% by weight or correspondingly smaller amounts are added to the last rinsing bath.
  • the textile softening agents can also be used in textile technology in the concentrations customary for this purpose, since they can easily be applied by customary methods such as pull-out, immersion centrifugal, padding or spraying methods.
  • Another object of the present invention relates to a process for the production of textile softening agents according to claim 1, characterized in that the alkyl, alkenyl and / or acyl residues with 8 to 24 carbon atoms are melted and melted with the katio ⁇ African Emulsifiers are added before they are then added to the aqueous solutions or dispersions of the nonionic emulsifiers.
  • Another subject relates to the use of alkyl, alkenyl and / or acyl radicals having sugar derivatives bearing 8 to 24 carbon atoms in a mixture with nonionic emulsifiers and cationic emulsifiers, selected from the group al), a2) and / or a3) from claim 1, in the form of their aqueous dispersions for softening household linen or as softening aftertreatment agent in textile technology.
  • an aqueous dispersion was prepared, but with 5 g of sucrose tetrastearate instead of the glucoside derivative.
  • Fresh standard tests must always be included to assess the soft grip.
  • the assessment itself was a subjective (haptic) test, in which at least 4 people grab the test tissue and place it on a scale from 1 to 5. 5 means the grip impression of the water standard, ie liquor without active ingredient and is synonymous with the worst grip. The better the grip, the higher the grades, whereby 1 is very good. The result represents the average of the ratings of all test subjects.

Abstract

L'invention concerne en général les agents de traitement de textiles, à usage domestique et destinés à l'industrie des textiles. L'invention concerne en particulier des agents conférant aux textiles une souplesse remarquable. Ces agents assouplissants pour textiles contiennent des assouplissants sous forme de dérivés de sucre comportant des radicaux alkyle, alcényle et/ou acyle, présentant une très bonne écocompatibilité, ainsi que des combinaisons spéciales d'émulsifiants non ioniques et cationiques. Cette combinaison d'émulsifiants non ioniques et cationiques sélectionnés dans le groupe des alkylamines alcoxylées quaternaires, des esters d'alcanolamines d'acide gras quaternaires et des alkylamines quaternaires n'entraîne pas de dégradation du pouvoir assouplissant des agents assouplissants et permet d'obtenir des dispersions aqueuses stables d'agents assouplissants sur une large plage de concentration.
PCT/EP1995/004349 1994-11-14 1995-11-06 Agents assouplissants pour textiles WO1996015213A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
DE59505051T DE59505051D1 (de) 1994-11-14 1995-11-06 Textile weichmachungsmittel
EP95937869A EP0792337B1 (fr) 1994-11-14 1995-11-06 Agents assouplissants pour textiles

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEP4440620.7 1994-11-14
DE4440620A DE4440620A1 (de) 1994-11-14 1994-11-14 Textile Weichmachungsmittel

Publications (1)

Publication Number Publication Date
WO1996015213A1 true WO1996015213A1 (fr) 1996-05-23

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ID=6533271

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP1995/004349 WO1996015213A1 (fr) 1994-11-14 1995-11-06 Agents assouplissants pour textiles

Country Status (5)

Country Link
EP (1) EP0792337B1 (fr)
AT (1) ATE176494T1 (fr)
DE (2) DE4440620A1 (fr)
ES (1) ES2128785T3 (fr)
WO (1) WO1996015213A1 (fr)

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WO1998016538A1 (fr) * 1996-10-16 1998-04-23 Unilever Plc Composition adoucissant les tissus
WO2000070004A1 (fr) * 1999-05-17 2000-11-23 Unilever Plc Compositions adoucissantes pour tissus
WO2001046359A1 (fr) * 1999-12-22 2001-06-28 Unilever Plc Compositions et composes adoucissants pour tissus
WO2001046360A1 (fr) * 1999-12-22 2001-06-28 Unilever Plc Procede de stabilisation des compositions assouplissantes pour tissus
WO2001046361A1 (fr) * 1999-12-22 2001-06-28 Unilever Plc Compositions d'assouplissement de tissu
US6436896B2 (en) * 1999-12-22 2002-08-20 Unilever Home & Personal Care Usa, A Divison Of Conopco, Inc. Method for preparing fabric softening compositions
WO2003104366A1 (fr) * 2002-06-10 2003-12-18 Unilever Plc Compositions detergentes liquides pour tissus
US6727220B1 (en) 1999-05-17 2004-04-27 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Fabric softening compositions
US7776813B2 (en) 2004-09-15 2010-08-17 The Procter & Gamble Company Fabric care compositions comprising polyol based fabric care materials and deposition agents

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US7135451B2 (en) 2003-03-25 2006-11-14 The Procter & Gamble Company Fabric care compositions comprising cationic starch

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EP0243735A2 (fr) * 1986-04-14 1987-11-04 Henkel Kommanditgesellschaft auf Aktien Adoncissant aqueux concentré pour matières textiles
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AU723907B2 (en) * 1996-10-16 2000-09-07 Unilever Plc Fabric softening composition
WO1998016538A1 (fr) * 1996-10-16 1998-04-23 Unilever Plc Composition adoucissant les tissus
US6727220B1 (en) 1999-05-17 2004-04-27 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Fabric softening compositions
WO2000070004A1 (fr) * 1999-05-17 2000-11-23 Unilever Plc Compositions adoucissantes pour tissus
CZ298908B6 (cs) * 1999-05-17 2008-03-12 Unilever N.V. Prostredek pro zmekcování tkanin
WO2001046359A1 (fr) * 1999-12-22 2001-06-28 Unilever Plc Compositions et composes adoucissants pour tissus
US6436896B2 (en) * 1999-12-22 2002-08-20 Unilever Home & Personal Care Usa, A Divison Of Conopco, Inc. Method for preparing fabric softening compositions
US6514931B2 (en) * 1999-12-22 2003-02-04 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Fabric softening compositions
WO2001046361A1 (fr) * 1999-12-22 2001-06-28 Unilever Plc Compositions d'assouplissement de tissu
WO2001046360A1 (fr) * 1999-12-22 2001-06-28 Unilever Plc Procede de stabilisation des compositions assouplissantes pour tissus
WO2003104366A1 (fr) * 2002-06-10 2003-12-18 Unilever Plc Compositions detergentes liquides pour tissus
US7012059B2 (en) 2002-06-10 2006-03-14 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Fabric detergent compositions
US7776813B2 (en) 2004-09-15 2010-08-17 The Procter & Gamble Company Fabric care compositions comprising polyol based fabric care materials and deposition agents

Also Published As

Publication number Publication date
DE4440620A1 (de) 1996-05-15
ES2128785T3 (es) 1999-05-16
EP0792337A1 (fr) 1997-09-03
ATE176494T1 (de) 1999-02-15
EP0792337B1 (fr) 1999-02-03
DE59505051D1 (de) 1999-03-18

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