EP0918901A1 - Textile finishing agent - Google Patents

Textile finishing agent

Info

Publication number
EP0918901A1
EP0918901A1 EP97937560A EP97937560A EP0918901A1 EP 0918901 A1 EP0918901 A1 EP 0918901A1 EP 97937560 A EP97937560 A EP 97937560A EP 97937560 A EP97937560 A EP 97937560A EP 0918901 A1 EP0918901 A1 EP 0918901A1
Authority
EP
European Patent Office
Prior art keywords
carbon atoms
alkyl
fatty acid
radical
composition according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP97937560A
Other languages
German (de)
French (fr)
Other versions
EP0918901B1 (en
Inventor
Bernd Wahle
Günter Uphues
Yvonne Reichert
Rafael Pi Subirana
Terese Copete Vidal
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF Personal Care and Nutrition GmbH
Original Assignee
Henkel AG and Co KGaA
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.)
Filing date
Publication date
Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP0918901A1 publication Critical patent/EP0918901A1/en
Application granted granted Critical
Publication of EP0918901B1 publication Critical patent/EP0918901B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • D06M13/461—Quaternised amin-amides from polyamines or heterocyclic compounds or polyamino-acids
    • 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
    • C11D1/645—Mixtures of compounds all of which are cationic
    • 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
    • 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
    • D06M13/47—Compounds containing quaternary nitrogen atoms derived from heterocyclic compounds
    • D06M13/473—Compounds containing quaternary nitrogen atoms derived from heterocyclic compounds having five-membered heterocyclic rings
    • 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
    • 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
    • D06M2200/25—Resistance to light or sun, i.e. protection of the textile itself as well as UV shielding materials or treatment compositions therefor; Anti-yellowing treatments
    • 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 relates to new agents for finishing textile fabrics based on esterquats and quaternized fatty acid imidazo and their use for softening and yellowing stabilization of fabrics.
  • finishing of yarns, fabrics, fabrics up to the finished textiles comprises a complex requirement profile.
  • the most important property that finishing agents must have is to give the textiles a pleasant soft feel.
  • cationic surfactants are generally used, among which the esterquats are particularly important because of their good ecological compatibility.
  • the finishing can take place both in the context of the textile pre- and post-treatment.
  • a further requirement then exists to protect textiles against soiling, for which purpose conventional laundry aftertreatment agents are added polymers of the so-called "soil repeilants" type.
  • a third important aspect is the stabilization of fabrics against the influence of ozone, which is very easy, especially with blue denim yellowing, but this requirement has so far not been satisfactorily met by the means of the prior art.
  • the object of the invention was therefore to provide new means which allow textile fabrics, ie yarns, fabrics and finished textiles, but in particular blue denim fabrics and jeans made therefrom, to be given a pleasant soft feel at the same time and against Equip yellowing Description of the invention
  • the invention relates to textile finishing agents containing
  • R CO is an acyl radical having 6 to 22 carbon atoms
  • R 2 and R 3 independently of one another are hydrogen or R 1 CO
  • R 4 is an alkyl radical having 1 to 4 carbon atoms or a (CH ⁇ CH ⁇ OJqH group, m, n and pm sum for 0 or numbers from 1 to 12, q for numbers from 1 to 12 and X for halide, alkyl sulfate or alkyl phosphate.
  • R 1 CO for an acyl radical having 6 to 22 carbon atoms, preferably for an acyl radical derived from tallow fatty acid
  • R 2 for hydrogen or R 1 CO
  • R 4 and R 5 independently of one another for alkyl radicals with 1 to 4 carbon atoms
  • m and n in total represents 0 or numbers from 1 to 12
  • X represents halide, alkyl sulfate or alkyl phosphate
  • R 1 CO is an acyl radical having 6 to 22 carbon atoms, preferably an acyl radical derived from the fatty acid mixture containing the tallow fatty acid
  • R 2 is hydrogen or R 1 CO
  • R 4 , R 6 and R 7 are, independently of one another, alkyl radicals having 1 up to 4 carbon atoms, m and n in total represent 0 or numbers from 1 to 12 and X represents halide, alkyl sulfate or alkyl phosphate.
  • Quaternized fatty acid imidazolines are also known cationic surfactants which are usually obtained by condensing fatty acids with diamines, preferably ethylenediamines and subsequent quaternization with alkyl halides or dialkyl sulfates.
  • Processes for producing the imidazolines and their quaternization products are known, for example, from the publications DE-A1 40 20 271, DE-A1 40 38 983 and DE-A1 41 16 648 (Henkel).
  • the imidazolines can also contain proportions of open-chain hydrolysis products. Usually they follow the formula (IV),
  • R 8 is an alkyl and / or alkenyl radical having 7 to 21, preferably 11 to 17 carbon atoms
  • R 9 is optionally hydroxyl-substituted alkyl radicals having 1 to 4 carbon atoms or a benzyl radical
  • R 10 is hydroxy-substituted alkyl radicals having 2 to 4 carbon atoms or a CH2CH2NHCOR 8 radical
  • X represents halide or alkyl sulfate.
  • products are used which are derived from oleic acid or a fatty acid cut containing predominantly oleic acid.
  • Quaternized fatty acid imidazolines which are obtained by condensation of oleic acid with diethylenetriamine or aminoethylethanolamine and subsequent quaternization with dimethyl sulfate or methyl chloride are particularly preferred.
  • the weight ratio of the two components (a) and (b) in the textile finishing agents according to the invention can be 90:10 to 10:90, preferably 15:85 to 50:50 and in particular 20:80 to 25:75.
  • the agents according to the invention not only give textile fabrics, preferably blue denim fabrics, a pleasant soft feel, but also provide reliable protection against yellowing. Another object of the invention therefore relates to the use of the mixtures as finishing agents for the simultaneous softening and yellowing stabilization of textile fabrics.
  • the agents themselves are usually in the form of aqueous solutions or pastes with an active substance content in the range from 5 to 30% by weight. To adjust the viscosity, they can also contain, for example, electrolyte salts.
  • the assessment of ozone stabilization was checked using blue denim fabric.
  • the evaluation is based on the ozone test according to AATCC 109-1992 using an ozone chamber of the type TriC-03 from Textile Innovators CorpVUSA.
  • the results are summarized in Table 1.
  • the following surfactants were used:
  • Methyl-quaternized fatty acid imidazoline produced from oleic acid of 90 to 100 iodine number and aminoethylethanolamine, in the form of the methyl sulfate salt;
  • Methyl-quaternized fatty acid minidazoline prepared from oleic acid of 85 to 90 iodine number and aminoethylethanolamine, in the form of the methyl sulfate salt;
  • Methylquaternized fatty acid minidazoline made from tall oil fatty acid and aminoethylethanolamine, in the form of the methyl isulfate acid;

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Detergent Compositions (AREA)

Abstract

New textile finishing agents contain (a) esterquats and (b) quaternary fatty acid imidazolines. These agents not only confer a soft, comfortable feel to flat textile structures, in particular blue denim fabrics, but also reliably stabilise them against yellowing.

Description

Textilausrüstungsmittel Textile finishing agents
Gebiet der ErfindungField of the Invention
Die Erfindung betrifft neue Mittel zur Ausrüstung von textilen Flächengebiiden auf Basis von Esterquats und quatemierten Fettsäureimidazo nen sowie deren Verwendung zur Avivage und Vergilbungsstabi- lisierung von Geweben.The invention relates to new agents for finishing textile fabrics based on esterquats and quaternized fatty acid imidazo and their use for softening and yellowing stabilization of fabrics.
Stand der TechnikState of the art
Die Ausrüstung von Garnen, Stoffen, Geweben bis hin zu den fertigen Textilien umfaßt ein komplexes Anforderungsprofil. Die wichtigste Eigenschaft, über die Ausrüstungsmittel verfügen müssen, besteht dann, den Textilien einen angenehmen Weichgπff zu verleihen. Für diesen Zweck werden in der Regel kationische Tenside eingesetzt, unter denen die Esterquats wegen ihrer guten ökologischen Vertraglichkeit eine besondere Bedeutung besitzen. Die Avivage kann dabei sowohl im Rahmen der textilen Vor- wie Nachbehandlung erfolgen. Eine weitere Forderung besteht dann, Textilien gegen Verschmutzung zu schützen, wozu man üblichen Wäschennachbehandlungsmitteln Polymere vom Typ der sogenannten „soil repeilants" zusetzt. Ein dritter wichtiger Gesichtspunkt ist die Stabilisierung von Geweben gegenüber dem Einfluß von Ozon, welcher insbesondere bei Blue Denim sehr leicht zu einer Vergilbung führt. Diese Anforderung erfüllen die Mittel des Stands der Technik bislang jedoch nicht zufriedenstellend.The finishing of yarns, fabrics, fabrics up to the finished textiles comprises a complex requirement profile. The most important property that finishing agents must have is to give the textiles a pleasant soft feel. For this purpose, cationic surfactants are generally used, among which the esterquats are particularly important because of their good ecological compatibility. The finishing can take place both in the context of the textile pre- and post-treatment. A further requirement then exists to protect textiles against soiling, for which purpose conventional laundry aftertreatment agents are added polymers of the so-called "soil repeilants" type. A third important aspect is the stabilization of fabrics against the influence of ozone, which is very easy, especially with blue denim yellowing, but this requirement has so far not been satisfactorily met by the means of the prior art.
Die Aufgabe der Erfindung hat somit darin bestanden, neue Mittel zur Verfügung zu stellen, die es erlauben, textilen Flächengebilden, also Garnen, Geweben und fertigen Textilien, insbesondere aber Blue Denim-Gewebe und daraus hergestellten Jeans, gleichzeitig einen angenehmen Weichgriff zu verleihen und gegen Vergilbung auszurüsten Beschreibung der ErfindungThe object of the invention was therefore to provide new means which allow textile fabrics, ie yarns, fabrics and finished textiles, but in particular blue denim fabrics and jeans made therefrom, to be given a pleasant soft feel at the same time and against Equip yellowing Description of the invention
Gegenstand der Erfindung sind Textilausrustungsmittel, enthaltendThe invention relates to textile finishing agents containing
(a) Esterquats und(a) Esterquats and
(b) quatemierte Fettsäureimidazoline(b) quaternized fatty acid imidazolines
Überraschenderweise wurde gefunden, daß Mischungen aus Esterquats und quaternierten Fett- saureimidazolinen, insbesondere dann, wenn sich der Fettsaurerest der Komponente (b) von der Olsaure ableitet, textilen Flächengebiiden und vorzugsweise Blue Denim-Gewebe nicht nur einen angenehmen Weichgriff verleiht, sondern diese auch zuverlässig gegen Vergilbung stabilisiertSurprisingly, it was found that mixtures of ester quats and quaternized fatty acid imidazolines, especially when the fatty acid residue of component (b) is derived from the oleic acid, not only gives textile fabrics and preferably blue denim fabrics a pleasant soft feel, but also reliably stabilized against yellowing
EsterquatsEsterquats
Unter der Bezeichnung „Esterquats" werden im allgemeinen quatemierte Fettsauretπethanoi- aminestersalze verstanden Es handelt sich dabei um bekannte Stoffe, die man nach den einschlagigen Methoden der praparativen organischen Chemie erhalten kann In diesem Zusammenhang sei auf die internationale Patentanmeldung WO 91/01295 (Henkel) verwiesen, nach der man Tπetha- nolamin in Gegenwart von unterphosphoriger Saure mit Fettsauren partiell verestert, Luft durchleitet und anschließend mit Dimethylsulfat oder Ethylenoxid quatemiert Stellvertretend für den umfangreichen Stand der Technik sei an dieser Stelle auf die Druckschriften US 3,915,867, US 4,370,272, EP- A2 0 239 910, EP-A2 0 293 955 A2, EP-A2 0 295 739 und EP-A2 0 309 052 A2 verwiesen Übersichten zum Thema Esterquats sind beispielsweise von O.Ponsati in C.R. CED-Kongress, Barcelona, 1992, S.167 , R Puchta et al in Tens.Surf.Det., 30, 186 (1993), M Brock in Tens.Surf.Det. 30, 394 (1993) und R Lagerman et al in J.Am.Oil.Chem.Soc, 71. 97 (1994) erschienenThe term “ester quats” is generally understood to mean quaternized fatty acid ethanoamine ester salts. These are known substances which can be obtained by the relevant methods of preparative organic chemistry. In this connection, reference is made to the international patent application WO 91/01295 (Henkel) , after which tπethanolamine is partially esterified with fatty acids in the presence of hypophosphorous acid, air is passed through and then quaternized with dimethyl sulfate or ethylene oxide. Representative of the extensive state of the art at this point is the publications US Pat 239 910, EP-A2 0 293 955 A2, EP-A2 0 295 739 and EP-A2 0 309 052 A2 referenced Overviews on the subject of ester quats are for example from O.Ponsati in CR CED Congress, Barcelona, 1992, p.167, R Puchta et al in Tens.Surf.Det., 30, 186 (1993), M Brock in Tens.Surf.Det. 30, 394 (1993) and R Lagerman et al in J.Am.Oil.Chem.Soc, 71, 97 (1994) appeared
Die quaternierten Fettsauretπethanolammestersalze folgen beispielsweise der Formel (I)The quaternized fatty acid ethanolamine ester salts follow, for example, the formula (I)
R«R «
II.
[RiCO-(OCH2CH2)mOCH2CH2-N+-CH2CH2θ-(CH2CH20)nR2] X" (I)[RiCO- (OCH2CH 2 ) m OCH 2 CH2-N + -CH 2 CH2θ- (CH 2 CH 2 0) nR 2 ] X "(I)
I CH2CH20(CH2CH2θ)pR3 in der R CO für einen Acylrest mit 6 bis 22 Kohlenstoffatomen, R2 und R3 unabhängig voneinander für Wasserstoff oder R1CO, R4 für einen Alkylrest mit 1 bis 4 Kohlenstoffatomen oder eine (CH∑CH∑OJqH- Gruppe, m, n und p m Summe für 0 oder Zahlen von 1 bis 12, q für Zahlen von 1 bis 12 und X für Halo- genid, Alkylsulfat oder Alkylphosphat steht Typische Beispiele für Esterquats, die im Sinne der Erfindung Verwendung finden können, sind Produkte auf Basis von Capronsaure, Caprylsaure, Capπn- saure, Launnsaure, Myπstinsaure, Palmitinsaure, Isosteannsaure, Stearinsäure, Olsaure, Elaidinsaure, Arachmsaure, Behensaure und Erucasaure sowie deren technische Mischungen, wie sie beispielsweise bei der Druckspaltung natürlicher Fette und Ole anfallen Vorzugsweise werden gesattigte oder überwiegend gesattigte Fettsauren wie z B Talg- oder Palmfettsaure eingesetzt Zur Herstellung der quaternierten Ester können die Fettsauren und das Tπethanolamin im molaren Verhältnis von 1 ,1 1 bis 3 1 eingesetzt werden Im Hinblick auf die anwendungstechnischen Eigenschaften der Esterquats hat sich ein Einsatzverhaltnis von 1 ,2 1 bis 2,2 1 , vorzugsweise 1 ,5 1 bis 1 ,9 1 als besonders vorteilhaft erwiesen Die bevorzugten Esterquats stellen technische Mischungen von Mono-, Di- und Tπ- estern mit einem durchschnittlichen Veresterungsgrad von 1 ,5 bis 1 ,9 dar und leiten sich von der Talgfettsaure ab Aus anwendungstechnischer Sicht haben sich quatemierte Fettsauretriethanolamm- estersalze der Formel (I) als besonders vorteilhaft erwiesen, in der R1CO für den Acylrest der Talgfettsaure, R2 für R1CO, R3 für Wasserstoff, R4 für eine Methylgruppe, m, n und p für 0 und X für Methylsulfat stehtI CH2CH 2 0 (CH 2 CH2θ) pR 3 in which R CO is an acyl radical having 6 to 22 carbon atoms, R 2 and R 3 independently of one another are hydrogen or R 1 CO, R 4 is an alkyl radical having 1 to 4 carbon atoms or a (CH∑CH ∑ OJqH group, m, n and pm sum for 0 or numbers from 1 to 12, q for numbers from 1 to 12 and X for halide, alkyl sulfate or alkyl phosphate. Typical examples of ester quats which can be used in the sense of the invention are products based on Caproic acid, caprylic acid, capric acid, launic acid, mypinic acid, palmitic acid, isosteanic acid, stearic acid, oleic acid, elaidic acid, arachidic acid, behenic acid and erucic acid, and their technical mixtures, which are predominantly obtained, for example, in the pressure cleavage of natural fats and fatty acids or fatty acids such as, for example, tallow or palm fatty acid , 1 1 to 3 1 are used With regard to the application properties of the ester quats, a ratio of 1, 2 1 to 2.2 1, preferably 1, 5 1 to 1, 9 1 has proven to be particularly advantageous. The preferred ester quats are technical Mixtures of mono-, di- and Tπ-esters with an average degree of esterification of 1.5 to 1.9 and are derived from tallow fatty acid. From an application point of view, quaternized fatty acid triethanolamm ester salts of the formula (I) have proven to be particularly advantageous, in which R 1 CO stands for the acyl residue of tallow fatty acid, R 2 for R 1 CO, R 3 for hydrogen, R 4 for a methyl group, m, n and p for 0 and X for methyl sulfate
Neben den quaternierten Fettsauretπethanolaminestersalzen kommen als Esterquats ferner auch quatemierte Estersalze von Fettsauren mit Diethanolalkylaminen der Formel (II) in Betracht,In addition to the quaternized fatty acid ethanolamine ester salts, quaternized ester salts of fatty acids with diethanolalkylamines of the formula (II) may also be used as ester quats.
R4 R 4
I ΪRiCO-(OCH2CH2)mOCH2CH2-N+-CH2CH2θ.(CH2CH20)nR2] X* (II) I ΪRiCO- (OCH2CH2) mOCH2CH2-N + -CH 2 CH2θ. (CH2CH 2 0) nR 2 ] X * (II)
in der R1CO für einen Acylrest mit 6 bis 22 Kohlenstoffatomen, vorzugsweise für einen Acylrest der sich von der Talgfettsaure ableitet, R2 für Wasserstoff oder R1CO, R4 und R5 unabhängig voneinander für Alkylreste mit 1 bis 4 Kohlenstoffatomen, m und n in Summe für 0 oder Zahlen von 1 bis 12 und X für Halogenid, Alkylsulfat oder Alkylphosphat stehtin which R 1 CO for an acyl radical having 6 to 22 carbon atoms, preferably for an acyl radical derived from tallow fatty acid, R 2 for hydrogen or R 1 CO, R 4 and R 5 independently of one another for alkyl radicals with 1 to 4 carbon atoms, m and n in total represents 0 or numbers from 1 to 12 and X represents halide, alkyl sulfate or alkyl phosphate
Als weitere Gruppe geeigneter Esterquats sind schließlich die quaternierten Estersalze von Fettsauren mit 1 ,2-Dιhydroxypropyldιalkylamιnen der Formel (III) zu nennen, R6 0-(CH2CH20)mOCRiFinally, as a further group of suitable ester quats, the quaternized ester salts of fatty acids with 1,2-dihydroxypropylalkylamines of the formula (III) are to be mentioned, R 6 0- (CH 2 CH 2 0) mOCRi
I I [R4-N+-CH2CHCH20-(CH2CH20)nR2] X" (|||)II [R 4 -N + -CH2CHCH 2 0- (CH2CH 2 0) nR 2 ] X "(|||)
II.
R'R '
in der R1CO für einen Acylrest mit 6 bis 22 Kohlenstoffatomen, vorzugsweise für einen Acylrest der sich von der Taigfettsäure enthaltenden Fettsäuremischung ableitet, R2 für Wasserstoff oder R1CO, R4, R6 und R7 unabhängig voneinander für Alkylreste mit 1 bis 4 Kohlenstoffatomen, m und n in Summe für 0 oder Zahlen von 1 bis 12 und X für Halogenid, Alkylsulfat oder Alkylphosphat steht.in which R 1 CO is an acyl radical having 6 to 22 carbon atoms, preferably an acyl radical derived from the fatty acid mixture containing the tallow fatty acid, R 2 is hydrogen or R 1 CO, R 4 , R 6 and R 7 are, independently of one another, alkyl radicals having 1 up to 4 carbon atoms, m and n in total represent 0 or numbers from 1 to 12 and X represents halide, alkyl sulfate or alkyl phosphate.
Hinsichtlich des optimalen Veresterungsgrades gelten die für (I) genannten Beispiele auch für die Esterquats der Formeln (II) und (III). Üblicherweise gelangen die Esterquats in Form 50 bis 90 Gew.- %iger alkoholischer Lösungen in den Handel, die bei Bedarf problemlos mit Wasser verdünnt werden können.With regard to the optimal degree of esterification, the examples given for (I) also apply to the esterquats of the formulas (II) and (III). The ester quats usually come in the form of 50 to 90% strength by weight alcoholic solutions, which can be diluted with water if necessary.
Quatemierte FettsäureimidazolineQuaternized fatty acid imidazolines
Quatemierte Fettsäureimidazoline stellen ebenfalls bekannte kationische Tenside dar, die man üblicherweise durch Kondensation von Fettsäuren mit Diaminen, vorzugsweise Ethylendiaminen und nachfolgende Quaternierung mit Alkylhalogeniden oder Dialkylsulfaten erhält. Verfahren zur Herstellung der Imidazoline und ihrer Quaternierungsprodukte sind beispielsweise aus den Druckschriften DE-A1 40 20 271, DE-A1 40 38 983 und DE-A1 41 16 648 (Henkel) bekannt. Die Imidazoline können dabei auch Anteile an offenkettigen Hydrolyseprodukten enthalten. Üblicherweise folgen sie aber der Formel (IV),Quaternized fatty acid imidazolines are also known cationic surfactants which are usually obtained by condensing fatty acids with diamines, preferably ethylenediamines and subsequent quaternization with alkyl halides or dialkyl sulfates. Processes for producing the imidazolines and their quaternization products are known, for example, from the publications DE-A1 40 20 271, DE-A1 40 38 983 and DE-A1 41 16 648 (Henkel). The imidazolines can also contain proportions of open-chain hydrolysis products. Usually they follow the formula (IV),
(IV)(IV)
in der R8 für einen Alkyl- und/oder Alkenylrest mit 7 bis 21 , vorzugsweise 11 bis 17 Kohlenstoffatomen, R9 für gegebenenfalls hydroxysubstituierte Alkylreste mit 1 bis 4 Kohlenstoffatomen oder einen Benzyl- rest, R10 für hydroxysubstituierte Alkylreste mit 2 bis 4 Kohlenstoffatomen oder einen CH2CH2NHCOR8- Rest und X für Halogenid oder Alkylsulfat steht. In einer besonderen Ausführungsform der Erfindung werden Produkte eingesetzt, die sich von der Ölsäure oder einem überwiegend Ölsäure enthaltenden Fettsäureschnitt ableiten. Besonders bevorzugt sind quatemierte Fettsäureimidazoline, die man durch Kondensation von Ölsäure mit Diethylentriamin oder Aminoethylethanolamin und nachfolgende Qua- temierung mit Dimethylsulfat oder Methylchlorid erhält. Das Gewichtsverhältnis der beiden Komponenten (a) und (b) in den erfindungsgemäßen Textilausrüstungsmitteln kann dabei 90 : 10 bis 10 : 90, vorzugsweise 15 :85 bis 50 : 50 und insbesondere 20 : 80 bis 25 : 75 betragen.in which R 8 is an alkyl and / or alkenyl radical having 7 to 21, preferably 11 to 17 carbon atoms, R 9 is optionally hydroxyl-substituted alkyl radicals having 1 to 4 carbon atoms or a benzyl radical, R 10 is hydroxy-substituted alkyl radicals having 2 to 4 carbon atoms or a CH2CH2NHCOR 8 radical and X represents halide or alkyl sulfate. In a special embodiment of the invention products are used which are derived from oleic acid or a fatty acid cut containing predominantly oleic acid. Quaternized fatty acid imidazolines which are obtained by condensation of oleic acid with diethylenetriamine or aminoethylethanolamine and subsequent quaternization with dimethyl sulfate or methyl chloride are particularly preferred. The weight ratio of the two components (a) and (b) in the textile finishing agents according to the invention can be 90:10 to 10:90, preferably 15:85 to 50:50 and in particular 20:80 to 25:75.
Gewerbliche AnwendbarkeitIndustrial applicability
Die erfindungsgemäßen Mittel verleihen textilen Flächengebilden, vorzugsweise Blue Denim-Gewebe, nicht nur einen angenehmen Weichgriff, sondern schützen auch zuverlässig gegen Vergilbung. Ein weiterer Gegenstand der Erfindung betrifft daher die Verwendung der Mischungen als Ausrüstungsmittel zur gleichzeitigen Avivage und Vergilbungsstabilisierung von textilen Flächengebilden. Die Mittel selbst liegen üblicherweise als wäßrige Lösungen oder Pasten mit einem Aktivsubstanzgehalt im Bereich von 5 bis 30 Gew.-% vor. Zur Viskositätseinstellung können sie femer beispielsweise Elektrolytsalze enthalten. The agents according to the invention not only give textile fabrics, preferably blue denim fabrics, a pleasant soft feel, but also provide reliable protection against yellowing. Another object of the invention therefore relates to the use of the mixtures as finishing agents for the simultaneous softening and yellowing stabilization of textile fabrics. The agents themselves are usually in the form of aqueous solutions or pastes with an active substance content in the range from 5 to 30% by weight. To adjust the viscosity, they can also contain, for example, electrolyte salts.
BeispieleExamples
Die Bewertung der Ozonstabilisierung wurde an Hand von Blue Denim Gewebe geprüft. Die Testsubstanzen wurden nach dem Foulard-Verfahren appliziert: Einsatzmenge 30 g/l, 20°C, Flottenaufnahme 70 %, pH = 5,5 bis 6,5. Das Aufziehen erfolgte in einer Horizontal-Waschmaschine, die Einsatzmenge betrug 4 Gew.-% vom Warengewicht (50°C, 20 min, pH = 5,5 bis 6,5, Flottenverhältnis 1 :20). Grundlage der Bewertung ist der Ozontest gemäß AATCC 109-1992 mittels einer Ozonkammer des Typs TriC-03 der Firma Textile Innovators CorpVUSA. Die Beurteilung des Ozonschutzes erfolgte an Hand eines Graumaßstabs, der Griff wurde im Paneltest bestimmt: 6 = sehr gut, 1 = schlecht. Die Ergebnisse sind in Tabelle 1 zusammengefaßt. Folgende Tenside wurden eingesetzt:The assessment of ozone stabilization was checked using blue denim fabric. The test substances were applied using the padding method: 30 g / l, 20 ° C., liquor pick-up 70%, pH = 5.5 to 6.5. The assembly was carried out in a horizontal washing machine, the amount used was 4% by weight of the product weight (50 ° C., 20 min, pH = 5.5 to 6.5, liquor ratio 1:20). The evaluation is based on the ozone test according to AATCC 109-1992 using an ozone chamber of the type TriC-03 from Textile Innovators CorpVUSA. The ozone protection was assessed using a gray scale, the grip was determined in the panel test: 6 = very good, 1 = bad. The results are summarized in Table 1. The following surfactants were used:
A1) Methylquaterniertes Fettsäureimidazolin, hergestellt aus Ölsäure der lodzahl 90 bis 100 und Aminoethylethanolamin, in Form des Methylsulfatsalzes;A1) Methyl-quaternized fatty acid imidazoline, produced from oleic acid of 90 to 100 iodine number and aminoethylethanolamine, in the form of the methyl sulfate salt;
A2) Methylquaterniertes Fettsäureminidazolin, hergestellt aus Ölsäure der lodzahl 85 bis 90 und Aminoethylethanolamin, in Form des Methylsulfatsalzes;A2) Methyl-quaternized fatty acid minidazoline, prepared from oleic acid of 85 to 90 iodine number and aminoethylethanolamine, in the form of the methyl sulfate salt;
A3) Methylquaterniertes Fettsäureminidazolin, hergestellt aus Tallölfettsäure und Aminoethylethanolamin, in Form des Methy Isulfatsaizes ;A3) Methylquaternized fatty acid minidazoline, made from tall oil fatty acid and aminoethylethanolamine, in the form of the methyl isulfate acid;
B1) Methylquatemierter Ditalgfettsäuretriethanolaminester in Form des Methylsulfatsalzes.B1) Methyl-quaternized ditallow fatty acid triethanolamine ester in the form of the methyl sulfate salt.
Tabelle 1Table 1
Vergrauung und Weichgriff (Mengenangaben als Gew.-%)Graying and soft handle (quantities as% by weight)
R1 R2 R3 R4R1 R2 R3 R4
Quat. Fettsäureimidazolin A1 12,3 . . .Quat. Fatty acid imidazoline A1 12.3. . .
Quat. Fettsäureimidazolin A2 . 12,3 _ _Quat. Fatty acid imidazoline A2. 12.3 _ _
Quat. Fettsäureimidazolin A3 . - 7,1 .Quat. Fatty acid imidazoline A3. - 7.1.
Esterquat B1 3,2 3,2 8,4 .Esterquat B1 3.2 3.2 8.4.
Wasser ad 00Water ad 00
Graumaßstab 4,0 4,5 3,5 2,5Gray scale 4.0 4.5 3.5 2.5
Weichgriff 4,5 5,0 5,5 1,0 Soft handle 4.5 5.0 5.5 1.0

Claims

Patentansprüche claims
1. Textilausrüstungsmittel, enthaltend1. Containing textile finishing agents
(a) Esterquats und(a) Esterquats and
(b) quatemierte Fettsäureimidazoline.(b) quaternized fatty acid imidazolines.
2. Mittel nach Anspruch 1 , dadurch gekennzeichnet, daß sie Esterquats der Formel (I) enthalten,2. Composition according to claim 1, characterized in that they contain esterquats of the formula (I),
R*R *
II.
[RiCO-(OCH2CH2)mOCH2CH2-N+-CH2CH20-(CH2CH2θ)nR2] X- (I)[RiCO- (OCH2CH2) mOCH2CH2-N + -CH 2 CH 2 0- (CH2CH2θ) nR 2 ] X- (I)
in der R1CO für einen Acylrest mit 6 bis 22 Kohlenstoffatomen, R2 und R3 unabhängig voneinander für Wasserstoff oder R1CO, R4 für einen Alkylrest mit 1 bis 4 Kohlenstoffatomen oder eine (CH∑CH∑OJqH-Gruppe, m, n und p in Summe für 0 oder Zahlen von 1 bis 12, q für Zahlen von 1 bis 12 und X für Halogenid, Alkylsulfat oder Alkylphosphat steht.in which R 1 CO for an acyl radical with 6 to 22 carbon atoms, R 2 and R 3 independently of one another for hydrogen or R 1 CO, R 4 for an alkyl radical with 1 to 4 carbon atoms or a (CH∑CH ∑ OJqH group, m , n and p in total stand for 0 or numbers from 1 to 12, q stands for numbers from 1 to 12 and X stands for halide, alkyl sulfate or alkyl phosphate.
3. Mittel nach Anspruch 1 , dadurch gekennzeichnet, daß sie Esterquats der Formel (II) enthalten,3. Composition according to claim 1, characterized in that they contain ester quats of the formula (II),
R*R *
I [RiCO-(OCH2CH2)mOCH2CH2-Nt-CH2CH2θ-(CH2CH2θ)nR2] X- (II) I [RiCO- (OCH2CH2) mOCH2CH 2 -N t -CH 2 CH2θ- (CH2CH2θ) nR 2 ] X- (II)
in der R1CO für einen Acylrest mit 6 bis 22 Kohlenstoffatomen, R2 für Wasserstoff oder R1CO, R4 und R5 unabhängig voneinander für Alkylreste mit 1 bis 4 Kohlenstoffatomen, m und n in Summe für 0 oder Zahlen von 1 bis 12 und X für Halogenid, Alkylsulfat oder Alkylphosphat steht.in which R 1 CO for an acyl radical with 6 to 22 carbon atoms, R 2 for hydrogen or R 1 CO, R 4 and R 5 independently of one another for alkyl radicals with 1 to 4 carbon atoms, m and n in total for 0 or numbers from 1 to 12 and X represents halide, alkyl sulfate or alkyl phosphate.
4. Mittel nach Anspruch 1 , dadurch gekennzeichnet, daß sie Esterquats der Formel (III) enthalten,4. Composition according to claim 1, characterized in that they contain ester quats of the formula (III),
R6 0-(CH2CH20)mOCR1 R 6 0- (CH 2 CH 2 0) m OCR 1
I II I
[R4-N+-CH2CHCH20-(CH2CH20)nR2] X" (III)[R 4 -N + -CH2CHCH 2 0- (CH2CH 2 0) nR 2 ] X "(III)
I R7 in der R'CO für einen Acylrest mit 6 bis 22 Kohlenstoffatomen, R2 für Wasserstoff oder R1CO, R4, R6 und R7 unabhängig voneinander für Alkylreste mit 1 bis 4 Kohlenstoffatomen, m und n in Summe für 0 oder Zahlen von 1 bis 12 und X für Halogenid, Alkylsulfat oder Alkylphosphat steht.IR 7 in the R'CO for an acyl radical having 6 to 22 carbon atoms, R 2 for hydrogen or R 1 CO, R 4 , R 6 and R 7 independently of one another for alkyl radicals with 1 to 4 carbon atoms, m and n in total for 0 or numbers from 1 to 12 and X represents halide, alkyl sulfate or alkyl phosphate.
5. Mittel nach den Ansprüchen 1 bis 4, dadurch gekennzeichnet, daß sie Esterquats der Formeln (I), (II) und/oder (III) enthalten, deren Acylrest R1CO sich ganz oder überwiegend von der Taigfettsäure ableitet.5. Composition according to claims 1 to 4, characterized in that they contain esterquats of the formulas (I), (II) and / or (III), the acyl radical R 1 CO is wholly or predominantly derived from the tallow fatty acid.
6. Mittel nach den Ansprüchen 1 bis 5, dadurch gekennzeichnet, daß sie quatemierte Fettsäureimidazoline der Formel (IV) enthalten,6. Composition according to claims 1 to 5, characterized in that they contain quaternized fatty acid imidazolines of the formula (IV),
(IV)(IV)
in der R8 für einen Alkyl- und/oder Alkenylrest mit 7 bis 21 Kohlenstoffatomen, R9 für gegebenenfalls hydroxysubstituierte Alkylreste mit 1 bis 4 Kohlenstoffatomen oder einen Benzylrest, R10 für hydroxysubstituierte Alkylreste mit 2 bis 4 Kohlenstoffatomen oder einen CH2CH2NHCOR8-Rest und X für Halogenid oder Alkylsulfat steht.in which R 8 is an alkyl and / or alkenyl radical having 7 to 21 carbon atoms, R 9 is optionally hydroxyl-substituted alkyl radicals having 1 to 4 carbon atoms or a benzyl radical, R 10 is hydroxy-substituted alkyl radicals having 2 to 4 carbon atoms or a CH2CH2NHCOR 8 radical and X represents halide or alkyl sulfate.
7. Mittel nach den Ansprüchen 1 bis 6, dadurch gekennzeichnet, daß sie die Komponenten (a) und (b) im Gewichtsverhältnis 90 : 10 bis 10 : 90 enthalten.7. Composition according to claims 1 to 6, characterized in that they contain the components (a) and (b) in a weight ratio of 90: 10 to 10: 90.
8. Verwendung von Mischungen nach Anspruch 1 als Ausrüstungsmittel zur gleichzeitigen Avivage und Vergilbungsstabilisierung von textilen Flächengebilden. 8. Use of mixtures according to claim 1 as a finishing agent for the simultaneous softening and yellowing stabilization of textile fabrics.
EP97937560A 1996-08-16 1997-08-07 Use of textile finishing agents Expired - Lifetime EP0918901B1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE19633104 1996-08-16
DE19633104A DE19633104C1 (en) 1996-08-16 1996-08-16 Use of detergent mixtures of ester-quat(s) and quaternised fatty acid imidazolines
PCT/EP1997/004304 WO1998007920A1 (en) 1996-08-16 1997-08-07 Textile finishing agent

Publications (2)

Publication Number Publication Date
EP0918901A1 true EP0918901A1 (en) 1999-06-02
EP0918901B1 EP0918901B1 (en) 2000-12-06

Family

ID=7802828

Family Applications (1)

Application Number Title Priority Date Filing Date
EP97937560A Expired - Lifetime EP0918901B1 (en) 1996-08-16 1997-08-07 Use of textile finishing agents

Country Status (9)

Country Link
US (1) US6402976B1 (en)
EP (1) EP0918901B1 (en)
BR (1) BR9711308A (en)
DE (2) DE19633104C1 (en)
DK (1) DK0918901T3 (en)
ES (1) ES2153683T3 (en)
PT (1) PT918901E (en)
TR (1) TR199900274T2 (en)
WO (1) WO1998007920A1 (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19829787A1 (en) * 1998-07-03 2000-01-05 Henkel Kgaa Finishing agent
DE50305183D1 (en) * 2003-06-24 2006-11-09 Cognis Ip Man Gmbh Pearlescent aqueous preparations
CN111778711B (en) * 2020-06-12 2022-12-23 鲁泰纺织股份有限公司 Production process for solving oxidative yellowing of jean shirts
JP2024517798A (en) 2021-05-04 2024-04-23 ニュートリション・アンド・バイオサイエンシーズ・ユーエスエー・フォー，インコーポレイテッド Compositions Comprising Insoluble Alpha-Glucans
CN117616054A (en) 2021-07-13 2024-02-27 营养与生物科学美国4公司 Cationic dextran ester derivatives
WO2023081341A1 (en) 2021-11-05 2023-05-11 Nutrition & Biosciences USA 4, Inc. Compositions comprising one cationic alpha- 1,6-glucan derivative and one alpha- 1,3-glucan
WO2023114942A1 (en) 2021-12-16 2023-06-22 Nutrition & Biosciences USA 4, Inc. Compositions comprising cationic alpha-glucan ethers in aqueous polar organic solvents
WO2024015769A1 (en) 2022-07-11 2024-01-18 Nutrition & Biosciences USA 4, Inc. Amphiphilic glucan ester derivatives
WO2024081773A1 (en) 2022-10-14 2024-04-18 Nutrition & Biosciences USA 4, Inc. Compositions comprising water, cationic alpha-1,6-glucan ether and organic solvent

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3915867A (en) 1973-04-24 1975-10-28 Stepan Chemical Co Domestic laundry fabric softener
GB1601360A (en) 1977-07-12 1981-10-28 Procter & Gamble Textile treatment composition
US4370272A (en) 1980-01-14 1983-01-25 Stepan Chemical Company Alkoxylated quaternary ammonium surfactants
GB2188653A (en) 1986-04-02 1987-10-07 Procter & Gamble Biodegradable fabric softeners
EP0293955B1 (en) 1987-05-01 1993-01-13 The Procter & Gamble Company Quaternary isopropyl ester ammonium compounds as fiber and fabric treatment compositions
EP0295739A3 (en) 1987-06-09 1990-01-17 The Procter & Gamble Company Method for preparing biodegradable fabric treatment compositions
DE3876196T2 (en) 1987-09-23 1993-04-15 Procter & Gamble LINEAR ALCOXYLATED ALCOHOLS CONTAINING STABLE, BIODEGRADABLE SOFTEN SOFTENER COMPOSITIONS.
JPH0756112B2 (en) * 1988-02-17 1995-06-14 花王株式会社 Concentrated softening agent for clothing
ES2021900A6 (en) 1989-07-17 1991-11-16 Pulcra Sa Process for preparing quaternary ammonium compounds.
DE3926740C2 (en) * 1989-08-12 1997-05-15 Witco Surfactants Gmbh Aqueous fabric softener and its use
US5116520A (en) * 1989-09-06 1992-05-26 The Procter & Gamble Co. Fabric softening and anti-static compositions containing a quaternized di-substituted imidazoline ester fabric softening compound with a nonionic fabric softening compound
DE4020271A1 (en) * 1990-06-26 1992-01-02 Henkel Kgaa SALTS OF FATTY ACID AMIDES AND FATTY ACID IMIDAZOLINES
DE4038983A1 (en) 1990-12-06 1992-06-11 Henkel Kgaa METHOD FOR THE PRODUCTION OF FLUID-LIQUID IMIDAZOLINIUM TENSIDES BY QUATERNATION OF 1-HYDROXYETHYL-2-ALKYLIMIDAZOLINES
DE4116648A1 (en) 1991-05-22 1992-11-26 Helmut Dipl Ing Wurster Self-cutting trocar insertable in sleeve for penetrating abdominal wall - has manual or motor driven cutting tool so hat power which is normally not used for inserting trocar is considerably reduced and insertion can be controlled
US5591186A (en) 1991-05-22 1997-01-07 Wurster; Helmut Self-cutting trocar
GB9122486D0 (en) * 1991-10-23 1991-12-04 Cussons Int Ltd Fabric softener composition
KR940006256B1 (en) * 1992-03-07 1994-07-13 재단법인 한국화학연구소 Fabric softner composition
EP0640121B2 (en) * 1992-05-12 2003-08-27 The Procter & Gamble Company Concentrated liquid fabric softener compositions containing biodegradable fabric softeners
US5397729A (en) 1992-06-15 1995-03-14 Asahi Kasei Microsystems Co., Ltd. Method for fabrication of semiconductor device having polycrystalline silicon and metal silicides
DE4243862A1 (en) 1992-12-23 1994-06-30 Huels Chemische Werke Ag Process for the quaternization of triethanolamine fatty acid esters and imidazoline amides in alkoxylated fats or oils as the reaction medium and the use of the reaction mixtures as fabric softening agent components
EP0607772A2 (en) * 1993-01-16 1994-07-27 Hüls Aktiengesellschaft Quaternary alkylamine alkoxylates as viscosity regulators for aqueous dispersions of nitrogen containing cationic active ingredients
DE4313085A1 (en) * 1993-04-21 1994-10-27 Stockhausen Chem Fab Gmbh Stable aqueous dispersions of quaternary ammonium compounds and imidazoline derivatives
US5652206A (en) * 1996-02-26 1997-07-29 The Procter & Gamble Company Fabric softener compositions with improved environmental impact
US5916863A (en) * 1996-05-03 1999-06-29 Akzo Nobel Nv High di(alkyl fatty ester) quaternary ammonium compound from triethanol amine

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9807920A1 *

Also Published As

Publication number Publication date
DE59702736D1 (en) 2001-01-11
EP0918901B1 (en) 2000-12-06
ES2153683T3 (en) 2001-03-01
PT918901E (en) 2001-04-30
WO1998007920A1 (en) 1998-02-26
BR9711308A (en) 1999-08-17
DE19633104C1 (en) 1997-10-16
TR199900274T2 (en) 1999-05-21
US6402976B1 (en) 2002-06-11
DK0918901T3 (en) 2001-03-05

Similar Documents

Publication Publication Date Title
EP1141189A1 (en) Clear softening agent formulations
EP0910338A1 (en) Cosmetic preparations based on cationic and non ionic surfactants
EP0918901B1 (en) Use of textile finishing agents
DE2812118A1 (en) TISSUE SOFTENING COMPOSITION WITH ANTISTATIC EFFECT
DE60126988T2 (en) AVIVISING COMPOSITIONS FOR FIBERS, CONTAINING NON-TENSIONS
DE4446137A1 (en) Quaternized triethanolamine difatty acid esters
EP0739976B1 (en) Brighteners
EP0861938A2 (en) Composition for finishing of textile- and keratin fibers
WO1991012364A1 (en) Active agent combination for textile treatment
DE3730444A1 (en) SOFTENER
DE69935337T3 (en) PLASTICISERS COMPOSITION
EP0230910B1 (en) Means for treating textiles
EP2909294B1 (en) Fabric softener composition with trialkanolamine-based ester quat
DE1619182C3 (en) Process for softening textiles
DE4215689A1 (en) Nitrogen-free active ingredient in fabric softener formulations
DE19714044C1 (en) Hydrophilic textile conditioners containing no polyolefin waxes
DE10054020B4 (en) Use of mixtures as textile treatment agents
DE10116491A1 (en) Textile conditioning composition, giving soft handle and increased hydrophilicity especially on polyacrylamide fabrics, comprising ester-quat, dimethyl diallylammonium chloride-acrylamide copolymer and water
EP1282739B1 (en) Use of surfactant mixtures as high speed textile fibre preparations
DE4413431A1 (en) Prepn. of quaternised aliphatic tri:ethanol:amine ester(s)
DD159263A3 (en) WEICHSPUELMITTELKONZENTRATE
DE2744021C3 (en) Concentrated aqueous agent for rendering synthetic fiber materials antistatic and its use
MXPA99001552A (en) Textile finishing agent
EP1314718A1 (en) Quaternised fatty acid amidoamines
EP0316701A2 (en) Quaternary amidoammonium salts, process for their preparation and their use

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19990208

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): BE DE DK ES FR IT PT

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: COGNIS DEUTSCHLAND GMBH

RTI1 Title (correction)

Free format text: USE OF TEXTILE FINISHING AGENTS

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

17Q First examination report despatched

Effective date: 20000118

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): BE DE DK ES FR IT PT

REF Corresponds to:

Ref document number: 59702736

Country of ref document: DE

Date of ref document: 20010111

ITF It: translation for a ep patent filed

Owner name: STUDIO JAUMANN P. & C. S.N.C.

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2153683

Country of ref document: ES

Kind code of ref document: T3

REG Reference to a national code

Ref country code: DK

Ref legal event code: T3

ET Fr: translation filed
REG Reference to a national code

Ref country code: PT

Ref legal event code: SC4A

Free format text: AVAILABILITY OF NATIONAL TRANSLATION

Effective date: 20010117

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
BECA Be: change of holder's address

Owner name: *COGNIS DEUTSCHLAND G.M.B.H. & CO. K.G.HENKELSTRAS

BECH Be: change of holder

Owner name: *COGNIS DEUTSCHLAND G.M.B.H. & CO. K.G.

BECN Be: change of holder's name

Owner name: *COGNIS DEUTSCHLAND G.M.B.H. & CO. K.G.HENKELSTRAS

REG Reference to a national code

Ref country code: PT

Ref legal event code: PD4A

Free format text: COGNIS DEUTSCHLAND GMBH & CO. KG DE

Effective date: 20030627

REG Reference to a national code

Ref country code: FR

Ref legal event code: TP

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: PT

Payment date: 20080808

Year of fee payment: 12

Ref country code: ES

Payment date: 20080922

Year of fee payment: 12

Ref country code: DK

Payment date: 20080815

Year of fee payment: 12

Ref country code: DE

Payment date: 20080821

Year of fee payment: 12

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IT

Payment date: 20080828

Year of fee payment: 12

REG Reference to a national code

Ref country code: PT

Ref legal event code: PC4A

Owner name: COGNIS IP MANAGEMENT GMBH, DE

Effective date: 20081215

REG Reference to a national code

Ref country code: FR

Ref legal event code: TP

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 20090119

Year of fee payment: 12

REG Reference to a national code

Ref country code: PT

Ref legal event code: MM4A

Free format text: LAPSE DUE TO NON-PAYMENT OF FEES

Effective date: 20100208

BERE Be: lapsed

Owner name: COGNIS IP MANAGEMENT G.M.B.H.

Effective date: 20090831

REG Reference to a national code

Ref country code: DK

Ref legal event code: EBP

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20100208

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20091201

Year of fee payment: 13

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090831

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090831

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20100302

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20090808

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090807

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20110819

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090808

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090831