EP1360364B1 - Verwendung von nicht-ionischen polysacchariden in einer zusammensetzung zur pflege von textilprodukten - Google Patents

Verwendung von nicht-ionischen polysacchariden in einer zusammensetzung zur pflege von textilprodukten Download PDF

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Publication number
EP1360364B1
EP1360364B1 EP02706853A EP02706853A EP1360364B1 EP 1360364 B1 EP1360364 B1 EP 1360364B1 EP 02706853 A EP02706853 A EP 02706853A EP 02706853 A EP02706853 A EP 02706853A EP 1360364 B1 EP1360364 B1 EP 1360364B1
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Prior art keywords
articles
nonionic
nonionic polysaccharide
composition
polysaccharide
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French (fr)
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EP1360364A1 (de
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Ian Harrison
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Rhodia Chimie SAS
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Rhodia Chimie SAS
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Classifications

    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/52Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
    • C11D1/526Carboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 are polyalkoxylated
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/38Cationic compounds
    • C11D1/52Carboxylic amides, alkylolamides or imides or their condensation products with alkylene oxides
    • C11D1/525Carboxylic amides (R1-CO-NR2R3), where R1, R2 or R3 contain two or more hydroxy groups per alkyl group, e.g. R3 being a reducing sugar rest
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/662Carbohydrates or derivatives
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/667Neutral esters, e.g. sorbitan esters

Definitions

  • the subject of the present invention is the use, in a composition for the care of articles made of textile fibers ("textile care"), in particular made of cotton, colored in particular, of at least one nonionic polysaccharide, as agent to prevent the degradation of these articles, to protect the colors of said articles and / or to provide them with anti-crease and / or softening properties.
  • textile care in particular made of cotton, colored in particular, of at least one nonionic polysaccharide
  • This degradation of the fibers leads to the formation of fibrils on the surface of the textile which finally gives a loss of brightness of the colored textiles. This degradation also induces a decrease in the resistance of the textile which has the extreme can lead to tearing of the tissues.
  • This degradation of textiles can be evaluated quantitatively either by a loss of colors of colored textiles or by a decrease in the breaking energy of the textile. It is usually necessary to carry out 10 to 20 cumulative machine washes to perceive this type of degradation.
  • Machine washing machine washing that systematically involves a spin operation also leads to a crumpled cloth that is accented during the drying, in particular by the formation of inter-fiber hydrogen bonds. An ironing operation is therefore necessary to obtain a presentable appearance of the laundry.
  • WO98 / 39401 discloses in particular the use of aminosilicone-type compounds as a softening and color-protecting agent in compositions for washing textiles in an aqueous medium.
  • JP 03 131695 A discloses the use, in a detergent composition for the care of textiles in an aqueous or wet medium, of a (poly) oxyalkylene, methyl or (poly) oxyalkylene methyl derivative of guar gum or starch, as anti-redeposition agent especially oils.
  • compositions for the treatment of textile articles especially cotton-based, colored in particular, certain non-ionic polysaccharides bearing hydrophobic substituents, soluble in the conditions of use (" Working conditions ") in aqueous or wet medium of said compositions avoided the degradation of these articles, allowed to protect colors and / or provided them with anti-crease and / or softening properties.
  • Such compositions may especially be compositions for washing and / or rinsing and / or softening articles made of textile fibers, for detaching articles made of pre-washing textile fibers ("prespotting"), for drying articles in textile fibers in tumble dryers or to facilitate the ironing of textile fiber articles.
  • the viscosity of an aqueous solution containing 1% by weight of said nonionic polysaccharides may preferably range from 200 to 5000 mPa.s.
  • the modification rate MS is expressed as the average number of moles of precursor of the nonionic modifying group reacted per anhydrohexose unit and / or anhydropentose unit.
  • the modification rate MS may vary according to the nature of the precursor of said modifying group. If said precursor is not capable of forming new reactive hydroxyl groups (alkylation precursor for example), the rate of modification by the nonionic groups is less than 3 by definition. If said precursor is capable of forming new reactive hydroxyl groups (hydroxyalkylation precursor for example), the modification rate MS is theoretically not limited; it can for example go up to 6, preferably up to 2.
  • the said nonionic groups are bonded to the carbon atoms of the sugar skeleton either directly or via -O- bonds.
  • the hexose units (similar or different) of the main backbone of the native skeleton can be D-glucose, D-or L-galactose, D-mannose, D- or L-fucose, L-rhamnose, etc.
  • the pentose and / or hexose units (similar or different) of the native backbone branches may be D-xylose ..., L- or D-arabinose, D-glucose, D- or L-galactose, D-mannose, D- or L-fucose, L-rhamnose ...
  • native skeleton there may be mentioned galactomannans, galactoglucomannans, xyloglucans, scleroglucannes ...
  • the native skeleton is a galactomannan.
  • Galactomannans are macromolecules comprising a main chain of ⁇ (1-4) -linked D-mannopyranose units substituted with D-galactopyranose units in the ⁇ (1-6) position.
  • ⁇ (1-4) -linked D-mannopyranose units substituted with D-galactopyranose units in the ⁇ (1-6) position.
  • gums guar, carob, tara there may be mentioned gums guar, carob, tara.
  • the native skeleton is a guar gum. Guar gums have a mannose / galactose ratio of 2.
  • the nonionic polysaccharides according to the invention can be obtained in known manner. These are mostly commercial products.
  • nonionic polysaccharides As examples of nonionic polysaccharides according to the invention, mention may be made of hydroxypropyl galactomannans, in particular hydroxypropyl guars. For a good realization of the invention, these can have a modification rate of the order of 0.1 to 6, preferably of 0.1 to 1.6, especially of 0.4 to 1.2. .
  • a second object of the invention is a method for improving the properties of a composition for the care of textile fiber articles in an aqueous or wet medium, by adding to said composition an effective amount of at least one non-polysaccharide. -ionic according to the invention to prevent the degradation of said articles and to protect the colors of said articles and / or to provide them with anti-crease and / or softening properties.
  • a third object of the invention consists in a method for preventing the degradation of textile fiber articles and protecting the colors of said articles and / or providing them with anti-crease and / or softening properties, by treatment of said articles. in an aqueous or wet medium, using a composition comprising at least one nonionic polysaccharide according to the invention.
  • composition of the invention is particularly well suited to the care of articles (linen) in particular cotton-based, in particular containing at least 35% cotton. It is particularly adapted to the care of colored articles.
  • the nonionic polysaccharides according to the invention are soluble under the conditions of use ("working conditions") in an aqueous or wet medium of said composition.
  • Said nonionic polysaccharides are considered soluble when more than 50%, preferably more than 70% of their weight are soluble in the aqueous or wet medium of use of the composition of the invention, that is to say especially in the conditions of temperature and pH of said medium.
  • the amount of nonionic polysaccharide present in the care composition according to the invention may range from 0.05 to 10% by dry weight of said composition in dry state, and this according to the desired application.
  • said nonionic polysaccharide (PN) can be implemented as follows: % of (PN) (in sec) in a care composition according to the invention used as 0.05 - 5 preferably 0.1 - 3 detergent formulation 0.05 - 3 preferably 0.1 - 2 rinse and / or softening formulation 0.05 - 10 drying additive 0.05 - preferably 0.1 - 5 repa-Issage formulation 0.05 - preferably 0.1 - 5 washing additive
  • compositions may contain at least one surfactant and / or a detergent and / or rinsing and / or softening additive for textile fiber articles and / or a solid support (textile in particular) of said nonionic polysaccharide.
  • surfactant and / or a detergent and / or rinsing and / or softening additive for textile fiber articles and / or a solid support (textile in particular) of said nonionic polysaccharide.
  • the detergent formulation may comprise surfactants in an amount corresponding to about 3 to 40% by weight, based on the detergent formulation, surfactants such as
  • Builder builders improving the properties of surfactants can be used in amounts of about 5-50%, preferably about 5-30% by weight for liquid detergent formulations or about 10% by weight. -80%, preferably 15-50% by weight for powder detergent formulations, detergency builders such as:
  • the detergent formulation may further comprise at least one oxygen-releasing bleaching agent comprising a percompound, preferably a persalt.
  • Said bleaching agent may be present in an amount corresponding to about 1 to 30%, preferably 4 to 20% by weight, based on the detergent formulation.
  • per-compounds which may be used as bleaching agents particular mention should be made of perborates such as sodium perborate monohydrate or tetrahydrate; peroxygen compounds such as sodium carbonate peroxyhydrate, pyrophosphate peroxyhydrate, urea peroxyhydrate, sodium peroxide, sodium persulfate.
  • perborates such as sodium perborate monohydrate or tetrahydrate
  • peroxygen compounds such as sodium carbonate peroxyhydrate, pyrophosphate peroxyhydrate, urea peroxyhydrate, sodium peroxide, sodium persulfate.
  • the preferred bleaching agents are sodium perborate, mono or tetrahydrate and / or sodium carbonate peroxyhydrate.
  • Said agents are generally associated with a bleaching activator generating in situ in the detergent medium, a peroxy carboxylic acid, in an amount corresponding to about 0.1 to 12%, preferably 0.5 to 8% by weight relative to the detergent formulation.
  • a bleaching activator generating in situ in the detergent medium, a peroxy carboxylic acid, in an amount corresponding to about 0.1 to 12%, preferably 0.5 to 8% by weight relative to the detergent formulation.
  • these activators mention may be made of tetraacetylethylenediamine, tetraacetylmethylenediamine, tetraacetylglycoluryl, sodium p-acetoxybenzenesulphonate, pentaacetylglucose and octaacetyllactose.
  • Non-oxygenated bleaches acting by photoactivation in the presence of oxygen agents such as aluminum phthalocyanines and / or sulphonated zinc.
  • the detergent formulation may further comprise soil release, anti-redeposition, chelant, dispersant, fluorescence, suds suppressor, softener, enzyme and other miscellaneous additives.
  • They can be used in amounts of about 0.01-10%, preferably about 0.1-5%, and more preferably of the order of 0.2-3% by weight.
  • the chelating agents of iron and magnesium may be present in amounts of the order of 0.1-10%, preferably of the order of 0.1-3% by weight.
  • agents such as: stilbene derivatives, pyrazoline, coumarin, fumaric acid, cinnamic acid, azoles, methinecyanines, thiophenes ...
  • stilbene derivatives pyrazoline, coumarin, fumaric acid, cinnamic acid, azoles, methinecyanines, thiophenes ...
  • agents such as clays.
  • a third embodiment of the care composition of the invention consists of a drying additive of textile fiber articles in a suitable drying machine.
  • Said additive comprises a flexible solid support consisting for example of a woven or non-woven textile web, a cellulose sheet, impregnated with said nonionic polysaccharide; said additive is introduced on drying in the wet laundry to be dried at a temperature of the order of 50 to 80 ° C for 10 to 60 minutes.
  • Said additive may further comprise cationic softening agents (up to 99%) and anti-color transfer agents (up to 80%) such as those mentioned above.
  • a fourth embodiment of the care composition of the invention consists of an ironing formulation which can be sprayed directly onto the dry cloth before the ironing operation.
  • Said formulation may further contain silicone-based polymers (from 0.2 to 5%), nonionic surfactants (from 0.5 to 5%) or anionic surfactants (from 0.5 to 5%), perfumes (0.1 to 3%), cellulose derivatives (0.1 to 3%) such as starch; spraying said formulation on the laundry makes it easier to iron and to limit the creasing of the laundry when worn.
  • silicone-based polymers from 0.2 to 5%
  • nonionic surfactants from 0.5 to 5%
  • anionic surfactants from 0.5 to 5%
  • perfumes 0.1 to 3%
  • cellulose derivatives 0.1 to 3%) such as starch
  • Washing temperature ° C 40 Duration: about 67 minutes Number of wash: 10 Laundry load: 3 kg dry (4 towels + 6 tea towels + colored fabrics) Volume of the bath: 13 liters ⁇ 1 liter Water hardness : about 23 ° TH french Concentration detergent formula: 5 ⁇ 0.1 g / l
  • the colors are measured on LUCI100 reflectometer:
  • the measuring system used is CIE-L * a * b * (DIN6174, CIE-LAB 1976).
  • Each tissue specimen is measured at 5 different points (one at the center and one at each corner) and the average of the L *, a * and b * components is calculated.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Detergent Compositions (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Cosmetics (AREA)

Claims (23)

  1. Verwendung, in einer Zusammensetzung zur Pflege von Gegenständen aus Textilfasern in wässrigem oder feuchtem Medium, mindestens eines nichtionischen Polysaccharids, das unter den Einsatzbedingungen der Zusammensetzung löslich ist, wobei das native Gerüst des Polysaccharids gebildet ist aus
    * einer Hauptkette, die gleiche oder verschiedene Anhydrohexoseeinheiten umfasst
    * und Verzweigungen, die mindestens eine Anhydropentose- und/oder Anhydrohexoseeinheit umfassen,
    wobei die Anhydrohexose- und/oder Anhydropentoseeinheiten des nativen Gerüsts durch mindestens eine nichtionische Gruppe modifiziert sind,
    wobei der Modifikationsgrad MS der Anhydrohexose-und/oder Anhydropentoseeinheiten durch die nichtionische(n) Gruppe(n) mindestens 0,001, bevorzugt mindestens 0,01 beträgt,
    als Mittel, das es ermöglicht, die Schädigung der Gegenstände zu verhindern und die Farben der Gegenstände zu schützen und/oder diesen Knitterfestigkeitseigenschaften und/oder weichmachende Eigenschaften zu verleihen.
  2. Verwendung nach Anspruch 1, dadurch gekennzeichnet, dass der Modifikationsgrad MS bis 6 reicht.
  3. Verwendung nach Anspruch 1 oder 2, dadurch gekennzeichnet, dass der Modifikationsgrad MS kleiner als 3 ist.
  4. Verwendung nach irgendeinem der Ansprüche 1 bis 3, dadurch gekennzeichnet, dass der Modifikationsgrad MS bis 2 reicht.
  5. Verwendung nach irgendeinem der Ansprüche 1 bis 4, dadurch gekennzeichnet, dass die nichtionischen Gruppen entweder direkt oder mittels -O--Bindungen an die Kohlenstoffatome des Zuckergerüsts gebunden sind.
  6. Verwendung nach irgendeinem der Ansprüche 1 bis 5, dadurch gekennzeichnet, dass die nichtionischen Gruppen folgende Formel haben:
    • -[-CH2-CH(R)-O]x-R1, worin
    R ein Wasserstoffatom oder ein Alkylrest ist, der 1 bis 4 Kohlenstoffatome enthält,
    x eine ganze Zahl zwischen 0 und 6 ist,
    R1 für Folgendes steht
    . ein Wasserstoffatom, wenn x ungleich 0 ist,
    . einen Alkylrest, der 1 bis 22 Kohlenstoffatome enthält, gegebenenfalls unterbrochen durch ein oder mehrere Sauerstoff- und/oder Stickstoffheteroatome, Cycloalkyl, Aryl, Arylalkyl, das 6 bis 12 Kohlenstoffatome enthält
    . einen Rest -(CH2)y-COOR2
    . einen Rest -(CH2)y-CN
    . einen Rest -(CH2)y-CONHR2
    wobei R2 für einen Alkyl-, Aryl oder Arylalkylrest steht, der 1 bis 22 Kohlenstoffatome enthält, und y eine ganze Zahl zwischen 0 und 5 ist,
    • -CO-NH-R1 mittels einer -O--Bindung an ein Kohlenstoffatom des Zuckergerüsts gebunden ist, wobei R1 die oben angegebene Definition hat.
  7. Verwendung nach irgendeinem der Ansprüche 1 bis 6, dadurch gekennzeichnet, dass die nichtionischen Gruppen
    . Methyl-, Ethyl-, Propyl-, Isopropyl-, Butyl-, Hexyl-, Octyl-, Dodecyl-, Octadecyl-, Phenyl-, Benzylgruppen sind, die mittels einer Ether-, Ester-, Amid- oder Urethanbindung an ein Kohlenstoffatom des Zuckergerüsts gebunden sind,
    . Cyanoethyl-, Hydroxyethyl-, Hydroxypropyl-, Hydroxybutylgruppen sind, die mittels einer -O--Bindung an ein Kohlenstoffatom des Zuckergerüsts gebunden sind.
  8. Verwendung nach irgendeinem der Ansprüche 1 bis 7, dadurch gekennzeichnet, dass die Hexoseeinheiten (gleich oder verschieden) der Hauptkette des nativen Gerüsts D-Glucose-, D- oder L-Galactose-, D-Mannose-, D- oder L-Fucose-, L-Rhamnoseeinheiten sind.
  9. Verwendung nach irgendeinem der Ansprüche 1 bis 8, dadurch gekennzeichnet, dass die Pentose- und/oder Hexoseeinheiten (gleich oder verschieden) der Verzweigungen des nativen Gerüsts D-Xylose-, L- oder D-Arabinose-, D-Glucose-, D- oder L-Galactose-, D-Mannose-, D- oder L-Fucose-, L-Rhamnoseeinheiten sind.
  10. Verwendung nach irgendeinem der Ansprüche 1 bis 9, dadurch gekennzeichnet, dass das native Gerüst ein Galactomannan, Galactoglucomannan, Xyloglucan, Scleroglucan ist.
  11. Verwendung nach Anspruch 10, dadurch gekennzeichnet, dass das native Gerüst ein Galactomannan ist.
  12. Verwendung nach Anspruch 11, dadurch gekennzeichnet, dass das nichtionische Polysaccharid ein Hydroxypropylgalactomannan ist.
  13. Verwendung nach Anspruch 12, dadurch gekennzeichnet, dass das nichtionische Polysaccharid ein Hydroxypropylguar ist.
  14. Verwendung nach Anspruch 13, dadurch gekennzeichnet, dass das Hydroxypropylguar einen Modifikationsgrad von 0,1 bis 6, bevorzugt 0,1 bis 1,6, insbesondere 0,4 bis 1,2 aufweist.
  15. Verwendung nach irgendeinem der Ansprüche 1 bis 14, dadurch gekennzeichnet, dass die Zusammensetzung die folgende Form aufweist:
    * eines Feststoffs, einer Dispersion oder einer konzentrierten wässrigen Lösung, die, nach Auflösung in Wasser, mit den zu behandelnden Gegenständen aus Textilfasern in Kontakt gebracht wird;
    * einer Dispersion oder einer konzentrierten wässrigen Lösung, die vor der Auflösung in Wasser auf den trockenen zu behandelnden Gegenständen aus Textilfasern aufgetragen wird;
    * einer Dispersion oder einer wässrigen Lösung, die direkt, ohne Auflösung, auf die trockenen zu behandelnden Gegenstände aus Textilfasern aufzutragen ist, oder eines festen Trägers, der das nichtionische Polysaccharid umfasst, der direkt auf die trockenen zu behandelnden Gegenstände aufzubringen ist;
    * oder eines unlöslichen festen Trägers, der das nichtionische Polysaccharid umfasst, der direkt mit den zu behandelnden Gegenständen aus Textilfasern in feuchtem Zustand in Kontakt gebracht wird.
  16. Verwendung nach irgendeinem der Ansprüche 1 bis 15, dadurch gekennzeichnet, dass die Zusammensetzung, bezogen auf die Trockensubstanz, 0,05 bis 10 % des nichtionischen Polysaccharids umfasst.
  17. Verwendung nach irgendeinem der Ansprüche 1 bis 16, dadurch gekennzeichnet, dass die Zusammensetzung Folgendes ist:
    - eine feste oder flüssige Waschmittelformulierung, die, bezogen auf die Trockensubstanz, 0,05 bis 5 %, bevorzugt 0,1 bis 3 % des nichtionischen Polysaccharids umfasst, die in der Lage ist, direkt durch Auflösung eine Waschflotte zu bilden;
    - eine flüssige Spül- und/oder Weichspülformulierung, die, bezogen auf die Trockensubstanz, 0,05 bis 3 %, bevorzugt 0,1 bis 2 % des nichtionischen Polysaccharids umfasst, die in der Lage ist, direkt durch Auflösung eine Spül- und/oder Weichspülflotte zu bilden;
    - ein festes, insbesondere textiles Material, das, bezogen auf die Trockensubstanz, 0,05 bis 10 %, bevorzugt 0,1 bis 5 % des nichtionischen Polysaccharids umfasst, das dazu bestimmt ist, mit Gegenständen aus feuchten Textilfasern in einem Wäschetrockner in Kontakt gebracht zu werden;
    - eine wässrige Bügelformulierung, die, bezogen auf die Trockensubstanz, 0,05 bis 10 %, bevorzugt 0,1 bis 5 % des nichtionischen Polysaccharids umfasst;
    - ein Waschzusatz, der, bezogen auf die Trockensubstanz, 0,05 bis 10 %, bevorzugt 0,1 bis 5 % des nichtionischen Polysaccharids umfasst, der dazu bestimmt ist, auf die trockenen Gegenstände aus Textilfasern vor einem Waschvorgang mit Hilfe einer Waschmittelformulierung, die das nichtionische Polysaccharid enthält oder nicht enthält, aufgetragen zu werden.
  18. Verwendung nach irgendeinem der Ansprüche 1 bis 17, dadurch gekennzeichnet, dass die Zusammensetzung mindestens ein Tensid und/oder einen Wasch- und/oder Spül- und/oder Weichspülzusatz für die Gegenstände aus Textilfasern und/oder einen festen Träger des nichtionischen Polysaccharids enthält.
  19. Verfahren zur Verbesserung der Eigenschaften einer Zusammensetzung zur Pflege von Gegenständen aus Textilfasern in wässrigem oder feuchtem Medium durch die Zugabe zu der Zusammensetzung mindestens eines nichtionischen Polysaccharids, dessen Verwendung Gegenstand irgendeines der Ansprüche 1 bis 14 ist, in einer Menge, die es ermöglicht, die Schädigung der Gegenstände zu verhindern und die Farben der Gegenstände zu schützen und/oder diesen Knitterfestigkeitseigenschaften und/oder weichmachende Eigenschaften zu verleihen.
  20. Verfahren zum Verhindern der Schädigung von Gegenständen aus Textilfasern und zum Schutz der Farben der Gegenstände und/oder zum Verleihen von Knitterfestigkeitseigenschaften und/oder weichmachenden Eigenschaften an diese durch Behandlung der Gegenstände in wässrigem oder feuchtem Medium mit Hilfe einer Zusammensetzung, die mindestens ein nichtionisches Polysaccharid umfasst, dessen Verwendung Gegenstand irgendeines der Ansprüche 1 bis 14 ist.
  21. Verfahren nach Anspruch 19 oder 20, dadurch gekennzeichnet, dass die Zusammensetzung folgende Form aufweist:
    * eines Feststoffs, einer Dispersion oder einer konzentrierten wässrigen Lösung, die, nach Auflösung in Wasser, mit den zu behandelnden Gegenständen aus Textilfasern in Kontakt gebracht wird;
    * einer Dispersion oder einer konzentrierten wässrigen Lösung, die vor der Auflösung in Wasser auf den trockenen zu behandelnden Gegenständen aus Textilfasern aufgebracht wird;
    * einer Dispersion oder einer wässrigen Lösung, die direkt, ohne Auflösung, auf die trockenen zu behandelnden Gegenstände aus Textilfasern aufzutragen ist, oder eines festen Trägers, der das nichtionische Polysaccharid umfasst, der direkt auf die trockenen zu behandelnden Gegenstände aufzubringen ist;
    * oder eines unlöslichen festen Trägers, der das nichtionische Polysaccharid umfasst, der direkt mit den zu behandelnden Gegenständen aus Textilfasern in feuchtem Zustand in Kontakt gebracht wird.
  22. Verfahren nach irgendeinem der Ansprüche 19 bis 21, dadurch gekennzeichnet, dass die Zusammensetzung Folgendes ist:
    - eine feste oder flüssige Waschmittelformulierung, die, bezogen auf die Trockensubstanz, 0,05 bis 5 %, bevorzugt 0,1 bis 3 % des nichtionischen Polysaccharids umfasst, die in der Lage ist, direkt durch Auflösung eine Waschflotte zu bilden;
    - eine flüssige Spül- und/oder Weichspülformulierung, die, bezogen auf die Trockensubstanz, 0,05 bis 3 %, bevorzugt 0,1 bis 2 % des nichtionischen Polysaccharids umfasst, die in der Lage ist, direkt durch Auflösung eine Spülflotte und/oder eine weichmachende Flotte zu bilden;
    - ein festes, insbesondere textiles Material, das, bezogen auf die Trockensubstanz, 0,05 bis 10 %, bevorzugt 0,1 bis 5 % des nichtionischen Polysaccharids umfasst, das dazu bestimmt ist, in einem Wäschetrockner mit feuchter Wäsche in Kontakt gebracht zu werden;
    - eine wässrige Bügelformulierung, die, bezogen auf die Trockensubstanz, 0,05 bis 10 %, bevorzugt 0,1 bis 5 % des nichtionischen Polysaccharids umfasst;
    - ein Waschzusatz, der, bezogen auf die Trockensubstanz, 0,05 bis 10 %, bevorzugt 0,1 bis 5 % des nichtionischen Polysaccharids umfasst, der dazu bestimmt ist, auf die trockenen Gegenstände aus Textilfasern vor einem Waschvorgang mit Hilfe einer Waschmittelformulierung, die das nichtionische Polysaccharid enthält oder nicht enthält, aufgetragen zu werden.
  23. Verfahren nach einem der Ansprüche 19 bis 22, dadurch gekennzeichnet, dass die Gegenstände mindestens 35 Gew.-% Baumwolle, bevorzugt farbige Baumwolle, enthalten.
EP02706853A 2001-02-15 2002-02-13 Verwendung von nicht-ionischen polysacchariden in einer zusammensetzung zur pflege von textilprodukten Expired - Lifetime EP1360364B1 (de)

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FR0102079 2001-02-15
FR0102079A FR2820747B1 (fr) 2001-02-15 2001-02-15 Composition a base de polysaccharide non-ionique pour le soin des articles en fibres textiles
PCT/FR2002/000549 WO2002064878A1 (fr) 2001-02-15 2002-02-13 Utilisation de polysaccharide non-ionique dans une composition pour le soin des articles en fibres textiles

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EP1360364B1 true EP1360364B1 (de) 2010-03-31

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8460477B2 (en) 2010-08-23 2013-06-11 Ecolab Usa Inc. Ethoxylated alcohol and monoethoxylated quaternary amines for enhanced food soil removal

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7666963B2 (en) * 2005-07-21 2010-02-23 Akzo Nobel N.V. Hybrid copolymers
US9321873B2 (en) 2005-07-21 2016-04-26 Akzo Nobel N.V. Hybrid copolymer compositions for personal care applications
US20080020961A1 (en) * 2006-07-21 2008-01-24 Rodrigues Klin A Low Molecular Weight Graft Copolymers
US8674021B2 (en) * 2006-07-21 2014-03-18 Akzo Nobel N.V. Sulfonated graft copolymers
FR2915824B1 (fr) * 2007-05-02 2009-06-05 Thales Sa Procede d'optimisation de la sortie d'un aeronef dans un circuit d'attente
JP4954798B2 (ja) * 2007-06-01 2012-06-20 花王株式会社 繊維製品処理剤組成物
WO2010139548A1 (de) * 2009-05-18 2010-12-09 Henkel Ag & Co. Kgaa Stabilisiertes flüssiges klebstoffkonzentrat
US11173106B2 (en) * 2009-10-07 2021-11-16 Johnson & Johnson Consumer Inc. Compositions comprising a superhydrophilic amphiphilic copolymer and a micellar thickener
US8258250B2 (en) * 2009-10-07 2012-09-04 Johnson & Johnson Consumer Companies, Inc. Compositions comprising superhydrophilic amphiphilic copolymers and methods of use thereof
US8399590B2 (en) * 2009-10-07 2013-03-19 Akzo Nobel Chemicals International B.V. Superhydrophilic amphiphilic copolymers and processes for making the same
US8636918B2 (en) 2011-08-05 2014-01-28 Ecolab Usa Inc. Cleaning composition containing a polysaccharide hybrid polymer composition and methods of controlling hard water scale
US8679366B2 (en) 2011-08-05 2014-03-25 Ecolab Usa Inc. Cleaning composition containing a polysaccharide graft polymer composition and methods of controlling hard water scale
US8841246B2 (en) 2011-08-05 2014-09-23 Ecolab Usa Inc. Cleaning composition containing a polysaccharide hybrid polymer composition and methods of improving drainage
US8853144B2 (en) 2011-08-05 2014-10-07 Ecolab Usa Inc. Cleaning composition containing a polysaccharide graft polymer composition and methods of improving drainage
IN2014DN03123A (de) 2011-11-04 2015-05-22 Akzo Nobel Chemicals Int Bv
CN103889395A (zh) 2011-11-04 2014-06-25 阿克佐诺贝尔化学国际公司 接枝树枝状共聚物及其制备方法
US8945314B2 (en) 2012-07-30 2015-02-03 Ecolab Usa Inc. Biodegradable stability binding agent for a solid detergent
WO2015074692A1 (en) * 2013-11-20 2015-05-28 Rhodia Operations Fabric softener composition
US9365805B2 (en) 2014-05-15 2016-06-14 Ecolab Usa Inc. Bio-based pot and pan pre-soak
US10435831B1 (en) * 2014-07-15 2019-10-08 Rita Harry-Ogiste Fabric treating accessories and associated use thereof
CN107558229A (zh) * 2017-08-24 2018-01-09 江苏澳洋世家服装有限公司 一种挺括型夹克面料的加工工艺
WO2020208052A1 (en) 2019-04-12 2020-10-15 Basf Se Method for providing laundry detergent with control and a laundry apparatus and a laundry detergent kit

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3226890A (en) * 1962-05-24 1966-01-04 William J Flajole House trailer having expansible room
DE1468014A1 (de) * 1964-01-29 1969-01-09 Henkel & Cie Gmbh Verfahren zur Herstellung von Hydroxyalkylaethern von Galactomannanen
US4169945A (en) * 1978-01-05 1979-10-02 Celanese Corporation Process for production of polygalactomannan ethers
DE3709698C1 (de) * 1987-03-25 1988-10-27 Diamalt Ag Schlichtemittel
US4918181A (en) * 1988-03-02 1990-04-17 Karcher Dennis J Tertiaryaminoalkyl-hydroxyalkyl ethers of polygalactomannans
JPH03131695A (ja) * 1989-10-17 1991-06-05 Sanyo Chem Ind Ltd 洗剤用添加剤および組成物
KR100304813B1 (ko) * 1992-12-28 2001-11-22 사와무라 시코 부성저항회로와이를사용한슈미트트리거회로
US5552462A (en) * 1993-11-22 1996-09-03 Rhone-Poulenc Inc. Compositions including cationic polymers and anionic xanthan gum
US5489674A (en) * 1994-06-09 1996-02-06 Rhone-Poulenc Inc. Guar gum composition and process for making it
DE69521170T2 (de) * 1994-06-09 2001-10-04 Rhodia Inc., Cranbury Guargummizusammensetzung und Verfahren zur deren Herstellung
US5948744A (en) * 1994-12-01 1999-09-07 Baillely; Gerard Marcel Detergent composition containing combination of nonionic polysaccharide ether with synthetic oxyalkylene-containing soil release agent
US5919271A (en) * 1994-12-31 1999-07-06 Procter & Gamble Company Detergent composition comprising cellulase enzyme and nonionic cellulose ether
AU4753296A (en) * 1995-01-19 1996-08-07 Rhone-Poulenc, Inc. Novel additive for textile and adhesive applications
US5801116A (en) * 1995-04-07 1998-09-01 Rhodia Inc. Process for producing polysaccharides and their use as absorbent materials
US5756720A (en) * 1996-10-25 1998-05-26 Rhodia Inc. Derivatized guar gum composition including nonionic and cationic groups which demonstrate excellent solution clarity properties
JPH11335698A (ja) * 1998-05-27 1999-12-07 Lion Corp 液体洗浄剤組成物の製造方法
US6197100B1 (en) * 1998-12-04 2001-03-06 Hercules Incorporated Dispersible water soluble polymers
DE19857543A1 (de) * 1998-12-14 2000-06-15 Henkel Kgaa Verwendung von Protease in flüssigen bis gelförmigen Wasch- und Reinigungsmitteln
US6485945B1 (en) * 1999-02-17 2002-11-26 Nurture, Inc. Polysaccharide compositions and uses thereof
US6387871B2 (en) * 2000-04-14 2002-05-14 Alticor Inc. Hard surface cleaner containing an alkyl polyglycoside
FR2815355B1 (fr) * 2000-10-18 2003-03-14 Rhodia Chimie Sa Composition a base de polysaccharide anionique pour le soin du linge
FR2818983B1 (fr) * 2000-12-28 2005-09-09 Rhodia Chimie Sa Polysaccharide amphotere et son utilisation pour le soin des articles en fibres textiles
US6395690B1 (en) * 2001-02-28 2002-05-28 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Process for making mild moisturizing liquids containing large oil droplet
US6897188B2 (en) * 2001-07-17 2005-05-24 Ecolab, Inc. Liquid conditioner and method for washing textiles
FR2828887B1 (fr) * 2001-08-22 2003-12-05 Rhodia Chimie Sa Additif preformule pour composition de traitement des articles en fibres textiles et utilisation dudit comme agent de soin
US6897189B2 (en) * 2001-12-07 2005-05-24 The Procter & Gamble Company Anti-wrinkle silicone polysaccharide compounds and compositions comprising said compounds

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8460477B2 (en) 2010-08-23 2013-06-11 Ecolab Usa Inc. Ethoxylated alcohol and monoethoxylated quaternary amines for enhanced food soil removal

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US20040067865A1 (en) 2004-04-08
JP2004528487A (ja) 2004-09-16
DE60235795D1 (de) 2010-05-12
ES2339534T3 (es) 2010-05-21
FR2820747B1 (fr) 2005-10-07
US20060162092A1 (en) 2006-07-27
FR2820747A1 (fr) 2002-08-16
EP1360364A1 (de) 2003-11-12
BR0207059A (pt) 2004-02-17
CA2437772A1 (fr) 2002-08-22
US7557077B2 (en) 2009-07-07
ATE462823T1 (de) 2010-04-15
WO2002064878A1 (fr) 2002-08-22

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