NO310420B1 - Pode-kopolymerer umettede monomerer og polyhydroksyforbindelser, fremgangsmåte for fremstilling, samtanvendelse av polymerene - Google Patents
Pode-kopolymerer umettede monomerer og polyhydroksyforbindelser, fremgangsmåte for fremstilling, samtanvendelse av polymerene Download PDFInfo
- Publication number
- NO310420B1 NO310420B1 NO19962656A NO962656A NO310420B1 NO 310420 B1 NO310420 B1 NO 310420B1 NO 19962656 A NO19962656 A NO 19962656A NO 962656 A NO962656 A NO 962656A NO 310420 B1 NO310420 B1 NO 310420B1
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- Norway
- Prior art keywords
- graft copolymers
- acid
- copolymers according
- weight
- monoethylenically unsaturated
- Prior art date
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- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- SZHIIIPPJJXYRY-UHFFFAOYSA-M sodium;2-methylprop-2-ene-1-sulfonate Chemical compound [Na+].CC(=C)CS([O-])(=O)=O SZHIIIPPJJXYRY-UHFFFAOYSA-M 0.000 description 1
- 239000008234 soft water Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 229940057429 sorbitan isostearate Drugs 0.000 description 1
- 229950006451 sorbitan laurate Drugs 0.000 description 1
- 235000011067 sorbitan monolaureate Nutrition 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 229950003429 sorbitan palmitate Drugs 0.000 description 1
- 229960005078 sorbitan sesquioleate Drugs 0.000 description 1
- 229950011392 sorbitan stearate Drugs 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- XXHDAWYDNSXJQM-ONEGZZNKSA-N trans-hex-3-enoic acid Chemical compound CC\C=C\CC(O)=O XXHDAWYDNSXJQM-ONEGZZNKSA-N 0.000 description 1
- YIYBQIKDCADOSF-ONEGZZNKSA-N trans-pent-2-enoic acid Chemical compound CC\C=C\C(O)=O YIYBQIKDCADOSF-ONEGZZNKSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- UGCDBQWJXSAYIL-UHFFFAOYSA-N vat blue 6 Chemical compound O=C1C2=CC=CC=C2C(=O)C(C=C2Cl)=C1C1=C2NC2=C(C(=O)C=3C(=CC=CC=3)C3=O)C3=CC(Cl)=C2N1 UGCDBQWJXSAYIL-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229920001221 xylan Polymers 0.000 description 1
- 150000004823 xylans Chemical class 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/56—Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F5/00—Softening water; Preventing scale; Adding scale preventatives or scale removers to water, e.g. adding sequestering agents
- C02F5/08—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents
- C02F5/10—Treatment of water with complexing chemicals or other solubilising agents for softening, scale prevention or scale removal, e.g. adding sequestering agents using organic substances
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F251/00—Macromolecular compounds obtained by polymerising monomers on to polysaccharides or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F291/00—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
- C08F291/06—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00 on to oxygen-containing macromolecules
- C08F291/08—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00 on to oxygen-containing macromolecules on to macromolecules containing hydroxy radicals
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3788—Graft polymers
-
- C—CHEMISTRY; METALLURGY
- C14—SKINS; HIDES; PELTS; LEATHER
- C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
- C14C3/00—Tanning; Compositions for tanning
- C14C3/02—Chemical tanning
- C14C3/28—Multi-step processes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L1/00—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods
- D06L1/12—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods using aqueous solvents
- D06L1/14—De-sizing
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/10—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen
- D06L4/12—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen combined with specific additives
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/46—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing natural macromolecular substances or derivatives thereof
- D06P1/48—Derivatives of carbohydrates
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/52—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
- D06P1/5207—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- D06P1/5214—Polymers of unsaturated compounds containing no COOH groups or functional derivatives thereof
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/52—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
- D06P1/5207—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- D06P1/5214—Polymers of unsaturated compounds containing no COOH groups or functional derivatives thereof
- D06P1/5228—Polyalkenyl alcohols, e.g. PVA
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/52—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing synthetic macromolecular substances
- D06P1/5207—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- D06P1/525—Polymers of unsaturated carboxylic acids or functional derivatives thereof
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4343993A DE4343993A1 (de) | 1993-12-22 | 1993-12-22 | Pfropf-Copolymerisate von ungesättigten Monomeren und Polyhydroxyverbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung |
PCT/EP1994/004187 WO1995017444A1 (fr) | 1993-12-22 | 1994-12-16 | Copolymerisats greffes de monomeres insatures et composes polyhydroxy, leur procede de preparation et leur utilisation |
Publications (3)
Publication Number | Publication Date |
---|---|
NO962656D0 NO962656D0 (no) | 1996-06-21 |
NO962656L NO962656L (no) | 1996-08-21 |
NO310420B1 true NO310420B1 (no) | 2001-07-02 |
Family
ID=6505872
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO19962656A NO310420B1 (no) | 1993-12-22 | 1996-06-21 | Pode-kopolymerer umettede monomerer og polyhydroksyforbindelser, fremgangsmåte for fremstilling, samtanvendelse av polymerene |
Country Status (22)
Country | Link |
---|---|
US (1) | US5760154A (fr) |
EP (1) | EP0737215B1 (fr) |
JP (1) | JPH09507871A (fr) |
CN (1) | CN1065543C (fr) |
AT (1) | ATE180798T1 (fr) |
AU (1) | AU698293B2 (fr) |
BR (1) | BR9408394A (fr) |
CA (1) | CA2179777A1 (fr) |
CZ (1) | CZ175896A3 (fr) |
DE (2) | DE4343993A1 (fr) |
DK (1) | DK0737215T3 (fr) |
ES (1) | ES2133718T3 (fr) |
FI (1) | FI962595A0 (fr) |
GR (1) | GR3030960T3 (fr) |
HU (1) | HU216286B (fr) |
MY (1) | MY111775A (fr) |
NO (1) | NO310420B1 (fr) |
PL (1) | PL315203A1 (fr) |
RO (1) | RO115055B1 (fr) |
SK (1) | SK281460B6 (fr) |
WO (1) | WO1995017444A1 (fr) |
ZA (1) | ZA9410201B (fr) |
Families Citing this family (61)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19516957C2 (de) | 1995-05-12 | 2000-07-13 | Stockhausen Chem Fab Gmbh | Wasserlösliche Copolymere und Verfahren zu ihrer Herstellung und ihre Verwendung |
DE19606899C2 (de) * | 1996-02-13 | 2002-11-21 | Fraunhofer Ges Forschung | Verfahren zur Herstellung von Dispersionen wasserlöslicher Vinylpolymere und Stabilisator zur Durchführung des Verfahrens |
JPH11500181A (ja) * | 1996-10-17 | 1999-01-06 | ザ、プロクター、エンド、ギャンブル、カンパニー | ターポリマーを含む洗剤組成物 |
CA2268531A1 (fr) * | 1996-10-17 | 1998-04-23 | Procter & Gamble Far East Inc. | Procede pour laver les textiles au moyen d'une composition detergente contenant un copolymere triple |
ES2218632T3 (es) | 1996-12-21 | 2004-11-16 | Clariant Gmbh | Componente pulverulento de agentes de lavado y limpieza. |
FR2774694B1 (fr) * | 1998-01-19 | 2003-08-08 | Rhodia Chimie Sa | Utilisation de copolymeres a base d'acides insatures ou leurs derives comme agents exhausteurs de mousse |
DE19819187A1 (de) | 1998-04-30 | 1999-11-11 | Henkel Kgaa | Festes maschinelles Geschirrspülmittel mit Phosphat und kristallinen schichtförmigen Silikaten |
FR2785629B1 (fr) | 1998-11-10 | 2000-12-22 | Coatex Sa | Composition polymerique retenteur d'eau et activateur d'azurants optiques, sauces de couchage pour papier, et feuilles de papier couche ainsi obtenues |
AU2455300A (en) * | 1999-04-06 | 2000-10-23 | Minerals Technologies Inc. | Bifunctional polymers |
SK285128B6 (sk) * | 1999-12-28 | 2006-07-07 | Zentiva, A. S. | Liečivý prípravok s riadeným uvoľňovaním obsahujúci tramadol hydrochlorid a spôsob jeho prípravy |
DE10027624A1 (de) * | 2000-06-02 | 2001-12-06 | Zschimmer & Schwarz Mohsdorf G | Verfahren zur Nachreinigung von gefärbten oder bedruckten polyesterhaltigen textilen Produkten und Mischung zur Durchführung des Verfahrens |
BR0207754A (pt) * | 2001-03-02 | 2004-04-27 | Unilever Nv | composição para tratamento de um tecido |
GB0117768D0 (en) * | 2001-07-20 | 2001-09-12 | Unilever Plc | Use of polymers in fabrics cleaning |
DE10225794A1 (de) * | 2002-06-10 | 2003-12-18 | Basf Ag | Verwendung von sulfonsäuregruppenhaltigen Copolymeren als Zusatz in Wasch- und Reinigungsmitteln |
US7345012B2 (en) * | 2004-12-15 | 2008-03-18 | Schlumberger Technology Corporation | Foamed viscoelastic surfactants |
US7378378B2 (en) * | 2002-12-19 | 2008-05-27 | Schlumberger Technology Corporation | Rheology enhancers |
US7387986B2 (en) * | 2004-01-21 | 2008-06-17 | Schlumberger Technology Corporation | Viscoelastic surfactant rheology modification |
GB0229806D0 (en) * | 2002-12-20 | 2003-01-29 | Unilever Plc | Fabric care composition |
GB0301020D0 (en) * | 2003-01-16 | 2003-02-19 | Unilever Plc | Detergent composition |
DE10334047A1 (de) * | 2003-07-25 | 2005-02-24 | Clariant Gmbh | Adsorbat aus Schichtsilicat und seine Verwendung |
DE10339332A1 (de) * | 2003-08-25 | 2005-04-21 | Basf Ag | Sulfonsäuregruppen- und carboxylgruppenhaltige Copolymere |
DE10342632A1 (de) * | 2003-09-15 | 2005-04-07 | Henkel Kgaa | Maschinelle Geschirrspülmittel mit speziellen Polymeren |
DE10350420A1 (de) * | 2003-10-28 | 2005-06-02 | Basf Ag | Verwendung von Alkylenoxideinheiten enthaltenden Copolymeren als belagsinhibierende Additive im Klarspülgang des maschinellen Geschirrspülers |
JP5463506B2 (ja) * | 2005-03-16 | 2014-04-09 | 国立大学法人山口大学 | グラフトポリマー、高分子電解質膜、これらの製造方法、及びそれを用いた燃料電池 |
US7666963B2 (en) * | 2005-07-21 | 2010-02-23 | Akzo Nobel N.V. | Hybrid copolymers |
DE102005041349A1 (de) * | 2005-08-31 | 2007-03-01 | Basf Ag | Reinigungsformulierungen für die maschinelle Geschirrreinigung enthaltend hydrophil modifizierte Polycarboxylate |
US20080020961A1 (en) * | 2006-07-21 | 2008-01-24 | Rodrigues Klin A | Low Molecular Weight Graft Copolymers |
US20080021167A1 (en) * | 2006-07-21 | 2008-01-24 | National Starch And Chemical Investment Holding Co | Sulfonated graft copolymers |
NO20073834L (no) * | 2006-07-21 | 2008-01-22 | Akzo Nobel Chemicals Int Bv | Sulfonerte podede kopolymerer |
CN100445345C (zh) * | 2006-10-13 | 2008-12-24 | 冀东石油勘探开发公司 | 钻井液用两性离子聚合醇及其制备方法 |
JP5275588B2 (ja) * | 2007-08-01 | 2013-08-28 | 花王株式会社 | 高分子ビルダー |
US8613834B2 (en) * | 2008-04-03 | 2013-12-24 | Basf Se | Paper coating or binding formulations and methods of making and using same |
DE502008002614D1 (de) * | 2008-06-24 | 2011-03-31 | Cognis Ip Man Gmbh | Reinigungsmittel enthaltend Pfropfcopolymere |
EP2370199A1 (fr) | 2008-12-29 | 2011-10-05 | Akzo Nobel N.V. | Particules de chélateur enrobées |
US20130137799A1 (en) | 2009-07-31 | 2013-05-30 | Akzo Nobel N.V. | Graft copolymers |
CH701769A1 (de) * | 2009-09-08 | 2011-03-15 | Schoeller Textil Ag | Wiederbeladbare Ausrüstungen für Textilien und Formulierungen zur Beladung solcher Ausrüstungen. |
US8895481B2 (en) * | 2009-12-21 | 2014-11-25 | Schlumberger Technology Corporation | Viscoelastic surfactant acid treatment |
BR112012015318A2 (pt) | 2009-12-28 | 2017-09-05 | Akzo Nobel Chemicals Int Bv | Material autossustentável, composição, artigo de fabricação e uso de um material autossustentável |
WO2012022034A1 (fr) | 2010-08-18 | 2012-02-23 | Unilever Plc | Améliorations apportées à des compositions de traitement des tissus comprenant des agents améliorants cibles |
BR112013030996B1 (pt) | 2011-06-02 | 2021-03-02 | Lanxess Deutschland Gmbh | polímero de enxerto de polissacarídeos e polipeptídeos ou os seus respectivos derivados, processo para a fabricação de polímeros de enxerto, processo para o autocurtimento, precurtimento ou curtimento assistido de couros não curtidos ou peles não curtidas ou para o recurtimento de couro ou peles, e couro auto-curtido, precurtido, de curtimento assistido ou recurtido |
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 |
US8853144B2 (en) | 2011-08-05 | 2014-10-07 | Ecolab Usa Inc. | Cleaning composition containing a polysaccharide graft polymer composition and methods of improving drainage |
US8841246B2 (en) | 2011-08-05 | 2014-09-23 | Ecolab Usa Inc. | Cleaning composition containing a polysaccharide hybrid polymer composition and methods of improving drainage |
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 |
ES2555605T3 (es) | 2011-08-24 | 2016-01-05 | Unilever N.V. | Partículas de suministro de agente de beneficio que comprenden dextrano |
WO2013064648A1 (fr) | 2011-11-04 | 2013-05-10 | Akzo Nobel Chemicals International B.V. | Copolymères dendritiques greffés, et procédés de production associés |
CN103945828A (zh) | 2011-11-04 | 2014-07-23 | 阿克佐诺贝尔化学国际公司 | 混杂树枝状共聚物、其组合物及其制备方法 |
US8945314B2 (en) | 2012-07-30 | 2015-02-03 | Ecolab Usa Inc. | Biodegradable stability binding agent for a solid detergent |
US8802617B2 (en) | 2012-11-08 | 2014-08-12 | Ecolab Usa Inc. | Polyglycerol graft polymers with low concentrations of carboxylic acid containing monomers and their applications |
US10167407B2 (en) * | 2014-04-11 | 2019-01-01 | Basf Se | Aqueous polymer dispersion for paper with a copolymer of vinyl acetate and an acrylate monomer prepared in the presence of a starch derivative |
US9365805B2 (en) | 2014-05-15 | 2016-06-14 | Ecolab Usa Inc. | Bio-based pot and pan pre-soak |
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US20170022314A1 (en) * | 2015-07-24 | 2017-01-26 | Weyerhaeuser Nr Company | Grafted crosslinked cellulose |
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CN113089321A (zh) * | 2021-04-07 | 2021-07-09 | 罗莱生活科技股份有限公司 | 乙烯基单体接枝改性的抗菌纤维及其制备方法和在抗菌袜中的用途 |
KR102649214B1 (ko) * | 2023-12-07 | 2024-03-19 | 임병열 | 소취기능이 우수한 섬유의 제조방법 |
Family Cites Families (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3709780A (en) * | 1971-11-04 | 1973-01-09 | Calgon Corp | Process and product for making paper products of improved dry strength |
FR2483932B1 (fr) * | 1980-06-09 | 1985-08-02 | Rhone Poulenc Spec Chim | Nouvelles compositions polymere acrylique, procede pour leur obtention, et application notamment comme agents antitartres |
ATE21109T1 (de) * | 1982-07-06 | 1986-08-15 | Ciba Geigy Ag | Wasserloesliche oder in wasser dispergierbare pfropfpolymerisate, deren herstellung und verwendung. |
DE3233777A1 (de) * | 1982-09-11 | 1984-03-15 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von copolymeren aus monoethylenisch ungesaettigten mono- und dicarbonsaeuren(anhydride) |
DE3248019A1 (de) * | 1982-12-24 | 1984-06-28 | Cassella Ag, 6000 Frankfurt | Wasserloesliche copolymerisate, ihre herstellung und ihre verwendung |
DE3413301A1 (de) * | 1984-04-09 | 1985-10-24 | Chemische Fabrik Stockhausen GmbH, 4150 Krefeld | Verfahren zum nachgerben von mineralisch oder kombiniert gegerbtem leder mit polymergerbstoffen |
NZ213578A (en) * | 1984-11-09 | 1988-04-29 | Calgon Corp | Inhibiting corrosion and scale deposition in aqueous systems by adding water soluble polymers |
US4657537A (en) * | 1985-05-15 | 1987-04-14 | The Procter & Gamble Company | Disposable absorbent articles |
DE3711296A1 (de) * | 1987-04-03 | 1988-10-13 | Basf Ag | Verwendung von alkoxylierten, carboxylgruppen enthaltenden polymerisaten in waschmitteln |
US4959409A (en) * | 1988-01-14 | 1990-09-25 | The Procter & Gamble Company | Amino-functional compounds as builder/dispersants in detergent compositions |
DE3818426A1 (de) * | 1988-05-31 | 1989-12-07 | Basf Ag | Verfahren zur herstellung von wasserloeslichen polymerisaten und ihre verwendung |
NL9001027A (nl) * | 1990-04-27 | 1991-11-18 | Tno | Werkwijze voor de bereiding van calciumbindende polycarboxyverbindingen op basis van polysacchariden, alsmede fosfaat-vervangers voor wasmiddelen op basis van deze polycarboxyverbindingen. |
CA2029631A1 (fr) * | 1989-11-22 | 1991-05-23 | Kathleen A. Hughes | Polymeres greffes utilises comme additifs de detergents biodegradables |
DE4003172A1 (de) * | 1990-02-03 | 1991-08-08 | Basf Ag | Pfropfcopolymerisate von monosacchariden, oligosacchariden, polysacchariden und modifizierten polysacchariden, verfahren zu ihrer herstellung und ihre verwendung |
DE4014628A1 (de) * | 1990-05-08 | 1991-11-14 | Starchem Gmbh | Verfahren zur herstellung von feinteiligen, wasserquellbaren polysaccharid-pfropfpolymeren |
FR2663940B1 (fr) * | 1990-07-02 | 1994-04-08 | Rhone Poulenc Chimie | Polysaccharides greffes, leur procede de preparation et leur application comme agents de sequestration. |
FR2663948B1 (fr) * | 1990-07-02 | 1994-06-03 | Rhone Poulenc Chimie | Composition detergente contenant un polysaccharide greffe biodegradable. |
JPH05132528A (ja) * | 1990-10-01 | 1993-05-28 | Phillips Petroleum Co | 電解質水溶液吸収性重合体 |
DE4038908A1 (de) * | 1990-12-06 | 1992-06-11 | Basf Ag | Verwendung von wasserloeslichen gepfropften naturstoffen als wasserbehandlungsmittel |
DE4141760A1 (de) * | 1991-12-18 | 1993-06-24 | Basf Ag | Waessrige polymerisatdispersion |
DE4201452A1 (de) * | 1992-01-21 | 1993-07-22 | Basf Ag | Polymere gerbstoffe |
DE4221381C1 (de) * | 1992-07-02 | 1994-02-10 | Stockhausen Chem Fab Gmbh | Pfropf-Copolymerisate von ungesättigten Monomeren und Zuckern, Verfahren zu ihrer Herstellung und ihre Verwendung |
US5264470A (en) * | 1992-12-30 | 1993-11-23 | Halliburton Company | Set retarding additives, cement compositions and methods |
DE4316740A1 (de) * | 1993-05-19 | 1994-11-24 | Huels Chemische Werke Ag | Polymerhaltige Universalreinigungsmittel |
-
1993
- 1993-12-22 DE DE4343993A patent/DE4343993A1/de not_active Withdrawn
-
1994
- 1994-12-16 RO RO96-01242A patent/RO115055B1/ro unknown
- 1994-12-16 BR BR9408394A patent/BR9408394A/pt not_active IP Right Cessation
- 1994-12-16 JP JP7517164A patent/JPH09507871A/ja not_active Ceased
- 1994-12-16 SK SK804-96A patent/SK281460B6/sk unknown
- 1994-12-16 PL PL94315203A patent/PL315203A1/xx unknown
- 1994-12-16 ES ES95904490T patent/ES2133718T3/es not_active Expired - Lifetime
- 1994-12-16 DK DK95904490T patent/DK0737215T3/da active
- 1994-12-16 AU AU13155/95A patent/AU698293B2/en not_active Ceased
- 1994-12-16 EP EP95904490A patent/EP0737215B1/fr not_active Expired - Lifetime
- 1994-12-16 HU HU9601724A patent/HU216286B/hu not_active IP Right Cessation
- 1994-12-16 US US08/392,791 patent/US5760154A/en not_active Expired - Fee Related
- 1994-12-16 DE DE59408372T patent/DE59408372D1/de not_active Expired - Fee Related
- 1994-12-16 AT AT95904490T patent/ATE180798T1/de not_active IP Right Cessation
- 1994-12-16 CZ CZ961758A patent/CZ175896A3/cs unknown
- 1994-12-16 CA CA002179777A patent/CA2179777A1/fr not_active Abandoned
- 1994-12-16 CN CN94195007A patent/CN1065543C/zh not_active Expired - Fee Related
- 1994-12-16 WO PCT/EP1994/004187 patent/WO1995017444A1/fr not_active Application Discontinuation
- 1994-12-21 ZA ZA9410201A patent/ZA9410201B/xx unknown
- 1994-12-21 MY MYPI94003454A patent/MY111775A/en unknown
-
1996
- 1996-06-20 FI FI962595A patent/FI962595A0/fi unknown
- 1996-06-21 NO NO19962656A patent/NO310420B1/no not_active IP Right Cessation
-
1999
- 1999-08-11 GR GR990402041T patent/GR3030960T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
SK80496A3 (en) | 1997-04-09 |
AU1315595A (en) | 1995-07-10 |
DE4343993A1 (de) | 1995-06-29 |
ZA9410201B (en) | 1995-08-31 |
RO115055B1 (ro) | 1999-10-29 |
US5760154A (en) | 1998-06-02 |
CZ175896A3 (en) | 1996-11-13 |
JPH09507871A (ja) | 1997-08-12 |
CN1142837A (zh) | 1997-02-12 |
HUT75506A (en) | 1997-05-28 |
HU9601724D0 (en) | 1996-08-28 |
ATE180798T1 (de) | 1999-06-15 |
NO962656L (no) | 1996-08-21 |
FI962595A (fi) | 1996-06-20 |
PL315203A1 (en) | 1996-10-14 |
EP0737215B1 (fr) | 1999-06-02 |
DE59408372D1 (de) | 1999-07-08 |
DK0737215T3 (da) | 1999-12-06 |
BR9408394A (pt) | 1997-08-19 |
EP0737215A1 (fr) | 1996-10-16 |
GR3030960T3 (en) | 1999-11-30 |
ES2133718T3 (es) | 1999-09-16 |
CN1065543C (zh) | 2001-05-09 |
HU216286B (hu) | 1999-06-28 |
NO962656D0 (no) | 1996-06-21 |
MY111775A (en) | 2000-12-30 |
AU698293B2 (en) | 1998-10-29 |
CA2179777A1 (fr) | 1995-06-29 |
FI962595A0 (fi) | 1996-06-20 |
SK281460B6 (sk) | 2001-03-12 |
WO1995017444A1 (fr) | 1995-06-29 |
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