ES2623261T3 - Aductos a base de isocianatoalquil-trialcoxisilanos y dioles o polioles alifáticos ramificados con alquilo - Google Patents

Aductos a base de isocianatoalquil-trialcoxisilanos y dioles o polioles alifáticos ramificados con alquilo Download PDF

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Publication number: ES2623261T3
Authority: ES; Spain
Prior art keywords: compounds; tetraethylammonium; tetrabutylammonium; tetramethylammonium; coating
Prior art date: 2012-03-19
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.): Active

Application number

ES13158701.6T

Other languages

English (en)

Spanish (es)

Inventor

Rainer Dr. Lomoelder

Andre Raukamp

Sabine Naumann

Christoph Nacke

Silvia Herda

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.)

Evonik Operations GmbH

Original Assignee

Evonik Degussa GmbH

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.)

2012-03-19

Filing date

2013-03-12

Publication date

2017-07-10

2013-03-12 Application filed by Evonik Degussa GmbH filed Critical Evonik Degussa GmbH

2017-07-10 Application granted granted Critical

2017-07-10 Publication of ES2623261T3 publication Critical patent/ES2623261T3/es

Status Active legal-status Critical Current

2033-03-12 Anticipated expiration legal-status Critical

Links

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125000003545 alkoxy group Chemical group 0.000 claims abstract description 12
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239000000126 substance Substances 0.000 claims abstract description 9
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WGYONVRJGWHMKV-UHFFFAOYSA-M tetrabutylazanium;benzoate Chemical compound [O-]C(=O)C1=CC=CC=C1.CCCC[N+](CCCC)(CCCC)CCCC WGYONVRJGWHMKV-UHFFFAOYSA-M 0.000 claims description 3
239000002023 wood Substances 0.000 claims description 3
SMKNBYSXDYPBME-UHFFFAOYSA-M butanoate;tetrabutylazanium Chemical compound CCCC([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC SMKNBYSXDYPBME-UHFFFAOYSA-M 0.000 claims description 2
BLWUXYZPUFJVSE-UHFFFAOYSA-M butanoate;tetraethylazanium Chemical compound CCCC([O-])=O.CC[N+](CC)(CC)CC BLWUXYZPUFJVSE-UHFFFAOYSA-M 0.000 claims description 2
OYGSFKZFXQKZDS-UHFFFAOYSA-M butanoate;tetramethylazanium Chemical compound C[N+](C)(C)C.CCCC([O-])=O OYGSFKZFXQKZDS-UHFFFAOYSA-M 0.000 claims description 2
KWAJGRXLJIZCBX-UHFFFAOYSA-M butanoate;tetrapropylazanium Chemical compound CCCC([O-])=O.CCC[N+](CCC)(CCC)CCC KWAJGRXLJIZCBX-UHFFFAOYSA-M 0.000 claims description 2
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ZEKIXPPWVVMOMQ-UHFFFAOYSA-M propanoate;tetraethylazanium Chemical compound CCC([O-])=O.CC[N+](CC)(CC)CC ZEKIXPPWVVMOMQ-UHFFFAOYSA-M 0.000 claims description 2
XNWSMNKRGNKRKP-UHFFFAOYSA-M propanoate;tetramethylazanium Chemical compound CCC([O-])=O.C[N+](C)(C)C XNWSMNKRGNKRKP-UHFFFAOYSA-M 0.000 claims description 2
MCZDHTKJGDCTAE-UHFFFAOYSA-M tetrabutylazanium;acetate Chemical compound CC([O-])=O.CCCC[N+](CCCC)(CCCC)CCCC MCZDHTKJGDCTAE-UHFFFAOYSA-M 0.000 claims description 2
SNMZANHSFVMKKA-UHFFFAOYSA-M tetrabutylazanium;formate Chemical compound [O-]C=O.CCCC[N+](CCCC)(CCCC)CCCC SNMZANHSFVMKKA-UHFFFAOYSA-M 0.000 claims description 2
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IEVVGBFMAHJELO-UHFFFAOYSA-M tetramethylazanium;benzoate Chemical compound C[N+](C)(C)C.[O-]C(=O)C1=CC=CC=C1 IEVVGBFMAHJELO-UHFFFAOYSA-M 0.000 claims description 2
WWIYWFVQZQOECA-UHFFFAOYSA-M tetramethylazanium;formate Chemical compound [O-]C=O.C[N+](C)(C)C WWIYWFVQZQOECA-UHFFFAOYSA-M 0.000 claims description 2
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150000003512 tertiary amines Chemical class 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/10—Compounds having one or more C—Si linkages containing nitrogen having a Si-N linkage
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/63—Additives non-macromolecular organic
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3203—Polyhydroxy compounds
- C08G18/3206—Polyhydroxy compounds aliphatic
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3203—Polyhydroxy compounds
- C08G18/3221—Polyhydroxy compounds hydroxylated esters of carboxylic acids other than higher fatty acids
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/71—Monoisocyanates or monoisothiocyanates
- C08G18/718—Monoisocyanates or monoisothiocyanates containing silicon
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/02—Polysilicates
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31609—Particulate metal or metal compound-containing
- Y10T428/31612—As silicone, silane or siloxane
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31652—Of asbestos
- Y10T428/31663—As siloxane, silicone or silane

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Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Life Sciences & Earth Sciences (AREA)
Polymers & Plastics (AREA)
Medicinal Chemistry (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Paints Or Removers (AREA)
Polyurethanes Or Polyureas (AREA)
Silicon Polymers (AREA)

ES13158701.6T 2012-03-19 2013-03-12 Aductos a base de isocianatoalquil-trialcoxisilanos y dioles o polioles alifáticos ramificados con alquilo Active ES2623261T3 (es)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE102012204290		2012-03-19
DE201210204290 DE102012204290A1 (de)	2012-03-19	2012-03-19	Addukte aus Isocyanatoalkyl-trialkoxysilanen und aliphatischen, alkyl-verzweigten Diolen oder Polyolen

Publications (1)

Publication Number	Publication Date
ES2623261T3 true ES2623261T3 (es)	2017-07-10

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ES13158701.6T Active ES2623261T3 (es)	2012-03-19	2013-03-12	Aductos a base de isocianatoalquil-trialcoxisilanos y dioles o polioles alifáticos ramificados con alquilo

Country Status (10)

Country	Link
US (1)	US20130244043A1 (2)
EP (1)	EP2641925B1 (2)
JP (1)	JP2013194055A (2)
KR (1)	KR20130106309A (2)
CN (1)	CN103319684A (2)
BR (1)	BR102013007461A2 (2)
CA (1)	CA2809720A1 (2)
DE (1)	DE102012204290A1 (2)
DK (1)	DK2641925T3 (2)
ES (1)	ES2623261T3 (2)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE102010041247A1 (de)	2010-09-23	2012-03-29	Evonik Degussa Gmbh	Verfahren zur Herstellung von lagerstabilen Polyurethan-Prepregs und daraus hergestellte Formkörper aus Polyurethanzusammensetzung in Lösung
EP2864383B1 (de)	2012-06-20	2019-10-02	Evonik Degussa GmbH	Beschichtungsmittel mit hoher kratzbeständigkeit
EP2905296B1 (de) *	2014-02-10	2015-12-23	Evonik Degussa GmbH	Copolymere aus Isocyanatoalkyltrialkoxysilanen und Urethandiolen
DE102014203865A1 (de) *	2014-03-04	2015-09-10	Henkel Ag & Co. Kgaa	Rohstoff und seine Verwendung
ES2707979T3 (es)	2015-04-09	2019-04-08	Evonik Degussa Gmbh	Aductos de isocianatoalquiltrimetoxisilanos y agentes ignífugos reactivos con éstos
DK3356444T3 (da) *	2015-09-30	2020-11-16	Evonik Operations Gmbh	Med silikoneharpiks modificerede isocyanatoalkylalkoxysilan-addukter og deres anvendelse
EP3263616B8 (de)	2016-06-27	2020-01-15	Evonik Operations GmbH	Alkoxysilan-funktionalisierte allophanat-haltige beschichtungsmittel
CN109642009B (zh)	2016-08-09	2021-12-10	科思创德国股份有限公司	硅烷官能的聚合聚氨酯
PL3404073T3 (pl) *	2017-05-19	2022-01-31	Evonik Operations Gmbh	Hydrofilowe izocyjanurany zawierające alkoksysilan
CN108504318B (zh) *	2018-03-13	2021-02-09	广东省石油与精细化工研究院	一种高透明度和高强度的硅烷改性聚醚弹性密封胶及其制备方法
US11326017B2 (en) *	2018-09-10	2022-05-10	Evonik Operations Gmbh	Tin-free catalysis of silane-functional polyurethane crosslinkers
WO2020089019A1 (de)	2018-10-30	2020-05-07	Covestro Deutschland Ag	Verfahren zur herstellung eines mehrschicht-lackaufbaus mit einer deckschicht aus silangruppen-enthaltenden prepolymeren
JP2022505990A (ja)	2018-10-30	2022-01-14	コベストロ・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング・アンド・コー・カーゲー	層接着が改善された複層ペイント構造
EP3722346A1 (de)	2019-04-09	2020-10-14	Covestro Deutschland AG	2-komponenten-polyurethanbeschichtungen mit verbesserter topfzeit ohne einbusse in der witterungsstabilität
EP3966271B1 (en)	2019-05-06	2023-09-27	BASF Coatings GmbH	Silane-based coating composition
AU2020384713A1 (en)	2019-11-15	2022-05-26	Basf Coatings Gmbh	Silane-based coating compositions comprising a metal alkoxide catalyst
EP4127012A1 (en)	2020-04-02	2023-02-08	BASF Coatings GmbH	Silane-based coating compositions comprising a metal alkoxide catalyst and an acid-functional polymer
WO2022102455A1 (ja) *	2020-11-13	2022-05-19	信越化学工業株式会社	コーティング剤組成物、該組成物を含む表面処理剤、及び該表面処理剤で表面処理された物品
WO2023285177A1 (en)	2021-07-13	2023-01-19	Evonik Operations Gmbh	Silane modified aliphatic polyurea
TW202528481A (zh) *	2023-09-11	2025-07-16	日商富士軟片股份有限公司	樹脂組成物、硬化物、積層體、硬化物之製造方法、積層體之製造方法、半導體元件之製造方法及半導體元件、以及化合物
KR102804536B1 (ko) *	2024-04-02	2025-05-12	주식회사 엔케이이노텍	도막식 방수 및 이를 이용한 복합식 방수공법

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2906136C2 (de) *	1979-02-17	1983-12-08	Fa. Carl Freudenberg, 6940 Weinheim	Verfahren zur Herstellung von niedrigschmelzenden Polyurethanen
US4540766A (en)	1983-10-03	1985-09-10	Ppg Industries, Inc.	Thermosetting high solids solvent-based polyester-urethane one-component coating compositions
JPH0232186A (ja) *	1988-07-21	1990-02-01	Kuraray Co Ltd	接着剤
DE69118915T2 (de)	1990-12-17	1996-10-31	E.I. Du Pont De Nemours & Co., Wilmington, Del.	Für kraftwagen geeignete beschichtungszusammensetzungen auf basis eines organosilan-polymers
DE4204518A1 (de)	1992-02-15	1993-08-19	Basf Lacke & Farben	Verfahren zur herstellung einer zweischichtigen lackierung und fuer dieses verfahren geeignete nicht-waessrige lacke
GB9210653D0 (en) *	1992-05-19	1992-07-01	Ici Plc	Silane functional oligomer
JPH0911406A (ja) *	1995-06-29	1997-01-14	Teijin Ltd	表面を保護されたプラスチック成形体及びその製造方法
DE19529124C1 (de)	1995-08-08	1996-11-21	Herberts Gmbh	Überzugsmittel und deren Verwendung in Verfahren zur Herstellung von Mehrschichtüberzügen
DE19714320A1 (de) *	1997-03-25	1998-10-01	Ivoclar Ag	Hydrolysierbare und polymerisierbare Vinylcyclopropansilane
BR9906377A (pt) *	1998-04-24	2000-07-11	Ck Witco Corp	Revestimentos ou adesivos em pó empregando silanos ou cargas tratadas com silano
DE10132938A1 (de)	2001-07-06	2003-01-16	Degussa	Nichtwässriges, wärmehärtendes Zweikomponenten-Beschichtungsmittel
JP2003089723A (ja) *	2001-09-18	2003-03-28	Kansai Paint Co Ltd	硬化性組成物及びその被膜形成方法
JP2004035612A (ja) *	2002-06-28	2004-02-05	Teijin Chem Ltd	表面を保護された透明プラスチック成形体およびオルガノシロキサン樹脂組成物用下塗り塗料組成物
DE10346958A1 (de) *	2003-10-09	2005-05-12	Degussa	Uretdiongruppenhaltige Polyurethanzusammensetzungen, welche bei niedriger Temperatur härtbar sind
JP2005128304A (ja) *	2003-10-24	2005-05-19	Dainippon Ink & Chem Inc	光ファイバー被覆用樹脂組成物及びそれを用いた光ファイバー素線
EP1783185B1 (en) *	2004-08-26	2009-11-11	Idemitsu Kosan Co., Ltd.	Coating composition and resin multilayer body
DE102004050747A1 (de)	2004-10-19	2006-04-27	Basf Coatings Ag	Beschichtungsmittel enthaltend Addukte mit Alkoxysilanfunktionalität
DE102004050748A1 (de)	2004-10-19	2006-04-20	Basf Coatings Aktiengesellschaft	Hochkratzfeste und hochelastische Beschichtungsmittel auf Basis von Alkoxysilanen
DE102007020404A1 (de)	2006-09-18	2008-10-30	Nano-X Gmbh	Verfahren zur Herstellung eines Beschichtungsmaterials
DE102006044310A1 (de)	2006-09-18	2008-03-27	Nano-X Gmbh	Silanbeschichtungsmaterial und Verfahren zur Herstellung eines Silanbeschichtungsmaterials
JP5637687B2 (ja)	2006-12-19	2014-12-10	ビーエーエスエフコーティングスゲゼルシャフトミットベシュレンクテルハフツングＢＡＳＦＣｏａｔｉｎｇｓＧｍｂＨ	高い引掻耐性及び耐候性を有する被覆剤
DE102007013262A1 (de)	2007-03-15	2008-09-18	Basf Coatings Ag	Beschichtungsmittel enthaltend Addukte mit Silanfunktionalität und daraus hergestellte hochkratzfeste Beschichtungen mit verbesserter Rissbeständigkeit
DE102007013242A1 (de)	2007-03-15	2008-09-18	Basf Coatings Ag	Hochkratzfeste Beschichtung mit guter Witterungs- und Rissbeständigkeit
KR101587666B1 (ko) *	2007-12-18	2016-01-21	다우 글로벌 테크놀로지스 엘엘씨	유리 결합용 접착제에 대한 접착성이 개선된 창 유리용 보호 코팅
JP2011514255A (ja) *	2008-03-18	2011-05-06	ナノ−エックスゲーエムベーハー	高耐摩耗性の乗り物用塗料の製造方法、乗り物用塗料、およびその使用
JP5316300B2 (ja) *	2009-08-07	2013-10-16	信越化学工業株式会社	耐摩耗性シリコーンコーティング組成物並びに被覆物品及びその製造方法

2012
- 2012-03-19 DE DE201210204290 patent/DE102012204290A1/de not_active Withdrawn
2013
- 2013-03-12 ES ES13158701.6T patent/ES2623261T3/es active Active
- 2013-03-12 DK DK13158701.6T patent/DK2641925T3/en active
- 2013-03-12 EP EP13158701.6A patent/EP2641925B1/de active Active
- 2013-03-13 US US13/799,626 patent/US20130244043A1/en not_active Abandoned
- 2013-03-15 CA CA 2809720 patent/CA2809720A1/en not_active Abandoned
- 2013-03-18 CN CN2013100857585A patent/CN103319684A/zh active Pending
- 2013-03-18 KR KR1020130028426A patent/KR20130106309A/ko not_active Ceased
- 2013-03-19 BR BRBR102013007461-6A patent/BR102013007461A2/pt not_active Application Discontinuation
- 2013-03-19 JP JP2013056814A patent/JP2013194055A/ja active Pending

Also Published As

Publication number	Publication date
EP2641925A1 (de)	2013-09-25
KR20130106309A (ko)	2013-09-27
DK2641925T3 (en)	2017-05-01
CA2809720A1 (en)	2013-09-19
DE102012204290A1 (de)	2013-09-19
EP2641925B1 (de)	2017-02-01
US20130244043A1 (en)	2013-09-19
CN103319684A (zh)	2013-09-25
JP2013194055A (ja)	2013-09-30
BR102013007461A2 (pt)	2015-06-16

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ES2623261T3 (es)	2017-07-10	Aductos a base de isocianatoalquil-trialcoxisilanos y dioles o polioles alifáticos ramificados con alquilo
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ES2211912T3 (es)	2004-07-16	Soluciones de resina de poliacrilato con indice de color mejorado y su utilizacion en productos de revestimiento.
US11359100B2 (en)	2022-06-14	Tin-free catalysis of silane-functional polyurethane crosslinkers
US20250171592A1 (en)	2025-05-29	Silicone modified polyol and applications thereof