NO312971B1 - Bindemiddelblanding, og dens anvendelse - Google Patents

Bindemiddelblanding, og dens anvendelse Download PDF

Info

Publication number: NO312971B1
Authority: NO; Norway
Prior art keywords: component; weight; molecular weight; mol; hydroxy
Prior art date: 1996-08-23

Application number

NO19973869A

Other languages

English (en)

Norwegian (no)

Other versions

NO973869L (no

NO973869D0 (no

Inventor

Martin Melchiors

Juergen Schwindt

Gerhard Ruttmann

Wieland Hovestadt

Joachim Probst

Josef Pedain

Original Assignee

Bayer Ag

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.)

1996-08-23

Filing date

1997-08-22

Publication date

2002-07-22

1997-08-22 Application filed by Bayer Ag filed Critical Bayer Ag

1997-08-22 Publication of NO973869D0 publication Critical patent/NO973869D0/no

1998-02-24 Publication of NO973869L publication Critical patent/NO973869L/no

2002-07-22 Publication of NO312971B1 publication Critical patent/NO312971B1/no

Links

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125000000753 cycloalkyl group Chemical group 0.000 description 1
XJOBOFWTZOKMOH-UHFFFAOYSA-N decanoyl decaneperoxoate Chemical compound CCCCCCCCCC(=O)OOC(=O)CCCCCCCCC XJOBOFWTZOKMOH-UHFFFAOYSA-N 0.000 description 1
LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 1
229940043276 diisopropanolamine Drugs 0.000 description 1
229940043279 diisopropylamine Drugs 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000006471 dimerization reaction Methods 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000002209 hydrophobic effect Effects 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
238000011068 loading method Methods 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
239000006224 matting agent Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
SZEGKVHRCLBFKJ-UHFFFAOYSA-N n-methyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCNC SZEGKVHRCLBFKJ-UHFFFAOYSA-N 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920005906 polyester polyol Polymers 0.000 description 1
239000011527 polyurethane coating Substances 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
239000001294 propane Substances 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000006798 ring closing metathesis reaction Methods 0.000 description 1
239000012266 salt solution Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000010959 steel Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 1
WYKYCHHWIJXDAO-UHFFFAOYSA-N tert-butyl 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)C WYKYCHHWIJXDAO-UHFFFAOYSA-N 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
238000005829 trimerization reaction Methods 0.000 description 1
LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
235000019871 vegetable fat Nutrition 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
238000004260 weight control Methods 0.000 description 1
239000004711 α-olefin Substances 0.000 description 1

Classifications

- 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
- C08G18/40—High-molecular-weight compounds
- C08G18/63—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers
- C08G18/632—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers onto polyethers
- 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
- C08G18/40—High-molecular-weight compounds
- C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
- C08G18/4063—Mixtures of compounds of group C08G18/62 with other macromolecular compounds
- 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
- C08G18/40—High-molecular-weight compounds
- C08G18/63—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers
- C08G18/638—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers characterised by the use of compounds having carbon-to-carbon double bonds other than styrene and/or olefinic nitriles
- 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
- C08G2150/00—Compositions for coatings
- C08G2150/90—Compositions for anticorrosive coatings

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Polyurethanes Or Polyureas (AREA)
Paints Or Removers (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Compositions Of Macromolecular Compounds (AREA)

NO19973869A 1996-08-23 1997-08-22 Bindemiddelblanding, og dens anvendelse NO312971B1 (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19634076A DE19634076A1 (de)	1996-08-23	1996-08-23	Bindemittelgemisch, Verfahren zu seiner Herstellung und seine Verwendung

Publications (3)

Publication Number	Publication Date
NO973869D0 NO973869D0 (no)	1997-08-22
NO973869L NO973869L (no)	1998-02-24
NO312971B1 true NO312971B1 (no)	2002-07-22

Family

ID=7803484

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO19973869A NO312971B1 (no)	1996-08-23	1997-08-22	Bindemiddelblanding, og dens anvendelse

Country Status (9)

Country	Link
US (1)	US6130285A (fr)
EP (1)	EP0825210B1 (fr)
JP (1)	JPH10101999A (fr)
AT (1)	ATE248198T1 (fr)
CA (1)	CA2213877A1 (fr)
DE (2)	DE19634076A1 (fr)
DK (1)	DK0825210T3 (fr)
ES (1)	ES2205099T3 (fr)
NO (1)	NO312971B1 (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA2236555C (fr) *	1997-06-05	2002-07-16	Joseph John Spanier	Composition de revetement thermodurcissable pauvre en cov mais a teneur ultra-elevee en solides; methode pour la preparer
KR100574482B1 (ko)	1999-09-07	2006-04-27	주식회사 하이닉스반도체	유기 난반사 방지막용 조성물과 이의 제조방법
EP1178080B1 (fr) *	2000-07-19	2007-04-25	Nippon Shokubai Co., Ltd.	Composition de résine durcissable utilisée dans un revêtement
DE10120083A1 (de) *	2001-04-17	2003-01-30	Nmi Univ Tuebingen	Meßelektrodenpaar, Biosensor mit einem solchen Meßelektrodenpaar und Verfahren zur Herstellung
DE10248618A1 (de) *	2002-10-18	2004-04-29	Bayer Ag	Hydrophobes Bindemittelgemisch mit niedriger Wasseraufnahme
US9732252B2 (en)	2012-05-15	2017-08-15	3M Innovative Properties Company	Polyurethane-based protective coatings for rotor blades
CN106008845B (zh) *	2016-06-21	2018-08-24	湖南本安亚大新材料有限公司	水性聚氨酯/聚丙烯酸酯核壳乳液的制备方法及其胶粘剂
CN110790886A (zh) *	2019-11-13	2020-02-14	浩力森涂料（上海）有限公司	单组份涂料及其成膜树脂和制备方法

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3523093A (en) *	1961-11-28	1970-08-04	Paul Stamberger	Method of producing polyurethanes by reacting polyisocyanate with a preformed polymer resulting from polymerization of ethylenically unsaturated monomers
US4065587A (en) *	1976-05-11	1977-12-27	Scm Corporation	U.V. Curable poly(ether-urethane) polyacrylates and wet-look polymers prepared therefrom
CA1145881A (fr) *	1980-11-17	1983-05-03	Som N. Khanna	Interpolymeres de polyurethanes et addition de monomeres polymerisables
DE3045788A1 (de) *	1980-12-04	1982-07-08	Bayer Ag, 5090 Leverkusen	Strahlenhaertbare urethangruppenhaltige acrylsaeureester und ihre verwendung
DE3047926C2 (de) *	1980-12-19	1985-05-15	Th. Goldschmidt Ag, 4300 Essen	Härtbares Klebmittel
DE3226131A1 (de) *	1982-07-13	1984-01-19	Basf Ag, 6700 Ludwigshafen	Verfahren zur herstellung von ueberzuegen
US5066733A (en) *	1989-04-03	1991-11-19	Ppg Industries, Inc.	Chip resistant coatings and methods of application
US5492731A (en) *	1991-05-17	1996-02-20	Ppg Industries, Inc.	Thermally curable coating composition
US5183831A (en) *	1991-08-22	1993-02-02	Ciba-Geigy Corporation	Radiation curable composition with high temperature oil resistance
US5248752A (en) *	1991-11-12	1993-09-28	Union Carbide Chemicals & Plastics Technology Corporation	Polyurethane (meth)acrylates and processes for preparing same
DE4224365A1 (de) *	1992-07-23	1994-01-27	Bayer Ag	Verfahren zur Herstellung von Polyhydroxylverbindungen und ihre Verwendung in Lacken
DE4228713A1 (de) *	1992-08-28	1994-03-03	Hoechst Ag	Wäßrige, strahlenhärtbare Bindemitteldispersionen
JP3288869B2 (ja) *	1994-10-14	2002-06-04	ジェイエスアール株式会社	液状硬化性樹脂組成物

1996
- 1996-08-23 DE DE19634076A patent/DE19634076A1/de not_active Withdrawn
1997
- 1997-08-14 DK DK97114061T patent/DK0825210T3/da active
- 1997-08-14 ES ES97114061T patent/ES2205099T3/es not_active Expired - Lifetime
- 1997-08-14 DE DE59710646T patent/DE59710646D1/de not_active Expired - Lifetime
- 1997-08-14 AT AT97114061T patent/ATE248198T1/de not_active IP Right Cessation
- 1997-08-14 EP EP97114061A patent/EP0825210B1/fr not_active Expired - Lifetime
- 1997-08-14 US US08/911,510 patent/US6130285A/en not_active Expired - Lifetime
- 1997-08-19 CA CA002213877A patent/CA2213877A1/fr not_active Abandoned
- 1997-08-21 JP JP9239153A patent/JPH10101999A/ja active Pending
- 1997-08-22 NO NO19973869A patent/NO312971B1/no not_active IP Right Cessation

Also Published As

Publication number	Publication date
ES2205099T3 (es)	2004-05-01
DK0825210T3 (da)	2003-11-24
ATE248198T1 (de)	2003-09-15
EP0825210B1 (fr)	2003-08-27
JPH10101999A (ja)	1998-04-21
DE19634076A1 (de)	1998-02-26
CA2213877A1 (fr)	1998-02-23
NO973869L (no)	1998-02-24
DE59710646D1 (de)	2003-10-02
NO973869D0 (no)	1997-08-22
EP0825210A2 (fr)	1998-02-25
US6130285A (en)	2000-10-10
EP0825210A3 (fr)	1998-03-04

Legal Events

Date	Code	Title	Description
2005-05-02	MM1K	Lapsed by not paying the annual fees

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CN110300771B (zh)	2022-04-01	水性涂料组合物
CA2549702C (fr)	2013-05-28	Compositions de revetement contenant des composes du type oligocarbonate pour la production de couches de finition resistant aux rayures
EP1923413A2 (fr)	2008-05-21	Agent de revêtement
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MXPA04009266A (es)	2005-05-17	Sistemas acuosos de poliuretano de dos componentes.
EP2426158B1 (fr)	2015-04-08	Compositions de revêtement
JP7398892B2 (ja)	2023-12-15	二液型ポリウレタンコーティング剤
NO312971B1 (no)	2002-07-22	Bindemiddelblanding, og dens anvendelse
JP2000507290A (ja)	2000-06-13	水性二成分系ポリウレタン塗料、その製法、仕上げ塗料又は透明塗料としての使用、及びプラスチック塗装のための使用
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KR100540410B1 (ko)	2006-03-23	결합제조성물,및금속기재및무기기재코팅을위한그의용도
US20040082711A1 (en)	2004-04-29	Hydrophobic binder mixture with low water absorption
CA2247959C (fr)	2006-08-08	Agent de recouvrement polyurethane a deux composants, aqueux, procede permettant de le produire et utilisation comme vernis de finition ou vernis clair et utilisation pour recouvrir des matieres plastiques
WO2001004172A1 (fr)	2001-01-18	Compositions de revetement a deux composants aqueux a base d'isocyanates et a faible teneur en cov accrue
HK1121770A (en)	2009-04-30	Aqueous two-component polyurethane systems containing hydroxy-functional polydimethylsiloxanes
PL190541B1 (pl)	2005-12-30	Emalia poliuretanowa
CA2261401A1 (fr)	1999-08-11	Composition de revetement, utilisation et procede de preparation
HK1095352B (en)	2013-03-01	Oligocarbonate-containing coating compositions for scratch-resistant topcoats