JP3883628B2 - Ｏｈ官能性ポリアクリレートグラフトコポリマーを含む高固形分バインダー組成物 - Google Patents
Ｏｈ官能性ポリアクリレートグラフトコポリマーを含む高固形分バインダー組成物 Download PDFInfo
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- JP3883628B2 JP3883628B2 JP34037596A JP34037596A JP3883628B2 JP 3883628 B2 JP3883628 B2 JP 3883628B2 JP 34037596 A JP34037596 A JP 34037596A JP 34037596 A JP34037596 A JP 34037596A JP 3883628 B2 JP3883628 B2 JP 3883628B2
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- 101000911390 Homo sapiens Coagulation factor VIII Proteins 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- QQWAKSKPSOFJFF-NSHDSACASA-N [(2S)-oxiran-2-yl]methyl 2,2-dimethyloctanoate Chemical compound CCCCCCC(C)(C)C(=O)OC[C@@H]1CO1 QQWAKSKPSOFJFF-NSHDSACASA-N 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- KYIKRXIYLAGAKQ-UHFFFAOYSA-N abcn Chemical compound C1CCCCC1(C#N)N=NC1(C#N)CCCCC1 KYIKRXIYLAGAKQ-UHFFFAOYSA-N 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- TUVYSBJZBYRDHP-UHFFFAOYSA-N acetic acid;methoxymethane Chemical compound COC.CC(O)=O TUVYSBJZBYRDHP-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000004705 aldimines Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229940009098 aspartate Drugs 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- RSOILICUEWXSLA-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(C)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(C)C(C)(C)C1 RSOILICUEWXSLA-UHFFFAOYSA-N 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-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
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000006221 furniture coating Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 150000004658 ketimines Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 150000007974 melamines Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- UJRDRFZCRQNLJM-UHFFFAOYSA-N methyl 3-[3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OC)=CC(N2N=C3C=CC=CC3=N2)=C1O UJRDRFZCRQNLJM-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- FIWHJQPAGLNURC-UHFFFAOYSA-N oxiran-2-ylmethyl 7,7-dimethyloctanoate Chemical compound CC(C)(C)CCCCCC(=O)OCC1CO1 FIWHJQPAGLNURC-UHFFFAOYSA-N 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- TWSRVQVEYJNFKQ-UHFFFAOYSA-N pentyl propanoate Chemical compound CCCCCOC(=O)CC TWSRVQVEYJNFKQ-UHFFFAOYSA-N 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- ZAKVZVDDGSFVRG-UHFFFAOYSA-N prop-1-en-2-ylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CC(=C)C1=CC=CC=C1 ZAKVZVDDGSFVRG-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- SWAXTRYEYUTSAP-UHFFFAOYSA-N tert-butyl ethaneperoxoate Chemical compound CC(=O)OOC(C)(C)C SWAXTRYEYUTSAP-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- 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
- C08F279/00—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
- C08F279/02—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/04—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to rubbers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Polyurethanes Or Polyureas (AREA)
- Ceramic Products (AREA)
- Nonmetallic Welding Materials (AREA)
- Compositions Of Oxide Ceramics (AREA)
- Glanulating (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19545634A DE19545634A1 (de) | 1995-12-07 | 1995-12-07 | Festkörperreiche Bindemittelkombinationen |
| DE19545634.3 | 1995-12-07 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JPH09176561A JPH09176561A (ja) | 1997-07-08 |
| JPH09176561A5 JPH09176561A5 (enExample) | 2004-11-25 |
| JP3883628B2 true JP3883628B2 (ja) | 2007-02-21 |
Family
ID=7779426
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP34037596A Expired - Fee Related JP3883628B2 (ja) | 1995-12-07 | 1996-12-06 | Ｏｈ官能性ポリアクリレートグラフトコポリマーを含む高固形分バインダー組成物 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US5733973A (enExample) |
| EP (1) | EP0778298B1 (enExample) |
| JP (1) | JP3883628B2 (enExample) |
| AT (1) | ATE200682T1 (enExample) |
| CA (1) | CA2191934C (enExample) |
| DE (2) | DE19545634A1 (enExample) |
| DK (1) | DK0778298T3 (enExample) |
| ES (1) | ES2158215T3 (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0861292B1 (en) * | 1995-11-16 | 2000-06-07 | Shell Internationale Researchmaatschappij B.V. | Crosslinkable hydroxy functional polydiene polymer coating compostions and a process for preparing them |
| DE19628444A1 (de) * | 1996-07-15 | 1998-01-22 | Bayer Ag | Neue festkörperreiche 2 K-PUR-Bindemittelkombinationen |
| DE19955129A1 (de) * | 1999-11-17 | 2001-05-23 | Bayer Ag | Neue, festkörperreiche Bindemittelkombinationen und deren Verwendung |
| DE10039675A1 (de) * | 2000-08-14 | 2002-02-28 | Basf Ag | Transparente Styrolcopolymerisate |
| US7151154B2 (en) * | 2004-01-13 | 2006-12-19 | Lexmark International, Inc. | Graft polymer curatives and polyurethanes formed therefrom |
| US7166358B2 (en) | 2004-01-13 | 2007-01-23 | Lexmark International, Inc. | Polyurethane rolls with graft polyacrylate curatives |
| US7034097B2 (en) * | 2004-01-13 | 2006-04-25 | Lexmark International, Inc. | Polyurethane elastomers with combination of curatives |
| US7347808B2 (en) * | 2004-01-13 | 2008-03-25 | Lexmark International, Inc. | Polyurethane rolls and methods of manufacturing |
| DE102005026863A1 (de) * | 2005-06-10 | 2006-12-14 | Bayer Materialscience Ag | Oligocarbonat-haltige Beschichtungsmittel für kratzfeste Decklacke |
| WO2007119305A1 (en) * | 2006-03-15 | 2007-10-25 | Kansai Paint Co., Ltd. | Coating composition and method of forming coating film |
| DE102006053740A1 (de) | 2006-11-15 | 2008-05-21 | Bayer Materialscience Ag | Beschichtungsmittel |
| DE102006053741A1 (de) * | 2006-11-15 | 2008-05-21 | Bayer Materialscience Ag | Beschichtungsmittel |
| CN102232091B (zh) * | 2008-10-31 | 2014-12-17 | 路博润高级材料公司 | 采用烯烃-丙烯酸系物共聚的杂化聚氨酯的分散体 |
| WO2018221199A1 (ja) * | 2017-05-30 | 2018-12-06 | Dic株式会社 | 水性樹脂組成物、水性塗料、及び物品 |
| JP2021038355A (ja) * | 2019-09-05 | 2021-03-11 | Dic株式会社 | 水性樹脂組成物、水性塗料、及び物品 |
Family Cites Families (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR943411A (fr) | 1941-11-13 | 1949-03-08 | American Cyanamid Co | Méthylol-mélamines méthylées solubles dans l'eau et leur procédé d'obtention |
| NL238495A (enExample) | 1958-04-24 | |||
| DE1090196B (de) | 1959-07-15 | 1960-10-06 | Bayer Ag | Verfahren zur Herstellung von physiologisch unbedenklichen Mono- oder Polyisocyanaten mit geringem Dampfdruck |
| DE1201992B (de) | 1963-04-11 | 1965-09-30 | Bayer Ag | Verfahren zur Herstellung von Polymeren mit Cyanuratstruktur |
| US3358010A (en) | 1964-03-11 | 1967-12-12 | Mobay Chemical Corp | Biuret polyisocyanates |
| DE1644809A1 (de) | 1967-08-04 | 1971-01-21 | Bayer Ag | Polyurethanlackueberzuege und Verfahren zu ihrer Herstellung |
| DE2308015B2 (de) | 1973-02-17 | 1980-07-31 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Polyisocyanaten mit Biuretstruktur |
| IE39205B1 (en) | 1973-04-19 | 1978-08-30 | Ciba Geigy Ag | New stabiliser system and its use for stabilising styrene polymers |
| CH589056A5 (enExample) | 1973-12-10 | 1977-06-30 | Ciba Geigy Ag | |
| US4010656A (en) | 1974-02-07 | 1977-03-08 | Borg-Warner Corporation | Power transmission drive |
| DE2417353C3 (de) | 1974-04-09 | 1979-11-29 | Ernst 4000 Duesseldorf Klein | Gliederkette |
| DE2551634C3 (de) | 1975-11-18 | 1980-07-17 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Isocyanuratgruppen aufweisenden Polyisocyanaten |
| DE2626900C2 (de) | 1976-06-16 | 1978-04-13 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung von hydroxylgruppenenthaltenden Mischpolymerisaten |
| DE2803103A1 (de) | 1978-01-25 | 1979-07-26 | Bayer Ag | Verfahren zur herstellung von biuret- und/oder harnstoffgruppen aufweisenden organischen polyisocyanaten |
| DE2806731A1 (de) | 1978-02-17 | 1979-08-23 | Bayer Ag | Verfahren zur herstellung von isocyanuratgruppen aufweisenden polyisocyanaten |
| CA1112243A (en) | 1978-09-08 | 1981-11-10 | Manfred Bock | Process for the preparation of polyisocyanates containing isocyanurate groups and the use thereof |
| DE2850872A1 (de) * | 1978-11-24 | 1980-06-04 | Bayer Ag | Wasserverduennbare lackbindemittel fuer chemikalienfeste beschichtungen |
| US4281078A (en) * | 1979-11-26 | 1981-07-28 | E. I. Du Pont De Nemours And Company | High-solids polyurethane enamel coating composition |
| DE3033860A1 (de) | 1980-09-09 | 1982-04-15 | Bayer Ag, 5090 Leverkusen | Neue isocyanato-isocyanurate, ein verfahren zu ihrer herstellung, sowie ihre verwendung als isocyanatkomponente in polyurethanlacken |
| DE3100262A1 (de) | 1981-01-08 | 1982-08-05 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von isocyanuratgruppen aufweisenden polyisocyanaten, als katalysator-komponente fuer dieses verfahren geeignete loesungen, sowie die verwendung der verfahrensprodukte als isocyanat-komponente bei der herstellung von polyurethanen |
| DE3100263A1 (de) | 1981-01-08 | 1982-08-12 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von isocyanuratgruppen aufweisenden polyisocyanaten und ihre verwendung bei der herstellung von polyurethanen |
| DE3120803A1 (de) * | 1981-05-25 | 1982-12-16 | Basf Ag, 6700 Ludwigshafen | Schlagzaehne thermoplastische formmassen |
| DE3144672A1 (de) | 1981-11-10 | 1983-05-26 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von mischtrimerisaten organischer isocyanate, die nach dem verfahren erhaltenen mischtrimerisate, sowie ihre verwendung zur herstellung von polyurethanen |
| EP0172589B1 (en) * | 1984-07-20 | 1988-11-23 | Akzo N.V. | Dispersion of addition (co)polymers in an organic liquid |
| US4855369A (en) * | 1985-12-11 | 1989-08-08 | Exxon Chemical Patents Inc. | High solids acrylic-based coatings |
| US4985517A (en) * | 1985-12-11 | 1991-01-15 | Exxon Chemical Patents, Inc. | High solids acrylic-based coatings |
| CA1325076C (en) | 1985-12-11 | 1993-12-07 | Albert Ilya Yezrielev | High solids acrylic-based coatings |
| US4758642A (en) | 1985-12-11 | 1988-07-19 | Exxon Chemical Patents Inc. | Process for preparing improved high solids acrylic-based coatings |
| FR2598427B1 (fr) * | 1986-05-09 | 1988-06-03 | Holden Europ Sa | Composition a base d'une resine phenolique et d'une resine epoxydique pour revetements, notamment metallises |
| DE3701067A1 (de) * | 1987-01-16 | 1988-07-28 | Bayer Ag | Wasserverduennbare, lufttrocknende pfropfcopolymerisate |
| DE3705090A1 (de) * | 1987-02-18 | 1988-09-01 | Bayer Ag | Neue lackbindemittel fuer die kunststofflackierung |
| ATE126256T1 (de) | 1989-05-19 | 1995-08-15 | Basf Corp | Festkörperreiche lackzusammensetzungen mit niedrigem gehalt an flüchtigem organischem kohlenstoff. |
| DK0408858T3 (da) | 1989-05-19 | 1994-04-11 | Basf Corp | Copolymerer til anvendelse til overtræk med ringe indhold af flygtige organiske bestanddele og højt faststofindhold |
| US5455306A (en) * | 1993-03-04 | 1995-10-03 | Toagosei Chemical Industry Co., Ltd. | Aqueous coating composition |
| DE4324801A1 (de) | 1993-07-23 | 1995-01-26 | Hoechst Ag | Verfahren zur Herstellung von OH-Gruppen enthaltenden Copolymerisaten und deren Verwendung in festkörperreichen Beschichtungsmitteln |
| DE4326656A1 (de) | 1993-08-09 | 1995-02-16 | Hoechst Ag | Hydroxylgruppen enthaltende Copolymerisate, ihre Herstellung und ihre Verwendung in festkörperreichen Beschichtungsmitteln |
-
1995
- 1995-12-07 DE DE19545634A patent/DE19545634A1/de not_active Withdrawn
-
1996
- 1996-11-25 DK DK96118831T patent/DK0778298T3/da active
- 1996-11-25 AT AT96118831T patent/ATE200682T1/de not_active IP Right Cessation
- 1996-11-25 ES ES96118831T patent/ES2158215T3/es not_active Expired - Lifetime
- 1996-11-25 EP EP96118831A patent/EP0778298B1/de not_active Expired - Lifetime
- 1996-11-25 DE DE59606798T patent/DE59606798D1/de not_active Expired - Lifetime
- 1996-12-02 US US08/755,878 patent/US5733973A/en not_active Expired - Fee Related
- 1996-12-03 CA CA002191934A patent/CA2191934C/en not_active Expired - Fee Related
- 1996-12-06 JP JP34037596A patent/JP3883628B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| DE19545634A1 (de) | 1997-06-12 |
| CA2191934C (en) | 2005-07-26 |
| CA2191934A1 (en) | 1997-06-08 |
| EP0778298A2 (de) | 1997-06-11 |
| EP0778298A3 (de) | 1997-10-01 |
| EP0778298B1 (de) | 2001-04-18 |
| ATE200682T1 (de) | 2001-05-15 |
| DK0778298T3 (da) | 2001-05-07 |
| JPH09176561A (ja) | 1997-07-08 |
| DE59606798D1 (de) | 2001-05-23 |
| US5733973A (en) | 1998-03-31 |
| ES2158215T3 (es) | 2001-09-01 |
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