JP2009510194A5 - - Google Patents
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- Publication number
- JP2009510194A5 JP2009510194A5 JP2008532455A JP2008532455A JP2009510194A5 JP 2009510194 A5 JP2009510194 A5 JP 2009510194A5 JP 2008532455 A JP2008532455 A JP 2008532455A JP 2008532455 A JP2008532455 A JP 2008532455A JP 2009510194 A5 JP2009510194 A5 JP 2009510194A5
- Authority
- JP
- Japan
- Prior art keywords
- resin substrate
- coating composition
- copolymer
- coating
- aliphatic group
- Prior art date
- 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.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 claims description 26
- 239000000758 substrate Substances 0.000 claims description 15
- 229920005989 resin Polymers 0.000 claims description 14
- 239000011347 resin Substances 0.000 claims description 14
- 239000008199 coating composition Substances 0.000 claims description 9
- 229920001577 copolymer Polymers 0.000 claims description 9
- 239000000178 monomer Substances 0.000 claims description 9
- 125000002723 alicyclic group Chemical group 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 7
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 6
- 239000011248 coating agent Substances 0.000 claims description 6
- 238000000576 coating method Methods 0.000 claims description 6
- 239000005056 polyisocyanate Substances 0.000 claims description 6
- 229920001228 polyisocyanate Polymers 0.000 claims description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- -1 polypropylene Polymers 0.000 claims description 4
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 4
- 239000000853 adhesive Substances 0.000 claims description 3
- 230000001070 adhesive effect Effects 0.000 claims description 3
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 2
- 239000004952 Polyamide Substances 0.000 claims description 2
- 239000004743 Polypropylene Substances 0.000 claims description 2
- 239000003677 Sheet moulding compound Substances 0.000 claims description 2
- 230000001464 adherent effect Effects 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 2
- 229930195729 fatty acid Natural products 0.000 claims description 2
- 239000000194 fatty acid Substances 0.000 claims description 2
- 150000004665 fatty acids Chemical class 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 229920001155 polypropylene Polymers 0.000 claims description 2
- 239000004711 α-olefin Substances 0.000 claims description 2
- 229920001955 polyphenylene ether Polymers 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 10
- 238000004132 cross linking Methods 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 3
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920000265 Polyparaphenylene Polymers 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical class OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 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
- 150000002148 esters Chemical class 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 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
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 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
- 150000002576 ketones 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
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 229920006250 telechelic polymer Polymers 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
- 239000013638 trimer Substances 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US71965705P | 2005-09-22 | 2005-09-22 | |
| PCT/US2006/037134 WO2007050213A2 (en) | 2005-09-22 | 2006-09-22 | Adherent coating compositions for resinous substrates |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009510194A JP2009510194A (ja) | 2009-03-12 |
| JP2009510194A5 true JP2009510194A5 (https=) | 2009-11-05 |
Family
ID=37781712
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008532455A Abandoned JP2009510194A (ja) | 2005-09-22 | 2006-09-22 | 樹脂基材用の付着コーティング組成物 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US7763679B2 (https=) |
| EP (1) | EP1954735A2 (https=) |
| JP (1) | JP2009510194A (https=) |
| CN (1) | CN101268112A (https=) |
| WO (1) | WO2007050213A2 (https=) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101611108A (zh) * | 2007-01-12 | 2009-12-23 | 纳幕尔杜邦公司 | 用于树脂基质的粘附性涂料组合物 |
| US8568888B2 (en) | 2007-03-15 | 2013-10-29 | Nanovere Technologies, Inc. | Dendritic polyurethane coating |
| US8206827B2 (en) * | 2007-03-15 | 2012-06-26 | Nanovere Technologies, Llc | Dendritic polyurethane coating |
| US11708470B2 (en) * | 2016-12-21 | 2023-07-25 | Ppg Industries Ohio, Inc. | Plastic substrate adhesion promoter with random copolymer |
| EP3381962A1 (de) * | 2017-03-29 | 2018-10-03 | Covestro Deutschland AG | Erzeugung von polyisocyanuratschichten durch getrennte auftragung von isocyanatkomponenten und katalysatoren |
| WO2019021259A1 (en) * | 2017-07-27 | 2019-01-31 | Magna Exteriors Inc. | PRIMER COATING FOR A PLASTIC SUBSTRATE FILLED WITH FIBERS |
| CN107895766A (zh) * | 2017-10-19 | 2018-04-10 | 中航锂电（洛阳）有限公司 | 一种涂覆耐高温涂层的电池隔膜及其制备方法 |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3652732A (en) | 1968-11-05 | 1972-03-28 | Exxon Research Engineering Co | Solventless encapsulating block copolymers |
| USRE27145E (en) | 1969-05-20 | 1971-06-22 | Side-chain | |
| US4039593A (en) | 1973-05-18 | 1977-08-02 | Lithium Corporation Of America | Preparation of hydroxy-terminated conjugated diene polymers |
| US4301053A (en) * | 1980-01-29 | 1981-11-17 | General Electric Company | Polyurethane resin coating composition |
| US4518753A (en) | 1982-04-26 | 1985-05-21 | National Research Development Corporation | Anionic polymerization of conjugated dienes in the presence of hindered triaryl boron or aluminum derivatives |
| JPS58221745A (ja) * | 1982-06-19 | 1983-12-23 | Japan Styrene Paper Co Ltd | 自動車のバンパ−用芯材 |
| US4439593A (en) * | 1983-05-26 | 1984-03-27 | Mobay Chemical Corporation | Polyurethane compositions with improved storage stability |
| DE3628119A1 (de) * | 1986-08-19 | 1988-02-25 | Herberts Gmbh | Fremdvernetzende bindemittelkombination, diese enthaltende waessriges ueberzugsmittel und dessen verwendung |
| US5306778A (en) * | 1988-08-24 | 1994-04-26 | Japan Synthetic Rubber Co., Ltd. | Process for producing rubber-modified thermoplastic resin |
| US4997882A (en) | 1989-07-07 | 1991-03-05 | Ppg Industries, Inc. | Acid or anhydride grafted chlorinated polyolefin reacted with monoalcohol and polyepoxide |
| US5221707A (en) | 1989-11-30 | 1993-06-22 | Gencorp Inc. | Coating blend compositions |
| US5115007A (en) * | 1989-11-30 | 1992-05-19 | Gencorp Inc. | Abrasion resistant polyurethane blend compositions |
| US5039755A (en) | 1990-05-29 | 1991-08-13 | Shell Oil Company | Selective hydrogenation of conjugated diolefin polymers |
| JP2893135B2 (ja) * | 1990-10-19 | 1999-05-17 | ジェイエスアール株式会社 | 光ファイバー被覆用液状硬化性樹脂組成物 |
| US5281443A (en) * | 1991-12-20 | 1994-01-25 | Basf Corporation | Coating method for one-component blocked isocyanate-crosslinked clearcoat |
| US5286782A (en) | 1992-08-31 | 1994-02-15 | E. I. Du Pont De Nemours And Company | Coating composition of an acrylic polymer, polyol and polyisocyanate crosslinking agent |
| US5319032A (en) | 1993-03-01 | 1994-06-07 | Ppg Industries, Inc. | Modified chlorinated polyolefins, aqueous dispersions thereof and their use in coating compositions |
| US5376745A (en) | 1993-12-01 | 1994-12-27 | Shell Oil Company | Low viscosity terminally functionalized isoprene polymers |
| US5486570A (en) | 1994-09-29 | 1996-01-23 | Shell Oil Company | Polyurethane sealants and adhesives containing saturated hydrocarbon polyols |
| US6025433A (en) * | 1995-12-20 | 2000-02-15 | Basf Coatings Ag | Thermosetting paint composition |
| US6001469A (en) * | 1996-03-28 | 1999-12-14 | Ppg Industries Ohio, Inc. | Thermosettable primer and topcoat for plastics, a method for applying and coated plastic articles |
| US6060560A (en) * | 1997-05-23 | 2000-05-09 | Shell Oil Company | Polyurethane compositions made from hydroxy-terminated polydiene polymers |
| US6203913B1 (en) | 1997-12-19 | 2001-03-20 | Ppg Industries Ohio, Inc. | Coating composition for plastic substrates |
| DE19846971A1 (de) * | 1998-10-12 | 2000-04-20 | Basf Coatings Ag | Beschichtungsmittel, Verfahren zu seiner Herstellung und seine Verwendung als Decklack oder Klarlack, insbesondere zur Beschichtung von Kunststoffen |
| US6221494B1 (en) | 1998-11-03 | 2001-04-24 | E.I. Du Pont De Nemours And Company | Reactive oligomers for isocyanate coatings |
| US7078474B2 (en) * | 2004-07-07 | 2006-07-18 | E. I. Dupont De Nemours And Company | Thermally curable coating compositions |
-
2006
- 2006-09-22 WO PCT/US2006/037134 patent/WO2007050213A2/en not_active Ceased
- 2006-09-22 EP EP20060844180 patent/EP1954735A2/en not_active Withdrawn
- 2006-09-22 US US11/526,038 patent/US7763679B2/en active Active
- 2006-09-22 JP JP2008532455A patent/JP2009510194A/ja not_active Abandoned
- 2006-09-22 CN CNA2006800346323A patent/CN101268112A/zh active Pending
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