JP2002523569A - 原子移動ラジカル重合を使用して調製されるカルバメート官能性ポリマーを含む熱硬化性組成物 - Google Patents
原子移動ラジカル重合を使用して調製されるカルバメート官能性ポリマーを含む熱硬化性組成物Info
- Publication number
- JP2002523569A JP2002523569A JP2000567579A JP2000567579A JP2002523569A JP 2002523569 A JP2002523569 A JP 2002523569A JP 2000567579 A JP2000567579 A JP 2000567579A JP 2000567579 A JP2000567579 A JP 2000567579A JP 2002523569 A JP2002523569 A JP 2002523569A
- Authority
- JP
- Japan
- Prior art keywords
- carbamate
- polymer
- group
- functional
- composition
- 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.)
- Pending
Links
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- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- IWTBVKIGCDZRPL-LURJTMIESA-N 3-Methylbutanol Natural products CC[C@H](C)CCO IWTBVKIGCDZRPL-LURJTMIESA-N 0.000 description 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
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- 125000001246 bromo group Chemical group Br* 0.000 description 1
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- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
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- 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
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- 238000004821 distillation Methods 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
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- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
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- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- MSYLJRIXVZCQHW-UHFFFAOYSA-N formaldehyde;6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound O=C.NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 MSYLJRIXVZCQHW-UHFFFAOYSA-N 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 150000002431 hydrogen Chemical group 0.000 description 1
- OUUQCZGPVNCOIJ-UHFFFAOYSA-N hydroperoxyl Chemical compound O[O] OUUQCZGPVNCOIJ-UHFFFAOYSA-N 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
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- 150000002500 ions Chemical class 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-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
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 238000010550 living polymerization reaction Methods 0.000 description 1
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- 239000008204 material by function Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- VPKDCDLSJZCGKE-UHFFFAOYSA-N methanediimine Chemical compound N=C=N VPKDCDLSJZCGKE-UHFFFAOYSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
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- 230000000269 nucleophilic effect Effects 0.000 description 1
- YJBMMHPCGWCCOH-UHFFFAOYSA-N octan-3-yl dihydrogen phosphate Chemical compound CCCCCC(CC)OP(O)(O)=O YJBMMHPCGWCCOH-UHFFFAOYSA-N 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
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- 239000003973 paint Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- GJVFBWCTGUSGDD-UHFFFAOYSA-L pentamethonium bromide Chemical compound [Br-].[Br-].C[N+](C)(C)CCCCC[N+](C)(C)C GJVFBWCTGUSGDD-UHFFFAOYSA-L 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 150000004032 porphyrins Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- ARJOQCYCJMAIFR-UHFFFAOYSA-N prop-2-enoyl prop-2-enoate Chemical compound C=CC(=O)OC(=O)C=C ARJOQCYCJMAIFR-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 238000007342 radical addition reaction Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 125000004354 sulfur functional group Chemical group 0.000 description 1
- 239000004094 surface-active agent Substances 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
- 238000010998 test method Methods 0.000 description 1
- 125000000858 thiocyanato group Chemical group *SC#N 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 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
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 229960002703 undecylenic acid Drugs 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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
- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
-
- 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
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3819—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen
- C08G18/3823—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen containing -N-C=O groups
- C08G18/3831—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen containing -N-C=O groups containing urethane groups
-
- 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
- C09D201/00—Coating compositions based on unspecified macromolecular compounds
- C09D201/02—Coating compositions based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
- C09D201/025—Coating compositions based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups containing nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
- Graft Or Block Polymers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymerization Catalysts (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Polyurethanes Or Polyureas (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9861698P | 1998-08-31 | 1998-08-31 | |
| US09/375,020 US6306965B1 (en) | 1998-08-31 | 1999-08-16 | Thermosetting compositions containing carbamate-functional polylmers prepared using atom transfer radical polymerization |
| US60/098,616 | 1999-08-16 | ||
| US09/375,020 | 1999-08-16 | ||
| PCT/US1999/019797 WO2000012566A1 (en) | 1998-08-31 | 1999-08-30 | Thermosetting compositions containing carbamate-functional polymers prepared using atom transfer radical polymerization |
Related Child Applications (1)
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|---|---|---|---|
| JP2004278575A Division JP3894933B2 (ja) | 1998-08-31 | 2004-09-24 | 原子移動ラジカル重合を使用して調製されるカルバメート官能性ポリマーを含む熱硬化性組成物 |
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| JP2002523569A true JP2002523569A (ja) | 2002-07-30 |
| JP2002523569A5 JP2002523569A5 (enExample) | 2005-12-22 |
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|---|---|---|---|
| JP2000567579A Pending JP2002523569A (ja) | 1998-08-31 | 1999-08-30 | 原子移動ラジカル重合を使用して調製されるカルバメート官能性ポリマーを含む熱硬化性組成物 |
| JP2004278575A Expired - Fee Related JP3894933B2 (ja) | 1998-08-31 | 2004-09-24 | 原子移動ラジカル重合を使用して調製されるカルバメート官能性ポリマーを含む熱硬化性組成物 |
| JP2006293357A Withdrawn JP2007070639A (ja) | 1998-08-31 | 2006-10-27 | 原子移動ラジカル重合を使用して調製されるカルバメート官能性ポリマーを含む熱硬化性組成物 |
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| Application Number | Title | Priority Date | Filing Date |
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| JP2004278575A Expired - Fee Related JP3894933B2 (ja) | 1998-08-31 | 2004-09-24 | 原子移動ラジカル重合を使用して調製されるカルバメート官能性ポリマーを含む熱硬化性組成物 |
| JP2006293357A Withdrawn JP2007070639A (ja) | 1998-08-31 | 2006-10-27 | 原子移動ラジカル重合を使用して調製されるカルバメート官能性ポリマーを含む熱硬化性組成物 |
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| Country | Link |
|---|---|
| US (1) | US6306965B1 (enExample) |
| EP (1) | EP1112290B1 (enExample) |
| JP (3) | JP2002523569A (enExample) |
| KR (1) | KR100420816B1 (enExample) |
| AU (1) | AU737520B2 (enExample) |
| BR (1) | BR9913485A (enExample) |
| CA (1) | CA2340703C (enExample) |
| DE (1) | DE69919180T2 (enExample) |
| ES (1) | ES2226436T3 (enExample) |
| MX (1) | MX224470B (enExample) |
| WO (1) | WO2000012566A1 (enExample) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005517789A (ja) * | 2002-02-15 | 2005-06-16 | ピーピージー インダストリーズ オハイオ， インコーポレイテッド | イソブチレンのコポリマーを含有する水系組成物 |
| JP2005517776A (ja) * | 2002-02-15 | 2005-06-16 | ピーピージー インダストリーズ オハイオ， インコーポレイテッド | イソブチレン型モノマーの交互コポリマーを含有する水系フィルム形成組成物 |
| US7009007B2 (en) | 2001-12-21 | 2006-03-07 | Canon Kabushiki Kaisha | Recyclable polymer, process for production thereof, and recycling treatment thereof |
| JP2009175551A (ja) * | 2008-01-25 | 2009-08-06 | Arisawa Mfg Co Ltd | 立体画像表示装置およびその製造方法 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6306965B1 (en) * | 1998-08-31 | 2001-10-23 | Ppg Industries Ohio, Inc. | Thermosetting compositions containing carbamate-functional polylmers prepared using atom transfer radical polymerization |
| US6355729B1 (en) | 1998-08-31 | 2002-03-12 | Ppg Industries Ohio, Inc. | Electrodepositable coating compositions comprising amine salt group-containing polymers prepared by atom transfer radical polymerization |
| US7205029B2 (en) * | 2000-12-19 | 2007-04-17 | Basf Corporation | Method of providing cured coating films free of popping defects |
| AU2003209067A1 (en) * | 2002-02-15 | 2003-09-09 | Ppg Industries Ohio, Inc. | Compositions containing copolymers of post-polymerization reacted (meth)acrylate monomers |
| US6784248B2 (en) | 2002-02-15 | 2004-08-31 | Ppg Industries Ohio, Inc. | Thermosetting compositions containing alternating copolymers of isobutylene type monomers |
| US6890994B2 (en) * | 2002-10-31 | 2005-05-10 | Basf Corporation | Curable coating compositions with carbamate-containing acrylic polymers |
| US20050032978A1 (en) * | 2003-08-06 | 2005-02-10 | O'dwyer James B. | Etherified carbamate functional copolymers of isobutylene type monomers, and their use in curable compositions |
| US7342077B2 (en) | 2004-06-04 | 2008-03-11 | Basf Corporation | Acrylic composition and a method of forming the same via free-radical polymerization |
| US7250480B2 (en) | 2004-03-04 | 2007-07-31 | Basf Corporation | Acrylic composition and a curable coating composition including the same |
| US7220811B2 (en) | 2004-03-04 | 2007-05-22 | Basf Corporation | Acrylic composition and a curable coating composition including the same |
| US7375174B2 (en) | 2004-03-04 | 2008-05-20 | Basf Corporation | Acrylic composition and a curable coating composition including the same |
| US7144966B2 (en) | 2004-03-04 | 2006-12-05 | Basf Corporation | Acrylic composition for use in coating applications and a method of forming the same |
| JP5094578B2 (ja) * | 2008-06-17 | 2012-12-12 | 花王株式会社 | グラフトポリマーの製造方法 |
| US9334234B2 (en) * | 2014-05-08 | 2016-05-10 | Basf Coatings Gmbh | Method using titanium catalyst for producing carbamate-functional materials |
| RU2562267C1 (ru) * | 2014-12-24 | 2015-09-10 | Сергей Вячеславович Штепа | Способ получения защитного композиционного термопластичного покрытия и способ его нанесения |
| EP3363835B1 (en) * | 2017-02-20 | 2023-10-11 | The Gillette Company LLC | Article comprising a polymer layer |
| CN110964175A (zh) * | 2019-11-20 | 2020-04-07 | 武汉科技大学 | 基于氨基甲酸叔醇酯交换的类玻璃聚氨酯弹性体、制备方法及应用 |
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|---|---|---|---|---|
| US3479328A (en) | 1966-11-18 | 1969-11-18 | Ashland Oil Inc | Novel monomers and polymers |
| US4147679A (en) | 1976-06-02 | 1979-04-03 | Ppg Industries, Inc. | Water-reduced urethane coating compositions |
| DE3166673D1 (en) | 1980-04-14 | 1984-11-22 | Ici Plc | Multi-layer coating process involving use of aqueous basecoat composition containing crosslinked polymer microparticles and having a pseudoplastic or thixotropic character |
| US5071904A (en) | 1989-05-30 | 1991-12-10 | Ppg Industries, Inc. | Waterborne coating compositions for automotive applications |
| US5605965A (en) * | 1992-10-23 | 1997-02-25 | Basf Corporation | High gloss and/or high DOI coating utilizing carbamate-functional polymer composition |
| ES2101353T3 (es) * | 1992-10-30 | 1997-07-01 | Ppg Industries Inc | Composiciones filmogenas endurecibles con aminoplastico que producen peliculas resistentes al ataque del acido. |
| US5384367A (en) * | 1993-04-19 | 1995-01-24 | Ppg Industries, Inc. | Carbamate urea or urethane-functional epoxy acrylic with polyacid |
| US5373069A (en) * | 1993-07-28 | 1994-12-13 | Basf Corporation | Curable carbamate-functional polymers |
| US5709950A (en) * | 1994-04-29 | 1998-01-20 | Ppg Industries, Inc. | Color-plus-clear composite coatings that contain polymers having carbamate functionality |
| DE4432897C2 (de) * | 1994-09-15 | 1999-05-20 | Dainippon Ink & Chemicals | Vernetzende Massen sowie Verfahren zur Herstellung vernetzter Materialien |
| US5552497A (en) * | 1994-12-29 | 1996-09-03 | Basf Corporation | Method of preparing carbamate-functional polymer |
| US5763548A (en) | 1995-03-31 | 1998-06-09 | Carnegie-Mellon University | (Co)polymers and a novel polymerization process based on atom (or group) transfer radical polymerization |
| US5807937A (en) | 1995-11-15 | 1998-09-15 | Carnegie Mellon University | Processes based on atom (or group) transfer radical polymerization and novel (co) polymers having useful structures and properties |
| US5789487A (en) | 1996-07-10 | 1998-08-04 | Carnegie-Mellon University | Preparation of novel homo- and copolymers using atom transfer radical polymerization |
| TW593347B (en) | 1997-03-11 | 2004-06-21 | Univ Carnegie Mellon | Improvements in atom or group transfer radical polymerization |
| US6306965B1 (en) * | 1998-08-31 | 2001-10-23 | Ppg Industries Ohio, Inc. | Thermosetting compositions containing carbamate-functional polylmers prepared using atom transfer radical polymerization |
-
1999
- 1999-08-16 US US09/375,020 patent/US6306965B1/en not_active Expired - Fee Related
- 1999-08-30 CA CA002340703A patent/CA2340703C/en not_active Expired - Fee Related
- 1999-08-30 AU AU57927/99A patent/AU737520B2/en not_active Ceased
- 1999-08-30 KR KR20017002612A patent/KR100420816B1/ko not_active Expired - Fee Related
- 1999-08-30 BR BR9913485-3A patent/BR9913485A/pt not_active Application Discontinuation
- 1999-08-30 JP JP2000567579A patent/JP2002523569A/ja active Pending
- 1999-08-30 ES ES99945306T patent/ES2226436T3/es not_active Expired - Lifetime
- 1999-08-30 WO PCT/US1999/019797 patent/WO2000012566A1/en not_active Ceased
- 1999-08-30 DE DE69919180T patent/DE69919180T2/de not_active Expired - Lifetime
- 1999-08-30 EP EP99945306A patent/EP1112290B1/en not_active Expired - Lifetime
- 1999-09-01 MX MXPA01001967 patent/MX224470B/es not_active IP Right Cessation
-
2004
- 2004-09-24 JP JP2004278575A patent/JP3894933B2/ja not_active Expired - Fee Related
-
2006
- 2006-10-27 JP JP2006293357A patent/JP2007070639A/ja not_active Withdrawn
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7009007B2 (en) | 2001-12-21 | 2006-03-07 | Canon Kabushiki Kaisha | Recyclable polymer, process for production thereof, and recycling treatment thereof |
| US7291679B2 (en) | 2001-12-21 | 2007-11-06 | Canon Kabushiki Kaisha | Recyclable polymer and process for production thereof |
| JP2005517789A (ja) * | 2002-02-15 | 2005-06-16 | ピーピージー インダストリーズ オハイオ， インコーポレイテッド | イソブチレンのコポリマーを含有する水系組成物 |
| JP2005517776A (ja) * | 2002-02-15 | 2005-06-16 | ピーピージー インダストリーズ オハイオ， インコーポレイテッド | イソブチレン型モノマーの交互コポリマーを含有する水系フィルム形成組成物 |
| JP2009175551A (ja) * | 2008-01-25 | 2009-08-06 | Arisawa Mfg Co Ltd | 立体画像表示装置およびその製造方法 |
| US8194316B2 (en) | 2008-01-25 | 2012-06-05 | Arisawa Mfg. Co., Ltd. | Three-dimensional image display apparatus |
| US8243367B2 (en) | 2008-01-25 | 2012-08-14 | Arisawa Mfg. Co., Ltd. | Manufacturing method of three-dimensional image display apparatus |
Also Published As
| Publication number | Publication date |
|---|---|
| AU5792799A (en) | 2000-03-21 |
| CA2340703A1 (en) | 2000-03-09 |
| US6306965B1 (en) | 2001-10-23 |
| KR100420816B1 (ko) | 2004-03-02 |
| MX224470B (es) | 2004-11-24 |
| ES2226436T3 (es) | 2005-03-16 |
| EP1112290A1 (en) | 2001-07-04 |
| CA2340703C (en) | 2004-11-02 |
| WO2000012566A1 (en) | 2000-03-09 |
| DE69919180D1 (de) | 2004-09-09 |
| EP1112290B1 (en) | 2004-08-04 |
| MXPA01001967A (es) | 2001-08-01 |
| BR9913485A (pt) | 2001-05-22 |
| JP3894933B2 (ja) | 2007-03-22 |
| KR20010074871A (ko) | 2001-08-09 |
| AU737520B2 (en) | 2001-08-23 |
| DE69919180T2 (de) | 2005-07-28 |
| JP2005089760A (ja) | 2005-04-07 |
| JP2007070639A (ja) | 2007-03-22 |
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