JP2003524683A5 - - Google Patents
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- JP2003524683A5 JP2003524683A5 JP2001511499A JP2001511499A JP2003524683A5 JP 2003524683 A5 JP2003524683 A5 JP 2003524683A5 JP 2001511499 A JP2001511499 A JP 2001511499A JP 2001511499 A JP2001511499 A JP 2001511499A JP 2003524683 A5 JP2003524683 A5 JP 2003524683A5
- Authority
- JP
- Japan
- Prior art keywords
- monomer
- functional
- polymer product
- weight
- reactor
- 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.)
- Granted
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- 239000000178 monomer Substances 0.000 description 93
- 238000000034 method Methods 0.000 description 34
- 238000006116 polymerization reaction Methods 0.000 description 32
- 229920000642 polymer Polymers 0.000 description 28
- 239000008199 coating composition Substances 0.000 description 20
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 13
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 13
- 239000002904 solvent Substances 0.000 description 12
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 11
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- 239000000463 material Substances 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical group C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 5
- 239000007870 radical polymerization initiator Substances 0.000 description 5
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 229920001002 functional polymer Polymers 0.000 description 4
- 230000000379 polymerizing effect Effects 0.000 description 4
- 238000010526 radical polymerization reaction Methods 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical group CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 3
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical group C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 description 2
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical group CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 description 2
- -1 acryl Chemical group 0.000 description 2
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 2
- 239000007863 gel particle Substances 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 229940119545 isobornyl methacrylate Drugs 0.000 description 2
- JJRDRFZYKKFYMO-UHFFFAOYSA-N 2-methyl-2-(2-methylbutan-2-ylperoxy)butane Chemical group CCC(C)(C)OOC(C)(C)CC JJRDRFZYKKFYMO-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 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
- 238000005406 washing Methods 0.000 description 1
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US21933499P | 1999-07-14 | 1999-07-14 | |
US35435099A | 1999-07-14 | 1999-07-14 | |
US09/354,350 | 1999-07-14 | ||
PCT/US2000/018890 WO2001005843A1 (en) | 1999-07-14 | 2000-07-12 | Process for the continuous production of epoxy-(meth)acrylic-styrene polymers and their use in coating |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2003524683A JP2003524683A (ja) | 2003-08-19 |
JP2003524683A5 true JP2003524683A5 (enrdf_load_stackoverflow) | 2007-03-22 |
JP5366347B2 JP5366347B2 (ja) | 2013-12-11 |
Family
ID=35965938
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2001511499A Expired - Fee Related JP5366347B2 (ja) | 1999-07-14 | 2000-07-12 | エポキシ化付加ポリマーの連続生産方法とエポキシ化付加ポリマーを含む粉体および液体コーティングへの応用 |
Country Status (2)
Country | Link |
---|---|
JP (1) | JP5366347B2 (enrdf_load_stackoverflow) |
MX (1) | MXPA02000469A (enrdf_load_stackoverflow) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE60015768T2 (de) * | 1999-07-14 | 2006-02-09 | Johnson Polymer, Inc., Sturtevant | Verfahren zur kontinuierlichen herstellung von gelfreien polymeren, pulverige und flüssige beschichtungsmasse enthaltend gelfreie polymere |
WO2003066704A1 (en) * | 2002-02-01 | 2003-08-14 | Johnson Polymer, Llc | Oligomeric chain extenders for processing, post-processing and recycling of condensation polymers, synthesis, compositions and applications |
JP2008094964A (ja) * | 2006-10-12 | 2008-04-24 | Toagosei Co Ltd | 粉体塗料用組成物 |
JP5941843B2 (ja) * | 2009-07-21 | 2016-06-29 | バスフ コーポレーションBasf Corporation | 反応器内鎖延長による縮合重合体生成のための方法、及びその生成物 |
JP2013072050A (ja) * | 2011-09-29 | 2013-04-22 | Toagosei Co Ltd | 側鎖に(メタ)アクリロイル基を有する(メタ)アクリル系重合体組成物の製造方法 |
JP2022075274A (ja) * | 2020-11-06 | 2022-05-18 | 東亞合成株式会社 | 活性エネルギー線硬化性組成物 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5474891A (en) * | 1977-11-29 | 1979-06-15 | Asahi Chem Ind Co Ltd | Continous preparation of copolymer having crosslinkable functional group |
US4529787A (en) * | 1982-06-15 | 1985-07-16 | S. C. Johnson & Son, Inc. | Bulk polymerization process for preparing high solids and uniform copolymers |
US4589999A (en) * | 1984-12-28 | 1986-05-20 | E. I. Du Pont De Nemours And Company | Electrically conductive coating composition of a glycidyl acrylic polymer and a reactive polysiloxane |
JPH03199211A (ja) * | 1989-12-27 | 1991-08-30 | Hitachi Chem Co Ltd | 塗料用アクリル系樹脂,その製造法及び塗料組成物 |
JP2805389B2 (ja) * | 1990-09-28 | 1998-09-30 | 日本ペイント株式会社 | 熱硬化性塗料組成物およびそれを用いた複合塗膜形成方法 |
CA2088129A1 (en) * | 1992-02-06 | 1993-08-07 | Fritz Erdmann Kempter | Continuous polymerization of vinyl monomers |
JPH06100605A (ja) * | 1992-09-18 | 1994-04-12 | Sanyo Chem Ind Ltd | アクリル系樹脂の製法 |
JPH09188833A (ja) * | 1995-11-09 | 1997-07-22 | Nippon Paint Co Ltd | 粉体塗料組成物および塗膜形成方法 |
JPH1160636A (ja) * | 1997-08-08 | 1999-03-02 | Kayaku Akzo Kk | アクリル樹脂の製造方法 |
DE19752747A1 (de) * | 1997-11-28 | 1999-06-24 | Herberts Gmbh | Verfahren zur Herstellung von Glycidyl(meth)acrylat-Copolymeren |
-
2000
- 2000-07-12 MX MXPA02000469A patent/MXPA02000469A/es active IP Right Grant
- 2000-07-12 JP JP2001511499A patent/JP5366347B2/ja not_active Expired - Fee Related
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