JP2005535737A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2005535737A5 JP2005535737A5 JP2003586199A JP2003586199A JP2005535737A5 JP 2005535737 A5 JP2005535737 A5 JP 2005535737A5 JP 2003586199 A JP2003586199 A JP 2003586199A JP 2003586199 A JP2003586199 A JP 2003586199A JP 2005535737 A5 JP2005535737 A5 JP 2005535737A5
- Authority
- JP
- Japan
- Prior art keywords
- solvent
- purification
- separation
- polymer
- product
- 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
Links
- 239000002904 solvent Substances 0.000 description 14
- 229920000642 polymer Polymers 0.000 description 11
- 238000000746 purification Methods 0.000 description 9
- FUGYGGDSWSUORM-UHFFFAOYSA-N 4-hydroxystyrene Chemical compound OC1=CC=C(C=C)C=C1 FUGYGGDSWSUORM-UHFFFAOYSA-N 0.000 description 7
- 238000000926 separation method Methods 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 229920001519 homopolymer Polymers 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 229920002120 photoresistant polymer Polymers 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 150000003440 styrenes Chemical class 0.000 description 2
- 229920001897 terpolymer Polymers 0.000 description 2
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 2
- 238000005809 transesterification reaction Methods 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000004377 microelectronic Methods 0.000 description 1
- 238000005580 one pot reaction Methods 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/126,563 US6864324B2 (en) | 2002-04-19 | 2002-04-19 | Anhydrous, liquid phase process for preparing hydroxyl containing polymers of enhanced purity |
| PCT/US2003/011261 WO2003089480A1 (en) | 2002-04-19 | 2003-04-10 | Anhydrous, liquid phase process for preparing hydroxyl containing polymers of enhanced purity |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005535737A JP2005535737A (ja) | 2005-11-24 |
| JP2005535737A5 true JP2005535737A5 (enExample) | 2008-09-11 |
| JP4261372B2 JP4261372B2 (ja) | 2009-04-30 |
Family
ID=29215054
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003586199A Expired - Lifetime JP4261372B2 (ja) | 2002-04-19 | 2003-04-10 | 純度の高いヒドロキシル含有ポリマーを調製するための無水液相方法 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US6864324B2 (enExample) |
| EP (1) | EP1497339B1 (enExample) |
| JP (1) | JP4261372B2 (enExample) |
| KR (1) | KR100965990B1 (enExample) |
| CN (1) | CN100564401C (enExample) |
| AR (1) | AR039433A1 (enExample) |
| AT (1) | ATE402962T1 (enExample) |
| AU (1) | AU2003221902A1 (enExample) |
| CA (1) | CA2482899A1 (enExample) |
| DE (1) | DE60322526D1 (enExample) |
| TW (1) | TWI250998B (enExample) |
| WO (1) | WO2003089480A1 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3841399B2 (ja) * | 2002-02-21 | 2006-11-01 | 富士写真フイルム株式会社 | ポジ型レジスト組成物 |
| US7312281B2 (en) * | 2002-04-19 | 2007-12-25 | Dupont Electronic Polymers L.P. | Anhydrous, liquid phase process for preparing hydroxyl containing polymers of enhanced purity |
| US20040242798A1 (en) * | 2003-05-08 | 2004-12-02 | Sounik James R. | Photoresist compositions and processes for preparing the same |
| JP2005350609A (ja) * | 2004-06-11 | 2005-12-22 | Daicel Chem Ind Ltd | 側鎖にアセタール構造を有する高分子化合物及びその製造法 |
| CN101331155A (zh) * | 2005-12-22 | 2008-12-24 | 杜邦电子聚合物公司 | 制备稳定的光致抗蚀剂组合物的方法 |
| JP4976229B2 (ja) * | 2007-08-03 | 2012-07-18 | 株式会社ダイセル | フォトレジスト用樹脂溶液の製造方法、フォトレジスト組成物およびパターン形成方法 |
| KR101314508B1 (ko) | 2008-08-25 | 2013-10-07 | 듀퐁 일렉트로닉 폴리머스 엘피 | 신규한 프로파노에이트 및 그의 제조 방법 |
| KR101111491B1 (ko) * | 2009-08-04 | 2012-03-14 | 금호석유화학 주식회사 | 신규 공중합체 및 이를 포함하는 포토레지스트 조성물 |
| FR2972193B1 (fr) | 2011-03-04 | 2014-07-04 | Setup Performance | Polyolefines modifiees, reticulables apres transformation, et procede de fabrication desdites polyolefines |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4491628A (en) | 1982-08-23 | 1985-01-01 | International Business Machines Corporation | Positive- and negative-working resist compositions with acid generating photoinitiator and polymer with acid labile groups pendant from polymer backbone |
| US4636540A (en) | 1985-07-08 | 1987-01-13 | Atlantic Richfield Company | Purification of polymer solutions |
| US4689371A (en) | 1986-07-07 | 1987-08-25 | Celanese Corporation | Process for the preparation of poly (vinylphenol) from poly (acetoxystyrene) |
| US4939070A (en) | 1986-07-28 | 1990-07-03 | Brunsvold William R | Thermally stable photoresists with high sensitivity |
| EP0260104A3 (en) | 1986-09-09 | 1989-03-15 | Celanese Corporation | Process for the preparation of poly (vinylphenol) by simultaneous methanolysis and polymerization of 4-acetoxystryene |
| US4678843A (en) | 1986-09-29 | 1987-07-07 | Celanese Corporation | Process for the ammonium hydroxide hydrolysis of polymers of acetoxystyrene to polymers of vinylphenol |
| US4931379A (en) | 1986-10-23 | 1990-06-05 | International Business Machines Corporation | High sensitivity resists having autodecomposition temperatures greater than about 160° C. |
| EP0277721A3 (en) | 1987-01-28 | 1989-03-15 | Hoechst Celanese Corporation | Emulsion polymerization of 4-acetoxystyrene and hydrolysis to poly(p-vinylphenol) |
| US4822862A (en) | 1987-01-28 | 1989-04-18 | Hoechst Celanese Corporation | Emulsion polymerization of 4-acetoxystyrene and hydrolysis to poly(p-vinylphenol |
| US4898916A (en) | 1987-03-05 | 1990-02-06 | Hoechst Celanese Corporation | Process for the preparation of poly(vinylphenol) from poly(acetoxystyrene) by acid catalyzed transesterification |
| US4877843A (en) | 1987-09-11 | 1989-10-31 | Hoechst Celanese Corporation | Selective hydrolysis of copolymers of para-acetoxy styrene and allyl esters of ethylenically unsaturated acids |
| US4912173A (en) | 1987-10-30 | 1990-03-27 | Hoechst Celanese Corporation | Hydrolysis of poly(acetoxystyrene) in aqueous suspension |
| US4962147A (en) | 1988-05-26 | 1990-10-09 | Hoechst Celanese Corporation | Process for the suspension polymerization of 4-acetoxystyrene and hydrolysis to 4-hydroxystyrene polymers |
| US5239015A (en) | 1990-06-29 | 1993-08-24 | Hoechst Celanese Corporation | Process for making low optical density polymers and copolymers for photoresists and optical applications |
| US5087772A (en) | 1990-11-16 | 1992-02-11 | Hoechst Celanese Corporation | Method for preparing 4-hydroxystyrene |
| JPH0768296B2 (ja) | 1991-11-28 | 1995-07-26 | 丸善石油化学株式会社 | ビニルフェノール系重合体の金属除去方法 |
| DE69322946T2 (de) | 1992-11-03 | 1999-08-12 | International Business Machines Corp., Armonk, N.Y. | Photolackzusammensetzung |
| WO1994014858A1 (en) | 1992-12-29 | 1994-07-07 | Hoechst Celanese Corporation | Metal ion reduction in polyhydroxystyrene and photoresists |
| US5304610A (en) | 1993-01-12 | 1994-04-19 | Hoechst Celanese Corporation | Amphoteric copolymer derived from vinylpyridine and acetoxystyrene |
| US5861231A (en) | 1996-06-11 | 1999-01-19 | Shipley Company, L.L.C. | Copolymers and photoresist compositions comprising copolymer resin binder component |
| US5789522A (en) | 1996-09-06 | 1998-08-04 | Shipley Company, L.L.C. | Resin purification process |
| US5888751A (en) * | 1997-07-15 | 1999-03-30 | Ludwig Institute For Cancer Research | Method for diagnosis and treating cancers, and methods for identifying pathogenic markers in a sample of normal cells |
| US5919597A (en) | 1997-10-30 | 1999-07-06 | Ibm Corporation Of Armonk | Methods for preparing photoresist compositions |
| EP1076667B1 (en) * | 1998-05-05 | 2004-03-24 | Triquest, L.P. | Preparation of co-and terpolymers of p-hydroxystyrene and alkyl acrylates |
| WO1999058579A1 (en) * | 1998-05-08 | 1999-11-18 | Arch Specialty Chemicals, Inc. | Process for producing purified solutions of blocked polyhydroxystyrene resin |
| US6414110B1 (en) * | 1999-11-12 | 2002-07-02 | Triquest Lp | Purification means |
| JP4129177B2 (ja) * | 2000-06-27 | 2008-08-06 | トリクエスト・リミテッド・パートナーシップ | 精製手段 |
-
2002
- 2002-04-19 US US10/126,563 patent/US6864324B2/en not_active Expired - Lifetime
-
2003
- 2003-04-10 KR KR1020047016757A patent/KR100965990B1/ko not_active Expired - Lifetime
- 2003-04-10 CA CA002482899A patent/CA2482899A1/en not_active Abandoned
- 2003-04-10 DE DE60322526T patent/DE60322526D1/de not_active Expired - Lifetime
- 2003-04-10 AT AT03718361T patent/ATE402962T1/de not_active IP Right Cessation
- 2003-04-10 WO PCT/US2003/011261 patent/WO2003089480A1/en not_active Ceased
- 2003-04-10 CN CNB038014459A patent/CN100564401C/zh not_active Expired - Lifetime
- 2003-04-10 JP JP2003586199A patent/JP4261372B2/ja not_active Expired - Lifetime
- 2003-04-10 AU AU2003221902A patent/AU2003221902A1/en not_active Abandoned
- 2003-04-10 EP EP03718361A patent/EP1497339B1/en not_active Expired - Lifetime
- 2003-04-16 AR ARP030101339A patent/AR039433A1/es not_active Application Discontinuation
- 2003-04-17 TW TW092108925A patent/TWI250998B/zh not_active IP Right Cessation
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4943616A (en) | Living cationic polymerization process | |
| JP6042340B2 (ja) | 末端二重結合含有ポリオレフィンとその製造方法 | |
| US3725505A (en) | Pyrene containing polymers prepared by anionic polymerization | |
| Farcet et al. | Polystyrene‐block‐poly (butyl acrylate) and polystyrene‐block‐poly [(butyl acrylate)‐co‐styrene] block copolymers prepared via controlled free‐radical miniemulsion polymerization using degenerative iodine transfer | |
| CA2098672C (en) | Butyl rubber with a bimodal molecular weight distribution | |
| MXPA01006720A (es) | Copolimeros de tri-bloque que incorporan un bloque medio de copolimero de estireno/iso-olefina. | |
| JP2005535737A5 (enExample) | ||
| JP2005526885A5 (enExample) | ||
| JPH08509779A (ja) | ビニル芳香族ポリマーおよびゴムを含む組成物およびその製法 | |
| JPH01284515A (ja) | ブタジエンから耐衝撃性芳香族ビニル樹脂を直接製造する方法 | |
| CA1336281C (en) | Polymerization process and catalyst system therefor | |
| TWI397538B (zh) | 高耐熱性壓克力共聚合物及其製備方法 | |
| CN109705251B (zh) | 具有交联结构的微球状离聚物及其制备方法和应用 | |
| US4908421A (en) | Production of terminally functional polymer by cationic polymerization | |
| Grishin et al. | Radical polymerization of acrylonitrile under the action of catalytic systems based on zero-valent copper | |
| RU2537002C1 (ru) | Способ получения триблоксополимеров метакриловых мономеров | |
| JPH05117306A (ja) | 高重合度ポリアクリル酸の製造方法 | |
| Sinniger et al. | Synthesis of poly (methyl methacrylate)-b-polyethylene (PMMA-b-PE) block copolymers via conventional emulsion polymerization | |
| Wu et al. | Synthesis of heteroarm star-shaped (polystyrene) n–[poly (ethyl acrylate)] m via atom transfer radical polymerization | |
| Bicu et al. | Allylic polymers from resin acids. Monomer synthesis at high temperature | |
| JP3490092B2 (ja) | ポリマーの凝固仕上げ方法 | |
| JP6829567B2 (ja) | 揮発成分を除去した重合体を製造する方法 | |
| JPH0632808A (ja) | 懸濁重合法 | |
| CA2424718A1 (en) | Process for devolatilizing an acrylic resin, process for preparing a powder coating composition and composition capable of being formed into a powder coating composition | |
| JP3313652B2 (ja) | 水溶性重合体の製法 |