JP2008517142A5 - - Google Patents
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- Publication number
- JP2008517142A5 JP2008517142A5 JP2007537934A JP2007537934A JP2008517142A5 JP 2008517142 A5 JP2008517142 A5 JP 2008517142A5 JP 2007537934 A JP2007537934 A JP 2007537934A JP 2007537934 A JP2007537934 A JP 2007537934A JP 2008517142 A5 JP2008517142 A5 JP 2008517142A5
- Authority
- JP
- Japan
- Prior art keywords
- reaction product
- initial reaction
- item
- acrylate
- unreacted polymerizable
- 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
- 239000007795 chemical reaction product Substances 0.000 claims description 32
- 239000000376 reactant Substances 0.000 claims description 15
- 229920000642 polymer Polymers 0.000 claims description 13
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 239000003638 chemical reducing agent Substances 0.000 claims description 5
- 238000010528 free radical solution polymerization reaction Methods 0.000 claims description 5
- 239000007800 oxidant agent Substances 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims 1
- 238000000034 method Methods 0.000 description 16
- 239000000463 material Substances 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical group CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 4
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical group NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- -1 alkyl hydroperoxide Chemical compound 0.000 description 3
- 230000001376 precipitating effect Effects 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 125000005250 alkyl acrylate group Chemical group 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- GCRIIVPDNWHODP-UHFFFAOYSA-N 2-(2-oxopyrrolidin-1-yl)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCN1CCCC1=O GCRIIVPDNWHODP-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- XRXANEMIFVRKLN-UHFFFAOYSA-N 2-hydroperoxy-2-methylbutane Chemical compound CCC(C)(C)OO XRXANEMIFVRKLN-UHFFFAOYSA-N 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
- NCTBYWFEJFTVEL-UHFFFAOYSA-N 2-methylbutyl prop-2-enoate Chemical compound CCC(C)COC(=O)C=C NCTBYWFEJFTVEL-UHFFFAOYSA-N 0.000 description 1
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
- CYUZOYPRAQASLN-UHFFFAOYSA-N 3-prop-2-enoyloxypropanoic acid Chemical compound OC(=O)CCOC(=O)C=C CYUZOYPRAQASLN-UHFFFAOYSA-N 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- DKCWBFMZNUOFEM-UHFFFAOYSA-L oxovanadium(2+);sulfate;hydrate Chemical compound O.[V+2]=O.[O-]S([O-])(=O)=O DKCWBFMZNUOFEM-UHFFFAOYSA-L 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US62008304P | 2004-10-19 | 2004-10-19 | |
| PCT/US2005/036924 WO2006044590A1 (en) | 2004-10-19 | 2005-10-13 | Method for the manufacture of pressure sensitive adhesives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008517142A JP2008517142A (ja) | 2008-05-22 |
| JP2008517142A5 true JP2008517142A5 (enExample) | 2008-10-02 |
Family
ID=35601758
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007537934A Pending JP2008517142A (ja) | 2004-10-19 | 2005-10-13 | 感圧接着剤の製造方法 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8039528B2 (enExample) |
| EP (1) | EP1802665B1 (enExample) |
| JP (1) | JP2008517142A (enExample) |
| CN (1) | CN101044169A (enExample) |
| AT (1) | ATE438664T1 (enExample) |
| CA (1) | CA2583963C (enExample) |
| DE (1) | DE602005015877D1 (enExample) |
| WO (1) | WO2006044590A1 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0700671D0 (en) | 2006-12-15 | 2007-02-21 | Innovision Res & Tech Plc | Nfc communicator and method of data communication |
| KR101678714B1 (ko) * | 2009-06-18 | 2016-11-23 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 고온 용융 감압 접착제의 제조 방법 |
| US8221994B2 (en) * | 2009-09-30 | 2012-07-17 | Cilag Gmbh International | Adhesive composition for use in an immunosensor |
| EP3517105B8 (en) * | 2010-07-21 | 2021-06-23 | Kindeva Drug Delivery L.P. | Transdermal adhesive compositions, devices, and methods |
| CN102175799B (zh) * | 2010-12-28 | 2014-11-19 | 西安航天三沃化学有限公司 | 气相色谱法测试丙烯酸酯压敏胶残留单体含量的方法 |
| CN104569248A (zh) * | 2014-12-08 | 2015-04-29 | 江苏泰洁检测技术有限公司 | 一种工作场所丙烯酸酯类中丙烯酸甲酯浓度测定方法 |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5228585A (en) | 1975-08-29 | 1977-03-03 | Toagosei Chem Ind Co Ltd | Process for the preparation of acrylamide containing little unreacted monomer |
| JPS5488985A (en) * | 1977-12-27 | 1979-07-14 | Toyo Ink Mfg Co Ltd | Preparation of aqueous dispersion of acrylic resin |
| AU529858B2 (en) * | 1979-05-24 | 1983-06-23 | Maltini Pty. Ltd. | Removal of free monomer for alkyl acrylate polymers |
| US4834979A (en) * | 1981-06-29 | 1989-05-30 | Alza Corporation | Medical bandage for administering beneficial drug |
| US4443568A (en) * | 1981-10-26 | 1984-04-17 | Scm Corporation | Polymerization process and product |
| US4751087A (en) * | 1985-04-19 | 1988-06-14 | Riker Laboratories, Inc. | Transdermal nitroglycerin delivery system |
| US4693776A (en) * | 1985-05-16 | 1987-09-15 | Minnesota Mining And Manufacturing Company | Macromer reinforced pressure sensitive skin adhesive |
| CA1299319C (en) * | 1986-10-23 | 1992-04-21 | Izumi Saitoh | Acrylic copolymer and skin protective |
| US4737577A (en) * | 1986-12-31 | 1988-04-12 | Minnesota Mining And Manufacturing Company | Method for removing monomer from an acrylate adhesive by reaction with a scavenger monomer |
| DE3724709A1 (de) * | 1987-07-25 | 1989-02-02 | Stockhausen Chem Fab Gmbh | Verfahren zur herstellung von polymerisaten mit niedrigem restmonomergehalt |
| US5656286A (en) * | 1988-03-04 | 1997-08-12 | Noven Pharmaceuticals, Inc. | Solubility parameter based drug delivery system and method for altering drug saturation concentration |
| DE3834734A1 (de) * | 1988-10-12 | 1990-04-19 | Basf Ag | Verfahren zur herstellung von polymerisaten aus olefinisch ungesaettigten monomeren |
| US5252334A (en) * | 1989-09-08 | 1993-10-12 | Cygnus Therapeutic Systems | Solid matrix system for transdermal drug delivery |
| EP0576128A1 (en) * | 1992-06-23 | 1993-12-29 | Rohm And Haas Company | Polymer blend containing an acid-rich polymer |
| JPH09118867A (ja) * | 1995-10-25 | 1997-05-06 | Sumitomo Chem Co Ltd | 接着剤 |
| US5641834A (en) * | 1995-12-11 | 1997-06-24 | Lord Corporation | Modified polyalkadiene-containing compositions |
| US6028155A (en) * | 1997-05-21 | 2000-02-22 | Eastman Chemical Company | Surfactant-containing acetoacetoxy-functional and enamine-functional polymers |
| US6365178B1 (en) * | 1996-09-06 | 2002-04-02 | Watson Pharmaceuticals, Inc. | Method of making pressure sensitive adhesive matrix patches for transdermal drug delivery using hydrophilic salts of drugs and hydrophobic pressure sensitive adhesive dispersions |
| ATE229817T1 (de) * | 1996-10-24 | 2003-01-15 | Alza Corp | Penetrationsfördernde substanzen für die transdermale verabreichung von wirkstoffen, vorrichtungen und verfahren zur herstellung |
| JP2000053719A (ja) * | 1998-08-11 | 2000-02-22 | Toagosei Co Ltd | アクリル系重合体の製造方法 |
| WO2001044400A1 (en) | 1999-12-14 | 2001-06-21 | Brady Worldwide, Inc. | Low outgassing pressure sensitive adhesives and method of use |
| DE10042543A1 (de) | 2000-08-30 | 2002-03-14 | Tesa Ag | Verfahren zur Verringerung des Restinitiatorgehaltes in Acrylathaftklebemassen |
| US20020065381A1 (en) | 2000-10-17 | 2002-05-30 | Lorah Dennis Paul | Redox process for preparing emulsion polymer having low formaldehyde content |
| US6696519B2 (en) * | 2000-10-17 | 2004-02-24 | Rohm And Haas Company | Redox process for preparing emulsion polymer having low residual monomer content |
| JP2004026855A (ja) * | 2002-06-21 | 2004-01-29 | Mitsubishi Chemicals Corp | 重合方法 |
| DE10241481B4 (de) | 2002-09-07 | 2006-07-06 | Celanese Emulsions Gmbh | Verfahren zum Herstellen von wässrigen Polymerdispersionen mit sehr niedrigen Restmonomergehalten und deren Verwendung |
-
2005
- 2005-10-13 EP EP05810291A patent/EP1802665B1/en not_active Expired - Lifetime
- 2005-10-13 CN CNA2005800358909A patent/CN101044169A/zh active Pending
- 2005-10-13 DE DE602005015877T patent/DE602005015877D1/de not_active Expired - Lifetime
- 2005-10-13 JP JP2007537934A patent/JP2008517142A/ja active Pending
- 2005-10-13 AT AT05810291T patent/ATE438664T1/de not_active IP Right Cessation
- 2005-10-13 CA CA2583963A patent/CA2583963C/en not_active Expired - Lifetime
- 2005-10-13 US US11/576,931 patent/US8039528B2/en active Active
- 2005-10-13 WO PCT/US2005/036924 patent/WO2006044590A1/en not_active Ceased
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