JP2520863B2 - 耐熱性に優れた共役ジエンとメチルメタクリレ―トとの熱可塑性弾性ブロック共重合体の製造方法 - Google Patents
耐熱性に優れた共役ジエンとメチルメタクリレ―トとの熱可塑性弾性ブロック共重合体の製造方法Info
- Publication number
- JP2520863B2 JP2520863B2 JP5321278A JP32127893A JP2520863B2 JP 2520863 B2 JP2520863 B2 JP 2520863B2 JP 5321278 A JP5321278 A JP 5321278A JP 32127893 A JP32127893 A JP 32127893A JP 2520863 B2 JP2520863 B2 JP 2520863B2
- Authority
- JP
- Japan
- Prior art keywords
- polymerization
- conjugated diene
- lithium
- copolymer
- methyl methacrylate
- 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.)
- Expired - Fee Related
Links
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 title claims abstract description 23
- 150000001993 dienes Chemical class 0.000 title claims abstract description 19
- 229920001169 thermoplastic Polymers 0.000 title claims abstract description 4
- 239000004416 thermosoftening plastic Substances 0.000 title claims abstract description 4
- 229920001400 block copolymer Polymers 0.000 title description 7
- 238000004519 manufacturing process Methods 0.000 title description 5
- 229920001577 copolymer Polymers 0.000 claims abstract description 28
- 238000000034 method Methods 0.000 claims abstract description 23
- 239000000178 monomer Substances 0.000 claims abstract description 20
- 239000003999 initiator Substances 0.000 claims abstract description 17
- 239000002904 solvent Substances 0.000 claims abstract description 9
- 239000003446 ligand Substances 0.000 claims abstract description 7
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 4
- 150000001340 alkali metals Chemical class 0.000 claims abstract description 4
- 125000000129 anionic group Chemical group 0.000 claims abstract description 4
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims abstract description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 27
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 22
- 239000004926 polymethyl methacrylate Substances 0.000 claims description 22
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 19
- 238000006116 polymerization reaction Methods 0.000 claims description 18
- 230000009477 glass transition Effects 0.000 claims description 10
- 239000004793 Polystyrene Substances 0.000 claims description 8
- 229920002223 polystyrene Polymers 0.000 claims description 8
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 7
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 claims description 7
- 238000010539 anionic addition polymerization reaction Methods 0.000 claims description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- -1 p-isopropenylphenyl Chemical group 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- QGOZVRUBHUDZFY-UHFFFAOYSA-N lithium;1-(2-methoxyethoxy)ethanolate Chemical compound [Li+].COCCOC(C)[O-] QGOZVRUBHUDZFY-UHFFFAOYSA-N 0.000 claims description 5
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 claims description 4
- WGOPGODQLGJZGL-UHFFFAOYSA-N lithium;butane Chemical compound [Li+].CC[CH-]C WGOPGODQLGJZGL-UHFFFAOYSA-N 0.000 claims description 4
- 239000012454 non-polar solvent Substances 0.000 claims description 4
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical group C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 claims description 4
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 3
- QHHUCCOZVUZUSR-UHFFFAOYSA-N C=1C=CC=CC=1C([Na])C1=CC=CC=C1 Chemical compound C=1C=CC=CC=1C([Na])C1=CC=CC=C1 QHHUCCOZVUZUSR-UHFFFAOYSA-N 0.000 claims description 2
- IRDQNLLVRXMERV-UHFFFAOYSA-N CCCC[Na] Chemical compound CCCC[Na] IRDQNLLVRXMERV-UHFFFAOYSA-N 0.000 claims description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- YCJDNDZTXMGKLM-UHFFFAOYSA-N lithium;1-methoxyethanolate Chemical compound [Li+].COC(C)[O-] YCJDNDZTXMGKLM-UHFFFAOYSA-N 0.000 claims description 2
- UUQLCJCZFWUWHH-UHFFFAOYSA-N lithium;1-phenylhexylbenzene Chemical compound [Li+].C=1C=CC=CC=1[C-](CCCCC)C1=CC=CC=C1 UUQLCJCZFWUWHH-UHFFFAOYSA-N 0.000 claims description 2
- XWRJSDBMRJIGSK-UHFFFAOYSA-N lithium;phenylmethylbenzene Chemical compound [Li+].C=1C=CC=CC=1[CH-]C1=CC=CC=C1 XWRJSDBMRJIGSK-UHFFFAOYSA-N 0.000 claims description 2
- 239000004417 polycarbonate Substances 0.000 claims description 2
- 229920000515 polycarbonate Polymers 0.000 claims description 2
- 239000004800 polyvinyl chloride Substances 0.000 claims description 2
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 2
- IRAPFUAOCHNONS-UHFFFAOYSA-N potassium;phenylmethylbenzene Chemical compound [K+].C=1C=CC=CC=1[CH-]C1=CC=CC=C1 IRAPFUAOCHNONS-UHFFFAOYSA-N 0.000 claims description 2
- 239000012429 reaction media Substances 0.000 claims description 2
- SXRLRTAOSJEJCG-UHFFFAOYSA-N C=1C=CC=CC=1C(C=1C=CC=CC=1)([Li])CCC([Li])(C=1C=CC=CC=1)C1=CC=CC=C1 Chemical group C=1C=CC=CC=1C(C=1C=CC=CC=1)([Li])CCC([Li])(C=1C=CC=CC=1)C1=CC=CC=C1 SXRLRTAOSJEJCG-UHFFFAOYSA-N 0.000 claims 1
- 229920000642 polymer Polymers 0.000 abstract description 8
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 229920001971 elastomer Polymers 0.000 abstract 1
- 239000000806 elastomer Substances 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- 239000005062 Polybutadiene Substances 0.000 description 7
- 229920002857 polybutadiene Polymers 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 5
- HIACAHMKXQESOV-UHFFFAOYSA-N 1,2-bis(prop-1-en-2-yl)benzene Chemical compound CC(=C)C1=CC=CC=C1C(C)=C HIACAHMKXQESOV-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 229920002725 thermoplastic elastomer Polymers 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 229920000359 diblock copolymer Polymers 0.000 description 3
- 125000004185 ester group Chemical group 0.000 description 3
- 229910052744 lithium Inorganic materials 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 229920000428 triblock copolymer Polymers 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical group [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 230000001588 bifunctional effect Effects 0.000 description 2
- 230000000977 initiatory effect Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000007086 side reaction Methods 0.000 description 2
- SDJHPPZKZZWAKF-UHFFFAOYSA-N 2,3-dimethylbuta-1,3-diene Chemical compound CC(=C)C(C)=C SDJHPPZKZZWAKF-UHFFFAOYSA-N 0.000 description 1
- 229920008712 Copo Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- BZEZSORUWZUMNU-UHFFFAOYSA-N [Li]CCCC[Li] Chemical compound [Li]CCCC[Li] BZEZSORUWZUMNU-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 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
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical class C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 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
- 239000003086 colorant Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- CJSBUWDGPXGFGA-UHFFFAOYSA-N dimethyl-butadiene Natural products CC(C)=CC=C CJSBUWDGPXGFGA-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- URMHJZVLKKDTOJ-UHFFFAOYSA-N lithium;(3-methyl-1-phenylpentyl)benzene Chemical compound [Li+].C=1C=CC=CC=1[C-](CC(C)CC)C1=CC=CC=C1 URMHJZVLKKDTOJ-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229910052700 potassium Chemical group 0.000 description 1
- 239000011591 potassium Chemical group 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Chemical group 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
-
- 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
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/02—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type
- C08F297/026—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type polymerising acrylic acid, methacrylic acid or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J153/00—Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Inorganic Chemistry (AREA)
- Graft Or Block Polymers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9214318 | 1992-11-27 | ||
| FR9214318A FR2698630B1 (fr) | 1992-11-27 | 1992-11-27 | Procédé de préparation de copolymères séquences élastomères thermoplastiques dérivés de diènes conjugués et de méthacrylate de méthyle, à tenue à la chaleur améliorée et produits obtenus. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH06206952A JPH06206952A (ja) | 1994-07-26 |
| JP2520863B2 true JP2520863B2 (ja) | 1996-07-31 |
Family
ID=9435994
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5321278A Expired - Fee Related JP2520863B2 (ja) | 1992-11-27 | 1993-11-26 | 耐熱性に優れた共役ジエンとメチルメタクリレ―トとの熱可塑性弾性ブロック共重合体の製造方法 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US5476904A (enExample) |
| EP (1) | EP0599671B1 (enExample) |
| JP (1) | JP2520863B2 (enExample) |
| KR (1) | KR0133492B1 (enExample) |
| CN (1) | CN1049666C (enExample) |
| AT (1) | ATE131501T1 (enExample) |
| AU (1) | AU5193893A (enExample) |
| CA (1) | CA2110080C (enExample) |
| DE (1) | DE69301022T2 (enExample) |
| ES (1) | ES2080598T3 (enExample) |
| FR (1) | FR2698630B1 (enExample) |
| MX (1) | MX9307450A (enExample) |
| TW (1) | TW269695B (enExample) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2729669A1 (fr) * | 1995-01-20 | 1996-07-26 | Atochem Elf Sa | Procede de preparation de polymeres de (meth) acrylates d'alkyle par polymerisation anionique |
| FR2762604B1 (fr) * | 1997-04-10 | 2001-01-05 | Atochem Elf Sa | Procede et systeme d'amorcage pour la (co)polymerisation anionique de monomeres (meth)acryliques, vinylaromatiques et/ou dieniques |
| US6734256B1 (en) * | 1998-12-29 | 2004-05-11 | 3M Innovative Properties Company | Block copolymer hot-melt processable adhesives, methods of their preparation, and articles therefrom |
| EP1591507A3 (en) * | 1998-12-29 | 2006-01-25 | Minnesota Mining And Manufacturing Company | Block copolymer hot-melt processable adhesives |
| FR2809741B1 (fr) * | 2000-05-31 | 2002-08-16 | Atofina | Materiaux thermodurs a tenue au choc amelioree |
| JP4554836B2 (ja) * | 2001-02-27 | 2010-09-29 | 株式会社クラレ | ゴム組成物 |
| FR2824834B1 (fr) * | 2001-05-18 | 2005-05-13 | Rhodia Elect & Catalysis | Procede de preparation de copolymeres blocs, copolymeres blocs ainsi obtenus et utilisation comme agents compatibilisants |
| JP2003082167A (ja) * | 2001-09-17 | 2003-03-19 | Kuraray Co Ltd | ゴム組成物 |
| JP4659303B2 (ja) * | 2001-09-18 | 2011-03-30 | 株式会社クラレ | ジエン系ゴム組成物 |
| KR20050057666A (ko) * | 2002-10-21 | 2005-06-16 | 아르끄마 | 무정형 매트릭스 및 블록 공중합체를 함유하는 연성의 투명열가소성 조성물 |
| US7951887B2 (en) | 2003-05-30 | 2011-05-31 | Nippon Soda Co., Ltd. | Process for producing a polymer |
| CN1312197C (zh) * | 2004-07-15 | 2007-04-25 | 复旦大学 | 改性软硬多嵌段共轭聚合物及其制备方法 |
| CN1315888C (zh) * | 2004-09-24 | 2007-05-16 | 奇美实业股份有限公司 | 以甲基丙烯酸甲酯为主成分的聚合物 |
| US8318459B2 (en) | 2011-02-17 | 2012-11-27 | Purecircle Usa | Glucosyl stevia composition |
| US9392799B2 (en) | 2011-02-17 | 2016-07-19 | Purecircle Sdn Bhd | Glucosyl stevia composition |
| US9107436B2 (en) | 2011-02-17 | 2015-08-18 | Purecircle Sdn Bhd | Glucosylated steviol glycoside as a flavor modifier |
| US9386797B2 (en) | 2011-02-17 | 2016-07-12 | Purecircle Sdn Bhd | Glucosyl stevia composition |
| US8257948B1 (en) | 2011-02-17 | 2012-09-04 | Purecircle Usa | Method of preparing alpha-glucosyl Stevia composition |
| EP2065442B1 (en) * | 2006-09-15 | 2013-03-27 | Kuraray Co., Ltd. | Methacrylic resin composition, resin modifier, and molded body |
| KR101605906B1 (ko) * | 2006-12-07 | 2016-03-23 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 블록 공중합체와 아크릴 접착제의 블렌드 |
| US8417312B2 (en) | 2007-10-25 | 2013-04-09 | Dexcom, Inc. | Systems and methods for processing sensor data |
| JP5186415B2 (ja) * | 2008-02-28 | 2013-04-17 | 株式会社クラレ | メタクリル系樹脂フィルム |
| JP5186416B2 (ja) * | 2008-02-28 | 2013-04-17 | 株式会社クラレ | 表示窓保護板 |
| JP5227847B2 (ja) * | 2008-02-29 | 2013-07-03 | 株式会社クラレ | メタクリル系樹脂組成物 |
| JP5317768B2 (ja) * | 2008-03-03 | 2013-10-16 | 株式会社クラレ | メタクリル系重合体組成物 |
| JP5237858B2 (ja) * | 2008-03-04 | 2013-07-17 | 株式会社クラレ | メタクリル系樹脂用改質剤 |
| EP2544538B1 (en) | 2010-03-12 | 2022-06-15 | PureCircle USA Inc. | High-purity steviol glycosides |
| US10696706B2 (en) | 2010-03-12 | 2020-06-30 | Purecircle Usa Inc. | Methods of preparing steviol glycosides and uses of the same |
| IT1402007B1 (it) * | 2010-10-06 | 2013-08-28 | Polimeri Europa Spa | Procedimento per la preparazione di polimeri dienici o copolimeri statistici vinilarene-diene |
| WO2012082587A2 (en) | 2010-12-13 | 2012-06-21 | Purecircle Usa | Highly soluble rebaudioside d |
| US9510611B2 (en) | 2010-12-13 | 2016-12-06 | Purecircle Sdn Bhd | Stevia composition to improve sweetness and flavor profile |
| US10362797B2 (en) | 2011-02-10 | 2019-07-30 | Purecircle Sdn Bhd | Stevia composition |
| US9474296B2 (en) | 2011-02-17 | 2016-10-25 | Purecircle Sdn Bhd | Glucosyl stevia composition |
| BR112014028819A2 (pt) | 2012-05-22 | 2017-07-25 | Purecircle Sdn Bhd | glicosídeos de esteviol de pureza elevada |
| TWI609912B (zh) * | 2012-06-29 | 2018-01-01 | Kuraray Co., Ltd. | （甲基）丙烯酸樹脂組成物之製造方法、光學構件之製造方法及偏光板之製造方法 |
| FR3029921B1 (fr) * | 2014-12-16 | 2018-06-29 | Arkema France | Procede de controle de la synthese d'un copolymere a blocs contenant au moins un bloc apolaire et au moins un bloc polaire et utilisation d'un tel copolymere a blocs dans des applications de nano-lithographie par auto-assemblage direct. |
| CN110799553B (zh) | 2017-07-14 | 2022-08-16 | 株式会社Lg化学 | 用于生产聚合物的方法 |
| CN110540610B (zh) * | 2018-05-28 | 2021-08-20 | 浙江省化工研究院有限公司 | 一种（甲基）丙烯酸酯类聚合物及其制备方法 |
| CN112480292A (zh) * | 2020-11-30 | 2021-03-12 | 沈阳化工研究院有限公司 | 一种丙烯酸烷基酯类极性单体阴离子聚合制备高分子聚合物的方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB138069A (en) * | 1919-01-11 | 1920-09-02 | Erwin Walter | Improvements in or relating to plaiting machines |
| GB138073A (en) * | 1920-01-17 | 1921-07-18 | George Macnair | Improvements in multiple pulley hoisting gears |
| DE1227235B (de) * | 1962-10-08 | 1966-10-20 | Ceskoslovenska Akademie Ved | Verfahren zur Herstellung von Polymeren oder Copolymeren durch anionische Polymerisation |
| US3285894A (en) * | 1963-10-11 | 1966-11-15 | Ceskoslovenska Akademie Ved | Polymerization initiators comprising alkali metal alcoholates |
| US3439064A (en) * | 1965-01-11 | 1969-04-15 | Exxon Research Engineering Co | Laminating varnish consisting of low viscosity,curable block copolymer |
| FR2387255A1 (fr) * | 1977-04-15 | 1978-11-10 | Anvar | Procede de preparation de copolymeres trisequences ou en etoile |
| FR2514011A1 (fr) * | 1981-10-02 | 1983-04-08 | Philippe Teyssie | Copolymeres sequences derives de dienes conjugues ou d'hydrocarbures aromatiques vinyl-substitues et d'esters acryliques et procede pour leur fabrication |
| ATE121104T1 (de) * | 1989-06-05 | 1995-04-15 | Atochem Elf Sa | Verfahren und anionische polymerisationskatalysatoren für acrylatmonomere. |
-
1992
- 1992-11-27 FR FR9214318A patent/FR2698630B1/fr not_active Expired - Fee Related
-
1993
- 1993-10-01 DE DE69301022T patent/DE69301022T2/de not_active Expired - Fee Related
- 1993-10-01 ES ES93402418T patent/ES2080598T3/es not_active Expired - Lifetime
- 1993-10-01 EP EP93402418A patent/EP0599671B1/fr not_active Expired - Lifetime
- 1993-10-01 AT AT93402418T patent/ATE131501T1/de not_active IP Right Cessation
- 1993-11-26 AU AU51938/93A patent/AU5193893A/en not_active Abandoned
- 1993-11-26 KR KR1019930025372A patent/KR0133492B1/ko not_active Expired - Fee Related
- 1993-11-26 CA CA002110080A patent/CA2110080C/fr not_active Expired - Fee Related
- 1993-11-26 JP JP5321278A patent/JP2520863B2/ja not_active Expired - Fee Related
- 1993-11-26 MX MX9307450A patent/MX9307450A/es unknown
- 1993-11-27 CN CN93120665A patent/CN1049666C/zh not_active Expired - Fee Related
- 1993-11-29 US US08/158,395 patent/US5476904A/en not_active Expired - Fee Related
-
1994
- 1994-02-03 TW TW083100901A patent/TW269695B/zh active
Also Published As
| Publication number | Publication date |
|---|---|
| FR2698630A1 (fr) | 1994-06-03 |
| TW269695B (enExample) | 1996-02-01 |
| MX9307450A (es) | 1994-08-31 |
| KR0133492B1 (ko) | 1998-04-21 |
| CA2110080A1 (fr) | 1994-05-28 |
| EP0599671B1 (fr) | 1995-12-13 |
| CN1049666C (zh) | 2000-02-23 |
| JPH06206952A (ja) | 1994-07-26 |
| KR940011511A (ko) | 1994-06-21 |
| AU5193893A (en) | 1994-06-09 |
| CN1089957A (zh) | 1994-07-27 |
| DE69301022D1 (de) | 1996-01-25 |
| US5476904A (en) | 1995-12-19 |
| DE69301022T2 (de) | 1996-09-05 |
| CA2110080C (fr) | 2000-02-15 |
| FR2698630B1 (fr) | 1995-01-06 |
| ATE131501T1 (de) | 1995-12-15 |
| ES2080598T3 (es) | 1996-02-01 |
| EP0599671A1 (fr) | 1994-06-01 |
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