ES2802457T3 - (Co)polímero aromático de vinilo reforzado con caucho, que tiene un equilibrio óptimo de propiedades fisico-mecánicas y un alto brillo - Google Patents
(Co)polímero aromático de vinilo reforzado con caucho, que tiene un equilibrio óptimo de propiedades fisico-mecánicas y un alto brillo Download PDFInfo
- Publication number
- ES2802457T3 ES2802457T3 ES09771310T ES09771310T ES2802457T3 ES 2802457 T3 ES2802457 T3 ES 2802457T3 ES 09771310 T ES09771310 T ES 09771310T ES 09771310 T ES09771310 T ES 09771310T ES 2802457 T3 ES2802457 T3 ES 2802457T3
- Authority
- ES
- Spain
- Prior art keywords
- rubber
- weight
- vinyl aromatic
- solution
- polymer
- 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.)
- Active
Links
- 229920002554 vinyl polymer Polymers 0.000 title claims abstract description 35
- 229920001577 copolymer Polymers 0.000 title claims abstract description 31
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 74
- 229920001971 elastomer Polymers 0.000 claims abstract description 52
- 239000005060 rubber Substances 0.000 claims abstract description 50
- 239000005062 Polybutadiene Substances 0.000 claims abstract description 37
- 229920003244 diene elastomer Polymers 0.000 claims abstract description 37
- 229920002857 polybutadiene Polymers 0.000 claims abstract description 37
- 239000000203 mixture Substances 0.000 claims abstract description 30
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 14
- 239000011159 matrix material Substances 0.000 claims abstract description 13
- 239000000243 solution Substances 0.000 claims description 52
- 239000000178 monomer Substances 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 5
- 238000012662 bulk polymerization Methods 0.000 claims description 2
- 239000000839 emulsion Substances 0.000 claims description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 claims 1
- 230000000379 polymerizing effect Effects 0.000 claims 1
- 238000010557 suspension polymerization reaction Methods 0.000 claims 1
- 229920000642 polymer Polymers 0.000 description 35
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 23
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 20
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 20
- 239000002904 solvent Substances 0.000 description 15
- 239000003963 antioxidant agent Substances 0.000 description 13
- 239000003999 initiator Substances 0.000 description 13
- 239000002245 particle Substances 0.000 description 13
- 230000003078 antioxidant effect Effects 0.000 description 12
- HSLFISVKRDQEBY-UHFFFAOYSA-N 1,1-bis(tert-butylperoxy)cyclohexane Chemical compound CC(C)(C)OOC1(OOC(C)(C)C)CCCCC1 HSLFISVKRDQEBY-UHFFFAOYSA-N 0.000 description 10
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 10
- 239000012467 final product Substances 0.000 description 10
- 238000002156 mixing Methods 0.000 description 10
- 238000003756 stirring Methods 0.000 description 10
- 238000012546 transfer Methods 0.000 description 10
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000007796 conventional method Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- 239000003643 water by type Substances 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- 238000012512 characterization method Methods 0.000 description 3
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical group C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 3
- 239000007822 coupling agent Substances 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 2
- 239000002879 Lewis base Substances 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-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
- 239000004793 Polystyrene Substances 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 229920005669 high impact polystyrene Polymers 0.000 description 2
- 239000004797 high-impact polystyrene Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 150000007527 lewis bases Chemical class 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- -1 lithium alcohols Chemical class 0.000 description 2
- 239000005055 methyl trichlorosilane Substances 0.000 description 2
- JLUFWMXJHAVVNN-UHFFFAOYSA-N methyltrichlorosilane Chemical group C[Si](Cl)(Cl)Cl JLUFWMXJHAVVNN-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000005049 silicon tetrachloride Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- SVHAMPNLOLKSFU-UHFFFAOYSA-N 1,2,2-trichloroethenylbenzene Chemical compound ClC(Cl)=C(Cl)C1=CC=CC=C1 SVHAMPNLOLKSFU-UHFFFAOYSA-N 0.000 description 1
- AUHKVLIZXLBQSR-UHFFFAOYSA-N 1,2-dichloro-3-(1,2,2-trichloroethenyl)benzene Chemical compound ClC(Cl)=C(Cl)C1=CC=CC(Cl)=C1Cl AUHKVLIZXLBQSR-UHFFFAOYSA-N 0.000 description 1
- XPXMCUKPGZUFGR-UHFFFAOYSA-N 1-chloro-2-(1,2,2-trichloroethenyl)benzene Chemical compound ClC(Cl)=C(Cl)C1=CC=CC=C1Cl XPXMCUKPGZUFGR-UHFFFAOYSA-N 0.000 description 1
- CTHJQRHPNQEPAB-UHFFFAOYSA-N 2-methoxyethenylbenzene Chemical compound COC=CC1=CC=CC=C1 CTHJQRHPNQEPAB-UHFFFAOYSA-N 0.000 description 1
- BTOVVHWKPVSLBI-UHFFFAOYSA-N 2-methylprop-1-enylbenzene Chemical compound CC(C)=CC1=CC=CC=C1 BTOVVHWKPVSLBI-UHFFFAOYSA-N 0.000 description 1
- FMFHUEMLVAIBFI-UHFFFAOYSA-N 2-phenylethenyl acetate Chemical compound CC(=O)OC=CC1=CC=CC=C1 FMFHUEMLVAIBFI-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- YMOONIIMQBGTDU-VOTSOKGWSA-N [(e)-2-bromoethenyl]benzene Chemical compound Br\C=C\C1=CC=CC=C1 YMOONIIMQBGTDU-VOTSOKGWSA-N 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- MPMBRWOOISTHJV-UHFFFAOYSA-N but-1-enylbenzene Chemical compound CCC=CC1=CC=CC=C1 MPMBRWOOISTHJV-UHFFFAOYSA-N 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-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
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000011258 core-shell material Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- MYRTYDVEIRVNKP-UHFFFAOYSA-N divinylbenzene Substances C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- KETWBQOXTBGBBN-UHFFFAOYSA-N hex-1-enylbenzene Chemical compound CCCCC=CC1=CC=CC=C1 KETWBQOXTBGBBN-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- WGOPGODQLGJZGL-UHFFFAOYSA-N lithium;butane Chemical compound [Li+].CC[CH-]C WGOPGODQLGJZGL-UHFFFAOYSA-N 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- VYMDGNCVAMGZFE-UHFFFAOYSA-N phenylbutazonum Chemical compound O=C1C(CCCC)C(=O)N(C=2C=CC=CC=2)N1C1=CC=CC=C1 VYMDGNCVAMGZFE-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229920006132 styrene block copolymer Polymers 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 238000004627 transmission electron microscopy Methods 0.000 description 1
- 239000005051 trimethylchlorosilane Substances 0.000 description 1
- 238000011179 visual inspection Methods 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
- C08F279/00—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
- C08F279/02—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes
-
- 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
- C08F279/00—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00
- C08F279/02—Macromolecular compounds obtained by polymerising monomers on to polymers of monomers having two or more carbon-to-carbon double bonds as defined in group C08F36/00 on to polymers of conjugated dienes
- C08F279/04—Vinyl aromatic monomers and nitriles as the only monomers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/04—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to rubbers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L55/00—Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
- C08L55/02—ABS [Acrylonitrile-Butadiene-Styrene] polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Graft Or Block Polymers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ITMI2008A002224A IT1393666B1 (it) | 2008-12-16 | 2008-12-16 | (co)polimero vinilaromatico rinforzato con gomma avente un ottimo bilancio di proprieta' fisico-meccaniche ed una elevata lucentezza |
| PCT/EP2009/008861 WO2010069515A1 (en) | 2008-12-16 | 2009-12-10 | Rubber-reinforced vinyl aromatic (co)polymer, having an optimum balance of physico-mechanical properties and a high gloss |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2802457T3 true ES2802457T3 (es) | 2021-01-19 |
Family
ID=41203793
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES09771310T Active ES2802457T3 (es) | 2008-12-16 | 2009-12-10 | (Co)polímero aromático de vinilo reforzado con caucho, que tiene un equilibrio óptimo de propiedades fisico-mecánicas y un alto brillo |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20120289660A1 (enExample) |
| EP (1) | EP2358773B1 (enExample) |
| JP (1) | JP5607065B2 (enExample) |
| CN (2) | CN103709332A (enExample) |
| BR (1) | BRPI0923456B1 (enExample) |
| ES (1) | ES2802457T3 (enExample) |
| HU (1) | HUE050825T2 (enExample) |
| IT (1) | IT1393666B1 (enExample) |
| MX (1) | MX2011006484A (enExample) |
| PL (1) | PL2358773T3 (enExample) |
| PT (1) | PT2358773T (enExample) |
| RU (1) | RU2506278C2 (enExample) |
| SI (1) | SI2358773T1 (enExample) |
| WO (1) | WO2010069515A1 (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY180377A (en) * | 2013-09-17 | 2020-11-28 | Ube Industries | Rubber composition and styrene resin composition using the same |
| CN105860406B (zh) * | 2015-01-20 | 2018-05-11 | 中国石油化工股份有限公司 | 一种烯烃聚合物及其制备方法和应用 |
| CN105860407B (zh) * | 2015-01-20 | 2018-05-11 | 中国石油化工股份有限公司 | 一种烯烃聚合物及其制备方法和应用 |
| CN105219012B (zh) * | 2015-11-09 | 2017-12-01 | 沈阳化工大学 | 一种接枝改性abs抗静电材料及其制备方法 |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1595203A1 (de) * | 1963-08-14 | 1970-04-16 | Rexall Drug Chemical | Pfropfpolymerisationsverfahren |
| US3309422A (en) * | 1963-09-03 | 1967-03-14 | Rexall Drug Chemical | Process for preparing interpolymers of styrene and rubbery diolefin polymers |
| US3487127A (en) * | 1965-12-13 | 1969-12-30 | Dart Ind Inc | Rubber-modified resinous polymers prepared in the presence of a polyphenylene oxide |
| NL154530B (nl) * | 1967-04-20 | 1977-09-15 | Rexall Drug Chemical | Werkwijze voor de bereiding van met rubber gemodificeerde polymeren. |
| US4183877A (en) * | 1975-05-12 | 1980-01-15 | Asahi Kasei Kogyo Kabushiki Kaisha | High-impact polystyrene composition and production thereof |
| US4524180A (en) * | 1982-05-21 | 1985-06-18 | The Dow Chemical Company | Rubber-modified, impact-resistant polymeric compositions |
| JPS60181112A (ja) * | 1984-02-28 | 1985-09-14 | Sumitomo Chem Co Ltd | ポリスチレンの製造方法 |
| JP2584211B2 (ja) * | 1986-06-30 | 1997-02-26 | 日本エラストマ−株式会社 | 耐衝撃性スチレン系樹脂組成物 |
| NL8700208A (nl) * | 1987-01-28 | 1988-08-16 | Dow Chemical Nederland | Verbeterde met rubber versterkte monovinylideen-aromatische polymeerharsen en een werkwijze voor de bereiding daarvan. |
| JP2802637B2 (ja) * | 1989-03-03 | 1998-09-24 | 日本エラストマー株式会社 | 物性バランスの優れた耐衝撃性スチレン系樹脂及びその製造方法 |
| GB8918157D0 (en) * | 1989-08-09 | 1989-09-20 | Dow Benelux | A process for the preparation of rubber-reinforced monovinylidene aromatic polymers |
| JPH05194676A (ja) * | 1991-10-24 | 1993-08-03 | Nippon Steel Chem Co Ltd | ゴム変性芳香族ビニル系共重合体樹脂及びその製造方法 |
| JPH05255458A (ja) * | 1991-11-22 | 1993-10-05 | Nippon Steel Chem Co Ltd | ゴム変性芳香族ビニル系共重合体樹脂及びその製造方法 |
| JPH05247149A (ja) * | 1991-12-28 | 1993-09-24 | Nippon Steel Chem Co Ltd | ゴム変性芳香族ビニル系共重合体樹脂及びその製造方法 |
| JPH06166729A (ja) * | 1992-09-30 | 1994-06-14 | Nippon Steel Chem Co Ltd | ゴム変性芳香族ビニル系共重合体樹脂及びその製造方法 |
| IT1274361B (it) * | 1995-02-16 | 1997-07-17 | Enichem Spa | Procedimento per la preparazione di copolimeri vinilaromatici rinforzati con gomma |
| IT1284599B1 (it) * | 1996-09-27 | 1998-05-21 | Enichem Spa | Procedimento per la preparazione di polimeri vinilaromatici rinforzati con gomma |
| US6306962B1 (en) * | 1999-09-30 | 2001-10-23 | The Dow Chemical Company | Flow carbonate polymer blends |
| WO2003011928A1 (en) * | 2001-08-02 | 2003-02-13 | Dow Global Technologies Inc. | Monovinylidene aromatic polymers based on highly linear high molecular weight polybutadiene rubbers and a process for their preparation |
| CA2515038A1 (en) * | 2003-02-05 | 2004-08-26 | Dow Global Technologies Inc. | High gloss rubber modified monovinylidene aromatic polymers produced by a mass polymerization process |
| ITMI20031420A1 (it) * | 2003-07-11 | 2005-01-12 | Polimeri Europa Spa | Polimeri vinilaromatici rinforzati con gomma |
| ITMI20040752A1 (it) * | 2004-04-16 | 2004-07-16 | Polimeri Europa Spa | Procedimento per la preparazione di co polimeri vinilaromatici aggraffati su elastometro in modo controllato |
| ITMI20042401A1 (it) * | 2004-12-16 | 2005-03-16 | Polimeri Europa Spa | Procedimento per la preparazione di co-polimeri vinilaromatici antiurto aggraffati su elastomero |
| CN101932652B (zh) * | 2006-07-27 | 2012-10-03 | 陶氏环球技术有限责任公司 | 含有小橡胶粒子和低橡胶粒子凝胶含量和嵌段共聚物的取向聚苯乙烯膜的收缩标签 |
-
2008
- 2008-12-16 IT ITMI2008A002224A patent/IT1393666B1/it active
-
2009
- 2009-12-10 CN CN201310275021.XA patent/CN103709332A/zh active Pending
- 2009-12-10 HU HUE09771310A patent/HUE050825T2/hu unknown
- 2009-12-10 PT PT97713101T patent/PT2358773T/pt unknown
- 2009-12-10 US US13/139,823 patent/US20120289660A1/en not_active Abandoned
- 2009-12-10 SI SI200932071T patent/SI2358773T1/sl unknown
- 2009-12-10 RU RU2011127683/04A patent/RU2506278C2/ru active
- 2009-12-10 JP JP2011541172A patent/JP5607065B2/ja active Active
- 2009-12-10 CN CN2009801550260A patent/CN102292364A/zh active Pending
- 2009-12-10 PL PL09771310T patent/PL2358773T3/pl unknown
- 2009-12-10 WO PCT/EP2009/008861 patent/WO2010069515A1/en not_active Ceased
- 2009-12-10 BR BRPI0923456-0A patent/BRPI0923456B1/pt active IP Right Grant
- 2009-12-10 EP EP09771310.1A patent/EP2358773B1/en active Active
- 2009-12-10 ES ES09771310T patent/ES2802457T3/es active Active
- 2009-12-10 MX MX2011006484A patent/MX2011006484A/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| JP5607065B2 (ja) | 2014-10-15 |
| PT2358773T (pt) | 2020-07-06 |
| MX2011006484A (es) | 2011-11-29 |
| CN103709332A (zh) | 2014-04-09 |
| IT1393666B1 (it) | 2012-05-08 |
| RU2011127683A (ru) | 2013-01-27 |
| EP2358773A1 (en) | 2011-08-24 |
| CN102292364A (zh) | 2011-12-21 |
| BRPI0923456A2 (pt) | 2016-01-12 |
| JP2012512288A (ja) | 2012-05-31 |
| BRPI0923456B1 (pt) | 2020-03-24 |
| US20120289660A1 (en) | 2012-11-15 |
| SI2358773T1 (sl) | 2020-10-30 |
| WO2010069515A1 (en) | 2010-06-24 |
| HUE050825T2 (hu) | 2021-01-28 |
| ITMI20082224A1 (it) | 2010-06-17 |
| RU2506278C2 (ru) | 2014-02-10 |
| EP2358773B1 (en) | 2020-04-01 |
| PL2358773T3 (pl) | 2020-10-05 |
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