CN1350560A - 采用橡胶溶液生产热塑性模塑组合物的方法 - Google Patents
采用橡胶溶液生产热塑性模塑组合物的方法 Download PDFInfo
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- CN1350560A CN1350560A CN 00807516 CN00807516A CN1350560A CN 1350560 A CN1350560 A CN 1350560A CN 00807516 CN00807516 CN 00807516 CN 00807516 A CN00807516 A CN 00807516A CN 1350560 A CN1350560 A CN 1350560A
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- HIDBROSJWZYGSZ-UHFFFAOYSA-N 1-phenylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1 HIDBROSJWZYGSZ-UHFFFAOYSA-N 0.000 description 1
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- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- SVMUEEINWGBIPD-UHFFFAOYSA-N dodecylphosphonic acid Chemical class CCCCCCCCCCCCP(O)(O)=O SVMUEEINWGBIPD-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- MGDOJPNDRJNJBK-UHFFFAOYSA-N ethylaluminum Chemical compound [Al].C[CH2] MGDOJPNDRJNJBK-UHFFFAOYSA-N 0.000 description 1
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- 230000002349 favourable effect Effects 0.000 description 1
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- 150000002220 fluorenes Chemical class 0.000 description 1
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- 238000005984 hydrogenation reaction Methods 0.000 description 1
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- 229910052740 iodine Inorganic materials 0.000 description 1
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- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 1
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- 238000004898 kneading Methods 0.000 description 1
- SORGMJIXNUWMMR-UHFFFAOYSA-N lanthanum(3+);propan-2-olate Chemical compound [La+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SORGMJIXNUWMMR-UHFFFAOYSA-N 0.000 description 1
- CTTNXIBRLSQXOB-KVVVOXFISA-N lanthanum;(z)-octadec-9-enoic acid Chemical compound [La].CCCCCCCC\C=C/CCCCCCCC(O)=O CTTNXIBRLSQXOB-KVVVOXFISA-N 0.000 description 1
- TXZLDPUFIHXKPH-UHFFFAOYSA-N lanthanum;octadecanoic acid Chemical compound [La].CCCCCCCCCCCCCCCCCC(O)=O TXZLDPUFIHXKPH-UHFFFAOYSA-N 0.000 description 1
- ILFMPHAXCBBTDW-UHFFFAOYSA-N lanthanum;propanoic acid Chemical compound [La].CCC(O)=O ILFMPHAXCBBTDW-UHFFFAOYSA-N 0.000 description 1
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- 238000012423 maintenance Methods 0.000 description 1
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- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
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- 229910052751 metal Inorganic materials 0.000 description 1
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- NFWSQSCIDYBUOU-UHFFFAOYSA-N methylcyclopentadiene Chemical compound CC1=CC=CC1 NFWSQSCIDYBUOU-UHFFFAOYSA-N 0.000 description 1
- ARWCRSVRKCNEDI-UHFFFAOYSA-K neodymium(3+);octanoate Chemical compound [Nd+3].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O.CCCCCCCC([O-])=O ARWCRSVRKCNEDI-UHFFFAOYSA-K 0.000 description 1
- XHUXUTOCAPVSKA-KVVVOXFISA-N neodymium;(z)-octadec-9-enoic acid Chemical compound [Nd].CCCCCCCC\C=C/CCCCCCCC(O)=O XHUXUTOCAPVSKA-KVVVOXFISA-N 0.000 description 1
- PJNIZDVDNWEBNQ-UHFFFAOYSA-N neodymium;octadecanoic acid Chemical compound [Nd].CCCCCCCCCCCCCCCCCC(O)=O PJNIZDVDNWEBNQ-UHFFFAOYSA-N 0.000 description 1
- FELXHLPDKXFOMC-UHFFFAOYSA-N neodymium;propanoic acid Chemical compound [Nd].CCC(O)=O FELXHLPDKXFOMC-UHFFFAOYSA-N 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- LBECSCQAAIRRIW-UHFFFAOYSA-N octadecanoic acid;praseodymium Chemical compound [Pr].CCCCCCCCCCCCCCCCCC(O)=O LBECSCQAAIRRIW-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 125000001190 organyl group Chemical group 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- MMCOUVMKNAHQOY-UHFFFAOYSA-L oxido carbonate Chemical compound [O-]OC([O-])=O MMCOUVMKNAHQOY-UHFFFAOYSA-L 0.000 description 1
- 150000002927 oxygen compounds Chemical class 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- ZXHSVNZCIHNAGM-UHFFFAOYSA-N pentane-2,3-dione praseodymium Chemical compound [Pr].C(C)C(=O)C(=O)C ZXHSVNZCIHNAGM-UHFFFAOYSA-N 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical group CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 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
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- LSSJKIHPAOAPCS-UHFFFAOYSA-N praseodymium;propanoic acid Chemical compound [Pr].CCC(O)=O LSSJKIHPAOAPCS-UHFFFAOYSA-N 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- MVCPDOUDYOUTKS-UHFFFAOYSA-N propanedithioic acid Chemical compound CCC(S)=S MVCPDOUDYOUTKS-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- XKXIQBVKMABYQJ-UHFFFAOYSA-N tert-butyl hydrogen carbonate Chemical compound CC(C)(C)OC(O)=O XKXIQBVKMABYQJ-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- RBNWAMSGVWEHFP-UHFFFAOYSA-N trans-p-Menthane-1,8-diol Chemical compound CC(C)(O)C1CCC(C)(O)CC1 RBNWAMSGVWEHFP-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- LFXVBWRMVZPLFK-UHFFFAOYSA-N trioctylalumane Chemical compound CCCCCCCC[Al](CCCCCCCC)CCCCCCCC LFXVBWRMVZPLFK-UHFFFAOYSA-N 0.000 description 1
- MGMXGCZJYUCMGY-UHFFFAOYSA-N tris(4-nonylphenyl) phosphite Chemical compound C1=CC(CCCCCCCCC)=CC=C1OP(OC=1C=CC(CCCCCCCCC)=CC=1)OC1=CC=C(CCCCCCCCC)C=C1 MGMXGCZJYUCMGY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
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)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerization Catalysts (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19922641 | 1999-05-18 | ||
| DE19922641.5 | 1999-05-18 | ||
| DE10001025.3 | 2000-01-13 | ||
| DE10001025A DE10001025A1 (de) | 1999-05-18 | 2000-01-13 | Verfahren zur Herstellung von thermoplastischen Formmassen unter Verwendung von Kautschuklösungen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN1350560A true CN1350560A (zh) | 2002-05-22 |
Family
ID=26003827
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 00807516 Pending CN1350560A (zh) | 1999-05-18 | 2000-05-05 | 采用橡胶溶液生产热塑性模塑组合物的方法 |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP1187862A1 (de) |
| JP (1) | JP2002544350A (de) |
| CN (1) | CN1350560A (de) |
| AU (1) | AU4755400A (de) |
| BR (1) | BR0010762A (de) |
| CA (1) | CA2372178A1 (de) |
| MX (1) | MXPA01011759A (de) |
| RU (1) | RU2001134206A (de) |
| WO (1) | WO2000069940A1 (de) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106661140A (zh) * | 2014-08-20 | 2017-05-10 | 株式会社普利司通 | 共轭二烯聚合物的制造方法、共轭二烯聚合物、橡胶组合物和轮胎 |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2002128724A (ru) * | 2000-03-24 | 2004-02-27 | Байер Акциенгезельшафт (De) | Способ полимеризации сопряженных диолефинов (диенов) с помощью редкоземельных катализаторов в присутствии винилароматических растворителей |
| CA2351957A1 (en) * | 2001-06-29 | 2002-12-29 | Akhtar Osman | Process for the preparation of diene polymers |
| EP2267046B1 (de) | 2003-02-21 | 2013-08-07 | Styron Europe GmbH | Verfahren zur Homo- oder Copolymerisation von konjugierten Olefinen |
| JP5251744B2 (ja) * | 2009-06-12 | 2013-07-31 | 宇部興産株式会社 | 共役ジエン重合体の製造方法 |
| JP5251806B2 (ja) * | 2009-09-24 | 2013-07-31 | 宇部興産株式会社 | 共役ジエン重合体の製造方法 |
| CN103772577A (zh) * | 2014-02-24 | 2014-05-07 | 大连理工大学 | 含氮功能化稀土苯乙烯/异戊二烯/丁二烯共聚物及其制备方法 |
| CN108341896A (zh) * | 2017-01-24 | 2018-07-31 | 中国石油化工股份有限公司 | 一种制备苯乙烯-乙苯胶液的方法和苯乙烯-乙苯胶液 |
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| DE19746266A1 (de) * | 1997-10-20 | 1999-04-22 | Bayer Ag | Katalysator auf Basis von Verbindungen der seltenen Erdmetalle für die Polymerisation von ungesättigten organischen Verbindungen |
| DE19832446A1 (de) * | 1998-07-18 | 2000-01-27 | Bayer Ag | Verfahren zur Polymerisation von konjugierten Diolefinen (Dienen) mit Katalysatoren der Seltenen Erden in Gegenwart vinylaromatischer Lösungsmittel |
-
2000
- 2000-05-05 JP JP2000618355A patent/JP2002544350A/ja active Pending
- 2000-05-05 CN CN 00807516 patent/CN1350560A/zh active Pending
- 2000-05-05 WO PCT/EP2000/004032 patent/WO2000069940A1/de not_active Application Discontinuation
- 2000-05-05 RU RU2001134206/04A patent/RU2001134206A/ru unknown
- 2000-05-05 AU AU47554/00A patent/AU4755400A/en not_active Abandoned
- 2000-05-05 BR BR0010762-0A patent/BR0010762A/pt not_active Application Discontinuation
- 2000-05-05 EP EP00929500A patent/EP1187862A1/de not_active Withdrawn
- 2000-05-05 MX MXPA01011759A patent/MXPA01011759A/es unknown
- 2000-05-05 CA CA002372178A patent/CA2372178A1/en not_active Abandoned
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106661140A (zh) * | 2014-08-20 | 2017-05-10 | 株式会社普利司通 | 共轭二烯聚合物的制造方法、共轭二烯聚合物、橡胶组合物和轮胎 |
| US10239964B2 (en) | 2014-08-20 | 2019-03-26 | Bridgestone Corporation | Method for manufacturing conjugated diene polymer, conjugated diene polymer, rubber composition, and tire |
| CN106661140B (zh) * | 2014-08-20 | 2019-04-19 | 株式会社普利司通 | 共轭二烯聚合物的制造方法、共轭二烯聚合物、橡胶组合物和轮胎 |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2372178A1 (en) | 2000-11-23 |
| RU2001134206A (ru) | 2004-02-27 |
| WO2000069940A1 (de) | 2000-11-23 |
| JP2002544350A (ja) | 2002-12-24 |
| AU4755400A (en) | 2000-12-05 |
| EP1187862A1 (de) | 2002-03-20 |
| MXPA01011759A (es) | 2002-05-14 |
| BR0010762A (pt) | 2002-02-19 |
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