CN100509879C - 含有环乙烯基单元的二烯高弹体及其制备工艺 - Google Patents
含有环乙烯基单元的二烯高弹体及其制备工艺 Download PDFInfo
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- CN100509879C CN100509879C CNB028142837A CN02814283A CN100509879C CN 100509879 C CN100509879 C CN 100509879C CN B028142837 A CNB028142837 A CN B028142837A CN 02814283 A CN02814283 A CN 02814283A CN 100509879 C CN100509879 C CN 100509879C
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- Prior art keywords
- diene elastomer
- line style
- side chain
- mol
- initiator
- 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 - Lifetime
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- 238000000034 method Methods 0.000 title claims abstract description 21
- 150000001993 dienes Chemical class 0.000 title claims abstract description 15
- 229920003244 diene elastomer Polymers 0.000 claims abstract description 57
- 239000003999 initiator Substances 0.000 claims abstract description 47
- -1 alicyclic hydrocarbon Chemical class 0.000 claims abstract description 41
- 239000000178 monomer Substances 0.000 claims abstract description 34
- 150000003839 salts Chemical class 0.000 claims abstract description 25
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 17
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 9
- 239000002904 solvent Substances 0.000 claims abstract description 9
- 238000002360 preparation method Methods 0.000 claims description 56
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 47
- 239000003153 chemical reaction reagent Substances 0.000 claims description 47
- 239000003054 catalyst Substances 0.000 claims description 42
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 claims description 27
- 238000006243 chemical reaction Methods 0.000 claims description 24
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 15
- 150000002191 fatty alcohols Chemical class 0.000 claims description 15
- 229910052744 lithium Inorganic materials 0.000 claims description 15
- 229910052783 alkali metal Inorganic materials 0.000 claims description 13
- 125000000129 anionic group Chemical group 0.000 claims description 10
- 125000004122 cyclic group Chemical group 0.000 claims description 8
- 229920002554 vinyl polymer Polymers 0.000 claims description 8
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 159000000000 sodium salts Chemical class 0.000 claims description 3
- 239000006085 branching agent Substances 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000007822 coupling agent Substances 0.000 claims description 2
- 150000004985 diamines Chemical class 0.000 claims description 2
- 238000010539 anionic addition polymerization reaction Methods 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 125000002723 alicyclic group Chemical group 0.000 abstract description 15
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 5
- 229930195733 hydrocarbon Natural products 0.000 abstract description 5
- 125000001931 aliphatic group Chemical group 0.000 abstract description 4
- 125000005842 heteroatom Chemical group 0.000 abstract description 4
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 125000001979 organolithium group Chemical group 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 36
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 25
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 22
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 16
- 238000005516 engineering process Methods 0.000 description 16
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 12
- 229910052708 sodium Inorganic materials 0.000 description 12
- 239000011734 sodium Substances 0.000 description 12
- 239000000203 mixture Substances 0.000 description 9
- 238000005070 sampling Methods 0.000 description 9
- 230000009466 transformation Effects 0.000 description 9
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound 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 8
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 8
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 8
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 7
- 239000005977 Ethylene Substances 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 238000001228 spectrum Methods 0.000 description 7
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 7
- 230000003064 anti-oxidating effect Effects 0.000 description 6
- 150000001721 carbon Chemical group 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 235000019587 texture Nutrition 0.000 description 6
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 5
- 239000012535 impurity Substances 0.000 description 5
- 238000006386 neutralization reaction Methods 0.000 description 5
- 239000012429 reaction media Substances 0.000 description 5
- 230000001105 regulatory effect Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 4
- IKEHOXWJQXIQAG-UHFFFAOYSA-N 2-tert-butyl-4-methylphenol Chemical compound CC1=CC=C(O)C(C(C)(C)C)=C1 IKEHOXWJQXIQAG-UHFFFAOYSA-N 0.000 description 4
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 4
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 4
- 238000005304 joining Methods 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 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 2
- MSXVEPNJUHWQHW-UHFFFAOYSA-N 2-methylbutan-2-ol Chemical compound CCC(C)(C)O MSXVEPNJUHWQHW-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- 244000246386 Mentha pulegium Species 0.000 description 2
- 235000016257 Mentha pulegium Nutrition 0.000 description 2
- 235000004357 Mentha x piperita Nutrition 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 238000000113 differential scanning calorimetry Methods 0.000 description 2
- 235000001050 hortel pimenta Nutrition 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 2
- JLUFWMXJHAVVNN-UHFFFAOYSA-N methyltrichlorosilane Chemical group C[Si](Cl)(Cl)Cl JLUFWMXJHAVVNN-UHFFFAOYSA-N 0.000 description 2
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 235000011164 potassium chloride Nutrition 0.000 description 2
- 239000001103 potassium chloride Substances 0.000 description 2
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 2
- 238000001542 size-exclusion chromatography Methods 0.000 description 2
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- ZUHZGEOKBKGPSW-UHFFFAOYSA-N tetraglyme Chemical compound COCCOCCOCCOCCOC ZUHZGEOKBKGPSW-UHFFFAOYSA-N 0.000 description 2
- 239000003643 water by type Substances 0.000 description 2
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
- PBBJBFOOHLPWOV-UHFFFAOYSA-N 1,1'-biphenyl;carbonic acid Chemical compound OC(O)=O.C1=CC=CC=C1C1=CC=CC=C1 PBBJBFOOHLPWOV-UHFFFAOYSA-N 0.000 description 1
- RYPKRALMXUUNKS-UHFFFAOYSA-N 2-Hexene Natural products CCCC=CC RYPKRALMXUUNKS-UHFFFAOYSA-N 0.000 description 1
- AIDLAEPHWROGFI-UHFFFAOYSA-N 2-methylbenzene-1,3-dicarboxylic acid Chemical compound CC1=C(C(O)=O)C=CC=C1C(O)=O AIDLAEPHWROGFI-UHFFFAOYSA-N 0.000 description 1
- CXURGFRDGROIKG-UHFFFAOYSA-N 3,3-bis(chloromethyl)oxetane Chemical compound ClCC1(CCl)COC1 CXURGFRDGROIKG-UHFFFAOYSA-N 0.000 description 1
- DXIJHCSGLOHNES-UHFFFAOYSA-N 3,3-dimethylbut-1-enylbenzene Chemical compound CC(C)(C)C=CC1=CC=CC=C1 DXIJHCSGLOHNES-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-OUBTZVSYSA-N Carbon-13 Chemical compound [13C] OKTJSMMVPCPJKN-OUBTZVSYSA-N 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 1
- 230000005526 G1 to G0 transition Effects 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- YLFSKHFWQGRUCI-UHFFFAOYSA-N [Li]CCc1ccccc1 Chemical compound [Li]CCc1ccccc1 YLFSKHFWQGRUCI-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- XZKRXPZXQLARHH-UHFFFAOYSA-N buta-1,3-dienylbenzene Chemical compound C=CC=CC1=CC=CC=C1 XZKRXPZXQLARHH-UHFFFAOYSA-N 0.000 description 1
- NPAXBRSUVYCZGM-UHFFFAOYSA-N carbonic acid;propane-1,2-diol Chemical compound OC(O)=O.CC(O)CO NPAXBRSUVYCZGM-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- LEKSIJZGSFETSJ-UHFFFAOYSA-N cyclohexane;lithium Chemical compound [Li]C1CCCCC1 LEKSIJZGSFETSJ-UHFFFAOYSA-N 0.000 description 1
- 125000002897 diene group Chemical group 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- DPUXQWOMYBMHRN-UHFFFAOYSA-N hexa-2,3-diene Chemical compound CCC=C=CC DPUXQWOMYBMHRN-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- DLEDOFVPSDKWEF-UHFFFAOYSA-N lithium butane Chemical compound [Li+].CCC[CH2-] DLEDOFVPSDKWEF-UHFFFAOYSA-N 0.000 description 1
- 150000002642 lithium compounds Chemical class 0.000 description 1
- UBJFKNSINUCEAL-UHFFFAOYSA-N lithium;2-methylpropane Chemical compound [Li+].C[C-](C)C UBJFKNSINUCEAL-UHFFFAOYSA-N 0.000 description 1
- WGOPGODQLGJZGL-UHFFFAOYSA-N lithium;butane Chemical compound [Li+].CC[CH-]C WGOPGODQLGJZGL-UHFFFAOYSA-N 0.000 description 1
- XBEREOHJDYAKDA-UHFFFAOYSA-N lithium;propane Chemical group [Li+].CC[CH2-] XBEREOHJDYAKDA-UHFFFAOYSA-N 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000005055 methyl trichlorosilane Substances 0.000 description 1
- UIUXUFNYAYAMOE-UHFFFAOYSA-N methylsilane Chemical compound [SiH3]C UIUXUFNYAYAMOE-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 150000002900 organolithium compounds Chemical class 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 230000010181 polygamy Effects 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- YFNKIDBQEZZDLK-UHFFFAOYSA-N triglyme Chemical compound COCCOCCOCCOC YFNKIDBQEZZDLK-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
- C08C19/30—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule
- C08C19/42—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with metals or metal-containing groups
- C08C19/44—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with metals or metal-containing groups of polymers containing metal atoms exclusively at one or both ends of the skeleton
-
- 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
- C08F36/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F36/02—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F36/04—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerization Catalysts (AREA)
Abstract
Description
化学位移 | 碳原子结构—序号 |
145-140.6116.6-113.2126.5-124.9132.9-126.9145-140.6147.1-145113.2-111 | V-3,VCP-6V-4S-6S-4,S-5,S-7,S-8C-2,C-3,T-2,T-3V-3,VCP-6S-3VCP-7 |
Claims (27)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR01/10287 | 2001-07-16 | ||
FR0110287 | 2001-07-16 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2009101183263A Division CN101503486B (zh) | 2001-07-16 | 2002-07-16 | 含有环乙烯基单元的二烯高弹体及其制备工艺 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1529721A CN1529721A (zh) | 2004-09-15 |
CN100509879C true CN100509879C (zh) | 2009-07-08 |
Family
ID=8866156
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2009101183263A Expired - Lifetime CN101503486B (zh) | 2001-07-16 | 2002-07-16 | 含有环乙烯基单元的二烯高弹体及其制备工艺 |
CNB028142837A Expired - Lifetime CN100509879C (zh) | 2001-07-16 | 2002-07-16 | 含有环乙烯基单元的二烯高弹体及其制备工艺 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2009101183263A Expired - Lifetime CN101503486B (zh) | 2001-07-16 | 2002-07-16 | 含有环乙烯基单元的二烯高弹体及其制备工艺 |
Country Status (5)
Country | Link |
---|---|
US (2) | US7470760B2 (zh) |
EP (1) | EP1423442B1 (zh) |
JP (1) | JP4391228B2 (zh) |
CN (2) | CN101503486B (zh) |
WO (1) | WO2003008470A1 (zh) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101503486B (zh) * | 2001-07-16 | 2012-01-11 | 米其林技术公司 | 含有环乙烯基单元的二烯高弹体及其制备工艺 |
WO2004065478A1 (fr) * | 2003-01-20 | 2004-08-05 | Societe De Technologie Michelin | Composition de caoutchouc pour bande de roulement de pneumatique et procede de preparation |
JP4716756B2 (ja) * | 2005-03-03 | 2011-07-06 | 旭化成ケミカルズ株式会社 | ランダム共重合体の製造方法 |
EP2716663B1 (en) | 2011-05-27 | 2015-06-24 | Asahi Kasei Chemicals Corporation | Method for manufacturing hydrogenated conjugated diene copolymer |
JP6211612B2 (ja) * | 2013-07-17 | 2017-10-11 | 旭化成株式会社 | 水素添加用触媒組成物の製造方法 |
JP6297041B2 (ja) * | 2013-07-17 | 2018-03-20 | 旭化成株式会社 | 重合体の製造方法 |
KR102315747B1 (ko) * | 2016-04-20 | 2021-10-20 | 알베마를 코포레이션 | 수소 매개 염유사 수소화물 개시된 음이온성 사슬 이동 중합을 위한 공정 및 촉매 |
US10899864B2 (en) | 2016-09-09 | 2021-01-26 | Dynasol Elastómeros, S.A. De C.V. | Polar modifier systems for high vinyl block copolymerization |
CN109485791B (zh) * | 2017-09-13 | 2021-10-19 | 中国石油化工股份有限公司 | 线形丁苯共聚物及其制备方法和组合物以及芳族乙烯基树脂及其制备方法 |
ES2960547T3 (es) | 2017-11-22 | 2024-03-05 | Kuraray Co | Copolímero de bloques o producto hidrogenado del mismo |
US11542355B2 (en) * | 2018-10-18 | 2023-01-03 | Dynasol Elastómeros, S.A. De C.V. | Polar modifier systems for high vinyl block copolymerization |
CN113698536B (zh) | 2020-05-21 | 2023-07-21 | 中国石油化工股份有限公司 | 液体丁苯聚合物及其制备方法和应用以及组合物和聚合物涂层和胶粘剂和交联剂 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3966691A (en) * | 1973-07-12 | 1976-06-29 | The Firestone Tire & Rubber Company | Polymerization of conjugated dienes with starved lithium, potassium or sodium catalyst |
US4316820A (en) * | 1979-02-15 | 1982-02-23 | Bayer Ag | Catalyst, preparation thereof and use thereof in the preparation of telomeric polybutadiene homo- or co-polymers |
US5620939A (en) * | 1995-09-22 | 1997-04-15 | The Goodyear Tire & Rubber Company | Initiative system |
US6140434A (en) * | 1999-01-08 | 2000-10-31 | The Goodyear Tire & Rubber Company | Synthesis of high vinyl rubber |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3294768A (en) | 1963-11-14 | 1966-12-27 | Phillips Petroleum Co | Preparation of conjugated diene polymers |
US3301840A (en) * | 1964-09-17 | 1967-01-31 | Phillips Petroleum Co | Preparation of polymers of conjugated dienes using organolithium/polar compound catalyst systems |
US3801554A (en) * | 1972-02-28 | 1974-04-02 | Phillips Petroleum Co | Lithium alkenoxides as modifiers in organolithium initiated polymerization |
GB2020670A (en) * | 1978-05-09 | 1979-11-21 | Polymer Investments Nv | Liquid polymer and liquid copolymers of Butadiene and the preparation thereof. |
JPS57117508A (en) * | 1981-01-14 | 1982-07-22 | Asahi Chem Ind Co Ltd | Preparation of conjugated diene polymer |
JPS5996112A (ja) * | 1982-11-26 | 1984-06-02 | Toyo Soda Mfg Co Ltd | 高純度イソプレン重合体環化物の製造方法 |
JPS6071616A (ja) * | 1983-09-29 | 1985-04-23 | Japan Synthetic Rubber Co Ltd | ホトレジスト用共役ジエン系重合体環化物の製造方法 |
JPS60206804A (ja) * | 1984-03-30 | 1985-10-18 | Japan Synthetic Rubber Co Ltd | 共役ジエン系重合体環化物の製法 |
DE3707434A1 (de) * | 1986-05-31 | 1987-12-03 | Huels Chemische Werke Ag | Polyisoprene mit einem hohen anteil von 1,2- und 3,4-struktureinheiten, verfahren zu ihrer herstellung und ihre verwendung |
US4696986A (en) | 1986-08-12 | 1987-09-29 | The Goodyear Tire & Rubber Company | Modifier for lithium catalysts |
JPH0637530B2 (ja) * | 1987-06-24 | 1994-05-18 | 日本ゼオン株式会社 | 新規な光学材料 |
DE3724870A1 (de) | 1987-07-28 | 1989-02-09 | Huels Chemische Werke Ag | Verfahren zur herstellung von polymerisaten auf basis von konjugierten dienen und ggf. monovinylaromatischen verbindungen |
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JP3319639B2 (ja) * | 1992-12-24 | 2002-09-03 | 株式会社ブリヂストン | 共役ジエン系重合体の製造方法、スチレン−ブタジエン系重合体及びそのゴム組成物 |
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FR2808025A1 (fr) | 2000-04-25 | 2001-10-26 | Michelin Soc Tech | Procede de preparation par voie anionique d'un elastomere dienique ramifie |
CN101503486B (zh) * | 2001-07-16 | 2012-01-11 | 米其林技术公司 | 含有环乙烯基单元的二烯高弹体及其制备工艺 |
-
2002
- 2002-07-16 CN CN2009101183263A patent/CN101503486B/zh not_active Expired - Lifetime
- 2002-07-16 EP EP02774485A patent/EP1423442B1/fr not_active Expired - Lifetime
- 2002-07-16 WO PCT/EP2002/007866 patent/WO2003008470A1/fr active Application Filing
- 2002-07-16 JP JP2003514025A patent/JP4391228B2/ja not_active Expired - Lifetime
- 2002-07-16 CN CNB028142837A patent/CN100509879C/zh not_active Expired - Lifetime
-
2004
- 2004-01-14 US US10/756,386 patent/US7470760B2/en not_active Expired - Lifetime
-
2008
- 2008-11-20 US US12/292,524 patent/US7763696B2/en not_active Expired - Lifetime
Patent Citations (4)
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US3966691A (en) * | 1973-07-12 | 1976-06-29 | The Firestone Tire & Rubber Company | Polymerization of conjugated dienes with starved lithium, potassium or sodium catalyst |
US4316820A (en) * | 1979-02-15 | 1982-02-23 | Bayer Ag | Catalyst, preparation thereof and use thereof in the preparation of telomeric polybutadiene homo- or co-polymers |
US5620939A (en) * | 1995-09-22 | 1997-04-15 | The Goodyear Tire & Rubber Company | Initiative system |
US6140434A (en) * | 1999-01-08 | 2000-10-31 | The Goodyear Tire & Rubber Company | Synthesis of high vinyl rubber |
Also Published As
Publication number | Publication date |
---|---|
CN101503486A (zh) | 2009-08-12 |
CN101503486B (zh) | 2012-01-11 |
CN1529721A (zh) | 2004-09-15 |
WO2003008470A1 (fr) | 2003-01-30 |
JP2005513172A (ja) | 2005-05-12 |
EP1423442A1 (fr) | 2004-06-02 |
EP1423442B1 (fr) | 2012-09-12 |
US20090082534A1 (en) | 2009-03-26 |
JP4391228B2 (ja) | 2009-12-24 |
US7763696B2 (en) | 2010-07-27 |
US20040147696A1 (en) | 2004-07-29 |
US7470760B2 (en) | 2008-12-30 |
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