CS240958B2 - Catalytic system for homopolymerisation of butadiene - Google Patents
Catalytic system for homopolymerisation of butadiene Download PDFInfo
- Publication number
- CS240958B2 CS240958B2 CS832713A CS271383A CS240958B2 CS 240958 B2 CS240958 B2 CS 240958B2 CS 832713 A CS832713 A CS 832713A CS 271383 A CS271383 A CS 271383A CS 240958 B2 CS240958 B2 CS 240958B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- component
- mmol
- butadiene
- compound
- range
- Prior art date
Links
- 230000003197 catalytic effect Effects 0.000 title claims abstract description 10
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 title claims description 39
- 150000001875 compounds Chemical class 0.000 claims abstract description 17
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 8
- 150000002484 inorganic compounds Chemical class 0.000 claims abstract description 6
- 229910010272 inorganic material Inorganic materials 0.000 claims abstract description 6
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 5
- 150000002367 halogens Chemical class 0.000 claims abstract description 5
- 239000003054 catalyst Substances 0.000 claims description 26
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 239000000460 chlorine Substances 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 7
- 150000001735 carboxylic acids Chemical class 0.000 claims description 6
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- -1 aluminum compound Chemical class 0.000 claims description 5
- 150000002798 neodymium compounds Chemical class 0.000 claims description 5
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- PLDDOISOJJCEMH-UHFFFAOYSA-N neodymium(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Nd+3].[Nd+3] PLDDOISOJJCEMH-UHFFFAOYSA-N 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 claims description 2
- 150000001993 dienes Chemical class 0.000 abstract description 8
- 238000000034 method Methods 0.000 abstract description 8
- 230000008569 process Effects 0.000 abstract description 6
- 239000002253 acid Substances 0.000 abstract description 4
- 238000000746 purification Methods 0.000 abstract description 4
- 239000003701 inert diluent Substances 0.000 abstract description 3
- 238000002360 preparation method Methods 0.000 abstract description 3
- 230000007935 neutral effect Effects 0.000 abstract 1
- 230000000737 periodic effect Effects 0.000 abstract 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 39
- 239000000243 solution Substances 0.000 description 15
- 229920000642 polymer Polymers 0.000 description 14
- 239000000178 monomer Substances 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
- 238000006116 polymerization reaction Methods 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 230000008901 benefit Effects 0.000 description 5
- 239000003085 diluting agent Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000001035 drying Methods 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 238000002329 infrared spectrum Methods 0.000 description 4
- 229920002857 polybutadiene Polymers 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 241001441571 Hiodontidae Species 0.000 description 3
- 239000005062 Polybutadiene Substances 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 150000003623 transition metal compounds Chemical class 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000005608 naphthenic acid group Chemical group 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- PMJHHCWVYXUKFD-PLNGDYQASA-N (3z)-penta-1,3-diene Chemical group C\C=C/C=C PMJHHCWVYXUKFD-PLNGDYQASA-N 0.000 description 1
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
- 102100021870 ATP synthase subunit O, mitochondrial Human genes 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241001547070 Eriodes Species 0.000 description 1
- 241000755093 Gaidropsarus vulgaris Species 0.000 description 1
- 229910052779 Neodymium Inorganic materials 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- QNRMTGGDHLBXQZ-UHFFFAOYSA-N buta-1,2-diene Chemical group CC=C=C QNRMTGGDHLBXQZ-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002602 lanthanoids Chemical group 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 108010007425 oligomycin sensitivity conferring protein Proteins 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical group 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 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
- 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)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT20746/82A IT1151542B (it) | 1982-04-15 | 1982-04-15 | Procedimento per la polimerizzazione di diolefine coniugate e mezzi adatti allo scopo |
Publications (2)
Publication Number | Publication Date |
---|---|
CS271383A2 CS271383A2 (en) | 1985-06-13 |
CS240958B2 true CS240958B2 (en) | 1986-03-13 |
Family
ID=11171451
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CS832713A CS240958B2 (en) | 1982-04-15 | 1983-04-15 | Catalytic system for homopolymerisation of butadiene |
Country Status (20)
Country | Link |
---|---|
US (1) | US4525549A (it) |
EP (1) | EP0092270B1 (it) |
JP (1) | JPS58187402A (it) |
AU (1) | AU565051B2 (it) |
BR (1) | BR8301824A (it) |
CA (1) | CA1205446A (it) |
CS (1) | CS240958B2 (it) |
DD (1) | DD209582A5 (it) |
DE (1) | DE3366688D1 (it) |
EG (1) | EG15942A (it) |
ES (1) | ES8502131A1 (it) |
IE (1) | IE56761B1 (it) |
IN (1) | IN161008B (it) |
IT (1) | IT1151542B (it) |
MX (1) | MX162409A (it) |
PL (1) | PL140562B1 (it) |
PT (1) | PT76555B (it) |
SU (1) | SU1396959A3 (it) |
YU (1) | YU44738B (it) |
ZA (1) | ZA832520B (it) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1164238B (it) * | 1983-05-25 | 1987-04-08 | Anic Spa | Procedimento per la polimerizzazione del butadiene |
IT1191612B (it) * | 1985-05-15 | 1988-03-23 | Enichem Elastomers | Procedimento migliorato per la polimerizzazione o copolimerizzazione del butadiene |
IT1191614B (it) * | 1985-05-15 | 1988-03-23 | Enichem Elastomers | Procedimento migliorato per la polimerizzazione o copolimerizzazione del butadiene |
IT1186730B (it) * | 1985-06-05 | 1987-12-16 | Enichem Elastomers | Procedimento per la polimerizzazione di isoprene |
IT1186747B (it) * | 1985-07-01 | 1987-12-16 | Enichem Elastomers | Procedimento migliorato per la polimerizzazione o copolimerizzazione del butadiene |
IT1230756B (it) * | 1989-02-17 | 1991-10-29 | Enichem Elastomers | Metodo per la preparazione di polibutadiene a lavorabilita' migliorata. |
US5405815A (en) * | 1993-06-17 | 1995-04-11 | The Goodyear Tire & Rubber Company | Process for preparing a catalyst system useful in the synthesis of isoprene-butadiene rubber |
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 |
KR100352764B1 (ko) * | 2000-03-16 | 2002-09-16 | 금호석유화학 주식회사 | 신규한 단분자 니오디뮴 카르복실레이트 화합물 및 이를포함하는 디엔 중합용 촉매 |
DE10115106A1 (de) * | 2001-03-27 | 2002-10-10 | Bayer Ag | Blockcopolymerisat auf Basis von konjugierten Diolefinen und polaren Monomeren |
KR100553249B1 (ko) | 2003-05-15 | 2006-02-20 | 금호석유화학 주식회사 | 고 1,4-시스 폴리부타디엔-폴리우레탄 공중합체 및 그 제조방법 |
US7094849B2 (en) * | 2003-12-15 | 2006-08-22 | Bridgestone Corporation | Bulk polymerization process for producing polydienes |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3297667A (en) * | 1963-02-28 | 1967-01-10 | Union Carbide Corp | Production of cis-1, 4-polydienes by polymerization of 1, 3-dienes |
US3803053A (en) * | 1968-05-08 | 1974-04-09 | Atlantic Richfield Co | Lanthanide oligomerization catalyst |
IT1085542B (it) * | 1976-05-14 | 1985-05-28 | Battelle Memorial Institute | Procedimento per la preparazione di catalizzatori di polimerizzazione di olefine |
DE2830080A1 (de) * | 1978-07-08 | 1980-01-17 | Bayer Ag | Katalysator, dessen herstellung und verwendung zur loesungspolymerisation von butadien |
US4384982A (en) * | 1981-05-18 | 1983-05-24 | Phillips Petroleum Company | Process and catalyst for olefin polymerization |
-
1982
- 1982-04-15 IT IT20746/82A patent/IT1151542B/it active
-
1983
- 1983-04-06 BR BR8301824A patent/BR8301824A/pt not_active IP Right Cessation
- 1983-04-08 AU AU13283/83A patent/AU565051B2/en not_active Expired
- 1983-04-11 MX MX196897A patent/MX162409A/es unknown
- 1983-04-11 ZA ZA832520A patent/ZA832520B/xx unknown
- 1983-04-11 EP EP83200504A patent/EP0092270B1/en not_active Expired
- 1983-04-11 DE DE8383200504T patent/DE3366688D1/de not_active Expired
- 1983-04-12 CA CA000425661A patent/CA1205446A/en not_active Expired
- 1983-04-13 EG EG234/83A patent/EG15942A/xx active
- 1983-04-14 IN IN437/CAL/83A patent/IN161008B/en unknown
- 1983-04-14 SU SU833584516A patent/SU1396959A3/ru active
- 1983-04-14 PT PT76555A patent/PT76555B/pt unknown
- 1983-04-14 IE IE846/83A patent/IE56761B1/en not_active IP Right Cessation
- 1983-04-14 US US06/484,956 patent/US4525549A/en not_active Expired - Lifetime
- 1983-04-15 ES ES521800A patent/ES8502131A1/es not_active Expired
- 1983-04-15 DD DD83249907A patent/DD209582A5/de not_active IP Right Cessation
- 1983-04-15 YU YU855/83A patent/YU44738B/xx unknown
- 1983-04-15 PL PL1983241513A patent/PL140562B1/pl unknown
- 1983-04-15 JP JP58065749A patent/JPS58187402A/ja active Granted
- 1983-04-15 CS CS832713A patent/CS240958B2/cs unknown
Also Published As
Publication number | Publication date |
---|---|
IN161008B (it) | 1987-09-12 |
US4525549A (en) | 1985-06-25 |
EG15942A (en) | 1986-12-30 |
EP0092270B1 (en) | 1986-10-08 |
IT8220746A0 (it) | 1982-04-15 |
PT76555A (en) | 1983-05-01 |
AU565051B2 (en) | 1987-09-03 |
JPS58187402A (ja) | 1983-11-01 |
CA1205446A (en) | 1986-06-03 |
ES521800A0 (es) | 1984-12-16 |
CS271383A2 (en) | 1985-06-13 |
PT76555B (en) | 1986-03-12 |
EP0092270A1 (en) | 1983-10-26 |
IE56761B1 (en) | 1991-12-04 |
IT1151542B (it) | 1986-12-24 |
SU1396959A3 (ru) | 1988-05-15 |
IE830846L (en) | 1983-10-15 |
MX162409A (es) | 1991-05-07 |
PL241513A1 (en) | 1984-04-24 |
AU1328383A (en) | 1983-10-20 |
PL140562B1 (en) | 1987-05-30 |
BR8301824A (pt) | 1983-12-20 |
YU85583A (en) | 1986-02-28 |
DE3366688D1 (en) | 1986-11-13 |
JPH0322887B2 (it) | 1991-03-27 |
ES8502131A1 (es) | 1984-12-16 |
YU44738B (en) | 1991-02-28 |
ZA832520B (en) | 1983-12-28 |
DD209582A5 (de) | 1984-05-16 |
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