DE69914095T2 - Verfahren zur herstellung eines dilithium initiators und dessen verwendung - Google Patents
Verfahren zur herstellung eines dilithium initiators und dessen verwendung Download PDFInfo
- Publication number
- DE69914095T2 DE69914095T2 DE69914095T DE69914095T DE69914095T2 DE 69914095 T2 DE69914095 T2 DE 69914095T2 DE 69914095 T DE69914095 T DE 69914095T DE 69914095 T DE69914095 T DE 69914095T DE 69914095 T2 DE69914095 T2 DE 69914095T2
- Authority
- DE
- Germany
- Prior art keywords
- alkyl
- diisopropenylbenzene
- lithium
- diethyl ether
- alkyl lithium
- 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
Links
- SMBQBQBNOXIFSF-UHFFFAOYSA-N dilithium Chemical compound [Li][Li] SMBQBQBNOXIFSF-UHFFFAOYSA-N 0.000 title claims description 18
- 238000004519 manufacturing process Methods 0.000 title claims description 10
- 239000003999 initiator Substances 0.000 title abstract description 25
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 75
- -1 diisopropenylbenzene compound Chemical class 0.000 claims abstract description 53
- 229910052744 lithium Inorganic materials 0.000 claims abstract description 44
- 238000000034 method Methods 0.000 claims abstract description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- 229920000642 polymer Polymers 0.000 claims description 14
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 10
- 239000005977 Ethylene Substances 0.000 claims description 10
- WGOPGODQLGJZGL-UHFFFAOYSA-N lithium;butane Chemical compound [Li+].CC[CH-]C WGOPGODQLGJZGL-UHFFFAOYSA-N 0.000 claims description 10
- UBJFKNSINUCEAL-UHFFFAOYSA-N lithium;2-methylpropane Chemical compound [Li+].C[C-](C)C UBJFKNSINUCEAL-UHFFFAOYSA-N 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 2
- 239000007858 starting material Substances 0.000 claims 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 abstract description 3
- HIACAHMKXQESOV-UHFFFAOYSA-N 1,2-bis(prop-1-en-2-yl)benzene Chemical class CC(=C)C1=CC=CC=C1C(C)=C HIACAHMKXQESOV-UHFFFAOYSA-N 0.000 description 26
- 238000006243 chemical reaction Methods 0.000 description 12
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 7
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- IBVPVTPPYGGAEL-UHFFFAOYSA-N 1,3-bis(prop-1-en-2-yl)benzene Chemical compound CC(=C)C1=CC=CC(C(C)=C)=C1 IBVPVTPPYGGAEL-UHFFFAOYSA-N 0.000 description 5
- 239000012190 activator Substances 0.000 description 5
- 239000003153 chemical reaction reagent Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- ABDKAPXRBAPSQN-UHFFFAOYSA-N veratrole Chemical compound COC1=CC=CC=C1OC ABDKAPXRBAPSQN-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000003607 modifier Substances 0.000 description 3
- 238000006384 oligomerization reaction Methods 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- FGQLGYBGTRHODR-UHFFFAOYSA-N 2,2-diethoxypropane Chemical compound CCOC(C)(C)OCC FGQLGYBGTRHODR-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229920006318 anionic polymer Polymers 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- 238000007306 functionalization reaction Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- WDDLHZXDSVMNRK-UHFFFAOYSA-N lithium;3-methanidylheptane Chemical compound [Li+].CCCCC([CH2-])CC WDDLHZXDSVMNRK-UHFFFAOYSA-N 0.000 description 2
- LTVBQYKXPQPFBJ-UHFFFAOYSA-N lithium;heptane Chemical compound [Li+].CCCCCC[CH2-] LTVBQYKXPQPFBJ-UHFFFAOYSA-N 0.000 description 2
- NHKJPPKXDNZFBJ-UHFFFAOYSA-N phenyllithium Chemical compound [Li]C1=CC=CC=C1 NHKJPPKXDNZFBJ-UHFFFAOYSA-N 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 125000006413 ring segment Chemical group 0.000 description 2
- JTBZFIJSFBPKNO-UHFFFAOYSA-N 1,2,3,4-tetramethyl-5,6-bis(prop-1-en-2-yl)benzene Chemical compound CC(=C)C1=C(C)C(C)=C(C)C(C)=C1C(C)=C JTBZFIJSFBPKNO-UHFFFAOYSA-N 0.000 description 1
- ISJYRTKOQVJTRP-UHFFFAOYSA-N 1,2,3,5-tetraethyl-4,6-bis(prop-1-en-2-yl)benzene Chemical compound CCC1=C(CC)C(C(C)=C)=C(CC)C(C(C)=C)=C1CC ISJYRTKOQVJTRP-UHFFFAOYSA-N 0.000 description 1
- ZDZMQOHBCHLKOZ-UHFFFAOYSA-N 1,2,4,5-tetrahexyl-3,6-bis(prop-1-en-2-yl)benzene Chemical compound CCCCCCC1=C(CCCCCC)C(C(C)=C)=C(CCCCCC)C(CCCCCC)=C1C(C)=C ZDZMQOHBCHLKOZ-UHFFFAOYSA-N 0.000 description 1
- KEJYHYCHSAIBAP-UHFFFAOYSA-N 1,2-dicyclohexyl-3,4-bis(prop-1-en-2-yl)benzene Chemical compound C1CCCCC1C1=C(C(C)=C)C(C(=C)C)=CC=C1C1CCCCC1 KEJYHYCHSAIBAP-UHFFFAOYSA-N 0.000 description 1
- GVLXIKYSWGGDLX-UHFFFAOYSA-N 1,4-bis(prop-1-en-2-yl)-2-(2-propylcyclopropyl)benzene Chemical compound CCCC1CC1C1=CC(C(C)=C)=CC=C1C(C)=C GVLXIKYSWGGDLX-UHFFFAOYSA-N 0.000 description 1
- ZENYUPUKNXGVDY-UHFFFAOYSA-N 1,4-bis(prop-1-en-2-yl)benzene Chemical compound CC(=C)C1=CC=C(C(C)=C)C=C1 ZENYUPUKNXGVDY-UHFFFAOYSA-N 0.000 description 1
- UZMWDTVBYPAEMH-UHFFFAOYSA-N 1,5-bis(prop-1-en-2-yl)naphthalene Chemical compound C1=CC=C2C(C(=C)C)=CC=CC2=C1C(C)=C UZMWDTVBYPAEMH-UHFFFAOYSA-N 0.000 description 1
- BVUFUXGQLRJYDA-UHFFFAOYSA-N 1-(3-methylcyclopentyl)-3,5-bis(prop-1-en-2-yl)benzene Chemical compound C1C(C)CCC1C1=CC(C(C)=C)=CC(C(C)=C)=C1 BVUFUXGQLRJYDA-UHFFFAOYSA-N 0.000 description 1
- VCNHLIDINGRNFS-UHFFFAOYSA-N 1-(cyclopentylmethyl)-2,5-bis(prop-1-en-2-yl)-4-propylbenzene Chemical compound C1=C(C(C)=C)C(CCC)=CC(C(C)=C)=C1CC1CCCC1 VCNHLIDINGRNFS-UHFFFAOYSA-N 0.000 description 1
- VCNONMCQKBPBCY-UHFFFAOYSA-N 1-ethyl-3,5-bis(prop-1-en-2-yl)benzene Chemical compound CCC1=CC(C(C)=C)=CC(C(C)=C)=C1 VCNONMCQKBPBCY-UHFFFAOYSA-N 0.000 description 1
- BPERVJJFOOSUPU-UHFFFAOYSA-N 2-methyl-1,4-bis(prop-1-en-2-yl)benzene Chemical compound CC(=C)C1=CC=C(C(C)=C)C(C)=C1 BPERVJJFOOSUPU-UHFFFAOYSA-N 0.000 description 1
- UXWXHEVHZVXRQU-UHFFFAOYSA-N 4-(2-cyclobutylethyl)-1,2-bis(prop-1-en-2-yl)benzene Chemical compound C1=C(C(C)=C)C(C(=C)C)=CC=C1CCC1CCC1 UXWXHEVHZVXRQU-UHFFFAOYSA-N 0.000 description 1
- UEAFNORNMPYBAU-UHFFFAOYSA-N 4-methyl-1,2-bis(prop-1-en-2-yl)benzene Chemical compound CC(=C)C1=CC=C(C)C=C1C(C)=C UEAFNORNMPYBAU-UHFFFAOYSA-N 0.000 description 1
- ZYWUIIGAFQRAGK-UHFFFAOYSA-N 5-hexyl-2-methyl-1,3-bis(prop-1-en-2-yl)benzene Chemical compound CCCCCCC1=CC(C(C)=C)=C(C)C(C(C)=C)=C1 ZYWUIIGAFQRAGK-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 1
- YNXURHRFIMQACJ-UHFFFAOYSA-N lithium;methanidylbenzene Chemical compound [Li+].[CH2-]C1=CC=CC=C1 YNXURHRFIMQACJ-UHFFFAOYSA-N 0.000 description 1
- SZAVVKVUMPLRRS-UHFFFAOYSA-N lithium;propane Chemical compound [Li+].C[CH-]C SZAVVKVUMPLRRS-UHFFFAOYSA-N 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- KZCIFCCRKCMKFH-UHFFFAOYSA-N naphthalene styrene Chemical compound C=CC1=CC=CC=C1.C1=CC=CC2=CC=CC=C21 KZCIFCCRKCMKFH-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical group [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic Table
- C07F1/02—Lithium compounds
-
- 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)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Polymerization Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Dental Preparations (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Nonmetallic Welding Materials (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10369598P | 1998-10-09 | 1998-10-09 | |
| US103695P | 1998-10-09 | ||
| PCT/EP1999/007758 WO2000022004A1 (en) | 1998-10-09 | 1999-10-07 | Process for making a dilithium initiator, and the use therof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69914095D1 DE69914095D1 (de) | 2004-02-12 |
| DE69914095T2 true DE69914095T2 (de) | 2004-06-09 |
Family
ID=22296568
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69914095T Expired - Lifetime DE69914095T2 (de) | 1998-10-09 | 1999-10-07 | Verfahren zur herstellung eines dilithium initiators und dessen verwendung |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US6217798B1 (https=) |
| EP (1) | EP1123320B1 (https=) |
| JP (1) | JP4445135B2 (https=) |
| KR (1) | KR100649780B1 (https=) |
| AT (1) | ATE257488T1 (https=) |
| AU (1) | AU6202899A (https=) |
| BR (1) | BR9914347A (https=) |
| DE (1) | DE69914095T2 (https=) |
| ES (1) | ES2211178T3 (https=) |
| TW (1) | TW539691B (https=) |
| WO (1) | WO2000022004A1 (https=) |
| ZA (1) | ZA200102901B (https=) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20010046938A1 (en) * | 2000-03-04 | 2001-11-29 | Halasa Adel Farhan | Synthesis of dilithium initiator |
| DE10036055A1 (de) * | 2000-07-25 | 2002-02-07 | Bayer Ag | Verfahren zur Herstellung von di- oder trifunktionellen Initiatorsystemen auf Lithiumbasis sowie deren Verwendung |
| WO2002020623A1 (fr) | 2000-09-11 | 2002-03-14 | Societe De Technologie Michelin | Procede de preparation d'un initiateur dilithie et procede de polymerisation anionique |
| GR1004163B (el) | 2001-11-01 | 2003-02-21 | Πολυκυκλικα παραγωγα τροποποιησης των οπτικων ιδιοτητων και των ιδιοτητων αντοχης στο πλασμα των πολυμερων λιθογραφιας | |
| EP1709090B1 (en) * | 2003-09-24 | 2016-03-23 | Kraton Polymers U.S. LLC | Anionic polymerization diinitiator and process for preparing same |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3734973A (en) | 1971-11-04 | 1973-05-22 | Phillips Petroleum Co | Multifunctional polymerization initiators from diisopropenylbenzene |
| US5393843A (en) * | 1992-08-31 | 1995-02-28 | Shell Oil Company | Butadiene polymers having terminal functional groups |
-
1999
- 1999-09-30 US US09/409,924 patent/US6217798B1/en not_active Expired - Lifetime
- 1999-10-07 BR BR9914347-0A patent/BR9914347A/pt not_active IP Right Cessation
- 1999-10-07 DE DE69914095T patent/DE69914095T2/de not_active Expired - Lifetime
- 1999-10-07 JP JP2000575906A patent/JP4445135B2/ja not_active Expired - Lifetime
- 1999-10-07 AT AT99948993T patent/ATE257488T1/de not_active IP Right Cessation
- 1999-10-07 ES ES99948993T patent/ES2211178T3/es not_active Expired - Lifetime
- 1999-10-07 WO PCT/EP1999/007758 patent/WO2000022004A1/en not_active Ceased
- 1999-10-07 EP EP99948993A patent/EP1123320B1/en not_active Expired - Lifetime
- 1999-10-07 AU AU62028/99A patent/AU6202899A/en not_active Abandoned
- 1999-10-07 KR KR1020017004334A patent/KR100649780B1/ko not_active Expired - Lifetime
- 1999-10-20 TW TW088118092A patent/TW539691B/zh not_active IP Right Cessation
-
2001
- 2001-04-09 ZA ZA200102901A patent/ZA200102901B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ZA200102901B (en) | 2002-01-30 |
| US6217798B1 (en) | 2001-04-17 |
| DE69914095D1 (de) | 2004-02-12 |
| JP4445135B2 (ja) | 2010-04-07 |
| KR20010080012A (ko) | 2001-08-22 |
| KR100649780B1 (ko) | 2006-11-24 |
| WO2000022004A1 (en) | 2000-04-20 |
| TW539691B (en) | 2003-07-01 |
| BR9914347A (pt) | 2001-11-27 |
| ATE257488T1 (de) | 2004-01-15 |
| AU6202899A (en) | 2000-05-01 |
| EP1123320B1 (en) | 2004-01-07 |
| EP1123320A1 (en) | 2001-08-16 |
| ES2211178T3 (es) | 2004-07-01 |
| JP2002527541A (ja) | 2002-08-27 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8328 | Change in the person/name/address of the agent |
Representative=s name: STOLMAR, HINKELMANN & PARTNER GBR, 80331 MUENCHEN |
|
| 8364 | No opposition during term of opposition | ||
| 8328 | Change in the person/name/address of the agent |
Representative=s name: STOLMAR SCHEELE & PARTNER, 80331 MUENCHEN |