GB1010029A - Process for the preparation of vulcanizable, essentially amorphous, olefinic terpolymers - Google Patents
Process for the preparation of vulcanizable, essentially amorphous, olefinic terpolymersInfo
- Publication number
- GB1010029A GB1010029A GB21317/64A GB2131764A GB1010029A GB 1010029 A GB1010029 A GB 1010029A GB 21317/64 A GB21317/64 A GB 21317/64A GB 2131764 A GB2131764 A GB 2131764A GB 1010029 A GB1010029 A GB 1010029A
- Authority
- GB
- United Kingdom
- Prior art keywords
- preferred
- terpolymers
- vulcanizable
- hbral
- alhcl2
- 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
Links
- 229920001897 terpolymer Polymers 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 3
- -1 cycloalkyl radical Chemical class 0.000 abstract 3
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 abstract 2
- 229910000091 aluminium hydride Inorganic materials 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- WADSLQQIOJIXTB-UHFFFAOYSA-L dichloroalumane Chemical compound Cl[AlH]Cl WADSLQQIOJIXTB-UHFFFAOYSA-L 0.000 abstract 2
- 150000005673 monoalkenes Chemical class 0.000 abstract 2
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 abstract 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- 239000002879 Lewis base Substances 0.000 abstract 1
- 229910010062 TiCl3 Inorganic materials 0.000 abstract 1
- 229910003074 TiCl4 Inorganic materials 0.000 abstract 1
- 229910021551 Vanadium(III) chloride Inorganic materials 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 238000007796 conventional method Methods 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 150000001993 dienes Chemical class 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 abstract 1
- 150000008282 halocarbons Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 150000004678 hydrides Chemical class 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 238000011065 in-situ storage Methods 0.000 abstract 1
- 150000007527 lewis bases Chemical class 0.000 abstract 1
- 239000000178 monomer Substances 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 230000000737 periodic effect Effects 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 238000006116 polymerization reaction Methods 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 238000000638 solvent extraction Methods 0.000 abstract 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 abstract 1
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 abstract 1
- 229910052723 transition metal Inorganic materials 0.000 abstract 1
- 150000003624 transition metals Chemical class 0.000 abstract 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 abstract 1
- HQYCOEXWFMFWLR-UHFFFAOYSA-K vanadium(iii) chloride Chemical compound [Cl-].[Cl-].[Cl-].[V+3] HQYCOEXWFMFWLR-UHFFFAOYSA-K 0.000 abstract 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
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
- C08F210/18—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers with non-conjugated dienes, e.g. EPT rubbers
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 |
|---|---|---|---|
| IT1072763 | 1963-05-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1010029A true GB1010029A (en) | 1965-11-17 |
Family
ID=11134403
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB21317/64A Expired GB1010029A (en) | 1963-05-24 | 1964-05-22 | Process for the preparation of vulcanizable, essentially amorphous, olefinic terpolymers |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3386975A (OSRAM) |
| BE (1) | BE662134A (OSRAM) |
| FR (1) | FR1397652A (OSRAM) |
| GB (1) | GB1010029A (OSRAM) |
| LU (1) | LU46144A1 (OSRAM) |
| NL (2) | NL6405719A (OSRAM) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3901862A (en) * | 1972-12-20 | 1975-08-26 | Snam Progetti | Process for the preparation of ethylene-butadiene copolymers |
| TR199900080T2 (xx) * | 1996-07-23 | 1999-04-21 | The Dow Chemical Company | Grup 13 bile�i�ini i�eren olefin polimerizasyon kataliz�r bile�imi. |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE614644A (OSRAM) * | 1957-07-17 | |||
| BE597929A (OSRAM) * | 1959-12-09 | |||
| BE623698A (OSRAM) * | 1961-10-18 | 1963-02-15 | Montecatina Societa Generale P |
-
0
- NL NL126040D patent/NL126040C/xx active
-
1964
- 1964-05-22 GB GB21317/64A patent/GB1010029A/en not_active Expired
- 1964-05-22 FR FR975489A patent/FR1397652A/fr not_active Expired
- 1964-05-22 US US369618A patent/US3386975A/en not_active Expired - Lifetime
- 1964-05-22 NL NL6405719A patent/NL6405719A/xx unknown
- 1964-05-23 LU LU46144D patent/LU46144A1/xx unknown
-
1965
- 1965-04-06 BE BE662134D patent/BE662134A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| LU46144A1 (OSRAM) | 1965-05-23 |
| NL126040C (OSRAM) | |
| BE662134A (OSRAM) | 1965-08-02 |
| NL6405719A (OSRAM) | 1964-11-25 |
| FR1397652A (fr) | 1965-04-30 |
| DE1520865B2 (de) | 1972-07-13 |
| DE1520865A1 (de) | 1970-01-29 |
| US3386975A (en) | 1968-06-04 |
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