DE3143595A1 - Aethylen- und propylen-terpolymere und verfahren zu deren herstellung - Google Patents
Aethylen- und propylen-terpolymere und verfahren zu deren herstellungInfo
- Publication number
- DE3143595A1 DE3143595A1 DE19813143595 DE3143595A DE3143595A1 DE 3143595 A1 DE3143595 A1 DE 3143595A1 DE 19813143595 DE19813143595 DE 19813143595 DE 3143595 A DE3143595 A DE 3143595A DE 3143595 A1 DE3143595 A1 DE 3143595A1
- Authority
- DE
- Germany
- Prior art keywords
- ethylene
- propylene
- dipl
- propenylnorbornene
- dicyclopentadiene
- 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.)
- Withdrawn
Links
- 229920001897 terpolymer Polymers 0.000 title claims description 16
- 238000000034 method Methods 0.000 title claims description 3
- 238000002360 preparation method Methods 0.000 title claims 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 title description 13
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 title description 13
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 title description 11
- 239000005977 Ethylene Substances 0.000 title description 11
- 239000000203 mixture Substances 0.000 claims description 18
- 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 claims description 11
- BSFWGXOMEGLIPL-UHFFFAOYSA-N 4-prop-1-enylbicyclo[2.2.1]hept-2-ene Chemical compound C1CC2C=CC1(C=CC)C2 BSFWGXOMEGLIPL-UHFFFAOYSA-N 0.000 claims description 11
- 238000006116 polymerization reaction Methods 0.000 claims description 10
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 9
- 150000001993 dienes Chemical class 0.000 claims description 8
- -1 ethylene, propylene Chemical group 0.000 claims description 7
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- 239000003607 modifier Substances 0.000 claims description 4
- 238000003786 synthesis reaction Methods 0.000 claims description 4
- 229910052720 vanadium Inorganic materials 0.000 claims description 4
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 239000011593 sulfur Substances 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 229920006125 amorphous polymer Polymers 0.000 claims description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 claims 1
- 229920000642 polymer Polymers 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 8
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- 230000003197 catalytic effect Effects 0.000 description 4
- 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
- 238000004519 manufacturing process Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 150000003682 vanadium compounds Chemical class 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- ZUHRGSQCGNLZFH-UHFFFAOYSA-N 1,3-benzothiazole-5-thiol Chemical compound SC1=CC=C2SC=NC2=C1 ZUHRGSQCGNLZFH-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- YNLAOSYQHBDIKW-UHFFFAOYSA-M diethylaluminium chloride Chemical compound CC[Al](Cl)CC YNLAOSYQHBDIKW-UHFFFAOYSA-M 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- RKQOSDAEEGPRER-UHFFFAOYSA-L zinc diethyldithiocarbamate Chemical compound [Zn+2].CCN(CC)C([S-])=S.CCN(CC)C([S-])=S RKQOSDAEEGPRER-UHFFFAOYSA-L 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
- 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 |
|---|---|---|---|
| RO10248980 | 1980-11-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE3143595A1 true DE3143595A1 (de) | 1982-05-27 |
Family
ID=20109116
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19813143595 Withdrawn DE3143595A1 (de) | 1980-11-03 | 1981-11-03 | Aethylen- und propylen-terpolymere und verfahren zu deren herstellung |
Country Status (9)
| Country | Link |
|---|---|
| AT (1) | AT377269B (cs) |
| BG (1) | BG40816A3 (cs) |
| CS (1) | CS245050B2 (cs) |
| DE (1) | DE3143595A1 (cs) |
| ES (1) | ES506777A0 (cs) |
| FR (1) | FR2493325B1 (cs) |
| HU (1) | HU192076B (cs) |
| LU (1) | LU83728A1 (cs) |
| PT (1) | PT73921B (cs) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3306488A1 (de) * | 1982-02-26 | 1983-09-15 | Industrie Pirelli S.p.A., 20100 Milano | Zahnriemen |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3472824A (en) * | 1966-11-22 | 1969-10-14 | Sumitomo Chemical Co | Sulfur curable copolymers of olefins and iso-ethenyl norbornenes and method for production thereof |
| US3903062A (en) * | 1973-08-08 | 1975-09-02 | Snam Progetti | Olefin tetrapolymer and process for the preparation thereof |
| JPS5948046B2 (ja) * | 1978-08-17 | 1984-11-24 | 三井化学株式会社 | エチレン共重合ゴム |
-
1981
- 1981-10-30 LU LU83728A patent/LU83728A1/fr unknown
- 1981-11-02 ES ES506777A patent/ES506777A0/es active Granted
- 1981-11-02 BG BG054036A patent/BG40816A3/xx unknown
- 1981-11-03 PT PT7392181A patent/PT73921B/pt unknown
- 1981-11-03 HU HU328481A patent/HU192076B/hu not_active IP Right Cessation
- 1981-11-03 FR FR8120570A patent/FR2493325B1/fr not_active Expired
- 1981-11-03 CS CS818079A patent/CS245050B2/cs unknown
- 1981-11-03 AT AT470881A patent/AT377269B/de not_active IP Right Cessation
- 1981-11-03 DE DE19813143595 patent/DE3143595A1/de not_active Withdrawn
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3306488A1 (de) * | 1982-02-26 | 1983-09-15 | Industrie Pirelli S.p.A., 20100 Milano | Zahnriemen |
Also Published As
| Publication number | Publication date |
|---|---|
| PT73921B (fr) | 1983-04-18 |
| PT73921A (fr) | 1981-12-01 |
| CS807981A2 (en) | 1985-08-15 |
| ES8303462A1 (es) | 1983-02-01 |
| CS245050B2 (en) | 1986-08-14 |
| FR2493325A1 (fr) | 1982-05-07 |
| ES506777A0 (es) | 1983-02-01 |
| BG40816A3 (bg) | 1987-02-16 |
| HU192076B (en) | 1987-05-28 |
| AT377269B (de) | 1985-02-25 |
| FR2493325B1 (fr) | 1986-04-04 |
| LU83728A1 (fr) | 1982-02-18 |
| ATA470881A (de) | 1984-07-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OP8 | Request for examination as to paragraph 44 patent law | ||
| 8128 | New person/name/address of the agent |
Representative=s name: VON FUENER, A., DIPL.-CHEM. DR.RER.NAT. EBBINGHAUS |
|
| 8130 | Withdrawal |