DE2237573A1 - Stabilisierte olefin-terpolymerisate und verfahren zu ihrer herstellung - Google Patents
Stabilisierte olefin-terpolymerisate und verfahren zu ihrer herstellungInfo
- Publication number
- DE2237573A1 DE2237573A1 DE2237573A DE2237573A DE2237573A1 DE 2237573 A1 DE2237573 A1 DE 2237573A1 DE 2237573 A DE2237573 A DE 2237573A DE 2237573 A DE2237573 A DE 2237573A DE 2237573 A1 DE2237573 A1 DE 2237573A1
- Authority
- DE
- Germany
- Prior art keywords
- terpolymers
- dienophilic
- stabilized
- olefin
- agent
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 14
- 229920001897 terpolymer Polymers 0.000 claims description 24
- 230000032683 aging Effects 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 150000001336 alkenes Chemical class 0.000 claims description 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 5
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 3
- 239000005977 Ethylene Substances 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000003342 alkenyl group Chemical group 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 150000004291 polyenes Chemical class 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims description 2
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- 150000002430 hydrocarbons Chemical class 0.000 claims description 2
- 229920002521 macromolecule Polymers 0.000 claims description 2
- 230000001590 oxidative effect Effects 0.000 claims description 2
- 230000006641 stabilisation Effects 0.000 claims description 2
- 238000011105 stabilization Methods 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 229920000642 polymer Polymers 0.000 description 14
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000003153 chemical reaction reagent Substances 0.000 description 5
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 3
- 238000004073 vulcanization Methods 0.000 description 3
- -1 methylcyclopentadienyl- Chemical group 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- WUIJTQZXUURFQU-UHFFFAOYSA-N 1-methylsulfonylethene Chemical compound CS(=O)(=O)C=C WUIJTQZXUURFQU-UHFFFAOYSA-N 0.000 description 1
- HIDBROSJWZYGSZ-UHFFFAOYSA-N 1-phenylpyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C1=CC=CC=C1 HIDBROSJWZYGSZ-UHFFFAOYSA-N 0.000 description 1
- LEHFKOPSVFOJDF-UHFFFAOYSA-N 2,3-dimethylidenebicyclo[2.2.1]hept-5-ene Chemical compound C1C2C=CC1C(=C)C2=C LEHFKOPSVFOJDF-UHFFFAOYSA-N 0.000 description 1
- VTWDKFNVVLAELH-UHFFFAOYSA-N 2-methylcyclohexa-2,5-diene-1,4-dione Chemical group CC1=CC(=O)C=CC1=O VTWDKFNVVLAELH-UHFFFAOYSA-N 0.000 description 1
- NCCTVAJNFXYWTM-UHFFFAOYSA-N 2-tert-butylcyclohexa-2,5-diene-1,4-dione Chemical group CC(C)(C)C1=CC(=O)C=CC1=O NCCTVAJNFXYWTM-UHFFFAOYSA-N 0.000 description 1
- OQNVBPKVFUOGQY-UHFFFAOYSA-N C(=O)(C=C)OS(=O)(=O)C#N Chemical compound C(=O)(C=C)OS(=O)(=O)C#N OQNVBPKVFUOGQY-UHFFFAOYSA-N 0.000 description 1
- YYBDEBBSYQNIDZ-UHFFFAOYSA-N C1C2C(C=CC)=CC1C=C2 Chemical compound C1C2C(C=CC)=CC1C=C2 YYBDEBBSYQNIDZ-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
- 229930192627 Naphthoquinone Natural products 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- CPEKAXYCDKETEN-UHFFFAOYSA-N benzoyl isothiocyanate Chemical compound S=C=NC(=O)C1=CC=CC=C1 CPEKAXYCDKETEN-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Substances CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- FRASJONUBLZVQX-UHFFFAOYSA-N naphthoquinone group Chemical group C1(C=CC(C2=CC=CC=C12)=O)=O FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000003878 thermal aging Methods 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
- C08F8/00—Chemical modification by after-treatment
- C08F8/34—Introducing sulfur atoms or sulfur-containing groups
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT2701471 | 1971-07-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2237573A1 true DE2237573A1 (de) | 1973-02-08 |
Family
ID=11220767
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2237573A Pending DE2237573A1 (de) | 1971-07-31 | 1972-07-31 | Stabilisierte olefin-terpolymerisate und verfahren zu ihrer herstellung |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US3892712A (en:Method) |
| JP (1) | JPS5222036B2 (en:Method) |
| AT (1) | AT315483B (en:Method) |
| BE (1) | BE786619A (en:Method) |
| CA (1) | CA984997A (en:Method) |
| CH (1) | CH549609A (en:Method) |
| CS (1) | CS178412B2 (en:Method) |
| DD (1) | DD100480A5 (en:Method) |
| DE (1) | DE2237573A1 (en:Method) |
| ES (1) | ES405704A1 (en:Method) |
| FR (1) | FR2149109A5 (en:Method) |
| GB (1) | GB1396333A (en:Method) |
| LU (1) | LU65793A1 (en:Method) |
| NL (1) | NL7210484A (en:Method) |
| PL (1) | PL70025B1 (en:Method) |
| RO (1) | RO63338A (en:Method) |
| ZA (1) | ZA725195B (en:Method) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1006626B (it) * | 1973-10-31 | 1976-10-20 | Snam Progetti | Materiali polimerici aventi pro prieta antiurto e loro procedi mento di preparazione |
| US4007121A (en) * | 1974-06-03 | 1977-02-08 | Texaco Inc. | Lubricating oil compositions containing a dispersant amount of aminated nitroketonized hydrocarbon terpolymers |
| JPS59227801A (ja) * | 1983-06-07 | 1984-12-21 | Akisuke Okubo | 植物保存用液及び植物保存用液を用いた乾燥植物の形成方法 |
| JPS60228401A (ja) * | 1984-04-26 | 1985-11-13 | Akisuke Okubo | 植物保存用液及び植物保存用液を用いた乾燥植物の形成方法 |
| US5616532A (en) * | 1990-12-14 | 1997-04-01 | E. Heller & Company | Photocatalyst-binder compositions |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3538193A (en) * | 1967-04-06 | 1970-11-03 | Copolymer Rubber & Chem Corp | Recovery of polymeric materials from organic reaction mixtures |
| GB1229399A (en:Method) * | 1968-09-05 | 1971-04-21 | ||
| NL135975C (en:Method) * | 1968-12-18 | |||
| CA978695A (en) * | 1970-01-22 | 1975-11-25 | Sebastiano Cesca | Curable amorphous olefinic terpolymers obtained from alpha-olefins and polyenes containing two conjugated double bonds and process for obtaining same |
-
0
- BE BE786619D patent/BE786619A/xx unknown
-
1972
- 1972-07-24 CH CH1103372A patent/CH549609A/fr not_active IP Right Cessation
- 1972-07-24 CA CA147,813A patent/CA984997A/en not_active Expired
- 1972-07-26 GB GB3504872A patent/GB1396333A/en not_active Expired
- 1972-07-26 FR FR7226806A patent/FR2149109A5/fr not_active Expired
- 1972-07-26 LU LU65793D patent/LU65793A1/xx unknown
- 1972-07-27 ZA ZA725195A patent/ZA725195B/xx unknown
- 1972-07-28 NL NL7210484A patent/NL7210484A/xx unknown
- 1972-07-28 ES ES405704A patent/ES405704A1/es not_active Expired
- 1972-07-28 AT AT652372A patent/AT315483B/de active
- 1972-07-28 DD DD164750A patent/DD100480A5/xx unknown
- 1972-07-28 US US275936A patent/US3892712A/en not_active Expired - Lifetime
- 1972-07-29 PL PL1972157018A patent/PL70025B1/pl unknown
- 1972-07-31 JP JP47076052A patent/JPS5222036B2/ja not_active Expired
- 1972-07-31 DE DE2237573A patent/DE2237573A1/de active Pending
- 1972-07-31 CS CS5352A patent/CS178412B2/cs unknown
- 1972-07-31 RO RO7200071806A patent/RO63338A/ro unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB1396333A (en) | 1975-06-04 |
| NL7210484A (en:Method) | 1973-02-02 |
| US3892712A (en) | 1975-07-01 |
| JPS4825091A (en:Method) | 1973-04-02 |
| AU4446872A (en) | 1974-01-17 |
| JPS5222036B2 (en:Method) | 1977-06-14 |
| FR2149109A5 (en:Method) | 1973-03-23 |
| CA984997A (en) | 1976-03-02 |
| RO63338A (fr) | 1978-09-15 |
| ES405704A1 (es) | 1975-09-01 |
| ZA725195B (en) | 1973-04-25 |
| AT315483B (de) | 1974-05-27 |
| DD100480A5 (en:Method) | 1973-09-20 |
| CH549609A (fr) | 1974-05-31 |
| CS178412B2 (en:Method) | 1977-09-15 |
| LU65793A1 (en:Method) | 1972-11-28 |
| PL70025B1 (en:Method) | 1973-12-31 |
| BE786619A (fr) | 1973-01-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69004712T2 (de) | Verfahren zur Herstellung von Polybutadien mit verbesserter Verarbeitkeit. | |
| DE2552617C2 (de) | Verfahren zur Herstellung eines modifizierten kautschukartigen Terpolymeren und seine Verwendung | |
| DE2713455C2 (en:Method) | ||
| DE2059378A1 (de) | Verfahren zur Herstellung von 1,2-Polybutadien | |
| DE2045574C3 (de) | Schwefelvulkanisierbare Masse | |
| DE60026035T2 (de) | Kautschukmischung | |
| DE3033175C2 (de) | Polybutadienkautschukzusammensetzungen | |
| DE2039394A1 (de) | Verfahren zur Herstellung von Pfropfmischpolymerisaten | |
| DE2237573A1 (de) | Stabilisierte olefin-terpolymerisate und verfahren zu ihrer herstellung | |
| DE3230744C2 (de) | Kautschukmassen | |
| DE1270820B (de) | Ver fahren zur Herstellung von Block Misch polymerisaten | |
| DE1142060B (de) | Verfahren zum Vulkanisieren von im wesentlichen amorphen hochmolekularen Mischpolymerisaten aus ª‡-Olefinen miteinander und/oder mit AEthylen | |
| DE2139888A1 (de) | Ozonbestandige Gemische aus natur hchem Kautschuk/Polychloropren/EPDM Copolymerem sowie Verfahren zu deren Herstellung | |
| DE1016262B (de) | Verfahren zur Herstellung des Perchlor-1, 1'-dihydrofulvalens | |
| DE1720142C3 (de) | Durch Luftfeuchtigkeit vulkanisierbare Masse aus einem flüssigen Polymerisat auf der Basis von Butadien-13 | |
| EP0301347A1 (de) | Polychloroprenmischungen | |
| DE1301093B (de) | Verfahren zur Herstellung von vulkanisierbaren sulfohalogenierten Olefin-Polymeren und -Copolymeren | |
| DE1816089B2 (de) | Verfahren zum herstellen von regellosen coplymeren aus conjugierten dienen mit 4 12 kohlenstoffatomen und vinylsubstitu ierten aromatischen kohlenwasserstoffen | |
| DE2626319C2 (de) | Verfahren zur Herstellung von modifizierten kautschukartigen Terpolymeren | |
| DE1251032B (de) | Verfahren zur Herstellung von hochmolekularem Polychloropren | |
| CH455293A (de) | Verfahren zur Herstellung von neuen olefinisch ungesättigten Carboxylgruppen aufweisenden Verbindungen mit hohem Molekulargewicht | |
| DE2622914C2 (de) | Brombutylkautschukmischungen | |
| DE1101763B (de) | Verfahren zur Herstellung von halogenierten Isoolefin-Polyolefin-Mischpolymerisaten | |
| DE2528852B2 (de) | Luftreifen | |
| DE852904C (de) | Verfahren zum Vulkanisieren eines synthetischen, mit Schwefel vulkanisierbaren, kautschukaehnlichen Mischpolymeren eines Butadien-1, 3-Kohlenwasserstoffs und einer Monovinylverbindung |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OGA | New person/name/address of the applicant | ||
| OHJ | Non-payment of the annual fee |