SU503529A3 - Способ получени сополимеров изобутилена - Google Patents
Способ получени сополимеров изобутиленаInfo
- Publication number
- SU503529A3 SU503529A3 SU1902141A SU1902141A SU503529A3 SU 503529 A3 SU503529 A3 SU 503529A3 SU 1902141 A SU1902141 A SU 1902141A SU 1902141 A SU1902141 A SU 1902141A SU 503529 A3 SU503529 A3 SU 503529A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- copolymerization
- isoprene
- polymer
- isobutylene copolymers
- isobutylene
- Prior art date
Links
- 229920001577 copolymer Polymers 0.000 title claims description 3
- 238000004519 manufacturing process Methods 0.000 title 1
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 18
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 6
- 239000003054 catalyst Substances 0.000 claims description 5
- 230000003197 catalytic effect Effects 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 238000007334 copolymerization reaction Methods 0.000 claims 4
- -1 alkylaluminum halide Chemical class 0.000 claims 1
- 150000008064 anhydrides Chemical class 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 229920000642 polymer Polymers 0.000 description 14
- 239000000203 mixture Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 238000004073 vulcanization Methods 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- 102100034535 Histone H3.1 Human genes 0.000 description 1
- 101001067844 Homo sapiens Histone H3.1 Proteins 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- CBHOOMGKXCMKIR-UHFFFAOYSA-N azane;methanol Chemical compound N.OC CBHOOMGKXCMKIR-UHFFFAOYSA-N 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000013213 extrapolation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 238000005406 washing 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
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
Landscapes
- 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)
- Polymerization Catalysts (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT23216/72A IT951473B (it) | 1972-04-17 | 1972-04-17 | Procedimento per la produzione di polimeri e copolimeri dell iso butilene |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU503529A3 true SU503529A3 (ru) | 1976-02-15 |
Family
ID=11204976
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1902141A SU503529A3 (ru) | 1972-04-17 | 1973-04-15 | Способ получени сополимеров изобутилена |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US3896097A (enExample) |
| JP (1) | JPS533424B2 (enExample) |
| AT (1) | AT327542B (enExample) |
| BE (1) | BE797842A (enExample) |
| CA (1) | CA1011900A (enExample) |
| CH (1) | CH569038A5 (enExample) |
| CS (1) | CS182784B2 (enExample) |
| DD (1) | DD105809A5 (enExample) |
| DE (1) | DE2319536C3 (enExample) |
| ES (1) | ES414371A1 (enExample) |
| FR (1) | FR2180724B1 (enExample) |
| GB (1) | GB1409337A (enExample) |
| HU (1) | HU167167B (enExample) |
| IN (1) | IN139842B (enExample) |
| IT (1) | IT951473B (enExample) |
| LU (1) | LU67394A1 (enExample) |
| NL (1) | NL153220B (enExample) |
| PL (1) | PL92998B1 (enExample) |
| RO (1) | RO63437A (enExample) |
| SU (1) | SU503529A3 (enExample) |
| TR (1) | TR18305A (enExample) |
| ZA (1) | ZA732563B (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2019075356A2 (en) | 2017-10-14 | 2019-04-18 | Tpc Group Llc | NON-RANDOM ISOBUTYLENE COPOLYMERS |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2220930A (en) * | 1938-11-03 | 1940-11-12 | Standard Oil Dev Co | Polymerization of hydrocarbons |
| US2536841A (en) * | 1945-12-04 | 1951-01-02 | Standard Oil Dev Co | Low-temperature olefin polymerization with sulfur containing friedel-crafts complex catalysts |
| US2581154A (en) * | 1948-07-01 | 1952-01-01 | Standard Oil Dev Co | Tertiary-butyl halide promoters in friedel-crafts catalyzed olefin polymerizations |
| US2670393A (en) * | 1952-01-10 | 1954-02-23 | Univ Notre Dame Du Lac | Polymerization of isobutene with anhydrous sulfur trioxide catalyst |
| US2931791A (en) * | 1955-05-23 | 1960-04-05 | Exxon Research Engineering Co | Polymerization of hydrocarbons with catalyst of bf3 and bci3 |
| US3024226A (en) * | 1959-11-23 | 1962-03-06 | Texaco Inc | Polymerization process |
| US3426007A (en) * | 1965-10-21 | 1969-02-04 | Exxon Research Engineering Co | Polymerization catalyst system |
-
1972
- 1972-04-17 IT IT23216/72A patent/IT951473B/it active
-
1973
- 1973-04-03 TR TR18305A patent/TR18305A/xx unknown
- 1973-04-05 FR FR7312240A patent/FR2180724B1/fr not_active Expired
- 1973-04-06 BE BE1004948A patent/BE797842A/xx unknown
- 1973-04-09 LU LU67394A patent/LU67394A1/xx unknown
- 1973-04-11 RO RO7300074446A patent/RO63437A/ro unknown
- 1973-04-13 ZA ZA732563A patent/ZA732563B/xx unknown
- 1973-04-13 DD DD170214A patent/DD105809A5/xx unknown
- 1973-04-14 CH CH537873A patent/CH569038A5/xx not_active IP Right Cessation
- 1973-04-15 SU SU1902141A patent/SU503529A3/ru active
- 1973-04-16 GB GB1830473A patent/GB1409337A/en not_active Expired
- 1973-04-16 JP JP4227373A patent/JPS533424B2/ja not_active Expired
- 1973-04-16 ES ES414371A patent/ES414371A1/es not_active Expired
- 1973-04-16 AT AT337773A patent/AT327542B/de not_active IP Right Cessation
- 1973-04-16 NL NL737305319A patent/NL153220B/xx unknown
- 1973-04-16 HU HUSA2485A patent/HU167167B/hu unknown
- 1973-04-16 CS CS7300002715A patent/CS182784B2/cs unknown
- 1973-04-16 PL PL1973161945A patent/PL92998B1/xx unknown
- 1973-04-17 US US352084A patent/US3896097A/en not_active Expired - Lifetime
- 1973-04-17 DE DE2319536A patent/DE2319536C3/de not_active Expired
- 1973-04-17 CA CA169,902A patent/CA1011900A/en not_active Expired
- 1973-04-24 IN IN963/CAL/73A patent/IN139842B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TR18305A (tr) | 1977-01-07 |
| ZA732563B (en) | 1974-03-27 |
| DE2319536C3 (de) | 1979-04-05 |
| CS182784B2 (en) | 1978-05-31 |
| DD105809A5 (enExample) | 1974-05-12 |
| DE2319536B2 (de) | 1978-08-03 |
| JPS533424B2 (enExample) | 1978-02-06 |
| RO63437A (fr) | 1978-05-15 |
| GB1409337A (en) | 1975-10-08 |
| FR2180724A1 (enExample) | 1973-11-30 |
| CA1011900A (en) | 1977-06-07 |
| AT327542B (de) | 1976-02-10 |
| CH569038A5 (enExample) | 1975-11-14 |
| BE797842A (fr) | 1973-07-31 |
| ES414371A1 (es) | 1976-02-01 |
| IT951473B (it) | 1973-06-30 |
| NL7305319A (enExample) | 1973-10-19 |
| AU5298573A (en) | 1974-09-12 |
| HU167167B (enExample) | 1975-08-28 |
| LU67394A1 (enExample) | 1973-06-18 |
| US3896097A (en) | 1975-07-22 |
| IN139842B (enExample) | 1976-08-07 |
| NL153220B (nl) | 1977-05-16 |
| DE2319536A1 (de) | 1973-10-31 |
| ATA337773A (de) | 1975-04-15 |
| FR2180724B1 (enExample) | 1976-09-10 |
| PL92998B1 (enExample) | 1977-04-30 |
| JPS4920289A (enExample) | 1974-02-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5247021A (en) | Process for preparation of a polymer having reactive terminal group | |
| Sen et al. | Kinetics of silane grafting and moisture crosslinking of polyethylene and ethylene propylene rubber | |
| EP1209170A1 (en) | Method of continuous cationic living polymerization | |
| SU503529A3 (ru) | Способ получени сополимеров изобутилена | |
| JPH0615609B2 (ja) | 狭い分子量分布を有するポリ(テトラメチレンエーテル)グリコールの製法 | |
| SU624577A3 (ru) | Способ получени карбоцепных сополимеров | |
| Kim et al. | Synthesis and crystallization behavior of regioregular-block-regiorandom poly (3-hexylthiophene) copolymers | |
| GB934742A (en) | Improvements in or relating to hydrocarbon copolymers | |
| Burrows et al. | Polymerization of tetrahydrofuran | |
| US3467637A (en) | Low molecular weight olefin interpolymers prepared in the presence of bicyclo(2.2.1)hepta-2,5-diene | |
| SU828973A3 (ru) | Способ получени эластомеров | |
| SU366723A1 (ru) | Способ получени статистических дивинилстирольных каучуков | |
| Park et al. | Effect of initiator end groups and trichlorethylene units on the dehydrochlorination of solution polymerized poly (vinyl chloride) | |
| RU2099359C1 (ru) | Способ получения цис-1,4-диенового каучука | |
| CA1042132A (en) | Production of polymeric compounds having functional end groups | |
| US3242147A (en) | Chlorosulfonate catalysts for polymerization | |
| US2962480A (en) | Chlorosulfonation of diolefin polymers | |
| US3853829A (en) | Copolymers of vinyl ethers and cyclic polyenes containing a system of conjugated double bonds and process for the preparation thereof | |
| SU418496A1 (ru) | Способ получения каучукоподобных полимеров | |
| US3940372A (en) | Modified molecular weight of polylactams | |
| SU493975A3 (ru) | Способ получени сополимеров изобутилена | |
| SU360850A1 (ru) | Способ получени статистических сополимеров бутадиена со стиролом | |
| Block et al. | Copolymerization of phenylethyne with maleic anhydride | |
| Furukawa et al. | Preparation of copolymer of acetylene and butadiene | |
| SU489339A3 (ru) | Способ получени сополимеров изобутилена |