GB1153775A - Process for the Production of Polybutadiene Oils - Google Patents
Process for the Production of Polybutadiene OilsInfo
- Publication number
- GB1153775A GB1153775A GB4466766A GB4466766A GB1153775A GB 1153775 A GB1153775 A GB 1153775A GB 4466766 A GB4466766 A GB 4466766A GB 4466766 A GB4466766 A GB 4466766A GB 1153775 A GB1153775 A GB 1153775A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- polymers
- butadiene
- compounds
- aliphatic
- 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
- 239000005062 Polybutadiene Substances 0.000 title 1
- 239000003921 oil Substances 0.000 title 1
- 229920002857 polybutadiene Polymers 0.000 title 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 239000000178 monomer Substances 0.000 abstract 3
- UNEATYXSUBPPKP-UHFFFAOYSA-N 1,3-Diisopropylbenzene Chemical compound CC(C)C1=CC=CC(C(C)C)=C1 UNEATYXSUBPPKP-UHFFFAOYSA-N 0.000 abstract 2
- SPPWGCYEYAMHDT-UHFFFAOYSA-N 1,4-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=C(C(C)C)C=C1 SPPWGCYEYAMHDT-UHFFFAOYSA-N 0.000 abstract 2
- XCYJPXQACVEIOS-UHFFFAOYSA-N 1-isopropyl-3-methylbenzene Chemical compound CC(C)C1=CC=CC(C)=C1 XCYJPXQACVEIOS-UHFFFAOYSA-N 0.000 abstract 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 abstract 2
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- NXLOLUFNDSBYTP-UHFFFAOYSA-N retene Chemical compound C1=CC=C2C3=CC=C(C(C)C)C=C3C=CC2=C1C NXLOLUFNDSBYTP-UHFFFAOYSA-N 0.000 abstract 2
- PBWHJRFXUPLZDS-UHFFFAOYSA-N (1-Ethylpropyl)benzene Chemical compound CCC(CC)C1=CC=CC=C1 PBWHJRFXUPLZDS-UHFFFAOYSA-N 0.000 abstract 1
- OKIRBHVFJGXOIS-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC=C1C(C)C OKIRBHVFJGXOIS-UHFFFAOYSA-N 0.000 abstract 1
- IAUKWGFWINVWKS-UHFFFAOYSA-N 1,2-di(propan-2-yl)naphthalene Chemical compound C1=CC=CC2=C(C(C)C)C(C(C)C)=CC=C21 IAUKWGFWINVWKS-UHFFFAOYSA-N 0.000 abstract 1
- BDJUQNIAPKYGNU-UHFFFAOYSA-N 1,4-di(propan-2-yl)naphthalene Chemical compound C1=CC=C2C(C(C)C)=CC=C(C(C)C)C2=C1 BDJUQNIAPKYGNU-UHFFFAOYSA-N 0.000 abstract 1
- FJMDMTMUYAPCLL-UHFFFAOYSA-N 1,4-dibutyl-2-ethylbenzene Chemical compound CCCCC1=CC=C(CCCC)C(CC)=C1 FJMDMTMUYAPCLL-UHFFFAOYSA-N 0.000 abstract 1
- MBEBPYJMHLBHDJ-UHFFFAOYSA-N 1,4-dimethyl-2,5-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC(C)=C(C(C)C)C=C1C MBEBPYJMHLBHDJ-UHFFFAOYSA-N 0.000 abstract 1
- ZTOFNRMEKUYYOE-UHFFFAOYSA-N 1-propan-2-yl-9h-carbazole Chemical compound C12=CC=CC=C2NC2=C1C=CC=C2C(C)C ZTOFNRMEKUYYOE-UHFFFAOYSA-N 0.000 abstract 1
- WQQVJVRRHCTWPP-UHFFFAOYSA-N 1-propan-2-yl-9h-fluorene Chemical compound C1C2=CC=CC=C2C2=C1C(C(C)C)=CC=C2 WQQVJVRRHCTWPP-UHFFFAOYSA-N 0.000 abstract 1
- PMPBFICDXLLSRM-UHFFFAOYSA-N 1-propan-2-ylnaphthalene Chemical compound C1=CC=C2C(C(C)C)=CC=CC2=C1 PMPBFICDXLLSRM-UHFFFAOYSA-N 0.000 abstract 1
- AJVJASHKSBJOOW-UHFFFAOYSA-N 9,10-di(propan-2-yl)anthracene Chemical compound C1=CC=C2C(C(C)C)=C(C=CC=C3)C3=C(C(C)C)C2=C1 AJVJASHKSBJOOW-UHFFFAOYSA-N 0.000 abstract 1
- 101100188555 Arabidopsis thaliana OCT6 gene Proteins 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 229910052792 caesium Inorganic materials 0.000 abstract 1
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 238000007796 conventional method Methods 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 229920001519 homopolymer Polymers 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
- -1 hydrogen halides Chemical class 0.000 abstract 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N itaconic acid Chemical class OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 150000002739 metals Chemical class 0.000 abstract 1
- 125000005395 methacrylic acid group Chemical class 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- 239000011591 potassium Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 229910052701 rubidium Inorganic materials 0.000 abstract 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 150000003440 styrenes Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 238000005406 washing Methods 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- 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)
- 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 |
|---|---|---|---|
| DE1965B0084014 DE1301900B (de) | 1965-10-07 | 1965-10-07 | Verfahren zur Herstellung von Polybutadienoelen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1153775A true GB1153775A (en) | 1969-05-29 |
Family
ID=6982236
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4466766A Expired GB1153775A (en) | 1965-10-07 | 1966-10-06 | Process for the Production of Polybutadiene Oils |
Country Status (6)
| Country | Link |
|---|---|
| AT (1) | AT268650B (enrdf_load_html_response) |
| BE (1) | BE687679A (enrdf_load_html_response) |
| CH (1) | CH460355A (enrdf_load_html_response) |
| DE (1) | DE1301900B (enrdf_load_html_response) |
| GB (1) | GB1153775A (enrdf_load_html_response) |
| NL (1) | NL6614168A (enrdf_load_html_response) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5717042A (en) * | 1991-05-06 | 1998-02-10 | Bridgestone/Firestone, Inc. | Process for preparing diene oligomers and copolymeric oligomers |
-
1965
- 1965-10-07 DE DE1965B0084014 patent/DE1301900B/de active Pending
-
1966
- 1966-09-30 BE BE687679D patent/BE687679A/xx unknown
- 1966-10-04 CH CH1427666A patent/CH460355A/de unknown
- 1966-10-06 GB GB4466766A patent/GB1153775A/en not_active Expired
- 1966-10-07 NL NL6614168A patent/NL6614168A/xx unknown
- 1966-10-07 AT AT941766A patent/AT268650B/de active
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5717042A (en) * | 1991-05-06 | 1998-02-10 | Bridgestone/Firestone, Inc. | Process for preparing diene oligomers and copolymeric oligomers |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1301900B (de) | 1969-08-28 |
| NL6614168A (enrdf_load_html_response) | 1967-04-10 |
| CH460355A (de) | 1968-07-31 |
| BE687679A (enrdf_load_html_response) | 1967-03-30 |
| AT268650B (de) | 1969-02-25 |
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