ES248458A1 - Un metodo de producir un polimero de eyileno normalmente sëlido - Google Patents
Un metodo de producir un polimero de eyileno normalmente sëlidoInfo
- Publication number
- ES248458A1 ES248458A1 ES0248458A ES248458A ES248458A1 ES 248458 A1 ES248458 A1 ES 248458A1 ES 0248458 A ES0248458 A ES 0248458A ES 248458 A ES248458 A ES 248458A ES 248458 A1 ES248458 A1 ES 248458A1
- Authority
- ES
- Spain
- Prior art keywords
- vanadyl
- acids
- acetate
- carboxylic acid
- salts
- 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
- 239000003054 catalyst Substances 0.000 title abstract 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 title abstract 4
- 239000005977 Ethylene Substances 0.000 title abstract 4
- 238000006116 polymerization reaction Methods 0.000 title 1
- 125000005287 vanadyl group Chemical group 0.000 abstract 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 6
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 abstract 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 6
- -1 alkenyl monocarboxylic acids Chemical class 0.000 abstract 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 5
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 abstract 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- 150000007513 acids Chemical class 0.000 abstract 3
- WIWVNQBYNTWQOW-UHFFFAOYSA-L oxovanadium(2+);diacetate Chemical compound [V+2]=O.CC([O-])=O.CC([O-])=O WIWVNQBYNTWQOW-UHFFFAOYSA-L 0.000 abstract 3
- OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical compound CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 abstract 2
- 101100058670 Aeromonas hydrophila subsp. hydrophila (strain ATCC 7966 / DSM 30187 / BCRC 13018 / CCUG 14551 / JCM 1027 / KCTC 2358 / NCIMB 9240 / NCTC 8049) bsr gene Proteins 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 2
- SHZIWNPUGXLXDT-UHFFFAOYSA-N caproic acid ethyl ester Natural products CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 abstract 2
- 239000006185 dispersion Substances 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 abstract 2
- 150000002899 organoaluminium compounds Chemical class 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 abstract 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 2
- OXQGTIUCKGYOAA-UHFFFAOYSA-N 2-Ethylbutanoic acid Chemical compound CCC(CC)C(O)=O OXQGTIUCKGYOAA-UHFFFAOYSA-N 0.000 abstract 1
- 150000001279 adipic acids Chemical class 0.000 abstract 1
- 150000001559 benzoic acids Chemical class 0.000 abstract 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- 150000001991 dicarboxylic acids Chemical class 0.000 abstract 1
- 150000002689 maleic acids Chemical class 0.000 abstract 1
- 150000002763 monocarboxylic acids Chemical class 0.000 abstract 1
- 239000002685 polymerization catalyst Substances 0.000 abstract 1
- 150000003839 salts Chemical class 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
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/02—Ethene
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)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Método de producir un polímero de etileno normalmente sólido, que comprende poner etileno en contacto con una composición catalítica que comprende un catalizador de trialquil-aluminio y una sal de vanadilo de un ácido carbonílico.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US731850A US3062803A (en) | 1958-04-30 | 1958-04-30 | Halogen-free catalyst for ethylene polymerization |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES248458A1 true ES248458A1 (es) | 1960-01-16 |
Family
ID=24941202
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0248458A Expired ES248458A1 (es) | 1958-04-30 | 1959-04-06 | Un metodo de producir un polimero de eyileno normalmente sëlido |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3062803A (es) |
| BE (1) | BE578220A (es) |
| DE (1) | DE1114035B (es) |
| ES (1) | ES248458A1 (es) |
| FR (1) | FR1223008A (es) |
| GB (1) | GB876532A (es) |
| NL (1) | NL238677A (es) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1317869A (es) * | 1961-03-20 | 1963-05-08 | ||
| DE2934277A1 (de) * | 1979-08-24 | 1981-03-26 | Dynamit Nobel Ag, 5210 Troisdorf | In organischen medien loesliche vanadium(iv)-verbindungen |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1012460B (de) * | 1953-11-17 | 1957-07-18 | Dr Dr E H Karl Ziegler | Verfahren zur Herstellung von hochmolekularen Polyaethylenen |
| DE973626C (de) * | 1953-11-17 | 1960-04-14 | Karl Dr Dr E H Ziegler | Verfahren zur Herstellung von hochmolekularen Polyaethylenen |
| NL206073A (es) * | 1955-04-07 | 1900-01-01 | Hercules Powder Co Ltd | |
| US3004963A (en) * | 1955-09-16 | 1961-10-17 | Dow Chemical Co | Purifying polymerized olefins prepared with catalytic metal compounds and compositions thereby obtained |
| US2881156A (en) * | 1956-03-28 | 1959-04-07 | Standard Oil Co | Catalytic conversion and catalysts |
| BE563686A (es) * | 1957-01-03 | |||
| US2933482A (en) * | 1957-07-19 | 1960-04-19 | Union Carbide Corp | Polypropylene |
-
0
- NL NL238677D patent/NL238677A/xx unknown
- BE BE578220D patent/BE578220A/xx unknown
-
1958
- 1958-04-30 US US731850A patent/US3062803A/en not_active Expired - Lifetime
-
1959
- 1959-04-06 ES ES0248458A patent/ES248458A1/es not_active Expired
- 1959-04-24 DE DEU6144A patent/DE1114035B/de active Pending
- 1959-04-28 FR FR793454A patent/FR1223008A/fr not_active Expired
- 1959-04-29 GB GB14571/59A patent/GB876532A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR1223008A (fr) | 1960-06-14 |
| NL238677A (es) | |
| BE578220A (es) | |
| GB876532A (en) | 1961-09-06 |
| US3062803A (en) | 1962-11-06 |
| DE1114035B (de) | 1961-09-21 |
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