ES252357A1 - Procedimiento de producciën de isopreno - Google Patents
Procedimiento de producciën de isoprenoInfo
- Publication number
- ES252357A1 ES252357A1 ES0252357A ES252357A ES252357A1 ES 252357 A1 ES252357 A1 ES 252357A1 ES 0252357 A ES0252357 A ES 0252357A ES 252357 A ES252357 A ES 252357A ES 252357 A1 ES252357 A1 ES 252357A1
- Authority
- ES
- Spain
- Prior art keywords
- neohexene
- butyl
- neohexane
- isomerization
- atmospheres
- 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
- PKXHXOTZMFCXSH-UHFFFAOYSA-N 3,3-dimethylbut-1-ene Chemical compound CC(C)(C)C=C PKXHXOTZMFCXSH-UHFFFAOYSA-N 0.000 title abstract 5
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 title abstract 4
- 238000005336 cracking Methods 0.000 title abstract 2
- HNRMPXKDFBEGFZ-UHFFFAOYSA-N 2,2-dimethylbutane Chemical compound CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 abstract 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 2
- 239000005977 Ethylene Substances 0.000 abstract 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical group CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 abstract 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 abstract 2
- 238000006317 isomerization reaction Methods 0.000 abstract 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 2
- VFWCMGCRMGJXDK-UHFFFAOYSA-N 1-chlorobutane Chemical compound CCCCCl VFWCMGCRMGJXDK-UHFFFAOYSA-N 0.000 abstract 1
- JMMZCWZIJXAGKW-UHFFFAOYSA-N 2-methylpent-2-ene Chemical class CCC=C(C)C JMMZCWZIJXAGKW-UHFFFAOYSA-N 0.000 abstract 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 abstract 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 abstract 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 230000018044 dehydration Effects 0.000 abstract 1
- 238000006297 dehydration reaction Methods 0.000 abstract 1
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 abstract 1
- 239000001282 iso-butane Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000003208 petroleum Substances 0.000 abstract 1
- 229910052697 platinum Inorganic materials 0.000 abstract 1
- WHFQAROQMWLMEY-UHFFFAOYSA-N propylene dimer Chemical class CC=C.CC=C WHFQAROQMWLMEY-UHFFFAOYSA-N 0.000 abstract 1
- 238000000197 pyrolysis Methods 0.000 abstract 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 abstract 1
- 229910010271 silicon carbide Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C11/00—Aliphatic unsaturated hydrocarbons
- C07C11/12—Alkadienes
- C07C11/173—Alkadienes with five carbon atoms
- C07C11/18—Isoprene
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C4/00—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms
- C07C4/02—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms by cracking a single hydrocarbon or a mixture of individually defined hydrocarbons or a normally gaseous hydrocarbon fraction
- C07C4/04—Thermal processes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C4/00—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms
- C07C4/08—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms by splitting-off an aliphatic or cycloaliphatic part from the molecule
- C07C4/10—Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms by splitting-off an aliphatic or cycloaliphatic part from the molecule from acyclic hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
- C07C5/327—Formation of non-aromatic carbon-to-carbon double bonds only
- C07C5/333—Catalytic processes
- C07C5/3332—Catalytic processes with metal oxides or metal sulfides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
- C07C5/327—Formation of non-aromatic carbon-to-carbon double bonds only
- C07C5/333—Catalytic processes
- C07C5/3335—Catalytic processes with metals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
- C07C5/327—Formation of non-aromatic carbon-to-carbon double bonds only
- C07C5/333—Catalytic processes
- C07C5/3335—Catalytic processes with metals
- C07C5/3337—Catalytic processes with metals of the platinum group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Procedimiento de producción de isopreno, caracterizado por comprender las etapas de deshidrogenar neohexano para formar una mezcla de neohexano y neohexeno; de separar el neohexano del neohexeno; de crakizar el neohexeno para producir una mezcla de isopreno y otros hidrocarburos, y de recuperar el isopreno.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US764876A US3115531A (en) | 1958-10-02 | 1958-10-02 | Cracking of neohexene to isoprene |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES252357A1 true ES252357A1 (es) | 1960-01-01 |
Family
ID=25072043
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0252357A Expired ES252357A1 (es) | 1958-10-02 | 1959-09-29 | Procedimiento de producciën de isopreno |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3115531A (es) |
| CH (1) | CH387614A (es) |
| ES (1) | ES252357A1 (es) |
| GB (1) | GB928932A (es) |
| NL (1) | NL6700037A (es) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3209048A (en) * | 1961-01-11 | 1965-09-28 | Sinclair Research Inc | Production of isoprene |
| US3274287A (en) * | 1964-04-21 | 1966-09-20 | Monsanto Co | Hydrocarbon conversion process and catalyst |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2162011A (en) * | 1934-12-27 | 1939-06-13 | Melle Usines Sa | Dehydrogenation of saturated hydrocarbons |
| US2217252A (en) * | 1937-08-14 | 1940-10-08 | Shell Dev | Process for isomerization of olefin hydrocarbons |
| US2184235A (en) * | 1937-12-06 | 1939-12-19 | Shell Dev | Catalytic dehydrogenation of organic compounds |
| US2339560A (en) * | 1941-05-27 | 1944-01-18 | Shell Dev | Production of dienes |
| US2396416A (en) * | 1942-02-16 | 1946-03-12 | Phillips Petroleum Co | Diolefin preparation |
| US2391158A (en) * | 1942-02-16 | 1945-12-18 | Phillips Petroleum Co | Manufacture of diolefins |
| US2406688A (en) * | 1942-12-03 | 1946-08-27 | Socony Vacuum Oil Co Inc | Process for producing olefinic hydrocarbons |
| US2417872A (en) * | 1942-12-19 | 1947-03-25 | Standard Oil Dev Co | Process for preparing a dimethyl butene from propylene |
| US2438315A (en) * | 1944-01-03 | 1948-03-23 | Phillips Petroleum Co | Dehydrogenation of 2, 3-dimethyl-butane |
| US2404056A (en) * | 1944-10-12 | 1946-07-16 | Socony Vacuum Oil Co Inc | Manufacture of isoprene |
| US2900429A (en) * | 1957-04-05 | 1959-08-18 | Houdry Process Corp | Preparation of isoprene |
-
1958
- 1958-10-02 US US764876A patent/US3115531A/en not_active Expired - Lifetime
-
1959
- 1959-09-29 ES ES0252357A patent/ES252357A1/es not_active Expired
- 1959-10-01 GB GB33348/59A patent/GB928932A/en not_active Expired
- 1959-10-01 CH CH7891559A patent/CH387614A/fr unknown
-
1967
- 1967-01-03 NL NL6700037A patent/NL6700037A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB928932A (en) | 1963-06-19 |
| NL6700037A (es) | 1967-03-28 |
| US3115531A (en) | 1963-12-24 |
| CH387614A (fr) | 1965-02-15 |
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