NO309857B1 - FremgangsmÕte for fremstilling av et isobutan- og isoheksanholdig produkt - Google Patents
FremgangsmÕte for fremstilling av et isobutan- og isoheksanholdig produkt Download PDFInfo
- Publication number
- NO309857B1 NO309857B1 NO955185A NO955185A NO309857B1 NO 309857 B1 NO309857 B1 NO 309857B1 NO 955185 A NO955185 A NO 955185A NO 955185 A NO955185 A NO 955185A NO 309857 B1 NO309857 B1 NO 309857B1
- Authority
- NO
- Norway
- Prior art keywords
- isobutane
- isopentane
- hydrocarbons
- disproportionation
- olefinic
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 15
- JZPXZBNKAIFFRE-UHFFFAOYSA-N 2-methylpentane 2-methylpropane Chemical compound CC(C)C.CCCC(C)C JZPXZBNKAIFFRE-UHFFFAOYSA-N 0.000 title description 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 claims description 32
- 229930195733 hydrocarbon Natural products 0.000 claims description 20
- 150000002430 hydrocarbons Chemical class 0.000 claims description 20
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 claims description 18
- 238000007323 disproportionation reaction Methods 0.000 claims description 13
- 150000001336 alkenes Chemical class 0.000 claims description 7
- 239000003054 catalyst Substances 0.000 claims description 4
- 150000003460 sulfonic acids Chemical class 0.000 claims description 4
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 claims description 3
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 claims description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000001282 iso-butane Substances 0.000 description 4
- YUHZIUAREWNXJT-UHFFFAOYSA-N (2-fluoropyridin-3-yl)boronic acid Chemical class OB(O)C1=CC=CN=C1F YUHZIUAREWNXJT-UHFFFAOYSA-N 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- -1 carbenium ions Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000001349 alkyl fluorides Chemical class 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000005504 petroleum refining Methods 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 230000005588 protonation Effects 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C6/00—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
- C07C6/08—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond
- C07C6/10—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond in hydrocarbons containing no six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- C07C2531/025—Sulfonic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DK146094A DK172069B1 (da) | 1994-12-21 | 1994-12-21 | Fremgangsmåde til fremstilling af et isobutan/isohexanholdigt produkt |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO955185D0 NO955185D0 (no) | 1995-12-20 |
| NO955185L NO955185L (no) | 1996-06-24 |
| NO309857B1 true NO309857B1 (no) | 2001-04-09 |
Family
ID=8105078
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO955185A NO309857B1 (no) | 1994-12-21 | 1995-12-20 | FremgangsmÕte for fremstilling av et isobutan- og isoheksanholdig produkt |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US5900522A (da) |
| EP (1) | EP0718259B1 (da) |
| JP (1) | JP3905147B2 (da) |
| CN (1) | CN1057990C (da) |
| AR (1) | AR000393A1 (da) |
| AT (1) | ATE179693T1 (da) |
| AU (1) | AU698190B2 (da) |
| DE (1) | DE69509486T2 (da) |
| DK (2) | DK172069B1 (da) |
| ES (1) | ES2132505T3 (da) |
| MX (1) | MX9505225A (da) |
| NO (1) | NO309857B1 (da) |
| RU (1) | RU2119474C1 (da) |
| TW (1) | TW300217B (da) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6573416B1 (en) * | 1999-11-19 | 2003-06-03 | Conocophillips Company | Hydrocarbon disproportionation |
| US6395945B1 (en) | 2000-03-31 | 2002-05-28 | Phillips Petroleum Company | Integrated hydroisomerization alkylation process |
| US6423880B1 (en) | 2000-06-19 | 2002-07-23 | Phillips Petroleum Company | Isopentane disproportionation |
| US20050033102A1 (en) * | 2003-08-06 | 2005-02-10 | Randolph Bruce B. | Supported ionic liquid and the use thereof in the disproportionation of isopentane |
| US20050288540A1 (en) * | 2004-06-28 | 2005-12-29 | Hommeltoft Sven I | Process for the preparation of a hydrocarbon product stream being rich in C6 and C7 iso-paraffins |
| WO2008012791A1 (en) * | 2006-07-24 | 2008-01-31 | Aquate Solar Ltd. | Water integrated photovoltaic system |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3668269A (en) * | 1970-06-26 | 1972-06-06 | Atlantic Richfield Co | A process for disproportionating paraffinic hydrocarbons to yield products containing iso-paraffinic hydrocarbons |
| US3766292A (en) * | 1970-11-23 | 1973-10-16 | Chevron Res | Process for obtaining isopentane from butane hexane or mixtures thereof |
| US3686354A (en) * | 1971-02-04 | 1972-08-22 | Universal Oil Prod Co | High octane paraffinic motor fuel production |
| JPS5384924A (en) * | 1977-07-25 | 1978-07-26 | Mitsubishi Chem Ind Ltd | Disproportionation of alkyl aromatic hydrocarbons |
| IT1129809B (it) * | 1979-03-26 | 1986-06-11 | Ugine Kuhlmann | Composizione catalitica per la conversione di idrocarburi e procedimento per la disidratazione di acidi perfluoroalcansolfonici destinati a fare parte bella composizione |
| DE3265069D1 (en) * | 1981-06-26 | 1985-09-05 | Inst Francais Du Petrole | Process for simultaneously obtaining high-purity butene-1 and a premium grade fuel from an olefinic c4 cut |
| US5396016A (en) * | 1993-08-19 | 1995-03-07 | Mobil Oil Corp. | MCM-36 as a catalyst for upgrading paraffins |
| US5489727A (en) * | 1994-10-28 | 1996-02-06 | Phillips Petroleum Company | Isopentane disproportionation |
-
1994
- 1994-12-21 DK DK146094A patent/DK172069B1/da not_active IP Right Cessation
-
1995
- 1995-12-13 TW TW084113276A patent/TW300217B/zh not_active IP Right Cessation
- 1995-12-13 MX MX9505225A patent/MX9505225A/es not_active IP Right Cessation
- 1995-12-16 AT AT95119903T patent/ATE179693T1/de active
- 1995-12-16 DK DK95119903T patent/DK0718259T3/da active
- 1995-12-16 DE DE69509486T patent/DE69509486T2/de not_active Expired - Fee Related
- 1995-12-16 EP EP95119903A patent/EP0718259B1/en not_active Expired - Lifetime
- 1995-12-16 ES ES95119903T patent/ES2132505T3/es not_active Expired - Lifetime
- 1995-12-19 AR AR33470495A patent/AR000393A1/es unknown
- 1995-12-19 JP JP33069995A patent/JP3905147B2/ja not_active Expired - Fee Related
- 1995-12-19 AU AU40536/95A patent/AU698190B2/en not_active Ceased
- 1995-12-20 RU RU95121110A patent/RU2119474C1/ru not_active IP Right Cessation
- 1995-12-20 NO NO955185A patent/NO309857B1/no unknown
- 1995-12-20 US US08/580,060 patent/US5900522A/en not_active Expired - Fee Related
- 1995-12-21 CN CN95121454A patent/CN1057990C/zh not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP3905147B2 (ja) | 2007-04-18 |
| AU698190B2 (en) | 1998-10-29 |
| DE69509486T2 (de) | 1999-09-02 |
| ATE179693T1 (de) | 1999-05-15 |
| JPH08268922A (ja) | 1996-10-15 |
| EP0718259B1 (en) | 1999-05-06 |
| TW300217B (da) | 1997-03-11 |
| ES2132505T3 (es) | 1999-08-16 |
| CN1130166A (zh) | 1996-09-04 |
| DE69509486D1 (de) | 1999-06-10 |
| DK0718259T3 (da) | 1999-11-15 |
| US5900522A (en) | 1999-05-04 |
| DK172069B1 (da) | 1997-10-13 |
| DK146094A (da) | 1996-06-22 |
| NO955185L (no) | 1996-06-24 |
| RU2119474C1 (ru) | 1998-09-27 |
| CN1057990C (zh) | 2000-11-01 |
| NO955185D0 (no) | 1995-12-20 |
| EP0718259A1 (en) | 1996-06-26 |
| AU4053695A (en) | 1996-06-27 |
| AR000393A1 (es) | 1997-06-18 |
| MX9505225A (es) | 1997-01-31 |
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