LU84823A1 - Procede d'isomerisation de la liaison olefinique - Google Patents
Procede d'isomerisation de la liaison olefinique Download PDFInfo
- Publication number
- LU84823A1 LU84823A1 LU84823A LU84823A LU84823A1 LU 84823 A1 LU84823 A1 LU 84823A1 LU 84823 A LU84823 A LU 84823A LU 84823 A LU84823 A LU 84823A LU 84823 A1 LU84823 A1 LU 84823A1
- Authority
- LU
- Luxembourg
- Prior art keywords
- moles
- catalyst
- alumina
- prepared
- sio
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 26
- 238000006317 isomerization reaction Methods 0.000 title claims description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 53
- 239000003054 catalyst Substances 0.000 claims description 48
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 45
- 229910052681 coesite Inorganic materials 0.000 claims description 27
- 229910052906 cristobalite Inorganic materials 0.000 claims description 27
- 229910052682 stishovite Inorganic materials 0.000 claims description 27
- 229910052905 tridymite Inorganic materials 0.000 claims description 27
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 19
- 239000000377 silicon dioxide Substances 0.000 claims description 17
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 11
- 229910052751 metal Inorganic materials 0.000 claims description 10
- 239000002184 metal Substances 0.000 claims description 10
- 150000001336 alkenes Chemical class 0.000 claims description 8
- MRELNEQAGSRDBK-UHFFFAOYSA-N lanthanum oxide Inorganic materials [O-2].[O-2].[O-2].[La+3].[La+3] MRELNEQAGSRDBK-UHFFFAOYSA-N 0.000 claims description 8
- 235000012239 silicon dioxide Nutrition 0.000 claims description 8
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 7
- 229910052788 barium Inorganic materials 0.000 claims description 6
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 6
- 229910052742 iron Inorganic materials 0.000 claims description 6
- 229910052746 lanthanum Inorganic materials 0.000 claims description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 5
- 229910052791 calcium Inorganic materials 0.000 claims description 5
- 239000011575 calcium Substances 0.000 claims description 5
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 claims description 5
- 150000002739 metals Chemical class 0.000 claims description 3
- 229910052747 lanthanoid Inorganic materials 0.000 claims description 2
- 150000002602 lanthanoids Chemical class 0.000 claims description 2
- 229910000311 lanthanide oxide Inorganic materials 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 29
- 239000000463 material Substances 0.000 description 9
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 8
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 8
- 239000000292 calcium oxide Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 7
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 5
- FYDKNKUEBJQCCN-UHFFFAOYSA-N lanthanum(3+);trinitrate Chemical compound [La+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O FYDKNKUEBJQCCN-UHFFFAOYSA-N 0.000 description 5
- 230000008929 regeneration Effects 0.000 description 5
- 238000011069 regeneration method Methods 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 4
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- IWOUKMZUPDVPGQ-UHFFFAOYSA-N barium nitrate Chemical compound [Ba+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O IWOUKMZUPDVPGQ-UHFFFAOYSA-N 0.000 description 2
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 description 2
- 239000013256 coordination polymer Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229910052761 rare earth metal Inorganic materials 0.000 description 2
- 229910052712 strontium Inorganic materials 0.000 description 2
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 101000912181 Arabidopsis thaliana Cysteine synthase, mitochondrial Proteins 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 101710094396 Hexon protein Proteins 0.000 description 1
- 101000820455 Homo sapiens Stonin-1 Proteins 0.000 description 1
- RSPISYXLHRIGJD-UHFFFAOYSA-N OOOO Chemical compound OOOO RSPISYXLHRIGJD-UHFFFAOYSA-N 0.000 description 1
- DTAFLBZLAZYRDX-UHFFFAOYSA-N OOOOOO Chemical compound OOOOOO DTAFLBZLAZYRDX-UHFFFAOYSA-N 0.000 description 1
- 229910020472 SiO7 Inorganic materials 0.000 description 1
- 102100021683 Stonin-1 Human genes 0.000 description 1
- 229910052770 Uranium Inorganic materials 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000010006 flight Effects 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- MVFCKEFYUDZOCX-UHFFFAOYSA-N iron(2+);dinitrate Chemical compound [Fe+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MVFCKEFYUDZOCX-UHFFFAOYSA-N 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- -1 rare earth acetate Chemical class 0.000 description 1
- 229910001404 rare earth metal oxide Inorganic materials 0.000 description 1
- 150000002910 rare earth metals Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000005372 silanol group Chemical group 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
Classifications
-
- 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
- C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
- C07C5/23—Rearrangement of carbon-to-carbon unsaturated bonds
- C07C5/25—Migration of carbon-to-carbon double bonds
-
- 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
- C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
- C07C5/23—Rearrangement of carbon-to-carbon unsaturated bonds
- C07C5/25—Migration of carbon-to-carbon double bonds
- C07C5/2506—Catalytic processes
- C07C5/2512—Catalytic processes with metal oxides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/02—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the alkali- or alkaline earth metals or beryllium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/08—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of gallium, indium or thallium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/10—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of rare earths
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/74—Iron group metals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT21511/82A IT1190839B (it) | 1982-05-27 | 1982-05-27 | Procedimento per la isomerizzazione di legame delle olefine |
| IT2151182 | 1982-05-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU84823A1 true LU84823A1 (fr) | 1984-03-07 |
Family
ID=11182885
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU84823A LU84823A1 (fr) | 1982-05-27 | 1983-05-26 | Procede d'isomerisation de la liaison olefinique |
Country Status (33)
| Country | Link |
|---|---|
| US (1) | US4814542A (cs) |
| JP (1) | JPS58219128A (cs) |
| KR (1) | KR870000055B1 (cs) |
| AT (1) | AT382864B (cs) |
| AU (1) | AU552806B2 (cs) |
| BE (1) | BE896849A (cs) |
| CA (1) | CA1199041A (cs) |
| CS (1) | CS244933B2 (cs) |
| DD (1) | DD209801A5 (cs) |
| DE (1) | DE3319171A1 (cs) |
| DK (1) | DK234583A (cs) |
| ES (1) | ES8500201A1 (cs) |
| FR (1) | FR2527596A1 (cs) |
| GB (1) | GB2121430B (cs) |
| GR (1) | GR81339B (cs) |
| HU (1) | HUT34419A (cs) |
| IN (2) | IN159131B (cs) |
| IT (1) | IT1190839B (cs) |
| LU (1) | LU84823A1 (cs) |
| MW (1) | MW2283A1 (cs) |
| NL (1) | NL8301872A (cs) |
| NO (1) | NO831847L (cs) |
| NZ (1) | NZ204340A (cs) |
| PH (1) | PH17965A (cs) |
| PL (1) | PL141424B1 (cs) |
| PT (1) | PT76764B (cs) |
| RO (1) | RO86409B (cs) |
| SE (1) | SE8302849L (cs) |
| SU (1) | SU1333231A3 (cs) |
| YU (1) | YU113083A (cs) |
| ZA (1) | ZA833396B (cs) |
| ZM (1) | ZM3683A1 (cs) |
| ZW (1) | ZW11283A1 (cs) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1190839B (it) * | 1982-05-27 | 1988-02-24 | Anic Spa | Procedimento per la isomerizzazione di legame delle olefine |
| EP0225407A1 (en) * | 1985-01-25 | 1987-06-16 | Council of Scientific and Industrial Research | Lanthanum silicate materials, their production and use |
| FR2584388B1 (fr) * | 1985-07-03 | 1991-02-15 | Rhone Poulenc Spec Chim | Composition a base d'oxyde cerique, sa preparation et ses utilisations |
| AU591208B2 (en) * | 1985-12-23 | 1989-11-30 | Nippon Shokubai Kagaku Kogyo Co. Ltd. | Catalyst for vapor-phase intramolecular dehydration reaction of alkanolamines |
| DE3677950D1 (de) * | 1985-12-27 | 1991-04-11 | Nippon Catalytic Chem Ind | Verfahren zur herstellung zyklischer amine. |
| US5507940A (en) * | 1991-08-30 | 1996-04-16 | Shell Oil Company | Hydrodenitrification catalyst and process |
| DE4445680A1 (de) * | 1994-12-21 | 1996-06-27 | Huels Chemische Werke Ag | Katalysator und Verfahren zur Isomerisierung von aliphatischen C¶4¶-C¶1¶¶0¶-Monoolefinen |
| IT1276802B1 (it) * | 1995-06-30 | 1997-11-03 | Enichem Spa | Procedimento integrato per la produzione di butene-1 |
| US6875901B2 (en) * | 2001-05-23 | 2005-04-05 | Abb Lummus Global Inc. | Olefin isomerization process |
| US6777582B2 (en) * | 2002-03-07 | 2004-08-17 | Abb Lummus Global Inc. | Process for producing propylene and hexene from C4 olefin streams |
| DE10311139A1 (de) | 2003-03-14 | 2004-09-23 | Basf Ag | Verfahren zur Herstellung von 1-Buten |
| US7638573B2 (en) * | 2006-04-07 | 2009-12-29 | Exxonmobil Chemical Patents Inc. | Butyl nanocomposite via low Mw elastomer pre-blend |
| MY162609A (en) | 2006-11-30 | 2017-06-30 | Basf Se | Method for the hydroformylation of olefins |
| DE102008036295A1 (de) * | 2008-08-04 | 2010-02-11 | Bayer Technology Services Gmbh | Katalysatorzusammensetzung zur Umesterung |
| US8586813B2 (en) | 2009-07-21 | 2013-11-19 | Lummus Technology Inc. | Catalyst for metathesis of ethylene and 2-butene and/or double bond isomerization |
| US8704028B2 (en) * | 2010-03-30 | 2014-04-22 | Uop Llc | Conversion of acyclic symmetrical olefins to higher and lower carbon number olefin products |
| DE102013226370A1 (de) | 2013-12-18 | 2015-06-18 | Evonik Industries Ag | Herstellung von Butadien durch oxidative Dehydrierung von n-Buten nach vorhergehender Isomerisierung |
| DE102015200702A1 (de) | 2015-01-19 | 2016-07-21 | Evonik Degussa Gmbh | Herstellung von Butadien aus Ethen |
| JP6571392B2 (ja) | 2015-05-29 | 2019-09-04 | Ｊｘｔｇエネルギー株式会社 | 異性化触媒、直鎖オレフィンの製造方法及び化合物の製造方法 |
| JP6736017B2 (ja) * | 2015-11-05 | 2020-08-05 | Ｅｎｅｏｓ株式会社 | 異性化触媒、直鎖オレフィンの製造方法及び化合物の製造方法 |
| RU2722665C1 (ru) * | 2016-07-28 | 2020-06-02 | Лионделл Кемикал Текнолоджи, Л.П. | Удаление парафина из потоков, имеющих в своем составе с4 |
| US10550048B2 (en) * | 2017-01-20 | 2020-02-04 | Saudi Arabian Oil Company | Multiple-stage catalyst system for self-metathesis with controlled isomerization and cracking |
| JP2020097544A (ja) * | 2018-12-18 | 2020-06-25 | Ｊｘｔｇエネルギー株式会社 | 直鎖モノオレフィンの製造方法及び化合物の製造方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3313858A (en) * | 1965-02-12 | 1967-04-11 | Phillips Petroleum Co | Isomerization of non-terminal olefins |
| US3467727A (en) * | 1966-10-10 | 1969-09-16 | Universal Oil Prod Co | Isomerization of 2,3-dimethylbutenes |
| US3479415A (en) * | 1967-05-12 | 1969-11-18 | Air Prod & Chem | Isomerization of olefinic hydrocarbons |
| GB1267719A (en) * | 1969-12-05 | 1972-03-22 | Exxon Research Engineering Co | Isomerization of olefins |
| US3864424A (en) * | 1973-04-30 | 1975-02-04 | Universal Oil Prod Co | Isomerization process |
| US4217244A (en) * | 1978-05-11 | 1980-08-12 | Phillips Petroleum Company | Regeneration of isomerization catalysts containing magnesium oxide |
| US4229610A (en) * | 1978-11-03 | 1980-10-21 | Phillips Petroleum Company | Olefin double bond isomerization |
| FR2506297B1 (fr) * | 1981-05-21 | 1986-05-02 | Inst Francais Du Petrole | Procede d'isomerisation d'olefines |
| IT1190839B (it) * | 1982-05-27 | 1988-02-24 | Anic Spa | Procedimento per la isomerizzazione di legame delle olefine |
-
1982
- 1982-05-27 IT IT21511/82A patent/IT1190839B/it active
-
1983
- 1983-05-11 ZA ZA833396A patent/ZA833396B/xx unknown
- 1983-05-12 ZW ZW112/83A patent/ZW11283A1/xx unknown
- 1983-05-13 AU AU14535/83A patent/AU552806B2/en not_active Ceased
- 1983-05-16 GR GR71362A patent/GR81339B/el unknown
- 1983-05-17 GB GB08313561A patent/GB2121430B/en not_active Expired
- 1983-05-18 PH PH28925A patent/PH17965A/en unknown
- 1983-05-19 SE SE8302849A patent/SE8302849L/ not_active Application Discontinuation
- 1983-05-20 YU YU01130/83A patent/YU113083A/xx unknown
- 1983-05-23 KR KR1019830002257A patent/KR870000055B1/ko not_active Expired
- 1983-05-24 RO RO111051A patent/RO86409B/ro unknown
- 1983-05-24 NZ NZ204340A patent/NZ204340A/en unknown
- 1983-05-25 NO NO831847A patent/NO831847L/no unknown
- 1983-05-25 DK DK234583A patent/DK234583A/da not_active Application Discontinuation
- 1983-05-25 FR FR8308648A patent/FR2527596A1/fr active Granted
- 1983-05-26 PT PT76764A patent/PT76764B/pt unknown
- 1983-05-26 PL PL1983242214A patent/PL141424B1/pl unknown
- 1983-05-26 SU SU833598342A patent/SU1333231A3/ru active
- 1983-05-26 CS CS833719A patent/CS244933B2/cs unknown
- 1983-05-26 LU LU84823A patent/LU84823A1/fr unknown
- 1983-05-26 BE BE0/210852A patent/BE896849A/fr not_active IP Right Cessation
- 1983-05-26 MW MW22/83A patent/MW2283A1/xx unknown
- 1983-05-26 AT AT0192583A patent/AT382864B/de not_active IP Right Cessation
- 1983-05-26 DE DE19833319171 patent/DE3319171A1/de active Granted
- 1983-05-26 NL NL8301872A patent/NL8301872A/nl not_active Application Discontinuation
- 1983-05-26 HU HU831864A patent/HUT34419A/hu unknown
- 1983-05-26 CA CA000428977A patent/CA1199041A/en not_active Expired
- 1983-05-27 JP JP58092563A patent/JPS58219128A/ja active Pending
- 1983-05-27 ES ES523076A patent/ES8500201A1/es not_active Expired
- 1983-05-27 IN IN671/CAL/83A patent/IN159131B/en unknown
- 1983-05-27 ZM ZM36/83A patent/ZM3683A1/xx unknown
- 1983-05-27 IN IN669/CAL/83A patent/IN158661B/en unknown
- 1983-05-27 DD DD83251340A patent/DD209801A5/de unknown
-
1988
- 1988-07-26 US US07/224,359 patent/US4814542A/en not_active Expired - Fee Related
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| LU84823A1 (fr) | Procede d'isomerisation de la liaison olefinique | |
| EP0474536B1 (fr) | Procédé d'aromatisation des hydrocarbures contenant 2 à 4 atomes de carbone par molécule | |
| EP0098622B1 (en) | Process for the preparation of a catalyst and process for the dehydrogenation of c2-c4 paraffins | |
| FR2662437A1 (fr) | Catalyseur contenant une zeolithe, un metal noble de la famille du platine, un metal alcalin ou alcalino terreux et un metal additionnel et son utilisation dans l'aromatisation des hydrocarbures contenant de 2 a 4 atomes de carbone par molecule. | |
| FR2617060A1 (fr) | Catalyseur de deshydrogenation, application a la preparation de styrene et styrene ainsi obtenu | |
| US3560408A (en) | Catalytic mineral fibers and their preparation | |
| GB2090595A (en) | Threo-3-amino-2-hydroxybutanoylacetice acid derivatives | |
| FR2641711A1 (fr) | Adsorbant pour purification de polyolefines et procede de fabrication de celui-ci | |
| US5011809A (en) | Preparation of a silver catalyst | |
| LU84824A1 (fr) | Catalyseur a base d'alumine gamma et son procede de preparation | |
| EP0241391B1 (fr) | Catalyseurs à base d'argent pour la fabrication d'oxyde d'éthylène | |
| EP0588680B1 (fr) | Procédé pour l'isomérisation des oléfines. | |
| JPH0455178B2 (cs) | ||
| CN1504261A (zh) | 一种催化正丁烷生产异丁烯的催化剂及制备方法和应用 | |
| Imbault et al. | Chloroplast leucyl-tRNA synthetase from Euglena gracilis. Purification, kinetic analysis, and structural characterization | |
| Rosenberg et al. | Reactivity of 2-furylethylenes with nucleophilic groups and its biological significance | |
| DE1443187A1 (de) | Verfahren zur Herstellung eines Fluorierungskatalysators | |
| SU1416171A1 (ru) | Катализатор дл гидрировани оксида углерода до метана | |
| EP0471599B1 (fr) | Procédé d'aromatisation des hydrocarbures contenant de 5 à 9 atomes de carbone par molécule | |
| RU2012395C1 (ru) | Катализатор для изомеризации c4-c7 - алкановых углеводородов и способ изомеризации c4-c7 - алкановых углеводородов | |
| JPH0472809B2 (cs) | ||
| SU407571A1 (ru) | Катализатор для гидрирования органических соединений | |
| JPH0516418B2 (cs) | ||
| SU1761740A1 (ru) | Способ получени изоамиленов | |
| EP0664278B1 (fr) | Procédé pour l'isomérisation des oléfines |