NO313621B1 - Katalysator for dehydrogenering av C3C20-paraffiner, samt fremstilling og anvendelse av katalysatorer - Google Patents
Katalysator for dehydrogenering av C3C20-paraffiner, samt fremstilling og anvendelse av katalysatorer Download PDFInfo
- Publication number
- NO313621B1 NO313621B1 NO19944855A NO944855A NO313621B1 NO 313621 B1 NO313621 B1 NO 313621B1 NO 19944855 A NO19944855 A NO 19944855A NO 944855 A NO944855 A NO 944855A NO 313621 B1 NO313621 B1 NO 313621B1
- Authority
- NO
- Norway
- Prior art keywords
- metal
- catalyst
- group
- catalyst according
- lithium
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title claims description 96
- 238000002360 preparation method Methods 0.000 title claims description 3
- 238000006356 dehydrogenation reaction Methods 0.000 title description 14
- 229910052751 metal Inorganic materials 0.000 claims description 36
- 239000002184 metal Substances 0.000 claims description 36
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 27
- 229910052744 lithium Inorganic materials 0.000 claims description 21
- 229930195733 hydrocarbon Natural products 0.000 claims description 20
- 150000002430 hydrocarbons Chemical class 0.000 claims description 18
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 17
- 229910052783 alkali metal Inorganic materials 0.000 claims description 16
- 150000001340 alkali metals Chemical class 0.000 claims description 16
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 13
- 229910052697 platinum Inorganic materials 0.000 claims description 13
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 12
- 229910052718 tin Inorganic materials 0.000 claims description 12
- 150000004645 aluminates Chemical class 0.000 claims description 8
- 150000001336 alkenes Chemical class 0.000 claims description 7
- 238000001354 calcination Methods 0.000 claims description 7
- 229910052738 indium Inorganic materials 0.000 claims description 7
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 6
- 229910052741 iridium Inorganic materials 0.000 claims description 6
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 5
- 238000000151 deposition Methods 0.000 claims description 5
- 229910052732 germanium Inorganic materials 0.000 claims description 5
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims description 5
- 229910052700 potassium Inorganic materials 0.000 claims description 5
- 239000011591 potassium Substances 0.000 claims description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 4
- 239000010970 precious metal Substances 0.000 claims description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 3
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 229910052804 chromium Inorganic materials 0.000 claims description 3
- 239000011651 chromium Substances 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 229910052762 osmium Inorganic materials 0.000 claims description 3
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 claims description 3
- 229910052763 palladium Inorganic materials 0.000 claims description 3
- 229910052702 rhenium Inorganic materials 0.000 claims description 3
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 claims description 3
- 229910052703 rhodium Inorganic materials 0.000 claims description 3
- 239000010948 rhodium Substances 0.000 claims description 3
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 3
- 229910052707 ruthenium Inorganic materials 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 3
- 229910052721 tungsten Inorganic materials 0.000 claims description 3
- 239000010937 tungsten Substances 0.000 claims description 3
- 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 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- 229910052792 caesium Inorganic materials 0.000 claims description 2
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 230000000737 periodic effect Effects 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 238000000034 method Methods 0.000 description 11
- 230000008929 regeneration Effects 0.000 description 10
- 238000011069 regeneration method Methods 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 8
- 230000003197 catalytic effect Effects 0.000 description 8
- 239000004215 Carbon black (E152) Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- -1 lithium aluminates Chemical class 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 238000002441 X-ray diffraction Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- KLFRPGNCEJNEKU-FDGPNNRMSA-L (z)-4-oxopent-2-en-2-olate;platinum(2+) Chemical compound [Pt+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O KLFRPGNCEJNEKU-FDGPNNRMSA-L 0.000 description 4
- 239000003513 alkali Substances 0.000 description 4
- XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 3
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 229940094933 n-dodecane Drugs 0.000 description 3
- YJGJRYWNNHUESM-UHFFFAOYSA-J triacetyloxystannyl acetate Chemical compound [Sn+4].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O YJGJRYWNNHUESM-UHFFFAOYSA-J 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- YQNQTEBHHUSESQ-UHFFFAOYSA-N lithium aluminate Chemical compound [Li+].[O-][Al]=O YQNQTEBHHUSESQ-UHFFFAOYSA-N 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- HDVLQIDIYKIVRE-UHFFFAOYSA-N tetrabutylgermane Chemical compound CCCC[Ge](CCCC)(CCCC)CCCC HDVLQIDIYKIVRE-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- XURCIPRUUASYLR-UHFFFAOYSA-N Omeprazole sulfide Chemical compound N=1C2=CC(OC)=CC=C2NC=1SCC1=NC=C(C)C(OC)=C1C XURCIPRUUASYLR-UHFFFAOYSA-N 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000001339 alkali metal compounds Chemical class 0.000 description 1
- 150000001341 alkaline earth metal compounds Chemical class 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 238000005899 aromatization reaction Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000011066 ex-situ storage Methods 0.000 description 1
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium oxide Inorganic materials O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 239000013528 metallic particle Substances 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 229940039748 oxalate Drugs 0.000 description 1
- PVADDRMAFCOOPC-UHFFFAOYSA-N oxogermanium Chemical compound [Ge]=O PVADDRMAFCOOPC-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229940127557 pharmaceutical product Drugs 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 229940071182 stannate Drugs 0.000 description 1
- 125000005402 stannate group Chemical group 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- AFCAKJKUYFLYFK-UHFFFAOYSA-N tetrabutyltin Chemical compound CCCC[Sn](CCCC)(CCCC)CCCC AFCAKJKUYFLYFK-UHFFFAOYSA-N 0.000 description 1
- DBGVGMSCBYYSLD-UHFFFAOYSA-N tributylstannane Chemical compound CCCC[SnH](CCCC)CCCC DBGVGMSCBYYSLD-UHFFFAOYSA-N 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
- C07C5/32—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
-
- 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
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/56—Platinum group metals
-
- 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
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/56—Platinum group metals
- B01J23/62—Platinum group metals with gallium, indium, thallium, germanium, tin or lead
- B01J23/622—Platinum group metals with gallium, indium, thallium, germanium, tin or lead with germanium, tin or lead
- B01J23/626—Platinum group metals with gallium, indium, thallium, germanium, tin or lead with germanium, tin or lead with tin
-
- 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
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S502/00—Catalyst, solid sorbent, or support therefor: product or process of making
- Y10S502/524—Spinel
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9315276A FR2713957B1 (fr) | 1993-12-16 | 1993-12-16 | Catalyseurs de déshydrogénation de paraffines C3-C20 et sa préparation. |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO944855D0 NO944855D0 (no) | 1994-12-14 |
| NO944855L NO944855L (no) | 1995-06-19 |
| NO313621B1 true NO313621B1 (no) | 2002-11-04 |
Family
ID=9454099
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19944855A NO313621B1 (no) | 1993-12-16 | 1994-12-14 | Katalysator for dehydrogenering av C3C20-paraffiner, samt fremstilling og anvendelse av katalysatorer |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US5536695A (fr) |
| JP (1) | JP3806808B2 (fr) |
| CN (1) | CN1057020C (fr) |
| CA (1) | CA2138357A1 (fr) |
| FR (1) | FR2713957B1 (fr) |
| GB (1) | GB2284769B (fr) |
| IT (1) | IT1271273B (fr) |
| MY (1) | MY114107A (fr) |
| NO (1) | NO313621B1 (fr) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2767721B1 (fr) * | 1997-08-29 | 1999-10-22 | Inst Francais Du Petrole | Nouveaux catalyseurs utilisables dans les reactions de transformation de composes organiques |
| FR2777806B1 (fr) * | 1998-04-22 | 2000-06-02 | Inst Francais Du Petrole | Procede de regeneration en mode degrade d'un catalyseur |
| JP4166333B2 (ja) * | 1998-07-24 | 2008-10-15 | 千代田化工建設株式会社 | 脱水素触媒 |
| US6559094B1 (en) * | 1999-09-09 | 2003-05-06 | Engelhard Corporation | Method for preparation of catalytic material for selective oxidation and catalyst members thereof |
| US6369000B1 (en) * | 1999-09-17 | 2002-04-09 | Phillips Petroleum Company | Process for producing a metal aluminate catalyst support |
| US6417136B2 (en) * | 1999-09-17 | 2002-07-09 | Phillips Petroleum Company | Hydrocarbon hydrogenation catalyst and process |
| US6764664B2 (en) * | 2002-04-22 | 2004-07-20 | Delphi Technologies, Inc. | Catalyst for the combustion of diesel soot, methods for making the catalyst and methods of using the catalyst |
| US6858769B2 (en) * | 2002-10-18 | 2005-02-22 | Uop Llc | Lithium aluminate layered catalyst and a selective oxidation process using the catalyst |
| CN1329286C (zh) * | 2002-12-20 | 2007-08-01 | 本田技研工业株式会社 | 生产富氢气体的方法和其中所使用的无贵金属催化剂配方 |
| US20050096217A1 (en) * | 2003-10-29 | 2005-05-05 | Sud-Chemie, Inc. | Selective hydrogenation catalyst |
| US7220701B2 (en) * | 2003-11-24 | 2007-05-22 | Exxonmobil Chemical Patents Inc. | Catalyst and process for selective hydrogenation |
| US7220700B2 (en) * | 2003-11-24 | 2007-05-22 | Exxonmobil Chemical Patents Inc. | Catalyst and process for selective hydrogenation |
| US7199273B2 (en) * | 2003-11-24 | 2007-04-03 | Exxonmobil Chemical Patents, Inc. | Selective hydrogenation of alkynes and/or diolefins |
| US20050113614A1 (en) * | 2003-11-24 | 2005-05-26 | Lowe David M. | Catalyst and process for selective hydrogenation |
| CN104177705A (zh) * | 2014-08-22 | 2014-12-03 | 华东理工大学 | 利用多金属复合催化剂制备无卤阻燃聚烯烃材料的方法 |
| CN106607100B (zh) * | 2015-10-22 | 2019-04-12 | 中国石油化工股份有限公司 | 低碳烷烃脱氢制低碳烯烃催化剂载体及其用途 |
| JP2017165667A (ja) * | 2016-03-15 | 2017-09-21 | Ｊｘｔｇエネルギー株式会社 | 共役ジエンの製造方法 |
| JP6770824B2 (ja) * | 2016-04-15 | 2020-10-21 | Ｅｎｅｏｓ株式会社 | 脱水素触媒の製造方法、不飽和炭化水素の製造方法、及び共役ジエンの製造方法 |
| JP2019137662A (ja) * | 2018-02-15 | 2019-08-22 | Ｊｘｔｇエネルギー株式会社 | アルケンの製造方法 |
| CN110560040B (zh) * | 2018-06-05 | 2021-10-01 | 中国石油化工股份有限公司 | 丙烷脱氢制丙烯的催化剂 |
| CN110560061B (zh) * | 2018-06-05 | 2021-10-01 | 中国石油化工股份有限公司 | 用于丙烷脱氢的方法 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1570521A (fr) * | 1967-02-10 | 1969-06-13 | ||
| GB1220389A (en) * | 1967-06-02 | 1971-01-27 | Catalysts & Chem Inc | Catalyst for hydrocarbon reforming |
| CA946364A (en) * | 1969-05-28 | 1974-04-30 | Lewis E. Drehman | Catalytic dehydrogenation process |
| JPS5274591A (en) * | 1975-12-17 | 1977-06-22 | Nippon Soken | Catalysts for reforming hydrocarbon fuels |
| GB2053712B (en) * | 1979-07-18 | 1983-10-26 | Exxon Research Engineering Co | Regenerable catalysts and process for the conversion of relatively low molecular weight hydrocarbons to higher molecular weight hydrocarbons |
| DE3064972D1 (en) * | 1979-11-20 | 1983-10-27 | Ici Plc | Hydrogenation catalyst material, a precursor thereto, method of making the latter and use of the catalyst for selective hydrogenation |
| US4486547A (en) * | 1981-11-05 | 1984-12-04 | Uop Inc. | Indium-containing dehydrogenation catalyst |
| AU562124B2 (en) * | 1984-06-19 | 1987-05-28 | Phillips Petroleum Co. | Dehydrogenation of butanes |
| US4608360A (en) * | 1985-07-02 | 1986-08-26 | Uop Inc. | Dehydrogenation catalyst compositions and method of preparing same |
| US4786625A (en) * | 1987-02-25 | 1988-11-22 | Uop Inc. | Dehydrogenation catalyst compositon |
| ES2024072B3 (es) * | 1988-02-11 | 1992-02-16 | Fina Research | Procedimiento para preparar catalizadores que contienen un metal del grupo del platino, y sus usos |
| JP2818171B2 (ja) * | 1988-09-09 | 1998-10-30 | 東洋シーシーアイ株式会社 | 炭化水素の水蒸気改質反応用触媒及びその製造方法 |
| US4914075A (en) * | 1988-12-05 | 1990-04-03 | Uop | Dehydrogenation catalyst composition |
| CA2019847A1 (fr) * | 1989-07-03 | 1991-01-03 | William C. Baird, Jr. | Catalyseurs a base d'iridium agglomere a du platine et procede de reformage |
| US5143888A (en) * | 1990-04-23 | 1992-09-01 | Phillips Petroleum Company | Group VIII catalyst supported on mixture of zinc aluminate and calcium aluminate |
| US5219816A (en) * | 1991-12-20 | 1993-06-15 | Exxon Research & Engineering Company | Dehydrogenation catalysts and process for preparing the catalysts |
| US5214227A (en) * | 1991-12-20 | 1993-05-25 | Exxon Research & Engineering Company | Low pressure dehydrogenation of light paraffins |
| FR2689419B1 (fr) * | 1992-04-02 | 1994-09-30 | Inst Francais Du Petrole | Catalyseur contenant un métal du groupe VIII et un métal de groupe III a déposés sur un support, applicable à l'hydrogénation sélective des hydrocarbures. |
-
1993
- 1993-12-16 FR FR9315276A patent/FR2713957B1/fr not_active Expired - Fee Related
-
1994
- 1994-12-14 MY MYPI94003342A patent/MY114107A/en unknown
- 1994-12-14 GB GB9425222A patent/GB2284769B/en not_active Expired - Fee Related
- 1994-12-14 NO NO19944855A patent/NO313621B1/no unknown
- 1994-12-15 IT ITMI942522A patent/IT1271273B/it active IP Right Grant
- 1994-12-16 CA CA002138357A patent/CA2138357A1/fr not_active Abandoned
- 1994-12-16 CN CN94120800A patent/CN1057020C/zh not_active Expired - Fee Related
- 1994-12-16 JP JP31311094A patent/JP3806808B2/ja not_active Expired - Fee Related
- 1994-12-16 US US08/357,026 patent/US5536695A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| GB9425222D0 (en) | 1995-02-08 |
| NO944855L (no) | 1995-06-19 |
| IT1271273B (it) | 1997-05-27 |
| FR2713957B1 (fr) | 1996-02-02 |
| JP3806808B2 (ja) | 2006-08-09 |
| NO944855D0 (no) | 1994-12-14 |
| MY114107A (en) | 2002-08-30 |
| GB2284769A (en) | 1995-06-21 |
| US5536695A (en) | 1996-07-16 |
| JPH07232065A (ja) | 1995-09-05 |
| CN1109857A (zh) | 1995-10-11 |
| CA2138357A1 (fr) | 1995-06-17 |
| GB2284769B (en) | 1998-02-11 |
| FR2713957A1 (fr) | 1995-06-23 |
| ITMI942522A0 (it) | 1994-12-15 |
| CN1057020C (zh) | 2000-10-04 |
| ITMI942522A1 (it) | 1996-06-15 |
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