EA011022B1 - Способ алкилирования с использованием катализатора, содержащего твердую кислоту и гидрирующий металл - Google Patents
Способ алкилирования с использованием катализатора, содержащего твердую кислоту и гидрирующий металл Download PDFInfo
- Publication number
- EA011022B1 EA011022B1 EA200601444A EA200601444A EA011022B1 EA 011022 B1 EA011022 B1 EA 011022B1 EA 200601444 A EA200601444 A EA 200601444A EA 200601444 A EA200601444 A EA 200601444A EA 011022 B1 EA011022 B1 EA 011022B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- catalyst
- alkylation
- water
- solid acid
- zeolites
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 126
- 238000005804 alkylation reaction Methods 0.000 title claims abstract description 54
- 239000011973 solid acid Substances 0.000 title claims abstract description 23
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 20
- 239000002184 metal Substances 0.000 title claims abstract description 20
- 238000005984 hydrogenation reaction Methods 0.000 title claims abstract description 4
- 238000000034 method Methods 0.000 claims abstract description 51
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 48
- 230000029936 alkylation Effects 0.000 claims abstract description 35
- 239000010457 zeolite Substances 0.000 claims description 27
- 238000011069 regeneration method Methods 0.000 claims description 16
- 230000008929 regeneration Effects 0.000 claims description 15
- 229910021536 Zeolite Inorganic materials 0.000 claims description 14
- 229940100198 alkylating agent Drugs 0.000 claims description 13
- 239000002168 alkylating agent Substances 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 10
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 9
- 150000001336 alkenes Chemical group 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 7
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 4
- 150000002739 metals Chemical class 0.000 claims description 4
- 229910000510 noble metal Inorganic materials 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 239000011733 molybdenum Substances 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 2
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 239000010937 tungsten Substances 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- 238000003723 Smelting Methods 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 abstract description 16
- 150000002430 hydrocarbons Chemical class 0.000 abstract description 16
- 239000004215 Carbon black (E152) Substances 0.000 abstract description 13
- 230000008569 process Effects 0.000 abstract description 7
- 230000000694 effects Effects 0.000 abstract description 5
- 230000002152 alkylating effect Effects 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 31
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 24
- 239000002245 particle Substances 0.000 description 13
- 239000001282 iso-butane Substances 0.000 description 12
- 239000011159 matrix material Substances 0.000 description 12
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 12
- 229910052739 hydrogen Inorganic materials 0.000 description 10
- 239000003502 gasoline Substances 0.000 description 9
- 239000001257 hydrogen Substances 0.000 description 9
- 238000012956 testing procedure Methods 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 230000009467 reduction Effects 0.000 description 7
- 230000003197 catalytic effect Effects 0.000 description 6
- 229910052697 platinum Inorganic materials 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- 239000003570 air Substances 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 5
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 5
- 239000011148 porous material Substances 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 4
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 4
- FLTJDUOFAQWHDF-UHFFFAOYSA-N 2,2-dimethylhexane Chemical compound CCCCC(C)(C)C FLTJDUOFAQWHDF-UHFFFAOYSA-N 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- 239000000571 coke Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 230000000737 periodic effect Effects 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 229910010271 silicon carbide Inorganic materials 0.000 description 3
- HNRMPXKDFBEGFZ-UHFFFAOYSA-N 2,2-dimethylbutane Chemical compound CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 description 2
- ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 2,3-dimethylbutane Chemical compound CC(C)C(C)C ZFFMLCVRJBZUDZ-UHFFFAOYSA-N 0.000 description 2
- WGECXQBGLLYSFP-UHFFFAOYSA-N 2,3-dimethylpentane Chemical compound CCC(C)C(C)C WGECXQBGLLYSFP-UHFFFAOYSA-N 0.000 description 2
- JVSWJIKNEAIKJW-UHFFFAOYSA-N 2-Methylheptane Chemical class CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- IAQRGUVFOMOMEM-ARJAWSKDSA-N cis-but-2-ene Chemical compound C\C=C/C IAQRGUVFOMOMEM-ARJAWSKDSA-N 0.000 description 2
- -1 clays Substances 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000012812 general test Methods 0.000 description 2
- 230000036571 hydration Effects 0.000 description 2
- 238000006703 hydration reaction Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- XTDQDBVBDLYELW-UHFFFAOYSA-N 2,2,3-trimethylpentane Chemical compound CCC(C)C(C)(C)C XTDQDBVBDLYELW-UHFFFAOYSA-N 0.000 description 1
- OKVWYBALHQFVFP-UHFFFAOYSA-N 2,3,3-trimethylpentane Chemical compound CCC(C)(C)C(C)C OKVWYBALHQFVFP-UHFFFAOYSA-N 0.000 description 1
- RLPGDEORIPLBNF-UHFFFAOYSA-N 2,3,4-trimethylpentane Chemical compound CC(C)C(C)C(C)C RLPGDEORIPLBNF-UHFFFAOYSA-N 0.000 description 1
- BZHMBWZPUJHVEE-UHFFFAOYSA-N 2,3-dimethylpentane Natural products CC(C)CC(C)C BZHMBWZPUJHVEE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- VIJYFGMFEVJQHU-UHFFFAOYSA-N aluminum oxosilicon(2+) oxygen(2-) Chemical compound [O-2].[Al+3].[Si+2]=O VIJYFGMFEVJQHU-UHFFFAOYSA-N 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical class [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000007613 slurry method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- ZISSAWUMDACLOM-UHFFFAOYSA-N triptane Chemical compound CC(C)C(C)(C)C ZISSAWUMDACLOM-UHFFFAOYSA-N 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/54—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
- C07C2/56—Addition to acyclic hydrocarbons
- C07C2/58—Catalytic processes
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
- C10G29/20—Organic compounds not containing metal atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G29/00—Refining of hydrocarbon oils, in the absence of hydrogen, with other chemicals
- C10G29/20—Organic compounds not containing metal atoms
- C10G29/205—Organic compounds not containing metal atoms by reaction with hydrocarbons added to the hydrocarbon oil
-
- 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
- B01J2229/00—Aspects of molecular sieve catalysts not covered by B01J29/00
- B01J2229/30—After treatment, characterised by the means used
- B01J2229/42—Addition of matrix or binder particles
-
- 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
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
- B01J29/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- B01J29/08—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the faujasite type, e.g. type X or Y
- B01J29/10—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the faujasite type, e.g. type X or Y containing iron group metals, noble metals or copper
- B01J29/12—Noble metals
- B01J29/126—Y-type faujasite
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/02—Gasoline
-
- 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
- Y10S585/00—Chemistry of hydrocarbon compounds
- Y10S585/8995—Catalyst and recycle considerations
- Y10S585/906—Catalyst preservation or manufacture, e.g. activation before use
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04075387 | 2004-02-09 | ||
| US54792304P | 2004-02-26 | 2004-02-26 | |
| PCT/EP2005/000929 WO2005075387A1 (en) | 2004-02-09 | 2005-01-26 | Alkylation process using a catalyst comprising a solid acid and a hydrogenation metal |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA200601444A1 EA200601444A1 (ru) | 2007-02-27 |
| EA011022B1 true EA011022B1 (ru) | 2008-12-30 |
Family
ID=34928095
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA200601444A EA011022B1 (ru) | 2004-02-09 | 2005-01-26 | Способ алкилирования с использованием катализатора, содержащего твердую кислоту и гидрирующий металл |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US7750197B2 (enExample) |
| EP (1) | EP1732866B1 (enExample) |
| JP (1) | JP5016927B2 (enExample) |
| KR (1) | KR101156299B1 (enExample) |
| CN (1) | CN1997610B (enExample) |
| AU (1) | AU2005211495B2 (enExample) |
| CA (1) | CA2555197C (enExample) |
| DK (1) | DK1732866T3 (enExample) |
| EA (1) | EA011022B1 (enExample) |
| ES (1) | ES2633798T3 (enExample) |
| HU (1) | HUE034363T2 (enExample) |
| MX (1) | MXPA06008943A (enExample) |
| PL (1) | PL1732866T3 (enExample) |
| TW (1) | TWI344949B (enExample) |
| WO (1) | WO2005075387A1 (enExample) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU188626U1 (ru) * | 2018-11-30 | 2019-04-18 | Федеральное государственное бюджетное учреждение науки Ордена Трудового Красного Знамени Институт нефтехимического синтеза им. А.В. Топчиева Российской академии наук (ИНХС РАН) | Устройство для алкилирования изобутана олефинами в реакторе со стационарным слоем катализатора |
| RU188625U1 (ru) * | 2018-11-30 | 2019-04-18 | Федеральное государственное бюджетное учреждение науки Ордена Трудового Красного Знамени Институт нефтехимического синтеза им. А.В. Топчиева Российской академии наук (ИНХС РАН) | Устройство для алкилирования изобутана олефинами в реакторе со стационарным слоем катализатора |
| RU2762589C2 (ru) * | 2017-03-01 | 2021-12-21 | Альбемарл Юроп Срл | Способ алкилирования с улучшенным октановым числом |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7425659B2 (en) | 2006-01-31 | 2008-09-16 | Exxonmobil Chemical Patents Inc. | Alkylaromatics production |
| TWI433829B (zh) * | 2007-01-26 | 2014-04-11 | Albemarle Netherlands Bv | 使用含稀土元素之沸石及氫化金屬之催化劑的烷化法 |
| WO2009050067A1 (en) * | 2007-10-17 | 2009-04-23 | Albemarle Netherlands, B.V. | Alkylation process using a catalyst comprising rare earth containing zeolites and reduced amount of noble metal |
| US20110313227A1 (en) | 2009-02-11 | 2011-12-22 | Albemarle Europe Sprl | Alkylation catalyst and related process |
| CN102574752A (zh) * | 2009-08-06 | 2012-07-11 | 中国石油大学(北京) | 制备烷基化油的方法 |
| AU2015286798B2 (en) * | 2014-07-07 | 2020-03-12 | Albemarle Europe Sprl | Alkylation process using a catalyst comprising cerium rich rare earth containing zeolites and a hydrogenation metal |
| CN111482194B (zh) * | 2019-01-25 | 2021-05-14 | 中国石油化工股份有限公司 | 一种烷基化催化剂及其应用 |
| CN111482195B (zh) * | 2019-01-25 | 2021-05-14 | 中国石油化工股份有限公司 | 一种固体酸催化剂 |
| CN111482193B (zh) * | 2019-01-25 | 2021-08-06 | 中国石油化工股份有限公司 | 一种固体酸催化剂的制备方法 |
| US11951461B2 (en) | 2019-01-25 | 2024-04-09 | China Petroleum & Chemical Corporation | Solid acid catalyst, preparation therefor and use thereof |
| US11078431B2 (en) | 2019-12-16 | 2021-08-03 | Saudi Arabian Oil Company | Modified ultra-stable Y (USY) zeolite catalyst for deolefinization of hydrocarbon streams |
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| US11484869B2 (en) | 2020-12-09 | 2022-11-01 | Saudi Arabian Oil Company | Modified ultra-stable Y (USY) zeolite catalyst for dealkylation of aromatics |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4300015A (en) * | 1966-08-25 | 1981-11-10 | Sun Oil Company Of Pennsylvania | Crystalline alumino-silicate zeolites containing polyvalent metal cations |
| US4992616A (en) * | 1988-07-15 | 1991-02-12 | Mobil Oil Corporation | Heterogeneous isoparaffin/olefin aklylation process |
| EP0456839A1 (en) * | 1989-12-05 | 1991-11-21 | Osaka Gas Co., Ltd. | Process for producing 4,4'-diisopropylbiphenyl |
| EP0842914A1 (en) * | 1996-11-18 | 1998-05-20 | Fina Technology, Inc. | Alkylation process with enhanced catalyst stability |
| WO2001091901A1 (en) * | 2000-05-30 | 2001-12-06 | Akzo Nobel N.V. | Novel alkylation catalyst and its use in alkylation |
| EP1308207A2 (en) * | 2001-11-06 | 2003-05-07 | Akzo Nobel N.V. | Sulfur-containing alkylation catalyst and use thereof |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3534115A (en) * | 1968-08-02 | 1970-10-13 | Sun Oil Co | Combination of dy alumino-silicate catalyst and hydrogenation catalyst |
| US3644565A (en) * | 1968-09-18 | 1972-02-22 | Union Oil Co | Alkylation process |
| NL171331C (nl) * | 1972-04-25 | 1983-03-16 | Shell Int Research | Werkwijze voor het activeren van katalysatoren die geschikt zijn voor het isomeriseren van alifatische verzadigde koolwaterstoffen. |
| NL171887C (nl) * | 1972-04-25 | 1983-06-01 | Shell Int Research | Werkwijze voor het isomeriseren van alifatische verzadigde koolwaterstoffen in aanwezigheid van waterstof. |
| US4604373A (en) * | 1984-08-24 | 1986-08-05 | Union Oil Company Of California | Hydrocracking catalyst of improved activity |
| JPH0626948B2 (ja) * | 1985-07-30 | 1994-04-13 | マツダ株式会社 | 車両用点滅装置 |
| DE68924165T2 (de) * | 1988-07-15 | 1996-02-29 | Mobil Oil Corp | Heterogenes isoparaffin/olefin-alkylierungsverfahren. |
| DE68910977T2 (de) * | 1988-07-15 | 1994-03-17 | Mobil Oil Corp | Heterogenes isoparaffin/olefin-alkylierungsverfahren. |
| US4918255A (en) * | 1988-07-15 | 1990-04-17 | Mobil Oil Corp. | Heterogeneous isoparaffin/olefin alkylation with isomerization |
| US5292981A (en) * | 1992-06-16 | 1994-03-08 | Mobil Oil Corporation | Isoparaffin-olefin alkylation process |
| US5705729A (en) * | 1995-11-22 | 1998-01-06 | Mobil Oil Corporation | Isoparaffin-olefin alkylation process |
| KR100533754B1 (ko) | 1996-11-27 | 2005-12-06 | 알베마를 네덜란드 비.브이. | 탄화수소의 알킬화 방법 |
-
2005
- 2005-01-26 CN CN2005800044348A patent/CN1997610B/zh not_active Expired - Fee Related
- 2005-01-26 EA EA200601444A patent/EA011022B1/ru not_active IP Right Cessation
- 2005-01-26 AU AU2005211495A patent/AU2005211495B2/en not_active Ceased
- 2005-01-26 EP EP05701274.2A patent/EP1732866B1/en not_active Expired - Lifetime
- 2005-01-26 US US10/588,106 patent/US7750197B2/en not_active Expired - Lifetime
- 2005-01-26 WO PCT/EP2005/000929 patent/WO2005075387A1/en not_active Ceased
- 2005-01-26 MX MXPA06008943A patent/MXPA06008943A/es active IP Right Grant
- 2005-01-26 KR KR1020067017504A patent/KR101156299B1/ko not_active Expired - Fee Related
- 2005-01-26 CA CA2555197A patent/CA2555197C/en not_active Expired - Lifetime
- 2005-01-26 DK DK05701274.2T patent/DK1732866T3/en active
- 2005-01-26 JP JP2006551778A patent/JP5016927B2/ja not_active Expired - Fee Related
- 2005-01-26 ES ES05701274.2T patent/ES2633798T3/es not_active Expired - Lifetime
- 2005-01-26 PL PL05701274T patent/PL1732866T3/pl unknown
- 2005-01-26 HU HUE05701274A patent/HUE034363T2/en unknown
- 2005-02-05 TW TW094104053A patent/TWI344949B/zh not_active IP Right Cessation
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4300015A (en) * | 1966-08-25 | 1981-11-10 | Sun Oil Company Of Pennsylvania | Crystalline alumino-silicate zeolites containing polyvalent metal cations |
| US4992616A (en) * | 1988-07-15 | 1991-02-12 | Mobil Oil Corporation | Heterogeneous isoparaffin/olefin aklylation process |
| EP0456839A1 (en) * | 1989-12-05 | 1991-11-21 | Osaka Gas Co., Ltd. | Process for producing 4,4'-diisopropylbiphenyl |
| EP0842914A1 (en) * | 1996-11-18 | 1998-05-20 | Fina Technology, Inc. | Alkylation process with enhanced catalyst stability |
| WO2001091901A1 (en) * | 2000-05-30 | 2001-12-06 | Akzo Nobel N.V. | Novel alkylation catalyst and its use in alkylation |
| EP1308207A2 (en) * | 2001-11-06 | 2003-05-07 | Akzo Nobel N.V. | Sulfur-containing alkylation catalyst and use thereof |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2762589C2 (ru) * | 2017-03-01 | 2021-12-21 | Альбемарл Юроп Срл | Способ алкилирования с улучшенным октановым числом |
| US11225614B2 (en) | 2017-03-01 | 2022-01-18 | Emanuel Hermanus Van Broekhoven | Alkylation process with improved octane number |
| RU188626U1 (ru) * | 2018-11-30 | 2019-04-18 | Федеральное государственное бюджетное учреждение науки Ордена Трудового Красного Знамени Институт нефтехимического синтеза им. А.В. Топчиева Российской академии наук (ИНХС РАН) | Устройство для алкилирования изобутана олефинами в реакторе со стационарным слоем катализатора |
| RU188625U1 (ru) * | 2018-11-30 | 2019-04-18 | Федеральное государственное бюджетное учреждение науки Ордена Трудового Красного Знамени Институт нефтехимического синтеза им. А.В. Топчиева Российской академии наук (ИНХС РАН) | Устройство для алкилирования изобутана олефинами в реакторе со стационарным слоем катализатора |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1997610B (zh) | 2010-09-15 |
| TWI344949B (en) | 2011-07-11 |
| US20070282149A1 (en) | 2007-12-06 |
| ES2633798T3 (es) | 2017-09-25 |
| KR20070015134A (ko) | 2007-02-01 |
| CA2555197C (en) | 2012-10-30 |
| EA200601444A1 (ru) | 2007-02-27 |
| AU2005211495B2 (en) | 2010-02-18 |
| HUE034363T2 (en) | 2018-02-28 |
| MXPA06008943A (es) | 2007-01-26 |
| PL1732866T3 (pl) | 2017-10-31 |
| US7750197B2 (en) | 2010-07-06 |
| JP5016927B2 (ja) | 2012-09-05 |
| WO2005075387A1 (en) | 2005-08-18 |
| KR101156299B1 (ko) | 2012-06-13 |
| CA2555197A1 (en) | 2005-08-18 |
| CN1997610A (zh) | 2007-07-11 |
| AU2005211495A1 (en) | 2005-08-18 |
| JP2007522140A (ja) | 2007-08-09 |
| EP1732866A1 (en) | 2006-12-20 |
| TW200606130A (en) | 2006-02-16 |
| DK1732866T3 (en) | 2017-09-11 |
| EP1732866B1 (en) | 2017-05-17 |
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