TW402587B - Process for converting C9+ aromatic hydrocarbons to lighter aromatic products - Google Patents
Process for converting C9+ aromatic hydrocarbons to lighter aromatic products Download PDFInfo
- Publication number
- TW402587B TW402587B TW087103842A TW87103842A TW402587B TW 402587 B TW402587 B TW 402587B TW 087103842 A TW087103842 A TW 087103842A TW 87103842 A TW87103842 A TW 87103842A TW 402587 B TW402587 B TW 402587B
- Authority
- TW
- Taiwan
- Prior art keywords
- benzene
- toluene
- stage catalyst
- catalyst composition
- zeolite
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 40
- 125000003118 aryl group Chemical group 0.000 title claims description 14
- 230000008569 process Effects 0.000 title description 11
- 150000004945 aromatic hydrocarbons Chemical class 0.000 title description 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims abstract description 153
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims abstract description 99
- 239000003054 catalyst Substances 0.000 claims abstract description 70
- 239000000203 mixture Substances 0.000 claims abstract description 51
- 239000010457 zeolite Substances 0.000 claims abstract description 28
- 229910021536 Zeolite Inorganic materials 0.000 claims abstract description 24
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims abstract description 24
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 13
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000011148 porous material Substances 0.000 claims abstract description 6
- 239000000047 product Substances 0.000 claims description 42
- 239000008096 xylene Substances 0.000 claims description 18
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 17
- 238000006243 chemical reaction Methods 0.000 claims description 15
- 238000010555 transalkylation reaction Methods 0.000 claims description 15
- 238000000605 extraction Methods 0.000 claims description 10
- 238000011049 filling Methods 0.000 claims description 10
- 239000004575 stone Substances 0.000 claims description 8
- 230000002079 cooperative effect Effects 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims description 5
- 238000006276 transfer reaction Methods 0.000 claims description 5
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 239000010455 vermiculite Substances 0.000 claims description 4
- 229910052902 vermiculite Inorganic materials 0.000 claims description 4
- 235000019354 vermiculite Nutrition 0.000 claims description 4
- 230000000737 periodic effect Effects 0.000 claims description 3
- MTFUEJNRJFNCRX-UHFFFAOYSA-N C1(=CC=CC=C1)C.C1=CC=CC=2C3=CC=CC=C3CC12 Chemical compound C1(=CC=CC=C1)C.C1=CC=CC=2C3=CC=CC=C3CC12 MTFUEJNRJFNCRX-UHFFFAOYSA-N 0.000 claims 2
- 150000007857 hydrazones Chemical class 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 239000013067 intermediate product Substances 0.000 claims 2
- PCTMTFRHKVHKIS-BMFZQQSSSA-N (1s,3r,4e,6e,8e,10e,12e,14e,16e,18s,19r,20r,21s,25r,27r,30r,31r,33s,35r,37s,38r)-3-[(2r,3s,4s,5s,6r)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-19,25,27,30,31,33,35,37-octahydroxy-18,20,21-trimethyl-23-oxo-22,39-dioxabicyclo[33.3.1]nonatriaconta-4,6,8,10 Chemical compound C1C=C2C[C@@H](OS(O)(=O)=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2.O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 PCTMTFRHKVHKIS-BMFZQQSSSA-N 0.000 claims 1
- 239000012467 final product Substances 0.000 claims 1
- 229910052702 rhenium Inorganic materials 0.000 claims 1
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 6
- 239000000377 silicon dioxide Substances 0.000 abstract description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 13
- 239000000463 material Substances 0.000 description 12
- 238000005804 alkylation reaction Methods 0.000 description 8
- 239000001301 oxygen Substances 0.000 description 7
- 229910052760 oxygen Inorganic materials 0.000 description 7
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 229910052697 platinum Inorganic materials 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- FYGHSUNMUKGBRK-UHFFFAOYSA-N 1,2,3-trimethylbenzene Chemical compound CC1=CC=CC(C)=C1C FYGHSUNMUKGBRK-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 239000000395 magnesium oxide Substances 0.000 description 4
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 4
- -1 poor Chemical compound 0.000 description 4
- 239000010970 precious metal Substances 0.000 description 4
- 239000012925 reference material Substances 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- LTPBRCUWZOMYOC-UHFFFAOYSA-N beryllium oxide Inorganic materials O=[Be] LTPBRCUWZOMYOC-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 210000004556 brain Anatomy 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 239000000779 smoke Substances 0.000 description 3
- 230000006641 stabilisation Effects 0.000 description 3
- 238000011105 stabilization Methods 0.000 description 3
- 150000003738 xylenes Chemical class 0.000 description 3
- GWHJZXXIDMPWGX-UHFFFAOYSA-N 1,2,4-trimethylbenzene Chemical compound CC1=CC=C(C)C(C)=C1 GWHJZXXIDMPWGX-UHFFFAOYSA-N 0.000 description 2
- KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-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
- FRWYFWZENXDZMU-UHFFFAOYSA-N 2-iodoquinoline Chemical compound C1=CC=CC2=NC(I)=CC=C21 FRWYFWZENXDZMU-UHFFFAOYSA-N 0.000 description 2
- VLJXXKKOSFGPHI-UHFFFAOYSA-N 3-methylhexane Chemical compound CCCC(C)CC VLJXXKKOSFGPHI-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 241000282320 Panthera leo Species 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 230000029936 alkylation Effects 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000001354 calcination Methods 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- QWHNJUXXYKPLQM-UHFFFAOYSA-N dimethyl cyclopentane Natural products CC1(C)CCCC1 QWHNJUXXYKPLQM-UHFFFAOYSA-N 0.000 description 2
- SQNZJJAZBFDUTD-UHFFFAOYSA-N durene Chemical compound CC1=CC(C)=C(C)C=C1C SQNZJJAZBFDUTD-UHFFFAOYSA-N 0.000 description 2
- 238000004945 emulsification Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052809 inorganic oxide Inorganic materials 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- OTUXRAAQAFDEQT-UHFFFAOYSA-N magnesium oxosilicon(2+) oxygen(2-) Chemical compound [O-2].[Mg+2].[Si+2]=O.[O-2] OTUXRAAQAFDEQT-UHFFFAOYSA-N 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- GDOPTJXRTPNYNR-UHFFFAOYSA-N methylcyclopentane Chemical compound CC1CCCC1 GDOPTJXRTPNYNR-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000002407 reforming Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- ZCUFMDLYAMJYST-UHFFFAOYSA-N thorium dioxide Chemical compound O=[Th]=O ZCUFMDLYAMJYST-UHFFFAOYSA-N 0.000 description 2
- 229910003452 thorium oxide Inorganic materials 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- HYFLWBNQFMXCPA-UHFFFAOYSA-N 1-ethyl-2-methylbenzene Chemical compound CCC1=CC=CC=C1C HYFLWBNQFMXCPA-UHFFFAOYSA-N 0.000 description 1
- JRLPEMVDPFPYPJ-UHFFFAOYSA-N 1-ethyl-4-methylbenzene Chemical compound CCC1=CC=C(C)C=C1 JRLPEMVDPFPYPJ-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
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 229910052693 Europium Inorganic materials 0.000 description 1
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical compound [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 description 1
- QWOHRPUHQYJPLB-UHFFFAOYSA-N [Si]=O.[O] Chemical compound [Si]=O.[O] QWOHRPUHQYJPLB-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 238000005269 aluminizing Methods 0.000 description 1
- 229940045985 antineoplastic platinum compound Drugs 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- QSKKXNSTGHZSQB-UHFFFAOYSA-N azane;platinum(2+) Chemical compound N.[Pt+2] QSKKXNSTGHZSQB-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- WQPDQJCBHQPNCZ-UHFFFAOYSA-N cyclohexa-2,4-dien-1-one Chemical class O=C1CC=CC=C1 WQPDQJCBHQPNCZ-UHFFFAOYSA-N 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000005194 ethylbenzenes Chemical class 0.000 description 1
- OGPBJKLSAFTDLK-UHFFFAOYSA-N europium atom Chemical compound [Eu] OGPBJKLSAFTDLK-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000002737 fuel gas Substances 0.000 description 1
- 239000003502 gasoline Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910000449 hafnium oxide Inorganic materials 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 150000002483 hydrogen compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000005172 methylbenzenes Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- SJLOMQIUPFZJAN-UHFFFAOYSA-N oxorhodium Chemical compound [Rh]=O SJLOMQIUPFZJAN-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000003348 petrochemical agent Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 150000003058 platinum compounds Chemical class 0.000 description 1
- CLSUSRZJUQMOHH-UHFFFAOYSA-L platinum dichloride Chemical compound Cl[Pt]Cl CLSUSRZJUQMOHH-UHFFFAOYSA-L 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 229910003450 rhodium oxide Inorganic materials 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 150000005201 tetramethylbenzenes Chemical class 0.000 description 1
- 150000005199 trimethylbenzenes Chemical class 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- 238000004804 winding Methods 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
- 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
-
- 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
- C07C6/12—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond of exclusively hydrocarbons containing a six-membered aromatic ring
- C07C6/126—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond of exclusively hydrocarbons containing a six-membered aromatic ring of more than one hydrocarbon
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2529/00—Catalysts comprising molecular sieves
- C07C2529/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites, pillared clays
- C07C2529/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2529/00—Catalysts comprising molecular sieves
- C07C2529/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites, pillared clays
- C07C2529/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- C07C2529/70—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups C07C2529/08 - C07C2529/65
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/874,875 US5942651A (en) | 1997-06-13 | 1997-06-13 | Process for converting C9 + aromatic hydrocarbons to lighter aromatic products by transalkylation in the prescence of two zeolite-containing catalysts |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW402587B true TW402587B (en) | 2000-08-21 |
Family
ID=25364770
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW087103842A TW402587B (en) | 1997-06-13 | 1998-03-16 | Process for converting C9+ aromatic hydrocarbons to lighter aromatic products |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US5942651A (https=) |
| EP (1) | EP0988265B1 (https=) |
| JP (1) | JP4021943B2 (https=) |
| KR (1) | KR100534062B1 (https=) |
| CN (1) | CN1111518C (https=) |
| AU (1) | AU738979B2 (https=) |
| BG (1) | BG103960A (https=) |
| CA (1) | CA2290694C (https=) |
| DE (1) | DE69807476T2 (https=) |
| ES (1) | ES2180181T3 (https=) |
| ID (1) | ID24255A (https=) |
| PL (1) | PL337778A1 (https=) |
| PT (1) | PT988265E (https=) |
| RU (1) | RU2183611C2 (https=) |
| TW (1) | TW402587B (https=) |
| WO (1) | WO1998056741A1 (https=) |
Families Citing this family (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7569136B2 (en) * | 1997-06-24 | 2009-08-04 | Ackerson Michael D | Control system method and apparatus for two phase hydroprocessing |
| US6750446B2 (en) * | 2001-01-17 | 2004-06-15 | Fuji Photo Film Co., Ltd. | Ultrasonic-welding apparatus, optical sensor and rotation sensor for the ultrasonic-welding apparatus |
| US6815570B1 (en) * | 2002-05-07 | 2004-11-09 | Uop Llc | Shaped catalysts for transalkylation of aromatics for enhanced xylenes production |
| US7553791B2 (en) * | 2002-11-14 | 2009-06-30 | Exxonmobil Chemical Patents Inc. | Heavy aromatics conversion catalyst composition and processes therefor and therewith |
| US7148391B1 (en) * | 2002-11-14 | 2006-12-12 | Exxonmobil Chemical Patents Inc. | Heavy aromatics processing |
| US6893624B2 (en) | 2002-11-15 | 2005-05-17 | Exxonmobil Chemical Patents Inc. | High activity small crystal ZSM-12 |
| ITMI20022712A1 (it) * | 2002-12-20 | 2004-06-21 | Polimeri Europa Spa | Composizione catalitica e processo per la transalchilazione di idrocarburi. |
| US6855854B1 (en) * | 2003-06-13 | 2005-02-15 | Uop Llc | Process and apparatus for ethylbenzene production and transalkylation to xylene |
| US6958425B1 (en) * | 2003-06-13 | 2005-10-25 | Uop Llc | Aromatics transalkylation to ethylbenzene and xylenes |
| US6872866B1 (en) * | 2003-12-15 | 2005-03-29 | Uop Llc | Liquid phase process for C8 alkylaromatic isomerization |
| US6972348B2 (en) | 2004-03-24 | 2005-12-06 | Uop Llc | Catalytic conversion of polycyclic aromatics into xylenes |
| FR2877665B1 (fr) * | 2004-11-09 | 2006-12-29 | Inst Francais Du Petrole | Procede de transalkylation d'hydrocarbures alkylaromatiques mis en oeuvre dans deux zones reactionnelles |
| US20070049780A1 (en) * | 2005-08-30 | 2007-03-01 | Schwartz Hilary E | Methods of making xylene isomers |
| WO2007114127A1 (ja) | 2006-03-29 | 2007-10-11 | Toray Industries, Inc. | エチルベンゼンの転化方法およびパラキシレンの製造方法 |
| US7566810B2 (en) * | 2006-09-12 | 2009-07-28 | Uop Llc | Xylene production processes employing rhenium-containing catalysts |
| US7776283B2 (en) * | 2007-07-30 | 2010-08-17 | Uop Llc | Xylene production apparatus with integrated feedstock treatment |
| US7847137B2 (en) * | 2007-07-30 | 2010-12-07 | Uop Llc | Xylene production processes with integrated feedstock treatment |
| CA2702423C (en) * | 2007-10-31 | 2015-04-28 | Exxonmobil Chemical Patents Inc. | Heavy aromatics processing catalyst and process of using the same |
| JP5340620B2 (ja) * | 2008-03-27 | 2013-11-13 | Ｊｘ日鉱日石エネルギー株式会社 | 触媒組成物及び芳香族炭化水素の製造方法 |
| US20100029467A1 (en) * | 2008-07-30 | 2010-02-04 | Tomoyuki Inui | Multiple zeolite catalyst |
| US8653315B2 (en) | 2008-07-30 | 2014-02-18 | King Fahd University Of Petroleum And Minerals | Multiple zeolite catalyst and method of using the same for toluene disproportionation |
| CN201340888Y (zh) * | 2009-01-08 | 2009-11-04 | 东莞新能源科技有限公司 | 锂离子电池 |
| US8163966B2 (en) * | 2009-11-30 | 2012-04-24 | Exxonmobil Chemical Patents Inc. | Aromatics processing catalyst system |
| US8183424B2 (en) * | 2010-02-03 | 2012-05-22 | Exxonmobil Chemical Patents Inc. | Transalkylation of heavy aromatic hydrocarbon feedstocks |
| US8071828B2 (en) * | 2010-02-03 | 2011-12-06 | Exxonmobil Chemical Patents Inc. | Transalkylation of heavy aromatic hydrocarbon feedstocks |
| US8586809B2 (en) | 2010-07-30 | 2013-11-19 | Exxonmobil Chemical Patents Inc. | Purification of transalkylation feedstock |
| CN103120952B (zh) * | 2011-11-18 | 2015-02-11 | 中国石油化工股份有限公司 | 歧化与烷基转移催化剂及其制备方法 |
| CN103120954B (zh) * | 2011-11-18 | 2015-04-08 | 中国石油化工股份有限公司 | 稠环芳烃制取单环芳烃催化剂 |
| WO2013095815A1 (en) | 2011-12-22 | 2013-06-27 | Uop Llc | Enhanced aromatics production by low pressure end point reduction and selective hydrogenation and hydrodealkylation |
| US9000247B2 (en) | 2012-04-19 | 2015-04-07 | Saudi Arabian Oil Company | Combined heavy reformate dealkylation-transalkylation process for maximizing xylenes production |
| US20140100403A1 (en) * | 2012-10-05 | 2014-04-10 | Uop Llc | Low pressure transalkylation process |
| US9522858B2 (en) | 2013-05-31 | 2016-12-20 | Exxonmobil Chemical Patents Inc. | Transalkylation system |
| CN103467238B (zh) * | 2013-08-23 | 2016-08-10 | 宁夏宝塔石化科技实业发展有限公司 | 一种对二甲苯的生产方法 |
| US9783462B2 (en) | 2013-09-10 | 2017-10-10 | Saudi Basic Industries Corporation | Toluene methylation with transalkylation of heavy aromatics |
| WO2015187363A1 (en) * | 2014-06-04 | 2015-12-10 | Exxonmobil Chemical Patents Inc. | Transalkylation of heavy aromatic hydrocarbon feedstocks |
| PL3185979T3 (pl) | 2014-08-06 | 2019-06-28 | Bp Corporation North America Inc. | Integracja ciepła w procesach dysproporcjonowania lub transalkilowania |
| RU2665477C2 (ru) * | 2014-10-31 | 2018-08-30 | Чайна Петролеум & Кемикал Корпорейшн | Способ получения ароматических углеводородов |
| US10781149B2 (en) | 2014-12-19 | 2020-09-22 | Exxonmobil Chemical Patents Inc. | Transalkylation process |
| US10450243B2 (en) | 2014-12-19 | 2019-10-22 | Exxonmobil Chemical Patents Inc. | Sulfiding process for aromatic transalkylations |
| US10053403B2 (en) | 2015-02-04 | 2018-08-21 | Exxonmobil Chemical Patents Inc. | Catalyst compositions and their use in transalkylation of heavy aromatics to xylenes |
| US10118165B2 (en) | 2015-02-04 | 2018-11-06 | Exxonmobil Chemical Patents Inc. | Catalyst compositions and use in heavy aromatics conversion processes |
| KR102252012B1 (ko) | 2016-10-04 | 2021-05-17 | 엑손모빌 케미칼 패턴츠 인코포레이티드 | 중질 방향족 탄화수소의 불균화 및 알킬교환 |
| BR112019004308A2 (pt) | 2016-10-10 | 2019-05-28 | Exxonmobil Chemical Patents Inc. | aromáticos pesados para processo de conversão de btx e composições catalisadoras usadas |
| US10173950B2 (en) | 2017-01-04 | 2019-01-08 | Saudi Arabian Oil Company | Integrated process for the production of benzene and xylenes from heavy aromatics |
| CN108264445B (zh) * | 2017-01-04 | 2021-02-09 | 中国石油化工股份有限公司 | 甲苯歧化与/或烷基转移反应的方法 |
| US10035742B1 (en) | 2017-05-26 | 2018-07-31 | Saudi Arabian Oil Company | Process for maximizing xylenes production from heavy aromatics for use therein |
| US10252958B2 (en) | 2017-05-26 | 2019-04-09 | Saudi Arabian Oil Company | Process for xylene production with energy optimization |
| US10464868B2 (en) | 2017-05-26 | 2019-11-05 | Saudi Arabian Oil Company | Process for maximizing production of xylenes from heavy reformate without purge |
| US10661260B2 (en) | 2017-06-15 | 2020-05-26 | King Fahd University Of Petroleum And Minerals | Zeolite composite catalysts for conversion of heavy reformate to xylenes |
| EP3539651B1 (en) | 2018-03-14 | 2025-09-17 | Saudi Arabian Oil Company | Method of heavy reformate conversion into btx over metal-impregnated zsm-5+layered mordenite zeolite composite catalyst; said composite catalyst |
| EP3539652A1 (en) | 2018-03-14 | 2019-09-18 | Saudi Arabian Oil Company | Method of heavy reformate conversion into btx over metal-impregnated zsm-5+mesoporous mordenite zeolite composite catalyst |
| EP3834931A1 (en) | 2018-03-14 | 2021-06-16 | Saudi Arabian Oil Company | Composite zeolite catalysts for heavy reformate conversion into xylenes |
| EP3539649B1 (en) | 2018-03-14 | 2020-11-18 | Saudi Arabian Oil Company | Methods of producing composite zeolite catalysts for heavy reformate conversion into xylenes |
| US10696609B2 (en) | 2018-10-15 | 2020-06-30 | Saudi Arabian Oil Company | Integrated process for maximizing production of para-xylene from full reformate |
| US10894755B2 (en) | 2018-10-15 | 2021-01-19 | Saudi Arabian Oil Company | Integrated process for optimum production of para-xylene |
| US10501389B1 (en) | 2018-10-25 | 2019-12-10 | Saudi Arabian Oil Company | Process and system for the production of para-xylene and benzene from streams rich in C6 to C12+ aromatics |
| US12239964B2 (en) | 2019-03-29 | 2025-03-04 | ExxonMobil Engineering & Technology Company | Catalysts and processes for converting aromatics |
| TWI749489B (zh) * | 2019-03-29 | 2021-12-11 | 美商艾克頌美孚化學專利股份有限公司 | 用於轉化芳族化合物之觸媒及方法 |
| CN112745926A (zh) * | 2019-10-30 | 2021-05-04 | 中国石油化工股份有限公司 | 处理催化裂解汽油的方法和系统、多产低碳烯烃和轻质芳烃的工艺和装置 |
| US10981160B1 (en) | 2019-12-19 | 2021-04-20 | Saudi Arabian Oil Company | Composite hierarchical zeolite catalyst for heavy reformate conversion to xylenes |
| KR20230079115A (ko) | 2020-09-27 | 2023-06-05 | 차이나 페트로리움 앤드 케미컬 코포레이션 | 불균등화 및 트랜스알킬화 촉매, 이의 제조 및 응용 |
| US12098121B2 (en) | 2023-02-07 | 2024-09-24 | Saudi Arabian Oil Company | Methods for producing xylenes with limited ethylbenzene production |
| CN117943109A (zh) * | 2024-01-29 | 2024-04-30 | 中国科学院山西煤炭化学研究所 | 一种用于多环芳烃加氢裂化制取苯及烷基苯的催化剂 |
Family Cites Families (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3308069A (en) * | 1964-05-01 | 1967-03-07 | Mobil Oil Corp | Catalytic composition of a crystalline zeolite |
| US3702886A (en) * | 1969-10-10 | 1972-11-14 | Mobil Oil Corp | Crystalline zeolite zsm-5 and method of preparing the same |
| US3729409A (en) * | 1970-12-24 | 1973-04-24 | Mobil Oil Corp | Hydrocarbon conversion |
| JPS517655B1 (https=) * | 1970-12-28 | 1976-03-10 | ||
| US3832449A (en) * | 1971-03-18 | 1974-08-27 | Mobil Oil Corp | Crystalline zeolite zsm{14 12 |
| US3767568A (en) * | 1971-03-19 | 1973-10-23 | Mobil Oil Corp | Hydrocarbon conversion |
| US3948758A (en) * | 1974-06-17 | 1976-04-06 | Mobil Oil Corporation | Production of alkyl aromatic hydrocarbons |
| US3957621A (en) * | 1974-06-17 | 1976-05-18 | Mobil Oil Corporation | Production of alkyl aromatic hydrocarbons |
| US3965208A (en) * | 1975-01-06 | 1976-06-22 | Mobil Oil Corporation | Methylation of toluene |
| US4100215A (en) * | 1974-09-25 | 1978-07-11 | Mobil Oil Corporation | Selective production of para-xylene |
| US4001346A (en) * | 1975-01-06 | 1977-01-04 | Mobil Oil Corporation | Selective production of para-xylene |
| US3965209A (en) * | 1975-01-06 | 1976-06-22 | Mobil Oil Corporation | Selective production of para-xylene |
| US4052476A (en) * | 1975-04-24 | 1977-10-04 | Mobil Oil Corporation | Toluene disproportionation over zeolite catalyst |
| US4016218A (en) * | 1975-05-29 | 1977-04-05 | Mobil Oil Corporation | Alkylation in presence of thermally modified crystalline aluminosilicate catalyst |
| US4016219A (en) * | 1975-08-22 | 1977-04-05 | Mobil Oil Corporation | Disproportionation of toluene |
| US4007231A (en) * | 1975-11-24 | 1977-02-08 | Mobil Oil Corporation | Selective production of para-xylene |
| US4029716A (en) * | 1975-12-08 | 1977-06-14 | Mobil Oil Corporation | Selective production of para-xylene |
| US4011276A (en) * | 1976-04-28 | 1977-03-08 | Mobil Oil Corporation | Disproportionation of toluene |
| US4117026A (en) * | 1976-05-12 | 1978-09-26 | Mobil Oil Corporation | Selective production of para dialkyl substituted benzenes |
| US4150062A (en) * | 1976-12-20 | 1979-04-17 | Mobil Oil Corporation | Light olefin processing |
| US4127471A (en) * | 1977-07-28 | 1978-11-28 | Texaco Inc. | Hydrocracking alkylaromatic-containing hydrocarbons at mild cracking conditions and then subjecting the alkylaromatic hydrocarbon to alkyl transfer |
| US4152364A (en) * | 1978-01-19 | 1979-05-01 | Mobil Oil Corporation | Selective production of para-xylene |
| US4418235A (en) * | 1980-02-14 | 1983-11-29 | Mobil Oil Corporation | Hydrocarbon conversion with zeolite having enhanced catalytic activity |
| US4380685A (en) * | 1980-05-19 | 1983-04-19 | Mobil Oil Corporation | Shape selective reactions with zeolite catalysts modified with iron and/or cobalt |
| DE3117135A1 (de) * | 1981-04-30 | 1982-11-18 | Bayer Ag, 5090 Leverkusen | Kristallines alumosilicat, verfahren zu dessen herstellung sowie dessen verwendung zur katalytischen umwandlung von methanol und/oder dimethylether in kohlenwasserstoffe |
| US4365104A (en) * | 1981-06-26 | 1982-12-21 | Mobil Oil Corporation | Para-selective zeolite catalysts treated with sulfur compounds |
| US4367359A (en) * | 1981-06-26 | 1983-01-04 | Mobil Oil Corporation | Para-selective zeolite catalysts treated with carbon dioxide |
| US4370508A (en) * | 1981-06-26 | 1983-01-25 | Mobil Oil Corporation | Para-selective zeolite catalysts treated with nitrogen compounds |
| ZA861382B (en) * | 1986-02-24 | 1987-10-28 | Mobil Oil Corp | Process for improving the octane number of cracked gasolines |
| US4954325A (en) * | 1986-07-29 | 1990-09-04 | Mobil Oil Corp. | Composition of synthetic porous crystalline material, its synthesis and use |
| US4812223A (en) * | 1987-05-01 | 1989-03-14 | Mobil Oil Corporation | Hydrocracking naphthas using mildly steamed, noble metal-containing zeolite beta |
| US4857666A (en) * | 1987-09-11 | 1989-08-15 | Uop | Alkylation/transalkylation process |
| US4891458A (en) * | 1987-12-17 | 1990-01-02 | Innes Robert A | Liquid phase alkylation or transalkylation process using zeolite beta |
| CA2042361C (en) * | 1989-12-13 | 2000-12-19 | Robert P. L. Absil | A process for the catalytic conversion of a c9+ aromatics feed |
| US5030787A (en) * | 1990-01-24 | 1991-07-09 | Mobil Oil Corp. | Catalytic disproportionation/transalkylation utilizing a C9+ aromatics feed |
| US5406016A (en) * | 1993-06-07 | 1995-04-11 | Exxon Research And Engineering Company | Transalkylation of benzene with heavy catalytic naphtha |
| TW504501B (en) * | 1995-02-10 | 2002-10-01 | Mobil Oil Corp | Process for converting feedstock comprising C9+ aromatic hydrocarbons to lighter aromatic products |
-
1997
- 1997-06-13 US US08/874,875 patent/US5942651A/en not_active Expired - Lifetime
-
1998
- 1998-03-16 TW TW087103842A patent/TW402587B/zh not_active IP Right Cessation
- 1998-06-12 ES ES98929047T patent/ES2180181T3/es not_active Expired - Lifetime
- 1998-06-12 CA CA002290694A patent/CA2290694C/en not_active Expired - Fee Related
- 1998-06-12 PL PL98337778A patent/PL337778A1/xx unknown
- 1998-06-12 DE DE69807476T patent/DE69807476T2/de not_active Expired - Fee Related
- 1998-06-12 RU RU2000100988/04A patent/RU2183611C2/ru not_active IP Right Cessation
- 1998-06-12 CN CN98805980A patent/CN1111518C/zh not_active Expired - Lifetime
- 1998-06-12 AU AU80705/98A patent/AU738979B2/en not_active Ceased
- 1998-06-12 KR KR10-1999-7011329A patent/KR100534062B1/ko not_active Expired - Lifetime
- 1998-06-12 ID IDW991593A patent/ID24255A/id unknown
- 1998-06-12 EP EP98929047A patent/EP0988265B1/en not_active Expired - Lifetime
- 1998-06-12 JP JP50328599A patent/JP4021943B2/ja not_active Expired - Lifetime
- 1998-06-12 WO PCT/US1998/012311 patent/WO1998056741A1/en not_active Ceased
- 1998-06-12 PT PT98929047T patent/PT988265E/pt unknown
-
1999
- 1999-12-07 BG BG103960A patent/BG103960A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP4021943B2 (ja) | 2007-12-12 |
| JP2002504946A (ja) | 2002-02-12 |
| CN1259930A (zh) | 2000-07-12 |
| DE69807476D1 (de) | 2002-10-02 |
| CA2290694C (en) | 2008-07-29 |
| PL337778A1 (en) | 2000-09-11 |
| ES2180181T3 (es) | 2003-02-01 |
| BG103960A (en) | 2000-06-30 |
| PT988265E (pt) | 2002-11-29 |
| US5942651A (en) | 1999-08-24 |
| EP0988265B1 (en) | 2002-08-28 |
| WO1998056741A1 (en) | 1998-12-17 |
| KR100534062B1 (ko) | 2005-12-07 |
| EP0988265A1 (en) | 2000-03-29 |
| KR20010013333A (ko) | 2001-02-26 |
| CN1111518C (zh) | 2003-06-18 |
| EP0988265A4 (en) | 2000-10-04 |
| AU738979B2 (en) | 2001-10-04 |
| CA2290694A1 (en) | 1998-12-17 |
| DE69807476T2 (de) | 2003-01-02 |
| RU2183611C2 (ru) | 2002-06-20 |
| ID24255A (id) | 2000-07-13 |
| AU8070598A (en) | 1998-12-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| TW402587B (en) | Process for converting C9+ aromatic hydrocarbons to lighter aromatic products | |
| TW504501B (en) | Process for converting feedstock comprising C9+ aromatic hydrocarbons to lighter aromatic products | |
| US3948758A (en) | Production of alkyl aromatic hydrocarbons | |
| TW492956B (en) | An improved process for the producing xylene | |
| CN102781889B (zh) | 重质芳族烃原料的烷基转移 | |
| TW518316B (en) | Para-xylene production process | |
| TWI375592B (en) | Heavy aromatics conversion catalyst composition and processes therefor and therewith | |
| WO1991011415A1 (en) | Dual function catalyst and isomerization therewith | |
| TW200530148A (en) | Method of converting C9 aromatics-comprising mixtures to xylene isomers | |
| JPS607603B2 (ja) | 熱処理変性した結晶性アルミノシリケート触媒の存在においてアルキル化を行う方法 | |
| JPH03503656A (ja) | アルカンおよびアルケンのハイオクタンガソリンへの転化 | |
| TW200418571A (en) | Heavy aromatics processing | |
| TWI332497B (en) | Method of conversion of heavy aromatics | |
| JP2019531298A (ja) | 重質芳香族炭化水素の不均化およびトランスアルキル化 | |
| JP2019529508A (ja) | 重質芳香族炭化水素の脱アルキル化およびトランスアルキル化 | |
| US4157950A (en) | Conversion of hydrocarbons | |
| TW527416B (en) | Processes and catalysts for the disproportion and conversion of toluene containing heavy aromatic hydrocarbons with nine and more than nine carbon atoms | |
| US4677240A (en) | Hydrocarbon conversion processes over crystalline borosilicate catalysts for pseudocumene recovery | |
| TW408033B (en) | A catalyst for the conversion of heavy aromatics to light aromatics and a process for the same conversion | |
| JP3554804B2 (ja) | 芳香族炭化水素化合物の転化用触媒および転化方法 | |
| JP2598127B2 (ja) | キシレンの異性化方法 | |
| JPS62285987A (ja) | 軽質パラフインの転化法 | |
| TW473464B (en) | Process for isomerising aromatic cuts containing eight carbon atoms using a catalyst containing a zeolite with structure type EUO | |
| JP3617416B2 (ja) | 芳香族炭化水素の転化方法 | |
| TW459039B (en) | Heavy aromatics processing |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| GD4A | Issue of patent certificate for granted invention patent | ||
| MK4A | Expiration of patent term of an invention patent |