KR20000052636A - Ｉｍ-5 제올라이트, 이의 제조 방법 및 촉매로서의 용도 - Google Patents
Ｉｍ-5 제올라이트, 이의 제조 방법 및 촉매로서의 용도 Download PDFInfo
- Publication number
- KR20000052636A KR20000052636A KR1019990703399A KR19997003399A KR20000052636A KR 20000052636 A KR20000052636 A KR 20000052636A KR 1019990703399 A KR1019990703399 A KR 1019990703399A KR 19997003399 A KR19997003399 A KR 19997003399A KR 20000052636 A KR20000052636 A KR 20000052636A
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- South Korea
- Prior art keywords
- zeolite
- group
- cation
- catalyst
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000010457 zeolite Substances 0.000 title claims abstract description 145
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 title claims abstract description 111
- 229910021536 Zeolite Inorganic materials 0.000 title claims abstract description 106
- 238000000034 method Methods 0.000 title claims abstract description 32
- 230000003197 catalytic effect Effects 0.000 title description 8
- 238000002360 preparation method Methods 0.000 title description 6
- 239000003054 catalyst Substances 0.000 claims abstract description 65
- 239000000203 mixture Substances 0.000 claims abstract description 63
- 150000001768 cations Chemical class 0.000 claims abstract description 46
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 26
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 25
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 23
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000010703 silicon Substances 0.000 claims abstract description 18
- 229910052733 gallium Inorganic materials 0.000 claims abstract description 14
- 229910052796 boron Inorganic materials 0.000 claims abstract description 13
- 229910052742 iron Inorganic materials 0.000 claims abstract description 13
- 239000000126 substance Substances 0.000 claims abstract description 13
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims abstract description 11
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract description 10
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052732 germanium Chemical group 0.000 claims abstract description 10
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical group [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 10
- 239000010936 titanium Substances 0.000 claims abstract description 10
- 150000008064 anhydrides Chemical class 0.000 claims abstract description 7
- 238000004519 manufacturing process Methods 0.000 claims abstract description 6
- 229910052751 metal Inorganic materials 0.000 claims description 35
- 239000002184 metal Substances 0.000 claims description 35
- 238000006243 chemical reaction Methods 0.000 claims description 32
- 239000001257 hydrogen Substances 0.000 claims description 21
- 229910052739 hydrogen Inorganic materials 0.000 claims description 21
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 16
- 238000001354 calcination Methods 0.000 claims description 15
- 238000000354 decomposition reaction Methods 0.000 claims description 15
- 125000001477 organic nitrogen group Chemical group 0.000 claims description 15
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 14
- -1 alkali metal cations Chemical class 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 14
- 239000013078 crystal Substances 0.000 claims description 14
- 150000002430 hydrocarbons Chemical class 0.000 claims description 13
- 229930195733 hydrocarbon Natural products 0.000 claims description 12
- 239000002243 precursor Substances 0.000 claims description 12
- 229910052697 platinum Inorganic materials 0.000 claims description 11
- 229910052702 rhenium Inorganic materials 0.000 claims description 11
- XXZFCJVFXKCILB-UHFFFAOYSA-N 1-methylpyrrolidine;hydrobromide Chemical compound [Br-].C[NH+]1CCCC1 XXZFCJVFXKCILB-UHFFFAOYSA-N 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 10
- 229910052759 nickel Inorganic materials 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 10
- 229910052783 alkali metal Inorganic materials 0.000 claims description 9
- 229910052763 palladium Inorganic materials 0.000 claims description 9
- 229910052703 rhodium Inorganic materials 0.000 claims description 7
- 229910052718 tin Inorganic materials 0.000 claims description 7
- 229910052745 lead Inorganic materials 0.000 claims description 6
- ZWVMLYRJXORSEP-LURJTMIESA-N (2s)-hexane-1,2,6-triol Chemical group OCCCC[C@H](O)CO ZWVMLYRJXORSEP-LURJTMIESA-N 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 5
- 150000001340 alkali metals Chemical class 0.000 claims description 5
- 229910052802 copper Inorganic materials 0.000 claims description 5
- 239000010949 copper Substances 0.000 claims description 5
- 230000000737 periodic effect Effects 0.000 claims description 5
- 150000001450 anions Chemical class 0.000 claims description 4
- 229910052787 antimony Inorganic materials 0.000 claims description 4
- 229910052804 chromium Inorganic materials 0.000 claims description 4
- 229910052698 phosphorus Inorganic materials 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 4
- 229910052720 vanadium Inorganic materials 0.000 claims description 4
- 229910052725 zinc Inorganic materials 0.000 claims description 4
- AVFZOVWCLRSYKC-UHFFFAOYSA-N 1-methylpyrrolidine Chemical compound CN1CCCC1 AVFZOVWCLRSYKC-UHFFFAOYSA-N 0.000 claims description 3
- 229910001413 alkali metal ion Inorganic materials 0.000 claims description 3
- 150000003863 ammonium salts Chemical class 0.000 claims description 3
- 239000011230 binding agent Substances 0.000 claims description 3
- 229910052793 cadmium Inorganic materials 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 229910052749 magnesium Inorganic materials 0.000 claims description 3
- 229910052748 manganese Inorganic materials 0.000 claims description 3
- 229910052709 silver Inorganic materials 0.000 claims description 3
- 229910052712 strontium Inorganic materials 0.000 claims description 3
- 239000012736 aqueous medium Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 31
- 238000005342 ion exchange Methods 0.000 description 24
- 239000000047 product Substances 0.000 description 23
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
- 238000006317 isomerization reaction Methods 0.000 description 17
- 239000011734 sodium Substances 0.000 description 15
- 239000008096 xylene Substances 0.000 description 13
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 12
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 12
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 238000005984 hydrogenation reaction Methods 0.000 description 12
- 239000011159 matrix material Substances 0.000 description 12
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 12
- 230000015572 biosynthetic process Effects 0.000 description 11
- 239000000377 silicon dioxide Substances 0.000 description 11
- 238000003786 synthesis reaction Methods 0.000 description 11
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 10
- 238000006356 dehydrogenation reaction Methods 0.000 description 10
- 239000007789 gas Substances 0.000 description 10
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 10
- 229910004298 SiO 2 Inorganic materials 0.000 description 8
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 8
- 239000003085 diluting agent Substances 0.000 description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 8
- 229910052708 sodium Inorganic materials 0.000 description 8
- 238000003756 stirring Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 229910001868 water Inorganic materials 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 238000002441 X-ray diffraction Methods 0.000 description 6
- 150000001336 alkenes Chemical class 0.000 description 6
- 150000001491 aromatic compounds Chemical class 0.000 description 6
- 238000007323 disproportionation reaction Methods 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000000499 gel Substances 0.000 description 6
- 150000002739 metals Chemical class 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 5
- 238000005804 alkylation reaction Methods 0.000 description 5
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 5
- 239000002808 molecular sieve Substances 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 5
- 238000010555 transalkylation reaction Methods 0.000 description 5
- 239000012808 vapor phase Substances 0.000 description 5
- 230000005260 alpha ray Effects 0.000 description 4
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 4
- 238000001636 atomic emission spectroscopy Methods 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 238000000921 elemental analysis Methods 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 238000005470 impregnation Methods 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 4
- 150000002736 metal compounds Chemical class 0.000 description 4
- 229910044991 metal oxide Inorganic materials 0.000 description 4
- 150000004706 metal oxides Chemical class 0.000 description 4
- 150000002894 organic compounds Chemical class 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 4
- 239000004810 polytetrafluoroethylene Substances 0.000 description 4
- 238000000634 powder X-ray diffraction Methods 0.000 description 4
- 229910001388 sodium aluminate Inorganic materials 0.000 description 4
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 4
- 235000011121 sodium hydroxide Nutrition 0.000 description 4
- 239000012265 solid product Substances 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229910000323 aluminium silicate Inorganic materials 0.000 description 3
- 238000005899 aromatization reaction Methods 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 238000004523 catalytic cracking Methods 0.000 description 3
- 239000007809 chemical reaction catalyst Substances 0.000 description 3
- 239000011651 chromium Substances 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052750 molybdenum Inorganic materials 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
- 238000006384 oligomerization reaction Methods 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- FYGHSUNMUKGBRK-UHFFFAOYSA-N 1,2,3-trimethylbenzene Chemical compound CC1=CC=CC(C)=C1C FYGHSUNMUKGBRK-UHFFFAOYSA-N 0.000 description 2
- 229910002014 Aerosil® 130 Inorganic materials 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 230000003321 amplification Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000004517 catalytic hydrocracking Methods 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000008119 colloidal silica Substances 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000008240 homogeneous mixture Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 230000000877 morphologic effect Effects 0.000 description 2
- 238000003199 nucleic acid amplification method Methods 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000006722 reduction reaction Methods 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000008247 solid mixture Substances 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- YFQBFBATCINSHI-BGERDNNASA-N (2s)-2,6-diamino-1-(2-diphenoxyphosphorylpyrrolidin-1-yl)hexan-1-one Chemical compound NCCCC[C@H](N)C(=O)N1CCCC1P(=O)(OC=1C=CC=CC=1)OC1=CC=CC=C1 YFQBFBATCINSHI-BGERDNNASA-N 0.000 description 1
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 description 1
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 1
- HYFLWBNQFMXCPA-UHFFFAOYSA-N 1-ethyl-2-methylbenzene Chemical compound CCC1=CC=CC=C1C HYFLWBNQFMXCPA-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004113 Sepiolite Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 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
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Inorganic materials O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- VXAUWWUXCIMFIM-UHFFFAOYSA-M aluminum;oxygen(2-);hydroxide Chemical compound [OH-].[O-2].[Al+3] VXAUWWUXCIMFIM-UHFFFAOYSA-M 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 150000003868 ammonium compounds Chemical class 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 238000006900 dealkylation reaction Methods 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 238000006477 desulfuration reaction Methods 0.000 description 1
- 230000023556 desulfurization Effects 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 150000002170 ethers Chemical group 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
- 238000007069 methylation reaction Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000002892 organic cations Chemical class 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 238000006798 ring closing metathesis reaction Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 150000004684 trihydrates Chemical class 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- 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
- C10G49/00—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00
- C10G49/02—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00 characterised by the catalyst used
- C10G49/08—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00 characterised by the catalyst used containing crystalline alumino-silicates, e.g. molecular sieves
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B39/00—Compounds having molecular sieve and base-exchange properties, e.g. crystalline zeolites; Their preparation; After-treatment, e.g. ion-exchange or dealumination
- C01B39/02—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof; Direct preparation thereof; Preparation thereof starting from a reaction mixture containing a crystalline zeolite of another type, or from preformed reactants; After-treatment thereof
- C01B39/46—Other types characterised by their X-ray diffraction pattern and their defined composition
- C01B39/48—Other types characterised by their X-ray diffraction pattern and their defined composition using at least one organic template directing agent
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Inorganic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9612873A FR2754809B1 (fr) | 1996-10-21 | 1996-10-21 | Zeolithe im-5, son procede de preparation et ses applications catalytiques |
| FR96/12873 | 1996-10-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20000052636A true KR20000052636A (ko) | 2000-08-25 |
Family
ID=9496909
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019990703399A Withdrawn KR20000052636A (ko) | 1996-10-21 | 1997-10-17 | Ｉｍ-5 제올라이트, 이의 제조 방법 및 촉매로서의 용도 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US6136290A (enExample) |
| EP (1) | EP0946416B1 (enExample) |
| JP (1) | JP4348651B2 (enExample) |
| KR (1) | KR20000052636A (enExample) |
| CN (1) | CN1234012A (enExample) |
| AU (1) | AU4872297A (enExample) |
| BR (1) | BR9712417A (enExample) |
| CA (1) | CA2268803A1 (enExample) |
| DE (1) | DE69710612T2 (enExample) |
| FR (1) | FR2754809B1 (enExample) |
| WO (1) | WO1998017581A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20140118994A (ko) * | 2011-11-10 | 2014-10-08 | 차이나 페트로리움 앤드 케미컬 코포레이션 | 중공 im-5 분자체 구 및 그 제조 방법 |
Families Citing this family (84)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2752567B1 (fr) * | 1996-08-23 | 1998-10-16 | Inst Francais Du Petrole | Zeolithe nu-88, son procede de preparation et ses applications catalytiques |
| FR2758817B1 (fr) * | 1997-01-24 | 1999-09-03 | Inst Francais Du Petrole | Procede de craquage de charges hydrocarbonees a l'aide d'un catalyseur comprenant une zeolithe im-5 eventuellement desaluminee |
| FR2758810B1 (fr) * | 1997-01-24 | 1999-02-19 | Inst Francais Du Petrole | Zeolithe im-5 desaluminee |
| FR2769919B1 (fr) * | 1997-10-16 | 1999-12-24 | Inst Francais Du Petrole | Procede pour l'amelioration du point d'ecoulement de charges paraffiniques avec un catalyseur a base de zeolithe im-5 |
| ES2155761B1 (es) * | 1998-12-22 | 2001-12-01 | Univ Valencia Politecnica | Zeolita itq-7. |
| FR2790001B1 (fr) * | 1999-02-24 | 2001-04-27 | Inst Francais Du Petrole | Procede d'hydrocraquage avec un catalyseur comprenant une zeolithe im-5 et catalyseur comprenant une zeolithe im-5 et un element promoteur |
| FR2790002B1 (fr) * | 1999-02-24 | 2003-10-24 | Inst Francais Du Petrole | Procede d'hydrocraquage de charges hydrocarbonees en presence d'un catalyseur comprenant une zeolithe im-5 et un element du groupe vb |
| NL1014299C2 (nl) * | 1999-02-24 | 2001-03-26 | Inst Francais Du Petrole | Werkwijze voor hydrokraken met een katalysator, die een zeoliet IM-5 bevat en katalysator, die een zeoliet IM-5 en een promotor-element bevat. |
| FR2794116B1 (fr) * | 1999-05-11 | 2001-07-20 | Inst Francais Du Petrole | Zeolithe im-5 au phosphore, composition catalytique, sa preparation et son utilisation en craquage catalytique |
| ES2160497B1 (es) * | 1999-06-17 | 2002-07-01 | Univ Valencia Politecnica | Catalizador para la eliminacion de oxidos de nitrogeno en presencia de oxigeno. |
| EP1958924B1 (en) * | 2000-12-08 | 2010-11-24 | ExxonMobil Chemical Patents Inc. | crystalline molecular sieves COK-5 |
| US6544495B1 (en) * | 2001-07-13 | 2003-04-08 | Chevron U.S.A. Inc. | Zeolite SSZ-57 composition of matter and synthesis thereof |
| FR2837489B1 (fr) * | 2002-03-20 | 2004-06-18 | Inst Francais Du Petrole | Solide cristallise im-6 de type metallophosphate et son procede de preparation |
| RU2328445C2 (ru) * | 2002-05-23 | 2008-07-10 | Консехо Супериор Де Инвестигасьонес Сьентификас | Микропористый кристаллический цеолитный материал (цеолит itq-22), способ его получения и применение в качестве катализатора |
| ES2208084B1 (es) * | 2002-05-23 | 2005-10-01 | Universidad Politecnica De Valencia | Material cristalino microporoso de naturaleza zeolitica (zeolita itq-22), su metodo de sintesis y su uso como catalizador. |
| ES2214141B1 (es) * | 2003-02-14 | 2005-12-01 | Universidad Politecnica De Valencia | Uso de zeolita itq-22 en procesos de craqueo catalitico de compuestos organicos. |
| ES2346521T3 (es) * | 2002-05-23 | 2010-10-18 | Consejo Superior De Investigaciones Cientificas | Material cristalino microporoso de naturaleza zeolitica (zeolita itq-22) su metodo de sintesis y su uso como catalizador. |
| ES2217980B1 (es) * | 2003-04-30 | 2005-12-16 | Universidad Politecnica De Valencia | Procedimiento para la alquilacion de compuestos aromaticos. |
| FR2852024B1 (fr) * | 2003-03-05 | 2005-04-15 | Inst Francais Du Petrole | Solide cristallise im-10 et son procede de preparation |
| FR2858334B1 (fr) * | 2003-07-30 | 2005-09-02 | Inst Francais Du Petrole | Solide cristallise im-11 de type structural lta et son procede de preparation |
| US7125821B2 (en) * | 2003-09-05 | 2006-10-24 | Exxonmobil Chemical Patents Inc. | Low metal content catalyst compositions and processes for making and using same |
| FR2860224B1 (fr) * | 2003-09-26 | 2006-06-02 | Inst Francais Du Petrole | Solide cristallise im-12 et son procede de preparation |
| US7615143B2 (en) * | 2004-07-30 | 2009-11-10 | Exxonmobil Chemical Patents Inc. | Hydrothermally stable catalyst and its use in catalytic cracking |
| 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 |
| EP1843975B1 (en) * | 2004-12-23 | 2014-06-11 | Chevron U.S.A. Inc. | Molecular sieve ssz-70 composition of matter and synthesis thereof |
| US7108843B2 (en) * | 2004-12-23 | 2006-09-19 | Chevron U.S.A. Inc. | Molecular sieve SSZ-70 composition of matter and synthesis thereof |
| US7083767B2 (en) * | 2004-12-23 | 2006-08-01 | Chevron U.S. A. Inc. | Reduction of oxides of nitrogen in a gas stream using molecular sieve SSZ-70 |
| US7084304B2 (en) * | 2004-12-23 | 2006-08-01 | Chevron U.S.A. Inc. | Acylation using molecular sieve SSZ-70 |
| US7084305B2 (en) * | 2004-12-23 | 2006-08-01 | Chevron U.S.A. Inc. | Partial oxidation using molecular sieve SSZ-70 |
| JP5475289B2 (ja) * | 2005-12-28 | 2014-04-16 | シェブロン ユー．エス．エー． インコーポレイテッド | 分子ふるいｓｓｚ−７４組成物及びその合成 |
| FR2908127B1 (fr) * | 2006-11-07 | 2009-02-06 | Inst Francais Du Petrole | Solide cristallise im-15 et son procede de preparation |
| FR2922546B1 (fr) | 2007-10-22 | 2010-02-12 | Inst Francais Du Petrole | Utilisation d'un catalyseur a base d'im-5 pour la transformation d'alcools ayant au moins deux atomes de carbone en base carburants diesel |
| US7651677B1 (en) * | 2008-09-12 | 2010-01-26 | Exxonmobil Research And Engineering Co. | Method of preparing SSZ-74 |
| FR2940266B1 (fr) * | 2008-12-18 | 2010-12-31 | Inst Francais Du Petrole | Solide cristallise im-20 et son procede de preparation |
| CA2693582A1 (en) * | 2009-02-27 | 2010-08-27 | Chevron U.S.A. Inc. | Synthesis of molecular sieve ssz-74 using a hydroxide-mediated gel |
| CN102040460B (zh) * | 2009-10-22 | 2014-08-20 | 中国石油化工股份有限公司 | 一种甲苯甲醇甲基化反应的方法 |
| CN102205251B (zh) * | 2010-03-31 | 2014-01-15 | 中国石油化工股份有限公司 | 一种p-im-5分子筛及其在甲苯烷基化反应中的应用 |
| FR2959749B1 (fr) | 2010-05-06 | 2012-06-01 | Inst Francais Du Petrole | Procede flexible de transformation de l'ethanol en distillats moyens. |
| CN102452666B (zh) * | 2010-10-21 | 2013-06-26 | 中国石油化工股份有限公司 | 一种合成im-5分子筛的方法 |
| CN102452667B (zh) * | 2010-10-21 | 2014-12-03 | 中国石油化工股份有限公司 | 一种复合模板剂合成im-5分子筛的方法 |
| KR101923248B1 (ko) | 2011-08-04 | 2018-11-28 | 엑손모빌 케미칼 패턴츠 인코포레이티드 | Emm-23 분자체 물질, 그의 합성 및 용도 |
| JP6065293B2 (ja) * | 2011-08-19 | 2017-01-25 | エクソンモービル ケミカル パテンツ インコーポレイテッド | Ｅｍｍ−２２分子篩材料、その合成および使用 |
| CN103101927B (zh) | 2011-11-10 | 2014-12-31 | 中国石油化工股份有限公司 | 一种im-5分子筛纤维及其合成方法 |
| CN103101928B (zh) * | 2011-11-10 | 2015-04-01 | 中国石油化工股份有限公司 | 一种超细纳米im-5分子筛及其合成方法 |
| JP5852749B2 (ja) | 2011-12-22 | 2016-02-03 | ユーオーピー エルエルシー | Ｕｚｍ−３９アルミノシリケートゼオライトを用いた芳香族化合物の転化反応 |
| CN104379507A (zh) | 2011-12-22 | 2015-02-25 | 环球油品公司 | 沸石的分层转化合成 |
| BR112014015231A8 (pt) * | 2011-12-22 | 2017-07-04 | Uop Llc | compósito, e, processos para preparar um compósito e para contactar pelo menos um primeiro componente com um compósito |
| CN103693654B (zh) * | 2012-09-28 | 2018-07-31 | 中国石油化工股份有限公司 | 一种合成im-5分子筛的方法 |
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| US8609921B1 (en) | 2012-12-12 | 2013-12-17 | Uop Llc | Aromatic transalkylation using UZM-44 aluminosilicate zeolite |
| US8609919B1 (en) | 2012-12-12 | 2013-12-17 | Uop Llc | Aromatic transformation using UZM-44 aluminosilicate zeolite |
| US8609910B1 (en) | 2012-12-12 | 2013-12-17 | Uop Llc | Catalytic pyrolysis using UZM-39 aluminosilicate zeolite |
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| US8618343B1 (en) | 2012-12-12 | 2013-12-31 | Uop Llc | Aromatic transalkylation using UZM-39 aluminosilicate zeolite |
| US8907151B2 (en) | 2012-12-12 | 2014-12-09 | Uop Llc | Conversion of methane to aromatic compounds using UZM-39 aluminosilicate zeolite |
| US8609911B1 (en) | 2012-12-12 | 2013-12-17 | Uop Llc | Catalytic pyrolysis using UZM-44 aluminosilicate zeolite |
| US8623321B1 (en) | 2012-12-12 | 2014-01-07 | Uop Llc | UZM-44 aluminosilicate zeolite |
| US8889939B2 (en) | 2012-12-12 | 2014-11-18 | Uop Llc | Dehydrocyclodimerization using UZM-44 aluminosilicate zeolite |
| US8912378B2 (en) | 2012-12-12 | 2014-12-16 | Uop Llc | Dehydrocyclodimerization using UZM-39 aluminosilicate zeolite |
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| JP6661615B2 (ja) * | 2014-09-03 | 2020-03-11 | エクソンモービル リサーチ アンド エンジニアリング カンパニーＥｘｘｏｎ Ｒｅｓｅａｒｃｈ Ａｎｄ Ｅｎｇｉｎｅｅｒｉｎｇ Ｃｏｍｐａｎｙ | 新規合成結晶材料のｅｍｍ−２６、その調製、およびその使用 |
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| CN107020145B (zh) * | 2016-01-29 | 2020-11-13 | 中国石油化工股份有限公司 | 一种介孔im-5分子筛及制备方法 |
| CN107311190B (zh) * | 2016-04-27 | 2020-06-16 | 中国石油化工股份有限公司 | 一种分子筛、其制造方法及其应用 |
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| CN109592697B (zh) * | 2017-09-30 | 2022-07-12 | 中国石油化工股份有限公司 | Im-5分子筛及其合成方法 |
| CN112090443B (zh) * | 2019-06-17 | 2023-03-10 | 中国石油化工股份有限公司 | 加氢脱氧催化剂及其应用和环己烷的制备方法 |
| FR3097856B1 (fr) * | 2019-06-28 | 2022-01-07 | Ifp Energies Now | Solide cristallise izm-5 et son procede de preparation |
| WO2021019314A1 (en) * | 2019-07-29 | 2021-02-04 | Chevron Usa Inc. | Molecular sieve ssz-118, its synthesis and use |
| KR102691228B1 (ko) * | 2019-08-27 | 2024-08-07 | 엑손모빌 테크놀로지 앤드 엔지니어링 컴퍼니 | 디쿼터너리 구조 지시제를 사용한 제올라이트 합성 |
| CN112679298B (zh) * | 2019-10-18 | 2022-12-13 | 中国石油化工股份有限公司 | 含乙烯的反应气气相法制乙苯的方法 |
| US11084766B1 (en) | 2020-02-18 | 2021-08-10 | Uop Llc | Toluene disproportionation using an enhanced UZM-39 aluminosilicate zeolite |
| CN111795985A (zh) * | 2020-07-03 | 2020-10-20 | 青海西钢特殊钢科技开发有限公司 | 一种炼钢用铝线中钛元素含量测定方法 |
| FR3135264A1 (fr) | 2022-05-06 | 2023-11-10 | Totalenergies Onetech | Procédé de fabrication d’un carburéacteur, carburéacteur et installation associés |
| FR3135263A1 (fr) | 2022-05-06 | 2023-11-10 | Totalenergies Onetech | Procédé de fabrication d’un carburéacteur comprenant une étape de conversion d’un flux d’alcool dans un lit fluidisé, carburéacteur et installation associés |
| FR3135265A1 (fr) | 2022-05-06 | 2023-11-10 | Totalenergies Onetech | Procédé d’obtention d’hydrocarbures, et installation associée |
| CN115364890B (zh) * | 2022-08-29 | 2024-03-19 | 中国石油大学(北京) | 一种负载型甲烷热催化裂解催化剂及其制备方法与应用 |
| CN117800357B (zh) * | 2024-01-05 | 2024-08-23 | 陕西探微日新化工有限公司 | 一种im-5分子筛合成方法及改性方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4557919A (en) * | 1983-04-12 | 1985-12-10 | Teijin Petrochemical Industries Ltd. | Production of crystalline zeolites |
| US4941963A (en) * | 1989-08-30 | 1990-07-17 | Mobil Oil Corp. | Synthesis of crystalline ZSM-11 structure |
| US5068096A (en) * | 1991-04-08 | 1991-11-26 | Mobil Oil Corporation | Synthesis of crystalline silicate MCM-47 |
-
1996
- 1996-10-21 FR FR9612873A patent/FR2754809B1/fr not_active Expired - Fee Related
-
1997
- 1997-10-17 KR KR1019990703399A patent/KR20000052636A/ko not_active Withdrawn
- 1997-10-17 DE DE69710612T patent/DE69710612T2/de not_active Expired - Lifetime
- 1997-10-17 BR BR9712417-6A patent/BR9712417A/pt not_active Application Discontinuation
- 1997-10-17 JP JP51903598A patent/JP4348651B2/ja not_active Expired - Fee Related
- 1997-10-17 AU AU48722/97A patent/AU4872297A/en not_active Abandoned
- 1997-10-17 CA CA002268803A patent/CA2268803A1/fr not_active Abandoned
- 1997-10-17 WO PCT/FR1997/001868 patent/WO1998017581A1/fr not_active Ceased
- 1997-10-17 CN CN97199011A patent/CN1234012A/zh active Pending
- 1997-10-17 EP EP97911293A patent/EP0946416B1/fr not_active Expired - Lifetime
- 1997-10-21 US US08/955,117 patent/US6136290A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20140118994A (ko) * | 2011-11-10 | 2014-10-08 | 차이나 페트로리움 앤드 케미컬 코포레이션 | 중공 im-5 분자체 구 및 그 제조 방법 |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2268803A1 (fr) | 1998-04-30 |
| WO1998017581A1 (fr) | 1998-04-30 |
| JP2001502652A (ja) | 2001-02-27 |
| US6136290A (en) | 2000-10-24 |
| CN1234012A (zh) | 1999-11-03 |
| DE69710612T2 (de) | 2002-11-28 |
| AU4872297A (en) | 1998-05-15 |
| EP0946416B1 (fr) | 2002-02-20 |
| DE69710612D1 (de) | 2002-03-28 |
| FR2754809B1 (fr) | 2003-04-04 |
| FR2754809A1 (fr) | 1998-04-24 |
| BR9712417A (pt) | 1999-10-26 |
| JP4348651B2 (ja) | 2009-10-21 |
| EP0946416A1 (fr) | 1999-10-06 |
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