CN111517337A - 一种ecnu-24分子筛及其制备方法和应用 - Google Patents
一种ecnu-24分子筛及其制备方法和应用 Download PDFInfo
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- CN111517337A CN111517337A CN202010294995.2A CN202010294995A CN111517337A CN 111517337 A CN111517337 A CN 111517337A CN 202010294995 A CN202010294995 A CN 202010294995A CN 111517337 A CN111517337 A CN 111517337A
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- Prior art keywords
- oxide
- molecular sieve
- ecnu
- acid
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- 239000002808 molecular sieve Substances 0.000 title claims abstract description 73
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 title claims abstract description 73
- 238000002360 preparation method Methods 0.000 title claims abstract description 18
- 239000002243 precursor Substances 0.000 claims abstract description 19
- 239000003054 catalyst Substances 0.000 claims abstract description 15
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims abstract description 12
- 150000001336 alkenes Chemical class 0.000 claims abstract description 11
- 230000003197 catalytic effect Effects 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims abstract description 10
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 8
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 8
- 238000005804 alkylation reaction Methods 0.000 claims abstract description 6
- 238000006735 epoxidation reaction Methods 0.000 claims abstract description 6
- 125000003118 aryl group Chemical group 0.000 claims abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 15
- 238000006243 chemical reaction Methods 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 11
- 238000002441 X-ray diffraction Methods 0.000 claims description 11
- 239000000243 solution Substances 0.000 claims description 11
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 8
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 7
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 6
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 claims description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 6
- 239000003513 alkali Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000010936 titanium Substances 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 5
- FYGHSUNMUKGBRK-UHFFFAOYSA-N 1,2,3-trimethylbenzene Chemical compound CC1=CC=CC(C)=C1C FYGHSUNMUKGBRK-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
- 239000003929 acidic solution Substances 0.000 claims description 4
- 150000001450 anions Chemical class 0.000 claims description 4
- 239000002585 base Substances 0.000 claims description 4
- -1 halogen ion Chemical class 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 4
- 150000003242 quaternary ammonium salts Chemical group 0.000 claims description 4
- 238000003756 stirring Methods 0.000 claims description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052796 boron Inorganic materials 0.000 claims description 3
- 229910052810 boron oxide Inorganic materials 0.000 claims description 3
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims description 3
- AJNVQOSZGJRYEI-UHFFFAOYSA-N digallium;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Ga+3].[Ga+3] AJNVQOSZGJRYEI-UHFFFAOYSA-N 0.000 claims description 3
- 238000001035 drying Methods 0.000 claims description 3
- 229910001195 gallium oxide Inorganic materials 0.000 claims description 3
- 229910003437 indium oxide Inorganic materials 0.000 claims description 3
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 claims description 3
- 239000012528 membrane Substances 0.000 claims description 3
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 3
- 229910001404 rare earth metal oxide Inorganic materials 0.000 claims description 3
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 3
- 229910052718 tin Inorganic materials 0.000 claims description 3
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims description 3
- 229910001887 tin oxide Inorganic materials 0.000 claims description 3
- 229910001935 vanadium oxide Inorganic materials 0.000 claims description 3
- 238000005406 washing Methods 0.000 claims description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 2
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 2
- 230000032683 aging Effects 0.000 claims description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 2
- 239000004327 boric acid Substances 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- XTEGARKTQYYJKE-UHFFFAOYSA-N chloric acid Chemical compound OCl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-N 0.000 claims description 2
- 229940005991 chloric acid Drugs 0.000 claims description 2
- 239000010408 film Substances 0.000 claims description 2
- 229910052733 gallium Inorganic materials 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 2
- 229940071870 hydroiodic acid Drugs 0.000 claims description 2
- 229910052738 indium Inorganic materials 0.000 claims description 2
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 229910017604 nitric acid Inorganic materials 0.000 claims description 2
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 238000000967 suction filtration Methods 0.000 claims description 2
- 229910052720 vanadium Inorganic materials 0.000 claims description 2
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 238000001914 filtration Methods 0.000 claims 1
- 150000007529 inorganic bases Chemical class 0.000 claims 1
- 239000002245 particle Substances 0.000 claims 1
- 239000008188 pellet Substances 0.000 claims 1
- 239000011148 porous material Substances 0.000 abstract description 11
- 239000000126 substance Substances 0.000 abstract description 7
- 230000002378 acidificating effect Effects 0.000 abstract description 2
- 125000004122 cyclic group Chemical group 0.000 abstract description 2
- 239000011973 solid acid Substances 0.000 abstract description 2
- 230000029936 alkylation Effects 0.000 abstract 1
- 229910001220 stainless steel Inorganic materials 0.000 description 6
- 239000010935 stainless steel Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000002425 crystallisation Methods 0.000 description 4
- 230000008025 crystallization Effects 0.000 description 4
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 239000004809 Teflon Substances 0.000 description 3
- 229920006362 Teflon® Polymers 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000018109 developmental process Effects 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- ZXIJMRYMVAMXQP-UHFFFAOYSA-N cycloheptene Chemical compound C1CCC=CCC1 ZXIJMRYMVAMXQP-UHFFFAOYSA-N 0.000 description 2
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 238000000547 structure data Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
- PCMIWASLPQNSCD-UHFFFAOYSA-N 1-cyclohexyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C1CCCCC1 PCMIWASLPQNSCD-UHFFFAOYSA-N 0.000 description 1
- ULBWADKCMNAMFJ-UHFFFAOYSA-N 1-cyclohexyl-3-methylbenzene Chemical compound CC1=CC=CC(C2CCCCC2)=C1 ULBWADKCMNAMFJ-UHFFFAOYSA-N 0.000 description 1
- GDFJTZFSMFVMKX-UHFFFAOYSA-N 1-cyclohexyl-4-methylbenzene Chemical compound C1=CC(C)=CC=C1C1CCCCC1 GDFJTZFSMFVMKX-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
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- 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
-
- 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
-
- 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
- B01J29/70—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65
- B01J29/7049—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of types characterised by their specific structure not provided for in groups B01J29/08 - B01J29/65 containing rare earth elements, titanium, zirconium, hafnium, zinc, cadmium, mercury, gallium, indium, thallium, tin or lead
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- 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
- C01B39/04—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 using at least one organic template directing agent, e.g. an ionic quaternary ammonium compound or an aminated compound
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- 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
- C01B39/06—Preparation of isomorphous zeolites characterised by measures to replace the aluminium or silicon atoms in the lattice framework by atoms of other elements, i.e. by direct or secondary synthesis
- C01B39/08—Preparation of isomorphous zeolites characterised by measures to replace the aluminium or silicon atoms in the lattice framework by atoms of other elements, i.e. by direct or secondary synthesis the aluminium atoms being wholly replaced
- C01B39/085—Group IVB- metallosilicates
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- 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
- C07C2/64—Addition to a carbon atom of a six-membered aromatic ring
- C07C2/66—Catalytic processes
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
- C07D301/02—Synthesis of the oxirane ring
- C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
- C07D301/19—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with organic hydroperoxides
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/04—Compounds containing oxirane rings containing only hydrogen and carbon atoms in addition to the ring oxygen atoms
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2002/00—Crystal-structural characteristics
- C01P2002/70—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data
- C01P2002/72—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data by d-values or two theta-values, e.g. as X-ray diagram
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- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
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Abstract
本发明公开了一种ECNU‑24分子筛及其制备方法和应用,其特点是该分子筛为“第一氧化物”或“第一氧化物·第二氧化物”所示式的化学组成,且骨架中含有Ti和Al等催化中心的ECNU‑24分子筛,其制备采用大尺寸环状有机模板剂获得前驱体后在酸性条件下进行化学处理的方法得到ECNU‑24新结构分子筛,含Ti和Al的ECNU‑24分子筛作为催化剂用于烯烃环氧化反应以及芳烃烷基化反应。本发明与现有技术相比具有原创性结构且为首次发现,能够丰富分子筛种类。基于该分子筛新颖的孔道结构,向其骨架中引入Al和Ti等催化中心构筑固体酸催化剂或氧化还原催化剂为开发新型环境友好催化体系提供了可能性。
Description
技术领域
本发明涉及分子筛技术领域,具体地说是一种新发现的具有优异催化性能且结构新型的ECNU-24分子筛及其制备方法和应用。
背景技术
微孔分子筛是以TO4(T=Si,Al,Ge,Ti,Sn,B等)四面体构建的具有独特的晶体结构、均匀的孔道结构、适宜的酸性以及良好的水热稳定性的无机多孔材料,被广泛应用于吸附分离、离子交换和催化等领域。分子筛广泛的应用得益于其独特的晶体结构和化学组成,随着化学化工发展的日新月异,对于催化剂的需求迅猛发展,因此合成新型孔道结构以及新化学组成的分子筛材料是一个重要的研究方向。
微孔分子筛按照孔道的开口是8元环、10元环、12元环和>12元环而分为小孔、中孔、大孔和超大孔分子筛。其中,大孔或超大孔的分子筛可以通过减小底物分子的扩散限制来有效催化一些大分子的反应。因此,合成大孔或超大孔分子筛材料已成为分子筛领域研究的热点之一。采用较大尺寸的有机碱、有机胺模板剂或添加具有结构导向能力的金属原子等是目前合成大孔径、新结构分子筛的重要方法。然而大孔径分子筛常常伴随着结构稳定性差的缺点,因此需在合成过程中对结构进行必要的化学修饰以改善其结构。
发明内容
本发明的目的是针对现有技术的不足而设计的一种ECNU-24分子筛及其制备方法和应用,采用大尺寸环状有机模板剂获得前驱体后在酸性条件下进行化学处理的方法,制得的新型分子筛经X-射线衍射谱图确认具有原创性结构以及新颖的孔道,骨架中含有Al、Ti等催化中心的ECNU-24分子筛材料,为首次发现且能够丰富分子筛种类,尤其提供了一种新结构分子筛的合成新思路,并为开发新型环境友好催化体系提供了可能性。
实现本发明目的的具体技术方案是:一种ECNU-24分子筛,其特点是该分子筛为“第一氧化物”或“第一氧化物·第二氧化物”所示式的化学组成,且具有下述表1所示的X射线(Cu-Kα,)表征的衍射谱线:表1:ECNU-24分子筛的X-射线衍射的结构数据表
其中:(a)为±0.30°;衍射峰相对强度w为小于20(弱),m为20~40(中等),s为40~70(强),vs为大于70(非常强)。
所述“第一氧化物·第二氧化物”组成的化合物,其骨架中含有铝、钛、硼、铁、镓、锡、稀土元素、铟、钒中一种或两种以上催化中心的ECNU-24分子筛材料;所述第一氧化物为氧化硅;所述第二氧化物为氧化铝、氧化钛、氧化硼、氧化铁、氧化镓、氧化锡、稀土氧化物、氧化铟和氧化钒中的一种或两种以上的混合;所述第一氧化物和第二氧化物的摩尔比为1:0~0.2。
一种ECNU-24分子筛的制备方法,其特点是所述ECNU-24分子筛按下述步骤制备:
(一)前驱体的制备
将第一氧化物源(以第一氧化物计)与第二氧化物源(以第二氧化物计)、有机模板剂、无机碱源和水按1:0~0.2:0.05~1.0:0~0.5:5~30摩尔比混合,在35~80℃温度下老化0.5~5小时,然后在120~180℃温度下晶化4~20天,晶化后的产物经过滤、洗涤、干燥,制得具有粉末、颗粒状或膜制品的分子筛母体;所述无机碱源为氢氧化钠、氢氧化钾、氢氧化锂一种或两种以上的混合;所述有机物模板剂为下述A结构式的化合物,其季铵盐或其季铵碱形式:
其中:R1和R2各自独立地为不同碳链个数的C1-6烷基,R1和R2优选C1-3烷基;n=4~8,优选6;作为所述A结构式化合物的季铵盐形式,该季氮(N+)结构的平衡阴离子为卤素离子(Br-)或氢氧根离子(OH-)等,但并不限于此;作为所述A结构式化合物的季铵碱形式,该季氮(N+)结构的平衡阴离子为氢氧根离子(OH-)。
(二)ECNU-24分子筛的制备
将上述前驱体置于pH值小于7的酸性溶液中,室温下磁力搅拌5~30分钟,然后在120~210℃温度下反应4~72小时,反应液经抽滤、洗涤、干燥后高温焙烧,得产物为ECNU-24分子筛,所述焙烧温度为500~650℃,焙烧时间为4~10小时;所述酸性溶液的溶质采用盐酸、磷酸、硝酸、硫酸、硼酸、氢碘酸、氢溴酸和氯酸中的一种或两种以上的混合,溶剂采用水、甲醇和乙醇的一种或两种以上的混合;所述酸性溶液的摩尔浓度为0.1~5M;所述前驱体和酸性溶液的固液质量比为1:10~100;所述ECNU-24分子筛的焙烧态为粉末状、颗粒状或膜制品状。
一种ECNU-24分子筛的应用,其特点是所述ECNU-24分子筛作为催化剂用于芳烃烷基化反应和烯烃环氧化反应。所述芳烃烷基化反应的催化剂为分子筛中第二氧化物是氧化铝的Al-ECNU-24,其中Al-ECNU-24分子筛与芳烃的用量比为1克(Al-ECNU-24):0.01~0.2摩尔(芳烃),所述芳烃为苯、甲苯、二甲苯、三甲苯、苯酚或萘;所述烯烃环氧化反应的催化剂为分子筛中第二氧化物是氧化钛的Ti-ECNU-24,其中Ti-ECNU-24分子筛与烯烃的用量比为1克(Ti-ECNU-24):0.02~0.5摩尔(烯烃),所述烯烃为碳数目不大于12的含C=C不饱和双键的直链或环状烯烃。
本发明与现有技术相比具有原创性结构且为首次发现,能够丰富分子筛种类,基于该分子筛新颖的孔道结构,向其骨架中引入Al,Ti等催化中心构筑固体酸催化剂或氧化还原催化剂,为开发新型环境友好催化体系提供了可能性。
附图说明
图1为实施例1制备的ECNU-24的X射线衍射谱图;
图2为实施例2制备的Ti-ECNU-24的X射线衍射谱图;
图3为实施例3制备的Al-ECNU-24的X射线衍射谱图。
具体实施方式
以下通过具体实施例对本发明的制备作进一步的详细说明。
实施例1
(一)前驱体的制备
将0.3克氢氧化钠溶于15克A结构式有机模板剂的季铵碱水溶液(R1,R2选取甲基,n=6,质量分数为25%)中搅拌至澄清,再将20克氧化硅(质量分数为30%的硅溶胶)加入到上述溶液中,在80℃温度下水浴除去多余的水,使得合成凝胶最终水和氧化硅的摩尔比为5。将该凝胶产物转移到带有聚四氟乙烯内衬的不锈钢高压反应釜中于150℃温度下晶化5天。晶化产物经过滤、洗涤、干燥后制得前驱体。
(二)ECNU-24分子筛的制备
将1克前驱体置于30克摩尔浓度为1M盐酸的乙醇溶液中并于室温下搅拌5分钟,将其转移到带有聚四氟乙烯内衬的不锈钢高压反应釜中于190℃温度下反应24小时,反应液经过滤、洗涤、干燥,在550温度下焙烧6小时,得粉末状焙烧态的产物为ECNU-24分子筛。
表1:ECNU-24分子筛的X-射线衍射的结构数据表
(a):±0.30°。衍射峰相对强度w为小于20(弱),m为20~40(中等),s为40~70(强),vs为大于70(非常强)。
实施例2
(一)前驱体的制备
将0.12克氢氧化钠和0.9克钛酸四丁酯依次溶于15克A结构式有机模板剂的季铵碱水溶液(R1选取甲基,R2选取乙基,n=6,质量分数为25%)中搅拌至澄清,再将16克氧化硅(质量分数为30%的硅溶胶)加入到上述溶液中,在70℃温度下水浴除去多余的水和醇,使得合成凝胶最终水和氧化硅的摩尔比值为7。将该凝胶产物转移到带有聚四氟乙烯内衬的不锈钢高压反应釜中于160℃温度下晶化7天。晶化产物经过滤、洗涤、干燥后制得含钛的前驱体。
(二)ECNU-24分子筛的制备
将1克前驱体分子筛置于30克摩尔浓度为2M盐酸的甲醇溶液中并于室温搅拌10分钟,再将其转移到带有聚四氟乙烯内衬的不锈钢高压反应釜中于200℃温度下反应30小时,经过滤、洗涤、干燥,在500温度下焙烧8小时,得颗粒状焙烧态的产物Ti-ECNU-24分子筛。
实施例3
(一)前驱体的制备
将0.6克氢氧化钠和0.16克偏铝酸钠依次溶于15克A结构式有机模板剂的季铵碱水溶液(R1,R2选取甲基,n=6,质量分数为25%)中搅拌至澄清,再将15克氧化硅(质量分数为30%的硅溶胶)加入到上述溶液中,在80℃温度下水浴除去多余的水,使得合成凝胶最终水和氧化硅的摩尔比值为7。将该凝胶产物转移到带有聚四氟乙烯内衬的不锈钢高压反应釜中于150℃温度下晶化5天。晶化产物经过滤、洗涤、干燥后制得含铝的前驱体。
(二)ECNU-24分子筛的制备
将1克前驱体分子筛置于50克摩尔浓度为3M盐酸的乙醇溶液中并于室温搅拌15分钟,再将其转移到带有聚四氟乙烯内衬的不锈钢高压反应釜中于210℃温度下反应24小时,经过滤、洗涤、干燥,在540温度下焙烧6小时,得膜制品状焙烧态的产物为Al-ECNU-24分子筛。
实施例5
将上述实施例2制备的Ti-ECNU-24分子筛应用于烯烃环氧化反应,其具体反应条件如下:
在圆底烧瓶中依次加入Ti-ECNU-24催化剂0.1克、乙腈10毫升、环庚烯10毫摩尔和过氧化氢叔丁醇(溶解在癸烷中,浓度5.5M)10毫摩尔,剧烈搅拌并于60℃的水浴中回流2小时。反应体系经充分冷却后加入0.1克内标环戊酮,使用气相色谱测定底物的转化率和产物的选择性,其环庚烯的转化率为16%。
实施例6
将上述实施例3制备的Al-ECNU-24催化剂应用于芳烃烷基化反应,其具体反应条件如下:
将11.27克甲苯、1克环己烯和0.1克Al-ECNU-24催化剂依次加入50毫升三颈烧瓶中,在机械搅拌、氮气气氛和110℃油浴下回流5小时。反应体系经充分冷却后进行取样分析,产物的定量分析通过高效液相色谱来完成。反应5小时后,得产物为邻环己基甲苯、间环己基甲苯和对环己基甲苯,环己烯的转化率为30%。
以上各实施例只是对本发明做进一步说明,并非用以限制本发明专利,凡为本发明等效实施,均应包含于本发明专利的权利要求范围之内。
Claims (6)
1.一种ECNU-24分子筛,其特征在于该分子筛的组成为“第一氧化物”或“第一氧化物·第二氧化物”,且具有下述表1所示的X射线表征的衍射谱线:
表1:ECNU-24分子筛的X-射线衍射的结构数据表
其中:(a)为±0.30°;衍射峰相对强度w为小于20(弱),m为20~40(中等),s为40~70(强),vs为大于70(非常强);
所述“第一氧化物·第二氧化物”组成的化合物,其骨架中含有铝、钛、硼、铁、镓、锡、稀土元素、铟、钒中一种或两种以上催化中心的ECNU-24分子筛材料;所述第一氧化物为氧化硅;所述第二氧化物为氧化铝、氧化钛、氧化硼、氧化铁、氧化镓、氧化锡、稀土氧化物、氧化铟和氧化钒中的一种或两种以上的混合;所述第一氧化物与第二氧化物的摩尔比为1:0~0.2。
2.一种权利要求1所述ECNU-24分子筛的制备方法,其特征在于所述ECNU-24分子筛按下述步骤制备:
(一)前驱体的制备
将第一氧化物与第二氧化物、有机模板剂、无机碱和水按1:0~0.2:0.05~1.0:0~0.5:5~30摩尔比混合,在35~80℃温度下老化0.5~5小时,然后在120~180℃温度下晶化4~20天,晶化后的产物经过滤、洗涤、干燥,制得具有粉末、颗粒状或膜制品的前驱体;所述第一类氧化物为氧化硅;所述第二类氧化物为氧化铝、氧化钛、氧化硼、氧化铁、氧化镓、氧化锡、稀土氧化物、氧化铟和氧化钒中的一种或两种以上的混合;所述无机碱为氢氧化钠、氢氧化钾和氢氧化锂一种或两种以上的混合;所述有机物模板剂为下述A结构式化合物的季铵盐或季铵碱形式:
其中:R1和R2各自独立地为不同碳链个数的C1-6烷基;n=4~8;
所述A结构式化合物的季铵盐形式,其季氮(N+)结构的平衡阴离子为卤素离子或氢氧根离子(OH-);所述A结构式化合物的季铵碱形式,其季氮(N+)结构的抗衡阴离子为氢氧根离子(OH-);
(二)ECNU-24分子筛的制备
将前驱体置于pH值小于7的酸性溶液中,室温下磁力搅拌5~30分钟,然后在120~210℃温度下反应4~72小时,其反应液经抽滤、洗涤、干燥后焙烧,得产物为焙烧态的ECNU-24分子筛,所述前驱体与酸性溶液的固液质量比为1:10~100;所述酸性溶液的摩尔浓度为0.1~5M;所述焙烧温度为500~650℃,焙烧时间为4~10小时。
3.根据权利要求2所述ECNU-24分子筛的制备方法,其特征在于所述酸性溶液的溶质采用盐酸、磷酸、硝酸、硫酸、硼酸、氢碘酸、氢溴酸和氯酸中的一种或两种以上的混合,溶剂采用水、甲醇和乙醇中的一种或两种以上的混合。
4.根据权利要求2所述ECNU-24分子筛的制备方法,其特征在于所述ECNU-24分子筛的焙烧态为粉末状、颗粒状或膜制品状。
5.一种权利要求1所述ECNU-24分子筛的应用,其特征在于所述ECNU-24分子筛作为催化剂用于芳烃烷基化反应和烯烃环氧化反应,所述芳烃烷基化反应中的催化剂,其第二氧化物为氧化铝的Al-ECNU-24分子筛;所述Al-ECNU-24分子筛与芳烃的重量摩尔比为1g:0.01~0.2摩尔;所述烯烃环氧化反应中的催化剂,其第二氧化物为氧化钛的Ti-ECNU-24分子筛;所述Ti-ECNU-24分子筛与烯烃的的重量摩尔比为1g:0.02~0.5摩尔。
6.根据权利要求5所述ECNU-24分子筛的应用,其特征在于所述芳烃为苯、甲苯、二甲苯、三甲苯、苯酚或萘;所述烯烃为碳数目不大于12的含C=C不饱和双键的直链或环状烯烃。
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