CN102319572B - Hydrotreating catalyst and preparation method thereof - Google Patents
Hydrotreating catalyst and preparation method thereof Download PDFInfo
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- CN102319572B CN102319572B CN 201110191663 CN201110191663A CN102319572B CN 102319572 B CN102319572 B CN 102319572B CN 201110191663 CN201110191663 CN 201110191663 CN 201110191663 A CN201110191663 A CN 201110191663A CN 102319572 B CN102319572 B CN 102319572B
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- Prior art keywords
- catalyst
- boehmite
- slurries
- amorphous aluminum
- aluminum silicide
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- 239000003054 catalyst Substances 0.000 title claims abstract description 107
- 238000002360 preparation method Methods 0.000 title claims abstract description 46
- 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 94
- 239000002002 slurry Substances 0.000 claims abstract description 77
- 229910052796 boron Inorganic materials 0.000 claims abstract description 50
- 230000032683 aging Effects 0.000 claims abstract description 42
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract description 33
- 238000000034 method Methods 0.000 claims abstract description 30
- 238000002156 mixing Methods 0.000 claims abstract description 29
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 27
- 150000001340 alkali metals Chemical class 0.000 claims abstract description 24
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 20
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 20
- 150000001342 alkaline earth metals Chemical class 0.000 claims abstract description 20
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims abstract description 17
- 229910017052 cobalt Inorganic materials 0.000 claims abstract description 17
- 239000010941 cobalt Substances 0.000 claims abstract description 17
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims abstract description 17
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract description 17
- 239000011733 molybdenum Substances 0.000 claims abstract description 17
- 238000001914 filtration Methods 0.000 claims abstract description 15
- 230000008569 process Effects 0.000 claims abstract description 8
- 239000011148 porous material Substances 0.000 claims abstract description 7
- 238000001035 drying Methods 0.000 claims abstract description 5
- 229910000272 alkali metal oxide Inorganic materials 0.000 claims abstract description 4
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 claims abstract description 4
- 229910052810 boron oxide Inorganic materials 0.000 claims abstract description 4
- 229910000428 cobalt oxide Inorganic materials 0.000 claims abstract description 3
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910000476 molybdenum oxide Inorganic materials 0.000 claims abstract description 3
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 claims abstract description 3
- LKTZODAHLMBGLG-UHFFFAOYSA-N alumanylidynesilicon;$l^{2}-alumanylidenesilylidenealuminum Chemical compound [Si]#[Al].[Si]#[Al].[Al]=[Si]=[Al] LKTZODAHLMBGLG-UHFFFAOYSA-N 0.000 claims description 86
- 229910001593 boehmite Inorganic materials 0.000 claims description 82
- FAHBNUUHRFUEAI-UHFFFAOYSA-M hydroxidooxidoaluminium Chemical compound O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 claims description 82
- 239000000243 solution Substances 0.000 claims description 63
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 55
- 229910001868 water Inorganic materials 0.000 claims description 48
- 239000003292 glue Substances 0.000 claims description 44
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 32
- 238000000465 moulding Methods 0.000 claims description 32
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 27
- 229910017604 nitric acid Inorganic materials 0.000 claims description 27
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 claims description 23
- 229910001388 sodium aluminate Inorganic materials 0.000 claims description 23
- 239000011734 sodium Substances 0.000 claims description 20
- 239000001569 carbon dioxide Substances 0.000 claims description 16
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 16
- 238000005406 washing Methods 0.000 claims description 13
- 239000000377 silicon dioxide Substances 0.000 claims description 12
- 229910052708 sodium Inorganic materials 0.000 claims description 11
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 10
- 239000007864 aqueous solution Substances 0.000 claims description 8
- 239000002210 silicon-based material Substances 0.000 claims description 6
- -1 boron oxide compound Chemical class 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 239000012752 auxiliary agent Substances 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 238000007598 dipping method Methods 0.000 claims description 4
- 239000012266 salt solution Substances 0.000 claims description 2
- 238000006386 neutralization reaction Methods 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 10
- 238000005984 hydrogenation reaction Methods 0.000 abstract description 9
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract description 3
- VXAUWWUXCIMFIM-UHFFFAOYSA-M aluminum;oxygen(2-);hydroxide Chemical group [OH-].[O-2].[Al+3] VXAUWWUXCIMFIM-UHFFFAOYSA-M 0.000 abstract description 3
- 239000010703 silicon Substances 0.000 abstract description 3
- 229910052710 silicon Inorganic materials 0.000 abstract description 3
- 239000002243 precursor Substances 0.000 abstract description 2
- 229910052814 silicon oxide Inorganic materials 0.000 abstract description 2
- 239000011959 amorphous silica alumina Substances 0.000 abstract 2
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000002994 raw material Substances 0.000 abstract 1
- 238000002407 reforming Methods 0.000 abstract 1
- APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 description 20
- 239000011609 ammonium molybdate Substances 0.000 description 20
- 235000018660 ammonium molybdate Nutrition 0.000 description 20
- 229940010552 ammonium molybdate Drugs 0.000 description 20
- 238000003756 stirring Methods 0.000 description 20
- 229910004298 SiO 2 Inorganic materials 0.000 description 19
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 18
- 239000004327 boric acid Substances 0.000 description 18
- 239000000284 extract Substances 0.000 description 18
- 238000002803 maceration Methods 0.000 description 18
- 230000000052 comparative effect Effects 0.000 description 17
- 229940011182 cobalt acetate Drugs 0.000 description 15
- QAHREYKOYSIQPH-UHFFFAOYSA-L cobalt(II) acetate Chemical compound [Co+2].CC([O-])=O.CC([O-])=O QAHREYKOYSIQPH-UHFFFAOYSA-L 0.000 description 15
- 239000003921 oil Substances 0.000 description 15
- 239000007789 gas Substances 0.000 description 14
- 229910002091 carbon monoxide Inorganic materials 0.000 description 13
- 239000008246 gaseous mixture Substances 0.000 description 13
- 229910052700 potassium Inorganic materials 0.000 description 13
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 12
- 239000002131 composite material Substances 0.000 description 11
- 229920006395 saturated elastomer Polymers 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 10
- 239000004115 Sodium Silicate Substances 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 229910052911 sodium silicate Inorganic materials 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- UFMZWBIQTDUYBN-UHFFFAOYSA-N cobalt dinitrate Chemical compound [Co+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O UFMZWBIQTDUYBN-UHFFFAOYSA-N 0.000 description 8
- 229910001981 cobalt nitrate Inorganic materials 0.000 description 8
- 239000008187 granular material Substances 0.000 description 8
- 229910052744 lithium Inorganic materials 0.000 description 8
- YIXJRHPUWRPCBB-UHFFFAOYSA-N magnesium nitrate Chemical compound [Mg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O YIXJRHPUWRPCBB-UHFFFAOYSA-N 0.000 description 8
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 8
- DHEQXMRUPNDRPG-UHFFFAOYSA-N strontium nitrate Chemical compound [Sr+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O DHEQXMRUPNDRPG-UHFFFAOYSA-N 0.000 description 8
- 239000008367 deionised water Substances 0.000 description 7
- 239000003595 mist Substances 0.000 description 7
- IATRAKWUXMZMIY-UHFFFAOYSA-N strontium oxide Inorganic materials [O-2].[Sr+2] IATRAKWUXMZMIY-UHFFFAOYSA-N 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 6
- 229910000323 aluminium silicate Inorganic materials 0.000 description 6
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 229910021641 deionized water Inorganic materials 0.000 description 5
- 239000011777 magnesium Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000011591 potassium Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 229910052712 strontium Inorganic materials 0.000 description 5
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 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 4
- 229910052749 magnesium Inorganic materials 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000004323 potassium nitrate Substances 0.000 description 4
- 235000010333 potassium nitrate Nutrition 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- 239000005864 Sulphur Substances 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 239000000084 colloidal system Substances 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000002808 molecular sieve Substances 0.000 description 3
- 239000012452 mother liquor Substances 0.000 description 3
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 239000004411 aluminium Substances 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 239000012065 filter cake Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229940071264 lithium citrate Drugs 0.000 description 2
- WJSIUCDMWSDDCE-UHFFFAOYSA-K lithium citrate (anhydrous) Chemical compound [Li+].[Li+].[Li+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O WJSIUCDMWSDDCE-UHFFFAOYSA-K 0.000 description 2
- IIPYXGDZVMZOAP-UHFFFAOYSA-N lithium nitrate Chemical compound [Li+].[O-][N+]([O-])=O IIPYXGDZVMZOAP-UHFFFAOYSA-N 0.000 description 2
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 description 2
- 229910017464 nitrogen compound Inorganic materials 0.000 description 2
- 150000002830 nitrogen compounds Chemical class 0.000 description 2
- 235000019353 potassium silicate Nutrition 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 229910001415 sodium ion Inorganic materials 0.000 description 2
- 239000004575 stone Substances 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 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
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 244000275012 Sesbania cannabina Species 0.000 description 1
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 238000007171 acid catalysis Methods 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- DCRIQAAPAFMPKP-UHFFFAOYSA-N aluminum oxygen(2-) titanium(4+) Chemical compound [O-2].[O-2].[Al+3].[Ti+4] DCRIQAAPAFMPKP-UHFFFAOYSA-N 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 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
- 230000008901 benefit Effects 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000004523 catalytic cracking Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000000975 co-precipitation Methods 0.000 description 1
- GVPFVAHMJGGAJG-UHFFFAOYSA-L cobalt dichloride Chemical compound [Cl-].[Cl-].[Co+2] GVPFVAHMJGGAJG-UHFFFAOYSA-L 0.000 description 1
- KTVIXTQDYHMGHF-UHFFFAOYSA-L cobalt(2+) sulfate Chemical compound [Co+2].[O-]S([O-])(=O)=O KTVIXTQDYHMGHF-UHFFFAOYSA-L 0.000 description 1
- HIYNGBUQYVBFLA-UHFFFAOYSA-D cobalt(2+);dicarbonate;hexahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Co+2].[Co+2].[Co+2].[Co+2].[Co+2].[O-]C([O-])=O.[O-]C([O-])=O HIYNGBUQYVBFLA-UHFFFAOYSA-D 0.000 description 1
- 229910000001 cobalt(II) carbonate Inorganic materials 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000004939 coking Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000002079 cooperative effect Effects 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000003009 desulfurizing effect Effects 0.000 description 1
- 229910001648 diaspore Inorganic materials 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000010931 ester hydrolysis Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000002779 inactivation Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 230000003606 oligomerizing 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
- 238000006213 oxygenation reaction Methods 0.000 description 1
- 238000001935 peptisation Methods 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229940093928 potassium nitrate Drugs 0.000 description 1
- 238000012797 qualification Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 150000003839 salts 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
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 238000002336 sorption--desorption measurement Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000005987 sulfurization reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 150000005622 tetraalkylammonium hydroxides Chemical class 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Landscapes
- Catalysts (AREA)
Abstract
The invention relates to a hydrotreating catalyst and a preparation method thereof. The catalyst is characterized in that silicon-containing alumina is used as a carrier, molybdenum and cobalt are used as active components, boron and alkali metal and/or alkaline earth metal are used as auxiliaries, and the total weight of the catalyst is 10-20 wt% of molybdenum oxide, 1-8 wt% of cobalt oxide, 0-5 wt% of boron oxide, 0-5 wt% of alkali metal and/or alkaline earth metal oxide and 3.25-35.6 wt% of silicon oxide. The specific surface area of the catalyst is 220-300 m2The pore volume is 0.55-0.75 ml/g. The silicon-containing alumina carrier precursor is pseudo-boehmite containing amorphous silica-alumina, which is obtained by firstly preparing amorphous silica-alumina slurry and pseudo-boehmite slurry, and then mixing, aging, filtering, drying and other post-treatment processes. The catalyst has high hydrodesulfurization and denitrification activity and good stability, and is suitable for the pre-hydrogenation treatment of reforming raw materials.
Description
Technical field
The present invention relates to a kind of hydrotreating catalyst and preparation method thereof, particularly a kind of preparation method of carrier of hydrogenating catalyst presoma.
Background technology
In recent years, along with the increasingly stringent of environmental legislation, more and more harsher to the requirement of sulfur content in the oil product and nitrogen content; Simultaneously since crude quality worse and worse, impurity contents such as sulphur, nitrogen are more and more higher, and are therefore also more and more higher to the requirement of hydrotreating catalyst.For example when coker gas oil is carried out hydrotreatment, the nitrogen compound of high level especially basic nitrogen compound can be adsorbed on the acidic site of catalyst, cause the catalyst desulfurizing denitrification activity to descend, be a kind of novel carriers material of exploitation or improve the catalyst activity constituent content and improve the emphasis that hydrotreating catalyst removes the impurity ability.People are when being optimized alumina support specific area, pore volume and aperture, by introducing modifying elements such as silicon, titanium, phosphorus, come the modulation alumina support surface acidity, improve the strong interaction between active component and alumina support or new cooperative effect occurs.Have the amorphous aluminum silicide specific area height that divergence hole distributes, anti-agglutinatting property can be good, and have certain acid catalysis activity, therefore often be used in the hydrotreating catalyst preparation process, but there is the relatively poor defective of mouldability in amorphous aluminosilicate.At present, the preparation method of siliceous aluminium oxide is a lot, concludes to get up to be mainly two kinds, and a kind of is to add a spot of aluminium oxide in alumino-silicate (2～10wt%) as structural promoter; Another kind is to add a spot of alumino-silicate in aluminium oxide, comes modulation alumina surface acidity, improves its specific area.
US4721696 discloses a kind of employing pH swing method and has prepared siliceous method of alumina, mainly be used as the carrier of sulfur-bearing and metal impurities material hydrotreating catalyst, silicone content generally is no more than 15wt%, and silica mainly is to be purpose as structural stabilizing agent rather than so that more acid centre to be provided.
CN1267187C discloses a kind of silica-alumina that contains structure of similar to thin diaspore, described carrier silica content height, and be with silicon-containing compound solution directly or and stream be incorporated in the boehmite slurries, purpose is that the aluminium content that increases four-coordination improves the amount of aluminium oxide acid strength and acid, the siliceous aluminium oxide of preparation has very high cracking activity, but higher cracking activity has reduced liquid yield as catalyst carrier for hydrgenating.
CN1074303C has proposed the manufacture method of a kind of aluminium oxide and monox composite oxides, it mixes the solution in salic source and the solution in silicon oxide-containing source earlier, in mixed solution, add hydrochloric acid then and obtain colloidal sol, in colloidal sol, add NaOH again and obtain gel, alumina source in the gel and silica source are reacted under high temperature, high pressure obtain the powdery alumino-silicate.But the composite oxides of this method preparation have a large amount of micropores, are unsuitable for the carrier as the medium-low distillate oil hydrotreating catalyst.
CN1048957C discloses and has prepared method amorphous, the catalytic activity silica-alumina, adopt tetraalkylammonium hydroxide, tri-alkoxy aluminium and positive silicic acid tetraalkyl ester hydrolysis and gel to obtain, this gel has the hole dimension that can control, and its specific area is at least 500m
2/ g, the mol ratio of silica and alundum (Al was at least 30: 1.This silica-alumina gel is mainly used in lighter hydrocarbons isomery and oligomerizing.
CN1306977C discloses a kind of silica-alumina and preparation method thereof, concrete steps are to adopt coprecipitation to prepare a kind of salic water mixed liquid earlier, introduce a kind of solution of silicon-containing compound again, be a kind of mother liquor of synthesis of molecular sieve, make silica-alumina through aging, drying.This carrier is mainly used in the preparation of catalytic cracking catalyst.
CN100487085C discloses a kind of method of poor petrol catalytic hydrofinishing, the catalyst that adopts is complex carrier with the aluminium oxide-titanium oxide, cobalt, molybdenum, tungsten are active component, and boron, strontium are auxiliary agent, and this catalyst mainly is applicable to the hydrofinishing of delayed coking gasoline, pressure gasoline.
Summary of the invention
The object of the present invention is to provide the Catalysts and its preparation method of a kind of hydrogenation activity height, good stability, the catalyst carrier presoma is the boehmite that contains amorphous aluminum silicide, the invention solves shortcomings such as poor, difficult moulding of amorphous aluminum silicide peptization and pure alumina support acidity be weak.
Hydrotreating catalyst of the present invention, with siliceous aluminium oxide is carrier, it is characterized in that catalyst is an active component with molybdenum, cobalt, boron and alkali metal and/or alkaline-earth metal in catalyst weight, contain molybdenum oxide 10～20wt% as auxiliary agent, cobalt oxide 1～8wt%, (preferably 0.5～5wt%), (preferably 1～5wt%), silica 3.25～35.6wt% (preferably 6～26wt%) for alkali metal and/or alkaline earth oxide 0～5wt% for boron oxide compound 0～5wt%.Specific surface area of catalyst 220～300m
2/ g, pore volume 0.55～0.75ml/g.The presoma of siliceous alumina support is the boehmite that contains amorphous aluminum silicide, it is by at first preparing amorphous aluminum silicide slurries and boehmite slurries, above-mentioned amorphous aluminum silicide slurries are mixed, wear out according to the ratio of silica content 5～40wt% with the boehmite slurries, ageing time is 10～30min, obtains containing the boehmite of amorphous aluminum silicide through the last handling process that comprises filtration, washing, drying then.
The most outstanding characteristics of hydrotreating catalyst of the present invention are that the presoma of the employed siliceous alumina support of catalytic amount is the boehmite that contains amorphous aluminum silicide, having selected it is to mix, wear out with preparing amorphous aluminum silicide slurries and boehmite slurries earlier, and include filtration, dry last handling process obtains, the mixed process of these amorphous aluminum silicide slurries and boehmite slurries, both being different from simple and mechanical mixing of two kinds of powders of amorphous aluminum silicide and boehmite, is not again the structure of amorphous aluminum silicide coated alumina type.With two bursts of mixing of materials, one side amorphous aluminum silicide and boehmite reciprocation; On the other hand, also be accompanied by reaction between a spot of free aluminum ion and the silicate ion.
The present invention also provides a kind of preparation method who contains the boehmite of amorphous aluminum silicide, it is characterized in that amorphous aluminum silicide slurries and boehmite slurries and stream mix or a kind of material joined in the another kind of material mixing, after mixing finishes, aging 10～30min, filter, wash to sodium ions content less than 0.5wt%, at 80～120 ℃ of down dry 2～20h, obtain containing the boehmite of amorphous aluminum silicide.Its specific area is preferably 250～400m
2/ g, pore volume is preferably 0.7～1.4ml/g, and infrared acidity is preferably 0.28～0.55mmol/g, so that the specific surface area of catalyst that makes at last, pore volume etc. satisfy requirement of the present invention.
The preparation process of pseudoboehmite that contains amorphous aluminum silicide provided by the invention comprises the preparation of amorphous aluminum silicide slurries and the preparation of boehmite slurries, and with these two kinds of slurries mixing, the mixing of two kinds of slurries can be adopted and flow to mix or a kind of slurries are joined in the another kind of slurries and mix, aging then, more after filtration, last handling processes such as washing, drying obtain containing the boehmite of amorphous aluminum silicide.PH value of solution is preferably 9.0～10.5 when aging, and temperature is preferably 20～65 ℃, and the time is preferably 10～25min.Baking temperature is preferably 80～120 ℃.
The present invention is not particularly limited the preparation method of amorphous aluminum silicide slurries and boehmite slurries, adopts current techique to get final product, and can adopt existing nitrate method or carbonizatin method as the preparation of boehmite slurries.
The present invention provides a kind of preparation method of amorphous aluminum silicide slurries simultaneously, comprising:
(a) compound concentration is 10～150gAl
2O
3The sodium metaaluminate of/L or sodium aluminate solution are added in the glue jar, are controlled to 15～50 ℃ of glue jar temperature.
(b) compound concentration is 50～200gSiO
2The silicon-containing compound solution of/L joins silicon-containing compound solution in the solution of (a), control pH value 11.5～13.
(c) under the condition of low whipping speed greater than 250r/min, feed the carbon dioxide of concentration greater than 20v% continuously, the flow of control carbon dioxide is at 1～10Nm
3/ h, with time 20～40min, control endpoint pH 7.5～9.5 neutralizes and finishes in the control.
(d) in pH value 7.5～9.5, the solution 5～20min of aging (c) preparation obtains the amorphous aluminum silicide slurries under the condition that temperature is 25～40 ℃.
Preferably with carbon dioxide process preparation, silicon-containing compound can be waterglass, Ludox to amorphous aluminum silicide slurries of the present invention, waterglass preferably, and concentration of sodium silicate is counted 50～200gSiO with silica
2/ L is preferably 80～120gSiO
2/ L; The concentration of sodium metaaluminate or sodium aluminate solution is counted 10～150gAl with aluminium oxide
2O
3/ L is preferably 35～110gAl
2O
3/ L; Ageing time preferably is controlled at 5～15min; Control silica alumina ratio 40～60wt% in the final amorphous aluminum silicide.
The present invention also provides a kind of preparation method of boehmite slurries.Sodium metaaluminate or sodium aluminate solution are added in the glue jar, feed carbon dioxide through becoming glue, the aging boehmite slurries that obtain with intermittence or continuous mode.The concentration of sodium metaaluminate or sodium aluminate solution is 20～150gAl
2O
3/ L; Concentration of carbon dioxide is preferably between 40～100v% greater than 20v%, and the flow of carbon dioxide is 1～10Nm
3/ h; Become 20～65 ℃ of glue temperature, best 30～45 ℃; Become glue endpoint pH 9.0～10.5; Become glue and ageing time preferably to be no more than 40min altogether, be advisable with 25～35min.
In the preparation process of boehmite slurries of the present invention, become glue terminal point pH preferably to be controlled at 9.0～10.5, the pH value is lower than at 9.0 o'clock, easy and the reaction of sodium bicarbonate generation silk sodium stone structure of the boehmite that forms, the silk sodium stone that generates is a kind of insoluble salt, hindered the washing of sodium ion, might influence the serviceability of aluminium oxide as carrier.
The boehmite best surfaces acidic site that contains amorphous aluminum silicide of the present invention's preparation is based on the weak acid position.
The boehmite that contains amorphous aluminum silicide that the present invention selects for use promptly has the high acidity of amorphous aluminum silicide, the characteristic of high-specific surface area, contains the advantage of boehmite simultaneously, has overcome the problem of amorphous aluminum silicide moulding difference.The aluminium oxide that contains amorphous aluminum silicide of preparation is specially adapted to do the carrier of hydrogenation catalyst.
Can contain alkali metal and/or alkaline-earth metal in the catalyst of the present invention, content is 0～5wt%, is preferably 1～5wt%.Alkali metal and/or alkaline-earth metal are among one among Li, Na, K, Be, Mg, Ca, the Sr or multiple, one or more among preferred Li, K, the Mg.When catalyst is used for the distillate hydrogenation processing, alkene is the one of the main reasons that causes catalysqt deactivation in the polymerisation of catalyst surface, the easy polymerization of alkene in the oil product forms colloid, covers on the hydrogenation sites of catalyst, has reduced the activated centre number of catalyst surface; On the other hand, the duct of the polymer plugging catalyst of generation influences the diffusion of reactant and product molecule.Therefore, hydrogenation activity and stabilized hydrogenation can be improved by adjusting the catalyst surface Acidity of Aikalinity,, the Acidity of Aikalinity on catalyst carrier surface can be changed by adding alkali metal and/or alkaline-earth metal, help reducing the deposition of carbonaceous in the hydrogenation process, colloid, thereby prolong the service life of catalyst.Alkali metal and/or alkaline-earth metal preferably add with the form of solubility nitrate, acetate or citrate among the present invention.
Can contain boron in the catalyst of the present invention, content is 0～5wt%, is preferably 0.5～5wt%.After adding boron, improve the quantity in low, the middle intensity acid site of catalyst, also effectively stoped the inactivation of catalyst.Boron adds with boric acid or boratory form among the present invention.
The present invention does not do detailed qualification to the Preparation of catalysts method, as adopting the equi-volume impregnating preparation.
Catalyst carrier of the present invention is to adopt the current techique preparation, and the present invention is not limited.Catalyst carrier can add one or more in boron, alkali metal, the alkaline-earth metal before extruded moulding.Recommend to adopt the method for one of the following to obtain:
Method one: will contain the boehmite of amorphous aluminum silicide and nitric acid, water mixer kneader, extruded moulding, 80～140 ℃ of oven dry, 400～700 ℃ of roasting 3～6h obtain catalyst carrier.
Method two: siliceous alumina support is by add one or more acquisitions in alkali metal, alkaline-earth metal, the boron element before extruded moulding.As the boehmite that will contain amorphous aluminum silicide and predecessor, nitric acid, the water mixer kneader of alkali metal, alkaline-earth metal and/or boron element, extruded moulding, 80～140 ℃ of oven dry, 400～700 ℃ of roasting 3～6h obtain catalyst carrier.
Method three: in containing the boehmite of amorphous aluminum silicide, add after nitric acid, water mediates, extruded moulding, 80～120 ℃ of oven dry, 300～600 ℃ of roasting 3～6h, flood the precursor solutions such as soluble-salt of alkali metal, alkaline-earth metal and/or boron element then, 80～140 ℃ of oven dry, 400～700 ℃ of roasting 3～6h make catalyst carrier.
The present invention also provides a kind of above-mentioned Preparation of catalysts method, and the aqueous solution that will contain molybdenum and cobalt soluble-salt impregnated on the carrier, and dry back is at 300～500 ℃ of following roasting 3～6h.
Alkali metal and/or alkaline-earth metal and auxiliary agent boron all can add when the preparation carrier, also can be after the carrier moulding, molybdenum, cobalt are added in the carrier before adding in advance, the aqueous solution that will contain molybdenum, cobalt soluble-salt again impregnated on the siliceous alumina support, dry back makes catalyst at 300～500 ℃ of following roasting 3～6h.Can also be when dipping molybdenum, cobalt, add simultaneously with molybdenum, cobalt, be about to alkali metal, alkaline-earth metal and/or boron element and be added to the aqueous solution that contains molybdenum, cobalt soluble-salt and impregnated on the siliceous alumina support, dry back makes catalyst at 300～500 ℃ of following roasting 3～6h.
Can be more specifically in containing the boehmite of amorphous aluminum silicide, add nitric acid, water carries out mixer kneader, extruded moulding, 80～120 ℃ of oven dry, 300～600 ℃ of roasting 3～6h flood the soluble-salt solution of alkali metal, alkaline-earth metal and/or P elements, 80～120 ℃ of oven dry then, 400～700 ℃ of roasting 4～6h, with the aqueous solution dipping that contains molybdenum, cobalt soluble-salt, dry back makes catalyst at 300～500 ℃ of following roasting 3～6h again.
The active component molybdenum is to add with the form of ammonium molybdate among the present invention; Cobalt is to add with the form of soluble-salt, as cobalt nitrate, cobalt acetate, cobalt chloride or cobaltous sulfate, and preferred cobalt nitrate, cobalt acetate.
Hydrotreating catalyst hydrodesulfurization of the present invention, denitrification activity height, chemical stability and Heat stability is good, coke content is low, long service life.
The specific embodiment
Preparation catalyst agents useful for same source:
Ammonium molybdate: Shanghai colloidization factory
Cobalt acetate: Shanghai reagent two factories
Industry amorphous aluminum silicide: the safe photoinitiator chemical in Zibo Co., Ltd, SiO
2Content 45%.
Industry boehmite: Zibo Wanlin Chemical Technology Co., Ltd.
Analytical method:
Oil distillation: adopt oil product test method SYB-2110-60 to measure;
Bromine valency: adopt the ICl method to measure, show with gram bromine/100 gram oil meters;
Arsenic: adopt the DV-4300 Atomic Emission Spectrometer AES to measure;
Sulphur: adopt the WK-2B Microcoulomb instrument to measure;
Nitrogen: adopt KY-3000N chemiluminescence azotometer to measure;
Catalyst crystalline phases: adopt BRUKER D
8ADVERCE type X-ray diffractometer is measured;
Infrared acidity: adopt pyridine-infrared mensuration;
Specific area, pore volume: adopt low temperature N
2The method of adsorption-desorption is measured.
Embodiment 1:
Configuration 2L concentration is 90gAl
2O
3The sodium aluminate solution of/L places in the glue jar, is controlled to 45 ℃ of glue jar temperature, under stirring condition, feeds 65v%CO
2+ 35v% Air mixing gas, the flow of carbon dioxide is 3Nm in the gaseous mixture
3/ h.Stop to feed mist when the pH value reaches 10.0, aging then 22min obtains the boehmite slurries.
Configuration 3L concentration is 100gAl
2O
3The sodium aluminate solution of/L places in the glue jar, adds 2L 80gSiO then
2The sodium silicate solution of/L is controlled to 30 ℃ of glue jar temperature, feeds 60v%CO
2+ 40v% Air mixing gas, CO in the gaseous mixture
2Flow be 3Nm
3/ h, the control endpoint pH is 9.0, aging 15min obtains the amorphous aluminum silicide slurries.
Under continuous stirring condition, 2L amorphous aluminum silicide slurries are joined in the 1L boehmite slurries, 40 ℃ of control mixing temperatures, aging 15min, filtration washing is to Na
+Content obtains containing the boehmite of amorphous aluminum silicide less than 0.5%, 120 ℃ of dry 10h.
To contain the boehmite of amorphous aluminum silicide and boric acid, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 550 ℃ of roasting 3h use the saturated impregnated carrier of potassium nitrate solution then, 120 ℃ of oven dry, 500 ℃ of roasting 4h obtain the alumina support of siliceous, boron and potassium.Cobalt acetate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 450 ℃ of roastings obtain containing CoO 3.0wt%, MoO
315wt%, SiO
218.0wt%, B
2O
33.0wt%, K
2The catalyst C-1 of O 2.0wt%.
Embodiment 2:
The preparation of amorphous aluminum silicide slurries is carried out according to embodiment 1.
Configuration 2L concentration is 100gAl
2O
3The sodium aluminate solution of/L places in the glue jar, is controlled to 40 ℃ of glue jar temperature, and under stirring condition, feeding concentration is 75v%CO
2+ 25v% Air mixing gas, the flow of carbon dioxide is 5Nm in the gaseous mixture
3/ h stops to feed mist when the pH value reaches 10.0, aging 28min obtains the boehmite slurries.
Under continuous stirring condition, 1.5L boehmite slurries are joined in the 1L amorphous aluminum silicide slurries, 45 ℃ of control mixing temperatures, aging 15min, filtration washing is to Na
+Content obtains containing the boehmite of amorphous aluminum silicide less than 0.5%, 120 ℃ of dry 9h.
To contain the boehmite of amorphous aluminum silicide and boric acid, lithium nitrate, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 520 ℃ of roasting 4h obtain the alumina support of siliceous, boron and lithium.Cobalt acetate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 480 ℃ of roasting 4h obtain containing CoO 3.5wt%, MoO
316.5wt%, SiO
210wt%, B
2O
32.5wt%, Li
2The catalyst C-2 of O 1.5wt%.
Embodiment 3:
Configuration 2L concentration is 100gAl
2O
3The sodium aluminate solution of/L places in the glue jar, is controlled to 40 ℃ of glue jar temperature, under stirring condition, feeds 60v%CO
2+ 40v% Air mixing gas, the flow of carbon dioxide is 5Nm in the gaseous mixture
3/ h.Stop to feed mist when the pH value reaches 10.0, aging then 25min obtains the boehmite slurries.
Configuration 2L concentration is 130gAl
2O
3The sodium aluminate solution of/L places in the glue jar, adds 2L 80gSiO then
2The sodium silicate solution of/L, 20 ℃ of control reaction temperatures feed 50v%CO
2+ 50v% Air mixing gas, CO in the mist
2Flow be 6Nm
3/ h, the control endpoint pH is 9.5, aging 18min obtains the amorphous aluminum silicide slurries.
Under continuous stirring condition, 1L boehmite slurries are joined in the glue jar with 3L amorphous aluminum silicide slurries and stream, 40 ℃ of control mixing temperatures, aging 15min, filtration washing is to Na
+Content obtains containing the boehmite of amorphous aluminum silicide less than 0.5%, 120 ℃ of dry 12h.
To contain the boehmite of amorphous aluminum silicide and boric acid, magnesium nitrate, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 550 ℃ of roasting 4h obtain the alumina support of siliceous, boron and magnesium.Cobalt acetate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 450 ℃ of roasting 4h obtain containing CoO 4.5wt%, MoO
315.5wt%, SiO
220.8wt%, B
2O
3The catalyst C-3 of 4.0wt%, MgO 4.0wt%.
Embodiment 4:
The preparation of amorphous aluminum silicide slurries is carried out according to embodiment 3.Configuration 2L concentration is 76gAl
2O
3The sodium aluminate solution of/L places in the glue jar, is controlled to 35 ℃ of glue jar temperature, under stirring condition, feeds 60v%CO
2+ 40v% Air mixing gas, the flow of carbon dioxide is 5Nm in the gaseous mixture
3/ h.Stop to feed mist when the pH value reaches 10.0, aging then 20min obtains the boehmite slurries.
Under continuous stirring condition, 2L boehmite slurries are joined in the glue jar with 1.6L amorphous aluminum silicide slurries and stream, 45 ℃ of control mixing temperatures, aging 20min, filtration washing is to Na
+Content obtains containing the boehmite of amorphous aluminum silicide less than 0.5%, 110 ℃ of dry 15h.
To contain the boehmite of amorphous aluminum silicide and boric acid, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 500 ℃ of roasting 4h use the saturated impregnated carrier of strontium nitrate solution then, 120 ℃ of oven dry, 550 ℃ of roasting 4h obtain the alumina support of siliceous, boron and strontium.Cobalt nitrate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 460 ℃ of roasting 4h obtain containing CoO 5.0wt%, MoO
316wt%, SiO
214.4wt%, B
2O
3The catalyst C-4 of 4.0wt%, SrO 3.0wt%.
Embodiment 5:
Configuration 2L concentration is 70gAl
2O
3The sodium aluminate solution of/L places in the glue jar, and being controlled to glue jar temperature is 50 ℃, and under continuous stirring condition, feeding concentration is 80v%CO
2+ 20v% Air mixing gas, the flow of carbon dioxide is 4Nm in the gaseous mixture
3/ h stops to feed mist when the pH value reaches 10.0, aging 20min obtains the boehmite slurries.
Configuration 3L concentration is 85gAl
2O
3The sodium aluminate solution of/L places in the glue jar, adds 2L65gSiO then
2The sodium silicate solution of/L, 30 ℃ of control reaction temperatures feed 60v%CO
2+ 40v% Air mixing gas, CO in the gaseous mixture
2Flow be 5Nm
3/ h, the control endpoint pH is 9.5, aging 18min obtains the amorphous aluminum silicide slurries.
Under continuous stirring condition, 2L boehmite slurries are joined in the glue jar with 2L amorphous aluminum silicide slurries and stream, 60 ℃ of control mixing temperatures, aging 10min, filtration washing is to Na
+Content obtains containing the boehmite of amorphous aluminum silicide less than 0.5%, 120 ℃ of dry 8h.
To contain the boehmite of amorphous aluminum silicide and boric acid, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 460 ℃ of roasting 4h use the saturated impregnated carrier of liquor kalii acetici then, 120 ℃ of oven dry, 520 ℃ of roasting 4h obtain the alumina support of siliceous, boron and potassium.Cobalt acetate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 450 ℃ of roasting 4h obtain containing CoO 2.0wt%, MoO
318wt%, SiO
213.3wt%, B
2O
33.5wt%, K
2The catalyst C-5 of O 1.5wt%.
Embodiment 6:
The configuration of boehmite slurries and amorphous aluminum silicide slurries is carried out according to embodiment 5.
Get 4L amorphous aluminum silicide slurries and join in the glue jar with 0.5L boehmite slurries and stream, 40 ℃ of control reaction temperatures, aging 10min, filtration washing is to Na
+Content obtains containing the boehmite of amorphous aluminum silicide less than 0.5%, 120 ℃ of following dry 10h.
To contain the boehmite of amorphous aluminum silicide and boric acid, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 500 ℃ of roasting 4h use the saturated impregnated carrier of lithium citrate solution then, 120 ℃ of oven dry, 600 ℃ of roasting 3h obtain the alumina support of siliceous, boron and lithium.Cobalt nitrate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 500 ℃ of roasting 3h obtain containing CoO 4.5wt%, MoO
314.5wt%, SiO
223.3wt%, B
2O
32.0wt%, Li
2The catalyst C-6 of O 2.0wt%.
Embodiment 7:
The preparation of boehmite slurries is carried out according to embodiment 5.
Configuration 2L concentration is 120gAl
2O
3The sodium aluminate solution of/L places in the glue jar, adds 1L60gSiO
2The sodium silicate solution of/L, 30 ℃ of control reaction temperatures feed 55v%CO
2+ 45v% Air mixing gas, CO in the gaseous mixture
2Flow be 6Nm
3/ h, the control endpoint pH is 10.0, aging 10min obtains the amorphous aluminum silicide slurries.
Under continuous stirring condition, 2L boehmite slurries are joined in the glue jar with 1L amorphous aluminum silicide slurries and stream, 40 ℃ of control mixing temperatures, aging 30min, filtration washing is to Na
+Content obtains containing the boehmite of amorphous aluminum silicide less than 0.5%, 120 ℃ of dry 8h.
To contain the boehmite of amorphous aluminum silicide and boric acid, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 550 ℃ of roasting 4h obtain siliceous alumina support.Cobalt acetate, ammonium molybdate, potassium nitrate and magnesium nitrate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 500 ℃ of roasting 4h obtain containing CoO 5.5wt%, MoO
312.5wt%, SiO
26.1wt%, B
2O
34.5wt%, K
2The catalyst C-7 of O 1.5wt%, MgO 2.0wt%.
Embodiment 8:
The preparation of boehmite that contains amorphous aluminum silicide is with embodiment 1.
To contain the boehmite of amorphous aluminum silicide and nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 550 ℃ of roasting 3h use the saturated impregnated carrier of potassium nitrate solution then, 120 ℃ of oven dry, and 500 ℃ of roasting 4h obtain siliceous and alumina support potassium.Cobalt acetate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 450 ℃ of roastings obtain containing CoO3.0wt%, MoO
315wt%, SiO
218.7wt%, K
2The catalyst C-8 of O 2.0wt%.
Embodiment 9:
The preparation of boehmite that contains amorphous aluminum silicide is with embodiment 6.
To contain the boehmite of amorphous aluminum silicide and boric acid, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 600 ℃ of roasting 3h obtain siliceous and alumina support boron.Cobalt nitrate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 500 ℃ of roasting 3h obtain containing CoO 4.5wt%, MoO
314.5wt%, SiO
223.9wt%, B
2O
3The catalyst C-9 of 2.0wt%.
Embodiment 10:
Configuration 2L concentration is 78gAl
2O
3The sodium aluminate solution of/L places in the glue jar, and being controlled to glue jar temperature is 50 ℃, and under continuous stirring condition, feeding concentration is 80v%CO
2+ 20v% Air mixing gas, the flow of carbon dioxide is 4Nm in the gaseous mixture
3/ h stops to feed mist when the pH value reaches 10.0, aging 20min obtains the boehmite slurries.
Configuration 3L concentration is 100gAl
2O
3The sodium aluminate solution of/L places in the glue jar, adds 2L 60gSiO then
2The sodium silicate solution of/L, 30 ℃ of control reaction temperatures feed 60v%CO
2+ 40v% Air mixing gas, CO in the gaseous mixture
2Flow be 5Nm
3/ h, the control endpoint pH is 9.5, aging 18min obtains the amorphous aluminum silicide slurries.
Under continuous stirring condition, 2L boehmite slurries are joined in the glue jar with 2L amorphous aluminum silicide slurries and stream, 60 ℃ of control mixing temperatures, aging 10min, filtration washing is to Na
+Content obtains containing the boehmite of amorphous aluminum silicide less than 0.5%, 120 ℃ of dry 8h.
To contain the boehmite of amorphous aluminum silicide and boric acid, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 460 ℃ of roasting 4h use the saturated impregnated carrier of strontium nitrate solution then, 120 ℃ of oven dry, 520 ℃ of roasting 4h obtain the alumina support of siliceous, boron and strontium.Cobalt acetate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 450 ℃ of roasting 4h obtain containing CoO 2.5wt%, MoO
314wt%, SiO
211.9wt%, B
2O
3The catalyst C-10 of 2.4wt%, SrO 0.8wt%.
Comparative Examples 1:
With 2L concentration is 100gAl
2O
3The sodium aluminate solution of/L places in the glue jar, is controlled to 40 ℃ of glue jar temperature, and under continuous stirring condition, feeding concentration is 60v%CO
2+ 40v% Air mixing gas, the flow of carbon dioxide is 2Nm in the gaseous mixture
3/ h stops to feed gaseous mixture when the pH value reaches 10.5, aging 25min obtains the boehmite slurries.
With 4L concentration is 150gAl
2O
3The sodium aluminate solution of/L places in the glue jar, adds 2L30gSiO then
2The sodium silicate solution of/L, 30 ℃ of control reaction temperatures feed 60v%CO
2+ 40v% Air mixing gas, CO in the gaseous mixture
2Flow be 3Nm
3/ h, the control endpoint pH is 9.5, aging 10min obtains the amorphous aluminum silicide slurries.
Under continuous stirring condition, 1L amorphous aluminum silicide slurries are joined in the 2L boehmite slurries, 40 ℃ of control mixing temperatures, aging 10min, filtration washing is to Na
+Content obtains containing the boehmite of amorphous aluminum silicide less than 0.5%, 120 ℃ of dry 8h.
To contain the boehmite of amorphous aluminum silicide and boric acid, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 550 ℃ of roasting 3h use the saturated impregnated carrier of potassium nitrate solution then, 120 ℃ of oven dry, 500 ℃ of roasting 4h obtain the alumina support of siliceous, boron and potassium.Cobalt acetate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 450 ℃ of roastings obtain containing CoO 3.0wt%, MoO
315wt%, SiO
22.5wt%, B
2O
33.0wt%, K
2The catalyst D-1 of O 2.0wt%.
Comparative Examples 2:
This Comparative Examples prepares silica-alumina according to the 3 described methods of embodiment among the CN1267187C, and concrete steps are as follows:
Take by weighing the 1000g aluminum nitrate, be dissolved into 2L aluminum nitrate solution a3 (Al with deionized water
2O
3Concentration is 65g/L); The 500ml concentrated ammonia liquor is diluted to 1500ml solution b3 with deionized water; Preparation 500ml89.6SiO
2The sodium silicate solution c3 of/L; Get 35g NaOH, be dissolved into 150ml solution d3 with deionized water.
In becoming the glue jar, add the 1.7L deionized water earlier, stirring also is heated to 40 ℃, then and stream add solution a3 and b3, regulating flow, to make the pH value of reaction system be 8, after the reaction end again pH be 8, aging 60min under 45 ℃ of conditions of temperature, behind aging the end, under stirring condition, add solution c3 and d3 successively, and control pH is 8.2,50 ℃ of temperature are warming up to 95 ℃ then and also filter behind the constant temperature 20h.Filter cake spends deionised water 4 times, and 120 ℃ of dry 15h obtain the silica-alumina composite granule.
With silica-alumina composite granule and boric acid, magnesium nitrate, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 550 ℃ of roasting 4h obtain the alumina support of siliceous, boron and magnesium.Cobalt acetate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 450 ℃ of roasting 4h obtain containing CoO 4.5wt%, MoO
315.5wt%, SiO
220.8wt%, B
2O
3The catalyst D-2 of 4.0wt%, MgO 4.0wt%.
Comparative Examples 3:
This Comparative Examples prepares the silica-alumina composite oxides according to the 1 described method of embodiment among the CN1074303C, and concrete steps are as follows:
Earlier in 150ml, 55 ℃ of distilled water with 30.5g sodium metasilicate (Na
2SiO
3) dissolving fully, with 152.5g sodium aluminate (NaAlO
2) also be dissolved in the 700ml distilled water.Then, sodium aluminate solution is slowly poured in the sodium silicate solution.In mixed process, mixed liquor is 55 ℃ of heating and stirrings simultaneously continuously.After two kinds of solution mixed fully, adding 6N HCl was transparent until reactant mixture.In clear solution, add 6N NaOH then and reach 10, keep 60min to obtain gel then until pH value of solution.Gel is put into reative cell keep 1h at 100 ℃ of pressure 100psi of temperature, product filters with vacuum equipment, is deposited in 100 ℃ of dry 24h and obtains the powdery alumino-silicate.
With powdery alumino-silicate and boric acid, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 500 ℃ of roasting 4h use the saturated impregnated carrier of strontium nitrate solution then, 120 ℃ of oven dry, 550 ℃ of roasting 4h obtain the alumina support of siliceous, boron and strontium.Cobalt nitrate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 460 ℃ of roasting 4h obtain containing CoO 5.0wt%, MoO
316wt%, SiO
214.4wt%, B
2O
3The catalyst D-3 of 4.0wt%, SrO 3.0wt%.
Comparative Examples 4:
This Comparative Examples prepares silica-alumina according to the 4 described methods of embodiment among the CN1306977C, and concrete steps are as follows:
Adopt water intaking glass 100ml, add high basicity sodium metaaluminate 75ml under the room temperature, stir 1h, leave standstill 6h, silica content is 235g/L in this solution, and alumina content is 6.7g/L.Get this solution 65ml, add water to 300ml, obtain the mother liquor of synthesis of molecular sieve, wherein SiO
2Content is 5.1g/100ml.
With concentration be 10% aluminum nitrate solution 385ml and concentration be 8% ammonia spirit 390ml and concentration be 8% ammonia spirit 390ml with and the mode of stream join simultaneously in the retort of a 2L, put into 0.5L water in advance in jar, the flow of aluminum nitrate solution is 1.1L/h, regulate the flow of ammonia spirit, the pH value that makes mixed liquor is 7.0 ± 0.3, and mixed liquor is collected in an ageing can.Under agitation the mother liquor with the 50ml synthesis of molecular sieve joins in this mixed liquor, makes silica-alumina colloid slurries, is warming up to 65 ℃, stir down aging 1h, after filtering, filter cake spends deionised water 3 times, 120 ℃ of dry 5h obtain the silica-alumina composite granule in baking oven.
With silica-alumina composite granule and boric acid, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 500 ℃ of roasting 4h use the saturated impregnated carrier of lithium citrate solution then, 120 ℃ of oven dry, 600 ℃ of roasting 3h obtain the alumina support of siliceous, boron and lithium.Cobalt nitrate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 500 ℃ of roasting 3h obtain containing CoO4.5wt%, MoO
314.5wt%, SiO
223.4wt%, B
2O
32.0wt%, Li
2The catalyst D-4 of O 2.0wt%.
Comparative Examples 5:
The preparation method of silica-alumina composite granule is with Comparative Examples 2.
With silica-alumina composite granule and magnesium nitrate, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 550 ℃ of roasting 4h obtain siliceous and alumina support magnesium.Cobalt acetate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 450 ℃ of roasting 4h obtain containing CoO 4.5wt%, MoO
315.5wt%, SiO
2The catalyst D-5 of 22wt%, MgO 4.0wt%.
Comparative Examples 6
The preparation method of silica-alumina composite granule is with Comparative Examples 4.
With silica-alumina composite granule and boric acid, nitric acid, water mixer kneader, behind the extruded moulding, 600 ℃ of roasting 3h obtain siliceous and alumina support boron.Cobalt nitrate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 500 ℃ of roasting 3h obtain containing CoO4.5wt%, MoO
314.5wt%, SiO
224wt%, B
2O
3The catalyst D-6 of 2.0wt%.
Comparative Examples 7:
With industrial amorphous aluminum silicide with boric acid, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 460 ℃ of roasting 4h use the saturated impregnated carrier of strontium nitrate solution then, 120 ℃ of oven dry, 520 ℃ of roasting 4h obtain the alumina support of siliceous, boron and strontium.Cobalt acetate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 450 ℃ of roasting 4h obtain containing CoO2.5wt%, MoO
314wt%, SiO
236.1wt%, B
2O
3The catalyst D-7 of 2.4wt%, SrO 0.8wt%.
Comparative Examples 8
With industrial boehmite and boric acid, nitric acid, water mixer kneader, behind the extruded moulding, 120 ℃ of oven dry, 460 ℃ of roasting 4h use the saturated impregnated carrier of liquor kalii acetici then, 120 ℃ of oven dry, 520 ℃ of roasting 4h, obtain siliceous, bump the alumina support with potassium.Cobalt acetate and ammonium molybdate be dissolved in the water jointly make maceration extract, be impregnated on the 100g carrier, 120 ℃ of oven dry, 450 ℃ of roasting 4h obtain containing CoO 2.0wt%, MoO
318wt%, B
2O
33.5wt%, K
2The catalyst D-8 of O 1.5wt%.
Comparative Examples 9
This Comparative Examples prepares catalyst according to the 3 described methods of embodiment among the CN100487085C, and concrete steps are as follows:
With the moulding that is mixed of 85g aluminum oxide dry glue powder, 15g titania powder, 1g strontium oxide strontia, 3g sesbania powder, 5g nitric acid, 65g deionized water,, at 450～600 ℃ of air atmosphere roasting 4～6h, make carrier then with the dry 3～20min that handles of micro-wave oven.Be made into alkaline solution with basic cobaltous carbonate, molybdenum trioxide, ammonium metatungstate, boric acid, flood above-mentioned carrier, health 2～3h under the room temperature, with the dry 3～20min that handles of micro-wave oven, 500～550 ℃ of air atmosphere roasting 4～6h obtain containing CoO 2.5wt%, MoO
314wt%, B
2O
32.4wt%, SrO 0.8wt%, TiO
211.9wt%, WO
3The catalyst D-9 of 1.2wt%.
Evaluating catalyst
With the reformer feed is feedstock oil (feedstock property sees Table 1), and embodiment catalyst C1-C10 and Comparative Examples catalyst D1-D9 are carried out activity rating at 100ml adiabatic reactor hydrogenation plant.Estimate 500h respectively, every 24h sample analysis sulphur, nitrogen content, average data sees Table 2.
Catalyst vulcanization: carbon disulfide is joined the sulfurized oil that is made in the cyclohexane about sulfur content 1000 μ g/g, and reactor is warmed up to 240 ℃ and begins into sulfurized oil, pressure 2.5Mpa, sulfurized oil volume space velocity 3.0h
-1, hydrogen/sulfurized oil volume ratio 300: 1, the heating rate with 10 ℃/h is warmed up to 350 ℃ then, keeps 25h, and sulfuration finishes.
Evaluating catalyst condition: pressure 2.5MPa, 240 ℃ of inlet temperatures, feedstock oil volume space velocity 8h
-1, hydrogen to oil volume ratio 70: 1.
Table 1 oxygenation feedstock oil index
The evaluating catalyst average data sees Table 2.
Embodiment and Comparative Examples catalyst composition and physico-chemical property are as shown in table 3.
Table 2 catalyst 500h estimates average data
The physico-chemical property of table 3 catalyst C1-C10 and D1-D9
Claims (16)
1. hydrotreating catalyst, with siliceous aluminium oxide is carrier, it is characterized in that catalyst is an active component with molybdenum, cobalt, boron and alkali metal and/or alkaline-earth metal be as auxiliary agent, in catalyst weight, and molybdenum oxide 10 ~ 20wt%, cobalt oxide 1 ~ 8wt%, boron oxide compound 0 ~ 5wt%, alkali metal and/or alkaline earth oxide 0 ~ 5wt%, silica 3.25 ~ 35.6wt%; Specific surface area of catalyst 220 ~ 300m
2/ g, pore volume 0.55 ~ 0.75ml/g; Siliceous alumina support presoma is the boehmite that contains amorphous aluminum silicide, it is by at first preparing amorphous aluminum silicide slurries and boehmite slurries, above-mentioned amorphous aluminum silicide slurries are mixed, wear out according to the ratio of silica content 5 ~ 40wt% with the boehmite slurries, ageing time is 10 ~ 30min, obtains through the last handling process that comprises filtration, washing, drying then.
2. hydrotreating catalyst according to claim 1 is characterized in that boron oxide compound content is 0.5 ~ 5wt%.
3. hydrotreating catalyst according to claim 1 is characterized in that alkali metal and/or alkaline earth oxide content are 1 ~ 5wt%.
4. according to claim 1 or 2 or 3 described hydrotreating catalysts, it is characterized in that silica content is 6 ~ 26wt%.
5. hydrotreating catalyst according to claim 1, the boehmite that it is characterized in that containing amorphous aluminum silicide is by with amorphous aluminum silicide slurries and boehmite slurries and stream mixes or a kind of slurries are joined in the another kind of slurries mix, after mixing was finished, pH value of solution was 9.0 ~ 10.5 when aging.
6. hydrotreating catalyst according to claim 1 or 5 is characterized in that temperature is 20 ~ 65 ℃ when aging.
7. hydrotreating catalyst according to claim 1 is characterized in that the amorphous aluminum silicide slurries obtain by following method:
(a) compound concentration is 10 ~ 150gAl
2O
3The sodium metaaluminate of/L or sodium aluminate solution join in the glue jar, are controlled to 15 ~ 50 ℃ of glue jar temperature;
(b) compound concentration is 50 ~ 200gSiO
2The silicon-containing compound solution of/L joins in the sodium aluminate solution of (a), control pH value 11.5 ~ 13;
(c) under the condition of low whipping speed greater than 250r/min, feed the carbon dioxide of concentration greater than 20v% continuously, the flow of control carbon dioxide is at 1 ~ 10Nm
3/ h, in and time 20 ~ 40min, endpoint pH 7.5 ~ 9.5, neutralization finishes;
(d) in pH value 7.5 ~ 9.5, product 5 ~ 20min that aging (c) step obtains under the condition that temperature is 25 ~ 40 ℃ obtains the amorphous aluminum silicide slurries.
8. hydrotreating catalyst according to claim 1, it is characterized in that the boehmite slurries obtain by following method: sodium metaaluminate or sodium aluminate solution are placed in the glue jar, feed carbon dioxide with intermittence or continuation mode and become glue, the aging boehmite slurries that obtain; The concentration of sodium metaaluminate or sodium aluminate solution is 20 ~ 150gAl
2O
3/ L; Gas concentration lwevel is greater than 20v%, flow 1 ~ 10Nm
3/ h; Become 20 ~ 65 ℃ of glue temperature; Become glue endpoint pH 9.0 ~ 10.5, become in the glue and time and ageing time sum less than 40min.
9. hydrotreating catalyst according to claim 1, it is characterized in that siliceous alumina support is boehmite by will containing amorphous aluminum silicide and nitric acid, water mixer kneader, extruded moulding, 80 ~ 140 ℃ of oven dry, 400 ~ 700 ℃ of roasting 3 ~ 6h make.
10. hydrotreating catalyst according to claim 1, it is characterized in that siliceous alumina support is to contain the boehmite of amorphous aluminum silicide and nitric acid, water mixer kneader, and add in alkali metal, alkaline-earth metal, the boron element one or more, extruded moulding, 80 ~ 140 ℃ of oven dry, 400 ~ 700 ℃ of roasting 3 ~ 6h make.
11. the described preparation method of hydrotreatment catalyst of claim 1 is characterized in that the aqueous solution that will contain molybdenum, cobalt soluble-salt impregnated on the siliceous alumina support, dry back makes catalyst at 300 ~ 500 ℃ of following roasting 3 ~ 6h.
12. hydrotreating catalyst preparation method according to claim 11 is characterized in that alkali metal, alkaline-earth metal and/or boron element add when the siliceous alumina support of preparation.
13. hydrotreating catalyst preparation method according to claim 11, it is characterized in that alkali metal, alkaline-earth metal and/or boron element are added in the siliceous alumina support before adding at molybdenum, cobalt in advance, again with the aqueous solution dipping that contains molybdenum, cobalt soluble-salt, dry back makes catalyst at 300 ~ 500 ℃ of following roasting 3 ~ 6h.
14. described preparation method of hydrotreatment catalyst of claim 1, it is characterized in that alkali metal, alkaline-earth metal and/or boron element are added to the aqueous solution that contains molybdenum, cobalt soluble-salt be impregnated on the siliceous alumina support, dry back makes catalyst at 300 ~ 500 ℃ of following roasting 3 ~ 6h.
15. hydrotreating catalyst preparation method according to claim 12, it is characterized in that siliceous alumina support is by add predecessor, nitric acid, the water mixer kneader of alkali metal, alkaline-earth metal and/or boron element at the boehmite of amorphous aluminum silicide, extruded moulding, 80 ~ 140 ℃ of oven dry, 400 ~ 700 ℃ of roasting 3 ~ 6h obtain.
16. hydrotreating catalyst preparation method according to claim 13, it is characterized in that in containing the boehmite of amorphous aluminum silicide, adding nitric acid, water carries out mixer kneader, extruded moulding, 80 ~ 120 ℃ of oven dry, 300 ~ 600 ℃ of roasting 3 ~ 6h, flood the soluble-salt solution of alkali metal, alkaline-earth metal and/or boron element then, 80 ~ 120 ℃ of oven dry, 400 ~ 700 ℃ of roasting 4 ~ 6h, again with the aqueous solution dipping that contains molybdenum, cobalt soluble-salt, dry back makes catalyst at 300 ~ 500 ℃ of following roasting 3 ~ 6h.
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| CN1218089A (en) * | 1997-11-24 | 1999-06-02 | 中国石油化工总公司 | Catalyst carrier containing difunctional amorphous aluminum silicide and preparation thereof |
| CN1250746A (en) * | 1998-10-13 | 2000-04-19 | 中国石油化工集团公司 | Process for preparing artificial diasporite and gamma-alumina |
| CN1351115A (en) * | 2000-10-26 | 2002-05-29 | 中国石油化工股份有限公司 | Demetalating and desulfurizing hydrocatalyst and its preparing process |
| CN1597093A (en) * | 2003-09-15 | 2005-03-23 | 中国石油化工股份有限公司 | Method of preparing amorphous silica-alumina using carbonization |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1218089A (en) * | 1997-11-24 | 1999-06-02 | 中国石油化工总公司 | Catalyst carrier containing difunctional amorphous aluminum silicide and preparation thereof |
| CN1250746A (en) * | 1998-10-13 | 2000-04-19 | 中国石油化工集团公司 | Process for preparing artificial diasporite and gamma-alumina |
| CN1351115A (en) * | 2000-10-26 | 2002-05-29 | 中国石油化工股份有限公司 | Demetalating and desulfurizing hydrocatalyst and its preparing process |
| CN1597093A (en) * | 2003-09-15 | 2005-03-23 | 中国石油化工股份有限公司 | Method of preparing amorphous silica-alumina using carbonization |
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