CN106669863A - Modification method of hydro-upgrading catalyst carrier - Google Patents
Modification method of hydro-upgrading catalyst carrier Download PDFInfo
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- CN106669863A CN106669863A CN201510757815.9A CN201510757815A CN106669863A CN 106669863 A CN106669863 A CN 106669863A CN 201510757815 A CN201510757815 A CN 201510757815A CN 106669863 A CN106669863 A CN 106669863A
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- 239000003054 catalyst Substances 0.000 title claims abstract description 100
- 238000002715 modification method Methods 0.000 title abstract 2
- 238000000034 method Methods 0.000 claims abstract description 73
- 238000010438 heat treatment Methods 0.000 claims abstract description 42
- 239000002253 acid Substances 0.000 claims abstract description 34
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims abstract description 32
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 32
- 150000001875 compounds Chemical class 0.000 claims abstract description 31
- 239000003921 oil Substances 0.000 claims description 45
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 43
- 239000002808 molecular sieve Substances 0.000 claims description 43
- 229910052710 silicon Inorganic materials 0.000 claims description 43
- 239000010703 silicon Substances 0.000 claims description 43
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 38
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims description 31
- 230000008569 process Effects 0.000 claims description 24
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 21
- 239000000377 silicon dioxide Substances 0.000 claims description 21
- 230000036541 health Effects 0.000 claims description 17
- 239000011148 porous material Substances 0.000 claims description 17
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 14
- OERNJTNJEZOPIA-UHFFFAOYSA-N zirconium nitrate Chemical compound [Zr+4].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O OERNJTNJEZOPIA-UHFFFAOYSA-N 0.000 claims description 14
- 229910052681 coesite Inorganic materials 0.000 claims description 13
- 229910052906 cristobalite Inorganic materials 0.000 claims description 13
- 229910052682 stishovite Inorganic materials 0.000 claims description 13
- 229910052905 tridymite Inorganic materials 0.000 claims description 13
- 238000002360 preparation method Methods 0.000 claims description 10
- 229910052593 corundum Inorganic materials 0.000 claims description 8
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 8
- 229910001845 yogo sapphire Inorganic materials 0.000 claims description 8
- 229910001928 zirconium oxide Inorganic materials 0.000 claims description 8
- 239000002671 adjuvant Substances 0.000 claims description 7
- 238000007598 dipping method Methods 0.000 claims description 7
- 238000001802 infusion Methods 0.000 claims description 6
- 229910052698 phosphorus Inorganic materials 0.000 claims description 6
- 238000005470 impregnation Methods 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 4
- 239000004033 plastic Substances 0.000 claims description 4
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
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- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 3
- 229910052796 boron Inorganic materials 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 238000010348 incorporation Methods 0.000 claims description 3
- 238000004898 kneading Methods 0.000 claims description 3
- CMOAHYOGLLEOGO-UHFFFAOYSA-N oxozirconium;dihydrochloride Chemical compound Cl.Cl.[Zr]=O CMOAHYOGLLEOGO-UHFFFAOYSA-N 0.000 claims description 3
- 239000011574 phosphorus Substances 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 3
- 239000010936 titanium Substances 0.000 claims description 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 229920000570 polyether Polymers 0.000 claims description 2
- 229920001296 polysiloxane Polymers 0.000 claims description 2
- 150000003376 silicon Chemical class 0.000 claims description 2
- DUNKXUFBGCUVQW-UHFFFAOYSA-J zirconium tetrachloride Chemical compound Cl[Zr](Cl)(Cl)Cl DUNKXUFBGCUVQW-UHFFFAOYSA-J 0.000 claims description 2
- ATYZRBBOXUWECY-UHFFFAOYSA-N zirconium;hydrate Chemical compound O.[Zr] ATYZRBBOXUWECY-UHFFFAOYSA-N 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 16
- 238000005984 hydrogenation reaction Methods 0.000 abstract description 13
- 238000009826 distribution Methods 0.000 abstract description 4
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- 239000002283 diesel fuel Substances 0.000 description 23
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- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
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- 238000001125 extrusion Methods 0.000 description 7
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- 238000012986 modification Methods 0.000 description 7
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 description 6
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- 239000011593 sulfur Substances 0.000 description 6
- 238000009833 condensation Methods 0.000 description 5
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
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- 238000007493 shaping process Methods 0.000 description 4
- 206010013786 Dry skin Diseases 0.000 description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 3
- 239000005864 Sulphur Substances 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- 230000001143 conditioned effect Effects 0.000 description 3
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- 238000005516 engineering process Methods 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052750 molybdenum Inorganic materials 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 229910017604 nitric acid Inorganic materials 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- HORCQSAKJDDBKB-UHFFFAOYSA-N 1-methyldibenzothiophene Chemical compound S1C2=CC=CC=C2C2=C1C=CC=C2C HORCQSAKJDDBKB-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Inorganic materials O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- -1 alkyl benzothiophenes Chemical class 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000006477 desulfuration reaction Methods 0.000 description 2
- 230000023556 desulfurization Effects 0.000 description 2
- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical class C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 description 2
- 230000008570 general process Effects 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
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- 241000894007 species Species 0.000 description 2
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- 239000003643 water by type Substances 0.000 description 2
- DGUACJDPTAAFMP-UHFFFAOYSA-N 1,9-dimethyldibenzo[2,1-b:1',2'-d]thiophene Natural products S1C2=CC=CC(C)=C2C2=C1C=CC=C2C DGUACJDPTAAFMP-UHFFFAOYSA-N 0.000 description 1
- MYAQZIAVOLKEGW-UHFFFAOYSA-N 4,6-dimethyldibenzothiophene Chemical compound S1C2=C(C)C=CC=C2C2=C1C(C)=CC=C2 MYAQZIAVOLKEGW-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 240000005702 Galium aparine Species 0.000 description 1
- 235000014820 Galium aparine Nutrition 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241000612118 Samolus valerandi Species 0.000 description 1
- 241000219793 Trifolium Species 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- PFRUBEOIWWEFOL-UHFFFAOYSA-N [N].[S] Chemical compound [N].[S] PFRUBEOIWWEFOL-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- HIGRAKVNKLCVCA-UHFFFAOYSA-N alumine Chemical compound C1=CC=[Al]C=C1 HIGRAKVNKLCVCA-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910021502 aluminium hydroxide Inorganic materials 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000011959 amorphous silica alumina Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910001593 boehmite Inorganic materials 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000004517 catalytic hydrocracking Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
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- 238000002474 experimental method Methods 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
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- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- FAHBNUUHRFUEAI-UHFFFAOYSA-M hydroxidooxidoaluminium Chemical compound O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000002803 maceration Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
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- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
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- ZULUUIKRFGGGTL-UHFFFAOYSA-L nickel(ii) carbonate Chemical compound [Ni+2].[O-]C([O-])=O ZULUUIKRFGGGTL-UHFFFAOYSA-L 0.000 description 1
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- 238000001935 peptisation Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
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- 239000011701 zinc Substances 0.000 description 1
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- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Catalysts (AREA)
Abstract
The invention discloses a modification method of a hydro-upgrading catalyst carrier. The method comprises the following steps: preparing the hydro-upgrading catalyst carrier, introducing water soluble silicone oil and a soluble zirconium containing compound into the hydro-upgrading catalyst carrier sequentially or simultaneously, and after heat treatment is carried out, obtaining a modified hydro-upgrading catalyst carrier. The modified carrier prepared by the method disclosed by the invention can provide more bronsted acid centers and reduce strong acid centers and further can adjust the distribution of acid centers and hydrogenation activity centers to be mutually coordinated to improve comprehensive performances of a catalyst. In addition, the modified carrier is suitable for being taken as a diesel hydro-upgrading catalyst carrier.
Description
Technical field
The present invention relates to a kind of method of modifying of catalyst for hydro-upgrading carrier, particularly for diesel oil hydrogenation modification catalyst carrier method of modifying.
Background technology
For cleaning diesel production, prior art mainly includes the technology such as hydrofinishing and MHUG.Hydrofinishing can reduce modifying the sulfur content of diesel oil, but limited to improving Cetane number and reduction T95 temperature capabilities.MHUG is using containing molecular sieve（Such as Y type molecular sieve, beta-molecular sieve）Catalyst for hydro-upgrading, aromatic hydrocarbons in diesel oil etc. is suitably cracked, while sulphur, nitrogen impurity content in reducing diesel oil, improve the combination properties such as diesel cetane-number.But using current catalyst for hydro-upgrading, the combination property to improve diesel oil（Sulphur nitrogen impurity content, Cetane number, T95 temperature, arene content etc.）, it usually needs higher cracking degree, can so make diesel yield relatively low, and the yield of diesel oil is kept, the combination property of diesel oil is again less than improvement well.
Sulfur-containing compound and aromatic hydrocarbons in diesel oil distillate, generally exist with complicated structure, such as dibenzothiophenes, alkyl benzothiophenes and methyldibenzothiophene etc., wherein be hydrogenated with more difficult removing is the thiophenes such as dibenzothiophenes, alkyl benzothiophenes and methyldibenzothiophene, especially with 4,6-
Dimethyl Dibenzothiophene（4,6- BMDBT）With
2,4,6- trimethyl dibenzothiophenes（2,4,6- BMDBT）Class formation is complicated and sulfur-containing compound that have space steric effect is most difficult to removing.Reach depth and ultra-deep desulfurization, it is accomplished by removing these complex structures and sterically hindered big sulfur-containing compound, and the generally more difficult removing under the harsh hydrofinishing operating condition such as HTHP of these sulfur-containing compounds, by being hydrocracked, diesel yield can be reduced.Therefore, in the case where keeping diesel yield higher, the impurity in diesel oil how is removed, while and the combination property of diesel oil can be improved, this is the important topic for being currently needed for studying.
Catalyst for hydro-upgrading is typically with the alumina support containing molecular sieve, at present, the method being modified to carrier is a lot, wherein introduce auxiliary agent such as silicon, phosphorus, fluorine, boron, zirconium, titanium, magnesium, gallium, vanadium, manganese, copper, zinc etc., can be used to improve the property of carrier, but because the consumption, the species that introduce auxiliary agent are different with mode, the property of alumina support can be made different, or even difference is very big.CN1184843A discloses a kind of catalyst for hydrocracking diesel oil, and the catalyst consists of 40～80wt% of aluminum oxide, 0～20wt% of amorphous silica-alumina, 5～30wt% of Y type molecular sieve.CN101463271A discloses a kind of catalyst for hydro-upgrading of inferior diesel and preparation method thereof, mainly the predecessor using silica-alumina, aluminum oxide and/or aluminum oxide and Y type molecular sieve mixing, shaping and roasting, introduce afterwards the hydrogenation metal of effective dose in shaping species.Above-mentioned catalyst has higher desulfurization and a denitrification activity, but the amplitude that the yield of diesel product is low, diesel oil Cetane number is improved is little, high condensation point and the shortcomings of big density.
CN201110350790.2 discloses a kind of diesel oil hydrogenation modification catalyst and preparation method thereof.The catalyst includes the carrier and hydrogenation active metals component being made up of modified beta molecular sieve and aluminum oxide.When being used for diesel oil hydrogenation modification using the catalyst, although the condensation point of diesel oil distillate can be reduced, the Cetane number of modification diesel oil is improved, but diesel yield is below 97%, it is still relatively low.
The content of the invention
For problems of the prior art, the invention provides a kind of method of modifying of catalyst for hydro-upgrading carrier.The be modified carrier of preparation of Jing the inventive method can provide more B acid sites, strong acid center is reduced, and the distribution of acid centre and hydrogenation sites can be adjusted so as to mutually coordinated effect, the combination property of catalyst is improved, the modified support is suitably as diesel oil hydrogenation modification catalyst carrier.
The method of the modified catalyst for hydro-upgrading carrier that the present invention is provided, including：The preparation of catalyst for hydro-upgrading carrier, by water-soluble silicon oil and soluble zirconium-containing compound catalyst for hydro-upgrading carrier is sequentially or simultaneously introduced, and after heat treatment, modified catalyst for hydro-upgrading carrier is obtained.
Catalyst for hydro-upgrading carrier of the present invention, it can be the catalyst for hydro-upgrading carrier of conventional method preparation, usually with aluminum oxide and molecular sieve as key component, adjuvant component can not contained, adjuvant component can also be contained, wherein adjuvant component can be one or more in fluorine, silicon, phosphorus, titanium, zirconium, boron etc., adjuvant component content in the carrier in below 15wt%, preferred below 10wt%.Catalyst for hydro-upgrading carrier of the present invention can be prepared using kneading method, mixing plastic method etc., and the general process of kneading method is as follows, by aluminium hydroxide（Such as boehmite）With obtain after high-temperature roasting after molecular sieve mixed-forming, the condition of high-temperature roasting is as follows：In 450 DEG C～1000 DEG C roasting 1.0h～20.0h, preferably 3.0 h ~ 8.0 h.The general process of mixing plastic method is that molecular sieve is introduced during alumine hydroxide colloid is prepared, and after plastic, the alumina dry glue containing molecular sieve is obtained, and Jing shapings are dried and roasting, make carrier, and the condition of wherein high-temperature roasting is as follows：In 450 DEG C～1000 DEG C roasting 1.0h～20.0h, preferably 3.0 h ~ 8.0 h.The shape of carrier can as needed make spherical, bar shaped（Such as clover, bunge bedstraw herb or cylindrical bars）Etc. suitable shape, conventional shaping assistant, such as the acid of extrusion aid, peptization, adhesive etc. can be added in forming process.The property of the catalyst for hydro-upgrading carrier is as follows：Specific surface area is 200 ~ 550m2/ g, preferably 280 ~ 450m2/g；Pore volume is 0.4 ~ 1.3mL/g, preferably 0.6 ~ 1.0mL/g.
Molecular sieve of the present invention is Y type molecular sieve and/or beta-molecular sieve.On the basis of the weight of catalyst for hydro-upgrading carrier, the content of molecular sieve is 3% ~ 35%, and the content of aluminum oxide is 65% ~ 97%, and preferably the content of molecular sieve is 3% ~ 20%, and the content of aluminum oxide is 80% ~ 97%.Wherein described molecular sieve is hydrogen type molecular sieve.Wherein beta-molecular sieve preferred property is as follows：SiO2/Al2O3Mol ratio is 30 ~ 150, specific surface area 400m2/ g～750m2/ g, total pore volume 0.30mL/g～0.55mL/g, meleic acid 0.1～0.8mmol/g of amount；Y type molecular sieve preferred property is as follows：SiO2/Al2O3Mol ratio is 5 ~ 50, specific surface area 450m2/ g～800m2/ g, total pore volume 0.30mL/g～0.60mL/g, meleic acid 0.2～0.9mmol/g of amount.Beta-molecular sieve of the present invention and Y type molecular sieve can be prepared using existing method.
In the inventive method, the silicone content being introduced into carrier by water-soluble silicon oil accounts for the 0.2%～7.0% of modified catalyst for hydro-upgrading vehicle weight in terms of silica, and preferably 0.3%～4.0%, more preferably 0.5% ~ 1.8%.
In the inventive method, the zirconium content being introduced into carrier by soluble zirconium-containing compound accounts for the 0.4%～10.0% of modified catalyst for hydro-upgrading vehicle weight in terms of zirconium oxide, and preferably 0.5%～5.0%, more preferably 0.5%～2.5%.
In the inventive method, mol ratio that the consumption of water-soluble silicon oil and soluble zirconium-containing compound counted with silica and zirconium oxide respectively is introduced as 0.04 ~ 36.0, preferably 0.12 ~ 16.0, more preferably 0.40 ~ 7.5.
Water-soluble silicon oil described in the inventive method, referring to can be dissolved in the silicone oil of water, and preferred property is as follows：Viscosity when 25 DEG C is 200 ~ 7000mPa.s, and preferably 500 ~ 5000mPa.s, cloud point is 30 ~ 100 DEG C, preferably 40 ~ 65 DEG C.What described water-soluble silicon oil was usually obtained using the method for group modified silicone oil, such as polyether modified silicon oil.
In the inventive method, soluble zirconium-containing compound refers to the combination of one or more in zirconium nitrate, zirconium chloride, zirconium oxychloride etc..
In the inventive method, water-soluble silicon oil and soluble zirconium-containing compound are sequentially or simultaneously incorporated on catalyst for hydro-upgrading carrier, first water-soluble silicon oil can be incorporated on catalyst for hydro-upgrading carrier, then soluble zirconium-containing compound is incorporated on catalyst for hydro-upgrading carrier again；Or simultaneously water-soluble silicon oil and soluble zirconium-containing compound are incorporated on catalyst for hydro-upgrading carrier, its incorporation way adopts infusion process, and infusion process can be incipient impregnation, or excessive dipping；Can be repeatedly dipping, or single-steeping.To improve efficiency, preferably using an incipient impregnation.
In the inventive method, described heat treatment is using two sections of heat treatments, first paragraph is 60 DEG C～150 DEG C in temperature, preferably 90 DEG C～120 DEG C, process time is 0.5h～20.0h, preferably 1.0h～6.0h, second segment is 180 DEG C～400 DEG C in temperature, preferably 200 DEG C～350 DEG C, process time is 0.5h～20.0h, preferably 1.0h～6.0h.Heat treatment can be carried out in oxygen-containing atmosphere, oxygen concentration is not particularly limited, such as air atmosphere, it is also possible to carry out in an inert atmosphere, such as nitrogen atmosphere etc..
Modified catalyst for hydro-upgrading carrier prepared by the inventive method, with a small amount of specific water-soluble silicon oil-impregnated catalyst for hydro-upgrading carrier, it is set to load on the ad-hoc location of catalyst for hydro-upgrading carrier surface using the effect of the hydrophilic and hydrophobic grouping of water-soluble silicon oil, and the zirconium-containing compound for impregnating simultaneously or afterwards is evenly spread to around silica group, by suitable heat treatment, the Si for being loaded, the more preferable coordinative role of Zr energy, the silicon zirconium hydroxyl being more evenly distributed is formed in carrier surface ad-hoc location, on the one hand carrier surface is made to form more acid suitable acid centres, and be engaged with the former acidic site in carrier, make the acidity and acid distribution of carrier more reasonable, reduce strong acid content, more B acid sites are provided, on the other hand, be conducive to adjusting the distribution of the hydrogenation sites that the follow-up active metal using infusion process load is formed, and the cooperation of the acid centre of hydrogenation sites and carrier, so as to improve the performance of catalyst.
Modified catalyst for hydro-upgrading carrier prepared by the inventive method, it is especially suitable as the carrier of diesel oil hydrogenation modification catalyst, the catalyst is used for during diesel oil hydrogenation modification, with deep hydrodesulfurizationof activity, and can keep improving the combination properties such as Cetane number in the case that diesel yield is higher.
Specific embodiment
In the present invention, cloud point refers to that the water-soluble silicon oil solution that mass concentration is 1% is heated to after muddiness and stops heating, temperature of the lower observation aqueous solution of stirring by muddy change when limpid.
The method of modifying of the catalyst for hydro-upgrading carrier provided according to the present invention, it can specifically adopt following steps：
1st, soluble zirconium-containing compound is configured into solution A, wherein zirconium-containing compound concentration is calculated as 0.1g/100mL ~ 32g/100mL with zirconium oxide；
2nd, water-soluble silicon oil is configured into solution B, wherein water-soluble silicon oil concentration is calculated as 0.1g/100mL ~ 20g/100mL with silica；
3rd, soluble zirconium-containing compound and water-soluble silicon oil are hybridly prepared into solution C, wherein zirconium-containing compound concentration is calculated as 0.1g/100mL ~ 16g/100mL with zirconium oxide, and water-soluble silicon oil concentration is calculated as 0.1g/100mL ~ 10g/100mL with silica；
4th, water-soluble silicon oil and zirconium-containing compound are guided on catalyst for hydro-upgrading carrier using a kind of at least following mode：
I, impregnate catalyst for hydro-upgrading carrier with solution C, preferably through health after, then by two sections of heat treatments, obtain modified catalyst for hydro-upgrading carrier；In wherein two sections heat treatments, first paragraph is 60 DEG C～150 DEG C in temperature, preferably 90 DEG C～120 DEG C, process time is 0.5h～20.0h, preferably 1.0h～6.0h, second segment is 180 DEG C～400 DEG C, preferably 200 DEG C～350 DEG C in temperature, process time is 0.5h～20.0h, preferably 1.0h～6.0h；
II, impregnate catalyst for hydro-upgrading carrier with solution B, preferably through health after, by Low Temperature Heat Treatment, then dipping solution A, preferably through health after, then by two sections of heat treatments, obtain modified catalyst for hydro-upgrading carrier；Wherein Low Temperature Heat Treatment is that process time is 0.5h～20.0h, preferably 1.0h～6.0h at 60 DEG C～150 DEG C, preferably 90 DEG C～120 DEG C；In two sections of heat treatments, first paragraph is 60 DEG C～150 DEG C in temperature, preferably 90 DEG C～120 DEG C, process time is 0.5h～20.0h, preferably 1.0h～6.0h, second segment is 180 DEG C～400 DEG C, preferably 200 DEG C～350 DEG C in temperature, process time is 0.5h～20.0h, preferably 1.0h～6.0h.
In the inventive method, heat treatment can be carried out in oxygen-containing atmosphere, oxygen concentration is not particularly limited, such as air atmosphere, it is also possible to be carried out in an inert atmosphere, such as nitrogen atmosphere etc..
The inventive method is not specifically limited to the conditioned time after dipping solution, conditioned time is defined by can guarantee that water-soluble silicon oil and the uniform adsorption of zirconium-containing compound component, those skilled in the art can be judged to determine conditioned time according to the absorption situation of the viscosity situation of solution and solution.
The technical scheme that the invention is further illustrated by the following examples, but invention should not be deemed limited in this embodiment.In the present invention, wt% is mass fraction, without specified otherwise, is air atmosphere.
In the present invention, meleic acid amount, B acid and L acid are determined using Pyridine adsorption IR spectra method, and wherein meleic acid amount is the sum of B acid and L acid acid amounts.
In embodiment, water-soluble silicon oil A used is by the industrial organosilicon new material company production in Qingdao, SiO2Content is 15wt%, viscosity（25℃）1500 ~ 5000 mPa.s, cloud point is 47 DEG C；Water-soluble silicon oil B is produced by Laiyang is along bright Chemical Co., Ltd, SiO2Content is 9wt%, viscosity（25℃）For 500～1500mPa.s, cloud point is 45～55 DEG C；Water-soluble silicon oil C is produced by Laiyang Sheng Bang organosilicons Science and Technology Ltd.,SiO2Content is 30wt%, viscosity（25℃）For 600～5000mPa.s, cloud point is 42～46 DEG C.
In embodiment, the property of beta-molecular sieve B1 used is as follows：SiO2/Al2O3Mol ratio is 40, specific surface area 530m2/ g, total pore volume 0.45mL/g, meleic acid amount 0.44mmol/g；The property of beta-molecular sieve B2 used is as follows：SiO2/Al2O3Mol ratio is 70, specific surface area 548m2/ g, total pore volume 0.46mL/g, meleic acid amount 0.39mmol/g.The property of Y type molecular sieve Y1 used is as follows：SiO2/Al2O3Mol ratio is 12, specific surface area 628m2/ g, total pore volume 0.48mL/g, meleic acid amount 0.49mmol/g；The property of Y type molecular sieve Y2 used is as follows：SiO2/Al2O3Mol ratio is 25, specific surface area 640m2/ g, total pore volume 0.49mL/g, meleic acid amount 0.45mmol/g.
The diameter of cylindrical vector used is about 1.2mm in embodiment, and length is about 3 ~ 5mm, and its physico-chemical property is as shown in table 1.
The preparation of Z1：By beta-molecular sieve B1, macroporous aluminium oxide (pore volume 1.0mL/g, specific surface area 400m2/ g), adhesive (mol ratio of nitric acid and little porous aluminum oxide is 0.3) be put into mixed grind in roller, add water, be rolled into paste, extrusion, extrusion bar then in 550 DEG C of roastings 4 hours, obtains carrier Z1 in 110 DEG C of dryings 4 hours.
The preparation of Z2：By beta-molecular sieve B1, Y type molecular sieve Y1, macroporous aluminium oxide (pore volume 1.0mL/g, specific surface area 400m2/ g), adhesive (mol ratio of nitric acid and little porous aluminum oxide is 0.3) be put into mixed grind in roller, add water, be rolled into paste, extrusion, extrusion bar then in 550 DEG C of roastings 4 hours, obtains carrier Z2 in 110 DEG C of dryings 4 hours.
The preparation of Z3：By beta-molecular sieve B2, Y type molecular sieve Y2, macroporous aluminium oxide (pore volume 1.0mL/g, specific surface area 400m2/ g), adhesive (mol ratio of nitric acid and little porous aluminum oxide is 0.3) be put into mixed grind in roller, add water, be rolled into paste, extrusion, extrusion bar then in 550 DEG C of roastings 4 hours, obtains carrier Z3 in 110 DEG C of dryings 4 hours.
The physico-chemical property of catalyst for hydro-upgrading carrier used in the embodiment of table 1
| Project | Z1 | Z2 | Z3 |
| Beta-molecular sieve content, wt% | _ | 4 | 6 |
| Y molecular sieve content, wt% | 10 | 6 | 6 |
| Aluminum oxide | Surplus | Surplus | Surplus |
| Specific surface area, m2/g | 350 | 341 | 362 |
| Pore volume, mL/g | 0.63 | 0.64 | 0.64 |
| Saturation liquid absorption, mL/100g | 72 | 73 | 73 |
Mo predecessors in the present embodiment in Mo, Ni, P maceration extract used are MoO3, Ni predecessors are basic nickel carbonate, and P predecessors are phosphoric acid.
Embodiment 1
Zirconium nitrate 18.6g is weighed, appropriate amount of deionized water dissolving is added, makes volume be 105mL, obtained solution A1.Water-soluble silicon oil A 21.0g are weighed, appropriate amount of deionized water dissolving is added, makes volume be 105mL, obtained solution B1.Under stirring, 35mL B1 solution is poured slowly into 35mL A1 solution, and adds appropriate amount of deionized water, make final volume be 72mL, be configured to C1 solution.
100g catalyst for hydro-upgrading carrier Z1 are taken, solution C 1 is uniformly sprayed on catalyst for hydro-upgrading carrier Z1, after health 10 hours, 100 DEG C of heat treatment 2h of Jing, 230 DEG C of heat treatment 2h obtain modified carrier S 1.
Take 100g catalyst for hydro-upgrading carrier Z1, the deionized water of 35mL solution Bs 1 is diluted into 72mL, uniformly it is sprayed on carrier Z1, health 10 hours, Jing after 100 DEG C are heat-treated 2h, again 35mL A1 solution deionized waters are diluted into 71mL, uniform sprinkling on this carrier, after health 3 hours, 100 DEG C of heat treatment 2h of Jing, 230 DEG C of heat treatment 2h, obtain modified carrier S 2.
Embodiment 2
Zirconium oxychloride 13.0g, water-soluble silicon oil B 36.0g are weighed, appropriate amount of deionized water dissolving is added, makes volume be 146mL, obtained solution C2.
100g catalyst for hydro-upgrading carrier Z1 are taken, 73mL solution Cs 2 are uniformly sprayed on catalyst for hydro-upgrading carrier Z1, after health 10 hours, 100 DEG C of heat treatment 2h of Jing, 230 DEG C of heat treatment 2h obtain modified carrier S 3.
100g catalyst for hydro-upgrading carrier Z1 are taken, 73mL solution Cs 2 are uniformly sprayed on catalyst for hydro-upgrading carrier Z1, after health 10 hours, in a nitrogen atmosphere, 100 DEG C of heat treatment 2h of Jing, 350 DEG C of heat treatment 2h obtain modified carrier S 4.
Embodiment 3
Zirconium nitrate 3.6g, water-soluble silicon oil C 2.7g are weighed, appropriate amount of deionized water dissolving is added, makes volume be 73mL, obtained solution C3.
100g catalyst for hydro-upgrading carrier Z2 are taken, solution C 3 is uniformly sprayed on catalyst for hydro-upgrading carrier Z2, after health 10 hours, 100 DEG C of heat treatment 2h of Jing, 260 DEG C of heat treatment 2h obtain modified carrier S 5.
Embodiment 4
Zirconium nitrate 16.5g, the g of water-soluble silicon oil C 12.5 are weighed, appropriate amount of deionized water dissolving is added, makes volume be 73mL, obtained solution C4.
100g catalyst for hydro-upgrading carrier Z2 are taken, solution C 4 is uniformly sprayed on catalyst for hydro-upgrading carrier Z2, after health 10 hours, 100 DEG C of heat treatment 2h of Jing, 260 DEG C of heat treatment 2h obtain modified carrier S 6.
Embodiment 5
Zirconium nitrate 7.2g, water-soluble silicon oil C 2.7g are weighed, appropriate amount of deionized water dissolving is added, makes volume be 73mL, obtained solution C5.
100g catalyst for hydro-upgrading carrier Z3 are taken, solution C 3 is uniformly sprayed on catalyst for hydro-upgrading carrier Z3, after health 10 hours, 100 DEG C of heat treatment 2h of Jing, 260 DEG C of heat treatment 2h obtain modified carrier S 7.
Comparative example 1
Water-soluble silicon oil A 7.0g are weighed, appropriate amount of deionized water dissolving is added, makes volume be 72mL, obtained solution B2.100g catalyst for hydro-upgrading carrier Z1 are taken, solution B 2 is uniformly sprayed on catalyst for hydro-upgrading carrier Z1, after health 10 hours, 100 DEG C of heat treatment 2h of Jing, 230 DEG C of heat treatment 2h obtain modified carrier DS1.
Comparative example 2
Zirconium nitrate 6.2g is weighed, appropriate amount of deionized water dissolving is added, makes volume be 72mL, be configured to A2 solution.100g catalyst for hydro-upgrading carrier Z1 are taken, solution A 2 is uniformly sprayed on catalyst for hydro-upgrading carrier Z1, after health 10 hours, 100 DEG C of heat treatment 2h of Jing, 230 DEG C of heat treatment 2h obtain modified carrier DS2.
Comparative example 3
Compared with the preparation method of carrier S 2 in embodiment 2, this comparative example is first to introduce zirconates, and water-soluble silicon oil is introduced afterwards, and detailed process is as follows：
Take 100g catalyst for hydro-upgrading carrier Z1,35mL A1 solution deionized waters are diluted into 72mL, uniform sprinkling on this carrier, after health 3 hours, 100 DEG C of heat treatment 2h of Jing, again the deionized water of 35mL solution Bs 1 is diluted into 71mL, uniformly it is sprayed on carrier Z1, health 10 hours, Jing after 100 DEG C are heat-treated 2h, 230 DEG C of heat treatment 2h, obtain modified carrier DS3.
Table 2
Embodiment and comparative example modified catalyst for hydro-upgrading carrier property
| Bearer number | S1 | S2 | S3 | S4 | S5 | S6 | S7 |
| Introduce ZrO2Amount, wt% | 1.7 | 1.7 | 2.3 | 2.3 | 1.0 | 4.4 | 2.0 |
| Introduce SiO2Amount, wt% | 1.0 | 1.0 | 1.5 | 1.5 | 0.8 | 3.5 | 0.8 |
| Specific surface area, m2/g | 304 | 302 | 295 | 292 | 312 | 279 | 311 |
| Pore volume, mL/g | 0.61 | 0.61 | 0.60 | 0.60 | 0.62 | 0.57 | 0.62 |
| Infrared total acid, mmol/g | 0.528 | 0.507 | 0.522 | 0.535 | 0.508 | 0.482 | 0.512 |
| B is sour, mmol/g | 0.122 | 0.119 | 0.125 | 0.131 | 0.118 | 0.110 | 0.119 |
| L is sour, mmol/g | 0.406 | 0.388 | 0.397 | 0.404 | 0.390 | 0.372 | 0.393 |
| Strong acid content *, % | 15.3 | 14.8 | 14.5 | 14.9 | 15.1 | 13.9 | 14.8 |
* note：In table 2, strong acid content refers to that acid amount when measuring using determination of infrared spectroscopy acid more than 450 DEG C accounts for the percentage of total acid content.
Continued 2
| Bearer number | Z1 | Z2 | Z3 | DS1 | DS2 | DS3 |
| Introduce ZrO2Amount, wt% | - | - | - | - | 1.7 | 1.7 |
| Introduce SiO2Amount, wt% | - | - | - | 1.0 | - | 1.0 |
| Specific surface area, m2/g | 350 | 341 | 362 | 321 | 323 | 303 |
| Pore volume, mL/g | 0.63 | 0.64 | 0.64 | 0.62 | 0.62 | 0.61 |
| Infrared total acid, mmol/g | 0.445 | 0.457 | 0.440 | 0.467 | 0.429 | 0.448 |
| B is sour, mmol/g | 0.075 | 0.078 | 0.076 | 0.080 | 0.061 | 0.071 |
| L is sour, mmol/g | 0.370 | 0.379 | 0.364 | 0.387 | 0.368 | 0.377 |
| Strong acid content *, % | 24.7 | 23.9 | 24.5 | 20.8 | 12.5 | 13.5 |
Embodiment 6 ~ 12
Take respectively carrier strip S1, S2 in the embodiment of the present invention, S3, S4, S5,
S6 and S7, is distinguished after incipient impregnation 2h with Mo, Ni, P solution, and 120 DEG C are dried 3h, 480 DEG C of roasting 2h, respectively obtain catalyst T1, T2, T3, T4, T5, T6 and T7.
Comparative example 4 ~ 8
Carrier strip DS1, DS2 and DS3 of comparative example of the present invention are taken respectively, and carrier Z1 and Z2 used in embodiment, with Mo, Ni, P solution difference incipient impregnation 2h after, 120 DEG C are dried 3h, 480 DEG C of roasting 2h, respectively obtain catalyst DT1, DT2, DT3, DT4 and DT5.
The composition of the catalyst of table 3
| Catalyst is constituted | T1 | T2 | T3 | T4 | T5 | T6 | T7 |
| MoO3, wt% | 23.52 | 23.54 | 23.71 | 23.80 | 23.75 | 23.81 | 23.73 |
| NiO, wt% | 3.97 | 4.11 | 3.98 | 3.96 | 4.08 | 4.06 | 4.05 |
| P, wt% | 1.25 | 1.26 | 1.22 | 1.23 | 1.25 | 1.23 | 1.24 |
Continued 3
| Catalyst is constituted | DT1 | DT2 | DT3 | DT4 | DT5 |
| MoO3, wt% | 23.85 | 23.77 | 23.81 | 23.79 | 23.88 |
| NiO, wt% | 3.99 | 3.95 | 4.07 | 4.09 | 3.98 |
| P, wt% | 1.23 | 1.25 | 1.22 | 1.24 | 1.23 |
Embodiment 13
The present embodiment is the henchnmrk test of catalyst.
Catalyst performance evaluation experiment is carried out on 100mL small hydrogenation devices, and presulfurization is carried out to catalyst before performance evaluation.Evaluating catalyst condition is in reaction stagnation pressure 10.0MPa, the h of volume space velocity 1.5 during liquid-1, hydrogen to oil volume ratio 800：1, reaction temperature is 365 DEG C.Henchnmrk test raw material oil nature is shown in Table 4, Evaluation results are shown in Table 5, from data in table, the catalyst for hydro-upgrading prepared with method of modifying of the present invention, catalyst it is desulphurizing activated apparently higher than comparative example catalyst, the Cetane number of diesel oil is improved into more than 10 units under conditions of diesel yield is kept not less than 98%, product quality has obtained good improvement.
Table
4
Raw material oil nature
| Feedstock oil | Catalytic diesel oil |
| Density (20 DEG C), g/cm3 | 0.9579 |
| Boiling range/DEG C | |
| IBP/ EBP | 188/375 |
| Condensation point, DEG C | 5 |
| Total sulfur, μ g/g | 8785 |
| 4,6-BMDBT contents, μ g/g | 100.5 |
| Nitrogen, μ g/g | 1158 |
| Cetane number | 27 |
| C, wt% | 87.63 |
| H, wt% | 11.05 |
Table
5
Catalyst performance
Evaluation result
| Catalyst is numbered | T1 | T2 | T3 | T4 | T5 | T6 | T7 |
| Diesel oil | |||||||
| Yield, wt% | 98.5 | 98.5 | 98.3 | 98.4 | 98.6 | 98.6 | 98.5 |
| Density (20 DEG C), g/cm3 | 0.8403 | 0.8402 | 0.8405 | 0.8402 | 0.8403 | 0.8401 | 0.8401 |
| T95, DEG C | 350 | 351 | 351 | 349 | 349 | 350 | 350 |
| Condensation point, DEG C | -21 | -22 | -21 | -20 | -22 | -21 | -22 |
| Cetane number | 47.9 | 48.1 | 48.0 | 48.2 | 48.3 | 47.7 | 48.1 |
| Sulphur, μ g/g | 7 | 6 | 6 | 5 | 6 | 6 | 6 |
Continued 5
| Catalyst is numbered | DT1 | DT2 | DT3 | DT4 | DT5 |
| Diesel oil | |||||
| Yield, wt% | 97.5 | 97.6 | 97.3 | 97.1 | 97.1 |
| Density (20 DEG C), g/cm3 | 0.8396 | 0.8415 | 0.8401 | 0.8378 | 0.8382 |
| T95, DEG C | 346 | 352 | 347 | 345 | 345 |
| Condensation point, DEG C | -20 | -17 | -19 | -21 | -22 |
| Cetane number | 45.6 | 43.0 | 44.5 | 44.8 | 45.0 |
| Sulphur, μ g/g | 10 | 19 | 14 | 13 | 12 |
Claims (21)
1. a kind of method of modifying of catalyst for hydro-upgrading carrier, including：The preparation of catalyst for hydro-upgrading carrier, by water-soluble silicon oil and soluble zirconium-containing compound catalyst for hydro-upgrading carrier is sequentially or simultaneously introduced, and after heat treatment, modified catalyst for hydro-upgrading carrier is obtained.
2. in accordance with the method for claim 1, it is characterised in that：Described catalyst for hydro-upgrading carrier, it is with aluminum oxide and molecular sieve as key component, with or without adjuvant component, wherein adjuvant component is one or more in fluorine, silicon, phosphorus, titanium, zirconium, boron, and content of the adjuvant component in terms of element in the carrier is in below 15wt%.
3. in accordance with the method for claim 1, it is characterised in that：The property of the catalyst for hydro-upgrading carrier is as follows：Specific surface area is 200 ~ 550m2/ g, pore volume is 0.4 ~ 1.3mL/g；It is preferably as follows：Specific surface area is 280 ~ 450m2/ g, pore volume is 0.6 ~ 1.0mL/g.
4. in accordance with the method for claim 1, it is characterised in that：Described catalyst for hydro-upgrading carrier is prepared using kneading method or mixing plastic method.
5. according to the method described in claim 1 or 4, it is characterised in that：Described catalyst for hydro-upgrading carrier is that Jing is molded and through the catalyst for hydro-upgrading carrier of high-temperature roasting, and the condition of high-temperature roasting is as follows：In 450 DEG C～1000 DEG C roasting 1.0h～20.0h.
6. in accordance with the method for claim 2, it is characterised in that：On the basis of the weight of catalyst for hydro-upgrading carrier, the content of molecular sieve is 3% ~ 35%, and the content of aluminum oxide is 65% ~ 97%, and preferably the content of molecular sieve is 3% ~ 20%, and the content of aluminum oxide is 80% ~ 97%.
7. according to the method described in claim 2 or 6, it is characterised in that：Described molecular sieve is Y type molecular sieve and/or beta-molecular sieve.
8. in accordance with the method for claim 7, it is characterised in that：Described molecular sieve is hydrogen type molecular sieve, and wherein beta-molecular sieve property is as follows：SiO2/Al2O3Mol ratio is 30 ~ 150, specific surface area 400m2/ g～750m2/ g, total pore volume 0.30mL/g～0.55mL/g, meleic acid 0.1～0.8mmol/g of amount；Y type molecular sieve property is as follows：SiO2/Al2O3Mol ratio is 5 ~ 50, specific surface area 450m2/ g～800m2/ g, total pore volume 0.30mL/g～0.60mL/g, meleic acid 0.2～0.9mmol/g of amount.
9. in accordance with the method for claim 1, it is characterised in that：The silicone content being introduced into carrier by water-soluble silicon oil accounts for the 0.2%～7.0% of modified catalyst for hydro-upgrading vehicle weight in terms of silica, and preferably 0.3%～4.0%, more preferably 0.5% ~ 1.8%.
10. according to the method described in claim 1 or 9, it is characterised in that：The zirconium content being introduced into carrier by soluble zirconium-containing compound accounts for the 0.4%～10.0% of modified catalyst for hydro-upgrading vehicle weight in terms of zirconium oxide, and preferably 0.5%～5.0%, more preferably 0.5%～2.5%.
11. according to the method described in claim 1 or 9, it is characterised in that：Mol ratio that the consumption of water-soluble silicon oil and soluble zirconium-containing compound counted with silica and zirconium oxide respectively is introduced as 0.04 ~ 36.0, preferably 0.12 ~ 16.0, more preferably 0.40 ~ 7.5.
12. in accordance with the method for claim 1, it is characterised in that：The property of described water-soluble silicon oil is as follows：Viscosity when 25 DEG C is 200 ~ 7000mPa.s, and cloud point is 30 ~ 100 DEG C, is preferably as follows：Viscosity when 25 DEG C is 500 ~ 5000mPa.s, and cloud point is 40 ~ 65 DEG C.
13. according to the method described in claim 1 or 12, it is characterised in that：Described water-soluble silicon oil is polyether modified silicon oil.
14. in accordance with the method for claim 1, it is characterised in that：Described soluble zirconium-containing compound is one or more in zirconium nitrate, zirconium chloride, zirconium oxychloride.
15. in accordance with the method for claim 1, it is characterised in that：Described heat treatment is 60 DEG C～150 DEG C in temperature using two sections of heat treatments, first paragraph, and process time is 0.5h～20.0h, and second segment is 180 DEG C～400 DEG C in temperature, and process time is 0.5h～20.0h, is preferably as follows：First paragraph is 90 DEG C～120 DEG C in temperature, and process time is 1.0h～6.0h, and second segment is 200 DEG C～350 DEG C in temperature, and process time is 1.0h～6.0h.
16. in accordance with the method for claim 1, it is characterised in that：Water-soluble silicon oil and soluble zirconium-containing compound are successively incorporated on carrier, its incorporation way adopts infusion process, first water-soluble silicon oil is impregnated on carrier, Jing after health, by Low Temperature Heat Treatment, then soluble zirconium-containing compound is impregnated on carrier again, by two sections of heat treatments, obtains modified catalyst for hydro-upgrading carrier；Wherein Low Temperature Heat Treatment is that process time is 0.5h～20.0h at 60 DEG C～150 DEG C.
17. in accordance with the method for claim 16, it is characterised in that：In the dipping solution that soluble zirconium-containing compound is made into, zirconium-containing compound concentration is calculated as 0.1g/100mL ~ 32g/100mL with zirconium oxide；In the dipping solution that water-soluble silicon oil is made into, water-soluble silicon oil concentration is calculated as 0.1g/100mL ~ 20g/100mL with silica.
18. in accordance with the method for claim 1, it is characterised in that：Water-soluble silicon oil and soluble zirconium-containing compound are incorporated on carrier simultaneously, its incorporation way adopts infusion process, will water-soluble silicon oil and soluble zirconium-containing compound be impregnated on carrier simultaneously, Jing after health, by two sections of heat treatments, modified catalyst for hydro-upgrading carrier is obtained.
19. in accordance with the method for claim 18, it is characterised in that：By in the dipping solution of soluble zirconium-containing compound and water-soluble silicon oil mixed preparing, zirconium-containing compound concentration is calculated as 0.1g/100mL ~ 16g/100mL with zirconium oxide, and water-soluble silicon oil concentration is calculated as 0.1g/100mL ~ 10g/100mL with silica.
20. according to the arbitrary described method of claim 16 ~ 19, it is characterised in that：Infusion process adopts an incipient impregnation.
21. according to the arbitrary described method of claim 16 ~ 19, it is characterised in that：Two sections of described heat treatments, first paragraph is 60 DEG C～150 DEG C in temperature, and process time is 0.5h～20.0h, and second segment is 180 DEG C～400 DEG C in temperature, and process time is 0.5h～20.0h, is preferably as follows：First paragraph is 90 DEG C～120 DEG C in temperature, and process time is 1.0h～6.0h, and second segment is 200 DEG C～350 DEG C in temperature, and process time is 1.0h～6.0h.
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| CN108786928A (en) * | 2017-07-05 | 2018-11-13 | 中国石油天然气股份有限公司 | Diesel hydrogenation catalyst carrier and preparation method thereof |
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| CN109772469A (en) * | 2017-11-13 | 2019-05-21 | 中国石油化工股份有限公司 | A kind of silicon modified zirconia catalyst carrier and its preparation method and application |
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| CN106669863B (en) | 2019-06-11 |
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