CN108620077A - Low-temperature Fischer-Tropsch synthesis catalyst and preparation method and application thereof - Google Patents
Low-temperature Fischer-Tropsch synthesis catalyst and preparation method and application thereof Download PDFInfo
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- CN108620077A CN108620077A CN201710161306.9A CN201710161306A CN108620077A CN 108620077 A CN108620077 A CN 108620077A CN 201710161306 A CN201710161306 A CN 201710161306A CN 108620077 A CN108620077 A CN 108620077A
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- catalyst
- temperature
- silicon source
- solution
- sio
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Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 161
- 230000015572 biosynthetic process Effects 0.000 title claims abstract description 33
- 238000003786 synthesis reaction Methods 0.000 title claims abstract description 33
- 238000002360 preparation method Methods 0.000 title claims abstract description 21
- 238000006243 chemical reaction Methods 0.000 claims abstract description 52
- 238000000034 method Methods 0.000 claims abstract description 46
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 39
- 239000010703 silicon Substances 0.000 claims abstract description 39
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 39
- 239000000243 solution Substances 0.000 claims abstract description 39
- 238000000975 co-precipitation Methods 0.000 claims abstract description 35
- 239000002002 slurry Substances 0.000 claims abstract description 33
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims abstract description 30
- 239000011591 potassium Substances 0.000 claims abstract description 30
- 229910052700 potassium Inorganic materials 0.000 claims abstract description 30
- 229910052751 metal Inorganic materials 0.000 claims abstract description 22
- 239000002184 metal Substances 0.000 claims abstract description 22
- 239000007864 aqueous solution Substances 0.000 claims abstract description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000007790 solid phase Substances 0.000 claims abstract description 16
- 230000001376 precipitating effect Effects 0.000 claims abstract description 15
- 238000005406 washing Methods 0.000 claims abstract description 14
- 150000003839 salts Chemical class 0.000 claims abstract description 13
- 239000007788 liquid Substances 0.000 claims abstract description 11
- 238000001694 spray drying Methods 0.000 claims abstract description 11
- 238000000926 separation method Methods 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims abstract description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 94
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 50
- 239000000377 silicon dioxide Substances 0.000 claims description 48
- 229910052681 coesite Inorganic materials 0.000 claims description 46
- 229910052906 cristobalite Inorganic materials 0.000 claims description 46
- 229910052682 stishovite Inorganic materials 0.000 claims description 46
- 229910052905 tridymite Inorganic materials 0.000 claims description 46
- 239000010949 copper Substances 0.000 claims description 38
- 239000011148 porous material Substances 0.000 claims description 26
- 230000032683 aging Effects 0.000 claims description 24
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 claims description 16
- 239000004111 Potassium silicate Substances 0.000 claims description 15
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 claims description 15
- 229910052913 potassium silicate Inorganic materials 0.000 claims description 15
- 235000019353 potassium silicate Nutrition 0.000 claims description 15
- 239000003153 chemical reaction reagent Substances 0.000 claims description 14
- 208000011580 syndromic disease Diseases 0.000 claims description 14
- 229910052742 iron Inorganic materials 0.000 claims description 13
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 11
- VCJMYUPGQJHHFU-UHFFFAOYSA-N iron(3+);trinitrate Chemical compound [Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VCJMYUPGQJHHFU-UHFFFAOYSA-N 0.000 claims description 8
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 8
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 6
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 6
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 5
- 239000000908 ammonium hydroxide Substances 0.000 claims description 5
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical group [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 4
- 239000001099 ammonium carbonate Substances 0.000 claims description 4
- 230000009467 reduction Effects 0.000 claims description 4
- 239000006188 syrup Substances 0.000 claims description 4
- 235000020357 syrup Nutrition 0.000 claims description 4
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 claims description 3
- 229910052684 Cerium Inorganic materials 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 229910052747 lanthanoid Inorganic materials 0.000 claims description 3
- 150000002602 lanthanoids Chemical group 0.000 claims description 3
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052779 Neodymium Inorganic materials 0.000 claims description 2
- 239000004115 Sodium Silicate Substances 0.000 claims description 2
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 claims description 2
- 235000012501 ammonium carbonate Nutrition 0.000 claims description 2
- VYLVYHXQOHJDJL-UHFFFAOYSA-K cerium trichloride Chemical compound Cl[Ce](Cl)Cl VYLVYHXQOHJDJL-UHFFFAOYSA-K 0.000 claims description 2
- OZECDDHOAMNMQI-UHFFFAOYSA-H cerium(3+);trisulfate Chemical compound [Ce+3].[Ce+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O OZECDDHOAMNMQI-UHFFFAOYSA-H 0.000 claims description 2
- 229910000333 cerium(III) sulfate Inorganic materials 0.000 claims description 2
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 claims description 2
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 claims description 2
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims description 2
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 claims description 2
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 claims description 2
- 229910000360 iron(III) sulfate Inorganic materials 0.000 claims description 2
- 229910052746 lanthanum Inorganic materials 0.000 claims description 2
- FYDKNKUEBJQCCN-UHFFFAOYSA-N lanthanum(3+);trinitrate Chemical group [La+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O FYDKNKUEBJQCCN-UHFFFAOYSA-N 0.000 claims description 2
- VQEHIYWBGOJJDM-UHFFFAOYSA-H lanthanum(3+);trisulfate Chemical compound [La+3].[La+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O VQEHIYWBGOJJDM-UHFFFAOYSA-H 0.000 claims description 2
- ICAKDTKJOYSXGC-UHFFFAOYSA-K lanthanum(iii) chloride Chemical compound Cl[La](Cl)Cl ICAKDTKJOYSXGC-UHFFFAOYSA-K 0.000 claims description 2
- CFYGEIAZMVFFDE-UHFFFAOYSA-N neodymium(3+);trinitrate Chemical compound [Nd+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O CFYGEIAZMVFFDE-UHFFFAOYSA-N 0.000 claims description 2
- OJSWEKSDNUORPG-UHFFFAOYSA-H neodymium(3+);trisulfate Chemical compound [Nd+3].[Nd+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O OJSWEKSDNUORPG-UHFFFAOYSA-H 0.000 claims description 2
- ATINCSYRHURBSP-UHFFFAOYSA-K neodymium(iii) chloride Chemical compound Cl[Nd](Cl)Cl ATINCSYRHURBSP-UHFFFAOYSA-K 0.000 claims description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 2
- 235000019795 sodium metasilicate Nutrition 0.000 claims description 2
- 229910052911 sodium silicate Inorganic materials 0.000 claims description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims 1
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims 1
- 239000000047 product Substances 0.000 abstract description 12
- 230000000694 effects Effects 0.000 abstract description 8
- 239000006227 byproduct Substances 0.000 abstract description 7
- 239000003795 chemical substances by application Substances 0.000 abstract description 4
- 239000012752 auxiliary agent Substances 0.000 abstract description 2
- 238000004537 pulping Methods 0.000 abstract 2
- 238000005299 abrasion Methods 0.000 abstract 1
- 150000001879 copper Chemical class 0.000 abstract 1
- 230000002431 foraging effect Effects 0.000 abstract 1
- 150000002505 iron Chemical class 0.000 abstract 1
- 238000000921 elemental analysis Methods 0.000 description 21
- 238000012876 topography Methods 0.000 description 21
- 230000000052 comparative effect Effects 0.000 description 12
- 238000005516 engineering process Methods 0.000 description 12
- 238000001914 filtration Methods 0.000 description 10
- 239000007789 gas Substances 0.000 description 10
- 238000001556 precipitation Methods 0.000 description 10
- 239000003643 water by type Substances 0.000 description 10
- 238000003756 stirring Methods 0.000 description 9
- 239000008367 deionised water Substances 0.000 description 8
- 229910021641 deionized water Inorganic materials 0.000 description 8
- 238000007599 discharging Methods 0.000 description 8
- 239000012065 filter cake Substances 0.000 description 7
- 239000000428 dust Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000013078 crystal Substances 0.000 description 5
- LDHBWEYLDHLIBQ-UHFFFAOYSA-M iron(3+);oxygen(2-);hydroxide;hydrate Chemical compound O.[OH-].[O-2].[Fe+3] LDHBWEYLDHLIBQ-UHFFFAOYSA-M 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 238000006722 reduction reaction Methods 0.000 description 5
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 4
- 235000011114 ammonium hydroxide Nutrition 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229910002651 NO3 Inorganic materials 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 238000005469 granulation Methods 0.000 description 3
- 230000003179 granulation Effects 0.000 description 3
- 239000004005 microsphere Substances 0.000 description 3
- 239000001103 potassium chloride Substances 0.000 description 3
- 235000011164 potassium chloride Nutrition 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 102100029203 F-box only protein 8 Human genes 0.000 description 2
- 101100334493 Homo sapiens FBXO8 gene Proteins 0.000 description 2
- 101000631695 Homo sapiens Succinate dehydrogenase assembly factor 3, mitochondrial Proteins 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 229910003205 Nd(NO3)3·6H2O Inorganic materials 0.000 description 2
- 102100028996 Succinate dehydrogenase assembly factor 3, mitochondrial Human genes 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- KMNWCNNLFBCDJR-UHFFFAOYSA-N [Si].[K] Chemical compound [Si].[K] KMNWCNNLFBCDJR-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 229910052738 indium Inorganic materials 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 235000011181 potassium carbonates Nutrition 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- 238000004438 BET method Methods 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 241000790917 Dioxys <bee> Species 0.000 description 1
- 229910017504 Nd(NO3)3 Inorganic materials 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- DQMUQFUTDWISTM-UHFFFAOYSA-N O.[O-2].[Fe+2].[Fe+2].[O-2] Chemical compound O.[O-2].[Fe+2].[Fe+2].[O-2] DQMUQFUTDWISTM-UHFFFAOYSA-N 0.000 description 1
- 229910003978 SiClx Inorganic materials 0.000 description 1
- DIFFLMNDXWOKQJ-UHFFFAOYSA-N [K].O[Si](O)(O)O Chemical compound [K].O[Si](O)(O)O DIFFLMNDXWOKQJ-UHFFFAOYSA-N 0.000 description 1
- 230000004308 accommodation Effects 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- PRKQVKDSMLBJBJ-UHFFFAOYSA-N ammonium carbonate Chemical class N.N.OC(O)=O PRKQVKDSMLBJBJ-UHFFFAOYSA-N 0.000 description 1
- 235000011162 ammonium carbonates Nutrition 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- HSJPMRKMPBAUAU-UHFFFAOYSA-N cerium(3+);trinitrate Chemical compound [Ce+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O HSJPMRKMPBAUAU-UHFFFAOYSA-N 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000010668 complexation reaction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000008246 gaseous mixture Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 238000005360 mashing Methods 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 239000010117 shenhua Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/83—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with rare earths or actinides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/002—Mixed oxides other than spinels, e.g. perovskite
-
- B01J35/51—
-
- B01J35/613—
-
- B01J35/615—
-
- B01J35/633—
-
- B01J35/635—
-
- B01J35/647—
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2/00—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon
- C10G2/30—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen
- C10G2/32—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen with the use of catalysts
- C10G2/33—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen with the use of catalysts characterised by the catalyst used
- C10G2/331—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen with the use of catalysts characterised by the catalyst used containing group VIII-metals
- C10G2/332—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen with the use of catalysts characterised by the catalyst used containing group VIII-metals of the iron-group
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2523/00—Constitutive chemical elements of heterogeneous catalysts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/70—Catalyst aspects
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/22—Higher olefins
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- General Chemical & Material Sciences (AREA)
- Catalysts (AREA)
Abstract
The invention relates to the field of Fischer-Tropsch synthesis, in particular to a low-temperature Fischer-Tropsch synthesis catalyst, and a preparation method and application thereof. The preparation method of the low-temperature Fischer-Tropsch synthesis catalyst comprises the following steps: (1) providing an aqueous solution containing iron salt, copper salt and auxiliary agent metal M salt, namely a first solution; providing an aqueous solution containing a precipitating agent and a silicon source, i.e. a second solution; carrying out coprecipitation reaction on the first solution and the second solution, then carrying out solid-liquid separation and washing the obtained solid phase; (2) pulping the washed solid phase with water to obtain slurry, introducing a potassium-containing silicon source, and adjusting the pH value of the obtained mixture to acidity for aging; (3) and carrying out solid-liquid separation on the aged slurry, pulping the obtained solid phase and water, and carrying out spray drying and roasting on the obtained slurry. The method can obtain high activity, low byproduct selectivity, and high C5+A low-temperature Fischer-Tropsch synthesis catalyst with product selectivity, high stability and high abrasion resistance.
Description
Technical field
The present invention relates to F- T synthesis fields, and in particular to Low Temperature Fischer Tropsch synthetic catalyst and its preparation method and application.
Background technology
Fischer-Tropsch synthesis refers to synthesis gas (H2+ CO) it is converted under the action of catalyst, under certain temperature and pressure
The reaction of hydrocarbon and other chemicals.Develop F- T synthesis technology to realizing that crude oil substitutes, ensures Chinese energy safety and Filter Tuber For Clean Coal
Trans-utilization has realistic meaning.F- T synthesis could only be realized under suitable catalyst action.The fifties in last century, south
Non- SASOL companies realize the quotient of Low Temperature Fischer Tropsch synthetic technology and high temperature fischer-tropsch synthesis using the patented technology of German Rule company
Industry application.For the reaction temperature of Low Temperature Fischer Tropsch synthetic technology between 210-280 DEG C, catalyst has precipitated iron catalyst and cobalt-based
Catalyst, reactor types have fixed bed reactors and paste state bed reactor.The reaction temperature of high temperature fischer-tropsch synthetic technology exists
Between 300-350 DEG C, reactor types are fixed fluidized bed and circulating fluid bed reactor.Precipitated iron catalyst is catalyzed with cobalt system
Agent is compared, and has cheap, in synthetic product alpha-olefin selection wider to the accommodation of reaction condition and synthesis gas composition
The higher feature of property.
Low Temperature Fischer Tropsch synthesis iron base catalyst passes through the development of many decades, and whole world technological development personnel are lasting to improve
Catalyst formulation and preparation method, many new useful auxiliary agents are added into Fe-Cu-K-SiO2Catalyst is improved in system
Performance.The Fe-Mn-Cu-K-SiO of more representational You Zhong sections synthetic oil exploitation2, the Fe-Cu-K-SiO of Yan Kuang exploitations2-
Na, the Fe-Co-Cu-K-SiO of Shenhua exploitation2Deng.
However, existing Low Temperature Fischer Tropsch synthesis Fe-series catalyst is still in activity, by-product selectivity, the selection of C5+ products
Property, have in many performances such as stability and wear resistence and need improvements.
Invention content
The purpose of the present invention is to provide a kind of high activity, low by-product selectivity, high C5+Selectivity of product, high stability
With the Low Temperature Fischer Tropsch synthetic catalyst of high-wearing feature and its preparation method and application.
To achieve the goals above, the first aspect of the present invention provides a kind of preparation side of Low Temperature Fischer Tropsch synthetic catalyst
Method, this method include：
(1) aqueous solution containing molysite, mantoquita and promoter metal M salt, i.e. the first solution are provided；There is provided containing precipitating reagent and
The aqueous solution of silicon source, i.e. the second solution；First solution and the second solution are subjected to coprecipitation reaction, are then separated by solid-liquid separation simultaneously
Washing gained solid phase；Temperature is 5-35 DEG C, pH value 4.5-9.5, time 5-60min；The pH for defining coprecipitation reaction is number
Value n, the temperature for defining coprecipitation reaction is numerical value T, and the temperature and pH of the coprecipitation reaction meet formula：N+0.16T=9-
14；The promoter metal M is lanthanide series metal；
(2) solid phase after washing is beaten with water, obtains slurries and introduces silicon source containing potassium, and adjust gained mixture
PH value to acidity to carry out aging；
(3) slurries after aging are separated by solid-liquid separation, gained solid phase is beaten with water, and it is dry that gained slurries carry out spraying
Dry and roasting；
Wherein, the dosage of the molysite, mantoquita, promoter metal M salt, silicon source and the silicon source containing potassium makes the catalyst of gained
In, Fe by weight2O3：Cu：K：M：SiO2=100：1-8：1-8：1-8：10-30.
Second aspect of the present invention provides the Low Temperature Fischer Tropsch synthetic catalyst made from the above method.
The present invention also provides a kind of method of synthesis gas through syrup state bed Fischer Tropsch synthetic reaction hydrocarbon compound, this method packets
It includes：In the presence of the reduction-state fischer-tropsch synthetic catalyst, CO and H will be contained2Synthesis gas temperature be 210-280 DEG C, pressure
Under power 1.0-5.0MPa, Fischer-Tropsch synthesis is carried out in paste state bed reactor；Wherein, the reduction-state fischer-tropsch synthetic catalyst
It is obtained through reduction by above-mentioned Low Temperature Fischer Tropsch synthetic catalyst.
The preparation method of the Low Temperature Fischer Tropsch synthetic catalyst of the present invention can obtain high activity, low by-product selectivity, height
C5+The Low Temperature Fischer Tropsch synthetic catalyst of selectivity of product, high stability and high-wearing feature.
Specific implementation mode
The endpoint of disclosed range and any value are not limited to the accurate range or value herein, these ranges or
Value should be understood as comprising the value close to these ranges or value.For numberical range, between the endpoint value of each range, respectively
It can be combined with each other between the endpoint value of a range and individual point value, and individually between point value and obtain one or more
New numberical range, these numberical ranges should be considered as specific open herein.
The first aspect of the present invention provides a kind of preparation method of Low Temperature Fischer Tropsch synthetic catalyst, and this method includes：
(1) aqueous solution containing molysite, mantoquita and promoter metal M salt, i.e. the first solution are provided；There is provided containing precipitating reagent and
The aqueous solution of silicon source, i.e. the second solution；First solution and the second solution are subjected to coprecipitation reaction, are then separated by solid-liquid separation simultaneously
Washing gained solid phase；Temperature is 5-35 DEG C, pH value 4.5-9.5, time 5-60min；The pH for defining coprecipitation reaction is number
Value n, the temperature for defining coprecipitation reaction is numerical value T, and the temperature and pH of the coprecipitation reaction meet formula：N+0.16T=9-
14；The promoter metal M is lanthanide series metal；
(2) solid phase after washing is beaten with water, obtains slurries and introduces silicon source containing potassium, and adjust gained mixture
PH value to acidity to carry out aging；
(3) slurries after aging are separated by solid-liquid separation, gained solid phase is beaten with water, and it is dry that gained slurries carry out spraying
Dry and roasting；
Wherein, the dosage of the molysite, mantoquita, promoter metal M salt, silicon source and the silicon source containing potassium makes the catalyst of gained
In, Fe by weight2O3：Cu：K：M：SiO2=100：1-8：1-8：1-8：10-30.
According to the present invention, in step (1), by the first solution containing metal salt and the second solution containing precipitating reagent into
Row coprecipitation reaction can obtain the precursor for preparing subsequent catalyst.It will be apparent to a skilled person that Fe3+It is heavy
Forming sediment, the product generated is sufficiently complex, and precipitation process is very sensitive to condition, the fluctuation (such as positive, reverse precipitation) of pH value, temperature
The fluctuation of degree, the length of ageing time can all influence the species of the precipitation particles generated, even if what is generated in precipitation is hydration
Iron oxide can also continue to be converted to other iron species, therefore the iron crystal grain generated in precipitation process is not single species, without
Same species and grain size affect the performance of final catalyst again.Wherein, full in the condition by controlling coprecipitation reaction
Sufficient temperature is 5-35 DEG C, pH value 4.5-9.5, and the time is 5-60min and meets formula n+0.16T=9-14 (preferably n+0.16T
=10-13) when, can obtain by hydrated ferric oxide be crystalline phase feature and with the characteristics of the multimodal pore distribution, superior performance urges
Agent precursor, to be conducive to obtain the catalyst of high activity and high-wearing feature energy.Especially in the item of control coprecipitation reaction
Part is in above range and under meeting the formula, and it is slower to play hydrated ferric oxide grain growth speed under low temperature in this way, and
It is not easy the di-iron trioxide crystal grain that dehydration generates, while the hydroxyl of aqua oxidation iron surface is more, is more conducive to hydrated ferric oxide
Intergranular reunion forms multiple dimensioned pore passage structure and reinforces intergranular bond strength, for the active surface of catalyst
Structure, pore size distribution structure and wear resistence have important contribution.Preferably, in step (1), the condition packet of the coprecipitation reaction
It includes：Temperature is 5-30 DEG C, pH value 5-9, time 10-50min.It is highly preferred that the temperature of the coprecipitation reaction is 8-20
℃。
According to the present invention, although the dosage control of the molysite, mantoquita, promoter metal M salt, silicon source and the silicon source containing potassium is existed
So that in the catalyst of gained, Fe by weight2O3：Cu：K：M：SiO2=100：1-8：1-8：1-8：10-30 can be obtained
The catalyst of effect needed for the present invention, but be to be able to obtain active higher, the lower, C of by-product selectivity5+Selectivity of product
Higher, stability higher and the higher Low Temperature Fischer Tropsch synthetic catalyst of wear resistence, it is preferable that the molysite, mantoquita, promoter metal
The dosage of M salt, silicon source and the sum of silicon source containing potassium make gained catalyst in, Fe by weight2O3：Cu：K：M：SiO2=100：
1-5：1-5：1-5：10-25, preferably Fe2O3：Cu：K：M：SiO2=100：1-4：1.5-4：2-5：10-23.
Wherein, there is no particular limitation to the molysite by the present invention, may be used this field routinely use it is various solvable
Property molysite, the specific example of the molysite for example can be it is one or more in ferric nitrate, ferric sulfate and iron chloride, preferably
Ferric nitrate.
Wherein, there is no particular limitation to the mantoquita by the present invention, may be used this field routinely use it is various solvable
Property mantoquita, the specific example of the mantoquita for example can be one or more in copper nitrate, copper sulphate and copper chloride.
Wherein, the promoter metal M is preferably one or more in La, Ce and Nd, it is highly preferred that the promoter metal
M salt is one kind in lanthanum nitrate, cerous nitrate, neodymium nitrate, lanthanum sulfate, cerous sulfate, Dineodymium trisulfate, lanthanum chloride, cerium chloride and neodymium chloride
Or it is a variety of.
Wherein, the silicon source may be used the various siliceous silicon sources that this field routinely uses, for example, can be potassium silicate,
It is one or more in sodium metasilicate, Ludox and Ludox containing potassium.Wherein, the Ludox containing potassium can be Ludox and/or
The mixture of potassium silicate and sylvite (such as one or more in potassium carbonate, potassium sulfate, potassium chloride and potassium nitrate), such as K2O：
SiO2For 50-200：100 Ludox and/or potassium silicate and the mixture of sylvite.The silicon source can provide in solid form,
It can also provide in form of an aqueous solutions, when providing as an aqueous solution, with SiO2The concentration of meter is, for example, 5-25 weights
Measure %.
Wherein, the various silicon sources containing potassium that this field routinely uses may be used in the silicon source containing potassium, such as can be silicic acid
Potassium and/or Ludox containing potassium.The Ludox containing potassium is as described above, and details are not described herein.
According to the present invention, the concentration of first solution can change in wider range, it was found by the inventors of the present invention that
When control in the first solution with Fe2O3When a concentration of 20-120g/L, especially 30-100g/L of the molysite of meter, it can obtain
The more excellent Low Temperature Fischer Tropsch synthetic catalyst of performance, the present inventor speculates the reason is that this concentration range is suitable for water
The growth of iron oxide nucleus is closed, concentration is excessive, and nucleus formation speed is too fast, and crystal grain is too small, influences the stability of catalyst；Concentration
It is too small, then a large amount of aqueous solution is consumed, hydrated ferric oxide nucleus is not easy to be molded.Most preferably, in the first solution with Fe2O3
A concentration of 30-60g/L of the molysite of meter.
Likewise, the concentration of second solution can also change in wider range, but the present inventor sends out
It is existing, as a concentration of 100-300g/L, especially 110-250g/L for controlling the precipitating reagent in the second solution, performance can be obtained
More excellent Low Temperature Fischer Tropsch synthetic catalyst, the present inventor speculate concentration and aqua oxidation the reason is that precipitating reagent
Iron crystal grain forms related, and when concentration is excessive, nucleus formation speed is too fast, and crystal grain is too small, influences the stability of catalyst；Concentration mistake
It is small, then a large amount of aqueous solution is consumed, hydrated ferric oxide nucleus is not easy to be molded.Most preferably, precipitating reagent in the second solution
A concentration of 120-200g/L.
Wherein, the various precipitating reagents that this field routinely uses may be used in the precipitating reagent, it is preferable that the precipitating reagent is
It is one or more in sodium carbonate, sodium bicarbonate, potassium carbonate, sodium hydroxide, potassium hydroxide, ammonium carbonate, ammonium hydrogen carbonate and ammonium hydroxide.
The concentration of the ammonium hydroxide for example can be that 20-28 weight % usually entirely calculate ammonium hydroxide when using ammonium hydroxide as precipitating reagent
For precipitating reagent, water therein is not removed.
According to the present invention, it is noted that silicon source containing potassium is divided into two parts (i.e. silicon source and silicon source containing potassium) in the present invention
Substep is introduced in catalyst, and the purpose done so is to enable to the gold in the Low Temperature Fischer Tropsch synthetic catalyst microballoon of gained
Belong to and layer distributed is presented, especially introduces part potassium and binder silica in follow-up step 2 so that potassium and dioxy
SiClx is formed as Low Temperature Fischer Tropsch synthetic catalyst microballoon outer layer, can more obtain the Low Temperature Fischer Tropsch synthesis iron of stability and wear resistence
Series catalysts, and coprecipitation process using low temperature, the aging in acidic environment after being introduced into silicon source containing potassium, also can iron,
Copper and M are uniformly distributed in the catalyst of kernel and form the channel that reactants and products pass in and out under permissible low temperature, to assign
Give high activity of catalyst, low by-product selectivity, high C5+Selectivity of product.Preferably, with SiO2Meter the silicon source and with
SiO2The weight ratio of the silicon source containing potassium of meter is 1：2-10, preferably 1：3-7.
According to the present invention, in step (1), the system after coprecipitation reaction be separated by solid-liquid separation filtering (example may be used
Such as filter, press filtration) mode, and gained solid phase is washed, for example, wash to filtrate conductivity be 1500 μ s/cm with
Under.
According to the present invention, the solid phase after washing is beaten with water in step (2), the slurries of gained in this way can be used for
Subsequent processing is carried out, in order to obtain stability and the higher catalyst of wear resistence, it is preferable that dosage of water makes at this
The ratio that a concentration of 4-9 weight % namely solid phase of the slurries of gained account for slurries is 4-9 weight %, preferably 4.5-8 weights
Measure %.
According to the present invention, potassium silicon source will be contained in step (2) and will be introduced into mashing gained slurries, to further be carried for catalyst
For potassium and silica.Wherein, the silicon source containing potassium can be introduced with the solid form of the silicon source containing potassium, can also be to contain potassium silicon source
Solution (such as with SiO2Meter a concentration of 10-25 weight %) form introduce, it is preferred to use the latter.It is stirred after introducing
Uniformly to mix, such as 5-120min is stirred under the mixing speed of 10-500rpm.
According to the present invention, needs to adjust pH before ageing to acidity, be convenient for precipitation to be impregnated with silicon source containing potassium in this way, also allow for
So that certain acid is soaked in precipitation, to which the microballoon with porous structure, formation and core can be formed in subsequent processing
The channel of the active metal contact of the heart.Preferably, in step (2), before aging adjust pH value to 4-6.5, more preferably to 4.5-6 this
Sample can not only keep the pore passage structure of catalyst appropriateness, can also keep the wear resistence and stability of catalyst appropriateness.Wherein,
It can be the inorganic acid that this field routinely uses, for example, hydrochloric acid, sulfuric acid, nitric acid etc. that system, which is adjusted to acid used in acidity, be somebody's turn to do
The concentration of acid for example can be 3-15 weight %.
According to the present invention, in order to coordinate the Coprecipitation of the present invention, aging condition of the invention is also relatively mild, in this way
Conducive to the catalyst of performance needed for the gained present invention.Under preferable case, in step (2), the condition of the aging includes：Temperature is
5-60 DEG C, time 30-150min.It is highly preferred that in step (2), the condition of the aging includes：Temperature is 15-55 DEG C, when
Between be 50-120min.According to the present invention, in step (3) by the system after aging carry out be separated by solid-liquid separation may be used filtering (such as
Suction filtration, press filtration etc.) mode, however gained solid phase is beaten, obtains slurries.The concentration of the slurries is preferably 12-25 weights
%, preferably 12-20 weight % are measured, subsequent spray drying and roasting are carried out using such slurries, with pattern needed for acquisition
Low Temperature Fischer Tropsch synthetic catalyst microballoon.
In the case of, according to the invention it is preferred to, the condition of the spray drying includes：Entrance wind-warm syndrome is 180-380 DEG C, outlet
Wind-warm syndrome is 70-180 DEG C.It is highly preferred that the condition of the spray drying includes：Entrance wind-warm syndrome is 220-380 DEG C, and outlet wind-warm syndrome is
100-140℃。
In the case of, according to the invention it is preferred to, the condition of the roasting includes：Temperature is 350-600 DEG C, time 1-15h.
It is highly preferred that the condition of the roasting includes：Temperature is 350-550 DEG C, and the time is 3-12h (more preferably 5-12h).
The present invention also provides the Low Temperature Fischer Tropsch synthetic catalysts made from the above method.
In the catalyst, Fe by weight2O3：Cu：K：M：SiO2=100：1-8：1-8：1-8：10-30, preferably with
The Fe of weight meter2O3：Cu：K：M：SiO2=100：1-5：1-5：1-5：10-25, it is highly preferred that Fe by weight2O3：Cu：K：
M：SiO2=100：1-4：1.5-4：2-5：10-23.
The catalyst is microspheroidal, the microballoon that for example, grain size is 30-150 μm.And the microballoon has the duct knot of appropriateness
Structure, it is preferable that total specific surface area of the catalyst is 60-185m2/ g, preferably 70-170m2/g；Its average pore size is preferably
10-25nm；It is preferably 0.2-0.8cm that its hole, which holds,3/ g, more preferably 0.2-0.7cm3/g。
The present invention also provides a kind of method of synthesis gas through syrup state bed Fischer Tropsch synthetic reaction hydrocarbon compound, this method packets
It includes：In the presence of the reduction-state fischer-tropsch synthetic catalyst, CO and H will be contained2Synthesis gas temperature be 210-280 DEG C, pressure
Under power 1.0-5.0MPa, Fischer-Tropsch synthesis is carried out in paste state bed reactor；Wherein, the reduction-state fischer-tropsch synthetic catalyst
It is obtained through reduction by above-mentioned Low Temperature Fischer Tropsch synthetic catalyst.
Wherein, the method that above-mentioned Low Temperature Fischer Tropsch synthetic catalyst restores may be used the method for this field routine into
Row, such as H may be used2, CO or arbitrary proportion H2, CO gaseous mixtures are as reducing agent.The condition of reduction may include：Temperature
For 200-300 DEG C (preferably 220-270 DEG C), pressure is 0.1-3MPa (preferably 0.1-2.9MPa), and the time is that 8-60h is (excellent
It is selected as 16-48h).
Wherein, the F- T synthesis condition may include：Temperature is 210-280 DEG C (preferably 240-270 DEG C), synthesis gas
Middle H2Molar ratio with CO is 1-5：1.The condition of the F- T synthesis may further include：Pressure be 0.5-6MPa (preferably
For 1.5-5MPa).
The Low Temperature Fischer Tropsch synthetic catalyst of the present invention has higher activity, stability and wear resistence, can be in synthesis gas
Through obtaining relatively low by-product and the C of higher yields in syrup state bed Fischer Tropsch synthetic reaction hydrocarbon compound5+Product.
The present invention will be described in detail by way of examples below.
In following embodiment and comparative example：
Total specific surface area, average pore size and the Kong Rong of catalyst are measured using BET method.
By the molal quantity of the CO in the reactor feed mouth measurement analysis charging for carrying out Fischer-Tropsch synthesis, and reacting
Device discharge port measures CO, CO in analysis discharging2、CH4Molal quantity, to CO conversion ratios %, CO2Selective %, CH4Selective %
It is calculate by the following formula respectively：
CO conversion ratios %=[CO molal quantitys in (CO molal quantitys in CO molal quantitys-discharging in charging)/charging] × 100%；
CO2Selective %=[CO in discharging2Molal quantity/(CO molal quantitys in CO molal quantitys-discharging in charging)] × 100%；
CH4Selective %=[CH in discharging4Molal quantity/(CO molal quantitys in CO molal quantitys-discharging in charging)] × 100%.
C5+ selectivity %=[C5+ molal quantitys/(CO molal quantitys in CO molal quantitys-discharging in charging) in discharging] ×
100%.
Catalyst wear resistence is measured by ASTM D5757-95 air gunitees.
Catalyst stability is the catalyst CO conversions by 100-500 hours sections under the conditions of measurement Fischer-Tropsch synthesis
For the rate of descent of rate come what is measured, unit is %/100h.
Embodiment 1
The present embodiment is used to illustrate the Low Temperature Fischer Tropsch synthetic catalyst and preparation method thereof of the present invention.
(1) by the Fe (NO of 303g3)3·9H2O, the Cu (NO of 7.95g3)2·3H2Nd (the NO of O and 3.7g3)3·6H2O adds
Enter the stirring and dissolving into 1700g deionized waters, obtains the first solution.By 251gNa2CO3With 30g potassium silicate aqueous solutions (with SiO2
A concentration of 5 weight % of meter) it is added to stirring and dissolving in 2000g deionized waters, obtain the second solution.Then it by the two and flows into
Enter and carry out coprecipitation reaction in the reaction kettle of stirring, which is：Temperature is 20 DEG C, pH value 8.5, when reaction
Between be 40min.After precipitation, precipitate slurry is subjected to press filtration, be used in combination deionized water repeatedly washing and filter pressing to filtrate conductivity
Terminate to wash when about 1400 μ S/cm.
(2) filter cake after washing is beaten (gained slurry solid content is 5 weight %) with 1600g deionized waters, and
The potassium silicate aqueous solution of 96g is added afterwards (with SiO2A concentration of 5 weight % of meter), and be stirred until homogeneous.5 weight % are prepared simultaneously
Dust technology.Potassium silicate slurries will be contained and dust technology cocurrent enters in reactor, temperature be 20 DEG C, pH be 5.5 times mixing
40min；Aging 120min is then stood at 20 DEG C of temperature；
(3) by after aging slurries carry out press filtration, obtain filter cake, with deionized water it is repulped obtain catalyst pulp (Gu
Content is 20 weight %)；Gained catalyst pulp is inputted in spray dryer, is 290 DEG C in entrance wind-warm syndrome, exports wind-warm syndrome
Spray drying forming (granulation) is carried out under conditions of 115 DEG C.Thus obtained microsphere catalyst is put into roaster, in 500 DEG C of constant temperature
6h is to get to final catalyst C1.
In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：K：Nd：SiO2=100：3.5：1.8：2：
10.5.The catalyst is spherical shape, and sphericity and surface topography are good, and grain size is 120 μm, and total specific surface area is 148m2/ g, hole
It is 0.66cm to hold3/ g, average pore size 21nm.
Embodiment 2
The present embodiment is used to illustrate the Low Temperature Fischer Tropsch synthetic catalyst and preparation method thereof of the present invention.
(1) by the Fe (NO of 303g3)3·9H2O, the Cu (NO of 2.3g3)2·3H2Nd (the NO of O and 7.3g3)3·6H2O is added
To stirring and dissolving in 1700g deionized waters, the first solution is obtained.By 251gNa2CO3With 7.5g potassium silicate solutions (with SiO2Meter
A concentration of 24 weight %) it is added to stirring and dissolving in 2000g deionized waters, obtain the second solution.Then the two cocurrent is entered
Coprecipitation reaction is carried out in the reaction kettle of stirring, which is：Temperature is 8 DEG C, and pH value 9, the reaction time is
30min.After precipitation, precipitate slurry is subjected to press filtration, deionized water is used in combination, and washing and filter pressing to filtrate conductivity is about repeatedly
Terminate to wash when 1000 μ S/cm.
(2) filter cake after washing is beaten (gained slurry solid content is 7 weight %) with 1000g deionized waters, and
48.8g potassium silicate aqueous solutions are added afterwards (with SiO2Meter a concentration of 24 weight %) and 40g K2CO3Aqueous solution (K2CO3Concentration
20 weight %), and to be stirred until homogeneous.The dust technology of 10 weight % is prepared simultaneously.Potassium silicate slurries and dust technology cocurrent will be contained
Into in reactor, temperature be 55 DEG C, pH be 6 times mixing 15min；Aging 90min is then stood at 55 DEG C of temperature；
(3) by after aging slurries carry out press filtration, obtain filter cake, with deionized water it is repulped obtain catalyst pulp (Gu
Content is 15 weight %)；Gained catalyst pulp is inputted in spray dryer, is 350 DEG C in entrance wind-warm syndrome, exports wind-warm syndrome
Spray drying forming (granulation) is carried out under conditions of 130 DEG C.Thus obtained microsphere catalyst is put into roaster, in 400 DEG C of constant temperature
12h is to get to final catalyst C2.
In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：K：Nd：SiO2=100：1：4：4：
22.5.The catalyst is spherical shape, and sphericity and surface topography are good, and total specific surface area is 91m2/ g, Kong Rongwei 0.33cm3/ g,
Average pore size is 22nm.
Embodiment 3
The present embodiment is used to illustrate the Low Temperature Fischer Tropsch synthetic catalyst and preparation method thereof of the present invention.
(1) by the Fe (NO of 303g3)3·9H2O, the Cu (NO of 6.8g3)2·3H2Nd (the NO of O and 11g3)3·6H2O is added
To stirring and dissolving in 1200g deionized waters, the first solution is obtained.By 180g ammonium carbonates and 15g Ludox (with SiO2The concentration of meter
For 10 weight %) it is added to stirring and dissolving in 1000g deionized waters, obtain the second solution.Then the two cocurrent is entered into stirring
Reaction kettle in carry out coprecipitation reaction, which is：Temperature is 18 DEG C, and pH value 8, the reaction time is
50min.After precipitation, precipitate slurry is subjected to press filtration, deionized water is used in combination, and washing and filter pressing to filtrate conductivity is about repeatedly
Terminate to wash when 1400 μ S/cm.
(2) filter cake after washing is beaten (gained slurry solid content is 4.5 weight %) with 1600g deionized waters,
The silicon sol solution of 75g is then added (with SiO2Meter a concentration of 10 weight %) and 60g K2CO3Aqueous solution (K2CO3Concentration
20 weight %), and be stirred until homogeneous.The dust technology of 15 weight % is prepared simultaneously.Slurries and dust technology cocurrent are entered into reactor
In, temperature be 35 DEG C, pH be 5.5 times mixing 30min；Aging 60min is then stood at 35 DEG C of temperature；
(3) by after aging slurries carry out press filtration, obtain filter cake, with deionized water it is repulped obtain catalyst pulp (Gu
Content is 20 weight %)；Gained catalyst pulp is inputted in spray dryer, is 300 DEG C in entrance wind-warm syndrome, exports wind-warm syndrome
Spray drying forming (granulation) is carried out under conditions of 120 DEG C.Thus obtained microsphere catalyst is put into roaster, in 350 DEG C of constant temperature
12h is to get to final catalyst C3.
In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：K：Nd：SiO2=100：3：3：6：15.
The catalyst is spherical shape, and sphericity and surface topography are good, and total specific surface area is 125m2/ g, Kong Rongwei 0.34cm3/ g, it is average
Aperture is 16nm.
Embodiment 4
The present embodiment is used to illustrate the Low Temperature Fischer Tropsch synthetic catalyst and preparation method thereof of the present invention.
According to method described in embodiment 1, the difference is that, the temperature of coprecipitation reaction is 35 DEG C in step (1), and pH value is
5.5；To obtain final catalyst C4.In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：K：Nd：
SiO2=100：3.5：1.8：2：10.5.The catalyst is spherical shape, and sphericity and surface topography are good, and total specific surface area is
164m2/ g, Kong Rongwei 0.79cm3/ g, average pore size 11nm.
Embodiment 5
The present embodiment is used to illustrate the Low Temperature Fischer Tropsch synthetic catalyst and preparation method thereof of the present invention.
According to method described in embodiment 1, the difference is that, the temperature of coprecipitation reaction is 25 DEG C in step (1), and pH value is
6；To obtain final catalyst C5.In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：K：Nd：
SiO2=100：3.5：1.8：2：10.5.The catalyst is spherical shape, and sphericity and surface topography are good, and total specific surface area is
155m2/ g, Kong Rongwei 0.61cm3/ g, average pore size 17nm,.
Embodiment 6
The present embodiment is used to illustrate the Low Temperature Fischer Tropsch synthetic catalyst and preparation method thereof of the present invention.
According to method described in embodiment 1, the difference is that, the deionized water that the first solution uses is prepared in step (1)
Amount is 600g；To obtain final catalyst C6.In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：
K：Nd：SiO2=100：3.5：1.8：2：10.5.The catalyst is spherical shape, and sphericity and surface topography are good, total specific surface
Product is 78m2/ g, Kong Rongwei 0.26cm3/ g, average pore size 15nm.
Embodiment 7
The present embodiment is used to illustrate the Low Temperature Fischer Tropsch synthetic catalyst and preparation method thereof of the present invention.
According to method described in embodiment 1, the difference is that, the deionized water that the first solution uses is prepared in step (1)
Amount is 2500g；To obtain final catalyst C7.In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：
K：Nd：SiO2=100：3.5：1.8：2：10.5.The catalyst is spherical shape, and sphericity and surface topography are good, total specific surface
Product is 185m2/ g, Kong Rongwei 0.7cm3/ g, average pore size 14nm.
Embodiment 8
The present embodiment is used to illustrate the Low Temperature Fischer Tropsch synthetic catalyst and preparation method thereof of the present invention.
According to method described in embodiment 1, the difference is that, step (2) is before introducing potassium silicate aqueous solution, after washing
Filter cake is beaten (gained slurry solid content is 10 weight %) with 800g deionized waters；To obtain final catalyst C8.
In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：K：Nd：SiO2=100：3.5：1.8：2：10.5.It should
Catalyst is spherical shape, and sphericity and surface topography are good, and total specific surface area is 156m2/ g, Kong Rongwei 0.65cm3/ g, average hole
Diameter is 19nm.
Embodiment 9
The present embodiment is used to illustrate the Low Temperature Fischer Tropsch synthetic catalyst and preparation method thereof of the present invention.
According to method described in embodiment 1, the difference is that, using the Ce (NO of 2.4g in step (1)3)3·6H2O replaces Nd
(NO3)3·6H2O；To obtain final catalyst C9.In the catalyst, through determination of elemental analysis, Fe by weight2O3：
Cu：K：Ce：SiO2=100：3.5：1.8：2：10.5.The catalyst is spherical shape, and sphericity and surface topography are good, always than table
Area is 143m2/ g, Kong Rongwei 0.59cm3/ g, average pore size 19nm.
Embodiment 10
The present embodiment is used to illustrate the Low Temperature Fischer Tropsch synthetic catalyst and preparation method thereof of the present invention.
According to method described in embodiment 1, the difference is that, using the La (NO of 3.2g in step (1)3)3·6H2O replaces Nd
(NO3)3·6H2O；To obtain final catalyst C10.In the catalyst, through determination of elemental analysis, Fe by weight2O3：
Cu：K：Ce：SiO2=100：3.5：1.8：2：10.5.The catalyst is spherical shape, and sphericity and surface topography are good, always than table
Area is 144m2/ g, Kong Rongwei 0.63cm3/ g, average pore size 20nm.
Comparative example 1
According to method described in embodiment 1, the difference is that, the temperature of coprecipitation reaction is 40 DEG C in step (1)；To
To final catalyst DC1.In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：K：Nd：SiO2=100：
3.5：1.8：2：10.5.The catalyst is spherical shape, and sphericity and surface topography are good, and total specific surface area is 150m2/ g, Kong Rong
For 0.38cm3/ g, average pore size 12nm.
Comparative example 2
According to method described in embodiment 1, the difference is that, the temperature of coprecipitation reaction is 90 DEG C in step (1)；To
To final catalyst DC2.In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：K：Nd：SiO2=100：
3.5：1.8：2：10.5.The catalyst is spherical shape, and sphericity and surface topography are good, and total specific surface area is 105m2/ g, Kong Rong
For 0.31cm3/ g, average pore size 13nm.
Comparative example 3
According to method described in embodiment 1, the difference is that, the temperature of coprecipitation reaction is 60 DEG C in step (1), co-precipitation
The pH value of reaction is 6；To obtain final catalyst DC3.In the catalyst, through determination of elemental analysis, by weight
Fe2O3：Cu：K：Nd：SiO2=100：3.5：1.8：2：10.5.The catalyst is spherical shape, and sphericity and surface topography are good,
Total specific surface area is 169m2/ g, Kong Rongwei 0.5cm3/ g, average pore size 10nm.
Comparative example 4
According to method described in embodiment 1, the difference is that, pH value is not adjusted before aging in step (2), pH value is at this time
7.8；To obtain final catalyst DC4.In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：K：Nd：
SiO2=100：3.5：1.8：2：10.5.The catalyst is spherical shape, and sphericity and surface topography are good, and total specific surface area is
107m2/ g, Kong Rongwei 0.39cm3/ g, average pore size 12nm.
Comparative example 5
According to method described in embodiment 1, the difference is that, in step (1), Cu (NO3)2·3H2The dosage of O is 1.2g, Nd
(NO3)3·6H2The dosage of O is 0.9g, to obtain final catalyst DC5.In the catalyst, through determination of elemental analysis, with
The Fe of weight meter2O3：Cu：K：Nd：SiO2=100：0.5：1：0.5：15.The catalyst is spherical shape, and sphericity and surface topography are good
Good, total specific surface area is 117m2/ g, Kong Rongwei 0.43cm3/ g, average pore size 13nm.
Comparative example 6
According to method described in embodiment 1, the difference is that, in step (1), Cu (NO3)2·3H2The dosage of O is 22.7g,
Nd(NO3)3·6H2The dosage of O is 18.2g, K2CO3The dosage of solution is 159g, to obtain final catalyst DC6.This is urged
In agent, through determination of elemental analysis, Fe by weight2O3：Cu：K：Nd：SiO2=100：10：10：10：10.5.The catalyst
For spherical shape, sphericity and surface topography are good, and total specific surface area is 158m2/ g, Kong Rongwei 0.61cm3/ g, average pore size are
17nm。
Comparative example 7
According to method described in embodiment 1, the difference is that, it is water-soluble to be added without potassium silicate in the second solution in step (1)
Liquid, the part potassium silicate aqueous solution are introduced together in step (2), i.e., potassium silicate aqueous solution is 126g in step (2)；To
To final catalyst DC7.In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：K：Nd：SiO2=100：
3.5：1.8：2：10.5.The catalyst is spherical shape, and sphericity and surface topography are general, and total specific surface area is 121m2/ g, Kong Rong
For 0.36cm3/ g, average pore size 14nm.
Comparative example 8
According to method described in embodiment 1, the difference is that, the temperature of coprecipitation reaction is 35 DEG C in step (1), and pH value is
9；To obtain final catalyst DC8.In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：K：Nd：
SiO2=100：3.5：1.8：2：10.5.The catalyst is spherical shape, and sphericity and surface topography are good, and total specific surface area is
147m2/ g, Kong Rongwei 0.65cm3/ g, average pore size 16nm.
Comparative example 9
According to method described in embodiment 1, the difference is that, step does not use Nd (NO in (1)3)3·6H2O, to obtain
Final catalyst DC9.In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：K：SiO2=100：3.5：
1.8：10.5.The catalyst is spherical shape, and sphericity and surface topography are good, and total specific surface area is 145m2/ g, Kong Rongwei
0.62cm3/ g, average pore size 19nm.
Comparative example 10
According to the method described in embodiment 2, the difference is that, the temperature of coprecipitation reaction is 35 DEG C in step (1), and pH value is
9.0；To obtain final catalyst DC10.In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：K：
Nd：SiO2=100：1：4：4：22.5.The catalyst is spherical shape, and sphericity and surface topography are good, and total specific surface area is
151m2/ g, Kong Rongwei 0.58cm3/ g, average pore size 16nm.
Comparative example 11
According to the method described in embodiment 2, the difference is that, the temperature of coprecipitation reaction is 15 DEG C in step (1), and pH value is
6；To obtain final catalyst DC11.In the catalyst, through determination of elemental analysis, Fe by weight2O3：Cu：K：Nd：
SiO2=100：1：4：4：22.5.The catalyst is spherical shape, and sphericity and surface topography are good, and total specific surface area is 135m2/
G, Kong Rongwei 0.47cm3/ g, average pore size 14nm.
Test case 1
Catalyst reaction performance evaluation is carried out in 1L stirred tank evaluating apparatus below.
(a) reduction reaction：With containing CO and H2Reducing atmosphere (CO and H2Molar ratio be 0.2：1) in 260 DEG C and pressure
Reduction reaction is carried out for 24 hours to above-mentioned catalyst C1-C10 and DC1-DC11 respectively under 0.1MPa；
(b) F- T synthesis：It is passed through synthesis gas (H2Molar ratio with CO is 2：1), at 250 DEG C, pressure 2.3MPa, when gas
Air speed is 4000mL/ (gh), carries out Fischer-Tropsch synthesis.
The reactivity worth for carrying out the catalyst of successive reaction the results are shown in Table 1.
Table 1
It can be seen from Table 1 that the Low Temperature Fischer Tropsch synthetic catalyst obtained by the present processes can obtain higher CO
Conversion ratio, lower CO2Selectivity, lower CH4Selectivity, higher C5+Selectivity.
Test case 2
Stability and wear resistence test are carried out to above-mentioned catalyst C1-C10 and DC1-DC8, DC10-DC11, result is such as
Shown in table 2：
Table 2
| Catalyst | The rate of descent of CO conversion ratios, %/100h | Wear resistence |
| C1 | 0.42 | 1.2 |
| C2 | 0.55 | 1.4 |
| C3 | 0.67 | 1.6 |
| C4 | 0.98 | 2.1 |
| C5 | 0.89 | 2.2 |
| C6 | 1.1 | 2.0 |
| C7 | 0.93 | 1.9 |
| C8 | 1.21 | 2.2 |
| C9 | 0.68 | 1.6 |
| C10 | 0.72 | 1.8 |
| DC1 | 3.14 | 4.3 |
| DC2 | 2.21 | 5.9 |
| DC3 | 1.82 | 4.8 |
| DC4 | 1.54 | 3.6 |
| DC5 | 1.64 | 3.7 |
| DC6 | 3.23 | 2.6 |
| DC7 | 1.67 | 2.7 |
| DC8 | 1.71 | 3.2 |
| DC10 | 1.52 | 2.5 |
| DC11 | 1.47 | 2.4 |
It can be seen from Table 2 that the Low Temperature Fischer Tropsch synthetic catalyst obtained by the present processes has higher stability
And wear resistence.
The preferred embodiment of the present invention has been described above in detail, and still, the present invention is not limited thereto.In the skill of the present invention
In art conception range, technical scheme of the present invention can be carried out a variety of simple variants, including each technical characteristic with it is any its
Its suitable method is combined, and it should also be regarded as the disclosure of the present invention for these simple variants and combination, belongs to
Protection scope of the present invention.
Claims (10)
1. a kind of preparation method of Low Temperature Fischer Tropsch synthetic catalyst, which is characterized in that this method includes：
(1) aqueous solution containing molysite, mantoquita and promoter metal M salt, i.e. the first solution are provided；It provides and contains precipitating reagent and silicon source
Aqueous solution, i.e. the second solution；First solution and the second solution are subjected to coprecipitation reaction, is then separated by solid-liquid separation and is washed
Gained solid phase；Temperature is 5-35 DEG C, pH value 4.5-9.5, time 5-60min；The pH for defining coprecipitation reaction is numerical value n,
The temperature for defining coprecipitation reaction is numerical value T, and the temperature and pH of the coprecipitation reaction meet formula：N+0.16T=9-14；Institute
It is lanthanide series metal to state promoter metal M；
(2) solid phase after washing is beaten with water, obtains slurries and introduces silicon source containing potassium, and adjust the pH of gained mixture
Value is to acidity to carry out aging；
(3) slurries after aging are separated by solid-liquid separation, gained solid phase is beaten with water, gained slurries carry out spray drying and
Roasting；
Wherein, the dosage of the molysite, mantoquita, promoter metal M salt, silicon source and the silicon source containing potassium makes in the catalyst of gained, with
The Fe of weight meter2O3：Cu：K：M：SiO2=100：1-8：1-8：1-8：10-30.
2. according to the method described in claim 1, wherein, the molysite, mantoquita, promoter metal M salt, silicon source and silicon source containing potassium and
Dosage make gained catalyst in, Fe by weight2O3：Cu：K：M：SiO2=100：1-5：1-5：1-5：10-25, it is excellent
Selection of land Fe2O3：Cu：K：M：SiO2=100：1-4：1.5-4：2-5：10-23.
3. method according to claim 1 or 2, wherein the molysite is one kind in ferric nitrate, ferric sulfate and iron chloride
Or a variety of, preferably ferric nitrate；
The mantoquita is one or more in copper nitrate, copper sulphate and copper chloride；
The promoter metal M is one or more in La, Ce and Nd, it is preferable that the promoter metal M salt is lanthanum nitrate, nitre
It is one or more in sour cerium, neodymium nitrate, lanthanum sulfate, cerous sulfate, Dineodymium trisulfate, lanthanum chloride, cerium chloride and neodymium chloride；
The silicon source is one or more in potassium silicate, sodium metasilicate, Ludox and Ludox containing potassium；
The silicon source containing potassium is potassium silicate and/or Ludox containing potassium.
4. according to the method described in any one of claim 1-3, wherein in first solution, with Fe2O3The molysite of meter
A concentration of 20-120g/L, preferably 30-100g/L, more preferably 30-60g/L；
Preferably, in second solution, a concentration of 100-300g/L of the precipitating reagent, preferably 110-250g/L are more excellent
It is selected as 120-200g/L；
Preferably, the precipitating reagent is sodium carbonate, sodium bicarbonate, potassium carbonate, sodium hydroxide, potassium hydroxide, ammonium carbonate, bicarbonate
It is one or more in ammonium and ammonium hydroxide；
Preferably, with SiO2Meter the silicon source and with SiO2The weight ratio of the silicon source containing potassium of meter is 1：2-10, preferably 1：3-7.
5. according to the method described in any one of claim 1-4, wherein in step (1), the condition of the coprecipitation reaction
Including：Temperature is 5-30 DEG C, pH value 5-9, time 10-50min；
Preferably, the temperature of the coprecipitation reaction is 8-20 DEG C.
6. according to the method described in any one of claim 1-5, wherein adjust pH value in step (2), before aging to 4-
6.5, preferably to 4.5-6；
Preferably, the condition of the aging includes：Temperature is 5-60 DEG C, time 30-150min；It is highly preferred that the aging
Condition include：Temperature is 15-55 DEG C, time 50-120min.
7. according to the method described in any one of claim 1-6, wherein in step (3), before carrying out the spray drying,
A concentration of 12-25 weight % of the slurries of gained；
Preferably, the condition of the spray drying includes：Entrance wind-warm syndrome is 180-380 DEG C, and outlet wind-warm syndrome is 70-180 DEG C；It is more excellent
The condition of selection of land, the spray drying includes：Entrance wind-warm syndrome is 220-380 DEG C, and outlet wind-warm syndrome is 100-140 DEG C；
Preferably, the condition of the roasting includes：Temperature is 350-600 DEG C, time 1-15h；It is highly preferred that the roasting
Condition includes：Temperature is 350-550 DEG C, time 3-12h.
8. the Low Temperature Fischer Tropsch synthetic catalyst made from the method described in any one of claim 1-7.
9. Low Temperature Fischer Tropsch synthetic catalyst according to claim 8, wherein the catalyst is that the total specific surface area of microspheroidal is
60-185m2/ g, preferably 70-170m2/ g, more preferably 100-165m2/g；
Preferably, average pore size 10-25nm；
Preferably, Kong Rongwei 0.2-0.8cm3/ g, preferably 0.2-0.7cm3/g。
10. a kind of method of synthesis gas through syrup state bed Fischer Tropsch synthetic reaction hydrocarbon compound, this method include：In the reduction-state
In the presence of fischer-tropsch synthetic catalyst, CO and H will be contained2Synthesis gas in temperature be 210-280 DEG C, under pressure 1.0-5.0MPa,
Fischer-Tropsch synthesis is carried out in paste state bed reactor；Wherein, the reduction-state fischer-tropsch synthetic catalyst is described in claim 9
Low Temperature Fischer Tropsch synthetic catalyst obtained through reduction.
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