CN107971031A - A kind of assistant for calalytic cracking for improving octane number bucket and preparation method thereof - Google Patents
A kind of assistant for calalytic cracking for improving octane number bucket and preparation method thereof Download PDFInfo
- Publication number
- CN107971031A CN107971031A CN201610921640.5A CN201610921640A CN107971031A CN 107971031 A CN107971031 A CN 107971031A CN 201610921640 A CN201610921640 A CN 201610921640A CN 107971031 A CN107971031 A CN 107971031A
- Authority
- CN
- China
- Prior art keywords
- molecular sieve
- acid
- phosphorus
- weight
- aluminum
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 title claims abstract description 45
- 238000002360 preparation method Methods 0.000 title claims abstract description 23
- 238000005336 cracking Methods 0.000 title abstract description 6
- 239000002808 molecular sieve Substances 0.000 claims abstract description 373
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims abstract description 369
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 101
- 239000011574 phosphorus Substances 0.000 claims abstract description 101
- 239000011230 binding agent Substances 0.000 claims abstract description 92
- 229910052751 metal Inorganic materials 0.000 claims abstract description 91
- 239000002184 metal Substances 0.000 claims abstract description 91
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 89
- 238000000034 method Methods 0.000 claims abstract description 72
- 239000003502 gasoline Substances 0.000 claims abstract description 69
- 239000004927 clay Substances 0.000 claims abstract description 67
- 238000004523 catalytic cracking Methods 0.000 claims abstract description 48
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 46
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 45
- 239000012752 auxiliary agent Substances 0.000 claims abstract description 27
- 229910052733 gallium Inorganic materials 0.000 claims abstract description 14
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 14
- 239000011701 zinc Substances 0.000 claims abstract description 14
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims abstract description 13
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 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 claims abstract description 13
- 239000004411 aluminium Substances 0.000 claims abstract description 12
- 239000002253 acid Substances 0.000 claims description 140
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 83
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 82
- 238000011282 treatment Methods 0.000 claims description 71
- 238000001914 filtration Methods 0.000 claims description 69
- 238000005406 washing Methods 0.000 claims description 60
- 239000002002 slurry Substances 0.000 claims description 58
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 57
- URRHWTYOQNLUKY-UHFFFAOYSA-N [AlH3].[P] Chemical compound [AlH3].[P] URRHWTYOQNLUKY-UHFFFAOYSA-N 0.000 claims description 56
- 239000013078 crystal Substances 0.000 claims description 51
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 50
- 239000011148 porous material Substances 0.000 claims description 48
- 238000003756 stirring Methods 0.000 claims description 48
- 239000007787 solid Substances 0.000 claims description 47
- 239000000654 additive Substances 0.000 claims description 46
- 230000000996 additive effect Effects 0.000 claims description 42
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 40
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 39
- 239000011734 sodium Substances 0.000 claims description 38
- 238000004537 pulping Methods 0.000 claims description 34
- 229910052593 corundum Inorganic materials 0.000 claims description 31
- 229910001845 yogo sapphire Inorganic materials 0.000 claims description 31
- 229910019142 PO4 Inorganic materials 0.000 claims description 27
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 25
- -1 rectorite Inorganic materials 0.000 claims description 25
- 150000007522 mineralic acids Chemical class 0.000 claims description 24
- 239000003513 alkali Substances 0.000 claims description 23
- 238000002156 mixing Methods 0.000 claims description 23
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 22
- 150000007524 organic acids Chemical class 0.000 claims description 22
- 238000009826 distribution Methods 0.000 claims description 20
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 19
- 239000005995 Aluminium silicate Substances 0.000 claims description 18
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 18
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 18
- 235000012211 aluminium silicate Nutrition 0.000 claims description 18
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 18
- 230000001965 increasing effect Effects 0.000 claims description 17
- 238000001694 spray drying Methods 0.000 claims description 16
- 239000002671 adjuvant Substances 0.000 claims description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 14
- VXAUWWUXCIMFIM-UHFFFAOYSA-M aluminum;oxygen(2-);hydroxide Chemical compound [OH-].[O-2].[Al+3] VXAUWWUXCIMFIM-UHFFFAOYSA-M 0.000 claims description 13
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 235000006408 oxalic acid Nutrition 0.000 claims description 13
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 12
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 claims description 11
- 150000002736 metal compounds Chemical class 0.000 claims description 11
- 239000012298 atmosphere Substances 0.000 claims description 10
- 238000012986 modification Methods 0.000 claims description 10
- 230000004048 modification Effects 0.000 claims description 10
- 229910052742 iron Inorganic materials 0.000 claims description 9
- 150000002739 metals Chemical class 0.000 claims description 9
- 229910052759 nickel Inorganic materials 0.000 claims description 9
- 150000002894 organic compounds Chemical class 0.000 claims description 9
- 239000002994 raw material Substances 0.000 claims description 9
- 239000004113 Sepiolite Substances 0.000 claims description 8
- 229960000892 attapulgite Drugs 0.000 claims description 8
- 239000002131 composite material Substances 0.000 claims description 8
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 claims description 8
- 229910052901 montmorillonite Inorganic materials 0.000 claims description 8
- 229910052625 palygorskite Inorganic materials 0.000 claims description 8
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 8
- 229910052624 sepiolite Inorganic materials 0.000 claims description 8
- 235000019355 sepiolite Nutrition 0.000 claims description 8
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims description 8
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 7
- 229910052708 sodium Inorganic materials 0.000 claims description 7
- 229910052718 tin Inorganic materials 0.000 claims description 7
- 239000011135 tin Substances 0.000 claims description 7
- 239000004254 Ammonium phosphate Substances 0.000 claims description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 6
- 229910000148 ammonium phosphate Inorganic materials 0.000 claims description 6
- 235000019289 ammonium phosphates Nutrition 0.000 claims description 6
- 229910052797 bismuth Inorganic materials 0.000 claims description 6
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 6
- 229910017052 cobalt Inorganic materials 0.000 claims description 6
- 239000010941 cobalt Substances 0.000 claims description 6
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 6
- 229910052802 copper Inorganic materials 0.000 claims description 6
- 239000010949 copper Substances 0.000 claims description 6
- 239000003292 glue Substances 0.000 claims description 6
- 239000010452 phosphate Substances 0.000 claims description 6
- 229910001948 sodium oxide Inorganic materials 0.000 claims description 6
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 5
- 239000005909 Kieselgur Substances 0.000 claims description 5
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 5
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 claims description 5
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 235000019837 monoammonium phosphate Nutrition 0.000 claims description 5
- 229910017604 nitric acid Inorganic materials 0.000 claims description 5
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 5
- 230000008093 supporting effect Effects 0.000 claims description 5
- 238000005342 ion exchange Methods 0.000 claims description 4
- 238000011068 loading method Methods 0.000 claims description 4
- WXHLLJAMBQLULT-UHFFFAOYSA-N 2-[[6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl]amino]-n-(2-methyl-6-sulfanylphenyl)-1,3-thiazole-5-carboxamide;hydrate Chemical compound O.C=1C(N2CCN(CCO)CC2)=NC(C)=NC=1NC(S1)=NC=C1C(=O)NC1=C(C)C=CC=C1S WXHLLJAMBQLULT-UHFFFAOYSA-N 0.000 claims description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 3
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical group [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 3
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 3
- 238000005470 impregnation Methods 0.000 claims description 3
- 235000019353 potassium silicate Nutrition 0.000 claims description 3
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 2
- 229910002651 NO3 Inorganic materials 0.000 claims description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 2
- 230000001976 improved effect Effects 0.000 abstract description 11
- 230000008569 process Effects 0.000 abstract description 11
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 abstract 1
- 239000012065 filter cake Substances 0.000 description 53
- 238000010438 heat treatment Methods 0.000 description 52
- 239000003054 catalyst Substances 0.000 description 46
- 239000000243 solution Substances 0.000 description 34
- 239000000706 filtrate Substances 0.000 description 31
- 230000007935 neutral effect Effects 0.000 description 31
- 239000010457 zeolite Substances 0.000 description 28
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 26
- 229910021536 Zeolite Inorganic materials 0.000 description 25
- 238000001035 drying Methods 0.000 description 24
- 230000000052 comparative effect Effects 0.000 description 23
- 239000003921 oil Substances 0.000 description 21
- 238000001816 cooling Methods 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 17
- 230000000694 effects Effects 0.000 description 17
- 239000000203 mixture Substances 0.000 description 16
- 239000000047 product Substances 0.000 description 16
- 239000012452 mother liquor Substances 0.000 description 15
- 230000015572 biosynthetic process Effects 0.000 description 14
- 235000021317 phosphate Nutrition 0.000 description 14
- 239000000523 sample Substances 0.000 description 14
- 238000002791 soaking Methods 0.000 description 14
- 238000003786 synthesis reaction Methods 0.000 description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 239000007864 aqueous solution Substances 0.000 description 12
- 238000004231 fluid catalytic cracking Methods 0.000 description 12
- 229930195733 hydrocarbon Natural products 0.000 description 10
- 150000002430 hydrocarbons Chemical class 0.000 description 10
- 239000004215 Carbon black (E152) Substances 0.000 description 9
- CSDREXVUYHZDNP-UHFFFAOYSA-N alumanylidynesilicon Chemical compound [Al].[Si] CSDREXVUYHZDNP-UHFFFAOYSA-N 0.000 description 9
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 9
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
- 239000007789 gas Substances 0.000 description 8
- 229910052710 silicon Inorganic materials 0.000 description 8
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 7
- 238000001354 calcination Methods 0.000 description 7
- 238000013329 compounding Methods 0.000 description 7
- 239000011159 matrix material Substances 0.000 description 7
- 239000004005 microsphere Substances 0.000 description 7
- 239000010703 silicon Substances 0.000 description 7
- 238000001179 sorption measurement Methods 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- 238000010009 beating Methods 0.000 description 5
- 238000003795 desorption Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 5
- 230000002829 reductive effect Effects 0.000 description 5
- 150000003863 ammonium salts Chemical class 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 229960001484 edetic acid Drugs 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- 238000006317 isomerization reaction Methods 0.000 description 4
- 238000002386 leaching Methods 0.000 description 4
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 4
- 238000009718 spray deposition Methods 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 3
- 150000001805 chlorine compounds Chemical class 0.000 description 3
- 229910000388 diammonium phosphate Inorganic materials 0.000 description 3
- 235000019838 diammonium phosphate Nutrition 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 150000007529 inorganic bases Chemical class 0.000 description 3
- 150000002484 inorganic compounds Chemical class 0.000 description 3
- 239000011806 microball Substances 0.000 description 3
- 150000002823 nitrates Chemical class 0.000 description 3
- 150000003018 phosphorus compounds Chemical class 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 238000010561 standard procedure Methods 0.000 description 3
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000000571 coke Substances 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 229910000373 gallium sulfate Inorganic materials 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 238000001027 hydrothermal synthesis Methods 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229910052680 mordenite Inorganic materials 0.000 description 2
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 2
- 150000007530 organic bases Chemical class 0.000 description 2
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical class O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 2
- 235000011007 phosphoric acid Nutrition 0.000 description 2
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 2
- 229910001392 phosphorus oxide Inorganic materials 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 230000009469 supplementation Effects 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- 229910018516 Al—O Inorganic materials 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical group [O+]#[C-] UGFAIRIUMAVXCW-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
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 1
- 239000006004 Quartz sand Substances 0.000 description 1
- 229910018557 Si O Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- HPTYUNKZVDYXLP-UHFFFAOYSA-N aluminum;trihydroxy(trihydroxysilyloxy)silane;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O[Si](O)(O)O HPTYUNKZVDYXLP-UHFFFAOYSA-N 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229910001593 boehmite Inorganic materials 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 238000004939 coking Methods 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000003009 desulfurizing effect Effects 0.000 description 1
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 1
- 229910001648 diaspore Inorganic materials 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000003546 flue gas Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 229910001679 gibbsite Inorganic materials 0.000 description 1
- 229910052621 halloysite Inorganic materials 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 239000002149 hierarchical pore Substances 0.000 description 1
- 229910001701 hydrotalcite Inorganic materials 0.000 description 1
- 229960001545 hydrotalcite Drugs 0.000 description 1
- FAHBNUUHRFUEAI-UHFFFAOYSA-M hydroxidooxidoaluminium Chemical compound O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 238000000696 nitrogen adsorption--desorption isotherm Methods 0.000 description 1
- 229910001682 nordstrandite Inorganic materials 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical class [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000012521 purified sample Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000005185 salting out Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910000275 saponite Inorganic materials 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
- 239000011949 solid catalyst Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 238000010408 sweeping Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- VSAISIQCTGDGPU-UHFFFAOYSA-N tetraphosphorus hexaoxide Chemical compound O1P(O2)OP3OP1OP2O3 VSAISIQCTGDGPU-UHFFFAOYSA-N 0.000 description 1
- 238000006276 transfer reaction Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J29/00—Catalysts comprising molecular sieves
- B01J29/82—Phosphates
- B01J29/84—Aluminophosphates containing other elements, e.g. metals, boron
- B01J29/85—Silicoaluminophosphates [SAPO compounds]
-
- 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
- C10G11/00—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils
- C10G11/02—Catalytic cracking, in the absence of hydrogen, of hydrocarbon oils characterised by the catalyst used
- C10G11/04—Oxides
- C10G11/05—Crystalline alumino-silicates, e.g. molecular sieves
-
- 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
- C10G2300/10—Feedstock materials
- C10G2300/1037—Hydrocarbon fractions
-
- 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
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/30—Physical properties of feedstocks or products
- C10G2300/305—Octane number, e.g. motor octane number [MON], research octane number [RON]
-
- 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
- C10G2400/02—Gasoline
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Materials Engineering (AREA)
- Crystallography & Structural Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Catalysts (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
The disclosure provides a kind of assistant for calalytic cracking for improving octane number bucket and preparation method thereof, on the basis of the butt weight of the auxiliary agent, the auxiliary agent is included with the phosphorous and carried metal MFI structure molecular sieve of 10 75 weight % of dry basis, with the phosphorus aluminium inorganic binder of 3 40 weight % of dry basis, other inorganic binders of in terms of oxide 1 30 weight %, with the metallic addition selected from least one of VIII race's metal and manganese, zinc, gallium of the second clay of 0 60 weight % of dry basis, and in terms of oxide 0.5 15 weight %.The auxiliary agent that the disclosure is provided is used for catalytic cracking process, and octane number is improved by improving the content of isohydrocarbon in gasoline, while keeps yield of gasoline to be basically unchanged, and then improves octane number bucket.
Description
Technical Field
The invention relates to a catalytic cracking auxiliary agent for improving the octane number of gasoline and a preparation method thereof.
Background
In recent years, the quantity of motor vehicles in China is continuously increased, and the demand for supporting the consumption of gasoline terminals in China is kept vigorous. The automobile sales volume is increased by 11% every year in the 'twelve five' period, the gasoline demand is driven to keep 5% stable increase every year, and the apparent gasoline consumption is estimated to reach 98Mt by 2015. With the new round of propylene production capacity, the global propylene supply will greatly exceed the demand increase in the next five years. It is predicted that the global propylene capacity will increase by 30Mt for the next five years, while the demand growth is expected to be only 22Mt, since this difference between supply and demand may lead to a lowering of the propylene price. Under the promotion of market demand and economic benefit, oil refining enterprises will adopt a production scheme of producing more gasoline and less liquefied gas. In order to realize the purpose of producing gasoline in a large amount, the technological parameters can be adjusted on one hand, and the formula of the catalyst can be adjusted on the other hand.
Under the requirements of environmental protection regulations and the trend that the requirement of the automobile industry on the quality of fuel is strict, the global quality of the automobile gasoline is rapidly improved in recent years, the upgrade pace of the quality of oil products in China is obviously accelerated, and especially when the new discharge regulations of the country VI are made, clean gasoline with high octane number and low olefin aromatic hydrocarbon content becomes a new oil production scheme. The foreign gasoline pool is characterized by comprising the following components: the proportion of the catalytic cracking gasoline is low, for example, the FCC gasoline in the United states accounts for only about 1/3; the average RON is high and is about 93-94; the development of other high-octane components, especially other high-octane components, is continuously promoting the improvement of the octane number of gasoline. However, the quality of the main oil products in China is still a certain gap compared with that of developed countries, currently, FCC (fluid catalytic cracking) gasoline in China accounts for more than 70% of the total amount of motor gasoline, the content of components of reformed gasoline and other high-quality gasoline with high octane number is too low and less than 9%, and the proportion of straight-run gasoline with low octane number is higher and reaches about 13%. Therefore, the octane number of FCC gasoline plays a significant role in the overall level of gasoline octane number. The highest octane number (RON) of FCC gasoline in China is 90-92, the lowest octane number (RON) of FCC gasoline in China is 87-88, and the average octane number (RON) of FCC gasoline in China is 89-90; the MON is 80.6 at the highest, 78 at the lowest and 79 on average, and has a larger gap compared with the gasoline quality of other developed countries, so that the octane number of the gasoline is improved, and the upgrading and updating of the gasoline are facilitated. In addition, in the process of cleaning gasoline, measures such as controlling the olefin content of the gasoline and desulfurizing all result in different degrees of octane number loss, and the contradiction of octane number shortage is more prominent.
Gasoline isomerization is an effective way to increase the octane number of gasoline. Because the isoolefine and isoalkane with side chain have higher octane number than the corresponding normal olefine, the cracking assistant containing molecular sieve with high silica-alumina ratio can properly reduce cracking activity and hydrogen transfer activity of the molecular sieve, and can raise isomerization capability, and the concentration of isoolefine and isoalkane in the product can be increased, so that it can raise gasoline octane number and reduce loss of light oil yield.
The ZSM-5 molecular sieve with high silica-alumina ratio is favorable for improving the octane number of gasoline and reducing the loss of light oil. This is because, as the silica-alumina ratio increases, the acid center density of the ZSM-5 molecular sieve can be reduced, and the acid strength can be increased, thereby reducing the cracking activity, inhibiting the hydrogen transfer reaction, and enhancing the isomerization ability. The ZSM-5 molecular sieve with high silica-alumina ratio is mainly used for isomerization reaction, so the octane number is improved mainly because the concentration of isoolefine and isoalkane in the product is increased, and the yield loss of light oil is low.
Aromatic hydrocarbons are one of the important high octane components in gasoline. At present, the aromatic hydrocarbon content of the domestic FCC gasoline is generally about 20 percent, and a certain distance is still left from the upper limit of 35 percent of the aromatic hydrocarbon content specified in the national V gasoline standard. The method can moderately improve the content of aromatic hydrocarbon in the gasoline and is an effective means for improving the octane number of the gasoline.
The ZSM-5 has a unique pore channel structure, so that on one hand, a better shape-selective effect is achieved, but on the other hand, larger reactant molecules are difficult to enter a crystal pore channel for reaction due to the narrow pore channel structure, the effective reaction area of the molecular sieve is reduced, and the reaction activity of the molecular sieve is reduced; meanwhile, the molecules of the larger products such as isoparaffin and aromatic hydrocarbon are not easy to diffuse out of the inside of the molecular sieve pore channel, thereby causing the molecular sieve to be deactivated due to coking. The introduction of the mesopores into the molecular sieve can well solve the problem of limitation in the mass transfer and diffusion processes of macromolecules in the pore channels of the molecular sieve. As can be seen from the above analysis, the ZSM-5 rich in mesopores with high silica-alumina ratio is beneficial to reducing the gasoline loss and improving the gasoline octane number in the catalytic cracking process.
In the prior art, in order to improve the silica-alumina ratio of a ZSM-5 molecular sieve, Chinese patent CN 101269340A discloses a ZSM-5 zeolite catalyst with high silica-alumina ratio and a preparation method thereof. The catalyst is prepared by taking an active pure silicon compound as a silicon source, adding trace aluminum and adopting a hydrothermal synthesis method. The zeolite skeleton has Si/Al ratio over 1000, submicron crystal grain, open pore passage, large specific surface area and high molecular diffusivity.
Chinese patent CN 1046922C discloses a method for improving the silica-alumina ratio of a ZSM-5 molecular sieve. The molecular sieve is a molecular sieve with high silicon-aluminum ratio and high crystallinity, is prepared by pressurized water-pressure heat treatment and acid treatment, and has no or only a small amount of non-framework aluminum in the product.
Chinese patent CN 103480411A discloses a molecular sieve catalyst containing mesoporous ZSM-5 and a preparation method thereof. According to the method, a cheap silicon-aluminum source, potassium salt and an organic template agent are dissolved in water, the system is subjected to heating ultrasonic auxiliary mechanical stirring by utilizing the cavitation action of ultrasonic waves, meanwhile, the salting-out effect of the potassium salt is utilized to generate a structure guiding effect, and finally, the mesoporous ZSM-5 with MFI structural property and high silicon-aluminum ratio is synthesized by a hydrothermal method.
Chinese patent CN 101857243A discloses a method for adjusting the surface aperture of a ZSM-5 molecular sieve by surface dealuminization and silicon supplementation, which adopts a treatment means of dealuminizing and silicon supplementation on the surface of the ZSM-5 zeolite molecular sieve by adopting an ammonium fluosilicate solution to realize the accurate control of the surface aperture. The ZSM-5 zeolite molecular sieve is modified by ammonium fluosilicate, Al in the surface framework of the molecular sieve is isomorphously replaced by Si, and the bond length of Si-O is less than that of Al-O, so that the diameter of the orifice on the surface of the molecular sieve can be reduced, and a silicon-rich ultrathin layer is formed on the surface of the molecular sieve. By fine control of the treatment conditions, the degree of shrinkage of the molecular sieve surface pores can be controlled.
Chinese patent CN 102851058A discloses a method for improving the octane number of catalytic cracking gasoline, wherein a ZSM-5 molecular sieve with a framework silica-alumina ratio of 30-150 is used as a catalytic cracking auxiliary agent prepared by the method, olefin in the gasoline can be converted into aromatic hydrocarbon, and the olefin content of the gasoline is reduced while the octane number of the gasoline is improved.
In the prior art, a template agent with high price is needed for directly synthesizing the ZSM-5 molecular sieve with high silica-alumina ratio, the cost is high, the production difficulty is high, the three wastes are discharged highly, and the synthesized ZSM-5 molecular sieve has the defects of fine crystal grain (100 plus 300nm) and poor hydrothermal stability, and is difficult to popularize and apply in a catalytic cracking catalyst.
Desiliconization is an effective method capable of generating mesopores in the ZSM-5 molecular sieve at present. The related domestic and foreign documents are reported more. Goen et al treated ZSM-5 molecular sieves with different silica-alumina ratios with sodium hydroxide alkali solution to obtain a mesoporous-rich ZSM-5 molecular sieve. In addition, researchers also treat the ZSM-5 molecular sieve by using an organic base or a composite system of organic and inorganic bases to obtain better pore-forming effect and higher crystallinity. During the alkaline treatment of ZSM-5, amorphous fragments are inevitably produced, clogging the channels, covering the active sites, and thus it is necessary to perform a subsequent dealumination treatment.
Chinese patents CN103818925A and CN104229824A disclose a method for preparing a hierarchical pore ZSM-5 molecular sieve by acid-base coupling, which comprises the steps of treating the ZSM-5 molecular sieve with inorganic base to prepare the ZSM-5 molecular sieve with a secondary pore structure, and then carrying out acid washing of strong acid solution such as hydrochloric acid and nitric acid and ion exchange of acidic ammonium salt to dissolve out an amorphous structure remained in a pore channel so as to improve the pore volume and the specific surface area and improve the distribution of aluminum outside the ZSM-5 molecular sieve.
Chinese patent CN103848438A discloses a method for preparing a modified ZSM-5 molecular sieve with a high mesoporous area, which comprises the steps of firstly exchanging and washing a roasted molecular sieve with acidic solutions such as nitric acid and hydrochloric acid for multiple times, drying, then roasting for the second time, desiliconizing the molecular sieve with inorganic base after roasting, washing the molecular sieve with dilute acid for multiple times after desiliconization and filtration, drying, roasting for the third time, exchanging ammonium salt ions for multiple times after roasting, and roasting for the fourth time after drying to obtain the molecular sieve with the high mesoporous area.
Although the ZSM-5 molecular sieve with the secondary holes can be obtained by the method, the desiliconization can obviously reduce the silica-alumina ratio of the molecular sieve, and although non-framework aluminum can be removed by acid washing, the acid washing step does not have obvious effect on improving the whole silica-alumina ratio of the molecular sieve. Therefore, in order to obtain more mesopores, the molecular sieve is subjected to desilication modification or the acid-base coupling treatment disclosed above, and the silica-alumina ratio of the molecular sieve is obviously lower than that of the molecular sieve raw material before modification. Therefore, in order to obtain a mesoporous molecular sieve with a high silica-alumina ratio, a molecular sieve raw material with a higher silica-alumina ratio needs to be used. As mentioned above, the synthesis of molecular sieve with high silica-alumina ratio is difficult to be widely applied in catalytic cracking catalyst due to the reasons of low production cost, environmental pollution, poor hydrothermal stability caused by fine crystal grains, etc.
Researches show that after the ZSM-5 molecular sieve is modified by a phosphorus compound and metal, or a phosphorus and metal modified binder is used in the catalyst, the phosphorus and metal modified binder has a positive effect on improving the octane number of gasoline, and meanwhile, the stability of an activator of the catalyst can be improved.
Chinese patent CN 102049291A discloses a molecular sieve auxiliary agent with high silica-alumina ratio, which takes phosphor-alumina gel as a binder, has higher strength and activity, improves the product distribution and simultaneously improves the gasoline octane number.
Chinese patent CN 1611299a discloses an MFI structure molecular sieve containing phosphorus and metal components, which has an anhydrous chemical expression, in terms of the weight of oxides: (0-0.3) Na2O(0.5-5.5)Al2O3(1.3-10)P2O5(0.7-15)M1xOy(0.01-5)M2mOn(70-97)SiO2Wherein M1 is selected from one of transition metals Fe, Co and Ni, and M2 is selected from any one of metals Zn, Mn, Ga and Sn. The molecular sieve has excellent performances of increasing the yield of low-carbon olefin and increasing the content of aromatic hydrocarbon in gasoline, and can be used as a shape-selective active component to be applied to a petroleum hydrocarbon catalytic cracking catalyst or an auxiliary agent.
Chinese patent CN 1057408A discloses a cracking catalyst containing high-silicon zeolite with high catalytic cracking activity, wherein the high-silicon zeolite is ZSM-5, β zeolite or mordenite containing 0.01-3.0 wt% of phosphorus, 0.01-1.0 wt% of iron or 0.01-10 wt% of aluminum, and the hydrogen type or potassium type ZSM-5 zeolite, β zeolite or mordenite with the silicon-aluminum ratio of more than 15 is heated to 350-820 ℃ for 0.1-10 hours-1The volume space velocity of the water-based catalyst is obtained after introducing an aluminum halide aqueous solution, an iron halide aqueous solution or an ammonium phosphate aqueous solution.
U.S. patent USP5,110,776 discloses a process for the preparation of a ZSM-5 zeolite catalyst modified with phosphorus. The phosphorus modification process comprises the steps of dispersing zeolite in a phosphorus compound aqueous solution with the pH value of 2-6, pulping the zeolite and a substrate, and carrying out spray drying and forming. The obtained catalyst can improve the octane number of gasoline without increasing the yield of dry gas and coke.
U.S. patent No. USP6,080,303 discloses a method for increasing the catalytic activity of small and medium pore zeolites. The process comprises treating small and medium pore zeolites with a phosphorus compound and then treating the zeolite with a phosphorus compoundPhosphorus treated zeolite with AlPO4And (4) combining the gel. The method can improve the activity and hydrothermal stability of small and medium pore zeolites.
Disclosure of Invention
The invention aims to provide a catalytic cracking auxiliary agent for improving the octane number of gasoline and a preparation method thereof.
In order to achieve the above object, the present disclosure provides a catalytic cracking promoter for increasing gasoline octane number, the promoter comprising 10-75 wt% of phosphorus-containing and supported metal MFI structure molecular sieve based on the dry weight of the promoter, 3-40 wt% of phosphorus-aluminum inorganic binder based on the dry weight, 1-30 wt% of other inorganic binder calculated by oxide, 0-60 wt% of second clay calculated by dry weight, and 0.5-15 wt% of metal additive selected from group viii metals and at least one of manganese, zinc and gallium calculated by oxide; wherein the phosphorus-aluminum inorganic binder is phosphorus-aluminum glue and/or phosphorus-aluminum inorganic binder containing first clay, and the phosphorus-aluminum inorganic binder containing first clay comprises Al based on the dry weight of the phosphorus-aluminum inorganic binder containing first clay2O315-40% by weight, calculated as P, of an aluminium component2O545-80 wt% of phosphorus component and more than 0 and not more than 40 wt% of first clay calculated on dry basis weight, and the P/Al weight ratio is 1.0-6.0, pH value is 1-3.5, solid content is 15-60 wt%; n (SiO) of the molecular sieve2)/n(Al2O3) Greater than 100; with P2O5The phosphorus content of the molecular sieve is 0.1-5 wt% based on the dry weight of the molecular sieve; the content of the supported metal of the molecular sieve is 0.1-5 wt% calculated by the oxide of the supported metal and based on the dry weight of the molecular sieve; the Al distribution parameter D of the molecular sieve meets the following requirements: d is more than or equal to 0.6 and less than or equal to 0.85, wherein,d ═ al (s)/al (c), al(s) represents the aluminum content in the region arbitrarily greater than 100 square nanometers within the distance H inward from the edge of the crystal face of the molecular sieve crystal grain measured by TEM-EDS, and al (c) represents the aluminum content in the region arbitrarily greater than 100 square nanometers within the distance H outward from the geometric center of the crystal face of the molecular sieve crystal grain measured by TEM-EDS, wherein H is 10% of the distance from a certain point of the edge of the crystal face to the geometric center of the crystal face; the proportion of the mesopore volume of the molecular sieve in the total pore volume is 40-80% by volume, and the proportion of the mesopore volume with the pore diameter of 2-20 nm in the total mesopore volume is more than 90% by volume; the ratio of the strong acid amount of the molecular sieve to the total acid amount is 60-80%, and the ratio of the acid amount of the B acid to the acid amount of the L acid is 15-80.
Preferably, n (SiO) of the molecular sieve2)/n(Al2O3) Greater than 120; with P2O5The phosphorus content of the molecular sieve is 0.2-4 wt% based on the dry weight of the molecular sieve; the content of the supported metal of the molecular sieve is 0.5-3 wt% calculated by the oxide of the supported metal and based on the dry weight of the molecular sieve; the Al distribution parameter D of the molecular sieve meets the following requirements: d is more than or equal to 0.65 and less than or equal to 0.80; the proportion of the mesopore volume of the molecular sieve in the total pore volume is 50-70% by volume, and the proportion of the mesopore volume with the pore diameter of 2-20 nm in the total mesopore volume is more than 92% by volume; the ratio of the strong acid amount of the molecular sieve to the total acid amount is 65-75%, and the ratio of the acid amount of the B acid to the acid amount of the L acid is 20-50.
Preferably, the supported metal is at least one selected from the group consisting of iron, cobalt, nickel, copper, manganese, zinc, tin, bismuth and gallium.
Preferably, the first clay is at least one selected from kaolin, sepiolite, attapulgite, rectorite, montmorillonite and diatomite; the second clay is at least one selected from kaolin, metakaolin, diatomite, sepiolite, attapulgite, montmorillonite and rectorite; the other inorganic binder is at least one selected from pseudo-boehmite, alumina sol, silica-alumina sol and water glass.
Preferably, the metal additive is introduced into the auxiliary in the form of a metal compound, the metal compound being at least one selected from the group consisting of an oxide, a hydroxide, a chloride, a nitrate, a sulfate, a phosphate and an organic compound.
Preferably, the auxiliary agent also contains P based on the dry weight of the auxiliary agent2O5Up to 5 wt% of a phosphorus additive.
Preferably, the adjuvant comprises 8-25 wt% of a phosphorus-aluminum inorganic binder, 20-60 wt% of a phosphorus-containing and metal-loaded MFI structure molecular sieve, 10-45 wt% of a second clay, 5-25 wt% of other inorganic binders, 1.0-10 wt% of a metal additive, and 0-3 wt% of a phosphorus additive.
The present disclosure also provides a method for preparing a catalytic cracking aid for increasing the octane number of gasoline, the method comprising: mixing the phosphorus-containing and metal-loaded MFI structure molecular sieve, the phosphorus-aluminum inorganic binder and other inorganic binders, adding or not adding second clay, pulping, and spray-drying; wherein, a metal additive is introduced, and a phosphorus additive is introduced or not introduced; based on the total dry basis weight of the preparation raw materials of the auxiliary agent, the preparation raw materials of the auxiliary agent comprise 10-75 wt% of phosphorus-containing and metal-loaded MFI structure molecular sieve based on the dry basis weight, 3-40 wt% of phosphorus-aluminum inorganic binder based on the dry basis weight, 1-30 wt% of other inorganic binders based on oxides, 0-60 wt% of second clay based on the dry basis weight, 0.5-15 wt% of metal additives selected from VIII group metals and at least one of manganese, zinc and gallium based on the oxides, and the additive or the additive does not comprise P2O5Up to 5 wt% of a phosphorus additive; wherein the phosphorus-aluminum inorganic binder is phosphorus-aluminum glue and/or phosphorus-aluminum inorganic binder containing first clay, and the phosphorus-aluminum inorganic binder containing first clay comprises Al based on the dry weight of the phosphorus-aluminum inorganic binder containing first clay2O315-40% by weight, calculated as P, of an aluminium component2O545-80 wt% of a phosphorus component and more than 0 and not more than 40 wt% of a first clay on a dry basis and having a P/Al weightThe weight ratio is 1.0-6.0, the pH value is 1-3.5, and the solid content is 15-60 wt%; n (SiO) of the molecular sieve2)/n(Al2O3) Greater than 100; with P2O5The phosphorus content of the molecular sieve is 0.1-5 wt% based on the dry weight of the molecular sieve; the content of the supported metal of the molecular sieve is 0.1-5 wt% calculated by the oxide of the supported metal and based on the dry weight of the molecular sieve; the Al distribution parameter D of the molecular sieve meets the following requirements: d is more than or equal to 0.6 and less than or equal to 0.85, wherein D is Al (S)/Al (C), Al (S) represents the aluminum content of a region which is arbitrarily more than 100 square nanometers in the inward H distance of the crystal face edge of the molecular sieve crystal grain measured by a TEM-EDS method, Al (C) represents the aluminum content of a region which is arbitrarily more than 100 square nanometers in the outward H distance of the geometric center of the crystal face of the molecular sieve crystal grain measured by the TEM-EDS method, wherein H is 10 percent of the distance from a certain point of the crystal face edge to the geometric center of the crystal face; the proportion of the mesopore volume of the molecular sieve in the total pore volume is 40-80% by volume, and the proportion of the mesopore volume with the pore diameter of 2-20 nm in the total mesopore volume is more than 90% by volume; the ratio of the strong acid amount of the molecular sieve to the total acid amount is 60-80%, and the ratio of the acid amount of the B acid to the acid amount of the L acid is 15-80.
Preferably, the preparation steps of the phosphorus-containing and metal-loaded MFI structure molecular sieve comprise: a. filtering and washing the crystallized MFI structure molecular sieve slurry to obtain a water-washed molecular sieve; wherein the sodium content of the washed molecular sieve is less than 3 wt% based on the total dry basis weight of the washed molecular sieve calculated as sodium oxide; b. b, carrying out desiliconization treatment on the washed molecular sieve obtained in the step a in an alkali solution, and filtering and washing to obtain a desiliconized molecular sieve; c. b, performing ammonium exchange treatment on the desiliconized molecular sieve obtained in the step b to obtain an ammonium exchange molecular sieve; wherein the ammonium exchanged molecular sieve has a sodium content of less than 0.2 wt.%, based on sodium oxide and based on total dry basis weight of the ammonium exchanged molecular sieve; d. c, dealuminizing the ammonium exchange molecular sieve obtained in the step c in a composite acid dealuminizing agent solution consisting of fluosilicic acid, organic acid and inorganic acid, and filtering and washing to obtain a dealuminized molecular sieve; e. and d, carrying out phosphorus modification treatment, load treatment of load metal and roasting treatment on the dealuminized molecular sieve obtained in the step d to obtain the MFI structure molecular sieve containing phosphorus and load metal.
Preferably, the alkali solution in step b is at least one selected from the group consisting of a sodium hydroxide solution, a potassium hydroxide solution and ammonia water.
Preferably, the conditions of the desilication treatment in the step b include: the weight ratio of the molecular sieve, the alkali in the alkali solution and the water in the alkali solution is 1: (0.1-2): (5-15); the desiliconization treatment is carried out at room temperature to 100 ℃ for 0.2 to 4 hours.
Preferably, the conditions of the desilication treatment in the step b include: the weight ratio of the molecular sieve, the alkali in the alkali solution and the water in the alkali solution is 1: (0.2-1): (5-15).
Preferably, the step of dealuminizing in step d further comprises: mixing organic acid with the ammonium exchange molecular sieve, and then mixing fluosilicic acid and inorganic acid with the ammonium exchange molecular sieve.
Preferably, the organic acid in step d is at least one selected from the group consisting of ethylenediaminetetraacetic acid, oxalic acid, citric acid and sulfosalicylic acid, and the inorganic acid is at least one selected from the group consisting of hydrochloric acid, sulfuric acid and nitric acid.
Preferably, the organic acid in step d is oxalic acid, and the inorganic acid is hydrochloric acid.
Preferably, the dealumination treatment conditions in step d include: the weight ratio of the molecular sieve, the organic acid, the inorganic acid and the fluosilicic acid is 1 (0.05-0.5) to 0.05-0.5): (0.02-0.5); the treatment temperature is 25-100 ℃, and the treatment time is 0.5-6 hours.
Preferably, the dealumination treatment conditions in step d include: the weight ratio of the molecular sieve, the organic acid, the inorganic acid and the fluosilicic acid is 1 (0.1-0.3) to 0.1-0.3) in terms of dry weight: (0.05-0.3).
Preferably, the phosphorus modification treatment in step e comprises: at least one phosphorus-containing compound selected from phosphoric acid, ammonium hydrogen phosphate, ammonium dihydrogen phosphate and ammonium phosphate is used to impregnate and/or ion-exchange the molecular sieve.
Preferably, the metal-supporting process in step e includes: loading a supported metal selected from at least one of iron, cobalt, nickel, copper, manganese, zinc, tin, bismuth and gallium on the molecular sieve by an impregnation method.
Preferably, the conditions of the calcination treatment include: the atmosphere of the roasting treatment is air atmosphere or water vapor atmosphere; the roasting temperature is 400-800 ℃, and the roasting time is 0.5-8 hours.
Preferably, the preparation step of the first clay-containing aluminophosphate inorganic binder comprises: (1) pulping and dispersing an alumina source, first clay and water into slurry with the solid content of 8-45 wt%; the alumina source is aluminum hydroxide and/or aluminum oxide which can be peptized by acid, first clay and Al which are calculated by dry weight2O3The weight ratio of the alumina source is (more than 0-40) to (15-40); (2) adding concentrated phosphoric acid into the slurry obtained in the step (1) according to the weight ratio of P/Al to 1-6 under stirring; (3) and (3) reacting the slurry obtained in the step (2) at the temperature of 50-99 ℃ for 15-90 minutes.
The catalytic cracking auxiliary agent provided by the disclosure has good catalytic cracking performance, can be used for catalytic cracking reaction of hydrocarbon oil after being mixed with a main agent, can improve the octane number of catalytic cracking gasoline, and can remarkably improve the content of isomeric hydrocarbon in gasoline so as to improve the octane number of the gasoline.
Additional features and advantages of the disclosure will be set forth in the detailed description which follows.
Detailed Description
The following describes in detail specific embodiments of the present disclosure. It should be understood that the detailed description and specific examples, while indicating the present disclosure, are given by way of illustration and explanation only, not limitation.
The present disclosure provides a catalytic cracking assistant for increasing gasoline octane number, which comprises, based on the dry weight of the assistant, 10-75 wt% of phosphorus-containing and metal-loaded MFI structure molecular sieve, 3-40 wt% of phosphorus-aluminum inorganic binder, 1-30 wt% of other inorganic binders, 0-60 wt% of second clay, and 0.5-15 wt% of metal additive selected from group VIII metals and at least one of manganese, zinc and gallium; wherein the phosphorus-aluminum inorganic binder is phosphorus-aluminum glue and/or phosphorus-aluminum inorganic binder containing first clay, and the phosphorus-aluminum inorganic binder containing first clay comprises Al based on the dry weight of the phosphorus-aluminum inorganic binder containing first clay2O315-40% by weight, calculated as P, of an aluminium component2O545-80 wt% of phosphorus component and more than 0 and not more than 40 wt% of first clay calculated on dry basis weight, and the P/Al weight ratio is 1.0-6.0, pH value is 1-3.5, solid content is 15-60 wt%; n (SiO) of the molecular sieve2)/n(Al2O3) Greater than 100; with P2O5The phosphorus content of the molecular sieve is 0.1-5 wt% based on the dry weight of the molecular sieve; the content of the supported metal of the molecular sieve is 0.1-5 wt% calculated by the oxide of the supported metal and based on the dry weight of the molecular sieve; the Al distribution parameter D of the molecular sieve meets the following requirements: d is more than or equal to 0.6 and less than or equal to 0.85, wherein D is Al (S)/Al (C), Al (S) represents the aluminum content of a region which is arbitrarily more than 100 square nanometers in the inward H distance of the crystal face edge of the molecular sieve crystal grain measured by a TEM-EDS method, Al (C) represents the aluminum content of a region which is arbitrarily more than 100 square nanometers in the outward H distance of the geometric center of the crystal face of the molecular sieve crystal grain measured by the TEM-EDS method, wherein H is 10 percent of the distance from a certain point of the crystal face edge to the geometric center of the crystal face; the proportion of the mesopore volume of the molecular sieve in the total pore volume is 40-80% by volume, and the proportion of the mesopore volume with the pore diameter of 2-20 nm in the total mesopore volume is more than 90% by volume; the strong acid content of the molecular sieve accounts for 60-80% of the total acid content, and B acidThe ratio of the acid amount to the L acid amount is 15-80. Preferably, n (SiO) of the molecular sieve2)/n(Al2O3) Greater than 120; with P2O5The phosphorus content of the molecular sieve is 0.2-4 wt% based on the dry weight of the molecular sieve; the content of the supported metal of the molecular sieve is 0.5-3 wt% calculated by the oxide of the supported metal and based on the dry weight of the molecular sieve; the Al distribution parameter D of the molecular sieve meets the following requirements: d is more than or equal to 0.65 and less than or equal to 0.80; the proportion of the mesopore volume of the molecular sieve in the total pore volume is 50-70% by volume, and the proportion of the mesopore volume with the pore diameter of 2-20 nm in the total mesopore volume is more than 92% by volume; the ratio of the strong acid amount of the molecular sieve to the total acid amount is 65-75%, and the ratio of the acid amount of the B acid to the acid amount of the L acid is 20-50.
According to the present disclosure, the aluminophosphate inorganic binder is a aluminophosphate inorganic binder and/or a aluminophosphate gel comprising a first clay.
In one embodiment, the phosphorus-aluminum inorganic binder comprises Al based on the dry weight of the phosphorus-aluminum inorganic binder2O315-40% by weight, calculated as P, of an aluminium component2O545-80 wt% of phosphorus component and 0-40 wt% of first clay calculated by dry basis weight, and the P/Al weight ratio is 1.0-6.0, pH value is 1-3.5, and solid content is 15-60 wt%; for example, including Al2O315-40% by weight, calculated as P, of an aluminium component2O545-80 wt% of a phosphorus component and 1-40 wt% of a first clay, based on dry weight; preferably contains Al2O315-35% by weight, calculated as P, of an aluminium component2O5A phosphorus component in an amount of 50 to 75 wt% and a first clay in an amount of 8 to 35 wt% on a dry basis, preferably having a P/Al weight ratio of 1.2 to 6.0, more preferably 2.0 to 5.0, and a pH value of 1.5 to 3.0.
In another embodiment, the phosphorus aluminum inorganic binder comprises Al based on the dry weight of the phosphorus aluminum inorganic binder2O320-40% by weight, calculated as P, of an aluminium component2O560-80% by weight of a phosphorus component.
According to the present disclosure, the supported metal refers to a metal supported on the molecular sieve by a supporting manner, and does not include aluminum and alkali metals such as sodium and potassium, and may include at least one selected from iron, cobalt, nickel, copper, manganese, zinc, tin, bismuth and gallium, and may also include other metals, and the present disclosure is not limited thereto.
According to the present disclosure, it is well known to those skilled in the art to determine the aluminum content of the molecular sieve by using the TEM-EDS method, wherein the geometric center is also well known to those skilled in the art, and can be calculated according to a formula, which is not repeated in the present disclosure, the geometric center of the general symmetric graph is an intersection point of connecting lines of respective opposite vertices, for example, the geometric center of the hexagonal crystal plane of the conventional hexagonal plate-shaped ZSM-5 is at an intersection point of connecting lines of three opposite vertices, the crystal plane is one surface of a regular crystal grain, and the inward and outward directions are both inward and outward directions on the crystal plane.
According to the present disclosure, the ratio of the mesopore volume of the molecular sieve, which is the pore volume having a pore diameter greater than 2 nanometers and less than 100 nanometers, to the total pore volume is measured using the nitrogen adsorption BET specific surface area method; the strong acid amount of the molecular sieve is NH in proportion to the total acid amount3The TPD method, the acid centre of which is NH3Desorbing the corresponding acid center at the temperature of more than 300 ℃; and the ratio of the acid amount of the B acid to the acid amount of the L acid is measured by adopting a pyridine adsorption infrared acidity method.
According to the present disclosure, the metal additive is added during the beating process, which may be introduced in the form of the metal compound in the preparation of the shaped aid, for example in the form of at least one selected from the group consisting of oxides, hydroxides, chlorides, nitrates, sulfates, phosphates and organic compounds, preferably in the form of one or more from the group consisting of oxides, orthophosphates, phosphites, basic phosphates and acid phosphates.
Clays are well known to those skilled in the art in light of this disclosure, and the first clay may be at least one selected from the group consisting of kaolin, sepiolite, attapulgite, rectorite, montmorillonite and diatomaceous earth, preferably including rectorite, more preferably rectorite; the second clay may be at least one selected from kaolin, metakaolin, sepiolite, attapulgite, montmorillonite, rectorite, diatomaceous earth, halloysite, saponite, bentonite and hydrotalcite, preferably at least one selected from kaolin, metakaolin, diatomaceous earth, sepiolite, attapulgite, montmorillonite and rectorite; the additional inorganic binder may be selected from one or more of the inorganic oxide binders conventionally used in catalytic cracking promoters or catalyst binder components other than the aluminophosphate and aluminophosphate inorganic binders, preferably from at least one of pseudoboehmite, alumina sol, silica alumina sol, and water glass, more preferably from at least one of pseudoboehmite and alumina sol.
In accordance with the present disclosure, the first clay-containing aluminophosphate inorganic binder preferably contains Al2O315-35% by weight, calculated as P, of an aluminium component2O5A phosphorus component in an amount of 50 to 75 wt% and a first clay in an amount of 8 to 35 wt% on a dry basis, preferably having a P/Al weight ratio of 1.2 to 6.0, more preferably 2.0 to 5.0, and a pH value of 1.0 to 3.5.
According to the disclosure, the adjuvant may further comprise P on a dry weight basis2O5Up to 5 wt% of a phosphorus additive. The phosphorus additive may be selected from phosphorus compounds, such as one or more of inorganic compounds and organic compounds including phosphorus, which may be readily soluble in water, or may be a poorly water-soluble or water-insoluble phosphorus compound, such as one or more selected from phosphorus oxides, phosphoric acid, orthophosphates, phosphites, hypophosphites, basic phosphates, acid phosphates, and phosphorus-containing organic compounds. Preferred phosphorus compounds are one or more of phosphoric acid, ammonium phosphate, ammonium dihydrogen phosphate, diammonium hydrogen phosphate and aluminum phosphate. The resulting adjuvant has a phosphorus additive in the form of a phosphorus compound such as phosphorus oxide, orthophosphate, phosphite, basic phosphate and acid phosphate. The phosphorus additive may beIs present in any location where the adjunct may be present, such as may be present inside the channels of the zeolite, on the surface of the zeolite, in the matrix material (i.e. the material of the adjunct other than the molecular sieve) and may also be present both inside the channels of the zeolite, on the surface of the zeolite and in said matrix material. The phosphorus additive is not included in the content of phosphorus in the molecular sieve, nor is the phosphorus introduced by the phosphorus-aluminum inorganic binder included.
In accordance with the present disclosure, the adjuvant preferably comprises 8-25 wt.% of a phosphorus aluminum inorganic binder, 20-60 wt.% of a phosphorus containing and metal loaded MFI structure molecular sieve, 10-45 wt.% of a second clay, 5-25 wt.% of other inorganic binders, 1.0-10 wt.% of a metal additive, and 0-3 wt.% of a phosphorus additive.
The present disclosure also provides a method for preparing a catalytic cracking aid for increasing the octane number of gasoline, the method comprising: mixing the phosphorus-containing and metal-loaded MFI structure molecular sieve, the phosphorus-aluminum inorganic binder and other inorganic binders, adding or not adding second clay, pulping, and spray-drying; wherein, a metal additive is introduced, and a phosphorus additive is introduced or not introduced; based on the total dry basis weight of the preparation raw materials of the auxiliary agent, the preparation raw materials of the auxiliary agent comprise 10-75 wt% of phosphorus-containing and metal-loaded MFI structure molecular sieve based on the dry basis weight, 3-40 wt% of phosphorus-aluminum inorganic binder based on the dry basis weight, 1-30 wt% of other inorganic binders based on oxides, 0-60 wt% of second clay based on the dry basis weight, 0.5-15 wt% of metal additives selected from VIII group metals and at least one of manganese, zinc and gallium based on the oxides, and the additive or the additive does not comprise P2O5Up to 5 wt% of a phosphorus additive; wherein the phosphorus-aluminum inorganic binder is phosphorus-aluminum glue and/or phosphorus-aluminum inorganic binder containing first clay, and the phosphorus-aluminum inorganic binder containing first clay comprises Al based on the dry weight of the phosphorus-aluminum inorganic binder containing first clay2O315-40% by weight, calculated as P, of an aluminium component2O545-80% by weight of a phosphorus component and more than 0 and not more than 40% by weight of a first clay, based on the weight of the dry basis, and its P/Al weightThe ratio is 1.0-6.0, the pH value is 1-3.5, and the solid content is 15-60 wt%; n (SiO) of the molecular sieve2)/n(Al2O3) Greater than 100; with P2O5The phosphorus content of the molecular sieve is 0.1-5 wt% based on the dry weight of the molecular sieve; the content of the supported metal of the molecular sieve is 0.1-5 wt% calculated by the oxide of the supported metal and based on the dry weight of the molecular sieve; the Al distribution parameter D of the molecular sieve meets the following requirements: d is more than or equal to 0.6 and less than or equal to 0.85, wherein D is Al (S)/Al (C), Al (S) represents the aluminum content of a region which is arbitrarily more than 100 square nanometers in the inward H distance of the crystal face edge of the molecular sieve crystal grain measured by a TEM-EDS method, Al (C) represents the aluminum content of a region which is arbitrarily more than 100 square nanometers in the outward H distance of the geometric center of the crystal face of the molecular sieve crystal grain measured by the TEM-EDS method, wherein H is 10 percent of the distance from a certain point of the crystal face edge to the geometric center of the crystal face; the proportion of the mesopore volume of the molecular sieve in the total pore volume is 40-80% by volume, and the proportion of the mesopore volume with the pore diameter of 2-20 nm in the total mesopore volume is more than 90% by volume; the ratio of the strong acid amount of the molecular sieve to the total acid amount is 60-80%, and the ratio of the acid amount of the B acid to the acid amount of the L acid is 15-80.
According to the present disclosure, the steps of preparing the phosphorus-containing and metal-loaded MFI structure molecular sieve may comprise: a. filtering and washing the crystallized MFI structure molecular sieve slurry to obtain a water-washed molecular sieve; wherein the sodium content of the washed molecular sieve is less than 3 wt% based on the total dry basis weight of the washed molecular sieve calculated as sodium oxide; b. b, carrying out desiliconization treatment on the washed molecular sieve obtained in the step a in an alkali solution, and filtering and washing to obtain a desiliconized molecular sieve; c. b, performing ammonium exchange treatment on the desiliconized molecular sieve obtained in the step b to obtain an ammonium exchange molecular sieve; wherein the ammonium exchanged molecular sieve has a sodium content of less than 0.2 wt.%, based on sodium oxide and based on total dry basis weight of the ammonium exchanged molecular sieve; d. c, dealuminizing the ammonium exchange molecular sieve obtained in the step c in a composite acid dealuminizing agent solution consisting of fluosilicic acid, organic acid and inorganic acid, and filtering and washing to obtain a dealuminized molecular sieve; e. and d, carrying out phosphorus modification treatment, load treatment of load metal and roasting treatment on the dealuminized molecular sieve obtained in the step d to obtain the MFI structure molecular sieve containing phosphorus and load metal.
The slurry of the MFI structure molecular sieve obtained by crystallization is well known to those skilled in the art according to the present disclosure, and the present disclosure is not repeated, wherein the MFI structure molecular sieve is also well known to those skilled in the art, and can be obtained by crystallization without amine, or can be a molecular sieve prepared by a template method, wherein the molecular sieve synthesized without amine does not need to be calcined, the molecular sieve prepared by the template method needs to be dried and then calcined in air, and the silica-alumina ratio of the ZSM-5 molecular sieve is generally less than 100.
According to the present disclosure, the desiliconization treatment using an alkaline solution is well known to those skilled in the art, the alkaline solution in step b may be at least one selected from the group consisting of a sodium hydroxide solution, a potassium hydroxide solution and ammonia water, preferably a sodium hydroxide solution, and the conditions of the desiliconization treatment may include: the weight ratio of the molecular sieve, the alkali in the alkali solution and the water in the alkali solution is 1: (0.1-2): (5-15), preferably 1: (0.2-1): (5-15); the desiliconization treatment is carried out at room temperature to 100 ℃ for 0.2 to 4 hours.
Ammonium exchange treatment is well known to those skilled in the art in light of this disclosure, for example, in step c, the base treated desilicated molecular sieve can be prepared according to the following molecular sieve: ammonium salt: h2O is 1: (0.1-1): (5-10) exchanging at room temperature to 100 ℃ for 0.5-2 hours, filtering to remove Na on the molecular sieve2The O content is less than 0.2 wt%. The ammonium salt may be a commonly used inorganic ammonium salt, for example, at least one selected from the group consisting of ammonium chloride, ammonium sulfate and ammonium nitrate.
Both organic and inorganic acids are well known to those skilled in the art in light of the present disclosure, for example, the organic acid in step d may be at least one selected from ethylenediaminetetraacetic acid, oxalic acid, citric acid, and sulfosalicylic acid, preferably oxalic acid; the inorganic acid may be at least one selected from hydrochloric acid, sulfuric acid and nitric acid, and is preferably hydrochloric acid.
Dealumination treatments are well known to those skilled in the art in light of this disclosure, but the use of inorganic acids, organic acids, and fluosilicic acid together for dealumination treatments has not been reported. The dealumination treatment can be carried out once or for multiple times, organic acid can be firstly mixed with the ammonium exchange molecular sieve, and then fluosilicic acid and inorganic acid are mixed with the ammonium exchange molecular sieve, namely, the organic acid is firstly added into the ammonium exchange molecular sieve, and then the fluosilicic acid and the inorganic acid are slowly and concurrently added, or the fluosilicic acid is firstly added and then the inorganic acid is added, preferably the fluosilicic acid and the inorganic acid are slowly and concurrently added. The dealumination treatment conditions may include: the weight ratio of the molecular sieve, the organic acid, the inorganic acid and the fluosilicic acid is 1 (0.05-0.5) to 0.05-0.5): (0.02-0.5), preferably 1 (0.1-0.3) to (0.1-0.3): (0.05-0.3); the treatment temperature is 25-100 ℃, and the treatment time is 0.5-6 hours.
The phosphorus modification treatment is well known to those skilled in the art in light of this disclosure, and the phosphorus modification treatment in step e may comprise: at least one phosphorus-containing compound selected from phosphoric acid, ammonium hydrogen phosphate, ammonium dihydrogen phosphate and ammonium phosphate is used to impregnate and/or ion-exchange the molecular sieve.
According to the present disclosure, the supporting treatment of the supported metal is well known to those skilled in the art, and means that the supported metal is supported on the molecular sieve by a supporting method, for example, the supported metal may be supported on the molecular sieve by an impregnation method using a compound containing at least one supported metal selected from iron, cobalt, nickel, copper, manganese, zinc, tin, bismuth and gallium; the loading method may also include other common metal loading methods, and the disclosure is not limited.
The calcination treatment is also well known to those skilled in the art in light of this disclosure, and may be performed under conditions such as: the atmosphere of the roasting treatment is air atmosphere or water vapor atmosphere; the roasting temperature is 400-800 ℃, and the roasting time is 0.5-8 hours.
The washing described in this disclosure is well known to those skilled in the art and can be done in the following manner: and (3) leaching the filtered molecular sieve by using water with the temperature of 30-60 ℃ which is 5-10 times that of the filtered molecular sieve.
According to the present disclosure, the step of preparing the first clay-containing aluminophosphate inorganic binder may comprise: (1) pulping and dispersing an alumina source, first clay and water into slurry with the solid content of 8-45 wt%; the alumina source is aluminum hydroxide and/or aluminum oxide which can be peptized by acid, first clay and Al which are calculated by dry weight2O3The weight ratio of the alumina source is (more than 0-40) to (15-40); (2) adding concentrated phosphoric acid into the slurry obtained in the step (1) according to the weight ratio of P/Al to 1-6 under stirring; wherein P in the P/Al is the weight of phosphorus in the phosphoric acid by simple substance, and Al is the weight of aluminum in the alumina source by simple substance; (3) and (3) reacting the slurry obtained in the step (2) at the temperature of 50-99 ℃ for 15-90 minutes.
According to the present disclosure, the alumina source may be at least one selected from the group consisting of rho-alumina, chi-alumina, η -alumina, gamma-alumina, kappa-alumina, delta-alumina, theta-alumina, gibbsite, surge, nordstrandite, diaspore, boehmite, and pseudoboehmite from which the aluminum component of the first clay-containing aluminophosphate inorganic binder is derived, the first clay may be one or more of kaolin, sepiolite, attapulgite, rectorite, montmorillonite, and diatomaceous earth, preferably rectorite, the concentrated phosphoric acid may have a concentration of 60 to 98 wt%, more preferably 75 to 90 wt%, a feeding rate of the phosphoric acid is preferably 0.01 to 0.10Kg phosphoric acid/min/Kg alumina source, more preferably 0.03 to 0.07Kg phosphoric acid/min/Kg alumina source.
According to the disclosure, due to the introduction of the clay, the phosphorus-aluminum inorganic binder containing the first clay not only improves mass transfer and heat transfer among materials in the preparation process, but also avoids binder solidification caused by nonuniform local instant violent reaction of the materials, heat release and overtemperature, and the obtained binder has the same binding performance as the phosphorus-aluminum binder prepared by a method without introducing the clay; in addition, the method introduces clay, especially rectorite with a layered structure, improves the heavy oil conversion capability of the catalyst composition, and enables the obtained auxiliary agent to have better selectivity.
The preparation method of the catalytic cracking assistant provided by the present disclosure mixes and pulps the phosphorus-containing and metal-loaded MFI structure molecular sieve, the phosphorus-aluminum inorganic binder and other inorganic binders, and the order of addition thereof has no special requirement, for example, the phosphorus-aluminum inorganic binder, other inorganic binders, the molecular sieve and the second clay can be mixed (when the second clay is not contained, the relevant addition step can be omitted) and then pulped, preferably, the second clay, the molecular sieve and other inorganic binders are mixed and pulped, and then the phosphorus-aluminum inorganic binder is added, which is beneficial to improving the activity and selectivity of the assistant.
The preparation method of the catalytic cracking assistant provided by the disclosure further comprises the step of spray drying the slurry obtained by pulping. Methods of spray drying are well known to those skilled in the art and no particular requirement of the present disclosure exists.
In the preparation method of the catalytic cracking assistant provided by the present disclosure, the metal additive can be introduced in the form of a metal compound, and the metal additive can be introduced by adding the metal compound to the slurry in any step before spray drying and forming in the preparation process of the assistant; or the promoter can be introduced by impregnating or chemically adsorbing the metal compound and then roasting after spray drying and molding, including the steps of impregnating or chemically adsorbing the promoter by using the aqueous solution of the metal-containing compound, and then carrying out solid-liquid separation (if needed), drying and roasting, wherein the drying temperature can be between room temperature and 400 ℃, preferably 100-300 ℃, the roasting temperature can be between 400-700 ℃, preferably 450-650 ℃, and the roasting time can be between 0.5 and 100 hours, preferably between 0.5 and 10 hours. The metal compound is selected from one or more of inorganic compounds and organic compounds thereof, and can be easily soluble in water, or can be hardly soluble in water or insoluble in water. Examples of the metal compound include oxides, hydroxides, chlorides, nitrates, sulfates, phosphates, organic compounds of metals, and the like of metals. Preferred metal compounds are selected from one or more of their chlorides, nitrates, sulfates and phosphates.
In the catalytic cracking promoter provided by the present disclosure, the metal additive may be present in any possible location of the promoter, such as may be present inside the pores of the zeolite, on the surface of the zeolite, in the matrix material, and may also be present both inside the pores of the zeolite, on the surface of the zeolite and in the matrix material, preferably in the matrix material. The metal additives may be present in the form of their oxides, orthophosphates, phosphites, basic phosphates and acid phosphates.
When the promoter contains the phosphorus additive, the phosphorus additive can be introduced by one of the following methods or a combination of several methods, but is not limited to the methods for introducing the phosphorus additive into the promoter:
1. adding a phosphorus compound to the slurry before the spray drying and forming of the auxiliary agent;
2. after the spray drying and forming of the auxiliary agent, the phosphorus compound is impregnated or chemically adsorbed, and the phosphorus compound is introduced through solid-liquid separation (if needed), drying and roasting processes, wherein the drying temperature can be between room temperature and 400 ℃, preferably 100-300 ℃, the roasting temperature can be between 400-700 ℃, preferably 450-650 ℃, and the roasting time can be between 0.5 and 100 hours, preferably between 0.5 and 10 hours. The phosphorus compound may be selected from one or more of various inorganic and organic compounds of phosphorus. The phosphorus compound may be either readily water-soluble or poorly water-soluble or water-insoluble. Examples of the phosphorus compound include oxides of phosphorus, phosphoric acid, orthophosphates, phosphites, hypophosphites, phosphorus-containing organic compounds, and the like. Preferred phosphorus compounds are selected from one or more of phosphoric acid, ammonium phosphate, ammonium dihydrogen phosphate, diammonium hydrogen phosphate and aluminum phosphate.
Thus, the phosphorus additive may be present in any location where an adjunct may be present, such as may be present inside the pores of the zeolite, on the surface of the zeolite, in the matrix material, and may also be present both inside the pores of the zeolite, on the surface of the zeolite and in the matrix material. The phosphorus additive is present in the form of a phosphorus compound (e.g., an oxide of phosphorus, an orthophosphate, a phosphite, a basic phosphate, an acid phosphate).
The catalytic cracking auxiliary agent provided by the disclosure is suitable for catalytic cracking of various hydrocarbon oils. When the catalyst is used in the catalytic cracking process, the catalyst can be added into a catalytic cracking reactor independently or can be mixed with a catalytic cracking catalyst for use. In general, the adjunct provided by the present disclosure comprises no more than 30 wt%, preferably 1 to 25 wt%, more preferably 3 to 15 wt% of the total amount of FCC catalyst and adjunct mixture provided by the present disclosure, and the hydrocarbon oil is selected from one or more of various petroleum fractions, such as crude oil, atmospheric residue, vacuum residue, atmospheric wax oil, vacuum wax oil, straight run wax oil, propane light/heavy deoiling, coker wax oil, and coal liquefaction products. The hydrocarbon oil may contain heavy metal impurities such as nickel and vanadium, and sulfur and nitrogen impurities, for example, the content of sulfur may be as high as 3.0 wt%, the content of nitrogen may be as high as 2.0 wt%, and the content of metal impurities such as vanadium and nickel may be as high as 3000 ppm.
The catalytic cracking auxiliary agent provided by the disclosure is used in a catalytic cracking process, and the catalytic cracking conditions of hydrocarbon oil are conventional catalytic cracking conditions. Generally, the hydrocarbon oil catalytic cracking conditions include: the reaction temperature is 400-600 ℃, the preferred temperature is 450-550 ℃, and the weight hourly space velocity is 8-120 h-1Preferably 8 to 80 hours-1The ratio of the solvent to the oil (weight ratio) is 1-20, preferably 3-15. The catalytic cracking auxiliary agent provided by the present disclosure can be used in various existing catalytic cracking reactors, such as in fixed bed reactors, fluidized bed reactors, riser reactors, multi-reaction zone reactors, and the like.
The present disclosure is further illustrated by the following examples, which are not intended to be limiting and the instruments and reagents used in the examples of the present disclosure are those commonly used by those skilled in the art unless otherwise specified.
The crystallinity of the present disclosure is determined using the standard method of ASTM D5758-2001(2011) e 1.
N (SiO) of the present disclosure2)/n(Al2O3) Namely, the silicon-aluminum ratio is calculated by the contents of silicon oxide and aluminum oxide, and the contents of the silicon oxide and the aluminum oxide are measured by the GB/T30905-2014 standard method.
The phosphorus content of the composition is determined by a GB/T30905-.
See methods for solid catalyst investigation, petrochemical, 29(3), 2000: 227.
total specific surface (S) of the present disclosureBET) Mesopore pore volume, total pore volume, and mesopore pore volume of 2-20 nm were measured by AS-3, AS-6 static nitrogen adsorption apparatus manufactured by Quantachrome instruments. The instrument parameters are as follows: the sample was placed in a sample handling system and evacuated to 1.33X 10 at 300 deg.C-2Pa, keeping the temperature and the pressure for 4h, and purifying the sample. Testing the purified samples at different specific pressures P/P at a liquid nitrogen temperature of-196 DEG C0The adsorption quantity and the desorption quantity of the nitrogen under the condition are obtained to obtain N2Adsorption-desorption isotherm curve. Then, the total specific surface area, the micropore specific surface area and the mesopore specific surface area are calculated by utilizing a two-parameter BET formula, and the specific pressure P/P is taken0The adsorption amount was 0.98 or less as the total pore volume of the sample, the pore size distribution of the mesopore portion was calculated using BJH formula, and the mesopore pore volume (2 to 100 nm) and the mesopore pore volume of 2 to 20nm were calculated by the integration method.
The acid content and total acid content of the strong acid disclosed by the disclosure are measured by an Autochem II 2920 temperature programmed desorption instrument of Michman, USA. And (3) testing conditions are as follows: weighing 0.2g of a sample to be detected, putting the sample into a sample tube, putting the sample tube into a thermal conductivity cell heating furnace, taking He gas as carrier gas (50mL/min), heating the sample tube to 600 ℃ at the speed of 20 ℃/min, and purging the sample tube for 60min to remove impurities adsorbed on the surface of the catalyst. Then cooling to 100 ℃, keeping the temperature for 30min, and switching to NH3-He mixed gas (10.02% NH)3+ 89.98% He) for 30min, and then continuously sweeping with He gas for 90min until the baseline is stable to desorbPhysically adsorbed ammonia gas. And (4) heating to 600 ℃ at the heating rate of 10 ℃/min for desorption, keeping for 30min, and finishing desorption. Detecting gas component change by TCD detector, automatically integrating by instrument to obtain total acid amount and strong acid amount, wherein acid center of strong acid is NH3The desorption temperature is higher than 300 ℃ of the corresponding acid center.
The amount of acid B and the amount of acid L of the present disclosure were measured by FTS3000 Fourier Infrared Spectroscopy manufactured by BIO-RAD, USA. And (3) testing conditions are as follows: pressing the sample into tablet, sealing in an in-situ cell of an infrared spectrometer, and vacuumizing to 10 deg.C at 350 deg.C-3Pa, keeping for 1h to enable gas molecules on the surface of the sample to be desorbed completely, and cooling to room temperature. Introducing pyridine vapor with pressure of 2.67Pa into the in-situ tank, balancing for 30min, heating to 200 deg.C, and vacuumizing to 10 deg.C-3Pa, keeping for 30min, cooling to room temperature at 1400-1700cm-1Scanning in wave number range, and recording infrared spectrogram of pyridine adsorption at 200 ℃. Then the sample in the infrared absorption cell is moved to a heat treatment area, the temperature is raised to 350 ℃, and the vacuum is pumped to 10 DEG-3Pa, keeping for 30min, cooling to room temperature, and recording the infrared spectrogram of pyridine adsorption at 350 ℃. And automatically integrating by an instrument to obtain the acid content of the B acid and the acid content of the L acid.
The D value is calculated as follows: selecting a crystal grain and a certain crystal face of the crystal grain in a transmission electron mirror to form a polygon, wherein the polygon has a geometric center, an edge and a 10% distance H (different edge points and different H values) from the geometric center to a certain point of the edge, any one of regions in the inward H distance of the edge of the crystal face which is larger than 100 square nanometers and any one of regions in the outward H distance of the geometric center of the crystal face which is larger than 100 square nanometers are respectively selected, measuring the aluminum content, namely Al (S1) and Al (C1), calculating D1 to Al (S1)/Al (C1), respectively selecting different crystal grains to measure for 5 times, and calculating the average value to be D.
When the auxiliary agent disclosed by the invention is used for evaluating the performance of catalytic cracking reaction, a reaction product is N2Carrying out gas-liquid separation in a liquid receiving bottle at the temperature of minus 10 ℃, and collecting a gas product to finish on-line analysis by an Agilent 6890GC (TCD detector); liquid product CollectionThen off-line weighing is carried out, simulated distillation and gasoline monomer hydrocarbon analysis (testing is carried out by adopting a RIPP81-90 testing method) are respectively carried out, and the cut points of the gasoline and the diesel are 221 ℃ and 343 ℃ respectively; the coke-forming catalyst is burnt and regenerated on line, and the coke mass is calculated according to the flow rate and the composition of the flue gas; the mass of all products is added to calculate the material balance, the octane number is determined by an RIPP 85-90 method, the gasoline PONA composition is determined by analyzing gasoline monomer hydrocarbon, and the octane number barrel is the octane number (RON) multiplied by the gasoline yield.
The RIPP standard method disclosed in the disclosure can be found in petrochemical analysis methods, edition such as Yangcui, 1990 edition.
Some of the raw materials used in the examples had the following properties:
the pseudoboehmite is an industrial product produced by Shandong aluminum industry company, and the solid content is 60 percent by weight; the aluminum sol is an industrial product, Al, produced by the Qilu division of the medium petrochemical catalyst2O3The content was 21.5 wt%; the silica sol is an industrial product, SiO, produced by the middle petrochemical catalyst Qilu division2The content was 28.9% by weight, Na2The O content is 8.9 percent; the kaolin is kaolin specially used for a catalytic cracking catalyst produced by Suzhou kaolin company, and the solid content is 78 weight percent. Hydrochloric acid concentration of 36 wt%, rectorite as product of Hubei Zhongxiang famous flow rectorite development Limited company, and quartz sand content<3.5 wt.% of Al2O339.0 wt.% of Fe2O3The content of Na was 2.0 wt%2The O content was 0.03% by weight, and the solid content was 77% by weight; SB aluminum hydroxide powder: al from Condex, Germany2O3The content was 75% by weight; gamma-alumina powder: al from Condex, Germany2O3The content was 95% by weight. Hydrochloric acid: chemical purity, concentration of 36-38 wt%, and is produced in Beijing chemical plant.
Examples 1-3 provide phosphorus-and metal-loaded MFI structure molecular sieves of the present disclosure, and comparative examples 1-13 provide comparative molecular sieves.
Example 1
Crystallizing ZSM-5 molecular sieve (produced by catalyst Qilu division, amine-free synthesis, n (SiO)2)/n(Al2O3) 27) the mother liquor was filtered off and washed with water to Na2The content of O is lower than 3.0 weight percent, and a filter cake is obtained by filtration; adding 100g (dry basis) of the molecular sieve into 1000g of 2.0% NaOH solution, heating to 65 ℃, reacting for 30min, rapidly cooling to room temperature, filtering, and washing until the filtrate is neutral. Then, the filter cake was added to 800g of water and slurried, 40g of NH was added4Cl, heating to 75 ℃, and carrying out exchange treatment for 1h until Na2The O content is lower than 0.2 weight percent, and a molecular sieve filter cake is obtained after filtering and washing; taking 50g (dry basis) of the molecular sieve, adding water to prepare molecular sieve slurry with the solid content of 10 weight percent, adding 11g of oxalic acid while stirring, then adding 110g of hydrochloric acid (mass fraction is 10 percent) and 92g of fluosilicic acid (mass fraction is 3 percent) in a concurrent flow manner, and adding for 30 min; heating to 65 ℃, stirring for 1h at constant temperature, filtering and washing until the filtrate is neutral; adding water into the filter cake, pulping to obtain molecular sieve slurry with solid content of 40 wt%, adding 1.2g H3PO4(concentration 85% by weight) and 3.3gZn (NO)3)2·6H2And O, uniformly mixing, soaking, drying and roasting at 550 ℃ for 2 hours. The molecular sieve A is obtained, and the physicochemical properties are shown in Table 1.
Comparative example 1
Crystallizing ZSM-5 molecular sieve (produced by catalyst Qilu division, amine-free synthesis, n (SiO)2)/n(Al2O3) 27) the mother liquor was filtered off and washed with water to Na2The content of O is lower than 3.0 weight percent, and a filter cake is obtained by filtration; adding 100g (dry basis) of the molecular sieve into 1000g of 2.0% NaOH solution, heating to 65 ℃, reacting for 30min, rapidly cooling to room temperature, filtering, and washing until the filtrate is neutral. Then, the filter cake was added to 800g of water and slurried, 40g of NH was added4Cl, heating to 75 ℃, and carrying out exchange treatment for 1h until Na2O content less than 0.2 wt%, filtering, washing to obtain moleculeScreening a filter cake; taking 50g (dry basis) of the molecular sieve, adding water to prepare molecular sieve slurry with the solid content of 10 weight percent, and adding 27g of oxalic acid while stirring; heating to 65 ℃, stirring for 1h at constant temperature, filtering and washing until the filtrate is neutral; adding water into the filter cake, pulping to obtain molecular sieve slurry with solid content of 40 wt%, adding 1.2gH3PO4(concentration 85% by weight) and 3.3gZn (NO)3)2·6H2And O, uniformly mixing, soaking, drying and roasting at 550 ℃ for 2 hours. Molecular sieve DA1 was obtained, and the physicochemical properties are shown in Table 1.
Comparative example 2
Crystallizing ZSM-5 molecular sieve (produced by catalyst Qilu division, amine-free synthesis, n (SiO)2)/n(Al2O3) 27) the mother liquor was filtered off and washed with water to Na2The content of O is lower than 3.0 weight percent, and a filter cake is obtained by filtration; adding 100g (dry basis) of the molecular sieve into 1000g of 2.0% NaOH solution, heating to 65 ℃, reacting for 30min, rapidly cooling to room temperature, filtering, and washing until the filtrate is neutral. Then, 50g (dry basis) of the molecular sieve is taken and added with water to prepare molecular sieve slurry with the solid content of 10 weight percent, and 215g of hydrochloric acid (the mass fraction is 10 percent) is added during stirring; heating to 65 ℃, stirring for 1h at constant temperature, filtering and washing until the filtrate is neutral; adding 1500g of water into the filter cake, pulping, adding 80g of NH4Heating Cl to 65 ℃, exchanging and washing for 40min, filtering, and leaching until the filtrate is neutral; adding water into the filter cake, pulping to obtain molecular sieve slurry with solid content of 40 wt%, adding 1.2gH3PO4(concentration 85% by weight) and 3.3gZn (NO)3)2·6H2And O, uniformly mixing, soaking, drying and roasting at 550 ℃ for 2 hours. Molecular sieve DA2 was obtained, and the physicochemical properties are shown in Table 1.
Comparative example 3
Crystallizing ZSM-5 molecular sieve (produced by catalyst Qilu division, amine-free synthesis, n (SiO)2)/n(Al2O3) 27) the mother liquor was filtered off and washed with water to Na2The content of O is lower than 3.0 weight percent, and a filter cake is obtained by filtration; adding 100g (dry basis) of the molecular sieve into 1000g of 2.0% NaOH solution, heating to 65 ℃, reacting for 30min, rapidly cooling to room temperature, filtering,washing until the filtrate is neutral. Then, the filter cake was added to 800g of water and slurried, 40g of NH was added4Cl, heating to 75 ℃, and carrying out exchange treatment for 1h until Na2The O content is lower than 0.2 weight percent, and a molecular sieve filter cake is obtained after filtering and washing; taking 50g (dry basis) of the molecular sieve, adding water to prepare molecular sieve slurry with the solid content of 10 weight percent, adding 370g (mass fraction of 3%) of fluosilicic acid while stirring, and adding for 30 min; heating to 65 ℃, stirring for 1h at constant temperature, filtering and washing until the filtrate is neutral; adding water into the filter cake, pulping to obtain molecular sieve slurry with solid content of 40 wt%, adding 1.2gH3PO4(concentration 85% by weight) and 3.3gZn (NO)3)2·6H2And O, uniformly mixing, soaking, drying and roasting at 550 ℃ for 2 hours. Molecular sieve DA3 was obtained, and the physicochemical properties are shown in Table 1.
Comparative example 4
Crystallizing ZSM-5 molecular sieve (produced by catalyst Qilu division, amine-free synthesis, n (SiO)2)/n(Al2O3) 27) the mother liquor was filtered off and washed with water to Na2The content of O is lower than 3.0 weight percent, and a filter cake is obtained by filtration; adding 100g (dry basis) of the molecular sieve into 1000g of 2.0% NaOH solution, heating to 65 ℃, reacting for 30min, rapidly cooling to room temperature, filtering, and washing until the filtrate is neutral. Then, the filter cake was added to 800g of water and slurried, 40g of NH was added4Cl, heating to 75 ℃, and carrying out exchange treatment for 1h until Na2The O content is lower than 0.2 weight percent, and a molecular sieve filter cake is obtained after filtering and washing; taking 50g (dry basis) of the molecular sieve, adding water to prepare molecular sieve slurry with the solid content of 10 weight percent, adding 11g of oxalic acid while stirring, then adding 110g of hydrochloric acid (the mass fraction is 10 percent), and adding for 30 min; heating to 65 ℃, stirring for 1h at constant temperature, filtering and washing until the filtrate is neutral; adding water into the filter cake, pulping to obtain molecular sieve slurry with solid content of 40 wt%, adding 1.2gH3PO4(concentration 85% by weight) and 3.3gZn (NO)3)2·6H2And O, uniformly mixing, soaking, drying and roasting at 550 ℃ for 2 hours. Molecular sieve DA4 was obtained, and the physicochemical properties are shown in Table 1.
Comparative example 5
Crystallizing ZSM-5 molecular sieve (produced by catalyst Qilu division, amine-free synthesis, n (SiO)2)/n(Al2O3) 27) the mother liquor was filtered off and washed with water to Na2The content of O is lower than 3.0 weight percent, and a filter cake is obtained by filtration; adding 100g (dry basis) of the molecular sieve into 1000g of 2.0% NaOH solution, heating to 65 ℃, reacting for 30min, rapidly cooling to room temperature, filtering, and washing until the filtrate is neutral. Then, the filter cake was added to 800g of water and slurried, 40g of NH was added4Cl, heating to 75 ℃, and carrying out exchange treatment for 1h until Na2The O content is lower than 0.2 weight percent, and a molecular sieve filter cake is obtained after filtering and washing; taking 50g (dry basis) of the molecular sieve, adding water to prepare molecular sieve slurry with the solid content of 10 weight percent, adding 11g of oxalic acid while stirring, then slowly adding 184g of fluosilicic acid (the mass fraction is 3 percent), and adding for 30 min; heating to 65 ℃, stirring for 1h at constant temperature, filtering and washing until the filtrate is neutral; adding water into the filter cake, pulping to obtain molecular sieve slurry with solid content of 40 wt%, adding 1.2gH3PO4(concentration 85% by weight) and 3.3gZn (NO)3)2·6H2And O, uniformly mixing, soaking, drying and roasting at 550 ℃ for 2 hours. Molecular sieve DA5 was obtained, and the physicochemical properties are shown in Table 1.
Comparative example 6
Crystallizing ZSM-5 molecular sieve (produced by catalyst Qilu division, amine-free synthesis, n (SiO)2)/n(Al2O3) 27) the mother liquor was filtered off and washed with water to Na2The content of O is lower than 3.0 weight percent, and a filter cake is obtained by filtration; adding 100g (dry basis) of the molecular sieve into 1000g of 2.0% NaOH solution, heating to 65 ℃, reacting for 30min, rapidly cooling to room temperature, filtering, and washing until the filtrate is neutral. Then, the filter cake was added to 800g of water and slurried, 40g of NH was added4Cl, heating to 75 ℃, and carrying out exchange treatment for 1h until Na2The O content is lower than 0.2 weight percent, and a molecular sieve filter cake is obtained after filtering and washing; taking 50g (dry basis) of the molecular sieve, adding water to prepare molecular sieve slurry with the solid content of 10 weight percent, and adding 110g (10 mass percent) of hydrochloric acid and 184g (3 mass percent) of fluosilicic acid in a concurrent flow manner for 30min under stirring; heating to 65 ℃, stirring for 1h at constant temperature, filtering and washing until the filtrate is neutral; will be provided withAdding water into the filter cake, pulping to obtain molecular sieve slurry with solid content of 40 wt%, adding 1.2gH3PO4(concentration 85% by weight) and 3.3gZn (NO)3)2·6H2And O, uniformly mixing, soaking, drying and roasting at 550 ℃ for 2 hours. Molecular sieve DA6 was obtained, and the physicochemical properties are shown in Table 1.
Comparative example 7
Crystallizing ZSM-5 molecular sieve (produced by catalyst Qilu division, amine-free synthesis, n (SiO)2)/n(Al2O3) 27) the mother liquor was filtered off and washed with water to Na2The content of O is lower than 3.0 weight percent, and a filter cake is obtained by filtration; adding 100g (dry basis) of the molecular sieve into 1000g of 2.0% NaOH solution, heating to 65 ℃, reacting for 30min, rapidly cooling to room temperature, filtering, and washing until the filtrate is neutral. Then, the filter cake was added to 800g of water and slurried, 40g of NH was added4Cl, heating to 75 ℃, and carrying out exchange treatment for 1h until Na2The O content is lower than 0.2 weight percent, and a molecular sieve filter cake is obtained after filtering and washing; adding water into 50g (dry basis) of the molecular sieve to prepare molecular sieve slurry with the solid content of 10 weight percent, slowly adding 733g (mass fraction of 3%) of fluosilicic acid under stirring for 30 min; heating to 65 ℃, stirring for 1h at constant temperature, filtering and washing until the filtrate is neutral; adding water into the filter cake, pulping to obtain molecular sieve slurry with solid content of 40 wt%, adding 0.75gH3PO4(concentration 85% by weight) and 3.3gZn (NO)3)2·6H2And O, uniformly mixing, soaking, drying and roasting at 550 ℃ for 2 hours. Molecular sieve DA7 was obtained, and the physicochemical properties are shown in Table 1.
Comparative example 8
The crystallized ZSM-5 molecular sieve (produced by catalyst Jianchangdian company, synthesized by amine method, n (SiO)2)/n(Al2O3) 310) the mother liquor was filtered off and washed with water to Na2The content of O is lower than 3.0 weight percent, the mixture is filtered, dried and roasted in the air at 550 ℃ for 2 hours to burn off the template agent; adding 100g (dry basis) of the molecular sieve into 1500g of NaOH aqueous solution (the solution concentration is 2.4%), stirring, heating to 65 ℃, reacting for 40min, cooling to room temperature, filtering, leaching until the filtrate is neutral,obtaining a filter cake; then 50g (dry basis) of the molecular sieve is taken and added with water to prepare molecular sieve slurry with the solid content of 10 weight percent, and 220g of hydrochloric acid (the mass fraction is 10 percent) is added under stirring; heating to 65 ℃, stirring for 1h at constant temperature, filtering and washing until the filtrate is neutral; adding 1500g of water into the filter cake, pulping, adding 80g of NH4Heating Cl to 65 ℃, exchanging and washing for 40min, filtering, and leaching until the filtrate is neutral; adding water into the filter cake, pulping to obtain molecular sieve slurry with solid content of 40 wt%, adding 1.0gH3PO4(concentration 85% by weight) and 3.3gZn (NO)3)2·6H2And O, uniformly mixing, soaking, drying and roasting at 550 ℃ for 2 hours. Molecular sieve DA8 was obtained, and the physicochemical properties are shown in Table 1.
Comparative example 9
The crystallized ZSM-5 molecular sieve (produced by catalyst Jianchangdian company, synthesized by amine method, n (SiO)2)/n(Al2O3) 72) the mother liquor was filtered off and washed with water to Na2The content of O is lower than 3.0 weight percent, the mixture is filtered, dried and roasted in the air at 550 ℃ for 2 hours to burn off the template agent; 100g (dry basis) of the molecular sieve is taken and added with water to prepare molecular sieve slurry with the solid content of 10 weight percent, 670g (mass fraction of 3 percent) of fluosilicic acid is added during stirring, and the adding time is 30 min; heating to 65 ℃, stirring for 1h at constant temperature, filtering and washing until the filtrate is neutral; adding the molecular sieve into 1000g of 2.0% NaOH solution, heating to 65 ℃, reacting for 30min, rapidly cooling to room temperature, filtering, and washing until the filtrate is neutral. Then with NH4Cl solution exchange washing to Na2The O content is lower than 0.1 weight percent, and a molecular sieve filter cake is obtained after filtering and washing; adding water into molecular sieve filter cake (dry basis 50g), pulping to obtain molecular sieve slurry with solid content of 40 wt%, adding 1.2g H3PO4(concentration 85% by weight) and 3.3gZn (NO)3)2·6H2And O, uniformly mixing, soaking, drying and roasting at 550 ℃ for 2 hours. Molecular sieve DA9 was obtained, and the physicochemical properties are shown in Table 1.
Comparative example 10
Crystallizing ZSM-5 molecular sieve (produced by catalyst Qilu division, amine-free synthesis, n (SiO)2)/n(Al2O3) 27) the mother liquor was filtered off and washed with water to Na2The content of O is lower than 3.0 weight percent, and a filter cake is obtained by filtration; taking 100g (dry basis) of the molecular sieve, adding water to prepare molecular sieve slurry with the solid content of 10 weight percent, adding 12g of ethylene diamine tetraacetic acid while stirring, then adding 1300g of fluosilicic acid (the mass fraction is 3%) in a concurrent flow manner for 30min, and finally adding 480g of hydrochloric acid (the mass fraction is 10%); heating to 85 ℃, stirring for 6 hours at constant temperature, filtering and washing until the filtrate is neutral; adding 1000g of 2.2% NaOH solution, heating to 60 ℃, reacting for 45min, rapidly cooling to room temperature, filtering, and washing until the filtrate is neutral. Then NH4Cl solution exchange washing to Na2The content of O is lower than 0.1 weight percent, and a molecular sieve filter cake is obtained by filtering; adding water into 50g (dry basis) of the molecular sieve filter cake, pulping to obtain molecular sieve slurry with the solid content of 40 weight percent, and adding 1.2g of H3PO4(concentration 85% by weight) and 3.3gZn (NO)3)2·6H2And O, uniformly mixing, soaking, drying and roasting at 550 ℃ for 2 hours. Molecular sieve DA10 was obtained, and the physicochemical properties are shown in Table 1.
Comparative example 11
The crystallized ZSM-5 molecular sieve (produced by catalyst Jianchangdian company, synthesized by amine method, n (SiO)2)/n(Al2O3) 210) mother liquor was filtered off and NH was used4Cl exchange washing to Na2The content of O is lower than 0.2 weight percent, the mixture is dried and roasted for 2 hours in the air at 550 ℃ to burn off the template agent; adding water into 100g (dry basis) of the molecular sieve, pulping to obtain molecular sieve pulp with the solid content of 40 weight percent, and adding 1.6g of H3PO4(concentration 85%) and 6.6gZn (NO)3)2·6H2O, dipping and drying; and roasting the obtained sample at 550 ℃ for 2 hours to obtain the molecular sieve DA 11. Physicochemical properties are shown in Table 1.
Comparative example 12
ZSM-5 molecular sieve (produced by catalyst Qilu division, Amineless synthesis, n (SiO)2)/n(Al2O3) 27) with NH4Cl solution exchange washing to Na2The content of O is lower than 0.2 weight percent, and a filter cake is obtained by filtration; taking 100g of the molecular sieve (A), (B), (C), (D), (C), (D), (CDry basis) adding water to prepare molecular sieve slurry with the solid content of 10 weight percent, adding 40g of citric acid while stirring, and then adding 100g of sulfuric acid (with the mass fraction of 10%) and 500g of fluosilicic acid (with the mass fraction of 3%) in a concurrent flow manner for 30 min; heating to 45 ℃, stirring for 1h at constant temperature, filtering and washing until the filtrate is neutral; adding water into the filter cake, pulping to obtain molecular sieve slurry with solid content of 40 wt%, adding 2.0gH3PO4(concentration 85% by weight) and 5.0 g Ga2(SO4)3·16H2And O, uniformly mixing, soaking, drying and roasting at 550 ℃ for 2 hours. Molecular sieve DA12 was obtained, and the physicochemical properties are shown in Table 1.
Example 2
Crystallizing ZSM-5 molecular sieve (produced by catalyst Qilu division, amine-free synthesis, n (SiO)2)/n(Al2O3) 27) the mother liquor was filtered off and washed with water to Na2The content of O is lower than 3.0 weight percent, and a filter cake is obtained by filtration; adding 100g (dry basis) of the molecular sieve into 1500g of 2.4% NaOH solution, heating to 60 ℃, reacting for 45min, rapidly cooling to room temperature, filtering, and washing until the filtrate is neutral. Then, the filter cake was added to 800g of water and slurried, 40g of NH was added4Cl, heating to 75 ℃, and carrying out exchange treatment for 1h until Na2The O content is lower than 0.2 weight percent, and a molecular sieve filter cake is obtained after filtering and washing; taking 50g (dry basis) of the molecular sieve, adding water to prepare molecular sieve slurry with the solid content of 10 weight percent, adding 22g of citric acid while stirring, then adding 55g of sulfuric acid (with the mass fraction of 10 percent) and 280g of fluosilicic acid (with the mass fraction of 3 percent) in a concurrent flow manner, and adding for 30 min; heating to 45 ℃, stirring for 1h at constant temperature, filtering and washing until the filtrate is neutral; adding water into the filter cake, pulping to obtain molecular sieve slurry with solid content of 40 wt%, adding 1.0gH3PO4(concentration 85% by weight) and 2.5 g Ga2(SO4)3·16H2And O, uniformly mixing, soaking, drying and roasting at 550 ℃ for 2 hours. The molecular sieve B is obtained, and the physicochemical properties are shown in Table 1.
Comparative example 13
Crystallizing the ZSM-5 molecular sieveProduced by chemical Qilu division, Amineless Synthesis of n (SiO)2)/n(Al2O3) 27) the mother liquor was filtered off and washed with water to Na2The content of O is lower than 3.0 weight percent, and a filter cake is obtained by filtration; adding 100g (dry basis) of the molecular sieve into 1500g of 2.4% NaOH solution, heating to 60 ℃, reacting for 45min, rapidly cooling to room temperature, filtering, and washing until the filtrate is neutral. Then, the filter cake was added to 800g of water and slurried, 40g of NH was added4Cl, heating to 75 ℃, and carrying out exchange treatment for 1h until Na2The O content is lower than 0.2 weight percent, and a molecular sieve filter cake is obtained after filtering and washing; taking 50g (dry basis) of the molecular sieve, adding water to prepare molecular sieve slurry with the solid content of 10 weight percent, adding 22g of citric acid while stirring, then adding 55g of sulfuric acid (with the mass fraction of 10 percent) and 280g of fluosilicic acid (with the mass fraction of 3 percent) in a concurrent flow manner, and adding for 30 min; heating to 45 ℃, stirring for 1h at constant temperature, filtering and washing until the filtrate is neutral; adding water into the filter cake, pulping to obtain molecular sieve slurry with solid content of 40 wt%, adding 1.0gH3PO4(concentration: 85 wt.%), mixing, immersing, baking, and calcining at 550 deg.C for 2 hr. Molecular sieve DB1 was obtained, and the physicochemical properties are shown in Table 1.
Example 3
Crystallizing ZSM-5 molecular sieve (produced by catalyst Qilu division, amine-free synthesis, n (SiO)2)/n(Al2O3) 27) the mother liquor was filtered off and washed with water to Na2The content of O is lower than 3.0 weight percent, and a filter cake is obtained by filtration; adding 100g (dry basis) of the molecular sieve into 1200g of 2.2% NaOH solution, heating to 55 ℃, reacting for 60min, rapidly cooling to room temperature, filtering, and washing until the filtrate is neutral. Then, the filter cake was added to 1000g of water and slurried, 50g of NH was added4Cl, heating to 75 ℃, and carrying out exchange treatment for 1h until Na2The O content is lower than 0.2 weight percent, and a molecular sieve filter cake is obtained after filtering and washing; adding water into 50g (dry basis) of the molecular sieve to prepare molecular sieve slurry with the solid content of 10 weight percent, adding 6g of ethylenediamine tetraacetic acid while stirring, then adding 550g (mass fraction of 3%) of fluosilicic acid in a concurrent flow manner for 30min, and finally adding 220g (mass fraction of mass fraction) of hydrochloric acid10%); heating to 85 ℃, stirring for 6 hours at constant temperature, filtering and washing until the filtrate is neutral; adding water into the filter cake, pulping to obtain molecular sieve slurry with solid content of 40 wt%, adding 0.8gH3PO4(concentration 85% by weight) and 4.1g Fe (NO)3)3·9H2And O, uniformly mixing, soaking, drying and roasting at 550 ℃ for 2 hours. The molecular sieve C was obtained, and the physicochemical properties are shown in Table 1.
As can be seen from the data in Table 1, for the ZSM-5 molecular sieve subjected to alkali treatment and desiliconization, Al in the molecular sieve cannot be effectively removed by adopting single organic acid oxalic acid for dealuminization (DA1), or adopting single inorganic acid hydrochloric acid for dealuminization (DA2) or adopting two acids of organic acid oxalic acid and inorganic acid hydrochloric acid for compounding (DA4), the molecular sieve still has aluminum-rich surface, and a good dealuminization effect can be obtained only after fluosilicic acid is used, so that the aluminum distribution of the molecular sieve is improved. When fluosilicic acid alone is used for dealumination (DA3 and DA7), the aluminum distribution of the molecular sieve can be improved, but the mesopores are relatively less, the proportion of strong acid in the total acid is lower, and the proportion of B acid/L acid is lower. The fluosilicic acid and organic acid composite oxalic acid dealumination (DA5) can not obtain higher mesopore proportion and better acidity distribution. Fluosilicic acid complex mineral acid salt dealumination (DA6) showed an increase in mesopore volume, but neither the proportion of strong acid in the total acid nor the B acid/L acid ratio was as high as the molecular sieve provided by the present disclosure. The ZSM-5 molecular sieve with high silicon-aluminum ratio is treated by alkali and then treated by inorganic acid hydrochloric acid (DA8), although a higher mesopore proportion can be obtained, the pore volume of the molecular sieve with the pore diameter of 2nm to 20nm accounts for the volume of the total mesopores, the pore diameter of the molecular sieve is enlarged, meanwhile, the Al distribution of the molecular sieve is still poor, strong acid is less, the ratio of B acid to L acid is low, the stability of the molecular sieve is poor, and the reaction activity is low. The ZSM-5 molecular sieve with higher silicon-aluminum ratio synthesized by adopting the acid-base treatment technology can obtain the ZSM-5 molecular sieve (DA9) containing mesopores according to the silicon-aluminum ratio range in the disclosure, but the molecular sieve has poorer Al distribution, less strong acid and low B acid/L acid ratio. By adopting the technical route of firstly dealuminizing and then desiliconizing, the silica-alumina ratio of the ZSM-5 molecular sieve is improved by using composite acid containing fluosilicic acid, and then the molecular sieve (DA10) obtained by desiliconizing treatment is low in crystallinity and mesopore ratio, the pore volume of the molecular sieve with the mesopore diameter of 2nm to 20nm accounts for the total mesopore volume, and the molecular sieve has relatively more Al on the outer surface and poor acidity distribution. The directly synthesized molecular sieve (DA11) with high silica-alumina ratio and the molecular sieve (DA12) obtained by dealuminizing and silicon supplementing with composite acid have no abundant secondary pores. According to the method, after the molecular sieve is subjected to desilication treatment, a composite acid system is used, and under the synergistic effect of three acids, the silicon-aluminum ratio of the molecular sieve can be effectively increased, the aluminum distribution is adjusted, and the acid distribution is improved on the premise of ensuring the integrity of the crystal structure and the mesoporous channel structure of the molecular sieve.
Examples 4-7 provide a phosphoaluminate inorganic binder for use in the present disclosure.
Example 4
This example prepared a phosphoaluminate inorganic binder as described in the present disclosure.
1.91 kg of pseudoboehmite (containing Al)2O31.19 Kg), 0.56 Kg kaolin (0.50 Kg on a dry basis) and 3.27 Kg decationized water, beating for 30 minutes, adding 5.37 Kg concentrated phosphoric acid (85% by mass) into the slurry under stirring, wherein the adding speed of the phosphoric acid is 0.04Kg phosphoric acid/min/Kg alumina source, heating to 70 ℃, and then reacting for 45 minutes at the temperature to obtain the phosphorus-aluminum inorganic binder. The material ratio is shown in Table 2, and the Binder Binder1 is obtained.
Examples 5 to 7
The phosphor-aluminum inorganic Binder was prepared by the method of example 4, and the material ratio is shown in table 2, to obtain Binder 2-4.
Examples 8-13 provide catalytic cracking aids of the present disclosure, and comparative examples 14-26 provide comparative catalytic cracking aids.
Example 8
Taking molecular sieve A, kaolin and pseudo-boehmite, adding decationized water and aluminum sol, pulping for 120 minutes, adding FeCl under stirring3·6H2Aqueous solution of O (FeCl)3Content 30 wt.%), adjusting pH to 3.0 with hydrochloric acid, beating for 45min, adding P-Al inorganic binder prepared in example 4, stirring for 30min, spray drying to obtain microballs, calcining at 500 deg.C for 1 hr to obtain ZJ1The compounding ratio is shown in Table 3.
Example 9
Taking molecular sieve B, kaolin and pseudo-boehmite, adding decationized water and aluminum sol, pulping for 120 minutes, adding FeCl under stirring3·6H2Aqueous solution of O (FeCl)3Content 30 wt.%), adjusting pH to 3.0 with hydrochloric acid, beating for 45min, adding P-Al inorganic binder prepared in example 4, stirring for 30min, spray drying to obtain microballs, calcining at 500 deg.C for 1 hr to obtain ZJ2The compounding ratio is shown in Table 3.
Example 10
Taking molecular sieve C, kaolin and pseudo-boehmite, adding decationized water and aluminum sol, pulping for 120 minutes, adding FeCl under stirring3·6H2Aqueous solution of O (FeCl)3Content 30 wt.%), adjusting pH to 3.0 with hydrochloric acid, beating for 45min, adding P-Al inorganic binder prepared in example 4, stirring for 30min, spray drying to obtain microballs, calcining at 500 deg.C for 1 hr to obtain ZJ3The compounding ratio is shown in Table 3.
Example 11
Adding decationized water and aluminum sol into molecular sieve A, kaolin and pseudo-boehmite, pulping for 120 minutes to obtain slurry with the solid content of 30 weight percent, adding hydrochloric acid to adjust the pH value of the slurry to be 3.0, continuing pulping for 45 minutes, adding the phosphorus-aluminum inorganic binder prepared in example 5, stirring for 30 minutes, spray-drying the obtained slurry to obtain microspheres, and roasting the microspheres for 1 hour at 500 ℃. Adding ZnCl into the obtained microsphere product2Heating the aqueous solution (with the concentration of 30 wt%) to 60 ℃ under stirring, reacting at the temperature for 20 minutes, vacuum-filtering and drying the slurry, and roasting at 500 ℃ for 2 hours to obtain the assistant ZJ4The mixture ratio is shown in Table 3
Example 12
Taking molecular sieve A, kaolin and pseudo-boehmite, adding decationized water and silica sol, pulping for 120 minutes, adding Co (NO) under stirring3)2·6H2O aqueous solution (concentration 30 wt%) to obtain slurry with solid content of 30 wt%, adding hydrochloric acid to adjust pH of the slurry to 3.0, continuing pulping for 45 minutes, adding the phosphorus-aluminum inorganic binder prepared in example 6, stirring for 30 minutes, spray-drying the obtained slurry to obtain microspheres, and roasting the microspheres at 500 ℃ for 1 hour to obtain ZJ5The compounding ratio is shown in Table 3.
Example 13
Taking molecular sieve A, kaolin and pseudo-boehmite, adding decationized water and alumina sol, pulping for 120 minutes, adding Ga (NO) under stirring3)3To obtain a slurry with a solid content of 30 wt%, adding hydrochloric acid to adjust the pH value of the slurry to 2.5, continuing to pulp for 45 minutes, adding the phosphorus-aluminum inorganic binder prepared in example 7, stirring for 30 minutes, and spray-drying the obtained slurry to obtain the aluminum-phosphorusAnd (3) microspheres. Adding the obtained microsphere product into 7.5 wt% diammonium hydrogen phosphate aqueous solution, heating to 60 deg.C under stirring, reacting at the temperature for 20 min, vacuum filtering the slurry, drying, and calcining at 500 deg.C for 2 hr to obtain auxiliary agent ZJ6The compounding ratio of the auxiliary is shown in Table 3.
Comparative examples 14 to 26
A catalytic cracking promoter was prepared as described in example 8, except that molecular sieves DA1, DA2, DA3, DA4, DA5, DA6, DA7, DA8, DA9, DA10, DA11, DA12 and DB1 were used instead of A, respectively, to prepare a promoter DZJ1-DZJ13The compounding ratio is shown in Table 4.
Blank test example, examples 14-19 use a small fixed fluidized bed reactor to incorporate 100% of the balancing agent and the adjuvant ZJ prepared in the examples of the present disclosure1-ZJ6The reaction performance evaluation was conducted to demonstrate the catalytic cracking reaction effect of the catalytic cracking aids provided by the present disclosure.
Blank test example, examples 14 to 19
Respectively mixing auxiliary agents ZJ1-ZJ6The aging treatment was carried out at 800 ℃ under a 100% steam atmosphere for 17 hours. Taking the aged ZJ1-ZJ6Separately mixed with an industrial FCC equilibrium catalyst (commercial grade DVR-3 FCC equilibrium catalyst, micro-reverse activity 63). 100 percent of balancing agent and catalyst mixture is loaded into a small-sized fixed fluidized bed reactor, and the raw oil shown in the table 5 is subjected to catalytic cracking under the following reaction conditions: the reaction temperature is 500 ℃, and the weight hourly space velocity is 8h-1And the weight ratio of the solvent to the oil is 6. The weight composition of the respective catalyst mixtures and the reaction results are given in table 6.
Comparative examples 27-39A small fixed fluidized bed reactor was used to incorporate the balancing agent DZJ prepared in the comparative examples of the present disclosure1-DZJ12Performance evaluations were conducted to illustrate the case where the comparative aid was used.
Comparative examples 27 to 39
The same feed oil was catalytically cracked by the same method as in example 14, except that DZJ which had been aged by the same aging method as in example 14 was used as the catalyst1-DZJ13Mixtures with commercial FCC equilibrium catalysts. The weight composition of the individual catalyst mixtures and the reaction results are given in Table 7.
As can be seen from tables 6 and 7, compared with the comparative assistant, the catalytic cracking reaction using the assistant provided by the present disclosure has a higher gasoline octane number while ensuring the gasoline yield, and particularly, the content of isomeric hydrocarbons in the gasoline component is increased, so that the gasoline composition is well improved, and further, the gasoline octane number is increased.
TABLE 1
TABLE 2
TABLE 3
TABLE 4
TABLE 5
| Density, g/cm3(20℃) | 0.9171 |
| Viscosity (100C), mm2/s | 10.61 |
| Freezing point, deg.C | 20 |
| Carbon residue, by weight% | 1.91 |
| Element content, wt% | |
| C | 85.96 |
| H | 12.37 |
| S | 1.0 |
| N | 0.35 |
| Metal content,. mu.g/g | |
| Ca | 8.3 |
| Fe | 12.3 |
| Na | 0.9 |
| Ni | 4.7 |
| V | 0.4 |
| Distillation range, deg.C | |
| Initial boiling point | 267 |
| 10％ | 371 |
| 50％ | 449 |
| 70％ | 486 |
| 86.9％ | 549 |
TABLE 6
TABLE 7
Claims (21)
1. A catalytic cracking promoter for increasing the octane number of gasoline is disclosed, which comprises 10-75 wt% of molecular sieve with MFI structure containing phosphorus and load metal, 3-40 wt% of inorganic binder containing phosphorus and aluminum, 1-30 wt% of other inorganic binder, 0-60 wt% of second clay, and 0.5-15 wt% of metal additive selected from VIII family metal and at least one of manganese, zinc and gallium; wherein,
the phosphor-aluminum inorganic bondThe agent is phosphor aluminum glue and/or phosphor aluminum inorganic binder containing first clay, and the phosphor aluminum inorganic binder containing the first clay comprises Al based on the weight of the phosphor aluminum inorganic binder containing the first clay2O315-40% by weight, calculated as P, of an aluminium component2O545-80 wt% of phosphorus component and more than 0 and not more than 40 wt% of first clay calculated on dry basis weight, and the P/Al weight ratio is 1.0-6.0, pH value is 1-3.5, solid content is 15-60 wt%;
n (SiO) of the molecular sieve2)/n(Al2O3) Greater than 100; with P2O5The phosphorus content of the molecular sieve is 0.1-5 wt% based on the dry weight of the molecular sieve; the content of the supported metal of the molecular sieve is 0.1-5 wt% calculated by the oxide of the supported metal and based on the dry weight of the molecular sieve; the Al distribution parameter D of the molecular sieve meets the following requirements: d is more than or equal to 0.6 and less than or equal to 0.85, wherein D is Al (S)/Al (C), Al (S) represents the aluminum content of a region which is arbitrarily more than 100 square nanometers in the inward H distance of the crystal face edge of the molecular sieve crystal grain measured by a TEM-EDS method, Al (C) represents the aluminum content of a region which is arbitrarily more than 100 square nanometers in the outward H distance of the geometric center of the crystal face of the molecular sieve crystal grain measured by the TEM-EDS method, wherein H is 10 percent of the distance from a certain point of the crystal face edge to the geometric center of the crystal face; the proportion of the mesopore volume of the molecular sieve in the total pore volume is 40-80% by volume, and the proportion of the mesopore volume with the pore diameter of 2-20 nm in the total mesopore volume is more than 90% by volume; the ratio of the strong acid amount of the molecular sieve to the total acid amount is 60-80%, and the ratio of the acid amount of the B acid to the acid amount of the L acid is 15-80.
2. The adjuvant of claim 1, wherein n (SiO) of the molecular sieve2)/n(Al2O3) Greater than 120; with P2O5The phosphorus content of the molecular sieve is 0.2-4 wt% based on the dry weight of the molecular sieve; the content of the supported metal of the molecular sieve is 0.5-3 wt% calculated by the oxide of the supported metal and based on the dry weight of the molecular sieve; the Al distribution parameter D of the molecular sieve meets the following requirements: d is more than or equal to 0.65 and less than or equal to 0.80; what is needed isThe proportion of the mesopore volume of the molecular sieve to the total mesopore volume is 50-70% by volume, and the proportion of the mesopore volume with the aperture of 2-20 nm to the total mesopore volume is more than 92% by volume; the ratio of the strong acid amount of the molecular sieve to the total acid amount is 65-75%, and the ratio of the acid amount of the B acid to the acid amount of the L acid is 20-50.
3. The adjuvant according to claim 1, wherein the supported metal is at least one selected from the group consisting of iron, cobalt, nickel, copper, manganese, zinc, tin, bismuth and gallium.
4. The adjuvant according to claim 1, wherein the first clay is at least one selected from kaolin, sepiolite, attapulgite, rectorite, montmorillonite and diatomaceous earth; the second clay is at least one selected from kaolin, metakaolin, diatomite, sepiolite, attapulgite, montmorillonite and rectorite; the other inorganic binder is at least one selected from pseudo-boehmite, alumina sol, silica-alumina sol and water glass.
5. The adjuvant according to claim 1, wherein the metal additive is introduced into the adjuvant in the form of a metal compound, the metal compound being at least one selected from the group consisting of an oxide, a hydroxide, a chloride, a nitrate, a sulfate, a phosphate and an organic compound.
6. The adjuvant according to any one of claims 1 to 5, wherein the adjuvant further comprises P based on the dry weight of the adjuvant2O5Up to 5 wt% of a phosphorus additive.
7. The adjuvant of claim 6 wherein the adjuvant comprises 8-25 wt% of a phosphorus aluminum inorganic binder, 20-60 wt% of a phosphorus containing and supported metal MFI structure molecular sieve, 10-45 wt% of a second clay, 5-25 wt% of other inorganic binders, 1.0-10 wt% of a metal additive, and 0-3 wt% of a phosphorus additive.
8. A preparation method of a catalytic cracking assistant for improving the octane number of gasoline comprises the following steps:
mixing the phosphorus-containing and metal-loaded MFI structure molecular sieve, the phosphorus-aluminum inorganic binder and other inorganic binders, adding or not adding second clay, pulping, and spray-drying; wherein, a metal additive is introduced, and a phosphorus additive is introduced or not introduced;
based on the total dry basis weight of the preparation raw materials of the auxiliary agent, the preparation raw materials of the auxiliary agent comprise 10-75 wt% of phosphorus-containing and metal-loaded MFI structure molecular sieve based on the dry basis weight, 3-40 wt% of phosphorus-aluminum inorganic binder based on the dry basis weight, 1-30 wt% of other inorganic binders based on oxides, 0-60 wt% of second clay based on the dry basis weight, 0.5-15 wt% of metal additives selected from VIII group metals and at least one of manganese, zinc and gallium based on the oxides, and the additive or the additive does not comprise P2O5Up to 5 wt% of a phosphorus additive; wherein,
the phosphorus-aluminum inorganic binder is phosphorus-aluminum glue and/or phosphorus-aluminum inorganic binder containing first clay, and the phosphorus-aluminum inorganic binder containing the first clay comprises Al based on the dry weight of the phosphorus-aluminum inorganic binder containing the first clay2O315-40% by weight, calculated as P, of an aluminium component2O545-80 wt% of phosphorus component and more than 0 and not more than 40 wt% of first clay calculated on dry basis weight, and the P/Al weight ratio is 1.0-6.0, pH value is 1-3.5, solid content is 15-60 wt%;
n (SiO) of the molecular sieve2)/n(Al2O3) Greater than 100; with P2O5The phosphorus content of the molecular sieve is 0.1-5 wt% based on the dry weight of the molecular sieve; the content of the supported metal of the molecular sieve is 0.1-5 wt% calculated by the oxide of the supported metal and based on the dry weight of the molecular sieve; the Al distribution parameter D of the molecular sieve meets the following requirements: 0.6. ltoreq. D.ltoreq.0.85, wherein D ═ Al (S)/Al (C), and Al (S) means that TEM-EDS method is usedMeasuring the aluminum content of a region with the crystal face edge being more than 100 square nanometers in the inward H distance, wherein Al (C) represents the aluminum content of the region with the crystal face being more than 100 square nanometers in the outward H distance of the geometric center of the crystal face of the molecular sieve crystal grain measured by a TEM-EDS method, wherein H is 10% of the distance from a certain point of the crystal face edge to the geometric center of the crystal face; the proportion of the mesopore volume of the molecular sieve in the total pore volume is 40-80% by volume, and the proportion of the mesopore volume with the pore diameter of 2-20 nm in the total mesopore volume is more than 90% by volume; the ratio of the strong acid amount of the molecular sieve to the total acid amount is 60-80%, and the ratio of the acid amount of the B acid to the acid amount of the L acid is 15-80.
9. The method of claim 8, wherein the step of preparing the phosphorus-containing and supported metal MFI structure molecular sieve comprises:
a. filtering and washing the crystallized MFI structure molecular sieve slurry to obtain a water-washed molecular sieve; wherein the sodium content of the washed molecular sieve is less than 3 wt% based on the total dry basis weight of the washed molecular sieve calculated as sodium oxide;
b. b, carrying out desiliconization treatment on the washed molecular sieve obtained in the step a in an alkali solution, and filtering and washing to obtain a desiliconized molecular sieve;
c. b, performing ammonium exchange treatment on the desiliconized molecular sieve obtained in the step b to obtain an ammonium exchange molecular sieve; wherein the ammonium exchanged molecular sieve has a sodium content of less than 0.2 wt.%, based on sodium oxide and based on total dry basis weight of the ammonium exchanged molecular sieve;
d. c, dealuminizing the ammonium exchange molecular sieve obtained in the step c in a composite acid dealuminizing agent solution consisting of fluosilicic acid, organic acid and inorganic acid, and filtering and washing to obtain a dealuminized molecular sieve;
e. and d, carrying out phosphorus modification treatment, load treatment of load metal and roasting treatment on the dealuminized molecular sieve obtained in the step d to obtain the MFI structure molecular sieve containing phosphorus and load metal.
10. The production method according to claim 9, wherein the alkali solution in step b is at least one selected from the group consisting of a sodium hydroxide solution, a potassium hydroxide solution and ammonia water.
11. The production method according to claim 9, wherein the conditions of the desiliconization treatment in step b include: the weight ratio of the molecular sieve, the alkali in the alkali solution and the water in the alkali solution is 1: (0.1-2): (5-15); the desiliconization treatment is carried out at room temperature to 100 ℃ for 0.2 to 4 hours.
12. The production method according to claim 9, wherein the conditions of the desiliconization treatment in step b include: the weight ratio of the molecular sieve, the alkali in the alkali solution and the water in the alkali solution is 1: (0.2-1): (5-15).
13. The method of claim 9, wherein the step of dealuminating in step d further comprises: mixing organic acid with the ammonium exchange molecular sieve, and then mixing fluosilicic acid and inorganic acid with the ammonium exchange molecular sieve.
14. The production method according to claim 9, wherein the organic acid in step d is at least one selected from the group consisting of ethylenediaminetetraacetic acid, oxalic acid, citric acid and sulfosalicylic acid, and the inorganic acid is at least one selected from the group consisting of hydrochloric acid, sulfuric acid and nitric acid.
15. The method according to claim 9, wherein the organic acid in step d is oxalic acid and the inorganic acid is hydrochloric acid.
16. The method of claim 9, wherein the dealumination treatment conditions in step d include: the weight ratio of the molecular sieve, the organic acid, the inorganic acid and the fluosilicic acid is 1 (0.05-0.5) to 0.05-0.5): (0.02-0.5); the treatment temperature is 25-100 ℃, and the treatment time is 0.5-6 hours.
17. The method of claim 9, wherein the dealumination treatment conditions in step d include: the weight ratio of the molecular sieve, the organic acid, the inorganic acid and the fluosilicic acid is 1 (0.1-0.3) to 0.1-0.3) in terms of dry weight: (0.05-0.3).
18. The method of claim 9, wherein the phosphorus modification treatment in step e comprises: at least one phosphorus-containing compound selected from phosphoric acid, ammonium hydrogen phosphate, ammonium dihydrogen phosphate and ammonium phosphate is used to impregnate and/or ion-exchange the molecular sieve.
19. The production method according to claim 9, wherein the supporting treatment of the supported metal in step e includes: loading a supported metal selected from at least one of iron, cobalt, nickel, copper, manganese, zinc, tin, bismuth and gallium on the molecular sieve by an impregnation method.
20. The production method according to claim 9, wherein the conditions of the baking treatment include: the atmosphere of the roasting treatment is air atmosphere or water vapor atmosphere; the roasting temperature is 400-800 ℃, and the roasting time is 0.5-8 hours.
21. The method of claim 8, wherein the first clay-containing aluminophosphate inorganic binder is prepared by a method comprising:
(1) pulping and dispersing an alumina source, first clay and water into slurry with the solid content of 8-45 wt%; the alumina source is aluminum hydroxide and/or aluminum oxide which can be peptized by acid, first clay and Al which are calculated by dry weight2O3The weight ratio of the alumina source is (more than 0-40) to (15-40);
(2) adding concentrated phosphoric acid into the slurry obtained in the step (1) according to the weight ratio of P/Al to 1-6 under stirring;
(3) and (3) reacting the slurry obtained in the step (2) at the temperature of 50-99 ℃ for 15-90 minutes.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610921640.5A CN107971031B (en) | 2016-10-21 | 2016-10-21 | A kind of assistant for calalytic cracking and preparation method thereof improving octane number bucket |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201610921640.5A CN107971031B (en) | 2016-10-21 | 2016-10-21 | A kind of assistant for calalytic cracking and preparation method thereof improving octane number bucket |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN107971031A true CN107971031A (en) | 2018-05-01 |
| CN107971031B CN107971031B (en) | 2019-11-15 |
Family
ID=62003901
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201610921640.5A Active CN107971031B (en) | 2016-10-21 | 2016-10-21 | A kind of assistant for calalytic cracking and preparation method thereof improving octane number bucket |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN107971031B (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114849769A (en) * | 2022-04-25 | 2022-08-05 | 安徽海华科技集团有限公司 | Catalyst for synthesizing thymol and preparation method and application thereof |
| CN115591573A (en) * | 2021-07-07 | 2023-01-13 | 中国石油化工股份有限公司（Cn） | Yield-increasing propylene additive and preparation method thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103785456A (en) * | 2012-10-26 | 2014-05-14 | 中国石油化工股份有限公司 | Cracking auxiliary agent for increasing low-carbon olefin concentration |
| CN103785454A (en) * | 2012-10-26 | 2014-05-14 | 中国石油化工股份有限公司 | Catalytic cracking catalyst and preparation method thereof |
-
2016
- 2016-10-21 CN CN201610921640.5A patent/CN107971031B/en active Active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103785456A (en) * | 2012-10-26 | 2014-05-14 | 中国石油化工股份有限公司 | Cracking auxiliary agent for increasing low-carbon olefin concentration |
| CN103785454A (en) * | 2012-10-26 | 2014-05-14 | 中国石油化工股份有限公司 | Catalytic cracking catalyst and preparation method thereof |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN115591573A (en) * | 2021-07-07 | 2023-01-13 | 中国石油化工股份有限公司（Cn） | Yield-increasing propylene additive and preparation method thereof |
| CN115591573B (en) * | 2021-07-07 | 2023-09-05 | 中国石油化工股份有限公司 | Yield-increasing propylene auxiliary agent and preparation method thereof |
| CN114849769A (en) * | 2022-04-25 | 2022-08-05 | 安徽海华科技集团有限公司 | Catalyst for synthesizing thymol and preparation method and application thereof |
| CN114849769B (en) * | 2022-04-25 | 2023-06-13 | 安徽海华科技集团有限公司 | Catalyst for synthesizing thymol and preparation method and application thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN107971031B (en) | 2019-11-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN107970990B (en) | Catalytic cracking auxiliary agent for increasing propylene yield and preparation method thereof | |
| CN112138711B (en) | Catalytic cracking auxiliary agent, preparation method thereof and method for catalytic cracking of hydrocarbon oil | |
| CN112138712B (en) | Catalytic cracking catalyst, preparation method thereof and hydrocarbon oil catalytic cracking method | |
| CN107971031B (en) | A kind of assistant for calalytic cracking and preparation method thereof improving octane number bucket | |
| CN107970978B (en) | Phosphorus-containing and metal-loaded MFI structure molecular sieve and preparation method thereof | |
| CN107970983B (en) | Catalytic cracking auxiliary agent for improving gasoline octane number barrel and preparation method thereof | |
| CN107973308B (en) | Phosphorus-containing MFI structure molecular sieve and preparation method thereof | |
| CN107970984B (en) | Catalytic cracking auxiliary agent for improving gasoline octane number barrel and preparation method thereof | |
| CN107970981B (en) | Catalytic cracking auxiliary agent for increasing propylene yield and preparation method thereof | |
| CN107970982B (en) | A kind of assistant for calalytic cracking of propylene enhancing and preparation method thereof | |
| CN107974274B (en) | Phosphorus-containing and metal-loaded MFI structure molecular sieve and preparation method thereof | |
| CN107971027B (en) | Aromatization auxiliary agent and preparation method thereof | |
| CN107971022B (en) | Catalytic cracking auxiliary agent for increasing propylene yield and preparation method thereof | |
| CN107971006B (en) | A kind of assistant for calalytic cracking of propylene enhancing and preparation method thereof | |
| CN107971032B (en) | Catalytic cracking auxiliary agent for improving gasoline octane number barrel and preparation method thereof | |
| CN107583666B (en) | A kind of assistant for calalytic cracking and preparation method thereof improving octane number bucket | |
| CN112138713B (en) | Catalytic cracking auxiliary agent and preparation method and application thereof | |
| CN107971029B (en) | A kind of assistant for calalytic cracking of propylene enhancing and preparation method thereof | |
| CN107583667B (en) | A kind of assistant for calalytic cracking and preparation method thereof improving octane number bucket | |
| CN107583670B (en) | A kind of assistant for calalytic cracking and preparation method thereof improving octane number bucket | |
| CN107970997B (en) | Catalytic cracking auxiliary agent for increasing propylene yield and preparation method thereof | |
| CN107583668B (en) | A kind of assistant for calalytic cracking and preparation method thereof improving octane number bucket | |
| CN107970979B (en) | Catalytic cracking auxiliary agent for increasing propylene yield and preparation method thereof | |
| CN107970998B (en) | Catalytic cracking auxiliary agent for increasing propylene yield and preparation method thereof | |
| CN107970980B (en) | Catalytic cracking auxiliary agent for increasing propylene yield and preparation method thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |