WO2019115627A1 - Composition de catalyseur et processus de production de 1,3-butadiene - Google Patents
Composition de catalyseur et processus de production de 1,3-butadiene Download PDFInfo
- Publication number
- WO2019115627A1 WO2019115627A1 PCT/EP2018/084588 EP2018084588W WO2019115627A1 WO 2019115627 A1 WO2019115627 A1 WO 2019115627A1 EP 2018084588 W EP2018084588 W EP 2018084588W WO 2019115627 A1 WO2019115627 A1 WO 2019115627A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- oxides
- catalyst composition
- butadiene
- weight
- carbon atoms
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 176
- 239000003054 catalyst Substances 0.000 title claims abstract description 111
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 title claims description 140
- 238000000034 method Methods 0.000 title claims description 59
- 238000004519 manufacturing process Methods 0.000 title claims description 23
- 229910052751 metal Inorganic materials 0.000 claims abstract description 41
- 239000002184 metal Substances 0.000 claims abstract description 41
- 239000002253 acid Substances 0.000 claims abstract description 17
- 230000009977 dual effect Effects 0.000 claims abstract description 17
- 230000000737 periodic effect Effects 0.000 claims abstract description 15
- 229910000510 noble metal Inorganic materials 0.000 claims abstract description 7
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 5
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 64
- 125000004432 carbon atom Chemical group C* 0.000 claims description 57
- 238000006243 chemical reaction Methods 0.000 claims description 52
- 229920006395 saturated elastomer Polymers 0.000 claims description 43
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 43
- 229930195733 hydrocarbon Natural products 0.000 claims description 32
- 150000002430 hydrocarbons Chemical class 0.000 claims description 32
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical class [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 30
- 238000006317 isomerization reaction Methods 0.000 claims description 30
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 26
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 26
- 238000000605 extraction Methods 0.000 claims description 24
- 238000006356 dehydrogenation reaction Methods 0.000 claims description 22
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 17
- 239000002245 particle Substances 0.000 claims description 17
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 16
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 claims description 16
- 238000005839 oxidative dehydrogenation reaction Methods 0.000 claims description 16
- 150000002739 metals Chemical class 0.000 claims description 14
- 238000000895 extractive distillation Methods 0.000 claims description 12
- 239000007858 starting material Substances 0.000 claims description 12
- IAQRGUVFOMOMEM-UHFFFAOYSA-N but-2-ene Chemical class CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 claims description 10
- 229910000323 aluminium silicate Inorganic materials 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- 239000001282 iso-butane Substances 0.000 claims description 8
- 229910052697 platinum Inorganic materials 0.000 claims description 8
- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical class [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 claims description 8
- 238000000926 separation method Methods 0.000 claims description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 6
- 239000000047 product Substances 0.000 claims description 6
- 239000010457 zeolite Substances 0.000 claims description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 5
- 229910000272 alkali metal oxide Inorganic materials 0.000 claims description 5
- 238000004438 BET method Methods 0.000 claims description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 4
- 230000001588 bifunctional effect Effects 0.000 claims description 4
- 230000003197 catalytic effect Effects 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 229910001950 potassium oxide Inorganic materials 0.000 claims description 4
- 230000003134 recirculating effect Effects 0.000 claims description 4
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical class [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims description 4
- 238000004230 steam cracking Methods 0.000 claims description 4
- -1 IVA metals Chemical class 0.000 claims description 3
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 3
- 239000012467 final product Substances 0.000 claims description 3
- 229910001195 gallium oxide Inorganic materials 0.000 claims description 3
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 230000001590 oxidative effect Effects 0.000 claims description 3
- 229910052763 palladium Inorganic materials 0.000 claims description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 3
- 238000007670 refining Methods 0.000 claims description 3
- 229910052703 rhodium Inorganic materials 0.000 claims description 3
- 239000010948 rhodium Substances 0.000 claims description 3
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims description 3
- 229910052707 ruthenium Inorganic materials 0.000 claims description 3
- 229910001948 sodium oxide Inorganic materials 0.000 claims description 3
- 229910001887 tin oxide Inorganic materials 0.000 claims description 3
- QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(ii) oxide Chemical class [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 claims description 3
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- KEZVEHRXAWUQOX-UHFFFAOYSA-N [O-2].[Fr+].[Fr+] Chemical class [O-2].[Fr+].[Fr+] KEZVEHRXAWUQOX-UHFFFAOYSA-N 0.000 claims description 2
- 238000000149 argon plasma sintering Methods 0.000 claims description 2
- KOPBYBDAPCDYFK-UHFFFAOYSA-N caesium oxide Chemical class [O-2].[Cs+].[Cs+] KOPBYBDAPCDYFK-UHFFFAOYSA-N 0.000 claims description 2
- 229910001942 caesium oxide Inorganic materials 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium oxide Inorganic materials O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 claims description 2
- 238000005984 hydrogenation reaction Methods 0.000 claims description 2
- 229910003437 indium oxide Inorganic materials 0.000 claims description 2
- 229910052741 iridium Inorganic materials 0.000 claims description 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 229910000464 lead oxide Inorganic materials 0.000 claims description 2
- FUJCRWPEOMXPAD-UHFFFAOYSA-N lithium oxide Chemical class [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 claims description 2
- 229910001947 lithium oxide Inorganic materials 0.000 claims description 2
- 229910052762 osmium Inorganic materials 0.000 claims description 2
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 claims description 2
- PVADDRMAFCOOPC-UHFFFAOYSA-N oxogermanium Chemical class [Ge]=O PVADDRMAFCOOPC-UHFFFAOYSA-N 0.000 claims description 2
- YIONJVUULJNSMK-UHFFFAOYSA-N oxygen(2-);rubidium(1+) Chemical class [O-2].[Rb+].[Rb+] YIONJVUULJNSMK-UHFFFAOYSA-N 0.000 claims description 2
- 239000001294 propane Substances 0.000 claims description 2
- 229910001952 rubidium oxide Inorganic materials 0.000 claims description 2
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical class [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 claims description 2
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 2
- 229910003438 thallium oxide Inorganic materials 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 32
- 239000000243 solution Substances 0.000 description 23
- 230000008929 regeneration Effects 0.000 description 14
- 238000011069 regeneration method Methods 0.000 description 14
- 239000000377 silicon dioxide Substances 0.000 description 13
- 239000007789 gas Substances 0.000 description 10
- 238000005516 engineering process Methods 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 8
- 239000002243 precursor Substances 0.000 description 8
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 8
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 229910052681 coesite Inorganic materials 0.000 description 6
- 229910052906 cristobalite Inorganic materials 0.000 description 6
- CHPZKNULDCNCBW-UHFFFAOYSA-N gallium nitrate Chemical compound [Ga+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O CHPZKNULDCNCBW-UHFFFAOYSA-N 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 229910052682 stishovite Inorganic materials 0.000 description 6
- 229910052905 tridymite Inorganic materials 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 235000013844 butane Nutrition 0.000 description 5
- 238000001354 calcination Methods 0.000 description 5
- 238000005336 cracking Methods 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 238000005470 impregnation Methods 0.000 description 5
- 229910052718 tin Inorganic materials 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical class [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 230000003071 parasitic effect Effects 0.000 description 4
- 229910003446 platinum oxide Inorganic materials 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 229960004543 anhydrous citric acid Drugs 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229940044658 gallium nitrate Drugs 0.000 description 3
- 239000000320 mechanical mixture Substances 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 230000001737 promoting effect Effects 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 2
- 239000012159 carrier gas Substances 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 239000000571 coke Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 230000002860 competitive effect Effects 0.000 description 2
- 229910052593 corundum Inorganic materials 0.000 description 2
- XNMQEEKYCVKGBD-UHFFFAOYSA-N dimethylacetylene Natural products CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 229910052733 gallium Inorganic materials 0.000 description 2
- 239000011551 heat transfer agent Substances 0.000 description 2
- 229910052738 indium Inorganic materials 0.000 description 2
- 239000003345 natural gas Substances 0.000 description 2
- 235000010333 potassium nitrate Nutrition 0.000 description 2
- 239000004323 potassium nitrate Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 2
- 229910001845 yogo sapphire Inorganic materials 0.000 description 2
- KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 description 1
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000010960 commercial process Methods 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000002737 fuel gas Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical class [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 238000006384 oligomerization reaction Methods 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 239000003348 petrochemical agent Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000007420 reactivation Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- NUMQCACRALPSHD-UHFFFAOYSA-N tert-butyl ethyl ether Chemical compound CCOC(C)(C)C NUMQCACRALPSHD-UHFFFAOYSA-N 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 230000036967 uncompetitive effect Effects 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
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/12—Silica and alumina
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/56—Platinum group metals
- B01J23/62—Platinum group metals with gallium, indium, thallium, germanium, tin or lead
- B01J23/622—Platinum group metals with gallium, indium, thallium, germanium, tin or lead with germanium, tin or lead
- B01J23/626—Platinum group metals with gallium, indium, thallium, germanium, tin or lead with germanium, tin or lead with tin
-
- 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/30—Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
-
- 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/40—Catalysts, in general, characterised by their form or physical properties characterised by dimensions, e.g. grain size
-
- 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
-
- 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
- B01J35/61—Surface area
- B01J35/613—10-100 m2/g
-
- 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
- B01J35/61—Surface area
- B01J35/615—100-500 m2/g
-
- 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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0201—Impregnation
-
- 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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0201—Impregnation
- B01J37/0203—Impregnation the impregnation liquid containing organic compounds
-
- 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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0201—Impregnation
- B01J37/0205—Impregnation in several steps
-
- 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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/08—Heat treatment
- B01J37/10—Heat treatment in the presence of water, e.g. steam
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
- C07C5/327—Formation of non-aromatic carbon-to-carbon double bonds only
- C07C5/333—Catalytic processes
- C07C5/3332—Catalytic processes with metal oxides or metal sulfides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/12—Silica and alumina
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
- C07C2523/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals combined with metals, oxides or hydroxides provided for in groups C07C2523/02 - C07C2523/36
- C07C2523/56—Platinum group metals
- C07C2523/62—Platinum group metals with gallium, indium, thallium, germanium, tin or lead
Definitions
- the present invention falls within the scope of the production of 1 ,3-butadiene from a mixture of unsaturated hydrocarbons having from 2 to 10 carbon atoms (described as “C2-C10 unsaturates” in this text), preferably unsaturated hydrocarbons having 4 carbon atoms (described as“C4 unsaturates” in this text), or mixtures of saturated and unsaturated hydrocarbons having from 2 to 10 carbon atoms (described as“mixtures of saturated and unsaturated C2-C10” in this text), preferably saturated and unsaturated hydrocarbons having 4 carbon atoms (described as“mixtures of saturated and unsaturated C4” in this text) originating from cracking plants that are either stand-alone, or incorporated into a selective extraction plant or the entire cycle for the utilization of said hydrocarbons.
- the present invention relates in particular to a dual catalyst composition which can be used in the process for the production of 1 ,3-butadiene.
- the present invention may advantageously be applied where there is an existing butadiene extraction plant or where such plant is newly constructed.
- Raffinate 1 or extraction raffinate is meant the resulting mixture after the starting materials have been treated with solvent for the extraction of 1 ,3-butadiene.
- intervals For the purposes of the present description definitions of intervals always comprise the end members unless specified otherwise.
- Any isobutene present in the C4 charge is almost inert with regard to dehydrogenation to 1 ,3-butadiene and is generally separated out by esterification of ethanol or methanol to obtain ETBE or MTBE. No applications providing for its conversion to butadiene are known.
- butadiene by extractive distillation has as its intrinsic limit the availability of the charge of saturated and unsaturated C2-C10 hydrocarbons, in particular saturated and unsaturated hydrocarbons having four carbon atoms (C4) originating from the cracking furnaces.
- Butadiene yields depend on the operating conditions of the cracking process, which is generally optimized for the production of lighter olefins.
- dehydrogenation technologies are economically uncompetitive in comparison with selective extraction of the C4 hydrocarbons fraction from cracking and are only capable of converting linear C4 compounds.
- isobutene cannot be converted into butadiene and has to be separated out using a dedicated process, with not always acceptable economic returns, or are isomerized to linear C4 hydrocarbons before being fed to a dehydrogenation plant for the production of 1 ,3-butadiene.
- said catalyst is used with a second catalyst comprising Boralite B or a granular support of porous gamma- alumina on the surface of which silica is deposited.
- Tin is present in quantities ranging from 0.1% to 1% by weight, indium is present in quantities ranging from 0.05% to 1%.
- Platinum/indium ratios by weight range from 0.3:1 to 1.5:1.
- Platinum/tin ratios range from 0.5:1 to 2:1.
- the Applicant has identified a dual catalyst composition capable of simultaneously promoting both isomerization of the chains of saturated and unsaturated hydrocarbons, having from 4 to 10 carbon atoms (C4-C10), including when mixed, preferably saturated and unsaturated hydrocarbons having from 4 to 6 carbon atoms (C4-C6), more preferably isobutene, including when mixed, in such a way that the branched isomers are converted into hydrocarbons having a linear structure, and dehydrogenation of the saturated and unsaturated linear hydrocarbons having from 2 to 10 carbon atoms (C2-C10), including when mixed, preferably saturated and unsaturated hydrocarbons having 4 carbon atoms (C4), including when mixed, to form 1 ,3-butadiene.
- Said dual catalyst composition comprises a component with acid moiety and a component with dehydrogenating moiety mechanically mixed or chemically bound together in a dual way.
- the active part having acid moiety and the active part having dehydrogenating moiety are located on separate catalyst elements, typically separate catalyst particles.
- the active parts may either interact physically or establish bonds of the ionic type.
- the dual catalyst composition described and claimed in the present patent application is very active, mechanically strong, and is suitable for operating with short contact times in fluidized bed or moving bed reactors, and in particular in reactors of the“Fast Riser Reactor” type which are more suitable for operating at shorter residence times to minimize parasitic reactions.
- the object of the present patent application thus constitutes a dual catalyst composition
- a dual catalyst composition comprising:
- a component with acid moiety selected from oxides and mixed oxides of aluminum, preferably selected from aluminosilicates, aluminum oxides or zeolites;
- a component with dehydrogenating moiety selected from oxides of a metal of Group IMA or IVA in the Periodic Table, said oxides having added noble metals belonging to Group VIIIB of the Periodic Table in a quantity ranging from 20 ppm to 500 ppm, preferably from 30 ppm to 200 ppm, more preferably from 30 ppm to 180 ppm, even more preferably from 30 ppm to 150 ppm of metal with respect to the total composition;
- a further object of the present invention constitutes a process for the production of 1 ,3- butadiene from mixtures of unsaturated hydrocarbons having from 2 to 10 carbon atoms, or mixtures of saturated and unsaturated hydrocarbons having from 2 to 10 carbon atoms, said process comprising the following stages:
- Raffinate 1 by extractive distillation in an extraction unit; c) subsequently to step (b), mixing Extraction Raffinate 1 with a reaction inert and sending such mixture to a non-oxidative isomerization and dehydrogenation reaction unit placed downstream of the extraction unit, wherein the mixture is simultaneously subjected to a non-oxidative dehydrogenation reaction and an isomerization reaction in a single-stage in the presence of a dual catalyst composition so as to form a reaction effluent containing from 4% to 25% by weight of 1 ,3-butadiene and possibly from 40% to 90% by weight of a mixture of unreacted unsaturated hydrocarbons having from 3 to 6 carbon atoms in the chain or a mixture of unreacted saturated and unsaturated hydrocarbons having from 3 to 6 carbon atoms in the chain, so as to form a stream of unreacted hydrocarbons containing unsaturated and saturated hydrocarbons having from 2 to 10 carbon atoms in the chain;
- reaction effluent then sending the reaction effluent to a physical separation section to separate the following streams:
- the catalyst composition constituting the subject matter of the present patent application is very active, non-toxic, and is used in a fluidized bed or“fast-riser” type reactor; it also performs the function of a heat transfer agent. In this way it supports the endothermic nature of the non-oxidative dehydrogenation reaction, which can thus maintain itself thermally, doing without auxiliary furnaces external to the plant. Through this aspect it overcomes the critical factor in present commercial technologies.
- One special feature of Fast Riser reactor technology comprises continuous catalyst regeneration as reaction volumes reduce, for the same productivity, at the same time avoiding the safety problems associated with air-hydrocarbon mixtures, in that regeneration of the catalyst system takes place in an operating unit, which is suitably intended for regeneration.
- the dual catalyst composition described and claimed in this text makes it possible to bring about the conversion of all unsaturated and saturated C2-C10 hydrocarbons (which may originate from steam cracking, petrochemical industry processes or refining processes) into 1 ,3-butadiene in a single stage, thus maximizing 1 ,3-butadiene yields, with overall investment costs and operating costs that are competitive in comparison with ordinary commercial dehydrogenation processes which otherwise require that said C4- C10 hydrocarbons or isobutene must first be removed or isomerized in a plant built for that purpose.
- Figure 1 illustrates a preferred embodiment of the process for the production of 1 ,3- butadiene.
- a mixture of hydrocarbons having 4 carbon atoms (1 ) is fed to an extractive distillation unit (A) which produces a Raffinate 1 (2) and 1 ,3-butadiene (3).
- Raffinate 1 (2) is fed directly to a unit in which an isomerization and non-oxidative dehydrogenation reaction (B) takes place in a single stage.
- a fraction (6) which is sent to other applications can be extracted from Raffinate 1.
- reaction unit (B) A mixture containing unreacted butenes and butanes (4) which is recycled to B, and a mixture containing concentrated 1 ,3-butadiene (5) which is recycled to the extractive distillation unit without further subsequent conversion or reaction stages is produced from reaction unit (B).
- the present invention is a dual catalyst composition comprising:
- a component with acid moiety selected from oxides and mixed oxides of aluminum, preferably selected from aluminosilicates, aluminum oxides or zeolites;
- a component with dehydrogenating moiety selected from metal oxides of a metal in Group IMA or IVA of the Periodic Table, said oxides having added noble metals belonging to Group VIIIB of the Periodic Table in a quantity ranging from 20 ppm to 500 ppm of metal with respect to the total composition;
- Preferred oxides may be aluminum oxides, aluminosilicates or zeolites; microspheroidal alumina having a specific surface area of between 50 m 2 /g and 150 m 2 /g measured according to the method in ASTM D-3037/89 (Brunauer, Emmett, Teller or BET method) and having an acidity of between 100 pmols/g and 500 pmols/g of pyridine adsorbed at 25°C may be more preferred.
- the noble metals belonging to Group VIIIB of the Periodic Table may be added in a quantity preferably ranging from 30 ppm to 200 ppm, more preferably from 30 ppm to 180 ppm, and even more preferably from 30 ppm to 150 ppm of metal with respect to the total composition.
- the oxides of metals in Group IMA in the Periodic Table may be selected from aluminum oxides, gallium oxides, indium oxides or thallium oxides; more preferably they may be selected from aluminum oxides or gallium oxides, even more preferably they may be AI2O3 or Ga 2 0 3 because they ensure a surprising balance in acidity values and at the same time have mechanical properties suitable for a Fast Riser type reactor.
- the oxides of metals in Group IVA of the Periodic Table may be selected from silicon oxides, tin oxides, lead oxides or germanium oxides; tin oxides SnO and/or Sn0 2 may be more preferred because they promote dehydrogenating catalytic activity.
- the concentrations of the oxides of metals in Group IIIA of the Periodic Table, and in particular Al 2 0 3 or Ga 2 0 3 may range from 0.1 % by weight to 34% by weight, more preferably they may range from 0.2% by weight to 3.8% by weight in comparison with the total weight of the catalyst composition.
- the concentrations of the oxides of metals in Group IVA of the Periodic Table, and in particular the Sn oxides, may range from 0.001 % by weight to 1 % by weight, more preferably they may range from 0.05% by weight to 0.4% by weight with respect to the total weight of the catalyst composition.
- the metals in Group VIIIB of the Periodic Table may be selected from iron, ruthenium, osmium, cobalt, rhodium, iridium, nickel, palladium or platinum; more preferably, they may be selected from ruthenium, rhodium, palladium, platinum, nickel; even more preferably it may be platinum, which enables the function promoting regeneration and reactivation of the dehydrogenating moiety.
- Supports suitable for the present invention may be selected from alumina or microspheroidal aluminosilicates, preferably they may be microspheroidal aluminas having a d (Delta) and/or Q (Theta) crystalline phase and aluminosilicates in the form of ZSM-5 zeolites.
- a support may be in the form of microspheroidal particles having the morphology below: mean particle diameter (D 5 o) ranging from 70 microns to 90 microns, measured using the Light Scattering technique according to ASTM standard D4464-15.
- the quantity of silica present in the support and/or the component having acid moiety ranges from 0.05% by weight to 10% by weight with respect to the support only, the remainder being alumina.
- the components having acid and dehydrogenating moieties may be located on separate and different catalyst particles, or on the same catalyst particle in a single bifunctional system.
- microspheroidal particles render the catalyst system described and claimed suitable for use in fluidized bed, moving bed or“Fast Riser” technology reactors.
- the oxides of the metals in Group IMA or IVA in the Periodic Table are deposited on a support having an acidity of between 100 pmols/g and 500 pmols/g of pyridine adsorbed at 25°C.
- the acidity of the support so obtained may optionally be suitably modulated through the addition of a quantity of alkali metal oxides which may range from 10 ppm to 5000 ppm, preferably from 50 ppm to 700 ppm, more preferably from 70 ppm to 200 ppm of metal with respect to the total composition in order to minimize parasitic reactions and maximize butadiene yield.
- the alkali metal oxides may be selected from lithium oxides, sodium oxides, potassium oxides, rubidium oxides, cesium oxides or francium oxides; sodium oxide Na 2 0 or potassium oxide K 2 0 may be more preferred. Potassium oxide K 2 O may be even more preferred.
- the quantity of alkali metal oxides, and in particular of the quantity of K 2 O oxide may range from 0.01% by weight to 5% by weight, more preferably from 0.01% by weight to 3% by weight with respect to the total weight of the catalyst composition.
- the dual catalyst composition or the dehydrogenating fraction of the catalyst mixture described and claimed in the present text is obtained by a process comprising dispersing the precursors of the active metals on microspheres of modified alumina.
- This dispersion treatment may be:
- a preferred technique is impregnation of the support with a volume of solution equal to that provided by the pores (the pore volume being calculated as the specific porosity of the support [cc/g] multiplied by the grams of support being impregnated) as appropriate for the quantity of support, which has to be treated.
- This impregnation procedure is known in the common state of the art as the“incipient wetness” procedure.
- Another preferred technique is immersion of the support in a volume of solution in excess with respect to that appropriate for the pores, in which the precursors of the active metals are dissolved, followed by evaporation and subsequent calcination.
- the active metal precursors may be dispersed simultaneously on the silica modified support in a single stage, or in several stages: • in the first stage the support, preferably modified with silica, is impregnated with a solution containing a precursor of the active metal, for example gallium and potassium, followed by drying and calcination; or the modified support, preferably modified with silica, is impregnated with a solution containing a precursor of the active metal, for example gallium, potassium and tin, followed by drying and calcination;
- the calcinate originating from the first stage is impregnated with a solution containing a precursor of platinum and tin, the impregnate being dried and finally calcined.
- Another object of the present invention is a process for the production of 1 ,3-butadiene.
- the starting materials used in the process for the production of 1 ,3-butadiene may be unsaturated C2-C10 or mixtures of saturated and unsaturated C2-C10.
- the starting materials may be mixtures of C4 unsaturates (“C4 butenes”), or mixtures of saturated and unsaturated C4 hydrocarbons (“mixtures of C4 butanes and butenes”).
- the starting materials may be mixtures of unsaturated hydrocarbons having from 2 to 8 carbon atoms, described as“C2-C8 unsaturates”; more preferably
- the starting materials may be mixtures of unsaturated and saturated hydrocarbons having from 2 to 8 carbon atoms, described as“mixtures of unsaturated and saturated C2-C8”; more preferably unsaturated and saturated hydrocarbons having from 2 to 5 carbon atoms, described as“mixtures of unsaturated and saturated C2-C5”.
- Preferred mixtures suitable for the purposes of the present invention contain from 1% to 18% of saturated C2-C10 components, more preferably from 4% to 13% of saturated C2- C10 components, and from 82% to 99% of unsaturated C2-C10 components, more preferably from 87% to 96% of unsaturated C2-C10 components calculated with respect to the mixture as a whole. As is obvious, the sum of the components must always be 100%.
- Saturated C2-C10 present in the starting mixtures may be selected from ethane, propane, n-butane, isobutane and their mixtures.
- Unsaturated C2-C10 present in the preferred starting mixtures may be selected from ethene, propene, 1 -butene, 2-butenes, isobutene and their mixtures.
- More preferred may be mixtures of saturated and unsaturated C4 containing n-butane, isobutane, 1 -butene, 2-butenes, isobutene.
- hydrocarbons having more than 4 carbon atoms in a quantity of 0.1 % w/w.
- the starting hydrocarbon mixtures are fed to an extractive distillation unit as separate flows.
- Such extraction units may comprise one or more extractors in series or in parallel.
- Raffinate 1 is a flow, which may comprise hydrocarbons having fewer than 4 carbon atoms, n-butane, isobutane, 1 -butene, 2-butenes, isobutene, and hydrocarbons having more than 4 carbon atoms.
- Raffinate 1 may contain:
- hydrocarbons having more than 4 carbon atoms in a quantity of 0.1 % w/w
- the reaction is carried out in the presence of a dual catalyst composition suitable for isomerization and non-oxidative dehydrogenation reactions to form a reaction effluent containing from 4% to 25% by weight of 1 ,3-butadiene and possibly 40 to 90% by weight for a mixture of unreacted unsaturated hydrocarbons having from 3 to 6 carbon atoms in the chain or a mixture of unreacted saturated and unsaturated hydrocarbons having from 3 to 6 carbon atoms in the chain, in such a way as to form a flow of unreacted hydrocarbons containing unsaturated and saturated hydrocarbons having from 2 to 10 carbon atoms in the chain.
- a dual catalyst composition suitable for isomerization and non-oxidative dehydrogenation reactions to form a reaction effluent containing from 4% to 25% by weight of 1 ,3-butadiene and possibly 40 to 90% by weight for a mixture of unreacted unsaturated hydrocarbons having from 3 to 6 carbon atoms in the chain or a mixture of unreacted saturated
- the catalyst composition used in the isomerization and non-oxidative dehydrogenation reaction unit is preferably the composition described and claimed in the present text.
- the hydrogenation and isomerization reaction can take place at a temperature ranging from 500°C to 700°C.
- the isomerization and dehydrogenation pressure may range from 0.2 atm to 2 atm absolute.
- the reaction inert/charge ratio (v/v) may range from 1 to 23, preferably from 1 to 9.
- Said reaction unit may comprise one or more reactors in series or in parallel, each operating as a single reaction stage, meaning that the isomerization and dehydrogenation reactions take place simultaneously in each individual reactor.
- the reactors which may preferably be used in the process described and claimed may be selected from fluidized bed reactors or moving bed reactors or“Fast Riser” type reactors.
- the inert has the function of lowering the partial pressure of the starting materials (reagents) and that of the reaction products with a view to increasing conversion and reducing the kinetics of parasitic reactions to preserve selectivity for the desired product.
- the inert may be selected from nitrogen, methane or another combustible gas having a maximum hydrogen content of 1% by weight and possibly oxygen. The latter may be present in traces as a typical residue of air distillation.
- the combustible gas offers the advantage in comparison with nitrogen that it can recover the calorific value of the hydrogen without the need for cryogenic separation.
- reaction effluent is then sent to a physical separation section to separate out the following flows:
- the flow containing from 13% to 30% by weight of 1 ,3-butadiene can be recirculated to the extraction unit without further subsequent reaction or processing stages, feeding it to the extraction unit separately from the starting materials (unsaturated C2-C10
- the mixture of unreacted unsaturated hydrocarbons having from 3 to 6 carbon atoms in the chain or a mixture of unreacted saturated and unsaturated hydrocarbons having from 3 to 6 carbon atoms in the chain can be recirculated directly to the isomerization and non- oxidative dehydrogenation unit.
- Fast-Riser technology comprises a reactor in the upper part of which there is a zone for separation of the catalyst and a stripping zone fed with inert, and in the lower part of which a regenerator in which there is a stripping zone.
- the regenerator is fed with a comburant, a fuel and an inert.
- the reactor and regenerator are connected together by means of a conduit for the passage of partly exhausted catalyst.
- the isomerization- dehydrogenation reaction effluent leaves the gas-solid separator at the top of the reactor.
- the hot regenerated catalyst leaves from the bottom of the regenerator and is
- the part of the catalyst which is sent to the regenerator ranges from 50% to 80% and as a consequence the part which is not regenerated ranges from 50% to 20%.
- the same carrier gas may be used to dilute the charge entering the reactor.
- the inert to dilute the charge may be selected from nitrogen, methane or another combustible gas having a maximum hydrogen content of 1 % by weight, and possibly oxygen. The latter may be present in traces, possibly as a typical residue of air distillation.
- the charge is mixed with the at least partly regenerated catalyst composition entering from the base of the reactor.
- the charge is progressively isomerized and dehydrogenated (by means of non-oxidative dehydrogenation) as it advances co- currently, until it passes through the entire reactor.
- the catalyst composition separates out from the gaseous effluent and at least part is sent to the regeneration device. The unregenerated part of the catalyst is directly recycled to the reactor. After regeneration the catalyst composition is recirculated to the reactor.
- the residence time of the gas phase may be a minute or less, and preferably in a range from 0.2 sec to 5 sec.
- the temperature may range from 450°C to 700°C.
- the pressure may preferably range from 0.2 atm absolute to 2 atm.
- the reaction inert/charge ratio (w/w) may range from 1 to 23, preferably from 1 to 9.
- Regeneration preferably takes place in a fluidized bed at a temperature higher than the operating temperature of the reaction section, preferably above 700°C.
- the pressure in the regeneration section may be equal to that in the isomerization and dehydrogenation section or atmospheric.
- the residence time of the catalyst composition during regeneration may range from 5 minutes to 60 minutes, preferably from 15 minutes to 40 minutes.
- the gas phase hourly space velocity (GHSV in Nl/h of air per liter of catalyst) may range from 1000 h 1 to 5000 h 1 , preferably from 2000 h 1 to 3000 h- 1 .
- the catalyst composition may be regenerated and the fuel gas may be burnt with a comburant selected from air, oxygen or any other gaseous comburant.
- a“Fast-Riser” reactor can be isomerized as follows:
- reaction and regeneration take place in physically separate zones and there can be no mixing of hydrocarbon flows with flows containing oxygen;
- composition described and claimed in the present patent application is very active and selective at low contact times for the isomerization of unsaturated C2-C10 hydrocarbons, in particular for the isomerization of isobutene, and for the
- the operating conditions used are typical of dehydrogenation processes (500°C-700°C).
- use of the“Fast-Riser” technology and the catalyst composition described and claimed make it possible to perform the isomerization reaction under more severe temperature conditions than in normal isomerization processes without significantly penalizing selectivity thanks to short contact times and an appropriate ratio between the concentrations of dehydrogenation and isomerization sites.
- the catalyst composition described and claimed in the present text constitutes the heat transfer agent for the isomerization and dehydrogenation reaction giving up sensible heat accumulated during regeneration.
- Combustion of the coke present in the spent catalyst composition generates heat which is wholly recovered for the reaction and incorporated with the proportions of combustible gases added to the regenerator to be able to completely balance the endothermic reactions.
- Natural gas or hydrogen, or combustible gas, including that obtained from a mixture of hydrogen and natural gas, can be used as combustible gas for the regeneration section.
- a mixture of C4 hydrocarbons comprising n-butane, isobutane, 1 -butene, 2-butene, isobutene, 1 ,3-butadiene (1 ) is fed separately to an extraction section (A) in which a flow containing 1 ,3-butadiene (3) and a Raffinate 1 (2) is extracted through extractive distillation.
- Raffinate 1 is fed directly to a reaction unit in which an isomerization reaction and a non-oxidative dehydrogenation reaction (B) which convert the C4 mixtures into a mixture containing 1 ,3-butadiene (5) in the presence of the catalyst system described and claimed take place simultaneously. Possibly some of Raffinate 1 is directed to other purposes (6).
- the unreacted flow (4) is recycled directly to the reaction section (B) feeding it as a separate flow, while the flow containing 1 ,3-butadiene (4) is recirculated directly to extractive distillation without further reaction and processing steps, feeding it separately.
- a catalyst composition was prepared as a mechanical mixture by mixing an acid component and a dehydrogenation catalyst in a stirred vessel in a 1 : 1 ratio by weight.
- the acid component was an aluminosilicate or microspheroidal alumina, modified with 5% by weight of silica, with average particles diameter (D50) equal to 70 pm and specific surface area of 120 m 2 /g.
- the dehydrogenation catalyst was a composition comprising Ga2C>3, in which Ga was present in a quantity amounting to 1.6% by weight, K 2 0 in which K was present in a quantity corresponding to 0.8% by weight, the % being calculated with reference to the total composition, SnO and/or Sn0 2 in which Sn was present in a quantity corresponding to 700 ppm by weight of metal with respect to the total composition and platinum oxides in which Pt was present in a quantity corresponding to 200 ppm by weight of metal with respect to the total composition, supported on microspheroidal alumina modified with 1.5% by weight of silica with respect to the total composition.
- the dehydrogenation catalyst was prepared in the following way.
- the impregnate was dried at 120°C for 4 hours and then calcined using the heating rate: from ambient temperature to 460°C in 530 minutes and an isothermal stage of 180 minutes at 460°C.
- the impregnate was dried at 120°C for 4 hours and then calcined in accordance with the heating rate: from 20° (ambient temperature) to 120°C in 120 minutes, followed by an isothermal stage at 120°C for 120 minutes, then from 120°C to 250°C in 120 minutes, from 250°C to 730°C in 210 minutes, followed by an isothermal stage at 730°C for 90 minutes.
- the composition by weight of the catalyst system was: Ga 2 0 3 in which Ga was present in a quantity corresponding to 1.6% by weight, K 2 0 in which K was present in a quantity corresponding to 0.8%, the % being calculated with respect to the total composition, SnO and/or Sn0 2 in which Sn was present in a quantity corresponding to 700 ppm by weight of metal with respect to the total composition, and platinum oxides in which Pt was present in a quantity corresponding to 200 ppm by weight of metal with respect to the total composition, the remaining part being Al 2 0 3 and Si0 2 .
- the catalyst showes average particles diameter (D50) equal to 80 pm and specific surface area of 80 m 2 /g,
- a catalyst composition comprising a bifunctional catalyst prepared by impregnation, using a microspheroidal alumina modified with 1.5% by weight of silica without the addition of potassium to modulate its acidity as a support and acid component was prepared by impregnation.
- the impregnate was dried at 120°C for 4 hours and finally calcined using the heating rate: from 20°C (ambient temperature) to 120°C in 120 minutes, followed by an isothermal stage at 120°C for 120 minutes, then from 120°C to 250°C in 120 minutes, from 250°C to 730°C in 210 minutes, followed by an isothermal stage at 730°C for 90 minutes.
- the composition by weight of the catalyst system was: Ga 2 C> 3 , in which Ga was present in a quantity corresponding to 1.6% by weight, the % being calculated with respect to the total composition, SnO and/or Sn0 2 in which Sn was present in a quantity corresponding to 700 ppm by weight of metal with respect to the total composition, and platinum oxides in which Pt was present in a quantity
- the catalyst showes average particles diameter (D50) equal to 80 pm and specific surface area of 80 m 2 /g.
- a catalyst composition comprising a bifunctional catalyst prepared by impregnation using a microspheroidal alumina modified with 1.2% by weight of silica, with the addition of potassium to modulate its acidity, being used as a support and acid component, was prepared.
- the impregnate was dried at 120°C for 4 hours and finally calcined using the heating rate: from ambient temperature to 460°C in 530 minutes and an isothermal stage of 180 minutes at 460°C.
- the composition by weight of the catalyst system was: Ga 2 0 3 in which Ga was present in a quantity corresponding to 1.6% by weight, K 2 O in which K was present in a quantity corresponding to 0.025% by weight, the % being calculated with respect to the total composition, SnO and/or Sn0 2 in which Sn was present in a quantity corresponding to 700 ppm by weight of metal with respect to the total composition, and platinum oxides in which Pt was present in a quantity
- the catalyst showes average particles diameter (D50) equal to 80 pm and specific surface area of 80 m 2 /g.
- the catalyst systems prepared in Examples 1-3 were tested for the isomerization and non-oxidative dehydrogenation reaction of a mixture of isobutene, linear butenes and n- butane (Raffinate 1 ) in a fixed bed laboratory microreactor, monitoring catalyst performance. All the tests were performed charging 0.5 cc catalyst, with a throughput of Raffinate 1 feed of 25 Nl/h diluted in nitrogen with a hydrocarbon concentration entering the reactor of 50% by weight; temperatures of 600°C and operating pressures of 0.6 and 1.1 atm absolute.
- Example 2 The data shown in Table 2 reveal that through operating in the presence of the dual catalyst composition both as a mechanical mixture (Example 1 ) and in the case where the active part with acid moiety and the active part with dehydrogenated moiety are located on the same element (Examples 2 and 3) it is possible to convert the isobutene present in the charge and at the same time dehydrogenate the linear butenes already present in the charge or formed by the conversion of isobutene into 1 ,3-butadiene.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
La présente invention concerne une composition de catalyseur double comprenant un composant avec des fractions acides choisies parmi des oxydes et des oxydes mixtes d'aluminium, un composant ayant une fraction déshydrogénante choisie parmi les oxydes d'un métal du Groupe IIIA ou IVA du tableau périodique, lesdits oxydes ayant des métaux nobles ajoutés appartenant au Groupe VIIIB du tableau périodique dans une quantité allant de 20 ppm à 500 ppm de métal par rapport à la composition totale, et un support.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT201700143763 | 2017-12-13 | ||
IT102017000143763 | 2017-12-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2019115627A1 true WO2019115627A1 (fr) | 2019-06-20 |
Family
ID=61656252
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2018/084588 WO2019115627A1 (fr) | 2017-12-13 | 2018-12-12 | Composition de catalyseur et processus de production de 1,3-butadiene |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2019115627A1 (fr) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112239391A (zh) * | 2019-07-16 | 2021-01-19 | 中国石油化工股份有限公司 | 丁烯脱氢制备1,3-丁二烯的方法 |
WO2023119131A1 (fr) * | 2021-12-22 | 2023-06-29 | Sabic Global Technologies B.V. | Catalyseur de déshydrogénation d'alcanes |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2246524A (en) | 1990-08-01 | 1992-02-05 | Eniricerche Spa | Dehydroisomerisation catalyst and its use in the preparation of isobutene from n-butane |
US20020198428A1 (en) * | 1993-08-06 | 2002-12-26 | Snamprogetti S.P.A. | Process for preparing light olefins by dehydrogenation of the corresponding paraffins |
EP2797863A1 (fr) * | 2011-12-28 | 2014-11-05 | Versalis S.p.A. | Procédé de production du 1,3-butadiène |
US20140378731A1 (en) * | 2011-12-28 | 2014-12-25 | Versalis S.P.A. | Catalytic composition and process for the dehydrogenation of butenes or mixtures of butanes and butenes to give 1,3-butadiene |
-
2018
- 2018-12-12 WO PCT/EP2018/084588 patent/WO2019115627A1/fr active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2246524A (en) | 1990-08-01 | 1992-02-05 | Eniricerche Spa | Dehydroisomerisation catalyst and its use in the preparation of isobutene from n-butane |
US20020198428A1 (en) * | 1993-08-06 | 2002-12-26 | Snamprogetti S.P.A. | Process for preparing light olefins by dehydrogenation of the corresponding paraffins |
EP2797863A1 (fr) * | 2011-12-28 | 2014-11-05 | Versalis S.p.A. | Procédé de production du 1,3-butadiène |
US20140378731A1 (en) * | 2011-12-28 | 2014-12-25 | Versalis S.P.A. | Catalytic composition and process for the dehydrogenation of butenes or mixtures of butanes and butenes to give 1,3-butadiene |
Non-Patent Citations (2)
Title |
---|
G.D. PIRNGRUBER; K. SESHAN, J.A., LERCHER (JOURNAL OF CATALYSIS, vol. 186, 1999, pages 188 - 200 |
XUEBING LI: "Catalytic dehydroisomerization of n-alkanes to isoalkenes", ENRIQUE IGLESIA (JOURNAL OF CATALYSIS, vol. 255, 2008, pages 134 - 137, XP022518272, DOI: doi:10.1016/j.jcat.2008.01.021 |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112239391A (zh) * | 2019-07-16 | 2021-01-19 | 中国石油化工股份有限公司 | 丁烯脱氢制备1,3-丁二烯的方法 |
CN112239391B (zh) * | 2019-07-16 | 2023-08-04 | 中国石油化工股份有限公司 | 丁烯脱氢制备1,3-丁二烯的方法 |
WO2023119131A1 (fr) * | 2021-12-22 | 2023-06-29 | Sabic Global Technologies B.V. | Catalyseur de déshydrogénation d'alcanes |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US10486140B2 (en) | Catalytic composition and process for the dehydrogenation of butenes or mixtures of butanes and butenes to give 1,3-butadiene | |
EP2834210B1 (fr) | Procédé de fabrication de xylenes et olefines légères à partir de composés aromatiques lourds | |
EP2834004B1 (fr) | Catalyseur zéolithique multimetallique de transalkylation de charges lourdes issues du reformage pour la production de xylenes et charges pétrochimiques | |
CN107428635B (zh) | 二烯的制造方法 | |
WO2019115627A1 (fr) | Composition de catalyseur et processus de production de 1,3-butadiene | |
Zhang et al. | Factors influencing 1, 3-butadiene formation for light alkane dehydrogenation | |
JP6446033B2 (ja) | 不飽和炭化水素の製造方法 | |
CN109092302B (zh) | 丁二烯选择加氢的方法 | |
US11383225B2 (en) | Hydrocarbon conversion catalyst system | |
US11285461B2 (en) | Catalyst system and process utilizing the catalyst system | |
CA3043512A1 (fr) | Systeme de catalyseur et procede de conversion d'une charge d'hydrocarbure utilisant le systeme de catalyseur | |
CN106365942B (zh) | 一种混合碳四转化方法 | |
CN110639517A (zh) | 丁二烯选择加氢的催化剂以及应用 | |
CN109092303B (zh) | 丁二烯选择加氢的催化剂 | |
CN106365948B (zh) | 一种混合碳四制备高辛烷值汽油组分及丁二烯的方法 | |
CN106365940B (zh) | 一种通过转化提高拔头油类轻烃附加值的工艺 | |
WO2023003624A1 (fr) | Catalyseur et processus de conversion d'alcanes en c2-c5 en composants de mélange d'essence | |
CN116920924A (zh) | 载体组合物及其制备方法与应用 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 18814644 Country of ref document: EP Kind code of ref document: A1 |
|
DPE1 | Request for preliminary examination filed after expiration of 19th month from priority date (pct application filed from 20040101) | ||
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 18814644 Country of ref document: EP Kind code of ref document: A1 |