SE438866B - Passiveringsmedelskomposition bestaende av en kiselhaltig krackningskatalysatorsvans, forfarande for dess framstellning samt anvendning derav vid krackning - Google Patents
Passiveringsmedelskomposition bestaende av en kiselhaltig krackningskatalysatorsvans, forfarande for dess framstellning samt anvendning derav vid krackningInfo
- Publication number
- SE438866B SE438866B SE7800244A SE7800244A SE438866B SE 438866 B SE438866 B SE 438866B SE 7800244 A SE7800244 A SE 7800244A SE 7800244 A SE7800244 A SE 7800244A SE 438866 B SE438866 B SE 438866B
- Authority
- SE
- Sweden
- Prior art keywords
- cracking
- antimony
- catalyst
- tail
- metals
- Prior art date
Links
- 238000005336 cracking Methods 0.000 title claims description 143
- 239000003054 catalyst Substances 0.000 title claims description 127
- 238000000034 method Methods 0.000 title claims description 56
- 239000000203 mixture Substances 0.000 title claims description 27
- 238000002360 preparation method Methods 0.000 title claims description 3
- 229920001296 polysiloxane Polymers 0.000 title 1
- 229910052787 antimony Inorganic materials 0.000 claims description 88
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 83
- 239000003921 oil Substances 0.000 claims description 56
- 229930195733 hydrocarbon Natural products 0.000 claims description 42
- 150000002430 hydrocarbons Chemical class 0.000 claims description 42
- 229910052751 metal Inorganic materials 0.000 claims description 35
- 239000002184 metal Substances 0.000 claims description 35
- 239000004215 Carbon black (E152) Substances 0.000 claims description 34
- 150000002739 metals Chemical class 0.000 claims description 29
- 239000003795 chemical substances by application Substances 0.000 claims description 28
- 150000001463 antimony compounds Chemical class 0.000 claims description 23
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 19
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 17
- 239000002994 raw material Substances 0.000 claims description 17
- 229910052759 nickel Inorganic materials 0.000 claims description 10
- 229910052720 vanadium Inorganic materials 0.000 claims description 10
- 229910052742 iron Inorganic materials 0.000 claims description 9
- 239000002245 particle Substances 0.000 claims description 9
- 239000002002 slurry Substances 0.000 claims description 9
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 claims description 9
- 238000004523 catalytic cracking Methods 0.000 claims description 8
- 230000000694 effects Effects 0.000 claims description 6
- 230000009931 harmful effect Effects 0.000 claims description 6
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims 2
- YPFNIPKMNMDDDB-UHFFFAOYSA-K 2-[2-[bis(carboxylatomethyl)amino]ethyl-(2-hydroxyethyl)amino]acetate;iron(3+) Chemical compound [Fe+3].OCCN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O YPFNIPKMNMDDDB-UHFFFAOYSA-K 0.000 claims 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 1
- 229910052710 silicon Inorganic materials 0.000 claims 1
- 239000010703 silicon Substances 0.000 claims 1
- 239000000725 suspension Substances 0.000 claims 1
- 235000013339 cereals Nutrition 0.000 description 59
- 230000008929 regeneration Effects 0.000 description 32
- 238000011069 regeneration method Methods 0.000 description 32
- 239000007789 gas Substances 0.000 description 19
- 239000010802 sludge Substances 0.000 description 17
- 241000196324 Embryophyta Species 0.000 description 13
- 239000010779 crude oil Substances 0.000 description 13
- 229910052739 hydrogen Inorganic materials 0.000 description 12
- 239000001257 hydrogen Substances 0.000 description 12
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 10
- 239000000571 coke Substances 0.000 description 10
- 238000002161 passivation Methods 0.000 description 10
- 239000007983 Tris buffer Substances 0.000 description 9
- 241000209219 Hordeum Species 0.000 description 8
- 235000007340 Hordeum vulgare Nutrition 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 8
- 239000000295 fuel oil Substances 0.000 description 8
- -1 hydrogen ions Chemical class 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 8
- 239000003546 flue gas Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 238000005194 fractionation Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 4
- 150000001462 antimony Chemical class 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 229910000323 aluminium silicate Inorganic materials 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000003502 gasoline Substances 0.000 description 3
- 229910001385 heavy metal Inorganic materials 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 239000010457 zeolite Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- IPSJOBCXDQJMFB-UHFFFAOYSA-K Cl[Sb](Cl)(Cl)=O Chemical compound Cl[Sb](Cl)(Cl)=O IPSJOBCXDQJMFB-UHFFFAOYSA-K 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910000410 antimony oxide Inorganic materials 0.000 description 2
- LJCFOYOSGPHIOO-UHFFFAOYSA-N antimony pentoxide Chemical compound O=[Sb](=O)O[Sb](=O)=O LJCFOYOSGPHIOO-UHFFFAOYSA-N 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- MVMLTMBYNXHXFI-UHFFFAOYSA-H antimony(3+);trisulfate Chemical class [Sb+3].[Sb+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O MVMLTMBYNXHXFI-UHFFFAOYSA-H 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical class [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 2
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical class C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- ODNBVEIAQAZNNM-UHFFFAOYSA-N 1-(6-chloroimidazo[1,2-b]pyridazin-3-yl)ethanone Chemical compound C1=CC(Cl)=NN2C(C(=O)C)=CN=C21 ODNBVEIAQAZNNM-UHFFFAOYSA-N 0.000 description 1
- LBMNROZFDOBCLI-UHFFFAOYSA-N 2,4,5-trioxa-1-phospha-3-stibabicyclo[1.1.1]pentane Chemical class P([O-])([O-])[O-].[Sb+3] LBMNROZFDOBCLI-UHFFFAOYSA-N 0.000 description 1
- RDFRTKTYYPFBKS-UHFFFAOYSA-H 2-[(4-sulfanylidene-1,3,2-dioxastibetan-2-yl)oxycarbothioyloxy]-1,3,2-dioxastibetane-4-thione Chemical class C([O-])([O-])=S.[Sb+3].C([O-])([O-])=S.C([O-])([O-])=S.[Sb+3] RDFRTKTYYPFBKS-UHFFFAOYSA-H 0.000 description 1
- CQOZJDNCADWEKH-UHFFFAOYSA-N 2-[3,3-bis(2-hydroxyphenyl)propyl]phenol Chemical class OC1=CC=CC=C1CCC(C=1C(=CC=CC=1)O)C1=CC=CC=C1O CQOZJDNCADWEKH-UHFFFAOYSA-N 0.000 description 1
- 229910021630 Antimony pentafluoride Inorganic materials 0.000 description 1
- GUNJVIDCYZYFGV-UHFFFAOYSA-K Antimony trifluoride Inorganic materials F[Sb](F)F GUNJVIDCYZYFGV-UHFFFAOYSA-K 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- APRJAPPXOAHJMR-UHFFFAOYSA-K O-[bis(butylcarbamothioyloxy)stibanyl] N-butylcarbamothioate Chemical compound [Sb+3].CCCCNC([O-])=S.CCCCNC([O-])=S.CCCCNC([O-])=S APRJAPPXOAHJMR-UHFFFAOYSA-K 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- VBVBHWZYQGJZLR-UHFFFAOYSA-I antimony pentafluoride Chemical compound F[Sb](F)(F)(F)F VBVBHWZYQGJZLR-UHFFFAOYSA-I 0.000 description 1
- PPKVREKQVQREQD-UHFFFAOYSA-N antimony pentasulfide Chemical compound S=[Sb](=S)S[Sb](=S)=S PPKVREKQVQREQD-UHFFFAOYSA-N 0.000 description 1
- 229960001283 antimony pentasulfide Drugs 0.000 description 1
- 229910000379 antimony sulfate Inorganic materials 0.000 description 1
- 229940045100 antimony triiodide Drugs 0.000 description 1
- ZSIZJCNPPZMOQY-UHFFFAOYSA-N antimony triselenide Chemical compound [Se-2].[Se-2].[Se-2].[SbH3+3].[SbH3+3] ZSIZJCNPPZMOQY-UHFFFAOYSA-N 0.000 description 1
- 229940007424 antimony trisulfide Drugs 0.000 description 1
- WAFWAXOYAJEMTA-UHFFFAOYSA-K antimony(3+) N-phenylcarbamodithioate Chemical compound [Sb+3].[S-]C(=S)Nc1ccccc1.[S-]C(=S)Nc1ccccc1.[S-]C(=S)Nc1ccccc1 WAFWAXOYAJEMTA-UHFFFAOYSA-K 0.000 description 1
- SHXXPUOHIKESCB-UHFFFAOYSA-K antimony(3+);4-methylbenzenesulfonate Chemical compound [Sb+3].CC1=CC=C(S([O-])(=O)=O)C=C1.CC1=CC=C(S([O-])(=O)=O)C=C1.CC1=CC=C(S([O-])(=O)=O)C=C1 SHXXPUOHIKESCB-UHFFFAOYSA-K 0.000 description 1
- XDEOZZDFNYGLHY-UHFFFAOYSA-K antimony(3+);octadecanoate Chemical compound [Sb+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XDEOZZDFNYGLHY-UHFFFAOYSA-K 0.000 description 1
- KIQKNTIOWITBBA-UHFFFAOYSA-K antimony(3+);phosphate Chemical class [Sb+3].[O-]P([O-])([O-])=O KIQKNTIOWITBBA-UHFFFAOYSA-K 0.000 description 1
- SICICTORIQWAKP-UHFFFAOYSA-K antimony(3+);thiophosphate Chemical class [Sb+3].[O-]P([O-])([O-])=S SICICTORIQWAKP-UHFFFAOYSA-K 0.000 description 1
- PALVEAZBDSAOLL-UHFFFAOYSA-K antimony(3+);tribenzoate Chemical compound [Sb+3].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 PALVEAZBDSAOLL-UHFFFAOYSA-K 0.000 description 1
- RPJGYLSSECYURW-UHFFFAOYSA-K antimony(3+);tribromide Chemical compound Br[Sb](Br)Br RPJGYLSSECYURW-UHFFFAOYSA-K 0.000 description 1
- SEKOGOCBEZIJIW-UHFFFAOYSA-H antimony(3+);tricarbonate Chemical class [Sb+3].[Sb+3].[O-]C([O-])=O.[O-]C([O-])=O.[O-]C([O-])=O SEKOGOCBEZIJIW-UHFFFAOYSA-H 0.000 description 1
- NJGBSFDVMQSDTF-UHFFFAOYSA-K antimony(3+);triformate Chemical compound [Sb+3].[O-]C=O.[O-]C=O.[O-]C=O NJGBSFDVMQSDTF-UHFFFAOYSA-K 0.000 description 1
- KWQLUUQBTAXYCB-UHFFFAOYSA-K antimony(3+);triiodide Chemical compound I[Sb](I)I KWQLUUQBTAXYCB-UHFFFAOYSA-K 0.000 description 1
- NVWBARWTDVQPJD-UHFFFAOYSA-N antimony(3+);trisulfide Chemical compound [S-2].[S-2].[S-2].[Sb+3].[Sb+3] NVWBARWTDVQPJD-UHFFFAOYSA-N 0.000 description 1
- VMPVEPPRYRXYNP-UHFFFAOYSA-I antimony(5+);pentachloride Chemical compound Cl[Sb](Cl)(Cl)(Cl)Cl VMPVEPPRYRXYNP-UHFFFAOYSA-I 0.000 description 1
- DAMJCWMGELCIMI-UHFFFAOYSA-N benzyl n-(2-oxopyrrolidin-3-yl)carbamate Chemical compound C=1C=CC=CC=1COC(=O)NC1CCNC1=O DAMJCWMGELCIMI-UHFFFAOYSA-N 0.000 description 1
- BXPINBZVBOJHGU-UHFFFAOYSA-K bis(benzenesulfonyloxy)stibanyl benzenesulfonate Chemical compound [Sb+3].[O-]S(=O)(=O)c1ccccc1.[O-]S(=O)(=O)c1ccccc1.[O-]S(=O)(=O)c1ccccc1 BXPINBZVBOJHGU-UHFFFAOYSA-K 0.000 description 1
- QFHODGUIDMNILD-UHFFFAOYSA-K bis(diethylcarbamoyloxy)stibanyl N,N-diethylcarbamate Chemical compound [Sb+3].CCN(CC)C([O-])=O.CCN(CC)C([O-])=O.CCN(CC)C([O-])=O QFHODGUIDMNILD-UHFFFAOYSA-K 0.000 description 1
- MIMGEWVRLQPMKW-UHFFFAOYSA-K bis(dipropylcarbamothioylsulfanyl)stibanyl N,N-dipropylcarbamodithioate Chemical compound [Sb+3].CCCN(CCC)C([S-])=S.CCCN(CCC)C([S-])=S.CCCN(CCC)C([S-])=S MIMGEWVRLQPMKW-UHFFFAOYSA-K 0.000 description 1
- VLPHFAGGIRDLBN-UHFFFAOYSA-K bis(ethanethioylsulfanyl)stibanyl ethanedithioate Chemical compound [Sb+3].CC([S-])=S.CC([S-])=S.CC([S-])=S VLPHFAGGIRDLBN-UHFFFAOYSA-K 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- NZNMSOFKMUBTKW-UHFFFAOYSA-M cyclohexanecarboxylate Chemical compound [O-]C(=O)C1CCCCC1 NZNMSOFKMUBTKW-UHFFFAOYSA-M 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- ALMJEOCNCLDGNJ-UHFFFAOYSA-K di(dodecanoyloxy)stibanyl dodecanoate Chemical compound [Sb+3].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O ALMJEOCNCLDGNJ-UHFFFAOYSA-K 0.000 description 1
- JVLRYPRBKSMEBF-UHFFFAOYSA-K diacetyloxystibanyl acetate Chemical compound [Sb+3].CC([O-])=O.CC([O-])=O.CC([O-])=O JVLRYPRBKSMEBF-UHFFFAOYSA-K 0.000 description 1
- KUMNEOGIHFCNQW-UHFFFAOYSA-N diphenyl phosphite Chemical compound C=1C=CC=CC=1OP([O-])OC1=CC=CC=C1 KUMNEOGIHFCNQW-UHFFFAOYSA-N 0.000 description 1
- RIBJLXBLWQKWLO-UHFFFAOYSA-N diphenylstiborylbenzene Chemical compound C=1C=CC=CC=1[Sb](C=1C=CC=CC=1)(=O)C1=CC=CC=C1 RIBJLXBLWQKWLO-UHFFFAOYSA-N 0.000 description 1
- QVKQJEWZVQFGIY-UHFFFAOYSA-N dipropyl hydrogen phosphate Chemical compound CCCOP(O)(=O)OCCC QVKQJEWZVQFGIY-UHFFFAOYSA-N 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- WPYVAWXEWQSOGY-UHFFFAOYSA-N indium antimonide Chemical compound [Sb]#[In] WPYVAWXEWQSOGY-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- CQDGTJPVBWZJAZ-UHFFFAOYSA-N monoethyl carbonate Chemical compound CCOC(O)=O CQDGTJPVBWZJAZ-UHFFFAOYSA-N 0.000 description 1
- 229910052680 mordenite Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- SSFPHCKFUBEAKZ-UHFFFAOYSA-N propoxymethanedithioic acid Chemical compound CCCOC(S)=S SSFPHCKFUBEAKZ-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 150000002910 rare earth metals Chemical class 0.000 description 1
- 239000003079 shale oil Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- YPMOSINXXHVZIL-UHFFFAOYSA-N sulfanylideneantimony Chemical class [Sb]=S YPMOSINXXHVZIL-UHFFFAOYSA-N 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- DUYAAUVXQSMXQP-UHFFFAOYSA-M thioacetate Chemical compound CC([S-])=O DUYAAUVXQSMXQP-UHFFFAOYSA-M 0.000 description 1
- LWRYDHOHXNQTSK-UHFFFAOYSA-N thiophene oxide Chemical compound O=S1C=CC=C1 LWRYDHOHXNQTSK-UHFFFAOYSA-N 0.000 description 1
- HVYVMSPIJIWUNA-UHFFFAOYSA-N triphenylstibine Chemical compound C1=CC=CC=C1[Sb](C=1C=CC=CC=1)C1=CC=CC=C1 HVYVMSPIJIWUNA-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US77323477A | 1977-03-01 | 1977-03-01 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SE7800244L SE7800244L (sv) | 1978-09-02 |
| SE438866B true SE438866B (sv) | 1985-05-13 |
Family
ID=25097609
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE7800244A SE438866B (sv) | 1977-03-01 | 1978-01-10 | Passiveringsmedelskomposition bestaende av en kiselhaltig krackningskatalysatorsvans, forfarande for dess framstellning samt anvendning derav vid krackning |
Country Status (18)
| Country | Link |
|---|---|
| US (2) | US4148712A (da) |
| JP (1) | JPS53106705A (da) |
| AU (1) | AU497417B1 (da) |
| BE (1) | BE864263A (da) |
| BR (1) | BR7801045A (da) |
| CA (1) | CA1098505A (da) |
| DE (1) | DE2808103C3 (da) |
| DK (1) | DK147451C (da) |
| ES (1) | ES466995A1 (da) |
| FR (1) | FR2382493A1 (da) |
| GB (1) | GB1592530A (da) |
| IN (1) | IN149751B (da) |
| IT (1) | IT1093808B (da) |
| MX (1) | MX147447A (da) |
| NL (1) | NL171720C (da) |
| SE (1) | SE438866B (da) |
| TR (1) | TR19957A (da) |
| ZA (1) | ZA78737B (da) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4169042A (en) * | 1978-03-13 | 1979-09-25 | Phillips Petroleum Company | Cracking process and catalyst for same containing tellurium |
| US4263130A (en) * | 1978-07-25 | 1981-04-21 | Phillips Petroleum Company | Process for cracking hydrocarbons with a catalyst passivated with an antimony tris (hydrocarbyl sulfide) |
| US4263131A (en) * | 1978-07-25 | 1981-04-21 | Phillips Petroleum Company | Passivation of metals contaminating a cracking catalyst with an antimony tris(dihydrocarbyl phosphite) catalyst and process of cracking therewith |
| US4257876A (en) * | 1978-07-25 | 1981-03-24 | Phillips Petroleum Company | Passivation of metals contaminating a cracking catalyst with trihydrocarbylantimony oxide and process for converting hydrocarbons |
| US4208302A (en) * | 1978-10-06 | 1980-06-17 | Phillips Petroleum Company | Passivating metals on cracking catalysts |
| US4256564A (en) * | 1979-04-03 | 1981-03-17 | Phillips Petroleum Company | Cracking process and catalyst for same containing indium to passivate contaminating metals |
| US4257919A (en) * | 1979-11-01 | 1981-03-24 | Phillips Petroleum Company | Method of transferring a passivating agent to or from a cracking catalyst |
| US4372840A (en) * | 1979-12-31 | 1983-02-08 | Exxon Research And Engineering Co. | Process for reducing coke formation in heavy feed catalytic cracking |
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| US4348273A (en) * | 1980-06-25 | 1982-09-07 | Phillips Petroleum Company | Treating cracking catalyst fines containing a passivating material |
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| EP0051689A1 (en) * | 1980-11-10 | 1982-05-19 | Phillips Petroleum Company | Method for passivating contaminant metals on a cracking catalyst and cracking process |
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| US3135683A (en) * | 1961-08-28 | 1964-06-02 | Phillips Petroleum Co | Double unit catalytic cracking |
| US3190828A (en) * | 1962-10-08 | 1965-06-22 | Phillips Petroleum Co | Catalytic process for cracking oils containing metallic contaminants |
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| US3591485A (en) * | 1969-09-10 | 1971-07-06 | Phillips Petroleum Co | Combination catalytic cracking process |
| CA942219A (en) * | 1969-09-19 | 1974-02-19 | Esso Research And Engineering Company | Fluid catalytic cracking process employing conventional cracking catalyst and superactive molecular sieve cracking catalyst |
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| DE2457963A1 (de) * | 1974-12-07 | 1976-06-16 | Interliz Anstalt | Heissgasgenerator |
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| US4111845A (en) * | 1977-02-11 | 1978-09-05 | Mckay Dwight L | Cracking catalyst modified by antimony thiophosphate |
-
1977
- 1977-11-22 CA CA291,499A patent/CA1098505A/en not_active Expired
-
1978
- 1978-01-10 SE SE7800244A patent/SE438866B/sv not_active IP Right Cessation
- 1978-01-31 IT IT19863/78A patent/IT1093808B/it active
- 1978-01-31 FR FR7802707A patent/FR2382493A1/fr active Granted
- 1978-02-07 ZA ZA00780737A patent/ZA78737B/xx unknown
- 1978-02-10 IN IN157/CAL/78A patent/IN149751B/en unknown
- 1978-02-10 AU AU33192/78A patent/AU497417B1/en not_active Expired
- 1978-02-15 ES ES466995A patent/ES466995A1/es not_active Expired
- 1978-02-21 TR TR19957A patent/TR19957A/xx unknown
- 1978-02-22 BR BR7801045A patent/BR7801045A/pt unknown
- 1978-02-23 BE BE185431A patent/BE864263A/xx not_active IP Right Cessation
- 1978-02-23 MX MX172528A patent/MX147447A/es unknown
- 1978-02-24 JP JP2082378A patent/JPS53106705A/ja active Granted
- 1978-02-24 DE DE2808103A patent/DE2808103C3/de not_active Expired
- 1978-02-28 GB GB7916/78A patent/GB1592530A/en not_active Expired
- 1978-02-28 DK DK91278A patent/DK147451C/da not_active IP Right Cessation
- 1978-02-28 NL NLAANVRAGE7802220,A patent/NL171720C/xx not_active IP Right Cessation
- 1978-06-29 US US05/920,618 patent/US4148712A/en not_active Expired - Lifetime
- 1978-06-30 US US05/920,885 patent/US4148714A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| BE864263A (fr) | 1978-08-23 |
| MX147447A (es) | 1982-12-03 |
| NL171720C (nl) | 1987-06-16 |
| US4148714A (en) | 1979-04-10 |
| FR2382493B1 (da) | 1980-04-04 |
| AU497417B1 (en) | 1978-12-14 |
| ZA78737B (en) | 1979-01-31 |
| DK91278A (da) | 1978-09-02 |
| JPS53106705A (en) | 1978-09-18 |
| NL7802220A (nl) | 1978-09-05 |
| DE2808103A1 (de) | 1978-09-07 |
| DE2808103C3 (de) | 1981-11-12 |
| SE7800244L (sv) | 1978-09-02 |
| IT1093808B (it) | 1985-07-26 |
| BR7801045A (pt) | 1978-11-28 |
| FR2382493A1 (fr) | 1978-09-29 |
| IN149751B (da) | 1982-04-03 |
| JPS5715798B2 (da) | 1982-04-01 |
| DE2808103B2 (de) | 1980-08-21 |
| CA1098505A (en) | 1981-03-31 |
| US4148712A (en) | 1979-04-10 |
| IT7819863A0 (it) | 1978-01-31 |
| GB1592530A (en) | 1981-07-08 |
| ES466995A1 (es) | 1978-10-16 |
| DK147451C (da) | 1985-05-28 |
| TR19957A (tr) | 1980-05-15 |
| DK147451B (da) | 1984-08-13 |
| NL171720B (nl) | 1982-12-01 |
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