DE69200450T2 - Ethylenoxidkatalysator und Verfahren zu seiner Herstellung und seiner Anwendung. - Google Patents
Ethylenoxidkatalysator und Verfahren zu seiner Herstellung und seiner Anwendung.Info
- Publication number
- DE69200450T2 DE69200450T2 DE69200450T DE69200450T DE69200450T2 DE 69200450 T2 DE69200450 T2 DE 69200450T2 DE 69200450 T DE69200450 T DE 69200450T DE 69200450 T DE69200450 T DE 69200450T DE 69200450 T2 DE69200450 T2 DE 69200450T2
- Authority
- DE
- Germany
- Prior art keywords
- oxide
- catalyst
- amount
- support
- weight
- 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.)
- Expired - Lifetime
Links
- 239000003054 catalyst Substances 0.000 title claims description 105
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 title claims description 22
- 238000000034 method Methods 0.000 title claims description 19
- 238000004519 manufacturing process Methods 0.000 title claims description 13
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 36
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 31
- 239000000203 mixture Substances 0.000 claims description 24
- 150000001875 compounds Chemical class 0.000 claims description 22
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 21
- 229910052709 silver Inorganic materials 0.000 claims description 21
- 239000004332 silver Substances 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- 239000000463 material Substances 0.000 claims description 20
- 239000001301 oxygen Substances 0.000 claims description 19
- 229910052760 oxygen Inorganic materials 0.000 claims description 19
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 18
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 18
- 229910052783 alkali metal Inorganic materials 0.000 claims description 17
- 239000007789 gas Substances 0.000 claims description 17
- 150000001340 alkali metals Chemical class 0.000 claims description 16
- 229910052702 rhenium Inorganic materials 0.000 claims description 16
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 claims description 16
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 14
- 239000005977 Ethylene Substances 0.000 claims description 14
- 239000000377 silicon dioxide Substances 0.000 claims description 14
- 238000001354 calcination Methods 0.000 claims description 12
- 239000011148 porous material Substances 0.000 claims description 10
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 8
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 8
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 8
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 8
- 229910052804 chromium Inorganic materials 0.000 claims description 8
- 239000011651 chromium Substances 0.000 claims description 8
- 239000011733 molybdenum Substances 0.000 claims description 8
- 229910052750 molybdenum Inorganic materials 0.000 claims description 8
- 239000000843 powder Substances 0.000 claims description 8
- 239000011593 sulfur Substances 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 8
- 239000010937 tungsten Substances 0.000 claims description 8
- 229910052721 tungsten Inorganic materials 0.000 claims description 8
- 229910052726 zirconium Inorganic materials 0.000 claims description 8
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 7
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 claims description 7
- 238000002156 mixing Methods 0.000 claims description 7
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 6
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 6
- 229910052710 silicon Inorganic materials 0.000 claims description 6
- 239000010703 silicon Substances 0.000 claims description 6
- 229910001928 zirconium oxide Inorganic materials 0.000 claims description 4
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 3
- 239000000292 calcium oxide Substances 0.000 claims description 3
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 3
- 229910052814 silicon oxide Inorganic materials 0.000 claims 3
- 239000011324 bead Substances 0.000 claims 2
- 239000012808 vapor phase Substances 0.000 claims 2
- 239000000395 magnesium oxide Substances 0.000 claims 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 17
- 239000011230 binding agent Substances 0.000 description 11
- 229910052792 caesium Inorganic materials 0.000 description 11
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 9
- 239000000378 calcium silicate Substances 0.000 description 9
- 229910052918 calcium silicate Inorganic materials 0.000 description 9
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 9
- -1 alkali metal salt Chemical class 0.000 description 8
- 235000012239 silicon dioxide Nutrition 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000002826 coolant Substances 0.000 description 6
- IIPYXGDZVMZOAP-UHFFFAOYSA-N lithium nitrate Chemical compound [Li+].[O-][N+]([O-])=O IIPYXGDZVMZOAP-UHFFFAOYSA-N 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- 229920002678 cellulose Polymers 0.000 description 5
- 235000010980 cellulose Nutrition 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 4
- HUCVOHYBFXVBRW-UHFFFAOYSA-M caesium hydroxide Inorganic materials [OH-].[Cs+] HUCVOHYBFXVBRW-UHFFFAOYSA-M 0.000 description 4
- 229910052791 calcium Inorganic materials 0.000 description 4
- 239000011575 calcium Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- INHCSSUBVCNVSK-UHFFFAOYSA-L lithium sulfate Inorganic materials [Li+].[Li+].[O-]S([O-])(=O)=O INHCSSUBVCNVSK-UHFFFAOYSA-L 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910052915 alkaline earth metal silicate Inorganic materials 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 229910000323 aluminium silicate Inorganic materials 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 3
- 239000010953 base metal Substances 0.000 description 3
- 239000001569 carbon dioxide Substances 0.000 description 3
- 229910002092 carbon dioxide Inorganic materials 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 229910001882 dioxygen Inorganic materials 0.000 description 3
- 229960003750 ethyl chloride Drugs 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 238000011065 in-situ storage Methods 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 150000003377 silicon compounds Chemical class 0.000 description 3
- MFGOFGRYDNHJTA-UHFFFAOYSA-N 2-amino-1-(2-fluorophenyl)ethanol Chemical compound NCC(O)C1=CC=CC=C1F MFGOFGRYDNHJTA-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 235000003276 Apios tuberosa Nutrition 0.000 description 2
- 235000010777 Arachis hypogaea Nutrition 0.000 description 2
- 235000010744 Arachis villosulicarpa Nutrition 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 240000007049 Juglans regia Species 0.000 description 2
- 235000009496 Juglans regia Nutrition 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- 244000133018 Panax trifolius Species 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 150000001341 alkaline earth metal compounds Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 description 2
- 239000003575 carbonaceous material Substances 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- MVLVMROFTAUDAG-UHFFFAOYSA-N ethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC MVLVMROFTAUDAG-UHFFFAOYSA-N 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000002386 leaching Methods 0.000 description 2
- 150000002823 nitrates Chemical class 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 229910052682 stishovite Inorganic materials 0.000 description 2
- RBTVSNLYYIMMKS-UHFFFAOYSA-N tert-butyl 3-aminoazetidine-1-carboxylate;hydrochloride Chemical compound Cl.CC(C)(C)OC(=O)N1CC(N)C1 RBTVSNLYYIMMKS-UHFFFAOYSA-N 0.000 description 2
- 229910052905 tridymite Inorganic materials 0.000 description 2
- 235000020234 walnut Nutrition 0.000 description 2
- 150000003755 zirconium compounds Chemical class 0.000 description 2
- OERNJTNJEZOPIA-UHFFFAOYSA-N zirconium nitrate Chemical compound [Zr+4].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O OERNJTNJEZOPIA-UHFFFAOYSA-N 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- 244000226021 Anacardium occidentale Species 0.000 description 1
- 244000068645 Carya illinoensis Species 0.000 description 1
- 235000009025 Carya illinoensis Nutrition 0.000 description 1
- 235000004035 Cryptotaenia japonica Nutrition 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 240000002913 Trifolium pratense Species 0.000 description 1
- 235000015724 Trifolium pratense Nutrition 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 150000001339 alkali metal compounds Chemical class 0.000 description 1
- 150000004645 aluminates Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000001479 atomic absorption spectroscopy Methods 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 229910052916 barium silicate Inorganic materials 0.000 description 1
- HMOQPOVBDRFNIU-UHFFFAOYSA-N barium(2+);dioxido(oxo)silane Chemical compound [Ba+2].[O-][Si]([O-])=O HMOQPOVBDRFNIU-UHFFFAOYSA-N 0.000 description 1
- QKYBEKAEVQPNIN-UHFFFAOYSA-N barium(2+);oxido(oxo)alumane Chemical compound [Ba+2].[O-][Al]=O.[O-][Al]=O QKYBEKAEVQPNIN-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 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
- 230000015572 biosynthetic process Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 235000011116 calcium hydroxide Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229920003064 carboxyethyl cellulose Polymers 0.000 description 1
- 235000020226 cashew nut Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- RKTYLMNFRDHKIL-UHFFFAOYSA-N copper;5,10,15,20-tetraphenylporphyrin-22,24-diide Chemical group [Cu+2].C1=CC(C(=C2C=CC([N-]2)=C(C=2C=CC=CC=2)C=2C=CC(N=2)=C(C=2C=CC=CC=2)C2=CC=C3[N-]2)C=2C=CC=CC=2)=NC1=C3C1=CC=CC=C1 RKTYLMNFRDHKIL-UHFFFAOYSA-N 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- CAMHHLOGFDZBBG-UHFFFAOYSA-N epoxidized methyl oleate Natural products CCCCCCCCC1OC1CCCCCCCC(=O)OC CAMHHLOGFDZBBG-UHFFFAOYSA-N 0.000 description 1
- 235000010944 ethyl methyl cellulose Nutrition 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000012633 leachable Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- WHXSMMKQMYFTQS-BKFZFHPZSA-N lithium-12 Chemical compound [12Li] WHXSMMKQMYFTQS-BKFZFHPZSA-N 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 229920003087 methylethyl cellulose Polymers 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 235000014571 nuts Nutrition 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-M octadecanoate Chemical class CCCCCCCCCCCCCCCCCC([O-])=O QIQXTHQIDYTFRH-UHFFFAOYSA-M 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- HPEUJPJOZXNMSJ-UHFFFAOYSA-N octadecanoic acid methyl ester Natural products CCCCCCCCCCCCCCCCCC(=O)OC HPEUJPJOZXNMSJ-UHFFFAOYSA-N 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000002926 oxygen Chemical class 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 102220059878 rs774989816 Human genes 0.000 description 1
- 102220061225 rs786201115 Human genes 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- XNGYKPINNDWGGF-UHFFFAOYSA-L silver oxalate Chemical compound [Ag+].[Ag+].[O-]C(=O)C([O-])=O XNGYKPINNDWGGF-UHFFFAOYSA-L 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000002798 spectrophotometry method Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000012086 standard solution Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 239000010457 zeolite 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
- 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
- B01J23/66—Silver or gold
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D301/00—Preparation of oxiranes
- C07D301/02—Synthesis of the oxirane ring
- C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
- C07D301/04—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with air or molecular oxygen
- C07D301/08—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with air or molecular oxygen in the gaseous phase
- C07D301/10—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with air or molecular oxygen in the gaseous phase with catalysts containing silver or gold
-
- 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
- B01J23/66—Silver or gold
- B01J23/68—Silver or gold with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/688—Silver or gold with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium with manganese, technetium or rhenium
-
- 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
- B01J21/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
- B01J21/066—Zirconium or hafnium; Oxides or hydroxides thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Catalysts (AREA)
- Epoxy Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US64360691A | 1991-01-22 | 1991-01-22 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69200450D1 DE69200450D1 (de) | 1994-11-03 |
| DE69200450T2 true DE69200450T2 (de) | 1995-02-23 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69200450T Expired - Lifetime DE69200450T2 (de) | 1991-01-22 | 1992-01-17 | Ethylenoxidkatalysator und Verfahren zu seiner Herstellung und seiner Anwendung. |
Country Status (20)
Families Citing this family (99)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5447897A (en) * | 1993-05-17 | 1995-09-05 | Shell Oil Company | Ethylene oxide catalyst and process |
| RU2129465C1 (ru) * | 1993-07-07 | 1999-04-27 | Шелл Интернэшнл Рисерч Маатсхаппий Б.В. | Катализатор эпоксидирования и способ его получения |
| US5573989A (en) * | 1993-08-06 | 1996-11-12 | Sumitomo Chemical Company, Limited | Process for producing olefin oxides |
| US5418202A (en) * | 1993-12-30 | 1995-05-23 | Shell Oil Company | Ethylene oxide catalyst and process |
| US5545603A (en) * | 1994-11-01 | 1996-08-13 | Shell Oil Company | Ethylene oxide catalyst and process |
| US5705661A (en) * | 1995-09-25 | 1998-01-06 | Mitsubishi Chemical Corporation | Catalyst for production of ethylene oxide |
| US5763630A (en) * | 1996-03-18 | 1998-06-09 | Arco Chemical Technology, L.P. | Propylene oxide process using alkaline earth metal compound-supported silver catalysts |
| US5733842A (en) * | 1996-04-30 | 1998-03-31 | Norton Checmical Process Products Corporation | Method of making porous catalyst carrier without the addition of pore forming agents |
| EP0915861B1 (en) * | 1996-07-01 | 2001-12-05 | The Dow Chemical Company | Process for the direct oxidation of olefins to olefin oxides |
| US5864047A (en) * | 1997-04-10 | 1999-01-26 | Arco Chemical Technology, L.P. | Propylene oxide process using alkaline earth metal compound-supported silver catalysts containing rhenium and potassium promoters |
| US5861519A (en) * | 1997-05-23 | 1999-01-19 | Arco Chemical Technology, L.P. | Propylene oxide process using alkaline earth metal compound-supported silver catalysts containing tungsten and potassium promoters |
| JPH11191963A (ja) * | 1997-12-25 | 1999-07-13 | Fujitsu Ltd | 電源装置 |
| US6455713B1 (en) | 1998-09-14 | 2002-09-24 | Eastman Chemical Company | Reactivation of Cs-promoted, Ag catalysts for the selective epoxidation of butadiene to 3,4-epoxy-1-butene |
| DE69924453T2 (de) * | 1998-11-17 | 2006-02-16 | Nippon Shokubai Co., Ltd. | Katalysatorträger zur Verwendung in der Herstellung von Ethylenoxid |
| RU2141378C1 (ru) * | 1999-02-22 | 1999-11-20 | Сотников Валерий Васильевич | Носитель серебросодержащего катализатора получения оксида этилена и способ его получения |
| US6172245B1 (en) | 1999-12-16 | 2001-01-09 | Eastman Chemical Company | Gas phase process for the epoxidation of non-allylic olefins |
| AU2001257241B2 (en) * | 2000-05-01 | 2006-04-27 | Sd Lizenzverwertungsgesellschaft Mbh & Co. Kg | Ethylene oxide catalyst |
| RU2190466C2 (ru) * | 2000-12-04 | 2002-10-10 | Открытое акционерное общество Научно-исследовательский институт "Ярсинтез" | Носитель для катализаторов |
| ZA200200049B (en) * | 2001-01-25 | 2002-07-16 | Nippon Catalytic Chem Ind | Fixed-bed shell-and-tube reactor and its usage. |
| JP4050041B2 (ja) * | 2001-11-06 | 2008-02-20 | 株式会社日本触媒 | 酸化エチレン製造用触媒、その製造方法および当該触媒による酸化エチレンの製造方法 |
| US7193094B2 (en) | 2001-11-20 | 2007-03-20 | Shell Oil Company | Process and systems for the epoxidation of an olefin |
| JP4335692B2 (ja) * | 2002-02-25 | 2009-09-30 | シエル・インターナシヨナル・リサーチ・マートスハツペイ・ベー・ヴエー | 担持された銀触媒およびその触媒を用いるエポキシ化方法 |
| US6831037B2 (en) * | 2002-02-25 | 2004-12-14 | Saint-Gobain Norpro Corporation | Catalyst carriers |
| DE60332457D1 (de) | 2002-06-28 | 2010-06-17 | Shell Int Research | Verfahren zur verbesserung der selektivität eines katalysators und verfahren zum epoxidieren eines olefins |
| US20040110973A1 (en) * | 2002-10-28 | 2004-06-10 | Marek Matusz | Olefin oxide catalysts |
| ATE376879T1 (de) * | 2003-04-01 | 2007-11-15 | Shell Int Research | Olefinepoxidationsverfahren und katalysator zur verwendung bei dem verfahren |
| US6858560B2 (en) | 2003-04-23 | 2005-02-22 | Scientific Design Co., Inc. | Ethylene oxide catalyst |
| US20040225138A1 (en) * | 2003-05-07 | 2004-11-11 | Mcallister Paul Michael | Reactor system and process for the manufacture of ethylene oxide |
| MX260863B (es) | 2003-05-07 | 2008-09-26 | Shell Int Research | Catalizadores que contienen plata, su elaboracion y uso de los mismos. |
| US20040224841A1 (en) * | 2003-05-07 | 2004-11-11 | Marek Matusz | Silver-containing catalysts, the manufacture of such silver-containing catalysts, and the use thereof |
| US8148555B2 (en) | 2003-06-26 | 2012-04-03 | Shell Oil Company | Method for improving the selectivity of a catalyst and a process for the epoxidation of an olefin |
| SG177010A1 (en) * | 2003-08-22 | 2012-01-30 | Dow Technology Investments Llc | Improved alumina carriers and silver-based catalysts for the production of alkylene oxides |
| EP2277622B1 (en) * | 2003-10-16 | 2013-01-09 | Dow Technology Investments LLC | Method for the preparation of catalysts having enhanced stability, efficiency and/or activity for alkylene oxide production |
| US6939979B2 (en) * | 2003-11-10 | 2005-09-06 | Scientific Design Co., Inc. | Oxidation process and catalyst |
| TW200600190A (en) * | 2004-04-01 | 2006-01-01 | Shell Int Research | Process for preparing a silver catalyst, the catalyst, and use thereof in olefin oxidation |
| TW200613056A (en) * | 2004-04-01 | 2006-05-01 | Shell Int Research | A process for preparing a silver catalyst, the catalyst, and a use of the catalyst for olefin oxidation |
| TW200602123A (en) * | 2004-04-01 | 2006-01-16 | Shell Int Research | Process for preparing a catalyst, the catalyst, and a use of the catalyst |
| CN100572370C (zh) | 2004-06-18 | 2009-12-23 | 国际壳牌研究有限公司 | 生产烯烃氧化物、1,2-二醇、1,2-二醇醚或链烷醇胺的方法 |
| EP1765799A1 (en) | 2004-06-18 | 2007-03-28 | Shell Oil Company | A process for the production of an olefin oxide, a 1,2-diol, a 1,2-diol ether, or an alkanolamine |
| US7767619B2 (en) * | 2004-07-09 | 2010-08-03 | Sud-Chemie Inc. | Promoted calcium-aluminate supported catalysts for synthesis gas generation |
| EP1796834A2 (en) * | 2004-08-12 | 2007-06-20 | Shell Oil Company | A method of preparing a shaped catalyst, the catalyst, and use of the catalyst |
| US7560411B2 (en) | 2004-09-01 | 2009-07-14 | Shell Oil Company | Olefin epoxidation process, a catalyst for use in the process, a carrier for use in preparing the catalyst, and a process for preparing the carrier |
| US8536083B2 (en) | 2004-09-01 | 2013-09-17 | Shell Oil Company | Olefin epoxidation process, a catalyst for use in the process, a carrier for use in preparing the catalyst, and a process for preparing the carrier |
| BRPI0515905A (pt) * | 2004-09-24 | 2008-08-12 | Shell Int Research | processo para selecionar partìculas moldadas, um processo para instalar um sistema, um processo para reagir uma carga de alimentação gasosa em um tal sistema, um produto de programa de computação e um sistema de computação |
| US7759284B2 (en) * | 2005-05-09 | 2010-07-20 | Scientific Design Company, Inc. | Calcination in an inert gas in the presence of a small concentration of an oxidizing component |
| DE102005023955A1 (de) * | 2005-05-20 | 2006-11-23 | Basf Ag | Inertmaterial für den Einsatz in exothermen Reaktionen |
| US8084390B2 (en) | 2005-06-07 | 2011-12-27 | Shell Oil Company | Catalyst, a process for preparing the catalyst and a process for the production of an olefin oxide, a 1,2-diol, a 1,2 diol ether, or an alkanolamine |
| US7825062B2 (en) | 2005-06-07 | 2010-11-02 | Saint-Gobain Ceramics & Plastics, Inc. | Catalyst carrier and a process for preparing the catalyst carrier |
| RU2008109027A (ru) * | 2005-08-11 | 2009-09-20 | Шелл Интернэшнл Рисерч Маатсхаппий Б.В. (NL) | Способ изготовления формованного катализатора, катализатор и использование такого катализатора |
| CN100577289C (zh) * | 2006-01-28 | 2010-01-06 | 中国石油化工股份有限公司 | 环氧乙烷生产用银催化剂的载体、其制备方法及其应用 |
| JP2009525848A (ja) * | 2006-02-03 | 2009-07-16 | シエル・インターナシヨナル・リサーチ・マートスハツペイ・ベー・ヴエー | 触媒の処理方法、触媒、および触媒の使用 |
| CA2641646A1 (en) * | 2006-02-10 | 2007-08-23 | Shell Internationale Research Maatschappij B.V. | A process for preparing a catalyst, the catalyst, and a process for the production of an olefin oxide, a 1,2-diol, a 1,2-diol ether, or an alkanolamine |
| CN101426573B (zh) * | 2006-04-18 | 2015-08-05 | 陶氏环球技术公司 | 环氧烷催化剂及其应用 |
| US20070280877A1 (en) * | 2006-05-19 | 2007-12-06 | Sawyer Technical Materials Llc | Alpha alumina supports for ethylene oxide catalysts and method of preparing thereof |
| DE102007017080A1 (de) | 2007-04-10 | 2008-10-16 | Basf Se | Verfahren zur Beschickung eines Längsabschnitts eines Kontaktrohres |
| WO2008141027A2 (en) | 2007-05-09 | 2008-11-20 | Shell Oil Company | An epoxidation catalyst, a process for preparing the catalyst, and a process for the production of an olefin oxide, a 1,2-diol, a 1,2-diol ether, a 1,2-carbonate, or an alkanolamine |
| CA2687234C (en) | 2007-05-11 | 2016-04-19 | Sd Lizenzverwertungsgesellschaft Mbh & Co. Kg | Start-up of high selectivity catalysts in olefin oxide plants |
| JP2010527758A (ja) | 2007-05-18 | 2010-08-19 | シエル・インターナシヨナル・リサーチ・マートスハツペイ・ベー・ヴエー | 反応器系、吸収剤および供給材料を反応させるための方法 |
| AR066574A1 (es) * | 2007-05-18 | 2009-08-26 | Shell Int Research | Un sistema reactor, un proceso de produccion de oxido de olefina 1,2-diol 1,2-diol eter , 1,2-carbonato o alcanolamina |
| DE102007028333A1 (de) | 2007-06-15 | 2008-12-18 | Basf Se | Verfahren zum Einbringen einer wenigstens einer Produktionscharge von ringförmigen Schalenkatalysatoren K entnommenen Teilmenge in ein Reaktionsrohr eines Rohrbündelreaktors |
| DE102007028332A1 (de) | 2007-06-15 | 2008-12-18 | Basf Se | Verfahren zum Beschicken eines Reaktors mit einem Katalysatorfestbett, das wenigstens ringförmige Katalysatorformkörper K umfasst |
| JP5581058B2 (ja) * | 2008-01-11 | 2014-08-27 | 株式会社日本触媒 | エチレンオキシド製造用触媒およびエチレンオキシドの製造方法 |
| CN102015101B (zh) | 2008-04-30 | 2013-11-06 | 陶氏技术投资有限公司 | 多孔体前体,成形多孔体,它们的制备方法和基于它们的终端产品 |
| EP2282832A1 (en) * | 2008-04-30 | 2011-02-16 | Dow Technology Investments LLC | Porous body precursors, shaped porous bodies, processes for making them, and end-use products based upon the same |
| CN102015095B (zh) * | 2008-04-30 | 2013-05-08 | 陶氏技术投资有限公司 | 多孔体前体，成形多孔体，它们的制备方法和基于它们的终端产品 |
| BRPI0912381A2 (pt) | 2008-05-07 | 2017-07-04 | Shell Int Research | processo para a partida de um processo de epoxidação, processo para a produção de óxido de etileno, 1,2-diol, 1, 2-diol éter, 1, 2-carbonato, ou uma alcanolamina |
| CA2723592C (en) * | 2008-05-07 | 2016-08-16 | Shell Internationale Research Maatschappij B.V. | A process for the production of an olefin oxide, a 1,2-diol, a 1,2-diol ether, a 1,2-carbonate, or an alkanolamine |
| CA2724084A1 (en) * | 2008-05-15 | 2009-11-19 | Shell Internationale Research Maatschappij B.V. | Process for the preparation of an alkylene carbonate and an alkylene glycol |
| JP2011520895A (ja) | 2008-05-15 | 2011-07-21 | シエル・インターナシヨナル・リサーチ・マートスハツペイ・ベー・ヴエー | アルキレンカーボネートおよび／またはアルキレングリコールの調製のための方法 |
| JPWO2010001732A1 (ja) | 2008-06-30 | 2011-12-15 | 株式会社日本触媒 | 固定床多管式反応器への固体粒状物の充填方法 |
| EP2300447A1 (en) * | 2008-07-14 | 2011-03-30 | Basf Se | Process for making ethylene oxide |
| CN102099345A (zh) * | 2008-07-14 | 2011-06-15 | 万罗赛斯公司 | 使用微通道工艺技术制造环氧乙烷的方法 |
| US8349765B2 (en) * | 2008-07-18 | 2013-01-08 | Scientific Design Company, Inc. | Mullite-containing carrier for ethylene oxide catalysts |
| JP2010234264A (ja) * | 2009-03-31 | 2010-10-21 | Nippon Shokubai Co Ltd | エチレンオキシド製造用触媒およびエチレンオキシドの製造方法 |
| WO2010113963A1 (ja) * | 2009-03-31 | 2010-10-07 | 株式会社日本触媒 | エチレンオキシド製造用触媒およびエチレンオキシドの製造方法 |
| EP2421841B1 (en) * | 2009-04-21 | 2018-12-26 | Dow Technology Investments LLC | Improved method of achieving and maintaining a specified alkylene oxide production parameter with a high efficiency catalyst |
| EP2421840B1 (en) * | 2009-04-21 | 2015-12-16 | Dow Technology Investments LLC | Simplified method for producing alkylene oxides with a high efficiency catalyst |
| EP2421842B1 (en) * | 2009-04-21 | 2018-05-30 | Dow Technology Investments LLC | Epoxidation reactions and operating conditions thereof |
| US8524927B2 (en) * | 2009-07-13 | 2013-09-03 | Velocys, Inc. | Process for making ethylene oxide using microchannel process technology |
| JP2011121048A (ja) | 2009-12-09 | 2011-06-23 | Rohm & Haas Co | 固体触媒物質をブレンドし、管状構造物に装填する方法 |
| KR101786935B1 (ko) * | 2009-12-28 | 2017-10-18 | 다우 테크놀로지 인베스트먼츠 엘엘씨. | 알킬렌 옥사이드의 제조시 은 촉매 상의 은 클로라이드의 생성을 제어하는 방법 |
| KR101822673B1 (ko) | 2010-03-01 | 2018-01-26 | 쉘 인터내셔날 리써취 마트샤피지 비.브이. | 에폭시화 촉매, 그 촉매의 제조 방법, 및 올레핀 옥시드의 제조 방법 |
| JP2013527803A (ja) * | 2010-05-10 | 2013-07-04 | アドバンスト・キャタリスト・テクノロジーズ・リミテッド・ライアビリティ・カンパニー | ナノ構造化触媒ペレット、触媒表面処理およびエチレンエポキシ化のための高選択性触媒 |
| US9018126B2 (en) | 2010-07-13 | 2015-04-28 | Shell Oil Company | Epoxidation catalyst, a process for preparing the catalyst, and a process for the production of an olefin oxide |
| US9649621B2 (en) | 2011-12-19 | 2017-05-16 | Dow Technology Investments Llc | Method of formulating alkylene oxide catalyst in relation to catalyst reference properties |
| CN103357437B (zh) * | 2012-03-28 | 2016-03-30 | 中国石油化工股份有限公司 | 制备用于银催化剂的氧化铝载体的方法及其银催化剂 |
| JP6090567B2 (ja) | 2012-12-18 | 2017-03-08 | 京進工業株式会社 | 拡管装置 |
| FR3001969B1 (fr) | 2013-02-12 | 2015-08-21 | IFP Energies Nouvelles | Procede de production d'oxyde d'ethylene a partir d'un flux d'ethanol thermiquement integre |
| FR3001968B1 (fr) | 2013-02-12 | 2015-02-27 | IFP Energies Nouvelles | Procede de production d'oxyde d'ethylene a partir d'un flux d'ethanol thermo-mecaniquement integre |
| TWI632138B (zh) * | 2013-05-16 | 2018-08-11 | 科學設計股份有限公司 | 具有降低鈉含量之建基於銀之環氧乙烷觸媒 |
| CN104549543B (zh) * | 2013-10-29 | 2017-08-25 | 中国石油化工股份有限公司 | 氧化铝载体、由其制成的银催化剂及其应用 |
| EP3496851A1 (en) | 2016-08-08 | 2019-06-19 | Basf Se | Catalyst for the oxidation of ethylene to ethylene oxide |
| KR102449657B1 (ko) | 2016-12-02 | 2022-09-29 | 쉘 인터내셔날 리써취 마트샤피지 비.브이. | 에틸렌 에폭시화 촉매를 컨디셔닝하는 방법 및 에틸렌 옥사이드의 생산을 위한 관련된 방법 |
| CN108283943B (zh) * | 2017-01-10 | 2021-07-02 | 中国石油化工股份有限公司 | 氧化铝载体及其制备方法、乙烯环氧化反应用银催化剂及乙烯环氧化制备环氧乙烷的方法 |
| TWI808125B (zh) * | 2018-02-07 | 2023-07-11 | 德商巴斯夫歐洲公司 | 有效地將乙烯氧化轉化為環氧乙烷之催化劑 |
| CN111072803B (zh) * | 2018-10-19 | 2022-07-12 | 中国石油化工股份有限公司 | 烯烃聚合催化剂载体及其制备方法和应用 |
| TW202239752A (zh) | 2020-12-29 | 2022-10-16 | 荷蘭商蜆殼國際研究所 | 用於生產環氧乙烷之製程 |
| TW202237260A (zh) * | 2021-01-19 | 2022-10-01 | 美商科學設計有限公司 | 用於製造管間距減小的立式沸騰反應器的管與管板焊接 |
| CN115382525B (zh) * | 2021-05-24 | 2024-05-10 | 中国石油化工股份有限公司 | 一种α-氧化铝载体及其制备方法和银催化剂和应用 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3725307A (en) * | 1967-01-30 | 1973-04-03 | Halcon International Inc | Process for preparing a silver-supported catalyst |
| US4428863A (en) * | 1982-07-06 | 1984-01-31 | The Dow Chemical Company | Alumina compositions of improved strength useful as catalyst supports |
| NL8501862A (nl) * | 1985-06-28 | 1987-01-16 | Shell Int Research | Werkwijze ter bereiding van een zilver-houdende katalysator. |
| JPH084745B2 (ja) * | 1986-05-09 | 1996-01-24 | 三菱化学株式会社 | エチレンオキシド製造用銀触媒 |
| US4820675A (en) * | 1986-10-31 | 1989-04-11 | Shell Oil Company | Ethylene oxide catalyst & process for preparing the catalyst |
| US4766105A (en) * | 1986-10-31 | 1988-08-23 | Shell Oil Company | Ethylene oxide catalyst and process for preparing the catalyst |
| IL84232A (en) * | 1986-10-31 | 1992-06-21 | Shell Int Research | Catalyst and process for the catalytic production of ethylene oxide |
| US4761394A (en) * | 1986-10-31 | 1988-08-02 | Shell Oil Company | Ethylene oxide catalyst and process for preparing the catalyst |
| GB8626687D0 (en) * | 1986-11-07 | 1986-12-10 | Shell Int Research | Preparing silver catalyst |
| GB8716653D0 (en) * | 1987-07-15 | 1987-08-19 | Shell Int Research | Silver-containing catalyst |
| US4874879A (en) * | 1988-07-25 | 1989-10-17 | Shell Oil Company | Process for starting-up an ethylene oxide reactor |
| DE68925767T2 (de) * | 1988-08-30 | 1996-08-14 | Union Carbide Corp | Katalysatoren für die Herstellung von Ethylenoxid und Verfahren zur deren Herstellung |
-
1991
- 1991-12-09 US US07/804,494 patent/US5145824A/en not_active Expired - Lifetime
- 1991-12-23 IN IN1271DE1991 patent/IN184775B/en unknown
-
1992
- 1992-01-17 DE DE69200450T patent/DE69200450T2/de not_active Expired - Lifetime
- 1992-01-17 BR BR929200166A patent/BR9200166A/pt not_active IP Right Cessation
- 1992-01-17 DK DK92200142.5T patent/DK0496470T3/da active
- 1992-01-17 ES ES92200142T patent/ES2061309T3/es not_active Expired - Lifetime
- 1992-01-17 EP EP92200142A patent/EP0496470B1/en not_active Expired - Lifetime
- 1992-01-18 KR KR1019920000684A patent/KR100225874B1/ko not_active Expired - Lifetime
- 1992-01-20 RU SU925010577A patent/RU2014114C1/ru active
- 1992-01-20 PL PL92293237A patent/PL174992B1/pl unknown
- 1992-01-20 ZA ZA92376A patent/ZA92376B/xx unknown
- 1992-01-20 TR TR92/0043A patent/TR25623A/xx unknown
- 1992-01-20 CA CA002059711A patent/CA2059711C/en not_active Expired - Lifetime
- 1992-01-20 CZ CS92166A patent/CZ281977B6/cs not_active IP Right Cessation
- 1992-01-20 MX MX9200243A patent/MX9200243A/es not_active IP Right Cessation
- 1992-01-20 CN CN92100325A patent/CN1035161C/zh not_active Expired - Lifetime
- 1992-01-20 AU AU10341/92A patent/AU641584B2/en not_active Ceased
- 1992-01-20 SK SK166-92A patent/SK279174B6/sk unknown
- 1992-01-20 JP JP02755792A patent/JP3302387B2/ja not_active Expired - Lifetime
- 1992-02-05 SA SA92120369A patent/SA92120369B1/ar unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0496470A1 (en) | 1992-07-29 |
| AU1034192A (en) | 1992-07-30 |
| DK0496470T3 (da) | 1994-10-24 |
| BR9200166A (pt) | 1992-10-06 |
| CN1035161C (zh) | 1997-06-18 |
| TR25623A (tr) | 1993-07-01 |
| JP3302387B2 (ja) | 2002-07-15 |
| JPH0584440A (ja) | 1993-04-06 |
| RU2014114C1 (ru) | 1994-06-15 |
| PL293237A1 (en) | 1992-11-02 |
| SA92120369B1 (ar) | 2004-07-12 |
| IN184775B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 2000-09-30 |
| CS16692A3 (en) | 1992-08-12 |
| US5145824A (en) | 1992-09-08 |
| PL174992B1 (pl) | 1998-10-30 |
| SK279174B6 (sk) | 1998-07-08 |
| CA2059711C (en) | 2002-07-30 |
| CZ281977B6 (cs) | 1997-04-16 |
| KR920014515A (ko) | 1992-08-25 |
| CA2059711A1 (en) | 1992-07-23 |
| ES2061309T3 (es) | 1994-12-01 |
| DE69200450D1 (de) | 1994-11-03 |
| CN1063427A (zh) | 1992-08-12 |
| MX9200243A (es) | 1992-07-01 |
| EP0496470B1 (en) | 1994-09-28 |
| ZA92376B (en) | 1992-09-30 |
| AU641584B2 (en) | 1993-09-23 |
| KR100225874B1 (ko) | 1999-10-15 |
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| 8364 | No opposition during term of opposition | ||
| 8328 | Change in the person/name/address of the agent |
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