RU2000101819A - METHOD OF EPOXIDATION WITH THE APPLICATION OF A SILVER CATALYST ON A MEDIA TREATED BY ORGANIC CHLORESETTING CONNECTION - Google Patents
METHOD OF EPOXIDATION WITH THE APPLICATION OF A SILVER CATALYST ON A MEDIA TREATED BY ORGANIC CHLORESETTING CONNECTIONInfo
- Publication number
- RU2000101819A RU2000101819A RU2000101819/04A RU2000101819A RU2000101819A RU 2000101819 A RU2000101819 A RU 2000101819A RU 2000101819/04 A RU2000101819/04 A RU 2000101819/04A RU 2000101819 A RU2000101819 A RU 2000101819A RU 2000101819 A RU2000101819 A RU 2000101819A
- Authority
- RU
- Russia
- Prior art keywords
- chlorine
- catalyst
- potassium
- propylene
- carrier
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 23
- 239000003054 catalyst Substances 0.000 title claims 16
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 title claims 11
- 229910052709 silver Inorganic materials 0.000 title claims 11
- 239000004332 silver Substances 0.000 title claims 11
- 238000006735 epoxidation reaction Methods 0.000 title claims 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 18
- 239000000460 chlorine Substances 0.000 claims 18
- 229910052801 chlorine Inorganic materials 0.000 claims 18
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims 8
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 6
- 229910001882 dioxygen Inorganic materials 0.000 claims 6
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 6
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 6
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 claims 6
- 230000003750 conditioning effect Effects 0.000 claims 5
- 239000001569 carbon dioxide Substances 0.000 claims 4
- 229910002092 carbon dioxide Inorganic materials 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims 4
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 claims 4
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 claims 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims 3
- 239000007787 solid Substances 0.000 claims 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical group [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 2
- AZFNGPAYDKGCRB-XCPIVNJJSA-M [(1s,2s)-2-amino-1,2-diphenylethyl]-(4-methylphenyl)sulfonylazanide;chlororuthenium(1+);1-methyl-4-propan-2-ylbenzene Chemical compound [Ru+]Cl.CC(C)C1=CC=C(C)C=C1.C1=CC(C)=CC=C1S(=O)(=O)[N-][C@@H](C=1C=CC=CC=1)[C@@H](N)C1=CC=CC=C1 AZFNGPAYDKGCRB-XCPIVNJJSA-M 0.000 claims 2
- -1 alkaline earth metal carbonate Chemical class 0.000 claims 2
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 claims 2
- 229960003750 ethyl chloride Drugs 0.000 claims 2
- 239000007789 gas Substances 0.000 claims 2
- 229910052751 metal Inorganic materials 0.000 claims 2
- 239000002184 metal Substances 0.000 claims 2
- 229910052750 molybdenum Inorganic materials 0.000 claims 2
- 239000011733 molybdenum Substances 0.000 claims 2
- 235000015497 potassium bicarbonate Nutrition 0.000 claims 2
- 239000011736 potassium bicarbonate Substances 0.000 claims 2
- 229910000028 potassium bicarbonate Inorganic materials 0.000 claims 2
- 229910000027 potassium carbonate Inorganic materials 0.000 claims 2
- 235000011181 potassium carbonates Nutrition 0.000 claims 2
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims 2
- 239000004323 potassium nitrate Substances 0.000 claims 2
- 235000010333 potassium nitrate Nutrition 0.000 claims 2
- 239000004304 potassium nitrite Substances 0.000 claims 2
- 235000010289 potassium nitrite Nutrition 0.000 claims 2
- 229910052702 rhenium Inorganic materials 0.000 claims 2
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 claims 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims 2
- 229910052721 tungsten Inorganic materials 0.000 claims 2
- 239000010937 tungsten Substances 0.000 claims 2
- 239000012808 vapor phase Substances 0.000 claims 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- FZRKAZHKEDOPNN-UHFFFAOYSA-N Nitric oxide anion Chemical compound O=[N-] FZRKAZHKEDOPNN-UHFFFAOYSA-N 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 claims 1
- 150000001342 alkaline earth metals Chemical class 0.000 claims 1
- 229910000019 calcium carbonate Inorganic materials 0.000 claims 1
- 239000011591 potassium Substances 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000002243 precursor Substances 0.000 claims 1
- 230000001737 promoting effect Effects 0.000 claims 1
Claims (20)
(a) контактирование серебряного катализатора на носителе с кондиционирующим потоком, содержащим в паровой фазе органическое хлорсодержащее соединение С1-С10 и молекулярный кислород, при температуре 150 - 350oС в течение времени, достаточного для включения хлорсодержащего соединения в серебряный катализатор на носителе с получением хлорсодержащего катализатора, в котором серебряный катализатор на носителе содержит (i) инертный огнеупорный твердый носитель, (ii) каталитически эффективное количество серебра и (iii) промотирующее количество калиевого промотора, полученного из соли калия, содержащей катион калия и азотно-оксидный анион либо его предшественник; и
(b) контактирование хлорсодержащего катализатора со входящим потоком, содержащим пропилен и молекулярный кислород, но практически не содержащим органического хлорсодержащего соединения С1-С10, в течение времени и при температуре, достаточных для образования оксида пропилена.1. The method of carrying out the process of epoxidation of propylene, including
(a) contacting a silver catalyst on a carrier with a conditioning stream containing in the vapor phase an organic chlorine-containing compound C 1 -C 10 and molecular oxygen, at a temperature of 150–350 o C for a time sufficient to turn the chlorine-containing compound into a silver catalyst on a carrier with obtaining a chlorine-containing catalyst, in which the silver catalyst on the carrier contains (i) an inert refractory solid carrier, (ii) a catalytically effective amount of silver and (iii) a promoter amount of a linear promoter derived from a potassium salt containing a potassium cation and a nitric oxide anion or its precursor; and
(b) contacting the chlorine-containing catalyst with an incoming stream containing propylene and molecular oxygen, but practically free of organic chlorine-containing compound C 1 -C 10 , for a time and at a temperature sufficient to form propylene oxide.
(а) контактирование серебряного катализатора на носителе с кондиционирующим потоком, содержащим в паровой фазе от 25 частей на млн. до 2000 частей на млн. органического хлорсодержащего соединения С1-С4 и молекулярный кислород, при температуре 220 - 280oС в течение времени, достаточного для включения хлорсодержащего соединения в серебряный катализатор на носителе с получением хлорсодержащего катализатора с содержанием хлора по крайней мере 0,1 мас.%, в котором серебряный катализатор на носителе содержит (i) инертный огнеупорный твердый носитель, содержащий карбонат щелочноземельного металла, (ii) 10 - 60 мас.% серебра и (iii) промотирующее количество калиевого промотора, полученного из соли калия, выбранной из группы, состоящей из нитрата калия, нитрита калия, карбоната калия, бикарбоната калия и их смесей; и
(b) контактирование хлорсодержащего катализатора со входящим потоком, содержащим пропилен и молекулярный кислород, но практически не содержащим органического хлорсодержащего соединения С1-С4, при температуре 220 - 280oС в течение времени, достаточного для образования оксида пропилена.13. The method of carrying out the process of epoxidation of propylene, including
(a) contacting a silver catalyst on a carrier with a conditioning stream containing in the vapor phase from 25 parts per million to 2000 parts per million of organic chlorine-containing compound C 1 -C 4 and molecular oxygen, at a temperature of 220–280 o C over time sufficient to include a chlorine-containing compound in a supported silver catalyst to obtain a chlorine-containing catalyst with a chlorine content of at least 0.1 wt.%, in which the supported silver catalyst contains (i) an inert refractory solid carrier, containing alkaline earth metal carbonate, (ii) 10 to 60 wt.% silver and (iii) a promoter amount of a potassium promoter derived from a potassium salt selected from the group consisting of potassium nitrate, potassium nitrite, potassium carbonate, potassium bicarbonate, and mixtures thereof; and
(b) contacting the chlorine-containing catalyst with the incoming stream containing propylene and molecular oxygen, but practically not containing the organic chlorine-containing compound C 1 -C 4 , at a temperature of 220-280 o C for a time sufficient to form propylene oxide.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/880,896 | 1997-06-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2000101819A true RU2000101819A (en) | 2001-11-10 |
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