NO794176L - Selektiv katalytisk oksydasjon av karbonmonoksyd i naervaer av olefinmonomer. - Google Patents
Selektiv katalytisk oksydasjon av karbonmonoksyd i naervaer av olefinmonomer.Info
- Publication number
- NO794176L NO794176L NO794176A NO794176A NO794176L NO 794176 L NO794176 L NO 794176L NO 794176 A NO794176 A NO 794176A NO 794176 A NO794176 A NO 794176A NO 794176 L NO794176 L NO 794176L
- Authority
- NO
- Norway
- Prior art keywords
- carbon monoxide
- ethylene
- approx
- oxidation
- stream
- Prior art date
Links
- 230000003647 oxidation Effects 0.000 title claims description 28
- 238000007254 oxidation reaction Methods 0.000 title claims description 28
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 title claims description 21
- 229910002091 carbon monoxide Inorganic materials 0.000 title claims description 21
- 239000000178 monomer Substances 0.000 title claims description 12
- 230000003197 catalytic effect Effects 0.000 title claims description 6
- 239000003054 catalyst Substances 0.000 claims description 26
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 22
- 239000005977 Ethylene Substances 0.000 claims description 22
- 239000002699 waste material Substances 0.000 claims description 20
- 238000000034 method Methods 0.000 claims description 19
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims description 9
- 150000001336 alkenes Chemical class 0.000 claims description 9
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 8
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims description 8
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims description 8
- 230000015572 biosynthetic process Effects 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- JGDFBJMWFLXCLJ-UHFFFAOYSA-N copper chromite Chemical compound [Cu]=O.[Cu]=O.O=[Cr]O[Cr]=O JGDFBJMWFLXCLJ-UHFFFAOYSA-N 0.000 claims description 6
- 238000003786 synthesis reaction Methods 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 3
- 239000000460 chlorine Substances 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 1
- 229910052802 copper Inorganic materials 0.000 claims 1
- 239000010949 copper Substances 0.000 claims 1
- 239000010795 gaseous waste Substances 0.000 claims 1
- 239000000463 material Substances 0.000 description 19
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 8
- 238000004064 recycling Methods 0.000 description 8
- 239000007789 gas Substances 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 4
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 4
- 229910002092 carbon dioxide Inorganic materials 0.000 description 4
- 239000001569 carbon dioxide Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000002808 molecular sieve Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910017813 Cu—Cr Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 238000007084 catalytic combustion reaction Methods 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 229940117927 ethylene oxide Drugs 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- -1 oxy- Chemical class 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- KFUSEUYYWQURPO-OWOJBTEDSA-N trans-1,2-dichloroethene Chemical compound Cl\C=C\Cl KFUSEUYYWQURPO-OWOJBTEDSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/15—Preparation of halogenated hydrocarbons by replacement by halogens with oxygen as auxiliary reagent, e.g. oxychlorination
- C07C17/152—Preparation of halogenated hydrocarbons by replacement by halogens with oxygen as auxiliary reagent, e.g. oxychlorination of hydrocarbons
- C07C17/156—Preparation of halogenated hydrocarbons by replacement by halogens with oxygen as auxiliary reagent, e.g. oxychlorination of hydrocarbons of unsaturated hydrocarbons
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Carbon And Carbon Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/972,770 US4185039A (en) | 1978-12-26 | 1978-12-26 | Selective catalytic oxidation of carbon monoxide in the presence of olefin monomer |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO794176L true NO794176L (no) | 1980-06-27 |
Family
ID=25520106
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO794176A NO794176L (no) | 1978-12-26 | 1979-12-19 | Selektiv katalytisk oksydasjon av karbonmonoksyd i naervaer av olefinmonomer. |
| NO834207A NO834207L (no) | 1978-12-26 | 1983-11-16 | Fremgangsmaate for syntese av etylendiklorid ved katalytisk oksyhydroklorering av etylen |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO834207A NO834207L (no) | 1978-12-26 | 1983-11-16 | Fremgangsmaate for syntese av etylendiklorid ved katalytisk oksyhydroklorering av etylen |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4185039A (de) |
| EP (1) | EP0013020B1 (de) |
| JP (1) | JPS5590411A (de) |
| AR (1) | AR221120A1 (de) |
| AU (2) | AU5306179A (de) |
| BR (1) | BR7908479A (de) |
| CA (1) | CA1115495A (de) |
| DE (1) | DE2964876D1 (de) |
| GR (1) | GR69728B (de) |
| IN (1) | IN152201B (de) |
| NO (2) | NO794176L (de) |
| PT (1) | PT70627A (de) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4400364A (en) * | 1981-07-17 | 1983-08-23 | The Halcon Sd Group, Inc. | Process for oxidizing carbon monoxide in the presence of methacrolein |
| US5157204A (en) * | 1991-06-14 | 1992-10-20 | Phillips Petroleum Company | Removal of impurities from hydrocarbon feeds |
| IT1251666B (it) * | 1991-10-08 | 1995-05-19 | Himont Inc | Processo per la depurazione di alfa-olefine e idrocarburi saturi dall`ossido di carbonio. |
| US5907076A (en) * | 1996-12-31 | 1999-05-25 | Exxon Chemical Patents Inc. | Process for selectively separating hydrogen, or both hydrogen and carbon monoxide from olefinic hydrocarbons |
| US6069288A (en) * | 1996-12-31 | 2000-05-30 | Exxon Chemical Patents Inc. | Process for selectively separating hydrogen, or both hydrogen and carbon monoxide from olefinic hydrocarbons |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1618701C3 (de) * | 1966-05-20 | 1974-10-17 | Mitsui Toatsu Chemicals, Inc., Tokio | Verfahren zur Herstellung von 1,2-Dichloräthan |
| NL156117B (nl) * | 1968-06-17 | 1978-03-15 | Stamicarbon | Werkwijze voor het zuiveren van etheen en/of propeen. |
| US4113786A (en) * | 1976-04-02 | 1978-09-12 | The Lummus Company | Hydrogen chloride recovery |
| ES468300A1 (es) * | 1977-04-28 | 1978-11-16 | Hoechst Ag | Procedimiento para la preparacion de 1,2-dicloroetano. |
-
1978
- 1978-12-26 US US05/972,770 patent/US4185039A/en not_active Expired - Lifetime
-
1979
- 1979-11-20 GR GR60555A patent/GR69728B/el unknown
- 1979-11-20 AR AR278956A patent/AR221120A1/es active
- 1979-11-21 AU AU53061/79A patent/AU5306179A/en not_active Abandoned
- 1979-11-24 IN IN1234/CAL/79A patent/IN152201B/en unknown
- 1979-11-28 CA CA340,802A patent/CA1115495A/en not_active Expired
- 1979-12-19 NO NO794176A patent/NO794176L/no unknown
- 1979-12-21 PT PT70627A patent/PT70627A/pt unknown
- 1979-12-21 BR BR7908479A patent/BR7908479A/pt unknown
- 1979-12-21 EP EP79105331A patent/EP0013020B1/de not_active Expired
- 1979-12-21 DE DE7979105331T patent/DE2964876D1/de not_active Expired
- 1979-12-24 AU AU54186/79A patent/AU530154B2/en not_active Ceased
- 1979-12-26 JP JP16847779A patent/JPS5590411A/ja active Pending
-
1983
- 1983-11-16 NO NO834207A patent/NO834207L/no unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0013020A1 (de) | 1980-07-09 |
| AU5306179A (en) | 1980-07-03 |
| CA1115495A (en) | 1982-01-05 |
| IN152201B (de) | 1983-11-12 |
| EP0013020B1 (de) | 1983-02-16 |
| US4185039A (en) | 1980-01-22 |
| GR69728B (de) | 1982-07-09 |
| AU5418679A (en) | 1980-07-03 |
| AR221120A1 (es) | 1980-12-30 |
| PT70627A (en) | 1980-01-01 |
| JPS5590411A (en) | 1980-07-09 |
| DE2964876D1 (en) | 1983-03-24 |
| NO834207L (no) | 1980-07-27 |
| AU530154B2 (en) | 1983-07-07 |
| BR7908479A (pt) | 1980-10-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN107400045B (zh) | 由低丁烯原料混合物制备正戊醛 | |
| Mimura et al. | Dehydrogenation of ethylbenzene to styrene over Fe2O3/Al2O3 catalysts in the presence of carbon dioxide | |
| KR930005947A (ko) | 저급 파라핀으로부터 올레핀을 제조하는 방법 | |
| KR19980033193A (ko) | 4개의 탄소 원자를 포함하는 탄화수소 분급물로부터 이소부텐및 프로필렌을 제조하는 신규한 방법 | |
| KR20030072541A (ko) | 이산화탄소 산화제를 사용한 알킬방향족 탄화수소의탈수소화 방법 | |
| ZA888821B (en) | Olefins production process | |
| JP2020513304A (ja) | 混合金属酸化物触媒及び酸化脱水素反応プロセスにおいてオレフィンを製造する方法 | |
| Su et al. | Simultaneous recovery of carbon and sulfur resources from reduction of CO2 with H2S using catalysts | |
| US3692859A (en) | Hydrogenation of oxidative dehydrogenation by-product | |
| NO794176L (no) | Selektiv katalytisk oksydasjon av karbonmonoksyd i naervaer av olefinmonomer. | |
| KR102413286B1 (ko) | 탈수소화 방법 | |
| EP0671394A1 (de) | Integrierte Herstellung von Propylenoxid und Methyl-Tert-Butylether | |
| ATE52102T1 (de) | Verfahren zur umwandlung von kohlenwasserstoffen mit kristallinen borsilikatkatalysatoren fuer die erholung von pseudokumeen. | |
| US6107526A (en) | Process for producing ethyl tertiary butyl ether | |
| US20200157023A1 (en) | Oxygenate separation following oxidative dehydrogenation of a lower alkane | |
| NO300320B1 (no) | Fremgangsmåte for overföring av metan til höyere hydrokarboner | |
| Park et al. | Potassium promoter for palladium on alumina selective hydrogenation catalysts | |
| CA1091694A (en) | Process for producing 1,4-glycol diester | |
| NO20025348D0 (no) | FremgangsmÕte for omdannelse av oksygenater til olefiner | |
| KR870001083B1 (ko) | 촉매탈수소화에 의한 이소부틸렌의 제조방법 | |
| Rihko-Struckmann et al. | Process configurations for the production of the 2-methoxy-2, 4, 4-trimethylpentane—a novel gasoline oxygenate | |
| Choudhary et al. | Energy efficient simultaneous oxidative conversion and thermal cracking of ethane to ethylene using supported BaO/La2O3 catalyst in the presence of limited O2 | |
| US20150133708A1 (en) | An apparatus for producing ethylene and a producing method thereof | |
| Yang et al. | The Catalytic Dehydrogenation of c 2 h 6 to c 2 h 4 under non-Oxidative Conditions over the 6cr/g-al 2 o 3 Catalyst | |
| EP3863997A1 (de) | Oxygenattrennung nach dehydrierung eines niederen alkans |