NO771875L - Fremgangsm}te ved forestring av umettede olefiner - Google Patents
Fremgangsm}te ved forestring av umettede olefinerInfo
- Publication number
- NO771875L NO771875L NO771875A NO771875A NO771875L NO 771875 L NO771875 L NO 771875L NO 771875 A NO771875 A NO 771875A NO 771875 A NO771875 A NO 771875A NO 771875 L NO771875 L NO 771875L
- Authority
- NO
- Norway
- Prior art keywords
- catalyst
- reactor
- mixture
- alcohol
- oxidation
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 26
- 150000001336 alkenes Chemical class 0.000 title claims description 13
- 239000003054 catalyst Substances 0.000 claims description 52
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 24
- 238000007254 oxidation reaction Methods 0.000 claims description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 17
- 230000003647 oxidation Effects 0.000 claims description 17
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 11
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 10
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 8
- 239000007789 gas Substances 0.000 claims description 8
- BAPJBEWLBFYGME-UHFFFAOYSA-N acrylic acid methyl ester Natural products COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 7
- 229910052742 iron Inorganic materials 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 7
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 5
- 239000005977 Ethylene Substances 0.000 claims description 5
- 229910052783 alkali metal Inorganic materials 0.000 claims description 5
- 150000001340 alkali metals Chemical class 0.000 claims description 5
- 229910052796 boron Inorganic materials 0.000 claims description 5
- 229910052748 manganese Inorganic materials 0.000 claims description 5
- 150000002734 metacrylic acid derivatives Chemical class 0.000 claims description 5
- 229910052698 phosphorus Inorganic materials 0.000 claims description 5
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 4
- 229910052770 Uranium Inorganic materials 0.000 claims description 4
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 4
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 4
- 229910052787 antimony Inorganic materials 0.000 claims description 4
- 229910052804 chromium Inorganic materials 0.000 claims description 4
- 229910001882 dioxygen Inorganic materials 0.000 claims description 4
- 229910052759 nickel Inorganic materials 0.000 claims description 4
- 229910052718 tin Inorganic materials 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
- 229910052772 Samarium Inorganic materials 0.000 claims description 2
- 229910052785 arsenic Inorganic materials 0.000 claims description 2
- 229910052793 cadmium Inorganic materials 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 229930195733 hydrocarbon Natural products 0.000 claims description 2
- 150000002430 hydrocarbons Chemical class 0.000 claims description 2
- 229910052758 niobium Inorganic materials 0.000 claims description 2
- 238000006709 oxidative esterification reaction Methods 0.000 claims description 2
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 2
- 150000002910 rare earth metals Chemical class 0.000 claims description 2
- 229910052716 thallium Inorganic materials 0.000 claims description 2
- 229910052721 tungsten Inorganic materials 0.000 claims description 2
- 229910052720 vanadium Inorganic materials 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- -1 ester methyl methacrylate Chemical class 0.000 claims 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 2
- 229910052749 magnesium Inorganic materials 0.000 claims 1
- 230000001590 oxidative effect Effects 0.000 claims 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 13
- 150000002148 esters Chemical class 0.000 description 13
- 150000001299 aldehydes Chemical class 0.000 description 10
- 235000019441 ethanol Nutrition 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 229910052797 bismuth Inorganic materials 0.000 description 3
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 3
- 230000032050 esterification Effects 0.000 description 3
- 238000005886 esterification reaction Methods 0.000 description 3
- 239000011572 manganese Substances 0.000 description 3
- 229910052750 molybdenum Inorganic materials 0.000 description 3
- 239000011733 molybdenum Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- STNJBCKSHOAVAJ-UHFFFAOYSA-N Methacrolein Chemical compound CC(=C)C=O STNJBCKSHOAVAJ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 239000004005 microsphere Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 230000007306 turnover Effects 0.000 description 2
- JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 description 2
- 239000012808 vapor phase Substances 0.000 description 2
- 229910052684 Cerium Inorganic materials 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- DKUYEPUUXLQPPX-UHFFFAOYSA-N dibismuth;molybdenum;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Mo].[Mo].[Bi+3].[Bi+3] DKUYEPUUXLQPPX-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005243 fluidization Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229940035429 isobutyl alcohol Drugs 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- NFIDBGJMFKNGGQ-UHFFFAOYSA-N isopropylmethylphenol Natural products CC(C)CC1=CC=CC=C1O NFIDBGJMFKNGGQ-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical class C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000006069 physical mixture Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/39—Preparation of carboxylic acid esters by oxidation of groups which are precursors for the acid moiety of the ester
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/691,052 US4060545A (en) | 1976-05-28 | 1976-05-28 | Preparation of unsaturated carboxylic esters from propylene or isobutylene |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO771875L true NO771875L (no) | 1977-11-29 |
Family
ID=24774973
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO771875A NO771875L (no) | 1976-05-28 | 1977-05-27 | Fremgangsm}te ved forestring av umettede olefiner |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US4060545A (xx) |
| JP (1) | JPS52144615A (xx) |
| AT (1) | AT358001B (xx) |
| BE (1) | BE855157A (xx) |
| BR (1) | BR7703184A (xx) |
| CA (1) | CA1114833A (xx) |
| CH (1) | CH631695A5 (xx) |
| CS (1) | CS199677B2 (xx) |
| DD (1) | DD132338A5 (xx) |
| DE (1) | DE2720861A1 (xx) |
| ES (1) | ES459224A1 (xx) |
| FR (1) | FR2352784A1 (xx) |
| GB (1) | GB1580743A (xx) |
| IT (1) | IT1074536B (xx) |
| MX (1) | MX144568A (xx) |
| NL (1) | NL7705770A (xx) |
| NO (1) | NO771875L (xx) |
| PT (1) | PT66580B (xx) |
| RO (1) | RO75590A (xx) |
| YU (1) | YU129877A (xx) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2070601B (en) * | 1980-03-05 | 1984-05-23 | Asahi Chemical Ind | Producing unsaturated carboxylic esters |
| CA1308737C (en) * | 1987-04-16 | 1992-10-13 | Syoichi Matsumoto | Process for producing methacrylic ester |
| EP0639553B1 (en) * | 1993-08-20 | 1998-01-14 | Nkk Corporation | Catalyst and method for producing phenols |
| EP1411043A1 (en) * | 2002-10-18 | 2004-04-21 | Rohm And Haas Company | Preparation of unsaturated carboxylic acids and unsaturated carboxylic acid esters from alkanes and/or alkenes |
| US7851397B2 (en) | 2005-07-25 | 2010-12-14 | Saudi Basic Industries Corporation | Catalyst for methacrolein oxidation and method for making and using same |
| US7649111B2 (en) | 2005-07-25 | 2010-01-19 | Saudi Basic Industries Corporation | Catalyst for the oxidation of a mixed aldehyde feedstock to methacrylic acid and methods for making and using same |
| US7649112B2 (en) | 2005-07-25 | 2010-01-19 | Saudi Basic Industries Corporation | Integrated plant for producing 2-ethyl-hexanol and methacrylic acid and a method based thereon |
| US7732367B2 (en) | 2005-07-25 | 2010-06-08 | Saudi Basic Industries Corporation | Catalyst for methacrolein oxidation and method for making and using same |
| EP1994978A1 (en) * | 2007-05-25 | 2008-11-26 | Evonik Röhm GmbH | Process for preparation of methyl methacrylate by esterification during oxidation |
| US8921257B2 (en) | 2011-12-02 | 2014-12-30 | Saudi Basic Industries Corporation | Dual function partial oxidation catalyst for propane to acrylic acid conversion |
| US8722940B2 (en) | 2012-03-01 | 2014-05-13 | Saudi Basic Industries Corporation | High molybdenum mixed metal oxide catalysts for the production of unsaturated aldehydes from olefins |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3293290A (en) * | 1963-03-04 | 1966-12-20 | Union Oil Co | Process for the production of unsaturated aldehydes and acids |
| BE776751A (fr) * | 1970-12-17 | 1972-06-15 | Nat Distillers Chem Corp | Procede de preparation des acrylates et des |
-
1976
- 1976-05-28 US US05/691,052 patent/US4060545A/en not_active Expired - Lifetime
-
1977
- 1977-05-09 GB GB19289/77A patent/GB1580743A/en not_active Expired
- 1977-05-10 DE DE19772720861 patent/DE2720861A1/de not_active Ceased
- 1977-05-10 CA CA278,088A patent/CA1114833A/en not_active Expired
- 1977-05-13 MX MX169125A patent/MX144568A/es unknown
- 1977-05-17 CH CH615377A patent/CH631695A5/de not_active IP Right Cessation
- 1977-05-17 BR BR3184/77A patent/BR7703184A/pt unknown
- 1977-05-20 JP JP5859377A patent/JPS52144615A/ja active Pending
- 1977-05-20 PT PT66580A patent/PT66580B/pt unknown
- 1977-05-20 AT AT364277A patent/AT358001B/de not_active IP Right Cessation
- 1977-05-20 IT IT23837/77A patent/IT1074536B/it active
- 1977-05-24 YU YU01298/77A patent/YU129877A/xx unknown
- 1977-05-25 NL NL7705770A patent/NL7705770A/xx not_active Application Discontinuation
- 1977-05-26 RO RO7790481A patent/RO75590A/ro unknown
- 1977-05-26 FR FR7716185A patent/FR2352784A1/fr active Granted
- 1977-05-26 DD DD7700199162A patent/DD132338A5/xx unknown
- 1977-05-27 BE BE178010A patent/BE855157A/xx unknown
- 1977-05-27 NO NO771875A patent/NO771875L/no unknown
- 1977-05-27 ES ES459224A patent/ES459224A1/es not_active Expired
- 1977-05-27 CS CS773511A patent/CS199677B2/cs unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FR2352784B1 (xx) | 1983-10-07 |
| CS199677B2 (en) | 1980-07-31 |
| US4060545A (en) | 1977-11-29 |
| GB1580743A (en) | 1980-12-03 |
| RO75590A (ro) | 1981-01-30 |
| CA1114833A (en) | 1981-12-22 |
| BR7703184A (pt) | 1978-01-31 |
| ATA364277A (de) | 1980-01-15 |
| BE855157A (fr) | 1977-09-16 |
| IT1074536B (it) | 1985-04-20 |
| PT66580B (en) | 1978-10-20 |
| CH631695A5 (de) | 1982-08-31 |
| MX144568A (es) | 1981-10-27 |
| ES459224A1 (es) | 1978-06-16 |
| YU129877A (en) | 1982-08-31 |
| NL7705770A (nl) | 1977-11-30 |
| DD132338A5 (de) | 1978-09-20 |
| AT358001B (de) | 1980-08-11 |
| JPS52144615A (en) | 1977-12-02 |
| PT66580A (en) | 1977-06-01 |
| FR2352784A1 (fr) | 1977-12-23 |
| DE2720861A1 (de) | 1977-12-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5925236B2 (ja) | グリセロールからのアクリル酸の製造方法 | |
| JP2574406B2 (ja) | メタクリル酸の製法 | |
| NO771875L (no) | Fremgangsm}te ved forestring av umettede olefiner | |
| CN100382889C (zh) | 复合氧化物催化剂以及使用该催化剂的丙烯酸制备方法 | |
| JPWO2003053570A1 (ja) | 酸化物触媒組成物 | |
| JP2001520976A5 (xx) | ||
| JPH07116070B2 (ja) | メチルタ−シャリ−ブチルエ−テルからメタクロレインおよびメタクリル酸の製法 | |
| CN104718182A (zh) | 具有用于预脱水塔的侧线式反应器的乙酸乙烯酯制造方法 | |
| US20040249000A1 (en) | Gas-phase catalytic oxidation process and process for producing (meth) acrolein or (meth) acrylic acid | |
| EP4003951B1 (en) | A process for the continuous production of either acrolein or acrylic acid as the target product from propene | |
| US20070106091A1 (en) | Integrated plant for producing 2-ethyl-hexanol and methacrylic acid and a method based thereon | |
| JP2509049B2 (ja) | メタクリル酸の製造方法 | |
| US20120190890A1 (en) | Method for producing bioresourced acrylic acid from glycerol | |
| US6274764B1 (en) | Process for one step gas phase production of acetic acid from ethylene | |
| EP1951650A1 (de) | Verfahren zur herstellung von acrolein, oder acrylsäure, oder deren gemisch aus propan | |
| NO147068B (no) | Fremgangsmaate for fremstilling av akrylsyre og metakrylsyre ved omsetning av propylen eller isobutylen med molekylaer oksygen | |
| US4564703A (en) | Process for preparing methacrylic acid | |
| EP1276559B1 (en) | Catalysts for the oxidation of unsaturated aldehydes to produce carboxylic acids, methods of making and using the same | |
| JPH1036311A (ja) | α，β−不飽和カルボン酸の製造方法 | |
| JPH05125010A (ja) | 不飽和アルデヒドまたは不飽和酸の製造用反応器 | |
| US4803302A (en) | Process for the production of methacrylic acid | |
| JP6762370B2 (ja) | 不飽和アルデヒド及び不飽和カルボン酸の製造方法 | |
| JP3523455B2 (ja) | 固定床反応器および不飽和カルボン酸の製造方法 | |
| KR810001558B1 (ko) | 프로필렌 또는 이소부틸렌으로부터 불포화카복실에스 테르의 제조방법 | |
| US4358622A (en) | Preparation of methacrolein and methacrylonitrile from tert-butyl alkanoates |