GB767290A - Production of aliphatic carboxylic acids - Google Patents
Production of aliphatic carboxylic acidsInfo
- Publication number
- GB767290A GB767290A GB11469/53A GB1146953A GB767290A GB 767290 A GB767290 A GB 767290A GB 11469/53 A GB11469/53 A GB 11469/53A GB 1146953 A GB1146953 A GB 1146953A GB 767290 A GB767290 A GB 767290A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxidation
- residues
- acid
- line
- products
- 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
Links
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 title abstract 2
- 238000009835 boiling Methods 0.000 abstract 15
- 239000000047 product Substances 0.000 abstract 13
- 230000003647 oxidation Effects 0.000 abstract 12
- 238000007254 oxidation reaction Methods 0.000 abstract 12
- 229930195733 hydrocarbon Natural products 0.000 abstract 9
- 150000002430 hydrocarbons Chemical class 0.000 abstract 9
- 239000004215 Carbon black (E152) Substances 0.000 abstract 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 6
- 125000001931 aliphatic group Chemical group 0.000 abstract 6
- 125000004432 carbon atom Chemical group C* 0.000 abstract 6
- 238000004821 distillation Methods 0.000 abstract 6
- 239000000463 material Substances 0.000 abstract 5
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract 4
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 abstract 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 3
- 229910001882 dioxygen Inorganic materials 0.000 abstract 3
- 239000007788 liquid Substances 0.000 abstract 3
- 239000007791 liquid phase Substances 0.000 abstract 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 abstract 2
- 235000011054 acetic acid Nutrition 0.000 abstract 2
- 230000002378 acidificating effect Effects 0.000 abstract 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 abstract 2
- 239000011260 aqueous acid Substances 0.000 abstract 2
- 235000019253 formic acid Nutrition 0.000 abstract 2
- 239000007789 gas Substances 0.000 abstract 2
- 239000012263 liquid product Substances 0.000 abstract 2
- 230000001590 oxidative effect Effects 0.000 abstract 2
- 239000012188 paraffin wax Substances 0.000 abstract 2
- 239000003208 petroleum Substances 0.000 abstract 2
- 235000019260 propionic acid Nutrition 0.000 abstract 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 abstract 2
- 238000000926 separation method Methods 0.000 abstract 2
- 239000001384 succinic acid Substances 0.000 abstract 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001336 alkenes Chemical class 0.000 abstract 1
- 230000029936 alkylation Effects 0.000 abstract 1
- 238000005804 alkylation reaction Methods 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000000706 filtrate Substances 0.000 abstract 1
- 229910001385 heavy metal Inorganic materials 0.000 abstract 1
- 238000005984 hydrogenation reaction Methods 0.000 abstract 1
- 238000006317 isomerization reaction Methods 0.000 abstract 1
- 150000002736 metal compounds Chemical class 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/215—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of saturated hydrocarbyl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB11469/53A GB767290A (en) | 1953-04-25 | 1953-04-25 | Production of aliphatic carboxylic acids |
| NL186540A NL95035C (OSRAM) | 1953-04-25 | 1954-04-06 | |
| US422932A US2800506A (en) | 1953-04-25 | 1954-04-13 | Production of aliphatic acids |
| DED17593A DE1019289B (de) | 1953-04-25 | 1954-04-17 | Verfahren zur Herstellung von essigsaeurereichen Gemischen niedermolekularer Fettsaeuren durch Paraffinoxydation |
| FR1099323D FR1099323A (fr) | 1953-04-25 | 1954-04-22 | Acides aliphatiques |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB11469/53A GB767290A (en) | 1953-04-25 | 1953-04-25 | Production of aliphatic carboxylic acids |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB767290A true GB767290A (en) | 1957-01-30 |
Family
ID=9986831
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB11469/53A Expired GB767290A (en) | 1953-04-25 | 1953-04-25 | Production of aliphatic carboxylic acids |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US2800506A (OSRAM) |
| DE (1) | DE1019289B (OSRAM) |
| FR (1) | FR1099323A (OSRAM) |
| GB (1) | GB767290A (OSRAM) |
| NL (1) | NL95035C (OSRAM) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL277161A (OSRAM) * | 1961-04-19 | |||
| US3347756A (en) * | 1962-11-08 | 1967-10-17 | Distillers Co Yeast Ltd | Production of pure acetic acid from methyl vinyl ketone by distillation |
| DE1301809B (de) * | 1966-06-01 | 1969-08-28 | Bayer Ag | Verfahren zur Herstellung von Essigsaeure |
| US3388157A (en) * | 1965-02-10 | 1968-06-11 | Ethyl Corp | Process for the production of dicarboxylic acids |
| DE1294361B (de) * | 1966-05-10 | 1969-05-08 | Bayer Ag | Verfahren zur Herstellung von Essigsaeure und Butylacetat |
| US3923882A (en) * | 1974-04-17 | 1975-12-02 | Union Carbide Corp | Production of acetic acid |
| US4337356A (en) * | 1980-03-20 | 1982-06-29 | Union Carbide Corporation | Catalytic liquid-phase oxidation of butane |
| US5300684A (en) | 1991-12-09 | 1994-04-05 | The Standard Oil Company | Process for the fluidized bed oxidation of ethane to acetic acid |
| SG46156A1 (en) * | 1994-06-02 | 1998-02-20 | Standard Oil Co Ohio | Fluid bed process for the acetoxylation of ethylene in the production of vinyl acetate |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE570732C (de) * | 1927-12-02 | 1933-02-22 | I G Farbenindustrie Akt Ges | Verfahren zur Herstellung wertvoller organischer Produkte durch Behandlung von fluessigen Kohlenwasserstoffen mit oxydierenden Gasen |
| US2287125A (en) * | 1938-10-12 | 1942-06-23 | Standard Oil Dev Co | Oxidation of low molecular weight hydrocarbons in liquid phase and catalyst therefor |
| US2241487A (en) * | 1939-02-18 | 1941-05-13 | Standard Oil Dev Co | Catalytic oxidation of ketones |
| US2265948A (en) * | 1939-08-02 | 1941-12-09 | Du Pont | Catalytic oxidation of lower aliphatic hydrocarbons |
| US2530512A (en) * | 1947-06-13 | 1950-11-21 | Celanese Corp | Oxidation of aliphatic esters |
| US2578306A (en) * | 1950-01-19 | 1951-12-11 | Eastman Kodak Co | Process for direct oxidation of aldehydes and alcohol to acid |
-
1953
- 1953-04-25 GB GB11469/53A patent/GB767290A/en not_active Expired
-
1954
- 1954-04-06 NL NL186540A patent/NL95035C/xx active
- 1954-04-13 US US422932A patent/US2800506A/en not_active Expired - Lifetime
- 1954-04-17 DE DED17593A patent/DE1019289B/de active Pending
- 1954-04-22 FR FR1099323D patent/FR1099323A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR1099323A (fr) | 1955-09-02 |
| NL95035C (OSRAM) | 1960-07-16 |
| DE1019289B (de) | 1957-11-14 |
| US2800506A (en) | 1957-07-23 |
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