GB1006945A - Production of adipic acid - Google Patents
Production of adipic acidInfo
- Publication number
- GB1006945A GB1006945A GB1298262A GB1298262A GB1006945A GB 1006945 A GB1006945 A GB 1006945A GB 1298262 A GB1298262 A GB 1298262A GB 1298262 A GB1298262 A GB 1298262A GB 1006945 A GB1006945 A GB 1006945A
- Authority
- GB
- United Kingdom
- Prior art keywords
- peak
- substrate
- rate
- reaction
- oxygen
- 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
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
- C07C51/31—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation of cyclic compounds with ring-splitting
- C07C51/313—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation of cyclic compounds with ring-splitting with molecular oxygen
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)
Abstract
Adipic acid is produced by contacting a cyclohexanone-containing substrate in an oxidation zone with a gaseous molecular oxygen stream in the presence of a manganese compound as catalyst at a temperature of from 60 DEG to 105 DEG C. and an oxygen partial pressure of from 1 to 30 p.s.i.a. and recovering adipic acid from the reaction mixture, the peak oxygen reaction rate being controlled such that it is at least 0.002 gm. mols./100 gms.substrate/min. when the reaction temperature prior to achieving the peak rate is 60 DEG C. or higher, at least 0.004 gm. mols./100 gms. substrate/min. when the reaction temperature prior to achieving the peak rate is 70 DEG C. or higher and at least 0.008 gm. mols./100 gms. substrate/min. when the reaction temperature prior to achieving the peak rate is 80 DEG C. or higher. The peak oxygen reaction rate may be controlled by altering the rate of flow of the molecular oxygen into the oxidation zone, or by adjusting the amount of mechanical agitation provided or by a combination of both methods. The substrate may be obtained by reacting cyclohexane with molecular oxygen at a temperature of from 125 DEG to 175 DEG C. at a pressure of 55 to 500 p.s.i.g., and removing unreacted cyclohexane; cyclohexanol and adipic acid are obtained in addition to cyclohexanone. The process of the invention is preferably carried out in the presence of a liquid reaction medium and the catalyst, which is normally a manganese salt and may include a copper salt as well, should be in a form soluble in the liquid reaction medium. Examples are given, together with comparative examples having peak oxygen reaction rates below the values specified above. Reference has been directed by the Comptroller to Specifications 941,662, 946,382 and 956,779.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12673061A | 1961-04-11 | 1961-04-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1006945A true GB1006945A (en) | 1965-10-06 |
Family
ID=22426386
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1298262A Expired GB1006945A (en) | 1961-04-11 | 1962-04-04 | Production of adipic acid |
Country Status (8)
Country | Link |
---|---|
BE (1) | BE616101A (en) |
CH (1) | CH427769A (en) |
DE (1) | DE1299624B (en) |
ES (1) | ES276341A1 (en) |
GB (1) | GB1006945A (en) |
LU (1) | LU41519A1 (en) |
NL (1) | NL277096A (en) |
SE (1) | SE311353B (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10184235B2 (en) | 2013-05-28 | 2019-01-22 | Falcon Waterfree Technologies, Llc | Directional fluid inlet |
US10182688B2 (en) | 2013-05-28 | 2019-01-22 | Falcon Waterfree Technologies, Llc | Splash-reducing and velocity-increasing cartridge exit |
US10197430B2 (en) | 2014-01-20 | 2019-02-05 | Falcon Waterfree Technologies, Llc | Visual indicator |
US10273675B2 (en) | 2013-04-26 | 2019-04-30 | Falcon Waterfree Technologies, Llc | Hybrid trap with water injection |
-
0
- NL NL277096D patent/NL277096A/xx unknown
-
1962
- 1962-04-04 GB GB1298262A patent/GB1006945A/en not_active Expired
- 1962-04-06 BE BE616101A patent/BE616101A/en unknown
- 1962-04-09 LU LU41519D patent/LU41519A1/xx unknown
- 1962-04-10 SE SE395662A patent/SE311353B/xx unknown
- 1962-04-10 ES ES276341A patent/ES276341A1/en not_active Expired
- 1962-04-11 DE DE1962S0078946 patent/DE1299624B/en active Pending
- 1962-04-11 CH CH440262A patent/CH427769A/en unknown
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10273675B2 (en) | 2013-04-26 | 2019-04-30 | Falcon Waterfree Technologies, Llc | Hybrid trap with water injection |
US10975560B2 (en) | 2013-04-26 | 2021-04-13 | Falcon Water Technologies, LLC | Hybrid trap with water injection |
US10184235B2 (en) | 2013-05-28 | 2019-01-22 | Falcon Waterfree Technologies, Llc | Directional fluid inlet |
US10182688B2 (en) | 2013-05-28 | 2019-01-22 | Falcon Waterfree Technologies, Llc | Splash-reducing and velocity-increasing cartridge exit |
US10197430B2 (en) | 2014-01-20 | 2019-02-05 | Falcon Waterfree Technologies, Llc | Visual indicator |
Also Published As
Publication number | Publication date |
---|---|
LU41519A1 (en) | 1963-10-09 |
CH427769A (en) | 1967-01-15 |
DE1299624B (en) | 1969-07-24 |
NL277096A (en) | |
BE616101A (en) | 1962-10-08 |
SE311353B (en) | 1969-06-09 |
ES276341A1 (en) | 1962-06-01 |
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