GB1429471A - Process for the production of phthalic acids - Google Patents
Process for the production of phthalic acidsInfo
- Publication number
- GB1429471A GB1429471A GB5149971A GB5149971A GB1429471A GB 1429471 A GB1429471 A GB 1429471A GB 5149971 A GB5149971 A GB 5149971A GB 5149971 A GB5149971 A GB 5149971A GB 1429471 A GB1429471 A GB 1429471A
- Authority
- GB
- United Kingdom
- Prior art keywords
- stage
- acid
- solvent
- oxidation
- weight
- 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
- C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
- C07C51/255—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of compounds containing six-membered aromatic rings without ring-splitting
- C07C51/265—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of compounds containing six-membered aromatic rings without ring-splitting having alkyl side chains which are oxidised to carboxyl 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)
Abstract
1429471 Iso- and terephthalic acids ATLANTIC RICHFIELD CO 5 Nov 1971 [29 Dec 1970] 51499/71 Heading C2C In a two-stage process for producing high purity terephthalic acid or isophahalic acid by oxidation with an oxygen-containing gas from C 8 hydrocarbon feedstock containing from 5 to 30% by weight of the isomer of xylene corresponding to the desired acid, the reaction mixture also containing from 70 to 95% by weight of a C 2-6 alkanoic acid solvent, said solvent containing a soluble metal compound catalyst in amounts from 0À2 to 2À0% by weight based on the weight of the reactants and the solvent, any water in the solvent being less than 10% by weight, said C 8 hydrocarbon feedstock is first oxidized substantially completely to the corresponding toluic acid at an essentially constant temperature in the range 200‹ to 280‹ F. while maintaining the pressure at about the vapour pressure of the reaction mixture, thereby producing a solvent-containing first stage effluent, some of the heat removal being attributable to the passage of inert gas through such first stage oxidation, such inert gas being admixed with the oxygen reactant and said effluent is advanced from the first stage oxidation to a second stage oxidation without subjecting said first stage effluent to liquid-liquid heat exchange and in said second stage oxidation, the product from the first oxidation stage is oxidized substantially completely to the desired benzene dicarboxylic acid at a temperature of from 230‹ to 280‹ F. and a pressure of from 200 to 800 p.s.i.g. A promoter may be employed in the process, e.g. an aldehyde, ketone, ozone or bromine. In the example isophthalic acid is obtained by oxidizing meta-xylene with air using acetic acid as solvent, cobalt acetate as catalyst and acetaldehyde as promoter.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10251470A | 1970-12-29 | 1970-12-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1429471A true GB1429471A (en) | 1976-03-24 |
Family
ID=22290267
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5149971A Expired GB1429471A (en) | 1970-12-29 | 1971-11-05 | Process for the production of phthalic acids |
Country Status (6)
Country | Link |
---|---|
BE (1) | BE776267A (en) |
DE (1) | DE2158279A1 (en) |
FR (1) | FR2120749A5 (en) |
GB (1) | GB1429471A (en) |
IT (1) | IT945355B (en) |
NL (1) | NL7116938A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005051881A1 (en) * | 2003-11-14 | 2005-06-09 | Bp Corporation North America Inc. | Staged countercurrent catalytic oxidation of disubstituted bemzene |
CN109369369A (en) * | 2018-12-18 | 2019-02-22 | 华东理工大学 | The preparation method of M-phthalic acid |
CN109485557A (en) * | 2018-12-18 | 2019-03-19 | 华东理工大学 | A kind of preparation process of M-phthalic acid |
CN109503369A (en) * | 2018-12-18 | 2019-03-22 | 华东理工大学 | A kind of preparation method of M-phthalic acid |
-
1971
- 1971-11-05 GB GB5149971A patent/GB1429471A/en not_active Expired
- 1971-11-24 DE DE19712158279 patent/DE2158279A1/en active Pending
- 1971-12-03 FR FR7143493A patent/FR2120749A5/fr not_active Expired
- 1971-12-06 BE BE776267A patent/BE776267A/en unknown
- 1971-12-09 NL NL7116938A patent/NL7116938A/xx unknown
- 1971-12-09 IT IT5463271A patent/IT945355B/en active
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005051881A1 (en) * | 2003-11-14 | 2005-06-09 | Bp Corporation North America Inc. | Staged countercurrent catalytic oxidation of disubstituted bemzene |
CN109369369A (en) * | 2018-12-18 | 2019-02-22 | 华东理工大学 | The preparation method of M-phthalic acid |
CN109485557A (en) * | 2018-12-18 | 2019-03-19 | 华东理工大学 | A kind of preparation process of M-phthalic acid |
CN109503369A (en) * | 2018-12-18 | 2019-03-22 | 华东理工大学 | A kind of preparation method of M-phthalic acid |
Also Published As
Publication number | Publication date |
---|---|
FR2120749A5 (en) | 1972-08-18 |
IT945355B (en) | 1973-05-10 |
NL7116938A (en) | 1972-07-03 |
DE2158279A1 (en) | 1972-07-06 |
BE776267A (en) | 1972-06-06 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |