GB743004A - Improvements in or relating to removal of salts from acetone-phenol mixtures - Google Patents
Improvements in or relating to removal of salts from acetone-phenol mixturesInfo
- Publication number
- GB743004A GB743004A GB6034/53A GB603453A GB743004A GB 743004 A GB743004 A GB 743004A GB 6034/53 A GB6034/53 A GB 6034/53A GB 603453 A GB603453 A GB 603453A GB 743004 A GB743004 A GB 743004A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acetone
- phase
- water
- phenol
- cumene hydroperoxide
- 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
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/53—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition of hydroperoxides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/08—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by decomposition of hydroperoxides, e.g. cumene hydroperoxide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/68—Purification; separation; Use of additives, e.g. for stabilisation
- C07C37/70—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment
- C07C37/72—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment by liquid-liquid treatment
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
In the production of phenol and acetone from cumene hydroperoxide by decomposing it in the presence of catalytic amounts of an acid (e.g. an inorganic acid such as sulphuric acid) and neutralizing the acid and acidic organic impurities in the oxidation mixture (e.g. with an aqueous solution of sodium phenolate), the salts produced by the neutralization are removed by adding, before or after the neutralization step, an amount of water sufficient to form, on neutralization and settling, an organic upper phase containing substantially all the phenol and acetone and some water, and an aqueous lower phase containing in solution substantially all the said salts and having a volume equal to at least 5 per cent (but preferably not exceeding about 50 per cent, e.g. about 8-20 per cent) of the organic phase, and separating the two phases. The addition of water and settling are advantageously effected at about 50-150 DEG F. (preferably 70-90 DEG F.). The aqueous phase, or part of it, may be recycled to the decomposition mixture, whilst the organic phase may be subjected to fractional distillation to recover the phenol and acetone. The cumene hydroperoxide may be obtained by oxidizing liquid-phase cumene with an oxygen-containing gas (e.g. air) in the presence of an aqueous alkali to form a mixture of cumene hydroperoxide and unreacted cumene. and removing substantially all of the latter. The decomposition of the cumene hydroperoxide may be effected at about 150-300 DEG F., advantageously in the presence of acetone or other inert diluent miscible with water and with acetone. Suitable arrangements of apparatus are described with the aid of flow sheets, and a detailed example is given. Reference has been directed by the Comptroller to Specifications 626,095, 629,429 and 684,039.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US743004XA | 1952-04-08 | 1952-04-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB743004A true GB743004A (en) | 1956-01-04 |
Family
ID=22118841
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB6034/53A Expired GB743004A (en) | 1952-04-08 | 1953-03-04 | Improvements in or relating to removal of salts from acetone-phenol mixtures |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB743004A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1128859B (en) * | 1957-07-31 | 1962-05-03 | Phenolchemie Ges Mit Beschraen | Process for the continuous neutralization of cleavage mixtures which have been obtained by cleaving alkyl aromatic hydroperoxides in the presence of acids |
EP0028910A1 (en) * | 1979-11-05 | 1981-05-20 | Mitsui Petrochemical Industries, Ltd. | Improved process for producing phenolic compounds from aralkyl hydroperoxides |
EP0952136A1 (en) * | 1998-04-23 | 1999-10-27 | Enichem S.p.A. | Process for the extraction of the salts contained in the neutralized separated product obtained in the preparation of phenol by the oxidation of cumene |
EP1411040A1 (en) * | 2002-10-15 | 2004-04-21 | Kellogg Brown & Root, Inc. | Low sodium cleavage product in phenol production |
WO2009080343A1 (en) | 2007-12-20 | 2009-07-02 | Borealis Technology Oy | Removal of a salt from a salt-containing organic mixture |
EP2769970A1 (en) | 2013-02-26 | 2014-08-27 | Borealis AG | Process for purifying hydrocarbons |
-
1953
- 1953-03-04 GB GB6034/53A patent/GB743004A/en not_active Expired
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1128859B (en) * | 1957-07-31 | 1962-05-03 | Phenolchemie Ges Mit Beschraen | Process for the continuous neutralization of cleavage mixtures which have been obtained by cleaving alkyl aromatic hydroperoxides in the presence of acids |
EP0028910A1 (en) * | 1979-11-05 | 1981-05-20 | Mitsui Petrochemical Industries, Ltd. | Improved process for producing phenolic compounds from aralkyl hydroperoxides |
US4328377A (en) | 1979-11-05 | 1982-05-04 | Mitsui Petrochemical Industries Ltd. | Process for producing phenolic compounds |
EP0952136A1 (en) * | 1998-04-23 | 1999-10-27 | Enichem S.p.A. | Process for the extraction of the salts contained in the neutralized separated product obtained in the preparation of phenol by the oxidation of cumene |
US6180834B1 (en) | 1998-04-23 | 2001-01-30 | Enichem S.P.A. | Process for the extraction of the salts contained in the neutralized separated product obtained in the preparation of phenol by the oxidation of cumene |
EP1411040A1 (en) * | 2002-10-15 | 2004-04-21 | Kellogg Brown & Root, Inc. | Low sodium cleavage product in phenol production |
US6825387B2 (en) | 2002-10-15 | 2004-11-30 | Kellogg Brown & Root, Inc. | Low sodium cleavage product |
WO2009080343A1 (en) | 2007-12-20 | 2009-07-02 | Borealis Technology Oy | Removal of a salt from a salt-containing organic mixture |
EP2769970A1 (en) | 2013-02-26 | 2014-08-27 | Borealis AG | Process for purifying hydrocarbons |
WO2014131800A1 (en) | 2013-02-26 | 2014-09-04 | Borealis Ag | Process for purifying hydrocarbons |
US10130896B2 (en) | 2013-02-26 | 2018-11-20 | Borealis Ag | Process for purifying hydrocarbons |
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