GB800763A - Purification of acetone - Google Patents
Purification of acetoneInfo
- Publication number
- GB800763A GB800763A GB2843/57A GB284357A GB800763A GB 800763 A GB800763 A GB 800763A GB 2843/57 A GB2843/57 A GB 2843/57A GB 284357 A GB284357 A GB 284357A GB 800763 A GB800763 A GB 800763A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acetone
- column
- tray
- crude
- aqueous
- 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
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/04—Saturated compounds containing keto groups bound to acyclic carbon atoms
- C07C49/08—Acetone
-
- 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
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring monocyclic with no unsaturation outside the aromatic ring
- C07C39/04—Phenol
-
- 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
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/81—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
- C07C45/82—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation by distillation
-
- 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
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/85—Separation; Purification; Stabilisation; Use of additives by treatment giving rise to a chemical modification
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Crude substantially phenol-free acetone obtained by the acid-catalysed decomposition of cumene hydroperoxide is purified by distillation in a fractionating column in the presence of an aqueous solution of an alkali metal hydroxide with removal of pure acetone as the overhead stream from the column. The crude acetone may be fed continuously into the column at an intermediate point and the aqueous alkali introduced at a point substantially below the column top. The aqueous alkali is suitably used in a concentration of about 1-25 w./v. per cent and at a feed rate of 5-1 gals. per hour for crude acetone rates of 5-10 gals. per minute. In examples: (1) a crude acetone fraction obtained by neutralization and then distillation of the acid catalyzed decomposition of cumene hydroperoxide in acetone (see Group IV (b)), is stripped of the bulk of aldehydic impurities and then introduced on to the 38th tray of a 55-tray column while aqueous NaOH is added at the 34th tray; a pure acetone fraction is removed overhead and a wet acetone is removed from the 20th tray and recycled to the decomposition zone; (2) the stripped acetone of (1) is fed with aqueous NaOH on to the 34th tray of the column operated under slight vacuum and specification acetone is distilled off; similar results are obtained when the aqueous NaOH is introduced a few trays above or below the acetone feed point.ALSO:Crude substantially phenol-free acetone obtained by the acid catalysed decomposition of cumene hydroperoxide is purified by distillation in a fractionating column in the presence of an aqueous solution of an alkali metal hydroxide with removal of pure acetone as the overhead stream from the column. The crude acetone, containing aldehydes, esters, acetals, mesityl oxide and sulphur compounds as impurities may be fed continuously into the column at an intermediate point and the aqueous caustic alkali solution introduced at a point substantially below the column top. Preferably, however, the aqueous alkali solution is added to the crude acetone immediately prior to its entering the fractionating column or prior to a preliminary stripping of the crude acetone of aldehyde impurities in a stripping column. The aqueous caustic alkali is suitably used in a concentration of about 1-25 w/v per cent and at a feed rate of 5-1 gallons per hour for crude acetone rates of 5 to 10 gallons per minute. In examples: (1) a cumene hydroperoxide concentrate containing some a :a -dimethylbenzyl alcohol, aceto phenone and cumene is continuously decomposed in a reaction medium of acetone and sulphuric acid under acetone reflux and product is withdrawn, neutralized and then distilled to recover a crude acetone fraction. Pure phenol is recovered from the residue. The crude acetone fraction is stripped of aldehydic impurities and then introduced into the 38th tray of a 55-tray column while aqueous NaOH is added at the 34th tray; a pure acetone fraction is removed as overheads and a wet acetone is removed from the 20th tray is recycled to the decomposition stage; (2) the stripped crude acetone of (1) is fed together with aqueous NaOH on to the 34th tray of the column operated under slight vacuum and specification acetone is distilled off; this process may be carried out with similar results by introducing the aqueous NaOH a few trays above or below the acetone feed point.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US800763XA | 1956-01-27 | 1956-01-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB800763A true GB800763A (en) | 1958-09-03 |
Family
ID=22155106
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2843/57A Expired GB800763A (en) | 1956-01-27 | 1957-01-25 | Purification of acetone |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB800763A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1185601B (en) * | 1960-07-01 | 1965-01-21 | It Resine Soc | Process for purifying acetone |
FR2202070A1 (en) * | 1972-10-04 | 1974-05-03 | Bp Chem Int Ltd |
-
1957
- 1957-01-25 GB GB2843/57A patent/GB800763A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1185601B (en) * | 1960-07-01 | 1965-01-21 | It Resine Soc | Process for purifying acetone |
FR2202070A1 (en) * | 1972-10-04 | 1974-05-03 | Bp Chem Int Ltd |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2737480A (en) | Recovery of acetone and phenol from cumene hydroperoxide decomposition product | |
US2757209A (en) | Recovery of phenol and alphamethylstyrene from cumene oxidation reaction mixtures | |
GB641250A (en) | Process for the manufacture of di-isopropyl-benzene hydro-peroxides and products resulting therefrom | |
US2971893A (en) | Phenol purification | |
JPS6412251B2 (en) | ||
US2856432A (en) | Aromatic dihydroperoxide production | |
US2906676A (en) | Process for purifying crude acetone | |
US4333801A (en) | Recovery of a cumene/alpha-methylstyrene fraction from a mixture thereof with phenol and water | |
US4262150A (en) | Process for the recovery of phenol from a reaction mixture resulting from the acid cleavage of cumene hydroperoxide | |
US4559110A (en) | Acetophenone recovery and purification | |
US2906789A (en) | Manufacture of phenol from cumene | |
US5567853A (en) | Purification of acetone | |
US4283568A (en) | Process for the recovery of phenol from a reaction mixture resulting from the acid cleavage of cumene hydroperoxide | |
CA1057313A (en) | Process for the continuous production of 2-ethyl hexanol | |
US3190924A (en) | Process for the production of organic dihydroperoxides | |
CA1158195A (en) | Process for the distillative separation of tertiary alkyl hydroperoxides and ditertiary alkyl peroxides | |
US2856433A (en) | Separation of organic compounds | |
GB800763A (en) | Purification of acetone | |
US4339615A (en) | Process for producing resorcinol | |
US3896006A (en) | Mesityl oxide removal from high-purity phenol | |
US3190923A (en) | Process for the recovery of dihydroperoxide content from aqueous alkali extraction solution of dialkylated aromatic hydrocarbon oxidation reaction mixtures | |
US4461676A (en) | Process for refining tetrahydrofuran | |
US2381032A (en) | Separation of organic compounds | |
US4370205A (en) | Recovery of cumene from a mixture thereof with phenol and water | |
GB1394452A (en) | Purification of phenol |