GB800763A - Purification of acetone - Google Patents

Purification of acetone

Info

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
Application number
GB2843/57A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Distillers Co Yeast Ltd
Distillers Co Ltd
Original Assignee
Distillers Co Yeast Ltd
Distillers Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Distillers Co Yeast Ltd, Distillers Co Ltd filed Critical Distillers Co Yeast Ltd
Publication of GB800763A publication Critical patent/GB800763A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/04Saturated compounds containing keto groups bound to acyclic carbon atoms
    • C07C49/08Acetone
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C37/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
    • C07C37/08Preparation 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C39/00Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
    • C07C39/02Compounds 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
    • C07C39/04Phenol
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/51Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
    • C07C45/53Preparation 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/78Separation; Purification; Stabilisation; Use of additives
    • C07C45/81Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
    • C07C45/82Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation by distillation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/78Separation; Purification; Stabilisation; Use of additives
    • C07C45/85Separation; 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.
GB2843/57A 1956-01-27 1957-01-25 Purification of acetone Expired GB800763A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (2)

* Cited by examiner, † Cited by third party
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

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