GB817149A - A method for the purification of acetone - Google Patents

A method for the purification of acetone

Info

Publication number
GB817149A
GB817149A GB40034/57A GB4003457A GB817149A GB 817149 A GB817149 A GB 817149A GB 40034/57 A GB40034/57 A GB 40034/57A GB 4003457 A GB4003457 A GB 4003457A GB 817149 A GB817149 A GB 817149A
Authority
GB
United Kingdom
Prior art keywords
acetone
alkali
per cent
time
mixing
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
GB40034/57A
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.)
Ineos Phenol GmbH
Original Assignee
Phenolchemie GmbH and Co KG
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 Phenolchemie GmbH and Co KG filed Critical Phenolchemie GmbH and Co KG
Publication of GB817149A publication Critical patent/GB817149A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C07C45/80Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
    • 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Acetone, which is contaminated with aldehydes, acids and esters, is purified by intimately mixing with a volumetric excess of 10-30 per cent w/w aqueous caustic solution, separating the phases before any substantial condensation of the acetone has taken place and distilling the acetone. The crude acetone may be derived, for example, from the acid cleavage of cumol hydroperoxide. The mixing is preferably effected in a centrifugal or turbo pump using at least 5 parts by volume of alkali to 1 part of acetone. After the separation step the alkali may be recycled, being replaced by fresh from time to time and the used alkali withdrawn. Water is preferably added to the acetone before treatment in order to replace that absorbed by the acetone from the alkali. It is expedient to add water (e.g. 1-2 per cent based on the acetone) to one of the lower plates of the distillation column above the inlet level. An example is given.
GB40034/57A 1957-01-16 1957-12-24 A method for the purification of acetone Expired GB817149A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE817149X 1957-01-16

Publications (1)

Publication Number Publication Date
GB817149A true GB817149A (en) 1959-07-22

Family

ID=6735160

Family Applications (1)

Application Number Title Priority Date Filing Date
GB40034/57A Expired GB817149A (en) 1957-01-16 1957-12-24 A method for the purification of acetone

Country Status (1)

Country Link
GB (1) GB817149A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3198837A (en) * 1965-08-03 Process for the purification of methyl ethyl ketone
US4722769A (en) * 1986-04-24 1988-02-02 Allied Corporation Process for recovery of acetone

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3198837A (en) * 1965-08-03 Process for the purification of methyl ethyl ketone
US4722769A (en) * 1986-04-24 1988-02-02 Allied Corporation Process for recovery of acetone

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