GB788931A - Improvements in or relating to the separation of organic mixtures - Google Patents

Improvements in or relating to the separation of organic mixtures

Info

Publication number
GB788931A
GB788931A GB2219854A GB2219854A GB788931A GB 788931 A GB788931 A GB 788931A GB 2219854 A GB2219854 A GB 2219854A GB 2219854 A GB2219854 A GB 2219854A GB 788931 A GB788931 A GB 788931A
Authority
GB
United Kingdom
Prior art keywords
ketone
acids
mixture
acid
formaldehyde
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
GB2219854A
Inventor
Andre Pacoud
Jacques Dallemagne
Albert Mercier
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.)
Rhone Poulenc SA
Original Assignee
Rhone Poulenc SA
Societe des Usines Chimiques Rhone Poulenc SA
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 Rhone Poulenc SA, Societe des Usines Chimiques Rhone Poulenc SA filed Critical Rhone Poulenc SA
Priority to GB2219854A priority Critical patent/GB788931A/en
Publication of GB788931A publication Critical patent/GB788931A/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
    • C07C45/84Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation by distillation by azeotropic distillation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42Separation; Purification; Stabilisation; Use of additives
    • C07C51/43Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
    • C07C51/44Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation by distillation
    • C07C51/46Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation by distillation by azeotropic distillation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The components of a mixture of one or more aliphatic carboxylic acids, water and formaldehyde are separated by rectifying the mixture in a distillation column in the presence of an auxiliary organic liquid which is insoluble in water and, which forms with water and formaldehyde, but not with the acid or acids, an azeotropic mixture having a boiling-point below that of the acid or acids, recovering anhydrous acid or acids from the base of the column and separating formaldehyde as an aqueous solution from a heterogeneous liquid phase condensed from the vapour phase of the column. The auxiliary organic liquid may be di-isopropyl ether, di-butyl ether, isopropyl or butyl formates or acetates, methyl isopropyl ketone, or methyl isobutyl ketone, when the acids are formic acid and acetic acid. A mixture also containing a ketone having a boiling-point below that of the acid or acids, such as acetone, may also be separated using an auxiliary organic liquid incapable of forming a binary azeotrope with the ketone or a ternary azeotrope with the ketone and water, and the boiling-point of the azeotropic mixture which it forms with formaldehyde and water must be between that of the ketone and the acid or acids; examples are isopropyl formate and isopropyl acetate. The ketone may be removed with the aqueous formaldehyde solution, or, using fractional distillation, pure ketone vapour may be withdrawn at the top of the column, and the azeotropic mixture vapour lower down. In examples: (1) isopropyl ether is used in the separation of a mixture of acetic and formic acids, formaldehyde and water, and (2) isopropyl acetate is used with a mixture also containing acetone.
GB2219854A 1954-07-29 1954-07-29 Improvements in or relating to the separation of organic mixtures Expired GB788931A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2219854A GB788931A (en) 1954-07-29 1954-07-29 Improvements in or relating to the separation of organic mixtures

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2219854A GB788931A (en) 1954-07-29 1954-07-29 Improvements in or relating to the separation of organic mixtures

Publications (1)

Publication Number Publication Date
GB788931A true GB788931A (en) 1958-01-08

Family

ID=10175534

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2219854A Expired GB788931A (en) 1954-07-29 1954-07-29 Improvements in or relating to the separation of organic mixtures

Country Status (1)

Country Link
GB (1) GB788931A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5980696A (en) * 1994-08-23 1999-11-09 E. I. Du Pont De Nemours And Company Dehydration of acetic acid by azeotropic distillation in the production of an aromatic acid
US6150553A (en) * 1998-08-11 2000-11-21 E. I. Du Pont De Nemours And Company Method for recovering methyl acetate and residual acetic acid in the production acid of pure terephthalic acid
WO2001007391A1 (en) * 1999-07-22 2001-02-01 Consortium für elektrochemische Industrie GmbH Method for separating and purifying an aqueous mixture that mainly consists of acetic acid and formic acid
WO2001007390A1 (en) * 1999-07-22 2001-02-01 Consortium für elektrochemische Industrie GmbH A method for the separation and purification of an aqueous mixture consisting of acetic acid and formic acid as the main components

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5980696A (en) * 1994-08-23 1999-11-09 E. I. Du Pont De Nemours And Company Dehydration of acetic acid by azeotropic distillation in the production of an aromatic acid
US6150553A (en) * 1998-08-11 2000-11-21 E. I. Du Pont De Nemours And Company Method for recovering methyl acetate and residual acetic acid in the production acid of pure terephthalic acid
WO2001007391A1 (en) * 1999-07-22 2001-02-01 Consortium für elektrochemische Industrie GmbH Method for separating and purifying an aqueous mixture that mainly consists of acetic acid and formic acid
WO2001007390A1 (en) * 1999-07-22 2001-02-01 Consortium für elektrochemische Industrie GmbH A method for the separation and purification of an aqueous mixture consisting of acetic acid and formic acid as the main components
US6695952B1 (en) 1999-07-22 2004-02-24 Consortium Fur Elektrochemische Industrie Gmbh Method for the separation of and purification of an aqueous mixture consisting of the main components acetic acid and formic acid
US6793777B1 (en) 1999-07-22 2004-09-21 Consortium für elektrochemische Industrie GmbH Method for separating and purifying an aqueous mixture that mainly consists of acetic acid and formic acid
CN1304352C (en) * 1999-07-22 2007-03-14 电化学工业有限公司(国际) Method for separating and purifying an aqueous mixture that mainly consists of acetic acid and formic acid

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