GB745594A - Recovery and preparation of lower percarboxylic acids - Google Patents

Recovery and preparation of lower percarboxylic acids

Info

Publication number
GB745594A
GB745594A GB30638/53A GB3063853A GB745594A GB 745594 A GB745594 A GB 745594A GB 30638/53 A GB30638/53 A GB 30638/53A GB 3063853 A GB3063853 A GB 3063853A GB 745594 A GB745594 A GB 745594A
Authority
GB
United Kingdom
Prior art keywords
acid
water
hydrogen peroxide
distilling
carboxylic acid
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
GB30638/53A
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.)
Evonik Operations GmbH
Original Assignee
Degussa GmbH
Deutsche Gold und Silber Scheideanstalt
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 Degussa GmbH, Deutsche Gold und Silber Scheideanstalt filed Critical Degussa GmbH
Publication of GB745594A publication Critical patent/GB745594A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C407/00Preparation of peroxy compounds
    • C07C407/003Separation; Purification; Stabilisation; Use of additives

Abstract

Lower aliphatic percarboxylic acids are concentrated by vacuum distillation of their aqueous solutions, which may also contain the corresponding carboxylic acid and hydrogen peroxide, in the presence of a substance which binds water, present in a quantity at least equal to the weight of water to be bound during the distillation. Suitable water-binding substances are sulphuric acid, phosphoric acid, phosphorus pentoxide, magnesium perchlorate or selenic acid. The process may also be applied to aqueous mixtures of hydrogen peroxide and carboxylic acid. In another embodiment a distilled vapour mixture of hydrogen peroxide, water and carboxylic acid is reacted in a suitable apparatus with the water-binding agent-thus vapours of hydrogen peroxide, water and acetic acid may pass up a tower down which sulphuric acid trickles. If desired, residual liquors from the manufacture of hydrogen peroxide from persulphuric acid or persulphates may be mixed with carboxylic acid and vacuum-distilled to yield the per acid. Distillate may be cooled by direct cotact with the corresponding carboxylic acid or anhydride to increase their stability. The process is particularly applicable to peracetic acid, and applicable to perpropionic or perbutyric acid. In examples 1-4, peracetic acid of up to 70 per cent strength is obtained by (1) distilling dilute aqueous peracetic acid with conc. H2SO4 at 40-50 DEG C. and 11 mms. pressure; (2) distilling a reaction mixture of acetic acid, aqueous hydrogen perxide and sulphuric acid; (3) distilling a mixture of water, acetic acid, hydrogen peroxide and metaphosphoric acid; (4) distilling a mixture of water, acetic acid, hydrogen peroxide and magnesium perchlorate. Examples 5 and 6 relate to perpropionic and perbutyric acids respectively.ALSO:Lower aliphatic percarboxylic acids are concentrated by vacuum distillation of their aqueous solutions, which may also contain the corresponding carboxylic acid and hydrogen peroxide, in the presence of a substance which bind water present in a quantity at least equal to the weight of water to be found during the distillation. Suitable water-binding substances are sulphuric acid, phosphoric acid, phosphorus pentoxide, magnesium perchlorate or selenic acid. The process may also be applied to aqueous mixtures of hydrogen peroxide and carboxylic acid. In another embodiment a distilled vapour mixture of hydrogen peroxide, water and carboxylic acid is reacted in a suitable apparatus with the water-binding agents, - thus vapours of hydrogen peroxide, water and acetic acid may pass up a tower down which sulphuric acid trickles. If desired residual liquors from the manufacture of hydrogen peroxide from persulphuric acid or persulphates may be mixed with carboxylic acid and vacuum-distilled to yield the per acid. Distillates may be cooled by direct contact with the corresponding carboxylic acid or anhydride to increase their stability. The process is particularly applicable to peracetic acid, and applicable to perpropionic or perbutyric acid. In Examples 1-4, peracetic acid of up to 70 per cent strength is obtained by (1) distilling dilute aqueous peracetic acid with conc. H2SO4 at 40-50 DEG C. and 11 mms. pressure; (2) distilling a reaction mixture of acetic acid, aqueous hydrogen peroxide and sulphuric acid; (3) distilling a mixture of water, acetic acid, hydrogen peroxide and metaphosphoric acid; and (4) distilling a mixture of water, acetic acid, hydrogen peroxide and magnesium perchlorate. Examples 5 and 6 relate to perpropionic and perbutyric acids respectively.
GB30638/53A 1952-11-12 1953-11-05 Recovery and preparation of lower percarboxylic acids Expired GB745594A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE745594X 1952-11-12

Publications (1)

Publication Number Publication Date
GB745594A true GB745594A (en) 1956-02-29

Family

ID=6648231

Family Applications (1)

Application Number Title Priority Date Filing Date
GB30638/53A Expired GB745594A (en) 1952-11-12 1953-11-05 Recovery and preparation of lower percarboxylic acids

Country Status (1)

Country Link
GB (1) GB745594A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4147720A (en) * 1977-12-30 1979-04-03 Fmc Corporation Process for preparing aliphatic diperoxydicarboxylic acids

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4147720A (en) * 1977-12-30 1979-04-03 Fmc Corporation Process for preparing aliphatic diperoxydicarboxylic acids

Similar Documents

Publication Publication Date Title
GB931119A (en) Improvements in processes for the production of peracids
US2877266A (en) Preparation of peracids
PHILLIPS et al. Preparation of aliphatic peroxyacids
GB949094A (en) Process for the production of solutions of pure peracetic acid
ES478961A1 (en) Process for the production of peracids and their use for the preparation of epoxides from olefins.
US2802025A (en) Process for the production of lower carboxylic peracids
GB745594A (en) Recovery and preparation of lower percarboxylic acids
GB872355A (en) Improvements in or relating to the production of a tetrabasic acid and esters thereof
ATE875T1 (en) PROCESS FOR THE PRODUCTION OF AROMATIC POXYCARBONIC ACIDS.
GB1014361A (en) Improvements in and relating to the production of aliphatic per-acids
US2454351A (en) Production of alicyclic carboxylic acids
GB700546A (en) Hydroperoxides
DE2603269C3 (en) Process for the production of cyclohexanone and methyl-substituted or unsubstituted phenol
ES483367A1 (en) Process for the preparation of glycidyl esters of aromatic polycarboxylic acids.
GB298137A (en) Improved process for concentrating acetic acid
US3214458A (en) Nitrite esters
US3478092A (en) Method of improving the color and color stability of benzoic acid
US2405471A (en) Manufacture of acetic anhydride
GB963359A (en) Chemical process for recovery of vanadium and copper catalysts
US1988611A (en) Process fob producing isopropyl
GB625131A (en) Improvements in or relating to the manufacture of diethyl acetal
GB824518A (en) A process of preparing colourless maleic acid anhydride of high purity
GB689095A (en) Manufacture of 2:4:4-trimethyl pentanal
GB1501356A (en) Process for the continuous preparation of organic solutions of percarboxylic acids
GB747417A (en) Improvements in or relating to the production of phthalic acids