GB294037A - Process for oxidising ethyl alcohol - Google Patents

Process for oxidising ethyl alcohol

Info

Publication number
GB294037A
GB294037A GB3048927A GB3048927A GB294037A GB 294037 A GB294037 A GB 294037A GB 3048927 A GB3048927 A GB 3048927A GB 3048927 A GB3048927 A GB 3048927A GB 294037 A GB294037 A GB 294037A
Authority
GB
United Kingdom
Prior art keywords
alcohol
acetaldehyde
gases
aldehyde
acetic 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
GB3048927A
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.)
HOLZVERKOHLUNGS IND ACTIEN GES
Otto Fuchs KG
Original Assignee
HOLZVERKOHLUNGS IND ACTIEN GES
Otto Fuchs 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 HOLZVERKOHLUNGS IND ACTIEN GES, Otto Fuchs KG filed Critical HOLZVERKOHLUNGS IND ACTIEN GES
Priority to GB3048927A priority Critical patent/GB294037A/en
Publication of GB294037A publication Critical patent/GB294037A/en
Expired legal-status Critical Current

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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
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/32Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/37Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of >C—O—functional groups to >C=O groups
    • C07C45/38Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of >C—O—functional groups to >C=O groups being a primary hydroxyl group

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

294,037. Holzverkohlungs-Industrie Akt.-Ges., and Fuchs, O. Nov. 14, 1927. Acetaldehyde and its polymers; acetic acid; ethyl acetate; diethyl acetal. - In the catalytic manufacture of acetaldehyde from ethyl alcohol and oxygen-containing gases, the reaction products are dehydrated by cooling and are then treated with an anhydrous, or practically anhydrous, solvent for the aldehyde. Preferably, the condensate obtained by cooling the gases is used to wash the gases prior to the solution of the aldehyde, and from this condensate, which contains unchanged alcohol, acetic acid, and some acetaldehyde, the aldehyde may be recovered by distillation, the acetic acid and part of the alcohol may be recovered as ethyl acetate, and the remaining alcohol may be recovered as such. For dissolving the acetaldehyde from the cooled gases, it is preferred to use solvents which permit the direct further treatment of the aldehyde. For example, the solvent may be ethyl alcohol, in which event the solution, after addition of a small amount of mineral acid, yields diethyl acetal on distillation. The initial material may be dilute alcohol, and the catalysts may be such as are unsuitable for treating absolute alcohol, e.g. finely divided or platinized silver. In one example, a mixture of ethyl alcohol vapour and air is passed over silver wire gauze and the reaction products are cooled to about 15‹ C. in two coolers arranged in series. The gases are then washed in a tower to which the condensate from the first cooler is led, whereafter the acetaldehyde remaining in the gases is removed by washing with aldol. The solution of acetaldehyde in aldol may be treated, e.g. with alkalies, to form aldol. The condensate from the coolers is fractionated in a column to separate acetaldehyde and is then fractionated in a second column, after addition of a small amount of sulphuric acid, a distillate containing ethyl acetate and alcohol being obtained. In another example, the aldehyde is absorbed in acetic acid and the solution is oxidized in known manner to form acetic acid. Reference is made also to the production of paraldehyde.
GB3048927A 1927-11-14 1927-11-14 Process for oxidising ethyl alcohol Expired GB294037A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3048927A GB294037A (en) 1927-11-14 1927-11-14 Process for oxidising ethyl alcohol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3048927A GB294037A (en) 1927-11-14 1927-11-14 Process for oxidising ethyl alcohol

Publications (1)

Publication Number Publication Date
GB294037A true GB294037A (en) 1928-07-19

Family

ID=10308472

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3048927A Expired GB294037A (en) 1927-11-14 1927-11-14 Process for oxidising ethyl alcohol

Country Status (1)

Country Link
GB (1) GB294037A (en)

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