GB598346A - Improved process and apparatus for the rectification of impure alcoholic liquids - Google Patents

Improved process and apparatus for the rectification of impure alcoholic liquids

Info

Publication number
GB598346A
GB598346A GB7283/39A GB728339A GB598346A GB 598346 A GB598346 A GB 598346A GB 7283/39 A GB7283/39 A GB 7283/39A GB 728339 A GB728339 A GB 728339A GB 598346 A GB598346 A GB 598346A
Authority
GB
United Kingdom
Prior art keywords
column
line
liquid
recovered
vapours
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
GB7283/39A
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.)
Dizem SA
Original Assignee
Dizem 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 Dizem SA filed Critical Dizem SA
Publication of GB598346A publication Critical patent/GB598346A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D3/00Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
    • B01D3/001Processes specially adapted for distillation or rectification of fermented solutions

Landscapes

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

Abstract

<PICT:0598346/III/1> <PICT:0598346/III/2> Pure 95 per cent. alcohol is recovered from raw alcoholic aqueous liquids obtained by fermentation and containing also other alcohols, esters, ketones, acids, amines and acetals, by introducing the impure liquid into the intermediate part of a first (distillation) column heated at its lower end and washed with a spray of hot aqueous liquid fed in at the top end, transferring the partly purified liquid from the bottom of the first column to a second (concentration) column from which purified concentrated alcohol is recovered at a point near the top while impurities collecting at the middle of the column are returned to the first column at a point a few plates above the point of introduction of the raw liquid. The vinasses recovered at the bottom of the second column are preferably used as the washing liquid for the first column while head impurities from the second column are returned to the first column. Vapours from the top of the first column are redistilled in a third column to recover aldehydes &c. Feed from a tank 1 flows through heat exchanger 4 and line 5 to the first column 6 and the partly concentrated alcohol is transferred through pipe 11 to the second column 12 from which the purified concentrated alcohol is recovered through line 12 and cooler 18. The exhausted vinasses are returned through lines 15, 15a to the top of column 6 to serve as washing liquid, while alcoholic &c. impurities collecting at the middle of the column are removed through taps R1, R2, R3, R4 and fed by emulsifier 21a to column 6. Vapours from top of column 12 pass through heat exchangers 4, 16, the condensate being in part recycled as reflux to column 12 through line 4a and in part being fed through line 10d to column 6. The vapours from column 6 are passed to the third column 7 surmounted by condenser 8 where they are fractionated to recover aldehydes esters and ketones through tap 9, and a liquid rich in propyl alcohol but also containing esters, ketones and acetals through tap 9a. Liquid recovered from the bottom of this column is cooled and passed to a separator 9c where separation into layers takes place. The upper layer rich in higher alcohols is removed through overflow 10 while the aqueous layer is mixed in a reheater 10c with the condensate in line 10d and fed back to the middle part of column 6. The Specification as open to inspection under Sect. 91 describes recovery of amines from the vapours issuing from the top of column 12 by passing these through line 25, Fig. 2 (Cancelled), into a column 26 where they are sprayed with dilute acid solution fed through 27 the amines being converted to non volatile salts the remaining vapours being condensed in cooler 28 and passed through line 29 to column 6. This subject-matter does not appear in the Specification as accepted.
GB7283/39A 1939-03-01 1939-03-06 Improved process and apparatus for the rectification of impure alcoholic liquids Expired GB598346A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
LU598346X 1939-03-01

Publications (1)

Publication Number Publication Date
GB598346A true GB598346A (en) 1948-02-17

Family

ID=19732945

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7283/39A Expired GB598346A (en) 1939-03-01 1939-03-06 Improved process and apparatus for the rectification of impure alcoholic liquids

Country Status (1)

Country Link
GB (1) GB598346A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2551593A (en) * 1947-01-28 1951-05-08 Standard Oil Dev Co Extractive distillation of alcohols from close-boiling aqueous mixtures
US2607719A (en) * 1949-04-15 1952-08-19 Stanolind Oil & Gas Co Extractive distillation of oxygenated organic compounds
US2729682A (en) * 1950-05-20 1956-01-03 Exxon Research Engineering Co Preparation of isopropanol of improved odor quality

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2551593A (en) * 1947-01-28 1951-05-08 Standard Oil Dev Co Extractive distillation of alcohols from close-boiling aqueous mixtures
US2607719A (en) * 1949-04-15 1952-08-19 Stanolind Oil & Gas Co Extractive distillation of oxygenated organic compounds
US2729682A (en) * 1950-05-20 1956-01-03 Exxon Research Engineering Co Preparation of isopropanol of improved odor quality

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