GB660773A - Improvements in or relating to the separation and purification of methanol - Google Patents

Improvements in or relating to the separation and purification of methanol

Info

Publication number
GB660773A
GB660773A GB31967/49A GB3196749A GB660773A GB 660773 A GB660773 A GB 660773A GB 31967/49 A GB31967/49 A GB 31967/49A GB 3196749 A GB3196749 A GB 3196749A GB 660773 A GB660773 A GB 660773A
Authority
GB
United Kingdom
Prior art keywords
column
methanol
liquid
zone
crude
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
GB31967/49A
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.)
Standard Oil Development Co
Original Assignee
Standard Oil Development Co
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 Standard Oil Development Co filed Critical Standard Oil Development Co
Publication of GB660773A publication Critical patent/GB660773A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/02Monohydroxylic acyclic alcohols
    • C07C31/04Methanol

Landscapes

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

Abstract

<PICT:0660773/IV (b)/1> Methanol is separated from a crude mixture containing neutral organic compounds normally boiling within the range of 10.8 DEG to 150 DEG C. by continuously introducing a feed mixture of the crude methanol into a fractional distillation zone, in which vapours of the neutral organic contaminants fractionally distilling from the mixture contact liquid reflux condensates of the vapours dissolved in at least 65 mole. per cent of water, continuously removing an aqueous vapour mixture of the neutral organic contaminants and continuously removing from the zone a residual portion of the liquid reflux which is a dilute aqueous solution of methanol. The crude mixture may contain methanol contaminated with aldehydes, ketones, other alcohols, carboxylic acids, ethers, esters, acetals, ketals and hydrocarbons in mixtures produced by various processes, as, for example, synthesis from carbon monoxide and hydrogen, oxidation of hydrocarbons, decomposition of alcohols, destructive distillation of wood &c. In the Figure, 1 is a fractional distillation column provided with means for obtaining efficient counter-current liquid-vapour phase contacting, e.g. by bubble plates or packing. The crude methanol feed is charged to column 1 at the bottom of the rectification zone 3. The water to be added continuously enters the column 1 at the upper part of the rectification zone 3. A portion of the condensate collected in receiver 7 is returned to the top part of column 1 as external reflux. A secondary rectifying zone 10 may be provided in the upper part of column 1. The internal liquid reflux flows downward from the feed-plate in column 1 through the stripping zone provided with means for obtaining liquid-vapour phase contacting. In this zone a sufficient number of contact stages is provided to strip the liquid reflux of neutral organic compounds which are rendered more volatile than the remaining methanol. The residual liquid reflux is withdrawn from the bottom part of the column and is passed through a reboiler 13. The heated and partially vaporized portion of the bottoms is recycled from the reboiler to the lower part of column 1. The remaining portion of the bottoms liquid is passed into the concentrating column 16 which is equipped with liquid-vapour phase contacting means and overhead line 17, for passing overhead purified methanol vapours. Some of the methanol distillate is passed as external reflux to the upper part of column 16 and a remaining portion of the purified methanol distillate is withdrawn to storage. Vapours from the dilute methanol feed to column 16 are rectified in the upper part of the column and the down-flowing internal reflux in column 16 is stripped of methanol. If the crude methanol feed contains carboxylic acid the acid will remain in the residual aqueous bottoms of the concentrator 16. In the example methanol is separated from a crude Fischer Synthesis water-layer product containing methanol, ethanol, isopropanol, methyl ethyl ketone, acetal, aldehyde and water. Specification 647,903 is referred to.ALSO:Methanol is separated from a crude mix<PICT:0660773/III/1> ture containing neutral organic compounds normally boiling with in the range of 108 DEG C. to 150 DEG C. by continuously introducing a feed mixture of the crude methanol into a fractional distillation zone, in which vapours of the neutral organic contaminants fractionally distilling from the mixture contact liquid reflux condensates of the vapours dissolved in at least 65 mol per cent of water, continuously removing an aqueous vapour mixture of the neutral organic contaminants and continuously removing from the zone a residual portion of the liquid reflux which is a dilute aqueous solution of methanol. The crude mixture may contain methanol contaminated with aldehydes, ketones, other alcohols, carboxylic acids, ethers, esters, acetals, ketals and hydrocarbons in mixtures produced by various processes, as, for example, synthesis from carbon monoxide and hydrogen, oxidation of hydrocarbons, decomposition of alcohols, destructive distillation of wood &c. In the Figure 1, is a fractional distillation column provided with means for obtaining efficient counter-current liquid-vapour phase contacting, e.g. by bubble plates or packing. The crude methanol feed is charged to column 1 at the bottom of the rectification zone 3. The water which is added continuously enters the column 1 at the upper part of the rectification zone 3. A portion of the condensate collected in receiver 7 is returned to the top part of column 1 as external reflux. A secondary rectifying zone 10 may be provided in the upper part of column 1. The internal liquid reflux flows downward from the feed plate in column 1 through the stripping zone provided with means for obtaining liquid-vapour phase contacting. In this zone a sufficient number of contact stages is provided to strip the liquid reflux of neutral organic compounds which are rendered more volatile than the remaining methanol. The residual liquid reflux is withdrawn from the bottom part of the column and is passed through a reboiler 13. The heated and partially vaporized portion of the bottoms is recycled from the reboiler to the lower part of column 1. The remaining portion of the bottoms liquid is passed into the concentrating column 16 which is equipped with liquid-vapour phase contacting means and overhead line 17 for passing overhead purified methanol vapours. Some of the methanol distillate is passed as external reflux to the upper part of column 16 and a remaining portion of the purified methanol distillate is withdrawn to storage. Vapours from the dilute methanol feed to column 16 are rectified in the upper part of the column and the downflowing internal reflux in column 16 is stripped of methanol. If the crude methanol feed contains carboxylic acid, the acid will remain in the residual aqueous bottoms of the concentator 16. In the example, methanol is separated from a crude Fischer synthesis water-layer product containing ethanol, isopropanol, methyl ethyl ketone, acetal, aldehyde and water. Specification 647,903 is referred to.
GB31967/49A 1949-01-08 1949-12-13 Improvements in or relating to the separation and purification of methanol Expired GB660773A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US660773XA 1949-01-08 1949-01-08

Publications (1)

Publication Number Publication Date
GB660773A true GB660773A (en) 1951-11-14

Family

ID=22067110

Family Applications (1)

Application Number Title Priority Date Filing Date
GB31967/49A Expired GB660773A (en) 1949-01-08 1949-12-13 Improvements in or relating to the separation and purification of methanol

Country Status (1)

Country Link
GB (1) GB660773A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3230156A (en) * 1961-09-08 1966-01-18 Chemical Construction Corp Purification of synthetic methanol by plural stage distillation
US3434937A (en) * 1966-10-06 1969-03-25 Allied Chem Distillation purification of crude synthetic methanol
US3442770A (en) * 1967-12-21 1969-05-06 Vulcan Cincinnati Inc Process for the purification of methanol by extractive distillation and plural stage distillation recovery
WO2001068215A1 (en) * 2000-03-10 2001-09-20 Siemens Axiva Gmbh & Co. Kg Rectifying separation of organic substances from water/methanol mixtures by addition of methanol or water
WO2009015614A1 (en) * 2007-07-30 2009-02-05 Kmps Financial Group, S.R.O. Method and equipment for production of glucose, ethanol, furfural, furane and lignin from renewable raw materials
DE102015102627A1 (en) 2015-02-24 2016-08-25 L'Air Liquide, Société Anonyme pour l'Etude et l'Exploitation des Procédés Georges Claude Plant and process for producing purified methanol
CN112159305A (en) * 2020-10-27 2021-01-01 湖南红宝科技开发有限公司 Method for purifying methanol
CN115724717A (en) * 2022-11-16 2023-03-03 厦门大学 Method for separating and co-producing methanol from low-carbon mixed alcohol

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3230156A (en) * 1961-09-08 1966-01-18 Chemical Construction Corp Purification of synthetic methanol by plural stage distillation
US3434937A (en) * 1966-10-06 1969-03-25 Allied Chem Distillation purification of crude synthetic methanol
US3442770A (en) * 1967-12-21 1969-05-06 Vulcan Cincinnati Inc Process for the purification of methanol by extractive distillation and plural stage distillation recovery
WO2001068215A1 (en) * 2000-03-10 2001-09-20 Siemens Axiva Gmbh & Co. Kg Rectifying separation of organic substances from water/methanol mixtures by addition of methanol or water
WO2009015614A1 (en) * 2007-07-30 2009-02-05 Kmps Financial Group, S.R.O. Method and equipment for production of glucose, ethanol, furfural, furane and lignin from renewable raw materials
EA017476B1 (en) * 2007-07-30 2012-12-28 Кмпс Файненсиал Груп, С.Р.О. Method and equipment for production of glucose, ethanol, furfural, furane and lignin from renewable raw materials
DE102015102627A1 (en) 2015-02-24 2016-08-25 L'Air Liquide, Société Anonyme pour l'Etude et l'Exploitation des Procédés Georges Claude Plant and process for producing purified methanol
WO2016134856A1 (en) 2015-02-24 2016-09-01 L'Air Liquide Société Anonyme pour l'Etude et l'Exploitation des Procédés Georges Claude Plant and process for producing purified methanol
RU2689594C2 (en) * 2015-02-24 2019-05-28 Л'Эр Ликид Сосьете Аноним Пур Л'Этюд Э Л'Эксплуатасьон Де Проседе Жорж Клод Apparatus and method for producing refined methanol
CN112159305A (en) * 2020-10-27 2021-01-01 湖南红宝科技开发有限公司 Method for purifying methanol
CN115724717A (en) * 2022-11-16 2023-03-03 厦门大学 Method for separating and co-producing methanol from low-carbon mixed alcohol
CN115724717B (en) * 2022-11-16 2024-04-05 厦门大学 Method for co-production of methanol by separating low-carbon mixed alcohol

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