GB467481A - Processes of removing water from aqueous aliphatic acids - Google Patents

Processes of removing water from aqueous aliphatic acids

Info

Publication number
GB467481A
GB467481A GB2536835A GB2536835A GB467481A GB 467481 A GB467481 A GB 467481A GB 2536835 A GB2536835 A GB 2536835A GB 2536835 A GB2536835 A GB 2536835A GB 467481 A GB467481 A GB 467481A
Authority
GB
United Kingdom
Prior art keywords
column
pipe
acid
entrainer
overflow
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
GB2536835A
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.)
Eastman Kodak Co
Original Assignee
Eastman Kodak 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 Eastman Kodak Co filed Critical Eastman Kodak Co
Priority to GB2536835A priority Critical patent/GB467481A/en
Publication of GB467481A publication Critical patent/GB467481A/en
Expired legal-status Critical Current

Links

Classifications

    • 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

Abstract

In the concentration of lower aliphatic acids (other than formic acid), an ester, ether, ketone, or alcohol-ester mixture is employed as entrainer having a boiling point between 25 DEG below and 30 DEG above the boiling point of the acid, and forming an azeotropic mixture with water boiling below 100 DEG C., the supply of entrainer and aqueous acid, and the heating of the column being so regulated that the lower part of the column is maintained free from entrainer and serves to rectify aqueous acid. The column may be in two parts, the upper one effecting the azeotropic distillation. The process may be effected in the one- or two-column apparatus shown in Specification 383,148 or more than two columns may be employed. Suitable entrainers are the alcohol-ester mixtures used in Specification 467,559, allyl, butyl, isobutyl, amyl, isoamyl, and crotonyl acetates, butyl, amyl, and isoamyl formates, propyl and butyl propionates, ethyl and butyl butyrates, dichloromethyl, ethyl isoamyl, allyl isoamyl, ethyl amyl, dibutyl, di-isobutyl, and di sec.-butyl ethers, chloroacetone, allyl acetone, mesityl oxide and ethyl <PICT:0467481/IV/1> propyl, methyl butyl, and dipropyl ketones. The process may be used for concentrating acetic, propionic and butyric acids or mixtures of them. In the apparatus shown, the azeotropic distillation is effected in a column 103 and simple distillation of the acid in a column 102. Most of the heat for the system is supplied by a " calendria " 104 connected with the column 102 by p pipes 106, 108. The liquid acid flows down by the pipe 106 and vaporized acid ascends by the pipe 108, but part is taken by a pipe 137 to a refining column 130 in which the concentrated acid is finally treated. Vaporized aqueous acid is supplied to the column 102 by a pipe 139 connected with vaporizers 146, 147. The vapour issues at the top of the column 102 by a pipe 161 leading to the column 103; from this latter column the azeotropic mixture passes to a condenser 164 and the condensate separates into two layers in a vessel 167, the entrainer returning to the column by an overflow 174, and pipe 177 while the aqueous layer is withdrawn at an overflow 176. The pipe 177 has a branch 179 connected through a sight-glass 181 and pipe 183 with the column 102. The overflow 176 carries the aqueous layer to a pipe 189 to provide a reflux in the column 103 or to a pipe 188 which may be connected with a flash column 191. When the process is effected in the apparatus shown in Fig. 2, of Specification 383,148, the column 41 contains an excess of water. Specification 356,787 also is referred to.ALSO:In the concentration of lower aliphatic acids such as acetic acid an entraining agent is used consisting of an ester, ether, ketone, or alcohol-ester mixture of a boiling point between 25 DEG C. lower and 30 DEG C. higher than the boiling-point of the acid, and forming an azeotropic mixture with water boiling below 100 DEG C., and the supply of entrainer and aqueous acid and the heating of the column are so regulated that the lower part of the column is maintained free from entraining agent and serves to rectify aqueous acid. The apparatus may have one, two or more columns. In the apparatus shown, the azeotropic distillation is effected in a column 103 and simple distillation in a column 102. Most of the heat for the system is supplied by a "calendria" 104 connected with the column 102 by pipes 106, 108. The liquid acid flows down by the pipe 106 and the vaporized acid ascends by the pipe 108, but part is taken by a pipe 137 to a refining column 130 in which the concentrated acid is finally treated. Vaporized aqueous acid is supplied to the column 102 by a pipe 139 connected with vaporizers 146, 147. The vapour issues at the top of the column 102 by a pipe 161 leading to the column 103; from this latter column the <PICT:0467481/III/1> azeotropic mixture passes to a condenser 164, and the condensate separates into two layers in a vessel 167, the entrainer returning to the column by an overflow 174 and pipe 177, while the aqueous layer is withdrawn at an overflow 176. The pipe 177 has a branch 179 connected through a sight-glass 181 and pipe 183 with the column 102. The overflow 176 carries the aqueous layer to a pipe 189 to provide a reflux in the column 103 or to a pipe 188 which may be connected to a flash column 191.
GB2536835A 1935-09-12 1935-09-12 Processes of removing water from aqueous aliphatic acids Expired GB467481A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2536835A GB467481A (en) 1935-09-12 1935-09-12 Processes of removing water from aqueous aliphatic acids

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2536835A GB467481A (en) 1935-09-12 1935-09-12 Processes of removing water from aqueous aliphatic acids

Publications (1)

Publication Number Publication Date
GB467481A true GB467481A (en) 1937-06-14

Family

ID=10226535

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2536835A Expired GB467481A (en) 1935-09-12 1935-09-12 Processes of removing water from aqueous aliphatic acids

Country Status (1)

Country Link
GB (1) GB467481A (en)

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006100311A2 (en) * 2005-05-20 2006-09-28 Solvay (Societe Anonyme) Method for making an epoxide
FR2885903A1 (en) * 2005-05-20 2006-11-24 Solvay 0rocess of manufacturing epoxide involving halo ketone formation as a by-product, comprises eliminating at least a part of the formed halo ketone
US7930651B2 (en) 2007-01-18 2011-04-19 Research In Motion Limited Agenda display in an electronic device
US7939696B2 (en) 2005-11-08 2011-05-10 Solvay Societe Anonyme Process for the manufacture of dichloropropanol by chlorination of glycerol
US8067645B2 (en) 2005-05-20 2011-11-29 Solvay (Societe Anonyme) Process for producing a chlorhydrin from a multihydroxylated aliphatic hydrocarbon and/or ester thereof in the presence of metal salts
US8124814B2 (en) 2006-06-14 2012-02-28 Solvay (Societe Anonyme) Crude glycerol-based product, process for its purification and its use in the manufacture of dichloropropanol
US8197665B2 (en) 2007-06-12 2012-06-12 Solvay (Societe Anonyme) Aqueous composition containing a salt, manufacturing process and use
US8258350B2 (en) 2007-03-07 2012-09-04 Solvay (Societe Anonyme) Process for the manufacture of dichloropropanol
US8273923B2 (en) 2007-06-01 2012-09-25 Solvay (Societe Anonyme) Process for manufacturing a chlorohydrin
US8314205B2 (en) 2007-12-17 2012-11-20 Solvay (Societe Anonyme) Glycerol-based product, process for obtaining same and use thereof in the manufacturing of dichloropropanol
US8378130B2 (en) 2007-06-12 2013-02-19 Solvay (Societe Anonyme) Product containing epichlorohydrin, its preparation and its use in various applications
US8415509B2 (en) 2003-11-20 2013-04-09 Solvay (Societe Anonyme) Process for producing dichloropropanol from glycerol, the glycerol coming eventually from the conversion of animal fats in the manufacture of biodiesel
US8471074B2 (en) 2007-03-14 2013-06-25 Solvay (Societe Anonyme) Process for the manufacture of dichloropropanol
US8507643B2 (en) 2008-04-03 2013-08-13 Solvay S.A. Composition comprising glycerol, process for obtaining same and use thereof in the manufacture of dichloropropanol
US8536381B2 (en) 2008-09-12 2013-09-17 Solvay Sa Process for purifying hydrogen chloride
US8715568B2 (en) 2007-10-02 2014-05-06 Solvay Sa Use of compositions containing silicon for improving the corrosion resistance of vessels
US8795536B2 (en) 2008-01-31 2014-08-05 Solvay (Societe Anonyme) Process for degrading organic substances in an aqueous composition
US9309209B2 (en) 2010-09-30 2016-04-12 Solvay Sa Derivative of epichlorohydrin of natural origin

Cited By (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8415509B2 (en) 2003-11-20 2013-04-09 Solvay (Societe Anonyme) Process for producing dichloropropanol from glycerol, the glycerol coming eventually from the conversion of animal fats in the manufacture of biodiesel
US9663427B2 (en) 2003-11-20 2017-05-30 Solvay (Société Anonyme) Process for producing epichlorohydrin
US7893193B2 (en) 2005-05-20 2011-02-22 Solvay (Société Anonyme) Method for making a chlorohydrin
WO2006100311A3 (en) * 2005-05-20 2006-11-23 Solvay Method for making an epoxide
US7615670B2 (en) 2005-05-20 2009-11-10 Solvay (Société Anonyme) Method for making chlorohydrin in liquid phase in the presence of heavy compounds
FR2885903A1 (en) * 2005-05-20 2006-11-24 Solvay 0rocess of manufacturing epoxide involving halo ketone formation as a by-product, comprises eliminating at least a part of the formed halo ketone
US7906691B2 (en) 2005-05-20 2011-03-15 Solvay (Societe Anonyme) Method for making chlorohydrin in corrosion-resistant equipment
US7906692B2 (en) 2005-05-20 2011-03-15 Solvay (Societe Anonyme) Method for making a chlorohydrin by chlorinating a polyhydroxylated aliphatic hydrocarbon
WO2006100311A2 (en) * 2005-05-20 2006-09-28 Solvay (Societe Anonyme) Method for making an epoxide
US8389777B2 (en) 2005-05-20 2013-03-05 Solvay (Société Anonyme) Continuous method for making chlorhydrines
US8067645B2 (en) 2005-05-20 2011-11-29 Solvay (Societe Anonyme) Process for producing a chlorhydrin from a multihydroxylated aliphatic hydrocarbon and/or ester thereof in the presence of metal salts
US8420871B2 (en) 2005-05-20 2013-04-16 Solvay (Societe Anonyme) Process for producing an organic compound
US8106245B2 (en) 2005-05-20 2012-01-31 Solvay (Société Anonyme) Method for preparing chlorohydrin by converting polyhydroxylated aliphatic hydrocarbons
US8344185B2 (en) 2005-05-20 2013-01-01 SOLVAY (Société Anonyme Method for making a chlorhydrine by reaction between a polyhydroxylated aliphatic hydrocarbon and a chlorinating agent
US8173823B2 (en) 2005-05-20 2012-05-08 Solvay (Société Anonyme) Method for making an epoxide
US7557253B2 (en) 2005-05-20 2009-07-07 Solvay (Societe Anonyme) Method for converting polyhydroxylated aliphatic hydrocarbons into chlorohydrins
US8591766B2 (en) 2005-05-20 2013-11-26 Solvay (Societe Anonyme) Continuous process for preparing chlorohydrins
EA018479B1 (en) * 2005-05-20 2013-08-30 Солвей (Сосьете Аноним) Method for making an epoxide
US8519198B2 (en) 2005-05-20 2013-08-27 Solvay (Societe Anonyme) Method for making an epoxide
US8106246B2 (en) 2005-11-08 2012-01-31 Solvay (Societe Anonyme) Process for the manufacture of dichloropropanol by chlorination of glycerol
US7939696B2 (en) 2005-11-08 2011-05-10 Solvay Societe Anonyme Process for the manufacture of dichloropropanol by chlorination of glycerol
US8124814B2 (en) 2006-06-14 2012-02-28 Solvay (Societe Anonyme) Crude glycerol-based product, process for its purification and its use in the manufacture of dichloropropanol
US7930651B2 (en) 2007-01-18 2011-04-19 Research In Motion Limited Agenda display in an electronic device
US8258350B2 (en) 2007-03-07 2012-09-04 Solvay (Societe Anonyme) Process for the manufacture of dichloropropanol
US8471074B2 (en) 2007-03-14 2013-06-25 Solvay (Societe Anonyme) Process for the manufacture of dichloropropanol
US8273923B2 (en) 2007-06-01 2012-09-25 Solvay (Societe Anonyme) Process for manufacturing a chlorohydrin
US8399692B2 (en) 2007-06-12 2013-03-19 Solvay (Societe Anonyme) Epichlorohydrin, manufacturing process and use
US8378130B2 (en) 2007-06-12 2013-02-19 Solvay (Societe Anonyme) Product containing epichlorohydrin, its preparation and its use in various applications
US8197665B2 (en) 2007-06-12 2012-06-12 Solvay (Societe Anonyme) Aqueous composition containing a salt, manufacturing process and use
US8715568B2 (en) 2007-10-02 2014-05-06 Solvay Sa Use of compositions containing silicon for improving the corrosion resistance of vessels
US8314205B2 (en) 2007-12-17 2012-11-20 Solvay (Societe Anonyme) Glycerol-based product, process for obtaining same and use thereof in the manufacturing of dichloropropanol
US8795536B2 (en) 2008-01-31 2014-08-05 Solvay (Societe Anonyme) Process for degrading organic substances in an aqueous composition
US8507643B2 (en) 2008-04-03 2013-08-13 Solvay S.A. Composition comprising glycerol, process for obtaining same and use thereof in the manufacture of dichloropropanol
US8536381B2 (en) 2008-09-12 2013-09-17 Solvay Sa Process for purifying hydrogen chloride
US9309209B2 (en) 2010-09-30 2016-04-12 Solvay Sa Derivative of epichlorohydrin of natural origin

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