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GB767103A - Electrolytic production of weak acids - Google Patents

Electrolytic production of weak acids

Info

Publication number
GB767103A
GB767103A GB27396/53A GB2739653A GB767103A GB 767103 A GB767103 A GB 767103A GB 27396/53 A GB27396/53 A GB 27396/53A GB 2739653 A GB2739653 A GB 2739653A GB 767103 A GB767103 A GB 767103A
Authority
GB
United Kingdom
Prior art keywords
acid
weak acid
compartments
compartment
salt
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
GB27396/53A
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.)
Rohm and Haas Co
Original Assignee
Rohm and Haas 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 Rohm and Haas Co filed Critical Rohm and Haas Co
Publication of GB767103A publication Critical patent/GB767103A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B33/00Silicon; Compounds thereof
    • C01B33/113Silicon oxides; Hydrates thereof
    • C01B33/12Silica; Hydrates thereof, e.g. lepidoic silicic acid
    • C01B33/14Colloidal silica, e.g. dispersions, gels, sols
    • C01B33/141Preparation of hydrosols or aqueous dispersions
    • C01B33/142Preparation of hydrosols or aqueous dispersions by acidic treatment of silicates
    • C01B33/143Preparation of hydrosols or aqueous dispersions by acidic treatment of silicates of aqueous solutions of silicates
    • C01B33/1435Preparation of hydrosols or aqueous dispersions by acidic treatment of silicates of aqueous solutions of silicates using ion exchangers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D61/00Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
    • B01D61/42Electrodialysis; Electro-osmosis ; Electro-ultrafiltration; Membrane capacitive deionization
    • B01D61/44Ion-selective electrodialysis
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B17/00Sulfur; Compounds thereof
    • C01B17/48Sulfur dioxide; Sulfurous acid

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Water Supply & Treatment (AREA)
  • Health & Medical Sciences (AREA)
  • Urology & Nephrology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • Water Treatment By Electricity Or Magnetism (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)

Abstract

767,103. Electrolytically preparing weak acids. ROHM & HAAS CO. Oct. 6, 1953 [Oct. 17, 1952], No. 27396/53. Drawings to Specification. Class 41. A water-soluble salt of a weak acid is converted into the weak acid by passing D.C. through a cell including one or more identical groups of two compartments, one containing a strong mineral acid, e.g. hydrochloric or sulphuric acid and the other the water-soluble salt of the weak acid, the first mineral acid compartment housing the anode and the last weak acid water-soluble salt compartment being adjacent a cathode compartment containing an aqueous electrolyte, e.g. of the hydroxide of the metal of weak acid salt typically an alkali metal, all of the compartments being separated by cationically permeable diaphragms containing a cation exchange resin. The process can be applied to the preparation of organic acids such as acetic, propionic, butyric, itaconic, maleic, fumaric, acrylic, tartaric, citric, sebacic, ascorbic, oleic, and stearic acids as well as of inorganic acids such as sulphurous, arsenious and silicic acids. Typically the strong mineral acid is sulphuric acid, the weak acid salt is sodium acetate, and the catholyte is caustic soda solution, hydrogen and oxygen being evolved. If only one weak acid salt compartment is employed between the anode and cathode compartments, it is only necessary to add water to the anolyte which may be removed at will, to add sodium acetate to the intermediate compartment and to remove acetic acid as a solution, and to add dilute electrolyte, e.g. sodium hydroxide, to the catholyte removing the more concentrated caustic soda solution formed. If hydrochloric acid is used in the anode compartment chlorine is evolved instead of oxygen and hydrochloric acid must be added. Valve supply pipes are provided above the levels of the solutions in the compartments and draw-off pipes are provided at the bottom of the compartments. If a number of weak acid salt and strong mineral acid compartments are provided, the weak acid and its salt are continuously successively transferred from the compartment nearest the cathode which receives further weak acid salt to those nearer the anode and the weak acid is removed from that adjacent the anode, water, if sulphuric acid is used, or hydrochloric acid being supplied to the intervening mineral acid compartments. The cationically permeable diaphragms are preferably of the kind described and claimed in Specification 719,315 typically of polyethylene, polyvinyl chloride, natural or synthetic rubber containing a sulphonated copolymer of styrene and divinyl benzene prepared by the process of U.S.A. Specification 2,366,007. A potential of 11-12 volts is applied to the cell to pass between platinum electrodes a current of 60 amps/sq. ft. initially, falling to 6 amps/sq. ft. at the end of operation. Specifications 489,437, 498,251, 515,517, 516,609, 521,207, [all in Group IV], 693,166, 720,002, and U.S.A. Specification 2,340,111 also are referred to.
GB27396/53A 1952-10-17 1953-10-06 Electrolytic production of weak acids Expired GB767103A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US315243A US2921005A (en) 1952-10-17 1952-10-17 Electrolytic conversions with permselective membranes

Publications (1)

Publication Number Publication Date
GB767103A true GB767103A (en) 1957-01-30

Family

ID=23223516

Family Applications (1)

Application Number Title Priority Date Filing Date
GB27396/53A Expired GB767103A (en) 1952-10-17 1953-10-06 Electrolytic production of weak acids

Country Status (7)

Country Link
US (1) US2921005A (en)
BE (1) BE523563A (en)
CH (1) CH327721A (en)
DE (1) DE1054068B (en)
FR (1) FR1084927A (en)
GB (1) GB767103A (en)
NL (1) NL82530C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4330378A (en) 1979-11-28 1982-05-18 Kernforschungsanlage Julich Gmbh Electrolysis cell and method for electrolytic production of hydrogen

Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3247133A (en) * 1956-06-18 1966-04-19 American Mach & Foundry Method of forming graft copolymer ion exchange membranes
US3330749A (en) * 1958-02-11 1967-07-11 Takeda Chemical Industries Ltd Process for treating amino acid solution
US3220941A (en) * 1960-08-03 1965-11-30 Hooker Chemical Corp Method for electrolysis
US3113911A (en) * 1960-09-06 1963-12-10 Armour Pharma Process of preparing aluminum chlorhydroxides and aluminum hydroxide
NL269837A (en) * 1960-10-04
US3193480A (en) * 1963-02-01 1965-07-06 Monsanto Co Adiponitrile process
US3105023A (en) * 1961-03-14 1963-09-24 Standard Oil Co Electrochemical manufacture of cyanogen halides
US3433726A (en) * 1962-06-08 1969-03-18 Ionics Method and apparatus for treating liquid milk products
US3335079A (en) * 1962-11-19 1967-08-08 American Mach & Foundry Electrodialysis apparatus including vertically suspended ion exchange membranes
US3250392A (en) * 1964-02-17 1966-05-10 Honeywell Inc Water softener system control apparatus
US3395087A (en) * 1964-06-09 1968-07-30 Sulphite Products Corp Electrodialysis cell
OA02233A (en) * 1965-07-01 1970-05-05 Ch Gervais S A Improvements made to the manufacture of cheese doughs and milk curds.
US3411998A (en) * 1966-04-06 1968-11-19 Gen Dynamics Corp Process for reclaiming spent alkali metal carboxylate solutions
US3776530A (en) * 1971-03-25 1973-12-04 Lau Inc Electrodialytic demineralizing unit for humidification purposes
US3964985A (en) * 1974-10-29 1976-06-22 Ionics, Incorporated Electrodialysis apparatus and process for ion modification
FR2434872A1 (en) * 1978-08-30 1980-03-28 Air Liquide PROCESS FOR THE PREPARATION OF PEROXYDISULFATE OF ALKALINE METALS AND AMMONIUM
FR2476077A1 (en) * 1980-02-19 1981-08-21 Rhone Poulenc Ind NEW PROCESS FOR THE PREPARATION OF METHIONINE
US4391841A (en) * 1980-03-28 1983-07-05 Kollmorgen Technologies Corporation Passivation of metallic equipment surfaces in electroless copper deposition processes
DE3126860A1 (en) * 1981-07-08 1983-01-27 BIOTRONIK Wissenschaftliche Geräte GmbH, 6000 Frankfurt METHOD AND DEVICE FOR QUANTITATIVELY DETERMINING CATIONS OR ANIONS BY ION CHROMATOGRAPHY
US4684453A (en) * 1984-10-26 1987-08-04 Vaughan Daniel J Purification of dye baths
US4566956A (en) * 1984-12-07 1986-01-28 The Dow Chemical Company Electrochemical conversion of soluble salts of insoluble acids to their acid form
EP0184381B1 (en) * 1984-12-07 1989-05-31 The Dow Chemical Company Electrochemical process and cell
US4652350A (en) * 1984-12-07 1987-03-24 The Dow Chemical Company Electrochemical process
JPS61261488A (en) * 1985-05-15 1986-11-19 Musashino Kagaku Kenkyusho:Kk Electrolyzing method for alkaline metallic salt of amino acid
DE3542861A1 (en) * 1985-12-04 1987-06-11 Huels Chemische Werke Ag METHOD FOR OBTAINING L-APPLE ACID
CA1337562C (en) * 1989-04-14 1995-11-14 Daniel A. D. Boateng Method for separating dissolved species by electrodialysis
US4985127A (en) * 1989-12-29 1991-01-15 Vaughan Daniel J Electrodialytic conversion of multivalent metal salts using sulfonate ions
US5310465A (en) * 1990-06-14 1994-05-10 Vaughan Daniel J Electrodialytic oxydation-reduction of metals
US6140428A (en) * 1992-06-17 2000-10-31 Basf Aktiengesellschaft Simultaneous production of dicarboxylic acids and diamines by splitting polyamides into their monomeric constituents
DE4342668A1 (en) * 1993-12-15 1995-06-22 Basf Ag Process for the recovery of carboxylic acids from their salts
CN105087677A (en) * 2014-04-21 2015-11-25 怀来县长城生物化学工程有限公司 D-(-)-tartaric acid clean production process based on bipolar membrane electroosmosis technology
CN105087676A (en) * 2014-04-21 2015-11-25 怀来县长城生物化学工程有限公司 L-(+)-tartaric acid clean production process based on bipolar membrane electroosmosis technology

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2592686A (en) * 1952-04-15 Electrolytic production of fatty
US634271A (en) * 1898-01-21 1899-10-03 Henri Plater-Syberg Process of extracting acetic acid from alkaline acetates.
US2033732A (en) * 1934-08-27 1936-03-10 Firm Hanseatische Muhlenwerke Process for the working up of soaps
US2636852A (en) * 1949-07-09 1953-04-28 Ionics Method of electrodialyzing aqueous solutions and apparatus therefor
NL96474C (en) * 1949-07-09
NL96481C (en) * 1950-07-21

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4330378A (en) 1979-11-28 1982-05-18 Kernforschungsanlage Julich Gmbh Electrolysis cell and method for electrolytic production of hydrogen

Also Published As

Publication number Publication date
NL82530C (en)
US2921005A (en) 1960-01-12
FR1084927A (en) 1955-01-25
CH327721A (en) 1958-02-15
DE1054068B (en) 1959-04-02
BE523563A (en)

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