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GB654655A - Electrolytic oxidation process - Google Patents

Electrolytic oxidation process

Info

Publication number
GB654655A
GB654655A GB18887/47A GB1888747A GB654655A GB 654655 A GB654655 A GB 654655A GB 18887/47 A GB18887/47 A GB 18887/47A GB 1888747 A GB1888747 A GB 1888747A GB 654655 A GB654655 A GB 654655A
Authority
GB
United Kingdom
Prior art keywords
acid
quinoline
anode
sulphuric acid
lead
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
GB18887/47A
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.)
Merck and Co Inc
Original Assignee
Merck and Co Inc
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 Merck and Co Inc filed Critical Merck and Co Inc
Publication of GB654655A publication Critical patent/GB654655A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/79Acids; Esters
    • C07D213/803Processes of preparation
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C11/00Multi-cellular glass ; Porous or hollow glass or glass particles
    • C03C11/005Multi-cellular glass ; Porous or hollow glass or glass particles obtained by leaching after a phase separation step
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C23/00Other surface treatment of glass not in the form of fibres or filaments
    • C03C23/008Other surface treatment of glass not in the form of fibres or filaments comprising a lixiviation step
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25BELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B3/00Electrolytic production of organic compounds
    • C25B3/20Processes
    • C25B3/23Oxidation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Electrochemistry (AREA)
  • Metallurgy (AREA)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)

Abstract

654,655. Electrolytic preparation of quinolinic. acid. MERCK & CO., Inc. July 16, 1947, No. 18887. Convention date, Nov. 6, 1941. [Class 41] A process of preparing quinolinic acid electrolytically comprises reacting quinoline with about four times its weight of 20 per cent oleum, preferably for about twenty minutes at about 180‹ C. diluting the resulting mixture of sulphonated quinoline and sulphuric acid to approximately twice its volume with water, and delivering it to the anode compartment of an electrolytic cell having a lead anode coated with lead dioxide, oxidizing the quinoline at a current density of 0.5 to 1.5 amperes per square decimetre, until approximately 370 ampere hours per mole. of sulphonated quinoline have been consumed, then reducing the current density to 0.5 to 0.75 amperes per square decimetre for approximately 220 ampere hours per mole., and recovering quinolinic acid from the anolyte. The cathode compartment may be packed with porous acid-resisting substance such as sand and kept filled with sulphuric acid. The cathode may be of acid-resisting metal such as copper, a highly-resistant steel, chromel alloy, or may be of graphite. The anode may be of lead coated with lead dioxide by electrolysis in sulphuric acid electrolyte, and may be a cylindrical sheet, a coil or a series of plates. It may be activated before use either by passing a current through the cell with the anode immersed in sulphuric acid containing a depolarizer such as quinoline or picoline, or by passing a current through the cell and reversing its direction for at least five intervals of ten minutes.
GB18887/47A 1941-11-06 1947-07-16 Electrolytic oxidation process Expired GB654655A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US262275XA 1941-11-06 1941-11-06

Publications (1)

Publication Number Publication Date
GB654655A true GB654655A (en) 1951-06-27

Family

ID=21830579

Family Applications (1)

Application Number Title Priority Date Filing Date
GB18887/47A Expired GB654655A (en) 1941-11-06 1947-07-16 Electrolytic oxidation process

Country Status (3)

Country Link
CH (1) CH262275A (en)
FR (1) FR939548A (en)
GB (1) GB654655A (en)

Also Published As

Publication number Publication date
CH262275A (en) 1949-06-30
FR939548A (en) 1948-11-17

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