GB608540A - Improvements in and relating to the production of tetrahydrofurfuryl alcohol - Google Patents

Improvements in and relating to the production of tetrahydrofurfuryl alcohol

Info

Publication number
GB608540A
GB608540A GB597946A GB597946A GB608540A GB 608540 A GB608540 A GB 608540A GB 597946 A GB597946 A GB 597946A GB 597946 A GB597946 A GB 597946A GB 608540 A GB608540 A GB 608540A
Authority
GB
United Kingdom
Prior art keywords
nickel
aluminium
foraminate
alkali
prepared
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
GB597946A
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB597946A priority Critical patent/GB608540A/en
Publication of GB608540A publication Critical patent/GB608540A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/04Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D307/10Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/12Radicals substituted by oxygen atoms

Landscapes

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

Abstract

Foraminate nickel catalysts (for use in the hydrogenation of furfural and furfuryl alcohol) may be prepared by alloying nickel with a metal which is more soluble in acid or alkali, converting the alloy into granular form, and treating the granules with acid or alkali so as to remove a part of the alloying metal. Suitable alloying metals are aluminium, zinc and silicon. Catalysts so prepared from nickel-aluminium and nickel-silicon alloys may be reactivated by treatment with a current of hot dilute caustic soda solution passed preferably in the opposite direction to the flow of the materials during the reaction. Examples are given in which furfural and a mixture thereof with tetrahydrofurfuryl alcohol are hydrogenated by passage through a tube packed with alternate layers of foraminate nickel-aluminium catalyst and silicon chips. Specifications 570,843 and 608,565, [Group IV (b)], are referred to.ALSO:Tetrahydrofurfuryl alcohol is prepared from furfural or furfuryl alcohol by a liquid-phase hydrogenation process in which the starting material and hydrogen are caused to flow at a raised temperature and pressure past a foraminate nickel catalyst. The process may be effected continuously at 50-200 DEG C. and 50-500 atm. pressure, and a part of the reaction product may be returned to the reaction zones. Hydrogen substantially free from carbon monoxide, sulphur and ammonia is preferably used, but the process may be effected either under anhydrous conditions or in the presence of water. An alkali, such as sodium carbonate, may also be present. Examples are given in which furfural and a mixture thereof with tetrahydrofurfuryl alcohol are hydrogenated by passage through a tube packed with alternate layers of foraminate nickel-aluminium catalyst and silicon chips. The Provisional Specification states that cobalt may also be used as the catalyst. Catalytic agents, preparation and treatment of. Foraminate nickel catalysts may be prepared by alloying nickel with a metal which is more soluble in acid or alkali, converting the alloy into granular form, and treating the granules with acid or alkali so as to remove a part of the alloying metal. Suitable alloying metals are aluminium, zinc and silicon. Catalysts so prepared from nickel-aluminium and nickel-silicon alloys may be reactivated by treatment with a current of hot dilute caustic soda solution passed preferably in the opposite direction to the flow of the materials during the reaction. Specifications 570,843, [Group III], and 608,565 are referred to.
GB597946A 1946-02-26 1946-02-26 Improvements in and relating to the production of tetrahydrofurfuryl alcohol Expired GB608540A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB597946A GB608540A (en) 1946-02-26 1946-02-26 Improvements in and relating to the production of tetrahydrofurfuryl alcohol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB597946A GB608540A (en) 1946-02-26 1946-02-26 Improvements in and relating to the production of tetrahydrofurfuryl alcohol

Publications (1)

Publication Number Publication Date
GB608540A true GB608540A (en) 1948-09-16

Family

ID=9806179

Family Applications (1)

Application Number Title Priority Date Filing Date
GB597946A Expired GB608540A (en) 1946-02-26 1946-02-26 Improvements in and relating to the production of tetrahydrofurfuryl alcohol

Country Status (1)

Country Link
GB (1) GB608540A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2763666A (en) * 1951-03-20 1956-09-18 Huillard Sa Ets Method for the catalytic hydrogenation of furfural

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2763666A (en) * 1951-03-20 1956-09-18 Huillard Sa Ets Method for the catalytic hydrogenation of furfural

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