GB311788A - Improvements in the production of mono or polyhydric alcohols - Google Patents

Improvements in the production of mono or polyhydric alcohols

Info

Publication number
GB311788A
GB311788A GB3255027A GB3255027A GB311788A GB 311788 A GB311788 A GB 311788A GB 3255027 A GB3255027 A GB 3255027A GB 3255027 A GB3255027 A GB 3255027A GB 311788 A GB311788 A GB 311788A
Authority
GB
United Kingdom
Prior art keywords
hydroxides
hydrogen
oxides
alcohols
per cent
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
GB3255027A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB3255027A priority Critical patent/GB311788A/en
Publication of GB311788A publication Critical patent/GB311788A/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
    • C07C31/18Polyhydroxylic acyclic alcohols

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Catalysts (AREA)

Abstract

311,788. Johnson, J. Y., (I. G. Farbenindustrie Akt.-Ges.). Dec. 2, 1927. Addition to 309,200. Alcohols.-In the process for the production of mono-and polyhydric alcohols by catalytic reduction with hydrogen of the condensation products of aldehydes or ketones or both described in the parent Specification, the condensing agent is removed from the condensation product prior to the reduction, either by precipitating the condensing agent with a suitable precipitant, such as sulphuric, oxalic or carbonic acid, or by purecipitating the condensation products, for instance in the form of saccharates, by adding metal oxides or hydroxides, especially alkaline earth oxides or hydroxides, or by extraction of the condensing agents or the condensation products with solvents such as water or alcohols. The condensing agents may be compounds of magnesium, barium, strontium, calcium, lithium, or lead, for instance the oxides, hydroxides, basic salts and salts with weak acids such as carbonates and formates and the catalysts for the reduction may be metals of the 1st and 8th groups of the periodic system, preferably with the addition of activators such as the oxides, hydroxides silicates and phosphates of the same or other elements, and preferably with a carrier such as kieselguhr or fullers' earth. In an example, a 3 per cent solution of formaldehyde is heated and stirred with lead hydroxide at 100‹ C. for an hour and after removing the undissolved lead hydroxide the dissolved lead is removed by adding dilute sulphuric acid; the filtrate is concentrated and reduced by hydrogen in presence of an activated nickel-kieselguhr catalyst, the products containing penta- and hexa-hydric alcohols together with glycol and glycerol. In another example, a 4 per cent solution of formaldehyde is heated and stirred with magnesia at 130‹ C. for 1¢ hours; the reaction mixture is concentrated to a syrup and the condensation product is extracted with alcohol, the solution being reduced with hydrogen at 25 atmospheres with a nickel-fullers' earth catalyst containing 40 per cent of nickel, which has been reduced in hydrogen at 450‹ C. The product is a mixture of polyhydric alcohols including glycol and glycerol, which are separated by distillation in vacuo.
GB3255027A 1927-12-02 1927-12-02 Improvements in the production of mono or polyhydric alcohols Expired GB311788A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3255027A GB311788A (en) 1927-12-02 1927-12-02 Improvements in the production of mono or polyhydric alcohols

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3255027A GB311788A (en) 1927-12-02 1927-12-02 Improvements in the production of mono or polyhydric alcohols

Publications (1)

Publication Number Publication Date
GB311788A true GB311788A (en) 1929-05-02

Family

ID=10340328

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3255027A Expired GB311788A (en) 1927-12-02 1927-12-02 Improvements in the production of mono or polyhydric alcohols

Country Status (1)

Country Link
GB (1) GB311788A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4247654A (en) * 1976-08-31 1981-01-27 Bayer Aktiengesellschaft Alkoxylated formose polyols and their use in polyurethane plastics

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4247654A (en) * 1976-08-31 1981-01-27 Bayer Aktiengesellschaft Alkoxylated formose polyols and their use in polyurethane plastics

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