GB802860A - Refining alcohols - Google Patents

Refining alcohols

Info

Publication number
GB802860A
GB802860A GB1094557A GB1094557A GB802860A GB 802860 A GB802860 A GB 802860A GB 1094557 A GB1094557 A GB 1094557A GB 1094557 A GB1094557 A GB 1094557A GB 802860 A GB802860 A GB 802860A
Authority
GB
United Kingdom
Prior art keywords
borohydride
sodium borohydride
alcohol
treated
colour
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
GB1094557A
Inventor
Robert H Wise
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.)
Standard Oil Co
Original Assignee
Standard Oil 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 Standard Oil Co filed Critical Standard Oil Co
Priority to GB1094557A priority Critical patent/GB802860A/en
Publication of GB802860A publication Critical patent/GB802860A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01GPRELIMINARY TREATMENT OF FIBRES, e.g. FOR SPINNING
    • D01G15/00Carding machines or accessories; Card clothing; Burr-crushing or removing arrangements associated with carding or other preliminary-treatment machines
    • D01G15/02Carding machines
    • D01G15/12Details
    • D01G15/46Doffing or like arrangements for removing fibres from carding elements; Web-dividing apparatus; Condensers
    • D01G15/62Slubbing-winding apparatus

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Water-immiscible synthetic C4-C15 alcohols, produced by reaction of mixtures containing carbon monoxide and hydrogen, are contacted with an alkali metal (or ammonium) borohydride or an alkaline earth metal borohydride to destroy undesirable impurities. The process is applicable to alcohols obtained by the Fischer-Tropsch and oxo processes. The purification may be carried out simultaneously with a distillation whereby the purified alcohol is separated from the crude alcohol feedstock, or may be used as a finishing process to improve the colour and remove colour-forming impurities from the previously distilled alcohol. The purified alcohols may be used to produce esters of improved colour or alternatively the borohydride may be added to the esterification mixture. The preferred borohydrides are those of lithium, sodium, potassium, calcium, magnesium and barium. The borohydrides may be used in the form of a dilute aqueous solution. If used in the solid form they may be mixed with an inert filtering medium such as clay or diatomaceous earth. A polyvalent metal halide, e.g. the chloride or bromide of calcium, aluminium, gallium, titanium or zirconium, may also be present. In the examples: (a) crude isooctylalcohol obtained by the oxo process is heated with sodium borohydride; (b) a crude C8 alcohol obtained by the oxo process is treated with (i) sodium borohydride, (ii) lithium borohydride, and (iii) a mixture of calcium chloride and sodium borohydride; (c) octyl alcohol obtained by the oxo process is treated with potassium borohydride; (d) octyl alcohol obtained by the oxo process is treated with sodium borohydride; the purified alcohol is esterified with phthalic acid in the presence of a trace of sulphuric acid; (e) octyl alcohol obtained by reacting carbon monoxide and hydrogen with a heptene fraction in the presence of a cobalt catalyst is treated with sodium borohydride; and (f) octyl alcohol obtained by the oxo process is esterified with phthalic anhydride, using sulphuric acid as catalyst, in the presence of sodium borohydride. In each case the colour of the product is improved.
GB1094557A 1957-04-03 1957-04-03 Refining alcohols Expired GB802860A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1094557A GB802860A (en) 1957-04-03 1957-04-03 Refining alcohols

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1094557A GB802860A (en) 1957-04-03 1957-04-03 Refining alcohols

Publications (1)

Publication Number Publication Date
GB802860A true GB802860A (en) 1958-10-15

Family

ID=9977188

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1094557A Expired GB802860A (en) 1957-04-03 1957-04-03 Refining alcohols

Country Status (1)

Country Link
GB (1) GB802860A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3373174A (en) * 1964-12-17 1968-03-12 Armour & Co A method for improving color and the color and odor stability of fatty amides
US4959468A (en) * 1987-06-12 1990-09-25 Henkel Kommanditgesellschaft Auf Aktien Color stabilization method for glycoside products

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3373174A (en) * 1964-12-17 1968-03-12 Armour & Co A method for improving color and the color and odor stability of fatty amides
US4959468A (en) * 1987-06-12 1990-09-25 Henkel Kommanditgesellschaft Auf Aktien Color stabilization method for glycoside products

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