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GB774855A - Improvements in or relating to the recovery of tocopherols from deodorizer sludges - Google Patents

Improvements in or relating to the recovery of tocopherols from deodorizer sludges

Info

Publication number
GB774855A
GB774855A GB25965/55A GB2596555A GB774855A GB 774855 A GB774855 A GB 774855A GB 25965/55 A GB25965/55 A GB 25965/55A GB 2596555 A GB2596555 A GB 2596555A GB 774855 A GB774855 A GB 774855A
Authority
GB
United Kingdom
Prior art keywords
tocopherol
sludge
per cent
concentrate
sterols
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
GB25965/55A
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.)
Eastman Kodak Co
Original Assignee
Eastman Kodak 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 Eastman Kodak Co filed Critical Eastman Kodak Co
Publication of GB774855A publication Critical patent/GB774855A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/58Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
    • C07D311/70Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4 with two hydrocarbon radicals attached in position 2 and elements other than carbon and hydrogen in position 6
    • C07D311/723,4-Dihydro derivatives having in position 2 at least one methyl radical and in position 6 one oxygen atom, e.g. tocopherols
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/352Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline 
    • A61K31/3533,4-Dihydrobenzopyrans, e.g. chroman, catechin
    • A61K31/355Tocopherols, e.g. vitamin E

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pyrane Compounds (AREA)

Abstract

Tocopherol concentrates are prepared by saponifying a vegetable oil deodorizer sludge containing 1 per cent or more of tocopherol, acidifying the resulting saponified composition, separating off the glycerine containing phase from the bottom of the reaction mixture, esterifying the fatty acids in the remaining composition with a lower monohydric alcohol, and thereafter separating from the resulting ester composition a tocopherol concentrate. The sludge may be derived from soya bean oil, or from cottonseed oil, or mixtures thereof. The saponification step may be carried out with an alkali metal hydroxide such as sodium or potassium hydroxide, in an aqueous medium or in a medium comprising a lower monohydric alcohol, preferably one containing between 1 and 4 carbon atoms such as methanol. The saponified sludge may be acidified with p-toluene-sulphonic acid or a mineral acid such as hydrochloric or sulphuric acid. After the separation of the glycerine containing phase, which settles to the bottom of the reaction mixture, the fatty acids in the remaining composition are preferably esterified with a lower monohydric alcohol containing 1 to 4 carbon atoms. The esterification is preferably effected in the presence of a catalyst such as a mineral acid-particularly hydrochloric acid in a quantity comprising 1 to 2 per cent by weight of the reaction mixture. A preferred method of operation is to use sulphuric acid to neutralize the saponified sludge and to catalyse the esterification with hydrochloric acid. The tocopherol concentrate, which at this stage is composed essentially of free tocopherols, lower monohydric alcohol esters of fatty acids and free sterols, may be separated from the ester composition by distillation, solvent extraction, crystallization, selective adsorption, or combinations thereof. The fatty acid esters are preferably removed by distillation prior to the separation of the tocopherol concentrate from the sterol fraction. The sterols are preferably separated by wintering and filtering off the relatively insoluble sterols, crystallization of the sterols being promoted by the addition of a small amount of a lower monohydric alcohol, and the resulting filtrate which usually contains tocopherols and fatty acid esters of lower monohydric alcohols may be subjected to vacuum distillation, thereby distilling off the esters followed by a tocopherol concentrate. Another method of separating a tocopherol concentrate is by distilling the crude reaction mixture to strip off the low-boiling esters, distilling off a fraction comprising essentially tocopherol and sterols, and leaching out a tocopherol concentrate with a solvent, e.g. acetone, acetonitrile, methyl ethyl ketone or isopropyl ether. The sludge treatment may be modified in that it is first enriched in alpha-tocopherol content, or the resulting tocopherol concentrate may be treated to increase the alpha-tocopherol content, e.g. methylation can be carried out by halomethylation and reduction, or by hydroxymethylation and reduction. The process is applicable to a sludge derived from soya bean oil to increase the tocopherol content from more than about 5 per cent by weight to more than about 20 per cent by weight -the tocopherol fraction in a soya bean oil sludge usually comprises 10 per cent alpha-tocopherol, 60 per cent gamma-tocopherol and 30 per cent delta-tocopherol. A number of detailed examples are given in which the sludge is derived from soya bean oil. Specification 548,731, [Group IV], is referred to.
GB25965/55A 1954-09-23 1955-09-12 Improvements in or relating to the recovery of tocopherols from deodorizer sludges Expired GB774855A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US774855XA 1954-09-23 1954-09-23

Publications (1)

Publication Number Publication Date
GB774855A true GB774855A (en) 1957-05-15

Family

ID=22138332

Family Applications (1)

Application Number Title Priority Date Filing Date
GB25965/55A Expired GB774855A (en) 1954-09-23 1955-09-12 Improvements in or relating to the recovery of tocopherols from deodorizer sludges

Country Status (1)

Country Link
GB (1) GB774855A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3335154A (en) * 1963-06-04 1967-08-08 Eastman Kodak Co Separation of tocopherols and sterols from deodorizer sludge and the like
EP0171009A2 (en) * 1984-08-02 1986-02-12 HENKEL CORPORATION (a Delaware corp.) Purification of tocopherols by extraction
ES2152856A1 (en) * 1998-10-08 2001-02-01 Biocaps S A Extraction of tocopherols from vegetable oil byproducts by catalyzed esterification of fatty acids by monohydroxylic alcohols with distillation and extraction

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3335154A (en) * 1963-06-04 1967-08-08 Eastman Kodak Co Separation of tocopherols and sterols from deodorizer sludge and the like
EP0171009A2 (en) * 1984-08-02 1986-02-12 HENKEL CORPORATION (a Delaware corp.) Purification of tocopherols by extraction
EP0171009A3 (en) * 1984-08-02 1986-06-25 Henkel Corporation Purification of tocopherols by extraction
ES2152856A1 (en) * 1998-10-08 2001-02-01 Biocaps S A Extraction of tocopherols from vegetable oil byproducts by catalyzed esterification of fatty acids by monohydroxylic alcohols with distillation and extraction

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