GB974432A - A process for the hydrogenation of phosphatides - Google Patents

A process for the hydrogenation of phosphatides

Info

Publication number
GB974432A
GB974432A GB4340261A GB4340261A GB974432A GB 974432 A GB974432 A GB 974432A GB 4340261 A GB4340261 A GB 4340261A GB 4340261 A GB4340261 A GB 4340261A GB 974432 A GB974432 A GB 974432A
Authority
GB
United Kingdom
Prior art keywords
phosphatide
catalyst
lecithin
hydrogenation
hydrogen
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
GB4340261A
Inventor
Paul Francis Davis
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.)
Central Soya Co Inc
Original Assignee
Central Soya 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 Central Soya Co Inc filed Critical Central Soya Co Inc
Priority to GB4340261A priority Critical patent/GB974432A/en
Publication of GB974432A publication Critical patent/GB974432A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/06Phosphorus compounds without P—C bonds
    • C07F9/08Esters of oxyacids of phosphorus
    • C07F9/09Esters of phosphoric acids
    • C07F9/10Phosphatides, e.g. lecithin
    • C07F9/103Extraction or purification by physical or chemical treatment of natural phosphatides; Preparation of compositions containing phosphatides of unknown structure

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Cosmetics (AREA)
  • Fats And Perfumes (AREA)
  • General Preparation And Processing Of Foods (AREA)

Abstract

Phosphatide (i.e. lecithin) material is hydrogenated by a process comprising first contacting a catalyst consisting of one or more of palladium, platinum, and rhodium, preferably dispersed on a carrier, with hydrogen in the absence of said phosphatide material and second contacting said phosphatide material with hydrogen in the presence of the catalyst to promote a decrease in the unsaturation of the phosphatide material. Both the pre-reduction of the catalyst and the hydrogenation of the phosphatide may be performed at 5 to 100 p.s.i.g. being preferably 45 p.s.i.g. and 15 p.s.i.a. respectively, and it is desirable to prevent contact of the catalyst with an oxidizing agent, e.g. air, between the two stages. The phosphatide may be pretreated with an acid, acid anhydride or a solvent comprising an alcohol to inhibit catalyst inactivation and, in general any solvent, or combination of solvents, in which the phosphatide is soluble but which will not inactivate the catalyst may be used for the reaction. It is desirable that such solvents should be removable under vacuum at temperatures lower than 95 DEG C. The phosphatide may also be bleached with an oxidizing agent, e.g. hydrogen peroxide, before or after hydrogenation in order to lighten the colour of the product. It is preferable to conduct the hydrogenation at below 70 DEG C. preferably 25 to 60 DEG C., and to filter off the catalyst at the end of the reaction after the addition of a filter acid. During this filtration the catalyst should be protected from oxygen and, in this connection, it is desirable to saturate the product solution with hydrogen or an inert gas, e.g. nitrogen, prior to filtration. The solvent is removed under reduced pressure and the product may be vacuum steam deodorized. Solutions of base, or aqueous suspensions of bases of limited water solubility, may be added to the product before or after deodorization to raise the aqueous pH to as high as 8.0, after which the water may be removed under vacuum. Numerous examples are given employing as the source of phosphatide commercial soybean lecithin, oil-free soybean phosphatides, alcohol-soluble or insoluble fractions of soybean phosphatides, peanut lecithin and com lecithin. The hydrogenated phosphatides obtained may be used as emulsifiers in the food and pharmaceutical industries (see Division A2).ALSO:Material obtained by the catalytic hydrogenation of phosphatide, e.g. lecithin, (see Division C2) is employed as an emulsifier in food preparations, such as ice-cream, cakes and biscuits.
GB4340261A 1961-12-05 1961-12-05 A process for the hydrogenation of phosphatides Expired GB974432A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4340261A GB974432A (en) 1961-12-05 1961-12-05 A process for the hydrogenation of phosphatides

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4340261A GB974432A (en) 1961-12-05 1961-12-05 A process for the hydrogenation of phosphatides

Publications (1)

Publication Number Publication Date
GB974432A true GB974432A (en) 1964-11-04

Family

ID=10428605

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4340261A Expired GB974432A (en) 1961-12-05 1961-12-05 A process for the hydrogenation of phosphatides

Country Status (1)

Country Link
GB (1) GB974432A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1543937A1 (en) * 1966-01-14 1970-01-08 Unilever Nv Process to improve the emulsifying effect of cephalin-containing phosphatide mixtures, especially for O / W emulsions

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1543937A1 (en) * 1966-01-14 1970-01-08 Unilever Nv Process to improve the emulsifying effect of cephalin-containing phosphatide mixtures, especially for O / W emulsions

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