US2218971A - Recovery of sterols - Google Patents
Recovery of sterols Download PDFInfo
- Publication number
- US2218971A US2218971A US266408A US26640839A US2218971A US 2218971 A US2218971 A US 2218971A US 266408 A US266408 A US 266408A US 26640839 A US26640839 A US 26640839A US 2218971 A US2218971 A US 2218971A
- Authority
- US
- United States
- Prior art keywords
- sterols
- quick lime
- water
- soaps
- porous mass
- 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 - Lifetime
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- 229930182558 Sterol Natural products 0.000 title description 58
- 150000003432 sterols Chemical class 0.000 title description 58
- 235000003702 sterols Nutrition 0.000 title description 58
- 238000011084 recovery Methods 0.000 title description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 56
- 239000000344 soap Substances 0.000 description 36
- 239000000203 mixture Substances 0.000 description 29
- 239000000292 calcium oxide Substances 0.000 description 28
- 235000012255 calcium oxide Nutrition 0.000 description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- 239000000463 material Substances 0.000 description 20
- 238000000034 method Methods 0.000 description 20
- 239000002904 solvent Substances 0.000 description 17
- 238000002156 mixing Methods 0.000 description 11
- 239000003513 alkali Substances 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 238000000605 extraction Methods 0.000 description 7
- 239000000284 extract Substances 0.000 description 6
- 239000003784 tall oil Substances 0.000 description 6
- 239000003549 soybean oil Substances 0.000 description 5
- 235000012424 soybean oil Nutrition 0.000 description 5
- LGJMUZUPVCAVPU-UHFFFAOYSA-N beta-Sitostanol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)CCC(CC)C(C)C)C1(C)CC2 LGJMUZUPVCAVPU-UHFFFAOYSA-N 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- OILXMJHPFNGGTO-UHFFFAOYSA-N (22E)-(24xi)-24-methylcholesta-5,22-dien-3beta-ol Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)C=CC(C)C(C)C)C1(C)CC2 OILXMJHPFNGGTO-UHFFFAOYSA-N 0.000 description 3
- OQMZNAMGEHIHNN-UHFFFAOYSA-N 7-Dehydrostigmasterol Natural products C1C(O)CCC2(C)C(CCC3(C(C(C)C=CC(CC)C(C)C)CCC33)C)C3=CC=C21 OQMZNAMGEHIHNN-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003518 caustics Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- NLQLSVXGSXCXFE-UHFFFAOYSA-N sitosterol Natural products CC=C(/CCC(C)C1CC2C3=CCC4C(C)C(O)CCC4(C)C3CCC2(C)C1)C(C)C NLQLSVXGSXCXFE-UHFFFAOYSA-N 0.000 description 3
- KZJWDPNRJALLNS-VPUBHVLGSA-N (-)-beta-Sitosterol Natural products O[C@@H]1CC=2[C@@](C)([C@@H]3[C@H]([C@H]4[C@@](C)([C@H]([C@H](CC[C@@H](C(C)C)CC)C)CC4)CC3)CC=2)CC1 KZJWDPNRJALLNS-VPUBHVLGSA-N 0.000 description 2
- CSVWWLUMXNHWSU-UHFFFAOYSA-N (22E)-(24xi)-24-ethyl-5alpha-cholest-22-en-3beta-ol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)C=CC(CC)C(C)C)C1(C)CC2 CSVWWLUMXNHWSU-UHFFFAOYSA-N 0.000 description 2
- KLEXDBGYSOIREE-UHFFFAOYSA-N 24xi-n-propylcholesterol Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)CCC(CCC)C(C)C)C1(C)CC2 KLEXDBGYSOIREE-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- LPZCCMIISIBREI-MTFRKTCUSA-N Citrostadienol Natural products CC=C(CC[C@@H](C)[C@H]1CC[C@H]2C3=CC[C@H]4[C@H](C)[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C)C(C)C LPZCCMIISIBREI-MTFRKTCUSA-N 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- ARVGMISWLZPBCH-UHFFFAOYSA-N Dehydro-beta-sitosterol Natural products C1C(O)CCC2(C)C(CCC3(C(C(C)CCC(CC)C(C)C)CCC33)C)C3=CC=C21 ARVGMISWLZPBCH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 229920001131 Pulp (paper) Polymers 0.000 description 2
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- HZYXFRGVBOPPNZ-UHFFFAOYSA-N UNPD88870 Natural products C1C=C2CC(O)CCC2(C)C2C1C1CCC(C(C)=CCC(CC)C(C)C)C1(C)CC2 HZYXFRGVBOPPNZ-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- MJVXAPPOFPTTCA-UHFFFAOYSA-N beta-Sistosterol Natural products CCC(CCC(C)C1CCC2C3CC=C4C(C)C(O)CCC4(C)C3CCC12C)C(C)C MJVXAPPOFPTTCA-UHFFFAOYSA-N 0.000 description 2
- NJKOMDUNNDKEAI-UHFFFAOYSA-N beta-sitosterol Natural products CCC(CCC(C)C1CCC2(C)C3CC=C4CC(O)CCC4C3CCC12C)C(C)C NJKOMDUNNDKEAI-UHFFFAOYSA-N 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- KZJWDPNRJALLNS-VJSFXXLFSA-N sitosterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CC[C@@H](CC)C(C)C)[C@@]1(C)CC2 KZJWDPNRJALLNS-VJSFXXLFSA-N 0.000 description 2
- 235000015500 sitosterol Nutrition 0.000 description 2
- 229950005143 sitosterol Drugs 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- HCXVJBMSMIARIN-PHZDYDNGSA-N stigmasterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)/C=C/[C@@H](CC)C(C)C)[C@@]1(C)CC2 HCXVJBMSMIARIN-PHZDYDNGSA-N 0.000 description 2
- 235000016831 stigmasterol Nutrition 0.000 description 2
- 229940032091 stigmasterol Drugs 0.000 description 2
- BFDNMXAIBMJLBB-UHFFFAOYSA-N stigmasterol Natural products CCC(C=CC(C)C1CCCC2C3CC=C4CC(O)CCC4(C)C3CCC12C)C(C)C BFDNMXAIBMJLBB-UHFFFAOYSA-N 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- RQOCXCFLRBRBCS-UHFFFAOYSA-N (22E)-cholesta-5,7,22-trien-3beta-ol Natural products C1C(O)CCC2(C)C(CCC3(C(C(C)C=CCC(C)C)CCC33)C)C3=CC=C21 RQOCXCFLRBRBCS-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- DNVPQKQSNYMLRS-NXVQYWJNSA-N Ergosterol Natural products CC(C)[C@@H](C)C=C[C@H](C)[C@H]1CC[C@H]2C3=CC=C4C[C@@H](O)CC[C@]4(C)[C@@H]3CC[C@]12C DNVPQKQSNYMLRS-NXVQYWJNSA-N 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 241000418087 Physostigma venenosum Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 210000004102 animal cell Anatomy 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- DNVPQKQSNYMLRS-SOWFXMKYSA-N ergosterol Chemical compound C1[C@@H](O)CC[C@]2(C)[C@H](CC[C@]3([C@H]([C@H](C)/C=C/[C@@H](C)C(C)C)CC[C@H]33)C)C3=CC=C21 DNVPQKQSNYMLRS-SOWFXMKYSA-N 0.000 description 1
- 239000012259 ether extract Substances 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 210000002683 foot Anatomy 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005325 percolation Methods 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/48—Fabaceae or Leguminosae (Pea or Legume family); Caesalpiniaceae; Mimosaceae; Papilionaceae
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/13—Coniferophyta (gymnosperms)
- A61K36/15—Pinaceae (Pine family), e.g. pine or cedar
Definitions
- Patented Oct. 22, 1940 PATENT cal-let.
- the present invention relates to the production of sterols, particularly of sterols and particularly relates to their extraction from plant and animal sources.
- sterols occur in many vegetable and animal products associated with fats and oils. Soybean oil contains an appreciable though small amount of sterols consisting principally of stigmasterol (16-20%) and larger amounts of sitosterol (8480%). The tall oil soaps and tall oil obtained from the digestion of wood pulp also contain an appreciable quantity sitosterol. Yeast is another common source of sterols, ergosterol being the principal one. Cholesterol is of animal origin and occurs in all animal tissues. These sterols occur in nature, partlyin the free condition and partly esterifled with higher fatty acids.
- the usual methods of isolation involve subjecting the fatty fraction containing the sterols ten saponiflcation step with alkali, preferably an alcoholic alkali solution and extracting the unsaponifiable sterols with a solvent such as ether,
- the soaps formed are of a gummy, heavy nature from which it is hard to extract all of the sterols. They are not of such a nature that they can be extracted by a continuous process, and large amounts of solvent are necessary.
- saponified material may be shaken with the solvent to facilitate the extraction but this results in the formation of stitl emulsions which are difllcult to separate, the only feasible procedure being to use large amounts of solvent and to dilute the solvent layer above the emulsion since a large amount of solvent is retained in the emulsion.
- drying of the soap is attempted other diiiiculties are encountered. As is known the drying of soaps is a diificult procedure and when vacuum drying is resorted to, there-ls a large amount of foaming and bubbling over of the foam.
- the saponi-' tied fatty materials-containing the sterols. are treated with quick lime. Water present in the mixture reacts with the quick lime, the heat produced resulting in converting additional water to steam. The steam generated in situ in the soap causes a pumng of the soap, producing a porous granular mass which is easily extracted with 'relatively small amounts of solvent. The porous character of the mass enables ready percolation'ot the solvent with free access'oi the solvent to all parts of the mass.
- the soapy material containing the sterols treatedin this manner can be readily extracted by a counter current extraction, a continuous extraction such as in a Soxhlet-tyriekxtractor, or by any other highly eillcient extraction method.
- the extract can,, then be evaporated to recover the sterols. in a fairly pure form.
- This fairly pure product may be further purified by crystallization of the sterols from'alcohol solution or by other well. known purification methods.
- Before evaporating the extract it is desirable but not necessary to wash the extract with an alkali solution to remove any traces of oil or soap which may be present.
- Example I 200 pounds of a concentrated traction of soy bean oil containing the sterols was treated with pounds of 50% caustic soda-solution, and the mixture heated to about F. for about 15 to 20 minutes, and l00pounds of quick lime added and the mixture agitated to mix in the quick lime. After a short additlonalwarming the mixture began to pufi up, and the agitation was continued. -The mixture heated up rapidly, and in a short time the entire mixture had been converted into a dry, crumbly, readily permeable the Example ll 100 pounds of soy bean 011 containing the sterols in higher concentration than in the original oil was heated'in a shallow pan to 180 F.
- the porous mass was then extracted with ether in a Soxhlet extractor.
- the ether extract was then dropped into hot alcohol, whereupon the ether was evaporated, the sterols went into solution, and the impurities precipitated. After filtering the alcoholic solution'hot, it was cooled and the sterols crystallized from solution.
- the sterols recovered were of substantially 100% purity and consistedprincipally of stigmasterol and sistosterol.
- Example III To 500 grams of crude tall oil soap containing 31% moisture as obtained from the treatment of wood pulp with caustic, was added 500 grams of quick lime, and the mixturewarmed to about 100 C. with agitation. Afters few minutes the -mixture began to pull up. Due to the excessive heat caused by the largeamount of water the mixture was cooled. In a few minutes the entire mass had been converted into a dry crumbly mass of porous granules from which the sterols were extracted and recrystallized as in Example I. About 15 grams of practically colorless once crystallized sterols were obtained. 4
- tall oil soap In place of tall oil soap the tall oil itself as obtainable on the market may be used and first saponified with alkali.
- the soaps used or formed for thetreatment with quick lime are liquid or soft soaps, such as sodium and potassium soaps. Harder soaps made with other basic radicals may be used however.
- the crude mixture of soap, sterol, and water to which the quick lime is added is of a soft or liquid consistency. Ammonium soaps or other soaps containing moieties volatile at the temperature generated by the reaction of the quick lime with water may be used and the gases so generated aid the pulling action. A dehydrated soap, however, should not be used as the reaction between the quick lime and water will not occur.
- Any suitable source of raw material containing sterols may be used, such as soy bean oil, Calabar beans, yeast, animal cells, tall oil and its soaps, soybean oil foots, 'etc.
- the amount of lime used should be sufiicient to produce the pulling action, and preferably is sumcientto convert. into steam all of the water not reacted with the lime. It need not be sumcient to completely form calcium soaps from all of the alkali soaps when such are used.
- the porous granular mass is a mixture of the sodium and calcium soaps containing the sterols. So far as is known the treatment with quick lime does not affect the sterols.
- sterol solvents which are nonsolvents for soap may be used such asprises providing a crude mixture containing soaps
- the process of recovering sterols which comprises providing a crude mixture containing alkali soaps, sterols and water, mixing suiiicient quick lime with said crude mixture to form a porous mass, and extracting the sterols from said porous mass.
- the step which comprises mixing suflicient quick lime with the saponifled material before drying or extracting the same to form a porous mass.
- the process of recovering sterols which comprises providing a crude mixture containing soaps, sterols and water, mixing sufficient quick lime with said crude mixture to cause substantial evaporation of water and to convert the mixture into a porous mass, extracting the sterols from said porous mass, washing the extract with an alkali solution, and recovering the sterols from the washed extract.
- the process of recovering sterols which comprises providing a crude mixture of soft consistency of soap, sterols and water, mixing sufficient quick lime with said crude mixture to form a porous mass, and extracting sterols from said porous mass.
- the steps which comprise providing a crude mixture of soap, sterols and water and mixing quick lime with said crude mixture.
- said soap mixture containing an ingredient in addition to the water which is volatile at the temperatures generated by the reaction of the quick lime and water whereby the steam formed and the gas generated by the heat of the reaction between the quick lime and water produces a porous mass readily extractible by solvents.
- the process of extraction comprising the steps of first providing a crude mixture of soap, water and a substance to be extracted, adding sumc'ient quick lime to the crude mixture to form a porous mass, and then extracting the porous mass with a. solvent for the material to be extracted'which is a nonsolvent for soap.
- the method of recovering sterols from fatty materials containing the same which comprises converting the fatty materials to soap. suflicient amounts of quick lime and water being reacted in the process to generate steam and to form a dry crumbly porous mass readily percolated by solvents, and extracting the sterols from the porous mass.
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- Health & Medical Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Alternative & Traditional Medicine (AREA)
- Biotechnology (AREA)
- Botany (AREA)
- Medical Informatics (AREA)
- Medicinal Chemistry (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Steroid Compounds (AREA)
- Fats And Perfumes (AREA)
Description
Patented Oct. 22, 1940 PATENT cal-let.
se i- RECOVERY OF STEBOLS' Percy L. Julian. and Edwin Wildfire: and Norman C. Krause, Chicago, IlL, assignorl Cleveland,
to The Glidden Company,
Ohio, a I
- lWo Drawing. hpplicatlonbm'll6i 1939,
sumxazestos is-cmmnlctzeo-m I 1 age of the original material' treated. since The present invention relates to the production of sterols, particularly of sterols and particularly relates to their extraction from plant and animal sources.
It is known that sterols occur in many vegetable and animal products associated with fats and oils. Soybean oil contains an appreciable though small amount of sterols consisting principally of stigmasterol (16-20%) and larger amounts of sitosterol (8480%). The tall oil soaps and tall oil obtained from the digestion of wood pulp also contain an appreciable quantity sitosterol. Yeast is another common source of sterols, ergosterol being the principal one. Cholesterol is of animal origin and occurs in all animal tissues. These sterols occur in nature, partlyin the free condition and partly esterifled with higher fatty acids.
The usual methods of isolation involve subjecting the fatty fraction containing the sterols ten saponiflcation step with alkali, preferably an alcoholic alkali solution and extracting the unsaponifiable sterols with a solvent such as ether,
trichlcrethylene, etc. However, considerable difliculty is encountered in extracting the soap formed, and none of the known methods are sufliciently simple and easy to enable the, sterols to be manufactured commercially at a price low enough to encourage their use.
The soaps formed are of a gummy, heavy nature from which it is hard to extract all of the sterols. They are not of such a nature that they can be extracted by a continuous process, and large amounts of solvent are necessary. The
saponified material may be shaken with the solvent to facilitate the extraction but this results in the formation of stitl emulsions which are difllcult to separate, the only feasible procedure being to use large amounts of solvent and to dilute the solvent layer above the emulsion since a large amount of solvent is retained in the emulsion. When drying of the soap is attempted other diiiiculties are encountered. As is known the drying of soaps is a diificult procedure and when vacuum drying is resorted to, there-ls a large amount of foaming and bubbling over of the foam.
In the latest published method of recoveringlowed by repeated was ings of the extract. As
is readily apparent this involves the use of much solvent, much time, and many operations, and greatly increases the cost of the sterols, which areat best only recovered in a small percent- According to the present invention the saponi-' tied fatty materials-containing the sterols. are treated with quick lime. Water present in the mixture reacts with the quick lime, the heat produced resulting in converting additional water to steam. The steam generated in situ in the soap causes a pumng of the soap, producing a porous granular mass which is easily extracted with 'relatively small amounts of solvent. The porous character of the mass enables ready percolation'ot the solvent with free access'oi the solvent to all parts of the mass. The soapy material containing the sterols treatedin this manner can be readily extracted by a counter current extraction, a continuous extraction such as in a Soxhlet-tyriekxtractor, or by any other highly eillcient extraction method.
The extract can,, then be evaporated to recover the sterols. in a fairly pure form. This fairly pure product may be further purified by crystallization of the sterols from'alcohol solution or by other well. known purification methods. Before evaporating the extract it is desirable but not necessary to wash the extract with an alkali solution to remove any traces of oil or soap which may be present.
The following examples illustrate the invention:
Example I 200 pounds of a concentrated traction of soy bean oil containing the sterols was treated with pounds of 50% caustic soda-solution, and the mixture heated to about F. for about 15 to 20 minutes, and l00pounds of quick lime added and the mixture agitated to mix in the quick lime. After a short additlonalwarming the mixture began to pufi up, and the agitation was continued. -The mixture heated up rapidly, and in a short time the entire mixture had been converted into a dry, crumbly, readily permeable the Example ll 100 pounds of soy bean 011 containing the sterols in higher concentration than in the original oil was heated'in a shallow pan to 180 F. 53.2 pounds of 37.5% 'caustic soda solution was added and the mixture well stirred until a semiplastic state had been obtained. 29.9 pounds of quick lime is then added and the mixture agitated to insure intimate contact between soaps and quick lime. After a few minutes, the mass begins to swell and puff up. In a short while the mixture is dry and of a porous nature.
The porous mass was then extracted with ether in a Soxhlet extractor. The ether extract was then dropped into hot alcohol, whereupon the ether was evaporated, the sterols went into solution, and the impurities precipitated. After filtering the alcoholic solution'hot, it was cooled and the sterols crystallized from solution. The sterols recovered were of substantially 100% purity and consistedprincipally of stigmasterol and sistosterol.
Example III To 500 grams of crude tall oil soap containing 31% moisture as obtained from the treatment of wood pulp with caustic, was added 500 grams of quick lime, and the mixturewarmed to about 100 C. with agitation. Afters few minutes the -mixture began to pull up. Due to the excessive heat caused by the largeamount of water the mixture was cooled. In a few minutes the entire mass had been converted into a dry crumbly mass of porous granules from which the sterols were extracted and recrystallized as in Example I. About 15 grams of practically colorless once crystallized sterols were obtained. 4
- In place of tall oil soap the tall oil itself as obtainable on the market may be used and first saponified with alkali.
Preferably the soaps used or formed for thetreatment with quick lime are liquid or soft soaps, such as sodium and potassium soaps. Harder soaps made with other basic radicals may be used however. Preferably the crude mixture of soap, sterol, and water to which the quick lime is added is of a soft or liquid consistency. Ammonium soaps or other soaps containing moieties volatile at the temperature generated by the reaction of the quick lime with water may be used and the gases so generated aid the pulling action. A dehydrated soap, however, should not be used as the reaction between the quick lime and water will not occur. Any suitable source of raw material containing sterols may be used, such as soy bean oil, Calabar beans, yeast, animal cells, tall oil and its soaps, soybean oil foots, 'etc.
The amount of lime used should be sufiicient to produce the pulling action, and preferably is sumcientto convert. into steam all of the water not reacted with the lime. It need not be sumcient to completely form calcium soaps from all of the alkali soaps when such are used. In the examples given the porous granular mass is a mixture of the sodium and calcium soaps containing the sterols. So far as is known the treatment with quick lime does not affect the sterols.
, In place of ether, other sterol solvents, which are nonsolvents for soap may be used such asprises providing a crude mixture containing soaps,
sterols and water, mixing suincient quick lime with said crude mixture to cause substantially complete removal of the water, whereby a porous mass is produced, and extracting the sterols from said porous mass.
3. The process of recovering sterols which comprises providing a crude mixture containing alkali soaps, sterols and water, mixing suiiicient quick lime with said crude mixture to form a porous mass, and extracting the sterols from said porous mass.
4. The process of recovering sterols from fatty materials containing the same which comprises saponifying the fatty material, mixing suflicient quick lime with the saponiiied material to form a porous crumbly mass, and extracting 'the sterols from said porous mass.
5. The process of recovering sterols from fatty materials containing the same which comprises saponifying thefatty material, mixing sufficient quick lime with the saponined material to cause substantially complete removal of the water present, whereby a porous mass is produced, and extracting the sterols from said porous mass.
6. The process of recovering sterols from fatty materials containing the same which comprises saponifying the fatty material with an alkali saponifying agent, mixing sufiicient quick lime with the saponifled material to form a porous mass, and extracting the sterols from said porous mass.
7. The process of recovering sterols which comprises saponifying-a fatty material of vegetable origin containing sterols, mixing sufficient quick lime with the saponified material to form a porous mass, and extracting the porous mass with a solvent for sterols.
8. The process of recovering sterols which comprises providing a crude mixture containing soap, sterols and water,-mixing quick lime with said crude mixture, the amount of quick -lime being suiiicient'to cause substantial evaporation of sensible water from the mass whereby it is converted into a porous mass and extracting the sterols from said porous mass. i
- 9. As an improvement in the process of recovering sterols from saponified material'containing the same by an extraction method, the step which comprises mixing suflicient quick lime with the saponifled material before drying or extracting the same to form a porous mass.
10. The process of recovering sterols which comprises providing a crude mixture containing soaps, sterols and water, mixing sufficient quick lime with said crude mixture to cause substantial evaporation of water and to convert the mixture into a porous mass, extracting the sterols from said porous mass, washing the extract with an alkali solution, and recovering the sterols from the washed extract.
11. The process of recovering sterols which comprises providing a crude mixture of soft consistency of soap, sterols and water, mixing sufficient quick lime with said crude mixture to form a porous mass, and extracting sterols from said porous mass.
12. In the process of recovering sterols the steps which comprise providing a crude mixture of soap, sterols and water and mixing quick lime with said crude mixture. said soap mixture containing an ingredient in addition to the water which is volatile at the temperatures generated by the reaction of the quick lime and water whereby the steam formed and the gas generated by the heat of the reaction between the quick lime and water produces a porous mass readily extractible by solvents.
13. The process of recovering sterols from soy bean oil containing the same which comprises saponitying the oil with an aqueous caustic alkali solution, adding sufiicien-t quick limeto the soaps thus formed to produce a porous mass, and extracting the porous mass with a solvent for-sterols which is ,a non-solvent for soaps.
14. The process of extraction comprising the steps of first providing a crude mixture of soap, water and a substance to be extracted, adding sumc'ient quick lime to the crude mixture to form a porous mass, and then extracting the porous mass with a. solvent for the material to be extracted'which is a nonsolvent for soap.
15. The method of recovering sterols from fatty materials containing the same which comprises converting the fatty materials to soap. suflicient amounts of quick lime and water being reacted in the process to generate steam and to form a dry crumbly porous mass readily percolated by solvents, and extracting the sterols from the porous mass.
PERCY L. JULIAN. EDWIN W. MEYER. NORMAN C. KRAUBE'.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US266408A US2218971A (en) | 1939-04-06 | 1939-04-06 | Recovery of sterols |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US266408A US2218971A (en) | 1939-04-06 | 1939-04-06 | Recovery of sterols |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2218971A true US2218971A (en) | 1940-10-22 |
Family
ID=23014451
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US266408A Expired - Lifetime US2218971A (en) | 1939-04-06 | 1939-04-06 | Recovery of sterols |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2218971A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2530809A (en) * | 1949-08-23 | 1950-11-21 | Pittsburgh Plate Glass Co | Fractionation of tall oil |
| US2530810A (en) * | 1949-08-23 | 1950-11-21 | Pittsburgh Plate Glass Co | Separation of unsaponifiable matter from tall oil residue |
| US2534809A (en) * | 1949-08-23 | 1950-12-19 | Fractionation of tall oil | |
| US2610195A (en) * | 1949-05-04 | 1952-09-09 | Colgate Palmolive Peet Co | Recovery of unsaponifiables from concentrates containing the same |
| US2910468A (en) * | 1955-11-10 | 1959-10-27 | Frederick E Dearborn | Sulfurized sterols |
| US20100316750A1 (en) * | 2000-12-01 | 2010-12-16 | N.V. Nutricia | Cholesterol lowering supplement |
-
1939
- 1939-04-06 US US266408A patent/US2218971A/en not_active Expired - Lifetime
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2610195A (en) * | 1949-05-04 | 1952-09-09 | Colgate Palmolive Peet Co | Recovery of unsaponifiables from concentrates containing the same |
| US2530809A (en) * | 1949-08-23 | 1950-11-21 | Pittsburgh Plate Glass Co | Fractionation of tall oil |
| US2530810A (en) * | 1949-08-23 | 1950-11-21 | Pittsburgh Plate Glass Co | Separation of unsaponifiable matter from tall oil residue |
| US2534809A (en) * | 1949-08-23 | 1950-12-19 | Fractionation of tall oil | |
| US2910468A (en) * | 1955-11-10 | 1959-10-27 | Frederick E Dearborn | Sulfurized sterols |
| US20100316750A1 (en) * | 2000-12-01 | 2010-12-16 | N.V. Nutricia | Cholesterol lowering supplement |
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