US2349274A - Antioxidant - Google Patents
Antioxidant Download PDFInfo
- Publication number
- US2349274A US2349274A US415425A US41542541A US2349274A US 2349274 A US2349274 A US 2349274A US 415425 A US415425 A US 415425A US 41542541 A US41542541 A US 41542541A US 2349274 A US2349274 A US 2349274A
- Authority
- US
- United States
- Prior art keywords
- tocopherol
- antioxidant
- oil
- vacuum
- steam
- 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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- 239000003963 antioxidant agent Substances 0.000 title description 37
- 230000003078 antioxidant effect Effects 0.000 title description 32
- 229930003799 tocopherol Natural products 0.000 description 38
- 239000011732 tocopherol Substances 0.000 description 38
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 37
- 235000006708 antioxidants Nutrition 0.000 description 36
- 235000010384 tocopherol Nutrition 0.000 description 33
- 229960001295 tocopherol Drugs 0.000 description 33
- 238000000034 method Methods 0.000 description 32
- 239000003921 oil Substances 0.000 description 31
- 235000019198 oils Nutrition 0.000 description 31
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 30
- 239000003925 fat Substances 0.000 description 27
- 235000019197 fats Nutrition 0.000 description 27
- 239000010802 sludge Substances 0.000 description 22
- 238000004332 deodorization Methods 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- 239000000126 substance Substances 0.000 description 18
- 238000011282 treatment Methods 0.000 description 18
- 239000000463 material Substances 0.000 description 17
- 239000000203 mixture Substances 0.000 description 16
- 239000011782 vitamin Substances 0.000 description 14
- 229940088594 vitamin Drugs 0.000 description 13
- 229930003231 vitamin Natural products 0.000 description 13
- 235000013343 vitamin Nutrition 0.000 description 13
- 230000008569 process Effects 0.000 description 11
- 238000007670 refining Methods 0.000 description 11
- 150000003722 vitamin derivatives Chemical class 0.000 description 10
- 235000021588 free fatty acids Nutrition 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 239000002253 acid Substances 0.000 description 8
- 238000009874 alkali refining Methods 0.000 description 8
- 230000000087 stabilizing effect Effects 0.000 description 8
- 235000014113 dietary fatty acids Nutrition 0.000 description 7
- 238000004821 distillation Methods 0.000 description 7
- 239000000194 fatty acid Substances 0.000 description 7
- 229930195729 fatty acid Natural products 0.000 description 7
- 150000004665 fatty acids Chemical class 0.000 description 7
- 235000013305 food Nutrition 0.000 description 7
- 235000010382 gamma-tocopherol Nutrition 0.000 description 7
- 239000000344 soap Substances 0.000 description 7
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 6
- 241001465754 Metazoa Species 0.000 description 6
- 229910052791 calcium Inorganic materials 0.000 description 6
- 239000011575 calcium Substances 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- 230000001877 deodorizing effect Effects 0.000 description 6
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 6
- 230000003647 oxidation Effects 0.000 description 6
- 238000007254 oxidation reaction Methods 0.000 description 6
- 239000012476 oxidizable substance Substances 0.000 description 6
- 238000004904 shortening Methods 0.000 description 6
- 125000002640 tocopherol group Chemical group 0.000 description 6
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 5
- 239000011261 inert gas Substances 0.000 description 5
- 235000019149 tocopherols Nutrition 0.000 description 5
- 235000013311 vegetables Nutrition 0.000 description 5
- 235000004835 α-tocopherol Nutrition 0.000 description 5
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 0.000 description 5
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 229930182558 Sterol Natural products 0.000 description 4
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 4
- 239000011149 active material Substances 0.000 description 4
- 235000012343 cottonseed oil Nutrition 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 150000003432 sterols Chemical class 0.000 description 4
- 235000003702 sterols Nutrition 0.000 description 4
- 235000019155 vitamin A Nutrition 0.000 description 4
- 239000011719 vitamin A Substances 0.000 description 4
- 229940045997 vitamin a Drugs 0.000 description 4
- 239000002699 waste material Substances 0.000 description 4
- 239000002478 γ-tocopherol Substances 0.000 description 4
- QUEDXNHFTDJVIY-DQCZWYHMSA-N γ-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-DQCZWYHMSA-N 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000011105 stabilization Methods 0.000 description 3
- 238000005292 vacuum distillation Methods 0.000 description 3
- 150000003772 α-tocopherols Chemical class 0.000 description 3
- 150000003785 γ-tocopherols Chemical class 0.000 description 3
- 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 2
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 244000000231 Sesamum indicum Species 0.000 description 2
- 235000003434 Sesamum indicum Nutrition 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
- 229930003427 Vitamin E Natural products 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 229940087168 alpha tocopherol Drugs 0.000 description 2
- 239000010775 animal oil Substances 0.000 description 2
- 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 2
- 239000012159 carrier gas Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- 239000002385 cottonseed oil Substances 0.000 description 2
- 239000010779 crude oil Substances 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000008157 edible vegetable oil Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229940013317 fish oils Drugs 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 159000000014 iron salts Chemical class 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 235000013310 margarine Nutrition 0.000 description 2
- 238000000199 molecular distillation Methods 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 235000013606 potato chips Nutrition 0.000 description 2
- 230000003389 potentiating effect Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000007127 saponification reaction Methods 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 238000001256 steam distillation Methods 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
- 150000003505 terpenes Chemical class 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- 229960000984 tocofersolan Drugs 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- 235000019165 vitamin E Nutrition 0.000 description 2
- 239000011709 vitamin E Substances 0.000 description 2
- 229940046009 vitamin E Drugs 0.000 description 2
- 239000002076 α-tocopherol Substances 0.000 description 2
- WIGIZIANZCJQQY-UHFFFAOYSA-N 4-ethyl-3-methyl-N-[2-[4-[[[(4-methylcyclohexyl)amino]-oxomethyl]sulfamoyl]phenyl]ethyl]-5-oxo-2H-pyrrole-1-carboxamide Chemical compound O=C1C(CC)=C(C)CN1C(=O)NCCC1=CC=C(S(=O)(=O)NC(=O)NC2CCC(C)CC2)C=C1 WIGIZIANZCJQQY-UHFFFAOYSA-N 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 description 1
- 240000008415 Lactuca sativa Species 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 241001125048 Sardina Species 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 235000013330 chicken meat Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 235000021323 fish oil Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000000687 hydroquinonyl group Chemical group C1(O)=C(C=C(O)C=C1)* 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000003264 margarine Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 235000012045 salad Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000019512 sardine Nutrition 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000035943 smell Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- -1 tocopherol quinones Chemical class 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 238000009489 vacuum treatment Methods 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 239000005418 vegetable material Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic 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
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
- C07D311/70—Benzo[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
- C07D311/72—3,4-Dihydro derivatives having in position 2 at least one methyl radical and in position 6 one oxygen atom, e.g. tocopherols
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic 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
- A61K31/352—Heterocyclic 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
- A61K31/353—3,4-Dihydrobenzopyrans, e.g. chroman, catechin
- A61K31/355—Tocopherols, e.g. vitamin E
Definitions
- This invention relates to improved procedure for preparing and employing antioxidants to improved antioxidant products and stabilized substances and the like.
- This invention has for its object to provide improved antioxidants. Another object is to provide antioxidants which are satisfactory for ediblc materials. A further object is to provide improved procedure for stabilizing unstable or oxidizable substances, part cularly foods and the like. Another object is to provide improved procedure for preparing antioxidants. Other objects are to provide improvements in the art of stabilizing materials and preparation of antioxidants. Other objects will appear hereinafter.
- the most common method of deodorizing oils involves vacuum treatment in the presence of steam.
- the vacuum is usually produced by means of a steam ejector and the steam is passed through the oil being refined.
- the steam which is passed through the oil is usually condensed in a barometric condenser and the condensed steam permitted to flow into a sump or condenser discharge.
- scum having high antioxidant qualities or potency is produced in relatively large amounts by this procedure and that it can be removed from mixed steam vapors, from the barometric condenser or from the sump into which the condenser discharges.
- the content of the scum in antioxidant potency vitamin E activity, and sterol and other accessory substance content is often many times that of the richest crude oils from which it is derived. The scum is thus a valuable primary concentrate of accessory substances in spite of it having been considered an annoying waste product for upwards of fifty years.
- vacuum deodorizing method Many variations of the vacuum deodorizing method are employed by the different oil manufacturers and it is to be understood that my invention is applicable to all methods of deodorization which involve the use of incipient distillations in combination with a carrier gas, and that my improved antioxidant can be separated from the vapors or gases derived from the refined oil. Separation may be accomplished in the manner set forth above but it is equally feasible to separate the vapors, sludge or scum at intermediate stages such as between the deodorizing vessel and the evacuating pumps by means of catching vessels or condensers. Such material is known as deodorizer trap sludge. It is to be understood that the word scum as used herein shall include volatilized matter produced by each of the foregoing methods.
- the antioxidant material is lighter than water and coats the surface of the condenser discharge or barometric sump with a thin scum.
- This material is known in industry as deodorizer hot well sludge.
- the simplest method employed is to skim the substance from the surface of the water intermittently. It also tends to collect on the walls of the tank and can be scraped therefrom.
- the discharge from the condenser is usually rather warm and the discharge tank is often quite small. For this reason the scum may not separate or considerable amounts of the active material remain in solution or suspension and flow to the Waste discharge. I have found that the yield of active substance can be considerably increased by completely cooling the condenser discharge or the contents of the discharge tank to approximately atmospheric temperature.
- the yield can also be increased by substantially increasing the size of the discharge tank pr even providing an outside pond to the still surface on which the scum can rise.
- the discharged condensate can also be treated with a solvent, scrubbers, or passed through filters or screens. Any one or all of the foregoing expedients can be employed to improve the yield of the active material.
- the scum can sometimes be employed eifec-- tively as an antioxidant in its original condition
- Calcium soaps are formed by this means and the antioxidant and the globules of oil, fatty acids, etc. are attracted to and precipitated in the calcium soaps.
- This product as removed from the deodorization procedure is a greasy, spongy substance.
- the scum may-also be distilled in a molecular or similar. still, under high vacuum, unobstructed path distillation conditions. A distillate having high antioxidant potency is obtained at about 120 to 220 C.
- the distillation treatment can be preceded by neutralization of the soaps and this procedure is usually desirable.
- the solvent extract can then be distilled either to remove the solvent or to also distill off the antioxidant from the accompanying extracted materials.
- the antioxidant of my invention namely, the sludge or the refined products derived therefrom, can be employed to stabilize a wide variety of substances.
- vitamin products such as fish oils and vitamin concentrates produced therefrom by high vacuumdistillation or saponification.
- It can be used in foods and in edible substances in general.
- it can be added to edible oils, shortenings, lard, margarines, etc. to protect them against rancidity.
- It can also be added to the fat employed to prepare foods such as potato chips and the potato chips are stabilized thereby. It is of particular interest in connection with foods because the antioxidant is derived from natural anim. nd vegetable materials and its presence in foods, therefore, would be free of objection.
- the antioxidant can be added to rubber, gasoline, or to crude materials treated to yield such substances.
- the antioxidant has particular-value for use in its crude condition for processes wherein an oxidizable substance is treated or purified, etc. For instance, if the crude sludge is adde to a fish oil which is then subjected to alkali refining, followed by molecular distillation, a' distillate containing the vitamins of the fish oils and the antioxidant of the sludge is obtained in relatively pure condition free from impurities accompanying the antioxident in the original sludge. This procedure has the added advantage that -the vitamin is. Ebrotec ted during the entire ,treatment. If desired the antioxidant can be returned to the oil from which it was derived in the'oil refinery. In this way the stability of-the original oil is made to compare favorably with that of the raw oil before it was introduced into the refinery.
- Example L-Treatment of corn oil deodorizer hotwell sludge to obtain materials of useful antioxidant value The sludge as recovered from the hotwell contains up to 50 percent free fatty acids and seldom less than 10 per cent.
- the pipes and vessels are generally made ofiron and the water from the ejector barometric is generally contains calcium.
- the sludgegtherefore contains calcium and iron salts, the latter being especially detrimental to its use as an antioxi nt. 1
- the sludge may bxzielted, the water separated, and then wet filtere from the debris and much of the soaps.
- the sludge may be melted, much of the water drained away, and the residue treated with an organic or inorganic acid, which may be acetic or some other strong organic acid, sulfuric, hydrochloric or other, acid giving soluble calcium and iron salts; sulfuric is widely used to liberate free fatty acids from crude soap-stocks but hydrochloric acid is the preferred acid for my purpose.
- an organic or inorganic acid which may be acetic or some other strong organic acid, sulfuric, hydrochloric or other, acid giving soluble calcium and iron salts; sulfuric is widely used to liberate free fatty acids from crude soap-stocks but hydrochloric acid is the preferred acid for my purpose.
- Example 1 In 'a substantially dry, bright oil of light brown color was secured. This oil contained approximately 2 per cent gamma tocopherol and was found suitable for addition to animal feeds without further treatment.
- Example 11 Before or during the boiling with hydrochloric acid as in Example la, zinc dust was added in the proportion of 5 pounds'to .100 gallons of oil. This resulted in a marked reduction in the color, and the tocopherol quinones present were altered to the reduced form of the substance, was worked up as before. Other metals which react with acid to give nascent hydrogen, such as iron can be used in place of zinc.
- the tocopheral in vegetable oil is present in the form of the quinone and hydroquinone form so that reduction of the quonine to the hydroquinone substantially reduces loss during subsequent procedures such as distillation.
- Example 1c The on were filtered on. The liquid portion was found to contain 2% per cent gamma tocopherol and had an acid value of 4. It was found suitable for addition to lard, edible vegetable oils, and vitamin-bearing products for the purpose of stabilization;
- Example 1d The oil from the preceding example instead of being withdrawn from the still after subjection to a temperature of 130 C. was continued under vacuum with the passage of steam while the temperature was raised to 170 C. Material which contained per cent free fatty acid and approximately 10 per cent tocopherol was collected from the barometric leg.
- This material was worked up separately for the production of pure tocopherol, or altematively it was returned to new batches of acidtreated sludge prior to deodorization.
- the temperature was now raised to 200 C. and a quantity of hotwell sludge collected which was substantially free from fatty acid and contained per cent gamma tocopherol.
- This material was entirely suitable for adding to margarine, salad Example 1e
- the sludge is treated exactly as in the foregoing example except that it is placed in the deodorizing kettle without any previous acid or other treatment except as a convenience for the removal of most of the water.
- Example 2a Recovery of tocopherol from hotwell sludge obtained from the deodorization of soybean oil Sludge is given acid treatment as in the previous example and is placed in a large vacuum kettle under a vacuum of 1 mm. of mercury. The temperature is raised to about 100, and a quantity of distillate withdrawn which smells strongly of terpenes. It contains free fatty acids and at least two unsaturated hydrocarbons. The fatty acids can be separated by crystallization or neutralization, and the hydrocarbons further purified by distillation. The temperature is now raised to 150 when more hydrocarbons of a similar nature come over together with a liberal proportion of free fatty acids. The temperature is now raised to 200 C.
- a mixture of residual free fatty acids comes over containing a mixture of alpha and gamma tocopherols.
- the distillate is cooled to separate th majority of acids, and the liquid filtered off containing 510 per cent tocopherols.
- the temperature is raised and further quantities of tocopherol solution substantially free from free fatty acids are removed.
- This solution may contain as much as per cent mixed alpha and gamma tocopherols. It is suitable for employment as such in medicinal preparations for vitamin E activity or for the stabilizing of oils and foods, or the distillates may be further worked up to produoe the further tocopherol or tocopherol palmitate.
- the acid-treated sludge after treatment in'a vacuum still at 130 may be transferred to a batch molecular still or a continuous molecular still or any form of high vacuum unobstructed or short-path still or to a continuous high-vacuum column still. and the tocopherols removed from the majority of the other constituents.
- the oil may be passed over the rotating plate of a centrifugal unobstructed path still operating at a pressure of three microns.
- the majority of the tocopherols will distill at 180 C. or between the limits 130-230" C. There will result a distillate containing from 10-30 per cent alpha and gamma tocopherols.
- concentrations as high as 50-60 per cent tocopherols may be obtained.
- Example 3 Alpha tocopherol from cottonseed deodorizer trap sludge
- the trap sludge is melted and filtered. If the fatty acid content is below 10 per cent, the fat is given an alkali refining at this stage. In either case, the melted sludge is allowed to enter a. vacuum degasser at 90 C. at a pressure of 10 mm.
- Example 4-Use of crude scam to stabilize vitamins during refining 5 parts of a deodorizer scum containing 2 per cent tocopherol is added to 97 parts of grayflshliver oil containing 15,000 units per gram vitamin A, and the mixture is given alkali refining. It is then distilled, under high vacuum, unobstructed path conditions yielding a fraction containing 230,000 units per gram of vitamin A and 14.5 per cent tocopherol.
- Example 7 A concentrate is made by vacuum distillation or steam distillation or.other means, consisting of tocopherol and hard fatty acids from deodorizer scum. This is blended with a vitamin A oil and is mechanically mixed with alkali, preferably lime in just sufficient quantity to neutralize all the free acid- The mixture sets to a hard cake which may then be pulverized and addedto the animal feed.
- the vitamin A is found to be extremely stable in such powders and th lime salts are definitely beneficial as a constituent of feed.
- Example 8Stabilization of rubber A low temperature distillate of tocopherol from I one of the preceding examples containing too much odor and fatty acid to be readily acceptable for edible pur ses is added to a rubber mix on the incorporating rolls in a rubber mill in the proportion of one part of distillate to 1000. parts of rubber. The mixture .is finished and moulded into commercial articles in the ordinary way.
- Example 9-Stabilization of lard One part of odorless distillate prepared as in the foregoing examples and containing approxi- ,mately per cent tocopherol is added to 200 parts of lard and thoroughly mixed and the mixture placed in containers for the commercial market.
- the active material can be obtained in. the manner described from the sludges and the like derived from any natural animal oil or fat or the like which contains the tocopherols.
- all oils do not contain it and for this reason all distillate by-products can not beusedvl'or instance sesame seed oil in its original condition or in hydrogenated condition is free of this materi- 3,1.
- I have found that most 01' these oils and fats do contain these substances and do yi l highly potent wastes. 0115 which give particularly active wastes are com, peanut, soybean and cottonseed oils.
- Patent 2,095,740 which describes the use of a heavier than water steam distillate of hydrogenated sesame seed 011.
- this oil does not. contain tocopherol.
- Tocopherol is lighter than water and is contained in the scum which separates at the top of steam condensate.
- the process for stabilizing a vitamin bearing substance which comprises adding thereto a lighter-than-water tocopherol-containing substance which has an antioxidant activity and which has. been separated from the class consisting of vapors and scum separated from a tocopherol-bearing fat during vacuum-inert gas deodorization of said fat.
- the method of stabilizing shortenings which comprises in combination subjecting a lighter-than-water tocopherol containing scum derived from the vacuum-inert gas deodorization of a tocopherol bearing fat to a refining treatment for the removal of impurities including free fatty acids, and incorporating the refined scum in the sh'ortening, said scum being condensed from the carrier gas utilized for the vacuum deodorization.
- the process of stabilizing an oxidizable substance which is unstable to atmospheric oxidation which comprises adding to the oxidizable substance a lighter-than-water tocopherol containing antioxidant comprising the matter volatilized during the steam-vacuum deodorization of a member of the group consisting of tocopherol-bearing vegetable and animal fats, and then subjecting this mixture of antioxidant and oxidizable substance to an alkali refining treatment whereby a refined oxidizable substance of high stability is obtained.
- the process of stabilizing a fat which is unstable to atmospheric oxidation which comprises adding to the fat an antioxidant comprising the lighter-than-water tocopherol-containing material volatilized during the steamvacuum deodorization of a member of the group consisting of tocopherol-bearing vegetable and animal fats, and then subjecting this mixture to an alkali refining treatment whereby a refined fat of high stability is obtained.
- the process of stabilizing a shortening which is unstable to atmospheric oxidation which comprises adding to the shortening an antioxidant comprising the lighter-than-water tocopheral containing material volatilized during the steam-vacuum deodorization of a member of the group consisting of tocopheral-bearing vegetable and animals fats, and then subjecting thi mixture to an alkali refining treatment whereby a refined shortening of high stability is obtained.
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Description
Patented May 23, 1944 AN TIOXIDAN T Kenneth C. D. Hickman, Rochester, N. Y., assignor to Distillation Products, Inc., Rochester, N. Y., a corporation of Delaware No Drawing. Original application March 2, 1940,
Serial No. 321,913. Divided and this application October 17, 1941, Serial No. 415,425
14 Claims.
This invention relates to improved procedure for preparing and employing antioxidants to improved antioxidant products and stabilized substances and the like.
It is common procedure to subject various vegetable and animal oils, fats, and the like to refining treatment in order to improve color, taste, odor, etc. It has been recognized that refined oils have rather poor keeping qualities and that they are decidedly inferior in this respect to the raw or crude oils. The refining treatments employed in most cases involved reaction with chemicals and deodorization in a vacuum with inert gases such as steam. The inert gas treatment in vacuum is usually the final step in the refining process with the possible exception of those cases where the oil is to be bleached.
This invention has for its object to provide improved antioxidants. Another object is to provide antioxidants which are satisfactory for ediblc materials. A further object is to provide improved procedure for stabilizing unstable or oxidizable substances, part cularly foods and the like. Another object is to provide improved procedure for preparing antioxidants. Other objects are to provide improvements in the art of stabilizing materials and preparation of antioxidants. Other objects will appear hereinafter.
It is well known that during the deodorization of fats and the like by vacuum and inert gas treatment, such as steam, a small amount of volatile matter is obtained as a distillate or impurity in the distillate. When steam is employed for deodorizing, the material separates as a scum on the top of the water in the discharge from the barometric condenser. I have discovered that this material when obtained from vegetable and marine oils contains substances having a high antioxidant activity. I have found that the material can be employed as an antioxidant in the original condition in which it is removed from the deodorizing equipment or it may be refined before use.
The most common method of deodorizing oils involves vacuum treatment in the presence of steam. The vacuum is usually produced by means of a steam ejector and the steam is passed through the oil being refined. The steam which is passed through the oil is usually condensed in a barometric condenser and the condensed steam permitted to flow into a sump or condenser discharge. I have found that scum having high antioxidant qualities or potency is produced in relatively large amounts by this procedure and that it can be removed from mixed steam vapors, from the barometric condenser or from the sump into which the condenser discharges. The content of the scum in antioxidant potency vitamin E activity, and sterol and other accessory substance content is often many times that of the richest crude oils from which it is derived. The scum is thus a valuable primary concentrate of accessory substances in spite of it having been considered an annoying waste product for upwards of fifty years.
Many variations of the vacuum deodorizing method are employed by the different oil manufacturers and it is to be understood that my invention is applicable to all methods of deodorization which involve the use of incipient distillations in combination with a carrier gas, and that my improved antioxidant can be separated from the vapors or gases derived from the refined oil. Separation may be accomplished in the manner set forth above but it is equally feasible to separate the vapors, sludge or scum at intermediate stages such as between the deodorizing vessel and the evacuating pumps by means of catching vessels or condensers. Such material is known as deodorizer trap sludge. It is to be understood that the word scum as used herein shall include volatilized matter produced by each of the foregoing methods.
The antioxidant material is lighter than water and coats the surface of the condenser discharge or barometric sump with a thin scum. This material is known in industry as deodorizer hot well sludge. In collecting the active material the simplest method employed is to skim the substance from the surface of the water intermittently. It also tends to collect on the walls of the tank and can be scraped therefrom. The discharge from the condenser is usually rather warm and the discharge tank is often quite small. For this reason the scum may not separate or considerable amounts of the active material remain in solution or suspension and flow to the Waste discharge. I have found that the yield of active substance can be considerably increased by completely cooling the condenser discharge or the contents of the discharge tank to approximately atmospheric temperature. The yield can also be increased by substantially increasing the size of the discharge tank pr even providing an outside pond to the still surface on which the scum can rise. The discharged condensate can also be treated with a solvent, scrubbers, or passed through filters or screens. Any one or all of the foregoing expedients can be employed to improve the yield of the active material.
The scum can sometimes be employed eifec-- tively as an antioxidant in its original condition,
Calcium soaps are formed by this means and the antioxidant and the globules of oil, fatty acids, etc. are attracted to and precipitated in the calcium soaps. This product as removed from the deodorization procedure is a greasy, spongy substance.
Numerous methods of refining are available but the ones which appear at the present time to oiler the best product are distillation, solvent extraction, neutralization or saponific-ation or combinations thereof preceded if necessary by a chemical treatment such as washing with mineral acid to remove iron or calcium soaps. Vace uum steam distillation analogous to that employed in the original deodorization, yields a distillate of the antioxidants relatively free of fatty acids, sterols, etc. and substantially free of soaps. Ordinary vacuum distillation of the scum can be employed and at a temperature of 150 to 330 a fraction of high antioxidant potency is obtained.
The scum may-also be distilled in a molecular or similar. still, under high vacuum, unobstructed path distillation conditions. A distillate having high antioxidant potency is obtained at about 120 to 220 C. The distillation treatment can be preceded by neutralization of the soaps and this procedure is usually desirable.
A portion of the antioxidant substance becomes entrained in' the soaps but it has been found that solvents can be employed to extract the antioxidant therefrom. The solvent extract can then be distilled either to remove the solvent or to also distill off the antioxidant from the accompanying extracted materials.
The antioxidant of my invention, namely, the sludge or the refined products derived therefrom, can be employed to stabilize a wide variety of substances. For instance, it can be added to vitamin products, such as fish oils and vitamin concentrates produced therefrom by high vacuumdistillation or saponification. It can be used in foods and in edible substances in general. For instance it can be added to edible oils, shortenings, lard, margarines, etc. to protect them against rancidity. It can also be added to the fat employed to prepare foods such as potato chips and the potato chips are stabilized thereby. It is of particular interest in connection with foods because the antioxidant is derived from natural anim. nd vegetable materials and its presence in foods, therefore, would be free of objection. The antioxidant can be added to rubber, gasoline, or to crude materials treated to yield such substances. The antioxidant has particular-value for use in its crude condition for processes wherein an oxidizable substance is treated or purified, etc. For instance, if the crude sludge is adde to a fish oil which is then subjected to alkali refining, followed by molecular distillation, a' distillate containing the vitamins of the fish oils and the antioxidant of the sludge is obtained in relatively pure condition free from impurities accompanying the antioxident in the original sludge. This procedure has the added advantage that -the vitamin is. Ebrotec ted during the entire ,treatment. If desired the antioxidant can be returned to the oil from which it was derived in the'oil refinery. In this way the stability of-the original oil is made to compare favorably with that of the raw oil before it was introduced into the refinery.
Example L-Treatment of corn oil deodorizer hotwell sludge to obtain materials of useful antioxidant value The sludge as recovered from the hotwell contains up to 50 percent free fatty acids and seldom less than 10 per cent. The pipes and vessels are generally made ofiron and the water from the ejector barometric is generally contains calcium. The sludgegtherefore, contains calcium and iron salts, the latter being especially detrimental to its use as an antioxi nt. 1 As a first stage in refining, the sludge may bxzielted, the water separated, and then wet filtere from the debris and much of the soaps. Alternatively, the sludge may be melted, much of the water drained away, and the residue treated with an organic or inorganic acid, which may be acetic or some other strong organic acid, sulfuric, hydrochloric or other, acid giving soluble calcium and iron salts; sulfuric is widely used to liberate free fatty acids from crude soap-stocks but hydrochloric acid is the preferred acid for my purpose.
Example In 'a substantially dry, bright oil of light brown color was secured. This oil contained approximately 2 per cent gamma tocopherol and was found suitable for addition to animal feeds without further treatment.
Example 11) Before or during the boiling with hydrochloric acid as in Example la, zinc dust was added in the proportion of 5 pounds'to .100 gallons of oil. This resulted in a marked reduction in the color, and the tocopherol quinones present were altered to the reduced form of the substance, was worked up as before. Other metals which react with acid to give nascent hydrogen, such as iron can be used in place of zinc. The tocopheral in vegetable oil is present in the form of the quinone and hydroquinone form so that reduction of the quonine to the hydroquinone substantially reduces loss during subsequent procedures such as distillation.
Example 1c The on were filtered on. The liquid portion was found to contain 2% per cent gamma tocopherol and had an acid value of 4. It was found suitable for addition to lard, edible vegetable oils, and vitamin-bearing products for the purpose of stabilization;
Example 1d The oil from the preceding example instead of being withdrawn from the still after subjection to a temperature of 130 C. was continued under vacuum with the passage of steam while the temperature was raised to 170 C. Material which contained per cent free fatty acid and approximately 10 per cent tocopherol was collected from the barometric leg.
This material was worked up separately for the production of pure tocopherol, or altematively it was returned to new batches of acidtreated sludge prior to deodorization. The temperature was now raised to 200 C. and a quantity of hotwell sludge collected which was substantially free from fatty acid and contained per cent gamma tocopherol. This material was entirely suitable for adding to margarine, salad Example 1e In this example the sludge is treated exactly as in the foregoing example except that it is placed in the deodorizing kettle without any previous acid or other treatment except as a convenience for the removal of most of the water.
Example 2aRecovery of tocopherol from hotwell sludge obtained from the deodorization of soybean oil Sludge is given acid treatment as in the previous example and is placed in a large vacuum kettle under a vacuum of 1 mm. of mercury. The temperature is raised to about 100, and a quantity of distillate withdrawn which smells strongly of terpenes. It contains free fatty acids and at least two unsaturated hydrocarbons. The fatty acids can be separated by crystallization or neutralization, and the hydrocarbons further purified by distillation. The temperature is now raised to 150 when more hydrocarbons of a similar nature come over together with a liberal proportion of free fatty acids. The temperature is now raised to 200 C. and the pressure reduced to .1 mm A mixture of residual free fatty acids comes over containing a mixture of alpha and gamma tocopherols. The distillate is cooled to separate th majority of acids, and the liquid filtered off containing 510 per cent tocopherols. The temperature is raised and further quantities of tocopherol solution substantially free from free fatty acids are removed. This solution may contain as much as per cent mixed alpha and gamma tocopherols. It is suitable for employment as such in medicinal preparations for vitamin E activity or for the stabilizing of oils and foods, or the distillates may be further worked up to produoe the further tocopherol or tocopherol palmitate.
All the distillates from this example when cooled separate into liquid and solid portions. Besides free fatty acids, a mixture of sterols which may contain as much as 50 per cent stigmasterol can be separated. Stigmasterol may be separated from this crude sterol by the preparation of the tetra-bromides. with subsequent hydrolysis. The residue left in the still is a low grade fat, the quality of which, however. is much higher than contained in the original sludge. It may be returned to the refinery cycle or may be used directly as a low grade fat.
Figure 2b The acid-treated sludge after treatment in'a vacuum still at 130, as in the above example, may be transferred to a batch molecular still or a continuous molecular still or any form of high vacuum unobstructed or short-path still or to a continuous high-vacuum column still. and the tocopherols removed from the majority of the other constituents. Thus, the oil may be passed over the rotating plate of a centrifugal unobstructed path still operating at a pressure of three microns. The majority of the tocopherols will distill at 180 C. or between the limits 130-230" C. There will result a distillate containing from 10-30 per cent alpha and gamma tocopherols. Where a grid or other fractionating device is employed, as in Patent 2,180,052 to Hickman and Hecker, concentrations as high as 50-60 per cent tocopherols may be obtained.
Example 3.Alpha tocopherol from cottonseed deodorizer trap sludge The trap sludge is melted and filtered. If the fatty acid content is below 10 per cent, the fat is given an alkali refining at this stage. In either case, the melted sludge is allowed to enter a. vacuum degasser at 90 C. at a pressure of 10 mm.
Volatile hydrocarbons and terpenes are separated I and from the third, a distillate of tocopherol which is substantially more potent than could be secured from a single molecular distillation. This apparatus with column still is described in detail in my application 187,454, filed 1/28/38.
Example 4-Use of crude scam to stabilize vitamins during refining 5 parts of a deodorizer scum containing 2 per cent tocopherol is added to 97 parts of grayflshliver oil containing 15,000 units per gram vitamin A, and the mixture is given alkali refining. It is then distilled, under high vacuum, unobstructed path conditions yielding a fraction containing 230,000 units per gram of vitamin A and 14.5 per cent tocopherol. This represents a higher concentration of tocopherol than could be obtained by distilling a blend of grayfish-liver oil afid 25 per cent of an average quality crude corn 0 One part of steam deodorized sludge prepared Example Example 6-Stabilization of vitamins Sardine oil is vacuum distilled to yield a concentrate containing 500 units per gram of vitamine D and 3,000 units per gram vitamin A. To 90 parts of this mixture is added parts of neutralized and filtered deodorizer scum. The mixture is used as a stable vitamin feed for chickens.
" Example 7 A concentrate is made by vacuum distillation or steam distillation or.other means, consisting of tocopherol and hard fatty acids from deodorizer scum. This is blended with a vitamin A oil and is mechanically mixed with alkali, preferably lime in just sufficient quantity to neutralize all the free acid- The mixture sets to a hard cake which may then be pulverized and addedto the animal feed. The vitamin A is found to be extremely stable in such powders and th lime salts are definitely beneficial as a constituent of feed.
Example 8Stabilization of rubber A low temperature distillate of tocopherol from I one of the preceding examples containing too much odor and fatty acid to be readily acceptable for edible pur ses is added to a rubber mix on the incorporating rolls in a rubber mill in the proportion of one part of distillate to 1000. parts of rubber. The mixture .is finished and moulded into commercial articles in the ordinary way.
Example 9-Stabilization of lard One part of odorless distillate prepared as in the foregoing examples and containing approxi- ,mately per cent tocopherol is added to 200 parts of lard and thoroughly mixed and the mixture placed in containers for the commercial market.
Example 10-Stabilizati0n of hardened fat as in Example 1 c, substantially free from taste and odor is added to parts of a hydrogenated cottonseed trying oil and is used for the frying of chipped potatoes.
In all the previous examples the starting materials and the methods of processing are interchangeable. Thus, the first examples have been given in connection with gamma tocopherol and corn oi1,.and the last with alpha tocopherol from cottonseed oil. Nevertheless, any one of the sludges could be handled according to any of the examples. a I
Due to thehigh stability of vitamin concentrates which are stabilized by this antioxidant, they can be dispersed in animal foodstuffs with out substantial loss. 'Heretofore this has been unsatisfactory procedure because the vitamin is necessarily exposed to atmospheric oxygen when distributed in the foods in this manner. Rapid loss was a consequence. However, with my highly active antioxidant this procedure is feasible and little loss results therefrom.
The active material can be obtained in. the manner described from the sludges and the like derived from any natural animal oil or fat or the like which contains the tocopherols. However, all oils do not contain it and for this reason all distillate by-products can not beusedvl'or instance sesame seed oil in its original condition or in hydrogenated condition is free of this materi- 3,1. However, I have found that most 01' these oils and fats do contain these substances and do yi l highly potent wastes. 0115 which give particularly active wastes are com, peanut, soybean and cottonseed oils.
' Since each stage in the refining treatment of an oil results in additional destruction of the antioxidant, I have found that it is best to modify the conventional refining scheme so that the deodorization step takes place at the first of the procedure and is then followed by the other refining steps such as alkali refining hydrogenation, bleaching, etc. In'this way the original antioxidant content of the oil is available for recovering in the manner described.
By another modification I have found that it is feasible to recover the antioxidant 01' my invention by providing means for collecting vapors removed from paint or drying oils, such as linseed oil, during the bodying or polymerization step in paint oil manufacture. If desired,'steam may be blown through the oil and/or vacuum may be applied. In the conventional polymerization procedure heretofore employed the active substance has been either decomposed completely or has been discharged into the atmosphere. The antioxidants are definitely detrimental to the drying oil and their removal is advantageous for this reason and also for the reason that the polymerization rate is increased.
I am aware of Patent 2,095,740, which describes the use of a heavier than water steam distillate of hydrogenated sesame seed 011. However, this oil does not. contain tocopherol. Tocopherol is lighter than water and is contained in the scum which separates at the top of steam condensate.
This application is a division of my application 321,913 filed March 2, 1940.
What I claim is:
1. The process for stabilizing a vitamin bearing substance which comprises adding thereto a lighter-than-water tocopherol-containing substance which has an antioxidant activity and which has. been separated from the class consisting of vapors and scum separated from a tocopherol-bearing fat during vacuum-inert gas deodorization of said fat.
2. The process which comprises adding to a vitamin bearing fat a lighter-than-water tocopherol containing crude vapor condensate derived from .the vacuum-steam deodorization of a tocopherol bearing fat, subjecting the mixture of vitamin bearing fate and vapor condensate to alkali refining and then subjecting the refined prises adding to the fat 9. lighter-than-water tocopherol containing vapor condensate derived from the vacuum-steam deodorization of a tocopherol bearing fat and then subjecting the mixture of vapor condensate and fat to a refining treatment whereby a refined fat of high stability is obtained.
6. The process of protecting a substance which is normally subject to oxidation which comprises adding thereto a relatively small amount of lighter-than-water tocopherol containing vapor condensate derived from the vacuum-steam deodorization of a fat which contains tocopherol, said vapor condensate being condensed and separated from the steam after it has been passed through the fat being deodorized.
7. The process defined in claim 6 in which the vapor condensate is first refined.
8. The process which comprises treating a lighter-than-water tocopherol containing scum which is condensed and separated from the steam utilized for the vacuum-steam deodorization treatment of a fat which contains tocopherol, in order to separate or concentrate the tocopherol content of the scum and then adding the concentrated material to an easily oxidizable organic material in order to protectit against oxidation.
9. As a new product an organic substance which is subject to oxidation to which has been added lighter-than-water tocopheral containing scum derived from the vacuum-steam deodorization of a vegetable fat which contains tocopheral, said scum being condensed from the steam used in the deodorization after the steam has been passed through the fat.
10. The method of stabilizing shortenings which comprises in combination subjecting a lighter-than-water tocopherol containing scum derived from the vacuum-inert gas deodorization of a tocopherol bearing fat to a refining treatment for the removal of impurities including free fatty acids, and incorporating the refined scum in the sh'ortening, said scum being condensed from the carrier gas utilized for the vacuum deodorization.
11. The process of claim 10 in which the short ening is lard.
12. The process of stabilizing an oxidizable substance which is unstable to atmospheric oxidation which comprises adding to the oxidizable substance a lighter-than-water tocopherol containing antioxidant comprising the matter volatilized during the steam-vacuum deodorization of a member of the group consisting of tocopherol-bearing vegetable and animal fats, and then subjecting this mixture of antioxidant and oxidizable substance to an alkali refining treatment whereby a refined oxidizable substance of high stability is obtained.
13. The process of stabilizing a fat which is unstable to atmospheric oxidation which comprises adding to the fat an antioxidant comprising the lighter-than-water tocopherol-containing material volatilized during the steamvacuum deodorization of a member of the group consisting of tocopherol-bearing vegetable and animal fats, and then subjecting this mixture to an alkali refining treatment whereby a refined fat of high stability is obtained.
14. The process of stabilizing a shortening which is unstable to atmospheric oxidation which comprises adding to the shortening an antioxidant comprising the lighter-than-water tocopheral containing material volatilized during the steam-vacuum deodorization of a member of the group consisting of tocopheral-bearing vegetable and animals fats, and then subjecting thi mixture to an alkali refining treatment whereby a refined shortening of high stability is obtained.
KENNETH C. D. HICKMAN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US415425A US2349274A (en) | 1940-03-02 | 1941-10-17 | Antioxidant |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US321913A US2349269A (en) | 1940-03-02 | 1940-03-02 | Recovery of tocopherol |
| US415425A US2349274A (en) | 1940-03-02 | 1941-10-17 | Antioxidant |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2349274A true US2349274A (en) | 1944-05-23 |
Family
ID=26983180
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US415425A Expired - Lifetime US2349274A (en) | 1940-03-02 | 1941-10-17 | Antioxidant |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2349274A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3153053A (en) * | 1962-04-26 | 1964-10-13 | Charles D Robeson | Chemistry of 6-chromanols |
-
1941
- 1941-10-17 US US415425A patent/US2349274A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3153053A (en) * | 1962-04-26 | 1964-10-13 | Charles D Robeson | Chemistry of 6-chromanols |
| US3153040A (en) * | 1962-04-26 | 1964-10-13 | Eastman Kodak Co | Piperazine complexes of 6-chromanols |
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