Classifications

• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
  • C11B3/00—Refining fats or fatty oils
  • C11B3/02—Refining fats or fatty oils by chemical reaction
  • C11B3/06—Refining fats or fatty oils by chemical reaction with bases

Definitions

• the present invention relates to an improved process for the purification and/or decolorization of natural oils such as the edible vegetable oils. It particularly relates to an improved process for alkali refining triglyceride oils into refined oils having improved color, color stability, odor and/or flavor.
• Crude vegetable glyceride oils as they are obtained from their natural sources by conventional extraction or pressing methods, normally contain various non-glyceride impurities.
• These non-glyceride substances include gross material from the source of the oil, such as xanthophyll or chlorophyll; products obtained by the breakdown of the glyceride oil during treatment such as free fatty acids and other derivatives of the glycerides such as phosphatides, sterols, aldehydes and ketones; peroxides; as well as various other impurities such as metal cations, metal complexes, various disulfides and related impurities.
• many vegetable oils normally contain natural waxes from the crushing of the coat of the oilseeds employed.
• alkali refining One technique for refining triglyceride oils heretofore developed by the prior art is alkali refining.
• the oil is treated with an aqueous solution of sodium hydroxide or some other strong alkali in an amount slightly in excess of the amount of the free fatty acids present in the oil to produce a refined oil and an impurity-containing soapstock.
• Typical alkali refining techniques which have previously been employed to refine triglyceride oils are described in U.S. Patent Nos. 2,702,813; 3,629,307; 3,943,155; 4,150,045 and 4,280,962; as well as in Sullivan, Journal Agricultural and Oil Chemists Society, page 845A (November 1980).
• mink oil a non-triglyceride oil
• NaBH 4 a non-triglyceride oil
• alkali metal borohydrides in order to improve the color and odor of soap has also been suggested in U .S. Patent No. 3,542,823.
• the alkali metal borohydride treatment is preferably conducted by treating the saponified soap charge immediately after leaving the washing unit with the alkali metal borohydride at a pH of at least 9.5.
• Use of such a treatment in the purification of triglyceride oils is undesirable, however, since this procedure requires the addition of a further expensive step to the already complicated triglyceride oil purification process.
• theri has been provided in accordance with the present invention an improved process for alkali refining natural oils, such as for example the triglyceride oils, wherein the efficiency of the refining process is improved by extracting the oil with alkali while in the presence of an alkali metal borohydride.
• the alkal: metal borohydride is generally employed during the alkali extraction treatment in an amount sufficient to effect the desired improvement in the quality of the triglyceride oil. Typically, from about 50 to about 2000 ppm of alkali metal borohydride (based on the weight of oil) are sufficient for most purposes.
• Oils of superior color and purity may be obtained by employing the alkali refining treatment of this invention in conjunction with a degumming pretreatment step and a bleaching step. If required, the bleaching treatment may be followed by a deodorization treatment as well as by any of the various other treatment steps conventional in the art.
• the present invention thus also provides a process for the purification of natural oils, such as the triglyceride oils, which comprises the steps of degumming a crude oil to produce a degummed oil; extracting the degummed oil with alkali while in the presence of an alkali metal borohydride to produce refined oil and a soapstock; bleaching the refined oil; and, if required, deodorizing, winterizing, hydrogenating and/or crystallizing the oil.
• natural oils such as the triglyceride oils
• oils of excellent purity and color may readily be obtained by a relatively simple procedure without the requirement for costly extra steps and the attendant capital investment outlays required therefor.
• Vegetable triglyceride oils exhibiting a Lovibond color characterized by a yellow value of 10 or less and a red value of 1 or less, a bland taste, a lack of any perceptible odor, and a significantly reduced peroxide content, for example may readily be obtained through the use of the process improvements of this invention.
• oils subjected to the alkali metal boroh y dride/alkali extraction of this invention have also been found to exhibit enhanced heat stability.
• the process improvements of this invention may be successfully utilized with any of the natural oils well known to those skilled in the art, such as the triglyceride oils.
• the edible vegetable oils are particularly amenable to processing according to this invention, examples of which include soybean oil, corn oil, cottonseed oil, peanut oil, sesame oil, rapeseed oil, canola oil, among others.
• such oils are frequently employed as salad oils, cooking oils, margarine constituents, and as constituents in various other food applications, and accordingly must meet stringent requirements in terms of color, flavor, odor and purity.
• the edible vegetable oils generally require that the purified oil exhibit a color, as evaluated by the Lovibond Color system, characterized by a yellow value of 10 or less and a red value of 1.0 or less.
• the edible vegetable oils must also desirably have a bland taste, a lack of any perceptible odor, and a peroxide value of 0 as determined by standard A.O.C.S. test Cd 8-53.
• the alkali metal borohydride treatment of this invention is preferably conducted during alkali refining of the triglyceride or other natural.oil. While the alkali metal borohydride treatment may be conducted at other points in the overall oil purification process, the low stability of the alkali metal borohydrides in non-alkaline environments requires that the alkali metal borohydride treatment be performed during the alkali refining step, or as a separate post-treatment step.
• the triglyceride oils or other natural oils utilized in the improved alkali refining procedure of this invention may comprise a crude oil or a pretreated oil, i.e., a degummed oil.
• D egumming of the oil may be accomplished by any of the various degumming procedures well known to those skilled in the art. The degumming process is primarily carried out at the extraction mill, where alkali refining may or may not be carried out. To a much lesser extent, degumming may be done by the refiner at another location. In general, degumming is accomplished by hydration of the mucilagineous product impurities contained in the vegetable oil with from about 1 to about 3% by weight water at elevated temperatures.
• a degumming agent such as for example acetic acid, acetic anhydride or phosphoric acid is employed during the degumming step in order to improve the efficiency thereof.
• the degumming agents are most easily employed by simply adding them to the crude vegetable oil prior to the addition of the hydrating water. The resulting admixture is thereafter introduced into a continuous centrifuge in which it is heated and caused to circulate continuously whereby the mucilagineous products are completely hydrated and the aqueous phase containing the precipitated hydrated mucilagineous products are separated from the oil.
• the alkali refining step is conducted according to conventional procedures with the exception that extraction of the oil with the alkali is performed in the presence of the alkali metal borohydride.
• Any of the various art recognized alkali refining procedures well known to those skilled in the art including any of the various procedures described in U.S. Patent Nos. 2,702,813; 3,629,307; 3,943,155; 4,150,045; and 4,280,962; as well as in Sullivan, Journal Agricultural and Oil Chemists Society, page 845A (November 1980), may thus be employed in conjunction with the alkali metal borohydride treatment of this invention.
• the particular operating procedures of this step will usually vary according to the particular type of oil to be refined, and the facilities and equipment wherein the oil is refined.
• the oil is refined by contacting the same with an aqueous solution of a suitable alkali, such as for example but not limited to sodium hydroxide, at temperatures which range from as low as 5°C to temperatures as high as about 100°C for an interval of from several seconds to several hours.
• a suitable alkali such as for example but not limited to sodium hydroxide
• the amount of alkali employed during the refining operation is preferably added in an amount which is only slightly in excess of that theoretically required (the stoichiometric amount) for neutralization of the free fatty acids in the oil, ah excess of 0.01% to 0.5%, and preferably from 0.01 to 0.3%, of alkali being preferred.
• the alkali metal borohydride may be added to the system by a variety of procedures. Typically, the alkali metal borohydride is added with the addition of the alkali solution to the oil. In this embodiment, the alkali metal borohydride may be employed in powdered form, or alternatively may be employed in the form of an alkaline aqueous alkali metal borohydride solution. Alkali metal borohydride solutions of this type are readily available commercially, for example, from the Morton- T hiokol Corporation under the trade designation SWS®. If an aqueous alkali metal borohydride solution is employed, it is necessary of course to adjust the amount of alkali admixed with the oil to compensate for the alkali present in the ⁇ alkali metal borohydride solution.
• the alkali may be divided into two portions with a first and larger portion being admixed with the oil.
• the alkali metal borohydride either in powdered form or in the form of an aqueous alkali metal borohydride solution, is admixed with the remaining portion of alkali, and the combined mixture thereafter added to the alkali deficient oil-alkali mixture.
• the reaction of the alkali with the oil during refining neutralizes the free fatty acids present in the oil and purifies and improves the flavor, odor and color of the same.
• This action of the alkali is enhanced by the alkali metal borohydride treatment of this invention. While not wishing to be bound by any particular theory or explanation, it is believed that the alkali metal borohydride reduces various impurities in the oil which are resistant to reduction with alkali, thereby improving the color, color stability, odor, and/or flavor of the refined oil.
• Such impurities comprise, for example, the various aldehydes, ketones, metal cations, metal complexes, disulfides, and related impurities present in the oil which are resistant to alkali attack. Reduction of these various impurities has been found to not only improve the quality of the refined oil, but in addition to retard the bui-ld-up of peroxides and other decomposition products during subsequent processing.
• the alkali metal borohydride may be, for example, lithium, potassium, or sodium borohydride. Of the alkali metal borohydrides, the sodium derivative is commercially readily available.
• the alkali metal borohydride may be added to the refining process of this invention either in solid form, or as discussed above, as an aqueous solution. If desired, the alkali metal borohydride may also be formed in situ from other borohydrides.
• the alkali metal borohydride is generally employed during the alkali refining step in an amount sufficient to effect the desired improvement in the quality of the purified oil.
• the exact amount required for this purpose varies with the particular vegetable oil being refined and with the particular characteristics of the oil which require improvement, e.g., color, flavor, odor, taste, etc.
• alkali metal borohydride typically, from about 50 to about 2000 ppm of alkali metal borohydride are sufficient for most purposes, with preferred amounts ranging from about 250 to 1000 ppm, and most preferably from about 250 to 500 ppm of alkali metal borohydride, based on the weight of the oil.
• the amount of alkali metal borohydride employed be sufficient to produce a purified oil having Lovibond color characterized by a yellow value of 10 or less and a red value of 1 or less, as measured by a Lovibond Tintometer using a 5 1/4" cell-at ambient temperature; a bland taste; a lack of any preceptible odor; and a peroxide value of 0.0 as measured by AOCS Standard Analytical Method Cd 8-53.
• these characteristics are based on the purified oil, i.e., after it has been degummed, refined, bleached, and if required deodorized and and/or
• the refined and purified oil is separated from the resulting soapstock by conventional separation procedures, such as for example, by centrifugation.
• the refined oil is thereafter typically washed with water to remove any residual traces of soap and then dried to remove any dissolved or emulsified water which may be present.
• the production of a purified oil having an acceptable color requires the use of a bleaching process in order to remove pigments remaining in the oil after the refining step, such as various carotenoids and chlorophyll, among others.
• the bleaching step is carried out under vacuum at a moderate temperature in the range of from about 50 to about 120°C in the presence of a bleaching clay.
• the oil is then filtered to remove the bleaching clay and pigment products adsorbed thereon.
• the oil may be thereafter subjected to a deodorization process, winterizing process, dewaxing process, etc. by conventional techniques well known to those skilled in the art in order to further improve the quality of the oil.
• Some oils may also require hydrogenation in order to reduce the polyunsaturates.
• a degummed soybean oil was alkali refined in accordance with the present invention.
• refining was carried out in the presence of 250 - 770 ppm of NaBH 4 , which was utilized in the form of an aqueous sodium borohydride solution comprising approximately 12% NaBH 4 and 40% by weight sodium hydroxide (SWS ® brand, available from the Morton-Thiokol Corporation) and in the presence of 1000 ppm NaBH 4 which was utilized in the form of a dry powder.
• SWS ® brand sodium hydroxide
• a further run was conducted by an identical procedure, but without the use of NaBH 4 during refining.
• each sample was allowed to sit overnight and then filtered through diatomaceous earth. All samples were then stirred for two hours with molecular sieve to remove any remaining water. Each of the resulting samples was then evaluated for peroxide value (A.O.C.S. method Cd 8-53), free fatty acids, FFA, (A.O.C.S. standard method Ca 5a 40, Ca 9a 52, B.3), odor, color (Lovibond system using a Lovibond Tintometer with a 5 1/4 inch cell at ambient temperature) and heat stability.
• the heat stability test comprised an accelerated heat aging process wherein the oil was heated for 2 hours at 205°C in air and then analyzed for color, peroxide value and FFA.
• This example demonstrates the effect of various NaBH 4 treatment levels during the alkali refining and subsequent bleaching at various bleaching clay levels of a partially degummed crude soybean oil.
• Example I The accelerated heat aging test of Example I was then performed on each sample and an analysis of % FFA, peroxide and .color made in order to evaluate to heat stability.

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Cited By (15)

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• 1983
  • 1983-12-15 IN IN841/DEL/83A patent/IN160358B/en unknown
• 1984
  • 1984-01-05 JP JP50584A patent/JPS59136398A/ja active Granted
  • 1984-01-10 EP EP84300145A patent/EP0116408A3/fr not_active Ceased

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