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
  • C11B3/04—Refining fats or fatty oils by chemical reaction with acids
• • 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
  • C11B3/006—Refining fats or fatty oils by extraction

Definitions

• the oxidation of polyunsaturated fatty substances is a critical problem because it modifies the quality of the oil since it leads to a bad taste, an unpleasant odor and a change in color.
• metals such as copper and iron act as powerful pro-oxidants.
• fatty substances free of metals are mainly present in the form of ions associated with phospholipids, themselves undesirable, with iron, calcium and magnesium.
• These salts are soluble complexes of phosphatidic acid and phosphatidylethanolamine. These complexes, called non-hydratable phospholipids, are difficult to remove and traditional degumming is not enough to reduce their concentrations to an acceptable level.
• Patents 4,069,686, 4,698,185 The phospholipid content can be reduced to around 20 ppm and the iron content to 0.2 ppm. These values remain high.
• Patent FR 1,388,567 and PCT application WO 950069 describe the refining of oil using organic acids and emulsifying agents. The fatty substance is suspended in an aqueous phase containing the acid and the emulsifier. The phospholipids are removed by complexing the polyvalent metals with acids, preferably polycarboxylic acids.
• emulsifiers require subsequent operations consisting, for example, of washing by centrifugation.
• the preferred emulsifier e.g. sodium lauryl sulfate is also not accepted in some countries due to the difficulty of removing it during refining.
• the present invention makes it possible to remedy the drawbacks mentioned above and to propose an economically valid method for completely ridding fatty substances, crude or delicithinated animal or vegetable fats, of their metals calcium, magnesium, iron as well as phospholipids.
• the iron content is indeed reduced from 8 to 0.05 ppm, in the same way the phosphorus content from 800 to 100 ppm at the origin can be reduced to less than 5 ppm even for oils bad qualities.
• a process for removing phospholipids and / or removing polyvalent metals from a fatty substance comprising the step of mixing the fatty substance with an aqueous solution of an acid salt.
• polycarboxylic or a mono salt, or corresponding polysodium characterized in that the mixing takes place in the form of fine droplets or in the micellar form of said aqueous solution in the fatty substance.
• the mixture thus occurs essentially or only in the so-called droplet or micellar form.
• the complexing agent is preferably an acid comprising at least 3 carboxylic functions, in the acid form or in the form of salts of monovalent cations.
• the preferred complexing agent is a sodium salt of ethylenediaminetetraacetic acid (EDTA).
• EDTA ethylenediaminetetraacetic acid
• a potassium salt or a mixed salt may also be suitable.
• the EDTA sodium solution used can also be a mixture of EDTA sodium salt with any other inorganic base.
• the fatty substance containing many non-hydratable phospholipids is previously intimately mixed with an organic or inorganic acid so as to dissociate the phospholipid-metal complexes and facilitate the co plexation of metals using '' an aqueous sodium solution of EDTA intimately mixed with the oil.
• the sodium solution of EDTA neutralizes the free hydroxyl functions phosphatidic acid (AP) and phosphatidylethanolamine (PE) to make them hydratable in sodium form.
• the organic acid chosen to dissociate the phospholipid-metal complex is, for example, citric, malic, ethylenediamine tetracetic, tartaric, oxalic, maleic acid or an inorganic acid such as phosphoric, hydrochloric or sulfuric acid.
• Concentrated acid is added in small amounts to the fatty substance. If added concentrated, the amount of acid can vary from 0.005 to 0.15% by weight relative to the oil but can be diluted up to 90%. This acid pretreatment is advantageously carried out at the same temperature as that of the addition of the complexing agent. In some cases, a different temperature is chosen.
• the acid is mixed for a very short time 3 to 4 seconds to 10 minutes using an emulsifier or homogenizer. It can also be mixed using a conventional shaker for more than 10 minutes.
• the aqueous solution of the complexing agent also comprises an electrolyte derived from monovalent cations, for example NaCl, KCl or Na2SO4.
• concentration of the electrolyte will preferably vary between 0.1 and 10%, typically between 0.5 and 5% by weight.
• the amount of complexing agent is close to the stoichiometric amount based on the estimated amount of metals in the oil to be refined.
• the EDTA salt perfectly chelates polyvalent metal cations (Fe ++ , Fe +++ , Ca ++ , Mg ++ ) and forms with them complexes much more stable than those obtained with phosphatidic acid or even phosphoric or citric acids which have a much lower stability constant.
• the EDTA complex is very stable, even at high temperatures. The separation of the aqueous phase can then be carried out at high temperature by decantation or centrifugation with the consequences of low losses of neutral oil and a high separation capacity.
• oils rich in metals and in phospholipids treated in this way can be bleached in a conventional manner with amounts of earth equivalent to those necessary for chemical refining and can be physically refined to generate oils of better quality from the point of view of stability to l oxidation at competitive prices.
• the removal of metals and phospholipids according to the invention can easily be carried out at the place of extraction, eg in the palm oil mill, during the removal of the "sludges oils" and give an oil which no longer requires only one step of deacidification-deodorization by steam entrainment.
• the invention therefore has a substantial economic advantage.
• the intimate mixing "aqueous phase in oil” is carried out for example using an emulsifier or homogenizer of the Ultraturax type between 50 and 20,000 revolutions per minute or using an ultrasonic device.
• the aqueous solution is from 0.5 to 30% by weight, preferably 3 to 15%, more preferably from 5 to 10% by weight of the fatty substance to be refined.
• the latter has most often already been degummed in a conventional manner in order to eliminate the hydratable phospholipids by delecithination, ie stirring in the presence of hot water then centrifugation.
• the reaction is preferably carried out at a temperature varying from 5 to 120 ° C., more preferably around 80 ° C.
• the reaction time will depend on the temperature, the reaction may take a few seconds, a few minutes or more than an hour.
• the preferred chelating agent is ethylene diaminetetracetic acid or one of its sodium, potassium or ammonium salts. This acid will preferably be in the disodium, trisodium or tetrasodium form.
• the amount of complexing agent in the aqueous phase is chosen according to the estimated amount of metals to be removed and the presence of carboxylic acids free from the oil to be refined, as well as according to the nature and form of the complexing agent.
• This quantity is advantageously close to the stoichiometric quantity, varying from 1 to 2, preferably from 1.2 to 1.5 equivalent.
• the free carboxylic acid will react first with tetrasodium EDTA to form the corresponding sodium salt and EDTA trisodium. The latter will then complex the metals associated with the phospholipids.
• fish and rapeseed oils rich in metals, phospholipids and sulfur products can be desulfurized simultaneously with the process of the invention.
• the crude corn and sunflower oils rich in iron, phospholipids and waxes can be dewaxed simultaneously with the process.
• the suspension After intimate mixing of the aqueous phase with the crude oil according to the invention, the suspension is cooled with less stirring between 5 and 90 ° C, preferably 5 to 50 ° C, before centrifugation.
• An oil purified from its waxes is thus obtained, the iron content of which is less than 0.05 ppm, and the phosphorus content is less than 5 ppm.
• palm fat can be treated with an aqueous solution containing the same reagents, then gradually cooled in a crystallizer before centrifugation.
• the result is a light phase, palm olein free of its metals, phospholipids and glucolipids and a heavy phase, containing the stearin crystals coated in the aqueous phase.
• palm fats can be degummed, demetallized and fractionated in one operation.
• the invention allows fats with a phosphorus content of less than 50 ppm or even 20 ppm, to be refined physically without the addition of bleaching earth or with a quantity of soil less than 0.5% to give an oil of maximum 3 red (Lovibond 5 1/4 ”) for palm oil.
• palm oil crystallizes better, is fractionated more easily and with better yield.
• aqueous phase consisting of 2.5 liters of water at 80 ° C in which 100 g of disodium salt of EDTA and 50 g of sodium chloride are dissolved, is added all at once to the soybean oil. After an agitation time of 10 min, the aqueous phase is centrifuged
• aqueous phase consisting of 5 liters of water at 80 ° C. in which 70 g of disodium salt of EDTA and 100 g of sodium chloride are dissolved, is added all at once to the cocoa butter. After an agitation time of 8 min, the aqueous phase is centrifuged.

Landscapes

• Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Microbiology (AREA)
• Engineering & Computer Science (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Wood Science & Technology (AREA)
• Organic Chemistry (AREA)
• General Chemical & Material Sciences (AREA)
• Fats And Perfumes (AREA)

Applications Claiming Priority (3)

Publications (1)

Family

ID=3890628

Family Applications (1)

Country Status (6)

Families Citing this family (21)

Family Cites Families (8)

• 1998
  • 1998-07-09 CA CA002296004A patent/CA2296004A1/fr not_active Abandoned
  • 1998-07-09 AU AU83267/98A patent/AU728062B2/en not_active Ceased
  • 1998-07-09 WO PCT/BE1998/000107 patent/WO1999002630A1/fr not_active Application Discontinuation
  • 1998-07-09 CN CN98806922A patent/CN1087339C/zh not_active Expired - Fee Related
  • 1998-07-09 EP EP98933382A patent/EP1000132A1/de not_active Withdrawn
  • 1998-07-09 US US09/462,423 patent/US6407271B1/en not_active Expired - Fee Related

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events