Palm oil fractionation and carotene extraction

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Date
1978-04
Authors
Boey, Peng Lim
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Publisher
Universiti Sains Malaysia
Abstract
A novel method of fractionation of vegetable, animal and fish oils and in particular palm oil is described. The method involves the a·ddition to the oils a medium made up of two common solvents. On centrifugation the olein and stearin are separated by tne medium in the middle. Twelve solvent systems or media which are made up of a combination of two from eight common solvents viz. water, propylene glycol, glycerine, acetone, ethanol, n-propanol, isopropanol and butanone are found to be effective in olein-stearin separation. However, the water-isopropanol system was studied in great details. The fractionation process can oe carried out at any suitable temperature and is independent of the method of crystal] isation of the oil. Fractionation of the Special Prime Bleached (SPB) crude palm oil at 16°C using the water-isopropanol system, yielded an olein fraction with a cloud point of 4.8°C. The used medium can be re-used up to seven times. Fractionation of hydrogenated palm kernel oil yielded a stearin fraction similar in melting characteristic (36°C) to that of cocoa butter. This fractionation process could also be extended with suitable modifications to include degumming and neutralisation. The olein fractions obtained after fractionation were found to be free from phosphatides and the free fatty acid content was reduced to as low as 0.02%. The development of this fractionation into a continuous process has been demonstrated using the Alfa-Laval LAPX 202 Separator. From the fractionation study of the various oil from hybrid palms, the Interspecific Hybrid F1 ( E. oleifera x E. guineensis (Pisifera based) ) was found to be promising. When the oil was fractionated at 15°C, the yield of olein was 87.7%, its cloud point 1.7°C and its iodine value 66.7 and the total unsaturation was 63% whilst the corresponding stearin obtained has a melting point of 49.0°C . Fractionation of crude palm oil using density graqients yielded six stearin fractions of different melting-characteristics (47.5°C to 55.3°C) and fatty acid composition (unsatur~tion 48.4% to 34.9%). Besides fractionation, this finding could also be applied to the determination of the olein content of palm oil. A reasonable relationship was found to exist between the percentage of olein thus determined at 29°C and the fatty acid composition. A mixture of 80% water and 20% isopropanol containing sodium hydroxide was found to effect neutralisation of palm oil and palm kernel oil without the formation of emulsion, while minimising oil loss to 4.8% . Oil loss using aqueous sodium hydroxide was 7.6% . A study on the synergistic effect-of lecithin with various common antioxidants in stabilising oils showed that the amount of antioxidants used could be very much reduced. It was found that when 0.05% of lecithin was added only 1/8 of the original concentration of buty hydroquinone (TBHQ) or 1/20 of the original concentration of butylated hydroxy anisole (BHA) or butylated hydroxy toluene (BHT) when used singly was required to give the same AOM-stabil ity. Normal refining of crude palm oil destroys the carotenes present in it. Here, a method of extracting the carotenes with locally produced activated carbons is described. The carotene extract obtained (using S51 I carbon) is about six times that of the concentration of carotene in the original oil. The extracted carotenes are biologically active and not toxic to animals as confirmed by feeding experiments using albino rats and a histological study of their organs. The sorption study on the activated carbons shows that carbons of pH around 10.8 ~ith large surface area and possessing large numbers of mesopores are suitable for carotene extraction.
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Keywords
Palm oil
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