OPTIMIZATION OF CHEMICAL TRANSESTERIFICATION OF PALM OIL USING RESPONSE SURFACE METHODOLOGY

The effect of catalyst concentration (0.1–0.5% methoxide powder), temperature (50–92C), and time (30–480 min) of chemical transesterification was studied to determine the optimum condition for maximizing concentration of triunsaturated and trisaturated triacylglycerols (TG) in palm oil. TG compositions of the oil were analysed using high-performance liquid chromatography. The optimum condition of the process was determined using statistical response surface methodology. The results showed that the triunsaturated and trisaturated TG responses followed a second order form of the treatments with R²= 0.83 and 0.85, respectively. The triunsaturated TG reached a maximum concentration by using 0.36% catalyst at 78C and 360 min reaction time, whereas the trisaturated TG with 0.36% catalyst at 81C and 325 min reaction time. Considering the two responses, it was concluded that the overall optimum condition could be achieved at 0.36% of catalyst at 78–81C and 325–360 min reaction time. Such conditions increased trisaturated TG in palm oil by 2.34 times and triunsaturated TG by 1.54 times.     

MONITORING OF TRANSESTERIFICATION OF PALM OIL BY DIFFERENTIAL SCANNING CALORIMETRY

Chemical transesterification was conducted to obtain triacylglycerol ( TG) containing maximum concentrations of trisaturated and triunsaturated TG in palm oil. Catalyst (sodium methoxide) concentration of 0.1–0.5%, reaction temperature of 50–92C and reaction time of 30–480 min were applied in 20 treatments. Concentrations of trisaturated and triunsaturated TG, as well as melting points and iodine values were monitored by differential scanning calorimetric (DSC) techniques. The results showed that maximum trisaturated and triunsaturated TG achieved for refined-bleached-deodorized (RBD) palm oil were 17.10 and 7.50%, respectively, using 0.42% catalyst, at 58C in 389 min. These amounts were higher compared to control (untransesterified) RBD palm oil i.e 7.45 and 4.92%, respectively. The melting points of the products were higher compared to the control, while the iodine values were not significantly changed in all of the treatments.     

Structured lipids obtained by chemical interesterification of olive oil and palm stearin

Interesterification of palm stearin (PS) with liquid vegetable oils could yield a good solid fat stock that may impart desirable physical properties, because PS is a useful source of vegetable hard fat, providing β′ stable solid fats. Dietary ingestion of olive oil (OO) has been reported to have physiological benefits such as lowering serum cholesterol levels. Fat blends, formulated by binary blends of palm stearin and olive oil in different ratios, were subjected to chemical interesterification with sodium methoxide. The original and interesterified blends were examined for fatty acid and triacylglycerol composition, melting point, solid fat content (SFC) and consistency. Interesterification caused rearrangement of triacylglycerol species, reduction of trisaturated and triunsaturated triacylglycerols content and increase in diunsaturated-monosaturated triacylglycerols of all blends, resulting in lowering of melting point and solid fat content. The incorporation of OO to PS reduced consistency, producing more plastic blends. The mixture and chemical interesterification allowed obtaining fats with various degrees of plasticity, increasing the possibilities for the commercial use of palm stearin and olive oil.     

Preparation of palm olein enriched with medium chain fatty acids by lipase acidolysis

Medium chain (MC) fatty acids, caprylic (C8:0) and capric (C10:0) were incorporated into palm olein by 1,3-specific lipase acidolysis, up to 36% and 43%, respectively, when added as mixtures or individually after 24 h. It was found that these acids were incorporated into palm olein at the expense of palmitic and oleic acids, the former being larger in quantity and reduction of 18:2 was negligible. The modified palm olein products showed reduction in higher molecular weight triacylglycerols (TGs) and increase in concentration of lower molecular weight TGs compared to those of palm olein. Fatty acids at sn-2 position in modified products were: C10:0, 4%; C16:0, 13%; C18:1, 66%; and C18:2, 15.4%. DSC results showed that the onset of melting and solids fat content were considerably reduced in modified palm olein products and no solids were found even at and below 10 °C and also the onset of crystallisation was considerably lowered. The cloud point was reduced and iodine value dropped from 55.4 to 38 in modified palm olein. Thus, nutritionally superior palm olein was prepared by introducing MC fatty acids with reduced palmitic acid through lipase acidolysis.     

Triglyceride composition of Buchanania lanzan seed oil

The fatty acid composition of Buchanania lanzan seed oil, determined by urea complex formation and gas liquid chromatography (g.l.c), was found to be: myristic, 0.6; palmitic, 33.4; stearic, 6.3; oleic, 53.7; and linoleic, 6.0%. Triglyceride compositions of the native seed oil and its randomised product were calculated from the fatty acid compositions of the triglycerides and of the corresponding 2-monoglycerides produced by pancreatic lipase hydrolysis. The oil is composed of 3.2, 35.8, 45.5 and 15.5% trisaturated, monounsaturated disaturated, diunsaturated monosaturated and triunsaturated glycerides respectively. The special characteristic of the B. lanzan seed oil is its content of 22.7, 31.0 and 11.3% dipalmitoolein, dioleopalmitin and triolein respectively. The percent GS₃ content in the oil increased from 3.2 to 7.5 by the process of randomisation. On directed interesterification the oil yielded a product with a slip point of 41.5°C which may be suitable as a coating material for delayed action tablets. The oil also appears to be a promising one as a commercial source of palmitic and oleic acids.     

A study on monitoring of frying performance and oxidative stability of cottonseed and palm oil blends in comparison with original oils

Blending polyunsaturated oils with highly saturated or monounsaturated oils has been studied extensively; however, in literature there is negligible information available on the blending of refined cottonseed oil with palm olein oil. Blending could enhance the stability and quality of cottonseed oil during the frying process. In the present study, the effects of frying conditions on physicochemical properties of the palm olein-cottonseed oil blends (1:0, 3:2, 1:1, 2:3, and 0:1, w/w) were determined and compared to the pure oils. The frying process of frozen French fries was performed in duplicate at 170 ± 5°C for 10 h without interruption. The oil degradations were characterized during deep-frying applications; peroxide, free fatty acid, and iodine value by standardized methods, fatty acid profile by using a gas chromatography-flame ionization detector, polar and polymeric compounds by using the high-performance size exclusion chromatography/evaporative light scattering detector technique. The present study clearly indicated that the oxidative and frying performances of pure palm olein oil and cottonseed oil significantly improved by blending application. Results clearly indicated that the frying performance of cottonseed oil significantly improved by the blending with palm olein oil. Except that free fatty acid content, all the physicochemical variables were significantly influenced by type of pure and blend oils. By increasing the proportion of palm olein oil in cottonseed oil, the levels of polyunsaturated fatty acids decreased, while saturated fatty acid content increased. The progression of oxidation was basically followed by detecting polar and polymeric compounds. The fastest increments for polar and polymeric compounds were found as 6.30% level in pure cottonseed oil and as 7.07% level in 40% cottonseed oil:60% palm olein oil blend. The least increments were detected as 5.40% level in 40% cottonseed oil:60% palm olein oil blend and 2.27% level in 50% cottonseed oil:50% palm olein oil blend. These levels were considerably below the acceptable levels recommended by the official codex. Therefore, the present study suggested that blending of cottonseed oil with palm olein oil provided the oil blends (50% cottonseed oil:50% palm olein oil and 40% cottonseed oil:60% palm olein oil, w/w) with more desirable properties for human nutrition.     

THE EFFECT OF DIFFERENT TYPES OF STIRRER AND FRACTIONATION TEMPERATURES DURING FRACTIONATION ON THE YIELD, CHARACTERISTICS AND QUALITY OF OLEINS

Refined, bleached and deodorized (RED) palm oil was fractionated by dry fractionation using two different types of stirrer at 3 fractionation temperatures to produce palm olein (POo). Statistical analysis by SAS showed significant differences (P < 0.05) between fractionation temperatures of 15C and 21C, and no significant differences between two types of stirrer on product yield. Iodine value showed significant differences between fractionation temperatures of 15C and 18C, and 15C and 21C but no significant difference was observed between the two types of stirrers. Analysis showed that palm olein fractionated at lower temperature contained less saturated fatty acids, more unsaturated fatty acids and lower solid fat than oleins fractionated at higher temperatures.     

Characterization of Low Saturation Palm Oil Products after Continuous Enzymatic Interesterification and Dry Fractionation

ABSTRACT:  The lipase-catalyzed interesterification of refined, bleached, deodorized palm olein with iodine value (IV) of 62 was studied in a pilot continuous packed-bed reactor operating at 65 °C. Sn- 1,3 specific immobilized enzyme; Lipozyme® TL IM ( Thermomyces Lanuginosa ) from Novozyme A/S was used in this study. The interesterification reaction produced fully solidified fats at ambient temperature due to the production of trisaturated triacylglycerols (TAG) (PPP and PPS, where P = palmitic acid, S = stearic acid). The reaction also increased the percentage of triunsaturated TAG (OLL, OLO, and OOO, where O = oleic acid, L = linoleic acid). The interesterified product was then dry fractionated at temperatures of 9, 12, 15, 18, and 21 °C to separate the saturated fats from the unsaturated. The results show that IV of olein increased when the fractionation temperature (T_FN) decreased. The highest IV of olein was 72, obtained from T_FN at 9 °C. After interesterification and laboratory-scale fractionation, the olein fractions contained higher unsaturation content ranging from 64.7% to 67.7% compared to the starting material (58.3%), while the saturation content was reduced from 41.7% to the range of 32.3% to 35.3%. The yields of these oleins were low with the range of 24.8% to 51.8% due to the limitation of the vacuum filtration. Ten kilograms of pilot-scale fractionation with membrane press filter was used to determine the exact olein yield. At T_FN of 12 °C, 67.1% of olein with saturation content of 33.9% was obtained.     

棕榈油与猪油在组成结构和功能特性上的比较

比较了3种棕榈油和6种猪油产品在理化指标、营养与功能特性指标以及脂肪酸组成及其在甘油三酯Sn-2位上的分布情况,以判断棕榈油对猪油的可替代性.结果表明,棕榈油和猪油的熔点、碘值、酸值、过氧化值等理化指标很接近;棕榈油不含胆固醇,具有比猪油较高的V_E含量和氧化稳定性;在可塑性方面,精炼棕榈油与猪板油相当,而且好于猪杂油和猪膘油,棕榈硬脂与猪骨油相当,棕榈液油与猪皮油相当;虽然棕榈油和猪油的脂肪酸组成具有相似性,猪油的不饱和脂肪酸含量略高于棕榈油的不饱和脂肪酸含量,但是棕榈油的Sn-2位上主要分布不饱和脂肪酸,而猪油的Sn-2位上主要分布饱和脂肪酸,使棕榈油比猪油更加容易消化吸收.     

RECOVERY OF PALM CAROTENE FROM PALM OIL AND HYDROLYZED PALM OIL BY ADSORPTION COLUMN CHROMATOGRAPHY

Crude palm oil and crude palm olein were hydrolyzed with lipase from Candida rugosa to produce a free fatty acid (FFA) rich oil. The percentages of FFA produced and carotene degradation after the hydrolysis process were determined. The palm oil and hydrolyzed palm oil were subsequently subjected to column chromatography. Diaion HP-20 adsorbent was used for reverse phase column chromatography at 50C. Isopropanol or ethanol, and n-hexane were used as the first and second eluting solvents, respectively. The objective of hydrolyzing the palm oil was to produce more polar FFA-rich oil in order to enhance the nonpolar carotene bind to the nonpolar HP-20 adsorbent in the column chromatography process. Hydrolyzing palm oil with lipase from Candida rugosa gave 30- and 60-fold, respectively, of FFA in the crude palm oil and crude palm olein in 24 h at 50C. Approximately, 15.56 and 17.48% of carotene degraded in crude palm oil and crude palm olein, respectively. For column chromatography, using isopropanol or ethanol as the first eluting solvent, unhydrolyzed oil and hydrolyzed oil showed the carotene recovery infraction two (carotene-rich fraction) of about 36–37 and 90–96%, respectively. Over 90% of carotene recovery was obtained from     

Deep Frying Performance of Enzymatically Synthesized Palm-Based Medium- and Long-Chain Triacylglycerols (MLCT) Oil Blends

The main aim of this work was to assess the frying strength of the enzymatically synthesized palm-based medium- and long-chain triacylglycerols (MLCT) oil with the aid of different antioxidants under deep-frying conditions. Palm-based MLCT oil in the presence of synthetic or natural antioxidants showed significantly better (P < 0.05) thermal resistance and oxidative strength than refined, bleached, and deodorized (RBD) palm olein throughout the five consecutive days of frying. Rancimat induction period, free fatty acid content, anisidine value, E^\text1% _1\textcm E^{{\text{1\% }}} _{1{\text{cm}}} at 232 and 268 nm, color, percentage of oil uptake, and viscosity measurement can be used as oil quality parameters to indicate the degree of oil deterioration under continuous stressed frying conditions. No significant changes (P > 0.05) in the saturated/unsaturated fatty acids ratio across frying periods indicated good oxidative stability of the palm-based MLCT oil. Due to the polarity of medium- and long-chain triacylglycerols in palm-based MLCT oil, total polar compounds determination may not be a suitable oil quality measures. Sensory evaluation of fried chips showed no significant differences (P > 0.05) between chips fried in RBD palm olein and palm-based MLCT oil over the 3-month storage period.     

Chemical interesterification of milkfat and milkfat-corn oil blends

Blending and chemical interesterification of fats have been used to modify physical and chemical properties of natural fats. The objective of this study was to produce binary mixtures of butterfat and corn oil that serve as a base for a tablespread, keeping the desirable organoleptic qualities of butter, yet with higher contents of ω-6 fatty acids. Chemical interesterification was performed to improve butter’s physical properties, such as better spreadability. Liquefied butterfat and corn oil were mixed in different proportions and then chemically interesterified. Butterfat consisted of 66.5% saturated fatty acids, with palmitic acid being predominant. Corn oil had more than 50% of linoleic acid in its composition. Interesterification significantly reduced trisaturated and triunsaturated triacylglycerol contents and increased softening points in all blends. The negative coefficients of the blends from multiple regression of the solid fat content revealed a monotectic interaction between butterfat and corn oil in temperatures ranging from 10 to 35 °C, before and after interesterification.     

Determination of the triacylglycerol content for the identification and assessment of purity of shea butter fat,peanut oil,and palm kernel oil using maldi-tof/tof mass spectroscopic technique

This article reports the rapid screening and identification of the triacylglycerol content of shea butter fat, palm kernel oil, and peanut oil sold in the local Ghanaian market for their characterization and identification. Samples were dissolved in chloroform with 2,5-dihydroxybenzoic acid as the matrix. After subjecting the samples to matrix-assisted laser desorption ionization-time-of-flight/mass spectrometry, the spectra obtained showed the characteristic triacylglycerols as sodium adducts. Seven major triacylglycerol species were identified as dipalmitoyl olein, palmitoyl diolein, palmitoyl stearoyl olein, linoleoyl diolein, triolein, stearoyl diolein, and distearoyl olein in all three samples. Palmitoyl linoleoyl olein and tristearin were also identified. Oxygenated triacylglycerols and other species from the fragmentation of triacylglycerols were also obtained. The presence of the oxygenated triacylglycerols and the triacylglycerol fragments may be a result of poor handling and production processes.     

巧克力涂层基料油的理化性质及其相容性研究

选用棕榈油中间分提物(PMF)、全氢化棕榈仁液油(HPKOL)、可可脂(CB)作为巧克力涂层的基料油,对其理化性质及其相容性进行分析。结果表明,当两相体系PMF-HPKOL中PMF含量在30%以下时,共晶现象较弱。PMF和HPKOL混合可以作为涂层油脂配方,用于开发无反式脂肪酸巧克力涂层。添加可可脂会导致三相体系(PMF-HPKOL-CB)严重的共晶现象,因此在代可可脂涂层配方中不宜再添加可可脂。     

Comparison of the stability of palm olein and a palm olein/canola oil blend during deep‐fat frying of chicken nuggets and French fries

Stability of palm olein (PO) and a blend 50% palm olein/50% canola oil (POC) during deep‐fat frying at 180 °C of French fries (FF) or chicken nuggets (CN) was studied through the determination of physical and chemical parameters in the fresh and used oils. Degradation at the end of the study resulted in total polar compounds of 12–13.5% for PO and 11.5–14.5% for POC and viscosity of 65–123.3 cP for PO and 63–72.8 cP for POC. Lower peroxide values (5.33–6.32) were obtained for the blend (PO had 5.21–8.55). Food type affected colour parameters and p‐anisidine value of the oils. For CN, the lowest fat content and higher hardness were obtained when they were fried in PO. CN caused a faster deterioration in the oils, in comparison with FF, especially in POC. Gas chromatography allowed to observe differences in fatty acids composition for both used oils.     

Discrimination of palm olein oil and palm stearin oil mixtures using a mass spectrometry based electronic nose

To discriminate mixing ratios for mixtures of palm olein oil and palm stearin oil, an electronic nose based on mass spectrometer (MS-electronic nose) and GC were used. The intensities of each fragment from the palm olein oil and palm stearin oil by the MS-electronic nose were used for discriminant function analysis (DFA). When palm olein oil is mixed with palm stearin oil, more than 3% of stearin oil can be estimated by DFA. The obtained data were used for DFA. DFA plot indicated a significant separation of pure palm olein oil and palm stearin oil. The added concentration of palm stearin oil to palm olein oil was highly correlated with the first discriminant function score (DF1). When palm stearin oil was added to palm olein oil, it was possible to predict the following equation; DF1= −0.112×(conc. of palm stearin oil)+0.416 (r²=0.95). When palm stearin oil was added to palm olein oil, peak area of GC was correlated to DF1 by MS-electronic nose with ratio of palm olein oil vs palm stearin oil. The MS-electronic nose system could be used as an efficient method for the authentication of oil.     

Tropical oils: nutritional and scientific issues.

Individually and in combination with other oils, the tropical oils impart into manufactured foods functional properties that appeal to consumers. The use of and/or labeling in the ingredient lists give the impression that these oils are used extensively in commercially processed foods. The estimated daily intake of tropical oils by adult males is slightly more than one fourth of a tablespoon (3.8 g), 75% of which consists of saturated fatty acids. Dietary fats containing saturated fatty acids at the beta-position tend to raise plasma total and LDL-cholesterol, which, of course, contribute to atherosclerosis and coronary heart disease. Health professionals express concern that consumers who choose foods containing tropical oils unknowingly increase their intake of saturated fatty acids. The saturated fatty acid-rich tropical oils, coconut oil, hydrogenated coconut oil, and palm kernel oil, raise cholesterol levels; studies demonstrating this effect are often confounded by a developing essential fatty acid deficiency. Palm oil, an essential fatty acid-sufficient tropical oil, raises plasma cholesterol only when an excess of cholesterol is presented in the diet. The failure of palm oil to elevate blood cholesterol as predicted by the regression equations developed by Keys et al. and Hegsted et al. might be due to the dominant alpha-position location of its constituent saturated fatty acids. If so, the substitution of interesterified artificial fats for palm oil in food formulations, a recommendation of some health professionals, has the potential of raising cholesterol levels. A second rationale addresses prospective roles minor constituents of palm oil might play in health maintenance. This rationale is founded on the following observations. Dietary palm oil does not raise plasma cholesterol. Single fat studies suggests that oils richer in polyunsaturated fatty acid content tend to decrease thrombus formation. Anomalously, palm oil differs from other of the more saturated fats in tending to decrease thrombus formation. Finally, in studies comparing palm oil with other fats and oils, experimental carcinogenesis is enhanced both by vegetable oils richer in linoleic acid content and by more highly saturated animal fats. The carotenoid constituents of red palm oil are potent dietary anticarcinogens. A second group of antioxidants, the tocotrienols, are present in both palm olein and red palm oil. These vitamin E-active constituents are potent suppressors of cholesterol biosynthesis; emerging data point to their anticarcinogenic and antithrombotic activities. This review does not support claims that foods containing palm oil have no place in a prudent diet.     

The impact of dietary oil source and frozen storage on the physical,chemical and sensorial quality of fillets from market-size red hybrid tilapia, Oreochromis sp.

Red hybrid tilapia (Oreochromis sp.) were fed one of four diets containing either fish oil, crude palm oil, palm fatty acid distillates or refined palm olein as the only added oil. Post-harvest fillet quality was then evaluated at 1, 10 and 30 weeks of frozen storage. Dietary oil source did not significantly (p > 0.05) influence the liquid holding capacity and texture of fillets but both these parameters were increased by frozen storage. Fillets from fish fed palm oil-based diets exhibited significantly higher oxidative stability during frozen storage, compared to fish fed the fish oil diet. Dietary oil source and frozen storage had little impact on sensory attributes. Unlike fillet proximate composition, fillet fatty acid composition was significantly affected by both diet and frozen storage. Total n-3 polyunsaturated fatty acids decreased significantly in the fillet lipids of all fish after 30 weeks of frozen storage.     

Physicochemical characteristics of palm oil and sunflower oil blends fractionated at different temperatures

This research was carried out to determine the effect of fractionation temperature on the physicochemical characteristics of refined, bleached and deodorized (RBD) palm oil and sunflower oil blends fractionated at different temperatures. Blends of 20% and 40% sunflower oil with 80% and 60% RBD palm oil, respectively, were fractionated at three different temperatures (15, 18 and 21 °C). The results showed that olein with higher iodine value was obtained at lower fractionation temperature. This was because, at lower fractionation temperature, more of the polyunsaturated fatty acid, namely linoleic acid (C18:2), went into the liquid fraction. On the other hand, more of the saturated fatty acid, namely palmitic acid (C16:0), went into the liquid fraction at higher fractionation temperature. Blending reduced the triacylglycerol composition, namely POP, POS, SOO and PLP, while OLO, PLL, OLL and LLL/LLnO increased. Lower fractionation temperature decreased the composition of monosaturated triacylglycerol and increased the composition of di- and polyunsaturated triacylglycerols. Lower fractionation temperature produced a liquid fraction with lower solid fat content and lower cloud point than did higher fractionation temperature.     

Interactions between tocopherols,tocotrienols and carotenoids during autoxidation of mixed palm olein and fish oil

Electron spin resonance (ESR) and spin trapping detection of radical formation showed that the oxidative stability of palm olein/fish oil mixtures increased with the amount of palm olein. Mixtures with red palm olein were less stable than were mixtures with yellow palm olein. Addition of ascorbyl palmitate and citric acid gave further reduction of radical formation, whereas no effect was observed by adding lecithins. Storage of palm olein/fish oil mixtures (4:1) at 30 °C confirmed that red palm olein mixtures were less stable than were yellow palm olein mixtures. Ascorbyl palmitate together with citric acid improved the stability in both cases. The concentrations of α-tocopherol and α-tocotrienol decreased during storage, whereas β-, γ-, and δ-tocotrienols were unaffected. Ascorbyl palmitate reduced the losses of α-tocopherol and α-tocotrienol. The rate of loss of carotenoids was independent of the presence of fish oil and, except for an initial fast drop, also of the presence of ascorbyl palmitate.