Composition, stability and acceptability of different vegetable oils used for frying peanuts

The purpose of this work was to determine the chemical stability of vegetable oils in the frying process and the consumer acceptance of fried-salted peanuts prepared in different vegetable oils. Fatty acids composition was determined in sunflower, corn, soybean, peanut and olive oils. A chemical study (free fatty acid and p-anisidine values) of these oils at frying temperature (170 °C) was developed during 96 h. Consumer test of fresh products was performed on fried-salted peanuts prepared in the different oils. Peanut oil and virgin olive oil presented oleic acid as predominant fatty acid (44.8% and 64.2%, respectively), making it more resistant to lipid oxidation at frying temperature than the other refined vegetable oils (sunflower, corn and soybean oils). Virgin olive and peanut oils showed less increment of free fatty acids and p-anisidine value than the other oils along the heating essay. In addition, fried-salted peanuts prepared with refined peanut oil showed higher consumer acceptance than those prepared with other vegetable oils such as sunflower, corn, soybean and olive oils. Peanut oil could be used to fry peanuts obtaining products with higher consumer acceptance and shelf-life, thus preventing loss of their sensory and nutritional quality.     

Temperature Dependence of Autoxidation of Perilla Oil and Tocopherol Degradation

Abstract: Temperature dependence of the autoxidation of perilla oil and tocopherol degradation was studied with corn oil as a reference. The oils were oxidized in the dark at 20, 40, 60, and 80 °C. Oil oxidation was determined by peroxide and conjugated dienoic acid values. Tocopherols in the oils were quantified by HPLC. The oxidation of both oils increased with oxidation time and temperature. Induction periods for oil autoxidation decreased with temperature, and were longer in corn oil than in perilla oil, indicating higher sensitivity of perilla oil to oxidation. However, time lag for tocopherol degradation was longer in perilla oil, indicating higher stability of tocopherols in perilla oil than in corn oil. Activation energies for oil autoxidation and tocopherol degradation were higher in perilla oil (23.9 to 24.2, 9.8 kcal/mol, respectively) than in corn oil (12.5 to 15.8, 8.8 kcal/mol, respectively) indicating higher temperature-dependence in perilla oil. Higher stability of tocopherols in perilla oil was highly related with polyphenols. The study suggests that more careful temperature control is required to decrease the autoxidation of perilla oil than that of corn oil, and polyphenols contributed to the oxidative stability of perilla oil by protecting tocopherols from degradation, especially at the early stage of oil autoxidation.     

Loss of tocopherols and formation of degradation compounds at frying temperatures in oils differing in degree of unsaturation and natural antioxidant content

Samples of oils of different degrees of unsaturation, namely palm olein, olive oil, high‐linoleic sunflower oil, high‐oleic sunflower oil, rapeseed oil and soybean oil, were heated at 180 °C for 2, 4, 6, 8 and 10 h in the presence or absence of their natural antioxidants. Also, tocopherol‐stripped oils were supplemented with α‐tocopherol (500 mg kg^?1), δ‐tocopherol (500 mg kg^?1) or a mixture of α‐, β‐, γ‐ and δ‐tocopherols (250 mg kg^?1 each) and heated under the same conditions. Losses of tocopherols and formation of polymeric triacylglycerols were followed. Total polar compounds were also evaluated after 10 h of heating. Results demonstrated that tocopherols were lost very rapidly, in the expected order, with α‐tocopherol being the least stable. Polymeric and polar compound formation during heating was inhibited to a variable extent, being more dependent on the natural content and type of tocopherols than on the degree of unsaturation of the oil. For example, polymeric and polar compound contents in soybean oil were significantly lower than those found in high‐linoleic sunflower oil. However, the expected influence of the degree of unsaturation was evident when oils were unprotected or possessed identical initial antioxidant contents. Finally, levels of degradation compounds after 10 h of heating were not dependent on the remaining content of antioxidants. © 2002 Society of Chemical Industry     

Effect of temperature on oxidation kinetics of walnut and grape seed oil

The effects of temperature on the oxidation of walnut oil (WO) and grape seed oil (GSO) were investigated. Both oils were stored at 25, 40, 60, and 80°C for 60, 30, 12, and 6 day, respectively. Degree of oxidation was measured in terms of peroxide value (POV), conjugated dienoic acid (CDA) value, and p-anisidine value (p-AV). The rates of increase in POV, CDA, and p-AV in both oils were strongly dependent on storage temperature. The induction period (IP) decreased gradually with increasing storage temperature in both oils. WO showed shorter IPs (23.0, 9.2, and 1.0 day at 25, 40, and 60°C, respectively) than those of GSO (41.5, 12.0, and 1.8 day at 25, 40, and 60°C, respectively), indicating the higher susceptibility of WO to oxidation. The activation energy (Ea) for the IP of WO and GSO autoxidation was similar (75.87 and 75.66 kJ/mol, respectively), revealing similar temperature dependence for autoxidation in WO and GSO.

     

Oxidative changes in hazelnut,olive, soybean,and sunflower oils during microwave heating

The effects of microwave heating for 3, 6, and 9 min at a frequency of 2450 MHz on fatty acid composition, tocopherols, iodine value, free fatty acids (%), peroxide value, conjugated dienes and trienes, and hexanal contents of refined hazelnut, soybean, sunflower, and virgin olive oils were investigated. A significant (p < 0.05) decrease was observed in linoleic and linolenic acids contents of soybean oil during exposure to microwave heating. Tocopherol contents of oil samples significantly decreased (p < 0.05) during microwave heating. Free fatty acids of the samples slightly increased and iodine value showed reduction throughout the process. Conjugated dienes contents of samples showed an increasing trend up to the 6 min, followed by a reduction at 9 min. Conjugated triene fatty acids of all the samples significantly increased (p < 0.05) throughout the application. While peroxide value showed increasing trend up to the 3 min and sharply decreased at 9 min, hexanal contents of refined hazelnut, virgin olive, soybean, and sunflower oils increased 63, 28, 55, and 389 fold, respectively, after 9 min exposure to microwave heating. Kinetic analysis of data showed that the reaction orders for peroxide and hexanal formation were zero and first order, respectively, and in the tested oils the reaction rate followed the order: soybean oil ? sunflower oil ? hazelnut oil ? virgin olive oil for peroxide, and sunflower oil ? soybean oil ? hazelnut oil ? virgin olive oil for hexanal formation. It was concluded that hexanal could be considered as a parameter for evaluation of the quality of oils exposed to microwave heating.     

Measurement of Thermal Conductivity of Edible Oils Using Transient Hot Wire Method

Thermal conductivities of three different edible oils, namely sunflower oil, corn oil and olive oil, were measured at temperatures 25, 40, 60, and 80°C. The measurements were carried out using a hot wire probe method. The calibration of the probe was performed using 0.3% agar gel with water and glycerin. In general, thermal conductivities of oils used in this study are found to be decreasing with temperature. The values of thermal conductivity measured are quite near to each other, the highest and the lowest being respectively 0.168 W/m K for sunflower oil at 25°C and 0.152 W/m K for corn oil at 80°C.     

Comparison of Oxidative Stability of Sesame (Sesamum Indicum), Soybean (Glycine Max) and Mahua (Mee) (Madhuca Longifolia) Oils Against Photo-Oxidation and Autoxidation

Lipid oxidation is one of the major causes of food spoilage. This study was conducted to evaluate and compare the oxidative stability of sesame (Sesamum indicum), soybean (Glycine max) and mahua (Madhuca longifolia) against photooxidation and autoxidation. Stability of oils against photo-oxidation and autoxidation was determined by exposing the oils to florescent light over 28 days and storing the oils at an elevated temperature (60 °C) for 28 days, respectively. The level of oxidation was determined by measuring peroxide value (PV), thiobarbituric acid reactive substances (TBARS), conjugated dienes (CD) and conjugated trienes (CT). Sesame oil exhibited the strongest oxidative stability against both photo-oxidation and autoxidation while Mahua oil exhibited the least stability highest both photo-oxidation and autoxidation as measured by primary oxidative products. However, Mahua oil showed the strongest stability against both photo-oxidation and autoxidation as measured by secondary oxidative products. In conclusion, higher oxidative stability was shown by the Mahua oil than sesame and soybean oils for photooxidation and autoxidation.     

Lipid oxidation-related characteristics of gim bugak (Korean fried cuisine with <Emphasis Type="Italic">Porphyra</Emphasis>) affected by frying oil

The effect of frying oil on the lipid oxidation, antioxidants, and in vitro antioxidant activity of gim bugak was studied. Bugak was prepared by pan-frying at 180 °C in unroasted sesame, soybean, extra virgin olive, or palm oil. The degree of lipid oxidation based on conjugated dienoic acid and p-anisidine values was higher in the bugak fried in soybean or sesame oil with high contents of polyunsaturated fatty acids and tocopherols. However, the oil oxidation was lower in olive and palm oils, which showed higher degradation of tocopherols and polyphenols than in sesame or soybean oil during frying. Although the bugak fried in palm oil contained less antioxidants than that fried in soybean or sesame oil, the in vitro antioxidant activity was not different (p > 0.05). Results suggest that palm oil can replace unroasted sesame oil for the preparation of gim bugak with improved lipid oxidative stability and health functionality.     

Chromatic parameters and oxidation indices for edible vegetable oils submitted to thermal oxidation

Peroxide values, TBA numbers and chromatic parameters of edible vegetable oils (olive, sunflower, corn oils) thermally oxidised (75°C, 100°C, 180°C) during 5 days were determined. For calculating chromatic parameters the recommended standard CIE methods and several simplified methods were employed. With olive oil a remarkable change in spectral characteristics occurred as the temperature and time of heating were increased. Thermal autoxidation, as assessed by peroxide value and TBA number, was only observed at 75°C (Schaal oven test). In none of the three types of vegetable oil was the dominant wavelength modified during the course of the heating process. Luminosity and hue angle showed slight increases in olive and sunflower oils. Colour saturation underwent a remarkable decrease in olive oil. From a comparison and a correlation study it is concluded that the simplified methods could be applied only for certain chromatic parameters and types of vegetable oil. For a comprehensive study of the diverse chromatic parameters the standard CIE methods should be applied.     

Use crude olive leaf juice as a natural antioxidant for the stability of sunflower oil during heating

Olive leaves (Kronakii cultivar) were obtained from the annual pruning of olive trees and pressed to obtain a crude juice. Aliquots from the concentrated crude olive leaf juice, representing 400, 800, 1600 and 2400 ppm as polyphenols, were added to sunflower oil. Samples of sunflower oil mixed with olive leaf juice were heated intermittently at 180 ± 5 °C for 5 h day^?1 and the heating process was repeated for five consecutive days. A control experiment was performed where butylated hydroxyl toluene (BHT) at 200 ppm was added to sunflower oil prior to intermittent heating in order to compare the antioxidant efficiency between the natural polyphenolics of olive leaf juice and synthetic antioxidant BHT. Some physical and chemical constants for the unheated and heated sunflower oil were determined. The data indicate that the addition of olive leaf juice to sunflower oil heated at 180 °C induced remarkable antioxidant activity and at 800 ppm level was superior to that of BHT in increasing sunflower oil stability.     

Antioxidant activity of grapefruit seed extract on vegetable oils

The antioxidant activities of a grapefruit seed extract (GFSE) which contains tocopherols, citric acid and ascorbic acid, were investigated in vegetable oils. Different amounts of GFSE in powder were dissolved in a mixture of soybean oil–sunflower oil. The oxidation was carried out in an AOM equipment at temperatures of 98·7°C, 75°C and 66·5°C. The results indicated prooxidant effects of GFSE at 97·8°C and 75°C possibly due to a blockade effect of a hydroxyl compound by tocopherol. The inhibitor reaction orders at these temperatures were 0·902 and 0·465, respectively, while at 66·5°C the oxidation rate was inverse to GFSE concentration with reaction order of −0·420. These results seem to indicate different reaction mechanisms depending on temperature conditions. The blockade effects were explained on the basis of a proposed complex between tocopherol and citric acid molecules. © 1998 SCI.     

Prooxidant Activity of Oxidized α-Tocopherol in Vegetable Oils

ABSTRACT:  The effect of oxidized α-tocopherol on the oxidative stabilities of soybean, corn, safflower, and olive oils and the oxidation of oleic, linoleic, and linolenic acids were studied. The 0, 650, 1300, and 2600 ppm oxidized α-tocopherol were added to soybean, corn, safflower, and olive oils and 10000 ppm oxidized α-tocopherol to the mixture of oleic, linoleic, and linolenic acids. Samples in the gas-tight vials were stored in the dark for 6 or 35 d at 55 °C. The oxidative stabilities of oils were determined by headspace oxygen with GC and peroxide value. Fatty acids were determined by GC. As the concentration of oxidized α-tocopherol in soybean, corn, safflower, and olive oils increased, the depletion of headspace oxygen and the peroxide values of oils increased during storage. The prooxidant effects of oxidized α-tocopherol on soybean and corn oils with about 55% linoleic acid were greater than those on safflower and olive oils with about 12% linoleic acid, respectively ( P  < 0.05). The changes of fatty acids during storage showed that the oxidation ratios of oleic, linoleic, and linolenic acids were 1 : 2 : 3, 1 : 12 : 26, and 1 : 8 : 16 after 5, 30, and 35 d of storage, respectively. The oxidation of α-tocopherol in oil should be prevented and the oxidized α-tocopherol should be removed to improve the oxidative stability of oils.     

Extra-Virgin Olive Oil and Cheap Vegetable Oils: Distinction and Detection of Adulteration as Determined by GC and Chemometrics

Refined oils including corn, sunflower, soybean, and palm oils as well as low-quality olive oil such as refined lampante and pomace olive oils are commonly used for extra-virgin olive oil (EVOO) adulteration. Indeed, K ₂₇₀ could be used as a parameter for the detection of EVOO fraud for each type of the studied refined oils, 10 % olive, 4 % pomace olive, 10 % palm, 5 % corn, and 2 % soybean oils. Moreover, the adulteration could also be detected by the increase of the trans fatty acid contents with 10 % pomace olive, 3 % soybean, 3 % sunflower, 2 % corn, and 10 % palm oils. Actually, stigmasta-3,5-diene content is one of the most effective means of detecting refined oils in EVOO at low levels: 2 % olive, 0.4 % pomace olive, 1 % palm, 0.2 % soybean, 0.5 % sunflower, and 0.1 % corn oils. Finally, the application of linear discriminant analysis could represent an alternative and innovative tool for faster and cheaper evaluation of EVOO adulteration.     

Contribution of minor compounds to the singlet oxygen-related photooxidation of olive and perilla oil blend

This study evaluated contribution of natural minor compounds including carotenoids, tocopherols, polyphenols, and phosphatidylcholine (PC) to the stability of chlorophyll sensitized oxidation of olive and perilla oil blend under 2,500 lx light at 25°C for 48 h. The oxidation of the oil blend was evaluated by headspace oxygen consumption and peroxide values (POV). Minor compounds were also monitored. The headspace oxygen consumption and POV of the oil blend were increased with oxidation time; however, fatty acid composition was not significantly changed. Carotenoids, tocopherols, polyphenols, and PC were degraded during the oil oxidation, which was closely related with their singlet oxygen quenching. Correlations of the oil oxidation were higher with contents of carotenoids and PC (r ²>0.93) than with those of tocopherols or polyphenols, suggesting high contribution of carotenoids and PC to decreasing singlet oxygen-related photooxidation of olive and perilla oil blend.     

Interaction of packaging materials and vegetable oils: oil stability

The effects of different plastic films (polyethyleneterephthalate, polyvinylchloride, polypropylene and polystyrene) on the stability of olive, sunflower and palm oils were studied at 24 and 37°C during 60 days of storage. The changes in peroxide value (PV) and thiobarbituric acid value (TBA) were significantly higher (p≤0.05) in the plastic bottles than in glass. Our study indicates that the plastic permeability has played a major role in oil stability. However, both butylated hydroxyanisole (BHA) and butylated hydroxytoluene (BHT) were found to leach out from plastics films into vegetable oils during storage. The rate of oxidation was not reduced by antioxidant migration from plastic films to oils. Natural antioxidant (vitamin E) retarded the oxidation rate, and this was dependent on its concentration in oils examined. The results showed that the ranking of stability of oil samples is PVC≥PET>PP≥PS. Further, the stability was dependent on the type of oil. Palm oil exibited high stability properties while the highest oxidation rate was observed in sunflower oil. In addition, increasing storage temperature accelerated the oxidation and limited the stability of vegetable oils.     

Antioxidant activity of ginger extract in sunflower oil

The antioxidant activity of dichloromethane extract from ginger was evaluated during 6 months of storage of refined sunflower oil at 25 and 45 °C. Free fatty acid (FFA) content, peroxide value (POV) and iodine value (IV) were used as criteria to assess ginger extract as an antioxidant. After 6 months of storage at 45 °C, sunflower oil containing 1600 and 2400 ppm ginger extract showed lower FFA contents (0.083 and 0.080%) and POVs (24.5 and 24.0 meq kg^?1) than the control sample (FFA contents 0.380%, POV 198.0 meq kg^?1). Sunflower oil containing 200 ppm butylated hydroxyanisole (BHA) and butylated hydroxytoluene (BHT) showed FFA contents of 0.089 and 0.072% and POVs of 26.5 and 24.7 meq kg^?1 respectively after 6 months of storage at 45 °C. Similarly, after 6 months of storage at 45 °C, IVs of sunflower oil containing 1600 and 2400 ppm ginger extract were 80 and 92 respectively, higher than that of the control sample (53). However, IVs of sunflower oil treated with 200 ppm BHA and BHT were 94 and 96 respectively after 6 months of storage at 45 °C. These results illustrate that ginger extract at various concentrations exhibited very strong antioxidant activity, almost equal to that of synthetic antioxidants (BHA and BHT). Ginger extract also showed good thermal stability and exhibited 85.2% inhibition of peroxidation of linoleic acid when heated at 185 °C for 120 min. Therefore the use of ginger extract in foods is recommended as a natural antioxidant to suppress lipid oxidation. © 2003 Society of Chemical Industry     

On the participation of fatty alcohols in the autoxidation of lipids

The influence of 1-tetradecanol, 1-hexadecanol, 1-octadecanol and 1-eicosanol in concentrations of 5 to 80 mmol kg^?1 on the autoxidation of various types of lipid systems (sunflower and olive oils, lard, tristearin and olive oil methyl esters) is investigated at 70–135°C. A pro-oxidative effect of the fatty alcohols introduced into the systems is established. The extent of this effect depends on the type and degree of unsaturation in the lipid system, its hydroperoxide content, and the chain length and concentration of the alcohols. A further factor is the valency of the alcohols with which the fatty acids are esterified; thus the pro-oxidative effect of the fatty alcohols is less pronounced with triacyl glycerols than with fatty acid methyl esters given the same oxidation rate. The results obtained are explained on the basis of the theory of a radical chain process of lipid oxidation.     

The tocopherol content of greek olive oils

Four types of Greek olive oil were analysed for α-and γ-tocopherols by high performance liquid chromatography. Certain seed oils widely consumed in Greece were also analysed for comparison with the olive oils. Virgin, pure, residual and refined oils contained an average of 113,81,156 and 37 mg kg^?1 of α-tocopherol, respectively. The α-tocopherol level within each type of olive oil appeared to be influenced by different factors. The content of y-tocopherol averaged 17 and 33 mg kg^?1of virgin and residual oil, respectively. Refined and pure olive oil contained very low levels of y-tocopherol. The α-tocopherol equivalent per gram of polyunsaturated fatty acids was calculated to be 1·48, 0·60, 0·88, 1·07 and 0·58 for edible olive oils, corn, cottonseed, sunflower and partially hydrogenated soya bean oil, respectively.     

The influence of phenolic extracts obtained from the olive plant (cvs. Picual and Kronakii), on the stability of sunflower oil

Summary The phenolic compounds of olive cultivars (Picual and Kronakii) were extracted. The total phenolic content of the extracts was estimated and their ability to reduce the oxidation of sunflower oil was tested at 100 °C by using a Rancimat^®. The fruits, leaves and pomaces were extracted separately with ethanol. Portions of the fruits were crushed to produce an oil/aqueous mixture, which was separated and the two fractions further processed. The oil fraction was extracted with 60% aqueous methanol and was separated further, by the method of Dabrowski & Sosulski (1984 ), into three major fractions. These contained mainly free phenols, soluble phenolic esters or bound phenolic acids, respectively. The phenolic concentrations were measured in all the fractions and were in accordance with expected amounts. When tested at 100, 200 or 400 ppm for their ability to stabilize sunflower oil the results showed that the vast majority of the anti‐oxidant activity found in the ‘total phenols’ fraction was because of a ‘free phenolic’ group. The free phenolics, at a 400‐ppm level, exhibited remarkable anti‐oxidant activity and were superior to that of butylated hydroxy toluene (BHT) in retarding sunflower oil oxidative rancidity. The mode of action is discussed.     

Thermal Stability Assessment of Vegetable Oils by Raman Spectroscopy and Chemometrics

Vegetable oils are widely used in culinary, e.g. in deep frying, cooking, and baking. During these processes, the oils are submitted to high temperatures, giving rise to unhealthy compounds. The risk for the health related to oil consumption resulted in a search for more healthy and stable oils, which could maintain their properties during the cooking process. The aim of this work was to evaluate the thermal stability of the most common oils used for cooking in Brazil by Raman spectroscopy. Eight types of vegetable oils (cotton, extra virgin olive oil, refined olive oil, canola, coconut, sunflower, corn, and soybean) were evaluated, heating them at temperatures ranging from 25 °C to 205 °C. The stability of oils presented high correlation with their smoke points. As expected, the more evident spectral changes were observed in the oils that present lower smoke points. The refined oils, which in general present higher smoke points, presented better stability. In this study, the more stable oils were sunflower, cotton, and canola. These results showed that Raman spectroscopy allied with chemometric tools as a fast and accurate method to evaluate the thermal stability of edible oils. At the same way, this technique could be employed to monitor and check the quality of oils used in restaurants.