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3. FOOD ChEMISTRy & bIOTEChNOLOGy 3.1. Lectures

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Chem. Listy, 102, s265–s1311 (2008) Food Chemistry & Biotechnology<br />

P97 STuDy OF OxIDATION STAbILITy<br />

OF SELECTED VEGETAGLE OILS<br />

HAnA ŠTOUDKOVá, MOnIKA MAXOVá, JIří<br />

KUČERíK and JAnA ZEMAnOVá<br />

Brno University of Technology, Faculty of Chemistry, Purkynova<br />

118, 61200 Brno, Czech Republic,<br />

stoudkova@fch.vutbr.cz<br />

Introduction<br />

Vegetable oils are obtained from different parts of oilseed<br />

plants by cold expression and subsequent extraction<br />

and purification. Since long ago, oils belong to among basic<br />

cosmetic preparations and use in pharmaceuticals, food industry<br />

and other industrial purposes. They embody the whole<br />

series of authenticated positive efects on human organism<br />

and they are used as a part of food supplements 1 .<br />

Food lipids undergo a chain of changes due to ripening,<br />

harvesting, processing and storage. These changes are caused<br />

by several factors including browning reactions, microbial<br />

spoilage and lipid autoxidation. Lipid oxidation is a free-radical<br />

chain reaction that causes a total change in the sensory<br />

properties and nutritive value of food products 2 .<br />

Oxidation processes influence quality of oils and fats.<br />

Characteristic changes associated with oxidative deterioration<br />

include development of unpleasant tastes and odours<br />

as well as changes in color, viskosity, density or solubility 3 .<br />

The others of the effects of lipid oxidation can be loss of vitamins,<br />

and damage to proteins 2 .<br />

Differential scanning calorimetry (DSC) is the technique<br />

used for establishing the oxidative stability of oils and fats<br />

and characterizion of their physical properties 4,5 . Oxidative<br />

stability and deterioration of oils depend on initial composition,<br />

concentration of minor compounds with antioxidant<br />

or prooxidant characteristics, degree of processing, and storage<br />

conditions 6 . Quality and stability of vegetable oils are<br />

important factors that influence its acceptability and market<br />

value.<br />

The induction period (IP) is measured as the time<br />

required to reach an endpoint of oxidation corresponding to<br />

either a level of detectable rancidity or a sudden change in the<br />

rate of oxidation 7 .<br />

Experimental<br />

S a m p l e s<br />

Different vegetable oils from various plant origins were<br />

used in this study. These were Grape Seed oil refined, Crude<br />

Linseed oil, Castor oil, Almond oil refined, Soya Bean oil<br />

refined, Avocado oil refined, Apricot Kernel oil refined, Corn<br />

oil refined and Olive oil refined.<br />

Samples were obtained from M + H, Míča and Harašta,<br />

s.r.o. After opening the bottles with oils there were stored<br />

at 4 °C.<br />

s795<br />

M e t h o d<br />

Differential Scanning Calorimetry (DSC) of each sample<br />

in oxygen atmosphere were performed several times until<br />

reproducible results were obtained. For this purpose Shimadzu<br />

DSC-60 (Kyoto, Japan) was used connected through<br />

TA-60WS with computer, where the data were collected.<br />

The furnace was calibrated by using transition temperatures<br />

of fusion of indium and zinc (melting point: 156.6 °C<br />

for indium, 419.6 °C for zinc).<br />

Samples were measured out 2.5 µl (0.2,<br />

0.5 °C min –1 ), 5.0 µl (1.0, <strong>3.</strong>0, 5.0, 7.0 °C min –1 ) and 10 µl<br />

(10.0, 15.0 °C min –1 ) and measured in open aluminum pan.<br />

Flow rate of oxygen was set at 15 ml min –1 and rate of heating<br />

0.2, 0.5, 1.0, <strong>3.</strong>0, 5.0, 7.0, 10.0 and 15.0 °C min –1 from<br />

room temperature (25 °C) to 300 °C was applied. Obtained<br />

results were treated by means of enclosed software TA-60.<br />

Results<br />

For the using vegetable oils, the kinetic parameters<br />

important to the determination of induction period were<br />

obtained for non-isothermal DSC measurements. The onset<br />

temperatures of oxidation for various using oils were measured<br />

with scan rates 0.2, 0.5, 1.0, <strong>3.</strong>0, 5.0, 7.0, 10.0 and<br />

15.0 °C min –1 .<br />

The parameters A and B were obtained by a comparison<br />

of experimental and theoretical values of onset temperatures<br />

of the oxidation peaks using the program TInD. The values<br />

of kinetic parameters A and B are listed in the Table I.<br />

Table I<br />

Values of the kinetic parameters A and B<br />

Oils A [min] B [K]<br />

Castor 2.72 × 10 –13 1.38 × 10 4<br />

Olive 6.62 × 10 –13 1.32 × 10 4<br />

Soya Bean 1.54 × 10 –11 1.16 × 10 4<br />

Avocado 4.69 × 10 –11 1.12 × 10 4<br />

Grape Seed 4.43 × 10 –12 1.19 × 10 4<br />

Almond 5.26 × 10 –11 1.10 × 10 4<br />

Corn 1.00 × 10 –10 1.08 × 10 4<br />

Apricot Kernel 1.29 × 10 –10 1.06 × 10 4<br />

Crude Linseed 8.99 × 10 –12 1.12 × 10 4<br />

The temperature dependence of the induction period can<br />

be expressed according to the Equation (1):<br />

t i = A exp (B/T) (1)<br />

Providing that parameters A [min] and B [K] were obtained<br />

by minimizing the sum of squares between experimental<br />

and theoretical values of heating rate and T [K] is specific<br />

temperature, induction period t i [min] can be determined.<br />

Induction period values (t i ) of various using vegetable<br />

oils calculated for temperature 25 °C and 100 °C are shown<br />

in Table II.

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