3. FOOD ChEMISTRy & bIOTEChNOLOGy 3.1. Lectures
3. FOOD ChEMISTRy & bIOTEChNOLOGy 3.1. Lectures
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.