EFFECT OF THE PHENOL ANTIOXIDANT TYPE ON THE KINETICS AND MECHANISM OF INHIBITED LIPID OXIDATION IN THE PRESENCE OF FATTY ALCOHOLS

Citation
Vd. Kortenska et Nv. Yanishlieva, EFFECT OF THE PHENOL ANTIOXIDANT TYPE ON THE KINETICS AND MECHANISM OF INHIBITED LIPID OXIDATION IN THE PRESENCE OF FATTY ALCOHOLS, Journal of the Science of Food and Agriculture, 68(1), 1995, pp. 117-126
Citations number
18
Categorie Soggetti
Agriculture,"Food Science & Tenology
ISSN journal
00225142
Volume
68
Issue
1
Year of publication
1995
Pages
117 - 126
Database
ISI
SICI code
0022-5142(1995)68:1<117:EOTPAT>2.0.ZU;2-K
Abstract
A kinetic analysis of inhibited lipid autoxidation in the presence of a phenol antioxidant and a hydroxy compound is proposed. It is based o n studies of the dependence of the W-inh(ROH)/W-inh ratio (between the inhibited oxidation rates in presence and absence of a hydroxy compou nd) on the hydroxy compound concentration. This analysis permits estab lishing the mechanism of action of the hydroxy compound in the presenc e of different types of phenol antioxidants during inhibited lipid oxi dation. The kinetic analysis has been applied to the oxidation at 80 d egrees C of triacylglycerols of sunflower oil (TGSO) inhibited by 0.1 mM hydroquinone, butylated hydroxytoluene (BHT) or alpha-tocopherol in the presence of different concentrations of 1-tetradecanol (1-TD) and 1-octadecanol (1-OD). A linear character of this dependence is establ ished during hydroquinone-inhibited oxidation of triacylglycerols of s unflower oil in presence of 1-TD. In the case of alpha-tocopherol this dependence is linear for both 1-TD and 1-OD. The equilibrium constant of interaction between the phenol antioxidant and the fatty alcohols is determined by the angle coefficient of the linear dependence. The h ydroquinone-inhibited autoxidation of TGSO in the presence of 1-OD has shown a non-linear character of the dependence under consideration. A kinetic model describing simultaneous participation of 1-OD in reacti on with both the phenol antioxidant and the lipid hydroperoxides is de duced. Studying the kinetics of BHT-inhibited autoxidation of TGSO in the presence of 1-OD, it has been shown that due to steric reasons the re is no interaction between 1-OD and BHT, 1-OD participating in the p rocess only by accelerating the decomposition of the lipid hydroperoxi des.