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
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.