Thermal stability and antioxidant ability of γ-oryzanol
in
oil have been widely studied. However, further research is needed
to explore its thermal degradation products and degradation pathways.
The thermal degradation products of γ-oryzanol in stripped soybean
oil were identified and quantified by employing high-performance liquid
chromatography (HPLC) and gas chromatography–mass spectrometry
(GC-MS) during heating at 180 °C. The results revealed that γ-oryzanol
undergoes ester bond cleavage to form trans-ferulic
acid and free sterols, and trans-ferulic acid generated
intermediate compound 4-vinylguaiacol, which ultimately generated
vanillin. Analysis of kinetic and thermodynamic parameters revealed
the thermal stability ranking of the four components of γ-oryzanol
as follows: CampFA > CAFA > 24MCAFA > SitoFA. Furthermore,
γ-oryzanol
exhibited superior antioxidant activity at lower temperatures. The
results of this study provide a theoretical basis for a better understanding
of the thermal stability and antioxidant properties of γ-oryzanol
in oil under thermal oxidation conditions.