Figures & data
Table 1. Color, refractive Index, saponification value (mg KOH/g oil), iodine value (gI2/100g oil), specific gravity, and moisture (%) of HEVCO, CEVCO, and CCO
Table 2. Fatty acid composition (%) of HEVCO, CEVCO, and CCO
Table 3. Tocopherol (μg/g), polyphenols (μg/g), antioxidant activity (%), monoglycerides (%), and phytosterol (μg/g) content in HEVCO, CEVCO, and CCO
Figure 1. Typical diagram of FTIR spectra for HEVCO, CEVCO, and CCO.
Table 4. Concentration of phenolic acids (μg/g) in HEVCO, CEVCO, and CCO
Figure 2. Typical diagram of DSC thermogram of crystallization peak (a) and melting peak (b) in HEVCO, CEVCO, and CCO.
Figure 3. HPLC chromatogram of the phenolic fraction of CEVCO (a), CCO (b), and HEVCO (c).
Figure 4. Reaction of hydroxyl groups of DG with 2-chloro4,4,5,5-tetramethyl-1,3-dioxa-2-phospholane (2-CITMDOP) & Structures of different phosphitylated mono and diesters of glycerol.
Figure 5. A typical 31P NMR spectrum of standard 1-monoglycerides (1-MG), 1, 2-diglycerides (1, 2-DGs), 1, 3-diglycerides (1, 3-DGs), and sterols.
Figure 6. A typical 31P NMR spectrum of HEVCO showing 1-monoglycerides (1-MG), 1, 2-diglycerides (1, 2-DGs), 1, 3-diglycerides (1, 3-DGs), and sterols.
Figure 7. A typical 31P NMR spectrum of CEVCO showing 1-monoglycerides (1-MG), 1, 2-diglycerides (1, 2-DGs), 1, 3-diglycerides (1, 3-DGS), and sterols.
Figure 8. A typical 31P NMR spectrum of CCO showing 1-monoglycerides (1-MG, 1, 2-diglycerides (1, 2-DGs), 1, 3-diglycerides (1, 3-DGS), and sterols.
