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Articles

Decomposition products of glycidyl esters of fatty acids by heating

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Pages 581-586 | Received 03 Aug 2016, Accepted 31 Oct 2016, Published online: 25 Nov 2016

Figures & data

Fig. 1. Changes in the weight of glycidyl palmitate (GP) and tripalmitin (TP) during heating at 180 and 200 °C. ● GP (200 °C), ▴ GP (180 °C), ■ TP (200 °C), and ♦ TP (180 °C). Data show the mean and standard deviation of triplicate.

Fig. 1. Changes in the weight of glycidyl palmitate (GP) and tripalmitin (TP) during heating at 180 and 200 °C. ● GP (200 °C), ▴ GP (180 °C), ■ TP (200 °C), and ♦ TP (180 °C). Data show the mean and standard deviation of triplicate.

Fig. 2. TLC-FID chromatograms of GP and TP after heating at 180 °C. A TP (2 h), B TP (4 h), C TP (8 h), D GP (2 h), E GP (4 h), and F GP (8 h). GP, glycidyl palmitate; TP, tripalmitin; PC, polar compounds.

Fig. 2. TLC-FID chromatograms of GP and TP after heating at 180 °C. A TP (2 h), B TP (4 h), C TP (8 h), D GP (2 h), E GP (4 h), and F GP (8 h). GP, glycidyl palmitate; TP, tripalmitin; PC, polar compounds.

Fig. 3. Changes in the relative ratio of GP, TP, and polar compounds (PC) to total peak areas during heating at 180 and 200 °C. ● GP (200 °C), ▴ GP (180 °C), ■ TP (200 °C), and ♦ TP (180 °C). Data shows the mean and standard deviation of triplicate.

Fig. 3. Changes in the relative ratio of GP, TP, and polar compounds (PC) to total peak areas during heating at 180 and 200 °C. ● GP (200 °C), ▴ GP (180 °C), ■ TP (200 °C), and ♦ TP (180 °C). Data shows the mean and standard deviation of triplicate.

Fig. 4. Gas chromatograms of head space gas from TP, GP, and glycidyl myristate after heating at 200 °C for 2 h.

Fig. 4. Gas chromatograms of head space gas from TP, GP, and glycidyl myristate after heating at 200 °C for 2 h.

Fig. 5. Changes in the contents of saturated aldehydes from GP and TP during heating at 180 and 200 °C. ● GP (200 °C), ▴ GP (180 °C), ■ TP (200 °C), and ♦ TP (180 °C). Data show the mean and standard deviation of triplicate.

Fig. 5. Changes in the contents of saturated aldehydes from GP and TP during heating at 180 and 200 °C. ● GP (200 °C), ▴ GP (180 °C), ■ TP (200 °C), and ♦ TP (180 °C). Data show the mean and standard deviation of triplicate.

Fig. 6. Changes in the contents of hydrocarbons from GP and TP during heating at 180 and 200 °C. ● GP (200 °C), ▴ GP (180 °C), ■ TP (200 °C), and ♦ TP (180 °C). Data show the mean and standard deviation of triplicate.

Fig. 6. Changes in the contents of hydrocarbons from GP and TP during heating at 180 and 200 °C. ● GP (200 °C), ▴ GP (180 °C), ■ TP (200 °C), and ♦ TP (180 °C). Data show the mean and standard deviation of triplicate.

Fig. 7. Changes in the relative ratio of pentadecane to peak areas of total hydrocarbons from GP and TP during heating at 180 and 200 °C. ● GP (200 °C), ▴ GP (180 °C), ■ TP (200 °C), and ♦ TP (180 °C). Data show the mean and standard deviation of triplicate.

Fig. 7. Changes in the relative ratio of pentadecane to peak areas of total hydrocarbons from GP and TP during heating at 180 and 200 °C. ● GP (200 °C), ▴ GP (180 °C), ■ TP (200 °C), and ♦ TP (180 °C). Data show the mean and standard deviation of triplicate.

Fig. 8. Changes in the contents of carbon dioxide (CO2) from GP (●) and TP (■) during heating at 200 °C. Data show the mean and standard deviation of triplicate.

Fig. 8. Changes in the contents of carbon dioxide (CO2) from GP (●) and TP (■) during heating at 200 °C. Data show the mean and standard deviation of triplicate.

Fig. 9. Conjectured mechanism for the formation of hydrocarbons, aldehydes, and polar compounds (polymers) from glycidyl esters (GEs) during heating at high temperature.

Fig. 9. Conjectured mechanism for the formation of hydrocarbons, aldehydes, and polar compounds (polymers) from glycidyl esters (GEs) during heating at high temperature.

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