The optimization and kinetics of the ring-opening reaction of an epoxidized biodiesel (epoxidized rapeseed oil methyl ester) (EBD) with 2-ethyl hexanol (2-EH) were studied. The determined optimum conditions were 4:1 2-EH/oil molar ratio, 90 °C, 18 h, and 7 wt%of Amberlyst D001 (dry) catalyst; the product's oxirane oxygen content was 0.081% with 38.32 mm2/s viscosity at 40 °C. The catalyst retained its high catalytic power after recycling five times. Furthermore, the determined non-catalyzed activation energy was 76 kJ. mol-1 and 54 kJ. mol-1 with the D001 resin catalyst. The product's chemical structure was investigated through FT-IR and 1H NMR. The viscosity, flash point, pour point, and anti-wear properties of the product were improved compared with those of epoxidized biodiesel.
CITATION STYLE
Ren, Q., Pan, J., Zhou, J., Na, Y., Chen, C., & Li, W. (2015). Synthesis and tribological studies of branched alcohol derived epoxidized biodiesel. Materials, 8(10), 6623–6632. https://doi.org/10.3390/ma8105326
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