Incorporation of Ce3+ ions into dodecatungstophosphoric acid for the production of biodiesel from waste cooking oil

Abstract A series of cerium-exchanged dodecatungstophosphates Ce x H 3-3x PW 12 O 40 (Ce x H 3-3x PW, x = 0.4, 0.6, 0.7, 0.8, 0.9, and 1.0) were designed and characterized by Fourier transform infrared spectroscopy (FT-IR), pyridine adsorption IR spectra, X-ray diffraction (XRD), and temperature programmed desorption of ammonia (NH 3 -TPD). The activity of these catalysts was evaluated for the generation of biodiesel from waste cooking oil (WCO) with 27 wt% of free fatty acids (FFAs) and 1 wt% of water. Compared to theri parent H 3 PW 12 O 40 , Ce x H 3-3x PW showed higher activity for esterification of FFAs and transesterification of triglyceride to mono-alkyl esters of fatty acids (FAMEs) in one-pot. The acidic properties of Ce x H 3-3x PW depended on the amount of Ce 3+ ions in the secondary structure of Keggin heteropolyacids, while conversion of triglycerides and FFAs depended on their increasing acid contents. Among Ce x H 3-3x PW, Ce 0.7 H 0.9 PW showed significant activity due to its high Bronsted acidity and Lewis acidity with 98% conversion of WCO and almost 100% selectivity to FAME at the molar ratio of methanol to WCO = 21:1 and 65 °C for 12 h. The reaction adhered to first-order kinetics with the activation energy (Ea) of 71 kJ/mol and the frequency factor (A) of 1.8 × 10 8  min −1 , while the reaction rates were not influenced by the internal mass transport. The catalyst behaved as a heterogeneous catalyst, which can achieve the regeneration and be used more than five runs but without obvious decrease in activity. The characteristics of the WCO methyl ester were found to be close to the engine requirement.