RESUMO
This study aims to synthesize a WO3/CuFe2O4 catalyst through a wet impregnation method and use it as a new magnetic acid catalyst in the transesterification process of waste cooking oil (WCO). The results of the characterization by XRD, FTIR, SEM, EDS, TG/DTG, VSM and Surface Acidity showed that the obtained bifunctional catalyst has been successfully synthesized. The study of the reaction parameters, such as reaction temperature (140-180 °C), reaction time (1-5 h), molar ratio MeOH : oil (25 : 1-45 : 1) and catalyst loading (2-10% m m-1) was performed in the conversion of WCO into biodiesel via transesterification. The reactional behavior showed the following optimal reaction conditions: reaction temperature of 180 °C, reaction time of 3 h, molar ratio MeOH : oil of 45 : 1 and catalyst loading of 6%. Based on the results, biodiesel with a maximum ester content of 95.2% was obtained using the WO3/CuFe2O4 magnetic catalyst under the optimal reaction conditions. The magnetic catalyst showed excellent catalytic and magnetic performance and it was applied in five reaction cycles with ester content above 80%. Biodiesel properties were found in accordance with ASTM limits. This research provided the development of a stable and reusable WO3/CuFe2O4 bifunctional catalyst for potential application in biodiesel production.
RESUMO
Two bentonites from Paraíba (Northeastern Brazil) were impregnated with heteropoly phosphomolybdic H3PMo12O40 (HPMo). The materials produced were characterized by various techniques such as N2 adsorption-desorption (specific surface area, SSA), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Thermogravimetric analysis (TGA/DTG), Scanning Electron Microscopy (SEM) equipped with Dispersive Energy X-ray spectroscopy (EDS), ultraviolet-visible spectroscopy (UV-vis), acid-base titration analysis. The catalytic activity of these materials was tested in the esterification of a waste from palm oil deodorization and the main results obtained (about 93.3% of conversion) indicated that these materials have potential to act as heterogeneous solid acid catalysts. The prepared materials exhibited satisfactory catalytic performance even after a very simple recycling process in three reuse cycles, without significant loss of their activities.