Abstract
AbstractBiodiesel has recently emerged as a renewable and environmentally benign fuel substitute for fossil‐derived energy sources. The use of heterogeneous solid catalysts for the generation of biodiesel from biomass‐derived fats and oils is sustainable. Among various reported catalyst supports, metal–organic frameworks (MOFs) have been popular choices for enhancing catalytic activity for biodiesel synthesis because of several outstanding features including porosity, high surface area, adjustable structures, and uniform pore sizes. In this research, the authors synthesized a novel nanocomposite of MOF‐supported hydroxyapatite (UiO‐66@HAp) using a facile impregnation technique and the characterization of the as‐synthesized catalyst was performed by different spectroscopic methods including powder X‐ray diffraction (PXRD), Fourier transform infrared (FTIR), X‐ray photoelectron spectroscopy (XPS), field emission gun‐scanning electron microscope (FEG‐SEM), energy dispersive X‐ray spectroscopy (EDS), high resolution transmission electron microscopy (HR‐TEM), thermogravimetric analysis (TGA), and N2 adsorption–desorption techniques. After successful synthesis, the catalytic property of the prepared material was evaluated in the palm oil transesterification into biodiesel. Product formation was confirmed by the 1H nuclear magnetic resonance (NMR) spectroscopy, 13C NMR, FTIR, and gas chromatography–mass spectrometry (GC–MS) of the biodiesel. The influence of different reaction variables such as catalyst dosage, methanol/oil molar ratio, temperature of the reaction, and reaction time was also studied. The outcomes revealed that the maximum biodiesel yield (∼97%) was obtained when 6 wt% catalyst was used with a 6:1 ratio of methanol/oil at 70 °C for 1 h. It was also observed that, even after 5 cycles of reuse, the catalyst was capable of producing significant amounts of biodiesel (over 90%). The results suggest that the synthesized novel catalyst holds a promising future in the sustainable production of biodiesel.
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