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Aluminosilicates with ordered hexagonal mesopores denoted as MAS-7 and MAS-9 with uniform size were synthesized from zeolite β assembly and ZSM-5 precursors, respectively, with P123 as a surfactant, via the cooperative self-assembly pathway. A series of 12 tungstophosphoric acid (TPA) supported on MAS-7 and MAS-9 (H 3 PW 12 O 40 /MAS-7/MAS-9) catalysts for biodiesel production were synthesized via the wet impregnation technique. The characterization of the supports and catalysts was done using N 2 adsorption-desorption analysis, X-ray diffraction (XRD), and pyridine adsorption Fourier transform infrared and Raman spectroscopies. Also, the 29 Si magic-angle spinning and cross-polarization/MAS nuclear magnetic resonance (NMR) techniques were employed to study MAS-7/MAS-9 and the supported solid acid catalyst surfaces. The nitrogen sorption analysis and XRD patterns indicated the formation of well-defined mesoporous materials, whereas IR spectroscopy confirmed the presence of four distinct types of OH groups with varying degrees of acidity. 29 Si MAS NMR signified a stronger interaction between the framework of mesoporous aluminosilicates and H 3 PW 12 O 40 . The X-ray absorption near-edge spectra of L 1 - and L 3 -edge tungsten showed that W in the H 3 PW 12 O 40 /MAS-9 sample exists as W 6+ , indicating the tungsten environment similar to that of H 2 WO 4 with O   h  symmetry. The catalytic activity of the synthesized catalysts was investigated for biodiesel synthesis using unrefined green seed canola oil as a feedstock, giving a methyl ester yield of 76.5-88.7 wt % under optimized reaction conditions. The catalyst activities were strongly correlated with the surface chemistry of the TPA-supported MAS-7 and MAS-9 catalysts.

Surface Investigation of Tungstophosphoric Acid Supported on Ordered Mesoporous Aluminosilicates for Biodiesel Synthesis