Preparation and Characterization of Cs2.8H1.2PMo11Fe(H2O)O39·6H2O and Investigation of Effects of Iron-Substitution on Heterogeneous Oxidative Dehydrogenation of 2-Propanol
datasetposted on 13.07.2004, 00:00 by Noritaka Mizuno, Joon-Seok Min, Akira Taguchi
Synthesis and characterization of mono-iron(III)-substituted molybdophosphate, the solidification as a heterogeneous catalyst, and the oxidative dehydrogenation of 2-propanol were reported. The catalyst was isolated as Cs2.8H1.2PMo11Fe(H2O)O39·6H2O, and characterized by elemental analysis and X-ray diffraction, infrared, 31P NMR, and ESR spectroscopy. The Fe3+ in Cs2.8H1.2PMo11Fe(H2O)O39·6H2O was incorporated into the molybdophosphate framework while that in Fe3+(2.5 wt %)/Cs3.0PMo12O40 existed as a countercation in a relatively distorted octahedral site. The seven water molecules were desorbed by the thermal treatment at 63 °C and the cesium hydrogen salt was stable below 210 °C. The cesium hydrogen salt was used for heterogeneous oxidative dehydrogenation of 2-propanol to acetone and intrinsically has a higher rate than those for the iron-impregnated Fe3+/Cs3.0PMo12O40 and Cs3.0PMo12O40 catalysts, showing the effectiveness of isolated iron in the PMo11O397- polyoxometalate on the oxidative dehydrogenation. The data for the stop of the supply of the oxygen at the stationary state in the flow experiment showed that acetone was produced by the reaction of 2-propanol with the cesium hydrogen salt. The correlation between intrinsic rates of oxidative dehydrogenation of 2-propanol and reducibility of catalysts, the rate equation of −d[2-PrOH]/dt = k·P2-PrOH0.80·PO2-0.06, and kinetic isotope effects of 1.6−1.9 showed that the reduction of the catalyst with the β-hydrogen elimination from 2-propanol was the rate-determining step.