Ultra-deep desulfurization via reactive adsorption on peroxophosphomolybdate/agarose hybrids

A catalyst system composed of peroxophosphomolybdates as catalytic center and agarose as matrix material had been designed. The [C16H33N(CH3)(3)](3)[PO4{MoO(O-2)(2)}(4)]/agarose (C16PMo(O-2)(2)/agarose) hybrid was found to be active for oxidation desulfurization (ODS) of dibenzothiophene (DBT) or real fuel into corresponding sulfone by H2O2 as an oxidant, while the sulfur content could be reduced to 5 ppm. The higher activity comes from its components including [PO4{MoO(O-2)(2)}(4)] catalytic sites, the hydrophobic quaternary ammonium cation affinity to low polarity substrates, and agarose matrix affinity to H2O2 and sulfone. During the oxidative reaction, the mass transfer resistance between H2O2 and organic sulfurs could be decreased and the reaction rate could increase by the assistance of agarose and hydrophobic tails of [C16H33N(CH3)(3)](3)[PO4{MoO(O-2)(2)}(4)]. Meanwhile, the oxidative products could be adsorbed by agarose matrix to give clean fuel avoiding the post-treatment. In addition, the hybrid was easily regenerated to be reused. (C) 2014 Elsevier Ltd. All rights reserved.