A MoO3-Metal-Organic Framework Composite as a Simultaneous Photocatalyst and Catalyst in the PODS Process of Light Oil

Photo-oxidative desulfurization (PODS) properties of MoO3-metal-organic framework composite photo catalysts were investigated by introducing the proper weight percent of MoO3 into a Zn(II)-based MOF, [Zn(oba)(4-bpdh)(0.5)]center dot 1.5DMF (TMU-5), for the mineralization of dibenzothiophene from model oil. The addition of 3 wt % of MoO3 into a TMU-5 host acting as a crystal growth inhibitor was confirmed by PXRD and BET results. For the first time, under mild and green reaction conditions, 5 wt % MoO3-TMU-S composite (MT-5) exhibited good photocatalytic activity in the model oil PODS reaction, which has no limitations in the current oxidative desulfurization catalytic systems. Only 3% of the total amount of MoO3 content in the MT catalyst is leached during the reaction. In addition, the rate of PODS of MT-5 obeys a pseudo-first-order equation with an apparent rate constant of 0.0305 min(-1) and half-life t(1/2) of 22.7 min. Radical scavenger experiments and terephthalic acid fluorescence techniques confirmed that OH center dot and O-2(center dot-) are the main reactive species in the dibenzothiophene photocatalytic degradation. The synergic effects of the active surface of TMU-5 (organic linkers as antennas) together with the active sites of MoO3 may lead to the further enhancement of the PODS activity of the MT-5 photocatalyst. Moreover, a possible photocatalytic desulfurization mechanism was proposed in the presence of MoO3-TMU-S composites.