On the effect of hafnium loading and location in mesoporous silica on the activity of catalysts in oxidation of dibenzothiophene

Oxidation of thiophenes to sulfones (easily extracted from fuel) is of crucial importance in petrochemical and automotive industry. The rational design and synthesis of stable catalysts of this process still remains one of the biggest challenges. In this work, a series of HfSBA-15 mesoporous materials with different hafnium content (3, 5 or 10 wt.%) has been prepared and studied in the liquid phase oxidation of dibenzothiophene (DBT) with H2O2. The activity of HfSBA-15 samples prepared by one-pot method was compared to that of Hf/SBA-15 synthesized by impregnation and that of HfMCF type of silica. It has been shown that hafnium loading and its location in the silica structure (framework and/or extra-framework positions) affect the efficiency of DBT oxidation. Moreover, the reaction conditions (i.e. oxidation temperature, reaction time, oxidant/sulfur ratio and catalyst amount) were optimized to achieve maximum conversion of dibenzothiophene (99 %). The location of hafnium species in SBA15 and MCF materials was influenced by the loading of the metal and the type of silica structure (determined by the preparation method). Hafnium located in the framework of SBA-15 promoted generation of a higher number of active Lewis acid sites (LAS) and higher activity in oxidation of dibenzothiophene compared to extraframework HfO2 species anchored in HfMCF material. It indicates that the location (framework vs extraframework) and formation of isolated Hf4+ species are decisive for high activity of hafnium-doped mesoporous molecular sieves. This finding opens up a pathway for the development of highly efficient, stable and relatively cheap solid acid catalyst for oxidation of thiophenes to sulfones.