“…Hydrogen peroxide was found to be the most suitable stoichiometric oxidant, although t-BuOOH was also used to oxidise DBT in the presence of Mo catalysts supported on Al 2 O 3 (16%) [7]. H 2 O 2 was used Scheme 1. together with organic acids to generate peroxoacids [4,8,9], Na 2 WO 4 /C 6 H 5 PO 3 H 2 /Me(n-octyl) 3 NHSO 4 [10], Mo(VI) and W(VI) catalysts [11], methyltrioxorhenium (MTO) [12,13], polyoxometalates [8], tungstophosphoric acid [14,15], TiO 2 -supported V 2 O 5 [16], Pd, Cr 2 O 3 , Mn oxides, Co-Mo/Al 2 O 3 [17], TS-1, Ti-beta, Ti-HMS [18]. Solid bases such as hydrotalcites and MgLa mixed oxides as catalysts and nitriles or methanol as solvents were also used to oxidise DBT to DBTSO 2 ; the efficiency of the process was hampered by the basecatalyzed H 2 O 2 unselective decomposition, thus requiring an excess of oxidant [19].…”