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   <subfield code="a">Catalytic oxidative desulfurization of diesel oil by Co/Mn/Al2O3 catalysts— tert -butyl hydroperoxide (TBHP) system: preparation, characterization, reaction, and mechanism</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Wan Wan Mokhtar, Wan Wan Abu Bakar, Rusmidah Ali, Abdul Abdul Kadir]</subfield>
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   <subfield code="a">The hydrodesulfurization (HDS) technique available is no longer suitable for the purpose of achieving ultra-low sulfur diesel. Therefore, in this study, the catalytic oxidative desulfurization of model diesel was carried out using tert-butyl hydroperoxide along with inexpensive alumina-supported manganese-based oxide catalysts, and later, the oxidized sulfur compounds were extracted by dimethylformamide, a polar solvent. The effect of dopant ratio, calcination temperature, reaction time, and reaction temperature were investigated in detail. The oxidation reactivity of different substrates was in the following order: DBT&gt;Th&gt;4,6-DMDBT. The best desulfurization efficiency of model diesel, under mild reaction conditions, was 85.3% thiophene, 85.0% dibenzothiophene, and 74.5% 4,6-dimethyldibenzothiophene using the 2.14%Co/13.17%Mn/Al2O3 catalyst calcined at 400°C. Besides, this catalyst retained a high conversion of sulfur after three rounds of reaction cycles and can be used as a reusable active catalyst in ODS treatment. Under the optimal conditions, the S-content in the commercial diesel could be decreased from 415 to less than 10ppmw. The oxidation mechanism was studied in detail, and TBHP-Co/Mn catalyst was the main active oxidizing species on the oxidation of DBT.</subfield>
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