Deep oxidative desulfurization of dibenzothiophene with {Mo132} nanoballs supported on activated carbon as an efficient catalyst at room temperature

被引:35
作者
Kermani, Ali Mojaverian [1 ]
Ahmadpour, Ali [1 ]
Bastami, Tahereh Rohani [2 ]
Ghahramaninezhad, Mahboube [2 ]
机构
[1] Ferdowsi Univ Mashhad, Fac Engn, Dept Chem Engn, Mashhad, Iran
[2] Quchan Univ Technol, Dept Chem Engn, Quchan, Iran
关键词
SELECTIVE OXIDATION; PERFORMANCE; ULTRASOUND; DIESEL; OPTIMIZATION; GASOLINE; REMOVAL; HYBRID; OIL;
D O I
10.1039/c8nj01735b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this paper, the Keplerate nanoball iso-polyoxomolybdate {Mo-132} supported on activated carbon (AC) has been synthesized and evaluated as a new, green and cost-effective catalyst for the oxidative desulfurization of a model fuel containing dibenzothiophene (DBT). The {Mo-132}/AC catalysts, which were prepared with various {Mo-132} contents, were characterized using FT-IR, XRD, SEM, EDX, ICP-OES, H-2-TPR and nitrogen adsorption/desorption isotherms. Experimental evaluations showed that the catalyst was highly efficient in the removal of DBT using hydrogen peroxide (H2O2) as the oxidant, which could result in a sulfur removal of up to 99.5% (or even more than that) under optimum reaction conditions. The factors affecting the process including catalyst dosage, temperature, O/S molar ratio, reaction time and initial sulfur content were evaluated, and the optimum operating conditions were determined. In addition, the new catalyst was recoverable and the recovered {Mo-132}/AC demonstrated a relatively similar catalytic activity to the fresh one. According to the results of GC-MS analysis, a sulfone species was found to be the only product of DBT oxidation by H2O2 over {Mo-132}/AC. Moreover, a mechanism for the oxidative desulfurization of DBT by the new catalyst was proposed. The present study suggested that the {Mo-132}/AC composite could be used as an efficient catalyst for the deep oxidative desulfurization and removal of refractory sulfur compounds in fossil fuels.
引用
收藏
页码:12188 / 12197
页数:10
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