期刊
FRONTIERS OF CHEMICAL SCIENCE AND ENGINEERING
卷 9, 期 3, 页码 336-348出版社
SPRINGER
DOI: 10.1007/s11705-015-1535-1
关键词
hydrodesulphurization (HDS); hydrogenation; dibenzothiophene (DBT); 4,6-dimethyldibenzothiophene (4,6-DMDBT); tetralin
资金
- Natural Resources Canada
- National Research Council (NRC) of Canada
- government of Canada's interdepartmental Program of Energy Research and Development (PERD)
A one-step synthesized Ni-Mo-S catalyst supported on SiO2 was prepared and used for hydrodesulphurization (HDS) of dibenzothiophene (DBT), and 4,6-dimethyl-dibenzothiophene (4,6-DMDBT), and for hydrogenation of tetralin. The catalyst showed relatively high HDS activity with complete conversion of DBT and 4,6-DMDBT at temperature of 280 A degrees C and a constant pressure of 435 psi. The HDS conversions of DBTand 4,6-DMDBT increased with increasing temperature and pressure, and decreasing liquid hourly space velocity (LHSV). The HDS of DBT proceeded mostly through the direct desulphurization (DDS) pathway whereas that of 4,6-DMDBT occurred mainly through the hydrogenationdesulphurization (HYD) pathway. Although the catalyst showed up to 24% hydrogenation/dehydrogenation conversion of tetralin, it had low conversion and selectivity for ring opening and contraction due to the competitive adsorption of DBTand 4,6-DMDBT and insufficient acidic sites on the catalyst surface.
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