HDS of dibenzothiophenes and hydrogenation of tetralin over a SiO2 supported Ni-Mo-S catalyst

被引:5
|
作者
Wei, Qiang [1 ]
Chen, Jinwen [1 ]
Song, Chaojie [2 ]
Li, Guangchun [2 ]
机构
[1] Nat Resources Canada, CanmetENERGY Devon, Devon, AB T9G 1A8, Canada
[2] Natl Res Council Canada, Energy Min & Environm, Vancouver, BC V6J 1W5, Canada
关键词
hydrodesulphurization (HDS); hydrogenation; dibenzothiophene (DBT); 4,6-dimethyldibenzothiophene (4,6-DMDBT); tetralin; DEEP DESULFURIZATION; GAS OIL; SIMULTANEOUS HYDRODESULFURIZATION; SULFIDE CATALYSTS; PROBE MOLECULES; COMO CATALYSTS; ALUMINA; DBT; MOLYBDENUM; 4,6-DMDBT;
D O I
10.1007/s11705-015-1535-1
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
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.
引用
收藏
页码:336 / 348
页数:13
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