Title of article :
The effect of boron addition on the hydrodesulfurization activity of MoS2/Al2O3 and Co–MoS2/Al2O3 catalysts
Author/Authors :
Usman، نويسنده , , Takeshi Kubota، نويسنده , , Yasuhiro Araki، نويسنده , , Katsuaki Ishida، نويسنده , , Yasuaki Okamoto، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2004
Pages :
7
From page :
523
To page :
529
Abstract :
The effect of boron addition was studied on the hydrodesulfurization (HDS) of thiophene over MoS2/B/Al2O3 and Co–MoS2/B/Al2O3 (CVD-Co/MoS2/B/Al2O3), which was prepared by a CVD technique using Co(CO)3NO as a precursor of Co. The catalysts were characterized by means of NO adsorption and TEM. The HDS activity of MoS2/B/Al2O3 catalysts kept constant up to a boron content of about 0.6 wt% and decreased with a further increase of boron content. With CVD-Co/MoS2/B/Al2O3 catalysts, the HDS activity significantly increased as the boron content increased up to about 0.6 wt% of boron, followed by a decrease with a further increase of boron loading. Despite the activity increase, the amount of NO adsorption on MoS2/B/Al2O3 steadily decreased with increasing boron loading, suggesting that the dispersion of MoS2 particles is decreased by the addition of boron. A selective formation of the CoMoS phase on CVD-Co/MoS2/B/Al2O3 was achieved by the CVD technique. The TOF of the HDS over the CVD-Co/MoS2/B/Al2O3 catalysts, defined by the activity per Co atom forming the CoMoS phase, increased as high as 1.6 times by the addition of boron, indicating that the active phase of the catalysts shifts from less active CoMoS Type I to more active CoMoS Type II. A TEM analysis showed that the number of stacking of MoS2 slabs was only slightly increased by the addition of boron. It is concluded that the activity increase of the CVD-Co/MoS2/B/Al2O3 catalyst is caused by the formation of CoMoS Type II because of weakened interaction strength between the CoMoS phase and the Al2O3 surface by the addition of boron.
Keywords :
FeMFI , N2O reduction , Framework composition , Iron species , Steam treatment , Mechanism , Kinetics , Active site , N2O decomposition
Journal title :
Journal of Catalysis
Serial Year :
2004
Journal title :
Journal of Catalysis
Record number :
1223437
Link To Document :
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