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首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Hydrodesulfurization of dibenzothiophene and hydrogenation of phenanthrene of alumina-supported Pt and Pd catalysts
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Hydrodesulfurization of dibenzothiophene and hydrogenation of phenanthrene of alumina-supported Pt and Pd catalysts

机译:二苯并噻吩的加氢脱硫和氧化铝负载的Pt和Pd催化剂的菲氢化

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摘要

Hydrodesulfurization (HDS) reactions of dibenzothiophene (DBT) and hydrogenation (HYD) of phenanthrene (PHE)were carried out over several alumina-supported noble metal catalysts at temperatures between 200 deg C and 400 deg C and under 50 kg/cm~2 pressure. A dual noble metal catalyst, Pt(2)-Pd(10), showed similar HDS results and better HYD promotion compared with a conventional Co-Mo catalyst. Further, ~(35)S radioisotope tracer method showed that almost no labile sulfur was accumulated on Pt/Al_2O_3 catalyst in the HDS of DBT or HYD of PHE, although this catalyst showed an HDS activity comparable to that of the Co-Mo catalyst. This indicated that the mechanism of DBT HDS on noble catalysts was different from that on the conventional Mo-based catalyst.
机译:在200至400摄氏度之间的温度和50 kg / cm〜2的压力下,在几种氧化铝负载的贵金属催化剂上进行了二苯并噻吩(DBT)的加氢脱硫(HDS)反应和菲(PHE)的氢化(HYD)反应。 。与传统的Co-Mo催化剂相比,双重贵金属催化剂Pt(2)-Pd(10)显示出相似的HDS结果和更好的HYD促进作用。此外,〜(35)S放射性同位素示踪法显示,在DBT的HDS或PHE的HYD中,Pt / Al_2O_3催化剂上几乎没有不稳定的硫积累,尽管该催化剂的HDS活性与Co-Mo催化剂相当。这表明DBT HDS在贵金属催化剂上的机理与在传统的Mo基催化剂上的机理不同。

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