首页> 外文期刊>Fuel Processing Technology >Oxygen free conversion of natural gas to useful hydrocarbons and hydrogen over monometallic Mo and bimetallic Mo-Fe, Mo-Co or Mo-Ni/HZSM-5 catalysts prepared by mechanical mixing
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Oxygen free conversion of natural gas to useful hydrocarbons and hydrogen over monometallic Mo and bimetallic Mo-Fe, Mo-Co or Mo-Ni/HZSM-5 catalysts prepared by mechanical mixing

机译:通过机械混合制备的单金属Mo和双金属Mo-Fe,Mo-Co或Mo-Ni / HZSM-5催化剂将天然气无氧转化为有用的烃和氢

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摘要

This work aims to approach a compromise of the activities of Mo/HZSM-5 catalyst as well known high performance aromatization catalyst after substituting half its Mo with Fe, Co or Ni (well known active hydrogen releasing metals) for hydrocarbons and hydrogen production. The catalysts were prepared by the mechanical mixing procedure in order to keep the zeolitic pores almost free of metal incorporation and hence reducing the metal/zeolite acid interaction. The catalytic performance of the catalysts was investigated during the non-oxidative conversion of natural gas to hydrocarbons and hydrogen in a fixed bed flow reactor at 700 °C and gas hourly space velocity (GHSV) of 1500 ml/g/h. The catalysts were characterized by XRD and TGA, where the results showed that the bimetallic 3%Mo-3%Fe, 3%Mo-3%Co or 3%Mo-3%Ni containing catalysts significantly decreased hydrocarbon (ethylene and aromatics) yield and selectivity as compared to the monometallic 6%Mo/HZSM-5 catalyst. The substitution of group VIII metals enhances the rate of coke and hydrogen formation in the direction of going from Fe → Co→ Ni. This behavior can be attributed to the electronic properties of these metals, where maximum reaction rates are exhibited by the metals with six to eight d-electrons.
机译:这项工作的目的是在将Mo / HZSM-5催化剂的一半Mo替换为Fe,Co或Ni(众所周知的释放活性氢的金属)形成碳氢化合物和氢之后,解决Mo / HZSM-5催化剂(众所周知的高性能芳构化催化剂)活性的折衷问题。通过机械混合程序制备催化剂,以保持沸石孔几乎没有金属结合,从而减少金属/沸石酸的相互作用。在固定床流动反应器中,在700°C和1500 ml / g / h的气时空速(GHSV)下,天然气非氧化转化为烃和氢的过程中,研究了催化剂的催化性能。通过XRD和TGA对催化剂进行了表征,结果表明,含双金属3%Mo-3%Fe,3%Mo-3%Co或3%Mo-3%Ni的催化剂显着降低了烃(乙烯和芳烃)的收率与单金属6%Mo / HZSM-5催化剂相比具有更高的选择性。 VIII族金属的取代沿从Fe→Co→Ni的方向提高了焦炭和氢形成的速率。这种行为可以归因于这些金属的电子特性,其中具有6至8个d电子的金属表现出最大的反应速率。

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