Production of syngas by CO2 reduction through Reverse Water–Gas Shift (RWGS) over catalytically-active molybdenum-based carbide, nitride and composite nanowires

催化作用 材料科学 水煤气变换反应 碳化物 氮化物 化学工程 物理吸附 合成气 化学吸附 纳米线 复合数 化学 纳米技术 冶金 复合材料 有机化学 图层(电子) 工程类
作者
Venkata D. B. C. Dasireddy,Damjan Vengust,Blaž Likozar,Janez Kovač,Aleš Mrzel
出处
期刊:Renewable Energy [Elsevier BV]
卷期号:176: 251-261 被引量:39
标识
DOI:10.1016/j.renene.2021.05.051
摘要

Transition metal carbides and nitrides with large surface areas are attractive for various catalytic reactions. The synthesis of molybdenum carbide, molybdenum nitride and nanocomposite mixed-phase nanowires with the preserved structural morphology of two different precursor reactant materials by heating in diverse gas mixtures is reported herein. Prepared heterogeneous catalysts were characterized using diffraction, physisorption, chemisorption and microscopic techniques. With XRD and interfacial elemental analysis, performed by a transmission electron microscope, the composition of starting intermediate moieties and products was determined. Ordered grain structure appeared almost independent of applied gaseous compounds and typical domain sizes were comparable. The conversions of CO2 during the reverse water–gas shift (RWGS) were calculated for all measured samples in a wide operation range. Composite Mo2C/Mo2N showed the highest conversion higher than the pure Mo2C with similar site amount and especially larger than Mo2N, which demonstrated a low activity throughout the process. The stability of Mo2C/Mo2N wires was tested at 300 °C and they exhibited an unchanged time-on-stream reactivity over a long period of time (>24 h), withstanding deactivation. In addition, the selectivity towards CO was maintained at around 99%. The comparison of catalyst characterisation before and after RWGS reaction show that there is no major difference in the physical and chemical characteristics of the materials further validate the use of the present catalysts.
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