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Effect of the surface state on the catalytic performance of a Co/CeO2 ethanol steam-reforming catalyst

机译:表面态对Co / CeO2乙醇蒸汽重整催化剂催化性能的影响

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摘要

This work examines the impact of the Co/CeO catalysts’ surface oxidation state and composition on the ethanol steam reforming (ESR) reaction performance. To this purpose, in situ and ex situ X-ray photoelectron spectroscopy (XPS) combined with on-line mass spectrometry were applied in a wide pressure range (0.2–20 mbar). When the reaction was performed at 0.2 mbar, metallic cobalt and partly reduced cerium oxide were found regardless of the catalysts’ pretreatment conditions. This surface state favors CO and H production, indicating that Csingle bondC bond cleavage is the most important pathway in this pressure regime. A higher reduction degree of ceria gave rise to a larger population of adsorbed hydroxyl groups, which, contrary to the expected behavior, suppressed the activity and the Csingle bondC bond cleavage yield. Under higher pressure (4–20 mbar), gradual oxidation of cobalt and ceria was noted. The presence of ionic cobalt species appears to enhance CO and acetaldehyde yields. On the basis of the present results and the available literature a plausible pressure-dependent reaction mechanism is proposed.
机译:本作品研究了CO / CEO催化剂表面氧化态和组合物对乙醇蒸汽重整(ESR)反应性能的影响。为此目的,原位和Ex原位X射线光电子能谱(XPS)与在线质谱相结合,施加在宽的压力范围内(0.2-20毫巴)。当反应在0.2毫巴进行时,无论催化剂的预处理条件如何,发现了金属钴和部分还原的氧化铈。这种表面状态有利于CO和H生产,表明Csingle BONDC键裂解是该压力方案中最重要的途径。较高的二氧化氮程度使得较大的吸附羟基群体,这与预期的行为相反,抑制活性和Csingle键合粘合产率。在较高的压力下(4-20毫巴),注意到钴和二氧化铈的逐渐氧化。似乎存在离子钴种类,以增强CO和乙醛产率。在本结果和可用文献的基础上提出了一种合理的压力依赖性反应机理。

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