催化作用
化学
硫黄
水煤气变换反应
X射线光电子能谱
无机化学
钼
化学工程
有机化学
工程类
作者
Joshua A. Schaidle,Adam C. Lausche,Levi T. Thompson
标识
DOI:10.1016/j.jcat.2010.04.004
摘要
Molybdenum carbide (Mo2C) and Pt/Mo2C catalysts were evaluated for the water gas shift reaction without and with 5 ppm H2S. The Mo2C catalyst was quickly poisoned by sulfur, achieving a rate that was ∼10% of that prior to sulfur exposure. The Pt/Mo2C catalyst was initially more active than the Mo2C catalyst and deactivated more gradually to a level similar to that for the Mo2C catalyst. X-ray photoelectron spectroscopy revealed Mo2C, MoS2, and S–Mo on the spent catalysts; the Pt/Mo2C catalyst also contained PtS. The results are consistent with Mo2C sites on the Mo2C and Pt/Mo2C catalysts being partially sulfur tolerant, in that these sites could be reactivated on treatment in 15% CH4/H2 at 590 °C. High activity sites associated with Pt nanoparticles were irreversibly deactivated. Residual activities for the Mo2C and Pt/Mo2C catalysts in the presence of H2S appeared to be associated primarily with the presence of MoS2 domains.
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