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CO removal for hydrogen purification via Water Gas Shift and COPROX reactions with monolithic catalysts

整体 水煤气变换反应 甲烷化 选择性 催化作用 近程 氢气净化器 化学工程 材料科学 水煤气 化学 分析化学(期刊) 合成气 制氢 一氧化碳 色谱法 有机化学 工程类
作者
Eduardo Poggio-Fraccari,Antonella Abele,Nicolas Zitta,Javier A. Francesconi,Fernando Mariño
出处
期刊:Fuel [Elsevier]
卷期号:310: 122419-122419 被引量:5
标识
DOI:10.1016/j.fuel.2021.122419
摘要

• Water Gas Shift and CO PROX reactions were studied for CO removal from H2-rich stream for PEMFC applications. • Cu and/or Ni over CeO2 or CePrOx coated honeycomb monoliths were successfully tested. • CFD simulation proved that canalizations are not present in monolith-loaded reactor. • CuNi/CePr15 sample for WGS reaction achieved >50% CO conversion, 100% selectivity in CO2-H2 rich stream. • Temperature, contact time, and O2/CO ratio were optimized for COPROX Cu/CeO2 catalyst. A combination of Water Gas Shift (WGS) and CO preferential oxidation (COPROX) reactions is considered a promising approach for CO removal in an H 2 feed employed for PEM fuel cells. Honeycomb monolithic catalysts were studied for this purpose, firstly coated with Ce or Ce-Pr, then with Cu or Cu-Ni, (mass gained ∼35%). Computational Fluid Dynamics simulation showed that outer channels (close to reactor wall) presented a slightly lower flow in comparison with flow in inner ones. The Pr content in WGS monoliths modulated the activity-selectivity ratio showing an optimal value for 15 at.% in case of Ni-containing samples due to a significant selectivity improvement towards WGS (hindering methanation). A Cu/ceria monolithic sample was tested as COPROX catalyst. The CO conversion presented a maximum value with the increase of the operation temperature. Besides, a larger contact time (achieved by modifying monolith length) also enhanced the undesired H 2 oxidation reaction as same as a larger O 2 /CO ratio. As a consequence, a temperature window around to 130 °C, a contact time close to 0.1 g.s/cm 3 , and a O 2 /CO = 1 M ratio was determined as the most adequate parameters set.
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