催化作用
水煤气变换反应
烧结
制氢
铜
吸附
化学工程
氢
微晶
材料科学
无机化学
化学
物理化学
冶金
有机化学
工程类
作者
Chongqi Chen,Yingying Zhan,Dalin Li,Yanjie Zhang,Xingyi Lin,Lilong Jiang,Qi Zheng
标识
DOI:10.1002/ente.201700750
摘要
Abstract CuO/CeO 2 is a promising catalyst for water–gas shift (WGS) reaction in H 2 production. Much effort has been devoted to improving its catalytic activity and stability by CeO 2 support modification or introduction of secondary active species. Here a method to enhance the catalytic performance by controlling the deposition rate of copper is reported. The nature of CuO and CuO‐CeO 2 synergetic interaction are modulated by using different copper sources (Cu(NO 3 ) 2 and Cu[(NH 3 ) ) and controlling reaction temperatures. The as‐prepared CuO‐CeO 2 catalysts show distinguish catalytic performances for the WGS reaction. The one prepared by using Cu[(NH 3 ) at the reaction temperature of 30 °C (CuCe‐ 30N ) shows superior catalytic activity and stability. The CuCe‐ 30N catalyst possesses the largest Cu 0 surface area (39.2 m 2 ) and strongest CuO‐CeO 2 synergetic interaction. The largest Cu 0 surface area provides the most active sites for CO adsorption thus leading to its highest activity. The strong synergetic interaction prevents Cu crystallites from sintering during the WGS reaction, thus improving its thermal stability.
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