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Preparation of CuO/CeO 2 Catalyst with Enhanced Catalytic Performance for Water–Gas Shift Reaction in Hydrogen Production
Author(s) -
Chen Chongqi,
Zhan Yingying,
Li Dalin,
Zhang Yanjie,
Lin Xingyi,
Jiang Lilong,
Zheng Qi
Publication year - 2018
Publication title -
energy technology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.91
H-Index - 44
eISSN - 2194-4296
pISSN - 2194-4288
DOI - 10.1002/ente.201700750
Subject(s) - catalysis , water gas shift reaction , sintering , hydrogen production , copper , adsorption , chemical engineering , hydrogen , crystallite , materials science , inorganic chemistry , chemistry , metallurgy , organic chemistry , engineering
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 ) ] 4 2 + ) 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 ) ] 4 2 +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 g cat - 1 ) 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.