CO reactive adsorption at low temperature over CuO/CeO2 structured catalytic monolith

被引:18
作者
Di Benedetto, Almerinda [1 ]
Landi, Gianluca [2 ]
Lisi, Luciana [2 ]
机构
[1] Univ Naples Federico II, Dipartimento Ingn Chim Mat & Prod Ind, Ple Tecchio 80, I-80125 Naples, Italy
[2] CNR, Inst Res Combust, Ple Tecchio 80, I-80125 Naples, Italy
关键词
CO-PROX; Hydrogen; Purification; Low temperature adsorption; CuO/CeO2; SOLUTION COMBUSTION SYNTHESIS; PREFERENTIAL OXIDATION; SELECTIVE OXIDATION; CUO-CEO2; CATALYSTS; CARBON-MONOXIDE; HIGH-PERFORMANCE; REDOX PROPERTIES; EXCESS HYDROGEN; H-2; FE;
D O I
10.1016/j.ijhydene.2017.03.077
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
CO adsorption on a copper/ceria nanopowder washcoated onto a cordierite monolith has been studied at low temperature by following the time evolution of the outlet concentration of CO and CO2 on nanometric CuO/CeO2 catalyst. The effects of adsorption time length, gas phase composition (H-2 or O-2 addition), temperature and contact time were investigated. Results showed that the high surface and the large availability of labile oxygen allows CO oxidation and CO2 release even at room temperature. Moreover, tests under transient conditions showed that i) interfacial copper/ceria sites re-oxidation can benefit of oxygen transfer from ceria depending on the operating conditions (O-2 partial pressure, temperature, etc.), hydroxyl groups, boosting CO2 production rate, can be formed over the catalyst surface by reaction with molecular H-2 at temperature above 80 degrees C, and iii) several CO and CO2 adsorbed species must be taken into account, covering not only copper but also ceria sites, some of them being spectators in the reaction pathway. Finally a novel strategy for CO removal based on CO trap is proposed. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:12262 / 12275
页数:14
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