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Tailoring catalytic performance of carbon nanotubes confined CuO-CeO_2 catalysts for CO preferential oxidation

机译:碳纳米管约束CuO-CeO_2催化剂对CO优先氧化的定制催化性能。

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Multi-wall carbon nanotubes confined CuO-CeO2 binary oxide catalysts (CuxCe1-xO/CNTs, x = 0, 0.2, 0.4, 0.6 and 1.0) have been prepared by a special ultrasound-aided impregnation. The effects of Cu-Ce molar ratios on the structure and catalytic performance for CO preferential oxidation have been systematically investigated. Judging from XRD patterns and Raman analysis, Cu2+ ions incorporate into CeO2 lattice to form ceria-base solid solution, accompanied by oxygen vacancies and an interaction produces between the catalyst particles and inner surface of carbon nanotubes. TEM microstructural analysis shows that CuO and CeO2 particles are uniformly dispersed in carbon nanotubes for the CuxCe1-xO/CNTs (x = 0.4) catalyst. Meanwhile, the reducibility of active copper species is enhanced markedly. In addition, the Cu0.4Ce0.6O/CNTs sample possesses more surface lattice oxygen and oxygen vacancies according to surface species characterization, which can provide more active oxygen species for CO oxidation and promote the mobility of lattice oxygen. The CuxCe1-xO/CNTs (x = 0.4) catalyst exhibits excellent activity, wide temperature span of full CO conversion (120-160 degrees C) and high selectivity especially above 110 degrees C (maintaining high selectivity until 140 degrees C). (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:通过特殊的超声浸渍法制备了多壁碳纳米管受限的CuO-CeO2二元氧化物催化剂(CuxCe1-xO / CNT,x = 0、0.2、0.4、0.6和1.0)。已经系统地研究了Cu-Ce摩尔比对CO优先氧化的结构和催化性能的影响。从X射线衍射图谱和拉曼分析来看,Cu2 +离子结合到CeO2晶格中形成二氧化铈基固溶体,并伴随着氧空位以及催化剂颗粒与碳纳米管内表面之间的相互作用。 TEM微观结构分析表明,对于CuxCe1-xO / CNTs(x = 0.4)催化剂,CuO和CeO2颗粒均匀分散在碳纳米管中。同时,活性铜的还原性显着提高。此外,根据表面物种的表征,Cu0.4Ce0.6O / CNTs样品具有更多的表面晶格氧和氧空位,可以为CO氧化提供更多的活性氧物种,并促进晶格氧的迁移。 CuxCe1-xO / CNTs(x = 0.4)催化剂表现出出色的活性,宽广的温度范围(可实现完全的CO转化)(120-160摄氏度)和高选择性,尤其是在110摄氏度以上(保持高选择性直至140摄氏度)。 (C)2018氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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