A novel W-doped Ni-Mg mixed oxide catalyst for CO2 methanation

被引:178
作者
Yan, Yong [1 ]
Dai, Yihu [1 ]
He, Hong [2 ,3 ]
Yu, Yunbo [2 ,3 ]
Yang, Yanhui [1 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, Singapore 637459, Singapore
[2] Chinese Acad Sci, Ecoenvironm Sci Res Ctr, State Key Joint Lab Environm Simulat & Pollut Con, Beijing 100085, Peoples R China
[3] Chinese Acad Sci, CAS Ctr Excellence Urban Atmospher Environm, Xiamen 361021, Peoples R China
基金
新加坡国家研究基金会;
关键词
CO2; methanation; Ni-W-Mg mixed oxide; Ni-Mg interactions; Monodentate formate; SUPPORTED NICKEL-CATALYSTS; TEMPERATURE-PROGRAMMED REDUCTION; CARBON-DIOXIDE; PARTICLE-SIZE; NI/MGO CATALYSTS; HYDROGENATION; SURFACE; SELECTIVITY; STABILITY; SILICA;
D O I
10.1016/j.apcatb.2016.05.016
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
Novel Ni-W-Mg mixed oxide catalysts (NiWMgOx) were prepared by homogeneous precipitation and attempted for the methanation of CO2. Adding W remarkably promoted the activity with improved stability, anti-CO-poisoning ability and resistance against coke formation compared to the undoped NiMgOx catalyst. The superior reactivity of monodentate formate towards hydrogenation than that of bidentate formate species was identified by DRIFTS analysis and the formation of more active monodentate formate species was indisputably facilitated by W additives, leading to the greatly enhanced catalytic activity. H-2-TPR and CO2-TPD characterization showed that doping W increased the number of stable CO2 adsorption sites and helped in anchoring the Ni sites as a result of strengthened Ni-Mg interaction, both of which were responsible for the enhanced CO2 methanation activity and the improved resistance against sintering. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:108 / 116
页数:9
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