Ni-Co catalyst derived from layered double hydroxides for dry reforming of methane

被引:66
|
作者
Zhang, Xiaoqing [1 ]
Yang, Chunhui [1 ]
Zhang, Yanping [1 ]
Xu, Yan [1 ]
Shang, Shuyong [2 ]
Yin, Yongxiang [1 ]
机构
[1] Sichuan Univ, Sch Chem Engn, Chengdu 610065, Peoples R China
[2] Yibin Univ, Inst Chem Engn Technol, Yibin 644000, Peoples R China
基金
中国国家自然科学基金;
关键词
LDH precursor; Ni-Co bimetallic catalyst; In-situ urea precipitation; Dry reforming of methane; Carbon deposition; CARBON-DIOXIDE; SYNGAS PRODUCTION; SYNTHESIS GAS; BIMETALLIC CATALYSTS; HYDROGEN-PRODUCTION; AL; DECOMPOSITION; DEACTIVATION; PERFORMANCE; FABRICATION;
D O I
10.1016/j.ijhydene.2015.09.150
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
Ni/Co monometallic and bimetallic layered double hydroxides (LDH) were in-situ synthesized on the surface of gamma-Al2O3 by urea precipitation method. Then they were decomposed and reduced by H-2/Ar atmospheric plasma jet at 400 degrees C for 15 min to become into catalysts. The LDH precursors were verified by XRD, SEM, FT-IR and Raman, while the catalysts were characterized by N-2 adsorption-desorption, XRD, TEM and H-2-TPR. After that their catalytic activity and stability were evaluated in dry reforming of methane (DRM) reaction. Both Ni and 2Ni-1Co showed better catalytic performance than other catalysts. Finally, the weight and species of carbon deposition on spent catalyst were tested by TG-DTA analysis. The deposition of inert carbon was the main reason for deactivation of catalysts in DRM. Moreover, a highly uniform dispersion and small particle size of active component are achieved by in situ co-precipitation method, and gamma-Al2O3 provided large specific surface area for these Ni/Co catalysts. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:16115 / 16126
页数:12
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