Attapulgite clay supported Ni nanoparticles encapsulated by porous silica: Thermally stable catalysts for ammonia decomposition to COx free hydrogen

被引:59
作者
Li, Lei [1 ]
Chen, Feng [2 ]
Shao, Jingling [1 ]
Dai, Yong [1 ]
Ding, Jianfei [1 ]
Tang, Zhe [1 ]
机构
[1] Yancheng Inst Technol, Sch Chem & Chem Engn, Yancheng 224051, Peoples R China
[2] Suzhou Univ Sci & Technol, Sch Chem Biol & Mat Engn, Suzhou 215009, Peoples R China
基金
中国国家自然科学基金;
关键词
Core-shell; Nickel catalyst; Attapulgite; Silica; Ammonia decomposition; PARTIAL OXIDATION; CARBON NANOFIBERS; NH3; DECOMPOSITION; SURFACE-AREA; FUEL-CELL; GENERATION; METHANE; PERFORMANCE; REDUCTION; SIZE;
D O I
10.1016/j.ijhydene.2016.08.156
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
Porous silica encapsulated attapulgite (ATP) clay supported nickel catalysts were prepared by successive precipitation-deposition method, which were tested in an ammonia decomposition for production of COx-free hydrogen. The textural and structure properties of Ni/ATP catalysts and silica encapsulated Ni/ATP catalysts were characterized by X-ray diffraction, scanning and transmission electron microscopy, N-2 sorption, thermogravimetry-differential thermal analysis, hydrogen temperature-programmed reduction. The results reveal that ATP supported Ni catalysts possess a suitable specific surface area and pore volume, as well as nano-structure. Ni nanoparticles are mostly located on the external surface of ATP supports. With an increase on Ni loading content from 10 to 50 wt % (theoretical value), the ammonia conversion increases gradually. Owning to porous silica enwrapping, the Ni-30/ATP@SiO2 catalysts show a higher specific activity (17.0 mol g(Ni)(-1) h(-1), 650 degrees C) and stability than Ni-30/ATP catalysts. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:21157 / 21165
页数:9
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