Transition metal nanoparticles dispersed in an alumina matrix as active and stable catalysts for COx-free hydrogen production from ammonia

被引:84
作者
Gu, Ying-Qiu [1 ]
Jin, Zhao [1 ]
Zhang, Hu [1 ]
Xu, Rong-Jie [1 ]
Zheng, Ming-Jiang [1 ]
Guo, Yu-Mei [1 ]
Song, Qi-Sheng [1 ]
Jia, Chun-Jiang [1 ]
机构
[1] Shandong Univ, Key Lab Colloid & Interface Chem, Key Lab Special Aggregated Mat, Sch Chem & Chem Engn, Jinan 250100, Peoples R China
基金
美国国家科学基金会;
关键词
FUEL-CELL; CARBON NANOTUBES; IRON CATALYSTS; DECOMPOSITION; GENERATION; SIZE; KINETICS; NITROGEN; SUPPORT; ETHANOL;
D O I
10.1039/c5ta04179a
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
Transition metal (Fe, Co, and Ni) nanoparticles dispersed in an alumina matrix as catalysts for NH3 decomposition have been synthesized by a facile co-precipitation method. The fresh and used catalysts were characterized by various techniques including powder X-ray diffraction (XRD), N-2 adsorption/desorption, and transmission electron microscopy (TEM). Also, temperature-programmed reduction by hydrogen (H-2-TPR) combining in situ XRD was performed to investigate the reducibility of the studied catalysts. For the ammonia decomposition reaction, 88% conversion of ammonia can be realized at the reaction temperature as low as 600 degrees C using a space velocity of 72 000 cm(3) g(cat)(-1) h(-1) NH3 during a long term (72 h) catalysis test without any observable deactivation. The small amount of alumina (low to 10 at%) can act as the matrix in which the catalytically active transition metal nanoparticles were stabilized. Thus, the agglomeration of active transition metals under reaction conditions was significantly suppressed and the high activity of catalysts was maintained.
引用
收藏
页码:17172 / 17180
页数:9
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