Catalytic evaluation of nickel nanoparticles in methane steam reforming

被引:61
作者
Ali, Sardar [1 ]
Al-Marri, Mohammed J. [1 ]
Abdelmoneim, Ahmed G. [1 ]
Kumar, Anand [2 ]
Khader, Mahmoud M. [1 ]
机构
[1] Qatar Univ, Coll Engn, Gas Proc Ctr, Doha 2713, Qatar
[2] Qatar Univ, Coll Engn, Dept Chem Engn, Doha 2713, Qatar
关键词
Methane steam reforming; Hydrogen production; Ni nanoparticles; Coke deposition; CARBON-DIOXIDE; SUPPORTED NI; HYDROGEN-PRODUCTION; METAL CATALYSTS; LOW-TEMPERATURE; COKING; DRY; CO2; HYDROCARBONS; RESISTANCE;
D O I
10.1016/j.ijhydene.2016.08.200
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
Development of a highly efficient and coke-resistant, nickel nanoparticles (Ni.NPs) based catalyst in the steam reformation reaction of methane is reported. The catalyst was prepared by dispersing Ni-nanoparticles over silica functionalized alumina support. The synthesized samples were characterized by a combination of analytical techniques of Xray diffraction (XRD), nitrogen physisorption (BET surface area), X-ray photoelectron spectroscopy (XPS), temperature programmed reduction (H-2-TPR) and temperature programmed oxidation (TPO). Characterization results revealed that functionalization of alumina resulted in improved physicochemical properties of Ni-nanoparticles catalyst compared to the conventional nickel based catalysts. More importantly, a clear improvement on the catalytic hydrogen production and resistance to coke was observed. At all temperature studied Ni.NPs catalyst exhibited high methane conversions which reached to 100% at 750 degrees C. Also, the Ni.NPs catalysts exhibited high H-2 selectivity and excellent thermal stability. The functionalization of alumina with silica improved the dispersion of Ni nano particles and prevented sintering and aggregation. Ni.NPs catalyst exhibited stable catalytic activities for a period of 48 h where no carbon deposition was evidenced neither by TPO nor XPS techniques. Contrary to Ni.NPs the conventional nickel catalyst suffered from severe deactivation due to deposition of filamentous carbon on the surface. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:22876 / 22885
页数:10
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