Methane cracking using Ni supported on porous and non-porous alumina catalysts

被引:43
作者
Amin, Ashraf M. [2 ]
Croiset, Eric [1 ]
Constantinou, Crystle [1 ]
Epling, William [1 ]
机构
[1] Univ Waterloo, Dept Chem Engn, Waterloo, ON N2L 3G1, Canada
[2] Natl Res Ctr, Chem Engn & Pilot Plant Dept, Giza, Egypt
基金
加拿大自然科学与工程研究理事会;
关键词
Hydrogen; Methane cracking; Nickel catalyst; HYDROGEN-PRODUCTION; CARBON NANOFIBERS; FILAMENTOUS CARBON; DECOMPOSITION; DEACTIVATION; REGENERATION; NI/SIO2; H-2; ECONOMY; CO;
D O I
10.1016/j.ijhydene.2012.02.001
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 and non-porous alumina catalysts were used as nickel supports to catalyze methane cracking. Different operating parameters were studied in a thermal gravimetric analyzer, including methane and hydrogen partial pressures, temperature and flow rate. During CH4 cracking, carbon builds up on the catalyst surface and therefore the catalyst requires periodic regeneration. Cycling tests were performed, using air during the regeneration phase to burn off the carbon. The results showed that the non-porous catalyst performed better than the porous catalyst in terms of cracking during the first cycle. Full regeneration of the catalysts by oxidizing the deposited carbon was achieved at 550 degrees C, while oxidation was very slow at 500 degrees C. After full regeneration, the performance of the porous catalyst became considerably better than the non-porous. The porous catalyst kept its activity for 24 cracking/regeneration cycles, while the non-porous catalyst lost half of its activity by the second cracking cycle and almost all of its activity after six cycles. NiAl2O4 formation and Ni sintering caused the non-porous catalyst activity loss. TPO results showed that two carbon types were deposited on the catalysts, namely C beta and C gamma, where CO is more active than C gamma. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
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页码:9038 / 9048
页数:11
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