Methane decomposition over Fe supported catalysts for hydrogen and nano carbon yield

A. Fakeeha, A. Ibrahim, M. Naeem, W. Khan, A. Abasaeed, Raja Alotaibi, A. Al‐Fatesh
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引用次数: 12

Abstract

Abstract Production of hydrogen, being an environmentally friendly energy source, has gained a lot of attention in the recent years. In this article, iron-based catalysts, with different active metal loadings, supported over magnesia and titania are investigated for hydrogen production via catalytic decomposition of methane. The catalytic activity and stability results revealed that magnesia supported catalysts performed better than titania supported catalysts. Hydrogen reduction temperature of 500°C was obtained suitable for catalyst activation. For magnesia supported catalysts, only higher loadings i.e., 30% and 40% Fe-Mg catalysts showed reasonable activity, while all titania supported catalysts presented less activity as well as deactivation. Among all the catalysts, 30% Fe/MgO catalyst displayed better activity. The formation of carbon nanofibers was evidenced from morphological analysis. FESEM and TEM images showed the generation of nonuniform carbon nanofibers with broader diameter. The catalysts were characterized using different techniques such as BET, H2-TPR, O2-TPO, XRD, TGA, FESEM and TEM.
铁负载催化剂上甲烷分解的氢和纳米碳产率
摘要氢气作为一种环保能源,近年来受到了广泛的关注。在本文中,研究了不同活性金属负载的铁基催化剂在氧化镁和二氧化钛上的负载,用于甲烷催化分解制氢。结果表明,氧化镁负载型催化剂的催化活性和稳定性优于二氧化钛负载型催化剂。得到了适宜催化剂活化的500℃氢还原温度。对于负载氧化镁的催化剂,只有较高的负载量,即30%和40%的Fe-Mg催化剂表现出合理的活性,而所有负载二氧化钛的催化剂都表现出较低的活性和失活。其中,30% Fe/MgO催化剂表现出较好的活性。形态分析证实了碳纳米纤维的形成。FESEM和TEM图像显示,制备出了直径更宽、不均匀的纳米碳纤维。采用BET、H2-TPR、O2-TPO、XRD、TGA、FESEM和TEM等技术对催化剂进行了表征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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