首页> 外文期刊>International journal of hydrogen energy >Non-oxidative thermocatalytic decomposition of methane into COx free hydrogen and nanocarbon over unsupported porous NiO and Fe2O3 catalysts
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Non-oxidative thermocatalytic decomposition of methane into COx free hydrogen and nanocarbon over unsupported porous NiO and Fe2O3 catalysts

机译:无载体多孔NiO和Fe2O3催化剂上甲烷的非氧化热催化分解为COx游离氢和纳米碳

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The non-oxidative thermal decomposition of methane is one of the most promising routes for the direct production of COx free hydrogen and nanocarbon. In this work, unsupported porous NiO and Fe2O3 catalysts were successfully synthesized by a facile precipitation method using ammonium carbonate as the precipitant and were used for the thermocatalytic decomposition of undiluted methane. The prepared catalysts were characterized for their crystalline, structural and textural properties. The pseudo spherical metal oxide nanoparticles with the size of 10-30 nm were highly inter-aggregated to provide a porous texture to the catalysts. A well packed particle arrangement was observed for the unsupported Fe2O3 catalyst whereas a loose aggregation was observed for the NiO clusters. The catalysts were found to be highly active and stable for the decomposition of methane at various reaction temperatures of 600 degrees C, 700 degrees C and 800 degrees C. A maximum hydrogen yield of 66% and 53% was observed for the NiO and Fe2O3 catalysts respectively for an undiluted methane feed of 150 ml/min at 800 degrees C. At the end of 360 min of time on stream, the hydrogen yield was measured to be 49% and 46% respectively without deactivation. Moreover, a high catalytic stability was observed for the iron catalyst due to its high carbon diffusion coefficient compared to the nickel catalyst. Bulk deposition of metal encapsulated carbon nanochunks and multilayer graphene sheets were observed over the Ni and Fe catalysts respectively. The structural, crystalline and morphological characterization of the metal dependent nanocarbon were performed by using X-ray diffraction, scanning and transmission electron microscopy, temperature programmed oxidation and Raman analysis. High oxidation stability, crystallinity and graphitization degree was observed for the metal encapsulated carbon nanochunks than the multilayer graphene sheets. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:甲烷的非氧化性热分解是直接生产COx游离氢和纳米碳的最有希望的途径之一。在这项工作中,使用碳酸铵作为沉淀剂,通过简便的沉淀方法成功地合成了无载体的多孔NiO和Fe2O3催化剂,并将其用于未稀释甲烷的热催化分解。所制备的催化剂的结晶,结构和结构性质对其进行表征。尺寸为10-30 nm的拟球形金属氧化物纳米粒子高度相互聚集,从而为催化剂提供了多孔质感。对于未负载的Fe2O3催化剂,观察到了堆积良好的颗粒排列,而对于NiO簇,观察到了松散的聚集。发现该催化剂在600℃,700℃和800℃的各种反应温度下对甲烷的分解具有很高的活性和稳定性。NiO和Fe2O3催化剂的最大氢产率为66%和53%对于在800摄氏度下150 ml / min的未稀释甲烷进料,分别进行测量。在运行360分钟的时间结束时,测得的氢产率分别为49%和46%,而没有失活。此外,由于铁催化剂的碳扩散系数比镍催化剂高,因此观察到铁催化剂的催化稳定性高。分别在Ni和Fe催化剂上观察到金属封装的碳纳米块和多层石墨烯片的本体沉积。金属依赖性纳米碳的结构,晶体和形态表征通过使用X射线衍射,扫描和透射电子显微镜,程序升温氧化和拉曼分析进行。与多层石墨烯片相比,金属包封的碳纳米块具有较高的氧化稳定性,结晶度和石墨化度。 (C)2016氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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