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首页> 外文期刊>Catalysts >In Situ Regeneration of Alumina-Supported Cobalt–Iron Catalysts for Hydrogen Production by Catalytic Methane Decomposition
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In Situ Regeneration of Alumina-Supported Cobalt–Iron Catalysts for Hydrogen Production by Catalytic Methane Decomposition

机译:用于催化甲烷分解制氢的氧化铝负载钴铁催化剂的原位再生

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摘要

A novel approach to the in situ regeneration of a spent alumina-supported cobalt–iron catalyst for catalytic methane decomposition is reported in this work. The spent catalyst was obtained after testing fresh catalyst in catalytic methane decomposition reaction during 90 min. The regeneration evaluated the effect of forced periodic cycling; the cycles of regeneration were performed in situ at 700 °C under diluted O 2 gasifying agent (10% O 2 /N 2 ), followed by inert treatment under N 2 . The obtained regenerated catalysts at different cycles were tested again in catalytic methane decomposition reaction. Fresh, spent, and spent/regenerated materials were characterized using X-ray powder diffraction (XRD), transmission electron microscopy (TEM), laser Raman spectroscopy (LRS), N 2 -physisorption, H 2 -temperature programmed reduction (H 2 -TPR), thermogravimetric analysis (TGA), and atomic absorption spectroscopy (AAS). The comparison of transmission electron microscope and X-ray powder diffraction characterizations of spent and spent/regenerated catalysts showed the formation of a significant amount of carbon on the surface with a densification of catalyst particles after each catalytic methane decomposition reaction preceded by regeneration. The activity results confirm that the methane decomposition after regeneration cycles leads to a permanent deactivation of catalysts certainly provoked by the coke deposition. Indeed, it is likely that some active iron sites cannot be regenerated totally despite the forced periodic cycling.
机译:在这项工作中,报道了一种新的方法来原位再生用过的氧化铝负载的钴铁催化剂催化甲烷的分解。在90分钟内在催化甲烷分解反应中测试新鲜催化剂后,获得了废催化剂。再生评估了强制周期性循环的效果。再生循环在稀释的O 2气化剂(10%O 2 / N 2)下于700°C原位进行,然后在N 2下进行惰性处理。在催化甲烷分解反应中再次测试在不同循环下获得的再生催化剂。使用X射线粉末衍射(XRD),透射电子显微镜(TEM),激光拉曼光谱(LRS),N 2-物理吸附,H 2-程序升温还原(H 2- TPR),热重分析(TGA)和原子吸收光谱(AAS)。用过的和用过的/再生过的催化剂的透射电子显微镜和X射线粉末衍射特性的比较表明,在每次催化甲烷分解反应进行再生之后,表面上会形成大量的碳,且催化剂颗粒会致密化。活性结果证实,再生循环后甲烷的分解导致了由焦炭沉积引起的催化剂的永久失活。确实,尽管有强制性周期性循环,某些活性铁位点仍可能无法完全再生。

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