单片Pt/Al2O3和Pt/ZrO2催化剂上甲烷氧化偶联生成乙炔

IF 5 Q2 ENERGY & FUELS
Sven Schardt , Ahmet Çelik , Simon Bastian , Suchada Sirisomboonchai , Maki Nakamura , Koyo Norinaga , Patrick Lott
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引用次数: 0

摘要

本研究考察了关键操作参数——包括空速、原料气氮稀释和碳氧比(C:O)对单片Pt/Al₂O₃和Pt/ZrO₂甲烷氧化偶联催化剂(OCM)的影响。确定了最佳操作条件,产生了高的碳2选择性,其中乙炔的比例明显很大。在理想条件下,Pt/ZrO₂催化剂的最大C₂选择性为11.3%,乙炔贡献为84%,甲烷转化率约为90%。与氧化铝相比,氧化锆在催化剂稳定性和寿命方面是一种优越的支撑材料。采用x射线衍射(XRD)、扫描电镜(SEM)和x射线光电子能谱(XPS)等表征技术,发现在温度超过1200℃的苛刻反应条件下,两种催化剂的形态和结构发生了显著变化。这些发现有助于开发更稳定的催化剂配方和优化OCM反应的工艺条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acetylene formation via oxidative coupling of methane over monolithic Pt/Al2O3 and Pt/ZrO2 catalysts
This study investigates the influence of key operational parameters – including space velocity, feed gas dilution with nitrogen, and the carbon-to-oxygen (C:O) ratio – on monolithic Pt/Al₂O₃ and Pt/ZrO₂ catalysts for the oxidative coupling of methane (OCM). Optimal operating conditions were identified that yielded high C₂ selectivities, with a notably large share of acetylene. Under ideal conditions, a Pt/ZrO₂ catalyst achieved a maximum C₂ selectivity of 11.3 %, with 84 % acetylene contribution and approximately 90 % methane conversion. Zirconia was found to be a superior support material compared to alumina in terms of catalyst stability and longevity. A number of characterization techniques including X-ray diffraction (XRD), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS) were applied and revealed significant morphological and structural changes in both catalyst types, induced by the harsh reaction conditions with temperatures exceeding 1200 °C. These findings contribute to the advancement of more robust catalyst formulations and optimized process conditions for the OCM reaction.
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CiteScore
4.20
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