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Lewis Acid Sites Stabilized Nickel Catalysts for Dry (CO2) Reforming of Methane

机译:Lewis酸部位稳定镍催化剂的干燥(CO2)重整甲烷

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摘要

Strong Lewis acid species [Al-F] were synthesized on a series of Al2O3-supported Ni catalysts modified with (0, 1, 5, and 10 wt.%) of KF to investigate the electronic and anchoring effect of [Al-F] on Ni catalysts in terms of catalytic activity, stability, and carbon resistance during dry reforming of methane (DRM) reaction. With the aids of XRD analysis, X-ray photoelectron spectroscopy, H-2 temperature-programmed reduction, and in situ diffuse reflectance infrared Fourier transform spectroscopy analyses, it was found that the activity and stability of KF-modified catalysts in the reaction was directly associated to the presence of [Al-F] sites. The [Al-F] Lewis acid sites not only stabilized the metal Ni from high-temperature sintering after reaction of 200 h through an enhanced metal-support interaction, but also reduced the electron density of Ni metal, which alleviated the fast decomposition of CH4 and subsequent carbon deposition on catalysts. Balancing the rates for CH4 dissociation and carbon removal would be promising steps in the design of active and stable Ni-based catalysts.
机译:在用(0,1,5和10wt.%)KF的一系列Al 2 O 3负载的Ni催化剂上合成强Lewis酸性物质[Al-F],以研究[Al-F]的电子和锚定效果在催化活性,稳定性和碳抗性期间的Ni催化剂在甲烷(DRM)反应中的干燥重整过程中。借助XRD分析的辅助性,X射线光电子能谱,H-2温度编程的降低,以及原位漫反射率红外傅里叶变换光谱分析,发现反应中Kf改性催化剂的活性和稳定性直接与[Al-F]网站的存在相关联。 [Al-F]路易斯酸部位不仅通过增强的金属 - 载体相互作用在200小时后从高温烧结中稳定金属Ni,而且还降低了Ni金属的电子密度,这缓解了CH4的快速分解并随后在催化剂上碳沉积。平衡CH4解离和碳去除率的速率将是有效和稳定的Ni基催化剂的设计。

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