时间分辨、原位漂移/EDE/MS研究氧化铝负载Rh催化剂:CO氧化过程中铈对Rh催化剂的影响

Q1 Materials Science Catalysis Structure & Reactivity Pub Date : 2017-02-14 DOI:10.1080/2055074X.2016.1266762
A. Kroner, M. Newton, M. Tromp, A. Russell, A. Dent, J. Evans
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引用次数: 1

摘要

摘要采用漫反射红外傅立叶变换光谱(DRIFTS)/能量分散X射线吸收精细结构/质谱联用技术,研究了氧化铈表面改性和可控金属表面改性对Rh/γ-Al2O3催化剂在CO氧化过程中结构-功能性能的影响在298–573 K的温度范围内,在时间分辨的原位条件下同时进行。CSM添加每种助催化剂元素对催化剂结构表现出多种影响。DRIFTS/XAS研究表明,CeOx有助于保护Rh颗粒免受空气、O2和CO环境中的广泛氧化,而不会降低可氧化吸附的CO的覆盖率。
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Time-resolved, in situ DRIFTS/EDE/MS studies on alumina supported Rh catalysts: effects of ceriation on the Rh catalysts in the process of CO oxidation
Abstract The effect of ceria doping by oxide surface modification and controlled metal surface modification (CSM) on the structure-function properties of Rh/γ-Al2O3 catalysts in the process of CO oxidation were studied by a combined array of Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS)/Energy Dispersive X-ray Absorption Fine Structure/Mass Spectrometry techniques applied simultaneously under time-resolved, in situ conditions in the temperature range of 298–573 K. The addition of each promoter element by CSM exhibits multiple effects on the catalysts structure. The DRIFTS/XAS studies indicate that CeOx facilitate the protection of Rh particles against extensive oxidation in atmospheres of air, O2 and CO, without reducing the coverage of oxidisable adsorbed CO.
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Catalysis Structure & Reactivity
Catalysis Structure & Reactivity CHEMISTRY, PHYSICAL-
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