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Ethanol dehydrogenation over copper catalysts on rice husk ash prepared by ion exchange

煅烧 脱氢 催化作用 乙醛 无机化学 去壳 X射线光电子能谱 化学 傅里叶变换红外光谱 核化学 氧化铜 材料科学 乙醇 化学工程 有机化学 工程类 生物 植物
作者
Feg-Wen Chang,Hanxi Yang,L. Selva Roselin,Wen-Yao Kuo
出处
期刊:Applied Catalysis A-general [Elsevier BV]
卷期号:304: 30-39 被引量:128
标识
DOI:10.1016/j.apcata.2006.02.017
摘要

Samples of copper on rice husk ash (Cu/RHA) have been prepared by the ion exchange method, with various copper loadings, and have been calcined at different temperatures. Such samples were tested for dehydrogenation of ethanol to acetaldehyde. The samples were characterized by DSC, XRD, FTIR, TEM, XPS, TPR, BET, and H2–N2O titration techniques. FTIR spectra illustrate the formation of chrysocolla in uncalcined and calcined Cu/RHA catalyst precursors. DSC, XRD and XPS analyses illustrate that, in Cu/RHA catalyst precursor after drying at 383 K, copper is present as Cu(OH)2 species. After calcination at 723 K, copper is present as Cu2+ ions and as CuO species. After reduction of the calcined Cu/RHA sample at 523–573 K, copper is present as Cu+ and/or Cu0 species along with unreduced Cu2+ species. TEM images show that copper crystallites are spherical in shape and are evenly distributed. TPR results reveal that various copper loadings in calcined Cu/RHA catalyst precursor exhibit similar metal-support interactions (MSI). Ethanol conversion for dehydrogenation of ethanol is found to be independent of calcination temperature and has little effect on Cu loading. Ethanol is selectively converted to acetaldehyde at the reaction temperature of 483–548 K. The Cu/RHA catalysts exhibit higher catalytic activity and lower deactivation rate than Cu/SiO2 catalysts. The activity of Cu/RHA catalysts is found to depend on Cu surface area.

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