煅烧
脱氢
铜
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
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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