乙醛
脱氢
催化作用
化学
乙醇
沸石
热重分析
漫反射红外傅里叶变换
无机化学
铜
核化学
有机化学
光催化
作者
Dongni Yu,Weili Dai,Guangjun Wu,Naijia Guan,Landong Li
标识
DOI:10.1016/s1872-2067(19)63378-4
摘要
The selective dehydrogenation of ethanol to acetaldehyde is a promising route for acetaldehyde production. Although Cu-based catalysts exhibit high activity in ethanol dehydrogenation, a rapid deactivation due to Cu sintering always occurs. In this study, highly dispersed Cu species were sta-bilized using the silanol defects in Beta zeolite (denoted as Beta) resulting from dealumination, and applied as robust catalysts for ethanol-to-acetaldehyde conversion. Typically, a long catalyst life-time of 100 h with an acetaldehyde yield of ∼70% could be achieved over 5% Cu/Beta. The pres-ence of Cu+ and Cu0 species and the agglomeration of Cu particles after a long-term reaction for 180 h were revealed by transmission electron microscopy, thermogravimetric analysis, and CO-diffuse-reflectance infrared Fourier transform spectroscopy, and were responsible for the deac-tivation of the Cu/Beta catalyst in the ethanol-to-acetaldehyde conversion.
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