二苯胺
脱氢
催化作用
化学
无机化学
化学吸附
吡啶
选择性
程序升温还原
吸附
环己酮
X射线光电子能谱
有机化学
化学工程
工程类
作者
Yuyao Zeng,Bowei Wang,Yang Li,Xilong Yan,Ligong Chen,Yue Wang
标识
DOI:10.1021/acs.iecr.9b04567
摘要
A series of alkaline-earth-metal-modified Pd/Al2O3 nanocatalysts were prepared by an impregnation and kneading method. It was found that all of the catalysts doped by alkaline metals exhibit better catalytic performance in the continuous dehydrogenative aromatization of the Schiff base derived from cyclohexanone and aniline to diphenylamine (DPA) than that of Pd/Al2O3, in which, Pd1/Al3BaO presents a remarkable catalytic performance. X-ray diffraction, CO chemisorption, transmission electron microscopy, X-ray photoelectron spectroscopy, temperature-programmed hydrogen reduction, NH3-temperature-programmed desorption, Fourier transform infrared spectroscopy of pyridine adsorption, and a N2 adsorption–desorption method were employed to explore their structure–activity relationship. It was found that the doped Ba in Pd1/Al3BaO could promote the dispersion of Pd nanoparticles and reduce its acidity compared with that of Pd1/Al2O3. Therefore, the better Pd dispersion facilitated the dehydrogenation of Schiff base to DPA and the lower acidity of catalysts restrained the hydrolysis of the Schiff base and other side reactions, achieving good DPA selectivity. Moreover, Pd1/Al3BaO exhibited good stability. This work provides a promising strategy for the highly selective continuous synthesis of diarylamine or its derivatives from nonaromatic compounds.
科研通智能强力驱动
Strongly Powered by AbleSci AI