催化作用
热重分析
铂金
化学吸附
无机化学
甲苯
傅里叶变换红外光谱
程序升温还原
粉末衍射
吸附
材料科学
选择性
化学
核化学
化学工程
有机化学
工程类
结晶学
作者
Marta Dobrosielska,Michał Zieliński,Miłosz Frydrych,Mariusz Pietrowski,Piotr Marciniak,Agnieszka Martyła,Bogna Sztorch,Robert E. Przekop
出处
期刊:Ceramics
[Multidisciplinary Digital Publishing Institute]
日期:2021-12-08
卷期号:4 (4): 667-680
被引量:4
标识
DOI:10.3390/ceramics4040047
摘要
Al2O3-TiO2 systems with Ti:Al 0.1, 0.5 and 1.0 molar ratio obtained by the sol–gel method have been used as a platinum support. As a precursor of alumina gel, aluminum isopropoxide has been chosen. Titanium tert-butoxylate was applied to obtain titania gel and hexachloroplatinic acid was applied as a source of platinum. The systems have been characterized by the following methods: thermogravimetric analysis (TGA), Fourier transformation infrared spectroscopy (FTIR), X-ray powder diffraction (XRPD), low-temperature nitrogen adsorption–desorption isotherms (BET, BJH), temperature-programmed reduction with hydrogen (TPR-H2) and hydrogen chemisorption. Reactions of toluene to methylcyclohexane and selective o-chloronitrobenzene (o-CNB) to o-chloroaniline (o-CAN) hydrogenation were used as the tests of systems’ catalytic activity. The application of Al2O3-TiO2 as a support has enabled the obtaining of platinum catalysts showing high activities for hydrogenation of toluene and selective hydrogenation of o-chloronitrobenzene to o-chloroaniline in the liquid phase. The highest activity in both reactions has been found for Pt/Al2O3-0.5TiO2 catalyst and the highest selectivity for Pt/Al2O3-. The activity of Pt/Al2O3-TiO2 catalysts was higher than that of alumina-supported ones.
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