首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Preparation of ultrafine Cu1.5Mn1.5O4 spinel nanoparticles and its application in p-nitrophenol reduction
Authors:Li  Fang  Zhang  Ruikai  Li  Qiming  Zhao  Shiduo
Institution:1.College of Chemistry, Chemical Engineering and Environmental Engineering, Liaoning Shihua University, Fushun, 113001, China
;2.Key Laboratory of Coal to Ethylene Glycol and Its Related Technology, Chinese Academy of Sciences, Fuzhou, 350002, Fujian, China
;
Abstract:

In this work, ultrafine Cu1.5Mn1.5O4 spinel nanoparticles were successfully synthesized by a sol–gel method combined with two complexing agents, which was firstly employed in the reductive transformation from p-nitrophenol into p-aminophenol. The effect of calcination temperature on the crystal phase and microstructure of Cu1.5Mn1.5O4 nanoparticles was investigated in this article. It was found that Cu1.5Mn1.5O4 nanoparticles with pure spinel phase can be obtained at 500 °C with the help of EDTA acid–citric acid complexing agents. Below 500 °C, there exists some Mn2O3 impure phase. SEM characterization indicated that the particle size of the spinel Cu1.5Mn1.5O4 rapidly increases above 600 °C. The catalytic experimental results show that the Cu1.5Mn1.5O4 nanoparticles prepared at 500 °C exhibit the highest catalytic activity which is even superior to some precious metal catalysts. With the calcination temperature increasing, the catalytic activity of Cu1.5Mn1.5O4 spinel nanoparticles gradually degrades which can be ascribed to the particle size growth of Cu1.5Mn1.5O4. It can also be observed that all the oxide samples, namely CuO, Mn2O3 and Cu1.5Mn1.5O4, possess certain catalytic ability for the transformation from p-nitrophenol into p-aminophenol. However, the catalytic activity of Cu1.5Mn1.5O4 spinel nanoparticles is obviously higher than CuO and Mn2O3. Especially, Mn2O3 alone has very poor catalytic activity in the reduction of p-nitrophenol.

Keywords:
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号