A simple granulation technique for preparing high-porosity nano copper oxide(II) catalyst beads

被引:23
作者
Ahmadi, Seyed Javad [1 ]
Outokesh, Mohammad [2 ]
Hosseinpour, Morteza [2 ]
Mousavand, Tahereh [3 ]
机构
[1] NSTRI, Jaber Ebne Hayyan Res Lab, Tehran, Iran
[2] Sharif Univ Technol, Sch Energy Engn, Tehran, Iran
[3] McGill Univ, Dept Mech Engn, Montreal, PQ H3A 2K6, Canada
关键词
CuO nanoparticles; Catalyst; Hydrothermal synthesis; Supercritical water; Granulation; Calcium alginate; SOLID-STATE REACTION; HYDROTHERMAL SYNTHESIS; ONE-STEP; CUO; CRYSTALLIZATION; PARTICLES; WATER;
D O I
10.1016/j.partic.2011.02.010
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A simple and efficient method was developed for fabricating spherical granules of CuO catalyst via a three-step procedure. In the first step, copper oxide nanoparticles were synthesized by hydrothermal decomposition of copper nitrate solution under supercritical condition. Then, they were immobilized in the polymeric matrix of calcium alginate. and followed by high-temperature calcination in an air stream as the third step, in which carbonaceous materials were oxidized, to result in a pebble-type catalyst of high porosity. The produced CuO nanoparticles were characterized by transmission electron microscopy (TEM) that revealed an average size of 5 nm, X-ray diffractometry (XRD), and thermo gravimetric (TG) analysis. The catalysts were further investigated by BET test for measurement of their surface area, and by temperature-programmed reduction analysis (H-2-TPR) for determination of catalytic activity. The results demonstrated that immobilization of the CuO nanoparticle in the polymeric matrix of calcium alginate, followed by calcination at elevated temperatures, could result in notable mechanical strength and enhanced catalytic activity due to preservation of the high surface area, both valuable for practical applications. (C) 2011 Chinese Society of Particuology and Institute of Process Engineering, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:480 / 485
页数:6
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