Effect of crystallinity on the catalytic performance of amorphous Co-B particles prepared from cobalt nitrate and potassium borohydride in the cinnamaldehyde hydrogenation

被引:36
作者
Tong, Dong-Ge [1 ]
Chu, Wei
Luo, Yong-Yue
Ji, Xiao-Yang
He, Yi
机构
[1] Sichuan Univ, Coll Chem Engn, Lab 230, Chengdu 610065, Peoples R China
[2] Sichuan Univ, State Key Lab Polymer Mat, Chengdu 610065, Peoples R China
[3] Sichuan Univ, Analyt & Testing Ctr, Chengdu 610064, Peoples R China
基金
中国国家自然科学基金;
关键词
amorphous Co-B particles; cinnamaldehyde; hydrogenation; crystallization; magnetic properties;
D O I
10.1016/j.molcata.2006.10.032
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The amorphous Co-B particles were prepared from cobalt nitrate and potassium borohydride. Ethanol-thermal treatment has been used to promote the crystallinity of Co-B particles. Both the amorphous and crystallized Co-B particles were characterized by X-ray powder diffraction (XRD), scanning electron micrograph (SEM), inductively coupled plasma (ICP), X-ray photoelectron spectroscopy (XPS), specific surface area (S-BET), CO temperature-programmed desorption (TPD), and magnetic performance test. After crystallization, the synergistic effect between Co and B, the structure stability, and the magnetic property of Co-B enhanced while the activation energy in cinnamaldehyde (CMA) hydrogenation decreased. Furthermore, the conversion of cinnamaldehyde (CMA) increased from 5% to 57%. The hydrogenation of the C=C bond in cinnamaldehyde (CMA) is favored for the amorphous Co-B particles while the hydrogenation of the C=O bond is preferred for the crystallized Co-B particles. After 13 cycles, the crystallized Co-B particles remain higher cinnamaldehyde (CMA) conversion and cinnamyl alcohol (CMO) selectivity, which is attributed to their good structure stability and the novel magnetic method for recycle; while the cycle performance of amorphous Co-B particles is poor due to their instable structure. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:195 / 204
页数:10
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