Immobilization of CoCl2 (cobalt chloride) on PAN (polyacrylonitrile) composite nanofiber mesh filled with carbon nanotubes for hydrogen production from hydrolysis of NaBH4 (sodium borohydride)

被引:48
|
作者
Li, Fang [1 ,2 ]
Arthur, Ernest Evans [1 ]
La, Dahye [1 ]
Li, Qiming [2 ]
Kim, Hem [1 ]
机构
[1] Myongi Univ, Dept Energy & Biotechnol, Energy & Environm Fus Technol Ctr, Yongin 449728, Kyonggi Do, South Korea
[2] Liaoning Shihua Univ, Coll Chem Chem Engn & Environm Engn, Fushun 113001, Liaoning, Peoples R China
基金
新加坡国家研究基金会; 中国国家自然科学基金;
关键词
PAN (polyacrylonitrile)/CoCl2 (cobalt chloride)/CNTs (carbon nanotubes); Composite nanofiber; Sodium borohydride; Hydrogen production; POLYMER NANOFIBERS; CO-B; GENERATION; CATALYSTS; PVDF;
D O I
10.1016/j.energy.2014.03.130
中图分类号
O414.1 [热力学];
学科分类号
摘要
Composite nanofiber sheets containing multiwalled carbon nanotubes and cobalt chloride dispersed in PAN (polyacrylonitrile) were produced by an electrospinning technique. The synthesized PAN/CoCl2/CNTs composite nanofiber was used as the catalyst for hydrogen production from the hydrolysis of sodium borohydride. FT-IR characterization showed that the pretreated CNTs possess different organic functional groups which help improve the compatibility between CNTs and PAN organic polymer. SEM (scanning electron microscopy), TEM (transmission electron microscopy) and EDX (energy-dispersive X-ray technique) were used to characterize the composite nanofiber and it was found that CNTs can be coaxially dispersed into the PAN nanofiber. During the hydrolysis of NaBH4, this PAN/CoCl2/CNTs composite nanofiber exhibited higher catalytic activity compared to the composite without CNTs doping. Kinetic analysis of NaBH4 hydrolysis shows that the reaction of NaBH4 hydrolysis based on this catalyst can be ascribed to the first-order reaction and the activation energy of the catalyst was approximately 52.857 kJ/mol. Meanwhile, the composite nanofiber catalyst shows excellent stability and reusability in the recycling experiment, (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:32 / 39
页数:8
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