Preparation of Y-zeolite/CoCl2 doped PVDF composite nanofiber and its application in hydrogen production

被引:35
作者
Li, Qiming [1 ]
Chen, Yingbo [2 ]
Lee, Dong Joo [1 ]
Li, Fang [1 ]
Kim, Hern [1 ]
机构
[1] Myongji Univ, Dept Environm Engn & Biotechnol, Energy & Environm Fus Technol Ctr, Yongin 449728, Kyonggi Do, South Korea
[2] Tianjin Polytech Univ, Sch Mat Sci & Engn, State Key Lab Hollow Fiber Membrane Mat & Proc, Tianjin 300160, Peoples R China
基金
新加坡国家研究基金会;
关键词
PVDF/CoCl2/Y-zeolite; Composite nanofiber; Co-electrospinning; Hydrogen; POLYMER-ELECTROLYTE; SODIUM-BOROHYDRIDE; CATALYTIC-ACTIVITY; GENERATION; NABH4; HYDROLYSIS; STORAGE; REDUCTION; HYDRIDE;
D O I
10.1016/j.energy.2011.12.021
中图分类号
O414.1 [热力学];
学科分类号
摘要
Hydrogen production from NaBH4 hydrolysis is very important for environment-friendly fuel cells. Here Y-zeolite/CoCl2 doped PVDF (Polyvinylidene fluoride) composite nanofibers were prepared by co-electrospinning method and successfully applied into hydrogen production from NaBH4 hydrolysis. The effect of Y-zeolite doping on properties of composite nanofibers was investigated in detail. SEM, EDX (Energy-dispersive X-ray spectroscopy) and FT-IR characterization showed that nanosized crystalline Y-zeolite can be doped into the bulk of composite nanofiber and high-quality composite nanofiber with fine morphologies can be obtained. The doping of Y-zeolite can improve the wetting ability of PVDF-based nanofiber and thus help to the diffusion rate of reactants. This Y-zeolite/CoCl2 doped electro-spun nanofiber as catalyst were applied into hydrogen production from NaBH4 hydrolysis and exhibits higher catalytic activity compared with that without Y-zeolite doping due to its improved surface hydrophilicity. Meanwhile, this composite nanofiber catalyst shows relatively good stability in hydrogen production without obvious loss of Y-zeolite. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:144 / 150
页数:7
相关论文
共 35 条
[1]   A multifactor study of catalyzed hydrolysis of solid NaBH4 on cobalt nanoparticles: Thermodynamics and kinetics [J].
Andrieux, Jerome ;
Swierczynski, Dariusz ;
Laversenne, Laetitia ;
Garron, Anthony ;
Bennici, Simona ;
Goutaudier, Christelle ;
Miele, Philippe ;
Auroux, Aline ;
Bonnetot, Bernard .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2009, 34 (02) :938-951
[2]   Carbon-supported platinum catalysts for on-site hydrogen generation from NaBH4 solution [J].
Bai, Ying ;
Wu, Chuan ;
Wu, Feng ;
Yi, Baolian .
MATERIALS LETTERS, 2006, 60 (17-18) :2236-2239
[3]   Highly active heteropolyanions supported Co catalysts for fast hydrogen generation in NaBH4 hydrolysis [J].
Bennici, Simona ;
Yu, Hao ;
Obeid, Emil ;
Auroux, Aline .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2011, 36 (13) :7431-7442
[4]   Metal-doped sodium aluminium hydrides as potential new hydrogen storage materials [J].
Bogdanovic, B ;
Brand, RA ;
Marjanovic, A ;
Schwickardi, M ;
Tölle, J .
JOURNAL OF ALLOYS AND COMPOUNDS, 2000, 302 (1-2) :36-58
[5]   Supported CoCl2 catalyst for NaBH4 dehydrogenation [J].
Cakanyildirim, Cetin ;
Guru, Metin .
RENEWABLE ENERGY, 2010, 35 (04) :839-844
[6]   Method of preparing Ru-immobilized polymer-supported catalyst for hydrogen generation from NaBH4 solution [J].
Chen, Ching-Wen ;
Chen, Chuh-Yung ;
Huang, Yao-Hui .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2009, 34 (05) :2164-2173
[7]   Preparation and application of sodium borohydride composites for portable hydrogen production [J].
Chen, Y. ;
Kim, H. .
ENERGY, 2010, 35 (02) :960-963
[8]   Use of a nickel-boride-silica nanocomposite catalyst prepared by in-situ reduction for hydrogen production from hydrolysis of sodium borohydride [J].
Chen, Yingbo ;
Kim, Hern .
FUEL PROCESSING TECHNOLOGY, 2008, 89 (10) :966-972
[9]   Ni/Ag/silica nanocomposite catalysts for hydrogen generation from hydrolysis of NaBH4 solution [J].
Chen, Yingbo ;
Kim, Hern .
MATERIALS LETTERS, 2008, 62 (8-9) :1451-1454
[10]   Preparation of PVDF nanofiber composites for hydrogen generation from sodium borohydride [J].
Chinnappan, Amutha ;
Kang, Hyuck-Chul ;
Kim, Hern .
ENERGY, 2011, 36 (02) :755-759