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International Journal of Photoenergy
Volume 2012, Article ID 121239, 8 pages
Research Article

Preparation of a Modified PTFE Fibrous Photo-Fenton Catalyst and Its Optimization towards the Degradation of Organic Dye

1Division of Textile Chemistry & Ecology, School of Textiles, Tianjin Polytechnic University, 399 Binshui Western Road, Xiqing District, Tianjin 300387, China
2State Key Laboratory Breeding Base of Photocatalysis, Fuzhou University, Fuzhou 350002, China

Received 22 May 2012; Accepted 30 July 2012

Academic Editor: Meenakshisundaram Swaminathan

Copyright © 2012 Zhizhong Ding et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Polytetrafluoroethylene (PTFE) fiber was grafted with acrylic acid to impart the carboxyl groups onto the fiber surface, which were used to coordinate with both transition metal ions Fe(III) and Cu(II) and a rare metal ion Ce(III) to prepare the metal grafted PTFE fiber complexes as the novel heterogeneous Fenton catalysts for the degradation of the azo dye in water under visible irradiation. Some factors affecting the preparation process, such as nature and concentration of metal ions in the coordination solution, grafting degree of PTFE and reaction temperature were optimized with respect to the content and strength of metal fixation on the fiber and dye degradation efficiency. The results indicated that increasing metal ion concentrations in solution and grafting degree of PTFE fiber as well as higher coordination temperature led to a significant increase in metal content, especially Fe(III) and Cu(II) content of the complexes. Fe(III) ions fixed on the fiber showed the better catalytic performance than Cu(II) and Ce(III) ions fixed when three different complexes with similar metal content being employed, respectively. Moreover, Increasing Fe content or incorporation of Cu(II) ions could significantly improve the catalytic activity of the complexes.