全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Photocatalytic BiFeO3 Nanofibrous Mats for Effective Water Treatment

DOI: 10.1155/2013/939531

Full-Text   Cite this paper   Add to My Lib

Abstract:

One-dimensional BiFeO3 (BFO) nanofibers fabricated by electrospinning of a solution of Nylon6/BFO followed by calcination were used for photocatalytic degradation of contaminants in water. The BFO fibers were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), and UV-Vis spectroscopy. The SEM images of the as-spun samples demonstrated the successful production of nanofibers and the SEM images of the samples after calcination confirmed the integrity of the continuous BFO nanofibers. XRD analysis indicated the dominant presence of BFO phase throughout the calcinated nanofibers. Photocatalytic activity of the nanofibers and their application in water purification were investigated against 4-chlorophenol (4CP) as a model water contaminant. The results of the UV-Vis spectroscopy show the degradation of the 4CP by means of the photocatalytic activity of the BFO nanofibers. The kinetics of the photodegradation of 4CP is believed to be governed by a pseudo-first-order kinetics model. 1. Introduction The presence of hazardous nondegradable contaminants in water such as pharmaceuticals [1] and organic and inorganic solutes [2] poses dangers of human and environmental exposure that result in health effects and environmental damage [3, 4]. A widespread need, therefore, exists for developing cost effective and scalable methods to reduce harmful compounds to a permitted amount or eliminate them entirely. Many methods such as the application of polymeric adsorbents, membrane separation, and oxidation treatments have been proposed [5]. Photocatalysis, a well-known oxidation treatment method, has the advantage of direct absorption of light at room temperature where there is no need for thermal activation to fully mineralize pollutants [6, 7]. Photocatalysis involves photolysis, the breaking down of a chemical compound by the assistance of light, which is accelerated by means of a catalyst. This process can occur in the form of homogeneous as well as heterogeneous photocatalysis. In the former, photocatalysts such as ozone are used and the reactants exist at the same phase as the catalyst. In the latter, however, the reactants are in a different phase from the reactive entity that triggers various oxidation and reduction reactions through which the contaminating agent is degraded [7]. Semiconductors are often applied in this type of photocatalysis. In this case, photocatalysis is activated when photons with sufficient energy excite the electrons of the valence band in the photocatalyst creating electron-hole pairs. Due to the presence of

References

[1]  T. Ternes and U. von Gunten, “Editorial to special issue in Water Research. Emerging contaminants in water,” Water Research, vol. 44, no. 2, p. 351, 2010.
[2]  N. Savage and M. S. Diallo, “Nanomaterials and water purification: opportunities and challenges,” Journal of Nanoparticle Research, vol. 7, no. 4-5, pp. 331–342, 2005.
[3]  M. Iscan, “Hazard identification for contaminants,” Toxicology, vol. 205, no. 3, pp. 195–199, 2004.
[4]  H. F. Schr?der, “Selective determination of non-biodegradable polar, organic pollutants in waste water related to functional groups using flow injection combined with tandem mass spectrometry,” Water Science and Technology, vol. 34, no. 7-8, pp. 21–28, 1996.
[5]  R. Hernandez, M. Zappi, J. Colucci, and R. Jones, “Comparing the performance of various advanced oxidation processes for treatment of acetone contaminated water,” Journal of Hazardous Materials, vol. 92, no. 1, pp. 33–50, 2002.
[6]  N. Keller, G. Rebmann, E. Barraud, O. Zahraa, and V. Keller, “Macroscopic carbon nanofibers for use as photocatalyst support,” Catalysis Today, vol. 101, no. 3-4, pp. 323–329, 2005.
[7]  J. M. Herrmann, “Heterogeneous photocatalysis: fundamentals and applications to the removal of various types of aqueous pollutants,” Catalysis Today, vol. 53, no. 1, pp. 115–129, 1999.
[8]  M. S. Lee, S. S. Park, G. D. Lee, C. S. Ju, and S. S. Hong, “Synthesis of TiO2 particles by reverse microemulsion method using nonionic surfactants with different hydrophilic and hydrophobic group and their photocatalytic activity,” Catalysis Today, vol. 101, no. 3-4, pp. 283–290, 2005.
[9]  M. Hussain, R. Ceccarelli, D. L. Marchisio, D. Fino, N. Russo, and F. Geobaldo, “Synthesis, characterization, and photocatalytic application of novel TiO2 nanoparticles,” Chemical Engineering Journal, vol. 157, no. 1, pp. 45–51, 2010.
[10]  S. Chuangchote, J. Jitputti, T. Sagawa, and S. Yoshikawa, “Photocatalytic activity for hydrogen evolution of electrospun TiO2 nanofibers,” ACS Applied Materials & Interfaces, vol. 1, no. 5, pp. 1140–1143, 2009.
[11]  Z. Liu, X. Zhang, S. Nishimoto, T. Murakami, and A. Fujishima, “Efficient photocatalytic degradation of gaseous acetaldehyde by highly ordered TiO2 nanotube arrays,” Environmental Science and Technology, vol. 42, no. 22, pp. 8547–8551, 2008.
[12]  K. Sunada, Y. Kikuchi, K. Hashimoto, and A. Fujishima, “Bactericidal and detoxification effects of TiO2 thin film photocatalysts,” Environmental Science and Technology, vol. 32, no. 5, pp. 726–728, 1998.
[13]  X. H. Xia, Y. Liang, Z. Wang, J. Fan, Y. S. Luo, and Z. J. Jia, “Synthesis and photocatalytic properties of TiO2 nanostructure,” Materials Research Bulletin, vol. 43, no. 8-9, pp. 2187–2195, 2008.
[14]  S. K. Choi, S. Kim, S. K. Lim, and H. Park, “Photocatalytic comparison of TiO2 nanoparticles and electrospun TiO2 nanofibers: effects of mesoporosity and interparticle charge transfer,” Journal of Physical Chemistry C, vol. 114, no. 39, pp. 16475–16480, 2010.
[15]  G. Laera, B. Jin, H. Zhu, and A. Lopez, “Photocatalytic activity of TiO2 nanofibers in simulated and real municipal effluents,” Catalysis Today, vol. 161, no. 1, pp. 147–152, 2011.
[16]  J. F. Ihlefeld, N. J. Podraza, Z. K. Liu et al., “Optical band gap of BiFeO3 grown by molecular-beam epitaxy,” Applied Physics Letters, vol. 92, no. 14, Article ID 142908, 2008.
[17]  A. J. Hauser, J. Zhang, L. Mier et al., “Characterization of electronic structure and defect states of thin epitaxial BiFeO3 films by UV-visible absorption and cathodoluminescence spectroscopies,” Applied Physics Letters, vol. 92, no. 22, Article ID 222901, 2008.
[18]  S. Li, Y. H. Lin, B. P. Zhang, C. W. Nan, and Y. Wang, “Photocatalytic and magnetic behaviors observed in nanostructured BiFeO3 particles,” Journal of Applied Physics, vol. 105, no. 5, Article ID 056105, 2009.
[19]  X. Xu, Y. H. Lin, P. Li, L. Shu, and C. W. Nan, “Synthesis and photocatalytic behaviors of high surface area BiFeO3 thin films,” Journal of the American Ceramic Society, vol. 94, no. 8, pp. 2296–2299, 2011.
[20]  F. Gao, X. Chen, K. Yin et al., “Visible-light photocatalytic properties of weak magnetic BiFeO3 nanoparticles,” Advanced Materials, vol. 19, no. 19, pp. 2889–2892, 2007.
[21]  E. Leyva, E. Moctezuma, M. G. Ruíz, and L. Torres-Martínez, “Photodegradation of phenol and 4-chlorophenol by BaO-Li2O-TiO2 catalysts,” Catalysis Today, vol. 40, no. 4, pp. 367–376, 1998.
[22]  N. Shakti and P. S. Gupta, “Structural and optical properties of sol-gel prepared ZnO thin film,” Applied Physics Research, vol. 2, no. 1, pp. 19–28, 2010.
[23]  K. Prashanthi, G. Thakur, and T. Thundat, “Surface enhanced strong visible photoluminescence from one-dimensional multiferroic BiFeO3 nanostructures,” Surface Science, vol. 606, pp. L83–L86, 2012.
[24]  M. Bertelli and E. Selli, “Reaction paths and efficiency of photocatalysis on TiO2 and of H2O2 photolysis in the degradation of 2-chlorophenol,” Journal of Hazardous Materials, vol. 138, no. 1, pp. 46–52, 2006.
[25]  K. V. Baiju, S. Shukla, K. S. Sandhya, J. James, and K. G. K. Warrier, “Photocatalytic activity of sol-gel-derived nanocrystalline titania,” Journal of Physical Chemistry C, vol. 111, no. 21, pp. 7612–7622, 2007.
[26]  I. Poulios and I. Tsachpinis, “Photodegradation of the textile dye Reactive Black 5 in the presence of semiconducting oxides,” Journal of Chemical Technology and Biotechnology, vol. 74, pp. 349–357, 1999.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133

WeChat 1538708413