Visible light photocatalytic activity of rutile TiO sub(2) fiber clusters in the degradation of terephthalic acid
Rutile TiO sub(2) nanoparticles, in different structural and morphological properties, were produced by the hydrolysis of titanium tetrachloride in a highly acidic reaction media at moderate temperatures without calcination. Their photocatalytic activities were investigated in the liquid-phase degra...
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Published in: | Applied physics. A, Materials science & processing Vol. 120; no. 3; pp. 967 - 976 |
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Main Authors: | , |
Format: | Journal Article |
Language: | English |
Published: |
01-09-2015
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Subjects: | |
Online Access: | Get full text |
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Summary: | Rutile TiO sub(2) nanoparticles, in different structural and morphological properties, were produced by the hydrolysis of titanium tetrachloride in a highly acidic reaction media at moderate temperatures without calcination. Their photocatalytic activities were investigated in the liquid-phase degradation of terephthalic acid under visible light illumination. The parameters, which are the concentration of the titanium tetrachloride solution (0.1-1 M) and reaction temperature (60-95 degree C), effective on the properties of the particles, and their photocatalytic performances, were investigated. The XRD patterns indicated a pure rutile crystal structure at moderate temperatures without need of calcination. The FEGSEM images showed the formation of flower-, pinecone-, and sphere-like clusters consisting of interconnected nanofibers. The N sub(2) adsorption-desorption isotherms pointed out the microporous structure of the clusters. Band gap energies were found to be varying between 3.02 and 3.08 eV due to the well-developed rutile crystallite structure. Systematic studies elucidated that the optimum reactant concentration and reaction temperature are 0.5 M TiCl sub(4) and 95 degree C, respectively. The rutile clusters synthesized at the optimum reaction conditions exhibited 99 % of the photocatalytic degradation of TPA under visible light illumination at shorter irradiation times compared with commercial P25 TiO sub(2). |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-2 |
ISSN: | 0947-8396 1432-0630 |
DOI: | 10.1007/s00339-015-9263-4 |