Comparative evaluation of anion doped photocatalysts on the mineralization and decolorization of natural organic matter

被引:24
作者
Birben, N. C. [1 ]
Uyguner-Demirel, C. S. [1 ]
Sen-Kayurmaci, S. [1 ]
Gurkan, Y. Y. [2 ]
Turkten, N. [2 ]
Cinar, Z. [2 ]
Bekbolet, M. [1 ]
机构
[1] Bogazici Univ, Inst Environm Sci, TR-34342 Istanbul, Turkey
[2] Yildiz Tech Univ, Dept Chem, TR-34220 Istanbul, Turkey
关键词
Doped TiO2; EEM fluorescence; Humic acid; Solar photocatalytic degradation; TIO2; PHOTOCATALYSTS; TITANIUM-DIOXIDE;
D O I
10.1016/j.cattod.2014.04.020
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The aim of this study was to assess photocatalytic performance of various anion doped TiO2 specimens on the degradation of natural organic matter represented by humic acids. Nitrogen doped (N-doped), sulfur doped (S-doped) and sulfur-nitrogen co-doped (S-N co-doped) TiO2 specimens were prepared according to a wet impregnation method. Their photocatalytic activities were evaluated with regard to degradation kinetics of humic acid in terms of UV-vis spectroscopic parameters (Color(436) and UV254) and dissolved organic carbon (DOC) as indicators of decolorization and mineralization respectively. The presence of different dopants in TiO2 structure ended up differences in terms of decolorization and mineralization kinetics of humic acids. Moreover, use of pure anatase form of TiO2 (Hombikat UV-100) for anion doping came up with higher photocatalytic activity than anion doped TiO2 specimens prepared by using TiO2 composed of mixture of anatase and rutile (Degussa P-25). Humic acid fluorescence excitation emission matrix (EEM) contour plots showed that solar photocatalytic degradation pathway was TiO2 type specific irrespective of dopants. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:125 / 131
页数:7
相关论文
共 23 条
[21]  
Yalçin Y, 2010, J ADV OXID TECHNOL, V13, P281
[22]   Single-step preparation, characterization and photocatalytic mechanism of mesoporous Fe-doped sulfated titania [J].
Yang, Ying ;
Zhong, Hui ;
Tian, Congxue ;
Jiang, Zhiqiang .
SURFACE SCIENCE, 2011, 605 (13-14) :1281-1286
[23]  
Zaleska Adriana., 2008, RECENT PATENTS ENG, V2, P157