Photodegradation of rhodamine B and methyl orange over one-dimensional TiO2 catalysts under simulated solar irradiation

被引:106
作者
Guo, Changsheng [1 ,2 ]
Xu, Jian [1 ]
He, Yan [1 ,2 ]
Zhang, Yuan [1 ]
Wang, Yuqiu [2 ]
机构
[1] Chinese Res Inst Environm Sci, Riverine Ecol Ctr, Beijing 100012, Peoples R China
[2] Nankai Univ, Coll Environm Sci & Engn, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
One-dimensional nanostructures; Titanium dioxide; Photocatalysis; Rhodamine B; Methyl orange; PHOTOCATALYTIC ACTIVITY; ANATASE TIO2; TITANATE NANOTUBES; DEGRADATION; ION; TEMPERATURE; NANOWIRES; OXIDATION; PHASE; DYES;
D O I
10.1016/j.apsusc.2010.11.152
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this paper, two one-dimensional (1D) TiO2 nanostructures, nanotube and nanowire were synthesized by a hydrothermal method using Degussa P25 TiO2 as a precursor. The synthesized anatase TiO2 nanotubes with the diameters of 10-20 nm and length of several hundred nanometers were formed from P25 and NaOH with the hydrothermal treatment temperature at 150 degrees C, and anatase TiO2 nanowires with the diameters of 10-40nm and length up to several micrometers were prepared at 180 degrees C. The photocatalytic activity of the two nanostructures was evaluated by degrading rhodamine B (RhB) and methyl orange (MO) in aqueous solutions under simulated solar light irradiation. The results suggested that the TiO2 nanocatalysts displayed higher degradation activity compared to P25. For RhB, 98.9% and 91.9% of RhB were removed by nanotubes and nanowires, respectively after 60 min irradiation in comparison to the 81.8% removal by P25. Similar trend was observed for MO, with the removal percentage of 95.6%, 88.3% and 74.9%, respectively by TiO2 nanotubes, nanowires and P25. Meanwhile, RhB and MO showed different photodegradation rates in nanotubes and nanowires suspensions, probably due to the morphology and crystal structure of the TiO2 nanocatalysts which play important roles in the degradation activity of the catalysts. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:3798 / 3803
页数:6
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