Difference in performance and mechanism for methylene blue when TiO2 nanoparticles are converted to nanotubes

被引:29
作者
Niu, Lin [1 ]
Zhao, Xiaoli [1 ]
Tang, Zhi [1 ]
Lv, Hongzhou [1 ]
Wu, Fengchang [1 ]
Wang, Xiaolei [1 ]
Zhao, Tianhui [1 ]
Wang, Junyu [1 ]
Wu, Aiming [1 ]
Giesy, John. P. [2 ]
机构
[1] Chinese Res Inst Environm Sci, State Key Lab Environm Criteria & Risk Assessment, Beijing 100012, Peoples R China
[2] Univ Saskatchewan, Toxicol Ctr, Saskatoon, SK, Canada
基金
中国国家自然科学基金;
关键词
TiO2; nanotubes; nanoparticles; Adsorption; Photocatalysis; Organic pollutants; ENHANCED PHOTOCATALYTIC DEGRADATION; ADSORPTION; DYE; REMOVAL; PHOTODEGRADATION; NANOCOMPOSITE; TEMPERATURE; SEPARATION; SHELL; WATER;
D O I
10.1016/j.jclepro.2021.126498
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
There are few reports on the diversification in adsorption and photo-catalysis caused by morphological changes. In this study, TiO2 nanotubes (TiO2 NTs) were synthesized by alkaline hydro-thermal method using commercial TiO2 nanoparticles (TiO2 NPs) as raw materials. When TiO2 nanoparticles are converted to nanotubes, the difference in adsorption and photocatalytic performance was analyzed using methylene blue (MB) as a model pollutant. The results showed that TiO2 NPs exhibited low adsorption capacity and greater photocatalytic activity for MB. In contrast, TiO2 NTs showed dual functions of adsorption and photo-catalysis. It exhibited better adsorption performance for MB and the maximum uptake was 102.41 mg/g. However, the photo-catalytic activity changed because the hydro-thermal method altered the crystal structure and increased the gap energy of TiO2 NTs, which led to the partial reduction of photo-catalytic activity compared to TiO2 NPs. The dominating free radicals were center dot OH, followed by center dot O-2(-) in the process of MB photodegradation by TiO2 NPs while center dot OH and center dot O-2(-) were main radicals in the process of MB photodegradation by TiO2 NTs. Moreover, 99% MB was degraded in 24 min via adsorption and photocatalysis synergy under the following optimal conditions: TiO2 NTs dose = 6 mg, pH = 9, and light intensity = 19 A. Compared with other photo-catalysts reported, TiO2 NTs exhibited a superior performance through adsorption and photo-catalysis synergy with advantages of faster degradation, less catalyst dose and high efficiency. This work hopes to provide reference for the design and synthesis of materials with dual functions of adsorption and photo-catalysis. (C) 2021 Elsevier Ltd. All rights reserved.
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页数:11
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