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[二氧化钛诱导左氧氟沙星的可见光光降解及其机制]

[TiO2-Induced Photodegradation of Levofloxacin by Visible Light and Its Mechanism].

作者信息

Guo Hong-sheng, Liu Ya-nan, Qiao Qi, Wei Hong, Dong Cheng-xing, Xue Jie, Li Ke-bin

出版信息

Huan Jing Ke Xue. 2015 May;36(5):1700-6.

PMID:26314119
Abstract

Levofloxacin is an emerging pollutant. Single levofloxacin and TiO2 have no visible-light activity. However, photodegradation of levofloxacin dramatically enhanced in the presence of TiO2 under visible light irradiation. Considering this finding, he photodegradation of levofloxacin over TiO2 was investigated under visible light irradiation. Effects of TiO2 dosage, levofloxacin concentration, and solution pH on levofloxacin photodegradation were examined by monitoring its concentration decay with time. The results showed that levofloxacin photodegradation fitted the Langmuir-Hinshelwood kinetic model. Solution pH, TiO2 dose, and levofloxacin concentration had significant effects on the photodegradation rates. In addition, batch adsorption experiments revealed that adsorption of levofloxacin on TiO2 conformed to the pseudo-second-order kinetics and the Langmuir isotherm. DRS spectrum of levofloxacin-adsorbed TiO2 suggested that a surface complex was formed between levofloxacin and TiO2. Addition of radical scavengers and N2-degassing affecting levofloxacin photodegradation indicated that the superoxide ion radical was mainly active species. UV-Vis spectra of a deaerated TiO2 and levofloxacin suspensions further confirmed that the electron injection into TiO2 conduction band took place under visible light irradiation. Based on these results, a charge-transfer mechanism initiated by photoexcitation of TiO2/ levofloxacin surface complex was proposed for levofloxacin photocatalytic degradation over TiO2 under visible light. This study indicates that the charge-transfer-complex-mediated photocatalytic technique has promising applications in the removal of colorless organic pollutants.

摘要

左氧氟沙星是一种新兴污染物。单一的左氧氟沙星和二氧化钛没有可见光活性。然而,在可见光照射下,二氧化钛存在时左氧氟沙星的光降解显著增强。基于这一发现,研究了可见光照射下左氧氟沙星在二氧化钛上的光降解。通过监测左氧氟沙星浓度随时间的衰减,考察了二氧化钛用量、左氧氟沙星浓度和溶液pH值对左氧氟沙星光降解的影响。结果表明,左氧氟沙星的光降解符合朗缪尔-欣谢尔伍德动力学模型。溶液pH值、二氧化钛用量和左氧氟沙星浓度对光降解速率有显著影响。此外,批量吸附实验表明,左氧氟沙星在二氧化钛上的吸附符合准二级动力学和朗缪尔等温线。吸附了左氧氟沙星的二氧化钛的漫反射光谱表明,左氧氟沙星与二氧化钛之间形成了表面络合物。添加自由基清除剂和氮气脱气对左氧氟沙星光降解的影响表明,超氧离子自由基是主要的活性物种。脱气后的二氧化钛和左氧氟沙星悬浮液的紫外-可见光谱进一步证实,在可见光照射下发生了电子注入二氧化钛导带的过程。基于这些结果,提出了一种由二氧化钛/左氧氟沙星表面络合物的光激发引发的电荷转移机制,用于可见光下左氧氟沙星在二氧化钛上的光催化降解。本研究表明,电荷转移络合物介导的光催化技术在去除无色有机污染物方面具有广阔的应用前景。

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