Photodegradation of nalidixic acid assisted by TiO2 nanorods/Ag nanoparticles based catalyst

被引:37
作者
Petronella, F. [1 ,2 ]
Diomede, S. [2 ,3 ]
Fanizza, E. [1 ,2 ]
Mascolo, G. [3 ]
Sibillano, T. [4 ]
Agostiano, A. [1 ,2 ]
Curri, M. L. [1 ]
Comparelli, R. [1 ,3 ]
机构
[1] CNR IPCF, Ist Proc Chim & Fis, Sez Bari, Dip Chim, I-70126 Bari, Italy
[2] Univ Bari, Dip Chim, I-70126 Bari, Italy
[3] CNR IRSA, Ist Ric Acque, I-70123 Bari, Italy
[4] CNR IC, Ist Cristallog, I-70126 Bari, Italy
关键词
Photocatalysis; TiO2/Ag nanoparticles; Antibiotics; Fluoroquinolone; Nalidixic acid; Recalcitrant pollutants; WASTE-WATER; PHOTOCATALYTIC ACTIVITY; DEGRADATION; ANTIBIOTICS; FILMS; NANOCOMPOSITE; TITANIUM; NANOCRYSTALS; REMOVAL;
D O I
10.1016/j.chemosphere.2013.01.107
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Two different nanosized TiO2-based catalysts supported onto glass with tailored photocatalytic properties upon irradiation by UV light were successfully employed for the degradation of nalidixid acid, a widely diffused antibacterial agent of environmental relevance known to be non-biodegradable. Anatase rod-like TiO2 nanocrystals (TiO(2)NRs) and a semiconductor oxide-noble metal nanocomposite TiO2 NRs/Ag nanoparticles (NPs), synthesized by colloidal chemistry routes, were cast onto glass slide and employed as photocatalysts. A commercially available catalyst (TiO2 P25), also immobilized onto a glass slide, was used as a reference material. It was found that both TiO2 NRs/Ag NPs composite and TiO2 NRs demonstrated a photocatalytic efficiency significantly higher than the reference TiO2 P25. Specifically, TiO2 NRs/Ag NPs showed a photoactivity in nalidixic acid degradation 14 times higher than TiO2 P25 and 4 times higher than bare TiO2 NRs in the first 60 min of reaction. Several by-products were identified by HPLC-MS along the nalidixic acid degradation, thus getting useful insight on the degradation pathway. All the identified by-products resulted completely removed after 6 h of reaction. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:941 / 947
页数:7
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