Solvothermal synthesis of C-N codoped TiO2 and photocatalytic evaluation for bisphenol A degradation using a visible-light irradiated LED photoreactor

被引:239
作者
Wang, Xiaoping [1 ]
Lim, Teik-Thye [1 ]
机构
[1] Nanyang Technol Univ, Div Environm & Water Resources Engn, Sch Civil & Environm Engn, Singapore 639798, Singapore
基金
新加坡国家研究基金会;
关键词
C-N codoping; LED photoreacror; Bisphenol A; Solvothermal; Inorganic ions; DOPED TIO2; HETEROGENEOUS PHOTOCATALYSIS; TITANIUM-DIOXIDE; INORGANIC-IONS; WATER; CARBON; OXIDATION; POWDERS; SILICATE; SYSTEMS;
D O I
10.1016/j.apcatb.2010.08.012
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 study, a highly visible-light photoactive carbon and nitrogen codoped TiO2 (CN-TiO2) was synthesized via a facile solvothermal method. The conditions for each synthesis step including selection of dopants, solvothermal treatment, and calcination temperatures were evaluated. X-ray photoelectron spectroscopy shows that the surface of TiO2 was modified by carbon and nitrogen via formation of Ti-C bonds, carbonate species and oxynitrides. The derived photocatalyst is predominantly of anatase phase. with well-developed mesoporosity and a large BET surface area (102 m(2)/g). The photocatalytic degradation (PCD) of bisphenol A (BPA) by CN-TiO2 was evaluated using a novel photoreactor irradiated with flexible strips of visible light-emitting diode (Vis-LED). The PCD of BPA was most favorable under circumneutral pH. Under 5 h of irradiation with white, blue, green and yellow LED lights, the extents of BPA degradation were >99%, >99%, 84% and 24% respectively, while the corresponding percentages of mineralization were 70%, 60%. 45% and 9%. Presence of sulfate, chloride and nitrate at 5.0 mM only slightly retarded BPA degradation, while bicarbonate and silica inhibited the process to a much larger extent. Deactivation of the CN-TiO2 by silica could be attributed to the formation of surface-bound silica species. By adjusting to acidic condition, the detrimental effect from silica could be significantly suppressed. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:355 / 364
页数:10
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