Journal
APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 100, Issue 1-2, Pages 355-364Publisher
ELSEVIER
DOI: 10.1016/j.apcatb.2010.08.012
Keywords
C-N codoping; LED photoreacror; Bisphenol A; Solvothermal; Inorganic ions
Funding
- National Research Foundation (NRF) of Singapore [EWI RFP 0802-11]
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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.
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