Institute of Chemistry, University of Campinas - UNICAMP, PO Box 6154, 13083-970 Campinas, SP, Brazil.
Faculty of Mechanical Engineering, University of Campinas - UNICAMP, PO Box 6122, 13083-970 Campinas, SP, Brazil.
Water Res. 2015 Apr 1;72:305-14. doi: 10.1016/j.watres.2014.08.042. Epub 2014 Sep 4.
TiO2 and TiO2/WO3 electrodes, irradiated by a solar simulator in configurations for heterogeneous photocatalysis (HP) and electrochemically-assisted HP (EHP), were used to remediate aqueous solutions containing 10 mg L(-1) (34 μmol L(-1)) of 17-α-ethinylestradiol (EE2), active component of most oral contraceptives. The photocatalysts consisted of 4.5 μm thick porous films of TiO2 and TiO2/WO3 (molar ratio W/Ti of 12%) deposited on transparent electrodes from aqueous suspensions of TiO2 particles and WO3 precursors, followed by thermal treatment at 450 (°)C. First, an energy diagram was organized with photoelectrochemical and UV-Vis absorption spectroscopy data and revealed that EE2 could be directly oxidized by the photogenerated holes at the semiconductor surfaces, considering the relative HOMO level for EE2 and the semiconductor valence band edges. Also, for the irradiated hybrid photocatalyst, electrons in TiO2 should be transferred to WO3 conduction band, while holes move toward TiO2 valence band, improving charge separation. The remediated EE2 solutions were analyzed by fluorescence, HPLC and total organic carbon measurements. As expected from the energy diagram, both photocatalysts promoted the EE2 oxidation in HP configuration; after 4 h, the EE2 concentration decayed to 6.2 mg L(-1) (35% of EE2 removal) with irradiated TiO2 while TiO2/WO3 electrode resulted in 45% EE2 removal. A higher performance was achieved in EHP systems, when a Pt wire was introduced as a counter-electrode and the photoelectrodes were biased at +0.7 V; then, the EE2 removal corresponded to 48 and 54% for the TiO2 and TiO2/WO3, respectively. The hybrid TiO2/WO3, when compared to TiO2 electrode, exhibited enhanced sunlight harvesting and improved separation of photogenerated charge carriers, resulting in higher performance for removing this contaminant of emerging concern from aqueous solution.
TiO2 和 TiO2/WO3 电极在异质光催化 (HP) 和电化学辅助 HP (EHP) 配置下受到太阳模拟器的辐照,用于修复含有 10mg/L(34μmol/L)17-α-乙炔基雌二醇 (EE2)(大多数口服避孕药的活性成分)的水溶液。光催化剂由 TiO2 和 TiO2/WO3(摩尔比 W/Ti 为 12%)的 4.5μm 厚多孔薄膜组成,这些薄膜沉积在透明电极上,由 TiO2 颗粒和 WO3 前体的水悬浮液制成,然后在 450°C 下进行热处理。首先,根据光电化学和紫外可见吸收光谱数据组织了一个能级图,并表明 EE2 可以通过半导体表面的光生空穴直接氧化,考虑到 EE2 和半导体价带边缘的相对 HOMO 能级。此外,对于辐照的混合光催化剂,TiO2 中的电子应转移到 WO3 导带,而空穴则向 TiO2 价带移动,从而改善电荷分离。通过荧光、HPLC 和总有机碳测量对修复后的 EE2 溶液进行了分析。正如能级图所预期的那样,两种光催化剂都在 HP 配置下促进了 EE2 的氧化;4 小时后,用辐照 TiO2 处理,EE2 浓度降至 6.2mg/L(EE2 去除率为 35%),而 TiO2/WO3 电极则导致 45%的 EE2 去除。在 EHP 系统中实现了更高的性能,此时引入一根 Pt 丝作为对电极,光电电极偏置在+0.7V;然后,EE2 的去除率分别为 TiO2 和 TiO2/WO3 的 48%和 54%。与 TiO2 电极相比,混合 TiO2/WO3 表现出增强的太阳光捕获和改善的光生载流子分离,从而提高了从水溶液中去除这种新兴关注污染物的性能。