Department of Civil and Environmental Engineering, School of Environment and Society, Tokyo Institute of Technology, 2-12-1, M1-4, Ookayama, Meguro-ku, Tokyo, 152-8552, Japan; Water and Wastewater Engineering Research Group, Faculty of Civil and Environmental Engineering, Institut Teknologi Bandung, Jl. Ganesha 10, Bandung, 40132, Indonesia.
Department of Chemistry, Northwestern University, Evanston, IL, 60208, United States.
Water Res. 2020 May 1;174:115643. doi: 10.1016/j.watres.2020.115643. Epub 2020 Feb 24.
Natural organic matter (NOM) can inhibit the photocatalytic degradation of organic micropollutants (OMPs) through inner filter effect, reactive oxygen species (ROS) scavenging, and competitive adsorption. However, previous studies have focused solely on the bulk properties of NOM and our understanding of the inhibition mechanism by NOM fractions during photocatalytic degradation of OMP is still fragmentary. In this study, five well-characterized different NOM samples (i.e., secondary treated wastewater, river water, and three standard NOM surrogates) were used to elucidate the inhibition mechanisms during photocatalytic degradation of carbamazepine (a model OMP) using TiO and its composites with carbon nanotubes (CNT-TiO) under UVC and solar-light irradiation. The results indicated that terrestrially derived NOM with high aromaticity, a low oxygen/carbon atom ratio, and large molecular weight is the major fraction that participates in ROS scavenging, competitive adsorption, and inner filter effect. Furthermore, the modeling analysis suggested that inner filter effect due to NOM and ROS scavenging was the most influential inhibitory mechanism. In the case of secondary treated wastewater, the presence of high concentrations of inorganic species (e.g., PO, Cl, and NO) together with NOM significantly reduced the photocatalytic degradation of carbamazepine. Overall, the methods and the results of this study provide a comprehensive understanding of the effects of NOM fractions on photocatalysis and highlight the need to further consider the interplay between NOM and background inorganic constituents in photocatalytic degradation of OMP.
天然有机物 (NOM) 可以通过内滤效应、活性氧物种 (ROS) 清除和竞争吸附来抑制有机微污染物 (OMP) 的光催化降解。然而,以前的研究仅关注 NOM 的整体性质,我们对 NOM 分数在 OMP 光催化降解过程中的抑制机制的理解仍然很零散。在这项研究中,使用了五种经过充分表征的不同 NOM 样品(即二级处理废水、河水和三种标准 NOM 替代物),以阐明在 UVC 和太阳光照射下使用 TiO 和 CNT-TiO (碳纳米管修饰的 TiO)光催化降解卡马西平(一种 OMP 模型)过程中的抑制机制。结果表明,具有高芳香度、低氧/碳原子比和大分子量的陆源 NOM 是参与 ROS 清除、竞争吸附和内滤效应的主要成分。此外,建模分析表明,由于 NOM 和 ROS 清除导致的内滤效应是最具影响力的抑制机制。在二级处理废水中,高浓度的无机物质(如 PO、Cl 和 NO)与 NOM 一起存在,会显著降低卡马西平的光催化降解。总的来说,本研究的方法和结果提供了对 NOM 分数对光催化影响的全面理解,并强调需要进一步考虑 NOM 和背景无机成分在 OMP 光催化降解过程中的相互作用。