化学
腐植酸
光催化
有机质
光敏剂
降级(电信)
膜
二氧化钛
水处理
环境化学
核化学
光化学
化学工程
有机化学
生物化学
环境工程
催化作用
电信
肥料
计算机科学
工程类
作者
Siqi Liu,Pattabhiramayya C. Edara,A.I. Schäfer
出处
期刊:Water Research
[Elsevier]
日期:2023-10-01
卷期号:245: 120438-120438
被引量:6
标识
DOI:10.1016/j.watres.2023.120438
摘要
Water treatment in photocatalytic membrane reactors (PMR) holds great promise for removing micropollutants from aquatic environments. Organic matter (OM) that is present in any water matrix may significantly interfere with the degradation of steroid hormone (SH) micropollutants in PMRs. In this study, the interference of various OM types, humic acid (HA), Australian natural organic matter (AUS), worm farm extract (WF), tannic acid (TA), and gallic acid (GA) with the SH degradation at its environmentally relevant concentration (100 ng/L) in a flow-through PMR equipped with a polyethersulphone-titanium dioxide (PES-TiO2) membrane operated under UV light (365 nm) was investigated. Results of this study showed that OM effects are complex and depend on OM type and concentration. The removal of β-estradiol (E2) was enhanced by HA at its levels below 5 mgC/L while the enhancement was abated at higher HA concentrations. The E2 removal was inhibited by TA, and GA, while no significant interference observed for AUS, and WF. The data demonstrated diverse roles of OM that acts in PMRs as a light screening agent, a photoreactive species scavenger, an adsorption alteration trigger, and a photosensitizer. The time-resolved fluorescence measurement showed that HA, acting as a photosensitizer, promoted the sensitization of TiO2 by absorbing light energy and transferring energy/electron to the TiO2 substrate. This pathway dominated the mechanism of the enhanced E2 degradation by HA. The favorable effect of HA was augmented as increasing the light intensity from 0.5 to 10 mW/cm2 and was weakened at higher light intensities due to the increased scavenging reactions and the limited amount of HA. This work clarifies the underlying mechanism of the OM interference on photocatalytic degradation of E2 by the PES-TiO2 PMR.
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