Influence of organic matter on the photocatalytic degradation of steroid hormones by TiO2-coated polyethersulfone microfiltration membrane

被引:16
作者
Liu, Siqi [1 ]
Edara, Pattabhiramayya C. [1 ]
Schaefer, Andrea I. [1 ]
机构
[1] Karlsruhe Inst Technol KIT, Inst Adv Membrane Technol IAMT, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
关键词
Micropollutant; Natural organic matter; photocatalytic membrane reactor; photosensitizer; time-resolved fluorescence; physico-chemical water treatment; HUMIC-ACID; TIO2; PHOTOCATALYSIS; ADVANCED OXIDATION; SINGLET OXYGEN; ENVIRONMENTAL PHOTOCHEMISTRY; REMOVAL MECHANISMS; ELECTRON-TRANSFER; WATER; NANOFILTRATION; PHOTODEGRADATION;
D O I
10.1016/j.watres.2023.120438
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
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 beta-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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页数:13
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