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Frontiers of Environmental Science & Engineering

ISSN 2095-2201

ISSN 2095-221X(Online)

CN 10-1013/X

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2018 Impact Factor: 3.883

Front. Environ. Sci. Eng.    2023, Vol. 17 Issue (6) : 69    https://doi.org/10.1007/s11783-023-1669-1
Photosensitivity sources of dissolved organic matter from wastewater treatment plants and their mediation effect on 17α-ethinylestradiol photodegradation
Zhicheng Liao1, Bei Li1, Juhong Zhan2(), Huan He1(), Xiaoxia Yang1, Dongxu Zhou1, Guoxi Yu1, Chaochao Lai1, Bin Huang1,3, Xuejun Pan1,3
1. Faculty of Environmental Science and Engineering, Kunming University of Science and Technology, Kunming 650500, China
2. Research Institute for Environmental Innovation (Suzhou), Tsinghua, Suzhou 215163, China
3. Yunnan Provincial Key Laboratory of Carbon Sequestration and Pollution Control in Soils, Kunming 650500, China
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Abstract

● EE2 photodegradation behavior in the presence of four WWTPs’ DOM was explored.

● The 3DOM* played a major role in the EE2 photodegradation mediated by WWTPs’ DOM.

● The A2/O process DOM contained more aromatic and oxygen-containing substances.

● Possible photosensitivity sources of DOM in the A2/O process were proposed.

Dissolved organic matter (DOM) from each treatment process of wastewater treatment plants (WWTPs) contains abundant photosensitive substances, which could significantly affect the photodegradation of 17α-ethinylestradiol (EE2). Nevertheless, information about EE2 photodegradation behavior mediated by DOM from diverse WWTPs and the photosensitivity sources of such DOM are inadequate. This study explored the photodegradation behavior of EE2 mediated by four typical WWTPs’ DOM solutions and investigated the photosensitivity sources of DOM in the anaerobic-anoxic-oxic (A2/O) process. The parallel factor analysis identified three varying fluorescing components of these DOM, tryptophan-like substances or protein-like substances, microbial humus-like substances, and humic-like components. The photodegradation rate constants of EE2 were positively associated with the humification degree of DOM (P < 0.05). The triplet state substances were responsible for the degradation of EE2. DOM extracted from the A2/O process, especially in the secondary treatment process had the fastest EE2 photodegradation rate compared to that of the other three processes. Four types of components (water-soluble organic matter (WSOM), extracellular polymeric substance, humic acid, and fulvic acid) were separated from the A2/O process DOM. WSOM had the highest promotion effect on EE2 photodegradation. Fulvic acid-like components and humic acid-like organic compounds in WSOM were speculated to be important photosensitivity substances that can generate triplet state substances. This research explored the physicochemical properties and photosensitive sources of DOM in WWTPs, and explained the fate of estrogens photodegradation in natural waters.

Keywords Photosensitivity sources      17α-ethinylestradiol      Photodegradation      Dissolved organic matter      Wastewater treatment plants     
Corresponding Author(s): Juhong Zhan,Huan He   
Issue Date: 03 January 2023
 Cite this article:   
Zhicheng Liao,Bei Li,Juhong Zhan, et al. Photosensitivity sources of dissolved organic matter from wastewater treatment plants and their mediation effect on 17α-ethinylestradiol photodegradation[J]. Front. Environ. Sci. Eng., 2023, 17(6): 69.
 URL:  
https://academic.hep.com.cn/fese/EN/10.1007/s11783-023-1669-1
https://academic.hep.com.cn/fese/EN/Y2023/V17/I6/69
Fig.1  Parallel factor analysis and wavelengths loadings (C1–C3) of the three components.
Fig.2  EE2 photodegradation behaviors in (a) SEDOM; (b) AEDOM; (c) DSDOM solutions. Experimental conditions: [DOM] = 5 mg C/L, [EE2] = 0.5 mg/L, pH = 8.0.
Fig.3  Relationships between the photodegradation rate constants of EE2 (kobs) and the values of (a) SUVA254 and (b) α280.
Fig.4  Electron paramagnetic resonance spectra of (a) •OH and (b) 1O2 in 5 mg C/L of DOM solution.
Fig.5  Steady-state concentrations of (a) •OH and (b) 1O2 in different reaction solutions.
WWTPs Treatment process DOM R[•OH] (%) R1 O2 (%) R3 D OM (%)
WW1 OD SEDOM 14.8 18.9 61.7
AEDOM 1.6 19.8 35.0
DSDOM 20.6 18.4 35.5
WW3 3AMBR SEDOM 13.0 30.1 43.0
AEDOM 0.5 22.4 50.8
DSDOM 16.7 20.4 32.5
WW4 ICEAS SEDOM 15.0 24.4 47.0
AEDOM 2.7 21.2 56.5
DSDOM 23.5 16.3 38.3
WW8 A2/O SEDOM 15.5 6.8 40.4
AEDOM 1.5 18.1 61.0
DSDOM 7.4 24.4 40.9
Tab.1  Percentage contributions of PPRI to EE2 photodegradation in diverse DOM solutions
Sample SUVA254 FI α280 E2/E3
Oxi-WDOM 2.8 6.8 23.9 6.4
Ano-WDOM 3.3 7.6 28.1 6.5
Ana-WDOM 2.3 7.7 19.6 6.6
Oxi-EPS 0.3 8.3 3.2 5.5
Ano-EPS 0.6 6.5 6.9 4.0
Ana-EPS 0.5 5.2 5.1 4.6
Oxi-HA 3.9 3.1 31.1 9.1
Ano-HA 4.4 3.2 35.9 7.7
Ana-HA 4.6 3.3 36.4 8.3
Oxi-FA 2.4 4.0 23.3 4.0
Ano-FA 1.0 4.5 9.4 5.7
Ana-FA 1.4 4.2 14.1 4.6
Tab.2  Calculated characteristic indexes of DOM extracted from A2/O process
Fig.6  FTIR spectra of the functional groups in DOM from A2/O process.
Fig.7  First order photodegradation rate constants (kobs) of EE2 in different DOM solutions and different matrixes. Experimental conditions: [DOM] = 5 mg C/L, [FFA] = 40 μmol/L, [SA] = 20 μmol/L, [TBA] = 30 μmol/L, pH = 8.0.
Fig.8  Possible photodegradation pathway of EE2.
A2/O Anaerobic-anoxic-oxic
DOM Dissolved organic matter
3DOM* Triplet state DOM
EDCs Endocrine disrupting chemicals
EE2 17α-ethinylestradiol
EPR Electron paramagnetic resonance
EPS Extracellular polymeric substance
FA Fulvic acid
FFA Furfuryl alcohol
FTIR Fourier transform infrared spectroscopy
HA Humic acid
HPLC High-performance liquid chromatograph
LC-MS Liquid chromatograph mass spectrometer
NOM Natural organic matter
3NOM* Triplet state NOM
1O2 Singlet oxygen
•OH Hydroxyl radicals
PPRIs Photochemically produced reactive intermediates
SA Sorbic acid
TBA Tert-butyl alcohol
•OH Hydroxyl radicals
PPRIs Photochemically produced reactive intermediates
SA Sorbic acid
TBA Tert-butyl alcohol
TOC Total organic carbon
TPA Terephthalic acid
WSOM Water-soluble organic matter
WWTPs Wastewater treatment plants
3D-EEMs Three-dimension excitation emission matrix fluorescence spectroscopy
  
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