UV/chlorine and chlorination of effluent organic matter fractions: tracing nitrogenous DBPs using FT-ICR mass spectrometry

UV/chlorine process is a promising advanced treatment to eliminate pathogen and remove refractory micropollutants for reclamation of municipal secondary effluent. However, effluent organic matter (EfOM) featuring high organic nitrogen content serves as a potential precursor for nitrogenous disinfect...

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Main Authors: Wang, Yuru, Xiang, Yingying, Dos Santos, Mauricius Marques, Wei, Gaoling, Jiang, Bin, Snyder, Shane, Shang, Chii, Croué, Jean-Philippe
Other Authors: Nanyang Environment and Water Research Institute
Format: Article
Language:English
Published: 2023
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Online Access:https://hdl.handle.net/10356/172050
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spelling sg-ntu-dr.10356-1720502023-11-20T08:20:21Z UV/chlorine and chlorination of effluent organic matter fractions: tracing nitrogenous DBPs using FT-ICR mass spectrometry Wang, Yuru Xiang, Yingying Dos Santos, Mauricius Marques Wei, Gaoling Jiang, Bin Snyder, Shane Shang, Chii Croué, Jean-Philippe Nanyang Environment and Water Research Institute Engineering::Environmental engineering Chlorination Effluent Organic Matter UV/chlorine process is a promising advanced treatment to eliminate pathogen and remove refractory micropollutants for reclamation of municipal secondary effluent. However, effluent organic matter (EfOM) featuring high organic nitrogen content serves as a potential precursor for nitrogenous disinfection byproducts (N-DBPs) of health concern. The molecular-level alteration of a hydrophobic (HPO) EfOM fraction and a transphilic (TPI) EfOM fraction isolated from the same municipal effluent and the formation of N-DBPs in the UV/chlorine were tracked by ultrahigh-resolution mass spectrometry. Compared with chlorination, UV/chlorine induced a significantly greater modification on the molecular composition of EfOM and resulted in formation of unique formulae and chlorinated molecules with higher degree of oxidation, lower aromaticity, and less carbon number due to the involvement of reactive radical species. For both EfOM fractions, UV/chlorine formed more diverse DBPs with higher intensity and Cl-incorporation than chlorination. The TPI fraction of EfOM characterized by higher O/C and N/C ratios generated more N-DBPs with higher intensity clustered in the high O/C region than the HPO fraction of EfOM by both UV/chlorine and chlorination. Totally, 207 and 117 nitrogen-containing chlorinated formulae were recorded after UV/chlorine treatment of TPI and HPO, respectively. Precursor tracking found a greater number of DBPs were originated from raw EfOM through electrophilic substitution pathway rather than chlorine addition. Toxicity bioassays demonstrated that DBPs can trigger oxidative stress-induced DNA damage, while HPO fraction of EfOM dominated the induction of cytotoxicity. However, no correlation could be established between the diversity/abundance of N-DBPs and the level of DNA damage. A total of 22 DBPs with a significant rank correlation with DNA damage were identified, while C8H6O5NCl was found as the N-DBP with the strongest correlation. The potential toxic chlorine-containing formula with the most abundant intensity was assigned to C5HO3Cl3. This study suggests that the character and transformation of EfOM and associated toxicity is critical to evaluate the UV/chlorine process toward practical application. This research was supported by the Fundamental Research Funds for the Central Universities (GK202103145) and Natural Science Basic Research Plan in Shaanxi Province of China (2021JM-192). 2023-11-20T08:10:46Z 2023-11-20T08:10:46Z 2023 Journal Article Wang, Y., Xiang, Y., Dos Santos, M. M., Wei, G., Jiang, B., Snyder, S., Shang, C. & Croué, J. (2023). UV/chlorine and chlorination of effluent organic matter fractions: tracing nitrogenous DBPs using FT-ICR mass spectrometry. Water Research, 231, 119646-. https://dx.doi.org/10.1016/j.watres.2023.119646 0043-1354 https://hdl.handle.net/10356/172050 10.1016/j.watres.2023.119646 36709566 2-s2.0-85147268234 231 119646 en Water Research © 2023 Elsevier Ltd. All rights reserved.
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Environmental engineering
Chlorination
Effluent Organic Matter
spellingShingle Engineering::Environmental engineering
Chlorination
Effluent Organic Matter
Wang, Yuru
Xiang, Yingying
Dos Santos, Mauricius Marques
Wei, Gaoling
Jiang, Bin
Snyder, Shane
Shang, Chii
Croué, Jean-Philippe
UV/chlorine and chlorination of effluent organic matter fractions: tracing nitrogenous DBPs using FT-ICR mass spectrometry
description UV/chlorine process is a promising advanced treatment to eliminate pathogen and remove refractory micropollutants for reclamation of municipal secondary effluent. However, effluent organic matter (EfOM) featuring high organic nitrogen content serves as a potential precursor for nitrogenous disinfection byproducts (N-DBPs) of health concern. The molecular-level alteration of a hydrophobic (HPO) EfOM fraction and a transphilic (TPI) EfOM fraction isolated from the same municipal effluent and the formation of N-DBPs in the UV/chlorine were tracked by ultrahigh-resolution mass spectrometry. Compared with chlorination, UV/chlorine induced a significantly greater modification on the molecular composition of EfOM and resulted in formation of unique formulae and chlorinated molecules with higher degree of oxidation, lower aromaticity, and less carbon number due to the involvement of reactive radical species. For both EfOM fractions, UV/chlorine formed more diverse DBPs with higher intensity and Cl-incorporation than chlorination. The TPI fraction of EfOM characterized by higher O/C and N/C ratios generated more N-DBPs with higher intensity clustered in the high O/C region than the HPO fraction of EfOM by both UV/chlorine and chlorination. Totally, 207 and 117 nitrogen-containing chlorinated formulae were recorded after UV/chlorine treatment of TPI and HPO, respectively. Precursor tracking found a greater number of DBPs were originated from raw EfOM through electrophilic substitution pathway rather than chlorine addition. Toxicity bioassays demonstrated that DBPs can trigger oxidative stress-induced DNA damage, while HPO fraction of EfOM dominated the induction of cytotoxicity. However, no correlation could be established between the diversity/abundance of N-DBPs and the level of DNA damage. A total of 22 DBPs with a significant rank correlation with DNA damage were identified, while C8H6O5NCl was found as the N-DBP with the strongest correlation. The potential toxic chlorine-containing formula with the most abundant intensity was assigned to C5HO3Cl3. This study suggests that the character and transformation of EfOM and associated toxicity is critical to evaluate the UV/chlorine process toward practical application.
author2 Nanyang Environment and Water Research Institute
author_facet Nanyang Environment and Water Research Institute
Wang, Yuru
Xiang, Yingying
Dos Santos, Mauricius Marques
Wei, Gaoling
Jiang, Bin
Snyder, Shane
Shang, Chii
Croué, Jean-Philippe
format Article
author Wang, Yuru
Xiang, Yingying
Dos Santos, Mauricius Marques
Wei, Gaoling
Jiang, Bin
Snyder, Shane
Shang, Chii
Croué, Jean-Philippe
author_sort Wang, Yuru
title UV/chlorine and chlorination of effluent organic matter fractions: tracing nitrogenous DBPs using FT-ICR mass spectrometry
title_short UV/chlorine and chlorination of effluent organic matter fractions: tracing nitrogenous DBPs using FT-ICR mass spectrometry
title_full UV/chlorine and chlorination of effluent organic matter fractions: tracing nitrogenous DBPs using FT-ICR mass spectrometry
title_fullStr UV/chlorine and chlorination of effluent organic matter fractions: tracing nitrogenous DBPs using FT-ICR mass spectrometry
title_full_unstemmed UV/chlorine and chlorination of effluent organic matter fractions: tracing nitrogenous DBPs using FT-ICR mass spectrometry
title_sort uv/chlorine and chlorination of effluent organic matter fractions: tracing nitrogenous dbps using ft-icr mass spectrometry
publishDate 2023
url https://hdl.handle.net/10356/172050
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