Comparison of monochloramination and chlorination of 1,3-diphenylguandine (DPG): kinetics, transformation products, and cell-based in-vitro testing
As a widely used secondary vulcanization accelerator in the rubber industry, 1,3-diphenylguanidine (DPG) poses risks to human health and the environment. To compare and comprehend the disinfection process of DPG, this work investigates the reaction kinetics, toxicity, and transformation products (TP...
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sg-ntu-dr.10356-1733092024-01-23T08:14:26Z Comparison of monochloramination and chlorination of 1,3-diphenylguandine (DPG): kinetics, transformation products, and cell-based in-vitro testing Ying, Lebing Dos Santos, Marques Mauricius Jia, Shenglan Li, Caixia Lee, Theodora Hui Yian Mensah, Anette Tele Snyder, Shane Allen School of Civil and Environmental Engineering Nanyang Environment and Water Research Institute Engineering::Environmental engineering Monochloramine Chorine As a widely used secondary vulcanization accelerator in the rubber industry, 1,3-diphenylguanidine (DPG) poses risks to human health and the environment. To compare and comprehend the disinfection process of DPG, this work investigates the reaction kinetics, toxicity, and transformation products (TPs) of DPG during chlorination and monochloramination. It has been revealed that the reactivity of monochloramine is significantly slower compared to chlorination of DPG, with the maximum efficiency observed at pH 7 to pH 8. Cytotoxicity assessment using HepG2 and THP-1 cells reveals that cytotoxicity hierarchy is as follows: chlorine TPs > monochloramine TPs > DPG. Moreover, oxidant-to-DPG molar ratios 10 and 20 lead to higher cytotoxicity in both chlorination and monochloramination compared to ratio 5 and 100. Additionally, cell bioenergetics experiments demonstrate that chlorine and monochloramine TPs induce mitochondrial dysfunction and enhance glycolytic function in HepG2 cells. The genotoxic response from p53 signaling further suggested genotoxic effects of certain TPs. Furthermore, analysis of TPs using high-resolution mass spectrometry (HRMS) identifies ten TPs, with chlorination yielding more TPs than monochloramination. Generally, a chlorine or monochloramine molar ratio to DPG of 10-20 results in an increased formation of TPs and heightened cytotoxicity. Notably, higher oxidant molar ratios increased the formation of monoguanidine TPs and DPG hydroxylation during chlorination, whereas monochloramination lead to DPG substitution predominantly generating chlorinated DPG due to weaker oxidation effects. These findings provide valuable information for the appropriate treatment of DPG and disinfection processes in water facilities to mitigate potential risks to human health and the ecosystem. National Research Foundation (NRF) Public Utilities Board (PUB) This research is supported by the National Research Foundation, Singapore, and PUB, Singapore’s National Water Agency under its RIE2025 Urban Solutions and Sustainability (USS) (Water) Centre of Excellence (CoE) Programme. Authors acknowledge and are thankful to Agilent Technologies Inc. for xCELLigence RTCA and Seahorse XFe 96 instrument and support through a research collaboration agreement (RCA-2019-0349). 2024-01-23T08:14:26Z 2024-01-23T08:14:26Z 2024 Journal Article Ying, L., Dos Santos, M. M., Jia, S., Li, C., Lee, T. H. Y., Mensah, A. T. & Snyder, S. A. (2024). Comparison of monochloramination and chlorination of 1,3-diphenylguandine (DPG): kinetics, transformation products, and cell-based in-vitro testing. Science of the Total Environment, 906, 167743-. https://dx.doi.org/10.1016/j.scitotenv.2023.167743 0048-9697 https://hdl.handle.net/10356/173309 10.1016/j.scitotenv.2023.167743 37838050 906 167743 en RCA-2019-0349 Science of the Total Environment © 2023 Elsevier B.V. All rights reserved. |
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Engineering::Environmental engineering Monochloramine Chorine Ying, Lebing Dos Santos, Marques Mauricius Jia, Shenglan Li, Caixia Lee, Theodora Hui Yian Mensah, Anette Tele Snyder, Shane Allen Comparison of monochloramination and chlorination of 1,3-diphenylguandine (DPG): kinetics, transformation products, and cell-based in-vitro testing |
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As a widely used secondary vulcanization accelerator in the rubber industry, 1,3-diphenylguanidine (DPG) poses risks to human health and the environment. To compare and comprehend the disinfection process of DPG, this work investigates the reaction kinetics, toxicity, and transformation products (TPs) of DPG during chlorination and monochloramination. It has been revealed that the reactivity of monochloramine is significantly slower compared to chlorination of DPG, with the maximum efficiency observed at pH 7 to pH 8. Cytotoxicity assessment using HepG2 and THP-1 cells reveals that cytotoxicity hierarchy is as follows: chlorine TPs > monochloramine TPs > DPG. Moreover, oxidant-to-DPG molar ratios 10 and 20 lead to higher cytotoxicity in both chlorination and monochloramination compared to ratio 5 and 100. Additionally, cell bioenergetics experiments demonstrate that chlorine and monochloramine TPs induce mitochondrial dysfunction and enhance glycolytic function in HepG2 cells. The genotoxic response from p53 signaling further suggested genotoxic effects of certain TPs. Furthermore, analysis of TPs using high-resolution mass spectrometry (HRMS) identifies ten TPs, with chlorination yielding more TPs than monochloramination. Generally, a chlorine or monochloramine molar ratio to DPG of 10-20 results in an increased formation of TPs and heightened cytotoxicity. Notably, higher oxidant molar ratios increased the formation of monoguanidine TPs and DPG hydroxylation during chlorination, whereas monochloramination lead to DPG substitution predominantly generating chlorinated DPG due to weaker oxidation effects. These findings provide valuable information for the appropriate treatment of DPG and disinfection processes in water facilities to mitigate potential risks to human health and the ecosystem. |
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School of Civil and Environmental Engineering |
author_facet |
School of Civil and Environmental Engineering Ying, Lebing Dos Santos, Marques Mauricius Jia, Shenglan Li, Caixia Lee, Theodora Hui Yian Mensah, Anette Tele Snyder, Shane Allen |
format |
Article |
author |
Ying, Lebing Dos Santos, Marques Mauricius Jia, Shenglan Li, Caixia Lee, Theodora Hui Yian Mensah, Anette Tele Snyder, Shane Allen |
author_sort |
Ying, Lebing |
title |
Comparison of monochloramination and chlorination of 1,3-diphenylguandine (DPG): kinetics, transformation products, and cell-based in-vitro testing |
title_short |
Comparison of monochloramination and chlorination of 1,3-diphenylguandine (DPG): kinetics, transformation products, and cell-based in-vitro testing |
title_full |
Comparison of monochloramination and chlorination of 1,3-diphenylguandine (DPG): kinetics, transformation products, and cell-based in-vitro testing |
title_fullStr |
Comparison of monochloramination and chlorination of 1,3-diphenylguandine (DPG): kinetics, transformation products, and cell-based in-vitro testing |
title_full_unstemmed |
Comparison of monochloramination and chlorination of 1,3-diphenylguandine (DPG): kinetics, transformation products, and cell-based in-vitro testing |
title_sort |
comparison of monochloramination and chlorination of 1,3-diphenylguandine (dpg): kinetics, transformation products, and cell-based in-vitro testing |
publishDate |
2024 |
url |
https://hdl.handle.net/10356/173309 |
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1789483165884088320 |