Loading…

Transformation of bisphenol A in water distribution systems: A pilot-scale study

[Display omitted] •The halogenations of BPA in a pilot-scale water distribution systems was studied.•The chlorinated mechanism of BPA in water distribution systems was proposed.•THMs and HAA formation in BPA chlorinated in water distribution systems were found. Halogenations of bisphenol A (BPA) in...

Full description

Saved in:
Bibliographic Details
Published in:Chemosphere (Oxford) 2015-04, Vol.125, p.86-93
Main Authors: Li, Cong, Wang, Zilong, Yang, Y. Jeffrey, Liu, Jingqing, Mao, Xinwei, Zhang, Yan
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c480t-271d3df2a0cde262f3ff75a68ca51dc734ddf85cf13d596c3d98a68d67d5f9213
cites cdi_FETCH-LOGICAL-c480t-271d3df2a0cde262f3ff75a68ca51dc734ddf85cf13d596c3d98a68d67d5f9213
container_end_page 93
container_issue
container_start_page 86
container_title Chemosphere (Oxford)
container_volume 125
creator Li, Cong
Wang, Zilong
Yang, Y. Jeffrey
Liu, Jingqing
Mao, Xinwei
Zhang, Yan
description [Display omitted] •The halogenations of BPA in a pilot-scale water distribution systems was studied.•The chlorinated mechanism of BPA in water distribution systems was proposed.•THMs and HAA formation in BPA chlorinated in water distribution systems were found. Halogenations of bisphenol A (BPA) in a pilot-scale water distribution system (WDS) of a cement-lined ductile cast iron pipe were investigated. The water in the pilot-scale WDS was chlorinated with a free chlorine concentration of 0.7mgL−1 using sodium hypochlorite, and with an initial BPA concentration of 100μgL−1 was spiked in the WDS. Halogenated compounds in the BPA experiments were identified using EI/GC/MS and GC. Several BPA congeners, including 2-chlorobisphenol A (MCBPA), dichlorobisphenol A (D2-CBPA), 2,2′,6-trichlorobisphenol A (T3CBPA), 2,2′,6,6′-tetrachlorobisphenol A (T4CBPA), 2-bromobisphenol A (MBBPA), and bromochlorobisphenol A (MBMCBPA) were found. Moreover, further halogenation yielded other reaction intermediates, including 2,4,6-trichlorophenol (T3CP), dichlorobisphenol A, bromodichlorophenol, and dibromochlorophenol. After halogenation for 120min, most of the abovementioned reaction intermediates disappeared and were replaced by trihalomethanes (THMs). Based on these experimental findings, the halogenation process of BPA oxidation in a WDS includes three stages: (1) halogenation on the aromatic ring; (2) chlorine or bromine substitution followed by cleavage of the α-C bond on the isopropyl moiety with a positive partial charge and a β′-C bond on the benzene moiety with a negative partial charge; and (3) THMs and a minor HAA formation from phenolic intermediates through the benzene ring opening with a chlorine and bromine substitution of the hydrogen on the carbon atoms. The oxidation mechanisms of the entire transformation from BPA to THM/HAA in the WDS were proposed.
doi_str_mv 10.1016/j.chemosphere.2014.11.047
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1770313825</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0045653514013708</els_id><sourcerecordid>1770313825</sourcerecordid><originalsourceid>FETCH-LOGICAL-c480t-271d3df2a0cde262f3ff75a68ca51dc734ddf85cf13d596c3d98a68d67d5f9213</originalsourceid><addsrcrecordid>eNqNkE1v1DAURS0EokPLX0BhxybBz47jhF014kuq1C7K2vLYz6pHSTz4OaD592Q6BbGD1Vu8c--VDmNvgTfAoXu_b9wDTokOD5ixERzaBqDhrX7GNtDroQYx9M_ZhvNW1Z2S6oK9ItpzvobV8JJdCKUUBxAbdnef7Uwh5cmWmOYqhWoXT8VzGqvrKs7VT1swVz5SyXG3PEJ0pIITfViBQxxTqcnZESsqiz9esRfBjoSvn-4l-_bp4_32S31z-_nr9vqmdm3PSy00eOmDsNx5FJ0IMgStbNc7q8A7LVvvQ69cAOnV0Dnph379-k57FQYB8pK9O_cecvq-IBUzRXI4jnbGtJABrbkE2Qv1b7TreAut0npFhzPqciLKGMwhx8nmowFuTu7N3vzl3pzcGwCzul-zb55mlt2E_k_yt-wV2J4BXL38iJgNuYizQx8zumJ8iv8x8wu2eJwF</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1660414577</pqid></control><display><type>article</type><title>Transformation of bisphenol A in water distribution systems: A pilot-scale study</title><source>ScienceDirect Freedom Collection</source><creator>Li, Cong ; Wang, Zilong ; Yang, Y. Jeffrey ; Liu, Jingqing ; Mao, Xinwei ; Zhang, Yan</creator><creatorcontrib>Li, Cong ; Wang, Zilong ; Yang, Y. Jeffrey ; Liu, Jingqing ; Mao, Xinwei ; Zhang, Yan</creatorcontrib><description>[Display omitted] •The halogenations of BPA in a pilot-scale water distribution systems was studied.•The chlorinated mechanism of BPA in water distribution systems was proposed.•THMs and HAA formation in BPA chlorinated in water distribution systems were found. Halogenations of bisphenol A (BPA) in a pilot-scale water distribution system (WDS) of a cement-lined ductile cast iron pipe were investigated. The water in the pilot-scale WDS was chlorinated with a free chlorine concentration of 0.7mgL−1 using sodium hypochlorite, and with an initial BPA concentration of 100μgL−1 was spiked in the WDS. Halogenated compounds in the BPA experiments were identified using EI/GC/MS and GC. Several BPA congeners, including 2-chlorobisphenol A (MCBPA), dichlorobisphenol A (D2-CBPA), 2,2′,6-trichlorobisphenol A (T3CBPA), 2,2′,6,6′-tetrachlorobisphenol A (T4CBPA), 2-bromobisphenol A (MBBPA), and bromochlorobisphenol A (MBMCBPA) were found. Moreover, further halogenation yielded other reaction intermediates, including 2,4,6-trichlorophenol (T3CP), dichlorobisphenol A, bromodichlorophenol, and dibromochlorophenol. After halogenation for 120min, most of the abovementioned reaction intermediates disappeared and were replaced by trihalomethanes (THMs). Based on these experimental findings, the halogenation process of BPA oxidation in a WDS includes three stages: (1) halogenation on the aromatic ring; (2) chlorine or bromine substitution followed by cleavage of the α-C bond on the isopropyl moiety with a positive partial charge and a β′-C bond on the benzene moiety with a negative partial charge; and (3) THMs and a minor HAA formation from phenolic intermediates through the benzene ring opening with a chlorine and bromine substitution of the hydrogen on the carbon atoms. The oxidation mechanisms of the entire transformation from BPA to THM/HAA in the WDS were proposed.</description><identifier>ISSN: 0045-6535</identifier><identifier>EISSN: 1879-1298</identifier><identifier>DOI: 10.1016/j.chemosphere.2014.11.047</identifier><identifier>PMID: 25550112</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Benzhydryl Compounds - chemistry ; Bisphenol A ; Bromine ; Bromine - chemistry ; Charge ; Chlorine ; Chlorine - chemistry ; Chlorophenols - analysis ; Gas Chromatography-Mass Spectrometry ; Halogenation ; Halogenations ; Mechanism ; Oxidation ; Phenols - chemistry ; Pilot Projects ; Sodium Hypochlorite - chemistry ; Transformations ; Trihalomethanes - analysis ; Water distribution ; Water distribution system ; Water Pollutants, Chemical - analysis ; Water Purification - methods ; Water Supply - analysis</subject><ispartof>Chemosphere (Oxford), 2015-04, Vol.125, p.86-93</ispartof><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c480t-271d3df2a0cde262f3ff75a68ca51dc734ddf85cf13d596c3d98a68d67d5f9213</citedby><cites>FETCH-LOGICAL-c480t-271d3df2a0cde262f3ff75a68ca51dc734ddf85cf13d596c3d98a68d67d5f9213</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25550112$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Cong</creatorcontrib><creatorcontrib>Wang, Zilong</creatorcontrib><creatorcontrib>Yang, Y. Jeffrey</creatorcontrib><creatorcontrib>Liu, Jingqing</creatorcontrib><creatorcontrib>Mao, Xinwei</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><title>Transformation of bisphenol A in water distribution systems: A pilot-scale study</title><title>Chemosphere (Oxford)</title><addtitle>Chemosphere</addtitle><description>[Display omitted] •The halogenations of BPA in a pilot-scale water distribution systems was studied.•The chlorinated mechanism of BPA in water distribution systems was proposed.•THMs and HAA formation in BPA chlorinated in water distribution systems were found. Halogenations of bisphenol A (BPA) in a pilot-scale water distribution system (WDS) of a cement-lined ductile cast iron pipe were investigated. The water in the pilot-scale WDS was chlorinated with a free chlorine concentration of 0.7mgL−1 using sodium hypochlorite, and with an initial BPA concentration of 100μgL−1 was spiked in the WDS. Halogenated compounds in the BPA experiments were identified using EI/GC/MS and GC. Several BPA congeners, including 2-chlorobisphenol A (MCBPA), dichlorobisphenol A (D2-CBPA), 2,2′,6-trichlorobisphenol A (T3CBPA), 2,2′,6,6′-tetrachlorobisphenol A (T4CBPA), 2-bromobisphenol A (MBBPA), and bromochlorobisphenol A (MBMCBPA) were found. Moreover, further halogenation yielded other reaction intermediates, including 2,4,6-trichlorophenol (T3CP), dichlorobisphenol A, bromodichlorophenol, and dibromochlorophenol. After halogenation for 120min, most of the abovementioned reaction intermediates disappeared and were replaced by trihalomethanes (THMs). Based on these experimental findings, the halogenation process of BPA oxidation in a WDS includes three stages: (1) halogenation on the aromatic ring; (2) chlorine or bromine substitution followed by cleavage of the α-C bond on the isopropyl moiety with a positive partial charge and a β′-C bond on the benzene moiety with a negative partial charge; and (3) THMs and a minor HAA formation from phenolic intermediates through the benzene ring opening with a chlorine and bromine substitution of the hydrogen on the carbon atoms. The oxidation mechanisms of the entire transformation from BPA to THM/HAA in the WDS were proposed.</description><subject>Benzhydryl Compounds - chemistry</subject><subject>Bisphenol A</subject><subject>Bromine</subject><subject>Bromine - chemistry</subject><subject>Charge</subject><subject>Chlorine</subject><subject>Chlorine - chemistry</subject><subject>Chlorophenols - analysis</subject><subject>Gas Chromatography-Mass Spectrometry</subject><subject>Halogenation</subject><subject>Halogenations</subject><subject>Mechanism</subject><subject>Oxidation</subject><subject>Phenols - chemistry</subject><subject>Pilot Projects</subject><subject>Sodium Hypochlorite - chemistry</subject><subject>Transformations</subject><subject>Trihalomethanes - analysis</subject><subject>Water distribution</subject><subject>Water distribution system</subject><subject>Water Pollutants, Chemical - analysis</subject><subject>Water Purification - methods</subject><subject>Water Supply - analysis</subject><issn>0045-6535</issn><issn>1879-1298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqNkE1v1DAURS0EokPLX0BhxybBz47jhF014kuq1C7K2vLYz6pHSTz4OaD592Q6BbGD1Vu8c--VDmNvgTfAoXu_b9wDTokOD5ixERzaBqDhrX7GNtDroQYx9M_ZhvNW1Z2S6oK9ItpzvobV8JJdCKUUBxAbdnef7Uwh5cmWmOYqhWoXT8VzGqvrKs7VT1swVz5SyXG3PEJ0pIITfViBQxxTqcnZESsqiz9esRfBjoSvn-4l-_bp4_32S31z-_nr9vqmdm3PSy00eOmDsNx5FJ0IMgStbNc7q8A7LVvvQ69cAOnV0Dnph379-k57FQYB8pK9O_cecvq-IBUzRXI4jnbGtJABrbkE2Qv1b7TreAut0npFhzPqciLKGMwhx8nmowFuTu7N3vzl3pzcGwCzul-zb55mlt2E_k_yt-wV2J4BXL38iJgNuYizQx8zumJ8iv8x8wu2eJwF</recordid><startdate>20150401</startdate><enddate>20150401</enddate><creator>Li, Cong</creator><creator>Wang, Zilong</creator><creator>Yang, Y. Jeffrey</creator><creator>Liu, Jingqing</creator><creator>Mao, Xinwei</creator><creator>Zhang, Yan</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>KR7</scope></search><sort><creationdate>20150401</creationdate><title>Transformation of bisphenol A in water distribution systems: A pilot-scale study</title><author>Li, Cong ; Wang, Zilong ; Yang, Y. Jeffrey ; Liu, Jingqing ; Mao, Xinwei ; Zhang, Yan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c480t-271d3df2a0cde262f3ff75a68ca51dc734ddf85cf13d596c3d98a68d67d5f9213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Benzhydryl Compounds - chemistry</topic><topic>Bisphenol A</topic><topic>Bromine</topic><topic>Bromine - chemistry</topic><topic>Charge</topic><topic>Chlorine</topic><topic>Chlorine - chemistry</topic><topic>Chlorophenols - analysis</topic><topic>Gas Chromatography-Mass Spectrometry</topic><topic>Halogenation</topic><topic>Halogenations</topic><topic>Mechanism</topic><topic>Oxidation</topic><topic>Phenols - chemistry</topic><topic>Pilot Projects</topic><topic>Sodium Hypochlorite - chemistry</topic><topic>Transformations</topic><topic>Trihalomethanes - analysis</topic><topic>Water distribution</topic><topic>Water distribution system</topic><topic>Water Pollutants, Chemical - analysis</topic><topic>Water Purification - methods</topic><topic>Water Supply - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Cong</creatorcontrib><creatorcontrib>Wang, Zilong</creatorcontrib><creatorcontrib>Yang, Y. Jeffrey</creatorcontrib><creatorcontrib>Liu, Jingqing</creatorcontrib><creatorcontrib>Mao, Xinwei</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Civil Engineering Abstracts</collection><jtitle>Chemosphere (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Cong</au><au>Wang, Zilong</au><au>Yang, Y. Jeffrey</au><au>Liu, Jingqing</au><au>Mao, Xinwei</au><au>Zhang, Yan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transformation of bisphenol A in water distribution systems: A pilot-scale study</atitle><jtitle>Chemosphere (Oxford)</jtitle><addtitle>Chemosphere</addtitle><date>2015-04-01</date><risdate>2015</risdate><volume>125</volume><spage>86</spage><epage>93</epage><pages>86-93</pages><issn>0045-6535</issn><eissn>1879-1298</eissn><abstract>[Display omitted] •The halogenations of BPA in a pilot-scale water distribution systems was studied.•The chlorinated mechanism of BPA in water distribution systems was proposed.•THMs and HAA formation in BPA chlorinated in water distribution systems were found. Halogenations of bisphenol A (BPA) in a pilot-scale water distribution system (WDS) of a cement-lined ductile cast iron pipe were investigated. The water in the pilot-scale WDS was chlorinated with a free chlorine concentration of 0.7mgL−1 using sodium hypochlorite, and with an initial BPA concentration of 100μgL−1 was spiked in the WDS. Halogenated compounds in the BPA experiments were identified using EI/GC/MS and GC. Several BPA congeners, including 2-chlorobisphenol A (MCBPA), dichlorobisphenol A (D2-CBPA), 2,2′,6-trichlorobisphenol A (T3CBPA), 2,2′,6,6′-tetrachlorobisphenol A (T4CBPA), 2-bromobisphenol A (MBBPA), and bromochlorobisphenol A (MBMCBPA) were found. Moreover, further halogenation yielded other reaction intermediates, including 2,4,6-trichlorophenol (T3CP), dichlorobisphenol A, bromodichlorophenol, and dibromochlorophenol. After halogenation for 120min, most of the abovementioned reaction intermediates disappeared and were replaced by trihalomethanes (THMs). Based on these experimental findings, the halogenation process of BPA oxidation in a WDS includes three stages: (1) halogenation on the aromatic ring; (2) chlorine or bromine substitution followed by cleavage of the α-C bond on the isopropyl moiety with a positive partial charge and a β′-C bond on the benzene moiety with a negative partial charge; and (3) THMs and a minor HAA formation from phenolic intermediates through the benzene ring opening with a chlorine and bromine substitution of the hydrogen on the carbon atoms. The oxidation mechanisms of the entire transformation from BPA to THM/HAA in the WDS were proposed.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>25550112</pmid><doi>10.1016/j.chemosphere.2014.11.047</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0045-6535
ispartof Chemosphere (Oxford), 2015-04, Vol.125, p.86-93
issn 0045-6535
1879-1298
language eng
recordid cdi_proquest_miscellaneous_1770313825
source ScienceDirect Freedom Collection
subjects Benzhydryl Compounds - chemistry
Bisphenol A
Bromine
Bromine - chemistry
Charge
Chlorine
Chlorine - chemistry
Chlorophenols - analysis
Gas Chromatography-Mass Spectrometry
Halogenation
Halogenations
Mechanism
Oxidation
Phenols - chemistry
Pilot Projects
Sodium Hypochlorite - chemistry
Transformations
Trihalomethanes - analysis
Water distribution
Water distribution system
Water Pollutants, Chemical - analysis
Water Purification - methods
Water Supply - analysis
title Transformation of bisphenol A in water distribution systems: A pilot-scale study
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T04%3A10%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Transformation%20of%20bisphenol%20A%20in%20water%20distribution%20systems:%20A%20pilot-scale%20study&rft.jtitle=Chemosphere%20(Oxford)&rft.au=Li,%20Cong&rft.date=2015-04-01&rft.volume=125&rft.spage=86&rft.epage=93&rft.pages=86-93&rft.issn=0045-6535&rft.eissn=1879-1298&rft_id=info:doi/10.1016/j.chemosphere.2014.11.047&rft_dat=%3Cproquest_cross%3E1770313825%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c480t-271d3df2a0cde262f3ff75a68ca51dc734ddf85cf13d596c3d98a68d67d5f9213%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1660414577&rft_id=info:pmid/25550112&rfr_iscdi=true