Loading…

Structural Modifications to Quaternary Ammonium Polymer Coagulants to Inhibit N‑Nitrosamine Formation

Quaternary ammonium cationic polymers, such as poly­(diallyldimethylammonium chloride) (polyDADMAC) and epichlorohydrin-dimethylamine (Epi-DMA), are commonly used by water utilities to enhance removal of particles and dissolved organic matter (DOM) from raw waters. Unfortunately, chloramination of w...

Full description

Saved in:
Bibliographic Details
Published in:Environmental science & technology 2016-05, Vol.50 (9), p.4778-4787
Main Authors: Zeng, Teng, Li, Russell Jingxian, Mitch, William A
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-a431t-8f8a05492e2dfe424ce2e70702ff45d10af357dcc90fc888e21941400c207eb93
cites cdi_FETCH-LOGICAL-a431t-8f8a05492e2dfe424ce2e70702ff45d10af357dcc90fc888e21941400c207eb93
container_end_page 4787
container_issue 9
container_start_page 4778
container_title Environmental science & technology
container_volume 50
creator Zeng, Teng
Li, Russell Jingxian
Mitch, William A
description Quaternary ammonium cationic polymers, such as poly­(diallyldimethylammonium chloride) (polyDADMAC) and epichlorohydrin-dimethylamine (Epi-DMA), are commonly used by water utilities to enhance removal of particles and dissolved organic matter (DOM) from raw waters. Unfortunately, chloramination of waters treated with quaternary ammonium polymers leads to the formation of carcinogenic N-nitrosodimethylamine (NDMA). In this study, two approaches were developed to modify polyDADMAC and Epi-DMA to inhibit N-nitrosamine formation. The first approach involved treatment of polymers with methyl iodide (MeI), an alkylating agent, to convert polymer-bound tertiary amine groups to less chloramine-reactive quaternary ammonium groups. The second approach involved synthesis of polymers bearing less chloramine-reactive quaternary ammonium groups with dipropylamino (DPA) substituents. Treatment with MeI reduced NDMA formation from polymers by ∼75%, while synthesis of DPA-based polymers eliminated NDMA formation and formed N-nitrosodipropylamine, which is 10-fold less carcinogenic than NDMA, at 20-fold lower yields. Bench-scale jar tests demonstrated that both MeI-treated and DPA-based polymers achieved similar removal of particles and DOM as the original polyDADMAC and Epi-DMA at both low and high doses, but formed significantly less N-nitrosamines. This work demonstrates two approaches for modifying quaternary ammonium cationic polymers, which may enable water utilities to meet potential future regulations on N-nitrosamines while maintaining polymer usage to meet existing regulations.
doi_str_mv 10.1021/acs.est.6b00602
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1808653903</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1808653903</sourcerecordid><originalsourceid>FETCH-LOGICAL-a431t-8f8a05492e2dfe424ce2e70702ff45d10af357dcc90fc888e21941400c207eb93</originalsourceid><addsrcrecordid>eNp1kUtPGzEUhS1UBGlgzQ6N1A1SNeHanoe9RBG0SOGltlJ3I8djU6PxGPxYZMdf6F_sL6lDUpAqsbqb75x77zkIHWGYYSD4VMgwUyHOmiVAA2QHTXBNoKxZjT-gCQCmJafNz330MYQHACAU2B7aJy3wJvMTdP8t-iRj8mIorlxvtJEiGjeGIrriLomo_Cj8qjiz1o0m2eLWDSurfDF34j4NYowv5OX4yyxNLK7_PP--NtG7IKwZVXHhvH3xO0C7WgxBHW7nFP24OP8-_1oubr5czs8WpagojiXTTEBdcaJIr1VFKqmIaqEFonVV9xiEpnXbS8lBS8aYIphXuAKQBFq15HSKTja-j949pRxNZ02QasiXKpdChxmwpqYcaEY__Yc-uJS_HTLVckJ5S3mVqdMNJfNTwSvdPXpjcyQdhm7dQZc76NbqbQdZcbz1TUur-lf-X-gZ-LwB1sq3ne_Y_QXu55Of</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1792397394</pqid></control><display><type>article</type><title>Structural Modifications to Quaternary Ammonium Polymer Coagulants to Inhibit N‑Nitrosamine Formation</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read &amp; Publish Agreement 2022-2024 (Reading list)</source><creator>Zeng, Teng ; Li, Russell Jingxian ; Mitch, William A</creator><creatorcontrib>Zeng, Teng ; Li, Russell Jingxian ; Mitch, William A</creatorcontrib><description>Quaternary ammonium cationic polymers, such as poly­(diallyldimethylammonium chloride) (polyDADMAC) and epichlorohydrin-dimethylamine (Epi-DMA), are commonly used by water utilities to enhance removal of particles and dissolved organic matter (DOM) from raw waters. Unfortunately, chloramination of waters treated with quaternary ammonium polymers leads to the formation of carcinogenic N-nitrosodimethylamine (NDMA). In this study, two approaches were developed to modify polyDADMAC and Epi-DMA to inhibit N-nitrosamine formation. The first approach involved treatment of polymers with methyl iodide (MeI), an alkylating agent, to convert polymer-bound tertiary amine groups to less chloramine-reactive quaternary ammonium groups. The second approach involved synthesis of polymers bearing less chloramine-reactive quaternary ammonium groups with dipropylamino (DPA) substituents. Treatment with MeI reduced NDMA formation from polymers by ∼75%, while synthesis of DPA-based polymers eliminated NDMA formation and formed N-nitrosodipropylamine, which is 10-fold less carcinogenic than NDMA, at 20-fold lower yields. Bench-scale jar tests demonstrated that both MeI-treated and DPA-based polymers achieved similar removal of particles and DOM as the original polyDADMAC and Epi-DMA at both low and high doses, but formed significantly less N-nitrosamines. This work demonstrates two approaches for modifying quaternary ammonium cationic polymers, which may enable water utilities to meet potential future regulations on N-nitrosamines while maintaining polymer usage to meet existing regulations.</description><identifier>ISSN: 0013-936X</identifier><identifier>EISSN: 1520-5851</identifier><identifier>DOI: 10.1021/acs.est.6b00602</identifier><identifier>PMID: 27096602</identifier><identifier>CODEN: ESTHAG</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Ammonia ; Ammonium Compounds ; Carcinogens ; Coagulation ; Dimethylnitrosamine - chemistry ; Nitrosamines - chemistry ; Polymers ; Polymers - chemistry ; Water Purification</subject><ispartof>Environmental science &amp; technology, 2016-05, Vol.50 (9), p.4778-4787</ispartof><rights>Copyright © 2016 American Chemical Society</rights><rights>Copyright American Chemical Society May 3, 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a431t-8f8a05492e2dfe424ce2e70702ff45d10af357dcc90fc888e21941400c207eb93</citedby><cites>FETCH-LOGICAL-a431t-8f8a05492e2dfe424ce2e70702ff45d10af357dcc90fc888e21941400c207eb93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27096602$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zeng, Teng</creatorcontrib><creatorcontrib>Li, Russell Jingxian</creatorcontrib><creatorcontrib>Mitch, William A</creatorcontrib><title>Structural Modifications to Quaternary Ammonium Polymer Coagulants to Inhibit N‑Nitrosamine Formation</title><title>Environmental science &amp; technology</title><addtitle>Environ. Sci. Technol</addtitle><description>Quaternary ammonium cationic polymers, such as poly­(diallyldimethylammonium chloride) (polyDADMAC) and epichlorohydrin-dimethylamine (Epi-DMA), are commonly used by water utilities to enhance removal of particles and dissolved organic matter (DOM) from raw waters. Unfortunately, chloramination of waters treated with quaternary ammonium polymers leads to the formation of carcinogenic N-nitrosodimethylamine (NDMA). In this study, two approaches were developed to modify polyDADMAC and Epi-DMA to inhibit N-nitrosamine formation. The first approach involved treatment of polymers with methyl iodide (MeI), an alkylating agent, to convert polymer-bound tertiary amine groups to less chloramine-reactive quaternary ammonium groups. The second approach involved synthesis of polymers bearing less chloramine-reactive quaternary ammonium groups with dipropylamino (DPA) substituents. Treatment with MeI reduced NDMA formation from polymers by ∼75%, while synthesis of DPA-based polymers eliminated NDMA formation and formed N-nitrosodipropylamine, which is 10-fold less carcinogenic than NDMA, at 20-fold lower yields. Bench-scale jar tests demonstrated that both MeI-treated and DPA-based polymers achieved similar removal of particles and DOM as the original polyDADMAC and Epi-DMA at both low and high doses, but formed significantly less N-nitrosamines. This work demonstrates two approaches for modifying quaternary ammonium cationic polymers, which may enable water utilities to meet potential future regulations on N-nitrosamines while maintaining polymer usage to meet existing regulations.</description><subject>Ammonia</subject><subject>Ammonium Compounds</subject><subject>Carcinogens</subject><subject>Coagulation</subject><subject>Dimethylnitrosamine - chemistry</subject><subject>Nitrosamines - chemistry</subject><subject>Polymers</subject><subject>Polymers - chemistry</subject><subject>Water Purification</subject><issn>0013-936X</issn><issn>1520-5851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp1kUtPGzEUhS1UBGlgzQ6N1A1SNeHanoe9RBG0SOGltlJ3I8djU6PxGPxYZMdf6F_sL6lDUpAqsbqb75x77zkIHWGYYSD4VMgwUyHOmiVAA2QHTXBNoKxZjT-gCQCmJafNz330MYQHACAU2B7aJy3wJvMTdP8t-iRj8mIorlxvtJEiGjeGIrriLomo_Cj8qjiz1o0m2eLWDSurfDF34j4NYowv5OX4yyxNLK7_PP--NtG7IKwZVXHhvH3xO0C7WgxBHW7nFP24OP8-_1oubr5czs8WpagojiXTTEBdcaJIr1VFKqmIaqEFonVV9xiEpnXbS8lBS8aYIphXuAKQBFq15HSKTja-j949pRxNZ02QasiXKpdChxmwpqYcaEY__Yc-uJS_HTLVckJ5S3mVqdMNJfNTwSvdPXpjcyQdhm7dQZc76NbqbQdZcbz1TUur-lf-X-gZ-LwB1sq3ne_Y_QXu55Of</recordid><startdate>20160503</startdate><enddate>20160503</enddate><creator>Zeng, Teng</creator><creator>Li, Russell Jingxian</creator><creator>Mitch, William A</creator><general>American Chemical Society</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>7QO</scope><scope>7ST</scope><scope>7T7</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>SOI</scope></search><sort><creationdate>20160503</creationdate><title>Structural Modifications to Quaternary Ammonium Polymer Coagulants to Inhibit N‑Nitrosamine Formation</title><author>Zeng, Teng ; Li, Russell Jingxian ; Mitch, William A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a431t-8f8a05492e2dfe424ce2e70702ff45d10af357dcc90fc888e21941400c207eb93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Ammonia</topic><topic>Ammonium Compounds</topic><topic>Carcinogens</topic><topic>Coagulation</topic><topic>Dimethylnitrosamine - chemistry</topic><topic>Nitrosamines - chemistry</topic><topic>Polymers</topic><topic>Polymers - chemistry</topic><topic>Water Purification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zeng, Teng</creatorcontrib><creatorcontrib>Li, Russell Jingxian</creatorcontrib><creatorcontrib>Mitch, William A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><jtitle>Environmental science &amp; technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zeng, Teng</au><au>Li, Russell Jingxian</au><au>Mitch, William A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural Modifications to Quaternary Ammonium Polymer Coagulants to Inhibit N‑Nitrosamine Formation</atitle><jtitle>Environmental science &amp; technology</jtitle><addtitle>Environ. Sci. Technol</addtitle><date>2016-05-03</date><risdate>2016</risdate><volume>50</volume><issue>9</issue><spage>4778</spage><epage>4787</epage><pages>4778-4787</pages><issn>0013-936X</issn><eissn>1520-5851</eissn><coden>ESTHAG</coden><abstract>Quaternary ammonium cationic polymers, such as poly­(diallyldimethylammonium chloride) (polyDADMAC) and epichlorohydrin-dimethylamine (Epi-DMA), are commonly used by water utilities to enhance removal of particles and dissolved organic matter (DOM) from raw waters. Unfortunately, chloramination of waters treated with quaternary ammonium polymers leads to the formation of carcinogenic N-nitrosodimethylamine (NDMA). In this study, two approaches were developed to modify polyDADMAC and Epi-DMA to inhibit N-nitrosamine formation. The first approach involved treatment of polymers with methyl iodide (MeI), an alkylating agent, to convert polymer-bound tertiary amine groups to less chloramine-reactive quaternary ammonium groups. The second approach involved synthesis of polymers bearing less chloramine-reactive quaternary ammonium groups with dipropylamino (DPA) substituents. Treatment with MeI reduced NDMA formation from polymers by ∼75%, while synthesis of DPA-based polymers eliminated NDMA formation and formed N-nitrosodipropylamine, which is 10-fold less carcinogenic than NDMA, at 20-fold lower yields. Bench-scale jar tests demonstrated that both MeI-treated and DPA-based polymers achieved similar removal of particles and DOM as the original polyDADMAC and Epi-DMA at both low and high doses, but formed significantly less N-nitrosamines. This work demonstrates two approaches for modifying quaternary ammonium cationic polymers, which may enable water utilities to meet potential future regulations on N-nitrosamines while maintaining polymer usage to meet existing regulations.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>27096602</pmid><doi>10.1021/acs.est.6b00602</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0013-936X
ispartof Environmental science & technology, 2016-05, Vol.50 (9), p.4778-4787
issn 0013-936X
1520-5851
language eng
recordid cdi_proquest_miscellaneous_1808653903
source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
subjects Ammonia
Ammonium Compounds
Carcinogens
Coagulation
Dimethylnitrosamine - chemistry
Nitrosamines - chemistry
Polymers
Polymers - chemistry
Water Purification
title Structural Modifications to Quaternary Ammonium Polymer Coagulants to Inhibit N‑Nitrosamine Formation
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T00%3A54%3A41IST&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=Structural%20Modifications%20to%20Quaternary%20Ammonium%20Polymer%20Coagulants%20to%20Inhibit%20N%E2%80%91Nitrosamine%20Formation&rft.jtitle=Environmental%20science%20&%20technology&rft.au=Zeng,%20Teng&rft.date=2016-05-03&rft.volume=50&rft.issue=9&rft.spage=4778&rft.epage=4787&rft.pages=4778-4787&rft.issn=0013-936X&rft.eissn=1520-5851&rft.coden=ESTHAG&rft_id=info:doi/10.1021/acs.est.6b00602&rft_dat=%3Cproquest_cross%3E1808653903%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a431t-8f8a05492e2dfe424ce2e70702ff45d10af357dcc90fc888e21941400c207eb93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1792397394&rft_id=info:pmid/27096602&rfr_iscdi=true