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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...
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Published in: | Environmental science & technology 2016-05, Vol.50 (9), p.4778-4787 |
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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 |
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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. 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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 & 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 & technology</jtitle><addtitle>Environ. 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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. 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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 |
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