Effect of resin charged functional group, porosity, and chemical matrix on the long-term pharmaceutical removal mechanism by conventional ion exchange resins

This study attempted to clarify the long-term pharmaceutical removal mechanism from sewage treatment plant effluent during the cyclical adsorption-regeneration operation of 5 commercial resin-based fixed-bed reactors with the simultaneous occurrence of electrostatic interactions and complex non-elec...

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Veröffentlicht in:Chemosphere (Oxford) 2016-10, Vol.160, p.71-79
Hauptverfasser: Wang, Wei, Li, Xiaofeng, Yuan, Shengliu, Sun, Jian, Zheng, Shaokui
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Li, Xiaofeng
Yuan, Shengliu
Sun, Jian
Zheng, Shaokui
description This study attempted to clarify the long-term pharmaceutical removal mechanism from sewage treatment plant effluent during the cyclical adsorption-regeneration operation of 5 commercial resin-based fixed-bed reactors with the simultaneous occurrence of electrostatic interactions and complex non-electrostatic interactions. It examined 12 pharmaceuticals belonging to 10 therapeutic classes with different predominant existing forms and hydrophobicities. Furthermore, the effect of the resin charged functional group (strong-base vs. strong-acid vs. non-ionic), porosity (macroporous vs. gel), and chemical matrix (polystyrenic vs. polyacrylic) on the mechanism was investigated to optimize resin properties and achieve higher pharmaceutical removal. The results reported herein indicate the importance of non-electrostatic interactions between pharmaceuticals and the resin backbone during short-term cyclical operation (i.e., the 1st adsorption-regeneration cycle). With the development of cyclical operation, however, non-electrostatic interaction-induced pharmaceutical removal generally decreased and even disappeared when equilibrium was achieved between the influent and the resin. Despite pharmaceutical therapeutic class or hydrophilicity, anion (or cation) exchange resin preferentially removed those pharmaceuticals that were predominantly present as organic anions (or cations) by ion exchange process during long-term cyclical operation (i.e., ≥6 adsorption-regeneration cycles). Besides pharmaceuticals predominantly present as undissociated molecules, some amphoteric pharmaceuticals containing large amounts of zwitterions were also difficult to remove by ion exchange resin. Additionally, neither resin porosity nor chemical matrix had any significant effect on the long-term pharmaceutical removal mechanism. [Display omitted] •Twelve pharmaceuticals (10 classes, varied existing forms and hydrophobicities) were included.•The long-term removal pharmaceutical mechanism by 5 resins during 8 cycles was clarified.•Complex non-electrostatic interactions and electrostatic interactions simultaneously occurred.•Non-electrostatic interactions resulted in differences in short- and long-term mechanisms.•Resin porosity and chemical matrix had insignificant effect on long-term removal mechanism.
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Despite pharmaceutical therapeutic class or hydrophilicity, anion (or cation) exchange resin preferentially removed those pharmaceuticals that were predominantly present as organic anions (or cations) by ion exchange process during long-term cyclical operation (i.e., ≥6 adsorption-regeneration cycles). Besides pharmaceuticals predominantly present as undissociated molecules, some amphoteric pharmaceuticals containing large amounts of zwitterions were also difficult to remove by ion exchange resin. Additionally, neither resin porosity nor chemical matrix had any significant effect on the long-term pharmaceutical removal mechanism. [Display omitted] •Twelve pharmaceuticals (10 classes, varied existing forms and hydrophobicities) were included.•The long-term removal pharmaceutical mechanism by 5 resins during 8 cycles was clarified.•Complex non-electrostatic interactions and electrostatic interactions simultaneously occurred.•Non-electrostatic interactions resulted in differences in short- and long-term mechanisms.•Resin porosity and chemical matrix had insignificant effect on long-term removal mechanism.</description><identifier>ISSN: 0045-6535</identifier><identifier>EISSN: 1879-1298</identifier><identifier>DOI: 10.1016/j.chemosphere.2016.06.073</identifier><identifier>PMID: 27367175</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adsorption ; Fixed-bed column ; Ion Exchange ; Ion exchange resin ; Ion Exchange Resins - chemistry ; Long-term removal mechanism ; Non-electrostatic interaction ; Pharmaceutical Preparations - chemistry ; Pharmaceuticals ; Porosity ; Static Electricity ; Water Pollutants, Chemical - chemistry ; Water Purification - methods</subject><ispartof>Chemosphere (Oxford), 2016-10, Vol.160, p.71-79</ispartof><rights>2016 Elsevier Ltd</rights><rights>Copyright © 2016 Elsevier Ltd. 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Despite pharmaceutical therapeutic class or hydrophilicity, anion (or cation) exchange resin preferentially removed those pharmaceuticals that were predominantly present as organic anions (or cations) by ion exchange process during long-term cyclical operation (i.e., ≥6 adsorption-regeneration cycles). Besides pharmaceuticals predominantly present as undissociated molecules, some amphoteric pharmaceuticals containing large amounts of zwitterions were also difficult to remove by ion exchange resin. Additionally, neither resin porosity nor chemical matrix had any significant effect on the long-term pharmaceutical removal mechanism. [Display omitted] •Twelve pharmaceuticals (10 classes, varied existing forms and hydrophobicities) were included.•The long-term removal pharmaceutical mechanism by 5 resins during 8 cycles was clarified.•Complex non-electrostatic interactions and electrostatic interactions simultaneously occurred.•Non-electrostatic interactions resulted in differences in short- and long-term mechanisms.•Resin porosity and chemical matrix had insignificant effect on long-term removal mechanism.</description><subject>Adsorption</subject><subject>Fixed-bed column</subject><subject>Ion Exchange</subject><subject>Ion exchange resin</subject><subject>Ion Exchange Resins - chemistry</subject><subject>Long-term removal mechanism</subject><subject>Non-electrostatic interaction</subject><subject>Pharmaceutical Preparations - chemistry</subject><subject>Pharmaceuticals</subject><subject>Porosity</subject><subject>Static Electricity</subject><subject>Water Pollutants, Chemical - chemistry</subject><subject>Water Purification - methods</subject><issn>0045-6535</issn><issn>1879-1298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc-O0zAQxi0EYsvCKyBz47ApthPHyRFVyx9pJS5wthx73LpK7GA71fZheFccWhDHlUa2NPOb-UbzIfSOki0ltP1w3OoDTCHNB4iwZSW1JSVE_QxtaCf6irK-e442hDS8annNb9CrlI6EFJL3L9ENE3UrqOAb9OveWtAZB4sjJOexPqi4B4Pt4nV2wasR72NY5js8hxiSy-c7rLzB6wZOl-qkcnSPOHicD4DH4PdVhjjhuQyalIYl_8FiWfi04lAUvEsTHs5YB38Cf5UpL4bHtbqHyzLpNXph1ZjgzfW_RT8-3X_ffakevn3-uvv4UOmGklxZDb1luuvBmqa2zLbMUDC9GphSltVGw0BMO-jaDqCA1bpnjeq44ZwCb0x9i95f5s4x_FwgZTm5pGEclYewJEk70rVCdKx5CsqbTrStKGh_QXU5XIpg5RzdpOJZUiJXI-VR_mekXI2UpISoS-_bq8wyTGD-df51rgC7CwDlLicHUSbtwGswLhZDpQnuCTK_AVWMusI</recordid><startdate>201610</startdate><enddate>201610</enddate><creator>Wang, Wei</creator><creator>Li, Xiaofeng</creator><creator>Yuan, Shengliu</creator><creator>Sun, Jian</creator><creator>Zheng, Shaokui</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>7ST</scope><scope>7TV</scope><scope>C1K</scope><scope>SOI</scope></search><sort><creationdate>201610</creationdate><title>Effect of resin charged functional group, porosity, and chemical matrix on the long-term pharmaceutical removal mechanism by conventional ion exchange resins</title><author>Wang, Wei ; 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Despite pharmaceutical therapeutic class or hydrophilicity, anion (or cation) exchange resin preferentially removed those pharmaceuticals that were predominantly present as organic anions (or cations) by ion exchange process during long-term cyclical operation (i.e., ≥6 adsorption-regeneration cycles). Besides pharmaceuticals predominantly present as undissociated molecules, some amphoteric pharmaceuticals containing large amounts of zwitterions were also difficult to remove by ion exchange resin. Additionally, neither resin porosity nor chemical matrix had any significant effect on the long-term pharmaceutical removal mechanism. [Display omitted] •Twelve pharmaceuticals (10 classes, varied existing forms and hydrophobicities) were included.•The long-term removal pharmaceutical mechanism by 5 resins during 8 cycles was clarified.•Complex non-electrostatic interactions and electrostatic interactions simultaneously occurred.•Non-electrostatic interactions resulted in differences in short- and long-term mechanisms.•Resin porosity and chemical matrix had insignificant effect on long-term removal mechanism.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>27367175</pmid><doi>10.1016/j.chemosphere.2016.06.073</doi><tpages>9</tpages></addata></record>
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subjects Adsorption
Fixed-bed column
Ion Exchange
Ion exchange resin
Ion Exchange Resins - chemistry
Long-term removal mechanism
Non-electrostatic interaction
Pharmaceutical Preparations - chemistry
Pharmaceuticals
Porosity
Static Electricity
Water Pollutants, Chemical - chemistry
Water Purification - methods
title Effect of resin charged functional group, porosity, and chemical matrix on the long-term pharmaceutical removal mechanism by conventional ion exchange resins
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