Removal of carbamazepine in aqueous solutions through solar photolysis of free available chlorine
Removal of a persistent antiepileptic drug carbamazepine (CBZ) in aqueous solutions was investigated by using solar photolysis combined with free available chlorine (FAC). The combination of chlorination with simulated or natural sunlight markedly enhanced removal of CBZ in 10 mM phosphate buffer so...
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description | Removal of a persistent antiepileptic drug carbamazepine (CBZ) in aqueous solutions was investigated by using solar photolysis combined with free available chlorine (FAC). The combination of chlorination with simulated or natural sunlight markedly enhanced removal of CBZ in 10 mM phosphate buffer solution (pH 7.0) and river water (pH 7.0) compared with sunlight or FAC alone. Further analysis indicated that the observed enhancements in CBZ removal can be attributed to the in situ hydroxyl radical (HO) and ozone (O3) production during FAC photolysis. During 70 min simulated sunlight photolysis combined with FAC treatment, HO reaction contributed to 35.8% removal of CBZ and O3 reaction contributed to 40.6% removal, while only 5.3% of CBZ was removed by HOCl reaction. The oxidation products of CBZ, epoxide CBZ, 10,11-dihydro-10,11-dihydroxy CBZ, 1-(2-benzaldehyde)-4-hydro-(1H,3H)-quinazoline-2-one (BQM), 1-(2-benzaldehyde)-(1H,3H)-quinazoline-2,4-dione (BQD) and 4-aldehyde-9-acridone, were mainly formed from the HO and O3 attack at the double bond on the central heterocyclic ring of CBZ. Formation of these oxidation products did not cause any increase or decrease in toxicity to microbial species tested through Microbial Assay for Toxicity Risk Assessment (MARA). The initial FAC concentration and pH had a major influence on the removal process of CBZ during FAC photolysis, while temperature had a minor effect only. The combination of chlorination with natural sunlight could provide an effective approach for removal of CBZ and other contaminants during water treatment.
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•Chlorination of carbamazepine was dramatically enhanced by sunlight photolysis.•These enhancements can be attributed to the in situ HO and O3 production.•Oxidation products were formed from HO and O3 attack at the double bond of carbamazepine.•Oxidation products did not cause any increase or decrease in toxicity to MARA microbial species.•Initial chlorine dosage and pH had a major influence on the removal processes. |
doi_str_mv | 10.1016/j.watres.2016.05.048 |
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[Display omitted]
•Chlorination of carbamazepine was dramatically enhanced by sunlight photolysis.•These enhancements can be attributed to the in situ HO and O3 production.•Oxidation products were formed from HO and O3 attack at the double bond of carbamazepine.•Oxidation products did not cause any increase or decrease in toxicity to MARA microbial species.•Initial chlorine dosage and pH had a major influence on the removal processes.</description><identifier>ISSN: 0043-1354</identifier><identifier>EISSN: 1879-2448</identifier><identifier>DOI: 10.1016/j.watres.2016.05.048</identifier><identifier>PMID: 27232985</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Carbamazepine ; Carbamazepine - chemistry ; Chlorination ; Chlorine ; Free available chlorine ; Microorganisms ; Oxidation ; Photolysis ; Simulation ; Sunlight ; Toxicity ; Water Pollutants, Chemical - chemistry</subject><ispartof>Water research (Oxford), 2016-09, Vol.100, p.413-420</ispartof><rights>2016 Elsevier Ltd</rights><rights>Copyright © 2016 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-bd894f4db77c71cee8811563385fc007a2d55d60a8bb54b893da667c60bb30b83</citedby><cites>FETCH-LOGICAL-c428t-bd894f4db77c71cee8811563385fc007a2d55d60a8bb54b893da667c60bb30b83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.watres.2016.05.048$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,782,786,3554,27933,27934,46004</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27232985$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Bin</creatorcontrib><creatorcontrib>Kookana, Rai S.</creatorcontrib><creatorcontrib>Williams, Mike</creatorcontrib><creatorcontrib>Du, Jun</creatorcontrib><creatorcontrib>Doan, Hai</creatorcontrib><creatorcontrib>Kumar, Anupama</creatorcontrib><title>Removal of carbamazepine in aqueous solutions through solar photolysis of free available chlorine</title><title>Water research (Oxford)</title><addtitle>Water Res</addtitle><description>Removal of a persistent antiepileptic drug carbamazepine (CBZ) in aqueous solutions was investigated by using solar photolysis combined with free available chlorine (FAC). The combination of chlorination with simulated or natural sunlight markedly enhanced removal of CBZ in 10 mM phosphate buffer solution (pH 7.0) and river water (pH 7.0) compared with sunlight or FAC alone. Further analysis indicated that the observed enhancements in CBZ removal can be attributed to the in situ hydroxyl radical (HO) and ozone (O3) production during FAC photolysis. During 70 min simulated sunlight photolysis combined with FAC treatment, HO reaction contributed to 35.8% removal of CBZ and O3 reaction contributed to 40.6% removal, while only 5.3% of CBZ was removed by HOCl reaction. The oxidation products of CBZ, epoxide CBZ, 10,11-dihydro-10,11-dihydroxy CBZ, 1-(2-benzaldehyde)-4-hydro-(1H,3H)-quinazoline-2-one (BQM), 1-(2-benzaldehyde)-(1H,3H)-quinazoline-2,4-dione (BQD) and 4-aldehyde-9-acridone, were mainly formed from the HO and O3 attack at the double bond on the central heterocyclic ring of CBZ. Formation of these oxidation products did not cause any increase or decrease in toxicity to microbial species tested through Microbial Assay for Toxicity Risk Assessment (MARA). The initial FAC concentration and pH had a major influence on the removal process of CBZ during FAC photolysis, while temperature had a minor effect only. The combination of chlorination with natural sunlight could provide an effective approach for removal of CBZ and other contaminants during water treatment.
[Display omitted]
•Chlorination of carbamazepine was dramatically enhanced by sunlight photolysis.•These enhancements can be attributed to the in situ HO and O3 production.•Oxidation products were formed from HO and O3 attack at the double bond of carbamazepine.•Oxidation products did not cause any increase or decrease in toxicity to MARA microbial species.•Initial chlorine dosage and pH had a major influence on the removal processes.</description><subject>Carbamazepine</subject><subject>Carbamazepine - chemistry</subject><subject>Chlorination</subject><subject>Chlorine</subject><subject>Free available chlorine</subject><subject>Microorganisms</subject><subject>Oxidation</subject><subject>Photolysis</subject><subject>Simulation</subject><subject>Sunlight</subject><subject>Toxicity</subject><subject>Water Pollutants, Chemical - chemistry</subject><issn>0043-1354</issn><issn>1879-2448</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1r3DAQhkVpaLZp_0EpPvZid_Rly5dCCekHBAohPQtJHne1yNZWsrckv74ym_ZYehpmeN75egl5Q6GhQNv3h-aXWRLmhpWsAdmAUM_Ijqqur5kQ6jnZAQheUy7FJXmZ8wEAGOP9C3LJOsZZr-SOmDuc4smEKo6VM8mayTzi0c9Y-bkyP1eMa65yDOvi45yrZZ_i-mO_VUyqjvu4xPCQfd7kY0KszMn4YGzAyu1DTKXRK3IxmpDx9VO8It8_3dxff6lvv33-ev3xtnaCqaW2g-rFKAbbda6jDlEpSmXLuZKjA-gMG6QcWjDKWims6vlg2rZzLVjLwSp-Rd6d-x5TLHvnRU8-OwzBzNsRmiomJS2X0_9AQbW8FwIKKs6oSzHnhKM-Jj-Z9KAp6M0HfdBnH_Tmgwapiw9F9vZpwmonHP6K_jy-AB_OAJaXnDwmnZ3H2eHgE7pFD9H_e8Jvv_eclg</recordid><startdate>20160901</startdate><enddate>20160901</enddate><creator>Yang, Bin</creator><creator>Kookana, Rai S.</creator><creator>Williams, Mike</creator><creator>Du, Jun</creator><creator>Doan, Hai</creator><creator>Kumar, Anupama</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>7QH</scope><scope>7TV</scope><scope>7UA</scope><scope>C1K</scope><scope>F1W</scope><scope>H97</scope><scope>L.G</scope><scope>8FD</scope><scope>FR3</scope><scope>KR7</scope></search><sort><creationdate>20160901</creationdate><title>Removal of carbamazepine in aqueous solutions through solar photolysis of free available chlorine</title><author>Yang, Bin ; Kookana, Rai S. ; Williams, Mike ; Du, Jun ; Doan, Hai ; Kumar, Anupama</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-bd894f4db77c71cee8811563385fc007a2d55d60a8bb54b893da667c60bb30b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Carbamazepine</topic><topic>Carbamazepine - chemistry</topic><topic>Chlorination</topic><topic>Chlorine</topic><topic>Free available chlorine</topic><topic>Microorganisms</topic><topic>Oxidation</topic><topic>Photolysis</topic><topic>Simulation</topic><topic>Sunlight</topic><topic>Toxicity</topic><topic>Water Pollutants, Chemical - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Bin</creatorcontrib><creatorcontrib>Kookana, Rai S.</creatorcontrib><creatorcontrib>Williams, Mike</creatorcontrib><creatorcontrib>Du, Jun</creatorcontrib><creatorcontrib>Doan, Hai</creatorcontrib><creatorcontrib>Kumar, Anupama</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aqualine</collection><collection>Pollution Abstracts</collection><collection>Water Resources Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Civil Engineering Abstracts</collection><jtitle>Water research (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Bin</au><au>Kookana, Rai S.</au><au>Williams, Mike</au><au>Du, Jun</au><au>Doan, Hai</au><au>Kumar, Anupama</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Removal of carbamazepine in aqueous solutions through solar photolysis of free available chlorine</atitle><jtitle>Water research (Oxford)</jtitle><addtitle>Water Res</addtitle><date>2016-09-01</date><risdate>2016</risdate><volume>100</volume><spage>413</spage><epage>420</epage><pages>413-420</pages><issn>0043-1354</issn><eissn>1879-2448</eissn><abstract>Removal of a persistent antiepileptic drug carbamazepine (CBZ) in aqueous solutions was investigated by using solar photolysis combined with free available chlorine (FAC). The combination of chlorination with simulated or natural sunlight markedly enhanced removal of CBZ in 10 mM phosphate buffer solution (pH 7.0) and river water (pH 7.0) compared with sunlight or FAC alone. Further analysis indicated that the observed enhancements in CBZ removal can be attributed to the in situ hydroxyl radical (HO) and ozone (O3) production during FAC photolysis. During 70 min simulated sunlight photolysis combined with FAC treatment, HO reaction contributed to 35.8% removal of CBZ and O3 reaction contributed to 40.6% removal, while only 5.3% of CBZ was removed by HOCl reaction. The oxidation products of CBZ, epoxide CBZ, 10,11-dihydro-10,11-dihydroxy CBZ, 1-(2-benzaldehyde)-4-hydro-(1H,3H)-quinazoline-2-one (BQM), 1-(2-benzaldehyde)-(1H,3H)-quinazoline-2,4-dione (BQD) and 4-aldehyde-9-acridone, were mainly formed from the HO and O3 attack at the double bond on the central heterocyclic ring of CBZ. Formation of these oxidation products did not cause any increase or decrease in toxicity to microbial species tested through Microbial Assay for Toxicity Risk Assessment (MARA). The initial FAC concentration and pH had a major influence on the removal process of CBZ during FAC photolysis, while temperature had a minor effect only. The combination of chlorination with natural sunlight could provide an effective approach for removal of CBZ and other contaminants during water treatment.
[Display omitted]
•Chlorination of carbamazepine was dramatically enhanced by sunlight photolysis.•These enhancements can be attributed to the in situ HO and O3 production.•Oxidation products were formed from HO and O3 attack at the double bond of carbamazepine.•Oxidation products did not cause any increase or decrease in toxicity to MARA microbial species.•Initial chlorine dosage and pH had a major influence on the removal processes.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>27232985</pmid><doi>10.1016/j.watres.2016.05.048</doi><tpages>8</tpages></addata></record> |
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subjects | Carbamazepine Carbamazepine - chemistry Chlorination Chlorine Free available chlorine Microorganisms Oxidation Photolysis Simulation Sunlight Toxicity Water Pollutants, Chemical - chemistry |
title | Removal of carbamazepine in aqueous solutions through solar photolysis of free available chlorine |
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