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Investigating the chlorination of acidic pharmaceuticals and by-product formation aided by an experimental design methodology

The degradation of seven acidic drugs and two metabolites during chlorination was investigated by liquid chromatography–mass spectrometry (LC–MS). A triple-quadrupole (QqQ) system was used to follow the time course of the pharmaceuticals and by-products, while a quadrupole time-of-flight (Q-TOF) sys...

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Published in:Water research (Oxford) 2010-01, Vol.44 (1), p.243-255
Main Authors: Quintana, José Benito, Rodil, Rosario, López-Mahía, Purificación, Muniategui-Lorenzo, Soledad, Prada-Rodríguez, Darío
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description The degradation of seven acidic drugs and two metabolites during chlorination was investigated by liquid chromatography–mass spectrometry (LC–MS). A triple-quadrupole (QqQ) system was used to follow the time course of the pharmaceuticals and by-products, while a quadrupole time-of-flight (Q-TOF) system was also used for the identification of the by-products. Under strong chlorination conditions (10mg/L Cl2, 24h), only four of the target compounds were significantly degraded: salicylic acid, naproxen, diclofenac and indomethacine. The degradation kinetics of these four compounds were investigated at different concentrations of chlorine, bromide and pH by means of a Box–Behnken experimental design. Depending on these factors, measured pseudo-first order half-lives were in the ranges: 23–573h for salicylic acid, 13–446min for naproxen, 5–328min for diclofenac and 0.4–13.4min for indomethacine. Also, it was observed that chlorine concentration was the overall most significant factor, followed by the bromide concentration (except for indomethacine), resulting in increased degradation kinetics as they are increased. The degradation path of salicylic acid, naproxen and diclofenac consisted of aromatic substitution of one or two hydrogens by chlorine and/or bromide. Moreover, for diclofenac, two other by-products corresponding to a decarboxylation/hydroxylation pathway from the monohalogenated products were also identified. On the other hand, indomethacine degradation did not lead to halogenation products but to oxidation ones. The investigation of these by-products in real samples by LC–MS/MS (QqQ) showed that the halogenated derivates of salicylic acid occurred in all the drinking water and wastewater samples analysed.
doi_str_mv 10.1016/j.watres.2009.09.018
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A triple-quadrupole (QqQ) system was used to follow the time course of the pharmaceuticals and by-products, while a quadrupole time-of-flight (Q-TOF) system was also used for the identification of the by-products. Under strong chlorination conditions (10mg/L Cl2, 24h), only four of the target compounds were significantly degraded: salicylic acid, naproxen, diclofenac and indomethacine. The degradation kinetics of these four compounds were investigated at different concentrations of chlorine, bromide and pH by means of a Box–Behnken experimental design. Depending on these factors, measured pseudo-first order half-lives were in the ranges: 23–573h for salicylic acid, 13–446min for naproxen, 5–328min for diclofenac and 0.4–13.4min for indomethacine. Also, it was observed that chlorine concentration was the overall most significant factor, followed by the bromide concentration (except for indomethacine), resulting in increased degradation kinetics as they are increased. 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A triple-quadrupole (QqQ) system was used to follow the time course of the pharmaceuticals and by-products, while a quadrupole time-of-flight (Q-TOF) system was also used for the identification of the by-products. Under strong chlorination conditions (10mg/L Cl2, 24h), only four of the target compounds were significantly degraded: salicylic acid, naproxen, diclofenac and indomethacine. The degradation kinetics of these four compounds were investigated at different concentrations of chlorine, bromide and pH by means of a Box–Behnken experimental design. Depending on these factors, measured pseudo-first order half-lives were in the ranges: 23–573h for salicylic acid, 13–446min for naproxen, 5–328min for diclofenac and 0.4–13.4min for indomethacine. Also, it was observed that chlorine concentration was the overall most significant factor, followed by the bromide concentration (except for indomethacine), resulting in increased degradation kinetics as they are increased. The degradation path of salicylic acid, naproxen and diclofenac consisted of aromatic substitution of one or two hydrogens by chlorine and/or bromide. Moreover, for diclofenac, two other by-products corresponding to a decarboxylation/hydroxylation pathway from the monohalogenated products were also identified. On the other hand, indomethacine degradation did not lead to halogenation products but to oxidation ones. 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Sewage sludge</topic><topic>Pharmaceuticals</topic><topic>Pollution</topic><topic>Salicylic acid</topic><topic>Salicylic Acid - analysis</topic><topic>Salicylic Acid - chemistry</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><topic>Tandem Mass Spectrometry</topic><topic>Time-of-flight (TOF)</topic><topic>Wastes</topic><topic>wastewater</topic><topic>Water Pollutants, Chemical - analysis</topic><topic>Water Pollutants, Chemical - chemistry</topic><topic>Water Supply - analysis</topic><topic>Water treatment and pollution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Quintana, José Benito</creatorcontrib><creatorcontrib>Rodil, Rosario</creatorcontrib><creatorcontrib>López-Mahía, Purificación</creatorcontrib><creatorcontrib>Muniategui-Lorenzo, Soledad</creatorcontrib><creatorcontrib>Prada-Rodríguez, Darío</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><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>Environment 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 &amp; Fisheries Abstracts (ASFA) 3: Aquatic Pollution &amp; Environmental Quality</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) Professional</collection><collection>Environment Abstracts</collection><collection>Environmental Engineering Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Water research (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Quintana, José Benito</au><au>Rodil, Rosario</au><au>López-Mahía, Purificación</au><au>Muniategui-Lorenzo, Soledad</au><au>Prada-Rodríguez, Darío</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigating the chlorination of acidic pharmaceuticals and by-product formation aided by an experimental design methodology</atitle><jtitle>Water research (Oxford)</jtitle><addtitle>Water Res</addtitle><date>2010-01</date><risdate>2010</risdate><volume>44</volume><issue>1</issue><spage>243</spage><epage>255</epage><pages>243-255</pages><issn>0043-1354</issn><eissn>1879-2448</eissn><coden>WATRAG</coden><abstract>The degradation of seven acidic drugs and two metabolites during chlorination was investigated by liquid chromatography–mass spectrometry (LC–MS). A triple-quadrupole (QqQ) system was used to follow the time course of the pharmaceuticals and by-products, while a quadrupole time-of-flight (Q-TOF) system was also used for the identification of the by-products. Under strong chlorination conditions (10mg/L Cl2, 24h), only four of the target compounds were significantly degraded: salicylic acid, naproxen, diclofenac and indomethacine. The degradation kinetics of these four compounds were investigated at different concentrations of chlorine, bromide and pH by means of a Box–Behnken experimental design. Depending on these factors, measured pseudo-first order half-lives were in the ranges: 23–573h for salicylic acid, 13–446min for naproxen, 5–328min for diclofenac and 0.4–13.4min for indomethacine. Also, it was observed that chlorine concentration was the overall most significant factor, followed by the bromide concentration (except for indomethacine), resulting in increased degradation kinetics as they are increased. The degradation path of salicylic acid, naproxen and diclofenac consisted of aromatic substitution of one or two hydrogens by chlorine and/or bromide. Moreover, for diclofenac, two other by-products corresponding to a decarboxylation/hydroxylation pathway from the monohalogenated products were also identified. On the other hand, indomethacine degradation did not lead to halogenation products but to oxidation ones. The investigation of these by-products in real samples by LC–MS/MS (QqQ) showed that the halogenated derivates of salicylic acid occurred in all the drinking water and wastewater samples analysed.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>19800649</pmid><doi>10.1016/j.watres.2009.09.018</doi><tpages>13</tpages></addata></record>
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source ScienceDirect Journals
subjects Acidic pharmaceuticals
Anti-Inflammatory Agents, Non-Steroidal - analysis
Anti-Inflammatory Agents, Non-Steroidal - chemistry
Applied sciences
Bromides
By-products
Byproducts
Chlorination
Chromatography, Liquid
Degradation
Diclofenac
Diclofenac - analysis
Diclofenac - chemistry
drinking water
drugs
Environmental fate
Exact sciences and technology
Halogenation
Hydrogen-Ion Concentration
indomethacine
Kinetics
liquid chromatography
Liquid chromatography–mass spectrometry (LC–MS)
Mass Spectrometry
methodology
Molecular Structure
Naproxen
Naproxen - analysis
Naproxen - chemistry
Non-steroidal anti-inflammatory drugs (NSAIDs)
Other industrial wastes. Sewage sludge
Pharmaceuticals
Pollution
Salicylic acid
Salicylic Acid - analysis
Salicylic Acid - chemistry
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Tandem Mass Spectrometry
Time-of-flight (TOF)
Wastes
wastewater
Water Pollutants, Chemical - analysis
Water Pollutants, Chemical - chemistry
Water Supply - analysis
Water treatment and pollution
title Investigating the chlorination of acidic pharmaceuticals and by-product formation aided by an experimental design methodology
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