Ultra high performance liquid chromatography tandem mass spectrometry for rapid analysis of trace organic contaminants in water
| dc.contributor.author | Anumol, Tarun | |
| dc.contributor.author | Merel, Sylvain | |
| dc.contributor.author | Clarke, Bradley | |
| dc.contributor.author | Snyder, Shane | |
| dc.date.accessioned | 2016-05-20T08:58:59Z | |
| dc.date.available | 2016-05-20T08:58:59Z | |
| dc.date.issued | 2013 | en |
| dc.identifier.citation | Anumol et al. Chemistry Central Journal 2013, 7:104 http://journal.chemistrycentral.com/content/7/1/104 | en |
| dc.identifier.doi | 10.1186/1752-153X-7-104 | en |
| dc.identifier.uri | http://hdl.handle.net/10150/610118 | |
| dc.description.abstract | BACKGROUND:The widespread utilization of organic compounds in modern society and their dispersion through wastewater have resulted in extensive contamination of source and drinking waters. The vast majority of these compounds are not regulated in wastewater outfalls or in drinking water while trace amounts of certain compounds can impact aquatic wildlife. Hence it is prudent to monitor these contaminants in water sources until sufficient toxicological data relevant to humans becomes available. A method was developed for the analysis of 36 trace organic contaminants (TOrCs) including pharmaceuticals, pesticides, steroid hormones (androgens, progestins, and glucocorticoids), personal care products and polyfluorinated compounds (PFCs) using a single solid phase extraction (SPE) technique with ultra-high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS). The method was applied to a variety of water matrices to demonstrate method performance and reliability.RESULTS:UHPLC-MS/MS in both positive and negative electrospray ionization (ESI) modes was employed to achieve optimum sensitivity while reducing sample analysis time (<20min) compared with previously published methods. The detection limits for most compounds was lower than 1.0 picogram on the column while reporting limits in water ranged from 0.1 to 15ng/L based on the extraction of a 1L sample and concentration to 1mL. Recoveries in ultrapure water for most compounds were between 90-110%, while recoveries in surface water and wastewater were in the range of 39-121% and 38-141% respectively. The analytical method was successfully applied to analyze samples across several different water matrices including wastewater, groundwater, surface water and drinking water at different stages of the treatment. Among several compounds detected in wastewater, sucralose and TCPP showed the highest concentrations.CONCLUSION:The proposed method is sensitive, rapid and robust | |
| dc.description.abstract | hence it can be used to analyze a large variety of trace organic compounds in different water matrixes. | |
| dc.language.iso | en | en |
| dc.publisher | Chemistry Central | en |
| dc.relation.url | http://journal.chemistrycentral.com/content/7/1/104 | en |
| dc.rights | © 2013 Anumol et al.; licensee Chemistry Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0). | en |
| dc.rights.uri | https://creativecommons.org/licenses/by/2.0/ | |
| dc.subject | Trace organic contaminant | en |
| dc.subject | Pharmaceutical | en |
| dc.subject | Personal-care product | en |
| dc.subject | Glucocorticoid | en |
| dc.subject | PFC | en |
| dc.subject | Solid-phase extraction | en |
| dc.subject | Ultra-high performance liquid chromatography | en |
| dc.subject | Tandem mass spectrometry | en |
| dc.subject | Water quality | en |
| dc.title | Ultra high performance liquid chromatography tandem mass spectrometry for rapid analysis of trace organic contaminants in water | en |
| dc.type | Article | en |
| dc.identifier.eissn | 1752-153X | en |
| dc.contributor.department | Department of Chemical & Environmental Engineering, University of Arizona, 1133 E James E Rogers Way, Harshbarger 108, Tucson, AZ, 85721-0011, USA | en |
| dc.contributor.department | School of Applied Sciences, RMIT University, 100 LaTrobe St, Melbourne, 3000, Australia | en |
| dc.identifier.journal | Chemistry Central Journal | en |
| dc.description.collectioninformation | This item is part of the UA Faculty Publications collection. For more information this item or other items in the UA Campus Repository, contact the University of Arizona Libraries at repository@u.library.arizona.edu. | en |
| dc.eprint.version | Final published version | en |
| refterms.dateFOA | 2018-06-17T00:35:56Z | |
| html.description.abstract | BACKGROUND:The widespread utilization of organic compounds in modern society and their dispersion through wastewater have resulted in extensive contamination of source and drinking waters. The vast majority of these compounds are not regulated in wastewater outfalls or in drinking water while trace amounts of certain compounds can impact aquatic wildlife. Hence it is prudent to monitor these contaminants in water sources until sufficient toxicological data relevant to humans becomes available. A method was developed for the analysis of 36 trace organic contaminants (TOrCs) including pharmaceuticals, pesticides, steroid hormones (androgens, progestins, and glucocorticoids), personal care products and polyfluorinated compounds (PFCs) using a single solid phase extraction (SPE) technique with ultra-high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS). The method was applied to a variety of water matrices to demonstrate method performance and reliability.RESULTS:UHPLC-MS/MS in both positive and negative electrospray ionization (ESI) modes was employed to achieve optimum sensitivity while reducing sample analysis time (<20min) compared with previously published methods. The detection limits for most compounds was lower than 1.0 picogram on the column while reporting limits in water ranged from 0.1 to 15ng/L based on the extraction of a 1L sample and concentration to 1mL. Recoveries in ultrapure water for most compounds were between 90-110%, while recoveries in surface water and wastewater were in the range of 39-121% and 38-141% respectively. The analytical method was successfully applied to analyze samples across several different water matrices including wastewater, groundwater, surface water and drinking water at different stages of the treatment. Among several compounds detected in wastewater, sucralose and TCPP showed the highest concentrations.CONCLUSION:The proposed method is sensitive, rapid and robust | |
| html.description.abstract | hence it can be used to analyze a large variety of trace organic compounds in different water matrixes. |
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Except where otherwise noted, this item's license is described as © 2013 Anumol et al.; licensee Chemistry Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0).