Magnetic stirring-assisted dispersive liquid–liquid microextraction followed by high performance liquid chromatography for determination of phthalate esters in drinking and environmental water samples
A simple, fast and efficient method for the preconcentration of phthalate esters (PEs) in water samples was developed using magnetic stirring-assisted dispersive liquid–liquid microextraction (MSA-DLLME) followed by high performance liquid chromatography coupled with ultraviolet detection (HPLC–UV)....
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Veröffentlicht in: | Talanta (Oxford) 2012-10, Vol.100, p.447-453 |
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description | A simple, fast and efficient method for the preconcentration of phthalate esters (PEs) in water samples was developed using magnetic stirring-assisted dispersive liquid–liquid microextraction (MSA-DLLME) followed by high performance liquid chromatography coupled with ultraviolet detection (HPLC–UV). This novel microextraction method is based on the fast injection of extracting solvent into the aqueous solution, which is being stirred by a magnetic stirrer, to form a cloudy binary component solvent (aqueous solution:extracting solvent) system. The extraction parameters such as type and volume of extracting solvent, pH of sample, salt addition, extraction time and stirring rate were optimized. Under the optimal conditions (extracting solvent: 200μL dodecane; pH of sample: 6.5; extraction time: 5min; stirring rate: 1000rpm), linearity was observed in the range of 2–1000μgL−1 for dimethyl phthalate (DMP) and 1–1000μgL−1 for diethyl phthalate (DEP), benzyl butyl phthalate (BBP) and di-n-butyl phthalate (DBP) with correlation determination values above 0.99 for them. The limits of detection and quantification were ranged from 0.13 to 0.38μgmL−1 and 0.43 to 1.27μgmL−1, respectively. The ranges of intra-day and inter-day precisions (n=5) at 100μgL−1 of PEs were 1.50–2.65% and 2.31–3.35%, respectively. Finally, the MSA-DLLME method was successfully applied for preconcentration of PEs in drinking and environmental water samples.
► MSA-DLLME–HPLC–UV has been applied for rapid determination of phthalates. ► Dodecane is safer than chlorinated solvents and has better chromatographic behavior. ► Using dodecane, elimination of the evaporation step results in excellent precision. ► Phthalates were determined in mineral, tap, well, river and sea water samples. |
doi_str_mv | 10.1016/j.talanta.2012.08.019 |
format | Article |
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► MSA-DLLME–HPLC–UV has been applied for rapid determination of phthalates. ► Dodecane is safer than chlorinated solvents and has better chromatographic behavior. ► Using dodecane, elimination of the evaporation step results in excellent precision. ► Phthalates were determined in mineral, tap, well, river and sea water samples.</description><identifier>ISSN: 0039-9140</identifier><identifier>EISSN: 1873-3573</identifier><identifier>DOI: 10.1016/j.talanta.2012.08.019</identifier><identifier>PMID: 23141363</identifier><identifier>CODEN: TLNTA2</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Analytical chemistry ; Applied sciences ; Chemistry ; Chromatographic methods and physical methods associated with chromatography ; Dispersive liquid–liquid microextraction ; Drinking water ; Environmental water ; Exact sciences and technology ; Global environmental pollution ; High performance liquid chromatography ; Magnetic stirring-assisted ; Other chromatographic methods ; Phthalate ester ; Pollution</subject><ispartof>Talanta (Oxford), 2012-10, Vol.100, p.447-453</ispartof><rights>2012 Elsevier B.V.</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-569f2fe2e97a7fca2d7d0c1b71044888154659732bb0bd5c4edf8ae8525e859c3</citedby><cites>FETCH-LOGICAL-c428t-569f2fe2e97a7fca2d7d0c1b71044888154659732bb0bd5c4edf8ae8525e859c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0039914012007072$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26640105$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23141363$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ranjbari, Elias</creatorcontrib><creatorcontrib>Hadjmohammadi, Mohammad Reza</creatorcontrib><title>Magnetic stirring-assisted dispersive liquid–liquid microextraction followed by high performance liquid chromatography for determination of phthalate esters in drinking and environmental water samples</title><title>Talanta (Oxford)</title><addtitle>Talanta</addtitle><description>A simple, fast and efficient method for the preconcentration of phthalate esters (PEs) in water samples was developed using magnetic stirring-assisted dispersive liquid–liquid microextraction (MSA-DLLME) followed by high performance liquid chromatography coupled with ultraviolet detection (HPLC–UV). This novel microextraction method is based on the fast injection of extracting solvent into the aqueous solution, which is being stirred by a magnetic stirrer, to form a cloudy binary component solvent (aqueous solution:extracting solvent) system. The extraction parameters such as type and volume of extracting solvent, pH of sample, salt addition, extraction time and stirring rate were optimized. Under the optimal conditions (extracting solvent: 200μL dodecane; pH of sample: 6.5; extraction time: 5min; stirring rate: 1000rpm), linearity was observed in the range of 2–1000μgL−1 for dimethyl phthalate (DMP) and 1–1000μgL−1 for diethyl phthalate (DEP), benzyl butyl phthalate (BBP) and di-n-butyl phthalate (DBP) with correlation determination values above 0.99 for them. The limits of detection and quantification were ranged from 0.13 to 0.38μgmL−1 and 0.43 to 1.27μgmL−1, respectively. The ranges of intra-day and inter-day precisions (n=5) at 100μgL−1 of PEs were 1.50–2.65% and 2.31–3.35%, respectively. Finally, the MSA-DLLME method was successfully applied for preconcentration of PEs in drinking and environmental water samples.
► MSA-DLLME–HPLC–UV has been applied for rapid determination of phthalates. ► Dodecane is safer than chlorinated solvents and has better chromatographic behavior. ► Using dodecane, elimination of the evaporation step results in excellent precision. ► Phthalates were determined in mineral, tap, well, river and sea water samples.</description><subject>Analytical chemistry</subject><subject>Applied sciences</subject><subject>Chemistry</subject><subject>Chromatographic methods and physical methods associated with chromatography</subject><subject>Dispersive liquid–liquid microextraction</subject><subject>Drinking water</subject><subject>Environmental water</subject><subject>Exact sciences and technology</subject><subject>Global environmental pollution</subject><subject>High performance liquid chromatography</subject><subject>Magnetic stirring-assisted</subject><subject>Other chromatographic methods</subject><subject>Phthalate ester</subject><subject>Pollution</subject><issn>0039-9140</issn><issn>1873-3573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqFkU1uFDEQhVsIRIbAEUDeILHpwT_9u0IogoAUxAbWltuunq6hu92xPRNmxx24VY7BSagwE1iysb34XvnVe1n2XPC14KJ6vV0nM5o5mbXkQq55s-aifZCtRFOrXJW1epitOFdt3oqCn2VPYtxyzqXi6nF2JpUohKrUKrv9ZDYzJLQsJgwB501uYsSYwDGHcYEQcQ9sxOsdul8_fh4fbEIbPHxPwdiEfma9H0d_Q5ruwAbcDIyEvQ-Tme29mNkh-MkkvwlmGQ4kCcxBgjDhbP4M8T1bhjTQWgkYkIUQGc7MkatvZIyZ2TGY9xj8PAFtPrIbIgOLZlpGiE-zR70ZIzw73efZ1_fvvlx8yK8-X368eHuV20I2KS-rtpc9SGhrU_fWSFc7bkVXC14UTdOIsqjKtlay63jnSluA6xsDTSlLOlqrzrNXx7lL8Nc78qknjBZGagP8LmohStFKKaqC0PKIUloxBuj1EnAy4aAF13c16q0-1ajvatS80VQj6V6cvth1E7i_qvveCHh5Aky0ZuwDBY3xH1dVBRe8JO7NkQMKZI8QdLQIVIrDADZp5_E_Vn4DYq3GqA</recordid><startdate>20121015</startdate><enddate>20121015</enddate><creator>Ranjbari, Elias</creator><creator>Hadjmohammadi, Mohammad Reza</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20121015</creationdate><title>Magnetic stirring-assisted dispersive liquid–liquid microextraction followed by high performance liquid chromatography for determination of phthalate esters in drinking and environmental water samples</title><author>Ranjbari, Elias ; Hadjmohammadi, Mohammad Reza</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-569f2fe2e97a7fca2d7d0c1b71044888154659732bb0bd5c4edf8ae8525e859c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Analytical chemistry</topic><topic>Applied sciences</topic><topic>Chemistry</topic><topic>Chromatographic methods and physical methods associated with chromatography</topic><topic>Dispersive liquid–liquid microextraction</topic><topic>Drinking water</topic><topic>Environmental water</topic><topic>Exact sciences and technology</topic><topic>Global environmental pollution</topic><topic>High performance liquid chromatography</topic><topic>Magnetic stirring-assisted</topic><topic>Other chromatographic methods</topic><topic>Phthalate ester</topic><topic>Pollution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ranjbari, Elias</creatorcontrib><creatorcontrib>Hadjmohammadi, Mohammad Reza</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Talanta (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ranjbari, Elias</au><au>Hadjmohammadi, Mohammad Reza</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Magnetic stirring-assisted dispersive liquid–liquid microextraction followed by high performance liquid chromatography for determination of phthalate esters in drinking and environmental water samples</atitle><jtitle>Talanta (Oxford)</jtitle><addtitle>Talanta</addtitle><date>2012-10-15</date><risdate>2012</risdate><volume>100</volume><spage>447</spage><epage>453</epage><pages>447-453</pages><issn>0039-9140</issn><eissn>1873-3573</eissn><coden>TLNTA2</coden><abstract>A simple, fast and efficient method for the preconcentration of phthalate esters (PEs) in water samples was developed using magnetic stirring-assisted dispersive liquid–liquid microextraction (MSA-DLLME) followed by high performance liquid chromatography coupled with ultraviolet detection (HPLC–UV). This novel microextraction method is based on the fast injection of extracting solvent into the aqueous solution, which is being stirred by a magnetic stirrer, to form a cloudy binary component solvent (aqueous solution:extracting solvent) system. The extraction parameters such as type and volume of extracting solvent, pH of sample, salt addition, extraction time and stirring rate were optimized. Under the optimal conditions (extracting solvent: 200μL dodecane; pH of sample: 6.5; extraction time: 5min; stirring rate: 1000rpm), linearity was observed in the range of 2–1000μgL−1 for dimethyl phthalate (DMP) and 1–1000μgL−1 for diethyl phthalate (DEP), benzyl butyl phthalate (BBP) and di-n-butyl phthalate (DBP) with correlation determination values above 0.99 for them. The limits of detection and quantification were ranged from 0.13 to 0.38μgmL−1 and 0.43 to 1.27μgmL−1, respectively. The ranges of intra-day and inter-day precisions (n=5) at 100μgL−1 of PEs were 1.50–2.65% and 2.31–3.35%, respectively. Finally, the MSA-DLLME method was successfully applied for preconcentration of PEs in drinking and environmental water samples.
► MSA-DLLME–HPLC–UV has been applied for rapid determination of phthalates. ► Dodecane is safer than chlorinated solvents and has better chromatographic behavior. ► Using dodecane, elimination of the evaporation step results in excellent precision. ► Phthalates were determined in mineral, tap, well, river and sea water samples.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>23141363</pmid><doi>10.1016/j.talanta.2012.08.019</doi><tpages>7</tpages></addata></record> |
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subjects | Analytical chemistry Applied sciences Chemistry Chromatographic methods and physical methods associated with chromatography Dispersive liquid–liquid microextraction Drinking water Environmental water Exact sciences and technology Global environmental pollution High performance liquid chromatography Magnetic stirring-assisted Other chromatographic methods Phthalate ester Pollution |
title | Magnetic stirring-assisted dispersive liquid–liquid microextraction followed by high performance liquid chromatography for determination of phthalate esters in drinking and environmental water samples |
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