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
Hauptverfasser: Ranjbari, Elias, Hadjmohammadi, Mohammad Reza
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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
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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. 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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. 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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. 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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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