Integration of the free liquid membrane into electrokinetic supercharging - capillary electrophoresis for the determination of paraquat and diquat in environmentalwater samples

A new approach based on the integration of the free liquid membrane (FLM) into electrokinetic supercharging (EKS) was demonstrated to be a new powerful tool used in order to enhance online preconcentration efficiency in capillary electrophoresis (CE). A small plug of water immiscible organic solvent...

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Main Author: Chui, Mei Qi
Format: Thesis
Language:English
Published: 2017
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Online Access:http://eprints.utm.my/id/eprint/77642/1/ChuiMeiQiMFS20171.pdf
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spelling my-utm-ep.776422018-06-26T07:37:21Z Integration of the free liquid membrane into electrokinetic supercharging - capillary electrophoresis for the determination of paraquat and diquat in environmentalwater samples 2017-06 Chui, Mei Qi QH301 Biology A new approach based on the integration of the free liquid membrane (FLM) into electrokinetic supercharging (EKS) was demonstrated to be a new powerful tool used in order to enhance online preconcentration efficiency in capillary electrophoresis (CE). A small plug of water immiscible organic solvent was used as a membrane interface during the electrokinetic sample injection step in EKS in order to significantly enhance the analyte stacking efficiency. The new online preconcentration strategy was evaluated for the determination of paraquat and diquat present in the environmental water samples. The optimised FLM-EKS conditions employed were as follows: hydrodynamic injection (HI) of 20 mM potassium chloride as leading electrolyte at 50 mbar for 75 s (3% of the total capillary volume) followed by the HI of tris(2-ethylhexyl) phosphate (TEHP) as FLM at a 1 mm length (0.1% of the capillary volume). The sample was injected at 10 kV for 360 s, followed by the HI of 20 mM cetyl trimethylammonium bromide (CTAB) as terminating electrolyte at 50 mbar for 50 s (2% of the total capillary volume). The separation was performed in 12 mM ammonium acetate and 30 mM NaCl containing 20% MeOH at +25 kV with UV detection at 205 nm. Under optimised conditions, the sensitivity was enhanced between 1500- and 1866-fold when compared with the typical HI at 50 mbar for 50 s. The detection limit of the method for paraquat and diquat was 0.15-0.20 ng/mL, with RSDs below 5.5%. Relative recoveries in spiked river water were in the range of 92-100%. A comparison was also made between the proposed approach with sole preconcentration of the fieldenhanced sample injection (FASI) and EKS in the absence of the FLM. 2017-06 Thesis http://eprints.utm.my/id/eprint/77642/ http://eprints.utm.my/id/eprint/77642/1/ChuiMeiQiMFS20171.pdf application/pdf en public http://dms.library.utm.my:8080/vital/access/manager/Repository/vital:105105 masters Universiti Teknologi Malaysia, Faculty of Science Faculty of Science
institution Universiti Teknologi Malaysia
collection UTM Institutional Repository
language English
topic QH301 Biology
spellingShingle QH301 Biology
Chui, Mei Qi
Integration of the free liquid membrane into electrokinetic supercharging - capillary electrophoresis for the determination of paraquat and diquat in environmentalwater samples
description A new approach based on the integration of the free liquid membrane (FLM) into electrokinetic supercharging (EKS) was demonstrated to be a new powerful tool used in order to enhance online preconcentration efficiency in capillary electrophoresis (CE). A small plug of water immiscible organic solvent was used as a membrane interface during the electrokinetic sample injection step in EKS in order to significantly enhance the analyte stacking efficiency. The new online preconcentration strategy was evaluated for the determination of paraquat and diquat present in the environmental water samples. The optimised FLM-EKS conditions employed were as follows: hydrodynamic injection (HI) of 20 mM potassium chloride as leading electrolyte at 50 mbar for 75 s (3% of the total capillary volume) followed by the HI of tris(2-ethylhexyl) phosphate (TEHP) as FLM at a 1 mm length (0.1% of the capillary volume). The sample was injected at 10 kV for 360 s, followed by the HI of 20 mM cetyl trimethylammonium bromide (CTAB) as terminating electrolyte at 50 mbar for 50 s (2% of the total capillary volume). The separation was performed in 12 mM ammonium acetate and 30 mM NaCl containing 20% MeOH at +25 kV with UV detection at 205 nm. Under optimised conditions, the sensitivity was enhanced between 1500- and 1866-fold when compared with the typical HI at 50 mbar for 50 s. The detection limit of the method for paraquat and diquat was 0.15-0.20 ng/mL, with RSDs below 5.5%. Relative recoveries in spiked river water were in the range of 92-100%. A comparison was also made between the proposed approach with sole preconcentration of the fieldenhanced sample injection (FASI) and EKS in the absence of the FLM.
format Thesis
qualification_level Master's degree
author Chui, Mei Qi
author_facet Chui, Mei Qi
author_sort Chui, Mei Qi
title Integration of the free liquid membrane into electrokinetic supercharging - capillary electrophoresis for the determination of paraquat and diquat in environmentalwater samples
title_short Integration of the free liquid membrane into electrokinetic supercharging - capillary electrophoresis for the determination of paraquat and diquat in environmentalwater samples
title_full Integration of the free liquid membrane into electrokinetic supercharging - capillary electrophoresis for the determination of paraquat and diquat in environmentalwater samples
title_fullStr Integration of the free liquid membrane into electrokinetic supercharging - capillary electrophoresis for the determination of paraquat and diquat in environmentalwater samples
title_full_unstemmed Integration of the free liquid membrane into electrokinetic supercharging - capillary electrophoresis for the determination of paraquat and diquat in environmentalwater samples
title_sort integration of the free liquid membrane into electrokinetic supercharging - capillary electrophoresis for the determination of paraquat and diquat in environmentalwater samples
granting_institution Universiti Teknologi Malaysia, Faculty of Science
granting_department Faculty of Science
publishDate 2017
url http://eprints.utm.my/id/eprint/77642/1/ChuiMeiQiMFS20171.pdf
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