scholarly journals Dispersive Liquid-Liquid Microextraction Based on Solidification of Floating Organic Drop Followed by Gas Chromatography-Electron Capture Detector for Determination of Some Pesticides in Water Samples

2011 ◽  
Vol 2011 ◽  
pp. 1-8 ◽  
Author(s):  
Mostafa Bashiri Juybari ◽  
Ali Mehdinia ◽  
Ali Jabbari ◽  
Yadollah Yamini

In this study dispersive liquid-liquid microextraction based on solidification of floating organic drop (DLLME-SFO) followed by gas chromatography-electron capture detection (GC-ECD) was developed for determination of some pesticides in the water samples. Some important parameters, such as type and volumes of extraction and disperser solvent and salt effect on the extraction recovery of analytes from aqueous solution were investigated. Under the optimum conditions (extraction solvent: 1-undecanol, 15.0 μL; disperser solvent: acetone, 1.0 mL, and without salt addition), the preconcentration factors were obtained ranged from 802 to 915 for analytes. The linear ranges were from 0.05 to 100 μg L−1, and detection limits ranged from 0.05 to 0.008 μg L−1. The relative standard deviations (RSDs%, ) were between 3.2% and 6.7%. The proposed method was successfully applied to the determination of target analytes in the tap, sea, and river water samples, and satisfactory recoveries were obtained.

2012 ◽  
Vol 518-523 ◽  
pp. 1379-1382
Author(s):  
Ying Chun Yang ◽  
Qian Sun ◽  
Chong Shu Yi ◽  
Zhi Xiang Ye ◽  
Li Mo

A rapid and effective method, the dispersive liquid-liquid microextraction(DLLME) with gas chromatography, has been developed for the extraction and determination of OCP in environmental water samples. The factors relevant to the efficiency of DLLME were investigated and optimized. Under the optimum conditions, such as 150μL of dichloromethane as extraction solvent, 1.2 mL acetone as dispersive agent, 8 minutes extraction time, and without salt addition, the linear response of this method was in the range of 0.5~5000μg L−1 (r = 0.9981), the relative standard deviation (RSD) for 500μg L−1 and 1000μg L−1 of OCP was 5.2% and 12.6% (n = 6), respectively. The detection limit (3σ) was 0.08 μg L−1. The developed method was successfully applied to the determination of trace amount of OCP in three kinds of real environmental water samples, the spiked recoveries were in the range of 87.4%~108.0%.


2014 ◽  
Vol 881-883 ◽  
pp. 631-634 ◽  
Author(s):  
Jian Qi Sun ◽  
Ming Tang ◽  
Jun Dai

A simple and reliable method combining dispersive liquid-liquid microextracion (DLLME) with gas chromatography (GC) using flame ionization detection (FID) was developed for the simultaneous determination of aniline (AL),o-toluidine (o-TLD),N,N-dimethylaniline (N,N-DAL),p-chloroaniline (p-CAL), andp-nitroaniline (p-NAL) in wastewater. For this purpose, dispersive liquid-liquid microextraction (DLLME) was applied as a sample preparation technique. The DLLME conditions such as the types and volume of extraction solvent, the types and volume of the disperser solvent, pH value and salt addition were studied and optimized. The method was linear in the ranges from 2.2×10-3to 100.0 μg·mL-1for aforementioned aromatic amines withR2≥ 0.9968. The DLLME procedure allowed efficient recovery of the investigated aromatic amines ranging between 82 % and 92 % with a relative standard deviation (RSD) ≤ 3.4 for actual wastewater samples spiked with 5, 10 and 20 μg·mL-1of aromatic amines, respectively. These results showed the potential of this technique for aromatic amines monitoring in wastewater samples. Furthermore, the investigated methods are simple, reproducible, and inexpensive.


2014 ◽  
Vol 1030-1032 ◽  
pp. 357-360 ◽  
Author(s):  
Jian Qi Sun

This study describes an analytical method employing capillary gas chromatography (GC) using flame ionization detection (FID) that has been developed for the simultaneous determination of food preservatives in drinks, including sorbic acid (SA), benzonic acid (BA) and methyl paraben (MP). For this purpose, dispersive liquid-liquid microextraction (DLLME) was applied as a sample preparation technique. The DLLME conditions such as the types and volume of extraction solvent, the types and volume of the disperser solvent, pH value and salt addition were investigated and optimized. The method was linear in the ranges from 0.5 to 100.0 μg·mL-1for abovementioned preservatives withR2≥ 0.9991. The DLLME procedure allowed efficient recovery of the analyted preservatives ranging between 91 % and 108 % with a relative standard deviation (RSD) ≤ 6.1 for the blank samples spiked with 20, 40 and 80 μg·mL-1of preservatives, respectively. The developed procedure was demonstrated to be a effective method for the analysis of preservatives in drinks. Furthermore, the method is simple, reproducible, envioronmentally friendly and inexpensive.


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