Evaluation of Mercury in Environmental Samples by a Supramolecular Solvent–Based Dispersive Liquid–Liquid Microextraction Method Before Analysis by a Cold Vapor Generation Technique

2017 ◽  
Vol 100 (3) ◽  
pp. 782-788 ◽  
Author(s):  
Jamshed Ali ◽  
Mustafa Tuzen ◽  
Tasneem G Kazi

Abstract Supramolecular solvent–based dispersive liquid–liquid microextraction was used as a preconcentration method for the determination of trace levels of Hg. This simple method accurately measured oxidized HgII content inclaystone and sandstone samples obtained from the Thar Coalfield in Pakistan. Cold vapor atomic absorption spectrometry was used as the detection technique because it is reliable and accurate. The HgII in acidic media forms a complexwith dithizone (DTz) in the presence of supramolecular solvent (tetrahydrofuran and 1-undecanol), forming reverse micelles. Formation of the Hg-DTz complex was achieved to increase the interactions with the supramolecular solvent phase at pH 2.5 under the optimized experimental conditions. After additionof the supramolecular solvent to the aqueous solution, the micelles were uniformly mixed using a vortex mixer. The cloudy solution was centrifuged, and the Hg-DTz complex was extracted into the supramolecular solvent phase. Under optimized experimental conditions, the LOD and enrichment factor were foundto be 5.61 ng/L and 77.8, respectively. Accuracy of the developed method was checked with Certified Reference Materials. The developed method was successfully applied for the determination of HgII in claystone and sandstone samples from the Block VII and Block VIII areas of the Thar Coalfield on the basis of depth.

2012 ◽  
Vol 95 (1) ◽  
pp. 227-231 ◽  
Author(s):  
Valfredo Azevedo Lemos ◽  
Liz Oliveira dos Santos ◽  
Eldevan dos Santos Silva ◽  
Emanuel Vitor dos Santos Vieira

Abstract A simple method for the determination of mercury in water samples after preconcentration using dispersive liquid–liquid microextraction is described. The procedure is based on the extraction of mercury in the form of a complex and its subsequent determination by spectrophotometry. The complex is formed between Hg(II) and 2-(2-benzothiazolylazo)-p-cresol. The detection at 650 nm is performed directly in the metal-rich phase, which is spread on a triacetylcellulose membrane. The method eliminates the need to use a cuvet or large quantities of samples and reagents. The parameters that influence the preconcentration were studied, and the analytical characteristics were determined. The enrichment factor and the consumptive index for this method were 64 and 0.16 mL, respectively. The LOD (3.3 μg/L) and LOQ (11.1 μg/L) were also determined. The accuracy of the method was tested by the determination of mercury in certified reference materials BCR 397 (Human Hair) and SRM 2781 (Domestic Sludge). The method was applied to the determination of mercury in samples of drinking water, sea water, and river water.


2016 ◽  
Vol 8 (18) ◽  
pp. 3795-3801 ◽  
Author(s):  
Monireh Majlesi ◽  
Mohamadreza Massoudinejad ◽  
Fateh Hosainzadeh ◽  
Nazir Fattahi

UA-DLLME-SFO combined with HPLC-UV is a fast and simple method for the determination of pesticides and herbicides in fresh vegetables.


2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
J. Pérez-Outeiral ◽  
E. Millán ◽  
R. Garcia-Arrona

A simple and inexpensive method for cadmium determination in water using dispersive liquid-liquid microextraction and ultraviolet-visible spectrophotometry was developed. In order to obtain the best experimental conditions, experimental design was applied. Calibration was made in the range of 10–100 μg/L, obtaining good linearity (R2 = 0.9947). The obtained limit of detection based on calibration curve was 8.5 μg/L. Intra- and interday repeatability were checked at two levels, obtaining relative standard deviation values from 9.0 to 13.3%. The enrichment factor had a value of 73. Metal interferences were also checked and tolerable limits were evaluated. Finally, the method was applied to cadmium determination in real spiked water samples. Therefore, the method showed potential applicability for cadmium determination in highly contaminated liquid samples.


2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Siroos Shojaei ◽  
Saeed Shojaei ◽  
Arezoo Nouri ◽  
Leila Baharinikoo

AbstractAs the world population continues to grow, so does the pollution of water resources. It is, therefore, important to identify ways of reducing pollution as part of our effort to significantly increase the supply of clean and safer water. In this study, the efficiency of ultrasound-assisted dispersive liquid–liquid microextraction (UA-DLLME) as a fast, economical, and simple method for extraction malachite green (MG) and rhodamine B (RB) dyes from water samples is investigated. In optimal conditions, the linear dynamic range (LDR) for RB and MG is 7.5–1500 ng mL−1 and 12–1000 ng mL−1, respectively. The limit of detection (LOD) is 1.45 ng mL−1 and 2.73 ng mL−1, and limit of quantification (LOQ) is 4.83 ng mL−1 and 9.10 ng mL−1 for RB and MG, respectively. Extraction efficiency is obtained in the range of 95.53–99.60%. The relative standard deviations (RSD) in real water and wastewater samples are less than 3.5. The developed method is used successfully in the determination of RB and MG dyes from water samples and there are satisfactory results.


2011 ◽  
Vol 94 (6) ◽  
pp. 1882-1890 ◽  
Author(s):  
Abdullah Akdoğan ◽  
Ümit Divrikli ◽  
Andlatif Elçi

Abstract A dispersive liquid–liquid microextraction (DLLME) procedure coupled with GC/MS detection is described for preconcentration and determination of some organophosphorus and azole group pesticides from water samples. Experimental conditions affecting the DLLME procedure were optimized by means of an experimental design. A mixture of 60 μL chlorobenzene (extraction solvent) and 750 μL acetonitrile (disperser solvent), 3.5 min extraction time, and 7.5 mL aqueous sample volume were chosen for the best recovery by DLLME. The linear range was 1.6–32 μg/L. The LOD ranged from 48.8 to 68.7 ng/L. The RSD values for organophosphorus and azole group pesticides at spiking levels of 3, 6, and 9 μg/L in water samples were in the range of 1.1 – 12.8%. The applicability and accuracy of the developed method were determined by analysis of spiked water samples, and the recoveries of the analyzed pesticides from artesian, stream, and tap waters at spiking levels of 3, 6, and 9 μg/L were 89.3–105.6, 89.5–103.0, and 92.0–111.3%, respectively.


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