Title : ( Determination of Hg(II) in Environmental Water Samples Using DLLME Method Prior to GC-FID )
Authors: Ali Sarafraz Yazdi , maryam abedi ostad , F. Mofazzeli ,Access to full-text not allowed by authors
Abstract
Abstract Mercury exists in two forms in environment, inorganic salts and organic compounds. Determination of mercury is very important, due to its health effects. In the present research, diphenylation of mercury using phenylboronic acid as a derivatization reagent was used for the determination of Hg(II) in real water samples. A simple, rapid and cheap method named dispersive liquid–liquid microextraction was used for the extraction of analyte under the following conditions: extraction solvent 16 lL of carbon tetrachloride, disperser solvent 1 mL of ethanol and sample volume 5 mL. Under the optimal conditions, the enrichment factor for diphenylmercury was 931 and the limit of detection calculated on the basis of five replicates was 0.004 lg mL-1. The repeatability of the method expresses as relative standard deviation was 5.1 (n = 6). The linear range was between 0.01 and 10 lg mL-1. The performance of the proposed technique was evaluated for the determination of mercury in different environmental water samples.
Keywords
, Gas chromatography, flame ionization detector (GC, FID) Dispersive liquid–liquid microextraction (DLLME) Mercury Diphenylmercury@article{paperid:1035058,
author = {Sarafraz Yazdi, Ali and Abedi Ostad, Maryam and F. Mofazzeli},
title = {Determination of Hg(II) in Environmental Water Samples Using DLLME Method Prior to GC-FID},
journal = {Chromatographia},
year = {2013},
volume = {76},
number = {6},
month = {June},
issn = {0009-5893},
pages = {861--865},
numpages = {4},
keywords = {Gas chromatography-flame ionization
detector (GC-FID) Dispersive liquid–liquid
microextraction (DLLME) Mercury Diphenylmercury},
}
%0 Journal Article
%T Determination of Hg(II) in Environmental Water Samples Using DLLME Method Prior to GC-FID
%A Sarafraz Yazdi, Ali
%A Abedi Ostad, Maryam
%A F. Mofazzeli
%J Chromatographia
%@ 0009-5893
%D 2013