Preconcentration of Copper Using 1,5‐Diphenyl Carbazide as the Complexing Agent via Dispersive Liquid‐Liquid Microextraction and Determination by Flame Atomic Absorption Spectrometry
Author(s) -
Reyhaneh Rahnama,
Elaheh Shafiei,
Mohammad Reza Jamali
Publication year - 2012
Publication title -
journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.436
H-Index - 50
eISSN - 2090-9063
pISSN - 2090-9071
DOI - 10.1155/2013/962365
Subject(s) - chemistry , detection limit , extraction (chemistry) , solvent , atomic absorption spectroscopy , analytical chemistry (journal) , calibration curve , enrichment factor , copper , chromatography , physics , organic chemistry , quantum mechanics
We report a simple and sensitive microextraction system for the preconcentration and determination of Cu (II) by flame atomic absorption spectrometry (FAAS). Dispersive liquid-liquid microextraction is a modified solvent extraction method and its acceptor-to-donor phase ratio is greatly reduced compared with other methods. In the proposed approach, 1,5-diphenyl carbazide (DPC) was used as a copper ion selective complexing agent. Several variables such as the extraction and dispersive solvent type and volume, pH of sample solution, DPC concentration, extraction time, and ionic strength were studied and optimized for a quantitative preconcentration and determination of copper (II) and at the optimized conditions: 60 μ L, 0.5 mL, and 5 mL of extraction solvent (chloroform), disperser solvent (ethanol), and sample volume, respectively, a linear calibration graph was obtained over the concentration range of 10–200 μ g L −1 for Cu (II) withR 2= 0.9966. The limit of detection (3S b /m), and preconcentration factor are 2 μ g L −1 and 25, respectively. The relative standard deviation ( n = 10 ) at 100 μ g L −1 of Cu (II) is 2.5%. The applicability of the developed technique was evaluated by application to spiked environmental water samples.
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