Determination of Trace Amounts of Gold in Electroplating Rinsing Bath by Slotted Quartz Tube Flame Atomic Absorption Spectrometry with Matrix Matching Calibration Strategy after Preconcentration with Vortex Assisted Dispersive Liquid–Liquid Microextraction

2020 ◽  
Vol 53 (14) ◽  
pp. 2191-2201 ◽  
Author(s):  
Duygu Terzioğlu ◽  
Merve Fırat ◽  
Dotse Selali Chormey ◽  
Sezgin Bakırdere
Keyword(s):  
Atomic Absorption Spectrometry ◽  
Atomic Absorption ◽  
Flame Atomic Absorption Spectrometry ◽  
Absorption Spectrometry ◽  
Quartz Tube ◽  
Flame Atomic Absorption ◽  
Slotted Quartz Tube ◽  
Dispersive Liquid Liquid Microextraction ◽  
Liquid Microextraction

scholarly journals Preconcentration of Copper Using 1,5-Diphenyl Carbazide as the Complexing Agent via Dispersive Liquid-Liquid Microextraction and Determination by Flame Atomic Absorption Spectrometry

2013 ◽  
Vol 2013 ◽  
pp. 1-7
Author(s):  
Reyhaneh Rahnama ◽  
Elaheh Shafiei ◽  
Mohammad Reza Jamali
Keyword(s):  
Atomic Absorption Spectrometry ◽  
Atomic Absorption ◽  
Flame Atomic Absorption Spectrometry ◽  
Absorption Spectrometry ◽  
Complexing Agent ◽  
Diphenyl Carbazide ◽  
Flame Atomic Absorption ◽  
Dispersive Liquid Liquid Microextraction ◽  
Liquid Microextraction

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 μL, 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 μg L−1for Cu (II) withR2= 0.9966. The limit of detection (3Sb/m), and preconcentration factor are 2 μg L−1and 25, respectively. The relative standard deviation (n=10) at 100 μg L−1of Cu (II) is 2.5%. The applicability of the developed technique was evaluated by application to spiked environmental water samples.

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