Extraction of Trace Quantities of Copper Using Novel Modified Magnetite Nanoparticles for Atomic Absorption Spectrometry Analysis

Author:

Pourbasheer Eslam1ORCID,Morsali Somayeh2,Ansari Samira3,Mirtamizdoust Babak4,Vojoudi Hossein5,Ganjali Mohammad Reza67ORCID

Affiliation:

1. Department of Chemistry, Faculty of Science, University of Mohaghegh Ardabili, P.O. Box 179, Ardabil, Iran

2. Department of Chemistry, Payame Noor University (PNU), P. O. Box 19395-3697, Tehran, Iran

3. CinnaGen Medical Biotechnology Research Center, Alborz University of Medical Sciences, Karaj, Iran

4. Department of Chemistry, Faculty of Science, University of Qom, Qom 37185359, Iran

5. School of Chemistry, College of Science, University of Tehran, Tehran, Iran

6. Center of Excellence in Electrochemistry, Faculty of Chemistry, University of Tehran, Tehran, Iran

7. National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran

Abstract

Background: Copper is one of several heavy metals. A low concentration of copper is vital for animals and plants, whereas it is highly toxic to aquatic plants and bacteria in a high concentration. Therefore, copper ions in water and food must be controlled, and as a result, the development of novel methods for the determination of copper in water samples is of interest. Objective: Different techniques have been proposed for copper ions extraction and determination. The magnetic solid-phase extraction method is considered superior to the other method for simplicity, its higher enrichment, and the need for lower quantities of solvents. The novel modified magnetite nanoparticles as the sorbent, along with the atomic absorption spectrometry analysis, can be a low-cost, simple and rapid method for this propose. Methods: Traces of Cu(II) in environmental samples were preconcentrated using a novel magnetic adsorbent developed based on 2,2´-((1E,1´E)-hydrazine-1,2-diylidenebis(methanylylidene)) diphenol coated magnetite nanoparticles. The influence of ligand concentration, amount of adsorbent, pH, type of eluent, sample volume, and effects of interfering ions were optimized. The adsorbed species were eluted for analysis through atomic absorption spectrometry. Results: A linear calibration curve was recorded from 2 to 40 μg ml-1 (r2= 0.999) under optimal conditions, and the detection limit of the method was as low as 1.6 μg ml-1. Also, good recoveries were obtained for the real sample analysis. Conclusion: The developed procedure constituted a rapid extraction, a low-cost and efficient method, and was used for the analysis of copper ions in the tap, river, and lake water.

Publisher

Bentham Science Publishers Ltd.

Subject

Analytical Chemistry

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