Published April 1, 2013 | Version v1
Journal article

Micro-electrodeposition in the presence of ionic liquid for the preconcentration of trace amounts of Fe, Co, Ni and Zn from aqueous samples

Description

The paper presents the preconcentration of trace elements via electrodeposition onto a (micro)aluminum cathode in the presence of ionic liquid 1-butyl-3-methylimidazolium hexafluorophosphate [BMIM][PF6] as a supporting electrolyte. The advantages of the proposed method include very simple instrumentation for the preconcentration of trace elements and low-cost reagents. The experiment showed that the use of ionic liquid in the electrodeposition process significantly improves sensitivity, recovery and detection limits for the determination of trace amounts of iron, cobalt, nickel and zinc. The preconcentrated metals were determined using X-ray fluorescence spectrometry. The optimum parameters for electrodeposition such as pH, the volume of the analyzed solution, the voltage and the deposition time were studied. Under the optimized conditions, the detection limits were 5, 2, 3 and 6 μg L−1 for iron, cobalt, nickel and zinc, respectively. The precision and recovery of the method were in the range of 3–5.5%, and 92–103%, respectively. The calibration was performed using aqueous standards of Fe(III), Co(II), Ni(II) and Zn(II) in the range 0.01–0.25 mg L−1. The method was applied successfully in water analysis. - Highlights: ► A novel method of micro sample preparation for XRF analysis is proposed. ► Electrodeposition is performed using microcathode. ► A novel modification of electrodeposition method is using ionic liquid. ► The method can be combined with many techniques for multielement trace analysis

Availability note (English)

Available from http://dx.doi.org/10.1016/j.sab.2013.01.003

Additional details

Identifiers

DOI
10.1016/j.sab.2013.01.003;
PII
S0584-8547(13)00005-0;

Publishing Information

Journal Title
Spectrochimica Acta. Part B, Atomic Spectroscopy
Journal Volume
82
Journal Page Range
p. 60-64
ISSN
0584-8547
CODEN
SAASBH

Optional Information

Copyright
Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.