Abstract

BackgroundThe aim of this paper was the validation of a new analytical method based on the high-resolution continuum source flame atomic absorption spectrometry for the fast-sequential determination of several hazardous/priority hazardous metals (Ag, Cd, Co, Cr, Cu, Ni, Pb and Zn) in soil after microwave assisted digestion in aqua regia. Determinations were performed on the ContrAA 300 (Analytik Jena) air-acetylene flame spectrometer equipped with xenon short-arc lamp as a continuum radiation source for all elements, double monochromator consisting of a prism pre-monocromator and an echelle grating monochromator, and charge coupled device as detector. For validation a method-performance study was conducted involving the establishment of the analytical performance of the new method (limits of detection and quantification, precision and accuracy). Moreover, the Bland and Altman statistical method was used in analyzing the agreement between the proposed assay and inductively coupled plasma optical emission spectrometry as standardized method for the multielemental determination in soil.ResultsThe limits of detection in soil sample (3σ criterion) in the high-resolution continuum source flame atomic absorption spectrometry method were (mg/kg): 0.18 (Ag), 0.14 (Cd), 0.36 (Co), 0.25 (Cr), 0.09 (Cu), 1.0 (Ni), 1.4 (Pb) and 0.18 (Zn), close to those in inductively coupled plasma optical emission spectrometry: 0.12 (Ag), 0.05 (Cd), 0.15 (Co), 1.4 (Cr), 0.15 (Cu), 2.5 (Ni), 2.5 (Pb) and 0.04 (Zn). Accuracy was checked by analyzing 4 certified reference materials and a good agreement for 95% confidence interval was found in both methods, with recoveries in the range of 94–106% in atomic absorption and 97–103% in optical emission. Repeatability found by analyzing real soil samples was in the range 1.6–5.2% in atomic absorption, similar with that of 1.9–6.1% in optical emission spectrometry. The Bland and Altman method showed no statistical significant difference between the two spectrometric methods for 95% confidence interval.ConclusionsHigh-resolution continuum source flame atomic absorption spectrometry can be successfully used for the rapid, multielemental determination of hazardous/priority hazardous metals in soil with similar analytical performances to those in inductively coupled plasma optical emission spectrometry.

Highlights

  • The aim of this paper was the validation of a new analytical method based on the high-resolution continuum source flame atomic absorption spectrometry for the fast-sequential determination of several hazardous/priority hazardous metals (Ag, Cd, Co, Cr, Cu, Ni, Pb and Zn) in soil after microwave assisted digestion in aqua regia

  • To face the challenges of the inductively coupled plasma optical emission spectrometry (ICP-Optical emission spectrometry (OES)), which imposed itself as a fast multielemental technique due to the charged-coupled device (CCD) technology, the need to increase the versatility of Low-resolution line source atomic absorption spectrometry (AAS) with respect to line selection, background correction and higher analysis speed became imperative

  • This paper reports on the validation of an analytical method for the fast-sequential determination of several hazardous/priority hazardous metals (Ag, Cd, Cr, Co, Cu, Ni, Pb and Zn) in soil based on the HR-CS High-resolution continuum source flame atomic absorption spectrometry (FAAS)

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Summary

Introduction

The aim of this paper was the validation of a new analytical method based on the high-resolution continuum source flame atomic absorption spectrometry for the fast-sequential determination of several hazardous/priority hazardous metals (Ag, Cd, Co, Cr, Cu, Ni, Pb and Zn) in soil after microwave assisted digestion in aqua regia. The extremely well acceptance of HR-CS AAS instrument after its introduction on the market together with the versatility of the analytical applications was reflected in several reviews [5,6,7,8,9,10,11] Both approaches of the technique, using either flame or electrothermal atomization, were used for multielemental determination in various complex matrices. HRCS GFAAS was mentioned for elemental determination in food after acidic digestion or extraction in tetramethylammonium hydroxide [12,13,14], airborne particulates [15,16,17,18], biological (beans and grain) samples using direct solid sampling [19,20,21], fertilizer by slurry sampling [22], crude oil [23,24,25,26], biodiesel [27] and in whole blood directly in diluted/undiluted samples [28]

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