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Validation of an analytical method based on the high-resolution continuum source flame atomic absorption spectrometry for the fast-sequential determination of several hazardous/priority hazardous metals in soil

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TLDR
High-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.
Abstract
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. 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. The 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. High-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.

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Journal ArticleDOI

High-resolution continuum source atomic absorption spectrometry for the simultaneous or sequential monitoring of multiple lines. A critical review of current possibilities

TL;DR: In this article, the capabilities and limitations of commercially available high-resolution continuum source atomic absorption spectrometry instrumentation for multi-line monitoring are examined, discussing in detail the possible strategies to develop multi-element methodologies that are truly simultaneous, or else sequential, but from the same sample aliquot.
Journal ArticleDOI

High-Resolution Continuum Source AAS: The Better Way to Do Atomic Absorption Spectrometry By Bernard Welz (Universdade Federal de Santa Caterina, Florianoplis, Brazil), Helmut Becker-Ross, Stefan Florek, and Uwe Heitmann (ISAS, Institute for Analytical Sciences, Berlin). Wiley-VCH Verlag GmbH & Co. KgaA: Weinheim, Germany. 2005. xii + 295 pp. $130.00. ISBN 3-527-30736-2.

TL;DR: Welz and Sperling as discussed by the authors provided the first complete and comprehensive discussion of high-resolution continuum source atomic absorption spectrometry (HR-CS AAS) and its application to the analysis of a variety of difficult matrices.
Journal ArticleDOI

Removal of Pb and Hg from marine intertidal sediment by using rhamnolipid biosurfactant produced by a Pseudomonas aeruginosa strain

TL;DR: In this article, two heavy metals, lead (Pb) and mercury (Hg), in marine intertidal sediment were removed by prepared rhamnolipid biosurfactant (RB) in laboratory scale.
Journal ArticleDOI

Use of High-Resolution Continuum Source Flame Atomic Absorption Spectrometry (HR-CS FAAS) for Sequential Multi-Element Determination of Metals in Seawater and Wastewater Samples

TL;DR: In this paper, a method for the determination of metals in saline matrices using high-resolution continuum source flame atomic absorption spectrometry (HR-CS FAAS) was developed.
Journal ArticleDOI

Application of low-cost electrothermal vaporization capacitively coupled plasma microtorch optical emission spectrometry for simultaneous determination of Cd and Pb in environmental samples

TL;DR: In this paper, the applicability and analytical capability of a laboratory miniaturized system including a small-sized electrothermal vaporizer with Rh filament and a low power (15W) and low Ar consumption (150mlmin−−1) capacitively coupled plasma microtorch interfaced with a low resolution microspectrometer for the simultaneous determination of Cd and Pb in environmental samples by optical emission spectrometry.
References
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Statistical methods for assessing agreement between two methods of clinical measurement.

TL;DR: An alternative approach, based on graphical techniques and simple calculations, is described, together with the relation between this analysis and the assessment of repeatability.
Journal ArticleDOI

Statistical methods for assessing agreement between two methods of clinical measurement

TL;DR: In this article, an alternative approach, based on graphical techniques and simple calculations, is described, together with the relation between this analysis and the assessment of repeatability, which is often used in clinical comparison of a new measurement technique with an established one.
Journal ArticleDOI

Measuring agreement in method comparison studies

TL;DR: The 95% limits of agreement, estimated by mean difference 1.96 standard deviation of the differences, provide an interval within which 95% of differences between measurements by the two methods are expected to lie.
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