Abstract

This work describes a method to determine Cu at wide range concentrations in a single run without need of further dilutions employing high-resolution continuum source flame atomic absorption spectrometry. Different atomic lines for Cu at 324.754 nm, 327.396 nm, 222.570 nm, 249.215 nm and 224.426 nm were evaluated and main figures of merit established. Absorbance measurements at 324.754 nm, 249.215 nm and 224.426 nm allows the determination of Cu in the 0.07 – 5.0 mg L-1, 5.0 – 100 mg L-1 and 100 – 800 mg L-1 concentration intervals respectively with linear correlation coefficients better than 0.998. Limits of detection were 21 μg L-1, 310 μg L-1 and 1400 μg L-1 for 324.754 nm, 249.215 nm and 224.426 nm, respectively and relative standard deviations (n = 12) were £ 2.7%. The proposed method was applied to water samples spiked with Cu and the results were in agreement at a 95% of confidence level (paired t-test) with those obtained by line-source flame atomic absorption spectrometry.

Highlights

  • Copper is usually present at different concentration levels in a variety of workable samples [1]

  • The elemental determination by atomic absorption spectrometry [2,3] is frequently performed by line source spectrometers

  • The line-source flame atomic absorption spectrometry (LS FAAS) [4] is a worldwide, robust and well-established technique, the single-element analysis and narrow range calibration may be considered the main drawbacks of the technique when several elements are required: the changing and conditioning of hollow cathode lamps and the need for adjusting analyte absorbance within the linear working range of calibrating plots are time consuming and lead to increased analytical cost in large scale routine analyses [5]

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Summary

Introduction

Copper is usually present at different concentration levels in a variety of workable samples [1]. Little attention has been given to the use secondary and alternating lines in flame AAS to reduce sensitivity and increase the dynamic working range to determine low, intermediate and high levels of an element in a single run without need of further dilutions.

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