Abstract

In this work, a new mathematical equation correction approach for overcoming spectral and transport interferences was proposed. The proposal was applied to eliminate spectral interference caused by PO molecules at the 217.0005 nm Pb line, and the transport interference caused by variations in phosphoric acid concentrations. Correction may be necessary at 217.0005 nm to account for the contribution of PO, since Atotal 217.0005 nm = A Pb 217.0005 nm + A PO 217.0005 nm. This may be easily done by measuring other PO wavelengths (e.g. 217.0458 nm) and calculating the relative contribution of PO absorbance (APO) to the total absorbance (Atotal) at 217.0005 nm: A Pb 217.0005 nm = Atotal 217.0005 nm - A PO 217.0005 nm = Atotal 217.0005 nm - k (A PO 217.0458 nm). The correction factor k is calculated from slopes of calibration curves built up for phosphorous (P) standard solutions measured at 217.0005 and 217.0458 nm, i.e. k = (slope217.0005 nm/slope217.0458 nm). For wavelength integrated absorbance of 3 pixels, sample aspiration rate of 5.0 ml min-1, analytical curves in the 0.1 – 1.0 mg L-1 Pb range with linearity better than 0.9990 were consistently obtained.

Highlights

  • Among many factors affecting the determination of lead (Pb) in phosphoric acid by flame atomic absorption spectrometry spectral and transport interferences are considered the more important ones [1], since the analytical line at 217.0005 nm overlaps with PO molecular absorption bands at 216.99 nm in the air-acetylene flame [2], the alternate line at 283.3060 nm is recommended

  • And upon the introduction of a highresolution continuum source atomic absorption spectrometry (HR-CS AAS) [7], this problem has been overcome as the whole spectral environment around the analytical line can be acquired [8,9]

  • The feasibility of using mathematical equation correction previously employed in inductively coupled plasma mass spectrometry (ICP-MS), to eliminate spectral interference caused by PO molecules at the 217.0005 nm Pb line and transport interference caused by variations in phosphoric acid concentrations in the determination of Pb in phosphoric acid has been investigated

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Summary

Introduction

Among many factors affecting the determination of lead (Pb) in phosphoric acid by flame atomic absorption spectrometry spectral and transport interferences are considered the more important ones [1], since the analytical line at 217.0005 nm overlaps with PO molecular absorption bands at 216.99 nm in the air-acetylene flame [2], the alternate line at 283.3060 nm is recommended. And upon the introduction of a highresolution continuum source atomic absorption spectrometry (HR-CS AAS) [7], this problem has been overcome as the whole spectral environment around the analytical line can be acquired [8,9]. Using this technique, the interference caused by PO molecules at the main line for Pb at 217.0005 nm may be eliminated using the least-squares background correction (LSBC) [1]. The feasibility of using mathematical equation correction previously employed in ICP-MS, to eliminate spectral interference caused by PO molecules at the 217.0005 nm Pb line and transport interference caused by variations in phosphoric acid concentrations in the determination of Pb in phosphoric acid has been investigated

Materials and methods
Measurement procedure
Results and discussion
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