2004Journal of Analytical Atomic SpectrometryRequires access

Speciation of selenium and tellurium in milk by hydride generation atomic fluorescence spectrometry

Patricia Cava‐Montesinos, Alberto Guardia, Carmen Teutsch, M. Luisa Cervera, Miguel de la Guárdia

Open publisher page 31 citations

Abstract

A simple, fast and highly sensitive method has been developed for the differentiation of Se and Te into their (IV) and (VI) oxidation states in milk samples by HG-AFS. This procedure involves a previous leaching of milk slurries by sonication with aqua regia for 10 min. Se(IV) and Te(IV) were determined by analysis of the samples without a pre-reduction step; being total Se and Te determined after reduction with KBr. The method provides limit of detection values (LOD) of 0.012 and 0.023 ng ml−1 for Se(IV) and Te(IV) respectively. Average relative standard deviation values of 10.5%, 3.9%, 12% and 12.5% were found for the determination of Se(IV), Se(VI), Te(IV) and Te(VI) in milk samples containing Se from 11.1 to 32.2 ng g−1 and Te from 1.1 to 10 ng g−1. Recovery experiments made on actual samples spiked with Se(IV), Se(VI), Te(IV) and Te(VI) evidenced that the sonication with aqua regia does not modify the oxidation state of the elements considered.

About this research paper

What this paper is about

A simple, fast and highly sensitive method has been developed for the differentiation of Se and Te into their (IV) and (VI) oxidation states in milk samples by HG-AFS. This procedure involves a previous leaching of milk slurries by sonication with aqua regia for 10 min. Se(IV) and Te(IV) were determined by analysis of the samples without a pre-reduction step; being total Se and Te determined after reduction with KBr. The method provides limit of detection values (LOD) of 0.012 and 0.023 ng ml−1 for Se(IV) and Te(IV) respectively. Average relative standard deviation values of 10.5%, 3.9%, 12% and 12.5% were found for the determination of Se(IV), Se(VI), Te(IV) and Te(VI) in milk samples containing Se from 11.1 to 32.2 ng g−1 and Te from 1.1 to 10 ng g−1. Recovery experiments made on actual samples spiked with Se(IV), Se(VI), Te(IV) and Te(VI) evidenced that the sonication with aqua regia does not modify the oxidation state of the elements considered.

Why it matters

OpenAlex reports 31 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

A simple, fast and highly sensitive method has been developed for the differentiation of Se and Te into their (IV) and (VI) oxidation states in milk samples by HG-AFS. This procedure involves a previous leaching of milk slurries by sonication with aqua regia for 10 min. Se(IV) and Te(IV) were determined by analysis of the samples without a pre-reduction step; being total Se and Te determined after reduction with KBr. The method provides limit of detection values (LOD) of 0.012 and 0.023 ng ml−1 for Se(IV) and Te(IV) respectively. Average relative standard deviation values of 10.5%, 3.9%, 12% and 12.5% were found for the determination of Se(IV), Se(VI), Te(IV) and Te(VI) in milk samples containing Se from 11.1 to 32.2 ng g−1 and Te from 1.1 to 10 ng g−1. Recovery experiments made on actual samples spiked with Se(IV), Se(VI), Te(IV) and Te(VI) evidenced that the sonication with aqua regia does not modify the oxidation state of the elements considered.

Key concepts: Aqua regia, Chemistry, Selenium, Detection limit, Tellurium, Hydride, Analytical Chemistry (journal), Sonication

Related papers

Back to paper searchBrowse research topicsOriginal source
Speciation of selenium and tellurium in milk by hydride generation atomic fluorescence spectrometry — Research Paper | ScholarLens