A Comparison of Reproducibility of Inductively Coupled Spectrometric Techniques in Soil Metal Analyses. Issue 12 (August 2019)

• Record Type: Journal Article
• Authors: Nyika, Joan; Onyari, Ednah; Dinka, Megersa Olumana; Mishra, Shivani Bhardwaj
• Is Part Of: Air, soil and water research. Volume 2019:Issue 12(2019)
• Publication Date: 2019-08
• Subjects: Bias -- errors -- spectrometry -- metals -- reproducibility -- soils; Air quality -- Research -- Periodicals; Soil science -- Periodicals; Water quality -- Research -- Periodicals; Conservation of natural resources -- Research -- Periodicals; Conservation of natural resources -- Periodicals; Agricultural conservation -- Research -- Periodicals; 363.7
• DOI: 10.1177/1178622119869002
• Languages: English
• ISSNs: 1178-6221

Abstract

Precise estimation of metals in samples remains a challenge as a result of analytical biases and errors, which occur at sample collection, preparation, and measurement stages. A poor understanding of the nature and occurrence of these errors further aggravates this challenge. This study aimed at comparing the effectiveness of inductively coupled plasma (ICP) mass spectrometry (MS) and optical emission spectrometry (OES) techniques in quantifying metals from contaminated soils of Roundhill landfill vicinity. Using statistical tools, the study evaluated biases of the 2 methods. High coefficients of variation were realized for V, Cr, and Pb concentrations varied at various sampling sites. Concentrations of elements obtained using the 2 methods had no significant differences using t -test analysis. Definitive agreement for the 2 methods was observed for V, Cr, Co, Ni, Cu, Zn, Sr, and Pb concentrations, whereas the concentrations of Mg, Ca, Ti, Mn, and Fe showed some deviations in their regression lines. Spectral, systematic, memory, and carry over errors could be attributable to these deviations. The errors promote chelation and adsorption of ions in samples to form insoluble compounds that cannot be quantified. Overall, ICP-MS had greater sensitivity than ICP-OES in trace elements analysis compared with major elements.