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Lanthanoid analysis in seawater by seaFAST-SP3™ system in off-line mode and magnetic sector high-resolution inductively coupled plasma source mass spectrometer

Analysis of lanthanoids in seawater is challenging due to the complex matrix (∼35 g L(−1) TDS) and low dissolved concentrations (in ng L(−1)). A 4-step strict analytical protocol and state-of-the-art technology were implemented and validated in this study. The 4-steps method involves the 1) sample f...

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Autores principales: Soto-Jiménez, M.F., Martinez-Salcido, A.I., Morton-Bermea, O., Ochoa-Izaguirre, M.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850790/
https://www.ncbi.nlm.nih.gov/pubmed/35198416
http://dx.doi.org/10.1016/j.mex.2022.101625
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author Soto-Jiménez, M.F.
Martinez-Salcido, A.I.
Morton-Bermea, O.
Ochoa-Izaguirre, M.J.
author_facet Soto-Jiménez, M.F.
Martinez-Salcido, A.I.
Morton-Bermea, O.
Ochoa-Izaguirre, M.J.
author_sort Soto-Jiménez, M.F.
collection PubMed
description Analysis of lanthanoids in seawater is challenging due to the complex matrix (∼35 g L(−1) TDS) and low dissolved concentrations (in ng L(−1)). A 4-step strict analytical protocol and state-of-the-art technology were implemented and validated in this study. The 4-steps method involves the 1) sample filtration and acidification (pH<2); 2) pre-concentration by the matrix separation system, 3) off-line injection of the eluted sample; and 4) determination of lanthanoids by high-resolution inductively coupled plasma mass spectrometer (HR-ICP-MS). Since there are no certified values for lanthanoids in seawater are available, the method validation was done by analyzing SLEW-3 (estuarine water reference samples) and comparing with other reports and artificial seawater (100 ng L(−1) lanthanoid multi-element standard solutions). SLEW-3 recovery varied from 78.6% to 106% and in artificial samples it ranged from 87 to 110%. Low recovery can be explained by complex organic in seawater, because the UV oxidation was not performed in the acidified samples. The variation was ≤10%, except for Gd, Tb, and Yb (11–13.75%). Blanks varied between 0.01 and 0.07 ng L(−1), except for La and Ce (0.13–0.21 ng L(−1)). Blanks represent <5% SLEW-3 values and <1% synthetic seawater. The procedural detection limit varied from 0.01 to 0.03 ng L(−1). • Lanthanoids as geochemical tracers in seawaters; • A 4-step strict analytical protocol and state-of-the-art technology for lanthanoids analyses in seawaters; • Sample pre-concentration system for matrix separation for the detection of ultra-low lanthanoids levels.
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spelling pubmed-88507902022-02-22 Lanthanoid analysis in seawater by seaFAST-SP3™ system in off-line mode and magnetic sector high-resolution inductively coupled plasma source mass spectrometer Soto-Jiménez, M.F. Martinez-Salcido, A.I. Morton-Bermea, O. Ochoa-Izaguirre, M.J. MethodsX Method Article Analysis of lanthanoids in seawater is challenging due to the complex matrix (∼35 g L(−1) TDS) and low dissolved concentrations (in ng L(−1)). A 4-step strict analytical protocol and state-of-the-art technology were implemented and validated in this study. The 4-steps method involves the 1) sample filtration and acidification (pH<2); 2) pre-concentration by the matrix separation system, 3) off-line injection of the eluted sample; and 4) determination of lanthanoids by high-resolution inductively coupled plasma mass spectrometer (HR-ICP-MS). Since there are no certified values for lanthanoids in seawater are available, the method validation was done by analyzing SLEW-3 (estuarine water reference samples) and comparing with other reports and artificial seawater (100 ng L(−1) lanthanoid multi-element standard solutions). SLEW-3 recovery varied from 78.6% to 106% and in artificial samples it ranged from 87 to 110%. Low recovery can be explained by complex organic in seawater, because the UV oxidation was not performed in the acidified samples. The variation was ≤10%, except for Gd, Tb, and Yb (11–13.75%). Blanks varied between 0.01 and 0.07 ng L(−1), except for La and Ce (0.13–0.21 ng L(−1)). Blanks represent <5% SLEW-3 values and <1% synthetic seawater. The procedural detection limit varied from 0.01 to 0.03 ng L(−1). • Lanthanoids as geochemical tracers in seawaters; • A 4-step strict analytical protocol and state-of-the-art technology for lanthanoids analyses in seawaters; • Sample pre-concentration system for matrix separation for the detection of ultra-low lanthanoids levels. Elsevier 2022-01-27 /pmc/articles/PMC8850790/ /pubmed/35198416 http://dx.doi.org/10.1016/j.mex.2022.101625 Text en © 2022 Published by Elsevier B.V. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Method Article
Soto-Jiménez, M.F.
Martinez-Salcido, A.I.
Morton-Bermea, O.
Ochoa-Izaguirre, M.J.
Lanthanoid analysis in seawater by seaFAST-SP3™ system in off-line mode and magnetic sector high-resolution inductively coupled plasma source mass spectrometer
title Lanthanoid analysis in seawater by seaFAST-SP3™ system in off-line mode and magnetic sector high-resolution inductively coupled plasma source mass spectrometer
title_full Lanthanoid analysis in seawater by seaFAST-SP3™ system in off-line mode and magnetic sector high-resolution inductively coupled plasma source mass spectrometer
title_fullStr Lanthanoid analysis in seawater by seaFAST-SP3™ system in off-line mode and magnetic sector high-resolution inductively coupled plasma source mass spectrometer
title_full_unstemmed Lanthanoid analysis in seawater by seaFAST-SP3™ system in off-line mode and magnetic sector high-resolution inductively coupled plasma source mass spectrometer
title_short Lanthanoid analysis in seawater by seaFAST-SP3™ system in off-line mode and magnetic sector high-resolution inductively coupled plasma source mass spectrometer
title_sort lanthanoid analysis in seawater by seafast-sp3™ system in off-line mode and magnetic sector high-resolution inductively coupled plasma source mass spectrometer
topic Method Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850790/
https://www.ncbi.nlm.nih.gov/pubmed/35198416
http://dx.doi.org/10.1016/j.mex.2022.101625
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