Nitric acid effect in inductively coupled plasma mass spectrometry: new insights on possible causes and correction

Fundamental aspects related to the analysis of nitric acid solutions by inductively coupled plasma mass spectrometry have been critically revisited in order to provide new insights into the possible sources of non-spectroscopic matrix effects and their correction by internal standardization. For ele...

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Published in:Journal of Analytical Atomic Spectrometry
Main Authors: Grotti, Marco, Todolí Torró, José Luis
Other Authors: Universidad de Alicante. Departamento de Química Analítica, Nutrición y Bromatología, Análisis de Polímeros y Nanomateriales
Format: Article in Journal/Newspaper
Language:English
Published: Royal Society of Chemistry 2020
Subjects:
Online Access:http://hdl.handle.net/10045/109046
https://doi.org/10.1039/D0JA00130A
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spelling ftunivalicante:oai:rua.ua.es:10045/109046 2023-05-15T13:46:48+02:00 Nitric acid effect in inductively coupled plasma mass spectrometry: new insights on possible causes and correction Grotti, Marco Todolí Torró, José Luis Universidad de Alicante. Departamento de Química Analítica, Nutrición y Bromatología Análisis de Polímeros y Nanomateriales 2020-06-19 http://hdl.handle.net/10045/109046 https://doi.org/10.1039/D0JA00130A eng eng Royal Society of Chemistry https://doi.org/10.1039/D0JA00130A info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PGC2018-100711-B-I00 Journal of Analytical Atomic Spectrometry. 2020, 35: 1959-1968. https://doi.org/10.1039/D0JA00130A 0267-9477 (Print) 1364-5544 (Online) http://hdl.handle.net/10045/109046 doi:10.1039/D0JA00130A © The Royal Society of Chemistry 2020 info:eu-repo/semantics/restrictedAccess Nitric acid effect Inductively coupled plasma Mass spectrometry Química Analítica info:eu-repo/semantics/article 2020 ftunivalicante https://doi.org/10.1039/D0JA00130A 2021-06-22T23:16:58Z Fundamental aspects related to the analysis of nitric acid solutions by inductively coupled plasma mass spectrometry have been critically revisited in order to provide new insights into the possible sources of non-spectroscopic matrix effects and their correction by internal standardization. For elements having first ionization potential (IP) lower than 7.5 eV, the increase in the signal due to nitric acid was ascribed to a delay in the ionization process, which resulted in a reduction of the ion lateral diffusion in the plasma. In contrast, for non-easily ionisable elements, signal depression was correlated with their IP value and attributed to the cooling effect due to the energy required for nitric acid dissociation. Moreover, the atomic mass did not show any significant effect, thus precluding the application of the widely accepted criterion of choice of internal standards based on matching of masses. The extent and sign of the acid effect also depended on the applied operating conditions. For elements with low IP (e.g. Co, Cs, In, Li, Pb, Y), nitric acid caused signal enhancement at high RF power and nebulizer gas flow rate values (i.e., plasma robust conditions) and signal depression under non-robust conditions. For elements with high IP (e.g. As, Be, Cd and Sb), the decreasing acid effect became stronger with increasing the nebulizer gas flow rate and decreasing the RF power. The acid effect was also influenced by the ion lens voltage, that significantly interacted with the RF power effect. Finally, a procedure for the selection of optimal internal standards by principal component analysis has been successfully applied for the correction of the nitric acid effect. This work has been funded by the Italian National Program of Research in Antarctica (projects PNRA14_00091 and PNRA16_00252) and the Spanish Ministry of Science, Innovation and Universities for the financial support (Project Ref. PGC2018-100711-B-I00). Article in Journal/Newspaper Antarc* Antarctica RUA - Repositorio Institucional de la Universidad de Alicante Journal of Analytical Atomic Spectrometry 35 9 1959 1968
institution Open Polar
collection RUA - Repositorio Institucional de la Universidad de Alicante
op_collection_id ftunivalicante
language English
topic Nitric acid effect
Inductively coupled plasma
Mass spectrometry
Química Analítica
spellingShingle Nitric acid effect
Inductively coupled plasma
Mass spectrometry
Química Analítica
Grotti, Marco
Todolí Torró, José Luis
Nitric acid effect in inductively coupled plasma mass spectrometry: new insights on possible causes and correction
topic_facet Nitric acid effect
Inductively coupled plasma
Mass spectrometry
Química Analítica
description Fundamental aspects related to the analysis of nitric acid solutions by inductively coupled plasma mass spectrometry have been critically revisited in order to provide new insights into the possible sources of non-spectroscopic matrix effects and their correction by internal standardization. For elements having first ionization potential (IP) lower than 7.5 eV, the increase in the signal due to nitric acid was ascribed to a delay in the ionization process, which resulted in a reduction of the ion lateral diffusion in the plasma. In contrast, for non-easily ionisable elements, signal depression was correlated with their IP value and attributed to the cooling effect due to the energy required for nitric acid dissociation. Moreover, the atomic mass did not show any significant effect, thus precluding the application of the widely accepted criterion of choice of internal standards based on matching of masses. The extent and sign of the acid effect also depended on the applied operating conditions. For elements with low IP (e.g. Co, Cs, In, Li, Pb, Y), nitric acid caused signal enhancement at high RF power and nebulizer gas flow rate values (i.e., plasma robust conditions) and signal depression under non-robust conditions. For elements with high IP (e.g. As, Be, Cd and Sb), the decreasing acid effect became stronger with increasing the nebulizer gas flow rate and decreasing the RF power. The acid effect was also influenced by the ion lens voltage, that significantly interacted with the RF power effect. Finally, a procedure for the selection of optimal internal standards by principal component analysis has been successfully applied for the correction of the nitric acid effect. This work has been funded by the Italian National Program of Research in Antarctica (projects PNRA14_00091 and PNRA16_00252) and the Spanish Ministry of Science, Innovation and Universities for the financial support (Project Ref. PGC2018-100711-B-I00).
author2 Universidad de Alicante. Departamento de Química Analítica, Nutrición y Bromatología
Análisis de Polímeros y Nanomateriales
format Article in Journal/Newspaper
author Grotti, Marco
Todolí Torró, José Luis
author_facet Grotti, Marco
Todolí Torró, José Luis
author_sort Grotti, Marco
title Nitric acid effect in inductively coupled plasma mass spectrometry: new insights on possible causes and correction
title_short Nitric acid effect in inductively coupled plasma mass spectrometry: new insights on possible causes and correction
title_full Nitric acid effect in inductively coupled plasma mass spectrometry: new insights on possible causes and correction
title_fullStr Nitric acid effect in inductively coupled plasma mass spectrometry: new insights on possible causes and correction
title_full_unstemmed Nitric acid effect in inductively coupled plasma mass spectrometry: new insights on possible causes and correction
title_sort nitric acid effect in inductively coupled plasma mass spectrometry: new insights on possible causes and correction
publisher Royal Society of Chemistry
publishDate 2020
url http://hdl.handle.net/10045/109046
https://doi.org/10.1039/D0JA00130A
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_relation https://doi.org/10.1039/D0JA00130A
info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PGC2018-100711-B-I00
Journal of Analytical Atomic Spectrometry. 2020, 35: 1959-1968. https://doi.org/10.1039/D0JA00130A
0267-9477 (Print)
1364-5544 (Online)
http://hdl.handle.net/10045/109046
doi:10.1039/D0JA00130A
op_rights © The Royal Society of Chemistry 2020
info:eu-repo/semantics/restrictedAccess
op_doi https://doi.org/10.1039/D0JA00130A
container_title Journal of Analytical Atomic Spectrometry
container_volume 35
container_issue 9
container_start_page 1959
op_container_end_page 1968
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