Low-level Ca-40 determinations using nitrous oxide with reaction cell inductively coupled plasma-tandem mass spectrometry

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Low-level Ca-40 determinations using nitrous oxide with reaction cell inductively coupled plasma-tandem mass spectrometry. / Lancaster, Shaun; Prohaska, Thomas; Irrgeher, Johanna.
In: Analytical and bioanalytical chemistry, Vol. 414.2022, No. October, 31.05.2022, p. 7495-7502.

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@article{72fffd0a421544f5ae2e0788e5467cd1,
title = "Low-level Ca-40 determinations using nitrous oxide with reaction cell inductively coupled plasma-tandem mass spectrometry",
abstract = "In inductively coupled plasma mass spectrometry, the most abundant Ca isotope ( 40Ca) suffers from isobaric interference with argon, hindering the potential for low detection limits of Ca. A powerful approach is to remove the interference by using a reaction gas in a reaction cell. Ammonia (NH 3) has proven to be an effective reaction gas by process of a charge transfer reaction. However, NH 3 is highly corrosive and toxic and cannot remove isobaric 40 K. Therefore, this work proposes the use of nitrous oxide (N 2O) to mass shift the target analyte 40Ca to 40Ca 16O + as a non-corrosive and non-toxic alternative. Instrument performance testing demonstrated that N 2O was capable of reaching equivalent detection limits (0.015 ng g −1) and background equivalence concentrations (0.041 ng g −1) to that of NH 3 and limited by the blank only. Further investigation of matrix interferences with synthetic standards highlighted that the N 2O approach supports the separation of potassium (K) and magnesium (Mg)–based interferences at tested concentrations of more than 600 times and almost 800 times higher than Ca respectively, whereas NH 3 was found to only support the removal of Mg. This work highlights a clear advantage of N 2O for low-level Ca determinations with high matrix loads, as well as compatibility with other instrumentation sensitive to corrosion that supports reaction cell technology. Graphical abstract: [Figure not available: see fulltext.]. ",
author = "Shaun Lancaster and Thomas Prohaska and Johanna Irrgeher",
note = "Publisher Copyright: {\textcopyright} 2022, The Author(s).",
year = "2022",
month = may,
day = "31",
doi = "10.1007/s00216-022-04146-9",
language = "English",
volume = "414.2022",
pages = "7495--7502",
journal = "Analytical and bioanalytical chemistry",
issn = "1618-2642",
publisher = "Springer Berlin",
number = "October",

}

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TY - JOUR

T1 - Low-level Ca-40 determinations using nitrous oxide with reaction cell inductively coupled plasma-tandem mass spectrometry

AU - Lancaster, Shaun

AU - Prohaska, Thomas

AU - Irrgeher, Johanna

N1 - Publisher Copyright: © 2022, The Author(s).

PY - 2022/5/31

Y1 - 2022/5/31

N2 - In inductively coupled plasma mass spectrometry, the most abundant Ca isotope ( 40Ca) suffers from isobaric interference with argon, hindering the potential for low detection limits of Ca. A powerful approach is to remove the interference by using a reaction gas in a reaction cell. Ammonia (NH 3) has proven to be an effective reaction gas by process of a charge transfer reaction. However, NH 3 is highly corrosive and toxic and cannot remove isobaric 40 K. Therefore, this work proposes the use of nitrous oxide (N 2O) to mass shift the target analyte 40Ca to 40Ca 16O + as a non-corrosive and non-toxic alternative. Instrument performance testing demonstrated that N 2O was capable of reaching equivalent detection limits (0.015 ng g −1) and background equivalence concentrations (0.041 ng g −1) to that of NH 3 and limited by the blank only. Further investigation of matrix interferences with synthetic standards highlighted that the N 2O approach supports the separation of potassium (K) and magnesium (Mg)–based interferences at tested concentrations of more than 600 times and almost 800 times higher than Ca respectively, whereas NH 3 was found to only support the removal of Mg. This work highlights a clear advantage of N 2O for low-level Ca determinations with high matrix loads, as well as compatibility with other instrumentation sensitive to corrosion that supports reaction cell technology. Graphical abstract: [Figure not available: see fulltext.].

AB - In inductively coupled plasma mass spectrometry, the most abundant Ca isotope ( 40Ca) suffers from isobaric interference with argon, hindering the potential for low detection limits of Ca. A powerful approach is to remove the interference by using a reaction gas in a reaction cell. Ammonia (NH 3) has proven to be an effective reaction gas by process of a charge transfer reaction. However, NH 3 is highly corrosive and toxic and cannot remove isobaric 40 K. Therefore, this work proposes the use of nitrous oxide (N 2O) to mass shift the target analyte 40Ca to 40Ca 16O + as a non-corrosive and non-toxic alternative. Instrument performance testing demonstrated that N 2O was capable of reaching equivalent detection limits (0.015 ng g −1) and background equivalence concentrations (0.041 ng g −1) to that of NH 3 and limited by the blank only. Further investigation of matrix interferences with synthetic standards highlighted that the N 2O approach supports the separation of potassium (K) and magnesium (Mg)–based interferences at tested concentrations of more than 600 times and almost 800 times higher than Ca respectively, whereas NH 3 was found to only support the removal of Mg. This work highlights a clear advantage of N 2O for low-level Ca determinations with high matrix loads, as well as compatibility with other instrumentation sensitive to corrosion that supports reaction cell technology. Graphical abstract: [Figure not available: see fulltext.].

UR - http://www.scopus.com/inward/record.url?scp=85131040497&partnerID=8YFLogxK

U2 - 10.1007/s00216-022-04146-9

DO - 10.1007/s00216-022-04146-9

M3 - Article

VL - 414.2022

SP - 7495

EP - 7502

JO - Analytical and bioanalytical chemistry

JF - Analytical and bioanalytical chemistry

SN - 1618-2642

IS - October

ER -