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
SN - 1618-2642
VL - 414.2022
SP - 7495
EP - 7502
JO - Analytical and bioanalytical chemistry
JF - Analytical and bioanalytical chemistry
IS - October
ER -