Research output: Contribution to journal › Article › peer-review
Selection of Internal Standards for Determining Rare-Earth Elements by Microwave Induced Plasma Optical Emission Spectrometry. / Kim, P. V.; Polyakova, E. V.; Nikolaev, R. E.
In: Journal of Analytical Chemistry, Vol. 79, No. 4, 04.2024, p. 440-446.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Selection of Internal Standards for Determining Rare-Earth Elements by Microwave Induced Plasma Optical Emission Spectrometry
AU - Kim, P. V.
AU - Polyakova, E. V.
AU - Nikolaev, R. E.
N1 - The work was supported by the Russian Science Foundation (project no. 22-43-02079) and the Ministry of Science and Higher Education of the Russian Federation.
PY - 2024/4
Y1 - 2024/4
N2 - Microwave plasma atomic emission spectrometry is used to determine the composition of lanthanum sulfide and europium-doped gadolinium oxide crystals, and also of elements in the melt (tin, boron, and lithium). Calibration dependencies for rare-earth elements were found to be nonlinear and did not meet the required accuracy. The internal standard method was used to minimize errors and linearize calibration dependences. Molecular species N2,, and OH did not affect plasma conditions or interelement influences. Internal standards were selected based on the proximity of their first ionization potential to that of the analytes; Ba, Al, Ga, and In were considered. Using these elements as internal standards enabled the linearization of the calibration dependences, achieving an recovery of 95–105%. The determined total mass of elements was 97–103% of the sample weight, with accuracy confirmed by the standard addition method.
AB - Microwave plasma atomic emission spectrometry is used to determine the composition of lanthanum sulfide and europium-doped gadolinium oxide crystals, and also of elements in the melt (tin, boron, and lithium). Calibration dependencies for rare-earth elements were found to be nonlinear and did not meet the required accuracy. The internal standard method was used to minimize errors and linearize calibration dependences. Molecular species N2,, and OH did not affect plasma conditions or interelement influences. Internal standards were selected based on the proximity of their first ionization potential to that of the analytes; Ba, Al, Ga, and In were considered. Using these elements as internal standards enabled the linearization of the calibration dependences, achieving an recovery of 95–105%. The determined total mass of elements was 97–103% of the sample weight, with accuracy confirmed by the standard addition method.
KW - MIP-OES
KW - REE
KW - calibration dependences
KW - internal standards
UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85190246092&origin=inward&txGid=74aaa5d8de3b6721498d91c38b01fa32
UR - https://www.mendeley.com/catalogue/fbaa4b12-8359-3740-90f2-87c9d75b1f69/
U2 - 10.1134/S1061934824040087
DO - 10.1134/S1061934824040087
M3 - Article
VL - 79
SP - 440
EP - 446
JO - Journal of Analytical Chemistry
JF - Journal of Analytical Chemistry
SN - 1061-9348
IS - 4
ER -
ID: 61072334