Possibility of isotopic analysis of lithium using an inductively coupled plasma and a selective interference spectrometer

1986 ◽  
Vol 44 (1) ◽  
pp. 10-14
Author(s):  
L. V. Egorova ◽  
M. A. Kartasheva ◽  
I. E. Leshcheva ◽  
M. E. Sidorenko
2021 ◽  
Vol 25 (2) ◽  
pp. 98-109
Author(s):  
P. A. Otopkova ◽  
◽  
A. M. Potapov ◽  
A. I. Suchkov ◽  
A. D. Bulanov ◽  
...  

In order to study the isotopic effects in semiconductor materials, single crystals of high chemical and isotopic purity are required. The reliability of the obtained data on the magnitude and the direction of isotopic shifts depends on the accuracy of determining the concentration of all stable isotopes. In the isotopic analysis of enriched “silicon-28” with a high degree of enrichment (> 99.99%), it is necessary to determine the impurities of 29Si and 30Si isotopes at the level of 10-3 ¸ 10-5 at. %. At this concentration level, these isotopes can be considered as impurities. It is difficult to achieve high measurement accuracy with simultaneous registration of the main and “impurity” isotopes in such a wide range of concentrations. The registration of analytical signals of silicon isotopes must be carried out in the solutions with different matrix concentrations. The use of the solutions with the high concentration of the matrix element requires the introduction of corrections for matrix noise and the drift of the instrument sensitivity during the measurement. It is possible to reduce the influence of the irreversible non-spectral interference and sensitivity drift by using the method of internal standardization. The inconsistency of the literature data on the selection criteria for the internal standard required studying the behavior of the signals of the “candidates for the internal standard” for the ELEMENT 2 single-collector high-resolution inductively coupled plasma mass spectrometer on the matrix element concentration and the nature of the solvent, as well as on the solution nebulizing time. Accounting for the irreversible non-spectral matrix noise and instrumental drift in isotopic analysis of enriched “silicon-28” and initial 28SiF4 by inductively coupled plasma mass spectrometry had allowed us to reduce by 3-5 times the random component and by more than an order of magnitude the systematic component of the measurement error in comparison with the external standard method. This made it possible to carry out, with sufficient accuracy, the operational control of the isotopic composition of enriched “silicon-28”, both in the form of silicon tetrafluoride and polycrystalline silicon obtained from it, using a single serial device in the range of isotopic concentrations 0.0001–99.999%.


2020 ◽  
Vol 35 (3) ◽  
pp. 560-566
Author(s):  
Jakub Karasiński ◽  
Cuc Thi Nguyen-Marcińczyk ◽  
Marcin Wojciechowski ◽  
Ewa Bulska ◽  
Ludwik Halicz

A robust and sensitive method for the precise isotopic analysis of 53Cr/50Cr during Cr(iii) oxidation by coupling ion pair reversed-phase chromatography and Multicollector Inductively Coupled Plasma Mass Spectrometry (MC-ICPMS) is presented.


2017 ◽  
Vol 32 (2) ◽  
pp. 314-321 ◽  
Author(s):  
Yulia Anoshkina ◽  
Marta Costas-Rodríguez ◽  
Frank Vanhaecke

The use of VAMS – volumetric absorptive microsampling – of finger-prick blood was evaluated in the context of high-precision isotopic analysis of whole blood Fe by multi-collector inductively coupled plasma-mass spectrometry.


2015 ◽  
Vol 30 (1) ◽  
pp. 296-309 ◽  
Author(s):  
M. Aramendía ◽  
L. Rello ◽  
S. Bérail ◽  
A. Donnard ◽  
C. Pécheyran ◽  
...  

This work presents a method that enables the direct elemental and isotopic analysis of dried blood spots using LA-ICPMS.


2016 ◽  
Vol 31 (7) ◽  
pp. 1459-1463 ◽  
Author(s):  
Jakub Karasinski ◽  
Ewa Bulska ◽  
Marcin Wojciechowski ◽  
Agnieszka Anna Krata ◽  
Ludwik Halicz

In this work a high throughput, robust and sensitive method for the precise isotopic analysis of 87Sr/86Sr by coupling Ion Chromatography (IC) and Multicollector Inductively Coupled Plasma Mass Spectrometry (MC-ICPMS) is presented.


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