scholarly journals Linearity testing and dead-time determination for MC-ICP-MS ion counters using the IRMM-072 series of uranium isotope reference materials

2016 ◽  
Vol 31 (8) ◽  
pp. 1647-1657 ◽  
Author(s):  
S. Richter ◽  
S. Konegger-Kappel ◽  
S. F. Boulyga ◽  
G. Stadelmann ◽  
A. Koepf ◽  
...  

The IRMM-072 series of reference materials is applied to perform linearity testing and dead time determinations for the ion counters on two MC-ICP-MS mass spectrometers at the IAEA.

2019 ◽  
Author(s):  
Ingo Strenge ◽  
Carsten Engelhard

<p>The article demonstrates the importance of using a suitable approach to compensate for dead time relate count losses (a certain measurement artefact) whenever short, but potentially strong transient signals are to be analysed using inductively coupled plasma mass spectrometry (ICP-MS). Findings strongly support the theory that inadequate time resolution, and therefore insufficient compensation for these count losses, is one of the main reasons for size underestimation observed when analysing inorganic nanoparticles using ICP-MS, a topic still controversially discussed.</p>


2019 ◽  
Vol 85 (6) ◽  
pp. 11-24
Author(s):  
I. V. Nikolaeva ◽  
A. A. Kravchenko ◽  
S. V. Palessky ◽  
S. V. Nechepurenko ◽  
D. V. Semenova

Two methods — ICP-MS and ICP-AES are used for certification of the new reference material — needles of Siberian pine (NSP-1). Techniques of the analysis include decomposition of plant samples in two different ways: acid digestion in a microwave system MARS-5 and lithium metaborate fusion followed by ICP-MS and ICP-AES analysis of the solutions. Simultaneous determinations of all the elements were carried out in low, medium and high resolution using SF-mass-spectrometer ELEMENT and atomic-emission spectrometer IRIS Advantage with external calibrations and internal standards (In — ICP-MS, Sc —ICP-AES). Middle and high resolutions of ICP mass spectrometer were used for interference corrections. Data obtained by ICP-MS and ICP-AES with different decomposition techniques are in good agreement. The ICP-MS and ICP-AES techniques have been validated by the analysis of three plant reference materials: LB-1 (leaf of a birch), Tr-1 (grass mixture) and EK-1 (Canadian pondweed). These techniques were used for the determination of 38 elements in the new reference material NSP-1. Relative standard deviations for most of the determined elements were below 10%. Combination of ICP-MS and ICP-AES techniques for certification of the new reference material makes it possible to expand the set of elements to be determined and to reduce the total analysis time.


Author(s):  
Lei Xu ◽  
Wen Zhang ◽  
Tao Luo ◽  
Jin-Hui Yang ◽  
Zhaochu Hu

High precise and accurate measurements of Fe isotope ratios for fourteen reference materials from the USGS, MPI-DING and CGSG were successfully carried out using a developed analytical technique by fs...


Author(s):  
Zhian Bao ◽  
Kaiyun Chen ◽  
Chunlei Zong ◽  
Honglin Yuan

Sulfur isotope is an important geochemical tracer in diverse fields of geosciences. Controlling the accuracy and precision of microanalysis of sulfur isotope requires well-characterized reference materials with matrices similar to...


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Richard M. Essex ◽  
Lav Tandon ◽  
Amy Gaffney ◽  
Cole R. Hexel ◽  
Debbie A. Bostick ◽  
...  

Abstract Two plutonium oxides were prepared as unique reference materials for measurement of actinide elements present as trace constituents. Each reference material unit is approximately 200 mg of PuO2 powder in a quartz glass bottle. Characterized attributes of the oxides included mass fractions of plutonium, americium, neptunium, and uranium. Isotope-amount ratios were also determined for plutonium and uranium, but neptunium and americium were observed to be monoisotopic 237Np and 241Am. Measurements for characterization and verification of the attributes show that plutonium and trace actinides are homogeneous with the exception of limited heterogeneity for uranium, primarily observed for the 238U isotope. Model purification ages calculated from measured americium and uranium attribute values are consistent with material histories and indicate that these impurities are predominantly due to the decay of plutonium isotopes.


Author(s):  
Sameer Amereih ◽  
Thomas Meisel ◽  
Wolfhard Wegsheider

Two independent digestion techniques (microwave acid digestion with HF and HCl, HNO3 and Na2O2 sintering, respectively) were applied to determine the total Sb concentration in a real soil sample and in reference materials: Icelandic Basalt (BIR-1), Cody Shale (SCo-1) and (Soil-7). ICP-MS was used to determine total antimony concentrations in the digested and the extracted solutions using external calibration and isotope dilution technique. The recoveries of Sb using HF in the acids digestion mixture in closed-vessels microwave digestion system were excellent and the concentrations are in very good agreement with certified or reported concentrations of reference materials. Using closed-vessels combined with microwave heating systems probably prevents the loss of volatile Sb compounds. The use of hydrogen fluoride with other strong acid can help dissociating insoluble antimony silicates. Different extraction reagents were tested for their ability to extract antimony using an ultrasonic bath namely: EDTA disodium salt, potassium hydroxide, citric acid monohydrate, pyridine-2,6-dicarboxylic acid, ammonium acetate, ammonium oxalate, ammonium thiocyanate, ammonium persulphate and di-ammonium hydrogen citrate. A 500 mmol L-1 solution of citric acid pH 1.08 proved to be the most efficient extractant. Optimization of the extraction conditions were investigated by studying the effect of pH, concentration, temperature, time of extraction, the ratio of sample mass to the volume of extractant and the number of consecutive extractions. As a result three consecutive extractions for a total time of 45 min at 80 ˚C was the most efficient condition for Sb extraction. Using these extraction conditions 61%, 3.7% RSD and 42%, 2.2% RSD (n=6) of the total antimony in the real soil and Soil-7 samples, respectively could be extracted.


2021 ◽  
Vol 5 ◽  
pp. 70-78
Author(s):  
T. K. Nurubeyli ◽  

The paper discusses the possibilities and limitations of the method of mass spectrometry with inductively coupled plasma on the example of elemental analysis of natural and drinking waters, soils and grounds. It is shown that the combination of this method with the simpler atomic emission method makes it possible to expand the range of determined elements, simplify the mass-spectral analysis and increase its reliability. It is shown that the use of the ICP-MS method in the analysis of various objects makes it possible to determine the majority of elements with extremely low detection limits. The reason for the manifestation of matrix effects is the positive space charge formed between the interface and the extractor, the composition of which is determined by the composition of singly charged argon ions. The increase in the concentration of ions in this region is the appearance of a matrix element, which facilitates the scattering of ions from this region. It was found that the heavier the ions of the matrix element, the more the space charge density increases and the scattering occurs. A serious limitation of the method is associated with interferences due to the presence of a certain amount of two and three-charged ions in the plasma. These ions, which have approximately the same mass as the isotopes of the element being determined, are formed as a result of various plasma-chemical reactions and interfere with the determination.


Author(s):  
Ruoxi Zhang ◽  
Kenny Nadeau ◽  
Eduardo Amilcar Gautier ◽  
Paola Alejandra Babay ◽  
José Luis Ramella ◽  
...  

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