Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2022Low-level Ca-40 determinations using nitrous oxide with reaction cell inductively coupled plasma-tandem mass spectrometry4citations

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Prohaska, Thomas
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Lancaster, Shaun
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2022

Co-Authors (by relevance)

  • Prohaska, Thomas
  • Lancaster, Shaun
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article

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

  • Prohaska, Thomas
  • Irrgeher, Johanna
  • Lancaster, Shaun
Abstract

<p>In inductively coupled plasma mass spectrometry, the most abundant Ca isotope (<sup>40</sup>Ca) 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<sub>3</sub>) has proven to be an effective reaction gas by process of a charge transfer reaction. However, NH<sub>3</sub> is highly corrosive and toxic and cannot remove isobaric<sup>40</sup> K. Therefore, this work proposes the use of nitrous oxide (N<sub>2</sub>O) to mass shift the target analyte<sup>40</sup>Ca to<sup>40</sup>Ca<sup>16</sup>O<sup>+</sup> as a non-corrosive and non-toxic alternative. Instrument performance testing demonstrated that N<sub>2</sub>O was capable of reaching equivalent detection limits (0.015 ng g<sup>−1</sup>) and background equivalence concentrations (0.041 ng g<sup>−1</sup>) to that of NH<sub>3</sub> and limited by the blank only. Further investigation of matrix interferences with synthetic standards highlighted that the N<sub>2</sub>O 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<sub>3</sub> was found to only support the removal of Mg. This work highlights a clear advantage of N<sub>2</sub>O 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.].</p>

Topics
  • impedance spectroscopy
  • corrosion
  • Magnesium
  • Magnesium
  • Potassium
  • spectrometry
  • inductively coupled plasma mass spectrometry
  • tandem mass spectrometry