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IDMS Training

  • Based on its proven records especially in reference material certification, isotope dilution mass spectrometry (IDMS) is considered as one of the most powerful and most accurate methods for determining amounts of substance. Contrary to other calibration approaches, IDMS does not directly suffer from long-time changes or drifts in instrument sensitivity. Moreover, provided isotopic exchange between the sample and spike is ensured, losses of analyte do not affect the analytical result. Both advantages are based on the fact that IDMS only requires isotope ratio measurements and isotope ratios are largely unaffected by instrumental drift, setup or by matrix, unless an isobaric interference is present. The Consultative Committee for Amount of Substance (CCQM), the world's highest institution for metrology in chemistry, considers IDMS as the most important “Primary Method of Measurement” for amount determination. The total combined uncertainty, according to ISO and EURACHEM guidelines, canBased on its proven records especially in reference material certification, isotope dilution mass spectrometry (IDMS) is considered as one of the most powerful and most accurate methods for determining amounts of substance. Contrary to other calibration approaches, IDMS does not directly suffer from long-time changes or drifts in instrument sensitivity. Moreover, provided isotopic exchange between the sample and spike is ensured, losses of analyte do not affect the analytical result. Both advantages are based on the fact that IDMS only requires isotope ratio measurements and isotope ratios are largely unaffected by instrumental drift, setup or by matrix, unless an isobaric interference is present. The Consultative Committee for Amount of Substance (CCQM), the world's highest institution for metrology in chemistry, considers IDMS as the most important “Primary Method of Measurement” for amount determination. The total combined uncertainty, according to ISO and EURACHEM guidelines, can easily be calculated via the IDMS equations. Applying it correctly, IDMS has the potential to be a primary method of measurement yielding SI traceable values in the most direct way with combined uncertainties significantly smaller than obtainable by other methods. In general it can be stated that IDMS is the most important reference method for elemental and elemental species analysis, offering highest accuracy and precision or smallest measurement uncertainties, when properly applied. Thus IDMS represents by far the best suited reference method for RM characterisation. Due to its universal applicability IDMS offers sufficient potential to follow future needs in analytical chemistry as well as in the RM sector. This presentation will demonstrate the basic principle of IDMS and will show its Pros and Cons as well as its pitfalls. Possible sources of errors and bias are mentioned and correction models will be discussed. Notice will be given to metrological aspects such as traceability and uncertainty. Differences in the application of thermal ionization mass spectrometry and inductively coupled plasma mass spectrometry are discussed as well as differences between different types of mass spectrometers. This will be illustrated by practical examples from various fields.zeige mehrzeige weniger

Volltext Dateien herunterladen

  • Vortrag_IDMS-Training-I-basics_Februar-2016.pdf
    eng
  • Vortrag_IDMS-Training-II-isotope ratios_Februar-2016.pdf
    eng
  • Vortrag_IDMS-Training-III-specifics_Februar-2016.pdf
    eng

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Metadaten
Autor*innen:Jochen VoglORCiD
Dokumenttyp:Vortrag
Veröffentlichungsform:Präsentation
Sprache:Englisch
Jahr der Erstveröffentlichung:2016
DDC-Klassifikation:Naturwissenschaften und Mathematik / Chemie / Analytische Chemie
Freie Schlagwörter:Certification; Isotope dilution mass spectrometry; Primary method of measurement
Veranstaltung:Workshop and practical training on isotope dilution mass spectrometry
Veranstaltungsort:Berlin, Germany
Beginndatum der Veranstaltung:22.02.2016
Enddatum der Veranstaltung:26.02.2016
Verfügbarkeit des Dokuments:Datei im Netzwerk der BAM verfügbar ("Closed Access")
Datum der Freischaltung:02.05.2017
Referierte Publikation:Nein
Eingeladener Vortrag:Nein
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