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Ultrahigh Sensitivity PTR-MS Instrument with a Well-Defined Ion Chemistry
[Image: see text] Proton-transfer-reaction mass spectrometry (PTR-MS) is widely used for measuring organic trace gases in air. In traditional PTR-MS, both nonpolar and polar analytes are ionized with unit efficiency, as predicted from ion-molecule collision theories. This well-defined ion chemistry...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433242/ https://www.ncbi.nlm.nih.gov/pubmed/37528801 http://dx.doi.org/10.1021/acs.analchem.3c02669 |
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author | Reinecke, Tobias Leiminger, Markus Jordan, Alfons Wisthaler, Armin Müller, Markus |
author_facet | Reinecke, Tobias Leiminger, Markus Jordan, Alfons Wisthaler, Armin Müller, Markus |
author_sort | Reinecke, Tobias |
collection | PubMed |
description | [Image: see text] Proton-transfer-reaction mass spectrometry (PTR-MS) is widely used for measuring organic trace gases in air. In traditional PTR-MS, both nonpolar and polar analytes are ionized with unit efficiency, as predicted from ion-molecule collision theories. This well-defined ion chemistry allows for direct quantification of analytes without prior calibration and therefore is an important characteristic of PTR-MS. In an effort to further increase the sensitivity, recently developed ultrahigh sensitivity chemical ionization mass spectrometry (CIMS) analyzers have, however, been reported to have sacrificed unit ionization efficiency for selected analytes or classes of analytes. We herein report on the development of a novel ultrasensitive PTR-MS instrument, the FUSION PTR-TOF 10k, which exhibits the same universal unit response as conventional PTR-MS analyzers. The core component of this analyzer is the newly designed FUSION ion-molecule reactor, which is a stack of concentric ring electrodes generating a static longitudinal electric field superimposed by a focusing transversal radiofrequency (RF) field. The FUSION PTR-TOF 10k instrument is equipped with an improved ion source, capable of switching between different reagent ions (H(3)O(+), O(2)(+), NO(+), NH(4)(+)) in less than one second. The improved time-of-flight mass spectrometer analyzes m/z signals with a mass resolution in the 10000–15000 range. FUSION PTR-TOF 10k achieves sensitivities up to 80000 cps ppbV(–1) and detection limits down to 0.5 pptV for a 1 s measurement time. We show time-series of naphthalene and (13)C-napthalene as measured in ambient air in Innsbruck for demonstrating the sub-pptV detection capability of this novel FUSION PTR-TOF 10k. |
format | Online Article Text |
id | pubmed-10433242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-104332422023-08-18 Ultrahigh Sensitivity PTR-MS Instrument with a Well-Defined Ion Chemistry Reinecke, Tobias Leiminger, Markus Jordan, Alfons Wisthaler, Armin Müller, Markus Anal Chem [Image: see text] Proton-transfer-reaction mass spectrometry (PTR-MS) is widely used for measuring organic trace gases in air. In traditional PTR-MS, both nonpolar and polar analytes are ionized with unit efficiency, as predicted from ion-molecule collision theories. This well-defined ion chemistry allows for direct quantification of analytes without prior calibration and therefore is an important characteristic of PTR-MS. In an effort to further increase the sensitivity, recently developed ultrahigh sensitivity chemical ionization mass spectrometry (CIMS) analyzers have, however, been reported to have sacrificed unit ionization efficiency for selected analytes or classes of analytes. We herein report on the development of a novel ultrasensitive PTR-MS instrument, the FUSION PTR-TOF 10k, which exhibits the same universal unit response as conventional PTR-MS analyzers. The core component of this analyzer is the newly designed FUSION ion-molecule reactor, which is a stack of concentric ring electrodes generating a static longitudinal electric field superimposed by a focusing transversal radiofrequency (RF) field. The FUSION PTR-TOF 10k instrument is equipped with an improved ion source, capable of switching between different reagent ions (H(3)O(+), O(2)(+), NO(+), NH(4)(+)) in less than one second. The improved time-of-flight mass spectrometer analyzes m/z signals with a mass resolution in the 10000–15000 range. FUSION PTR-TOF 10k achieves sensitivities up to 80000 cps ppbV(–1) and detection limits down to 0.5 pptV for a 1 s measurement time. We show time-series of naphthalene and (13)C-napthalene as measured in ambient air in Innsbruck for demonstrating the sub-pptV detection capability of this novel FUSION PTR-TOF 10k. American Chemical Society 2023-08-02 /pmc/articles/PMC10433242/ /pubmed/37528801 http://dx.doi.org/10.1021/acs.analchem.3c02669 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Reinecke, Tobias Leiminger, Markus Jordan, Alfons Wisthaler, Armin Müller, Markus Ultrahigh Sensitivity PTR-MS Instrument with a Well-Defined Ion Chemistry |
title | Ultrahigh Sensitivity PTR-MS Instrument with a Well-Defined
Ion Chemistry |
title_full | Ultrahigh Sensitivity PTR-MS Instrument with a Well-Defined
Ion Chemistry |
title_fullStr | Ultrahigh Sensitivity PTR-MS Instrument with a Well-Defined
Ion Chemistry |
title_full_unstemmed | Ultrahigh Sensitivity PTR-MS Instrument with a Well-Defined
Ion Chemistry |
title_short | Ultrahigh Sensitivity PTR-MS Instrument with a Well-Defined
Ion Chemistry |
title_sort | ultrahigh sensitivity ptr-ms instrument with a well-defined
ion chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433242/ https://www.ncbi.nlm.nih.gov/pubmed/37528801 http://dx.doi.org/10.1021/acs.analchem.3c02669 |
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