current state of the manuscript - early stage
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\documentclass[%
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% Conference Proceedings
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]{revtex4-2}
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\usepackage{booktabs}
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\usepackage[exponent-product=\cdot]{siunitx}
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\usepackage{chemformula}
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\begin{document}
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\preprint{PREPRINT: DRAFT}
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\title[Test operation of a novel Time-Of-Flight mass spectrometer on the gas exhaust of Wendelstein 7-X]{Test operation of a novel Time-Of-Flight mass spectrometer on the gas exhaust of Wendelstein 7-X}
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\author{G. Schlisio}
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\email{georg.schlisio@ipp.mpg.de}
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\affiliation{
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Max-Planck-Institut für Plasmaphysik, Wendelsteinstra{\ss}e 1, 17491 Greifswald, Germany
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}
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\author{S. Gasc}
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\affiliation{
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Spacetek Technology AG, Brüggliweg 18, 3073 Gümligen, Switzerland
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}
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\author{L. Hofer}
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\affiliation{
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Spacetek Technology AG, Brüggliweg 18, 3073 Gümligen, Switzerland
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}
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\author{C.C. Klepper}
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\affiliation{
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Oak Ridge National Laboratory, Oak Ridge, Tennesse 37831, USA
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}
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\author{the W7-X team\footnote{See author list of Thomas Sunn Pedersen et al 2022 Nucl. Fusion 62 042022}}
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\date{\today}% It is always \today, today
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\begin{abstract}
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A novel time-of-flight mass spectrometer was operated in Wendelstein 7-X, a magnetic confinement fusion (MCF) experiment, to assess the suitability and limitations in the use for gas exhaust analysis in MCF devices.
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With a focus on high mass resolution sufficient for isotope separation, the permanent presence of magnetic field and a need for fast time resolution MCF presents a challenging environment for the operation of such devices.
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% TODO continue
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\end{abstract}
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\maketitle
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%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%%
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\section{\label{sec:intro}Introduction}
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Mass spectrometers of various measurement principles are indispensable in many applications, vacuum quality monitoring and gas composition being a prominent one.
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Wendelstein 7-X (W7X) is an optimized modular stellarator experiment dedicated to magnetic confinement fusion research in high-temperature plasmas [TODO reference]. %TODO
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Time-of-flight mass spectrometers (TOF-MS) measure mass to charge ratio m/z by accelerating ions against a retarding field and measure the response time in a detector.
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The flight time is directly proportional to the ions m/z ratio, which allows the mass-resolved measurement of the injected ions.
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The IonTamer® FA (ITFA) is a novel TOF-MS <put properties here>. %TODO
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Possible applications of a fast high-resolution mass spectrometer in magnetic confinement fusion (MCF) research and future fusion reactors:
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\begin{itemize}
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\item Gas exhaust monitoring, especially accounting of DT fuel
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\item He exhaust monitoring, e.g. for divertor effectiveness and efficiency
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\item Impurity monitoring, e.g. for assessment of plasma chemistry and vacuum quality
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\end{itemize}
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\section{Residual magnetic field influence on the TOF-MS measurement}
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Many mass analyzers require free-streaming charged particles, and TOF-MS share this property. Fast free streaming particles are subject to a Lorentz force in a magnetic field. While MCF employs toroidal fields with a quadrupole far field characteristics, residual fields of several mT cannot entirely be avoided at reasonable distance of the torus system.
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Therefore, magnetic shielding is frequently employed to reduce the residual magnetic field down to an acceptable level.
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Over the test duration, we successively improved the magnetic shielding in steps and document the effect below.
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While the residual field could not be measured in-situ, calculation of the residual field vectors were performed and the shielding structure was subjected to measurements in a test magnet setup thereafter.
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\section{Dynamic range dependence on pressure}
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The TOF-MS is designed for pressures up to \SI{1e-3}{\pascal}.
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Higher pressure means higher signal
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Sudden changes in pressure can lead to safety deactivation of the instrument
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%(ANALYSIS HINT: take data from 20230307 where we reach transient saturation at some point and a short pumpdown at ~12:57CET reduces pressure and signal drastically; see also data taken on 2023-03-09: stepwise h2 pressure increase up to saturation, subsequent tuning-down of the gain, and pressure increase up to 1e-5mbar, gain scan at elevated pressures and a comparison with the ITMS and its spectra; see also 50ks=13.9h integration spectrum @~2e-8mbar 20230309)
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\section{Time response}
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Observing gas dynamics in the fusion exhaust requires a sub-second time resolution, which is often detrimental to dynamic range of instruments, as longer integration times give higher signal-to-noise ratio.
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The ITFA in its present hard- and software configuration has a minimum integration time of \SI{0.1}{\second}, which in turn already contains the average of 1000 scans.
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\section{Mass range}
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The mass range of the ITFA is defined by hardware settings to ~\SI{1300}{u}.
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Most of this range is of interest only for analysis of larger compounds, as found in chemistry analysis \cite{Gasc2022}.
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For the purpose of fusion gas exhaust monitoring, a mass range up to \SI{100}{u} is mostly sufficient and a limitation of the mass range leads - due to the nature of a TOF - to significantly reduce data data footprint and lead to a speed-up, improving the time response.
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\section{Observation of isotopes in common molecules}
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While W7X does currently only run Hydrogen, and neither Deuterium nor Tritium is present in the machine, the question of deuterated and tritiated molecules poses itself in view of Deuterium-Tritium fuel foreseen for reactors. W7X is planning for Deuterium operation in the next years, Tritium will be utilized in ITER and beyond.
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Identifying fuel-carrying molecules and precisely accounting for fuel will be a relevant and challenging part of the fusion fuel cycle.
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While new developments \cite{Day2019,Haertl2022} promise to extract over 90\% of the Tritium via direct internal recycling, the remaining mixture remains to be analyzed and monitored.
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Due to the unavailability of D and T in the experimental setup, simulations have been performed and are presented here along with measurements as a prediction of the TOF-MS capabilities in this regard.
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\section{Other notable findings}
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During operation of the ITFA in hydrogen-dominated sampling gas a prominent mass peak at $ \text{m}/\text{Z} = 3.024$ was reliably observed.
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This corresponds to thrice the hydrogen mass and relates to \ch{H3+}, a molecule long known \cite{Thomson1911} and special relevance in astrophysics.
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According to literature, it forms with a proton transfer process \ch{H2 + H2+ -> H3+ + H} which occurs in the ITFA analyzer.
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This effect is well-documented \cite{Gauthier1995} but not common knowledge.
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\section{Discussion}
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Future development of the ITFA and its analysis tools are planned, with features like mass range selection.
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\section*{Declaration of the authors}
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The authors declare that SG and LH are employed by Spacetek Technologies AG, manufacturer and marketer of the discussed ITFA.
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\begin{acknowledgments}
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The authors wish to acknowledge the support of S. Vartanian and E. Gauthier for discussions on H3+.
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The authors further wish to acknowledge the fine lab work of A. Graband in support of the ITFA test, especially with regard to the magnetic shielding.
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This work has been carried out within the framework of the EUROfusion
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Consortium and has received funding from the Euratom research and
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training programme 2014-2018 and 2019-2020 under grant agreement No
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633053. The views and opinions expressed herein do not necessarily
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reflect those of the European Commission.
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\end{acknowledgments}
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\appendix
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\nocite{*}
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\begin{thebibliography}{10}
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\bibitem{Gasc2022}
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S. Gasc, L. Hofer, Chimia 2022, DOI: 10.2533/chimia.2022.52
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\bibitem{Schlisio2019}
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G. Schlisio et al, RSI 2019, DOI: 10.1063/1.5098125
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\bibitem{Schlisio2021}
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G. Schlisio et al, NF 2021, DOI: 10.1088/1741-4326/abd63f
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\bibitem{Thomson1911}
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Thomson, J. J. (1911). XXVI. Rays of positive electricity. The London, Edinburgh, and Dublin Philosophical Magazine and Journal of Science, 21(122), 225-249.
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\bibitem{Gauthier1995}
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E. Gauthier, (1995). Quantitative analysis of deuterium and helium after plasma shots by means of resolved mass spectrometry (EUR-CEA-FC--1557). France %(https://inis.iaea.org/search/search.aspx?orig_q=RN:27073670)
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\bibitem{McCall2000}
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McCall Phil.Trans.R.Soc.Lond.A 2000, DOI: 10.1098/rsta.2000.0655 (H3+ spectroscopy)
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\bibitem{Day2019}
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Day FusEngDes2019 https://doi.org/10.1016/j.fusengdes.2019.04.019
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\bibitem{Haertl2022}
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Haertl FusEngDes22 https://doi.org/10.1016/j.fusengdes.2021.112969
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%\bibitem{loarer2005} % no DOI found, see https://inis.iaea.org/search/search.aspx?orig_q=RN:36078348
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%T. Loarer, et al., 20th IAEA fusion energy conference proceedings (2005): 36078348.
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% \bibitem{Grote2003} % DOI https://doi.org/10.1016/S0022-3115(02)01503-9
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% H. Grote, et al., J.Nuc.Mat. Volumes 313–316, March 2003, Pages 1298-1303
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% \bibitem{Haas1998}
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% G. Haas, H.-S. Bosch, Vacuum 51.1 (1998): 39-46. % DOI https://doi.org/10.1016/S0042-207X(98)00131-6
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% \bibitem{Wenzel2019}
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% U. Wenzel, et al., RSI (2019) % DOI https://doi.org/10.1063/1.5121203
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% \bibitem{Kremeyer2020}
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% T. Kremeyer, et al., RSI (2020) % https://doi.org/10.1063/1.5125863
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\end{thebibliography}
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\end{document}
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