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      Conservation of the Charge in Signal from Drift Tube Ion Mobility Spectrometers

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      Analytical Chemistry
      American Chemical Society

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          Abstract

          Quantitative information obtained from drift tube detectors used in ion mobility spectrometry is contained in the area of peaks forming the drift time spectrum. The area of all peaks corresponds to the total charge of ions entering the drift section of the spectrometer. It was found that this charge is not conserved when the ion composition changes. This work is devoted to studying the causes of this phenomenon. Experimental research consisted of recording drift time spectra for 2-pentanone and n-heptanone, at various analyte concentrations and different opening times of the shutter grid. Measurements of the total ion current were also performed in static mode with an open grid. The research results indicated that the reasons for the lack of ion charge conservation in the drift time spectrum are ion recombination, mutual repulsion, and mobility-dependent transmission of ions through the shutter grid. The explanation of the relationships obtained experimentally was based on a simple theoretical model, which considered the phenomenon of ion transport along the reaction section and the penetration of ions through the shutter. The developed model provides a good description of the measurement results and allows the estimation of ion currents and ion concentrations in the reaction section upstream of the grid. This information is important for proper quantitative analysis as well as when the ion mobility spectrometer is used in quantitative studies of chemical ionization processes.

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          Absolute Values of the Electron Mobility in Hydrogen

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            Ion mobility spectrometry for the detection of volatile organic compounds in exhaled breath of patients with lung cancer: results of a pilot study.

            Analysis of exhaled breath, especially of volatile organic compounds (VOCs), is of increasing interest in the diagnosis of lung cancer. Compared with other methods of breath analysis, ion mobility spectrometry (IMS) offers a tenfold higher detection rate of VOCs. By coupling the ion mobility spectrometer with a multicapillary column as a pre-separation unit, IMS offers the advantage of an immediate twofold separation of VOCs with visualisation in a three-dimensional chromatogram. The total analysis time is about 500 s compared with gas chromatography/mass spectrometry (GC/MS) of about 1 h. It therefore seemed reasonable to test IMS in breath analysis. In a pilot study, 32 patients with lung cancer were subjected to a breath analysis by IMS. Their IMS chromatograms were compared with those of 54 healthy controls. An IMS that was built for special clinical application was used to identify characteristic peaks of VOCs which might be relevant for the diagnosis of lung cancer in exhaled air of 10 ml volume. By a combination of 23 peak regions within the IMS chromatogram, patients with lung cancer, including a patient with carcinoma in situ, were classified and differentiated from healthy persons with an error rate of zero. Breath analysis by IMS can detect a discriminating combination of VOCs in patients with lung cancer. By pattern recognition without the need for chemical analysis of the underlying VOCs, IMS has the potential to facilitate lung cancer diagnosis.
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              Process analysis using ion mobility spectrometry.

              Ion mobility spectrometry, originally used to detect chemical warfare agents, explosives and illegal drugs, is now frequently applied in the field of process analytics. The method combines both high sensitivity (detection limits down to the ng to pg per liter and ppb(v)/ppt(v) ranges) and relatively low technical expenditure with a high-speed data acquisition. In this paper, the working principles of IMS are summarized with respect to the advantages and disadvantages of the technique. Different ionization techniques, sample introduction methods and preseparation methods are considered. Proven applications of different types of ion mobility spectrometer (IMS) used at ISAS will be discussed in detail: monitoring of gas insulated substations, contamination in water, odoration of natural gas, human breath composition and metabolites of bacteria. The example applications discussed relate to purity (gas insulated substations), ecology (contamination of water resources), plants and person safety (odoration of natural gas), food quality control (molds and bacteria) and human health (breath analysis).
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                Author and article information

                Journal
                Anal Chem
                Anal Chem
                ac
                ancham
                Analytical Chemistry
                American Chemical Society
                0003-2700
                1520-6882
                16 October 2024
                29 October 2024
                : 96
                : 43
                : 17337-17344
                Affiliations
                Faculty of Advanced Technologies and Chemistry, Military University of Technology , ul. gen. Sylwestra Kaliskiego 2, Warsaw 00-908, Poland
                Author notes
                Author information
                https://orcid.org/0000-0003-4110-0377
                Article
                10.1021/acs.analchem.4c03825
                11525926
                39413290
                1ce25c20-dbd6-4925-b6a4-6a4a44fefbd5
                © 2024 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 23 July 2024
                : 09 October 2024
                : 01 October 2024
                Funding
                Funded by: Narodowe Centrum Badan i Rozwoju, doi 10.13039/501100005632;
                Award ID: DOB-SZAFIR/09/A/010/01/2021
                Categories
                Article
                Custom metadata
                ac4c03825
                ac4c03825

                Analytical chemistry
                Analytical chemistry

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