Fast Orthogonal Separation by Superposition of Time of Flight and Field Asymmetric Ion Mobility Spectrometry

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OriginalspracheEnglisch
Seiten (von - bis)1114-1121
Seitenumfang8
FachzeitschriftAnalytical chemistry
Jahrgang90
Ausgabenummer2
PublikationsstatusVeröffentlicht - 22 Dez. 2017

Abstract

Ion mobility spectrometry is a powerful and low-cost technique for the identification of chemical warfare agents, toxic chemicals, or explosives in air. Drift tube ion mobility spectrometers (DT-IMS) separate ions by the absolute value of their low field ion mobility, while field asymmetric ion mobility spectrometers (FAIMS) separate them by the change of their ion mobility at high fields. However, using one of these devices alone, some common and harmless substances show the same response as the hazardous target substances. In order to increase the selectivity, orthogonal data are required. Thus, in this work, we present for the first time an ambient pressure ion mobility spectrometer which is able to separate ions both by their differential and low field mobility, providing additional information for selectivity enhancement. This novel field asymmetric time of flight ion mobility spectrometer (FAT-IMS) allows high repetition rates and reaches limits of detection in the low ppb range common for DT-IMS. The device consists of a compact 44 mm drift tube with a tritium ionization source and a resolving power of 70. An increased separation of four substances with similar low field ion mobility is shown: phosgene (K0 = 2.33 cm2/(V s)), 1,1,2-trichlorethane (K0 = 2.31 cm2/(V s)), chlorine (K0 = 2.24 cm2/(V s)), and nitrogen dioxide (K0 = 2.25 cm2/(V s)). Furthermore, the behavior and limits of detection for acetonitrile, dimethyl methylphosphonate, diisopropyl methyl phosphonate in positive polarity and carbon dioxide, sulfur dioxide, hydrochloric acid, cyanogen chloride, and hydrogen cyanide in negative polarity are investigated.

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Fast Orthogonal Separation by Superposition of Time of Flight and Field Asymmetric Ion Mobility Spectrometry. / Bohnhorst, Alexander; Kirk, Ansgar T.; Berger, Marc et al.
in: Analytical chemistry, Jahrgang 90, Nr. 2, 22.12.2017, S. 1114-1121.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Bohnhorst A, Kirk AT, Berger M, Zimmermann S. Fast Orthogonal Separation by Superposition of Time of Flight and Field Asymmetric Ion Mobility Spectrometry. Analytical chemistry. 2017 Dez 22;90(2):1114-1121. doi: 10.1021/acs.analchem.7b03200
Bohnhorst, Alexander ; Kirk, Ansgar T. ; Berger, Marc et al. / Fast Orthogonal Separation by Superposition of Time of Flight and Field Asymmetric Ion Mobility Spectrometry. in: Analytical chemistry. 2017 ; Jahrgang 90, Nr. 2. S. 1114-1121.
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abstract = "Ion mobility spectrometry is a powerful and low-cost technique for the identification of chemical warfare agents, toxic chemicals, or explosives in air. Drift tube ion mobility spectrometers (DT-IMS) separate ions by the absolute value of their low field ion mobility, while field asymmetric ion mobility spectrometers (FAIMS) separate them by the change of their ion mobility at high fields. However, using one of these devices alone, some common and harmless substances show the same response as the hazardous target substances. In order to increase the selectivity, orthogonal data are required. Thus, in this work, we present for the first time an ambient pressure ion mobility spectrometer which is able to separate ions both by their differential and low field mobility, providing additional information for selectivity enhancement. This novel field asymmetric time of flight ion mobility spectrometer (FAT-IMS) allows high repetition rates and reaches limits of detection in the low ppb range common for DT-IMS. The device consists of a compact 44 mm drift tube with a tritium ionization source and a resolving power of 70. An increased separation of four substances with similar low field ion mobility is shown: phosgene (K0 = 2.33 cm2/(V s)), 1,1,2-trichlorethane (K0 = 2.31 cm2/(V s)), chlorine (K0 = 2.24 cm2/(V s)), and nitrogen dioxide (K0 = 2.25 cm2/(V s)). Furthermore, the behavior and limits of detection for acetonitrile, dimethyl methylphosphonate, diisopropyl methyl phosphonate in positive polarity and carbon dioxide, sulfur dioxide, hydrochloric acid, cyanogen chloride, and hydrogen cyanide in negative polarity are investigated.",
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AU - Bohnhorst, Alexander

AU - Kirk, Ansgar T.

AU - Berger, Marc

AU - Zimmermann, Stefan

N1 - Funding information: We would like to thank Airsense Analytics for providing the laboratory for the measurements. This work has been supported by the German Federal Ministry of Economics and Technology (BMWi), under the Grant KF3238301NT3 upon decision of the German Bundestag.

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N2 - Ion mobility spectrometry is a powerful and low-cost technique for the identification of chemical warfare agents, toxic chemicals, or explosives in air. Drift tube ion mobility spectrometers (DT-IMS) separate ions by the absolute value of their low field ion mobility, while field asymmetric ion mobility spectrometers (FAIMS) separate them by the change of their ion mobility at high fields. However, using one of these devices alone, some common and harmless substances show the same response as the hazardous target substances. In order to increase the selectivity, orthogonal data are required. Thus, in this work, we present for the first time an ambient pressure ion mobility spectrometer which is able to separate ions both by their differential and low field mobility, providing additional information for selectivity enhancement. This novel field asymmetric time of flight ion mobility spectrometer (FAT-IMS) allows high repetition rates and reaches limits of detection in the low ppb range common for DT-IMS. The device consists of a compact 44 mm drift tube with a tritium ionization source and a resolving power of 70. An increased separation of four substances with similar low field ion mobility is shown: phosgene (K0 = 2.33 cm2/(V s)), 1,1,2-trichlorethane (K0 = 2.31 cm2/(V s)), chlorine (K0 = 2.24 cm2/(V s)), and nitrogen dioxide (K0 = 2.25 cm2/(V s)). Furthermore, the behavior and limits of detection for acetonitrile, dimethyl methylphosphonate, diisopropyl methyl phosphonate in positive polarity and carbon dioxide, sulfur dioxide, hydrochloric acid, cyanogen chloride, and hydrogen cyanide in negative polarity are investigated.

AB - Ion mobility spectrometry is a powerful and low-cost technique for the identification of chemical warfare agents, toxic chemicals, or explosives in air. Drift tube ion mobility spectrometers (DT-IMS) separate ions by the absolute value of their low field ion mobility, while field asymmetric ion mobility spectrometers (FAIMS) separate them by the change of their ion mobility at high fields. However, using one of these devices alone, some common and harmless substances show the same response as the hazardous target substances. In order to increase the selectivity, orthogonal data are required. Thus, in this work, we present for the first time an ambient pressure ion mobility spectrometer which is able to separate ions both by their differential and low field mobility, providing additional information for selectivity enhancement. This novel field asymmetric time of flight ion mobility spectrometer (FAT-IMS) allows high repetition rates and reaches limits of detection in the low ppb range common for DT-IMS. The device consists of a compact 44 mm drift tube with a tritium ionization source and a resolving power of 70. An increased separation of four substances with similar low field ion mobility is shown: phosgene (K0 = 2.33 cm2/(V s)), 1,1,2-trichlorethane (K0 = 2.31 cm2/(V s)), chlorine (K0 = 2.24 cm2/(V s)), and nitrogen dioxide (K0 = 2.25 cm2/(V s)). Furthermore, the behavior and limits of detection for acetonitrile, dimethyl methylphosphonate, diisopropyl methyl phosphonate in positive polarity and carbon dioxide, sulfur dioxide, hydrochloric acid, cyanogen chloride, and hydrogen cyanide in negative polarity are investigated.

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SN - 0003-2700

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ER -

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