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    Condensed phase membrane introduction mass spectrometry with in situ liquid reagent chemical ionization in a liquid electron ionization source (CP-MIMS-LEI/CI)

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    Date
    2020-03-02
    Author
    Vandergrift, Gregory W.
    Lattanzio-Battle, William
    Krogh, Erik T.
    Gill, Chris G.
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    Abstract
    Direct mass spectrometry has grown significantly due to wide applicability, relative ease of use, and high sample throughput. However, many current direct mass spectrometry methods are largely based on ambient ionization techniques that can suffer from matrix effects and poor selectivity. A strategy that addresses these shortcomings is condensed phase membrane introduction mass spectrometry-liquid electron ionization utilizing in situ liquid reagent chemical ionization (CP-MIMS-LEI/CI). In CP-MIMS measurements, a semipermeable hollow fibre polydimethylsiloxane membrane probe is directly immersed into a complex sample. Neutral, hydrophobic analytes permeating the membrane are entrained by a continuously flowing liquid acceptor phase (nL/min) to an LEI/CI source, where the liquid is nebulized, followed by analyte vaporization and ionization. This study marks the first intentional exploitation of the liquid CP-MIMS acceptor phase as an in situ means of providing liquid chemical ionization (CI) reagents for improved analyte sensitivity and selectivity (CP-MIMSLEI/ CI). Acetonitrile and diethyl ether were used as a combination acceptor phase/CI proton transfer reagent system for the direct analysis of dialkyl phthalates. Using isotopically labeled reagents, the gas phase ionization mechanism was found to involve reagent autoprotonation, followed by proton transfer to dialkyl phthalates. A demonstration of the applicability of CP-MIMS-LEI/CI for rapid and sensitive screening of bis(2-ethylhexyl) phthalate in house dust samples is presented. The detection limit in house dust (6 mg/kg) is comparable to that obtained by conventional analyses, but without time-consuming sample work up or chromatographic separation steps.
    Description
    This document is the Accepted Manuscript version of a Published Work that appeared in final form in the Journal of the American Society for Mass Spectrometry, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see: http://dx.doi.org/10.1021/jasms.9b00143
    URI
    https://viurrspace.ca/handle/10613/24435
    http://dx.doi.org/10.25316/IR-16261
    Identifier (Other)
    DOI: http://dx.doi.org/10.1021/jasms.9b00143
    DOI: 10.25316/IR-16261
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    • Gill, Chris
    • Krogh, Erik
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