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Ion chemistry at elevated ion–molecule interaction energies in a selected ion flow-drift tube: reactions of H3O+, NO+ and O2+ with saturated aliphatic ketones

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F17%3A00482892" target="_blank" >RIV/61388955:_____/17:00482892 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1039/C7CP05795D" target="_blank" >http://dx.doi.org/10.1039/C7CP05795D</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/C7CP05795D" target="_blank" >10.1039/C7CP05795D</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Ion chemistry at elevated ion–molecule interaction energies in a selected ion flow-drift tube: reactions of H3O+, NO+ and O2+ with saturated aliphatic ketones

  • Original language description

    The reactions of H3O+, NO+ and O2+ ions with a homologous series of six aliphatic ketones, viz. acetone through 2-octanone, have been investigated in a helium-buffered selected ion flow-drift tube, SIFDT, in order to reveal their dependencies on ion–molecule interaction energies, Er, and to gain insight into their mechanisms. The ultimate motivation is to allow analysis and absolute quantification of trace amounts of ketones and other volatile organic compounds in air using selected ion flow-drift tube mass spectrometry, SIFDT-MS. The reactions of H3O+ with the ketone molecules, M, proceed via exothermic proton transfer producing MH+ ions, the collisional rate coefficients, kc, for which can be calculated as a function of Er and are seen to reduce by about one third over the Er range from 0.05 eV up to 0.5 eV. The rate coefficients, k, and product ion distributions for the NO+ and O2+ reactions with M had to be obtained experimentally relative to the calculated kc for the H3O+ reactions. The product ions of the NO+/ketones reactions initially proceed via the formation of excited (NO+M)* adduct ions that partially fragment, and the k reduces with Er as much as four times for the acetone reactions but remains close to their respective kc for the higher-order ketones indicating long lifetimes of the (NO+M)* ions with respect to the stabilising collision times with He atoms. The k for the O2+/ketones dissociative charge transfer reactions are observed to be greater than their calculated kc implying that long distance electron transfer occurs.n

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10403 - Physical chemistry

Result continuities

  • Project

    <a href="/en/project/GJ17-13157Y" target="_blank" >GJ17-13157Y: New ion chemistry methods for rapid mass spectrometric monitoring of atmospheric biogenic volatile organic compounds responsible for air pollution</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2017

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Physical Chemistry Chemical Physics

  • ISSN

    1463-9076

  • e-ISSN

  • Volume of the periodical

    19

  • Issue of the periodical within the volume

    47

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    10

  • Pages from-to

    31714-31723

  • UT code for WoS article

    000417295800021

  • EID of the result in the Scopus database

    2-s2.0-85038352492