Solvated Positron Chemistry. II. The Reaction of Hydrated Positrons with C1-, Br- and I-Ions

O. E. Mogensen

    Research output: Contribution to journalJournal articleResearchpeer-review

    Abstract

    The reaction of the hydrated positron, eaq+ with Cl−, Br−, and I− ions in aqueous solutions was studied by means of positron The measured angular correlation curves for [Cl−, e+], [Br−, e+, and [I−, e+] bound states were in good agreement with th Because of this agreement and the fact that the calculated positron wavefunctions penetrate far outside the X− ions in the [X−, e+] sta propose that a bubble is formed around the [X−, e+] state, similar to the Ps bubble found in nearly all liquids. F−ions did not react w Preliminary results showed that CN− ions react with eaq+ while OH−ions are non reactive. The rate constants were 3.9 × 1010 M−1 s−1, 4.4 × 1010 M−1 s−1, and 6.3 × 1010 M−1 s−1 for Cl−, Br−, and I−, respectively, at low (less, approximate 0.03 M) X− concentrations. A 25% decrease in the rate constant caused by the addition of 1 M ethanol to the I− solutions was i The influence of halide ions on the positronium (Ps) yields in pure water was studied by use of lifetime measurements. The Cl−, Br−, and I− ions reduced the Ps yields at low concentrations (less, approximate 0.03 M), while F− ions only reduced the Ps-yield However, the Ps yields saturated (e.g. at ≈ 21% ortho-Ps yield in the Cl− case) at higher concentrations. This saturation and the high-concentration effects-in the angular correlation results were interpreted as caused by rather complicated spur effects, wh It is proposed that spur electrons may pick off the positron from the [X−, e+ states with an efficiency which depends on the structure of the
    Original languageEnglish
    JournalChemical Physics
    Volume37
    Issue number1
    Pages (from-to)139-158
    ISSN0301-0104
    DOIs
    Publication statusPublished - 1979

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