Literature DB >> 21359353

A kinetic study of Mg+ and Mg-containing ions reacting with O3, O2, N2, CO2, N2O and H2O: implications for magnesium ion chemistry in the upper atmosphere.

Charlotte L Whalley1, Juan C Gómez Martín, Timothy G Wright, John M C Plane.   

Abstract

Reactions between Mg(+) and O(3), O(2), N(2), CO(2) and N(2)O were studied using the pulsed laser photo-dissociation at 193 nm of Mg(C(5)H(7)O(2))(2) vapour, followed by time-resolved laser-induced fluorescence of Mg(+) at 279.6 nm (Mg(+)(3(2)P(3/2)-3(2)S(1/2))). The rate coefficient for the reaction Mg(+) + O(3) is at the Langevin capture rate coefficient and independent of temperature, k(190-340 K) = (1.17 ± 0.19) × 10(-9) cm(3) molecule(-1) s(-1) (1σ error). The reaction MgO(+) + O(3) is also fast, k(295 K) = (8.5 ± 1.5) × 10(-10) cm(3) molecule(-1) s(-1), and produces Mg(+) + 2O(2) with a branching ratio of (0.35 ± 0.21), the major channel forming MgO(2)(+) + O(2). Rate data for Mg(+) recombination reactions yielded the following low-pressure limiting rate coefficients: k(Mg(+) + N(2)) = 2.7 × 10(-31) (T/300 K)(-1.88); k(Mg(+) + O(2)) = 4.1 × 10(-31) (T/300 K)(-1.65); k(Mg(+) + CO(2)) = 7.3 × 10(-30) (T/300 K)(-1.59); k(Mg(+) + N(2)O) = 1.9 × 10(-30) (T/300 K)(-2.51) cm(6) molecule(-2) s(-1), with 1σ errors of ±15%. Reactions involving molecular Mg-containing ions were then studied at 295 K by the pulsed laser ablation of a magnesite target in a fast flow tube, with mass spectrometric detection. Rate coefficients for the following ligand-switching reactions were measured: k(Mg(+)·CO(2) + H(2)O → Mg(+)·H(2)O + CO(2)) = (5.1 ± 0.9) × 10(-11); k(MgO(2)(+) + H(2)O → Mg(+)·H(2)O + O(2)) = (1.9 ± 0.6) × 10(-11); k(Mg(+)·N(2) + O(2)Mg(+)·O(2) + N(2)) = (3.5 ± 1.5) × 10(-12) cm(3) molecule(-1) s(-1). Low-pressure limiting rate coefficients were obtained for the following recombination reactions in He: k(MgO(2)(+) + O(2)) = 9.0 × 10(-30) (T/300 K)(-3.80); k(Mg(+)·CO(2) + CO(2)) = 2.3 × 10(-29) (T/300 K)(-5.08); k(Mg(+)·H(2)O + H(2)O) = 3.0 × 10(-28) (T/300 K)(-3.96); k(MgO(2)(+) + N(2)) = 4.7 × 10(-30) (T/300 K)(-3.75); k(MgO(2)(+) + CO(2)) = 6.6 × 10(-29) (T/300 K)(-4.18); k(Mg(+)·H(2)O + O(2)) = 1.2 × 10(-27) (T/300 K)(-4.13) cm(6) molecule(-2) s(-1). The implications of these results for magnesium ion chemistry in the atmosphere are discussed.

Entities:  

Year:  2011        PMID: 21359353     DOI: 10.1039/c0cp02637a

Source DB:  PubMed          Journal:  Phys Chem Chem Phys        ISSN: 1463-9076            Impact factor:   3.676


  5 in total

1.  The mesosphere and metals: chemistry and changes.

Authors:  John M C Plane; Wuhu Feng; Erin C M Dawkins
Journal:  Chem Rev       Date:  2015-03-09       Impact factor: 60.622

2.  Meteoric Metal Chemistry in the Martian Atmosphere.

Authors:  J M C Plane; J D Carrillo-Sanchez; T P Mangan; M M J Crismani; N M Schneider; A Määttänen
Journal:  J Geophys Res Planets       Date:  2018-03-06       Impact factor: 3.755

3.  Carbon Dioxide Activation at Metal Centers: Evolution of Charge Transfer from Mg .+ to CO2 in [MgCO2 (H2 O)n ].+ , n=0-8.

Authors:  Erik Barwa; Tobias F Pascher; Milan Ončák; Christian van der Linde; Martin K Beyer
Journal:  Angew Chem Int Ed Engl       Date:  2020-03-12       Impact factor: 15.336

4.  CO2/O2 Exchange in Magnesium-Water Clusters Mg+(H2O) n.

Authors:  Erik Barwa; Milan Ončák; Tobias F Pascher; Thomas Taxer; Christian van der Linde; Martin K Beyer
Journal:  J Phys Chem A       Date:  2018-12-19       Impact factor: 2.781

5.  Electronic spectroscopy and nanocalorimetry of hydrated magnesium ions [Mg(H2O)n]+, n = 20-70: spontaneous formation of a hydrated electron?

Authors:  Thomas Taxer; Milan Ončák; Erik Barwa; Christian van der Linde; Martin K Beyer
Journal:  Faraday Discuss       Date:  2019-07-18       Impact factor: 4.008

  5 in total

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