Metal ion-molecule kinetics at combustion temperatures:: The reaction of Ca+ with O2

被引:2
|
作者
Cosic, Bjana [1 ]
Ermoline, Alexandre [1 ]
Fontijn, Arthur [1 ]
Marshall, Paul [2 ]
机构
[1] Rensselaer Polytech Inst, Isermann Dept Chem & Biol Engn, High Temp React Kinet, Troy, NY 12180 USA
[2] N Texas State Univ, Dept Chem, Ctr Adv Sci Comp & Modeling, Denton, TX 76203 USA
基金
美国国家科学基金会;
关键词
metal ions; elementary reactions; temperature dependence; high-temperature reactors;
D O I
10.1016/j.proci.2006.07.047
中图分类号
O414.1 [热力学];
学科分类号
摘要
The high-temperature photochemistry (HTP) technique, previously used for reactions of neutral species, has been adapted to the study of atomic metal ion-molecule reactions. Ca+ ions were generated by 193 nut multi-photon photolysis of calcium acetyl acetonate and its pyrolysis fragments. The relative ion concentrations were monitored by laser-induced fluorescence at 393.4 min. Ar was used as the bath gas. The data for the Ca+ + O-2 + M-6 --> CaO2+ + M association reaction (1) are fitted by k(1)(907-1425 K) = 3.5 x 10(-32) exp(+3161 K/T) cm(6) molecule(-2) s(-1). Combining with an approximate k(1)(296 K) value in the literature leads to k(1)(296-1425 K) = 5.8 x 10(-22) (T/K)(-2.9) exp(-601 K/T cm(6) molecule(-2) s(-1). Over much of the observed temperature range reaction (1) has much smaller rate coefficients than the corresponding neutral Ca association reaction. Reaction (1) is shown to behave very similarly to the O-2 association reaction with neutral K atoms, with which Ca+ is iso-electronic. This suggests that the initial step is ion-pair complex formation of the superoxide Ca2+(O-2)(-), which is also consistent with results from density functional calculations. The k(1) values are rationalized via Troe's unimolecular formalism, which leads to good accord with the experiments. (C) 2006 The Combustion Institute. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:349 / 356
页数:8
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