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A study of the reaction Li+HCl by the technique of time-resolved laser-induced fluorescence spectroscopy of Li (22PJ-2 2S1/2, λ=670.7 nm) between 700 and 1000 K

  • Author(s): Plane, JMC;
  • Saltzman, ES
  • et al.

Published Web Location

https://doi.org/10.1063/1.452871Creative Commons 'BY' version 4.0 license
Abstract

A kinetic study is presented of the reaction between lithium atoms and hydrogen chloride over the temperature range 700-1000 K. Li atoms are produced in an excess of HCl and He bath gas by pulsed photolysis of LiCl vapor. The concentration of the metal atoms is then monitored in real time by the technique of laser-induced fluorescence of Li atoms at λ= 670.7 nm using a pulsed nitrogen-pumped dye laser and box-car integration of the fluorescence signal. Absolute second-order rate constants for this reaction have been measured at T = 700, 750, 800, and 900 K. At T = 1000 K the reverse reaction is sufficiently fast that equilibrium is rapidly established on the time scale of the experiment. A fit of the data between 700 and 900 K to the Arrhenius form, with 2σ errors calculated from the absolute errors in the rate constants, yields k(T) = (3.8±1.1)×10-10exp[ - (883 ± 218)/T] cm3 molecule-1 s-1. This result is interpreted through a modified form of collision theory which is constrained to take account of the conservation of total angular momentum during the reaction. Thereby we obtain an estimate for the reaction energy threshold, E0 = 8.2 ± 1.4 kJ mol-1 (where the error arises from uncertainty in the exothermicity of the reaction), in very good agreement with a crossed molecular beam study of the title reaction, and substantially lower than estimates of E0 from both semiempirical and ab initio calculations of the potential energy surface. © 1987 American Institute of Physics.

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