Design of and initial results from a highly instrumented reactor for atmospheric chemistry (HIRAC)
Author:
Glowacki D. R.,Goddard A.,Hemavibool K.,Malkin T. L.,Commane R.,Anderson F.,Bloss W. J.,Heard D. E.,Ingham T.,Pilling M. J.,Seakins P. W.
Abstract
Abstract. The design of a Highly Instrumented Reactor for Atmospheric Chemistry (HIRAC) is described and initial results obtained from HIRAC are presented. The ability of HIRAC to perform in-situ laser-induced fluorescence detection of OH and HO2 radicals with the Fluorescence Assay by Gas Expansion (FAGE) technique establishes it as internationally unique for a chamber of its size and pressure/temperature variable capabilities. In addition to the FAGE technique, HIRAC features a suite of analytical instrumentation, including: a multipass FTIR system; a conventional gas chromatography (GC) instrument and a GC instrument for formaldehyde detection; and NO/NO2, CO, O3, and H2O vapour analysers. Ray tracing simulations and measurements of the blacklamp flux have been utilized to develop a detailed model of the radiation field within HIRAC. Comparisons between the analysers and the FTIR coupled to HIRAC have been performed, and HIRAC has also been used to investigate pressure dependent kinetics of the chlorine atom reaction with ethene and the reaction of O3 and t-2-butene. The results obtained are in good agreement with literature recommendations and Master Chemical Mechanism predictions. HIRAC thereby offers a highly instrumented platform with the potential for: (1) high precision kinetics investigations over a range of atmospheric conditions; (2) detailed mechanism development, significantly enhanced according to its capability for measuring radicals; and (3) field instrument intercomparison, calibration, development, and investigations of instrument response under a range of atmospheric conditions.
Publisher
Copernicus GmbH
Reference77 articles.
1. Akimoto, H., Hoshino, M., Inoue, G., Sakamaki, F., Washida, N., and Okuda, M.: Design and characterization of the evacuable and bakable photochemical smog chamber, Environ. Sci. Tech., 13(4), 471–475, 1979. 2. Atkinson, R. and Aschmann, S. M.: Kinetics of the gas phase reaction of chlorine atoms with a series of organics at 296+-2 K and atmospheric pressure, Int. J. Chem. Kin., 17(1), 33–41, 1985. 3. Bailey, A. E., Heard, D. E., Paul, P. H., and Pilling, M. J.: Collisional quenching of OH (A 2S+, n'=0) N2, O2 and CO2 between 204 and 294 K: Implications for atmospheric measurements of OH by laser-induced fluorescence, J. Chem. Soc. Faraday T., 93(16), 2915–2920, 1997. 4. Baltensperger, U., Kalberer, M., Dommen, J., Paulsen, D., Alfarra, M. R., Coe, H., Fisseha, R., Gascho, A., Gysel, M., Nyeki, S., Sax, M., Steinbacher, M., Prevot, A. S. H., Sjogren, S., Weingartner, E., and Zenobi, R.: Secondary organic aerosols from anthropogenic and biogenic precursors, Faraday Discuss., 130, 265–278, 2005. 5. Barnes, I., Becker, K. H., and Mihalopoulos, N.: An FTIR Product Study of the Photooxidation of Dimethyl Disulfide, J. Atmos. Chem., 18(3), 267–289, 1994.
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|