4.6 Article

Experimental Study of the Rate of OH + HO2 → H2O + O2 at High Temperatures Using the Reverse Reaction

Journal

JOURNAL OF PHYSICAL CHEMISTRY A
Volume 114, Issue 17, Pages 5520-5525

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jp100739t

Keywords

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Funding

  1. National Science Foundation [0649936]
  2. Department of Energy, Office of Basic Energy Sciences
  3. Department of Energy [National Nuclear Security Administration] [NA28614]
  4. Div Of Chem, Bioeng, Env, & Transp Sys
  5. Directorate For Engineering [0649936] Funding Source: National Science Foundation

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The rate constant of the reaction OH + HO2 -> H2O + O-2 (1) can be inferred at high temperatures from measurements of the rate of its reverse reaction H2O + O-2 -> OH + HO2 (-1). In this work, we used laser absorption of both H2O and OH to study the reverse reaction in shock-heated H2O/O-2/Ar mixtures over the temperature range 1600-2200 K. Initial H2O concentrations were determined using tunable diode laser absorption near 2.5 mu m, and OH concentration time-histories were measured using UV ring dye laser absorption near 306.7 nm. Detailed kinetic analysis of the OH time-history profiles yielded a value for the rate constant k(1) of (3.3 +/- 0.9) x 10(13) [cm(3) mol(-1) s(-1)] between 1600 and 2200K. The results of this study agree well with those reported by Srinivasan et al. (Srinivasan, N.K.; Su, M.-C.; Sutherland, J.W.; Michael, J.V.; Ruscic, B. J. Phys. Chem. A 2006, 110, 6602-6607) in the temperature regime between 1200 and 1700 K. The combination of the two studies suggests only a weak temperature dependence of k(1) above 1200 K. Data from the current study and that of Keyser (Keyser, L.F.J. Phys. Chem. 1988, 92, 1193-1200) at lower temperatures can be described by the k(1) expression proposed by Baulch et al. (Baulch, D.L.; Cobos, C.J.; Cox, R.A.; Esser, C.; Frank, P.; Just, Th.; Kerr, J.A.; Pilling, Mi.; Troe, J.; Walker, R.W.; Warnatz, J. J. Phys. Chem. Ref Data 1992, 21, 411), k(1) = 2.89 x 10(13) exp(252/T) [cm(3) mol(-1) s(-1)]. However, it should be noted that some previous studies suggest a k(1) minimum around 1250 K (Hippler, H.; Neunaber, H.; Troe, J. J. Chem. Phys. 1995, 103, 3510-3516) or 1000 K (Kappel, C.; Luther, K.; Troe, J. Phys. Chem. Chem. Phys. 2002, 4, 4392-4398).

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