Initiation in H2/o2: Rate Constants for H2 O2 → H Ho2 at High Temperature
نویسندگان
چکیده
The reaction between H2 and O2 has been studied in a reflected shock tube apparatus between temperatures of 1662–2097 K and pressures of 400–570 torr with Kr as the diluent gas. O atom atomic resonance absorption spectrometry (ARAS) was used to observe absolute [O]t under conditions of low [H2]0 so that most secondary reactions were negligible. Hence, the observed [O]t was the direct result of the rate controlling reaction between H2 and O2. Three different reactions were considered, but experimental and ab initio theoretical results both indicated that the process, H2 O2 → H HO2, is the most probable reaction. After rapid HO2 dissociation, O atoms are then instantaneously produced by H O2 → O OH. Using the ab initio result, conventional transition state theoretical calculations (CTST) with tunneling corrections give the expression T2.4328 exp( 26,926 K/T) cm3 molth 18 k 1.228 10 1 ecule 1 s 1, applicable between 400 and 2300 K. This theoretical result agrees with the present experimental determinations and those at lower temperature, derived from earlier work on the reverse reaction.
منابع مشابه
Assessment of kinetic modeling for lean H2/CH4/O2/diluent flames at high pressures
Experimental measurements of burning rates, analysis of key reactions and kinetic pathways, and modeling studies were performed for H2/CH4/O2/diluent flames spanning a wide range of fuel-lean conditions: equivalence ratios from 0.30 to 1.0, flame temperatures from 1400 to 1800 K, pressures from 1 to 25 atm, CH4 fuel fractions from 0 to 0.1. The experimental data show negative pressure dependenc...
متن کاملExperimental and modeling study of the effect of elevated pressure on lean high-hydrogen syngas flames
New laminar burning velocity measurements of 85:15% (by volume) H2–CO and H2–N2 mixtures with O2–He oxidizer are reported at lean conditions and elevated pressures (1–10 atm). Experiments are conducted using the heat flux method at initial temperature of 298 K. In this technique a near adiabatic flame is stabilized by balancing the heat loss from the flame to the burner with heat gain to the un...
متن کاملMicrokinetic modeling of the oxygen reduction reaction at the Pt(111)/gas interface
A microkinetic model of the oxygen reduction reaction (ORR) on Pt(111) under a gaseous H2 and O2 atmosphere is used to predict and explain which compositions of H2 and O2 lead to the fastest rate of water formation for temperatures between 600 and 900 K. For a stoichiometric (2:1) mixture of H2 and O2 the rate-determing step is found to transition from O hydrogenation to O2 H dissociation over ...
متن کاملKinetics of HO 2 + HO 2 ! H 2 O 2 + O 2 : Implications for Stratospheric H
[1] The reaction HO2 + HO2 ! H2O2 + O2 (1) has been studied at 100 Torr and 222 K to 295 K. Experiments employing photolysis of Cl2/CH3OH/O2/N2 and F2/H2/O2/N2 gas mixtures to produce HO2 confirmed that methanol enhanced the observed reaction rate. At 100 Torr, zero methanol, k1 = (8.8 ± 0.9) 10 13 exp[(210 ± 26)/T] cm molecule 1 s 1 (2s uncertainties), which agrees with current recommendations...
متن کاملEpoxidation of Alkenes and Oxidation of Alcohols with Hydrogen Peroxide Catalyzed by a Fe (Br8TPPS) Supported on Amberlite IRA-400
Iron (III) meso-tetrakis(p-sulfonatophenyl)-β-octabromoporphyrin supported on Amberlite IRA- 400 [Fe(Br8 TPPS)-Ad-400] is a robust and efficient catalyst for oxidation of alkenes and alcohols at room temperature. The catalyst exhibits a high activity and stability in hydrocarbon oxidation by H2 O2 . The method was useful in the oxidation of various primary, secondary-aliphatic, alicyclic and ar...
متن کامل