Kinetics and mechanism of the reaction of CH3O with NO

Article abstract of DOI:10.1002/kin.550260903

The kinetics of the reaction of CH₃O with NO and the branching ratio for HCHO product formation, obtained as Γ_HCHO = (Rate of HCHO formation) / (Rate of CH₃O decay), have been studied using a discharge flow reactor. Laser induced fluorescence has been used to monitor the decay of the CH₃O radical and the build-up of the HCHO product. Overall rate constants and product branching ratios were measured at room temperature over the pressure range of 0.72-8.5 torr He. Three reaction mechanisms were considered which differed in the routes of HCHO formation: (i) direct disproportionation; (ii) via an energized collision complex; or (iii) both reaction routes. It has been shown that data on the pressure dependence of the overall rate constant are not sufficient to distinguish between these mechanisms. In addition, an accurate value of Γ_HCHO^∞ is required. Analysis of the available experimental data provided 0.0 and about 0.1 as the lower and upper limit for Γ_HCHO^∞, respectively. Since the rate constants derived for CH₃ONO formation were not sensitive to the value assumed for Γ_HCHO^∞, k_CH(3)ONO⁰ = (1.69 ± 0.69) × 10^-29 cm⁶ molecule^-2 s^-1 and k_CH(3)ONO^∞ = (2.45 ± 0.31) × 10^-11 cm³ molecule^-1 s^-1 could be derived. The rate constant obtained for formaldehyde formation when extrapolated to zero pressure is k_HCHO⁰ = (3.15 ± 0.92) × 10^-12 cm³ molecule^-1 s^-1.