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The OH-initiated heterogeneous oxidation of mixed saccharide aqueous aerosols is investigated using an atmospheric-pressure flow tube coupled to off-line analysis of the particle composition. For equimolar monosaccharide/disaccharide aqueous aerosol mixtures, the decay of the disaccharide is found to be significantly slower than that of the monosaccharide. Molecular dynamics simulations of the mixed aqueous solutions reveal the formation of a ∼10 Å disaccharide exclusion layer below the water surface. A simple chemical model is developed to discuss the possible effect of the disaccharide surface partitioning on the heterogeneous kinetics. The observed decays are consistent with a poor spatial overlap of the OH radical at the interface with the disaccharide in the particle bulk. The effect of partitioning on the heterogeneous oxidation of atmospheric organic aerosols is discussed. 

Abstract The gas phase reaction of the ground state cyano‐radical (CN (X²∑⁺)) with 2‐methylfuran (2‐MF) is investigated in a quasi‐static reaction cell at pressures ranging from 2.2 to 7.6 Torr and temperatures ranging from 304 to 440 K. The CN radicals are generated in their ground electronic state by pulsed laser photolysis of gaseous cyanogen iodide (ICN) at 266 nm. Their concentration is monitored as a function of reaction time using laser‐induced fluorescence at 387.3 nm on the B²∑⁺(ν′ = 0) ← X²∑⁺(ν″ = 0) vibronic band. The reaction rate coefficient is found to be rapid and independent of pressure and temperature. Over the investigated temperature and pressure ranges, the rate coefficient is measured to be 2.83 (± 0.18) × 10⁻¹⁰cm³molecules s⁻¹. The enthalpies of the stationary points and transition states on the CN + 2‐MF potential energy surface are calculated using the CBS‐QB3 computational method. The kinetic results suggest the lack of a prereactive complex on the reaction entrance channel with either a very small or nonexistent entrance energy barrier. In addition, the potential energy surface calculations reveal only submerged barriers along the minimum energy path. Based on comparisons between previous CN reactions with unsaturated hydrocarbons, the most likely reaction pathway is CN addition onto one of the unsaturated carbons followed by either H or methyl elimination. The implications for the transformation of biomass‐derived fuels in nitrogen‐rich flames is discussed.