Using a relative rate technique, kinetic studies on the gas-phase reactions of OH radicals, ozone, and NO(3) radicals with iso-butyl vinyl ether (iBVE) and tert-butyl vinyl ether (tBVE) have been performed in a 405 L Duran glass chamber at (298 ± 3) K and atmospheric pressure (750 ± 10 Torr) in synthetic air using in situ FTIR spectroscopy to monitor the reactants. The following rate coefficients (in units of cm(3) molecule(-1) s(-1)) have been obtained: (1.08 ± 0.23) × 10(-10) and (1.25 ± 0.32) × 10(-10) for the reactions of OH with iBVE and tBVE, respectively; (2.85 ± 0.62) × 10(-16) and (5.30 ± 1.07) × 10(-16) for the ozonolysis of iBVE and tBVE, respectively; and (1.99 ± 0.56) × 10(-12) and (4.81 ± 1.01) × 10(-12) for the reactions of NO(3) with iBVE and tBVE, respectively. The rate coefficients for the NO(3) reactions are first-time determinations. The measured rate coefficients are compared with estimates using current structure activity relationship (SAR) methods and the effects of the alkoxy group on the gas-phase reactivity of the alkyl vinyl ethers toward the oxidants are compared and discussed. In addition, estimates of the tropospheric lifetimes of iBVE and tBVE with respect to their reactions with OH, ozone, and NO(3) for typical OH radical, ozone, and NO(3) radical concentrations are made, and their relevance for the environmental fate of compounds is considered.
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http://dx.doi.org/10.1021/jp305992a | DOI Listing |
J Phys Chem A
September 2012
Bergische Universitaet Wuppertal, Physikalische Chemie/FBC, Gauss Strasse 20, D-42119 Wuppertal, Germany.
Using a relative rate technique, kinetic studies on the gas-phase reactions of OH radicals, ozone, and NO(3) radicals with iso-butyl vinyl ether (iBVE) and tert-butyl vinyl ether (tBVE) have been performed in a 405 L Duran glass chamber at (298 ± 3) K and atmospheric pressure (750 ± 10 Torr) in synthetic air using in situ FTIR spectroscopy to monitor the reactants. The following rate coefficients (in units of cm(3) molecule(-1) s(-1)) have been obtained: (1.08 ± 0.
View Article and Find Full Text PDFChemosphere
August 2012
Environment Research Institute, Shandong University, Jinan 250100, PR China.
Density functional theory (DFT) and ab initio method are employed to elucidate the mechanisms for O(3)-initiated oxidation of n-butyl vinyl ether (n-BVE) and its isomers (i-BVE and t-BVE). For each BVE, the reactions proceed via O(3) cycloaddition resulting in the formation of primary ozonides (POZs) and then two self-decomposition pathways of POZs are followed. Major products are identified to be formaldehyde and butyl formates (CH(3)CH(2)CH(2)CH(2)OCHO for n-BVE, (CH(3))(2)CHCH(2)OCHO for i-BVE and (CH(3))(3)COCHO for t-BVE).
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