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Kinetic and mechanistic study of the atmospheric reaction of MBO331 with Cl atoms
Authors:Diana Rodríguez  Ana Rodríguez  Andrés Garzón  José M Granadino-Roldán  Amparo Soto  Alfonso Aranda
Institution:1. Faculty of Environmental Sciences , University of Castilla La Mancha , Avenida Carlos III, s/n, 45071 Toledo , Spain diana.rodriguez@uclm.es;3. Faculty of Environmental Sciences , University of Castilla La Mancha , Avenida Carlos III, s/n, 45071 Toledo , Spain;4. Faculty of Pharmacy , University of Castilla La Mancha , Paseo de los estudiantes, s/n, 02071 Albacete , Spain;5. Department of Physical and Analytical Chemistry. Faculty of Experimental Sciences , University of Jaén. Paraje las Lagunillas , s/n., 23071, Jaén , Spain;6. Faculty of Chemical Sciences , University of Castilla La Mancha, Avenida Camilo José Cela , n° 10, 13071?-?Ciudad Real , Spain
Abstract:The present work deals with the reaction of 3-methyl-3-buten-1-ol (MBO331) with Cl atoms, which has been investigated by gas chromatography with flame ionization detection (GC-FID) at atmospheric pressure in N2 or air, using the relative rate technique. The rate constant reaction at 298?±?1?K was found to be (5.01?±?0.70)?×?10?10?cm3 molecule?1?s?1, using cyclohexane, octane and 1-butene as a reference compounds. The temperature dependence for the reaction was studied within the 298?333?K range. Additionally, a product identification under atmospheric conditions has been performed for the first time by GC-MS, with 3-methyl-3-butenal, methacrolein and chloroacetone being observed as degradation products. A theoretical study on the reaction at the QCISD(T)/6-311G**//MP2/6-311G** level was also carried out to obtain more information on the mechanism. From the theoretical study it can be predicted that Cl addition to the double bond proceeds through lower energy barriers than H-abstraction pathways and therefore is energetically favoured. Finally, atmospheric implications of the results obtained are discussed.
Keywords:3-methyl-3-buten-1-ol  kinetics  chlorine atom  troposphere  oxidation
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