Rate Constants and Branching Ratios in the Oxidation of Aliphatic Aldehydes by OH Radicals under Atmospheric Conditions

Authors

  • Romina Castañeda Universidad Nacional Autónoma de México
  • Cristina Iuga Universidad Autónoma Metropolitana-Azcapotzalco
  • J. Raúl Álvarez-Idaboy Universidad Nacional Autónoma de México
  • Annik Vivier-Bunge Universidad Autónoma Metropolitana-Iztapalapa

DOI:

https://doi.org/10.29356/jmcs.v56i3.296

Keywords:

Radical-Molecule Reactions, Atmospheric Reactions, Reaction. Mechanism, Negative Activation Energy, Reactant Complexes

Abstract

In this work, a theoretical study is presented on the mechanism of OH reactions with C1-C5 aliphatic aldehydes. We have shown that, starting from butanal, the Cβ H-abstraction channel becomes relatively important and it contributes moderately to the total rate constant. Calculated overall rate coefficients at the CCSD(T)/6-311++G**//BHandHLYP/6-311++G** level are in excellent agreement with experimental data, supporting the proposed mechanisms. Negative activation energies are found to be in agreement with the temperature dependence observed for aldehydes. The branching ratio between the aldehydic and Cβ hydrogen abstraction is not significantly modified as temperature increases from 230 to 330 K.

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Author Biographies

Romina Castañeda, Universidad Nacional Autónoma de México

Facultad de Química, Departamento de Física y Química Teórica

Cristina Iuga, Universidad Autónoma Metropolitana-Azcapotzalco

Departamento de Ciencias Básicas

J. Raúl Álvarez-Idaboy, Universidad Nacional Autónoma de México

Facultad de Química, Departamento de Física y Química Teórica

Annik Vivier-Bunge, Universidad Autónoma Metropolitana-Iztapalapa

Departamento de Química

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Published

2017-10-12