Can a single water molecule catalyze the OH+CH2CH2 and OH+CH2O reactions?

Add time:08/26/2019    Source:sciencedirect.com

The reaction of OH radicals with ethylene (CH2CH2) and formaldehyde (CH2O) molecules with and without water have been investigated using ab initio/DFT potential energy surfaces (PESs) at CCSD(T)/aug-cc-pVTZ//BHandHLYP//aug-cc-pVTZ levels of theory. The rate coefficients for the bimolecular reaction pathways OH + CH2X···H2O (X = CH2, O) and CH2X + H2O⋯HO were calculated using canonical variational transition state theory (CVT) with small curvature tunneling (SCT) correction. The kinetic results show that OH radical adds to C=C bond in CH2CH2, and abstract the hydrogen atoms from CH2O, similar to its isoelectronic analogous OH + CH2NH (+H2O) reaction. The catalytic effect of a single water molecule on OH + CH2X (X = CH2, O) reaction system shows that the initial water complexation step is essential in the rate coefficients calculation. The calculated rate coefficient for the OH + CH2CH2(+H2O) reaction at 300K is 6 × 10−16 cm3 molecule−1 s−1 and for OH + CH2O(+H2O) reaction at 300K is 8.1 × 10−14 cm3 molecule−1 s−1. The rate coefficient for OH + CH2CH2(+H2O) reaction is at least two orders of magnitude smaller than OH + CH2NH(+H2O) reaction (at 300K is 5.1 × 10−14 cm3 molecule−1 s−1) and rate coefficient for OH + CH2O reaction is in good agreement with OH + CH2NH reaction. In general, the rate coefficients for OH + CH2X (X = CH2, O)⋯H2O and for CH2X + H2O⋯HO reactions are ∼3–4 orders of magnitude smaller than reaction without water molecule. Our results predict that catalytic effect of single water molecule on OH + CH2CH2 and OH + CH2O reactions can make a negligible contribution to the gas phase removal of CH2CH2 and CH2O by OH radicals because the dominated water-assisted process depends parametrically on water concentration. As a result, the overall reaction rate coefficients are smaller. The present results provide a better understanding of gas phase catalytic effect of a water molecule on the most important atmospheric and combustion reaction prototypes.

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