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A Proposal for the Mechanism of the CH + CO2 Reaction
Author(s) -
Rafael M. Vichietti,
Rene F. K. Spada,
Albérico B. F. da Silva,
Francisco B. C. Machado,
Roberto L. A. Haiduke
Publication year - 2019
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.9b02530
Subject(s) - arrhenius equation , kinetic energy , reaction mechanism , chemistry , decomposition , mechanism (biology) , elementary reaction , thermodynamics , reaction rate , computational chemistry , activation energy , kinetics , catalysis , physics , organic chemistry , quantum mechanics
Few experimental studies on the CH + CO 2 global reaction propose H, CO, and HCO as major products. However, the reaction mechanisms behind this process have not yet been elucidated. Moreover, some intriguing kinetic particularities were noticed in these previous investigations. The advanced theoretical study performed here shows that a CH insertion mechanism is capable of explaining all the experimental data available. Hence, the strong deviations from a traditional Arrhenius behavior ascribed to the rate-determining elementary reaction (the CH insertion step) account for the kinetic particularities observed experimentally. A change in the preferred product channel as temperatures increase (from HCO + CO to H + 2CO) is also predicted to occur due to the HCO decomposition, although the CH depletion rates in typical conditions are not affected by this additional step.

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