CRAHCN-O: A Consistent Reduced Atmospheric Hybrid Chemical Network Oxygen Extension for Hydrogen Cyanide and Formaldehyde Chemistry in CO2-, N2-, H2O-, CH4-, and H2-Dominated Atmospheres
Ben K. D. Pearce, Paul W. Ayers, Ralph E. Pudritz

TL;DR
This paper develops an extended chemical network model to accurately simulate the formation and destruction of HCN and H2CO in diverse planetary atmospheres, incorporating newly identified reactions validated against experimental data.
Contribution
It introduces CRAHCN-O, a novel oxygen extension to the existing chemical network, including 45 new reactions crucial for modeling planetary atmospheric chemistry.
Findings
126 reactions with calculated rate coefficients, mostly within a factor of 2 of experimental data
Identification of 6 key reactions dominating HCN and H2CO chemistry
Development of a versatile model applicable to various atmospheric compositions
Abstract
Hydrogen cyanide (HCN) and formaldehyde (H2CO) are key precursors to biomolecules such as nucleobases and amino acids in planetary atmospheres; However, many reactions which produce and destroy these species in atmospheres containing CO2 and H2O are still missing from the literature. We use a quantum chemistry approach to find these missing reactions and calculate their rate coefficients using canonical variational transition state theory and Rice-Ramsperger-Kassel-Marcus/master equation theory at the BHandHLYP/aug-cc-pVDZ level of theory. We calculate the rate coefficients for 126 total reactions, and validate our calculations by comparing with experimental data in the 39% of available cases. Our calculated rate coefficients are most frequently within an factor of 2 of experimental values, and generally always within an order of magnitude of these values. We discover 45 previously…
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