Methanol Formation in Hyperthermal Oxygen Collisions with Methane Clathrate Ice.

J Phys Chem A

Materials and Process Simulation Center, California Institute of Technology, Pasadena, California 91125, United States.

Published: November 2024

AI Article Synopsis

  • - The study investigates how hyperthermal reactive ions, specifically water group molecules, affect the organic chemistry of icy bodies, which could be important for understanding prebiotic conditions.
  • - Molecular dynamics simulations reveal that irradiating carbon-bearing ice with atomic oxygen primarily produces methanol, suggesting a unique hot-atom reaction mechanism, especially at lower doses.
  • - At higher irradiation doses, the chemical composition shifts towards more oxidized carbon compounds, with formaldehyde becoming more prevalent than methanol, indicating varying effects of different impactors and guest species on the ice chemistry.

Article Abstract

The presence of small organic molecules at airless icy bodies may be significant for prebiotic chemistry, yet uncertainties remain about their origin. Here, we consider the role of hyperthermal reactive ions in modifying the organic inventory of ice. We employ molecular dynamics using the ReaxFF formalism to simulate bombardment of carbon-bearing ice by hyperthermal water group molecules (HO, = 0-2) with kinetic energy between 2 and 58 eV. Methanol is the dominant closed-shell organic product for a CH clathrate irradiated at low dose by atomic oxygen. It is produced at yields as high as 10%, primarily by a novel hot-atom reaction mechanism, while radiolysis makes a secondary contribution. At high irradiation doses (≳1.4 × 10 cm), the composition is driven toward greater carbon oxidation states with formaldehyde being favored over methanol production. Other water group impactors are less efficient at inducing chemistry in the ice, and alternate clathrate guest species (CO, CO) are very robust against hydrogenation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11613570PMC
http://dx.doi.org/10.1021/acs.jpca.4c06078DOI Listing

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