The first computational model of solid-phase chemistry in cometary nuclear ices is presented. An astrochemical kinetics model, , is adapted to trace the chemical evolution in multiple layers of cometary ice, over a representative period of 5 Gyr. Physical conditions are chosen appropriate for "cold storage" of the cometary nucleus in the outer Solar System, prior to any active phase. The chemistry is simulated at a selection of static temperatures in the range 5 - 60 K, while the ice is exposed to the interstellar radiation field, inducing a photo-chemistry in the outer ice layers that produces significant formation of complex organic molecules. A treatment for the chemistry resulting from cosmic-ray bombardment of the ices is also introduced into the model, along with a new formulation for low-temperature photo-chemistry. Production of simple and complex molecules to depth on the order of 10 m or more is achieved, with local fractional abundances comparable to observed values in many cases. The production of substantial amounts of O (and HO) is found, suggesting that long-term processing by high-energy cosmic rays of cometary ices , over a period on the order of 1 Gyr, may be sufficient to explain the large observed abundances of O, if the overall loss of material from the comet is limited to a depth on the order of 10 m. Entry into the inner solar system could produce a further enhancement in the molecular content of the nuclear ices that may be quantifiable using this modeling approach.
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http://dx.doi.org/10.3847/1538-4357/ab418e | DOI Listing |
Proc Natl Acad Sci U S A
December 2024
Department of Chemistry and Biochemistry, University of California San Diego, La Jolla, CA 92093.
The origin of water in the Earth-Moon system is a pivotal question in planetary science, particularly with the need for water resources in the race to establish lunar bases. The candidate origins of lunar water are an indigenous lunar component, solar wind water production, and the delivery of meteoritic and cometary material. Characterizing the oxygen isotopic composition of water provides information on lunar oxygen sources.
View Article and Find Full Text PDFChem Commun (Camb)
October 2024
Physical and Materials Chemistry Division, CSIR-National Chemical Laboratory, Pune 411008, India.
J Phys Chem Lett
August 2024
Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry Chinese Academy of Sciences, Beijing 100190, China.
The radiative and photodissociative properties of the dicarbon molecule, C, in high-lying electronic states are of utmost importance for modeling the photochemical processes that occur in various astronomical environments. Despite extensive spectroscopic studies in the last two centuries, the photodissociation properties of C are still largely unknown, particularly for quantum states in the vacuum ultraviolet (VUV) region. Here, the lifetimes of C for each individual rovibrational level in the recently identified 2Σ state are measured for the first time using a VUV-pump-UV-probe photoionization scheme.
View Article and Find Full Text PDFOpen Res Eur
April 2024
Rosseland Centre for Solar Physics, University of Oslo, Oslo, N-0315, Norway.
Spectrochim Acta A Mol Biomol Spectrosc
October 2024
Centre for Astrophysics and Planetary Science, School of Physics and Astronomy, University of Kent, Canterbury CT2 7NH, United Kingdom; HUN-REN Institute for Nuclear Research (Atomki), Debrecen H-4026, Hungary. Electronic address:
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