Journal
ASTROPHYSICAL JOURNAL
Volume 850, Issue 1, Pages -Publisher
IOP PUBLISHING LTD
DOI: 10.3847/1538-4357/aa93d9
Keywords
astrochemistry; ISM: abundances; ISM: clouds; ISM: molecules; molecular processes
Categories
Funding
- European Research Council (NANOCOSMOS) [SyG-610256]
- Spanish Ministry of Science and Innovation (ASTROMOL) [CSD2009-00038]
- Spanish Ministry of Economy and Competitiveness (MINECO) under the GASSOL [CGL2013-43227-R]
- MINECO [AYA2012-32032, AYA2016-75066-C2-1-P, RyC-2014-16277, FIS2014-52172-C2]
- UCLM (Plan Propio de Investigacion)
- Institut National des Sciences de l'Univers (INSU)
- European COST [CM1401]
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The chemical kinetics of neutral-neutral gas-phase reactions at ultralow temperatures is a fascinating research subject with important implications on the chemistry of complex organic molecules in the interstellar medium (T similar to 10-100 K). Scarce kinetic information is currently available for these kinds of reactions at T < 200 K. In this work, we use the Cinetique de Reaction en Ecoulement Supersonique Uniforme (CRESU; Reaction Kinetics in a Uniform Supersonic Flow) technique to measure for the first time the rate coefficients (k) of the gas-phase OH+H2CO reaction between 22 and 107 K. The k values greatly increase from 2.1. x. 10(-11) cm(3) s(-1) at 107 K to 1.2. x. 10(-10) cm(3) s(-1) at 22 K. This is also confirmed by quasi-classical trajectories (QCT) at collision energies down to 0.1 meV performed using a new full dimension and ab initio potential energy surface that generates highly accurate potential and includes long-range dipole-dipole interactions. QCT calculations indicate that at low temperatures HCO is the exclusive product for the OH+H2CO reaction. In order to revisit the chemistry of HCO in cold dense clouds, k is reasonably extrapolated from the experimental results at 10 K (2.6 x 10(-10) cm(3) s(-1)). The modeled abundances of HCO are in agreement with the observations in cold dark clouds for an evolving time of 10(5) - 10(6) yr. The different sources of production of HCO are presented and the uncertainties in the chemical networks are discussed. The present reaction is shown to account for a few percent of the total HCO production rate. This reaction can be expected to be a competitive process in the chemistry of prestellar cores. Extensions to photodissociation regions and diffuse cloud environments are also addressed.
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