Experimental and Theoretical Study of the Chemical Network of the Hydrogenation of NO on Interstellar Dust Grains

Autor: Thanh Nguyen, E. Congiu, Dahbia Talbi, Amir Karton, Jean-Christophe Loison, S. Baouche, François Dulieu
Přispěvatelé: LERMA Cergy (LERMA), Laboratoire d'Etude du Rayonnement et de la Matière en Astrophysique (LERMA (UMR_8112)), Institut national des sciences de l'Univers (INSU - CNRS)-Observatoire de Paris, Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-CY Cergy Paris Université (CY)-Institut national des sciences de l'Univers (INSU - CNRS)-Observatoire de Paris, Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-CY Cergy Paris Université (CY), Laboratoire Univers et Particules de Montpellier (LUPM), Université Montpellier 2 - Sciences et Techniques (UM2)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS), The University of Western Australia (UWA), Institut des Sciences Moléculaires (ISM), Université Montesquieu - Bordeaux 4-Université Sciences et Technologies - Bordeaux 1-École Nationale Supérieure de Chimie et de Physique de Bordeaux (ENSCPB)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Rok vydání: 2019
Předmět:
Zdroj: ACS Earth and Space Chemistry
ACS Earth and Space Chemistry, ACS, 2019, 3 (7), pp.1196-1207. ⟨10.1021/acsearthspacechem.9b00063⟩
ISSN: 2472-3452
DOI: 10.1021/acsearthspacechem.9b00063
Popis: International audience; Nitrogen Monoxide (NO) is observed in the gas phase of molecular clouds. It may accrete on dust grains and there its hydrogenation should lead to hydroxylamine (NH 2 OH), the same way that CO is transformed in methanol (CH 3 OH) on the surface dust grains. NO hydrogenation has been said barrier-less, whereas CO hydrogenation proceed through quantum tunneling, and is thus slower. However, CH 3 OH is widely observed and is considered as a proxy of complex organic molecules while hydroxy-lamine remains undetected. We aim at studying, analyzing, and understanding the 1 chemical network of NO hydrogenation on cold surfaces. Experiments are carried out using a new Ultra-Hight Vacuum (UHV) setup named VENUS. NO molecules and H atoms are co-deposited on a golden mirror at different temperatures. Infrared spectroscopy as well as Temperature Programmed Desorption (TPD) are used to follow the NO reactivity, with both H and D, and in presence or absence of water substrate. Quantum calculations on water ice cluster models are computed separately. During the hydrogenation of NO, 10 reactions proceed concurrently. They are identified and constrained by changing physical conditions in experiments or in calculations. Among them, we demonstrate that the HNO+H addition reaction has a barrier which is probably crossed via quantum tunneling at 10 K. Moreover, abstraction reactions are occurring although they are limited by H and O bonding with their environment. Chemical desorption should occur especially in absence of water which enhances the total production of hydroxylamine. The chemical network of the hydrogenation of NO has been re-investigated. Each of the 10 reactions are sorted by efficiency. We exclude the possibility of a chemical loop between NO and HNO, especially in presence of water. Therefore hydroxylamine remains the main product of the hydrogenation of NO on grains and the question of its non-detection in ices or in the gas phase, specifically in shocked regions where ice mantles should be sputtered, is still open.
Databáze: OpenAIRE
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