• Bassas, A.
• Bonnin, M.
• Dulieu, F.
• Noble, J. A.
• Danger, Gregoire
• Chiavassa, T.
• Congiu, E.
• Theule, P.
• Duvernay, F.

Abstract

Context. It is generally agreed that hydrogenation reactions dominate chemistry on grain surfaces in cold, dense molecular cores, saturating the molecules present in ice mantles. <BR /> Aims: We present a study of the low temperature reactivity of solid phase isocyanic acid (HNCO) with hydrogen atoms, with the aim of elucidating its reaction network. <BR /> Methods: Fourier transform infrared spectroscopy and mass spectrometry were employed to follow the evolution of pure HNCO ice during bombardment with H atoms. Both multilayer and monolayer regimes were investigated. <BR /> Results: The hydrogenation of HNCO does not produce detectable amounts of formamide (NH<SUB>2</SUB>CHO) as the major product. Experiments using deuterium reveal that deuteration of solid HNCO occurs rapidly, probably via cyclic reaction paths regenerating HNCO. Chemical desorption during these reaction cycles leads to loss of HNCO from the surface. <BR /> Conclusions: It is unlikely that significant quantities of NH<SUB>2</SUB>CHO form from HNCO. In dense regions, however, deuteration of HNCO will occur. HNCO and DNCO will be introduced into the gas phase, even at low temperatures, as a result of chemical desorption....

Topics

• impedance spectroscopy
• surface
• grain
• experiment
• mass spectrometry
• Hydrogen
• gas phase
• Fourier transform infrared spectroscopy
• spectrometry