Carbon, hydrogen, nitrogen, oxygen, and sulfur are the main elements involved in the solid-phase chemistry of various astrophysical environments. Among these elements, sulfur chemistry is probably the least well understood. We investigated whether sulfur ion bombardment within simple astrophysical ice analogs (originating from H2O:CH3OH:NH3, 2:1:1) could trigger the formation of complex organosulfur molecules. Over 1100 organosulfur (CHNOS) molecular formulas (12% of all assigned signals) were detected in resulting refractory residues within a broad mass range (from 100 to 900 amu, atomic mass unit). This finding indicates a diverse, rich and active sulfur chemistry that could be relevant for Kuiper Belt objects (KBO) ices, triggered by high-energy ion implantation. The putative presence of organosulfur compounds within KBO ices or on other icy bodies might influence our view on the search of habitability and biosignatures.

We use a laboratory facility to study the sputtering properties of centimeter-thick porous water ice subjected to the bombardment of ions and electrons to better understand the formation of exospheres of the icy moons of Jupiter. Our ice samples are as similar as possible to the expected moon surfaces but surface charging of the samples during ion irradiation may distort the experimental results. We therefore monitor the time scales for charging and discharging of the samples when subjected to a beam of ions. These experiments allow us to derive an electric conductivity of deep porous ice layers. The results imply that electron irradiation and sputtering play a non-negligible role for certain plasma conditions at the icy moons of Jupiter. The observed ion sputtering yields from our ice-samples are similar to previous experiments where compact ice films were sputtered off a micro-balance. (C) 2016 Elsevier Ltd. All rights reserved.

We conducted a qualitative study to simulate the flux of volatile gases expected to occur at the lunar surface due to cometary impact or lunar outgassing events. A small sample cell containing 8.8 g of JSC-1A lunar soil simulant in a vacuum system with a base pressure of 1.5 x 10(-8) Torr was exposed to various gases using dynamic pressure dosing at room temperature to observe any retention of those gases as a function of the exposure times, temperatures and pressures used. Gases included pure argon, a five-component gas mixture (H-2, He, Ne, N-2, Ar), a simulated Mars atmospheric mixture (CO2, N-2, Ar CO, O-2), and a simulated Titan mixture (N-2, CH4). Results at exposure pressures of approximately 1.5 x 10(-8) Torr above background showed no observable retention of rare gases, slight retention of molecular gases, but surface retention of the triatomic gas CO2 occurred at room temperature with a time to reach equilibrium of greater than 10 min, which was an unanticipated result. Despite several bakeouts and months under ultrahigh vacuum (UHV) conditions, trace levels of atmospheric gases continued to evolve from the simulant. Mechanical and optical probing of the simulant surface increased this latent gas evolution, particularly for CO2 and CO, with some evidence also for the release of CH4. We assert our results are, by analogy, applicable to protocols and instrumentation needed for conducting analytical chemistry aboard future landed lunar missions. (c) 2015 Elsevier Inc. All rights reserved.