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Browsing by Author "Vignoli Muniz, Gabriel S."

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    Irradiation of nitrogen-rich ices by swift heavy ions: clues for the formation of ultracarbonaceous micrometeorites
    (2015) Mejía Guamán, Christian Fernando; Martinez Rodrigues, Rafael; Dartois, Emmanuel; Vignoli Muniz, Gabriel S.; Engrand, Cecile; Godard, Marie; Delauche, L.; Auge, Basile; Bardin, Nathalie; Rothard, H.; Boduch, Philippe; Domaracka, Alicja; Duprat, Jean
    Context. Extraterrestrial materials, such as meteorites and interplanetary dust particles, provide constraints on the formation and evolution of organic matter in the young solar system. Micrometeorites represent the dominant source of extraterrestrial matter at the Earth’s surface, some of them originating from large heliocentric distances. Recent analyses of ultracarbonaceous micrometeorites recovered from Antarctica (UCAMMs) reveal an unusually nitrogen-rich organic matter. Such nitrogen-rich carbonaceous material could be formed in a N2-rich environment, at very low temperature, triggered by energetic processes. Aims. Several formation scenarios have been proposed for the formation of the N-rich organic matter observed in UCAMMs. We experimentally evaluate the scenario involving high energy irradiation of icy bodies subsurface orbiting at large heliocentric distances. Methods. The effect of Galactic cosmic ray (GCR) irradiation of ices containing N2 and CH4 was studied in the laboratory. The N2-CH4 (90:10 and 98:2) ice mixtures were irradiated at 14 K by 44 MeV Ni11+ and 160 MeV Ar15+ swift heavy ion beams. The evolution of the samples was monitored using in-situ Fourier transform infrared spectroscopy. The evolution of the initial ice molecules and new species formed were followed as a function of projectile fluence. After irradiation, the target was annealed to room temperature. The solid residue of the whole process left after ice sublimation was characterized in-situ by infrared spectroscopy, and the elemental composition was measured ex-situ. Results. The infrared bands that appear during irradiation allow us to identify molecules and radicals (HCN, CN−, NH3, ...). The infrared spectra of the solid residues measured at room temperature show similarities with that of UCAMMs. The results point towards the efficient production of a poly-HCN-like residue from the irradiation of N2-CH4 rich surfaces of icy bodies. The room temperature residue provides a viable precursor for the N-rich organic matter found in UCAMMs.
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    Radiolysis of cytosine at cryogenic temperatures by swift heavy ion bombardments
    (2022) Agníhotri, Aditya; Vignoli Muniz, Gabriel S.; Domaracka, Alicja; Rothard, Hermann; Martinez, Rafael; Mejía Guamán, Christian Fernando; Boduch, Philippe; Augé, Basile
    We investigated the radiolysis effects on the cytosine in the solid phase irradiated by swift heavy ions as galactic cosmic ray analogues (GCRs). Infrared (IR) absorption spectroscopy was employed to monitor the physical and chemical radiolytic modifications. The targets were prepared on ZnSe in two different ways: (1) by dropping a nucleobase-water-ethanol solution on the substrate and evaporating the solvent and (2) by sublimation of nucleobase powders in an oven and condensation on the windows. Both types of samples present similar IR absorption spectra. From the exponential decrease of the areas of IR absorption bands as a function of projectile fluence, apparent destruction cross sections (σd) were determined and were found to be very similar for samples prepared using both techniques. The destruction cross section of solid cytosine at cryogenic temperatures follows an electronic stopping (Se) power law: σd = C Sen, where C is a constant and the exponential n is a dimensionless quantity. We determined σd = (3 ± 1) × 10-17 Se (1.25 ±0.06). New absorption features emerge from cytosine degradation, which can be attributed to OCN-, H2CO, and HNCO. By using the observed power law, the half-life of cytosine exposed to galactic cosmic rays was estimated in the order of Mega years. The findings reported here may help a better understanding of complex organic molecule radiostability.
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    Radioresistance of adenine to cosmic rays
    (2017) Domaracka, Alicja; Rothard, Hermann; Vignoli Muniz, Gabriel S.; Mejía Guamán, Christian Fernando; Martinez, Rafael; Auge, Basile; Boduch, Philippe
    The presence of nucleobases in carbonaceous meteorites on Earth is an indication of the existence of this class of molecules in outer space. However, space is permeated by ionizing radiation, which can have damaging effects on these molecules. Adenine is a purine nucleobase that amalgamates important biomolecules such as DNA, RNA, and ATP. Adenine has a unique importance in biochemistry and therefore life. The aim of this work was to study the effects of cosmic ray analogues on solid adenine and estimate its survival when exposed to corpuscular radiation. Adenine films were irradiated at GANIL (Caen, France) and GSI (Darmstadt, Germany) by 820 MeV Kr³³⁺, 190 MeV Ca¹⁰⁺, 92 MeV Xe²³⁺, and 12 MeV C⁴⁺ ion beams at low temperature. The evolution of adenine molecules under heavy ion irradiation was studied by IR absorption spectroscopy as a function of projectile fluence. It was found that the adenine destruction cross section (σd) follows an electronic stopping power (Se) power law under the form: CSeⁿ; C is a constant, and the exponential n is a dimensionless quantity. Using the equation above to fit our results, we determined σd = 4 × 10⁻¹⁷ Se1.17, with Se in kiloelectronvolts per micrometer (keV μm⁻¹). New IR absorption bands arise under irradiation of adenine and can be attributed to HCN, CN⁻, C2H4N4, CH3CN, and (CH3)3CNC. These findings may help to understand the stability and chemistry related to complex organic molecules in space. The half-life of solid adenine exposed to the simulated interstellar medium cosmic ray flux was estimated as (10 ± 8) × 10⁶ years.
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    Swift heavy ion irradiation of thymine at cryogenic temperature
    (2022) Trautmann, Christina; Vignoli Muniz, Gabriel S.; Mejía Guamán, Christian Fernando; Rothard, Hermann; Severin, Daniel; Augé, Basile; Domaracka, Alicja; Boduch, Philippe; Agníhotri, Aditya; Bender, Markus
    Thymine (C5H6N2O2) is a basic N-heterocyclic nucleobase in all known organisms, and this molecule is also found in meteoritic materials. This study aims to investigate thymine's physical and chemical modifications under ion irradiation in cryogenic conditions. Space radiation was simulated by exposing thymine at 27 K to 230 MeV 48Ca10+ ions. Fourier transform infrared spectroscopy (FTIR) was employed to monitor the degradation of a 2.8 μm thick sample film under irradiation. From the intensity decrease of the infrared absorptions as a function of ion fluence, the destruction cross-section (σ), required to dissociate or eject a thymine molecule, is deduced by an exponential function. The physical and chemical modifications induced by energetic projectiles can be related to the electronic stopping power Se as σ=Se/D0, where D0=9.6±0.4 eV/molecule is the effective mean dose needed to destroy the thymine molecule at 27 K. Also, new molecular species formed under irradiation are observed and, based on infrared spectra, identified as CN−, OCN−, HCNO, and CO.

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