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  • EDP Sciences  (4)
  • 1
    In: Astronomy & Astrophysics, EDP Sciences, Vol. 553 ( 2013-5), p. A50-
    Type of Medium: Online Resource
    ISSN: 0004-6361 , 1432-0746
    RVK:
    RVK:
    Language: English
    Publisher: EDP Sciences
    Publication Date: 2013
    detail.hit.zdb_id: 1458466-9
    SSG: 16,12
    Location Call Number Limitation Availability
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  • 2
    In: Astronomy & Astrophysics, EDP Sciences, Vol. 598 ( 2017-2), p. A18-
    Abstract: Context. Almost 20% of the ~200 different species detected in the interstellar and circumstellar media present a carbon atom linked to nitrogen by a triple bond. Among these 37 molecules, 30 are nitrile R-CN compounds, the remaining seven belonging to the isonitrile R-NC family. How these species behave in presence of the grain surfaces is still an open question. Aims. In this contribution we investigate whether the difference between nitrile and isonitrile functional groups may induce differences in the adsorption energies of the related isomers at the surfaces of interstellar grains of different nature and morphologies. Methods. The question was addressed by means of a concerted experimental and theoretical study of the adsorption energies of CH 3 CN and CH 3 NC on the surface water ice and silica. The experimental determination of the molecule – surface interaction energies was carried out using temperature programmed desorption (TPD) under an ultra-high vacuum (UHV) between 70 and 160 K. Theoretically, the question was addressed using first principle periodic density functional theory (DFT) to represent the organized solid support. Results. The most stable isomer (CH 3 CN) interacts more efficiently with the solid support than the higher energy isomer (CH 3 NC) for water ice and silica. Comparing with the HCN and HNC pair of isomers, the simulations show an opposite behaviour, in which isonitrile HNC are more strongly adsorbed than nitrile HCN provided that hydrogen bonds are compatible with the nature of the model surface. Conclusions. The present study confirms that the strength of the molecule surface interaction between isomers is not related to their intrinsic stability but instead to their respective ability to generate different types of hydrogen bonds. Coupling TPD to first principle simulations is a powerful method for investigating the possible role of interstellar surfaces in the release of organic species from grains, depending on the environment.
    Type of Medium: Online Resource
    ISSN: 0004-6361 , 1432-0746
    RVK:
    RVK:
    Language: English
    Publisher: EDP Sciences
    Publication Date: 2017
    detail.hit.zdb_id: 1458466-9
    SSG: 16,12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    In: Astronomy & Astrophysics, EDP Sciences, Vol. 608 ( 2017-12), p. A50-
    Abstract: Context. Almost 20% of the ~200 different species detected in the interstellar and circumstellar media present a carbon atom linked to nitrogen by a triple bond. Of these 37 molecules, 30 are nitrile R-CN compounds, the remaining 7 belonging to the isonitrile R-NC family. How these species behave in their interactions with the grain surfaces is still an open question. Aims. In a previous work, we have investigated whether the difference between nitrile and isonitrile functional groups may induce differences in the adsorption energies of the related isomers at the surfaces of interstellar grains of various nature and morphologies. This study is a follow up of this work, where we focus on the adsorption on carbonaceous aromatic surfaces. Methods. The question is addressed by means of a concerted experimental and theoretical approach of the adsorption energies of CH 3 CN and CH 3 NC on the surface of graphite (with and without surface defects). The experimental determination of the molecule and surface interaction energies is carried out using temperature-programmed desorption in an ultra-high vacuum between 70 and 160 K. Theoretically, the question is addressed using first-principle periodic density functional theory to represent the organised solid support. Results. The adsorption energy of each compound is found to be very sensitive to the structural defects of the aromatic carbonaceous surface: these defects, expected to be present in a large numbers and great diversity on a realistic surface, significantly increase the average adsorption energies to more than 50% as compared to adsorption on perfect graphene planes. The most stable isomer (CH 3 CN) interacts more efficiently with the carbonaceous solid support than the higher energy isomer (CH 3 NC), however.
    Type of Medium: Online Resource
    ISSN: 0004-6361 , 1432-0746
    RVK:
    RVK:
    Language: English
    Publisher: EDP Sciences
    Publication Date: 2017
    detail.hit.zdb_id: 1458466-9
    SSG: 16,12
    Location Call Number Limitation Availability
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  • 4
    Online Resource
    Online Resource
    EDP Sciences ; 2017
    In:  Astronomy & Astrophysics Vol. 603 ( 2017-7), p. A61-
    In: Astronomy & Astrophysics, EDP Sciences, Vol. 603 ( 2017-7), p. A61-
    Abstract: Context. Methane is among the main components of the ice mantles of interstellar dust grains, where it is at the start of a rich solid-phase chemical network. Quantification of the photon-induced desorption yield of these frozen molecules and understanding of the underlying processes is necessary to accurately model the observations and the chemical evolution of various regions of the interstellar medium. Aims. This study aims at experimentally determining absolute photodesorption yields for the CH 4 molecule as a function of photon energy. The influence of the ice composition is also investigated. By studying the methane desorption from layered CH 4 :CO ice, indirect desorption processes triggered by the excitation of the CO molecules are monitored and quantified. Methods. Tunable monochromatic vacuum ultraviolet light (VUV) light from the DESIRS beamline of the SOLEIL synchrotron is used in the 7–13.6 eV (177–91 nm) range to irradiate pure CH 4 or layers of CH 4 deposited on top of CO ice samples. The release of species in the gas phase is monitored by quadrupole mass spectrometry, and absolute photodesorption yields of intact CH 4 are deduced. Results. CH 4 photodesorbs for photon energies higher than ~9.1 eV (~136 nm). The photodesorption spectrum follows the absorption spectrum of CH 4 , which confirms a desorption mechanism mediated by electronic transitions in the ice. When it is deposited on top of CO, CH 4 desorbs between 8 and 9 eV with a pattern characteristic of CO absorption, indicating desorption induced by energy transfer from CO molecules. Conclusions. The photodesorption of CH 4 from pure ice in various interstellar environments is around 2.0 ± 1.0 × 10 -3 molecules per incident photon. Results on CO-induced indirect desorption of CH 4 provide useful insights for the generalization of this process to other molecules co-existing with CO in ice mantles.
    Type of Medium: Online Resource
    ISSN: 0004-6361 , 1432-0746
    RVK:
    RVK:
    Language: English
    Publisher: EDP Sciences
    Publication Date: 2017
    detail.hit.zdb_id: 1458466-9
    SSG: 16,12
    Location Call Number Limitation Availability
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