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Register a new userInteractions of adsorbed CO$_2$ on water ice at low temperatures
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Added by
Leendertjan Karssemeijer
Publication date
2014
fields
Physics
and research's language is
English
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We present a computational study into the adsorption properties of CO$_2$ on amorphous and crystalline water surfaces under astrophysically relevant conditions. Water and carbon dioxide are two of the most dominant species in the icy mantles of interstellar dust grains and a thorough understanding of their solid phase interactions at low temperatures is crucial for understanding the structural evolution of the ices due to thermal segregation. In this paper, a new H$_2$O-CO$_2$ interaction potential is proposed and used to model the ballistic deposition of CO$_2$ layers on water ice surfaces, and to study the individual binding sites at low coverages. Contrary to recent experimental results, we do not observe CO$_2$ island formation on any type of water substrate. Additionally, density functional theory calculations are performed to assess the importance of induced electrostatic interactions.
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The optical properties of ice in the far infrared are important for models of protoplanetary and debris disks. In this report we derive a new set of data for the absorption (represented by the imaginary part of the refractive index $kappa$) of crystalline water ice in this spectral range, including a detailed inspection of the temperature dependence, which had not been done in such detail before. We measured the transmission of three ice layers with different thicknesses at temperatures $vartheta = 10...250$K and present data at wavelengths $lambda=80...625$ microns. We found a change in the spectral dependence of $kappa$ at a wavelength of $175 pm 6$ microns. At shorter wavelengths, $kappa$ exhibits a constant flat slope and no significant temperature dependence. Long-ward of that wavelength, the slope gets steeper and has a clear, approximately linear temperature dependence. This change in the behaviour is probably caused by a characteristic absorption band of water ice. The measured data were fitted by a power-law model that analytically describes the absorption behaviour at an arbitrary temperature. This model can readily be applied to any object of interest, for instance a protoplanetary or a debris disk. To illustrate how the model works, we simulated the spectral energy distribution (SED) of the resolved, large debris disk around the nearby solar-type star HD 207129. Replacing our ice model by another, commonly used data set for water ice results in a different SED slope at longer wavelengths. This leads to changes in the characteristic model parameters of the disk, such as the inferred particle size distribution, and affects the interpretation of the underlying collisional physics of the disk.
Water is the main constituent of interstellar ices, and it plays a key role in the evolution of many regions of the interstellar medium, from molecular clouds to planet-forming disks. In cold regions of the ISM, water is expected to be completely frozen out onto the dust grains. Nonetheless, observations indicate the presence of cold water vapor, implying that non-thermal desorption mechanisms are at play. Photodesorption by UV photons has been proposed to explain these observations, with the support of extensive experimental and theoretical work on ice analogues. In contrast, photodesorption by X-rays, another viable mechanism, has been little studied. The potential of this process to desorb key molecules, such as water, intact rather than fragmented or ionised, remains unexplored. We experimentally investigated X-ray photodesorption from water ice, monitoring all desorbing species. We find that desorption of neutral water is efficient, while ion desorption is minor. We derive for the first time yields that can be implemented in astrochemical models. These results open up the possibility of taking into account the X-ray photodesorption process in the modelling of protoplanetary disks or X-ray dominated regions.
The work is devoted to the adaptation of the results of laboratory studies of the laser-induced dissociation of molecules of benzene adsorbed on a quartz substrate to the conditions of the interstellar medium. Adsorption was performed under conditions of low temperature and deep vacuum. The difference between the photolysis of adsorbed molecules and molecules in the gas phase is identified. Significance of process of photolytic desorption in the interstellar conditions is analyzed, in particular, in the conditions of photodissociation regions. It is shown that the efficiency and dissociation channels of photolysis of adsorbed and gas phase benzene differ substantially. It is concluded that the photolysis of aromatic hydrocarbons adsorbed on the interstellar dust grains contributes a negligible fraction to the abundance of small hydrocarbons in the interstellar medium.
CO$_2$ ice is an important reservoir of carbon and oxygen in star and planet forming regions. Together with water and CO, CO$_2$ sets the physical and chemical characteristics of interstellar icy grain mantles, including desorption and diffusion energies for other ice constituents. A detailed understanding of CO$_2$ ice spectroscopy is a prerequisite to characterize CO$_2$ interactions with other volatiles both in interstellar ices and in laboratory experiments of interstellar ice analogs. We report laboratory spectra of the CO$_2$ longitudinal optical (LO) phonon mode in pure CO$_2$ ice and in CO$_2$ ice mixtures with H$_2$O, CO, O$_2$ components. We show that the LO phonon mode position is sensitive to the mixing ratio of various ice components of astronomical interest. In the era of JWST, this characteristic could be used to constrain interstellar ice compositions and morphologies. More immediately, LO phonon mode spectroscopy provides a sensitive probe of ice mixing in the laboratory and should thus enable diffusion measurements with higher precision than has been previously possible.
We report results of MD simulations of amorphous ice in the pressure range 0 - 22.5 kbar. The high-density amorphous ice (HDA) prepared by compression of Ih ice at T = 80 K is annealed to T = 170 K at intermediate pressures in order to generate relaxed states. We confirm the existence of recently observed phenomena, the very high-density amorphous ice and a continuum of HDA forms. We suggest that both phenomena have their origin in the evolution of the network topology of the annealed HDA phase with decreasing volume, resulting at low temperatures in the metastability of a range of densities.
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