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Register a new userOxygen atom reactions with C2H6, C2H4, and C2H2 in ices
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Oxygen atom addition and insertion reactions may provide a pathway to chemical complexity in ices that are too cold for radicals to diffuse and react. We have studied the ice-phase reactions of photo-produced oxygen atoms with C2 hydrocarbons under ISM-like conditions. The main products of oxygen atom reactions with ethane are ethanol and acetaldehyde; with ethylene are ethylene oxide and acetaldehyde; and with acetylene is ketene. The derived branching ratio from ethane to ethanol is ~0.74 and from ethylene to ethylene oxide is ~0.47. For all three hydrocarbons there is evidence of an effectively barrierless reaction with O(^1D) to form oxygen-bearing organic products; in the case of ethylene, there may be an additional barriered contribution of the ground-state O(^3P) atom. Thus, oxygen atom reactions with saturated and unsaturated hydrocarbons are a promising pathway to chemical complexity even at very low temperatures where the diffusion of radical species is thermally inaccessible.
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We have analysed the ISO-SWS spectrum of Jupiter in the 12-16 micron range, where several hydrocarbons exhibit rovibrational bands. Using temperature information from the methane and hydrogen emissions, we derive the mixing ratios (q) of acetylene and ethane at two independent pressure levels. For acetylene, we find $q=(8.9^{+1.1}_{-0.6})times10^{-7}$ at 0.3 mbar and $q=(1.1^{+0.2}_{-0.1})times10^{-7}$ at 4 mbar, giving a slope $-dln q / dln P=0.8pm0.1$, while for ethane $q=(1.0pm0.2)times10^{-5}$ at 1 mbar and $q=(2.6^{+0.5}_{-0.6})times10^{-6}$ at 10 mbar, giving $-dln q / dln P=0.6pm0.2$. The ethane slope is consistent with the predictions of Gladstone et al. (1996), but that predicted for acetylene is larger than we observe. This disagreement is best explained by an overestimation of the acetylene production rate compared to that of ethane in the Gladstone et al. (1996) model. At 15.8 micron, methylacetylene is detected for the first time at low jovian latitudes, and a stratospheric column density of $(1.5pm0.4)times10^{15}$ molecule.cm-2 is inferred. We also derive an upper limit for the diacetylene column density of $7times10^{13}$ molecule.cm-2.
Molecular oxygen, nitrogen, and ozone have been detected in the Solar System. They are also expected to be present in ice-grain mantles within star-forming regions. Laboratory experiments that simulate energetic processing (ions, photons, and electrons) of ices are essential for interpreting and directing future astronomical observations. We provide VUV photoabsorption spectroscopic data of energetically processed nitrogen- and oxygen-rich ices that will help to identify absorption bands and/or spectral slopes observed on icy objects in the Solar System and on ice-grain mantles of the interstellar medium. We present VUV photoabsorption spectra of frozen O2 and N2, a 1:1 mixture of both, and a new systematic set of pure and mixed nitrogen oxide ices. Spectra were obtained at 22 K before and after 1 keV electron bombardment of the ice sample. Ices were then annealed to higher temperatures to study their thermal evolution. In addition, Fourier-transform infrared spectroscopy was used as a secondary probe of molecular synthesis to better identify the physical and chemical processes at play. Our VUV data show that ozone and the azide radical (N3) are observed in our experiments after electron irradiation of pure O2 and N2 ices, respectively. Energetic processing of an O2:N2 = 1:1 ice mixture leads to the formation of ozone along with a series of nitrogen oxides. The electron irradiation of solid nitrogen oxides, pure and in mixtures, induces the formation of new species such as O2, N2 , and other nitrogen oxides not present in the initial ice. Results are discussed here in light of their relevance to various astrophysical environments. Finally, we show that VUV spectra of solid NO2 and water can reproduce the observational VUV profile of the cold surface of Enceladus, Dione, and Rhea, strongly suggesting the presence of nitrogen oxides on the surface of the icy Saturn moons.
The validity of the widely used linear mixing approximation for the equations of state (EOS) of planetary ices is investigated at pressure-temperature conditions typical for the interior of Uranus and Neptune. The basis of this study are ab initio data ranging up to 1000 GPa and 20 000 K calculated via density functional theory molecular dynamics simulations. In particular, we calculate a new EOS for methane and EOS data for the 1:1 binary mixtures of methane, ammonia, and water, as well as their 2:1:4 ternary mixture. Additionally, the self-diffusion coefficients in the ternary mixture are calculated along three different Uranus interior profiles and compared to the values of the pure compounds. We find that deviations of the linear mixing approximation from the results of the real mixture are generally small; for the thermal EOS they amount to 4% or less. The diffusion coefficients in the mixture agree with those of the pure compounds within 20% or better. Finally, a new adiabatic model of Uranus with an inner layer of almost pure ices is developed. The model is consistent with the gravity field data and results in a rather cold interior ($mathrm{T_{core}} mathtt{sim}$ 4000 K).
Ices are an important constituent of protoplanetary disks. New observational facilities, notably JWST, will greatly enhance our view of disk ices by measuring their infrared spectral features. We present a suite of models to complement these upcoming observations. Our models use a kinetics-based gas-grain chemical evolution code to simulate the distribution of ices in a disk, followed by a radiative transfer code using a subset of key ice species to simulate the observations. We present models reflecting both molecular inheritance and chemical reset initial conditions. We find that H$_2$O, CO$_2$, and CH$_3$OH near-to-mid-IR absorption features are readily observable in disk-integrated spectra of highly-inclined disks while CO, NH$_3$, and CH$_4$ ice do not show prominent features. CH$_3$OH ice has low abundance and is not observable in the reset model, making this species an excellent diagnostic of initial chemical conditions. CO$_2$ ice features exhibit the greatest change over disk lifetime: decreasing and increasing for the inheritance and reset models, respectively. Spatially-resolved spectra of edge-on disks, possible with JWSTs integral field unit observing modes, are ideal for constraining the vertical distribution of ices and may be able to isolate features from ices closer to the midplane (e.g., CO) given sufficient sensitivity. Spatially-resolved spectra of face-on disks can trace scattered-light features from H$_2$O, CO$_2$, and CH$_3$OH, plus CO and CH$_4$ from the outermost regions. We additionally simulate far-IR H$_2$O ice emission features and find they are strongest for disks viewed face-on.
The fundamental band for the OC-C2H2 dimer and two combination bands involving the intermolecular bending modes nu9 and nu8 in the carbon monoxide CO stretch region are re-examined. Spectra are obtained using a pulsed supersonic slit jet expansion probed with a mode-hop free tunable infrared quantum cascade laser. Analogous bands for OC-C2D2 and the fundamental for OC-DCCH as an impurity are also observed and analysed. A much weaker band in the same spectral region is assigned to a new mixed trimer, CO-(C2H2)2. The trimer band is composed uniquely of a-type transitions, establishing that the CO monomer is nearly aligned with the a-inertial axis. The observed rotational constants agree well with ab initio calculations and a small inertial defect value indicates that the trimer is planar. The structure is a compromise between the T-shaped structure of free acetylene dimer and the linear geometry of free OC-C2H2. A similar band for the fully deuterated isotopologue CO-(C2D2)2 confirms our assignment.
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