Radiation Products in Processed Ices Relevant to Edgeworth-Kuiper-Belt Objects

Near the inner edge of the Edgeworth-Kuiper Belt (EKB) are Pluto and Charon, which are known to have N₂- and H₂O-dominated surface ices, respectively. Such non-polar and polar ices, and perhaps mixtures of them, also may be present on other trans-Neptunian objects. Pluto, Charon, and all EKB objects reside in a weak, but constant UV-photon and energetic ion radiation environment that drives chemical reactions in their surface ices. Effects of photon and ion processing include changes in ice composition, volatility, spectra, and albedo, and these have been studied in a number of laboratories. This paper focuses on ice processing by ion irradiation and is aimed at understanding the volatiles, ions, and residues that may exist on outer solar system objects. We summarize radiation chemical products of N₂-rich and H₂O-rich ices containing CO or CH₄, including possible volatiles such as alcohols, acids, and bases. Less-volatile products that could accumulate on EKB objects are observed to form in the laboratory from acid-base reactions, reactions promoted by warming, or reactions due to radiation processing of a relatively pure ice (e.g., CO → C₃O₂). New IR spectra are reported for the 1–5 mu;m region, along with band strengths for the stronger features of carbon suboxide, carbonic acid, the ammonium and cyanate ions, polyoxymethylene, and ethylene glycol. These six materials are possible contributors to EKB surfaces, and will be of interest to observers and future missions.     

Extreme Ultraviolet Photon-Induced Chemical Reactions in the C2H2-H2O Mixed Ices at 10 K

Experimental results on the spectral identification of new infrared absorption features and the changes of their absorbances produced through vacuum ultraviolet-extreme ultraviolet (VUV-EUV) photon-induced chemical reactions in the C₂H₂-H₂O mixed ices at 10 K are obtained. To the best of our knowledge, this is the first time that EUV photons have been employed in the study of the photolysis of ice analogues. Two different compositions, i.e., C₂H₂:H₂O=1:4 and 1:1, were investigated in this work. A tunable intense synchrotron radiation light source available at the Synchrotron Radiation Research Center, Hsinchu, Taiwan, was employed to provide the required VUV-EUV photons. In this study, the photon wavelengths selected to irradiate the icy samples corresponded to the prominent solar hydrogen, helium, and helium ion lines at 121.6 nm, 58.4 nm, and 30.4 nm, respectively. The photon dosages used were typically in the range of 1×10¹⁵ to 2×10¹⁷ photons. Molecular species produced and identified in the ice samples at 10 K resulting from VUV-EUV photon irradiation are mainly CO, CO₂, CH₄, C₂H₆, CH₃OH, and H₂CO. In addition to several unidentified features, we have tentatively assigned several absorption features to HCO, C₃H₈, and C₂H₅OH. While new molecular species were formed, the original reactants, i.e., H₂O and C₂H₂, were detectably depleted due to their conversion to other species. The new chemical species produced by irradiation of photons at 30.4 nm and 58.4 nm can be different from those produced by the 121.6-nm photolysis. In general, the product column density of CO reaches saturation at a lower photon dosage than that of CO₂. Furthermore, the production yield of CO is higher than that of CO₂ in the photon irradiation. In the present study, we also observe that the photon-induced chemical reaction yields are high using photons at 30.4 and 58.4 nm. The results presented in this work are essential to our understanding of chemical synthesis in ice analogues, e.g., the cometary-type ices and icy satellites of planetary systems.     

Infrared Observations Of Volatile Molecules In Comet Hale-Bopp

Infrared observations of comets C/1996 B2 (Hyakutake) and C/1995 O1 (Hale-Bopp) benefited from the high spectral resolution and sensitivity of échelle spectrometers now equipping ground-based telescopes and from the availability of the Infrared Space Observatory (ISO). From the ground, several hydrocarbons were unambiguously detected for the first time: CH₄, C₂H₂, C₂H₆. Water was observed through several of its hot vibrational bands, escaping telluric absorption. CO, HCN, NH₃ and OCS were also observed, as well as several radicals. This permitted the evaluation of molecular production rates, of rotational temperature, and — taking advantage of the 1-D imaging of long-slit spectroscopy — of the space distribution of these species. With ISO, carbon dioxide was directly observed for the second time in a comet (after its detection from the Vega probes in P/Halley). The spectrum of water was investigated in detail (several bands of vibration and far-infrared rotational lines), permitting the evaluation of the rotational temperature of water, and of it spin temperature from the ortho-to-para ratio. Water ice was identified in the grains of Hale-Bopp as far as 7 AU from the ground and possibly at 3 AU with ISO. The composition of cometary volatiles appears to be strikingly similar to that of interstellar ices. This revised version was published online in July 2006 with corrections to the Cover Date.     

Gas trapping in water ice at very low deposition rates and implications for comets

The effect of water ice formation temperature and rate of ice deposition on a cold plate on the amount of trapped argon (equivalent to CO), and the ratios of Ar/Kr/Xe trapped in the water ice were studied at 50, 27 and 22 K and at ice formation rates ranging over four orders of magnitude, from 10⁻¹ to 10⁻⁵ μm min⁻¹. Contrary to our previous conclusions that cometary ices were formed at 50-60 K, we now conclude that these ices were formed at about 25 K. At 25 K the enrichment ratios for Ar, Kr, and Xe remained the same as those at 50 K, reinforcing our suggestion of cometary contribution of these noble gases to the atmospheres of Earth and Mars.     

On liquid phases in cometary nuclei

In this paper we review the relevant literature and investigate conditions likely to lead to melting of H₂O ice, methanol (CH₃OH) ice, ethane (C₂H₆) ice and other volatile ices in cometary nuclei. On the basis of a heat balance model which takes account of volatiles loss, we predict the formation of occasional aqueous and hydrocarbon liquid phases in subsurface regions at heliocentric distances, r_h of 1–3 AU, and 5–12 AU, respectively. Low triple-point temperatures and low vapour pressures of C₂H₆, C₃H₈, and some higher-order alkanes and alkenes, favour liquid phase formation in cometary bodies at high r_h. Microporosity and the formation of a stabilization crust occluding the escape of volatiles facilitate liquid-phase formation. Characteristics of the near-surface which favour subsurface melting include; low effective surface emissivity (at low r_h), high amorphous carbon content, average pore sizes of ～10 μm or less, presence of solutes (e.g. CH₃OH), mixtures of C₂–C₆ hydrocarbons (for melting at high r_h), diurnal thermal cycling, and slow rotation rate. Applying the principles of soil mechanics, capillary forces are shown to initiate pre-melting phenomena and subsequent melting, which is expected to impart considerable strength of ～10⁴ Pa in partially saturated layers, reducing porosity and permeability, enhancing thermal conductivity and heat transfer. Diurnal thermal cycling is expected to have a marked effect on the composition and distribution of H₂O ice in the near-surface leading to frost heave-type phenomena even where little if any true melting occurs. Where melting does take place, capillary suction in the wetted zone has the potential to enhance heat transfer via capillary wetting in a low-gravity environment, and to modify surface topography creating relatively smooth flat-bottomed features, which have a tendency to be located within small depressions. An important aspect of the “wetted layer” model is the prediction that diurnal melt–freeze cycles alter the mixing ratio vs. depth of solutes present, or of other miscible components, largely through a process of fractional crystallization, but also potentially involving frost heave. Wetted layers are potentially durable and can involve significant mass transport of volatile materials in the near-surface, increasing in extent over many rotations of the nucleus prior to and just after perihelion passage, and causing stratification and trapping of the lowest-melting mixtures at depths of several metres. A possible mechanism for cometary outbursts is proposed involving a heat pulse reaching the liquid phase in the deepest wetted zone, leading to supersaturation and triggering the sudden release under pressure of dissolved gases, in particular CO₂, CO, CH₄ or N₂, contained beneath a consolidated near-surface layer. This study indicates that liquid water can persist for long periods of time in the near-surface of some intermediate-sized bodies (10²–10³ km radius) within protoplanetary discs.     

S.E.M.A.Ph.Or.E COMETAIRE,a tool for the study of the photochemical decomposition of probable large organic molecules in comets. first application: Polyoxymethylene

This paper presents a current experimental program concerning the study of the photochemical evolution of the organic matter ejected from the cometary nucleus. The aim of the work is to better understand, using laboratory simulations, the mechanisms which are involved in the degradation of the high molecular weight organics in cometary ices and dust when they are submitted to the warming up and to the bombardment of photons in the surrounding area of the Sun. This experimental study will establish correlations between the nucleus and the molecular composition of the coma. Furthermore, experimental data will provide useful information to bring to a close the question of the origin of the extended sources of H₂CO and CO. Polyoxymethylene, suspected to be present in the cometary nucleus, is often mentioned as a possible parent molecule for the extended source of H₂CO. In order to test this hypothesis, irradiation of POM has been performed at 147 nm. The preliminary results show effectively H₂CO as one photodegradation product as well as CO. C0₂ and HCOOH. Tentative detections of CH₃0CH₃, CH₃OCH₂OCH₃, CH₃OCHO and C₃H₆O₃ are also presented.     

Laboratory studies of the interaction of carbon monoxide with water ice

The interaction of carbon monoxide (CO) with vapour-deposited water(H₂O) ices has been studied using temperature programmed desorption (TPD) and Fourier transform reflection-absorption infrared spectroscopy (FT-RAIRS) over a range of astrophysically relevant temperatures. Such measurements have shown that CO desorption from amorphous H₂Oices is a much more complex process than current astrochemical models suggest. Re-visiting previously reported laboratory experiments (Collings et al., 2003), a rate model has been constructed to explain, in a phenomenological manner, the desorption of CO over astronomically relevant time scales. The model presented here can be widely applied to a range of astronomical environments where depletion of CO from the gas phase is relevant. The model accounts for the two competing processes of CO desorption and migration, and also enables the entrapment of some of the CO in the ice matrix and its subsequent release as the water ice crystallises and then desorbs. The astronomical implications of this model are discussed. This revised version was published online in July 2006 with corrections to the Cover Date.     

Carbon dioxide segregation in 1:4 and 1:9 CO2:H2O ices

The mid-infrared spectra of mixed vapor deposited ices of CO₂ and H₂O were studied as a function of both deposition temperature and warming from 15 to 100 K. The spectra of ices deposited at 15 K show marked changes on warming beginning at 60 K. These changes are consistent with CO₂ segregating within the ice matrix into pure CO₂ domains. Ices deposited at 60 and 70 K show a greater degree of segregation, as high as 90% for 1:4 CO₂:H₂O ice mixtures deposited at 70 K. As the ice is warmed above 80 K, preferential sublimation of the segregated CO₂ is observed. The kinetics of the segregation process is also examined. The segregation of the CO₂ as the ice is warmed corresponds to temperatures at which the structure of the water ice matrix changes from the high density amorphous phase to the low density amorphous phase. We show how these microstructural changes in the ice have a profound effect on the photochemistry induced by ultraviolet irradiation. These experimental results provide a framework in which observations of CO₂ on the icy bodies of the outer Solar System can be considered.     

Models of P/Wirtanen nucleus: active regions versus non-active regions

From the current understanding we know that comet nuclei have heterogeneous compositions and complex structures. It is believed that cometary activity is the result of a combination of physical processes in the nucleus, like sublimation and recondensation of volatile ices, dust grains release, phase transition of water ice, depletion of the most volatile components in the outer layers and interior differentiation.The evolution of the comet depends on the sublimation of ices and the release of different gases and dust grains: the formation of a dust crust, the surface erosion and the development of the coma are related to the gas fluxes escaping from the nucleus. New observations, laboratory experiments and numerical simulations suggest that the gas and dust emissions are locally generated, in the so-called active regions. This localized activity is probably superimposed to the global nucleus activity. The differences between active and inactive regions can be attributed to differences in texture and refractory material content of the different areas.In this paper we present the results of numerical models of cometary nucleus evolution, developed in order to understand which are the processes leading to the formation of active and non-active regions on the cometary surface. The used numerical code solves the equations of heat transport and gas diffusion within a porous nucleus composed of different ices—such as water (the dominant constituent), CO₂, CO- and of dust grains embedded in the ice matrix.By varying the set of physical parameters describing the initial properties of comet P/Wirtanen, the different behaviour of the icy and dusty areas can be followed.Comet P/Wirtanen is the target of the international ROSETTA mission, the cornerstone ESA mission to a cometary nucleus. The successful design of ROSETTA requires some knowledge of comet status and activity: surface temperatures, amount of active and inactive surface areas, gas production rate and dust flux.     

Studies of proton-irradiated cometary-type ice mixtures

Radiation synthesis has been proposed as a mechanism for changing the nature of the outer few meters of ice in a comet stored 4.6 billion years in the Oort cloud and may explain some of the differences observed between new and more evolved comets. Cometary-type ice mixtures were studied in a laboratory experiment designed to approximately simulate the expected temperature, pressure, and radiation environment of the interstellar Oort cloud region. The 2.5- to 15-μm infrared absorption features of thin ice films were analyzed near 20°K before and after 1 MeV proton irradiation. Various ice mixtures included the molecules H₂O, NH₃, CH₄, N₂, C₃H₈, CO, and CO₂. All experiments confirm the synthesis of new molecular species in solid phase mixtures at 20°K. The synthesized molecules, identified by their infrared signatures, are C₂H₆, CO₂, CO, N₂O, NO, and CH₄ (weak). Synthesized molecules, identified by gas chromatographic (GC) analysis of the volatile fraction of the warmed irradiated ice mixture, are C₂H₄ or C₂H₆, and C₃H₈. When CH₄ is present in the irradiated ice mixture, long-chained volatile hydrocarbons and CO₂ are synthesized along with high-molecular-weight carbon compounds present in the room temperature residue. Irradiated mixtures containing CO and H₂O synthesize CO₂ and those CO₂ and H₂O synthesize CO. Due to radiation synthesis, ～1% of the ice was converted into a nonvolatile residue containing complicated carbon compounds not present in blank samples. These results suggest that irrespective of the composition of newly accreted comets, initial molecular abundances can be altered and new species created as a result of radiation synthesis. Irradiated mixtures exhibited thermoluminescence and pressure enhancements during warming; these phenomena suggest irradiation synthesis of reactive species. Ourbursts in new comets resulting from similar radiation induced exothermic activity would be expected to occur beginning at distances of the order of 100 AU.     

Evolution of density in solar system ICES

Pores present in ices in the solar system do not remain unchanged. In isothermal conditions they shrink while in a thermal gradient they migrate towards the higher temperature and escape so that the ice densifies. This motion has been investigated for pure H₂O- and CO₂-ices in a very simple one-dimensional model assuming uniform thermal conductivity and temperature gradient. The results indicate that the densification of H₂O-ice is so slow that it could be significant only for icy satellites having an internal heat source. On the other hand, CO₂-ice densifies orders of magnitude faster and the effect should be important for the CO₂ component of cometary nuclei. No effect is expected for icy planetary rings.     

C/1995 O1 (Hale-Bopp): Gas Production Curves And Their Interpretation

The discovery of C/1995 O1 (Hale-Bopp) at 7 AU from the Sun provided the first opportunity to follow the activity of a bright comet over a large range of heliocentric distances r_h. Production rates of a number of parent molecules and daughter species have been monitored both pre- and postperihelion. CO was found to be the major driver of the activity far from the Sun, surpassed by water within 3 AU whose production rate reached 10³¹ s⁻¹ at perihelion. Gas production curves obtained for various species show several behaviours with r_h. Gas production curves contain important information concerning the physical state of cometary ices, the structure of the nucleus and all the processes taking place inside the nucleus leading to outgassing. They are relevant to the study of several other phenomena such as the sublimation from icy grains, dust mantling or seasonal effects. For some species, such as H₂CO or HNC, they permit to constrain their origin in the coma. We discuss models of subsurface gas production in distant comets and predictions of how such a source may vary as the comet moves along its orbit, approaching perihelion and receding again. Features in the observed gas production curves of comet Hale-Bopp are generally interpretable in terms of either subsurface production (typical example: CO at large r_h) or free sublimation (typical example: H₂O). Possible implications for the vertical stratification of the cometary ices are reviewed, and preference is found for a model with crystallization of amorphous ice close to the nuclear surface. This revised version was published online in July 2006 with corrections to the Cover Date.     

UV photolysis of quinoline in interstellar ice analogs

Abstract— The polycyclic aromatic nitrogen heterocycle (PANH) quinoline (C₉H₇N) was frozen at 20 K in interstellar ice analogs containing either pure water or water mixed with methanol or methane and exposed to ultraviolet (UV) radiation. Upon warming, the photolysis products were analyzed by high‐performance liquid chromatography and nanoscale liquid chromatography‐electrospray ionization mass spectrometry. A suite of hydroxyquinolines, which were formed by the addition of oxygen atoms to quinoline, was observed as the primary product in all the ices. Quinoline N oxide was not formed, but five hydroxyquinoline isomers were produced with no clear dominance of one isomer. Reduction products, formed by hydrogen atom addition, were also created. Ices created at 20 K with H₂O: quinoline ratios of 10:1 to 100:1 showed similar product distributions to those at 122 K, with no apparent temperature or concentration dependence. Increasing the UV dose led to a decrease in overall yield, indicating that quinoline and its products may be photo‐destroyed. Methylquinolines were formed upon photolysis of the methanol‐ and methane‐containing ices. In addition, possible methoxyquinolines or quinoline methylene alcohols were formed in the methanol‐containing ice, while methylhydroxyquinolines were created in the methane‐containing ice. This work indicates that oxidation of PANHs could occur in icy extraterrestrial environments and suggests that a search for such compounds in carbonaceous meteorites could illuminate the possible link between interstellar ice chemistry and meteoritic organics. Given the importance of oxidized and alkylated PANHs to biochemistry, the formation and delivery of such molecules to the early Earth may have played a role in the origin and evolution of life.     

Experimental impact shock chemistry on planetary icy satellites

We present new experimental results on impact shock chemistry into icy satellites of the outer planets. Icy mixtures of pure water ice with CO₂, Na₂CO₃, CH₃OH, and CH₃OH/(NH₄)₂SO₄ at 77 K were ablated with a powerful pulsed laser—a new technique used to simulate shock processes which can occur during impacts. New products were identified by GC-MS and FTIR analyses after laser ablation. Our results show that hydrogen peroxide is formed in irradiated H₂O/CO₂ ices with a final concentration of 0.23%. CO and CH₃OH were also detected as main products. The laser ablation of frozen H₂O/Na₂CO₃ generates only CO and CO₂ as destruction products from the salt. Pulsed irradiation of water ice containing methanol leads also to the formation of CO and CO₂, generates methane and more complex molecules containing carbonyl groups like acetaldehyde, acetone, methyl formate, and a diether, dimethyl formal. The last three compounds are also produced when adding ammonium sulfate to H₂O/CH₃OH ice, but acetone is more abundant. The formation of two hydrocarbons, CH₄ and C₂H₆ is observed as well as the production of three nitrogen compounds, nitrous oxide, hydrogen cyanide, and acetonitrile.     

Production,processing and characterization techniques for cosmic dust analogues

Abstract— The laboratory analyses of cosmic dust analogues—that in the context of this paper include interstellar, circumstellar as well as cometary dust—have a critical role in the study of circumstellar and cometary dust. The morphological, structural and chemical characterization of these analogues are critical for comparisons of their infrared and ultraviolet spectra with those obtained by astronomical observations, as well as for modeling purposes. Besides, the results from these laboratory studies are important to the success of space missions to comets when testing and calibrating the payload instruments. The interpretations of returned scientific data would benefit from the comparison with data recorded by the instruments in a laboratory setting for different classes of previously characterized analogues. We produced various types of condensed samples: (1) Mg,Fe‐silicates, (olivine, pyroxene), (2) carbon‐rich dust, and (3) mixed carbon‐silicate dust. The samples were prepared using different techniques, viz. (1) laser bombardment of solid targets in an Ar and O₂ atmosphere, (2) arc discharge in an Ar and H₂ atmosphere, and (3) grinding powders of natural minerals. We simulated various post‐condensation processes, such as thermal annealing, ultraviolet irradiation, ion bombardment and exposure to atomic hydrogen. These processes produced compound samples of a wide range of physico‐chemical properties. To identify their textures, morphologies, grain compositions and crystallographic properties we used electron microscopy and far‐ultraviolet to far‐infrared (millimeter range) spectroscopy.     

The loss and depth of CO2 ice in comet nuclei

An analytical model has been developed to simulate the chemical differentiation of a homogeneous, initially unmantled cometary nucleus composed of water ice, putative unclathrated CO₂ ice, and silicate dust in specified proportions. Selective sublimation of any free CO₂ ice present in a new comet should produce a surface layer of water ice and dust overlying the undifferentiated core. This surface layer modifies the temperature of buried CO₂ ice and restricts the outflow of gaseous CO₂. On each orbit, water sublimation closer to perihelion temporarily reduces the thickness of the water ice and dust layer and liberates dust. Most of the dust is blown off the nucleus, but a small amount of residual dust remains on the surface (cf. H. L. F. Houpis, W. H. Ip, and D. A. Mendis, 1986, Astrophys. J., in press). Our model includes the effects of nucleus rotation, arbitrary orientation of the rotation axis, latitude, heat conduction into the interior of the nucleus, restriction of CO₂ gas outflow by the water ice and dust layer, and the use of thermal conductivities for both amorphous and crystalline water ice as appropriate, featuresthat were not included in the Houpis et al. model. The model also accounts for the erosion of the water ice surface, which Houpis et al. appear to have accounted for and which is an important effect. Specifically, we investigate the effects of varying the permeability of the surface water ice layer, the mass fraction of CO₂, the orbit and the latitude, using the orbital parameters of Comets Halley and Tempel 2. It is found that CO₂ gas production should exceed H₂O gas production beyond ∼3 AU, and at 1 AU CO₂ gas production should be between 20 to 25% of H₂O gas production. The depth of CO₂ ice and the variation in the depth of CO₂ ice throughout an orbit are affected significantly by the perihelion of the orbit. The effects due to water ice permeability are significant but much less than expected on the basis of flow area. Latitude and CO₂ concentration produce relatively small effects. Under all conditions considered here, CO₂ ice should always be found within ∼1 m from the surface of comet nuclei if it is present as a free species to begin with. This result is probably generally valid for unmantled portions of most comets and qualitatively simulates the behavior of an abundant, highly volatile component in an H₂O/silicate matrix. Comparison of these and similar results with observations could yield information regarding the permeability and chemical composition of cometary material and suggest sampling strategies to minimize fractionation effects. The method is applicable to other nonwater ices.     

Near-infrared spectral monitoring of Triton with IRTF/SpeX II: Spatial distribution and evolution of ices

This report arises from an ongoing program to monitor Neptune’s largest moon Triton spectroscopically in the 0.8 to 2.4 μm range using IRTF/SpeX. Our objective is to search for changes on Triton’s surface as witnessed by changes in the infrared absorption bands of its surface ices N₂,CH₄,H₂O, CO, and CO₂. We have recorded infrared spectra of Triton on 53 nights over the ten apparitions from 2000 to 2009. The data generally confirm our previously reported diurnal spectral variations of the ice absorption bands (Grundy and Young, 2004). Nitrogen ice shows a large amplitude variation, with much stronger absorption on Triton’s Neptune-facing hemisphere. We present evidence for seasonal evolution of Triton’s N₂ ice: the 2.15 μm absorption band appears to be diminishing, especially on the Neptune-facing hemisphere. Although it is mostly dissolved in N₂ ice, Triton’s CH₄ ice shows a very different longitudinal variation from the N₂ ice, challenging assumptions of how the two ices behave. Unlike Triton’s CH₄ ice, the CO ice does exhibit longitudinal variation very similar to the N₂ ice, implying that CO and N₂ condense and sublimate together, maintaining a consistent mixing ratio. Absorptions by H₂O and CO₂ ices show negligible variation as Triton rotates, implying very uniform and/or high latitude spatial distributions for those two non-volatile ices.     

Combustion as the cause of comet P/Halley's activity

The totality of the results obtained in the VEGA, GIOTTO and SUISEI projects does not lend itself to interpretation within the old sublimation models of comet activity considering solar radiation as the sole source of energy. Among them are the systematic excess of the velocity and temperature of the gas escaping from the nucleus over the theoretical values, the outflow being concentrated in several ( ~ 12–15) narrow ( ~ 300 m in size at the nucleus) hypersonic jets carrying very large amounts of remarkably fine CHON dust and located along continuous lines on the nuclear surface, intense release from the nucleus or very close to it (2 × 10³km) of CO (Q _Co/Q _{H2 O} = 0.05–0.2) with a smaller amount of CO₂ (Q _{CO 2}/ Q _{H2 O} 0.015), large near-nucleus abundances of C, C⁺ (Q _C/Q _CO 0.29), etc.The new observations, together with some earlier data still poorly understood (e.g. the appearance in the coma of large amounts of C₃) can be accounted for by assuming the cometary ices to contain, apart from hydrocarbons, nitrogen-containing compounds, etc. also of free oxygen ( ~ 15 wt.%). Under these conditions, burning should occur in the products of sublimation under deficiency of oxidizer accompanied by the production of soot, smoke, etc. The burning should propagate under the surface crust and localize primarily at a few sites.The presence of oxygen in cometary ices follows from a new eruption theory assuming the minor bodies of the Solar System to have formed in explosions of the massive ice envelopes saturated by electrolysis products on distant moonlike bodies of the type of Ganymede and Callisto.     

Light scattering by fluffy Mg-Fe-SiO and C mixtures as cometary analogs (PROGRA experiment)

Cometary particles mainly consist of silicates and carbon compounds; they seem to be fluffy aggregates of tiny grains, as found in some IDPs. The linear polarization of the scattered light is an efficient method to characterize their physical properties. Laboratory simulations of light scattering by cometary analog particles help to disentangle different physical parameters by comparison with observational data. We present here polarization laboratory results with nine samples levitating particles: five samples of vapor-condensed magnesiosilica, one ferrosilica smoke, a mixture of magnesio-ferrosilica smokes, one mixture of ferrosilica with carbon and one mixture of magnesio-ferrosilica with carbon. The phase curves are bell-shaped with a maximum polarization at a phase range of (80°-100°). A shallow negative branch can be present at phase angles smaller than 20°. The different characteristics of the phase curves are discussed considering the size and the structure of the constituent grains and the size of the particles. For the five magnesiosilica samples, the maximum in polarization is in the 40% range (close to cometary values), and no wavelength dependence is detected; the negative branch, whose presence seems to be linked to the presence of large aggregates of fine silica (SiO₂) grains, does not always exist. For the ferrosilica smoke, the maximum in polarization is about 30% in red light (632.8 nm) and 40% in green light (543.5 nm); the negative branch occurs for phase angles smaller than 20°. For the two mixtures with carbon black, the polarization spectral gradient is positive, as expected for cometary analog particles. Finally, the phase curves obtained for agglomerates of magnesio-ferrosilica and carbon (expected to be the main components of cometary particles) are comparable to those obtained by remote observations of dust in cometary comae.     

CO/CO2 Molecular Number Ratio Produced by ion Irradiation of Ices

We have quantitatively studied, by infrared absorption spectroscopy, the CO/CO₂ molecular number ratio after ion irradiation of ices and mixtures containing astrophysically relevant species such as CO, CO₂, H₂O, CH₄, CH₃OH, NH₃, O₂, and N₂ at 12–15 K. The ratios have also been measured after warm up to temperatures between 12 and 200 K. As a general result we find that the CO/CO₂ ratio decreases with the irradiation dose (amount of energy deposited on the sample). In all of the studied mixtures, as expected, it decreases with increasing temperature because of CO sublimation. However the temperature where CO sublimes strongly depends on the initial mixture, remaining at a temperature over 100 K in some cases. Our results might be relevant to interpret the observed CO/CO₂ ratio in several astrophysical scenarios such as planetary icy surfaces and ice mantles on grains in the interstellar medium. This revised version was published online in July 2006 with corrections to the Cover Date.