Near-infrared spectral monitoring of Triton with IRTF/SpeX I: establishing a baseline for rotational variability

We present eight new 0.8 to 2.4 μm spectral observations of Neptune's satellite Triton, obtained at IRTF/SpeX during 2002 July 15-22 UT. Our objective was to determine how Triton's near-infrared spectrum varies as Triton rotates, and to establish an accurate baseline for comparison with past and future observations. The most striking spectral change detected was in Triton's nitrogen ice absorption band at 2.15 μm; its strength varies by about a factor of two as Triton rotates. Maximum N₂ absorption approximately coincides with Triton's Neptune-facing hemisphere, which is also the longitude where the polar cap extends nearest Triton's equator. More subtle rotational variations are reported for Triton's CH₄ and H₂O ice absorption bands. Unlike the other ices, Triton's CO₂ ice absorption bands remain nearly constant as Triton rotates. Triton's H₂O ice is shown to be crystalline, rather than amorphous. Triton's N₂ ice is confirmed to be the warmer, hexagonal, β N₂ phase, and its CH₄ is confirmed to be highly diluted in N₂ ice.     

Large seasonal variations in Triton's atmosphere

Triton's seasons differ materially from those of Pluto owing to four important differences in the governing physics: First, the obliquity of Triton is significantly less than Pluto's obliquity. Second, Triton's inclined orbit precesses rapidly about Neptune so that a complicated seasonal variation in the latitude of the Sun occurs for Triton. Third, Neptune's orbit is much more circular than Pluto's orbit so that the sunlight intercepted by Triton's disk does not vary seasonally. Finally, Triton's atmosphere cannot be saturated at the lower latitudes so that the mass of the atmosphere is controlled by the temperature of the high-latitude ices or liquids (polar caps), as for CO₂ on Mars. The consequences of Triton's entire surface being covered with volatile substances have been examined. It is found that the circularity of Neptune's orbit then implies that Triton would have hardly any seasonal variation at all in surface temperature or atmospheric bulk, in spite of the complicated precessional effects of Triton's orbit. The only seasonal effect would be the migration of surface ices and liquids. This scenario is ruled out because it implies a column CH₄ abundance much higher than that observed and because it quickly depletes the lower latitudes of volatiles. It is concluded that Triton's most volatile surface substances are probably relegated to latitudes higher than 35° and probably form polar caps. The temperature of the polar caps should be nearly equal, even during midwinter/midsummer when the insolation of the summer pole is greatest. If the summer pole completely sublimates during one of the “major” summers, Triton's atmosphere may begin to freeze out over the winter caps. It is therefore expected that Triton's atmosphere undergoes large and complex seasonal variations. Triton is currently approaching a “maximum southern summer”, and over the remainder of this century, a dramatic increase in CH₄ abundance above the current upper limit of 1 m-Am may be witnessed.     

Discovery of co2 ice and leading-trailing spectral asymmetry on the uranian satellite ariel

New 0.8- to 2.4-μm spectral observations of the leading and trailing hemispheres of the uranian satellite Ariel were obtained at IRTF/SpeX during 2002 July 16 and 17 UT. The new spectra reveal contrasts between Ariel’s leading and trailing hemispheres, with the leading hemisphere presenting deeper H₂O ice absorption bands. The observed dichotomy is comparable to leading-trailing spectral asymmetries observed among jovian and saturnian icy satellites. More remarkably, the trailing hemisphere spectrum exhibits three narrow CO₂ ice absorption bands near 2 μm. This discovery of CO₂ ice on one hemisphere of Ariel is its first reported detection in the uranian system.     

Remote sensing D/H ratios in methane ice: Temperature-dependent absorption coefficients of CH3D in methane ice and in nitrogen ice

The existence of strong absorption bands of singly deuterated methane (CH₃D) at wavelengths where normal methane (CH₄) absorbs comparatively weakly could enable remote measurement of D/H ratios in methane ice on outer Solar System bodies. We performed laboratory transmission spectroscopy experiments, recording spectra at wavelengths from 1 to 6 μm to study CH₃D bands at 2.47, 2.87, and 4.56 μm, wavelengths where ordinary methane absorption is weak. We report temperature-dependent absorption coefficients of these bands when the CH₃D is diluted in CH₄ ice and also when it is dissolved in N₂ ice, and describe how these absorption coefficients can be combined with data from the literature to simulate arbitrary D/H ratio absorption coefficients for CH₄ ice and for CH₄ in N₂ ice. We anticipate these results motivating new telescopic observations to measure D/H ratios in CH₄ ice on Triton, Pluto, Eris, and Makemake.     

Distributions of H2O and CO2 ices on Ariel, Umbriel, Titania, and Oberon from IRTF/SpeX observations

We present 0.8-2.4 μm spectral observations of uranian satellites, obtained at IRTF/SpeX on 17 nights during 2001-2005. The spectra reveal for the first time the presence of CO₂ ice on the surfaces of Umbriel and Titania, by means of 3 narrow absorption bands near 2 μm. Several additional, weaker CO₂ ice absorptions have also been detected. No CO₂ absorption is seen in Oberon spectra, and the strengths of the CO₂ ice bands decline with planetocentric distance from Ariel through Titania. We use the CO₂ absorptions to map the longitudinal distribution of CO₂ ice on Ariel, Umbriel, and Titania, showing that it is most abundant on their trailing hemispheres. We also examine H₂O ice absorptions in the spectra, finding deeper H₂O bands on the leading hemispheres of Ariel, Umbriel, and Titania, but the opposite pattern on Oberon. Potential mechanisms to produce the observed longitudinal and planetocentric distributions of the two ices are considered.     

Infrared study of ion-irradiated N2-dominated ices relevant to Triton and Pluto: formation of HCN and HNC

Infrared spectra and radiation chemical behavior of N₂-dominated ices relevant to the surfaces of Triton and Pluto are presented. This is the first systematic IR study of proton-irradiated N₂-rich ices containing CH₄ and CO. Experiments at 12 K show that HCN, HNC, and diazomethane (CH₂N₂) form in the solid phase, along with several radicals. NH₃ is also identified in irradiated N₂ + CH₄ and N₂ + CH₄ + CO. We show that HCN and HNC are made in irradiated binary ice mixtures having initial N₂/CH₄ ratios from 100 to 4, and in three-component mixtures have an initial N₂/(CH₄ + CO) ratio of 50. HCN and HNC are not detected in N₂-dominated ices when CH₄ is replaced with C₂H₆, C₂H₂, or CH₃OH.The intrinsic band strengths of HCN and HNC are measured and used to calculate G(HCN) and G(HNC) in irradiated N₂ + CH₄ and N₂ + CH₄ + CO ices. In addition, the HNC/HCN ratio is calculated to be ∼1 in both icy mixtures. These radiolysis results reveal, for the first time, solid-phase synthesis of both HCN and HNC in N₂-rich ices containing CH₄.We examine the evolution of spectral features due to acid-base reactions (acids such as HCN, HNC, and HNCO and a base, NH₃) triggered by warming irradiated ices from 12 K to 30-35 K. We identify anions (OCN⁻, CN⁻, and N3−) in ices warmed to 35 K. These ions are expected to form and survive on the surfaces of Triton and Pluto. Our results have astrobiological implications since many of these products (HCN, HNC, HNCO, NH₃, NH₄OCN, and NH₄CN) are involved in the syntheses of biomolecules such as amino acids and polypeptides.     

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.     

Methane on Triton: Physical state and distribution

Infrared spectrophotometric measurements of Neptune's satellite Triton obtained between 1980 and 1982 in the spectral range 0.8–2.5 μm show six individual absorption bands attributable to methane. An additional band in the Triton data is not methane. The Triton spectral data conform more closely to a laboratory spectrum of frozen methane than to a synthetic spectrum of methane gas computed for conditions of low temperature expected at the satellite. Additionally, the strength of the bands vary with Triton's orbital position. The data thus suggest that methane in the ice phase is mostly responsible for the bands in Triton's spectrum, and that the ice is distributed nonuniformly around the satellite's surface.     

Evidence of N2-ice on the surface of the icy dwarf Planet 136472 (2005 FY9)

We present high signal precision optical reflectance spectra of 2005 FY9 taken with the Red Channel Spectrograph and the 6.5-m MMT telescope on 2006 March 4 UT (5000-9500 Å; 6.33 Å pixel⁻¹) and 2007 February 12 UT (6600-8500 Å; 1.93 Å pixel⁻¹). From cross-correlation experiments between the 2006 March 4 spectrum and a pure CH₄-ice Hapke model, we find the CH₄-ice bands in the MMT spectrum are blueshifted by 3 ± 4 Å relative to bands in the pure CH₄-ice Hapke spectrum. The higher resolution MMT spectrum of 2007 February 12 UT enabled us to measure shifts of individual CH₄-ice bands. We find the 7296, 7862, and 7993 Å CH₄-ice bands are blueshifted by 4 ± 2, 4 ± 4, and 6 ± 5 Å. From four measurements we report here and one of our previously published measurements, we find the CH₄-ice bands are shifted by 4 ± 1 Å. This small shift is important because it suggest the presence of another ice component on the surface of 2005 FY9. Laboratory experiments show that CH₄-ice bands in spectra of CH₄ mixed with other ices are blueshifted relative to bands in spectra of pure CH₄-ice. A likely candidate for the other component is N₂-ice because its weak 2.15 μm band and blueshifted CH₄ bands are seen in spectra of Triton and Pluto. Assuming the shift is due to the presence of N₂, spectra taken on two consecutive nights show no difference in CH₄/N₂. In addition, we find no measurable difference in CH₄/N₂ at different depths into the surface of 2005 FY9.     

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.     

Dione’s spectral and geological properties

We present a detailed analysis of the variations in spectral properties across the surface of Saturn’s satellite Dione using Cassini/VIMS data and their relationships to geological and/or morphological characteristics as seen in the Cassini/ISS images. This analysis focuses on a local region on Dione’s anti-saturnian hemisphere that was observed by VIMS with high spatial resolution during orbit 16 in October 2005. The results are incorporated into a global context provided by VIMS data acquired within Cassini’s first 50 orbits. Our results show that Dione’s surface is dominated by at least one global process. Bombardment by magnetospheric particles is consistent with the concentration of dark material and enhanced CO₂ absorption on the trailing hemisphere of Dione independent of the geology. Local regions within this terrain indicate a special kind of resurfacing that probably is related to large-scale impact process. In contrast, the enhanced ice signature on the leading side is associated with the extended ejecta of the fresh impact crater Creusa (∼49°N/76°W). Although no geologically active regions could be identified, Dione’s tectonized regions observed with high spatial resolution partly show some clean H₂O ice implying that tectonic processes could have continued into more recent times.     

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.     

The Temperature-Dependent Spectrum of Methane Ice I between 0.7 and 5 μm and Opportunities for Near-Infrared Remote Thermometry

New infrared absorption coefficient spectra of pure methane ice I were measured at temperatures between 30 and 90 K, over wavelengths from 0.7 to 5 μm, along with spectra of methane ice II at 20 K and liquid methane at 93 K. The spectra were derived from transmission measurements through monocrystalline samples grown in a series of closed cells having interior dimensions ranging from 100 μm to 1 cm. The thicker samples permitted measurement of extremely weak absorption bands, with absorption coefficients as small as 0.003 cm⁻¹. We report 14 new absorption bands, which we tentatively assign to specific vibrational transitions. Two of the new bands are attributed to CH₃D. Measurements of the weaker CH₄ bands are particularly needed for interpreting spectral observations of Pluto and Triton, where a number of weak CH₄-ice absorption bands have been observed. The data presented in this paper complement studies of spectral transmission by thin films of methane ice, which are most suitable for measuring the stronger absorption bands. Temperature-dependent spectral features revealed by the new data offer the opportunity to determine CH₄-ice temperatures remotely, via near-infrared reflectance spectroscopy. This approach could prove particularly valuable for future spacecraft exploration of Pluto.     

Formation of radical species in photolyzed CH4:N2 ices

We report photochemical studies of thin cryogenic ice films composed of N₂, CH₄ and CO in ratios analogous to those on the surfaces of Neptune’s largest satellite, Triton, and on Pluto. Experiments were performed using a hydrogen discharge lamp, which provides an intense source of ultraviolet light to simulate the sunlight-induced photochemistry on these icy bodies. Characterization via infrared spectroscopy showed that C₂H₆ and C₂H₂, and HCO are formed by the dissociation of CH₄ into H, CH₂ and CH₃ and the subsequent reaction of these radicals within the ice. Other radical species, such as C₂, , CN, and CNN, are observed in the visible and ultraviolet regions of the spectrum. These species imply a rich chemistry based on formation of radicals from methane and their subsequent reaction with the N₂ matrix. We discuss the implications of the formation of these radicals for the chemical evolution of Triton and Pluto. Ultimately, this work suggests that , CN, HCO, and CNN may be found in significant quantities on the surfaces of Triton and Pluto and that new observations of these objects in the appropriate wavelength regions are warranted.     

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.     

Spatial and Compositional Constraints on Non-ice Components and H2O on Pluto's Surface

We present four new near-infrared spectra of Pluto, measured separately from its satellite Charon during four HST/NICMOS observations in 1998, timed to sample four evenly spaced longitudes on Pluto. Being free of contamination by telluric absorptions or by Charon light, the new data are particularly valuable for studies of Pluto's continuum absorption. Previous studies of the major volatile species indicate the existence of at least three distinct terrains on Pluto's surface: N₂-rich, CH₄-rich, and volatile-depleted. The new data provide evidence that each of these three terrains has distinct near-infrared continuum absorption features. CH₄-rich regions appear to show reddish continuum absorption through the near-infrared spectral range. N₂-rich regions have very little continuum absorption. Visually dark, volatile-depleted regions exhibit intermediate continuum albedos with a bluish continuum slope. By analogy with Triton, we expected that careful spectral modeling would reveal strong evidence for the existence of H₂O ice on Pluto's surface, but we found only very weak evidence for its existence in the volatile-depleted regions. These data require H₂O ice to play a much less prominent role on Pluto's surface than it does on Triton's.     

A spectroscopic study of the surfaces of Saturn's large satellites: H2O ice, tholins, and minor constituents

We present spectra of Saturn's icy satellites Mimas, Enceladus, Tethys, Dione, Rhea, and Hyperion, 1.0-2.5 μm, with data extending to shorter (Mimas and Enceladus) and longer (Rhea and Dione) wavelengths for certain objects. The spectral resolution (R=λ/Δλ) of the data shown here is in the range 800-1000, depending on the specific instrument and configuration used; this is higher than the resolution (R=225 at 3 μm) afforded by the Visual-Infrared Mapping Spectrometer on the Cassini spacecraft. All of the spectra are dominated by water ice absorption bands and no other features are clearly identified. Spectra of all of these satellites show the characteristic signature of hexagonal H₂O ice at 1.65 μm. We model the leading hemisphere of Rhea in the wavelength range 0.3-3.6 μm with the Hapke and the Shkuratov radiative transfer codes and discuss the relative merits of the two approaches to fitting the spectrum. In calculations with both codes, the only components used are H₂O ice, which is the dominant constituent, and a small amount of tholin (Ice Tholin II). Tholin in small quantities (few percent, depending on the mixing mechanism) appears to be an essential component to give the basic red color of the satellite in the region 0.3-1.0 μm. The quantity and mode of mixing of tholin that can produce the intense coloration of Rhea and other icy satellites has bearing on its likely presence in many other icy bodies of the outer Solar System, both of high and low geometric albedos. Using the modeling codes, we also establish detection limits for the ices of CO₂ (a few weight percent, depending on particle size and mixing), CH₄ (same), and NH₄OH (0.5 weight percent) in our globally averaged spectra of Rhea's leading hemisphere. New laboratory spectral data for NH₄OH are presented for the purpose of detection on icy bodies. These limits for CO₂, CH₄, and NH₄OH on Rhea are also applicable to the other icy satellites for which spectra are presented here. The reflectance spectrum of Hyperion shows evidence for a broad, unidentified absorption band centered at 1.75 μm.     

Trapping and release of gases by water ice and implications for icy bodies

The trapping and release of H₂, CO, CO₂, CH₄, Ar, Ne, and N₂ by amorphous water ice was studied experimentally under dynamic conditions, at low temperatures starting at 16°K, with gas pressure of 5 × 10^?8?10^?6 Torr. CO, CH₄, Ar, and N₂ were found to be released in three or four distinct temperature ranges, each resulting from a different trapping mechanism: (a) 30–55°K, where the gas frozen on the water ice evaporates; (b) 135–155°K, where gas is squeezed out of the water ice during the transformation of amorphous ice to cubic ice; (c) 165–190°K, where gas and water are released simultaneously, probably by the evaporation of a clathrate hydrate, and, occasionally (d) 160–175°K, where deeply buried gas is released during the transformation of cubic ice to hexagonal ice. If the third range is indeed due to clathrate formation, CO was found to form this compound. CO₂ did not form a clathrate under the experimental conditions. Excess hydrogen did not affect the occlusion of other gases. Hydrogen itself was trapped only at 16°K. Neon was not trapped at 25°K. With cubic ice, the only trapping mechanism is freezing of gas on the ice surface. No fractionation between the gas phase and the ice was observed with a mixture of CO and Ar. Massive ejection of ice grains was observed during the evaporation of the gas in three (a,c,d) out of the four ranges. The experimental results are used to explain several cometary phenomena, especially those occurring at large heliocentric distances, and are applied also to Titan's atmospheric composition and to the possible ejection of ice grains from Enceladus.     

Density and refractive index of binary CH4, N2 and CO2 ice mixtures

In this work we present the results of a series of laboratory experiments performed to obtain the density and the real part of the refractive index of binary mixtures of ices of astrophysical interest. Densities of CO₂:CH₄ mixtures obey the expected weighted mean and the other binary mixtures have densities up to 20% lower than expected. Refractive index for all the binary mixtures deviates up to 5% from the theoretical, obtaining higher values than expected for CO₂:CH₄ and lower values than predicted for CO₂:N₂ and CH₄:N₂.     

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.