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1.
The condensation and vaporization behavior of ices containing SO2, H2S, and CO2: implications for Io
In an extension of previously reported work on ices containing CO, CO2, H2O, CH3OH, NH3, and H2, measurements of the physical and infrared spectral properties of ices containing molecules relevant to Jupiter's moon Io are presented. These include studies on ice systems containing SO2, H2S, and CO2. The condensation and sublimation behaviors of each ice system and surface binding energies of their components are discussed. The surface binding energies can be used to calculate the residence times of the molecules on a surface as a function of temperature and thus represent important parameters for any calculation that attempts to model the transport of these molecules on Io's surface. The derived values indicate that SO2 frosts on Io are likely to anneal rapidly, resulting in less fluffy, "glassy" ices and that H2S can be trapped in the SO2 ices of Io during night-time hours provided that SO2 deposition rates are on the order of 5 micrometers/hr or larger. 相似文献
2.
In an extension of previously reported work on ices containing H2O, CO, CO2, SO2, H2S, and H2, we present measurements of the physical and infrared spectral properties of ices containing CH3OH and NH3. The condensation and sublimation behavior of these ice systems is discussed and surface binding energies are presented for all of these molecules. The surface binding energies can be used to calculate the residence times of the molecules on grain surfaces as a function of temperature. It is demonstrated that many of the molecules used to generate radio maps of and probe conditions in dense clouds, for example CO and NH3, will be significantly depleted from the gas phase by condensation onto dust grains. Attempts to derive total column densities solely from radio maps that do not take condensation effects into account may vastly underestimate the true column densities of any given species. Simple CO condensation onto and vaporization off of grains appears to be capable of explaining the observed depletion of gas phase CO in cold, dense molecular cores. This is not the case for NH3, however, where thermal considerations alone predict that all of the NH3 should be condensed onto grains. The fact that some gas phase NH3 is observed indicates that additional desorption processes must be involved. The surface binding energies of CH3OH, in conjunction with this molecule's observed behavior during warm up in H2O-rich ices, is shown to provide an explanation of the large excess of CH3OH seen in many warm, dense molecular cores. The near-infrared spectrum and associated integrated band strengths of CH3OH-containing ice are given, as are middle infrared absorption band strengths for both CH3OH and NH3. 相似文献
3.
Both laboratory measurements and theory indicate that CO2 should be a common component in interstellar ices. We show that the exact band position, width, and profile of the solid-state 12CO2 infrared bands near 3705, 3600, 2340, and 660 cm-1 (2.70, 2.78, 4.27, and 15.2 micrometers) and the 13CO2 band near 2280 cm-1 (4.39 micrometers) are dependent on the matrix in which the CO2 is frozen. Measurements of these bands in astronomical spectra can be used to determine column densities of solid-state CO2 and provide important information on the physical conditions present in the ice grains of which the CO2 is a part. Depending on the composition of the ice, the CO2 asymmetric stretching band was observed to vary from 2328.7 to 2346.0 cm-1 and have full widths at half-maxima (FWHMs) ranging from 4.7 to 29.9 cm-1. The other CO2 bands showed similar variations. Both position and width are also concentration dependent. Absorption coefficients were determined for the five CO2 bands. These were found to be temperature independent for CO2 in CO and CO2 matrices but varied slightly with temperature for CO2 in H2O-rich ices. For all five bands this variation was found to be less than 15% from 10 to 150 K, the temperature at which H2O ice sublimes. A number of parameters associated with the physical behavior of CO2 in CO2- and H2O-rich ices were also determined. The CO2-CO2 surface binding energy in pure CO2 ices is found to be (delta Hs/k) = 2690 +/- 50 K. CO2-H2O and CO-H2O surface binding energies were determined to be (delta Hs/k) = 2860 +/- 200 K and 1740 +/- 100 K, respectively. Under our experimental conditions, CO2 condenses in measurable quantities into H2O-rich ices at temperatures up to 100 K, only slightly higher than the temperature at which pure CO2 condenses. Once frozen into an H2O-rich ice, the subsequent loss of CO2 upon warming is highly dependent on concentration. For ices with H2O/CO2 > 20, the CO is physically trapped within the H2O lattice, and little CO2 is lost until the sublimation temperature of the H2O matrix is reached. In contrast, in ices having H2O/CO2 < 5, the CO2 remains only to temperatures of about 90 K. Above this point the CO2 readily diffuses out of the H2O matrix. These results suggest that two different forms of H2O lattice are produced. The implications of these data for cometary models and our understanding of cometary formation are considered. 相似文献
4.
Infrared spectra of Io in the region 2.5-5.0 micrometers, including new observational data, are analyzed using detailed laboratory studies of plausible surface ices. Besides the absorption bands attributable to sulfur dioxide frosts, four infrared spectral features of Io are shown to be unidentified. These unidentified features show spatial and temporal band strength variations. One pair is centered around 3.9 micrometers (3.85 and 3.91 micrometers) and the second pair is centered around 3.0 micrometers (2.97 and 3.15 micrometers). These absorptions fall close to the fundamental stretching modes in H2S and H2O, respectively. The infrared absorption spectra of an extensive set of laboratory ices ranging from pure materials, to binary mixtures of H2S and H2O (either mixed at different concentrations or layered), to H2O:H2S:SO2 mixtures are discussed. The effects of ultraviolet irradiation (120 and 160 nm) and temperature variation (from 9 to 130 K) on the infrared spectra of the ices are examined. This comparative study of Io reflectance spectra with the laboratory mixed ice transmission data shows the following: (1) Io's surface most likely contains H2S and H2O mixed with SO2. The 3.85- and 3.91-micrometers bands in the Io spectra can be accounted for by the absorption of the S-H stretching vibration (nu 1) in H2S clusters and isolated molecules in an SO2-dominated ice. The weak 2.97- and 3.15-micrometers bands which vary spatially and temporally in the Io spectra coincide with the nu 3 and nu 1 O-H stretching vibrations of clusters of H2O molecules complexed, through hydrogen bonding and charge transfer interactions, with SO2. (2) The observations are well matched qualitatively by the transmission spectra of SO2 ices containing about 3% H2S and 0.1% H2O which have been formed by the condensation of a mixture of the gases onto a 100 K surface. (3) No new features are produced in the region 2.5 to 5.0 micrometers in the spectrum of these ices under prolonged ultraviolet irradiation or temperature variation up to 120 K. (4) Comparison of the Io spectra to transmission spectra of both mixed molecular ices and layered ices indicates that only the former can explain the shifts and splitting of the absorption bands seen in the Io spectrum and additionally can account for the fact that solid H2S is observed in the surface material of Io at temperature and pressure conditions above the sublimation point of pure H2S. 相似文献
5.
The infrared transmission spectra and photochemical behavior of various organic compounds isolated in solid N2 ices, appropriate for applications to Triton and Pluto, are presented. It is shown that excess absorption in the surface spectra of Triton and Pluto, i.e., absorption not explained by present models incorporating molecules already identified on these bodies (N2, CH4, CO, and CO2), that starts near 4450 cm-1 (2.25 micrometers) and extends to lower frequencies, may be due to alkanes (C(n)H2n+2) and related molecules frozen in the nitrogen. Branched and linear alkanes may be responsible. Experiments in which the photochemistry of N2:CH4 and N(2):CH4:CO ices was explored demonstrate that the surface ices of Triton and Pluto may contain a wide variety of additional species containing H, C, O, and N. Of these, the reactive molecule diazomethane, CH2N2, is particularly important since it may be largely responsible for the synthesis of larger alkanes from CH4 and other small alkanes. Diazomethane would also be expected to drive chemical reactions involving organics in the surface ices of Triton and Pluto toward saturation, i.e., to reduce multiple CC bonds. The positions and intrinsic strengths (A values) of many of the infrared absorption bands of N2 matrix-isolated molecules of relevance to Triton and Pluto have also been determined. These can be used to aid in their search and to place constraints on their abundances. For example, using these A values the abundance ratios CH4/N2 approximately 1.3 x 10(-3), C2H4/N2 < or = 9.5 x 10(-7) and H2CO/N2 < or = 7.8 x 10(-7) are deduced for Triton and CH4/N2 approximately 3.1 x 10(-3), C2H4/N2 < or = 4.1 x 10(-6), and H2CO/N2 < or = 5.2 x 10(-6) deduced for Pluto. The small amounts of C2H4 and H2CO in the surface ices of these bodies are in disagreement with the large abundances expected from many theoretical models. 相似文献
6.
H2O, CO and CO2 ices are condensed on carbonaceous and silicate dust grains in dense interstellar clouds and circumstellar environments. The presence of these ices is inferred by analysing their infrared (IR) spectra. The upcoming Herschel space observatory (HERSCHEL) and ground-based astronomy project (ALMA) will provide new spectral data in the unexplored far infrared (FIR) and sub-millimetre range. In our laboratory we are developing instrumentation to study ices at IR region. One of the key components of our laboratory is a silicon composite bolometer in our IFS. This detector allows us to obtain spectra with a sensitivity much greater than that obtained with a standard deuterated triglycine sulphate (DTGS) detector working at room temperature and under vacuum conditions. We plan to collect mid infrared (MIR) and FIR spectra of simple ices and their mixtures and compare these with observational data. It is also planned to do a systematic laboratory study of the effects that ultraviolet (UV) photolysis and thermal annealing have on the ice band profiles and their structure. 相似文献
7.
We present the database of maser sources in H2 O, OH and Si O lines that can be used to identify and study variable stars at evolved stages. Detecting the maser emission in H2 O, OH and Si O molecules toward infrared-excess objects is one of the methods for identifing long-period variables(LPVs, including miras and semiregulars), because these stars exhibit maser activity in their circumstellar shells. Our sample contains 1803 known LPV objects. Forty-six percent of these stars(832 objects) manifest maser emission in the line of at least one molecule: H2 O, OH or Si O. We use the database of circumstellar masers in order to search for LPVs which are not included in the General Catalogue of Variable Stars(GCVS). Our database contains 4806 objects(3866 objects without associations in GCVS) with maser detection in at least one molecule. Therefore it is possible to use the database in order to locate and study the large sample of LPV stars. The database can be accessed at http://maserdb.net. 相似文献
8.
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. 相似文献
9.
E. Dartois 《Icarus》2011,212(2):950-956
Carbon monoxide is the second most abundant molecule after H2 in the molecular universe, and as such an abundant constituent of interstellar and Solar System ices. To trace the possibility of this molecule to be found in a clathrate hydrate inclusion compound, its pure phase FTIR spectrum is investigated. We confirm the formation of a type I clathrate structure whereas simple guest size estimates would favour a type II clathrate hydrate, revealing interactions of this molecule with its water network during clathrate formation. The observed cage vibrational downshift with respect to pure CO ice is within 5 cm−1. The temperature dependent wavenumber separation between the two enclathrated CO vibrational transitions in the two distinct type I clathrate cages is less than a wavenumber below 140 K, implying that the spectral simplification for detailed spectroscopic analysis of the individual profiles is a difficult task. The dynamics of the CO molecules in its cage change considerably from 5 K to 140 K. At temperatures above 30 K, the molecule is extremely mobile in the cages, as revealed by the infrared profile, significantly different from CO entrapped in water ice and different from observed profiles in astrophysical objects. 相似文献
10.
We have detected a new interstellar molecule, H2CN (methylene amidogen), in the cold, dark molecular cloud TMC-l. The column density of H2CN is estimated to be approximately 1.5 x 10(11) cm-2 by assuming an excitation temperature of 5 K. This column density corresponds to a fractional abundance relative to H2 of approximately 1.5 x 10(-11). This value is more than three orders of magnitude less than the abundance of the related molecule HCN in TMC-1. We also report a tentative detection of H2CN in Sgr B2(N). The formation mechanism of H2CN is discussed. Our detection of the H2CN molecule may suggest the existence of a new series of carbon-chain molecules, CH2CnN (n = 0, 1, 2,...). 相似文献
11.
Carl Sagan 《Icarus》1973,18(4):649-656
Both non-gray radiative equilibrium and gray convective equilibrium calculations for Titan indicate that the discrepancy between the equilibrium temperature of an atmosphereless Titan and the observed infrared temperatures can be explained by a massive molecular hydrogen greenhouse effect. The convective calculations indicate a probable minimum optical depth of 14, corresponding to many tens of km-atm of H2, and total pressures of ～0.1 bar. The tropopause is several hundred km above the Titanian surface and at a temperature of about 90°K. Methane condensation is likely at this level. Such an atmosphere is unstable against atmospheric blow-off unless typical mesosphere scale heights are < 25km, an unlikely situation. Blow-off can also be circumvented by exospheric temperatures near the freezing point of hydrogen. It is considered more plausible that the present atmosphere is in equilibrium between outgassing and blow-off of the one hand and accretion from protons trapped in a hypothetical Saturnian magnetic field on the other; or exhibits uncompensated blow-off of outgassing products. To maintain the present blow-off rate without compensation for all of geological time requires an outgassing equivalent to the volatilization of a few km of subsurface ices. Photo-dissociation of these volatilized ices produces the observed high abundance of H2 as well as large quantities of complex organic chromophores which may explain the reddish coloration of the Titanian cloud deck. An extensive circum-Titanian hydrogen corona is postulated. Surface temperatures as high as 200°K are not excluded. Because of its high temperatures and pressures and the probable large abundance of organic compounds, Titan is a prime target for spacecraft exploration in the outer solar system. 相似文献
12.
Recently published laboratory measurements of the isotopic exchange rate constant k−(T) between CD4 and H2 are used to calculate f(z)—the isotopic enrichment factor between CH4 and H2—at every level in the outer atmosphere of the giant planets. The variation of f(z) with local vertical velocity, temperature and pressure has been calculated under the assumption that atmospheres are convective and uncertainties have been calculated by error propagation. Considering only the random errors—mainly the uncertainty on k−(T)—the f values in the observable upper atmospheres of giant planets (i.e. at z = 0, P = 1 bar) are: f(0) = 1.25 ± 0.05, 1.38 ± 0.06, 1.68 ± 0.09, and 1.61 ± 0.08 for Jupiter, Saturn, Uranus, and Neptune, respectively. Additional systematic errors due to the uncertainty in calculating the vertical velocity in the framework of the mixing length Prandtl theory lead to an overall uncertainty on f(0) of ±0.12, ±0.15, ±0.23, and ±0.21 for each planet, respectively. The D/H ratios in H2 derived from the measured CH3D/CH4 ratios in the upper atmosphere of the four giant planets are then recalculated. Uranus and Neptune seem to be enriched in deuterium with respect to the protosolar nebula but depleted relative to the Standard Mean Oceanic Water on the Earth (SMOW). However calculations based on current interior models of Neptune suggest that ices which formed the core of the planet had a D/H ratio of the order of the SMOW. The deuterium abundance in proto-Uranian ices remains uncertain. The case where water is a major constituent of the fluid envelope of Neptune is discussed. It is shown that the D/H ratio of the planet would then be higher than the value measured in hydrogen. Even in this case, the D/H ratio in proto-Neptunian ices is less than the recently revised value in P/Halley and less than the value measured in water of the Semarkona meteorite. These results suggest that the ices which formed the core of Neptune did not have an interstellar origin. Similarly, the comparison of the most recent determination of the D/H ratio in the atmosphere of Titan with the value of D/H in P/Halley suggests that this atmosphere was not formed by infalling comets but more likely from grains embedded in the sub-nebula of Saturn. 相似文献
13.
We present a series of models of Uranus and Neptune in which the relative amounts of (1) rock, (2) ices, and (3) hydrogen and helium are allowed to vary. By fitting the density and the gravitational quadruppole moment, the model composition can be determined. Because of the ambiguity in the rotation periods of these planets, several possible models are presented and discussed. 相似文献
14.
We have conducted a search for emissivity features in the thermal infrared spectrum of the icy satellites of Saturn, Phoebe, Iapetus, Enceladus, Tethys, and Hyperion, observed by the Composite Infrared Spectrometer (CIRS) on board the Cassini spacecraft. Despite the heterogeneity of the composition of these bodies depicted by Earth-based and Cassini/VIMS observations, the CIRS spectra of all satellites are undistinguishable from black-body spectra, with no detectable emissivity feature. However, several materials, which have been detected on the surface of the same bodies, present emissivity features in the analyzed spectral range. In particular, water ice presents features with sufficient contrast to be detected by CIRS. Here we study the physical causes of the absence of features by simulating the effects of intimate mixtures using models of directional emissivity for optically thick surfaces for different particle sizes and abundances, and porosities. The simulations include a set of materials detected on the Phoebe's surface, like water ice, hydrated silicates, and organics. We find that featureless spectra can be produced in three scenarios: (1) ice particles with large sizes, (2) mixtures of ices dominated by dark contaminants, and (3) small particles with large porosity. Constraints imposed by the NIR spectra of the satellites favors the latter scenario as the more likely explanation to the absence of emissivity features on the icy satellites of Saturn. 相似文献
15.
Konstantinos S. Kalogerakis Jochen Marschall Patricia A. Engel Rhiannon T. Meharchand Michael H. Wong 《Icarus》2008,196(1):202-215
We report laboratory experiments and modeling calculations investigating the effect of a hydrocarbon coating on ammonia ice spectral signatures. Observational evidence and thermochemical models indicate an abundance of ammonia ice clouds in Jupiter's atmosphere. However, spectrally identifiable ammonia ice clouds are found covering less than 1% of Jupiter's atmosphere, notably in areas of strong vertical transport, indicating a short lifetime for the signature of ammonia absorption on condensed ammonia particles [Baines, K.H., Carlson, R.W., Kamp, L.W., 2002. Icarus 159, 74-94]. Current literature has suggested coating of ammonia ice particles by a hydrocarbon haze as a possible explanation for this paradox. The work presented here supports the inference of a coating effect that can alter or suppress ammonia absorption features. In the experiments, thin films of ammonia ices are deposited in a cryogenic apparatus, coated with hydrocarbons, and characterized by reflection-absorption infrared spectroscopy. We have observed the effects on the ammonia ice absorption features near 3 and 9 μm with coverage by thin layers of hydrocarbons. Modeling calculations of these multilayer thin films assist in the interpretation of the experimental results and reveal the important role of optical interference in altering the aforementioned ammonia spectral features. Mie and T-matrix scattering calculations demonstrate analogous effects for ammonia ice particles and investigate the relative effects of ammonia ice particle size, shape, and coating layer thickness on the ice particle spectral signatures. 相似文献
16.
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. 相似文献
17.
M.E. Van Den Ancker P.R. Wesselius A.G.G.M. Tielens L.B.F.M. Waters 《Astrophysics and Space Science》1997,255(1-2):69-75
We present SWS grating scans of pure H2 rotational lines, as well as several infrared fine-structure lines for two embedded
Young Stellar Objects, S106 IR and Cep A East. Excitation temperatures and masses were derived from the low-lying pure rotational
levels of H2 and are 490 and 740 K and 0.04 and 0.007 M⊙ for S106 and Cep A, respectively. The observations were compared
to theoretical models for PDRs and dissociative and non-dissociative shocks. The infrared spectrum of S106 IR is dominated
by PDR emission while that of Cep A East has a large shock component. We suggest that the difference between these two objects
could reflect an evolutionary trend.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
18.
At present, there are few laboratory spectra of analogs of astrophysical interest in the far-infrared range (FIR). Laboratory infrared (IR) spectra of simple ices and its mixtures obtained at low temperature and pressure are found mainly up to 25 μm, and few up to 200 μm. On the other hand, there are some spectra for carbonaceous material and silicates up to 2000 μm. Our laboratory is equipped with an IR spectrometer that integrates a Michelson interferometer with a resolution better than 0.25 cm−1 and that operates under vacuum conditions of 10−1 mbar. There is also a silicon bolometer, a very high-sensitivity detector in comparison with the standard deuterated triglycine sulfate (DTGS) detectors. The use of the bolometer and the possibility of working under vacuum conditions inside the optics and the sample compartment of the spectrometer allow obtaining high-sensitivity spectra free from H2O vapor and CO2 gas bands. Those conditions are necessary to obtain high-quality spectra in the FIR where absorption bands are much less intense than those in the mid-IR region. In our laboratory there is also a high-vacuum chamber that allows different studies on ices deposited onto a cold finger. We have already carried out experiments on the study of ice density as a function of temperature, UV irradiation of ices, temperature-programmed desorption (TPD) and UV-vis reflectance. In this work, we present the design of the experimental setup we are building to carry out different experiments simultaneously on the same ice sample, including spectra measurements in the mid-IR range (MIR) and the FIR. This design integrates jointly the IR spectrometer, the high-vacuum chamber and the silicon bolometer. Lastly, we show a spectrum we have obtained of a solid of astrophysical interest such as crystalline forsterite grains by using the polyethylene pellet technique. 相似文献
19.
We use the clathrate hydrate trapping theory and gas drag formalism to calculate the composition of ices incorporated in the interior of Ceres. Utilizing a time-dependent solar nebula model, we show that icy solids can drift from beyond 5 au to the present location of the asteroid and be preserved from vaporization. We argue that volatiles were trapped in the outer solar nebula in the form of clathrate hydrates, hydrates and pure condensates prior to having been incorporated in icy solids and subsequently in Ceres. Under the assumption that most of volatiles were not vaporized during the accretion phase and the thermal evolution of Ceres, we determine the per mass abundances with respect to H2 O of CO2 , CO, CH4 , N2 , NH3 , Ar, Xe and Kr in the interior of the asteroid. The Dawn space mission, scheduled to explore Ceres in August 2014, may have the capacity to test some predictions. We also show that an in situ measurement of the D/H ratio in H2 O in Ceres could constrain the distance range in the solar nebula where its icy planetesimals were produced. 相似文献
20.
Dickens JE Irvine WM Ohishi M Ikeda M Ishikawa S Nummelin A Hjalmarson A 《The Astrophysical journal》1997,489(2):753-757
We report the identification of 10 transitions that support the detection of the small cyclic molecule ethylene oxide (c-C2H4O) in Sgr B2N. Although one of these transitions is severely blended, so that an accurate intensity and line width could not be determined, and two other lines are only marginally detected, we have done Gaussian fits to the remaining seven lines and have performed a rotation diagram analysis. Our results indicate a rotation temperature T(rot) = 18 K and a molecular column density N(c-C2H4O) = 3.3 x 10(14) cm-2, corresponding to a fractional abundance relative to molecular hydrogen of order 6 x 10(-11). This is a factor of more than 200 higher than the abundance for this molecule suggested by the "new standard" chemistry model of Lee, Bettens, & Herbst. This result suggests that grain chemistry might play an effective role in the production of c-C2H4O. No transitions of this molecule were detected in either Sgr B2M or Sgr B2NW. 相似文献