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1.
The transition 111 ? 110 at 4.829 GHz of formaldehyde (H2CO) was the first one showing the anomalous absorption, i.e., the absorption against the cosmic microwave background. Anomalous absorption is an unusual phenomena. Structure of H2CC is very similar to that of H2CO and H2CS. Both H2CO and H2CS have already been identified in a number of cosmic objects. Though H2CC is not yet identified in the cosmic objects, we propose that H2CC may be identified in cool cosmic objects through its transition 111 ? 110 at 4.85 GHz in anomalous absorption.  相似文献   

2.
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.  相似文献   

3.
W.M. GrundyM.W. Buie 《Icarus》2002,157(1):128-138
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.  相似文献   

4.
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.  相似文献   

5.
C.A. Hibbitts  J. Szanyi 《Icarus》2007,191(1):371-380
CO2 is known to adsorb onto clay and other minerals when a significant atmospheric pressure is present. We have found that CO2 can also adsorb onto some clays when the CO2 partial pressure is effectively zero under ultra-high vacuum (UHV) if cooled to the surface temperatures of the icy satellites of Jupiter and Saturn. The strength of adsorption and the spectral characteristics of the adsorbed CO2 infrared (IR) ν3 absorption band near 4.25 μm depend on the composition and temperature of the adsorbent. CO2 remains adsorbed onto the clay mineral montmorillonite for >10 s of min when exposed to a vacuum of ∼1×10−8 Torr at ∼125 K. CO2 does not adsorb onto serpentine, goethite, or palagonite under these conditions. A small amount may adsorb onto kaolinite. When heated above 150 K under vacuum, the CO2 desorbs from the montmorillonite within a few minutes. The ν3 absorption band of CO2 adsorbed onto montmorillonite at 125 K is similar to that of the CO2 detected on the saturnian and Galilean satellites and is markedly different from CO2 adsorbed onto montmorillonite at room temperature. We infer the adsorption process is physisorption and postulate that this mechanism may explain the presence and spectral characteristics of the CO2 detected in the surfaces of these outer satellites.  相似文献   

6.
We report observation and analysis of a high-resolution 2.87-3.54 μm spectrum of the southern temperate region of Saturn obtained with NIRSPEC at Keck II. The spectrum reveals absorption and emission lines of five molecular species as well as spectral features of haze particles. The ν2+ν3 band of CH3D is detected in absorption between 2.87 and 2.92 μm; and we derived from it a mixing ratio approximately consistent with the Infrared Space Observatory result. The ν3 band of C2H2 also is detected in absorption between 2.95 and 3.05 μm; analysis indicates a sudden drop in the C2H2 mixing ratio at 15 mbar (130 km above the 1 bar level), probably due to condensation in the low stratosphere. The presence of the ν3+ν9+ν11 band of C2H6 near 3.07 μm, first reported by Bjoraker et al. [Bjoraker, G.L., Larson, H.P., Fink, U., 1981. Astrophys. J. 248, 856-862], is confirmed, and a C2H6 condensation altitude of 10 mbar (140 km) in the low stratosphere is determined. We assign weak emission lines within the 3.3 μm band of CH4 to the ν7 band of C2H6, and derive a mixing ratio of 9±4×10−6 for this species. Most of the C2H6 3.3 μm line emission arises in the altitude range 460-620 km (at ∼μbar pressure levels), much higher than the 160-370 km range where the 12 μm thermal molecular line emission of this species arises. At 2.87-2.90 μm the major absorber is tropospheric PH3. The cloud level determined here and at 3.22-3.54 is 390-460 mbar (∼30 km), somewhat higher than found by Kim and Geballe [Kim, S.J., Geballe, T.R., 2005. Icarus 179, 449-458] from analysis of a low resolution spectrum. A broad absorption feature at 2.96 μm, which might be due to NH3 ice particles in saturnian clouds, is also present. The effect of a haze layer at about 125 km (∼12 mbar level) on the 3.20-3.54 μm spectrum, which was not apparent in the low resolution spectrum, is clearly evident in the high resolution data, and the spectral properties of the haze particles suggest that they are composed of hydrocarbons.  相似文献   

7.
Sulfur dioxide has a strong and complex rotational spectrum in the microwave and far infrared regions. The microwave absorption due to SO2 in a CO2 mixture is calculated for conditions applicable to the Venus atmosphere. It is shown that at the concentrations detected by Pioneer-Venus in situ measurements, SO2 may be expected to contribute significantly to the microwave opacity of the Venus atmosphere. In particular, SO2 might provide the major source of opacity in the atmospheric region immediately below the main sulfuric acid cloud deck. The spectrum is largely nonresonant at the pressures where SO2 is expected to occur, however.  相似文献   

8.
W.M Grundy  L.A Young  E.F Young 《Icarus》2003,162(1):222-229
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.  相似文献   

9.
Simultaneous measurements of NO and NO2 in the stratosphere leading to an NOx determination have been performed by means of i.r. absorption spectrometry using the Sun as a source in the 5·2 μm band of NO and in the 6·2 μm band of NO2. The observed abundance of NOP peaks at 26 km where it is equal to (4·2 ± 1) × 109 cm?3. The volume mixing ratio of NOp was observed to vary from 1·3 × 10?9 at 20 km to 1·3 × 10?8 at 34 km.  相似文献   

10.
Three organic compounds (HC3N, C6H2, and C4N2) relevant of Titan's atmosphere have been studied within the framework of the SIPAT (Spectroscopie UV d'Intérêt Prébiologique dans l'Atmosphère de Titan) program. Since this facility is still unable to reach the very low temperatures (170 K) of Titan's high atmosphere, spectra have to be obtained at several absorption-cell temperatures, and the data extrapolated towards lower temperatures. Previously published HC3N and C6H2 absorption coefficient data are reviewed, while new spectroscopic data are presented on C4N2. Integrated intensity calculations over the vibrational bands are performed apart from the background continuum. Thus, only the band contrast is considered here. While, the temperature dependence of the hot-band integrated intensity follows a Boltzmann distribution, we have enhanced the fit through an empirical parametrisation to account for the observed temperature dependence of the C4N2 and HC3N absorption coefficients, and to extrapolate those data to the low temperature conditions of Titan's high atmosphere. Finally, we discuss the implications of the results to possible detection by remote sensing observations of these minor compounds in Titan's atmosphere.  相似文献   

11.
Ultraviolet absorption by H2O and other species in the comae of comets could be detected by studying, with satellite telescope-spectrometers, the occultation of hot stars by comets. Such observations could produce the first direct detection of H2O, the fundamental parent molecule in comet comae, and give measures of molecular level populations. The first instrument suitable for such observations will be the High Resolution Spectrograph on Space Telescope and, therefore, we consider its capabilities. We have used a Haser model to estimate the molecular column densities and to predict equivalent widths for lines of H2O, OH, CO, and O as functions of time and angular distance from a comet with a high H2O production rate. We have determined the minimum detectable equivalent widths, and therefore, the maximum angular separation from such a comet at which H2O, OH, and CO could be studied. A conservative, statistical estimate shows that comets with high water production rates should pass near enough to about 10 to 100 stars suitable for absorption studies of the CX band of H2O (1240 Å). Estimated equivalent widths for CO, OH, and the resonance lines of C and O indicate that these species may also be detected.  相似文献   

12.
Hydrocarbons such as acetylene (C2H2) and ethane (C2H6) are important tracers in Jupiter's atmosphere, constraining our models of the chemical and dynamical processes. However, our knowledge of the vertical and meridional variations of their abundances has remained sparse. During the flyby of the Cassini spacecraft in December 2000, the Composite Infrared Spectrometer (CIRS) instrument was used to map the spatial variation of emissions from 10 to 1400 cm−1 (1000-7 μm). In this paper we analyze a zonally averaged set of CIRS spectra taken at the highest (0.48 cm−1) resolution, firstly to infer atmospheric temperatures in the stratosphere at 0.5-20 mbar via the ν4 band of CH4, and in the troposphere at 150-400 mbar, via the H2 absorption at 600-800 cm−1. Stratospheric temperatures at 5 mbar are generally warmer in the north than the south by 7-8 K, while tropospheric temperatures show no such asymmetry. Both latitudinal temperature profiles however do show a pattern of maxima and minima which are largely anti-correlated between the two levels. We then use the derived temperature profiles to infer the vertical abundances of C2H2 and C2H6 by modeling tropospheric absorption (∼200 mbar) and stratospheric emission (∼5 mbar) in the C2H2ν5 and C2H6ν9 bands, and also emission of the acetylene (ν4+ν5)−ν4 hotband (∼0.1 mbar). Acetylene shows a distinct north-south asymmetry in the stratosphere, with 5 mbar abundances greatest close to 20° N and decreasing from there towards both poles by a factor of ∼4. At 200 mbar in contrast, acetylene is nearly flat at a level of ∼3×10−9. Additionally, the abundance gradient of C2H2 between 10 and 0.1 mbar is derived, based on interpolated temperatures at 0.1 mbar, and is found to be positive and uniform with latitude to within errors. Ethane at both 5 and 200 mbar shows increasing VMR towards polar regions of ∼1.75 towards 70° N and ∼2.0 towards 70° S. An explanation for the meridional trends is proposed in terms of a combination of photochemistry and dynamics. Poleward, the decreasing UV flux is predicted to decrease the abundances of C2H2 and C2H6 by factors of 2.7 and 3.5, respectively, at latitude 70°. However, the lifetime of C2H6 in the stratosphere (3×1010 s at 5 mbar) is much longer than the dynamical timescale for meridional mixing inferred from Comet SL-9 debris (5-50×108 s), and therefore the rising abundance towards high latitudes likely indicates that meridional mixing dominates over photochemical effects. For C2H2, the opposite occurs, with the relatively short photochemical lifetime (3×107 s), compared to meridional mixing times, ensuring that the expected photochemical trends are visible.  相似文献   

13.
Absorption against the Cosmic Microwave Background (CMB), called the anomalous absorption, is an unusual phenomenon. The transition 111–110 at 4.829 GHz of formaldehyde (H2CO) was the first one showing the anomalous absorption. The c-C3H2 is the second molecule showing anomalous absorption through its transition 220–211 at 21.590 GHz. Structure of thioformaldehyde (H2CS) is very similar to that of the H2CO. Therefore, we have investigated about the physical conditions under which the transition 111– 110 at 1.0465 GHz of H2CS would be found in anomalous absorption in cool cosmic objects. As in case of H2CO, the anomalous absorption of 111–110 of H2CS is found sensitive to the relative collisional rates and it requires that the collisional rate for the transition 111–211 must be smaller than that for the transition 110–212.  相似文献   

14.
A general analysis of the absorption of the Schumann-Runge bands of molecular oxygen has been made in order to compare the various experimental and theoretical results which have been obtained for an application to the O2 atmospheric absorption and its photodissociation in the mesosphere and stratosphere. The different values of the oscillator strengths deduced from the laboratory absorption spectra and of the predissociation linewidths used for the calculation of the absorption have been compared.Calculations based on a Voight profile of the O2 rotational lines have led to simple formulas for atmospheric applications taking into account that the total photodissociation rate in the stratosphere depends strongly on the absorption of solar radiation in the spectral range of the O2 Herzberg continuum. Specific examples are given.  相似文献   

15.
R.T Clancy  B.J Sandor 《Icarus》2004,168(1):116-121
The 362.156 GHz absorption spectrum of H2O2 in the Mars atmosphere was observed on September 4 of 2003, employing the James Clerk Maxwell Telescope (JCMT) sub-millimeter facility on Mauna Kea, Hawaii. Radiative transfer analysis of this line absorption yields an average volume mixing ratio of 18±0.4 ppbv within the lower (0-30 km) Mars atmosphere, in general accordance with standard photochemical models (e.g., Nair et al., 1994, Icarus 111, 124-150). Our derived H2O2 abundance is roughly three times greater than the upper limit retrieved by Encrenaz et al. (2002, Astron. Astrophys. 396, 1037-1044) from infrared spectroscopy, although part of this discrepancy may result from the different solar longitudes (Ls) of observation. Aphelion-to-perihelion thermal forcing of the global Mars hygropause generates substantial (>200%) increases in HOx abundances above ∼10 km altitudes between the Ls=112° period of the Encrenaz et al. upper limit measurement and the current Ls=250° period of detection (Clancy and Nair, 1996, J. Geophys. Res. 101, 12785-12590). The observed H2O2 line absorption weakens arguments for non-standard homogeneous (Encrenaz et al., 2002, Astron. Astrophys. 396, 1037-1044) or heterogeneous (Krasnopolsky, 2003a, J. Geophys. Res. 108; 2003b, Icarus 165, 315-325) chemistry, which have been advocated partly on the basis of infrared (8 μm) non-detections for Mars H2O2. Observation of Mars H2O2 also represents the first measurement of a key catalytic specie in a planetary atmosphere other than our own.  相似文献   

16.
An ultraviolet spectral probe for a hydrogen-rich planetary atmosphere, such as that of Jupiter, is suggested, utilizing discrete lines in the H2staggered+ 2pπu?1sσg electronic transition. For the Jovian atmosphere, the dominant mechanism for exciting H2+ to its 2pπu state appears to be photoexcitation, principally through absorption of the solar Lyman-α line. We estimate that the Jovian column emission rate of the H2+ 2pπu(ν′ = 2, J′ = 1) →1sσg(ν″ = 18,J″ = 0) fluorescent line at 1236.6 Å is if1 photon cmsu-2 secsu-1; i.e., that if1 photon secsu-1 of this radiation would strike a 15-cm diameter mirror in a Jupiter fly-by at an impact parameter of 3 × 105km. The critical role of corrections to the Born-Oppenheimer approximation in the use of an H2+ probe is discussed.  相似文献   

17.
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.  相似文献   

18.
W.M. Grundy  L.A. Young 《Icarus》2004,172(2):455-465
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.  相似文献   

19.
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.  相似文献   

20.
Marla H. Moore 《Icarus》1984,59(1):114-128
The infrared absorption spectrum from 3.3 to 27 μm (3030-370 cm?) of SO2 ice films has been measured at 20 and 88°K before and after 1-MeV proton irradiation. The radiation flux was chosen to simulate the estimated flux of Jovian magnetospheric 1-MeV protons incident on Io. After irradiation, SO3 is identified as the dominant molecule synthesized in the SO2 ice. This is also the case after irradiation of composite samples of SO2 with sulfur, or disulfites. Darkening was observed in irradiated SO2 ice and in irradiated S8 pellets. Photometric and spectral measurements of the thermoluminescence of irradiated SO2 have been made during warming. The spectrum appears as a broad band with a maximum at 4450 Å. Analysis of the luminescence data suggests that, at Ionian temperatures, irradiated SO2 ice would not be a dominant contributor to posteclipse brightening phenomena. After warming to room temperature, a form of SO3 remains along with a sulfate and S8. Based on these experiments, it is reasonable to propose that small amounts of SO3 may exist on the surface of Io as a result of irradiation synthesis in SO2 frosts.  相似文献   

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