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At least 721 records · Page 40
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NASA NTRS1994

A perspective of landing-site selection

The problems that now confront Mars Pathfinder are much the same as those that confronted Viking, but more and better information exists today. Like Viking, Mars Pathfinder must select a landing site compatible with lander and rover designs as evidenced by available data (Viking images, radar and thermal observations, albedo and color observations, visible-infrared spectra, etc.). Most regions at low elevations probably contain favorable sites, but some sites at low elevations with weak quasispecular echoes and low thermal inertias may be unfavorable.

Moore, Henry J.↗
NASA NTRS1995

Weightless Environment Training Facility (WETF) materials coating evaluation, volume 2

This volume consists of Appendices A and B to the report on the Weightless Environment Training Facility Materials Coating Evaluation project. The project selected 10 coating systems to be evaluated in six separate exposure environments, and subject to three tests for physical properties. Appendix A holds the coating system, surface preparation, and application data. Appendix B holds the coating material infrared spectra.

Source record↗
NASA NTRS1995

Hubble Space Telescope observations of C2 molecules in diffuse interstellar clouds

Interstellar C2 F-X (1342 A) and D-X (2313 A) bands in the spectrum of zeta Oph were detected using the Goddard High-Resolution Spectrograph (GHRS) on the Hubble Space Telescope (HST). The total C2 column density is (1.79 +/- 0.06) 10(exp 13)/sq cm for an adopted f-value of 0.0545 for the 2313 A band of the Mulliken (D-X) system. Relative f-values for the 0-0 F-X, 0-0 D-X, and 2-0 A-X (Phillips) bands are derived by combining ultraviolet and near-infrared spectra: f(sub 00 sup FX)/f(sub 00 sup DX) = 1.83 +/- 0.18 and f(sub 20 sup AX)/f(sub 00 sup DX) = 0.0226 +/- 0.0029. For the Mulliken system, lines are detected up to a rotational level J double prime = 24. The relative populations along the rotational ladder are shown to be consistent with the physical and environmental conditions suggested by other diagnostics. Interstellar C2 molecules were detected towards zeta Per (N(C2) = (0.80 +/- 0.23) 10(exp 13)) but not towards Beta(sup 1), pi, and omega(sup 1) Sco(N(C2) less than or equal to 0.17 x 10(exp 13)/sq cm.

Lambert, David L.↗
NASA NTRS1995

The temporal evolution of the 1-5 micron spectrum of V1974 CYGNI (Nova Cygni 1992)

We present 1-5 micrometer moderate- and high-resolution infrared spectra of the ONeMg nova V1974 (Nova Cygni 1992) obtained at multiple epochs during an approximately 500 day period after outburst. During the first 80 days, the spectra exhibited continuum emission from thermal bremsstrahlung (free-free radiation) with prominent recombination line emission from hydrogen, helium, nitrogen, and oxygen. The measurement Full Width at Half Maximum (FWHM) of these recombination lines suggests that the initial velocity of the ejecta was approximately equals 2400-3400 km/s. We estimate from the hydrogen recombination line ratios that the density of the ionized shell at this epoch was approximately equals 10(exp 9), with an effective electron temperature of approximately equals 5 x 10(exp 3) K. As the temporal evolution of the ejecta progressed, the hydrogen and helium lines diminished in intensity, and coronal lines of aluminum, calcium, magnesium, neon, and sulfur appeared by approximately day 80. The coronal line emission phase persisted for over 400 days. During this epoch, no significant dust formation occurred. We find that the ejecta of V1974 Cyg were overabundant in aluminum with respect to silicon by a factor of approximately equals 5 and in magnesium with respect to silicon by a factor of greater than or equal to 3 relative to the solar photosphere. Comparison of our observed overabundances with recent model predictions of elemental synthesis in ONeMg outbursts suggests that the accreted envelope on V1974 Cyg was close to solar composition and that the precursor ONeMg white dwarf had a mass of approximately equals 1 solar mass.

Woodward, Charles E.↗
NASA NTRS1994

Relative emission-line strengths for the 146 and 63 micron transitions in O I and a comparison with far-infrared observations of photodissociation regions

Theoretical O I density-sensitive emission-line ratios R = I(2s(sup 2))(2p(sup 4))((sup 3)P(sub 0))-((2s(sup 2))(2p(sup 4))((sup 3)P(sub 1)))/I((2s(sup 2))(2p(sup 4))((sup 3)P(sub 1))-(2s(sup 2))(2p(sup 4))((sup 3)P(sub 2))) = I(146 micrometers)/I(63 micrometers) are presented for a range of temperatures (T = 100-10,000 K), neutral hydrogen densities (N(sub H) = 10(exp -2) to 10(exp 7)/cu cm) and radiation fields (G(sub 0) = 1-10(exp 6)) applicable to both photodissociation regions (PDRs) and H II regions and the diffuse ionized medium (DIM). The observed values of R for several PDRs, measured from far-infrared spectra obtained with the Kuiper Airborne Observatory (KAO), imply hydrogen densities which are in good agreement with those determined using other methods. This provides observational support for the validity of the theoretical O I line ratios, and hence the atomic data used in their derivation.

Keenan, F. P.↗
NASA NTRS1994

Real refractive indices of infrared-characterized nitric-acid/ice films: Implications for optical measurements of polar stratospheric clouds

The infrared spectra of nitric-acid/ice films representative of polar stratospheric clouds (PSCs) were collected with simultaneous optical interference measurements to determine the real refractive indices at lambda = 632 nm. Ice and amphorous nitric-acid/ice films were prepared by condensation of water and nitric acid vapors onto a wedged Al2O3 substrate. The real refractive indices of these films were determined from the optical interference of a reflected helium-neon laser during film growth. The indices of the amphorous films varied smoothly from n = 1.30 for ice to n = 1.49 for nitric acid, similar to observations in previous work. We were unable to obtain the refractive index of crystlline films during adsorption because of optical scattering caused by surface roughness. Therefore crystlline nitric acid hydrate films were prepared by annealing amphorous nitric-acid/ice films. Further heating caused desorption of the crystalline hydrate films. During desorption, the refractive indices for ice, NAM (nitric acid monohydrate), alpha- and beta-NAT (nitric acid trihydrate) films were measured using the optical interference technique. In agreement with earlier data, the real refractive indices for ice and NAM determined in desorption were n = 1.30 +/- 0.01 and n = 1.53 +/- 0.03, respectively. The real refractive indices for alpha- and beta-NAT were found to be n = 1.51 +/- 0.01 and n greater than or equal to 1.46, respectively. Our measurements also suggest that the shape of crystalline nitric acid particles may depend on whether they nucleate from the liquid or by vapor deposition. If confirmed by future studies, this observation may provide a means of distinguishing the nucleation mechanism of crystalline PSCs.

Middlebrook, Ann M.↗
NASA NTRS1995

A luminous companion to SGR 1806-20

We have obtained infrared spectra of the star suggested to be the counterpart of the soft gamma-ray repeater (SGR) 1806-20. We found strong emission lines similar to those seen in the spectra of the rare luminous blue variables and B(e) stars. A He I absorption line is also seen, from which we infer a spectral type O9-B2. This classification, in combination with the minimum distance of greater than or approximately = 6 kpc inferred from its extinction, makes the star one of the most luminous in the Galaxy. We infer that it is a companion to SGR 1806-20 and suggest that the presence of a companion is somehow related to the SGR phenomenon.

Van Kerkwijk, M. H.↗
NASA NTRS1994

Origin of organic matter in the protosolar nebula and in comets

Comet organics are traced to their origin in interstellar space. Possible sources of comet organics from solar nebula chemistry are briefly discussed. The infrared spectra of interstellar dust are compared with spectra of solar (space) irradiated laboratory organic residues and with meteorites. The spectra compare very favorably. The atomic composition of first generation laboratory organic residues compares favorably with that of comet Halley organics if divided into approrpriate 'volatile' (less refreactory) and 'refractory' (more refractory) complex organics.

Greenberg, J. M.↗
NASA NTRS1992

The tropospheric emission spectrometer (TES) for the Earth Observing System (EOS)

In recent years, increasing concern has been expressed about Global Change - the natural and anthropogenic alteration of the Earth's environment involving global greenhouse warming and the associated climate change, urban and regional atmospheric pollution, acid deposition, regional increases in tropospheric zone, and the decrease in stratospheric ozone. A common theme among these problems is that they all involve those tropospheric trace gases which are fundamental to the biosphere-troposphere interaction, the chemistry of the free troposphere itself, and troposphere-stratosphere exchange. The chemical species involved all have spectral signatures within the near and mid infrared that can now be measured by advanced techniques of remote-sensing infrared spectroradiometry. Such a system is the Tropospheric Emission Spectrometer (TES), now in Phase B definition for the Earth Observing System (EOS) polar platforms. TES addresses these objectives by obtaining radiometrically calibrated, linewidth-limited spectral resolution, infrared spectra of the lower atmosphere using both natural thermal emission and reflected sunlight (where appropriate) in three different, but fully programmable, modes: a gobal mode, a pointed mode, and a limb-viewing mode. The goals of TES, its instrumentation, operational modes, sensitivity and data handling are discussed.

Beer, R.↗
NASA NTRS1995

Spectroscopic detection of the secondaries of the Hyades interferometric spectroscopic binary theta(sup 2) Tauri and of the interferometric spectroscopic binary alpha Andromedae

We report new high-resolution, wide-wavelength-coverage CCD observations of the visual and near-infrared spectra of the interferometric spectroscopic binaries theta(sup 2) Tau (primary spectral type A 7 III) and alpha And (primary spectral type B8 IVpMnHg), which allow the first direct spectroscopic detection of their secondaries. We have measured primary and secondary radial velocities and used them to redetermine the spectroscopic orbits of the primaries, make an improved determination of K(sub 2) for theta(sup 2) Tau, and measure K(sub 2) for alpha And for the first time. The spectroscopic orbits combined with the interferometrically measured visual orbits of theta(sup 2) Tau and alpha And provide masses and distances, M(sub 1) = 2.1 +/- 0.3 solar mass, M(sub 2) = 1.6 +/- 0.2 solar mass, and d = 44.1 +/- 2.2 pc for theta(sup 2) Tau and M(sub 1) = 5.5 +/- 0.5 solar mass, M(sub 2) = 2.3 +/- 0.2 solar mass, and d = 34.0 +/- 1.3 pc for alpha And. The distance to theta(sup 2) Tau and a foreground correction of 0.07 +/- 0.05 mag set the distance to the center of the Hyades cluster at 45.5 +/- 2.5 pc, or m - M = 3.29 +/- 0.12. Indirect estimates of the mass of theta(sup 2) Tau's primary, made via the mass-luminosity relation and via the Hyades cluster turnoff mass, are consistent with these dynamical masses for its primary and secondary. But in the case of alpha And, the mass-luminosity relation suggests that our dynamical masses for its primary and secondary may be too large. For alpha And somewhat smaller dynamical masses (4.0 and 1.9 solar mass) and the correspondingly smaller distance (31 pc), required by the corresponding larger orbital parallax, provide results consistent with the mass-luminosity relation for normal stars.

Tomkin, Jocelyn↗
NASA NTRS1995

Crystal Growth and Spectroscopy of Diglycine

Raman and infrared spectra have been obtained for alpha-diglycine (C4H8N2O3) single crystals. These dipeptide crystals are being grown as a models system for protein crystal growth studies. There have been previous Raman measurements on diglycine powder samples recorded, but there is no reference to measurements on oriented diglycine single crystals. Diglycine can grow in one of three forms, alpha, beta, or gamma.

Taylor, Taravia M.↗
NASA NTRS1995

Infrared Spectroscopy of Matrix-Isolated Polycyclic Aromatic Hydrocarbon Cations

Gaseous, ionized polycyclic aromatic hydrocarbons (PAHs) are thought to be responsible for a very common family of interstellar infrared emission bands. Here the near- and mid-infrared spectra of the cations of the five most thermodynamically favored PAHs up to coronene: phenanthrene, pyrene, benzo(e)pyrene, benzo-(ghi)perylene, and coronene, are presented to test this hypothesis. For those molecules that have been studied previously (pyrene, pyrene-d(sub 10), and coronene), band positions and relative intensities are in agreement. In all of these cases we report additional features. Absolute integrated absorbance values are given for the phenanthrene, perdeuteriophenanthrene, pyrene, benzo(ghi]perylene, and coronene cations. With the exception of coronene, the cation bands corresponding to the CC modes are typically 2-5 times more intense than those of the CH out-of-plane bending vibrations. For the cations, the CC stretching and CH in-plane bending modes give rise to bands that are an order of magnitude stronger than those of the neutral species, and the CH out-of-plane bends produce bands that are 5-20 times weaker than those of the neutral species. This behavior is similar to that found in most other PAH cations studied to date. The astronomical implications of these PAH cation spectra are also discussed.

Hudgins, D. M.↗
NASA NTRS1995

Infrared Spectroscopy of Matrix-Isolated Polycyclic Aromatic Hydrocarbon Cations: The Polyacenes Anthracene, Tetracence, and Pentacene - 3

Gaseous, ionized polycyclic aromatic hydrocarbons (PAHS) are thought to be responsible for a very common family of interstellar infrared emission bands. Unfortunately, very little infrared spectroscopic data are available on ionized PAHS. Here we present the near- and mid-infrared spectra of the polyacene cations anthracene, tetracene, and pentacene. We also report the vibrational frequencies and relative intensities of the pentacene anion. The cation bands corresponding to the CC modes are typically about 10-20 times more intense than those of the CH out-of-plane bending vibrations. For the cations the CC stretching and CH in-plane bending modes give rise to bands which are an order of magnitude stronger than for the neutral species, and the CH out-of-plane bends produce bands which are 3-20 times weaker than in the neutral species. This behavior is similar to that found for most other PAH cations. The most intense PAH cation bands fall within the envelopes of the most intense interstellar features. The strongest absorptions in the polyacenes anthracene, tetracene, and pentacene tend to group around 1400/cm (between about 1340 and 1500/cm) and near 1180/cm, regions of only moderate interstellar emission. These very strong polyacene bands tend to fall in gaps in the spectra of the other PAH cations studied to date suggesting that while PAHs with polyacene structures may contribute to specific regions of the interstellar emission spectra, they are not dominant members of the interstellar PAH family.

Hudgins, D. M.↗
NASA NTRS1995

Infrared Spectroscopy of Matrix-Isolated Polycyclic Aromatic Hydrocarbon Cations. 3. The Polyacenes Anthracene, Tetracene, and Pentacene

Gaseous, ionized Polycyclic Aromatic Hydrocarbons (PAH's) are thought to be responsible for a very common family of interstellar infrared emission bands. Unfortunately, very little infrared spectroscopic data are available on ionized PAH's. Here we present the near- and mid-infrared spectra of the polyacene cations anthracene, tetracene, and pentacene. We also report the vibrational frequencies and relative intensities of the pentacene anion. The cation bands corresponding to the CC modes are typically about 10-20 times more intense than those of the CH out-of-plane bending vibrations. For the cations the CC stretching and CH in-plane bending modes give rise to bands which are an order of magnitude stronger than for the neutral species, and the CH out-of-plane bends produce bands which are 3-20 times weaker than in the neutral species. This behavior is similar to that found for most other PAH cations. The most intense PAH cation bands fall within the envelopes of the most intense interstellar features. The strongest absorptions in the polyacenes anthracene, tetracene, and pentacene tend to group around 1400 / cm (between about 1340 and 1500 / cm) and near 1180 /cm, regions of only moderate interstellar emission. These very strong polyacene bands tend to fall in gaps in the spectra of the other PAH cations studied to date suggesting that while PAHs with polyacene structures may contribute to specific regions of the interstellar emission spectra, they are not dominant members of the interstellar PAH family.

Hudgins, D. M.↗
NASA NTRS1995

Spectroscopic Evidence Against Nitric Acid Trihydrate in Polar Stratospheric Clouds

Heterogeneous reactions on polar stratospheric clouds (PSC's) play a key role in the photochemical mechanism thought to be responsible for ozone depletion in the Antarctic and Arctic. Reactions of PSC particles activate chlorine to forms that are capable of photochemical ozone destruction, and sequester nitrogen oxides (NOx) that would otherwise deactivate the chlorine. Although the heterogeneous chemistry is now well established, the composition of the clouds themselves is uncertain. It is commonly thought that they are composed of nitric acid trihydrate, although observations have left this question unresolved. Here we reanalyse infrared spectra of type 1 PSCs obtained in Antarctica in September 1987, using recently measured optical constants of the various compounds that might be present in PSCs. We find these PSCs were not composed of nitric acid trihydrate but instead had a more complex compositon, perhaps that of a ternary solution. Because cloud formation is sensitive to their composition, this finding will alter our understanding of the locations and conditions in which PSCs form. In addition, the extent of ozone loss depends on the ability of the PSCs to remove NOx permanently through sedimentation, The sedimentation rates depend on PSC particle size which in turn is controlled by the composition and formation mechanism.

Toon, Owen B.↗
NASA NTRS1995

Spectroscopic Evidence Against Nitric Acid Trihydrate in Polar Stratospheric Clouds

Heterogeneous reactions on polar stratospheric clouds (PSC's) play a key role in the photochemical mechanisms thought to be responsible for ozone depletion in the Antarctic and the Arctic. Reactions on PSC particles activate chlorine to forms that are capable of photochemical ozone destruction, and sequester nitrogen oxides (NOx) that would otherwise deactivate the chlorine. Although the heterogeneous chemistry is now well established, the composition of the clouds themselves is uncertain. It is commonly thought that they are composed of nitric acid trihydrate, although observations have left this question unresolved. Here we reanalyse infrared spectra of type I PCS's obtained in Antarctica in September 1987, using recently measured optical constraints of the various compounds that might be present in PSC's. We find that these PSC's were not composed of nitric acid trihydrate but instead had a more complex composition perhaps that of a ternary solution. Because cloud formation is sensitive to their composition, this finding will alter our understanding of the locations and conditions in which PSCs form. In addition, the extent of ozone loss depends on the ability of the PSC's to remove NOx permanently through sedimentation. The sedimentation rates depend on PSC particle size which in turn is controlled by the composition and formation mechanism.

Toon, Owen B.↗
NASA NTRS1991

Constraints on the Parent Bodies of Collected Interplanetary Dust Particles

Samples of Interplanetary Dust Particles (IDPs) have now been collected from the stratosphere, from the Earth's ocean beds, and from the ice caps of Greenland and Antarctica. The most likely candidates for the sources of these particles are comets and asteroids. Comparison of the infrared spectra, elemental compositions, and mineralogy of the collected dust with atmospheric entry models and data obtained from cometary probes and telescopic observations has provided important constraints on the possible sources of the various types of collected dust. These constraints lead to the following conclusions. First, most of the deep sea, Greenland, and Antarctic spherules larger than 100 microns are derived from asteroids. Second, the stratospheric IDPs dominated by hydrated layer-lattice silicate minerals are also most likely derived from asteroids. Finally, the stratospheric IDPs dominated by the anhydrous minerals olivine and pyroxene are most likely from comets. The consequences of these parent body assignments are discussed.

Sandford, S. A.↗
NASA NTRS1992

Grain Spectroscopy

Our fundamental knowledge of interstellar grain composition has grown substantially during the past two decades thanks to significant advances in two areas: astronomical infrared spectroscopy and laboratory astrophysics. The opening of the mid-infrared, the spectral range from 4000-400 cm(sup -1) (2.5-25 microns), to spectroscopic study has been critical to this progress because spectroscopy in this region reveals more about a materials molecular composition and structure than any other physical property. Infrared spectra which are diagnostic of interstellar grain composition fall into two categories: absorption spectra of the dense and diffuse interstellar media, and emission spectra from UV-Vis rich dusty regions. The former will be presented in some detail, with the latter only very briefly mentioned. This paper summarized what we have learned from these spectra and presents 'doorway' references into the literature. Detailed reviews of many aspects of interstellar dust are given.

Allamandola, L. J.↗