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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 19 records
All sourcesNASA NTRSDOE OSTI
NASA NTRS1979

Physical characteristics of ionized gaseous nebulae

The high angular resolution and the capability of the space telescope to observe ultraviolet radiation are discussed in relation to investigating planetary nebulae. The physical characteristics of planetary nebulae particulary the abundances of the common light elements, the H2 regions, the angular size, and the surface brightness are reviewed. Differences between supernova remants and planetary nebulae and H2 regions are discussed.

Osterbrock, D. E.↗
NASA NTRS2004

Imaging Spectrophotometry of the Jet/ISM Interaction in IC5063

IC5063 is a somewhat dusty z=0.0110 S0 galaxy with a Seyfert 2 nucleus. It has a triple radio source that spans 3 arcsec, mostly blueshifted H I absorption that spans 700 km/s, and ionization cones that extend for more than 2 arcmins. We obtained fully sampled [O III]\lambda5007 grids at 0."9 and 70 km/s FWHM resolution using the Rutgers Fabry-Perot system on the Blanco 4m telescope. Complementary long-slit spectra using the RC spectrograph on the Blanco, and Taurus Tunable Filter spectral images in H\alpha and [N II]\lambda6583, were also obtained to assess gaseous ionization conditions. We present the results of our analysis, and correlate spectral structures to those visible in archival WFPC2 images. We find that, in the region near the radio triple, gaseous ionization and line velocity width is tightly correlated, in excellent quantitative agreement with the high-velocity shock regime in the diagnostic emission-line ratio diagrams of Dopita & Sutherland. We separate kinematically gas in normal disk rotation that is illuminated by the AGN in the ionization cones from that agitated mechanically by the jet, and assess the energy input from both processes.

Cecil, G.↗
NASA NTRS1994

Infrared Spectroscopy of Polycyclic Aromatic Hydrocarbon Cations: The Members - 3

In spite of the fact that the infrared spectroscopic properties of only a few isolated ionized polycyclic aromatic hydrocarbons (PAHs) are known, gaseous, ionized PAHs are thought to be responsible for a very common family of infrared interstellar emission bands. In order to provide a data base to test this hypothesis and, if borne out, to use this emission band family as a probe of many different interstellar environments, we are carrying out a thorough study of the infrared spectroscopic properties of neutral and ionized PAHs in argon matrices. Here we present 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[ghilperylene, and coronene. The properties of naphthalene, the first member of the series, are given elsewhere. The spectra of perdeuterated phenanthrene and pyrene are also reported. For those molecules which have been previously studied (pyrene, d(10)-pyrene, and coronene), band positions and relative intensities are in agreement. In all cases we report additional features. Absolute integrated absorbance values are given for the phenanthrene, perdeutero-phenanthrene, 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 which are an order of magnitude stronger than for the neutral species, and the CH out-of-plane bends produce bands which are 5-20 times weaker than in 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

Ionization Nebulae Surrounding CAL 83 and Other Supersoft X-ray Sources

We present the results of an optical search for ionized gaseous nebulae surrounding luminous, "supersoft" X-ray sources in the Large and Small Magellanic Clouds. This relatively new and mysterious X-ray class has characteristic luminosities approximately 10(exp 37) - 10(exp 38) ergs/s with effective temperatures in the range of 2 - 6 x 10(exp 5) K. The presence of a large flux of UV and soft X-ray photons from these objects has led to predictions of bright optical emission lines from the local interstellar medium. One such object, CAL 83 in the LMC, was known to have an associated nebula, and we quantify here the asymmetry and luminosity of this remarkable nebula. Deep images were made using narrowband filters to isolate the emission lines of H.alpha and [O III] (lamda5007). In these emission lines, the nebula is detected out to distances as far as 25 pc from the central object, and the integrated luminosity in each line is of order approximately 100 solar luminosity. Model calculations of such nebulae for chemical abundances characteristic of the LMC indicate that approximately 1% of the X-ray luminosity of the central source is reprocessed into the nebular H.alpha and [O III] lamda5007 emission lines, from which we conclude that the time-averaged X-ray luminosity of the central source, CAL 83, is greater than 3 x 10(exp 37) ergs/s. The bright inner nebula contains approximately 150 solar mass within 7.5 pc of CAL 83, which clearly indicates that the nebular material has its origin in the interstellar medium. In sharp contrast, there were null detections for nebulae associated with nine other luminous, supersoft X-ray sources in the LMC and SMC, with upper limits for the [O III] luminosity that are a factor of approximately 10 below that for CAL 83. For eight of these latter sources, we conclude that either their time-averaged luminosity is substantially below that of CAL 83, or that the local interstellar medium is much less dense. The latter effect may be enhanced by expansion of the ionized nebula during the last several million years.

Remillard, R. A.↗
NASA NTRS1995

Ionization nebulae surrounding CAL 83 and other supersoft X-ray sources

We present the results of an optical search for ionized gaseous nebulae surrounding luminous, 'supersoft' X-ray sources in the Large and Small Magellanic Clouds. This relatively new and mysterious X-ray class has characteristic luminosities approximately 10(exp 37)-10(exp 38) ergs/s with effective temperatures in the range of 2-6 x 10(exp 5) K. The presence of a large flux of UV and soft X-ray photons from these objects has led to predictions of bright optical emission lines from the local interstellar medium. One such object, CAL 83 in the LMC, was known to have an associated nebula, and we quantify here the asymmetry and luminosity of this remarkable nebula. Deep images were made using narowband filters to isolate the emission lines of H alpha and (O III) (lambda 5007). In these emission lines, the nebula is detected out to distances as far as 25 pc from the central object, and the integrated luminositu in each line is of order approximately 100 solar luminosity. Model calculations of such nebulae for chemical abundances characteristic of the LMC indicate that approximately 1% of the X-ray luminosity of the central source is reprocessed into the nebular H-alpha and (O III) lambda 5007 emission lines, from which we conclude that the time-averaged X-ray luminosity of the central source, CAL 83, is greater than 3 x 10(exp 37) ergs/s. The bright inner nebula contains approximately 150 solar mass within 7.5 pc of CAL 83, which clearly indicates that the nebular material has its origin in the interstelar medium. In sharp contrast, there were null detections for nebulae associated with nine other luminous, supersoft X-ray sources in the LMC and SMC, with upper limits for the (O III) luminosity that are a factor of approximately 10 below that for CAL 83. For eight of these latter sources, we conclude that either their time-averaged luminosity is substantially below that of CAL 83, or that the local interstellar medium is much less dense. The latter effect may be enhanced by expansion of the ionized nebula during the last several million years.

Remillard, R. A.↗
NASA NTRS1979

Scientific Research with the Space Telescope: International Astronomical Union Colloquium No. 54

The application of the space telescope for extragalactic astronomy, planetary research, and stellar, interstellar, and galactic structural problems is discussed. Topics include investigations of small solar system objects, the physical characteristics of ionized gaseous nebulae, the central regions of active galaxies and quasars, problems of cosmology, and the distribution and composition of interstellar matter.

Longair, M. S.↗
NASA NTRS1983

Active lamp pulse driver circuit

A flashlamp drive circuit is described which uses an unsaturated transistor as a current mode switch to periodically subject a partially ionized gaseous laser excitation flashlamp to a stable, rectangular pulse of current from an incomplete discharge of an energy storage capacitor. A monostable multivibrator sets the pulse interval, initiating the pulse in response to a flash command by providing a reference voltage to a non-inverting terminal of a base drive amplifier; a tap on an emitter resistor provides a feedback signal sensitive to the current amplitude to an inverting terminal of amplifier, thereby controlling the pulse amplitude. The circuit drives the flashlamp to provide a squarewave current flashlamp discharge.

Logan, K. E.↗
NASA NTRS1989

Extent of warm haloes around medium-redshift galaxies

The properties of low-to-medium ionization gaseous haloes around galaxies are briefly reviewed. New observations concerning such haloes are presented. For the galaxy-QSO pair in the field of the radio source 3C303, the higher-redshift QSO has been found to show Mg II absorption at the lower redshift of the faint nearby galaxy. Secondly, new data are presented on one of the galaxies in the environment of the well-known BL Lac object AO 0235 + 164.

Burbidge, E. 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

Infrared Spectroscopy of Matrix-Isolated Polycyclic Aromatic Hydrocarbon Cations: The Members of the Thermodynamically Most Favorable Series through Coronene - Part 2

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. 2. The members of the thermodynamically most favorable series through coronene

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-d10, 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.

NASA Discipline Exobiology↗