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Allamandola, L. J.

Publications and source records attributed to Allamandola, L. J..

At least 127 records · Page 7
All sourcesNASA NTRSDOE OSTI
NASA NTRS1987

Airborne and groundbased spectrophotometry of comet P/Halley from 5-13 micrometers

Spectrophotometry of comet Halley from 5-13 microns was obtained from the Kuiper Airborne Observatory and from the Lick Observatory Nickel Telescope, revealing a strong broad emission band at 10 microns and a weak feature at 6.8 microns. The 10-micron band is identified with silicate materials, and the primary component of the silicate emission is suggested to be due to olivine. The 6.8 micron feature may be due either to carbonates or the C-H deformation mode in organic molecules. The data indicate that small particles are abundant in the coma and that the dust contains at least two physically separate components. Significant spatial and temporal variations are also noted in the spectrum.

Bregman, J. D.↗
NASA NTRS1987

Interstellar polycyclic aromatic hydrocarbons and carbon in interplanetary dust particles and meteorites

Raman spectra of interplanetary dust particles (IDPs) and meteorites containing material similar to polycyclic aromatic hydrocarbons (PAHs) show features that are similar in position and relative strength to interstellar IR emission features attributable to vibrational transitions in free molecular-sized PAHs. In addition, these spectra sometimes show red photoluminescence that has elsewhere been attributed to PAHs, and a part of the carbonaceous phase in IDPs and meteorites contain a degree of deuterium enrichment anticipated in small, free PAHs that are exposed to ISM UV radiation. These observations suggest that some of the IDPs' carbonaceous material may have been produced in circumstellar dust shells, and only slightly modified in interstellar space.

Allamandola, L. J.↗
NASA NTRS1987

Anharmonicity and the interstellar polycyclic aromatic hydrocarbon infrared emission spectrum

The hypothesis that interstellar infrared emission originates from vibrationally excited polycyclic aromatic hydrocarbons (PAHs) requires that emission can arise from all vibrational levels that are energetically accessible. Due to anharmonicity, the emission from the upper vibrational levels is shifted to longer wavelengths from that of the v = 1-0 transition. It is shown that structure in the 3-micron region is readily and quantitatively explained by emission from upper vibrational levels of excited PAHs that contain a maximum of 20-30 carbon atoms. The asymmetrical broadening of the 11.3-micron emission band may also be due to anharmonicity.

Barker, John R.↗
NASA NTRS1987

The IR emission features - Emission from PAH molecules and amorphous carbon particles

Techniques for the assessment of the importance of the various forms of PAHs, and recent infrared observations concerning the PAH problem, are considered. Spectroscopic data suggest that the observed interstellar spectrum is due to both free molecule-sized PAHs producing the narrow features, and amorphous carbon particles contributing to the broad underlying components. Explanations for the multicomponent emission spectrum are discussed. A model of the emission mechanism for the example of chrysene is presented, and an exact treatment of the IR fluorescence from highly vibrationally excited large molecules shows that species containing 20-30 carbon atoms are responsible for the narrow features, although the spectra more closely resemble those of amorphous carbon particles. It is suggested that future emphasis should be placed on the spatial characteristics of the component spectra.

Allamandola, L. J.↗
NASA NTRS1987

The IR emission features - Emission from PAH molecules and amorphous carbon particles

Given the current understanding of polycyclic aromatic hydrocarbons (PAHs), the spectroscopic data suggest that are at least two components which contribute to the interstellar emission spectrum: (1) free molecule-sized PAHs producing the narrow features and (2) amorphous carbon particles (which are primarily composed of an irregular 'lattice' of PAHs) contributing to the broad underlying components. An exact treatment of the IR fluorescence from highly vibrationally excited large molecules demonstrates that species containing between 20 and 30 carbon atoms are responsible for the narrow features, although the spectra match more closely with the spectra of amorphous carbon particles. It is concluded that, since little is known about the spectroscopic properties of free PAHs and PAH clusters, much laboratory work is required along with an observational program focusing on the spatial characteristics of the spectra.

Allamandola, L. J.↗
NASA NTRS1987

The hydrogen coverage of interstellar PAHs

The rate at which the CH bond in interstellar Polycyclic Aromatic Hydrocarbons (PAHs) rupture due to the absorption of a UV photon has been calculated. The results show that small PAHs (less than or equal to 25 carbon atoms) are expected to be partially dehydrogenated in regions with intense UV fields, while large PAHs (greater than or equal to 25 atoms) are expected to be completely hydrogenated in those regions. Because estimate of the carbon content of interstellar PAHs lie in the range of 20 to 25 carbon atoms, dehydrogenation is probably not very important. Because of the absence of other emission features besides the 11.3 micrometer feature in ground-based 8 to 13 micrometer spectra, it has been suggested that interstellar PAHs are partially dehydrogenated. However, IRAS 8 to 22 micrometer spectra of most sources that show strong 7.7 and 11.2 micrometer emission features also show a plateau of emission extending from about 11.3 to 14 micrometer. Like the 11.3 micrometer feature, this new feature is attributed to the CH out of plane bending mode in PAHs. This new feature shows that interstellar PAHs are not as dehydrogenated as estimated from ground-based 8 to 13 micrometer spectra. It also constrains the molecular structure of interstellar PAHs. In particular, it seems that very condensed PAHs, such as coronene and circumcoronene, dominate the interstellar PAH mixture as expected from stability arguments.

Tielens, A. G. G. M.↗
NASA NTRS1987

Composition, structure, and chemistry of interstellar dust

Different dust components present in the interstellar medium (IM) such as amorphous carbon, polycyclic aromatic hydrocarbons, and those IM components which are organic refractory grains and icy grain mantles are discussed as well as their relative importance. The physical properties of grain surface chemistry are discussed with attention given to the surface structure of materials, the adsorption energy and residence time of species on a grain surface, and the sticking probability. Consideration is also given to the contribution of grains to the gas-phase composition of molecular clouds.

Tielens, A. G. G. M.↗
NASA NTRS1987

Infrared absorption and emission characteristics of interstellar PAHs

The mid-infrared interstellar emission spectrum with features at 3.28, 6.2, 7.7, 8.7 and 11.3 microns is discussed in terms of the Polycyclic Aromatic Hydrocarbon (PAH) hypothesis, which is based on the suggestive, but inconclusive comparison between the interstellar emission spectrum with the infrared absorption and Raman spectra of a few PAHs. The fundamental vibrations of PAHs and PAH-like species which determine the IR and Raman properties are discussed. Interstellar IR band emission is due to relaxation from highly vibrationally excited PAHs excited by ultraviolet photons. The excitation/emission process is described and the IR fluorescence from one PAH, chrysene, is traced. Generally, there is sufficient energy to populate several vibrational levels in each mode. Molecular vibrational potentials are anharmonic and emission from these higher levels will fall at lower frequencies and produce weak features to the red of the stronger fundamentals. This process is also described and can account for some spectroscopic details of the interstellar emission spectra previously unexplained. Analysis of the interstellar spectrum shows that PAHs contain between 20 and 30 carbon atoms and are responsible for the emission.

Allamandola, L. J.↗
NASA NTRS1987

Infrared emission from interstellar PAHs

The mid-IR absorption and Raman spectra of polycyclic aromatic hydrocarbons (PAHs) and the mechanisms determining them are reviewed, and the implications for observations of similar emission spectra in interstellar clouds are considered. Topics addressed include the relationship between PAHs and amorphous C, the vibrational spectroscopy of PAHs, the molecular emission process, molecular anharmonicity, and the vibrational quasi-continuum. Extensive graphs, diagrams, and sample spectra are provided, and the interstellar emission bands are attributed to PAHs with 20-30 C atoms on the basis of the observed 3.3/3.4-micron intensity ratios.

Allamandola, L. J.↗
NASA NTRS1987

Evolution of interstellar dust

The composition, origins, and evolution of interstellar dust (ISD) are examined, reviewing the results of recent observational and theoretical investigations. Topics discussed include amorphous and polycrystalline structures; the relationship between amorphous C, graphite, and polycyclic aromatic hydrocarbons; observational techniques for determining ISD structure and composition; ISD formation in outflows from late-type giants, planetary nebulae, and novae; destruction of ISD by shocks; the formation of ISD in the ISM; and the relationship between ISD and interplanetary dust. IR spectroscopy of molecular ices and icy grain mantles is considered in detail, and it is shown that typical grain mantles consist of a 1/0.6/0.05/0.05 mixture of H2O, CH3OH, CO, and NH3.

Tielens, A. G. G. M.↗
NASA NTRS1986

Infrared spectra of WC10 planetary nebulae nuclei

The 5.2 to 8.0 micron spectra are presented for two planetary nebulae nuclei Hen1044 (He2-113) and CPD-56 8032. The unidentified infrared (UIR) emission bands at 6.2 microns, 6.9 microns, 7.7 microns are present in the spectra of Hen1044 and in CPD-56 8032, and the 8.6 micron band is present in the long wavelength shoulder of the 7.7 micron band in the spectrum of CPD-56 8032. The 8 to 13 micron spectra of these two stars by Aitken et. al. clearly show the presence of the 8.6 micron band in He2-113 while weakly resolving this feature in the spectra of CPD-56 8032. In their spectra the 11.3 micron band is also clearly detected in both objects. The 6.2 micron and 7.7 micron bands are characteristic of the infrared active C-C stretching modes in polycyclic aromatic hydrocarbons (PAHs); the 3.3 micron, 8.6 micron, and 11.3 micron bands are respectively assigned to the in-plane stretching mode, the in-plane bending mode, and the out-of-plane bending mode of the aromatic CH bond. The weak 6.9 micron emission feature is attributed to the UIR spectrum by Bregman et. al. The IRAS LRS spectra of He2-113 (IRAS 14562-5406) and CPD-56 8032 (IRAS 17047-5650) are presented. Cohen et. al. identify the broad plateau from 11.3 to 13.0 microns in the spectrum of He2-113 with increased hydrogenation of PAHs. This broad plateau is not seen in the LRS spectrum of CPD-56 8032. Also, He2-113 has greater infrared excess emission in the 17-22 micron region than does CPD-56 8032.

Wooden, D. H.↗
NASA NTRS1986

A research proposal on spectroscopy of gases and solids observed in the solar system

It is well recognized and accepted that the interpretation and analysis of any type of remote planetary spectroscopic observation requires that basic molecular parameters be available. Furthermore, the newly developed capabilities of air, ground, and space borne spectrometers trained on bodies in the solar system are producing results which are extremely difficult to understand on the basis of available data. This is particularly true in the case of spectral features arising from gases and volatiles condensed as ices. With the objective to continue to extend the understanding of spectroscopic observations of solar system objects (including comets) , laboratory studies of both gas phase molecules and ices and dusts are proposed.

Valero, F. P. J.↗
NASA NTRS1986

Laser induced fluorescence and phosphorescence of matrix isolated glyoxal - Evidence for exciplex formation in the A 1Au and a 3Au states

Laser-induced fluorescence and phosphorescence as well as infrared and visible absorption spectra of glyoxal in Ar, N2, and CO matrices are presented and analyzed. Glyoxal in its first excited electronic state is shown to form an exciplex with its nearest neighbors in all three matrices, and transitions normally forbidden dominate the emission spectra. The spectral characteristics of these complexes are similar to those of the Ar-glyoxal complex found in supersonic beam experiments. Due to the matrix cage effect, no vibrational predissociation is observed. The phosphorescence lifetime is determined and an upper limit is given for the fluorescence lifetime. This, in combination with the relative intensities of fluorescence and phosphorescence, can be used to place limits on the quantum yields of the various relaxation processes.

Van Ijzendoorn, L. J.↗
NASA NTRS1986

Time dependent chemistry in dense molecular clouds. III - Infrared band cross sections of molecules in the solid state at 10 K

Thin film transmission infrared spectra and a list of integrated absorbance values (band strengths) of bands in the 2.5 to 20 micron range of various molecular solids deposited on a CsI window cooled to 10 K are presented. These solids include molecules known or suspected to be present on interstellar grains such as H2O, CO, NH3 and CH4 and mixtures of these molecules as well as various hydrocarbons. The method is described by which the absorbance values derived can be used to estimate column densities of species adsorbed on interstellar grains and other solids associated with celestial IR sources.

Dhendecourt, L. B.↗
NASA NTRS1986

Polycyclic aromatic hydrocarbons and the diffuse interstellar bands

The profiles, widths and positions of the Diffuse Interstellar Bands (DIB's) are discussed. It is shown that the carriers of the DIB's are molecular rather than impurities in grains. Polycyclic Aromatic Hydrocarbons (PAH's) are attractive candidates for the DIB's, in view of their likely abundance, their extreme stability, and the fact that these molecules, and their corresponding radicals, show visible transitions.

Van Der Zwet, G. P.↗
NASA NTRS1985

A new emission feature in IRAS spectra and the polycyclic aromatic hydrocarbon spectrum

IRAS spectra of those sources which show strong 7.7 and 11.3 micron emission features also show a plateau of emission extending from 11.3 to about 13.0 microns. Like the 11.3 micron feature, this new feature is attributed to the CH out-of-plane bending mode in polycyclic aromatic hydrocarbons (PAHs). Its discovery reinforces the identification of the 'unidentified infrared emission features' as emission from PAHs. The wavelength of this new feature suggests that interstellar PAHs are not as partially hydrogenated as hitherto thought. It also constrains their molecular structure.

Cohen, M.↗
NASA NTRS1985

Emission features in the 4-13 micron spectra of the reflection nebulae NGC 7023 and NGC 2023

Spectroscopy from 4 to 13 microns of the visual reflection nebulae NGC 7023 and NGC 2023 has been obtained. These data, together with previous work from 1 to 4 microns, show that the spectra of these sources consist of a relatively flat continuum from 1 to 13 microns and six emission features at 3.3, 3.4, 6.2, 7.7, 8.6, and 11.3 microns. The observations rule out equilibrium thermal emission for the features and continuum in reflection nebulae, and point toward a nonequilibrium emission mechanism such as thermal emission from thermally fluctuating small grains or fluorescence from large molecules. The similarity of the emission feature spectra in reflection nebulae to those in other sources suggests a universal emission mechanism, thus implying nonequilibrium emission mechanisms in other sources.

Sellgren, K.↗