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Chackerian, C., Jr.

Publications and source records attributed to Chackerian, C., Jr..

At least 55 records · Page 3
All sourcesNASA NTRSDOE OSTI
NASA NTRS1982

Gaseous infrared absorption in the lower atmosphere of Venus

Possibly important sources of infrared opacity in the Venusian atmosphere was identified. It is shown that which is the major atmospheric constituent comprising about 97 percent of the atmosphere, is the dominant infrared opacity source. Not shown is N2 which comprises about 3 percent of the atmosphere. The mixing ratio of water vapor varies considerably with altitude but falls in the range of about 20 to 200 parts per million (ppm). The mixing ratio of SO2 falls in the range of 100-200 ppm. This number is about 5000 times larger than estimates obtained earlier via Earth-based observations. The abundance of some of the other minor constituents is also shown.

Chackerian, C., Jr.↗
NASA NTRS1981

Vibration-rotation intensities of SiO

Dipole moment matrix elements have been computed for a large number of transitions of astrophysical interest for the more abundant isotopes of SiO. The wave functions utilized were obtained from a direct solution of the Schroedinger equation with an accurate RKR potential. The dipole moment function, in the form of a Pade approximant, was chosen to reproduce the experimental measurements near equilibrium, to have the proper united and separated atom limits, and to have the correct long-range asymptotic dependence on internuclear separation. Because of the large number of transitions involved, and to facilitate applications, the squares of the dipole moment matrix elements were fitted by a least-squares procedure to polynomials in v and J. In addition, Einstein A coefficients are given for observed maser transitions and for selected vibrational bands. These latter are compared with previous calculations, and it is concluded that for the higher Delta v transitions, the present results represent a significant improvement.

Tipping, R. H.↗
NASA NTRS1980

Vibration-rotation line shifts for 1 sigma g + H2/V,J/-1S/0/ He computed via close coupling - Temperature dependence

The density shifting of vibration-rotation transitions of H2 perturbed by He was computed (as a function of temperature) with no adjustable parameters. The calculation was carried out using the framework of the impact theory of Baranger with S-matrix elements obtained via close coupling calculations which incorporated the ab initio H2-H2 system potential of Tsapline et al.(1977). Vibrational and rotational inelasticity were neglected in the calculations; nevertheless good agreement with experimental data was obtained, up to moderate temperatures, for the density shift. A much poorer comparison was obtained for the density broadening.

Hahne, G. E.↗
NASA NTRS1980

Integrated band intensities of gaseous N/2/O/5/

Values for mid-IR integrated band intensities of gaseous N2O5 were determined at room temperature. The absorptions studied were at 1720, 1246, 743, and 557/cm. The integrated intensities were 2204, 581, 685, and 699/atm cm, respectively. Implications of these results for the stratospheric detection of N(2)O(5) are discussed.

Lovejoy, R. W.↗
NASA NTRS1980

Ground-state rotational constants of /C-13/H3D

Rotational constants for the vibrational ground state of (C-13)H3D, which has been detected in the atmospheres of Jupiter and Saturn, are reported. High-resolution spectra of monodeuteromethane were obtained in the region 1800 to 2500 kaysers by a vacuum Fourier interferometer, and the values of the rotational constants B0, D0J, D0JK, H0JJJ, H0JJK and H0JKK were calculated by an analysis of ground-state combination differences in the nu 2(A1) band. The calculated frequency and intensity of this transition are found to be in agreement with the observed values.

Chackerian, C., Jr.↗
NASA NTRS1977

Theoretical brightness temperature profiles of atmospheric pure H2 rotational quadrupole lines - Jupiter and Uranus

With the advent of high-resolution instruments and their use high above most of the telluric water vapor, the hydrogen pure rotational quadrupole lines at 28, 17, and 12 microns from the atmospheres of the outer planets may be observed. Best values for the line strengths, pressure-broadening coefficients, diffusion constants, and pressure shifts for these rotational transitions are calculated. The collisionally narrowed Galatry profile is used to calculate brightness temperature line profiles for these H2 transitions for the outer planets, Jupiter and Uranus. The effects of the H2 rotational-translational continuum and of the NH3 v2 band are also included.

Goorvitch, D.↗
NASA NTRS1976

Electric dipole moment function of the X1 Sigma/+/ state of CO - Vibration-rotation matrix elements for transitions of gas laser and astrophysical interest

The electric dipole moment function of the ground electronic state of carbon monoxide has been determined by combining numerical solutions of the radial Schrodinger equation with absolute intensity data of vibration-rotation bands. The derived dipole moment function is used to calculate matrix elements of interest to stellar astronomy and of importance in the carbon monoxide laser.

Chackerian, C., Jr.↗
NASA NTRS1976

Absolute intensity measurement of the 4-0 vibration-rotation band of carbon monoxide

The absolute intensity of the 4-0 vibration band of CO is measured in spectra obtained using a 25-m base-path multiple-traversal absorption cell and a 5-m scanning spectrometer. The intensities of individual vibration-rotation lines in this band are determined from measurements of their equivalent widths, and absolute values for the rotationless transition moment and the vibration-rotation interaction factor are derived from the measured line strengths. The experimentally obtained vibration-rotation function is compared with a theoretical curve; agreement between theory and experiment is found to be good for the P-branch but poor for the R-branch. It is noted that numerical solutions to the radial Schroedinger equation lead to vibration-rotation function values that are in good agreement with the experiment.

Chackerian, C., Jr.↗
NASA NTRS1975

Density-dependent frequency shift of the hydrogen S2/1/ quadrupole line

An optical parametric oscillator pumped with an Nd:YAG laser was used in the investigations along with a White cell and a scanning spectrometer. The frequency of the S2(1) line was measured at a temperature of about 293 K over the density range from 1 to 4.3 amagat with the aid of a technique reported by Douglas and Sharma (1953). It was found that the obtained data are in good agreement with measurements conducted by Fink et al. (1965).

Chackerian, C., Jr.↗
NASA NTRS1974

Aircraft observations of Venus' near-infrared reflection spectrum - Implications for cloud composition

A comparison of aircraft-based measurement data on Venus' near-infrared (1.2- to 4.1-micron) reflection spectrum with computer generated spectra of a number of cloud candidates shows a 75-% or more concentrated water solution of sulfuric acid to give the only acceptable match to the profile of Venus' strong 3-micron absorption feature. However, the measurement data obtained also show a modest decline in reflectivity from 2.3-micron to 1.2-micron wavelength, which is inconsistent with the flat spectrum of sulfuric acid in this spectral region. It is hypothesized that this decline is due to impurities in the sulfuric acid droplets.

Pollack, J. B.↗
NASA NTRS1973

Vibrational relaxation of carbon monoxide studied by two-wavelength infrared emission

Experimental results are presented for the vibrational relaxation of pure carbon monoxide behind incident shock waves over the temperature range 4000 to 6300 K. The data were obtained as infrared emission from the fundamental and overtone vibrational band systems (in some of the experiments the two-band systems were recorded simultaneously). The data are consistent with present theories for the vibrational relaxation of diatomic molecules and can be interpreted in terms of an initial Boltzmann vibrational distribution relaxing toward final equilibrium via a continuous sequence of intermediate Boltzmann distributions.

Chackerian, C., Jr.↗
NASA NTRS1973

Relaxation of the V = 4,5,6,7, Sigma g/+/ vibrational levels of carbon monoxide studied by laser absorption.

The vibrational relaxation of individual vibration rotation levels of carbon monoxide behind incident shock waves of carbon monoxide has been studied by the method of laser absorption. For the particular vibrational states (V = 4 to 7) and temperature range (2500 to 5500 K) studied, it is concluded that the characteristic relaxation times are in excellent agreement with those obtained via previous measurements of 'bulk' gas properties. Further, the data furnish strong corroboration of the idea that the individual levels are in Boltzmann vibrational equilibrium during the relaxation process.

Chackerian, C., Jr.↗
NASA NTRS1973

Amplified laser absorption - Detection of nitric oxide.

Experimental results are reported for the power loss of a carbon monoxide gas laser due to the absorption of small amounts of nitric oxide placed in an intra-laser-cavity absorption cell. It was found, for the particular experimental conditions employed, that the absorption coefficient of nitric oxide at 1900.04/cm is enhanced more than two orders of magnitude when it is in the intracavity cell. Finally, the experimental results are compared with theoretical calculations.

Chackerian, C., Jr.↗
NASA NTRS1973

Detection of nitric oxide pollution

Studies of absorption spectra enhancement of certain atomic and molecular species inserter in dye-laser cavities have indicated that nitric oxide can be determined at low concentrations. Absorption coefficient of small amounts of nitric oxide in intra-laser-cavity absorption cell containing helium is enhanced by more than two orders of magnitude.

Chackerian, C., Jr.↗
NASA NTRS1972

CW operation in some CO lines below 5.0 microns.

CW laser emission has been observed from a He-N2-O2-CO laser on six vibration-rotation lines of carbon monoxide that lie below 5.0 microns. The lines correspond to V = 4:3 transitions.

Weisbach, M. F.↗