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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 199 records · Page 11
All sourcesNASA NTRSDOE OSTI
NASA NTRS1988

Dependence of rate constants on vibrational temperatures - An Arrhenius description

An interpretation of the variation of rate constants with vibrational temperature is proposed which introduces parameters analogous to those of the classical Arrhenius expression. The constancy of vibrational activation energy is studied for the dissociaton of NO, the ion-molecular reaction of O(+) with N2, and the atom exchange reaction of I with H2. It is found that when a Boltzmann distribution for vibrational states is applicable, the variation of the rate constant with the vibrational temperature can be used to define a vibrational activation energy. The method has application to exchange reactions where a vibrational energy threshold exists.

Ford, D. I.↗
NASA NTRS1988

Chemical abundance of comets

Observations of NH2, (OI) and molecular ion spectra in comets represent virtually all of the volatile fraction of a comet nucleus. Their study leads to the N2, NH3, H2O, CO2, CO content of the nucleus, and thus to important constraints on models of comet formation and chemical processing in the primitive solar nebula. The observations of Comet Halley provide the opportunity for the first comprehensive determination of the abundances in a comet nucleus. The carbon isotope abundance ratio 12 C/13 C = 65 plus or minus 8 has been determined for Comet Halley from resolved rotational line structure in the CN B-X (0,0) band. The ratio is approximately 30 pct lower than the solar system value, 89, indicating either an enhancement of 13CN or a depletion of 12CN in the comet. Scenarios consistent with the observed carbon isotope ratio are: (1) formation of the comet at the periphery of the solar nebula in a fractionation-enriched 13CN region, or hidden from 12CN enrichment sources, and (2) capture of an interestellar comet. Long-slit charge coupled device (CCD) spectra obtained at the time of the spacecraft encounter of Comet Halley have also been analyzed. Scale lengths, production rates and column densities of CH, CN, C2 and NH2 were determined.

Wyckoff, Susan↗
NASA NTRS1989

Introduction to dissociative recombination

Dissociative recombination (DR) of molecular ions with electrons has important consequences in many areas of physical science. Ab-initio calculations coupled with resonant scattering theory and multichannel quantum defect studies have produced detailed results illuminating the role of ion vibrational excitation, the quantum yields of the DR products, and the role of Rydberg states. The theoretical and experimental results are discussed.

Guberman, Steven L.↗
NASA NTRS1988

Deexcitation of muonic molecules by internal conversion

Deexcitation rates, lifetimes, and branching ratios are calculated for all the J = 0, J = 1, and J = 2 bound states of the muonic molecular ion td(mu) when it serves as the nucleus of a hydrogen atom. The J = 2 binding energy (E2 = 101.59 eV) is the first reported variational result for this state. It is found that the excited J = 0 state is populated several hundred times as often as the ground state.

Bhatia, A. K.↗
NASA NTRS1989

Vibrational temperature from measurements of N2 and N2(+) shock layer radiation

Measurements of the vibrational temperature in a shock layer produced by a cylindrical blunt body in an arc jet nitrogen flow are made for both the neutral molecule and the molecular ion. Spectra were obtained at two locations in the shock layer produced by a 20-cm long cylindrical blunt body inserted in the arc jet conical flow. The technique used for determining the temperatures from the spectral radiation involves obtaining ratios of integrated intensities for certain spectral regions of the measured spectrum and making a comparison with computed ratios as a function of temperature for the same spectral regions. The technique is difficult to apply due to radiation overlapping bands from other species. However, using a trial and error procedure, the vibrational and rotational temperatures at the two locations are inferred. The results indicate that the shock layer is significantly out of thermal equilibrium.

Blackwell, Harvel E.↗
NASA NTRS1989

Effect of rotational and vibrational excitation on interaction of diatomic molecules

A general and computationally efficient approach evaluating the central-force potentials for interaction of rotationally and vibrationally excited molecules and molecular ions is presented. Examples of numerical calculations are given for interactions of diatomic systems (H2, N2 and O2) in ground electronic states. The approach can be applied in straightforward way to interaction of atoms and atomic ions with diatomic molecules in arbitrary rotational-vibrational states.

Kunc, Joseph A.↗
NASA NTRS1989

Fast molecular shocks. II - Emission from fast dissociative shocks

The line radiations emitted in the cooling gas behind a fast dissociative shock are studied. The intensities emitted in high rotational transitions of the neutral molecules CO, SiO, HCN, CN, NO, and SO are estimated, as well as in rovibrational transitions of the molecular ions HeH(+) and OH(+) in radio recombination lines of atomic hydrogen and in fine-structure transitions of C, C(+), O, and Si(+). The predictions are compared with the observed intensities of line emission from the Orion-KL region. For Orion-KL the observations do not exclude, but probably do not require, the presence of a fast dissociative shock. Emission from SiO in high-J rotational states and from vibrationally excited OH(+), HeH(+), HeH(+), and SO(+) may be detectable from dissociative shocks under suitable conditions of preshock density and shock velocity; such emission may prove to be a useful diagnostic probe of fast shock activity.

Neufeld, David A.↗
NASA NTRS1990

Vibrationally excited H2 in the upper atmosphere of Saturn

The impact of resonance fluorescense of solar EUV radiation by H2 on the distribution of the vibrational levels of H2 in the upper atmosphere of Saturn is considered. It appears that, for vibration levels, v not smaller than 3, this is the most important source, more important than those due to photoelectron induced fluorescence, recombination of molecular ions such as H3(+), and vibrational excitation of H2 by photoelectron impact. Based on the Voyager limb observations of H2 band emission, it is estimated that some of the higher vibrational levels may have effective temperatures about 3500 K. Such high vibrational densities may have an impact on ionospheric densities.

Majeed, Tariq↗
NASA NTRS1990

Comparison of the bonding between ML(+) and ML2(+) (M = metal, L = noble gas)

Ab initio calculations are reported of the spectroscopic constants for the low-lying states of the molecular ions ML2(+), where M = Li, Na, Mg, V, Fe, Co, Ni and Cu, and where L is usually Ar. Comparison with existing analogous calculations on the ML(+) ions shows how the bonding and binding energy change with the addition of a second noble gas atom. The second binding energy is predicted to be essentially the same as the first for the Li, Na, Mg, and V ions, but larger for the Fe, Co, Ni and Cu ions. The binding energies of the transition metal noble gas ions are not accurately predicted at the SCF level, because correlation is required to describe their M(0)Ln(+) character. All trends can be explained in terms of promotion and hybridization on the metal ion.

Bauschlicher, Charles W., Jr.↗
NASA NTRS1990

Observations of the H2S toward OMC-1

Observations of the 1(10) - 1(01) transition of interstellar H2S and its isotopes toward OMC-1 are reported. The fractional abundance of H2S in the quiescent regions of OMC-1 seems difficult to explain by currently known ion-molecular reactions. The fractional abundance of H2S relative to H2 is enhanced by a factor of 1000 in the hot core and the plateau relative to the quiescent clouds. The (HDS)/(H2S) abundance ratio in the hot core is estimated at 0.02 or less.

Minh, Y. C.↗
NASA NTRS1990

Central-force potentials for interaction of rotationally and vibrationally excited molecules

A general and computationally efficient approach evaluating the central-force potentials for interaction of rotationally and vibrationally excited molecules and molecular ions is presented. Examples of numerical calculations are given for interactions of diatomic systems (H2, N2 and O2) in ground electronic states. The approach can be applied in a straightforward way to interactions of atoms and atomic ions with diatomic molecules in arbitrary rotational-vibrational states.

Kunc, Joseph A.↗
NASA NTRS1990

LIF and emission studies of copper and nitrogen

A technique is developed to determine the rotational temperature of nitrogen molecular ion, N2(+), from the emission spectra of B-X transition, when P and R branches are not resolved. Its validity is tested on simulated spectra of the 0-1 band of N2(+) produced under low resolution. The method is applied to experimental spectra of N2(+) taken in the shock layer of a blunt body at distances of 1.91, 2.54, and 3.18 cm from the body. The laser induced fluorescence (LIF) spectra of copper atoms is analyzed to obtain the free stream velocities and temperatures. The only broadening mechanism considered is Doppler broadening. The temperatures are obtained by manual curve fitting, and the results are compared with least square fits. The agreement on the average is within 10 percent.

Akundi, Murty A.↗
NASA NTRS1991

Tunable far infrared laser spectrometers

The state of the art in far infrared (FIR) spectroscopy is reviewed. The development of tunable, coherent FIR radiation sources is discussed. Applications of tunable FIR laser spectrometers for measurement of rotational spectra and dipole moments of molecular ions and free radicals, vibration-rotation-tunneling spectra of weakly bound complexes, and vibration-rotation spectra of linear carbon clusters are presented. A detailed description of the Berkeley tunable FIR laser spectrometers is presented.

Blake, G. A.↗
NASA NTRS1991

Micrometeorite erosion of the man rings as a source of plasma in the inner Saturnian plasma torus

Micrometeorite bombardment is presently suggested to be a source of water molecules and molecular ions in the region between the outer edge of the main rings of Saturn and Encedalus, adding to those neutrals and plasma that are generated by the sputtering of icy satellites. In view of uncertainties concerning the magnitude and distribution of the ring source, an examination is conducted of limiting cases. The implications of such cases for the Cassini division are calculated, and a discussion of their possible relevance to the region's neutral and plasma cloud is presented.

Pospieszalska, M. K.↗
NASA NTRS1991

Small-scale plasma irregularities in the nightside Venus ionosphere

The individual volt-ampere curves from the Pioneer Venus Orbiter electron temperature probe showed evidence for small-scale density irregularities, or short-period plasma waves, in regions of the nightside ionosphere where the Orbiter electric field detector observed waves in its 100-Hz channel. A survey of the nightside volt-ampere curves has revealed several hundred examples of such irregularities. The I-V structures correspond to plasma density structure with spatial scale sizes in the range of about 100-2000 m, or alternatively they could be viewed as waves having frequencies extending toward 100 Hz. They are often seen as isolated events, with spatial extent along the orbit frequently less than 80 km. The density irregularities or waves occur in or near prominent gradients in the ambient plasma concentrations both at low altitudes where molecular ions are dominant and at higher altitudes in regions of reduced plasma density where O(+) is the major ion. Electric field 100-Hz bursts occur simultaneously, with the majority of the structured I-V curves providing demonstrative evidence that at least some of the E field signals are produced within the ionosphere.

Grebowsky, J. M.↗
NASA NTRS1992

Relaxation of higher vibrational states in diatomic gases

A general and computationally efficient approach evaluating the transition probabilities for the V-T exchange, involving highly excited levels and the transitions of delta-v of more than 1, in diatomic gases is presented. The role of the repulsive part of the intermolecular potential on the transition probability is also investigated. Examples of numerical results are given for number of transitions in nitrogen and oxygen molecules in the ground electronic states. The approach can be used for interactions involving diatomic molecular ions.

Kunc, J. A.↗
NASA NTRS1992

Measured rotational and vibrational temperature differences in arc jet shock layers

Shock-layer-radiation emission spectra from the first negative system of the nitrogen molecular ion N2(+) are analyzed over the wavelength region between 370 and 430 nm. The shock layer is produced by a blunt body placed in the expanded flow from an arc heater employing either pure nitrogen or a nitrogen-oxygen air mixture. A rotational temperature is obtained from analysis of (0,1) band emission from N2(+). Vibrational temperatures are extracted from population distributions obtained through spectral fitting of the N2(+) (B-X) band sequences. Rotational temperatures up to 9500 K near the front of the shocks are determined for different energy and flow conditions. The rotational temperatures are found to be lower than those obtained for vibration confirming previous measurements and contrary to expectation based on theory.

Blackwell, Harvel E.↗
NASA NTRS1991

The V-T energy transfer in collisions of diatomics

A general approach evaluating the transition probabilities for the V-T exchange, involving highly excited levels and the Delta-v greater than 1 transitions, in diatomic gases is presented. Examples of numerical results are given for a number of transitions in nitrogen and oxygen molecules in the ground electronic states. The approach can be used for the V-T exchange involving diatomic molecular ions.

Kunc, Joseph A.↗