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Prasad, S. S.

Publications and source records attributed to Prasad, S. S..

At least 55 records · Page 3
All sourcesNASA NTRSDOE OSTI
NASA NTRS1979

Some aspects of stratospheric chemical response to solar particle precipitations. I - Potential roles of N2/A3Sigma/ and ion-chemistry

Large amounts of long lived N2(A3Sigma) are created by the energy degradation of precipitating solar particles. Laboratory data suggest that in the stratosphere N2(A3Sigma) are efficiently converted into N2O. Through reactions with O(1D), N2O may gradually release NO and thereby influence the long term aspects of stratospheric chemical response. During the daytime, negative ions may transform an active NO(x) into an inactive HNO3. At night both negative and positive ion chemistry generate HO(x). Omission of ionic chemistry results in considerable underestimation of O3 depletion during the initial phases of solar particle events, and thereby introduces significant error in the estimation of the nature of the prompt response.

Prasad, S. S.↗
NASA NTRS1978

Reservoirs of atmospheric chlorine - Prospects for HOCl revisited

Possible effects of HOCl aeronomy in the terrestrial stratosphere are reexamined. Chemical kinetics data for HOCl are analyzed which are required in aeronomical studies, and the possible role of HOCl as a reservoir of atmospheric chlorine is evaluated. Chemical production and loss of HOCl in the stratosphere is considered, along with photolysis of HOCl and prospects for HOCl as an inert chlorine reservoir. It is shown that a recent theoretical calculation of the HOCl photodissociation cross section suggests this species as a possible significant reservoir of atmospheric chlorine, but that the theoretical calculations are in sharp disagreement with some experimental measurements. Laboratory and atmospheric experiments to clarify the uncertainties of HOCl aeronomy are proposed.

Prasad, S. S.↗
NASA NTRS1977

The ionospheres of Saturn, Uranus, and Neptune

Models of the ionospheres of Saturn, Uranus, and Neptune are presented. It is postulated that galactic cosmic-ray ionization is an important component of these ionospheres. For example, in the case of Neptune, the level of ionization caused by cosmic rays is comparable with that due to solar extreme-ultraviolet (EUV) radiation. The existence of cosmic-ray, as well as solar EUV-produced ionization, could be a valuable diagnostic tool for investigating the atmospheric thermal structure of those planets.

Capone, L. A.↗
NASA NTRS1976

Some aspects of the stratospheric Cl-ClO-Cl cycle - Possible roles of ClO, ClNO3 and HOCl

The possible inhibitory effect of excited ClO produced during chlorine-sensitized ozone decomposition on the stratospheric Cl-ClO-Cl cycle is investigated. Collisional deactivation of excited ClO is discussed, chemical reactions involving excited ClO are examined, and the possible roles of HO2 and NO2 in weakening the Cl-ClO-Cl cycle are evaluated. It is noted that the formation of HOCl through a reaction between ClO and HO2 implies that the Cl-ClO-Cl cycle has not been completed.

Prasad, S. S.↗
NASA NTRS1976

Heat budget of ionospheric electrons

Heat input calculations were detached from solar extreme UV data and monatomic oxygen densities were derived from simultaneously measured data sets (ion composition 146-191 km) in a study of the heat budget of ionosphere electrons. Earlier inferences that cooling predominates over heating are supported. A search for additional heat sources or a revision of the cooling rates is recommended, by way of balancing the heat budget. Importance is attached to electron cooling by fine structure excitation of monatomic oxygen.

Prasad, S. S.↗
NASA NTRS1976

The photochemistry of ammonia in the Jovian atmosphere

A reinvestigation of the ammonia photochemistry in the Jovian lower atmosphere above the cloud tops is conducted in connection with certain questions concerning the model proposed by Strobel (1973). Chemical reactions and their rate coefficients are considered along with the model atmosphere, solar fluxes, the continuity equations, and numerical details. Differences between the newmodel and Strobel's model are related to more moderate ammonia depletion relations. The height profiles of H, NH2, N2H3, N2H4, and NH3 concentrations are presented in a graph.

Prasad, S. S.↗
NASA NTRS1976

The lower ionosphere of Titan

Ionization of the atmosphere of Titan by galactic cosmic rays is a very significant process throughout the altitude range from 100 to 400 km. An approximate form of the Boltzmann equation for cosmic-ray transport has been used to obtain local ionization rates. Models of both ion and neutral chemistry have been employed to compute electron and ion density profiles for three different values of the H2/CH4 abundance ratio. The peak electron density is of the order of 1000 per cu cm. The most abundant positive ions are C2/H9(+) and C3H9(+), while the predicted densities of the negative ions H(-) and CH3(-) are very small (less than one ten-thousandth that of the positive ions). It is suggested that inclusion of the ion chemistry is important in the computation of the H and CH3 density profiles in the lower ionosphere.

Capone, L. A.↗
NASA NTRS1975

Possible new Jovian thermospheric models

Possibilities of models for the Jovian thermosphere, based upon mechanical heating, have been explored. Under certain reasonable assumptions about the magnitude of the critical Richardson number, the correction to the conventional expression for the eddy heat flux, and the height dependence of the eddy diffusion coefficient, a very hot thermosphere could result, yielding exospheric temperatures more in tune with the bounds being suggested by the recent optical and radio occultation experiments.

Prasad, S. S.↗
NASA NTRS1975

Photochemistry of hydrocarbons in the Jovian upper atmosphere

The possibility of catalytic destruction of H by C2H2 in the Jovian upper atmosphere is investigated, and other photochemical hydrocarbon reactions are presented. It is shown that the catalytic action of C2H2 can destroy or preserve atomic hydrogen, depending on the branching ratio of an intermediate reaction and the temperature dependence of various reaction rates. A model Jovian atmosphere is constructed, and the altitude profiles of some species are plotted. It is noted that this model has a greater atomic hydrogen abundance and a lower concentration of C2H2 than previous ones, and that the H profile should be considered as an upper limit for the Jovian atmosphere.

Prasad, S. S.↗
NASA NTRS1973

Jovian ionospheric models

This paper reports results obtained on ionosphere formation in the Jovian upper atmosphere with special reference to some of the recently available reaction rates, and to recent models of the Jovian neutral atmosphere based on the possibility of a warmer mesopause. In the older models of the Jovian ionosphere, the major ions were H+ which were lost only by pure radiative recombination. This led to high electron densities and practically no diurnal change. In contrast, recent models have relatively much smaller electron densities, especially in lower regions, and may be susceptible to significant diurnal variation.

Capone, L. A.↗
NASA NTRS1972

Upper atmospheric spectroscopy

Atomic physics is so intimately entwined with planetary aeronomy that progress in this geophysical-astronomical discipline is dependent in large measure upon progress in certain phases of atomic physics. The interdependence is illustrated by a discussion of photon, electron, and proton stimulation of the dayglow and the aurora. Calculations are given for the excitation of various states in N2, O2, and O as a result of electron energy degradation, assuming a gas mixture appropriate to 120 km. Emphasis is given to the O2(a 1 Delta g) 1.27 micron emission and to the low energy region in areas where many competing mechanisms enhance or inhibit certain spectral emissions.

Green, A. E. S.↗
NASA NTRS1969

Escaping photoelectron and dayglow.

Dayglow O I lambda 1304 and 1356 A radiations photoelectron excitation rates theoretical calculation and experimental data on altitude dependence characteristics

Prasad, S. S.↗