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At least 397 records · Page 22

Stratospheric distributions of odd nitrogen and odd hydrogen in a two-dimensional model

A two-dimensional pole-to-pole chemical model of the stratosphere is developed which extends from 8 to 38 km in altitude. Atmospheric motions are simulated by mean vertical and meridional winds and eddy diffusion coefficients. Seasonally averaged distributions of important odd nitrogen (NO, NO2, and HNO3) and odd hydrogen (H, OH, HO2, H2O2) compounds are computed. Photodissociation of N2O leads to production of odd nitrogen in the stratosphere, and the odd nitrogen is ultimately removed by downward transport into the troposphere and by rain-out (modeled by a rain-out lifetime of 30 days below 8-km altitude). Results are presented for a quasi-steady state in which seasonal cycles repeat themselves. These results show significant latitudinal as well as vertical variations in the predicted species which emphasize the need for at least two dimensions in accurate stratospheric modeling. Computed concentrations are compared with observations when they exist.

Prinn, R. G.↗

Diurnal and seasonal variations in atomic and molecular oxygen inferred from Atmosphere Explorer-C

Mass-spectrometer measurements of O and N2, obtained with the Atmosphere Explorer-C satellite during December 1974 and January 1975, are used to derive the O2 concentration near 250 km from several ionization reactions. In order to separate temperature effects from diffusion effects, the measured O and inferred O2 concentrations are employed to determine, under the assumption of diffusive equilibrium, the O/N2 and O2/N2 ratios at 120 km. It is found that the latitudinal and diurnal variations in the O concentration at 120 km are consistent with previous results obtained with OGO 6 and that the O2 concentration in the Northern (winter) Hemisphere is about twice as high as that in the Southern (summer) Hemisphere. The possible importance of photodissociation in the diurnal O2 variations is discussed.

Mayr, H. G.↗

Absorption coefficient of HCl in the region 1400 to 2200 A

The results of absorption coefficient measurements of HCl in the region 1400 to 2200 A are reported and compared with those previously published. It is concluded that the present results represent the best compromise of all measurements and should be used for any calculations on the photodissociation rate of HCl in planetary atmospheres.

Inn, E. C. Y.↗

Nitric oxide formation by meteoroids in the upper atmosphere

The process of nitric oxide formation during atmospheric entry of meteoroids is analyzed theoretically. An ablating meteoroid is assumed to be a point source in a uniform flow with a continuum regime evolving in its wake. The amount of nitric oxide produced by high-temperature reactions of air in the continuum regime is calculated by numerical integration of chemical-rate equations. The results, when summed over the observed mass, velocity, and entry-angle distributions of meteoroids, provide annual global production rates of nitric oxide as a function of altitude. The peak production of nitric oxide is found to occur at altitudes between 90 and 100 km, the total annual rate being about 40 million kg. The present results suggest that the large concentration of nitric oxide observed below 95 km could be attributed to meteoroids instead of photodissociation of nitrogen.

Menees, G. P.↗

The structure of cometary ionospheres. I - H2O dominated comets

A hydrodynamic description of the density distributions of the ionic products of H2O and CO in the atmosphere of an H2O-dominated comet having 10% CO is given. Two models are discussed. In the first, the effecs of photodissociation, photoionization, and gas-phase reactions are considered. In the second, the effect of an internal ionization source is also included. It is found that while the observed morphology of the H2O(+) coma of Comet Kohoutek (1973f) cannot be explained by gas-phase reactions alone, it is consistent with the presence of a strong internal source of ionization, presumably an electric current flowing through the inner coma. In the latter case the number densities of H2O(+) and CO(+) remain more or less constant within the scale lengths against collisional dissociation by the electron flux of their neutrals. While the abundance ratio of CO(+) to H2O(+) remains considerably less than unity when the internal ionization source is neglected, it is significantly larger than unity when the internal ionization source is included. Consequently, even the so-called 'CO-rich' comets may in reality be H2O-dominated, provided a strong internal source of ionization is operative.

Ip, W.-H.↗

Radiative processes affecting the abundance of interstellar OH

Photodissociation of OH dominates its destruction for a significant range of density and shielding in H I regions. Although inverse predissociation may provide an observable flux of ultraviolet recombination photons, it can provide only a small fraction of the total observed OH in most H I regions.

Smith, w. H.↗

Chlorofluoromethanes in the stratosphere and some possible consequences for ozone

Inert chlorofluoromethanes are used by man as refrigerants and aerosol propellants. These substances eventually escape and diffuse upward into the stratosphere. At great enough heights, UV sunlight can photodissociate these chlorofluorocarbons into chlorine atoms which will catalytically destroy ozone molecules. Chlorofluoromethane production has been increasing steadily in recent years to its present level of about a megaton per year, and chlorofluorocarbon usage will probably continue to grow in the future. Calculations with a one-dimensional time-dependent atmospheric model suggests that, if projected increases in chlorofluoromethane use materialize and there is no tropospheric destruction mechanism for these gases, the total global abundance of ozone may be reduced by more than 20 per cent over the next 50 years. If the residence times for these fluorocarbons in the troposphere are in the range of 10-30 years, however, predicted ozone depletions would be significantly smaller.

Turco, R. P.↗

Carbon production in comet West 1975n

Rocket-ultraviolet spectra of comet West 1975n are reported which were obtained with scanning spectrophotometers in the wavelength range from 1200 to 1300 A. The principal emission features observed include lines of C, O, and C(+), as well as bands of OH, CO, CO(+). The estimated fluxes of the C, O, H, CO, and OH features are found to be consistent with a photodissociation source in which the CO evaporation rate is about one-third that of water. The presence of a large number of carbon atoms in the metastable 1D state is indicated and taken to suggest that dissociative recombination is important near the cometary nucleus, that CO must originate in the nucleus, and that CO is the primary carbon constituent of the comet.

Feldman, P. D.↗

Laboratory measurements

A compilation of chemical and photochemical data that are relevant to stratospheric modeling is presented. There are three broad categories of data: (1) rate constants for chemical reactions, including temperature and pressure dependencies along with product distributions; (2) absorption cross sections, photodissociation quantum yield, and photolysis; (3) heterogeneous chemical processes.

Source record↗

On the detection of newly created CN radicals and comets

Laboratory investigations of CN radical formation by photodissociation of parent molecules have suggested the possibility of observing emission lines in cometary spectra from newly formed CN radicals. These laboratory studies have shown that high initial internal excitation of CN is the rule with excitation of rotational levels N up to 70. In the collisionless environment of the cometary atmosphere this initial excitation would yield a corresponding distribution for the lowest vibrational level of the ground X(2) Sigma (+) state. Our calculations show that it is feasible with present observational techniques to detect photochemically excited lines with N approx. equal to 30 in the 0-0 band of the violet system.

Donn, B.↗

The NASA Ames Research Center one- and two-dimensional stratospheric models. Part 1: The one-dimensional model

A one-dimensional model of stratospheric trace constituents is described in detail. Specifically, the numerical solution of the species continuity equations, including a technique for treating the stiff differential equations representing the chemical kinetic terms, and an appropriate method for simulating the diurnal variations of the species concentrations, are discussed. A specialized treatment of atmospheric photodissociation rates is outlined in the text. The choice of a vertical eddy diffusivity profile and its success in predicting the vertical tracer distributions (carbon 14, methane, and nitrous oxide) are also discussed.

Turco, R. P.↗

Chemistry and spectroscopy of the Jovian atmosphere

A comprehensive review is given of the chemistry and spectroscopic studies of the Jovian atmosphere. Thermochemical equilibrium models for determining atmospheric composition are considered along with possible disequilibrating processes, and studies of the photochemistry of H2, CH4, NH3, H2S, and PH3 using the modeling methods are summarized. It is shown that photodissociation and advection are the major disequilibrating processes in Jupiter's atmosphere, that lightning and charged-particle bombardment are relatively minor factors in the planet's bulk chemistry, and that the existence of living organisms on the planet is highly improbable. Spectroscopic investigations of Jupiter are discussed, emphasizing recent observations of absorption bands due to CH4, NH3, H2, He, and D. Spectroscopic abundance determinations are examined for H2, HD, CH4, CH3D, NH3, C2H6, C2H2, and PH3. Upper limits are given for the abundances of several unobserved gases in the visible atmosphere, including H2S, HCl, SiH4, benzene, purines, pyrimidines, and their derivatives.

Prinn, R. G.↗

OH emission intensity measurements during the 1969 NASA Airborne Auroral Expedition

Absolute intensity measurements of the (8, 6) OH band obtained during 10 flights of the December 1969 NASA Auroral Airborne Expedition are presented. Nightglow intensities higher by a factor of 2 than the usual values are recorded during flights 8, 14, and 15. The OH variations are compared with the evolution of the green line and O2(1 Delta g) emissions measured by other experimenters on board the aircraft. Before sunrise the twilight variations of OH down to a solar depression angle of 5 deg show a rapid decrease. A theoretical prediction of the OH, O I 5577 A, and O2(1 Delta g) emissions is evaluated by means of an extensive time-dependent oxygen-hydrogen model of the 25- to 150-km region. Twilight decrease of the OH emission is interpreted in terms of mesospheric ozone photodissociation. Nighttime variations of the emissions may be reproduced if modifications of the dynamic regime are introduced into the model.

Moreels, G.↗

Interpretation of high-resolution spectra of Mars. IV - New calculations of the CO abundance

Recent measurements of the half-widths of lines, pressure broadened by CO2 at a temperature of 200 K, in the 0-2 band of CO are used to reestimate the amount of CO in the atmosphere of Mars. Assuming an air-mass factor of 3.5, the amount of CO in a vertical path through the Martian atmosphere is estimated to be approximately 5.6 cm-atm. A comparison of CO and O2 abundances indicates that there is about 3.4 times as much molecular oxygen on Mars than expected. It is suggested that the extra oxygen may come from photodissociation of water.

Young, L. D. G.↗

The structure of cometary ionospheres. II - CO-rich comets

The structure of the ionosphere of a CO-rich comet is computed using two different models. The first one, the photochemical model, assumes that the dissociation and ionization of cometary neutrals and ions are due to photoionization, and photodissociation by solar UV radiation together with dissociative recombinations and ion-neutral reactions. The second one, the internal source model, also incorporates the ionization and dissociation effects of an electric current discharging through the inner coma. The generation of this current has been discussed in earlier papers. It is concluded that the internal source model can explain qualitatively the basic morphology of the ionospheres of CO-rich comets such as Humason (1962, VIII) and Morehouse (1908, III), whereas the photochemical model cannot. The main aim of this paper is not so much to provide accurate numerical estimates as to draw attention to a process which may very well dominate the structures of cometary ionospheres.

Ip, W.-H.↗

Ultraviolet absorption spectrum of chlorine nitrite, ClONO

The near-ultraviolet absorption spectrum of chlorine nitrite (ClONO) has been quantitatively investigated over the wavelength range 230-400 nm at 231 K. An absorption maximum was observed at 290 nm with a cross section of 1.5 by 10 to the -18th power sq cm. The calculated lifetime against photodissociation for ClONO in the atmosphere is 2 to 3 minutes. The large photolysis rate indicates that ClONO does not play a significant role in the stratosphere as a temporary holding tank for chlorine.

Molina, L. T.↗

Laser-induced fluorescence of CN/X2 Sigma +/ produced by photolysis of C2N2 at 160 nm

The paper reports laser-induced fluorescence measurements of the initial product state distributions of CN(X2 Sigma +) produced during the photolysis of C2N2 at a wavelength of 160 nm. The parent molecules were photodissociated by an argon flash lamp, and saturated solutions of BBD in p-dioxane were used as a laser dye to produce radiation that excited CN radicals in the (upsilon-double-prime, N-prime) vibrational-rotational sublevels of the X state to the B-state sublevels. Spectral-line identification is discussed along with the observed rotational, electronic, and vibrational energy partitionings. The effect of added buffer gas (N2 or He) on the observed product state distributions is examined in order to monitor collisional energy transfer from CN(A2 Pi, upsilon = 0) to CN(X2 Sigma +, upsilon-double-prime = 4). It is found that both buffer gases produce population inversion between the upsilon-double-prime = 4 and upsilon-double-prime = 3 levels of the X state.

Cody, R. J.↗

The yield of N/2D/ atoms in the dissociative recombination of NO/+/

The quantum yield or branching ratio of N(2D) atoms formed in the reaction e + NO(+) yields N + O was measured to be 76% plus or minus 6%. Photoionization of buffered nitric oxide by a flash lamp was studied using time-resolved atomic absorption. Atoms were produced both by direct photodissociation and by dissociative recombination, and these two effects were separated by means of SF6 as an electron scavenger.

Kley, D.↗