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At least 199 records · Page 11

Excitation of Na D-line radiation in collisions of sodium atoms with internally excited H2, D2, and N2

Excitation of D-line radiation in collisions of Na atoms with vibrationally excited N2, H2 and D2 was studied in two modulated crossed beam experiments. In both experiments, the vibrational excitation of the molecules was provided by heating the molecular beam source to temperatures in the range of 2000 to 3000 K, which was assumed to give populations according to the Boltzmann expression. In the first experiment, a total rate coefficient was measured as a function of molecular beam temperature, with absolute calibration of the photon detector being made using the black body radiation from the heated molecular beam source. Since heating affects both the internal energy and the collisional kinetic energy, the first experiment could not determine the relative contributions of internal energy transfer versus collisional excitation. The second experiment achieved partial separation of internal versus kinetic energy transfer effects by using a velocity-selected molecular beam. Using two simple models for the kinetic energy dependence of the transfer cross section for a given change in vibrational quantum number, the data from both experiments were used to determine parameters in the models.

Krause, H. F.↗

A curve of growth determination of the f-values for the fourth positive system of CO and the Lyman-Birge-Hopfield system of N2.

The curve of growth method has been employed to determine f-values for the fourth positive system of CO and the magnetic dipole and electric quadrupole components of the Lyman-Birge-Hopfield system of N2. No significant dependence on r-centroid was found. The mean value of the ratio of the electric quadrupole to magnetic dipole f-values was 0.076.

Pilling, M. J.↗

Vibrational population of the A super 3 sigma sub u/+/ and B super 3 pi sub g states of N2 in normal auroras.

Use of new electron impact excitation cross sections for the six lowest triplet states (A, B, W, C, E, D) of N2, and solution of the coupled equations of statistical equilibrium to obtain the vibrational population of each electronic state. The results show that cascade from high levels of the A super 3 sigma sub u(+) state and from the W super 3 delta sub u state is significant in populating the lower vibrational levels of the B state and hence the character of its ?apparent' excitation cross sections. For the B state excited under auroral conditions, the fraction of the total population due to cascade processes exceeds 25% for all levels lower than 7 and is greater than 80% for B(v' = 0). For the A state under similar conditions, cascade from the B state contributes 50% or more of the total vibrational population for levels lower than 7, and 80% or more for levels below 4. For levels of the A state greater than 7, the A yields B transitions depopulate the levels rapidly and indicate that the Vegard-Kaplan emissions from these higher levels will be weak or totally absent in normal auroras.

Cartwright, D. C.↗

Physisorption of Ar, Kr, CH4, and N2 on 304 stainless steel at very low pressures.

Determination of physisorption isotherms of these gases on stainless steel by pressure change measurements in very low pressure cryogenic baths where a steel nipple was brought in contact with the test gas at 77 to 90 K in a sealed constant-volume system. The position of the nipple in the gas was changed in such a manner that gas adsorption on a 47.5 sq cm area of the steel surface could be measured. The Dubinin-Radushkevich (DR) equation (1947) was used for an empirical description of isotherms at different temperatures. The mean adsorption energies calculated from the DR plots were 1290, 1545, 1490 and 1903 cal/mol for Ar, Kr, CH4 and N2, respectively, being about 10% higher than the corresponding values on Pyrex.

Troy, M.↗

Excitation of sodium D-line radiation in collisions of sodium atoms with internally excited H2, D2 and N2.

Excitation of D-line radiation in collisions of Na atoms with vibrationally excited N2, H2, and D2 was studied in two modulated crossed-beam experiments. In both experiments, the molecular excitation was provided by heating the molecular beam to temperatures which were assumed to give populations corresponding to the Boltzmann distribution. In the first experiment, a total rate coefficient was measured as a function of molecular beam temperature. The second experiment achieved partial separation of internal vs kinetic energy transfer effects by using a velocity-selected molecular beam. The data from both experiments were used to determine parameters for the dependence of the transfer cross section upon the kinetic energy for a given change in the vibrational quantum number. Results indicate that most of the Na excitation energy comes from internal vibrational energy, with the remainder coming from kinetic energy.

Krause, H. F.↗

High energy-resolution studies of electron impact optical excitation functions. I - The second positive system of N2.

The relative emission cross section for the N2 second positive system (0,0) and (1,0) bands excited by electron impact was measured for incident electron energies from threshold to 17 eV. The use of a high energy-resolution electron spectrometer coupled to an optical detection system made it possible to obtain the measurements with an incident electron beam having an energy half width of 50 meV. Calibration of the incident electron energy was provided by observing the scattering resonances in nitrogen and helium. The maximum of the (0,0) and (1,0) bands were found to be at approximately 14.02 and 14.3 eV, respectively. A small structural feature that was pressure-independent appeared only in the (0,0) band emission cross section. Another such feature was pressure-dependent and appeared more strongly in the (1,0) band cross section.

Finn, T. G.↗

Excitation of the W triplet Delta (U), W singlet Delta (U), B prime triplet Sigma (U) (minus), and A prime singlet Epsison (U) (minus) states of N2 by electron impact

Electron energy-loss spectra have been obtained for N2 at 20.6 eV impact energy, and scattering angles of 10-138 deg. The differential cross section for excitation of the W triplet Delta(U) state is the largest triplet-state cross section at all scattering angles, and is the largest inelastic cross section at angles greater than 70 degrees. (Author Modified Abstract)

Cartwright, D. C.↗

Photodissociation continuums of N2 and O2.

Dissociation continuum cross sections for N2 and O2 have been determined from previously measured total absorption and ionization cross sections. Several dissociation continuums were found for each molecule. Some of these continuums were attributed to specific dissociation products in which the dissociation products are in excited states. The upper-atmosphere emission rates resulting from these photodissociative excitation processes have been calculated for the N I 10,400-A and O I 1356-A lines. The results indicate, particularly for the oxygen line, that these photodissociative processes may be important in the dayglow.

Cook, G. R.↗

Photoionization branching ratios and vibrational intensity distribution for N2, CO; and CO2 between 53 and 75 nm

The probability of radiation producing ions in specific electronic and vibrational levels was documented. For example, when a narrow band-pass of solar ionizing photons is incident on an atmospheric species it is now possible to describe, accurately, how the radiant energy is shared among the various electronic states of the ions produced. The molecules studied were N2, CO, and CO2. These molecules were photoionized by radiation between 53 and 75 nm. The effects of autoionization are discussed and continuum vibrational intensities are tabulated and compared with theoretical Franck-Condon factors where available. The branching ratios and partial cross sections for ionization into various electronic states are tabulated.

Samson, J. A. R.↗

Crossed beam study of the reaction O/+/ + N2 yields NO/+/ + N

The kinematics of the reaction O(+)(4 S) + N2 yields NO(+) + N were studied using crossed molecular beams. Product angular and energy distributions were measured for the initial relative translational energy range from 1.5 to 15.8 eV. The products are formed in their ground electronic states. The product distributions are described, with some deviations, by the spectator stripping model. No evidence was found for a persistent complex or for a second mechanism. A scattering chamber study of 0 deg lab was made of the related reactions 15N(+) + 14NO yields 15N14N(+), 15NO(+), 14NO(+). The results obtained are discussed in terms of possible surface hopping effects.

Smith, G. P. K.↗

Hybrid theory and calculation of e-N2 scattering

A theory of electron-molecule scattering is developed which is a synthesis of close-coupling and adiabatic-nuclei theories. Specifically, the theory is close-coupling with respect to vibrational degrees of freedom and adiabatic-nuclei with respect to rotation. It can be applied to any number of partial waves required; the remaining ones can be calculated purely in one or the other approximation. A theoretical criterion based on fixed-nuclei calculations is given which indicates those partial waves and energy domains requiring the various approximations. The theory allows all cross sections (pure rotational, vibrational, simultaneous vibration-rotation, differential, and total) to be calculated, and explicit formulas for all these cross sections are given. The theory is applied to low-energy e-N2 scattering. The fixed-nuclei results are such that the criterion shows clearly that vibrational close coupling is necessary, but only for the Pi sub g partial wave. It is found that the close-coupling calculation for this wave gives rise to the substructure as well as the gross structure of the 2.4-eV resonance and that vibrational excitation cross sections are about twice as large as previously inferred.

Chandra, N.↗

Measurement of the 13 to 100 eV electron impact excitation cross section for the X 1Sigma /+/-g yields a 1Pi-g transition in N2

An inelastic scattering technique was used to measure the electron impact excitation cross section for the X 1Sigma (+)-g yields a 1Pi-g transition in N2 in the energy range 13 to 100 eV. The relative excitation cross section was calculated by integration of the relative differential scattering cross sections at various energies and the relative values of the excitation cross section were put on an absolute scale by comparing the relative cross sections to those for excitation of the X 1Sigma (+)-g yields C 3Pi-u transition and those of the electron impact optical emission cross section for the C 3Pi-u yields B 3Pi-g transition as a secondary standard. The excitation cross section was found to vary from a maximum value of 3.6 x 10 to the -17 cu cm between 15 and 18 eV to 5.2 x 10 to the -18 cu cm at 100 eV.

Finn, T. G.↗

Ion chemistry of N2/+/ and the solar ultraviolet flux in the thermosphere

We have analyzed daytime composition measurements in the thermosphere from Atmosphere Explorer-C by use of a theory of the ion chemistry. Predicted and measured N2(+) densities are compared to infer global variation of the solar ionizing flux. Results indicate that the solar flux of Hinteregger measured on Atmosphere Explorer-C provides an adequate basis for the calculation of solar ultraviolet photoionization rates. The role of metastable species is examined, and theoretical O+(2D) densities are presented.

Oppenheimer, M.↗

Tabulation of hybrid theory calculated e-N2 vibrational and rotational cross sections

Vibrational excitation cross sections of N2 by electron impact are tabulated. Integrated cross sections are given for transitions v yields v prime where o=or v=or 8 in the energy range 0.1 eV=or E=or 10 eV. The energy grid is chosen to be most dense in the resonance region (2 to 4 eV) so that the substructure is present in the numerical results. Coefficients in the angular distribution formula (differential scattering cross section) for transitions v=0 yields v prime = or 8 are also numerically given over the same grid of energies. Simultaneous rotation-vibration coefficients are also given for transitions v=o,j=o; 1 yields v prime=o, j=o,2,4; 1,3,5. All results are obtained from the hybrid theory.

Chandra, N.↗

Hybrid theory calculation of electron-N2 scattering at 5 and 10 eV

Hybrid theory results pertaining to e-N2 scattering have been evaluated for differential elastic and first vibrational excitation cross sections at 5 and 10 eV. Comparison with the recent experiment of Chutjian, Srivastava, and Trajmar is good (1976), although there is an indication that the calculated nonresonant (adiabatic-nuclei) contribution is somewhat too small. A short discussion engendered by this point is given.

Chandra, N.↗

Effects of soft electron precipitation on the distribution of vibrational energy of N2

The paper investigates the direct effect of soft electron precipitation on the nitrogen vibrational distribution and on the rate coefficient for the ion-atom interchange reaction between O(+) and N2, using a spectrum of the precipitating electrons characteristic of the dayside cusp region. Substantial increases in the nitrogen vibrational temperature and in the rate of the O(+) destruction reaction do not occur unless the flux of incident electrons is as large as 1 trillion per sq cm/sec. For such large fluxes, departures of the vibrational distribution from a Boltzmann distribution have a significant effect on the rate coefficient. Incident fluxes less than 100 billion per sq cm/sec, such as are usually observed, have little direct effect on nitrogen vibration, although the indirect effect resulting from enhanced electron temperatures might be important.

Newton, G. P.↗

Determination of the rate coefficient for the N2/+/ + O reaction in the ionosphere

Using approximately 400 simultaneous measurements of ion and neutral densities and temperatures, and the spectrum of the solar flux measured by the Atmosphere Explorer C satellite, we have determined the rate constant k1 for the reaction between N2(+) and O in the ionosphere for ion temperatures between 600 and 700 K. We find that k1 = 1.1 x 10 to the minus 10th power cu cm per sec, with a standard deviation of + or - 15%. If we use the temperature dependence for this reaction determined in the laboratory then at 300 K we find excellent agreement with the recommended laboratory value.

Torr, D. G.↗

The rate coefficient for the O/+/ + N2 reaction in the ionosphere

The rate coefficient for the reaction O(+) + N2 yields NO(+) + N is determined as a function of temperature from the photochemistry of NO(+) for both day and night conditions by using a large sample of simultaneous measurements of ion and neutral concentrations and temperatures made by the Atmosphere Explorer C satellite. The results cover the ion temperature range from 500 to 1200 K. Using recent flow-drift-tube results, the rate coefficient is calculated as a function of ion temperature and mean ion drift velocity for ionospheric conditions. The satellite and laboratory determinations are found to be in good agreement. Using this temperature dependence, an earlier determination of the dissociative recombination coefficient of NO(+) with electrons is refined.

Torr, M. R.↗