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At least 217 records · Page 12

Diagrammatic perturbation theory - N2 X1 Sigma/plus/g

The diagrammatic many-body perturbation theory is used to calculate the correlation energy of the nitrogen molecule in its electronic ground state. Using the algebraic approximation, the energy is evaluated through third order, including all many-body effects. (2/1) Pade approximants and variational upper bounds are constructed. For one of the perturbation expansions considered, the (2/1) Pade approximant leads to the recovery of 79.5 percent of the empirical correlation energy, while the variational upper bound recovers 72.0 percent. Three-body effects are examined in some detail. The relationships with previous work on N2 are discussed.

Wilson, S.↗

Review of the absorption spectra of solid O2 and N2 as they relate to contamination of a cooled infrared telescope

During contamination studies for the liquid helium cooled shuttle infrared telescope facility, a literature search was conducted to determine the absorption spectra of the solid state of homonuclear molecules of O2 and N2, and ascertain what laboratory measurements of the solid have been made in the infrared. With the inclusion of one unpublished spectrum, the absorption spectrum of the solid oxygen molecule has been thoroughly studied from visible to millimeter wavelengths. Only two lines appear in the solid that do not also appear in the gas or liquid. A similar result is implied for the solid nitrogen molecule because it also is homonuclear. The observed infrared absorption lines result from lattice modes of the alpha phase of the solid, and disappear at the warmer temperatures of the beta, gamma, and liquid phases. They are not observed from polycrystalline forms of O2, while strong scattering is. Scattering, rather than absorption, is considered to be the principal natural contamination problem for cooled infrared telescopes in low earth orbit.

Smith, S. M.↗

Electron impact excitation of the electronic states of N2. III - Transitions in the 12.5-14.2-eV energy-loss region at incident energies of 40 and 60 eV

Analysis of electron energy-loss data at incident electron energies of 40 and 60 eV has led to the determination of normalized absolute differential cross sections for electron-impact excitation of five optically-allowed singlet states, two known triplet states, and two unknown triplet-like states of N2, lying in the energy-loss range 12.5-14.2 eV. The range of scattering angles was 5 to 138 deg. The optically allowed transitions and the known triplet excitations are identified. Cross sections for excitation to two unidentified triplet-like states at 13.155 and 13.395 eV were also obtained. The relationship of the generalized oscillator strength for the dipole-allowed states obtained from the described data to known optical oscillator strengths is discussed.

Chutjian, A.↗

Determination of the N2 recombination rate coefficient in the ionosphere

Measurements of aeronomic parameters made by the Atmosphere Explorer-C satellite are used to determine the recombination rate coefficient of N2(+) in the ionosphere. The rate is found to increase significantly with decreasing electron density. Values obtained range from approximately 1.4 x 10 to the -7th to 3.8 x 10 to the -7th cu cm/sec. This variation is explained in a preliminary way in terms of an increase in the rate coefficient with vibrational excitation. Thus, high electron densities depopulate high vibrational levels reducing the effective recombination rate, whereas, low electron densities result in an enhancement in the population of high vibrational levels, thus, increasing the effective recombination rate.

Orsini, N.↗

Vibrational intensity distributions for the various electronic states of O2/+/, N2/+/ and CO/+/ produced by photoionization

Vibrational intensity distributions obtained with many discrete emission lines are presented for all major electronic states of O2(+), N2(+) and CO(+) subjected to photoionization. The vibrational distributions are reported as a function of wavelength between 745 and 304 A. The data, provided by photoelectron spectroscopy with an electron energy analyzer of known luminosity, appear to be consistent with calculated Franck-Condon Factors. Evidence for autoionization in the data is also discussed.

Gardner, J. L.↗

Measurement at different temperatures of absolute intensities, line half-widths, and broadening by Ar and N2 for the 30 0 1 II--00 0 0 band of CO2

Vibration-rotation line intensities, self-broadening coefficients, and foreign-gas-broadening (Ar and N2) coefficients were measured at 197, 233, and 294 K for the 30 0 1 II--00 0 0 band of CO2 at 6348/cm. Values for the total band intensity, purely vibrational transition moment, and vibration-rotation interaction factor were deduced from the measurements.

Valero, F. P. J.↗

Two-potential approach for electron-molecular collisions at intermediate and high energies - Application to e-N2 scatterings

A general theoretical approach is proposed for the calculation of elastic, vibrational, and rotational transitions for electron-molecule scattering at intermediate and high-electron-impact energies. In this formulation, contributions to the scattering process come from the incoherent sum of two dominant potentials: a short-range shielded nuclear Coulomb potential from individual atomic centers, and a permanent/induced long-range potential. Application to e-N2 scattering from 50-500 eV incident electron energies has yielded good agreement with absolutely calibrated experiments. Comparisons with other theoretical approaches are made. The physical picture as well as the general features of electron-molecule scattering process are discussed within the framework of the two-potential approach.

Choi, B. H.↗

SCF treatment of charge polarization effects in intermediate-energy electron scattering calculations with applications to N2

Converged rotational close coupling calculations of differential, integral, and momentum-transfer cross sections are obtained for seven model potentials for electron-N2 scattering at an impact energy of 30 eV. The model potentials involve a static potential calculated by the INDO/1s or INDOXI/1s method, and exchange potential calculated by the semiclassical exchange approximation from the INDO/1s or INDOXI/1s unperturbed electron density and a polarization potential. The polarization potentials used include the Buckley-Burke semiempirical one and various modifications of the INDOXI and INDO SCF (self-consistent-field) adiabatic polarization potentials. Without adjustment of parameters, good agreement is obtained with the angle dependence of the experimentally measured sum of the elastic and rotational excitation differential cross sections; however, the absolute value of the calculated cross sections is about 20-30% larger than the measured values in the best case, perhaps indicating that the model potentials are too strong or should have a nonzero imaginary part.

Onda, K.↗

Intensities and N2 collision-broadening coefficients measured for selected H2O absorption lines between 715 and 732 nm

Intensities and N2 collision-broadening coefficients are measured for 62 water vapor absorption lines between 715 and 732 nm potentially applicable to laser remote sensing of atmospheric water vapor. Absolute line strengths and widths were determined from spectra corrected for instrument resolution, air-path absorption and Lorentz and Doppler broadening for pure water vapor and water vapor-nitrogen mixtures in a multipass absorption cell with a base path length of 25 m (White cell). Line strengths are observed to range from 4 x 10 to the -25th to 4 x 10 to the -23rd kayser/molecule per sq cm, and collision broadening coefficients are found to be approximately equal to 0.1 kayser/atm.

Wilkerson, T. D.↗

Temperature dependence of the rate coefficient for charge exchange of metastable O/+//2D/ with N2

Using a data base of aeronomical parameters measured on board the Atmosphere Explorer-C satellite, temperature dependence of the reaction rate coefficient is deduced for the charge exchange of O(+)(2D) with N2. The results indicate the Explorer values determined over the temperature range from 700 to 1900 K are not in conflict with laboratory measurements made at higher temperatures.

Torr, M. R.↗

Charge transfer coefficients for the O+/2D/ + N2 and O+/2D/ + O2 excited ion reactions at thermal energy

An investigation of the reactions of metastable O(+) ions and O2 using drift tube-mass spectrometer techniques is presented. It was shown that ordinary charge transfer is the dominant reaction branch in both cases; it occurs with large rate coefficients, k(N2) = (8 + or - 2) x 10 to the -10th cu cm/s and k(O2) = (7 + or - 2) x 10 to the -10th cu cm/s, at an effective ion temperature of about 550 K. The reaction He(+) + O2 is used as a source of metastable O(+) ions, and evidence is presented that the O(+) ions so produced are in the 2D state rather than the 2P state. The results are compared with previous measurements, and inferences drawn from ionospheric observations.

Johnsen, R.↗

Single-pulse broad-band rotational CARS thermometry of cold N2 gas

Coherent anti Stokes Raman scattering (CARS) from the pure rotational Raman lines of N2 was employed to measure the instantaneous (10 nsec) rotational temperature of the gas at room temperature and below. An entire rotational CARS spectrum was generated by a single laser pulse using a broad bandwidth dye laser and was recorded on an optical multichannel analyzer. A best fit temperature obtained for individual experimental spectra by comparison with calculated spectra. Good agreement between CARS temperatures and thermocouple temperatures was observed.

Chang, R. K.↗

Reactions of ground-state and metastable O/2+/ ions with He, O2, N2, and CO2 at thermal energies

Evidence is presented that some previous studies of reactions of O(2+) ions with various atoms and molecules referred to ion samples composed in part of ions in metastable (1D and/or 1S) states. This finding resolves the 3 orders of magnitude discrepancy between previous experimental and calculated rate coefficients for the O(2+)(3P) + He charge transfer process. Using a drift tube to distinguish, via arrival time differences, groundstate O(+)(3P) and metastable ions, a rate coefficient of (3.5 plus or minus 1.5) x 10 to the -11th cu cm/sec is obtained for the reaction, in good agreement with that obtained from ab initio theoretical calculations. Previous conclusions concerning reactions of O(2+) with O2 and N2, however, remain valid since the difference in reactivity of ground-state and metastable O(2+) ions appears to be negligible in this case. The rate coefficient for the reaction O(2+) + CO2 has been determined to be (2 plus or minus 0.5) x 10 to the -9th cu cm/sec for ions either in the ground-state or in metastable states.

Johnsen, R.↗

O1, P1, N2 models of the global ocean tide on an elastic earth plus surface potential and spherical harmonic decompositions for M2, S2, and K1

The models of M2, S2, and K1 presented in Parke and Hendershott (1980) are supplemented with models of O1, P1, and N2. The models satisfy specified elevation boundary conditions and are generated by fighting a small number of test functions to island data. Maps are presented of the geocentric tide, the induced free space potential, the induced vertical component of the solid earth tide, and the induced vertical component of the gravitational field for each new component. Maps of the tidal potential seen by an observer fixed to the surface of the solid earth are also presented for all six constituents. Spherical harmonic coefficients up to order four and the rms magnitude of the coefficients to order fifteen are presented for each constituent. The rms magnitudes of the P1 and K1 coefficients normalized by their respective equilibrium amplitudes are compared to determine the effect of the diurnal core resonance.

Parke, M. E.↗

Atomic nitrogen emissions from photodissociation of N2

Cross sections for the production of N I emissions at 1412, 1493, and 1743 A and the undispersed fluorescence in the range 1050-1800 A produced through photodissociative excitation of N2 have been determined at selected intense atomic emission lines and throughout the synchrotron radiation continuum from 500 to 620 A. The neutral excited atomic nitrogen fragments are produced through direct dissociation processes as well as predissociation from the well-known two-electron excited Rydberg states. The yield for photodissociative excitation processes is found to have the same magnitude as that for photodissociative ionization processes reported by other investigators. The Doppler shifts of the excited atomic fragments have been calculated, and the relevance to atmospheric observations is discussed.

Wu, C. Y. R.↗

EUV studies of N2 and O2 produced by low energy electron impact

The emission spectra resulting from electron impact excitation on molecular nitrogen and oxygen in the 500-1200 A spectral region are investigated. Electron energies are from 0 to 300 eV. Numerous bands of N2 are found between 800 and 1000 A. Excitation functions are measured for the NII 916 A, the OI 879 A, and the OII 834 multiplets, and nitrogen band emission. Cross sections were measured at 200 eV for several of the band emissions plus the NI 1135 A, NI 1164 A, NI 1177 A, NII 776 A, NII 1084 A, OI 1152 A, OI 1041 A, OI 999 A, OI 989 A, OI 879 A, OII 834 A, OII 616 A, OII 555 A, OII 539 A, and OII 718 A multiplets.

Morgan, H. D.↗

Transport properties for the nitrogen system - N2, N, N(+) and E

The transport properties of the 'nitrogen system' (N2, N, N(+), and e) are important in a variety of applications, including atmospheric entry of the Shuttle and other re-entry vehicles. The kinetic theory of gases has been used to calculate the conductive transport properties for this system. The best available two-body interaction potentials have been used to calculate the transport collision integrals for each of the ten interactions which can occur in this system. Results are presented for the pure species and for the gas mixture from 600K-14000K.

Biolsi, L.↗

N2 broadening parameters of ozone at 9.6 microns

Pressure-broadening coefficients were determined for 156 O3 absorption lines made with the Fourier-transform spectrometer at the McMath Solar Telescope of the Kitt Peak National Observatory in the 9-micron region, with a resolution of 0.005/cm. O3 prepared from O2 by silent arc discharge and collected on cold silica gel was held at stable concentrations over 50 percent in a glass or stainless-steel cell with a rock-salt window, and broadened with dry N2. Interferograms were made in several scans of the interferometer during 30 min. The pressure-broadening coefficients were calculated by an iterative least-squares approach, a synthetic spectrum was constructed and compared to the actual spectrum, and the parameters were varied to achieve the best fit. It is shown that the estimated precision of the values reported is about 7 percent, and that the deviation from the theoretical calculations of Tejwani and Yeung (1975) averaged 7.6 percent (a small number of large discrepancies having been excluded).

Margolis, J. S.↗