Isentropic flow solutions for reacting gas mixtures in thermochemical equilibrium
Isentropic flow solutions for reacting gas mixtures in thermochemical equilibrium
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Isentropic flow solutions for reacting gas mixtures in thermochemical equilibrium
Kinetic theory of bimolecular chemical reaction and diffusive drag in gas mixtures
The stagnation-point convective heat transfer to an axisymmetric blunt body for arbitrary gases in chemical equilibrium was investigated. The gases considered were base gases of nitrogen, oxygen, hydrogen, helium, neon, argon, carbon dioxide, ammonia, and methane and 22 gas mixtures composed of the base gases. Enthalpies ranged from 2.3 to 116.2 MJ/kg, pressures ranged from 0.001 to 100 atmospheres, and the wall temperatures were 300 and 1111 K. A general equation for the stagnation-point convective heat transfer in base gases and gas mixtures was derived and is a function of the mass fraction, the molecular weight, and a transport parameter of the base gases. The relation compares well with present boundary-layer computer results and with other analytical and experimental results. In addition, the analysis verified that the convective heat transfer in gas mixtures can be determined from a summation relation involving the heat transfer coefficients of the base gases. The basic technique developed for the prediction of stagnation-point convective heating to an axisymmetric blunt body could be applied to other heat transfer problems.
The effects of molecular angular momentum (spin polarization) on the thermal conductivity of a multicomponent gas mixture are considered. The Wang Chang-Uhlenbeck approach to the kinetic theory of gases with internal states is used. Formal results are obtained for the thermal conductivity of a gas mixture of uniform composition. These results are given in terms of the quantum mechanical degeneracy-averaged cross section.
Probe measurements using a continuous wave CO2 laser have been carried out on a He-3 - CO2 gas mixture directly excited by the He-3(n,p)H-3 reaction. At a gas pressure of 1 atm and thermal neutron flux up to 10 to the 17th n/sq cm sec, total extinction of the probe beam was observed. Addition of N2 to the gas mixture (up to 20%) produced a media such as is used in electric discharge CO2 lasers. However, this mixture produced the same results as the He-3 - CO2 mixture. Absorption of the laser beam indicates that with direct nuclear excitation, it is the lower laser level which is excited. Therefore direct nuclear pumping of a CO2 laser does not appear feasible.
Results are presented which detail the performance of proportional counters when filled with a wide variety of argon- and xenon-based gas mixtures. It is shown that alternative gas mixtures can offer considerable advantages in the counters. The mixtures of argon plus 10 percent propane and xenon plus 10 percent propylene look particularly attractive in terms of operating voltage and energy resolution. The quench gas CO2 returns the poorest results in all areas except aging.
Corrosion of SAE 310 stainless steel in H2-H2O-H2S gas mixtures was studied at a constant temperature of 1150 K. Reactive gas mixtures were chosen to yield a constant oxygen potential of approximately 6 x 10 to the minus 13th power/cu Nm and sulfur potentials ranging from 0.19 x 10 to the minus 2nd power/cu Nm to 33 x 10 to the minus 2nd power/cu Nm. The kinetics of corrosion were determined using a thermobalance, and the scales were analyzed using metallography, scanning electron microscopy, and energy dispersive X-ray analysis. Two corrosion regimes, which were dependent on sulfur potential, were identified. At high sulfur potentials (p sub S sub 2 less than or equal to 2.7 x 10 to the minus 2nd power/cu Nm) the corrosion rates were high, the kinetics obeyed a linear rate equation, and the scales consisted mainly of sulfide phases similar to those observed from pure sulfication. At low sulfur potentials (P sub S sub 2 less than or equal to 0.19 x 10 to the minus 2nd power/cu Nm) the corrosion rates were low, the kinetics obeyed a parabolic rate equation, and scales consisted mainly of oxide phases.
Approximate methods for predicting viscosities of gas mixtures involving both polar and nonpolar gases
Qualitative analysis of gas mixtures by microwave spectroscopy
In considering transfer phenomena in reacting gas mixtures, the following topics are discussed: (1) dynamics of paired collisions; (2) Enskog method for solving the Boltzmann equation, taking into account inelastic collisions; (3) use of the variation principle for approximate solutions; (4) computations of inelastic bracketed expressions; (5) calculation of collision integrals; and (6) formulas for transfer coefficients.
Magnetohydrodynamic (MHD) centrifuge utilizing electric currents and magnetic fields produces a magnetic force which develops supersonic rotational velocities in gas mixtures. Device is superior to ordinary centrifuges because rotation of gas mixture is produced by MHD force rather than mechanical means.
A method is proposed for predicting the translational component of the thermal conductivity of partially ionized gas mixtures. It is approximate but simple in form and offers a significant improvement over commonly utilized approximations. It does not require large computer run times nor storage, thus it is suitable for use with complex flow fields and heat transfer calculations. Results for gas mixtures which are representative of the atmosphere of Jupiter, Earth, and Venus are presented and they compare favorably with results from detailed kinetic theory analyses.
A method for calculating viscosity and thermal conductivity of a helium-xenon (He-Xe) gas mixture was employed, and results were compared to AiResearch (part of Honeywell) analytical data. The method of choice was that presented by Hirschfelder with Singh's third-order correction factor applied to thermal conductivity. Values for viscosity and thermal conductivity were calculated over a temperature range of 400 to 1200 K for He-Xe gas mixture molecular weights of 20.183, 39.94, and 83.8 kg/kmol. First-order values for both transport properties were in good agreement with AiResearch analytical data. Third-order-corrected thermal conductivity values were all greater than AiResearch data, but were considered to be a better approximation of thermal conductivity because higher-order effects of mass and temperature were taken into consideration. Viscosity, conductivity, and Prandtl number were then compared to experimental data presented by Taylor.
Theory for calculating heat conductivity of polyatomic and polar gases and gas mixtures
A review of the convolution theorem for obtaining the cumulative k-distribution of a gas mixture proven in Goody et al. (1989) and a discussion of its application to natural spectra are presented. Computational optimizations for use in analyzing high-altitude gas mixtures are introduced. Comparisons of the results of the optimizations, and criteria for deciding what altitudes are 'high' in this context are given. A few relevant features of the testing support software are examined. Some spectrally integrated results, and the circumstances the might permit substituting the method of principal absorbers are examined.
A procedure has been developed whereby nitrogen can be incorporated into an organic film from an ethylene-nitrogen gas mixture using an internal electrode capacitively coupled radio frequency reactor. The presence of nitrogen has been shown directly by infrared transmittance spectra and electron spectroscopic chemical analysis data, and further indirect evidence was provided by dielectric measurements and by the reverse osmosis properties of the film. Preparation of a nitrogen containing film did not require vapor from an organic nitrogen containing liquid monomer. Some control over the bonding and stoichiometry of the polymer film was provided by the added degree of freedom of the nitrogen partial pressure in the gas mixture. This new parameter strongly affected the dielectric properties of the plasma polymerized film and could affect the reverse osmosis behavior.
Approximate formula for viscosity of binary polar gas mixtures confirmed for unlike cross sections
Centered one-dimensional unsteady expansion calculated for reacting gas mixture subject to vibrational and chemical nonequilibrium