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At least 1,081 records · Page 60

Tables and charts of equilibrium thermodynamic properties of ammonia for temperatures from 500 to 50,000 K.

Equilibrium thermodynamic properties for pure ammonia were generated for a range of temperature from 500 to 50,000 K and pressure from 0.01 to 40 MN/sq m and are presented in tabulated and graphical form. Properties include pressure, temperature, density, enthalpy, speed of sound, entropy, molecular-weight ratio, specific heat at constant pressure, specific heat at constant volume, isentropic exponent, and species mole fractions. These properties were calculated by the method which is based on minimization of the Gibbs free energy. The data presented herein are for an 18-species ammonia model. Heats of formation and spectroscopic constants used as input data are presented. Comparison of several thermodynamic properties calculated with the present program and a second computer code is performed for a range of pressure and for temperatures up to 30,000 K.

Simmonds, A. L.↗

The use of the ion probe mass spectrometer in the measurement of hydrogen concentration gradients in Monel K 500

The ion probe mass spectrometer was used to measure hydrogen concentration gradients in cathodically charged Monel K 500. Initial work with the ion probe involved the calibration of the instrument and the establishment of a suitable experimental procedure for this application. Samples of Monel K 500 were cathodically charged in a weak sulfuric acid solution. By varying the current density, different levels of hydrogen were introduced into the samples. Hydrogen concentration gradients were taken by ion sputtering on the surface of these samples and monitoring the behavior of the hydrogen mass peak as a function of time. An attempt was made to determine the relative amounts of hydrogen in the bulk and grain boundaries by analyzing a fresh fracture surface with a higher proportion of grain boundary area. It was found that substantially more hydrogen was detected in the grain boundaries than in the bulk, confirming the predictions of previous workers. A sputter rate determination was made in order to establish the rate of erosion.

Truhan, J. J., Jr.↗

Measurement of hydrogen- and self-broadened half-widths of ammonia at 200 and 300 K

The hydrogen- and self-broadened half-widths have been measured for the (nu1 + nu2) and (nu2 + nu3) bands of ammonia at 300 and 207 K. Measurement of hydrogen-broadened widths has been restricted to J and K values not exceeding 6, but that of self-broadened widths is done for a few lines outside that range. Assuming a power-law dependence of half-width on temperature, the average value of the index alpha for the lines measured is found to be 0.57 for hydrogen broadening.

Margolis, J. S.↗

Absolute rate of the reaction of O/3-P/ with hydrogen sulfide over the temperature range 263 to 495 K

The technique of flash photolysis coupled with time resolved detection of O via resonance fluorescence has been used to obtain rate constants for the reaction of O(3-P) with H2S at temperatures from 263 to 495 K and at pressures in the range 10-400 torr. Under conditions where secondary reactions are avoided, the measured rate constants for the primary step obey the Arrhenius equation k = (7.24 plus or minus 1.07) x 10 to the -12th exp(-3300 plus or minus 100/1.987 T) cu cm/molecules/s. Experiments with D2S show that the reaction exhibits a primary isotope effect, in support of a hydrogen abstraction mechanism.

Whytock, D. A.↗

Creep and tensile properties of several oxide-dispersion-strengthened nickel-base alloys at 1365 K

The tensile properties at room temperature and at 1365 K and the tensile creep properties at low strain rates at 1365 K were measured for several oxide-dispersion-strengthened (ODS) alloys. The alloys examined included ODS Ni, ODS Ni-20Cr, and ODS Ni-16Cr-Al. Metallography of creep tested, large grain size ODS alloys indicated that creep of these alloys is an inhomogeneous process. All alloys appear to possess a threshold stress for creep. This threshold stress is believed to be associated with diffusional creep in the large grain size ODS alloys and normal dislocation motion in perfect single crystal (without transverse low angle boundaries) ODS alloys. Threshold stresses for large grain size ODS Ni-20Cr and Ni-16Cr-Al type alloys are dependent on the grain aspect ratio. Because of the deleterious effect of prior creep on room temperature mechanical properties of large grain size ODS alloys, it is speculated that the threshold stress may be the design limiting creep strength property.

Wittenberger, J. D.↗

K I 7699 A emission from the Betelgeuse shell

A map of the circumstellar gas shell around Betelgeuse is presented from observations of the fluorescent emission in the K I 7699 A resonance line. The observations obtained at 3 sec and 5 sec from the star indicate approximate spherical symmetry in the 10 km/s expanding shell responsible for the blueshifted sharp cores seen in strong resonance and low excitation lines. Calculations show that the density of neutral K atoms is approximately constant between 3 sec and 5 sec from the star. The emission profiles in the west show a second, higher velocity, component at 5 sec from the star.

Bernat, A. P.↗

Spectroscopic studies of O-type stars. VIII - Radial velocities and the K-term

Radial velocities are measured on coude spectrograms of over 200 O-type stars in both hemispheres. The selection of effective wavelengths for the stellar lines to be measured is reviewed, and the measured velocities are compared with those available in a catalog of O stars. The Trumpler (1935) effect (a reported anomalous redshift in certain O stars) is inconclusively reinvestigated, atmospheric motions in Of stars are examined, and some kinematic properties of O stars are discussed statistically. It is found that 58% of all O stars and 41% of all the Of stars considered are certain or probable binaries. A K-term in the range from 1 to 2 km/s is derived for the O stars, but the Of stars are shown to have a highly significant negative K-term. It is suggested that the systematically negative peculiar velocities of the Of stars are due to outflow of material beginning at the photospheric level.

Conti, P. S.↗

The Raman spectra of N-14O2 and N-15O2 solids at 20 K

The Raman spectra of N-14O2 and N-15O2 have been studied at 20 K. The far infrared of N-14O2 at 20 K was also measured. The data were assigned on the basis of a C-sub 2 nu molecular model. Normal coordinate calculations were performed for a variety of assignments. The assignment that yielded the best fit is presented. The solid state effects are discussed.

Durig, J. R.↗

Absolute rate of the reaction of hydrogen atoms with ozone from 219-360 K

Absolute rate constants for the reaction of atomic hydrogen with ozone were obtained over the temperature range 219-360 K by the flash photolysis-resonance fluorescence technique. The results can be expressed in Arrhenius form by K = (1.33 plus or minus 0.32)x10 to the minus 10 power exp (-449 plus or minus 58/T) cu cm/molecule/s (two standard deviations). The present work is compared to two previous determinations and is discussed theoretically.

Lee, J. H.↗

Calculated rate constants for the reaction ClO + O yields Cl + O2 between 220 and 1000 deg K

Classical trajectory calculations are presented for the reaction ClO + O yields Cl + O2, a reaction which is an important step in the chlorine-catalyzed destruction of ozone which is thought to occur in the 220 and 1000 K. The calculated rate constant is 4.36 x 10 to the minus 11th power exp (-191/T)cu cm molecule (-1)s(-1) and its value at 300 K is 2.3 plus or minus 10 to the 11th power cu cm molecule (-1)s(-1), about a factor of 2 lower than recent experimental data. The empirical potential energy surface used in the calculations was constructed to fit experimental data for ClO, O2 and ClOO molecules. Other important features of this potential surface, such as the barrier to reaction, were varied systematically and calculations were performed for a range of conditions to determine the best theoretical rate constants. Results demonstrate the utility of classical trajectory methods for determining activation energies and other kinetic data for important atmospheric reactions.

Jaffee, R. L.↗

High-resolution optical observations of Ca II K in Deneb and Aldebaran

High-spectral-resolution echellograms confirm the existence of an asymmetric emission core in the K line of Deneb that may be due to chromospheric emission from this A-type supergiant or that may be due to scattering from a circumstellar shell. If the core is due to chromospheric emission, its width does not agree with what is predicted using the Wilson-Bappu relation for late-type stars. This would indicate that the chromospheres of hotter stars are qualitatively different from those of cooler stars. A K-emission-core profile for Aldebaran is also presented.

Mcclintock, W.↗

Tensile and creep properties of the experimental oxide dispersion strengthened iron-base sheet alloy MA-956E at 1365 K

A study of the 1365 K tensile properties, creep characteristics and residual room temperature properties after creep testing of the experimental oxide dispersion strengthened iron-base alloy MA-956E (Fe-20Cr-4.5Al-0.5Ti-0.5Y2O3) was conducted. The 1365 K tensile properties, particularly ductility, are strongly dependent on strain rate. It appears that MA-956E does not easily undergo slow plastic deformation. Rather than deform under creep loading conditions, the alloy apparently fails by a crack nucleation and growth mechanism. Fortunately, there appears to be a threshold stress below which crack nucleation and/or growth does not occur.

Whittenberger, J. D.↗

Temporal evolution of the equatorial K-corona

Variation of the equatorial K-corona radiance at 2.5 solar radii from the sun center was studied on a daily basis during the Skylab mission (May 1973 to February 1974). The radiance data may be divided into three periods, the first characterized by a smooth variation in time, the second by a signal that is neither persistent in the short term nor recurrent from one limb passage to the next, and the third (and longest period) by a signal exhibiting an orderly, periodically increasing intensity. The data may be interpreted as indicating a general simplification of the coronal magnetic field; harmonic analysis of the surface field provides additional information on the evolution of the equatorial K-corona structures.

Macqueen, R. M.↗

Absolute rate of the reaction of bromine atoms with ozone from 200 to 360 K

The rate constant for the reaction Br + O3 yields BrO + O2 has been measured from 200 to 360 K by the technique of flash photolysis coupled to time resolved detection of bromine atoms by resonance fluorescence (FP-RF). Br atoms were produced by the flash photolysis of CH3Br at a wavelength of 165 nm. O3 concentration was monitored continuously under reaction conditions by absorption at 253.7 nm. At each of five temperatures the results were independent of substantial variations in O3 concentration, total pressure (Ar), and limited variations in flash intensity (i.e., initial Br concentration). The measured rate constants obey the Arrhenius expression, k = (7.74 plus or minus 0.50) x 10 to the -12th exp(-603 plus or minus 16/T) cu cm/molecule/sec, where the error quoted is two standard deviations.

Michael, J. V.↗

Absolute rate of the reaction of hydrogen atoms with ozone from 219-360 K

Absolute rate constants for the reaction of atomic hydrogen with ozone were obtained over the temperature range 219-360 K by the flash photolysis-resonance fluorescence (FP-RF) technique. The results can be expressed in Arrhenius form by k = (1.33 + or - 0.32) times (10 to the minus tenth power) exp(-449 + or - 58/T) cu cm/molecule per sec (two standard deviations). The present work is compared to two previous determinations and is theoretically discussed.

Lee, J. H.↗

Absolute rate constants for the reaction of atomic hydrogen with ketene from 298 to 500 K

Rate constants for the reaction of atomic hydrogen with ketene have been measured at room temperature by two techniques, flash photolysis-resonance fluorescence and discharge flow-resonance fluorescence. The measured values are (6.19 + or - 1.68) x 10 to the -14th and (7.3 + or - 1.3) x 10 to the -14th cu cm/molecule/s, respectively. In addition, rate constants as a function of temperature have been measured over the range 298-500 K using the FP-RF technique. The results are best represented by the Arrhenius expression k = (1.88 + or - 1.12) x 10 to the -11th exp(-1725 + or - 190/T) cu cm/molecule/s, where the indicated errors are at the two standard deviation level.

Michael, J. V.↗

Rate constant for the reaction H + NO2 from 195 to 400 K with FP-RF and DF-RF techniques

Measurements are made of the rate constant for the reaction H + NO2 yielding OH + NO over significant temperature ranges with the flash photolysis-resonance fluorescence (FP-RF) technique and also with the discharge flow-resonance fluorescence (DF-RF) technique. Since it is important to study chemical reactions with more than one technique, the above reaction is investigated with the FP-RF technique over the temperature range 230-400 K. The results reported do not agree with earlier determinations. Accordingly, a separate set of measurements is made with the DF-RF technique over the temperature range 195-368 K; the results are also reported. The reaction is also considered theoretically, especially with regard to the question of temperature dependence and absolute magnitude of the rate constant.

Michael, J. V.↗

Absolute rate constant of the reaction between chlorine /2P/ atoms and hydrogen peroxide from 298 to 424 K

The absolute rate constant of the reaction between chlorine (2P) atoms and hydrogen peroxide was determined from 298 to 424 K, using the discharge flow resonance fluorescence technique. Pseudo-first-order conditions were used with hydrogen peroxide in large excess. A fast flow-sampling procedure limited hydrogen peroxide decomposition to less than 5% over the temperature range studied. At 298 K, the rate constant is (4.1 plus or minus 0.2) x 10 to the minus 13th cu cm/molecule-sec.

Keyser, L. F.↗