The nocturnal inversion and its effect on the dispersion of carbon monoxide at ground level in Hampton, Virginia
Explore the source record for details and available documents.
SEARCH · Engineering Papers
Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.
Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.
Explore the source record for details and available documents.
Autoradiographic analysis and gas chromatography were used to measure the solubility in silicate melts of CO-CO2 vapors (30 to 40% CO by thermodynamic calculation) in equilibrium with graphite at temperatures up to 1700 deg C and pressures to 30 kbar. At near-liquidus temperatures CO-CO2 vapors were found to be slightly more soluble than CO2 alone. As a result of the apparently negative temperature dependence of CO solubility, the solubility of CO-CO2 at superliquidus temperatures is less than that of CO2. Melting points of two silicates were depressed more by CO than by CO2. Phase boundary orientations suggest that CO/CO + CO2 is greater in the liquid than in the vapor. The effect of the presence of CO on periodotite phase relations was investigated, and it was found that melts containing both CO and CO2 are nearly as polymerized as those containing only CO2. These results suggest that crystallization processes in planetary interiors can be expected to be about the same, whether the melts contain CO2 alone or CO2 and CO.
During the period 28-30 October 1977, a Pan American 747-SP aircraft flew around the world with an automated instrument package that included measurements of atmospheric CO made every 4 sec. The flight path extended from San Francisco, over the North Pole to London, south to Capetown, over the South Pole to Auckland, and back to San Francisco. The data collected show large changes with longitude, which are interpreted as direct evidence of interhemispheric mixing. Possible sources for CO are discussed.
Explore the source record for details and available documents.
Accurate theoretical collisional excitation rates are used to determine the emissivities of CO rotational lines 10 to the 4th power/cu cm n(H2), 100 K T 2000 K, and J 50. An approximate analytic expression for the emissitivities which is valid over most of this region is obtained. Population inversions in the lower rotational levels occur for densities n(H2) approximately 10 (to the 3rd to 5th power)/cu cm and temperatures T approximately 50 K. Interstellar shocks observed edge on are a potential source of millimeter wave CO maser emission. The CO rotational cooling function suggested by Hollenbach and McKee (1979) is verified, and accurate numerical values given. Application of these results to other linear molecules should be straightforward.
CO emission has been sought in 52 directions toward six irregular, Magellanic-type galaxies, with null results at a typical detection limit of 0.04 K for a line width of 10 km/s. The positions searched correspond to those of bright OB star clusters, H II regions, H I peaks, and dark clouds. In two cases, one-third of the optical galaxy was covered by the observations. CO has been detected at 2.6 mm toward the nucleus of the low-mass SA(s)dm galaxy NGC 7793. The results imply that the mean surface brightness of CO emission in Magellanic irregulars is less than that of the Galaxy and other spirals which have been studied. Two categories of explanations for this are discussed, including (1) those based on a lower heating rate for interstellar clouds in irregulars, and thus a lower CO temperature, and (2) those based on a lower CO abundance.
Observations of the fundamental 4.6 micron band of CO in nine red giants are presented. A common feature is multiple absorption lines which are identified as products of separate components or shells. Column densities are derived; the relative values should be free of the uncertainties inherent in determining the absolute scale. These column densities are well fitted by single excitation temperatures for each absorption component; these excitation temperatures are identified with the local kinetic temperatures. There is no correlation of CO column density with either gas or dust column density nor of the expansion velocity of the component with its distance from the star. The evidence is reviewed, and it is concluded that mass loss from red giants is most likely episodic in nature.
An observational program to study variations of the vertical distribution of CO in the Venus atmosphere is presented. Measurements of the J = 0 - 1 absorption line at 2.6 mm wavelength are reported for two phase angles in 1977, one near eastern elongation (February) and the other near inferior conjunction (April). The two spectra are significantly different, with the April absorption line being narrower and deeper. The results of numerical inversion calculations show that the CO mixing ratio increases by a factor of approximately 100 between 78 and 100 km and that the CO abundance above approximately 100 km is greatest on the night-side hemisphere. These conclusions are in qualitative agreement with theoretical models. In addition to the CO observations, a search for other molecules was made to provide further information on the composition of the Venus middle atmosphere. The J = 0 - 1 transition of (C-13)O was detected and upper limits were derived for nine other molecules.
The two-dimensional distributions of CO and O3 in the free troposphere during July and August, 1974, are discussed. The data confirm the previous findings that both of these gases are considerably more abundant in the northern hemisphere, but the degree of the asymmetry is somewhat different from what had been reported previously, especially for CO. When examined with respect to other available data sets, the conclusion is drawn that a pronounced seasonal cycle exists for CO in both hemispheres which may be driven by the likely seasonal cycle of the OH radical. The data also indicate that CO concentrations exhibit significant variability with height in the northern hemisphere, whereas southern hemispheric concentrations are quite constant with altitude except in cases where interhemispheric exchange of air may be occurring. A discussion on the vertical and horizontal transport processes inferred from the CO and O3 measurements is presented. The possible interdependence of the photochemical cycles of these two trace gases is also discussed.
The catalytic activity of cupric oxide activated with ceric oxide in a braod interval of volumetric velocities was investigated. It was determined that for practical catalysts used in the diffuse region, dilution of the active substance by an inert diluent increases the effectiveness of the catalysts.
Recent observations of the Venus dayglow spectrum from 1200 to 1800 A are discussed, and identifications of the CO4+ bands are given using synthetic spectra. The main excitation mechanism is found to be resonant and fluorescent scattering of solar radiation, so the theory for this process is covered in some detail. A synthetic fluorescence spectrum is generated with the aid of high-resolution solar flux data, and emission rate factors are calculated. The influence of solar emission line excitation on this spectrum is demonstrated. In particular, it is shown that the uncertainties in interpreting the Venus dayglow are overcome by the identification of CO4+ bands in the v prime = 14 progression resulting from the fluorescent scattering by CO of solar Lyman alpha radiation.
Accurate theoretical collisional excitation rates are used to determine the emissivities of CO rotational lines for an H2 molecule content of at least 10,000/cu cm, temperature in the range 100-3000 K, and J not more than 60 under the assumption that the lines are optically thin. An approximate analytic expression for the emissivities which is valid in this region is obtained. Population inversions in the lower rotational levels occur for densities of molecular H2 around 1000-100,000/cu cm and temperatures T not more than about 50 K provided photon trapping is unimportant. Interstellar shocks observed edge-on are a potential source of weak millimeter-wave CO maser emission.
First order RKR turning points were computed for (C-12)O16, (C-12)O17, (C-13)O16, (C-12)O18, and (C-13)O18 for vibrational levels up to v = 40. These turning points should be useful in the numerical computation of matrix elements of powers of the internuclear separation.
The results of trials with a staged combustor designed to use coal-derived gaseous fuels and reduce the NO(x) emissions from nitrogen-bound fuels to 75 ppm and 37 ppm without bound nitrogen in 15% O2 are reported. The combustor was outfitted with primary zone regenerative cooling, wherein the air cooling the primary zone was passed into the combustor at 900 F and mixed with the fuel. The increase in the primary air inlet temperature eliminated flashback and autoignition, lowered the levels of CO, unburned hydrocarbons, and smoke, and kept combustion efficiencies to the 99% level. The combustor was also equipped with dual fuel injection to test various combinations of liquid/gas fuel mixtures. Low NO(x) emissions were produced burning both Lurgi and Winkler gases, regardless of the inlet pressure and temperature conditions. Evaluation of methanation of medium energy gases is recommended for providing a fuel with low NO(x) characteristics.
Approximately 35 hours of radiometric measurements were obtained of the CO mixing ratio in the middle troposphere, upper troposphere, and lower stratosphere, by means of the Measurement of Air Pollution from Satellites (MAPS) experiment carried in the OSTA-1 payload of the second Space Shuttle flight. In view of gas filter radiometer data in the 4.67-micron band, gathered over the 38 N-38 S latitude region during both daytime and nighttime, the performance of MAPS was excellent. Significant gradients have been found in the middle tropospheric CO mixing ratio with both latitude and longitude over the North Atlantic, the Mediterranean Sea, and the Middle East.
The small-scale vertical variability of troposheric O3 and CO is examined using a set of simultaneous measurements obtained in July and August 1974 between 55 deg S and 67 deg N. From this set of vertical profiles, it is found that many of the fluctuations are coincident in both species, and a method is presented that quantifies the correlation between the observed O3 and CO variability. A two-dimensional depiction of the distribution of these O3-CO correlations reveals that there are regions in the troposphere where these trace gases are positively correlated and that, at the same time, there are preferred locations where these two species are primarily anticorrelated. The regions of anticorrelation are found to be consistent with the traditional picture of the tropospheric ozone cycle, suggesting that this gas is chemically unreactive in the troposphere. On the other hand, the location and magnitude of the region in which these two species are positively correlated indicates that there is considerable in situ production of tropospheric ozone.
Recent measurements and reanalyses of past measurements are used to derive estimates of the variability of CO concentrations in the Martian atmosphere. The J = 1 - 2 rotational transition of CO in the microwave spectrum of Mars was observed in January, 1982, and abundances were calculated through surface and atmospheric temperature modeling. A column density of 4.6 + or - 2.0 x 10 to the 20th/sq cm is obtained, which is contrasted with values of 3.0 + or - 1.0 x 10 to the 20th/sq cm in 1980 and 1.7 x + or - 0.9 x 10 to the 20th/sq cm in 1975 obtained by reanalysis of the J = 0 - 1 transition observed by Good and Schloerb (1981) and Kakar et al. (1977), respectively. It is noted that due to the uncertainties in global atmospheric average temperatures, results are consistent with a CO variability of from 0 to 100 percent over a time scale of several years. It is suggested that simultaneous measurements of the J = 0 - 1 and J = 1 - 2 transitions may provide stronger constraints on the CO abundance and atmospheric temperature of Mars.
The four-to-fivefold difference in water abundance between the earth and Venus may reflect either initial differences in the bulk volatile content of the two planets, or massive water loss mechanisms on Venus. These two possibilities were investigated by performing thermodynamic calculations on the heterogeneous system C-O-H-N-S, varying C/H upward from its 0.033 terrestrial value. While atmospheric H2O decreases as bulk C/H increases, the latter would have to rise to an improbably high value in order to account for the low water abundance on Venus through initial deficiency alone. Calculations suggest that if the outgassed C/H on Venus was higher than on earth by even a factor of 5, it would have been sufficient for CO to become competitive with FeO as a sink for oxygen. Together with the lower initial water abundance value that follows from a higher C/H ratio, water loss due to CO may have been a major factor.