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Vapor phase deposition process forms a heavily doped n-region on a melt-grown p-type gallium antimonide substrate. HCl transports gallium to the reaction zone, where it combines with antimony hydride and the dopant carrier, hydrogen telluride. Temperatures as low as 400 degrees C are required.
Epitaxial surface morphology layer electrical properties and autodoping at GaAs-Ge heterojunctions as function of substrate temperature, orientation and HCl concentration
Direct sensitized photolysis of various dichlorobutanes yielding HCl
Photolysis of HCl photosensitized evolution from dichlorobutane in solution by aliphatic ketones
Exponential approximation of rotational relaxation of polar HCl and DCl at 300 and 500 K by molecular dynamics, comparing with perturbation calculations
IR chemiluminescence from HCl formed in atomic hydrogen reaction with sulfur dichloride, noting energy distribution among reaction products
The activities of the Toxic Hazards Research Unit (THRU) for the period of June 1970 through May 1971 reviewed. Modification of the animal exposure facilities primarily for improved human safety but also for experimental integrity and continuity are discussed. Acute toxicity experiments were conducted on hydrogen fluoride (HF), hydrogen chloride (HCl), nitrogen dioxide (NO2), and hydrogen cyanide (HCN) both singly and in combination with carbon dioxide (CO). Additional acute toxicity experiments were conducted on oxygen difluoride (OF2) and chlorine pentafluoride (ClF5). Subacute toxicity studies were conducted on methylisobutylketone and dichloromethane (methylene dichloride). The interim results of further chronic toxicity experiments on monomethylhydrazine (MMH) are also described.
The spectral and polarization data for Venus are consistent with micron-sized, aerosol cloud particles of hydrochloric acid containing soluble and insoluble iron compounds, whose source could be volcanic or crustal dust. The ultraviolet features could arise from variations in the Fe-HCl concentration in the cloud particles.
The influence of multipole interactions on exchanges of rotational energy in molecular collisions was investigated by means of a simple two-state impact parameter approximation. The calculations are restricted to linear molecules and to dipole and quadrupole fields. The effects of such exchanges on the thermal conductivity of gases and of gaseous mixtures was investigated, after correcting the kinetic theory of mixtures to include exchanges between unlike molecules. It was found that dipole-quadrupole and quadrupole-quadrupole interactions may have a significant effect for molecules with low moments of inertia. In particular, quadrupole interactions are important in the hydrogen isotopes, and the calculated corrections for H2 are consistent with recent experimental work by Harris. The theory seems capable of accounting for the anomalies observed in HF + DF and HCl + DCl mixtures in terms of multipolar accidental resonances.
The absorption of solar ultraviolet radiation in the wavelength range 2000 to 2200 A by CO2 strongly reduces the dissociation rate of HCl on Venus. The Cl catalytic reaction for the rapid recombination of O and CO and the yellow coloration of the Venus haze by OCl(-) and Cl3(-) appears to be unlikely. At the time of the Martian dust storm, the dissociation of H2O in the vicinity of the surface may vanish. The increase of dissociation at high altitudes, however, can be the source of H atoms in the upper atmosphere. The H atoms from the dissociation of hydrides may catalyze the recombination of CO and O in the lower atmospheres of these planets according to the following scheme: H + CO + M yields HCO + M, and HCO + O yields H + CO2. In the case of Venus, there may be other kinds of sinks for the photodissociation products, and its chemical environment might be more complex than that of Mars.
The design of a mass spectrometer, based on the results of the Venera and Mariner probes, with sensitivity high enough to detect the HCl in the Venus atmosphere is discussed. One way to analyze the clouds is by the introduction of the atmosphere with cloud particles through a molecular leak into the mass spectrometer. The analysis can be performed in regular Nier-type ion sources with the electrodes of materials which are completely free of Cl and F. The problem of preventing the blockage of the capillaries to the Nier type ion source is also considered.
The observed chemical composition of the atmosphere near the Venus cloud tops, the refractive index of cloud particles as deduced from polarization data, and the 3-4-micron reflectivity of the clouds are discussed. The data are shown to be consistent with and to strongly support the possibility that the topmost clouds of Venus are composed of concentrated aqueous HCl solutions.
The Cr2O3 content of powder metallurgy nickel-20 chromium-3 thoria was reduced with atmospheres consisting of hydrogen plus hydrogen chloride (HCl) or hydrogen bromide (HBr). The nonthoria oxygen content or 'oxygen excess' was reduced from an initial amount of greater than 50,000 ppm to less than 100 ppm. Low temperatures were effective, but lowest oxygen levels were achieved with the highest cleaning temperature of 1200 C.
The existing high resolution spectra of Venus show considerable variations in the abundance of CO2. As this is the major constituent of the atmosphere, these day-to-day variations indicate the effective reflecting cloud layer is undergoing substantial vertical displacements over a relatively short time scale. The published observations indicate that CO is uniformly mixed with the CO2, but that the lines of HF may be formed deeper in the atmosphere and HCl lines considerably deeper. These conclusions are based on extrapolations of laboratory measurements and could be considerably altered by new laboratory measurements made under conditions similar to those near the tropopause in Venus.
The Mariner 6 and 7 infrared spectrometers provided data which, in principle, determine upper limits on the possible atmospheric abundance of every gaseous substance that was undetected but which has recognized absorptions in the accessible spectral region, 1.9 to 14.4 microns. Through supporting laboratory determinations of curves of growth under pressure-broadening conditions appropriate to Mars, upper limits can be specified (expressed first in cm-atm, STP, for a vertical column and then in parts per million) for NO2, NH3, C3O2, SO2, OCS, NO, O3, CH4, N2O, HCL, HBr, and H2S. In addition, considerations of band contours, moments of inertia, and experimental absorption coefficients make it possible to place useful upper limits on 27 additional substances that were not detected and for which curves of growth have not been measured.
Calculation of the reflectivity of Lewis' (1969) mercury cloud systems to determine the limits placed upon such models by the requirement that they reproduce the observed high albedo of Venus. In this way an upper limit is placed on the mercury droplet cloud mass. This limit is a function of the droplet size. If the droplets are less than 10 microns in radius, models with mercury clouds of mass greater than 0.005 g/sq cm are excluded the values for the masses of the Hg2Cl2 and HCl-H2O clouds given by Lewis are adopted. Relations are given which make it possible to determine whether a particular model satisfies the constraints imposed by the requirement that it produce the high albedo of Venus.
The activities of the Toxic Hazards Research Unit (THRU) for the period of June 1971 through May 1972 are reviewed in this report. Acute inhalation toxicity experiments were conducted on hydrogen chloride (HCl) gas and aerosol, ethyl bromide (C2H5Br), hydrogen bromide (HBr), hydrogen sulfide (H2S), ammonia (NH3), chlorine (CL2), and silane (SiH4). Subacute toxicity studies were conducted on chlorine pentafluoride (ClF5), dichloromethane (CH2Cl2) and coal tar volatiles. Further toxicity studies of subacute and chronic responses to inhaled monomethylhydrazine (MMH) are also described.
The existing high-resolution spectra of Venus show considerable variations in the abundance of CO2. As this is the major constituent of the atmosphere, these day-to-day variations indicate that the effective reflecting cloud layer is undergoing substantial vertical displacements over a relatively short time scale. The published observations indicate that CO is uniformly mixed with the CO2, but that the lines of HF may be formed deeper in the atmosphere and HCl lines considerably deeper. These conclusions are based on extrapolations of laboratory measurements and could be considerably altered by new laboratory measurements made under conditions similar to those near the tropopause in Venus.