A study of the intensity of the self-broadened fundamental band of hydrogen chloride
Intensity study of self-broadened fundamental band of hydrogen chloride
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Intensity study of self-broadened fundamental band of hydrogen chloride
Ethylene oxide and vinyl chloride adsorption on iron /011/ surface, and surface film effect on adhesion
Research and developments in electrochemistry of aluminum chloride melts
Nitrosyl chloride reagent effects on phenylalanine peptides
Vibrational spectra and structure of oxalyl chloride in crystalline and fluid states, discussing molecular and space group symmetry
Modulation of carbon dioxide laser with Stark cell internal to cavity, using methyl chloride electrooptical gas
Hydrogen chloride self broadened fundamental vibration rotation band intensity variation with pressure investigated by absorption spectroscopy analysis
Experimental and computerized electrochemical measurements in fused sodium aluminum chlorides
Aluminum chloride containing solvent systems as organic reactions media - literature survey
Polyvinyl chloride nonlinear viscoelastic behavior by multiple integral representation, determining kernel functions for mixed time parameters from tension/torsion creep experiments
Porous glass hyperfiltration membranes stabilization by aluminum chloride solution, noting retreatment need
Nonactomyosin component differentiation in potassium chloride insoluble myofilaments in vertebrate smooth muscle cells
The sliding of polyvinyl chloride on nickel, iron and S-Monel has been studied by Auger electron spectroscopy. Polymer was not transferred to the metals, rather shear appeared to take place at the interface. The metal was progressively chlorinated as the polymer made multiple passes on the surface. The thickness of this chlorine film was the order of one atomic layer. Electron-induced desorption studies indicate that the chlorine is chemisorbed to the metal. These results are interpreted as evidence for mechanically induced and/or thermal degradation of the polymer during sliding. Degradation products of HCl and Cl2 which chemisorb to the metal are evolved near the interface.
On the basis of measurements of the velocity of ultrasounds in aqueous solutions of some alkaline-earth chlorides (MgCl2, CaCl2, BaCl2) the concentration and temperature dependences of the internal pressure were determined. Using these results, as well as surface tension measurements, the mean diameters of the molecular species as a function of concentration and temperature, were determined.
Cellulose acetate butyrate (CAB) membranes are shown to give high salt and urea rejection with water flux of about 3 gallons/sq ft per day at 600 psig. Membranes prepared from a formulation containing glyoxal show a significant increase in flux and decrease in salt and urea rejection with drying time. Zero drying time gives maximum urea and salt rejection and is therefore most suitable for hyperfiltration of sodium chloride and urea feed solution.
A copper vapor laser utilizing copper chloride as a lasant in a heated discharge tube has been studied. The lasing action was observed only when two successive discharge current pulses at suitable time intervals were applied. The first pulse is considered to be a dissociation pulse to produce copper and chlorine atoms; the second to be a pumping pulse to produce population inversion. The maximum energy density measured to date was 17 microjoule/cu cm.
A manganese vapor laser utilizing manganese chloride as a lasant has been observed and investigated. Lasing is attained by means of two consecutive electrical discharges. The maximum laser output is obtained at a vapor pressure of about 3 torr, a temperature of 680 C, and a time delay between electrical discharges of 150 microsec. The maximum energy density is 1.3 microjoule per cu cm.
Ti-8 Al-1 Mo-1 V was tested in solvents containing chloride, bromide or iodide ions. It was found that the region II plateau velocity could be correlated with the inverse of the viscosity for several solvents. It seems most likely that this reflects the influence of the viscosity on the diffusion coefficient of some species involved in a mass transfer process which limits the crack growth. Associated tests were performed in which the potential, pH and concentration of Cl- were varied, in some of the same solutions as used for the viscosity tests. It is concluded from these tests that the absence of cathodic protection against cracking in solutions of low pH arises from an ohmic effect which isolates the crack tip from external potential control.