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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of chemical & engineering data 8 (1963), S. 564-567 
    ISSN: 1520-5134
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 9 (1963), S. 121-128 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: An elution gas that might be either a single component or a binary mixture, but which in any case was appreciably soluble in the fixed liquid phase on the column matrix material, was used to form a multicomponent liquid phase within the chromatographic column. Vapor-liquid equilibrium was studied both with the solute of interest at essentially infinite dilution conditions and with the solute present at some finite concentration in both phases. From the elution data vapor-liquid equilibrium ratios, or K values, were calculated by expressions relating the solute retention volume to the solute K value in the vapor-liquid system maintained within the chromatographic column.Data were taken for the solutes ethane, propane, and n-butane at infinite dilution in the methane-n-decane system at 160°, 70°, 40°, 0°, and -20°F from 20 to 2,000 lb./sq. in.; for propane at infinite dilution in methane-n-hexadecane at 70°F and 20 to 200 lb./sq. in.; and propane in the system methane-propane-n-decane at 40°F from 20 to 460 lb./sq. in. The univariant gas-liquid-solid locus was experimentally determined for the methane-n-decane binary system.The chromatographically determined K values for n-butane at infinite dilution in methane-n-decane were compared with published static equilibrium values and found to be in substantial agreement. Activity coefficients calculated from the data for all the solute isotherms were compared at atmospheric pressure with the results of the Brönsted and Koefoed relation for estimating activity coefficients of hydrocarbons, and close agreement was again found.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 9 (1963), S. 106-108 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The characteristic velocities in binary and particular ternary cases allow straightforward calculation of equilibrium partition coefficients for components present in both flowing and fixed phases. It is shown in the case of a general N-component flowing phase that N-1 characteristic velocities arise. In theory N-1 equilibrium partition coefficients can be obtained from measurements of these velocities. It is also shown that radioactive tagging of one component provides a distinct characteristic velocity, which can be used either to obtain the Nth equilibrium coefficient or to eliminate a parameter which is especially subject to experimental error.The analytically determined characteristic velocities are compared with pulse velocities obtained from numerical solution of the original balance equations. The agreement over a range of solute concentrations is excellent.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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