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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 7 (1978), S. 525-531 
    ISSN: 1572-8927
    Schlagwort(e): Electrophoretic effect ; mixed electrolytes ; Chen effect ; unsymmetrical electrolytes ; conductance theory
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The ionic electrophoretic effect for solutions of mixed electrolytes of any type is calculated. The calculation is based on the well-known treatment due to Chen with the same distance of closest approach for all the ions in solution. The improved iterative method used for the relaxation-field treatment is applied. For the latter the electrophoretic velocity results are derived to the second iteration in the perturbation method.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 7 (1978), S. 533-548 
    ISSN: 1572-8927
    Schlagwort(e): Electrical conductivity ; mixed electrolytes ; conductivity equation ; unsymmetrical electrolytes ; conductance theory
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract An analytical expression for the electrical conductance of a mixed electrolyte solution of any type is derived. A general expression giving the equivalent ionic conductance is derived. This expression is also valid for the case of a pure electrolyte, whether asymmetrical or symmetrical. A comparison is made with the results obtained by other authors in the particular case of symmetrical electrolytes.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    ISSN: 1572-8927
    Schlagwort(e): Flow calorimetry ; vibrating tube densimetry ; heat of mixing ; volume of mixing ; high temperature ; high pressure
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract A new instrument combining a flow-mixing calorimeter and a vibrating tube densimeter inside a thermostatted environment has been constructed. The instrument is designed for simultaneous measurements of calorimetric and volumetric properties at superambient conditions on mixtures for which both pure components are liquid at room temperature or one component is a liquid and the other is gaseous. The system yields simultaneously two properties: (1) the enthalpy of mixing determined in a heat-leak calorimeter with power compensation; (2) the density difference between a mixture (solution) and a reference liquid measured as a change in frequency of a tube vibrating in a field of permanent magnets. The instrument was tested in the full concentration range using aqueous ethanol and aqueous methanol. The results are presented at temperatures between 348 and 573 K and pressures from 5 to 20 MPa for mixing enthalpies ΔH mix ranging from −160 to 5700 J-mol−1. The corresponding heating powers are between −60 and 850 mW, respectively. The results for ΔV mix of mixing volumes were measurable from 348 K to 523 and between 5 and 13 MPa with the maximum volume change being −4.0 cm3-mol−1. The errors in ΔH mix and ΔV mix near mole fraction of 0.5 are believed to be less than 5% over the temperature and pressure ranges given above.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 7 (1978), S. 137-153 
    ISSN: 1572-8927
    Schlagwort(e): Relaxation field ; mixed electrolytes ; kinetic effect ; unsymmetrical electrolytes ; conductance theory
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The relaxation field for solutions of mixed electrolytes of any type is calculated. the calculation is based on the well-known treatment due to Fuoss-Onsager with the same distance parameter for all the ions in solution. A general conductance-continuity equation has been established and an improved iterative method of calculation, using Laplace transforms, is proposed. The relaxation-field results are derived to the second iteration in the perturbation method of integration.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 1229-1242 
    ISSN: 0887-6266
    Schlagwort(e): polyethylenes ; thermal expansion ; pressure-controlled scanning calorimetry ; high pressure ; crystallinity ; amorphous ; equation of state ; Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A pressure-controlled scanning calorimeter (PCSC) has been applied for measuring the isobaric volume thermal expansivities (αp) of crystalline polymers as a function of pressure up to 300 MPa at various temperatures. The measurements have been performed for several well-defined polyethylenes with various degrees of crystallinity at 302.6, 333.0, 362.6, and 393.0 K. The results are reported as values of coefficients in a correlation equation, which facilitates the use of reported data over large ranges of temperature and pressure. The general pressure-temperature behavior of αp for all polyethylenes under study is such that αp increases with temperature and decreases with pressure. The increase with temperature is smaller at high pressures and the isotherms of αp have a tendency to converge at high pressures; αp decreases linearly with the crystallinity of the polyethylene over the whole range of pressure and temperature under investigation. From the linear approximation of experimental data for polyethylenes with various crystallinities the estimated αp for both crystal and amorphous phases of polyethylenes have been determined as a function of pressure up to 300 MPa at 302.6, 333.0, and 362.5 K. The obtained results have been compared with available literature crystallographic data and with the values derived from the Pastine theoretical equation of state for both crystalline and amorphous phases. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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