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  • 1
    ISSN: 1435-1536
    Keywords: Microgels ; thermal diffusion ; self diffusion ; forced Rayleigh scattering
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Thermal diffusion in solutions of polystyrene micro-network spheres (microgels) in toluene has been studied by the holographic scattering technique of thermal diffusion forced Rayleigh scattering (TDFRS) and by photon correlation spectroscopy (PCS). Size distributions of microgels of different crosslink ratios are obtained from TDFRS measurements on dilute solutions at very lowq-values around 4000cm−1. At low concentrations a single diffusive mode is observed and the diffusion coefficient increases with concentration. It is attributed to the collective diffusion of the microgels and the solvent. At high concentrations an additional slow mode appears whose diffusion coefficient decreases with increasing concentration. Both diffusive modes are observed with PCS and TDFRS. Contrary to PCS, heterodyne TDFRS-measurements reveal a negative amplitude of the slow mode. We attribute the slow mode to self-diffusion of the microgels, made visible by the polydispersity of their size distribution. It is discussed in terms of a fast coupled thermal diffusion with subsequent decoupling of the individual microgels and relaxation into a new Soret equilibrium by self-diffusion of the microgels.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 20 (1999), S. 1-18 
    ISSN: 1572-9567
    Keywords: diffusion ; forced Rayleigh scattering ; Fourier transform ; Ludwig–Soret effect ; polymer solutions ; stochastic excitation ; thermal diffusion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The holographic grating technique of thermal-diffusion forced Rayleigh scattering (TDFRS) utilizes the Ludwig–Soret effect to induce a concentration modulation within a binary liquid. The signal generation is described in terms of a linear response formalism, and the memory function for the concentration mode g(t) and its Fourier transform, the diffusion susceptibility, are measured by means of pseudostochastic random binary sequences with flat power spectra in combination with fast Fourier transform and correlation techniques. For polydisperse polymer solutions the individual modes contribute proportional to their concentration to g(t), contrary to photon-correlation spectroscopy, where the correlation function is dominated by the high molar mass components. Other advantages of stochastic TDFRS are time-scale delocalization of dust spikes and frequency multiplexing. Measurements are reported on monodisperse and bimodal polystyrene in toluene.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    International journal of thermophysics 16 (1995), S. 11-21 
    ISSN: 1572-9567
    Keywords: diffusion ; forced Rayleigh scattering ; holography ; polymer solution ; thermal diffusion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The transient grating technique of thermal diffusion forced Rayleigh scattering (TDFRS) has been employed to study translational and thermal diffusion of polystyrene in toluene. Different molar masses and concentrations below or slightly above (lie overlap concentrationc * have been investigated. The translational diffusion coefficients agree well with results obtained from photon correlation spectroscopy. Small remaining diferences can be attributed to sample polydispersity. The molar mass independence of the thermal diffusion coefficient is confirmed, and thermal diffusion and Soret coefficients are compared with data obtained from thermal field flow fractionation and diffusion cell experiments.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 13 (1989), S. 217-229 
    ISSN: 1434-6079
    Keywords: 31.20.D ; 34.20
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The successfully tested interaction potential of H2-H2 obtained from quantum chemical calculations (M 80) has been used again as input in the attempt of determining a fit interaction potential of the H2-H2 system. It does not only give quantitative agreement with measurements as obtained previously, but also reproduces the second virial coefficients at low temperatures, calculated via quantum mechanical pair correlation functions, as measured in several independent experiments. Since the unique determination of this fit is not possible in principle, we have chosen a final version by means of plausible estimates of the limitations of previous ab initio calculations. The new potential is included in this paper in a table. Our isotropic rigid rotor potential term will be discussed in comparisons with experimentally determined potential fits. More tests of our fit potential have already been completed and can be used for a final judgement.
    Type of Medium: Electronic Resource
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