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  • 1975-1979  (3)
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  • 1
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We have studied the effects of temperature, EDTA, and ionic strength on C-polysaccharides in solution by examining the details of the time-correlation function using a 96-channel single-clipped photon correlation spectrometer. Our linewidth results have shown that the C-polysaccharides in buffer solution form aggregates of very broad distributions. Thus, fractionation by gel-filtration chromatography is only mildly effective. Although the aggregate sizes seem to remain relatively constant from 4 to 25°C, a fraction of those aggregates break up to form smaller fragments or monomers at higher temperatures. However, the dissolution-association process is quite slow and takes days even at room temperatures before the equilibrium is reached. We have also shown that by adding an excess amoutn of EDTA, the aggregates can be broken up. Again the dramatic changes occur only at short delay times suggesting that a protion of the larger aggregates remains. Finally, the amount and size of aggregates depend upon the ionic strength which exhibit a maximum ΓT/sin2 (θ/2) around 0.1-0.2 M KCl.If the activities of polysaccharides in solution depend upon molecular size, the standard techniques such as gel-permeation chromatography and ultracentrifugation cannot properly characterize the detailed size distribution. Quasielastic laser light scattering can provide us with a qualitative model. The quantitative details must necessarily await more extensive investigations using a combination of the techniques and better fractionation procedures in an appropriate buffer solution.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 14 (1975), S. 93-109 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We report measurements of the diffusion coefficient of β-lactoglobulin A (βLG-A) at pH = 5.60 and 4.58 in 0.10 ionic strength acetate buffer by the techniques of analog photocurrent signal correlation and digital single-clipped photon correlation. At a concentration of 21 mg/ml and a pH of 4.58, the self-association of β-lactoglobulin can be represented by a simple dimer-octamer equilibrium model. We determined the translational diffusion coefficient of the dimer and that of the octamer using the scattering results of Kumosinski and Timasheff in a dimer-octamer mixture. Our analysis shows that the dimer βLG-A does not change its size if the pH is varied from 5.60 to 4.58 and both species remain constant in size for temperature changes from 3.5° to 25°C Hydrodynamically, the octamers behave like closed-packed spheres with an effective radius of about 45 Å according to the Stokes-Einstein relation.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 17 (1979), S. 87-94 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Heat capacities of poly(vinylidene fluoride) (PVF2) and polytetrafluoroethylene (PTFE) have been measured between 5 and 100°K with an accuracy of (1-5)% by adiabatic calorimetry. Calculations based on contributions from known optical lines and the Tarasov continuum model are in good agreement with experimental results down to 30°K for PVF2 and 10°K for PTFE, and yield characteristic temperatures θ1 and θ3 which are consistent with previous values determined from high-temperature (100 - 350°K) data. At lower temperature the measured heat capacity is significantly higher [(30-100)%] than the model prediction, and can be satisfactorily accounted for by the introduction of localized vibrators at a concentration of about 1% as compared to acoustical oscillators and at a characteristic temperature of about 20°K. Using established data on polyethylene for comparison, the principle of additivity for heat capacities is found to be valid down to at least 20°K, convering the region (〈60°K) where interchain vibrations contribute significantly to the heat capacity. Possible reasons for this unexpected behavior are discussed.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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