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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 14 (1975), S. 409-417 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The storage and loss shear moduli, G′ and G″, have been measured for dilute solutions of unaggregated and aggregated tobacco mosaic virus samples in glycerol-water mixtures, by the Birnboim-Schrag multiple-lumped resonator modified for use with aqueous solvents. The frequency range was 100-5800 Hz, the concentration range 0.6-2.1 × 10-3 g/ml, and the temperatures 25.0° and 37.8°C. The number-average and weight-average molecular weights of the aggregated sample were estimated as 1.4 and 2.0 × 108, respectively, from electron microscopy. The extrapolated intrinsic moduli [G′] and [G″] were compared with the predictions of the Kirkwood-Auer theory for rigid rodlike molecules. For the unaggregated sample, the frequency dependence of [G′] and [G″] agreed well with the theory assuming the intrinsic viscosity to be 27 ml/g, though the asymptotic limit of [G′]M/RT at higher frequencies was slightly larger than the theoretical value of 3/5. For the aggregated sample, the data agreed with theory for rigid rods as modified to account for molecular-weight distribution.
    Additional Material: 3 Ill.
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  • 2
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dynamic light scattering measurements were performed on dilute aqueous solutions of native ovalbumin (OA) and on those of linear OA aggregates induced by thermal denaturation at low ionic strength and neutral pH. The weight-average molecular weight Mw of four aggregates tested ranged from 1,700,000 to 5,500,000. The translational diffusion coefficient D0 of native OA at infinite dilution was estimated as 8.70 × 10 -7 cm2/s, which gave 56.0 Å as the diameter of the rigid spherical particle. The intensity autocorrelation function of linear OA polymers was analyzed with the cumulant method to obtain the first cumulant Λe. The dependence of Λe on the scattering vector q at very low polymer concentration was found intermediate between those of a flexible chain and a rigid rod. The translational diffusion coefficient Dtr [≡ (Te/q2)q → 0] was in proportion to Mw-0.55, and the magnitude was in good agreement with a value calculated from the wormlike cylinder model with values of three parameters determined in an earlier study, ML = 1600 Å-1, d = 120 Å, and Q = 230 Å, where ML, d, and Q are the molecular weight per unit length, diameter, and persistence length, respectively. Based on these results, a new model, to be called as the dimer model, was proposed to interpret the formation mechanism of linear OA polymers induced by thermal denaturation. © 1993 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 3
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The storage and loss shear moduli, G′ and G″, have been measured for dilute solutions of bovine fibrinogen in 68% aqueous glycerol and of intermediate fibrin polymer in 6M hexamethylene glycol, by the Birnboim-Schrag multiple-lumped resonator apparatus with titanium alloy resonators. The frequency range was 100-5800 Hz, the concentration range 1-6 g/l., and the temperatures 10.0 and 25.0°C. The shear moduli G′ and G″ at finite concentration, and the extrapolated instrinsic shear moduli [G′] and [G″], as functions of frequency, were compared with the predictions of various molecular theories. For fibrinogen, the frequency dependence agreed quite well with the calculations of Hassager for a trinodular rod as modified for the presence of small amounts of dimeric and trimeric aggregates which were deduced from parallel measurements of oscillatory flow birefringence. It was not possible, however, to distinguish between a linearly rigid configuration and one which is freely jointed at the central nodule. A model of a soft elastic sphere (simulating the cage model of Köppel) appeared to be very unlikely. The relaxation time for a rigid trinodular rod and the longest relaxation time for a jointed trinodular rod, calculated from molecular dimensions on the basis of electron microscope measurements, are somewhat smaller than the corresponding observed values; the discrepancy suggests that the molecule is swollen in solution. For the intermediate polymer (which was formed under conditions where ligation is expected), the frequency dependence agreed quite well with that predicted either for a prolate ellipsoid (Cerf-Scheraga-Saitō) or for a cylindrical rod (Yamakawa). The relaxation time obtained by fitting to theory agrees quite well with that calculated for a cylindrical rod with molecular dimensions based on a degree of polymerization of 20 and lateral binary association with staggered overlapping.
    Additional Material: 5 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 17 (1977), S. 527-534 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The diffusion, solution, and permeation behavior of a series of inert gases (helium, argon, nitrogen, krypton, and xenon) in S-B block copolymer films was studied by transient permeability measurements and by the equilibrium desorption method. The morphologies of most of the samples used in the measurements were (a) polystyrene rods dispersed in a polybutadiene matrix and (b) alternating lamellae of styrene and butadiene components. It was indicated, as far as the kinetic nature at lower temperatures is concerned, that the diffusion and permeation processes of gases, except for helium, are governed primarily by behavior in the polybutadiene matrix. At lower temperatures, it was shown that the transient method counts only the mobile penetrant in the polybutadiene matrix, while the equilibrium method counts less diffusive species in the polystyrene domains as well. The diffusion behavior in the copolymer films was compared with that in homopolybutadiene and discussed in terms of two impedance factors: the tortuosity and the chain immobilization factors. From the homopolymer-block copolymer comparison along with results obtained from diffusion experiments using n-hexane as the penetrant, it was indicated that segmental motions in the polybutadiene phase in the copolymers are restricted relative to motions in homopolybutadiene. Also, from data on gas sorption in samples of various styrene contents, involving both S-B block copolymers and binary mixtures with homopolystyrene, it was suggested that the partial mixing of component block chains occurs at the interface between the domains, resulting in rather diffuse domain boundaries.
    Additional Material: 6 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 21 (1983), S. 531-537 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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