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  • 1975-1979  (6)
  • 1978  (6)
  • Polymer and Materials Science  (6)
  • 1
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A thermal perturbation curve (TPC) is defined to be the derivative of the fractional degree of saturation, f, with respect to temperature, considered as a function of the natural logarithm of free ligand concentration, y. The theoretical framework for the use of such curves in the thermodynamic analysis of ligand binding to macromolecules is presented. The thermal perturbation curve either provides or complements the information obtained from the derivative binding isotherm ∂f/∂y. For a single set of identical and independent sites the TPC is identical to the derivative binding isotherm. Analysis of such a curve directly yield ΔH0 and ΔG0 for the binding reaction. In actual experimental work, however, the TPC can only be approximated because of “self-buffering” effects relations between the parameter of the approximate curve and the thermodynamic quantities have been developed. This technique is applied to the proflavin-α-chymotryspin system to demonstrate its usefulness. The general features of thermal perturbation curves for cases of multiple sets of independent sites and cooperatively interacting sites have also been developed. The analysis of thermal perturbation curves in combination with other methods should provide a more powerful approach to the characterization of ligand-macromolecule interactions.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 17 (1978), S. 2601-2608 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermodynamics of the partition of chondroitin sulfate-hexadecylpyridinium complexes wee studied in order to gain further insight into the mechanisms responsible for the sensitivity of the relative solubility of these complexes in aqueous slat and butanol phases to small changes in slat concentration. The dependence of the partition coefficient was measured as a function of temperature at three different salt concentrations. Increasing the temperature was found to favor the form of the complex which was soluble n the aqueous phase. Although the transition could be induced by temperature changes, he transition occurred over a 20°C range in temperature. The transition from the aqueous phase to the butanol phase was strongly exothermic, with ΔH = -22.3 kcal/mol polymer. The value of ΔS was found to be dependent on the salt concentration, ranging from -72.7 e.u./mol polymer in 0.05125M NaCl to -77.1 e.u./mol polymer in 0.05375M MaCl. When placed on a disaccharide basis, the corresponding values are ΔH = -402 cal/mol and ΔS = -1.31 to -1.3 e.u./mol. The sharpness of he transition was found to be due t the similarity in magnitude of ΔH and TΔS, and on the dependence of the later upon the salt concentration.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 2387-2389 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 2533-2542 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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 conditions under which cellulose-cellulose triacetate (CTA) and cellulose-poly(acrylonitrile) (PAN) blends can be prepared from solution, are described in this paper. These two systems form transparent films when the blend contains less than 50% PAN or 60% CTA. Young's modulus, tensile strength, and elongation at rupture were measured for these blends. These values usually are between those of the corresponding homopolymers, except for the blend containing 10% polymer (PAN or CTA) which has a tensile strength value larger than that of cellulose. This result seems to indicate a certain level of compatibility for this blend. However, x-ray measurements indicate the presence of two crystal structures for these systems, suggesting that compatibility does not exist at the molecular level, in the crystalline fraction of the samples.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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: ABA-type “tapered” block copolymers of α-methylstyrene (monomer A) and butadiene were prepared using four commercially available dilithio initiators. Polymerizations were run at 25°C in benzene solvent, or at 40°C with butadiene dissolved in neat α-methylstyrene. Although α-methylstyrene has a rather low ceiling temperature, triblock copolymers could be made at these temperatures by using α-methylstyrene concentrations well in excess of the [M]e values at the respective temperatures. Its concentration was such that molecular weights of at least 15,000-20,000 for the A blocks could be attained. The course of the copolymerization at 40°C was followed, showing that copolymers containing about 40% α-methylstyrene could be formed in 4-8 hr, depending on the initiator used. They showed the usual behavior of triblock thermoplastic elastomers, with tensile strengths 〉 3000 lb/in.2 at 24°C. However, because of the high Tg of poly(α-methylstyrene) (172°C), they also had tensiles of several hundred lb/in.2 at 100°C, unlike comparable polymers with polystyrene end blocks, which have practically no strength at this temperature. Microstructures of polybutadienes made with these initiators are also given.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Biomedical Materials Research 12 (1978), S. 361-366 
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The production and decay of forces produced by Alastik modules was studied under conditions simulating clinical usage over a time period of 2 hr to 4 weeks. Force decay was moderate and all Kx modules tested produced approximately 1 lb of force at the end of the 4-week test period. Therefore, from a clinical standpoint, modules need not be changed more frequently than once every 4 weeks.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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