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  • 1
    ISSN: 1573-904X
    Keywords: captopril ; organic volatile impurities ; gas chromatography ; Fourier transform infrared
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 747-752 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Growth rates of G of low-melting spherulites in fractions of trans-1,4-polyisoprene have been measured. The data were analyzed by use of an equation, ln G = ln G0 - ΔF*/RTc, valid at temperatures close to the equilibrium melting point. Plots of ln G against a function of the critical free energy of nucleation ΔF* result in a family of straight lines having a common intercept, ln G0, which is independent of molecular weight. The slope of these lines is a measure of the interfacial free energy of the crystallites and increases with the molecular weight, reflecting increasing irregularity in the structure of the semicrystalline mass. Comparison of growth rates of low-melting and high-melting trans-1,4-polyisoprene indicates that G0 does not, to a first approximation, depend on the nature of the crystals growing from the melt. The temperature at which spherulites of the two crystalline forms grow at equal rates has been calculated.
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 7 (1969), S. 1639-1649 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The melting transitions of both crystalline forms of trans-1,4-polyisoprene, as detected by differential thermal analysis, have been identified by attendant studies with optical microscopy and x-ray diffraction. The lower-melting (LM) form melts initially at a temperature which depends upon the crystallization temperature but which, under our experimental conditions, is between 45 and 53°C. If recrystallization is allowed to occur, the apparent final melting point, which depends upon the recrystallization temperature, is about 58°C. The initial melting point of the higher-melting (HM) form, also crystallization temperature-dependent, is upwards of 57°C. Under the most easily accessible experimental conditions, it may be obscured by the final melting of the LM-form. The apparent final melting point of the HM form is approximately 66°C. Conversion of the LM form into the HM form occurs only by fusion and crystallization. No evidence of a solid-solid transition was found. The rate of conversion is governed principally by the rate of nucleation at the conversion temperature. If fusion of the LM form is incomplete, recrystallization of the LM form takes place instead of conversion to the HM form.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1697-1701 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Middle range fractions of mimusops balata, a natural trans-1,4-polyisoprene, exhibit transcrystallinity when crystallized in the 35-40°C range. The presence of transcrystallinity was established by x-ray diffraction and optical microscopy. Diffraction peak intensities change due to transcrystallinity, suggesting x-rays be used to detect transcrystallinity and that caution be exercised in using x-ray diffraction techniques to determine the phases present in bulk material and in calculating the degree of crystallinity. The tendency toward transcrystallinity may depend upon molecular weight.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 175-179 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Equilibrium melting points in trans-1,4-polyisoprene were calculated from plots of crystallization temperature versus the experimentally measured melting points. The melting points were found to be 78 ± 1.7°C for the low-melting crystalline form and 87 ± 1.3°C for the high-melting form. Within the experimental error, melting points were independent of molecular weight above a number-average weight of 33,000.
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 2197-2201 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 1831-1835 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Average polymer segment densities and thermodynamic properties of polymer adsorbed at liquid-solid interfaces were computed by extension of the polymer adsorption theory of Forsman and Hughes. Expressions were derived for the total free energy of adsorbed polymer chains by using the Flory-Huggins theory to represent free energy of mixing. A square-well potential was used to represent segment-surface interaction, and configurational entropy was calculated from the probability density function for the radius of gyration of random-flight chains. For each specified amount of surface coverage the free energy of the adsorbed polymer was minimized by varying the density of segments normal to the adsorbing surface and using a modified gradient search algorithm on a digital computer. Two different segment densities were considered, and they both gave qualitatively the same results. The two densities were (1) the sum of two Gaussian distributions and (2) a two-step density distribution. Isotherms were then calculated by equating the partial molal free energy of polymer at the surface to that of polymer in bulk solution for each specified amount of surface coverage. The results showed that for the initial region of the isotherms the distribution of polymer segments normal to the surface consisted of a high-density layer adjacent to the surface and a low-density “tail” extending far out into the solution. At higher amounts of adsorbed polymer, i.e., in the general concentration range of the pseudo-plateau, the tail of the polymer density distribution was predicted to thicken, and a single Gaussian distribution best described the segment density. Predicted adsorptions were in good agreement with reported experimental values.
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 6 (1968), S. 2221-2235 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of isoprene polymerization catalyzed by VCl3 and Et3Al were studied by measuring fractional conversions, polymer composition, and molecular weight distributions at a series of reaction times and temperatures. The rate of polymerization plotted against temperature shows an inflection point with a minimum and maximum in the 60-90°C range. The isomeric composition of the polymer changes with temperature but not with reaction time, while the molecular weight distribution undergoes substantial change with both of these variables. The rate of polymerization at sites producing low molecular weight polymers was measured, and the activation energy calculated to be about 10 kcal/mole. The active sites were found to deactivate at different rates. The results support the hypothesis that several species of active sites are present in the system and that these exhibit characteristic polymerization behavior.
    Additional Material: 14 Ill.
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