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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 24 (1979), S. 1169-1178 
    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: New polyol containing aromatic rings was prepared from BHET, or BHET/ethylene glycol mixtures and adipic acid. In this new system, the kinetics of polyesterification were investigated and were shown to follow the kinetic equations proposed by Lin and his co-workers which were obtained by modifying Flory's theory. Polyurethane elastomers were prepared by reacting these polyols and toluene diisocyanate (TDI) in DMF solution with NaCN as a crosslinking catalyst at room temperature. Their physical properties such as density, gel fraction, swelling ratio, mechanical properties, etc., were measured. High values of elastic modulus are due to the rigid segment of BHET. By varying the molar ratio of diisocyanate and polyester, polyurethanes with different crosslinking densities can be obtained. The relationship between physical properties and crosslinking density was shown to follow the general theory of rubber elasticity.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 25 (1980), S. 565-574 
    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: A new mathematical model with a correction for radical capturing efficiency in a continuous emulsion polymerization with recycle flow has been proposed. These performance equations predict the conversion as well as molecular weight distribution of the polymer product during the continuous-flow operation. Experimental results obtained with vigorous mixing associated with a premixer are in best agreement with the theoretical prediction. In certain situations, the recycling provides a means for obtaining a higher degree of back-mixing with a normal flow reactor. However, it is difficult to obtain a high conversion of monomer by a continuous emulsion polymerization operation even with a long residence time. Theoretical and experimental average degrees of polymerization of polymer leaving the reactor are progressively displaced toward smaller values with greater mean residence time. According to the calculations based on our kinetic model the ratio M̄w/M̄n in the continuous emulsion polymerization remains constant regardless of mean residence time.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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