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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 192 (1991), S. 1811-1820 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The preparation of various polyamides, polyureas and polyurethanes by polymerization reactions with diphenylphosphoryl azide (DPPA) was investigated. Various polyamides were obtained very conveniently by polymerization of aminocarboxylic acids or copolymerization of dicarboxylic acids and diamines. Polyureas were mainly obtained by conversion of dicarboxylic acids to acyl azides with DPPA and then to isocyanates, followed by copolymerization of these diisocyanates with diamines. Further, the polymerization of some aminocarboxylic acids that have an amino group of low nucleophilicity (such as p-aminobenzoic acid) was found to give polyureas instead of polyamides by direct polymerization. Polyurethanes were also obtained from dicarboxylic acids and diols through the Curtius rearrangement of acyl azides, similarly as in the polyurea preparations. The products were identified with the help of IR spectra and elemental analyses, and their molecular weights were evaluated viscometrically.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 2 (1991), S. 41-47 
    ISSN: 1042-7147
    Keywords: Polyurethane ; Solvolysis lignin ; Tensile properties ; Diphenylmethane diisocyanate ; Crosslinking ; 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
    Notes: In order to study the tensile properties of solvolysis lignin polyurethanes, polyurethane (PU) films were prepared from the solvolysis lignin (SL)-polyethylene glycol (PEG)-diphenylmethane diisocyanate (MDI) system, and in addition to this further PU films were also prepared from the SL-MDI system. In the SL-PEG-MDI system, the SL content, the molecular weight of PEG and the NCO:OH ratio were varied in order to control the physical properties. The tensile stress and Young's modulus of the PUs of the SL-PEG-MDI type increased with increasing SL content and NCO:OH ratio. The tensile properties of the PUs from the SL-MDI system showed no NCO:OH ratio dependency; i.e. the mechanical properties of PUs are not influenced by the change in crosslinking. It is possible to control the tensile properties of PUs of the SL-PEG-MDI type by changing the content of PEG and SL at a constant NCO:OH ratio.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 137-149 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The complex compliance in extension of gels of poly(vinyl chloride) (PVC) in di(2-ethylhexyl) phthalate (DOP) and in tricresyl phosphate (TCP) was measured over the frequency range from 0.6 to 0.006 cps and the temperature range from -66 to 65°C: the weight fractions of DOP and TCP in the gels were 0.32, 0.40, 0.49, and 0.59. Measurements were carried out in an apparatus using forced low-frequency longitudinal osillations. Data for the gels could not be combined by the method of reduced variables, since there were gradual changes with decreasing temperature, attributable to an increase in crystallinity. Application of the reduction method of Ninomiya and Ferry for solutions of crystalline polymers was found to be successful. The apparent melting temperatures (T′m) were obtained from the temperature dependence of the vertical shift factors. An apparent heat of fusion of ca. 120 cal/mole of monomer unit was found. This melting range was in agreement with that of secondary crystallinity in plasticized PVC reported in calorimetric studies by Juijn. With decreasing temperature, two phenomena occurred in the temperature range from Tg + ca. 80°C to Tg: the vitrification of a concentrated amorphous solution and the slight crystallization of the polymeric component. The larger the difference between Tg and T′m the broader the primary dispersion zone on the frequency scale. This broadening effect was explained as due to the difference in dependence of Tg and T′m on plasticizer concentration, without any need to consider any specific interaction between plasticizer and PVC.
    Additional Material: 12 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 2299-2311 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Homogeneous and heterogeneous poly(2-hydroxyethyl methacrylate) hydrogels were prepared by copolymerization of 2-hydroxyethyl methacrylate and small amounts of ethylene glycol dimethacrylate in the presence of water; concentrations of water (V1) in the polymerization mixture and the volume fractions of water (v1) of the gels swollen to equilibrium were 40, 50, 60, 70% by volume, and 0.475, 0.541, 0.669, 0.778, respectively. From the homogeneous (clear) hydrogel (V1 = 40%) preparation, four hydrogels were prepared with v1 = 0.434, 0.418, 0.378, 0.326. Tensile dynamic moduli were measured in the frequency range from 0.006 to 0.6 cps and the temperature range from 0 to 40°C. In these cases, the influence of swelling on the shape of the relaxation spectra and on the monomeric unit friction coefficient was studied. The dependence of the friction coefficient on water concentration was interpreted in terms of free volume. In the heterogeneous (opaque) gel preparations (V1 = 50, 60, 70%), the effect of the aqueous phase in the system on the mechanical behavior was described by a modification of the blending law of Ninomiya. For the systems with V1 = 60% and 70% the shapes of the storage and loss moduli in the main transition region and the friction coefficient were similar to those of the homogeneous gel with V1 = 40%, except for the decrease in absolute value of the storage moduli. For the system with V1 = 50% the shape of the relaxation spectrum changes appreciably and the wedge distribution does not hold.
    Additional Material: 12 Ill.
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