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  • 1995-1999  (4)
  • 1975-1979  (2)
  • Chemistry  (6)
  • Chemical Engineering  (1)
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  • 1
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: This question was addressed using various methods to monitor the process of curing and state of the final network. Attention was particularly focused on the possible inhomogeneous network formation as a consequence of the crosslinking process. An analysis of experimental data has revealed that some cured resins can be considered as homogeneous as the corresponding uncrosslinked materials. Resins cured by simple stepwise alternating chemistries, with good compatibility of components, usually fulfill the criterion of homogeneity. A family of epoxy resins cured with polyamines belongs to this category. Nodular structures seen by electron microscopy are a result of interaction of the electron beam or etching. Such structures are also observed for uncrosslinked polymers investigated under the same conditions. Formation of inhomogeneities in a number of thermoset systems is due to (a) chainwise mechanism of network formation with fast propagation inducing cyclization and steric volume exclusion and (b) poor compatibility of components of the system made stronger by increasing molecular weights and crosslinking during curing. Networks formed by freeradical polymerization and copolymerization of polyvinyl monomers can serve as an example of crosslinking-driven formation of inhomogeneities.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 2 (1979), S. 35-49 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Theoretical treatments of network formation and the applicability of the tree-like models to the calculation of structural parameters in the post-gel state and to more complex systems of practical importance are discussed. The unseparability of structural interpretation of network properties from network formation is stressed.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 461-472 
    ISSN: 0887-624X
    Keywords: reaction mechanism ; curing of epoxides ; theory of structure development ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A complex mechanism of the reaction of diglycidylamine (DGA)-based epoxides with primary amines is described and the kinetic model is developed. The reaction mechanism involves the addition of amine, etherification, and also formation of small cycles and anionic homopolymerization of the epoxide compound including transfer and termination. The polymer structure was theoretically described by distribution of structural fragments determined using the kinetic model. Simulation of the structure evolution during the DGA-aniline reaction at varying molar ratios of reagents and dilution of the system was performed. The effect of the reaction conditions on the distribution of structural fragments, such as branching units and cyclic structures, was determined. © 1995 John Wiley & Sons, Inc.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 33 (1995), S. 473-480 
    ISSN: 0887-624X
    Keywords: epoxides ; reaction mechanism ; cyclization ; structure development ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of diepoxides, diglycidylaniline (DGA), or diglycidyl ether of Bisphenol A (DGEBA) with aniline was followed using HPLC and SEC. The effect of molar ratio of reagents, dilution of the system, reaction temperature, and the difference between the reaction mechanisms for DGA and DGEBA systems on the reaction kinetics and molecular weight evolution is discussed. Molecular weights of the DGA-aniline polymers were by an order of magnitude lower than those of the DGEBA-aniline polymers due to the formation of small cyclic products in the former case. Also, a reduction in Mn with increasing temperature, dilution, and diluent polarity is brought about by a greater tendency toward cyclization under these conditions. Theoretically calculated molecular weight evolution during the reaction is in satisfactory agreement with the experiment. © 1995 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Chemistry and Physics 197 (1996), S. 1577-1586 
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The polymerization of a bismaleimide-styrene system was studied by using a model compound, p-maleimidobenzoic anhydride, that can be split by simple hydrolysis. Compared to known divinyl systems, a decreased reactivity of the pendant double bonds is observed, probably as a result of cyclization and the steric excluded volume effect. The use of a solvent causes an additional shift of the gel point towards higher conversion. Hydrolysis of gelled material affords soluble p-maleimidobenzoic acid-alt-styrene copolymers. Compared to a linear system, methyl p-maleimidobenzoate and styrene, the primary chains obtained by hydrolysis show an increased polydispersity, probably due to retardation of bimolecular termination of the free radicals that are attached to the polymer network (gel effect).
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 19 (1979), S. 246-253 
    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: Problems of the characterization of network structure by investigating the network formation and its response to mechanical stress have been analyzed. Attention has been devoted to the effect of reactivity of functional groups and cyclization on the formation of network structure and to problems of obtaining the equilibrium modulus and its relation to the concentration of elastically active network chains (EANCs). It has been demonstrated that a theoretical description of network formation must be based on reliable information on the rules of joining of functional groups and on their relative reactivity; the tree-like approximation offers a number of structural parameters of the sol and gel including, e.g, chemical clustering of units of a certain type. The main obstacles to reaching the equilibrium modulus are long relaxation, times of lightly crosslinked networks and the occurrence of secondary relaxations. In correlating the equilibrium modulus and the concentration of EANCs, it is necessary to find conditions under which the Mooney-Rivlin constant C2 can be neglected and to carry out the required corrections of the modulus, if experimental conditions differ from those of network formation.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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