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  • Polymer and Materials Science  (3)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 42 (1991), S. 2933-2941 
    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 preparation and properties of some new saturated and unsaturated esters of 2-cyano-2,4-pentadienoic acid (CPDA) are described. A comparison is also made with the known CPDA monomers synthesized under identical conditions. It was found that the monomer yields are dependent on the structure of the corresponding CPDA esters. This fact was explained with solvatation effects, occurring during the isolation procedures. The base-catalyzed anionic bulk polymerization of CPDA esters was studied by means of spectral methods. The data indicated that during the homopolymerization 1,4-addition of monomer molecules takes place to give a steric copolymer consisting of 1,4-cis and 1,4-trans structural units. The ability of poly-CPDA esters was also followed to form crosslinks at room and higher temperatures.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 44 (1992), S. 1829-1835 
    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 aim of the present study is to clarify some problems concerning the synthesis of additional quantities of ethyl-2-cyanoacrylate monomer (ECA) utilizing the waste residue (WR) from the large-scale depolymerization of ECA oligomers. The composition of WR was established by GPC and IR spectroscopy. WR was found to consist mostly of diethyl dicyanoglutarate (DEDCG) and low molecular weight products of its condensation with paraformaldehyde (pFA). The DEDCG&-pFA interaction was studied as a model, and the influence of DEDCG conversion on the average degree of polymerization (xn and xw) of the oligomers formed was also followed. On this basis, it was found that oligomer formation in condensation of WR with pFA is consistent with a stepgrowth mechanism, the polymer chain length being determined by steric hindrance and destructive reactions.
    Additional Material: 7 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 47 (1993), S. 1019-1026 
    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: Cured adhesive layers produced from ethyl-(ECA), allyl-(ACA), and allyloxyethyl-(AOECA) 2-cyanoacrylates were studied by means of thermogravimetry and differential scanning calorimetry. Polymer films of ECA-based adhesive compositions comprising various amounts and types of 2-cyano-2,4-pentadienoic acid (CPDA) esters were also examined. The influence of the modifier type, as well as the chemical structure of the cyanoacrylates used, was followed upon the glass transition temperatures (Tg) and the rates of thermal degradation of the corresponding polymers. In the case of cured adhesive mixtures containing unsaturated CPDA esters and when poly(ACA) and poly(AOECA) were studied, a significant increase of their heat resistance was established, as compared with poly(ECA). This fact was explained with the formation of three-dimensional structure of the polymer film due to crosslinking reactions. A different course and character of these reactions were found comparing the thermal behavior of poly(ACA) and cured compositions containing unsaturated CPDA esters. A good agreement was found between data from the thermal analyses and the tensile shear and impact strength tests. It was shown that the modification of ECA with unsaturated CPDA esters is a possible way of increasing the heat resistance of the basic adhesive. © 1993 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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