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  • 1
    Publication Date: 1996-04-01
    Print ISSN: 0170-0839
    Electronic ISSN: 1436-2449
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Published by Springer
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Polymer bulletin 36 (1996), S. 455-462 
    ISSN: 1436-2449
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Summary Block copolymers containing polyester and polyamide blocks have been prepared by the bulk reaction of the corresponding carboxy-terminated polymers with 2,2′-bis(2-oxazoline) or 2,2′-bis(5,6-dihydro-(4H)-1,3-oxazine) as chain-coupling reagents (CC). A two-step reaction has been used, involving (i) the reaction of polyamide with CC excess, and (ii) the addition of polyester, leading to a random distribution of blocks in the final block-copolymer. 1H and 13C NMR studies show that the coupling reaction takes place in the expected way. The stability of the resulting polymers is higher than that of the starting oligomers, and DSC indicates a phase separation between polyester and polyamide phases.
    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. 691-699 
    ISSN: 0887-624X
    Keywords: chain coupling reactions ; bisoxazoline ; bisoxazine ; carboxy end groups ; polyester ; polyamide ; bulk reaction ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2,2′-Bis(2-oxazoline) and 2,2′-bis[5,6-dihydro-(4H)-1,3-oxazine] have been used as chain coupling reagents (CC) and reacted in the bulk with α,ω-dicarboxy-poly(2,2′-oxydiethylene adipate) (PS) or with α,ω-dicarboxy-polyamide 12 (PA). The reactions have been followed by viscosimetry, titration of COOH groups and 1H- and 13C-NMR spectroscopy. Either with the PS/CC or PA/CC systems, or with the model system dodecanoic acid (DA)/CC, the reactions were fast, since in most cases 80% conversion was reached after 15 min reaction. The expected DA dimer or high molar mass PA or PS polymers were obtained. No significant side reaction has been detected. The thermal stability of the resulting polymers is higher than that of starting oligomers. Due to the introduction of CC units in the chains, the crystallinity of PA/CC is slower than that of starting PA. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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