淡江大學機構典藏:Item 987654321/92460
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    Please use this identifier to cite or link to this item: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/92460


    Title: Green PU resin from an accelerated Non-isocyanate process with microwave radiation
    Authors: Hwang, Jing-Zhong;Chen, Chieh-Ling, Huang, Chi-Yuan;Yeh, Jen-Taut, Chen, Kan-Nan
    Contributors: 淡江大學化學學系;淡江大學化學工程與材料工程學系
    Keywords: PU;Cyclic carbonate;Diamine;Non-isocyanate;Microwave radiation
    Date: 2013-06
    Issue Date: 2013-10-14 22:09:16 (UTC+8)
    Publisher: Dordrecht: Springer Netherlands
    Abstract: The ring opening between BCC with di-amine by conventional heating (130 °C for 48 h) is a time-consuming and non-efficient process. This work has been aiming at accelerating its ring-opening reaction by a microwave radiation process. Besides, catalyst and solvent selections of this PU reaction system, the microwave power output, radiation time, catalyst and reaction media were major consideration of this research. A catalyst, TBAC or LiBr had been applied on each microwave-assisted ring-opening polymerization of BCC with Jeffamine D-2000. A similar average molecular weight of NH2-PU oligomer was obtained from a 50 min microwave radiation by using 50 W power output. The radiation system with TBAC as catalyst, and it resulted in a formation of NH2-PU oligomer with Mn and Mw were 12,997 and 15,580, and that of 10,882 and 13,508 with LiBr as catalyst. The solvent polarity, catalyst solubility and microwave output energy in this radiation system were considered as important factors for this new green process.
    Relation: Journal of Polymer Research 20(7), 195(10pages)
    DOI: 10.1007/s10965-013-0195-4
    Appears in Collections:[Graduate Institute & Department of Chemistry] Journal Article
    [Graduate Institute & Department of Chemical and Materials Engineering] Journal Article

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