English  |  正體中文  |  简体中文  |  Items with full text/Total items : 62796/95837 (66%)
Visitors : 3641379      Online Users : 370
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library & TKU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/44127


    Title: A kinetic study on the autocatalytic cure reaction of a cyanate ester resin
    Authors: Chen, Ching-chung;董崇民;Don, Trong-ming;Lin, Tai-hung;Cheng, Liao-ping
    Contributors: 淡江大學化學工程與材料工程學系
    Date: 2004-06
    Issue Date: 2010-03-09 09:54:42 (UTC+8)
    Publisher: Wiley-Blackwell
    Abstract: The cure of a novolac-type cyanate ester monomer, which reacts to form a polycyanurate network, was investigated by using differential scanning calorimeter. The conversions and the rates of cure were determined from the exothermic curves at several isothermal temperatures (513–553 K). The experimental data, showing an autocatalytic behavior, conforms to the kinetic model proposed by Kamal, which includes two reaction orders, m and n, and two rate constants, k1 and k2. These kinetic parameters for each curing temperature were obtained by using Kenny's graphic-analytical technique. The overall reaction order was about 1.99 (m = 0.99, n = 1.0) and the activation energies for the rate constants, k1 and k2, were 80.9 and 82.3 kJ/mol, respectively. The results show that the autocatalytic model predicted the curing kinetics very well at high curing temperatures. However, at low curing temperatures, deviation from experimental data was observed after gelation occurred. The kinetic model was, therefore, modified to predict the cure kinetics over the whole range of conversion. After modification, the overall reaction order slightly decreased to be 1.94 (m = 0.95, n = 0.99), and the activation energies for the rate constants, k1 and k2, were found to be 86.4 and 80.2 kJ/mol.
    Relation: Journal of applied polymer science 92(5), pp.3067-3079
    DOI: 10.1002/app.20314
    Appears in Collections:[化學工程與材料工程學系暨研究所] 期刊論文

    Files in This Item:

    File Description SizeFormat
    0KbUnknown545View/Open
    index.html0KbHTML241View/Open

    All items in 機構典藏 are protected by copyright, with all rights reserved.


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library & TKU Library IR teams. Copyright ©   - Feedback