English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 80990/80990 (100%)
造訪人次 : 41638406      線上人數 : 1728
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋


    請使用永久網址來引用或連結此文件: http://ir.lib.ncu.edu.tw/handle/987654321/28303


    題名: Highly Thermally Stable Novolac Derivatives and Their Properties in Epoxy Composites
    作者: Wu,HH;Chu,PP
    貢獻者: 中央大學
    關鍵詞: FLAME-RETARDANT THERMOSETS;PHENOLIC RESINS;CURING AGENT;PHOSPHORUS;MECHANISMS;POLYMERS
    日期: 2009
    上傳時間: 2010-06-29 19:45:47 (UTC+8)
    出版者: 化學研究所
    摘要: Two diazo-coupling novolac derivative resins (carbonyl phenyl azo novolac resin and carbonyl phenol-biphenylene azo novolac resin) were used as flame retardants. The cured resins exhibited elevated glass-transition temperatures from 115 degrees C (blank) to 195 and 167 degrees C, respectively. The char yield at 800 degrees C was increased, which elaborated the effectiveness of flame retardancy with evaluated limiting oxygen indices around 36 to 40. This was mainly attributed to the increased crosslink densities and highly aromatic contents in the modified phenol novolac derivative resins, which exhibited higher thermal degradation energies. Furthermore, the more effective flame retardancy was expected because of the loss of nitrogen during combustion. Through the evaluation of the cooperative flame retardancy in the organic/inorganic hybrid with char yield and increasing limiting oxygen index percentage, the effects of the filler showed cooperative flame retardancy only with the appropriate addition and with a difference in the crosslinking densities. (C) 2009 Wiley Periodicals, Inc. J Appl Polyni Sci 113: 3782-3790, 2009
    關聯: JOURNAL OF APPLIED POLYMER SCIENCE
    顯示於類別:[化學研究所] 期刊論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    index.html0KbHTML488檢視/開啟


    在NCUIR中所有的資料項目都受到原著作權保護.

    社群 sharing

    ::: Copyright National Central University. | 國立中央大學圖書館版權所有 | 收藏本站 | 設為首頁 | 最佳瀏覽畫面: 1024*768 | 建站日期:8-24-2009 :::
    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 隱私權政策聲明