淡江大學機構典藏:Item 987654321/19518
English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 62805/95882 (66%)
造訪人次 : 3928861      線上人數 : 777
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library & TKU 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: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/19518


    題名: Convenient post-curing reactions for aqueous-based polyurethane anionomers
    作者: Chen, Guan-nan;Liu, Po-hong;Chen, Maw-shuh;Chen, Kan-nan
    貢獻者: 淡江大學化學學系
    關鍵詞: Aqueous-based PU anionomers;Aziridinyl;Epoxide;Ambient temperature curing
    日期: 1997-07-01
    上傳時間: 2009-11-04 16:52:26 (UTC+8)
    出版者: Springer
    摘要: Anionic aqueous-based polyurethane (PU) dispersions were prepared by introducing carboxylic groups into a conventional PU backbone, followed by a water dispersion process. The resulting carboxylic groups containing aqueous-based PUs were amino-terminated anionomers. Two model reactions between an amino and a carboxylic group containing compounds with an epoxide and an aziridinyl compound, respectively were carried out at ambient temperature. Di-functional epoxide and aziridinyl compound were employed as the convenient single post-curing and dual-curing agents for these prepared PU dispersions. Di-aziridinyl compound was stable in aqueous PU dispersions as a latent curing agent when the pH value of the system was 8.0 or above. The curing behaviors of each PU curing system were monitored by measurements of the gel content, average particle size, zeta potential, and fluorescence spectra. The mechanical and thermal properties of these post-cured PUs were evaluated.
    關聯: Journal of Polymer Research 4(3), pp.165-175
    DOI: 10.1007/s10965-006-0022-2
    顯示於類別:[化學工程與材料工程學系暨研究所] 期刊論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    1022-9760_4(3)p165-175.pdf692KbAdobe PDF309檢視/開啟

    在機構典藏中所有的資料項目都受到原著作權保護.

    TAIR相關文章

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