English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 78937/78937 (100%)
造訪人次 : 39422257      線上人數 : 430
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/987654321/26719


    題名: THE INFLUENCE OF THE CATALYST PREPARATION ON THE CATALYTIC PROPERTIES OF ZEOLITE-SUPPORTED CATALYSTS
    作者: CHEN,YW;WANG,WJ
    貢獻者: 化學工程與材料工程學系
    關鍵詞: CARBON-MONOXIDE HYDROGENATION;COBALT
    日期: 1993
    上傳時間: 2010-06-29 17:35:06 (UTC+8)
    出版者: 中央大學
    摘要: Two preparation techniques (incipient-wetness impregnation and ion exchange) have been used to prepare NaX and NaY zeolite-supported cobalt catalysts. These catalysts were characterized by X-ray diffraction, temperature-programmed reduction, and temperature-programmed desorption of hydrogen. The Fischer-Tropsch synthesis was examined at temperatures in the range of 220-300-degrees-C, a pressure of 1 atm, a CO/H-2 ratio of 1, and flow rate of GHSV=1200. The mobility of cobalt ions inside the zeolite cages in the ion-exchanged samples caused the difficulty in reduction and less active sites for the access of CO to the metals which are entraped in the sodalite cage. The ion-exchaned catalyst thus disclosed a low catalytic activity. The absence of hydroxyl group in the impregnated catalysts results in the stabilization of the metallic form of cobalt on the external surface of zeolite which cause catalytic activity in the FT reaction. The Co/X catalysts always exhibited higher activities than the Co/Y catalysts, no matter what preparation method was followed.
    關聯: STUDIES IN SURFACE SCIENCE AND CATALYSIS
    顯示於類別:[化學工程與材料工程研究所] 期刊論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    index.html0KbHTML514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