高等学校化学学报 ›› 2003, Vol. 24 ›› Issue (6): 977.

• 研究快报 • 上一篇    下一篇

大晶粒钛硅沸石TS-1晶貌的离子蚀刻改性

郭洪臣1, 刘娜1, 周军成1, 郭明星1, 王祥生1, 陈黎行1, 邹龙江2   

  1. 1. 大连理工大学化工学院催化化学与工程系, 大连 116012;
    2. 大连理工大学材料测试与分析中心, 大连 116023
  • 收稿日期:2003-01-08 出版日期:2003-06-24 发布日期:2003-06-24
  • 通讯作者: 郭洪臣(1964年出生),男,博士,副教授,主要从事沸石分子筛多相催化研究.
  • 基金资助:

    国家自然科学基金重点项目(批准号:20233050)资助

Morphological Modification of Large Crystal TS-1 by Ion Etching

GUO Hong-Chen1, LIU Na1, ZHOU Jun-Cheng1, GUO Ming-Xing1, WANG Xiang-Sheng1, CHEN Li-Xing1, ZOU Long-jiang2   

  1. 1. Department of Catalytic Chemistry and Engineering, Dalian University of Technology, Dalian 116012, China;
    2. Center of Measurement and Analysis of Materials, Dalian University of Technology, Dalian 116012, China
  • Received:2003-01-08 Online:2003-06-24 Published:2003-06-24

关键词: 离子蚀刻, 晶貌, TS-1, 结晶度, 活性位

Abstract: A post-synthesis modification method, named ion etching, is proposed to adjust the morphology of titanium silicalite TS-1 for a better catalytic activity. The new method mainlYINvolves treating titanium silicalite TS-1 with an ammonia-containing aqueous solution in autoclave under the conditions of ca. ammonia aqueous solution concentration 0.5-14 mol/L NH3, volume ratio of liquid/solid 20-100, hydrothermal temperature 100-180 ℃ and contact time 24-500 h. According to the characterizations by SEM, XRF, XRD, FTIR and UV-Vis, the modification can transform a well-defined large crystal TS-1[1 μm×2 μm×6 μm, n(Si)/n(Ti)=53.62] into fine grains which can avoid falling off from the matrix if the conditions of the treatment are properly controlled. The effect of ion etching upon TS-1 morphology is attributed to the OH -ion(derives from NH3·H2O) catalyzed hydrolysis of the T-O-T bridge bond of the silicic zeolitic framework. Its main advantages over mechanical ball-millingthe conventional zeolitic morphology modification method, include actually fully retained crystallinity and almost intact coordination state of the active Ti sites of the remained framework, as confirmed by XRD, FTIR and UV-Vis. Probe reaction shows that, the large crystal TS-1 modified by the present method at 170 ℃ for 129 h, when used as the catalyst for epoxidation of propylene, could be operated at propylene weight hourly space velocity of 0.5h-1, and 97.85% hydrogen peroxide conversion and 96.87% propylene oxide selectivity were obtained. However, to reach comparative hydrogen peroxide conversion, the intact zeolite could only be operated under propylene weight hourly space velocity of 0.2h-1. The remarkable increase of the catalytic activity of the modified TS-1 may be attributed to the improved intra-crystal diffusivity and the excellent preservation of the crystallinity and active Ti sites by the present modification.

Key words: Ion etching, Morphology, TS-1, Crystallinity, Active site

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