杨建华

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:女

毕业院校:日本广岛大学

学位:博士

所在单位:化工学院

学科:化学工艺. 功能材料化学与化工. 膜科学与技术

办公地点:西部新校区化工楼C223

联系方式:电话:041184986147

电子邮箱:yjianhua@dlut.edu.cn

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Synthesis of silicalite-1 membrane with two silicon source by secondary growth method and its pervaporation performance

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论文类型:期刊论文

发表时间:2011-01-14

发表刊物:SEPARATION AND PURIFICATION TECHNOLOGY

收录刊物:SCIE、EI

卷号:76

期号:3

页面范围:308-315

ISSN号:1383-5866

关键字:Silicalite-1 membrane; Two silicon source; Secondary growth; Pervaporation

摘要:Silicalite-1 membranes supported on macroporous alumina (alpha-Al(2)O(3)) tubes for pervaporation were successfully prepared by introducing ethyl triethoxysilane (ETES) during the preparation of synthesis solutions. The effects of synthesis parameters (i.e., FETES] content, crystallization time, and crystallization temperature) on the membranes thickness and pervaporation performance were investigated for silicalite-1 membranes grown onto seeded supports. The as-synthesized membranes were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and pervaporation testing. The results indicated that the as-synthesized membranes were typical MFI-type zeolite membranes and the ETES promoted the crystal growth of the silicalite-1 membranes. The optimum molar composition (1TEOS:0.17TPAOH:120H(2)O:[0.02-0.04]ETES:4EtOH), more than 16h crystallization time at low-temperature (413K) was better for obtaining a dense and continuous silicalite-1 membranes with a good pervaporation performance. The M(3) membrane shows a relatively low selectivity for ethanol/water system but a high selectivity for acetone/water and butanol/water systems. The total fluxes of the M(3) membrane were 1.55, 0.10, and 1.51 kg m(-2) h(-1) towards acetone/H(2)O, butanol/H(2)O and ethanol/H(2)O mixtures, respectively for 3 wt.% acetone/water, 2 wt.% butanol/water and 5 wt.% ethanol/water mixture, respectively and the corresponding separation factor was 211, 150, and 39, respectively. (C) 2010 Elsevier B.V. All rights reserved.