Functional defect-patching of a zeolite membrane for the dehydration of acetic acid by pervaporation

被引:30
|
作者
Chen, Zan [1 ]
Yin, Dehong [1 ]
Li, Yinhui [1 ]
Yang, Jianhua [1 ]
Lu, Jinming [1 ]
Zhang, Yan [1 ]
Wang, Jinqu [1 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, Inst Adsorpt & Inorgan Membrane, State Key Lab Fine Chem, Dalian 116012, Peoples R China
关键词
Pervaporation; Zeolite membrane; Grain boundary defects; Poly(4-vinylpyridine); Water/acetic acid mixture; MORDENITE MEMBRANES; HIGH-PERMEANCE; SEPARATION; THIN; MIXTURES; SUPPORTS; GROWTH; PERFORMANCE; COMPOSITE; FILMS;
D O I
10.1016/j.memsci.2010.12.034
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Pervaporation (PV) using zeolite membrane is one of the emerging technologies undergoing a rapid growth in recent years, regarded as an alternative method to distillation for its energy-efficient. However, grain boundary defects, especially for hydrophilic zeolite membranes, inevitably formed due to their polycrystalline structures and strong negative surface charges of Al-containing zeolites during hydrothermal synthesis, degrade their selectivity by providing nonselective transport pathway for permeating species. We show that functional defect-patching (FDP) can improve the PV performances of thin columnar membrane of a certain zeolite (mordenite) by eliminating grain boundary defects, by grafting functional polymer groups onto grain boundaries. This methodology enables the preparation of mordenite zeolite membrane (MZM) with high PV performances for the dehydration of acetic acid (AcOH) and holds promise for realizing high-throughput and scalable production of the membrane with improved energy efficiency. Furthermore, durable tests for acid stability showed that the FDP-treated membrane displayed a reasonably strong acid resistance. Finally, the products fabricated were characterized by a variety of techniques such as scanning electron microscopy (SEM). X-ray diffraction (XRD), diffuse reflectance FT-IR spectroscopy (DRIFTS) and thermogravimetric analysis (TGA). (C) 2011 Published by Elsevier B.V.
引用
收藏
页码:506 / 513
页数:8
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