Novel anion-exchange organic–inorganic hybrid membranes prepared through sol–gel reaction of multi-alkoxy precursors
A series of anion-exchange organic–inorganic hybrid membranes were prepared through sol–gel process from different precursors such as the copolymer of glycidylmethacrylate (GMA) and γ-methacryloxypropy trimethoxy silane (γ-MPS) (multi-silicon), N-triethoxysilylpropyl-N,N,N-trimethylammonium iodine (...
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Published in | Journal of membrane science Vol. 329; no. 1; pp. 236 - 245 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
05.03.2009
|
Subjects | |
Online Access | Get full text |
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Summary: | A series of anion-exchange organic–inorganic hybrid membranes were prepared through sol–gel process from different precursors such as the copolymer of glycidylmethacrylate (GMA) and γ-methacryloxypropy trimethoxy silane (γ-MPS) (multi-silicon), N-triethoxysilylpropyl-N,N,N-trimethylammonium iodine (A-1100(+), mono-silicon) and monophenyltriethoxysilane (EPh) (mono-silicon). Influence of the copolymer's molecular weight on the sol–gel process and membrane formation is primarily investigated. It is demonstrated that copolymer with lower molecular weight (number average molecular weight,
M
n, 8248) is more desirable to obtain homogenous and flexible hybrid membranes. Results also show that increasing the content of A-1100(+) could increase the membrane water uptake (
W
R), ion exchange capacity (IEC) and membrane potential (
E
m), while decrease in EPh content can result in an increase in
W
R,
E
m, and elongation at break (
E
b). Generally speaking, the membranes have relatively strong hydrophobicity and high mechanical strength. The tensile strength (TS) can reach up to 88
MPa, and the
E
b is in the range of 34–41%. Morphology studies show all the hybrid membranes are compact and homogenous even though they have high silica content (27.0–29.8%). |
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ISSN: | 0376-7388 1873-3123 |
DOI: | 10.1016/j.memsci.2008.12.056 |