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Description of the preferential transport of monovalent salts through Na-mordenite membrane: Physico-chemical aspects
被引:7
作者:
Limousy, L.
[1
]
Dutournie, P.
[1
]
Chevereau-Landais, E.
[2
]
机构:
[1] Univ Haute Alsace, Lab Gest Risques & Environm, F-68093 Mulhouse, France
[2] Univ Bretagne S, Lab Ingn Mat Bretagne LIMATB EA 4250, F-56321 Lorient, France
关键词:
Na-mordenite membrane;
Halide salts;
Preferential transport;
Van der Waals forces;
ZEOLITE;
WATER;
NANOCRYSTALS;
DEHYDRATION;
CATALYSTS;
D O I:
10.1016/j.micromeso.2012.01.025
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
A Na-mordenite membrane was prepared by using sol-gel synthesis protocol, and spin-coating was chosen as the impregnation methodology. The gel was impregnated onto commercial ceramic tubular support (alpha-alumina) and surface characterizations were carried out on Na-mordenite powder prepared with the same gel. The Na-mordenite surface charge is not appreciably modified by a contact with monovalent or divalent salts. The average pore diameter was estimated in the range of 8 nm. Previous results showed that monovalent salts were not retained by the stabilized Na-mordenite membrane while after an alkaline treatment, rejections were observed according to the order of hydration energies (NaF > NaCl > NaBr > NaI). After an acid cleaning, the membrane recovered its initial properties. A new estimation of average pore radius proved that steric effects were not responsible for rejection themselves. A new filtration test of mixed monovalent salt solution was carried out. Fluoride ions were retained by a majority while the others were almost not retained. Infrared characterizations indicate that, after an alkaline treatment, surface chemistry modifications may be at the origin of these interactions. Especially, the apparition of an ultrapolar layer all over the Na-mordenite surface greatly modifies Van der Waals interactions between the hydrated anions and the Na-mordenite surface. (C) 2012 Elsevier Inc. All rights reserved.
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页码:133 / 136
页数:4
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