Water sorption in hybrid silica gels containing colloidal nontronite

被引:3
作者
Oulkadi, Djihad [1 ]
Desobry, Stephane [2 ]
Mustin, Christian [1 ]
Desobry-Banon, Sylvie [1 ]
机构
[1] Univ Lorraine, Fac Sci & Technol, LIMOS, UMR CNRS 7137, F-54506 Vandoeuvre Les Nancy, France
[2] Univ Lorraine, Lab Ingn Biomol LIBio, ENSAIA, F-54505 Vandoeuvre Les Nancy, France
关键词
Hybrid material; Silica; Sorption; Isotherm; Nontronite; DISSOLUTION; ADSORPTION; KINETICS; SOILS; SIZE; CLAY;
D O I
10.1007/s10971-012-2898-0
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Hybrid silica gels (HSGs) were prepared according to an acid-catalyzed sol-gel method using tetraethoxysilane (TEOS) as silica precursors and colloidal suspension of nontronite clay mineral. The silica surfaces were hydrophilic in relation to silanol groups and it was of interest to increase hydrophobicity by substituting silanol by methylated groups through addition of methyltrimethoxysilane (MTMS) in a molar ratio TEOS: MTMS equaled to 1:0.4. The aim of the present paper was to predict effects of water content in soil on HSG hydration by characterizing HSG water desorption and sorption with dynamic vapor sorption device. From desorption kinetics, TEOS HSGs showed higher ability to water surface evaporation and diffusion compared to the TEOS-MTMS HSGs. After complete dehydration, water sorption isotherms Type II were obtained for HSGs. Isotherms were fitted with Brunauer-Emmett-Tellet (BET) and Guggenheim, Andersen, de Boer (GAB) models. The higher monolayer values of water adsorbed for HSGs containing nontronite suggested a major influence of clay minerals on overall hydration. However, the water binding energy depended upon the nature of silica matrix indicating weaker bonds with methylated groups at solid surface in MTMS-TEOS HSGs. Apparent water sorption diffusivities, D-app were calculated according to Fick's diffusion model. Maximal D-app values were obtained in the range 0.2-0.3 a(w) after which the D-app decreased in relation with capillary condensation.
引用
收藏
页码:653 / 660
页数:8
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