DLS and SAXS investigations of organic gels and aerogels

被引:42
作者
Berthon, S
Barbieri, O
Ehrburger-Dolle, F
Geissler, E
Achard, P
Bley, F
Hecht, AM
Livet, F
Pajonk, GM
Pinto, N
Rigaci, A
Rochas, C
机构
[1] CNRS, UPR 9069, ICSI, F-68057 Mulhouse, France
[2] Ecole Mines, CENERG, F-06904 Sophia Antipolis, France
[3] UJF Grenoble, UMR 5588, LSP, CNRS, F-38402 St Martin Dheres, France
[4] INPG, CNRS, UMR 5614, LTPCM, F-38402 St Martin Dheres, France
[5] Univ Lyon 1, CNRS, LACE, F-69622 Villeurbanne, France
关键词
D O I
10.1016/S0022-3093(01)00447-1
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
Recent investigations have shown that the structure of organic aerogels can be significantly modified by changing the precursors, the solvent and the nature of the catalyst involved in the sol-gel reaction. it is therefore highly desirable to investigate the sol-gel mechanism. For this purpose, dynamic light scattering (DLS) measurements have been performed at different stages of the reaction for base- or acid-catalyzed gelation of resorcinol formaldehyde (RF) using water or acetone as solvents. The structure of aged gels was investigated by small-angle X-ray scattering (SAXS) and compared to that of the aerogels obtained after exchange of solvent by supercritical COL and drying of the aged gels. It is shown that acid-catalyzed gelation of RF in acetone can be described by percolation, which explains that this series of aerogels consists of mass fractal aggregates (D-m = 2.5). The partial collapse of this polymeric gel yielding colloidal particles in the aerogel can be attributed to deswelling in supercritical CO2. DLS indicates that gelation of RF with a base catalyst yields a colloidal gel whose structure remains practically unchanged in the aerogel, as shown by SAXS. (C) 2001 Elsevier Science B,V. All rights reserved.
引用
收藏
页码:154 / 161
页数:8
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