Mesoporous silica matrices derived from sol-gel process assisted by low power ultrasonic activation
Author(s) -
Cecilia Savii,
László Almásy,
Claudia Ionescu,
Noemi Szekély,
Corina Enache,
M. Popovici,
Ioan Şora,
Dan Nicoară,
Gustav Savii,
Daniela Susan-Resiga,
Ján Šubrt,
Václav Štengl
Publication year - 2009
Publication title -
processing and application of ceramics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.326
H-Index - 15
eISSN - 2406-1034
pISSN - 1820-6131
DOI - 10.2298/pac0902059s
Subject(s) - materials science , mesoporous material , microstructure , sonication , ultrasonic sensor , porosity , chemical engineering , adsorption , texture (cosmology) , specific surface area , fractal dimension , sol gel , composite material , fractal , nanotechnology , organic chemistry , catalysis , chemistry , mathematical analysis , physics , image (mathematics) , mathematics , artificial intelligence , computer science , acoustics , engineering
The present work contributes to elucidating the differences between silica gels obtained by low doses ultrason- ic activation, and those obtained by the conventional method, termed as classical sol gel. Silica matrices were produced by sol-gel synthesis process, assisted and non-assisted by an ultrasonic fi eld, and subsequently char- acterized by various methods. Nitrogen adsorption and small-angle neutron scattering (SANS) measurements provided texture and microstructure of the dried gels. The adsorption results show that the sample sonicated for 2 hours presents the most ordered microstructure, characterized by pore shape close to spherical and the narrowest size distribution - about 90 % of the pores for this sample fall into the mesopore range (2-50 nm). SANS data reveal the formation of primary structural units of sizes around 1.5-2 nm which are small linear or branched polymeric species of roughly spherical shape and with rough surface. They are generated in the very early stage of sol gel process, as a result of hydrolysis and condensation reactions. The aggregated primary units form the secondary porous structure which can be described as a rough surface with fractal dimension above 2. The best porosity characteristics were obtained for the sample activated for 2 hours, indicating the optimal doses of sonication in the present conditions. Our results demonstrate the possibility of tailoring the pore size distribution using a low power ultrasonic bath.
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