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pubmed-article:12914071pubmed:abstractTextSilica xerogels were prepared by a sol-gel process catalyzed by acid with tetraethylorthosilicate, and using an organic covalent ligand template (methyltriethoxysilane) or a noncovalent template C6 surfactant (triethylhexylammonium bromide). The influence of hydrotreatment on the structure of templated xerogels is examined in terms of surface area, micropore volume, average pore size, and pore size distribution, and compared against a blank xerogel (nontemplated). The role of surface functional groups was evaluated using 29Si nuclear magnetic resonance. The structural integrity of the xerogel was maintained to a large extent in samples that had a high contribution of Q4 species (siloxane groups). Xerogel matrix densification occurred when there was a large concentration of Q3 and Q2 species (silanol groups), which also were responsible for increased hydrophilicity. The templated xerogels resulted in up to a 25% concentration of methyl functional groups (T3 and T2 species), leading to hydrophobic xerogels. The best results in terms of structural integrity and hydrophobicity were obtained with templated xerogels prepared with the C6 surfactant. The results in this study suggest that surfactant-enhanced condensation reactions lead to structures with a high contribution of Q4 groups, which are not susceptible to water attack, but are strong enough to oppose matrix densification during rehydration.lld:pubmed
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pubmed-article:12914071pubmed:dateRevised2010-11-18lld:pubmed
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pubmed-article:12914071pubmed:articleTitleHydrophobicity of templated silica xerogels for molecular sieving applications.lld:pubmed
pubmed-article:12914071pubmed:affiliationNanomaterials Centre, Department of Chemical Engineering, University of Queensland, Brisbane, Queensland, 4072, Australia.lld:pubmed
pubmed-article:12914071pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12914071pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:12914071pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
pubmed-article:12914071pubmed:publicationTypeEvaluation Studieslld:pubmed