One-pot synthesis of silica monoliths with hierarchically porous structure

被引:20
作者
Drisko, Glenna L. [2 ]
Zelcer, Andres [1 ,3 ]
Caruso, Rachel A. [2 ,4 ]
Soler-Illia, Galo J. de A. A. [1 ,5 ]
机构
[1] Comis Nacl Energia Atom, RA-1650 San Martin, Buenos Aires, Argentina
[2] Univ Melbourne, Sch Chem, Particulate Fluids Proc Ctr, Melbourne, Vic 3010, Australia
[3] Univ Nacl San Martin, Escuela Ciencia & Tecnol, San Martin, Argentina
[4] Commonwealth Sci & Ind Res Org, Clayton, Vic 3169, Australia
[5] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Quim Inorgan Analit & Quim Fis, RA-1053 Buenos Aires, DF, Argentina
基金
澳大利亚研究理事会;
关键词
Polymerization-induced phase separation; Monolith; Hierarchical pore structures; Silica; Furfuryl alcohol; PORE-SIZE DISTRIBUTION; SOL-GEL PROCESS; PHASE-SEPARATION; MESOPOROUS SILICA; INTEGRATIVE-CHEMISTRY; ADSORPTION PROPERTIES; AQUEOUS-SOLUTIONS; CROSS-LINKING; POROSITY; CARBON;
D O I
10.1016/j.micromeso.2011.08.007
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Poly(furfuryl alcohol) (PFA) and block copolymer Pluronic F127 were used as pore templates to create mechanically robust silica monoliths with a hierarchical and interconnected macro-mesoporous network in an easy, reproducible bimodal scale templating process. Control over the morphology was obtained by varying the reactant ratios. Phase separation on the submicrometer scale occurred when furfuryl alcohol was cationically polymerized and therefore became immiscible with the solvent and the silica precursor. Upon a subsequent sol-gel reaction, a silica-F127 matrix formed around the PFA spheres, leading to macropore structures with mesoporous walls. Surface areas of the final structures ranged from 500 to 989 m(2) g(-1) and a maximum pore volume of 4.5 mL g(-1) was achieved. Under mildly acidic conditions, micelle-templated mesopores resulted. Interconnected macropores could be obtained by increasing the pH or the block copolymer concentration. The formation mechanism and the relationship between PFA, Pluronic F127 and acidity are discussed in detail. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:137 / 144
页数:8
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