Article ID Journal Published Year Pages File Type
66970 Journal of Molecular Catalysis A: Chemical 2009 10 Pages PDF
Abstract

Nanometric Fe2O3 particles could be inserted inside the internal pore volume of SBA-15 mesoporous silica when Fe(III) chelates (EDTA, gluconate and citrate) were used as impregnating precursors. Fe(III) nitrate preferentially yields 8 nm uniformly sized Fe2O3 clusters that selectively plug the SBA-15 channels through a geometric confinement effect. An oxidative degradation of Fe-chelate precursors yielded Fe(III) oxidic particles of various sizes and dispersion, depending on the nature and geometry of chelate anion. Fe(EDTA) precursors specifically generated Fe2O3 nanoparticles that selectively migrate towards two types of positions where the silica surface exhibits a high curvature. In samples involving low Fe loadings, Fe2O3 particles first creep towards the silica micropore mouths (nests), in which they are readily confined and stabilized. For higher Fe loadings, when most of the micropore nests were filled, oxidic particles eventually settle as a superficial film on the mesopore walls and undergo stabilization onto the surface roughness that can also favors their confinement, as theoretically predicted by Derouane and co-workers. Upon further reduction, as selectively followed by combined cyclic voltammetry and TPR, Fe2O3 readily yield FeO nanoslabs that remain even more efficiently confined within their respective nest positions through a further acid–base type stabilization.

Graphical abstractMechanism illustrating schematically different steps of the thermal decomposition of Fe2O3/SBA-15 composite synthesized using the chelate route, yielding nanosized Fe2O3 particles confined at the micropore mouth levels inside the SBA-15 mesopores.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
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