Please use this identifier to cite or link to this item:
|Title:||Template synthesis and adsorption properties of hierarchically porous zirconium titanium oxides.|
|Publisher:||American Chemical Society|
|Citation:||Drisko, G. L., Luca, V., Sizgek, E., Scales, N., & Caruso, R. A. (2009). Template synthesis and adsorption properties of hierarchically porous zirconium titanium oxides. Langmuir, 25(9), 5286-5293.|
|Abstract:||Hierarchical morphologies in metal oxides are advantageous for many applications, including controlled drug release, photocatalysis, catalysis, synthetic biomaterials, and adsorption and separation technologies. In this study, agarose gel has been used as a template to prepare zirconium titanium mixed oxide pellets with bimodal porosity. Sol−gel chemistry conducted within the agarose gel produced "coral-like" interconnected networks of oxide nanoparticles with controllable quantities of zirconium and titanium. The materials were characterized using N2 sorption, extended X-ray absorption fine structure, X-ray diffraction, TEM, SEM, zeta potential, and thermogravimetric analysis (to measure surface hydroxyl group density). The oxides were then tested for the adsorption of vanadyl and vanadate to determine which Zr mole fraction exhibited the highest capacity and fastest kinetics. The material containing 25 mol % Zr exhibited the highest surface area (322 ± 8 m2/g) of the compositions investigated and also displayed a superior adsorption rate and capacity. Vanadate adsorption occurred with faster kinetics than did vanadyl adsorption. A comparative study demonstrated that the macro/meso pore structure had improved transport properties over a monomodal mesopore structure of similar Zr/Ti composition. The faster vanadate adsorption kinetics is attributed to enhanced surface accessibility in a hierarchical material. © 2009, American Chemical Society|
|Gov't Doc #:||1587|
|Appears in Collections:||Journal Articles|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.