A hierarchical structure of mesoporous−macroporous phosphated aluminum (oxyhydr)oxide (PAl) materials was prepared via a simple self-assembly process with the use of precursor aluminum sec-butoxide in a mixed solution of H3PO4 and Na2HPO4. Direct phosphation resulted in the incorporation of phosphorus into the inorganic framework of aluminum (oxyhydr)oxides by the Al−O−P bonds. The X-ray diffraction (XRD) patterns revealed that, despite slight phosphorus incorporation or phosphation, the frameworks of the as-synthesized autoclaved PAl samples remained in a crystalline phase of boehmite AlOOH-type, and their calcined products had a phase of γ-Al2O3-type. The macroporous structures are uniform, with sizes of 500−1800 nm, and the macropore walls are composed of accessible mesopores of a scaffold-like nanoparticle assembly. It is shown that the direct incorporation of phosphorus from a phosphate solution of the synthesis system can stabilize the framework of mesoporous−macroporous aluminum oxides with high surface areas and acidic properties. The present study also demonstrated that the surfactant (Brij 56) did not seem to have a direct role in the formation of macroporous structures, but significantly influenced the textural properties of the resultant PAl materials. The surface areas of surfactant-synthesized PAl exceeded 700 m2/g, which is almost two times of that of surfactantless-synthesized samples. The synthesized hierarchical PAl exhibited high thermal stability (at least 800 °C), possessing surface hydroxyl groups and acid sites, which may attract much interest for practical applications, including catalysis.
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Yuan et al. (2006) studied this question.
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