Macroporous alumina monoliths prepared by filling polymer foams with alumina hydrosols

被引:57
|
作者
Zhang, Yuan [1 ]
Liang, Hao [1 ]
Zhao, Cun Yu [1 ]
Liu, Yuan [1 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Dept Catalysis Sci & Technol, Tianjin Key Lab Appl Catalysis Sci & Engn, Tianjin 300072, Peoples R China
关键词
SOL-GEL PROCESS; PREFERENTIAL OXIDATION; CARBON MONOLITHS; HIERARCHICAL POROSITY; CATALYSTS; MONOXIDE; FABRICATION; CERAMICS; CRYSTALS; SUPPORTS;
D O I
10.1007/s10853-008-3189-6
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Macroporous alumina monoliths have been prepared for the first time by filling polystyrene foam templates with alumina hydrosols which were prepared from pseudo-boehmite. Polystyrene foam templates were obtained by polymerization in highly concentrated water-in-oil (W/O) emulsions. The organic templates were subsequently removed by calcination. The effects of filling times of the alumina hydrosols, calcination temperature, and CTAB surfactant addition in the hydrosols on the properties of the monolith have been investigated. TG, FT-IR, SEM, TEM, N-2 adsorption-desorption, and XRD techniques were used for characterization. The so prepared monoliths are the replicas of the polystyrene foams and are characterized with hierarchically porous structure. The macropores are interconnected and the macropore walls contain many meso and/or micropores. The hierarchically macro-meso-microporous structure can be controlled and tailored by adjusting the preparation conditions stated above and by addition of surfactant, and the organic components can be eliminated by high temperature calcination. When the calcination temperatures are 600 A degrees C and 900 A degrees C, the gamma-Al2O3 phases are obtained, with S-BET of 228 and 85 m(2) g(-1), respectively. When calcined at 1100 A degrees C, the alumina monolith presents a single theta-Al2O3 phase with S-BET of 80 m(2) g(-1). The 1300 A degrees C calcined sample takes on the single alpha-Al2O3 phase with S-BET of 5 m(2) g(-1) and compressive strength of 3.1 MPa.
引用
收藏
页码:931 / 938
页数:8
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