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Iron(III) oxyhydroxide and oxide monoliths with controlled multiscale porosity: synthesis and their adsorption performance
被引:17
|作者:
Hara, Yosuke
[1
]
Kanamori, Kazuyoshi
[1
]
Morisato, Kei
[1
,2
]
Miyamoto, Riichi
[1
,3
]
Nakanishi, Kazuki
[1
]
机构:
[1] Kyoto Univ, Grad Sch Sci, Dept Chem, Sakyo Ku, Kyoto 6068502, Japan
[2] GL Sci Inc, 237-2 Sayamagahara, Iruma, Saitama 3580032, Japan
[3] SnG Inc, Nishikyo Ku, 1-39 Goryo Ohara, Kyoto 6158245, Japan
基金:
日本科学技术振兴机构;
关键词:
SOL-GEL SYNTHESIS;
POROUS MATERIALS;
MESOPOROUS FE2O3;
PHASE-SEPARATION;
CONGO RED;
HYDROXIDE;
NANOSTRUCTURES;
NANOPARTICLES;
CONVERSION;
CATALYSIS;
D O I:
10.1039/c8ta01691g
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Iron(III) oxyhydroxide and oxide monoliths with controlled multiscale porosity have been successfully fabricated via the sol-gel process accompanied by phase separation. The size of macropores was controlled by synthesis parameters such as starting compositions. The as-dried iron(III) oxyhydroxide monoliths were amorphous and possessed surface areas over 340 m(2) g(-1), of which mesostructures could be further controlled by a heat-treatment at 250-350 degrees C without collapse of macrostructures and monolithic forms. When the as-dried gel was heated at 300 degrees C, the resultant gel transformed to crystalline alpha-Fe2O3 and exhibited a specific surface area of 124 m(2) g(-1). Heat-treatment at 350 degrees C resulted in the broadened size distribution of mesopores. The adsorption behavior of Congo red has revealed that the interconnected macroporous structure contributed to faster diffusion and better accessibility in a continuous flow-through set up, and the crack-free monolithic forms accounted for an advantageous use of the flow-through adsorbents.
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页码:9041 / 9048
页数:8
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