期刊
MICROPOROUS AND MESOPOROUS MATERIALS
卷 113, 期 1-3, 页码 305-314出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.micromeso.2007.11.028
关键词
mesoporous carbon; thermal stability; pore structure; porosity; self-assembly
Mesoporous carbons FDU-15 with ordered hexagonal structure were prepared by using triblock copolymer Pluronic F127 as a template and resol as a carbon precursor via evaporation induced organic-organic assembly method. The pore structure evolution and stability of FDU-15 functioned with the treatment temperature and time were systematically investigated in CO2, O-2 or water vapor atmospheres. A variety of techniques such as powder X-ray diffraction (XRD), nitrogen sorption and transmission electron microscopy (TEM) were used to characterize the thermal stability of the carbon mesostructure. N-2 sorption measurements show that the activation process can simply increase the specific surface area and pore volume of the mesoporous carbons. The effect of structural regularity, pore size, meso- or microporosity, and wall thickness on the thermal stability at different treatment temperature and time was discussed. The results show that mesoporous carbon FDU-15 materials after the carbonization at 900 degrees C have a good thermal stability under CO2 at 750 degrees C, O-2 at 350 degrees C and water vapor at 800 degrees C for at least 3 h. Nevertheless, CO2, O-2 or water vapor develops the pore system through different ways. For CO2, the thermal treatment leads to large mesopore volumes while the micropores are slightly increased during the carbon burn-off. Different from CO2, water vapor activation renders a continuous increase of micropore volumes as well as the total pore volumes with increasing the carbon burn-off. Under O-2-treatment at 350 degrees C, the ordered mesostructures can be rapidly destroyed due to the fast burning reactions of oxygen with mesoporous carbons. (C) 2007 Elsevier Inc. All rights reserved.
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