A review of the control of pore structure in MgO-templated nanoporous carbons

被引:270
作者
Morishita, T. [1 ]
Tsumura, T. [2 ]
Toyoda, M. [2 ]
Przepiorski, J. [3 ]
Morawski, A. W. [3 ]
Konno, H. [4 ]
Inagaki, M.
机构
[1] Toyo Tanso Co Ltd, Adv Carbon Technol Ctr, Nishiyodogawa Ku, Osaka 5550011, Japan
[2] Oita Univ, Fac Engn, Oita 8701192, Japan
[3] W Pomeranian Univ Technol, PL-70322 Szczecin, Poland
[4] Hokkaido Univ, Grad Sch Engn, Sapporo, Hokkaido 0608628, Japan
关键词
SOL-GEL POLYCONDENSATION; ORDERED MICROPOROUS CARBONS; ANATASE-TYPE TIO2; MESOPOROUS CARBONS; COATED ANATASE; POROUS CARBON; IMINOCTADINE TRIACETATE; PHOTOCATALYTIC ACTIVITY; METHYLENE-BLUE; GRAPHITE;
D O I
10.1016/j.carbon.2010.03.064
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
Nanoporous carbons with a high surface area were directly prepared from various carbon precursors without any stabilization and activation processes. Various carbon precursors, including poly(vinyl alcohol), poly(ethylene terephthalate), polyimide, coal tar pitch, were used and MgO itself, Mg acetate, Mg citrate, Mg gluconate and Mg hydroxy-carbonate were employed as MgO precursor. Carbon precursor was mixed with MgO precursor in different ratios either in powder (powder mixing) or in solution (solution mixing), and heat-treated at 900 degrees C in inert atmosphere. MgO formed in the carbonization products was dissolved out using a diluted acid. BET surface area of the carbons obtained could be reached to high value, as high as 2000 m(2)/g, even though any activation process was not applied. Most carbons prepared through this method were rich in mesopores. Size of mesopores in the resultant carbons was tunable by selecting MgO precursor and relative volume between mesopores and micropores was controlled by carbon precursor. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2690 / 2707
页数:18
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