Production of micro- and mesoporous carbons by pyrolysis of the lithium salts of aromatic acids

被引:7
作者
Kamegawa, K [1 ]
Kodama, M
Nishikubo, K
Yamada, H
Adachi, Y
Yoshida, H
机构
[1] Natl Inst Adv Ind Sci & Technol AIST Kyushu, Sensing & Diag Res Lab, Tosu, Saga 8410052, Japan
[2] AIST, Tsukuba, Ibaraki 3058569, Japan
[3] Kurume Inst Technol, Dept Environm Symbiosis Engn, Kurume, Fukuoka 8300052, Japan
关键词
phthalic acid; aromatic acid; pyrolysis; mesoporous carbon; lithium compound;
D O I
10.1016/j.micromeso.2005.07.031
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
As a new process for the production of micro- and mesoporous carbon materials, the thermal decomposition of the lithium salts of aromatic acids (terephthalic acid, 1,3,5-benzenetricarboxylic acid, and 1,2,4,5-benzenetetracarboxylic acid) was followed by TGA, MS, SEM, TEM, elemental analysis, and N-2 adsorption. The lithium salt of terephthalic acid was decomposed at temperatures above 550 degrees C and then converted into a composite of amorphous carbon and microcrystalline lithium carbonate (600-700 degrees C) or oxide (800-900 degrees C). The amorphous carbons produced by washing out the lithium compounds showed surface areas of 480-780 m(2) g(-1), and the micro- and mesopore volumes attained 0.27 and 0.93 cm(3) g(-1), respectively, at the pyrolytic temperature of 850 degrees C. The mesopores were distributed from ca. 20 to 100 nm in size, and the distribution was independent of the pyrolytic temperatures. The pore size was, however, increased when larger-size crystals of the lithium salt were employed as the starting material. Both porous carbons prepared from the lithium salts of 1,3,5-benzenetricarboxylic acid and 1,2,4,5-benzenetetracarboxylic acid showed similar surface areas and pore size distributions to those from terephthalic acid. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:118 / 123
页数:6
相关论文
共 27 条
[1]   Template synthesis of mesoporous carbons with tailorable pore size and porosity [J].
Alvarez, S ;
Fuertes, AB .
CARBON, 2004, 42 (02) :433-436
[2]  
Bansal R. C., 1988, ACTIVE CARBON, P27
[3]   MODIFIED CARBON-BLACK IN HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
COLIN, H ;
EON, C ;
GUIOCHON, G .
JOURNAL OF CHROMATOGRAPHY, 1976, 119 (APR28) :41-54
[4]   POROUS GLASSY-CARBON, A NEW COLUMNS PACKING MATERIAL FOR GAS-CHROMATOGRAPHY AND HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
GILBERT, MT ;
KNOX, JH ;
KAUR, B .
CHROMATOGRAPHIA, 1982, 16 :138-148
[5]  
Hatori H, 2001, J APPL POLYM SCI, V79, P836, DOI 10.1002/1097-4628(20010131)79:5<836::AID-APP80>3.0.CO
[6]  
2-1
[7]  
Hu ZH, 2000, ADV MATER, V12, P62, DOI 10.1002/(SICI)1521-4095(200001)12:1<62::AID-ADMA62>3.0.CO
[8]  
2-B
[9]   Ordered nanoporous arrays of carbon supporting high dispersions of platinum nanoparticles [J].
Joo, SH ;
Choi, SJ ;
Oh, I ;
Kwak, J ;
Liu, Z ;
Terasaki, O ;
Ryoo, R .
NATURE, 2001, 412 (6843) :169-172
[10]   Preparation and characterization of swelling porous carbon beads [J].
Kamegawa, K ;
Yoshida, H .
CARBON, 1997, 35 (05) :631-639