Acid-catalyzed reactions on flexible polycyclic aromatic carbon in amorphous carbon

被引:519
作者
Okamura, Mai
Takagaki, Atsushi
Toda, Masakazu
Kondo, Junko N.
Domen, Kazunari
Tatsumi, Takashi
Hara, Michikazu
Hayashi, Shigenobu
机构
[1] Tokyo Inst Technol, Chem Res Lab, Midori Ku, Yokohama, Kanagawa 2268503, Japan
[2] Natl Inst Adv Ind Sci & Technol, Res Inst Instrumentat Frontier, AIST, Tsukuba, Ibaraki 3058565, Japan
[3] Univ Tokyo, Sch Engn, Dept Chem Syst Engn, Bunkyo Ku, Tokyo 1138656, Japan
[4] Japan Sci & Technol Co, SORST, JST, Taito Ku, Tokyo 1100015, Japan
关键词
D O I
10.1021/cm0605623
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
Carbonization of D-glucose at 573-723 K followed by sulfonation produces a functionalized amorphous carbon material with acid catalytic activity as a solid-acid replacement for sulfuric acid. The carbon material contains phenolic hydroxyl, carboxylic acid, and sulfonic acid groups and exhibits high catalytic performance for liquid-phase acid-catalyzed reactions. Carbonization at higher temperature followed by sulfonation also results in amorphous carbon, but the resultant does not exhibit catalytic activity although the amorphous carbon has sufficient amount of sulfonic acid groups. Structural and active site analyses suggest that the marked difference in catalytic activity is due to the accessibility of reactants to sulfonic acid groups in the carbon structure.
引用
收藏
页码:3039 / 3045
页数:7
相关论文
共 17 条
[1]   Origins, current status, and future challenges of green chemistry [J].
Anastas, PT ;
Kirchhoff, MM .
ACCOUNTS OF CHEMICAL RESEARCH, 2002, 35 (09) :686-694
[2]   Design through the 12 principles of green engineering [J].
Anastas, PT ;
Zimmerman, JB .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2003, 37 (05) :94A-101A
[3]   Solid acids for green chemistry [J].
Clark, JH .
ACCOUNTS OF CHEMICAL RESEARCH, 2002, 35 (09) :791-797
[4]   Practical approaches to green solvents [J].
DeSimone, JM .
SCIENCE, 2002, 297 (5582) :799-803
[5]   A carbon material as a strong protonic acid [J].
Hara, M ;
Yoshida, T ;
Takagaki, A ;
Takata, T ;
Kondo, JN ;
Hayashi, S ;
Domen, K .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (22) :2955-2958
[6]   Green chemistry puts down roots [J].
Horton, B .
NATURE, 1999, 400 (6746) :797-799
[7]   NMR characterization of Bronsted acid sites in faujasitic zeolites with use of perdeuterated trimethylphosphine oxide [J].
Karra, MD ;
Sutovich, KJ ;
Mueller, KT .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (06) :902-903
[8]   Low temperature mechanism for the formation of polycyclic aromatic hydrocarbons from the pyrolysis of cellulose [J].
McGrath, TE ;
Chan, WG ;
Hajaligol, MR .
JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 2003, 66 (1-2) :51-70
[9]   Friedel crafts acylation of aromatic compounds over arenesulfonic containing mesostructured SBA-15 materials [J].
Melero, JA ;
van Grieken, R ;
Morales, G ;
Nuño, V .
CATALYSIS COMMUNICATIONS, 2004, 5 (03) :131-136
[10]   Acid catalysts for clean production. Green aspects of heteropolyacid catalysts [J].
Misono, M .
COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE II FASCICULE C-CHIMIE, 2000, 3 (06) :471-475