Amorphous Carbon Bearing Sulfonic Acid Groups in Mesoporous Silica as a Selective Catalyst

被引:130
作者
Nakajima, Kiyotaka [1 ]
Okamura, Mai [1 ]
Kondo, Junko N. [2 ]
Domen, Kazunari [4 ]
Tatsumi, Takashi [2 ]
Hayashi, Shigenobu [3 ]
Hara, Michikazu [1 ,5 ]
机构
[1] Tokyo Inst Technol, Mat & Struct Lab, Midori Ku, Yokohama, Kanagawa 2268503, Japan
[2] Tokyo Inst Technol, Chem Resources Lab, Midori Ku, Yokohama, Kanagawa 2268503, Japan
[3] Natl Inst Adv Ind Sci & Technol, Res Inst Instrumentat Frontier, Tsukuba, Ibaraki 3058565, Japan
[4] Univ Tokyo, Dept Chem Syst Engn, Bunkyo Ku, Tokyo 1138656, Japan
[5] Kanagawa Acad Sci & Technol, Takatsu Ku, Kawasaki, Kanagawa 2130012, Japan
基金
日本学术振兴会;
关键词
ION-EXCHANGE-RESINS; STRONG SOLID-ACID; TRIMETHYLPHOSPHINE OXIDE; GREEN CHEMISTRY; P-31; NMR; ZEOLITES; DIMERIZATION; SITES; COPOLYMER; TRIBLOCK;
D O I
10.1021/cm801441c
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
Sulfonic acid group (SO3H)-bearing amorphous carbon/mesoporous silica composites were studied for use as solid acid catalysts. Sugar-derived amorphous carbon with SO3H cannot catalyze hydrophobic acid-catalyzed reactions, such as the dimerization of alpha-methyl styrene, because of the small surface area. However, SO3H-bearing sugar-derived amorphous carbon supported on mesoporous silica exhibits remarkable catalytic performance for the dimerization of alpha-methylstyrene. Under optimal conditions, the selectivity of the composite catalysts for unsaturated dimers exceeds 98%. Structural and reaction analyses revealed that SO3H-bearing carbon particles with large surface areas are formed in the mesopores and prevent intramolecular Friedel-Crafts alkylation, resulting in high catalytic activity.
引用
收藏
页码:186 / 193
页数:8
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