Graphene oxide mediated cellulose-derived carbon as a highly selective catalyst for the hydrolysis of cellulose to glucose

被引:38
|
作者
Zhang, Meng [1 ]
Wu, Minghui [1 ]
Liu, Qing [1 ]
Wang, Xin [1 ]
Lv, Tao [1 ]
Jia, Lishan [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem & Biochem Engn, Xiamen 361005, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Graphene oxide; Carbon-based solid acid; Hydrothermal carbonization; Lamellar structure; SOLID ACID; MICROCRYSTALLINE CELLULOSE; HYDROTHERMAL CARBONIZATION; EFFICIENT HYDROLYSIS; IONIC LIQUIDS; BEARING SO3H; OH GROUPS; COOH;
D O I
10.1016/j.apcata.2017.06.033
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
A novel graphene oxide mediated flake carbon-based solid acid bearing -SO3H, -COOH, and -OH groups was synthesized via hydrothermal carbonization of cellulose with a small amount of graphene oxide (GO) as a structure-directing agent and subsequent sulfonation. A series of characterization results show that with a certain addition of GO, the carbonized samples can transform from micron carbon spheres into crumpling layers, and the hydrophilcity of the GO induced catalysts also get increased. The prepared solid acid with 10 wt% addition of GO (10-SGOC) exhibits excellent glucose selectivity (94.22%) at a moderate temperature (160 degrees C). The catalytic performance of 10-SGOC is attributed to its lamellar structure with good hydrophilcity and the existence of functional OH, COOH and -SO3H groups. The unique structure and hydrophilcity could improve the dispersion of the catalyst and provide effective interaction between reactants and functional groups on the solid acid, then OH groups adsorb cellulose on surface of the catalyst and acidic sites hydrolyze cellulose to glucose. Moreover, the catalyst displays good stability in catalytic activity; the selectivity of glucose could remain above 92.48% after four cycling experiments.
引用
收藏
页码:218 / 224
页数:7
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