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Structure and Catalysis of Cellulose-Derived Amorphous Carbon Bearing SO3H Groups

机译:纤维素衍生的无定形碳轴承SO3H基团的结构和催化

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The correlation between catalytic performance and structure of a cellulose-derived and carbon-based solid acid (CCSA), an amorphous carbon bearing SO3H, COOH, and phenolic OH groups, was investigated. Sulfonation of partially carbonized cellulose under a N-2 atmosphere resulted in the formation of a CCSA, which was amorphous carbon consisting of small polycyclic aromatic carbon sheets with a high density of SO3H groups (ca. 2 mmol g(-1)). CCSAs were prepared from carbon precursors, which were obtained at temperatures = 723 K, and exhibited a high catalytic performance for the esterification of acetic acid with ethanol and for the hydrolysis of cellobiose, although the surface areas were small (5 m(2)g(-1)). In contrast, CCSAs, which were prepared from carbon precursors obtained at = 823 K, exhibited much lower catalytic activities for both reactions, although the CCSAs had sufficient amounts of SO3H groups. Structural analyses, including spectroscopic analysis of CCSAs with adsorbed probe molecules, revealed that cross-linking between the polycyclic aromatic carbon sheets caused the sharp decrease in activity.
机译:研究了纤维素衍生和碳基固体酸(CCSA),无定形碳轴承SO3H,COOH和酚类OH基团之间的催化性能和结构之间的相关性。在N-2气氛下部分碳化纤维素的磺化导致CCSA的形成,其是由具有高密度的小密度(约2mmol g(-1))组成的无定形碳。 CCSA由碳前体制备,其在温度下获得,并在温度下获得,并且表现出乙酸酯化的高催化性能,乙醇与纤维二糖水解,尽管表面积小(<5米) (2)G(-1))。相反,由&gt的碳前体制备的CCSA = 823 k,虽然CCSA具有足够量的SO 3 H,但表现出较低的催化活性。结构分析,包括具有吸附探针分子的CCSA的光谱分析,显示多环芳族碳板之间的交联导致活性急剧下降。

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