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Adsorption-Enhanced Hydrolysis of β-1,4-Glucan on Graphene-Based Amorphous Carbon Bearing SO3H, COOH, and OH Groups

化学 水解 糖苷键 催化作用 纤维素 碳纤维 吸附 纤维二糖 硫酸 有机化学 氢键 葡聚糖 分子 无机化学 纤维素酶 材料科学 复合数 复合材料 酶
作者
Masaaki Kitano,Daizo Yamaguchi,Satoshi Suganuma,Kiyotaka Nakajima,Hideki Kato,Shigenobu Hayashi,Masahiko Hara
出处
期刊:Langmuir [American Chemical Society]
卷期号:25 (9): 5068-5075 被引量:282
标识
DOI:10.1021/la8040506
摘要

The reaction mechanism of the hydrolysis of cellulose by a carbon-based solid acid, amorphous carbon containing graphene sheets bearing SO(3)H, COOH, and phenolic OH groups, has been investigated in detail through the hydrolysis of water-soluble beta-1,4-glucan. Whereas a range of solid strong Brønsted acid catalysts (inorganic oxides with acidic OH groups, SO(3)H-bearing resins, and the carbon-based solid acid) can hydrolyze the beta-1,4-glycosidic bonds in cellobiose (the shortest water-soluble beta-1,4-glucan), the tested solid acids except for the carbon material, consisting of conventional solid acids, cannot function as effective catalysts for the hydrolysis of cellohexaose (a long-chain water-soluble beta-1,4-glucan). However, the carbon material exhibits remarkable catalytic performance for the hydrolysis of cellohexaose: the turnover frequency (TOF) of SO(3)H groups in the carbon material exceeds ca. 20 times those of the conventional solid acids, reaching that of sulfuric acid, which is the most active catalyst. Experimental results revealed that inorganic oxides with acidic OH groups are not acidic enough to decompose the hydrogen and beta-1,4-glycosidic bonds in cellohexaose molecules aggregated by strong hydrogen bonds as well as cellulose and that the SO(3)H groups of the resins that do not adsorb beta-1,4-glucan are unable to attack the hydrogen and beta-1,4-glycosidic bonds in cellohexaose molecules effectively. In contrast, the carbon material is capable of adsorbing beta-1,4-glucan by phenolic OH or COOH groups in the carbon material, and SO(3)H groups bonded to the carbon therefore function as effective active sites for both decomposing the hydrogen bonds and hydrolyzing the beta-1,4-glycosidic bonds in the adsorbed long-chain water-soluble beta-1,4-glucan aggregate. These results suggest that the synergetic combination of high densities of the functional groups bonded to amorphous carbon causes the efficient hydrolysis of beta-1,4-glucan, including cellulose, on the carbon material.
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