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Preparation of a Sulfonated Porous Carbon Catalyst with High Specific Surface Area

机译:高比表面积磺化多孔碳催化剂的制备

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摘要

A sulfonated (SO3H-bearing) carbon catalyst with mesoporous structure and high specific surface area is successfully prepared by impregnating the cellulosic precursor (wood powder) with ZnCl2 prior to activation and sulfonation. The specific surface area of the porous carbon catalyst thus prepared is also found to increase with carbonization temperature to a maximum of 1,560 m~2 g~(-1) at ca. 773 K. Structural analyses reveal that the porous carbon catalysts carbonized at temperatures higher than 723 K contain high densities of micro- and mesopores. The porous carbon catalyst exhibits high catalytic performance for the esterification of acetic acid (343 K), the activity for which is dependent only on the acid density. The porous carbon catalyst also exhibits high catalytic activity for the benzylation of toluene, whereas non-porous sulfonated carbon has very limited activity for this reaction. The activity for the benzylation of toluene is dependent on both the specific surface area and the acid density of the sulfonated porous carbon catalyst.
机译:通过在活化和磺化之前用ZnCl2浸渍纤维素前体(木粉),成功制备了具有介孔结构和高比表面积的磺化(含SO3H)碳催化剂。还发现由此制得的多孔碳催化剂的比表面积随碳化温度在约200℃下增加至最大1,560m〜2g〜(-1)。 773K。结构分析表明,在高于723 K的温度下碳化的多孔碳催化剂含有高密度的微孔和中孔。多孔碳催化剂对乙酸(343 K)的酯化反应显示出高催化性能,其活性仅取决于酸密度。多孔碳催化剂对甲苯的苄基化也显示出高催化活性,而无孔磺化碳对该反应的活性非常有限。甲苯苄基化的活性取决于磺化多孔碳催化剂的比表面积和酸密度。

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