木质素
碳化
碳纤维
半纤维素
多孔性
材料科学
纤维素
化学工程
介孔材料
溶解
生物炭
生物量(生态学)
热解
扩散
化学
复合材料
有机化学
催化作用
扫描电子显微镜
复合数
工程类
地质学
物理
海洋学
热力学
作者
Huiying Xing,Guancong Jiang,Jingjing Xiong,Zetao Zhu,Lilong Zhang,Minjiao Chen,Jiahua Zhu
标识
DOI:10.1016/j.micromeso.2023.112653
摘要
The natural hierarchical pore structure existing in biomass provides favorable foundation for the design and preparation of carbon materials with 3D structure. However, it remains a challenge to understand the structure evolution from intrinsic micro-nano skeleton of natural wood to hierarchical porous carbon. In this study, a unique delignification process was used to remove lignin and hemicellulose without damaging the bulk structure of cellulose. The effects of the delignification process on pore structure during carbonization and activation were examined. It was found that biochar with fine micropores and hierarchical pores could be prepared through controlled dissolution of lignin, resulting in an SBET and Vtotal of 880 m2/g and 0.36 cm3/g respectively. The developed micropores then contributed to improved gas diffusion during the activation process, leading to mesoporous carbon materials with an SBET of 1310 m2/g and Vtotal of 1.08 cm3/g after 30 min. This research shed light on understanding how natural wood can be converted into hierarchical porous carbon by removing lignin followed by CO2 activation, significantly improving its potential for use as a porous material.
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