Tian Wenjie, Sun Hongqi, Duan Xiaoguang, Zhang Huayang, Ren Yongxiang, Wang Shaobin
School of Chemical Engineering and Advanced Materials, The University of Adelaide, Adelaide, SA 5005, Australia.
School of Engineering, Edith Cowan University, 270 Joondalup Drive, Joondalup, WA 6027, Australia.
J Hazard Mater. 2020 May 5;389:121881. doi: 10.1016/j.jhazmat.2019.121881. Epub 2019 Dec 11.
The biomass, bottlebrush flower, is exploited for the preparation of functionalized porous carbons by one-pot thermal activation using NaHCO and dicyandiamide. An intensified cross-linking effect among the precursors boosts pore (especially mesopore) formation in the pyrolysis process, producing N-doped porous carbons (NPCs) with a large specific surface area (SSA, up to 2025 m g). The biomass-derived carbon samples turn out to be highly effective in adsorption, and catalytic activation of peroxymonosulfate for degradation of aqueous phenol and p-hydroxybenzoic acid (HBA) in single and binary systems. The effects of N content, porous structure, and trace Ni species on the adsorptive and catalytic behavior of carbon are investigated. It is found that the porous structure plays a more critical role in adsorption than surface N functionality, while the contributions of various reactive species for phenol and HBA degradation are different.
生物质“瓶刷花”通过使用碳酸氢钠和双氰胺进行一锅法热活化来制备功能化多孔碳。前驱体之间增强的交联效应促进了热解过程中孔(特别是中孔)的形成,从而制备出具有大比表面积(高达2025 m²/g)的氮掺杂多孔碳(NPCs)。结果表明,生物质衍生的碳样品在单体系和双体系中对水中苯酚和对羟基苯甲酸(HBA)的吸附以及过一硫酸盐的催化活化降解方面具有高效性。研究了氮含量、多孔结构和痕量镍物种对碳的吸附和催化行为的影响。结果发现,多孔结构在吸附中比表面氮官能团起更关键的作用,而各种活性物种对苯酚和HBA降解的贡献则有所不同。