Biomass-derived functional porous carbons for adsorption and catalytic degradation of binary micropollutants in water

被引:0
|
作者
Tian, Wenjie [1 ]
Sun, Hongqi [2 ]
Duan, Xiaoguang [1 ]
Zhang, Huayang [1 ]
Ren, Yongxiang [3 ]
Wang, Shaobin [1 ]
机构
[1] Univ Adelaide, Sch Chem Engn & Adv Mat, Adelaide, SA 5005, Australia
[2] Edith Cowan Univ, Sch Engn, 270 Joondalup Dr, Joondalup, WA 6027, Australia
[3] Xian Univ Architecture & Technol, Key Lab Northwestern Water Resource & Environm Ec, Shaanxi Key Lab Environm Engn, Minist Educ, Xian 710055, Peoples R China
基金
澳大利亚研究理事会;
关键词
Biomass; Functionalized porous carbon; Adsorption; Advanced oxidation processes; Multicomponent system; REDUCED GRAPHENE OXIDE; ADVANCED OXIDATION; CO2; CAPTURE; ACTIVATION; OXYGEN; PORES; PEROXYMONOSULFATE; PHENOL; CONTAMINANTS; POLLUTANTS;
D O I
10.1016/j.jhazmat.2019.121881
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The biomass, bottlebrush flower, is exploited for the preparation of functionalized porous carbons by one-pot thermal activation using NaHCO3 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 2025m(2) g(-1)). 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.
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页数:9
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