Porous hydrochar loaded nZVI as an efficient catalyst to activate persulfate for phenol degradation: Performance and mechanism

被引:7
|
作者
Cao, Bo [1 ]
Qu, Jianhua [1 ]
Bian, Wenhui [1 ]
Hu, Qiqi [1 ]
Fu, Xinyan [1 ]
Zhang, Guangshan [2 ]
Zhang, Yuezhi [1 ]
Tao, Yue [1 ]
Jiang, Zhao [1 ]
Zhang, Ying [1 ]
机构
[1] Northeast Agr Univ, Sch Resources & Environm, Harbin 150030, Peoples R China
[2] Qingdao Agr Univ, Coll Resource & Environm, Qingdao Engn Res Ctr Rural Environm, Qingdao 266109, Peoples R China
基金
中国博士后科学基金;
关键词
nZVI; Porous hydrochar; Persulfate activation; Degradation; BIOCHAR;
D O I
10.1016/j.jclepro.2024.141221
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Persulfate (PS) activation by nano zerovalent iron (nZVI) is promising for water purification, which is restricted due to its easy agglomeration and oxidation. Herein, porous hydrochar loaded nZVI (nZVI@PHC) was successfully synthesized by one-step process. nZVI@PHC not only had excellent adsorption capacity (178.6 mg/g) and abundant functional groups, but also possessed highly dispersed nZVI for PS activation to produce reactive oxygen species. Impressively, 0.2 g/L of nZVI@PHC (PHC/nZVI = 5:3) and 0.4 g/L of PS could achieve 99.7 % of phenol removal within 10 min. Moreover, nZVI@PHC/PS system showed superior applicability among wide range of initial pH (3.0-9.0) and temperatures (25-55 degrees C). Phenol removal mechanisms were elaborated by dissolved iron ions, scavenging experiments, and electronic paramagnetic spectrometer. As a result, both non-free radical pathway mediated by O-1(2) and free radical pathway (SO4 center dot-, HO center dot, and O-2(center dot-)) participated in phenol degradation. Additionally, nZVI@PHC/PS system had favorable reusability and high tolerance to co-existing substance and different water bodies. This study provides a promising strategy to tailor highly active nZVI for PS activation to organic contaminants degradation.
引用
收藏
页数:10
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