过硫酸盐
2,4-二氯苯酚
化学
碳纤维
纳米颗粒
催化作用
吸附
化学工程
纳米复合材料
木质素
无机化学
有机化学
材料科学
生物
复合数
细菌
工程类
复合材料
遗传学
作者
Chengfang Zhang,Danni Feng,Dong Wang,Lin-Lin Wang,Linan Liu,Jingchun Tang
标识
DOI:10.1016/j.jece.2023.110661
摘要
In this study, taking advantage of the amphiphilic properties of alkali lignin, carbon shell-encapsulated nano-zero-valent iron particles (AL@nZVI) anchored in a porous carbon framework were firstly synthesized by a combination of antisolvent reaction and carbothermal reduction method. AL@nZVI exhibited efficient catalytic performance for the activation of persulfate for the complete removal of 2,4-dichlorophenol at 30 min. The formation of a porous carbon skeleton and carbon shell enhanced the dispersibility and antioxidation of Fe0 nanoparticles and enabled long-term storage of AL@nZVI in air for more than 60 days. Furthermore, oxidation was mainly responsible for the removal of 2,4-dichlorophenol. The adsorption was determined to be 26.9% by analyzing the 2,4-dichlorophenol content in the used material. The generation of O2·−, SO4·−, 1O2 and·OH, was confirmed by EPR and scavenging experiments, and O2·− and 1O2 played dominant roles in the AL@nZVI+ persulfate system. The O2·−-guided free radical pathway was induced by activation of persulfate by Fe0 nanoparticles, while O2·− acted as a precursor to induce the 1O2-guided non-radical pathway. It is worth noting that CO may be favourable for the generation of 1O2. Moreover, the graphitized carbon, micropores, and structural defects contained in AL@nZVI created an electron-rich environment to facilitate the interaction between 2,4-dichlorophenol and reactive oxygen species. Therefore, the free radical and non-radical pathways were coupled to work together to degrade 2,4-dichlorophenol. This work not only develops a new synthesis method for core-shell structured carbon-coated nZVI composites, but also open the way for the high-value utilization of industrial by-products and the advanced oxidation degradation of organic pollutants in environmental remediation.
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