过氧二硫酸盐
稻草
学位(音乐)
多孔性
比表面积
碳纤维
固碳
化学工程
化学
材料科学
废物管理
环境科学
农学
二氧化碳
冶金
无机化学
复合材料
生物
催化作用
有机化学
工程类
物理
钾
复合数
声学
作者
Xiaodan Tang,Tingting Dong,Mengya Wang,Shuanglong Ma,Shengjun Xu,Jingzhen Wang,Boqiang Gao,Yan Huang,Qiuyun Yang,Dangling Hua,Sihui Zhan
标识
DOI:10.1016/j.jhazmat.2024.134422
摘要
Electron transfer pathways have been verified as overriding regimes when peroxydisulfate (PDS) was activated by porous carbon. The incorporation of graphitic structure into carbon matrix was favorable to the rapid electron transfer, but excessive graphitization would deteriorate the specific surface area (SSA), weakening the catalytic performance. The reasonable trade-off between SSA and graphitization degree was necessary and challenging for the preparation of efficient carbon based PS-activators. Herein, a series of graphitic porous carbon with discrepant SSA and graphitic structure were fabricated. The incorporation of graphitization tracks into ultra-thin edges on porous carbon film was verified by multifarious structural characterization. After trade-off, the optimum catalyst exhibited superior catalytic performance with degradation rate constant (kobs) exceeding that of ungraphitized precursor by up to 16.0 times. Mechanistic investigations substantiated that the sufficient SSA of catalyst provided favorable conditions for its affinity towards PDS and sulfadiazine (SDZ), resulting in the formation of PDS* complexes and SDZ adsorption, while the appropriate graphitization degree ensured the reinforced electron transfer rate, which collectively accelerated SDZ oxidation through electron-transfer pathway. The multivariate linear regression model linking kobs to SSA and graphitization degree was established providing basis to construct efficient catalysts for PDS activation.
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