磺胺嘧啶
碳化
硝酸盐
吸附
杂原子
金属有机骨架
兴奋剂
碳纤维
化学
降级(电信)
化学工程
氧化剂
无机化学
材料科学
复合材料
烷基
有机化学
复合数
生物化学
光电子学
工程类
抗生素
电信
计算机科学
作者
Da Li,Kehan Li,Liang Zhou,Juying Lei,Lingzhi Wang,Jinlong Zhang,Yongdi Liu
标识
DOI:10.1016/j.seppur.2023.123556
摘要
Using nitrate saturated metal–organic frameworks (MOFs) MIL-101-NH2(Fe) as precursors, N, O co-doped carbon/Fe composites (NOC/Fe-MIL) were synthesized by carbonization for activating peroxymonosulfate (PMS) to degrade sulfadiazine (SDZ). N and O species were doped into the carbon matrix by adsorbed nitrate, increasing the degradation rate of SDZ by 2.80 times compared to the original materials (NC/Fe-MIL). N, O co-doping not only increased the charge transfer rate on the materials surface, but also provided more pyridine N, CO groups and defects as main active sites for enhancing the adsorption to PMS indicated by DFT calculations, thus promoting the generation of O2− and 1O2 to degrade SDZ. More importantly, the NOC/Fe-MIL/PMS system still exhibited stable degradation performance in a wide pH range and in the presence of background anions, which can be used in a variety of complex water matrices and regenerated by heating, enabling it to be applied to practical wastewater treatment. This work will provide a general approach for preparing heteroatom modified materials and new insights for exploring critical roles of N and O species in PMS activation.
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