二硫化钼
化学
钼
盐度
废水
降级(电信)
电子顺磁共振
激活剂(遗传学)
水溶液中的金属离子
核化学
无机化学
环境化学
离子
化学工程
有机化学
环境工程
生态学
电信
生物化学
物理
核磁共振
计算机科学
基因
工程类
生物
作者
Yang Ye,Xiaonan Hu,Chuan Pu,Gang Ren,Gang Lu,Mingshan Zhu
出处
期刊:Chemosphere
[Elsevier]
日期:2023-06-15
卷期号:336: 139245-139245
被引量:2
标识
DOI:10.1016/j.chemosphere.2023.139245
摘要
Drawing on the robust activation activity and affinity that transition metal ions and MoS2 exhibit towards peroxymonosulfate (PMS), 1T/2H hybrid molybdenum disulfide doped with Fe3+ (Fe3+/N–MoS2) was synthesized to activate PMS for the treatment of organic wastewater. The ultrathin sheet morphology and 1T/2H hybrid nature of Fe3+/N–MoS2 were confirmed by characterization. The (Fe3+/N–MoS2 + PMS) system demonstrated excellent performance in the degradation of carbamazepine (CBZ) above 90% within 10 min even under high salinity conditions. By electron paramagnetic resonance and active species scavenging experiments, it was inferred that SO4•─ palyed a dominant role in the treatment process. The strong synergistic interactions between 1T/2H MoS2 and Fe3+ efficiently promoted PMS activation and generated active species. Additionally, the (Fe3+/N–MoS2 + PMS) system was found to be capable of high activity for CBZ removal in high salinity natural water, and Fe3+/N–MoS2 exhibited high stability during recycle tests. This new strategy of Fe3+ doped 1T/2H hybrid MoS2 for more efficient PMS activation provides valuable insights for the removal of pollutants from high salinity wastewater.
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