Yang Wenning, Yang Jie, Liu Erkang, Xing Ningning, Wang Dong, Yang Hua, Li Yongfei, Zhang Pengfang, Dou Jianmin
Shandong Provincial Key Laboratory of Chemical Energy Storage and Novel Cell Technology, School of Chemistry and Chemical Engineering, Liaocheng University, Liaocheng 252059, China.
Department of Pharmaceutical and Bioengineering, ZiBo Vocational Institute, ZiBo 255000, China.
J Colloid Interface Sci. 2025 Aug;691:137428. doi: 10.1016/j.jcis.2025.137428. Epub 2025 Mar 23.
The rational design and exploitation of cost-effective and robust catalysts for peroxymonosulfate (PMS) activation is of great significance. Herein, MnO/MnS nanoparticles encapsulated in Nitrogen-doped porous carbon skeleton (abbreviated as MnO/MnS@NPC) were first constructed through an easy two-step of impregnation along with subsequent pyrolysis technique and utilized to activate PMS for the elimination and mineralization of tetracycline (TC). Benefiting from the strong coupling of transition metal Mn with carbon-based material, the co-doping of heteroatom N and S, the enhanced electrical conductivity, and the hierarchical porous microarchitecture, the obtained MnO/MnS@NPC composite has been expected to present superior PMS activation capacity and pollutant elimination efficiency to its benchmark NPC and MnO@NPC, with 92.5 % degradation rate of TC within 60 min. Comprehensive investigations, involving quenching experiments, electron paramagnetic resonance (EPR) studies, in situ Raman identification, and electrochemical tests, jointly indicated that the non-radical pathways including electron-transfer, single oxygen (O) and the high-valent Mn-oxo species, especially the electron transfer process (ETP) from TC molecule to the metastable MnO/MnS@NPC-PMS* complex were dominantly responsible for PMS activation and further decomposition of TC, which greatly enhanced the selective removal of TC and the anti-interference capacity of the PMS system. Furthermore, the possible TC degradation routes were predicted by Density Functional Theory (DFT) calculation and the toxicity of degradation intermediates were also analyzed by toxicity assessment software. In addition, the heterogeneous catalyst displayed outstanding stability and reusability owing to the shield effect of NPC framework to MnO/MnS nanoparticles. Overall, this work proposed a prospective strategy for rationally designing and exploring heterogeneous PMS activator towards wastewater purification.
合理设计和开发用于过一硫酸盐(PMS)活化的具有成本效益且稳定的催化剂具有重要意义。在此,通过简单的两步浸渍法以及随后的热解技术,首次构建了包裹在氮掺杂多孔碳骨架中的MnO/MnS纳米颗粒(简称为MnO/MnS@NPC),并将其用于活化PMS以去除和矿化四环素(TC)。得益于过渡金属Mn与碳基材料的强耦合、杂原子N和S的共掺杂、增强的电导率以及分级多孔微结构,预期所制备的MnO/MnS@NPC复合材料相对于其对照材料NPC和MnO@NPC具有优异的PMS活化能力和污染物去除效率,在60分钟内TC的降解率达到92.5%。综合研究,包括猝灭实验、电子顺磁共振(EPR)研究、原位拉曼鉴定和电化学测试,共同表明包括电子转移、单线态氧(O)和高价锰氧物种在内的非自由基途径,特别是从TC分子到亚稳态MnO/MnS@NPC-PMS*复合物的电子转移过程(ETP),是PMS活化和TC进一步分解的主要原因,这极大地增强了TC的选择性去除和PMS系统的抗干扰能力。此外,通过密度泛函理论(DFT)计算预测了可能的TC降解途径,并通过毒性评估软件分析了降解中间体的毒性。此外,由于NPC骨架对MnO/MnS纳米颗粒的屏蔽作用,该非均相催化剂表现出出色的稳定性和可重复使用性。总体而言,这项工作为合理设计和探索用于废水净化的非均相PMS活化剂提出了一种前瞻性策略。