Lei Chao, Mao Mufan, Wang Xuxu, Chen Wenqian, Lei Xiaojia, Xie Jituo, Hu Yongyou, Feng Chunhua, Huang Binbin
School of Hydraulic Engineering, Changsha University of Science & Technology, Changsha 410114, China.
School of Hydraulic Engineering, Changsha University of Science & Technology, Changsha 410114, China; Key Laboratory of Environmental Biology and Pollution Control, Ministry of Education, College of Environmental Science and Engineering, Hunan University, Changsha 410082, China.
J Colloid Interface Sci. 2025 Dec 15;700(Pt 3):138602. doi: 10.1016/j.jcis.2025.138602. Epub 2025 Jul 30.
Permanganate (PM)-based advanced oxidation process (AOP) is a promising methodology for the efficient degradation of organic pollutants and water purification. Photocatalytic PM activation is an attractive strategy by using clean sustainable solar irradiation, but still faces great challenges in terms of energy source (i.e., ultraviolet light) and catalyst recovery. Here we report a visible light (VL)-driven photocatalytic PM activation strategy as a new platform technology that enables highly efficient degradation of organic pollutants by coupling PM oxidation with photocatalysis. This platform technology is compatible with a wide range of photocatalysts, refractory organic pollutants, pH conditions, and real-water systems. Using micron‑bismuth vanadate (BiVO) and ciprofloxacin (CIP) as the model catalyst and pollutant, a rapid and complete degradation of CIP was achieved within 7 min with an apparent rate constant of 0.52 min, which was 40 and 9 times higher than those of the PM oxidation and VL-assisted PM oxidation processes, respectively. Physical, theoretical, and in situ spectroscopy investigations showed that the thermodynamically favorable adsorption of PM on BiVO significantly enhanced the separation and utilization of photogenerated electrons, resulting in the concurrent formations of reactive manganese and oxygen species with the former as the primary oxidizing species, and hence contributed to the superior oxidation performance. This strategy achieves a synergy between PM oxidation and photocatalysis that can address their respective critical challenges. Importantly, a horizontal-flow photocatalytic reactor was designed that enabled a continuous degradation of CIP with water treatment capacity of 20 L h under outdoor solar irradiation. This study provides new insight into photocatalytic PM activation and offers a robust AOPs for water purification.
基于高锰酸盐(PM)的高级氧化工艺(AOP)是一种用于高效降解有机污染物和水净化的有前景的方法。光催化PM活化是一种利用清洁可持续的太阳辐射的有吸引力的策略,但在能源(即紫外光)和催化剂回收方面仍面临巨大挑战。在此,我们报告一种可见光(VL)驱动的光催化PM活化策略,作为一种新的平台技术,通过将PM氧化与光催化耦合,能够高效降解有机污染物。该平台技术与多种光催化剂、难降解有机污染物、pH条件和实际水系统兼容。以微米级钒酸铋(BiVO)和环丙沙星(CIP)作为模型催化剂和污染物,在7分钟内实现了CIP的快速完全降解,表观速率常数为0.52 min,分别比PM氧化和VL辅助PM氧化过程高40倍和9倍。物理、理论和原位光谱研究表明,PM在BiVO上的热力学有利吸附显著增强了光生电子的分离和利用,导致同时形成活性锰和氧物种,前者为主要氧化物种,从而有助于优异的氧化性能。该策略实现了PM氧化和光催化之间的协同作用,可以解决它们各自的关键挑战。重要的是,设计了一种水平流光催化反应器,在室外太阳辐射下能够连续降解CIP,水处理能力为20 L h。本研究为光催化PM活化提供了新的见解,并为水净化提供了一种强大的AOPs。