摘要
Advanced oxidation processes (AOPs) surpass photocatalytic methods in energy efficiency, enabling organic dye degradation under mild conditions without light activation. In this study, we crafted a highly effective Zr(WO 4 ) 2 catalyst for AOPs, rigorously characterized through SEM, TEM, TG-DTA, N 2 -sorption, XRD, and XPS analyses. The system demonstrated exceptional catalytic performance, achieving 95.62 % phenol removal (2 mg/L) within 60 min using only 0.1 g/L Zr(WO 4 ) 2 and 1 mM PMS, with singlet oxygen ( 1 O 2 ) identified as the dominant reactive species. Crucially, the synergistic redox interplay between Zr 4+ and WO 4 2− surface species emerged as the critical driver for efficient PMS activation. Beyond its catalytic prowess, the Zr(WO 4 ) 2 system exhibited remarkable reusability and versatility across multiple applications, while generating treated water with minimal toxicity, positioning it as an environmentally promising solution.
危险品化学品经营许可证(带存储)