Schroeder Chelsea M, Denucci Lucas W, Leadbeater Nicholas E
Department of Chemistry, University of Connecticut 55 North Eagleville Road Storrs Connecticut 06269 USA
RSC Adv. 2025 Sep 1;15(38):31289-31295. doi: 10.1039/d5ra04183j. eCollection 2025 Aug 29.
This study explores a phosphate-based electrochemical advanced oxidation process (EAOP) for the decolourisation of synthetic dyes in wastewater. A real-time UV-Vis spectrophotometric system enabled continuous monitoring of dye decolourisation, allowing for high-throughput optimisation of reaction conditions using phenol red as a model compound. The optimised system demonstrated superior performance compared to anodic oxidation and electrochemically activated persulphate systems. Further analysis of six triarylmethane dyes revealed that structural features, such as substitution near the central carbon and halogenation, significantly impact decolourisation efficiency. Among the dyes studied, bromocresol purple exhibited the fastest decolourisation, reaching 99% colour removal in 19 min, while tetrabromophenol blue was the slowest, requiring 34 min to reach a smilar level of decolourisation. Overall, this system offers an effective, pH-stable, and environmentally conscious alternative for wastewater remediation.
本研究探索了一种基于磷酸盐的电化学高级氧化工艺(EAOP)用于废水中合成染料的脱色。一个实时紫外可见分光光度系统能够连续监测染料脱色情况,从而可以使用酚红作为模型化合物对反应条件进行高通量优化。与阳极氧化和电化学活化过硫酸盐系统相比,优化后的系统表现出卓越的性能。对六种三芳基甲烷染料的进一步分析表明,诸如中心碳附近的取代和卤化等结构特征对脱色效率有显著影响。在所研究的染料中,溴甲酚紫脱色最快,在19分钟内达到99%的脱色率,而四溴酚蓝最慢,需要34分钟才能达到类似的脱色水平。总体而言,该系统为废水修复提供了一种有效、pH稳定且环保的替代方案。