Peroxydisulfate activation by sulfur-doped ordered mesoporous carbon: Insight into the intrinsic relationship between defects and 1O2 generation

过氧二硫酸盐 过硫酸盐 硫黄 化学 可重用性 碳纤维 催化作用 降级(电信) 分解 介孔材料 水处理 化学工程 无机化学 材料科学 有机化学 环境工程 环境科学 计算机科学 软件 电信 程序设计语言 复合材料 复合数 工程类
作者
Shiyu Liu,Cui Lai,Xuerong Zhou,Chen Zhang,Liang Chen,Huchuan Yan,Lei Qin,Danlian Huang,Haoyang Ye,Wenfang Chen,Ling Li,Mingming Zhang,Lin Tang,Fuhang Xu,Dengsheng Ma
出处
期刊:Water Research [Elsevier BV]
卷期号:221: 118797-118797 被引量:185
标识
DOI:10.1016/j.watres.2022.118797
摘要

The carbon-catalyzed persulfate-based advanced oxidation process (PS-AOP) has recently received much focus owing to the green, economical, and sustainable nature of carbon catalysts. In this study, sulfur-doped ordered mesoporous carbons (S-OMCs) were utilized to activate peroxydisulfate (PDS) for ciprofloxacin (CIP) removal. A synthesis temperature gradient was set to regulate the defect level of S-OMCs, since the thermal decomposition of oxygen- and sulfur-containing groups at different temperatures could release S and O and then create defects. In all S-OMCs/PDS systems, 1O2 dominated CIP degradation. Interestingly, a high linear correlation (R2 = 0.9091) between defect level and 1O2 yield was found, confirming the structure-activity relationship between defects and 1O2 generation. Moreover, the impacts of several important reaction conditions and water matrix on S-OMC-1000/PDS activation system were surveyed. In the S-OMC-1000/PDS activation system, CIP removal could attain 85.84% under the condition of unadjusted pH (pH = 5.3) and small amount of S-OMC-1000 (50 mg/L). The S-OMC-1000/PDS activation system also exhibited relatively stable or even better performance in the presence of common inorganic anions and natural organic matter (NOM), manifesting its good potential for practical applications. In addition, the reusability of S-OMC-1000 was investigated. This study provides a practical and high-efficiency way for decontaminating antibiotic-polluted water, and gives an alternative approach for identifying the active site of catalysts.
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