用 Fe-BiOCl 空心微球高效活化过一硫酸盐以去除卡马西平†。

Liyong Ding, Xuejuan Huang, Yuqin Liu, Qingqing Jiang and Juncheng Hu
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引用次数: 0

摘要

制备高效稳定的光催化剂,在可见光驱动下活化过一硫酸盐(PMS)以去除难处理的有机污染物,是一项极具吸引力的研究。本文通过常规的一步溶热法制备了一系列具有中空结构的 Fe-BiOCl 光催化剂,并将其用于活化 PMS 以降解卡马西平(CBZ)。得益于光催化和 PMS 活化的协同效应,3% Fe-BiOCl/PMS 系统在可见光照射下表现出更高的 CBZ 去除能力,相应的表观速率常数(k = 0.0449 min-1)是单个 BiOCl(k = 0.0037 min-1)的 12 倍。进一步的实验验证了掺入 Fe 和构建中空结构的 BiOCl 能够提高光的吸收和利用效率。更重要的是,引入的 Fe3+ 可以促进光生载流子的快速分离和 PMS 的活化。捕获实验和 EPR 测试表明,多种活性物种(OH˙、SO4˙-、1O2 和 O2˙-)参与了 CBZ 降解过程中 PMS 的活化,其中 SO4˙- 是主要的活性物种。此外,还探讨了光催化剂用量、PMS 浓度、初始溶液 pH 值和共存阴离子对 CBZ 去除的影响。还提出了光催化去除 CBZ 的可能机制。此外,3% 的 Fe-BOC 在连续四个循环中显示出卓越的光催化活性,这表明它可以成为实际应用中消除 CBZ 的可靠 PMS 活性剂。这项工作为构建高效、稳定的基于生物OCl 的催化系统提供了新思路,该系统可在可见光驱动下去除新出现的污染物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Efficient peroxymonosulfate activation by Fe–BiOCl hollow microspheres for carbamazepine removal†

Efficient peroxymonosulfate activation by Fe–BiOCl hollow microspheres for carbamazepine removal†

The preparation of highly effective and stable photocatalysts for visible-light-driven activation of peroxymonosulfate (PMS) to remove refractory organic contaminants is an attractive study. Herein, a series of Fe–BiOCl photocatalysts with a hollow structure were prepared through a regular one-step solvothermal approach and applied to activate PMS for carbamazepine (CBZ) degradation. Benefiting from the synergistic effect of photocatalysis and PMS activation, the 3% Fe–BiOCl/PMS system exhibits a higher CBZ removal ability under visible irradiation, with the corresponding apparent rate constant (k = 0.0449 min−1) being 12 times higher than that of individual BiOCl (k = 0.0037 min−1). Further experiments verify that the doping of Fe and the construction of the hollow structure of BiOCl can improve light absorption and utilization efficiency. More importantly, the introduced Fe3+ can facilitate the fast separation of photogenerated carriers and the activation of PMS. Capture experiments and EPR tests demonstrate that multiple active species (OH˙, SO4˙, 1O2 and O2˙) participate in the PMS activation for the CBZ degradation process, with SO4˙ being the primary active species. Furthermore, the effects of photocatalyst amount, PMS concentration, initial solution pH, and co-existing anions on CBZ removal were explored. A possible mechanism for the photocatalytic removal of CBZ is also proposed. In addition, the 3% Fe-BOC displays outstanding photocatalytic activity over four consecutive cycles, indicating that it could be a reliable PMS activator for CBZ elimination in practical application. This work provides new ideas for constructing efficient and stable BiOCl-based catalytic systems for visible-light-driven removal of emerging contaminants.

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