用g-C3N4/硅藻土复合材料调控Fe0@Fe3O4的结晶,增强光催化过氧单硫酸盐活化

Xinlin Wang, Xiangwei Zhang, Haiqin Zhou, Chunquan Li, Zhiming Sun
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摘要

光催化和过硫酸盐协同催化是近年来污水中难降解有机污染物的重要技术。在这项工作中,Fe0@Fe3O4通过简单的自组装过程成功地固定在缺氮g-C3N4/硅藻土复合材料(NGD)上。详细探讨了该复合材料的结构特点和在可见光下的过氧单硫酸盐活化能力。值得注意的是,NGD的引入影响了Fe0@Fe3O4的结晶度和形貌,形成了均匀分布的纳米颗粒,而不是不规则的、团块的棒状结构晶体。合成的Fe0@Fe3O4/缺氮g-C3N4/硅藻土复合材料(FNGD)对双酚a的去除率在15 min内达到95%以上。其降解速率常数(k)分别是NGD和裸Fe0@Fe3O4的59倍和27倍。通过径向猝灭实验和电子顺磁共振谱分析发现,空穴(hvb+)、单线态氧(1O2)和超氧自由基(•O2-)在FNGD/过氧单硫酸根/可见光体系中起主要作用。总的来说,本研究为g-C3N4/矿物基复合材料在废水处理中的可见光辅助过氧单硫酸盐活化提供了新的见解。
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Crystallization regulation of Fe0@Fe3O4 using a g-C3N4/diatomite composite for enhancing photocatalytic peroxymonosulfate activation
Photocatalysis and persulfate synergistic catalysis have recently become promising technologies for degrading refractory organic contaminants in effluents. In this work, Fe0@Fe3O4 is successfully immobilized on a N-deficient g-C3N4/diatomite composite (NGD) via a simple self-assembly process. The structural characteristics and peroxymonosulfate activation ability of the composite under visible-light irradiation are explored in detail. Notably, the introduction of NGD affects the crystallinity and morphology of Fe0@Fe3O4, forming homogenously distributed nanoparticles rather than irregular and agglomerated crystals with rod-like structures. The synthesized Fe0@Fe3O4/N-deficient g-C3N4/diatomite composite (FNGD) exhibits a superior removal percentage of bisphenol A (> 95% within 15 min). Furthermore, its degradation rate constant (k) is ~59 and ~27 times higher than those of NGD and bare Fe0@Fe3O4, respectively. Moreover, holes (hvb+), singlet oxygen (1O2) and superoxide free radicals (•O2-) play a major role in the FNGD/peroxymonosulfate/visible system based on radial quenching experiments and electron paramagnetic resonance spectra. Overall, this study provides novel insights into visible light-assisted peroxymonosulfate activation by the g-C3N4/mineral-based composite for wastewater treatment.
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