Fe3+和H2O2辅助多巴胺在三聚氰胺泡沫上快速聚合以激活PMS降解有机污染物†

IF 3.5 4区 环境科学与生态学 Q3 ENGINEERING, ENVIRONMENTAL
Haoxiang Yan, Jianzheng Zhen and Yuyuan Yao
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引用次数: 0

摘要

开发一种简便的制备方法来构建可分离和可回收的类芬顿催化剂在环境修复领域具有重要意义。本文提出了一种快速多巴胺(DA)聚合改性三聚氰胺泡沫(MF)的策略,用于构建块状泡沫催化材料,并进一步用于过一硫酸盐(PMS)活化降解有机污染物。利用多巴胺的儿茶酚基团与 Fe3+ 之间的螯合作用以及 H2O2 提供的氧化环境,DA 可在 2 小时内包覆并聚合在 MF 表面,从而获得 MF@Fe@PDA 催化剂。详细的实验结果表明,MF@Fe@PDA 可高效活化 PMS,在 20 分钟内实现对双酚 A(BPA)近 100%的去除,其相应的翻转频率(TOF)值比均相(Fe2+、Fe3+)和纳米颗粒(Fe0)催化剂高出一个数量级。MF@Fe@PDA/PMS体系的高活性源于Fe位点和羰基(CO)可诱导PMS活化,快速生成单线态氧(1O2)、硫酸根自由基(SO4˙-)和羟自由基(˙OH)。同时,MF@Fe@PDA/PMS 系统中共存的碳酸氢根离子(HCO3-)可促进 1O2 的生成,从而加速双酚 A 的降解。此外,在块状 MF@Fe@PDA 催化剂的辅助下,还构建了一个用于降解有机污染物的流经系统。总之,这些发现为开发用于废水修复的高效催化剂提供了新的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fe3+ and H2O2 assisted dopamine rapid polymerization on melamine foam to activate PMS for organic pollutant degradation†

Fe3+ and H2O2 assisted dopamine rapid polymerization on melamine foam to activate PMS for organic pollutant degradation†

Developing a facile preparation method to construct separable and recyclable Fenton-like catalysts holds great significance in the field of environmental remediation. Herein, a rapid dopamine (DA) polymerization strategy to modify melamine foam (MF) was proposed for the construction of bulk foam catalytic materials, which was further utilized for peroxymonosulfate (PMS) activation to degrade organic pollutants. Taking advantage of the chelation between dopamine's catechol group and Fe3+, as well as the oxidative environment provided by H2O2, DA could encapsulate and polymerize on the surface of MF within 2 h to obtain the MF@Fe@PDA catalyst. Detailed experimental results demonstrated that MF@Fe@PDA could efficiently activate PMS to achieve almost 100% removal of bisphenol A (BPA) in 20 min, and the corresponding turnover frequency (TOF) value was one order of magnitude higher than that of the homogeneous (Fe2+, Fe3+) and nanoparticle (Fe0) catalysts. The high activity of the MF@Fe@PDA/PMS system stemmed from the Fe sites and carbonyl group (CO), which could induce the activation of PMS for the rapid generation of singlet oxygen (1O2), sulfate radical (SO4˙) and hydroxyl radicals (˙OH). Meanwhile, the coexisting bicarbonate ions (HCO3) in the MF@Fe@PDA/PMS system could enhance the generation of 1O2, thereby accelerating the degradation of BPA. Moreover, a flow-through system assisted by the bulk MF@Fe@PDA catalyst was constructed for organic pollutant degradation. Overall, these findings may open up new possibilities for developing highly efficient catalysts for wastewater remediation.

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来源期刊
Environmental Science: Water Research & Technology
Environmental Science: Water Research & Technology ENGINEERING, ENVIRONMENTALENVIRONMENTAL SC-ENVIRONMENTAL SCIENCES
CiteScore
8.60
自引率
4.00%
发文量
206
期刊介绍: Environmental Science: Water Research & Technology seeks to showcase high quality research about fundamental science, innovative technologies, and management practices that promote sustainable water.
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