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在纳滤膜分解过程中不产生羟基自由基的芬顿反应机制。

Fenton reaction mechanism generating no OH radicals in Nafion membrane decomposition.

作者信息

Tsuneda Takao

机构信息

Graduate School of Science, Technology, and Innovation, Kobe University, Kobe, 657-8501, Japan.

Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo, 060-0810, Japan.

出版信息

Sci Rep. 2020 Oct 23;10(1):18144. doi: 10.1038/s41598-020-74646-0.

Abstract

Mechanism of Fenton reaction, which is a most widely-used degradation test for organic materials using hydrogen peroxide (H[Formula: see text]O[Formula: see text]) and iron (Fe) cations, is revealed for the decomposition of hydrated Nafion membrane. This reaction mechanism has been assumed to generate OH radicals. For a doubly-hydrated Nafion membrane model, Fenton reaction with divalent and monovalent Fe (Fe[Formula: see text] and Fe[Formula: see text]) cation hydration complexes is explored for experimentally-supported hydration numbers using long-range correction for density functional theory. As a result, it is found that H[Formula: see text]O[Formula: see text] coordinating to the Fe[Formula: see text] hydration complexes first approaches Nafion side chains in high humidity, then leads to the C-S bond dissociation of the side chain to produce carbonic acid group and sulfonic acid ion. On the other hand, once electron transfer proceeds between iron ions, the O-O bond of the coordinating H[Formula: see text]O[Formula: see text] is extended, then the C-S bond is dissociated to produce trihydroxymethyl group and sulfur trioxide, which are rapidly transformed to carboxyl group and sulfonic acid ion in aquo. This mechanism is confirmed by the vibrational spectrum analysis of the decomposed product. Collective Nafion decomposition mechanisms also suggest that the decomposition reaction uses the recycle of generated Fe cation hydration complexes under acidic condition near membrane surface.

摘要

芬顿反应是一种使用过氧化氢(H₂O₂)和铁(Fe)阳离子对有机材料进行降解的广泛应用的测试方法,本文揭示了其对水合Nafion膜的分解机制。该反应机制被认为会产生羟基自由基。对于双水合Nafion膜模型,利用密度泛函理论的长程校正,探索了二价和一价铁(Fe²⁺和Fe³⁺)阳离子水合络合物的芬顿反应,以获得实验支持的水合数。结果发现,与Fe²⁺水合络合物配位的H₂O₂在高湿度下首先接近Nafion侧链,然后导致侧链的C-S键断裂,生成碳酸基团和磺酸离子。另一方面,一旦铁离子之间发生电子转移,配位的H₂O₂的O-O键就会伸长,然后C-S键断裂,生成三羟甲基和三氧化硫,它们在水中迅速转化为羧基和磺酸离子。通过对分解产物的振动光谱分析证实了这一机制。Nafion的集体分解机制还表明,分解反应利用了膜表面附近酸性条件下生成的Fe阳离子水合络合物的循环。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/211a/7584670/9765b564eb7e/41598_2020_74646_Fig1_HTML.jpg

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