过氧二硫酸盐
化学
试剂
过氧化物
猝灭(荧光)
电子转移
氧化还原
反应机理
亲核细胞
催化作用
过氧化氢
组合化学
无机化学
光化学
荧光
有机化学
物理
量子力学
作者
Hongyu Zhou,Heng Zhang,Yongli He,Bingkun Huang,Chenying Zhou,Gang Yao,Bo Lai
标识
DOI:10.1016/j.apcatb.2021.119900
摘要
Abstract In this review, we systematically summarized the origins, development, basic mechanism and limits of reductant-enhanced iron-based peroxide activation processes (including H2O2, peroxymonosulfate and peroxydisulfate). Notably, the use of reductants would simultaneously accelerate the reduction of Fe3+ and quench the production of reactive species. This trade-off between Fe3+ reduction and reactive species consumption is mainly determined by two aspects, i.e. (i) intrinsic chemical properties like electron transfer pathways and reaction rates with reactive species, and (ii) experimental conditions like reagent dosage ratio, dissolved O2 and pH. Therefore, we first reviewed the characteristics of different iron/peroxide/reductant systems in terms of the above two aspects. Then, we evaluated the practical application potential of different reductants based on their toxicity, costs and self-transformation products. Finally, newly-emerging enhancement strategies like multiple dosing and regulation of phase and crystalline degree were summarized, and future research needs were proposed.
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