化学
电子转移
铜
金属
硫酸盐
降级(电信)
激活剂(遗传学)
无机化学
光化学
有机化学
生物化学
基因
电信
计算机科学
作者
Haoran Song,Shiting Pan,Yuwei Wang,Yanfei Cai,Wei Zhang,Yongming Shen,Changping Li
标识
DOI:10.1016/j.seppur.2022.121428
摘要
There exists an obvious contradiction between Cu(III) generation and Cu(I) contribution in reductants enhanced Cu(II)/peroxymonosulfate (PMS) process because the involved electron transfer pathways were always ignored in previous studies. This study investigated the MXene-mediated electron transfer mechanism in Cu(II)/PMS for the first time. The introduction of MXene significantly promoted atrazine degradation under acidic condition because the in-situ generation of Cu(I) was an excellent activator for PMS. Under alkaline condition, although addition of MXene generated a large amount of Cu(I), the degradation of atrazine was inhibited due to that the conversion of Cu(I) to Cu(III) was interrupted. The strong metal-support interaction (SMSI) altered the reactive intermediate species from Cu(III) (two-electron transfer) to hydroxyl radical (HO•) and sulfate radical (SO4•-) (one-electron transfer) under alkaline condition. This work proposed a novel MXene-mediated electron transfer mechanism and improved the understanding of Cu(III)/Cu(I) transformation pathway.
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