石墨烯
阳极
氯化物
无机化学
氧化物
电解质
化学工程
电化学
材料科学
电极
化学
有机化学
纳米技术
工程类
物理化学
作者
Luis Baptista‐Pires,Giannis-Florjan Norra,Jelena Radjenović
出处
期刊:Water Research
[Elsevier BV]
日期:2021-08-02
卷期号:203: 117492-117492
被引量:60
标识
DOI:10.1016/j.watres.2021.117492
摘要
Graphene-based sponges doped with atomic nitrogen and boron were applied for the electrochemical degradation of persistent organic contaminants in one-pass, flow-through mode, and in a low-conductivity supporting electrolyte. The B-doped anode and N-doped cathode was capable of >90% contaminant removal at the geometric anodic current density of 173 A m2. The electrochemical degradation of contaminants was achieved via the direct electron transfer, the anodically formed O3, and by the OH radicals formed by the decomposition of H2O2 produced at the cathode. The identified transformation products of iopromide show that the anodic cleavage of all three C-I bonds at the aromatic ring was preferential over scissions at the alkyl side chains, suggesting a determining role of the pi-pi interactions with the graphene surface. In the presence of 20 mM sodium chloride (NaCl), the current efficiency for chlorine production was <0.04%, and there was no chlorate and perchlorate formation, demonstrating a very low electrocatalytic activity of the graphene-based sponge anode towards chloride. Graphene-based sponges were produced using a low-cost, bottom-up method that allows easy introduction of dopants and functionalization of the reduced graphene oxide coating, and thus tailoring of the material for the removal of specific contaminants.
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