Low consumption Fenton-like water purification through pollutants as electron donors substituting H2O2 consumption via twofold cation-π over MoS2 cross-linking g-C3N4 hybrid

羟基化 污染物 化学 催化作用 瓶颈 分解 化学工程 计算机科学 有机化学 嵌入式系统 工程类
作者
Lai Lyu,Chao Lu,Yingtao Sun,Wenrui Cao,Tingting Gao,Chun Hu
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:320: 121871-121871 被引量:59
标识
DOI:10.1016/j.apcatb.2022.121871
摘要

A twofold cation-π-assembled catalyst consisting of honeycomb microsphere-like MoS 2 cross-linking g-C 3 N 4 hybrid (HM-MS/CN) is first developed to address the bottleneck of excessive resource and energy consumption in Fenton chemistry. A series of modern characterization techniques combined with theoretical calculation are used to reveal and verify the twofold cation-π interaction (Mo-O-C and Mo-S-C bonding bridges). It is found that the electrons of pollutants can be captured by H 2 O 2 and O 2 through the twofold cation-π interaction during Fenton-like reaction, which inhibits the oxidative decomposition of H 2 O 2 and promotes its hydroxylation. As a result, HM-MS/CN shows excellent performance for water purification by initiating pollutants as electron donors substituting H 2 O 2 consumption under mild natural conditions, and the actual consumption of H 2 O 2 in this system is only 6-8% of that in the common Fenton systems. This discovery is of great significance for the development of novel water purification technology with high efficiency and low consumption. • A twofold cation-π-assembled catalyst consisting of HM-MS/CN is first prepared. • HM-MS/CN shows excellent performance for actual water purification. • The actual consumption of H 2 O 2 is only 6-8% of that in the common Fenton systems. • Twofold cation-π interaction based on Mo-O-C and Mo-S-C is responsible for excellent performance. • Pollutants act as electron donors substituting H 2 O 2 consumption via twofold cation-π.
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