The global shortage of freshwater and inadequate supply of clean water have necessitated the implementation of robust technologies for wastewater purification, and Fenton-like chemistry is a highly-promising approach. However, realizing the rapid Fenton-like chemistry for high-efficiency degradation of organic micropollutants (OMs) remains challenging. Herein, one novel system was constructed by a Co single-atom catalyst activating peroxymonosulfate (PMS), and the optimal system (SA-Co-NBC-0.2/PMS) achieved unprecedented catalytic performance towards a model OM [Iohexol (IOH)], i.e., almost 100% decay ratio in only 10 min (the observed rate constant: 0.444 min -1 ) with high electrophilic species 1 O 2 (singlet oxygen) generation. Theoretical calculations unveiled that Co-N 4 sites preferred to adsorb the terminal-O of PMS (more negative adsorption energy than other O sites: -32.67 kcal/mol), promoting the oxidation of PMS to generate 1 O 2 . Iodine (I)23 (0.1097), I24 (0.1154) and I25 (0.0898) on IOH with higher f - electrophilic values were thus identified as the main attack sites. Furthermore, 16S ribosomal RNA high-throughput sequencing and quantitative structure-activity relationship analysis illustrated the environmentally-benign property of the SA-Co-NBC-0.2 and the tapering ecological risk during IOH degradation process. Significantly, this work comprehensively checked the competence of the SA-Co-NBC-0.2/PMS system for organics abatement in practical wastewater.
Keyphrases
- wastewater treatment
- high efficiency
- molecular dynamics
- hydrogen peroxide
- reduced graphene oxide
- structure activity relationship
- high throughput sequencing
- room temperature
- metal organic framework
- visible light
- healthcare
- primary care
- water soluble
- gold nanoparticles
- molecular dynamics simulations
- density functional theory
- climate change
- computed tomography
- electron transfer
- nitric oxide
- carbon dioxide
- risk assessment
- mass spectrometry
- data analysis
- nucleic acid
- energy transfer