Single-atom catalysis steers polymerization pathways in water treatment: from atomic-level mechanisms to low-carbon engineering
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Updated: Nov 9, 2026

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
Published on: April 22, 2016
Sen Feng1, Wenqian Wu1, Dan Sheng1
1Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resource Reuse, School of Environmental and Chemical Engineering, Nanchang Hangkong University, Nanchang 330063, China.
Abstract:
Unlike mineralization, polymerization pathways can convert wastewater pollutants into recoverable solid polymers, cutting oxidant use and carbon emissions while recovering carbon. Single-atom catalysts (SACs), featuring atomically dispersed metal centers, tunable coordination environments, and maximal atomic utilization, are ideal for steering polymerization pathways. Although research on SACs in polymerization pathways continues to advance, a multi scale framework that systematically integrates their electronic structure design with engineering applications is still lacking. To fill this gap, this review presents such a framework across microscopic, mesoscopic, and macroscopic scales. At the microscopic level, d-band center, spin-state, and coordination microenvironment are regulated to confine reactive species within the polymerization-favorable thermodynamic window. From a mesoscopic perspective, nanoconfinement, forced convection, and multi active site synergy overcome mass transfer and radical-collision bottlenecks. As for a macroscopic level, reactor scale up, polymer product separation/recovery, resource utilization, and economic assessment are discussed. This review provides theoretical guidance and design principles for advancing SACs driven polymerization pathways from fundamental research toward low-carbon water treatment technologies.
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