Deep Oxidation Removal of Nitric Oxide and SO(2) via Singlet Oxygen and Hydroxyl Radicals in the LaCoO(3‑δ)/H(2)O(2) System

LaCoO(3-δ)/H(2)O(2)体系中单线态氧和羟基自由基对一氧化氮和二氧化硫的深度氧化去除

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Abstract

This study proposes a novel LaCoO(3‑δ)/H(2)O(2) Fenton-like process for the efficient generation of nonradical singlet oxygen ((1)O(2)) and hydroxyl radicals ((•)OH), enabling the deep oxidation of nitric oxide (NO), as well as simultaneous denitrification and desulfurization. A LaCoO(3‑δ) perovskite material enriched with Co(3+) ions and oxygen vacancies (OV) was successfully synthesized by using a one-step citric acid sol-gel method. OV enhances electron mobility and expedites the redox cycling of surface Co(2+)/Co(3+) pairs, thereby promoting the generation of (•)OH and (•)O(2) (-). The high Co(3+) content further facilitates the transformation of (•)O(2) (-) into (1)O(2). Moreover, electron-rich centers and highly reactive lattice oxygen (O(2-)) induced by abundant OV also contribute to the activation of H(2)O(2), enhancing the production of (•)OH and (1)O(2). When combined with a comprehensive Na(2)SO(3)/NaOH absorption system, simultaneous removal efficiencies of 91.2% for NO and 100% for SO(2) were achieved under optimal experimental conditions while ensuring good operational stability. This innovative noniron-based Fenton-like system not only rivals the performance of typical iron-based Fenton-like systems but also provides new insights into the development of multipollutant deep oxidation removal technologies for application in coal-fired power plants.

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