化学
臭氧
离解(化学)
分解
氧化还原
化学工程
化学反应
化学稳定性
纳米技术
化学分解
反应条件
氢氧化物
反应机理
化学能
工作(物理)
能量转换
化学过程
电场
科技与社会
碘
作者
Bosheng Chen,Cheng Ni,Lin Ding,Lei Miao,Zhu Luo,Jinlong Wang,Yanbing Guo
摘要
Microdroplet chemistry offers a promising platform for advancing green chemical processes; however, its limited reaction efficiency has restricted practical applications. Herein, we report a scalable iodide-mediated microdroplet system that markedly enhances stability and rate. The iodide-mediated microdroplet system (0.1 wt %) can achieve 100% ozone (O 3 ) decomposition at the gas–liquid interface for 120 h and exhibits continuous and stable characteristics. Experiments proved that compared with bulk solution, I – enrichment and strong O 3 affinity at microdroplet interfaces promote the accumulation of reactants and stabilize transition states. Moreover, the strong interfacial electric field induces hydroxide dissociation and drives electron-mediated regeneration of I – from iodine species, thereby sustaining continuous O 3 reduction. Compared with the spray reactor, the iodide-mediated microdroplet reactor achieves a 100% O 3 conversion, above 5-fold longer operational stability, 8.0% cost, and 10.4% energy consumption. Life cycle assessment further confirms its superior environmental and economic performance. This work provides a mechanistic understanding of the iodide-driven interfacial redox reaction and offers a scalable, green approach for O 3 purification.
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