硝化作用
逆流交换
化学
选择性
动力学
相(物质)
反应条件
溶解
反应速率
组合化学
化学动力学
水溶液
反应中间体
催化作用
分析物
微流控
色谱法
反应机理
动能
化学工程
作者
Jing Song,Yongqi Pan,Ruobing Xin,Zifei Yan,Tianyao Tang,Kai Yu Wang,Yujun Wang,Jian Deng,Guangsheng Luo
标识
DOI:10.1038/s41467-026-69902-2
摘要
Aromatic nitration, a hazardously complex process, poses serious risks. A major challenge for the reaction is the trade-off effect between spatiotemporal conversion rate and selectivity, particularly the over-nitration side reactions that have plagued the field for nearly 200 years. We propose a countercurrent microflow mode between two microreactors, which boosts spatiotemporal conversion rate by over five times compared to the normal single-stage co-current microflow mode, and two orders of magnitude compared to traditional batch reactors. Meanwhile, we identify an inhibition mechanism of over-nitration. The generated H2O in the main reaction can in situ reduce the dissolution of nitroaromatics in the aqueous phase and effectively prevent over-nitration. Through synergistic control of both kinetics and thermodynamics in the microreaction process, high spatiotemporal conversion and selectivity are achieved simultaneously, overcoming the trade-off effect. Furthermore, we demonstrate the broad applicability of the microflow strategy across various aromatic nitration processes.
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