Elevated Pressure Effects on Plasma-Driven Ammonia Synthesis: Insights from Experiments and Kinetic Modeling

化学 氨 等离子体 离解(化学) 氨生产 动力学 化学动力学 非热等离子体 介质阻挡放电 化学反应 动能 反应机理 氮气 大气压等离子体 反应速率 环境压力 激发态 分析化学(期刊) 分子 电子 化学平衡 化学物理 热力学平衡 电场 产量(工程) 活化能 激进的 无机化学 等离子体处理 化学工程
作者
Jintao Sun,Weitao Wang,Chunqiang Lu,Xin Tu
出处
期刊:ACS Sustainable Chemistry & Engineering [American Chemical Society]
卷期号:13 (37): 15576-15587 被引量:8
标识
DOI:10.1021/acssuschemeng.5c06251
摘要

High Resolution Image Download MS PowerPoint Slide Nonthermal plasma (NTP) presents a promising pathway for sustainable ammonia synthesis under mild conditions, enabling activation of nitrogen without the need for high thermal input. While most studies to date have focused on plasma ammonia synthesis under ambient pressure, the potential benefits of elevated pressure, such as improved thermodynamic favorability and enhanced compatibility with downstream ammonia separation technologies, remain underexplored. In this work, we investigate plasma-driven ammonia synthesis under elevated pressure by combining experimental measurements with detailed plasma chemical kinetics modeling. A dielectric barrier discharge plasma reactor was employed, with the system pressure controlled up to 3 bar using a high-pressure regulator. Contrary to thermodynamic expectations, the experimental results reveal that increasing pressure suppresses ammonia yield in the plasma environment, primarily due to a reduction in the reduced electric field (E/N), which diminishes the energy of electrons available for molecule activation. The underlying reaction mechanism was elucidated using in situ optical diagnostics and chemical kinetics simulations. Path flux analysis confirms that N 2 is dissociated by energetic electrons into N and excited N( 2 D) species, which are subsequently hydrogenated to form NH and NH 2 radicals. These intermediates recombine via NH 2 + H(+M) → NH 3 (+M) and NH + H 2 + M → NH 3 + M to form ammonia. Notably, elevated pressure does not alter the dominant reaction pathways but significantly influences the reaction rates and plasma characteristics. Sensitivity analysis highlights that the electron-impact dissociation of N 2 [e + N 2 → e + N + N( 2 D)] is the rate-limiting step and has the greatest promoting effect on ammonia formation. These insights offer guidance for optimizing plasma operating conditions and advancing the practical application of plasma-assisted ammonia synthesis under pressurized conditions.
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