等离子体
微波食品加热
化学
化学物理
工作(物理)
氮氧化物
扩散
原子物理学
激发
等离子体诊断
等离子体参数
氮气
电子密度
机制(生物学)
氧气
红外线的
等离子体化学
等离子体参数
动力学
动能
芯(光纤)
离子
电子
化学动力学
等离子体稳定性
喷射(流体)
等离子体处理
多普勒效应
大气压等离子体
化学反应
化学过程
纳米技术
作者
Q. Shen,Lex Kuijpers,J. Gans,Serguei Starostine,Vasco Manuel Domingues Carvalho Guerra,M. C. M. van de Sanden
标识
DOI:10.1021/acssuschemeng.5c08163
摘要
Microwave plasma has emerged as one of the most energy-efficient approaches for nitrogen fixation. To elucidate the underlying mechanisms at intermediate pressure, a quasi-1.5D physicochemical multitemperature model is developed under varying N2–O2 compositions. The plasma shape and radial gas temperature profile, derived from the emission intensity distribution and the Doppler broadening of the 777 nm O(5S ←5P) atomic oxygen triplet, serve as key model inputs for determining the power density profile and turbulent viscosity, respectively. The model captures the coupled interplay among vibrational, chemical, and electron kinetics in microwave plasma NOx synthesis, with particular emphasis on the role of vibrational excitation at 80 mbar. The energy costs predicted by the model show good agreement with the experimental results measured using Fourier-transform infrared spectroscopy. Nonthermal behavior within the plasma core is found to strongly promote NO formation. Radial diffusion emerges as a key mechanism for sustaining chemical nonequilibrium, and improving overall NO yield. Key reactions involved in NO formation and destruction under different initial gas mixtures are discussed. Finally, it is suggested that the energy cost can be improved by optimizing the plasma shape. This work offers fundamental insights into the underlying plasma–chemical mechanisms and establishes a predictive framework to guide the future design and optimization of energy-efficient microwave plasma technologies for nitrogen fixation.
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