氧化磷酸化
氮气
硝酸盐
化学
等离子体
机制(生物学)
非热等离子体
活性氮物种
反应机理
环境化学
氧化应激
催化作用
有机化学
生物化学
哲学
物理
认识论
量子力学
作者
Yue‐Qin Tang,Jianxiong Dai,Pei Zhang,Guanghui Niu,Yixiang Duan,Yonghui Tian
标识
DOI:10.1021/acssuschemeng.4c03296
摘要
Plasma/liquid (P/L) reaction is an emerging green chemical process for nitrogen fixation into ammonia or nitrogen oxides directly from air and water. On the other hand, the P/L synthesis is often limited by product nonselectivity. Mechanistic understanding is essential to achieve selective nitrate synthesis in P/L reactions, which would also be profitable in practice. In this study, selective NO3– synthesis from nitrogen gas and liquid water was achieved via a cold microwave plasma (CMP) at ambient temperature and pressure. The product yield and selectivity were found to be controlled by tuning the types of discharge gases as well as the treatment time. The results demonstrate that NO3– was exclusively produced in nitrogen discharge at an extended treatment time of 20 min. Various spectroscopy characterizations and reactive nitrogen or oxygen species measurements were conducted to understand the underlying mechanism. In the nitrogen plasma, the abundant metastable N2(A) species were suggested to be responsible for the ample hydroxyl radicals generated from water, which in turn plays a key role for the high NO3– selectivity. The results in this work not only give insight into the nitrogen fixation process in plasma and liquid water systems but also have a more general relevance to the understanding of P/L based chemical transformation.
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