Selective synthesis of nitrate from air using a plasma-driven gas-liquid relay reaction system

IF 14 1区 化学 Q1 CHEMISTRY, APPLIED 能源化学 Pub Date : 2023-10-01 DOI:10.1016/j.jechem.2023.06.021
Sibo Chen , Kai Mei , Yaru Luo , Liang-Xin Ding , Haihui Wang
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Abstract

The direct oxidation of nitrogen is a potential pathway to achieving the zero-carbon-emission synthesis of nitric acid or nitrate, because it does not involve ammonia synthesis and additional ammonia oxidation processes. However, the slow kinetics of nitrogen oxidation and the difficult selective control of oxidation products hinder the development of this process. In this study, a plasma-driven gas-liquid relay reaction system was developed to overcome these limitations. A typical feature of this reaction system is that it can efficiently generate NOx under plasma exposure; moreover, the specific anions in the absorption solution can be oxidized to strong oxidants capable of relay oxidation of low-valence nitrogen oxides. This feature allows for the deep oxidation of nitrogen, thus enabling the oxidation products of nitrogen to exist in high-valence states in the absorption solution. For experimental verification, we achieved the 100% selective synthesis of nitrate under plasma exposure, with air as the supply gas and a sodium sulfate solution as the absorption solution.

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等离子体驱动气液中继反应系统从空气中选择性合成硝酸盐
氮的直接氧化是实现硝酸或硝酸盐零碳排放合成的潜在途径,因为它不涉及氨合成和额外的氨氧化过程。然而,氮氧化的缓慢动力学和氧化产物的难以选择性控制阻碍了该工艺的发展。在本研究中,开发了一种等离子体驱动的气液中继反应系统来克服这些限制。该反应系统的一个典型特征是,它可以在等离子体暴露下有效地产生NOx;此外,吸收溶液中的特定阴离子可以被氧化为能够中继氧化低价氮氧化物的强氧化剂。该特征允许氮的深度氧化,从而使氮的氧化产物以高价态存在于吸收溶液中。为了进行实验验证,我们在等离子体暴露下实现了硝酸盐的100%选择性合成,空气作为供应气体,硫酸钠溶液作为吸收溶液。
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2875
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