离子液体
化学
无机化学
氧化物
一氧化氮
化学工程
材料科学
核化学
水溶液
吸收(声学)
作者
Shenyao Wang,Xiaoyu Lv,Zhenyu Zhao,Yi-Xin Chen,Zhong Chen,Wenjun Lin,Haoran Li,Congmin Wang
标识
DOI:10.1021/acssuschemeng.1c01597
摘要
A novel method of using anion-functionalized ionic liquids (ILs) with high NO absorption capacity and reversibility for the capture and in situ oxidation of low-concentration NO was established. For the mixed gas containing 0.25% NO, the accumulation rate of nitric acid in these ILs was significantly higher than that in the conventional ILs; after absorption and oxidation reached equilibrium, the molar ratio of HNO 3 to [P 4446 ][PhSO 3 ] was 0.86, which was 5 times as high as that of the conventional IL. Therefore, the problems of low efficiency and poor reversibility of traditional ILs in the absorption and oxidation process were solved. Through absorption and oxidation experiments, quantum chemical calculation, NMR, and time-resolved in situ ATR-FTIR spectroscopic investigation, the results demonstrated that such a high accumulation rate of HNO 3 originated from high uptake of NO through multiple-site interaction. Moreover, high reversibility is attributed to low volatility of conjugated acid of anions and decreased basicity of O sites on anions. We believe that such highly efficient and reversible conversion of low-concentration NO to HNO 3 by ILs provides a new strategy for improving atomic economy of fossil fuel combustion, that is, converting post-combustion pollutants to good valuable chemicals.
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