Efficient cavity-enhanced adsorption and recovery of low-concentration ammonia on pillar[5]arenes

被引:7
作者
Gong, Wen-Qiang [1 ]
Fu, Yu-Xuan [1 ]
Zhou, Yan [1 ]
Sun, Ming-Shuai [1 ]
Li, Zhang-Min [1 ]
Lu, Nai-Hao [1 ]
Tao, Duan- Jian [1 ]
机构
[1] Jiangxi Normal Univ, Coll Chem & Chem Engn, Natl Engn Res Ctr Carbohydrate Synth, Key Lab Fluorine & Silicon Energy Mat & Chem,Minis, Nanchang 330022, Peoples R China
关键词
Ammonia capture; NH3; Pillar[5]arenes; Solid adsorbent; METAL-ORGANIC FRAMEWORKS; SYNTHETIC FERTILIZERS; BASIS-SETS; CAPTURE; HYDROGEN; REMOVAL; DENSITY; QUALITY; PHENOL; GAS;
D O I
10.1016/j.seppur.2023.124304
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Ammonia (NH3) capture has great implications for environmental protection and resource recovery. Developing effective and recyclable adsorbent materials to remove low-concentration NH3 in industrial waste gas is critical. Here, solid adsorbents per-hydroxylated pillar[5]arene (OHP[5]) and pillar[5]quinone (P[5]Q) with welldesigned functional groups were synthesized and evaluated for NH3 adsorption. The results showed that both materials have high NH3 uptake capacity and excellent cycle stability. P[5]Q showed higher NH3 capacity (15.4 mmol/g) than OHP[5] (11.5 mmol/g) at ambient conditions (293.2 K and 1.0 bar). Dynamic breakthrough experiments showed that P[5]Q had good separation performance on low concentration NH3. Characterizations (including FTIR, SEM, and XPS) and density functional theory (DFT) studies revealed that the adsorption strength for NH3 on P[5]Q possessing C--O groups was stronger than OHP[5] composed of phenolic hydroxyls. Also, the electron-accepting C--O groups on P[5]Q could change the intramolecular charge distribution, in which an amount of NH3 enters and stores in the electron-deficient internal cavity of P[5]Q. It is demonstrated that P[5]Q with the suitable cavity has good potential for separating low concentration NH3 from industrial waste gas.
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页数:8
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