中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly efficient and reversible absorption of NH3 by dual functionalised ionic liquids with protic and Lewis acidic sites

文献类型:期刊论文

作者Shang, Dawei2,3; Zeng, Shaojuan3; Zhang, Xiangping1,3; Zhang, Xiaochun3; Bai, Lu3; Dong, Haifeng3
刊名JOURNAL OF MOLECULAR LIQUIDS
出版日期2020-08-15
卷号312页码:7
关键词Dual functionalised Protic ionic liquids Li+-based anion NH3 absorption Multiple interactions
ISSN号0167-7322
DOI10.1016/j.molliq.2020.113411
英文摘要Ammonia (NH3) pollution poses a serious environmental threat. Ionic liquids (ILs) are regarded as potential solvents to treat NH3-containing gases because of their unique properties, including tunable structures and high affinity for NH3 molecules. In order to achieve an efficient and reversible absorption of NH3, a series of profit ionic liquids (PILs) with multiple active sites were designed by introducing acidic protons, as well as the Li+ ion into ILs, resulting in PILs with two acidic protons on cations ([2-Mim][NTf2] and [Im][NTf2]), as well as dual functionalised PILs with a Lewis acidic Li+-based anion and acidic protons on cations, namely, [2-Mim][Li (NTf2)(2)] and [Eim][Li(NTf2)(2)]. The NH3 absorption capacity of [Im][NTf2] was found to be 3.46 mol NH3/mol which is the highest among the NH3 absorption capacities of all known nonmetallic ILs, and is ascribed to the hydrogen bonding interactions between the NH3 and PIL molecules. Furthermore, [2-Mim][Li(NTf2)(2)] exhibited the highest NH3 absorption capacity, with a value of 7.01 mol NH3/mol IL, which is about 30 times higher than that of conventional ILs. The superior NH3 absorption performance of the dual functionalised PILs is attributed to the combination of hydrogen bonding interactions between the protons and the NH3 molecules, and the formation of coordination complexes between the Li+-based anion and the NH3 molecules. Moreover, the ILs studied here exhibited excellent recyclability, indicating a great potential for their use in applications involving efficient and reversible NH(3 )absorption from NH3-containing industrial gases. (C) 2020 Elsevier B.V. All rights reserved.
WOS关键词DEEP EUTECTIC SOLVENTS ; CO2 CAPTURE ; AMMONIA ; SO2 ; SOLUBILITIES ; SIMULATION ; SEPARATION
资助项目National Key Research and Development Program of China[2017YFB0603401-03] ; National Natural Science Foundation of China[21890764] ; National Natural Science Foundation of China[21776277] ; National Natural Science Foundation of China[U1704251] ; National Natural Science Foundation of China[21978306] ; Beijing Municipal Natural Science Foundation[2182071] ; Hebei Natural Science Foundation[B2019103011]
WOS研究方向Chemistry ; Physics
语种英语
WOS记录号WOS:000559968600010
出版者ELSEVIER
资助机构National Key Research and Development Program of China ; National Natural Science Foundation of China ; Beijing Municipal Natural Science Foundation ; Hebei Natural Science Foundation
源URL[http://ir.ipe.ac.cn/handle/122111/41726]  
专题中国科学院过程工程研究所
通讯作者Zeng, Shaojuan
作者单位1.Univ Chinese Acad Sci, Sch Chem Engn, Beijing 100049, Peoples R China
2.Sinopec Shanghai Res Inst Petrochem Technol, Shanghai 201208, Peoples R China
3.Chinese Acad Sci, State Key Lab Multiphase Complex Syst, Key Lab Green Proc & Engn, Beijing Key Lab Ion Liquids Clean Proc,Inst Proc, Beijing 100190, Peoples R China
推荐引用方式
GB/T 7714
Shang, Dawei,Zeng, Shaojuan,Zhang, Xiangping,et al. Highly efficient and reversible absorption of NH3 by dual functionalised ionic liquids with protic and Lewis acidic sites[J]. JOURNAL OF MOLECULAR LIQUIDS,2020,312:7.
APA Shang, Dawei,Zeng, Shaojuan,Zhang, Xiangping,Zhang, Xiaochun,Bai, Lu,&Dong, Haifeng.(2020).Highly efficient and reversible absorption of NH3 by dual functionalised ionic liquids with protic and Lewis acidic sites.JOURNAL OF MOLECULAR LIQUIDS,312,7.
MLA Shang, Dawei,et al."Highly efficient and reversible absorption of NH3 by dual functionalised ionic liquids with protic and Lewis acidic sites".JOURNAL OF MOLECULAR LIQUIDS 312(2020):7.

入库方式: OAI收割

来源:过程工程研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。