Water Sorption in Amino Acid Ionic Liquids: Kinetic, Mechanism, and Correlations between Hygroscopicity and Solvatochromic Parameters

被引:42
作者
Cao, Yuanyuan [1 ]
Sun, Xiaofu [1 ]
Chen, Yu [1 ]
Mu, Tiancheng [1 ]
机构
[1] Renmin Univ China, Dept Chem, Beijing 100872, Peoples R China
来源
ACS SUSTAINABLE CHEMISTRY & ENGINEERING | 2014年 / 2卷 / 02期
基金
中国国家自然科学基金;
关键词
Amino acid ionic liquids; Water; Hygroscopicity; Modified two-step sorption model; Arrow-shooting ball mechanism; Solvatochromic parameters; Correlation; THERMAL-STABILITY; ORGANIC-SOLVENTS; BINARY-SYSTEMS; TEMPERATURE; POLARITY; CO2; CATION; ABSORPTION; ANIONS; SCALE;
D O I
10.1021/sc4003246
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Amino acid ionic liquids (ILs) are biocompatible, biodegradable, and easy to synthesis, thus resulting in many potentially sustainable applications (e.g., sour gases capture and biomass dissolution). If mixed or contaminated with water, their properties would be altered and degradation may be induced, hence influencing their applications. Therefore, the hygroscopicity of nine amino acid ILs was investigated in this study. Furthermore, an arrow-shooting ball mechanism was proposed to simulate the interaction mechanism of water sorption. Namely, a fragile melon ILs ball would easily be split by the water arrow, i.e., a weaker cation anion interaction induces a stronger ion water interaction, hence producing greater hygroscopicity. Instead, a hard golden ILs ball with a higher ILs ILs interaction would disfavor the ILs water interaction, hence producing lower hygroscopicity. Finally, the correlations between the hygroscopicity of amino acid ILs and the solvatochromic parameters were investigated. The results showed that hygroscopicity had no direct correlation with the solvatochromic parameters, whereas it did have a close relationship with the polarity depending on the region of hydrogen-bonding basicity. Therefore, hygroscopicity could be designed by three procedures: (1) estimating the hydrogen-bonding basicity, (2) determining the region of hydrogen-bonding basicity, and (3) decreasing (increasing) the polarity, which would lead to more hydrophobic ILs in a + (-) region, where "+" and "-" indicate a positive and negative correlation between polarity and hygroscopicity parameters in a specific region of hydrogen-bonding basicity, respectively.
引用
收藏
页码:138 / 148
页数:11
相关论文
共 63 条
  • [1] Understanding the polarity of ionic liquids
    Ab Rani, M. A.
    Brant, A.
    Crowhurst, L.
    Dolan, A.
    Lui, M.
    Hassan, N. H.
    Hallett, J. P.
    Hunt, P. A.
    Niedermeyer, H.
    Perez-Arlandis, J. M.
    Schrems, M.
    Welton, T.
    Wilding, R.
    [J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2011, 13 (37) : 16831 - 16840
  • [2] How polar are room-temperature ionic liquids?
    Aki, SNVK
    Brennecke, JF
    Samanta, A
    [J]. CHEMICAL COMMUNICATIONS, 2001, (05) : 413 - 414
  • [3] Experimental and Computational Study on the Properties of Pure and Water Mixed 1-Ethyl-3-methylimidazolium L-(+)-Lactate Ionic Liquid
    Aparicio, Santiago
    Alcalde, Rafael
    Atilhan, Mert
    [J]. JOURNAL OF PHYSICAL CHEMISTRY B, 2010, 114 (17) : 5795 - 5809
  • [4] Thermal stability and moisture uptake of 1-alkyl-3-methylimidazolium bromide
    Arellano, Ian Harvey J.
    Guarino, Jeiel G.
    Paredes, Fiona U.
    Arco, Susan D.
    [J]. JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY, 2011, 103 (02) : 725 - 730
  • [5] Amino-functionalized ionic liquid as an efficient and recyclable catalyst for Knoevenagel reactions in water
    Cai, YQ
    Peng, YQ
    Song, GH
    [J]. CATALYSIS LETTERS, 2006, 109 (1-2) : 61 - 64
  • [6] Cammarata L, 2001, PHYS CHEM CHEM PHYS, V3, P5192, DOI 10.1039/b106900d
  • [7] Water Sorption in Functionalized Ionic Liquids: Kinetics and Intermolecular Interactions
    Cao, Yuanyuan
    Chen, Yu
    Lu, Liyi
    Xue, Zhimin
    Mu, Tiancheng
    [J]. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2013, 52 (05) : 2073 - 2083
  • [8] Water sorption in ionic liquids: kinetics, mechanisms and hydrophilicity
    Cao, Yuanyuan
    Chen, Yu
    Sun, Xiaofu
    Zhang, Zhongmin
    Mu, Tiancheng
    [J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2012, 14 (35) : 12252 - 12262
  • [9] Carmichael AJ, 2000, J PHYS ORG CHEM, V13, P591, DOI 10.1002/1099-1395(200010)13:10<591::AID-POC305>3.0.CO
  • [10] 2-2