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Effect of cationic structure of ionic liquids on dissolution and regeneration of white hide powder

Journal 2017 · IF 1.113 · 18(8): 1512-1522 · 发表于 2017 年 10 月 13 日
作者: Li Qiaoping,Xu Bin,Wang Yan,Zhuang Linghua,Wang Qiang,Li Chao,Xu Xiaoqing,Wang Guowei
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摘要

3-methyl-1-ethoxycarbonylimidazolium chloride ([EtMIM]Cl), was synthesized for white hide powder dissolution. White hide powder was successfully dissolved in [EtMIM]Cl, and regenerated from methanol. The dissolution data and thermodynamic parameter of white hide powder in [EtMIM]Cl and [BMIM]Cl were studied. Hydrogen bond basicity (β) and general polarizability (π*) of ILs were determined. The white hide powders were characterized by FT-IR, XRD, and TGA. The results showed that the maximum solubility of white hide powder in [EtMIM]Cl was higher than that in [BMIM]Cl at same dissolution temperature. At same temperature and same solid content, the dissolution time of white hide powder in [EtMIM]Cl was shorter than that in [BMIM]Cl. Density functional theory (DFT) simulation showed that two kinds of hydrogen bonds (C-H/O and C-H/Cl) and eight strong hydrogen bonds are found in [EtMIM]Cl/GPH, while seven hydrogen bonds are found in [BMIM]Cl/GPH. The carboxylic acid ester cationic group in [EtMIM] + has more electronegative ester groups and stronger electronic cloud density oxygen atoms than alkyl group in [BMIM] + , [EtMIM]Cl is easier to destroy the intermolecular or intramolecular hydrogen bonds in white hide powder, so as to accelerate the dissolution of white hide powder in [EtMIM]Cl. The molecular simulation results indicated that both Cl − anions and [EtMIM] + cation played important roles in the white hide powder dissolution.

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