Functional Comparison of Polar Ionic Liquids and Onium Hydroxides for Chitin Dissolution and Deacetylation to Chitosan

被引:36
|
作者
Shimo, Mizuki [1 ,2 ]
Abe, Mitsuru [1 ,2 ,3 ]
Ohno, Hiroyuki [1 ,2 ]
机构
[1] Tokyo Univ Agr & Technol, Dept Biotechnol, 2-24-16 Naka Cho, Koganei, Tokyo 1848588, Japan
[2] Tokyo Univ Agr & Technol, Grad Sch Engn, Funct Ion Liquid Labs, 2-24-16 Naka Cho, Koganei, Tokyo 1848588, Japan
[3] Kyoto Univ, Grad Sch Agr, Div Forest & Biomat Sci, Kyoto 6068502, Japan
来源
ACS SUSTAINABLE CHEMISTRY & ENGINEERING | 2016年 / 4卷 / 07期
基金
日本学术振兴会;
关键词
Hydrogen bond; Proton-accepting ability; Hydroxide anion; Ethylenediamine; Mild conditions; Deacetylation; ALPHA-CHITIN; CELLULOSE; BIOMASS; WOOD;
D O I
10.1021/acssuschemeng.6b00368
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of ionic liquids (ILs) have been synthesized, and the dissolution ability of chitin has been evaluated under mild conditions. We have focused on tris(2-hydroxyethyl)methylammonium (THEMA) type ILs. These [THEMA]-type ILs partly dissolved chitin, and addition of ethylenediamine (EDA) was confirmed to improve the chitin dissolution. Relatively high hydrogen bond accepting ability of the IL/EDA mixtures was required to dissolve chitin. Among these mixtures, the [THEMA] [OAc]/EDA mixture dissolved chitin completely without heating. As other potential solvents, a series of tetraalkylammonium hydroxides/water mixtures was also found to dissolve chitin without heating. Conversion of chitin to chitosan during the dissolution process has been found in such tetraalkylammonium hydroxides/water mixtures in spite of the fact that almost no deacetylation was found in the IL/EDA mixture. The effect of ILs and onium hydroxides on both chitin dissolution and deacetylation ability was discussed.
引用
收藏
页码:3722 / 3727
页数:6
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