Structural Changes of Bagasse during the Homogeneous Esterification with Maleic Anhydride in Ionic Liquid 1-Allyl-3-methylimidazolium Chloride

被引:22
|
作者
Wang, Huihui [1 ]
Chen, Wei [1 ]
Zhang, Xueqin [1 ]
Wei, Yi [1 ]
Zhang, Aiping [2 ]
Liu, Shijie [1 ,3 ]
Wang, Xiaoying [1 ]
Liu, Chuanfu [1 ]
机构
[1] South China Univ Technol, State Key Lab Pulp & Paper Engn, Guangzhou 510640, Guangdong, Peoples R China
[2] South China Agr Univ, Coll Forestry & Landscape Architecture, Guangzhou 510642, Guangdong, Peoples R China
[3] SUNY Syracuse, Dept Paper & Bioproc Engn, Coll Environm Sci & Forestry, Syracuse, NY 13210 USA
基金
中国国家自然科学基金;
关键词
bagasse; maleic anhydride; structural changes; AmimCl; SUGARCANE BAGASSE; PHTHALIC-ANHYDRIDE; ARUNDO-DONAX; CELLULOSE; LIGNIN; COMPOSITES; HEMICELLULOSES; LIGNOCELLULOSE; DISSOLUTION; SEPARATION;
D O I
10.3390/polym10040433
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The maleation of bagasse could greatly increase the compatibility between bagasse and composite matrixes, and the percentage of substitution (PS) of bagasse maleates could be regulated in the homogeneous system. However, due to the complicated components and the linkages of bagasse, it was difficult to control the reaction behaviors of each component. In this paper, the detailed structural changes of bagasse during the homogeneous maleation in ionic liquid 1-allyl-3-methylimidazolium chloride (AmimCl) were comparatively investigated with the three main components (cellulose, hemicelluloses, and lignin) from bagasse. The PS of the maleated bagasse was 12.52%, and the PS of the maleated cellulose, hemicelluloses, and lignin were 13.50%, 10.89%, and 14.03%, respectively. Fourier translation infrared (FT-IR) and NMR analyses confirmed that the three main components were all involved in the homogeneous maleation. H-1-C-13 HSQC analysis indicated that the predominant monoesterification of cellulose, diesterification of hemicelluloses and lignin, and the degradation of the three main components simultaneously occurred. Besides, the quantitative analysis from 1H-13C HSQC revealed the relative PS of reactive sites in each component. P-31 NMR results showed that the reactivity of lignin aliphatic hydroxyls was higher than that of phenolic ones, and the reactivity of phenolic hydroxyls followed the order of p-hydroxyphenyl hydroxyls > guaiacyl hydroxyls > syringyl hydroxyls.
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页数:15
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