Characterization of the regenerated cellulose films in ionic liquids and rheological properties of the solutions

被引:135
作者
Liu, Zhen [1 ]
Wang, Hui [1 ]
Li, Zengxi [1 ]
Lu, Xingmei [2 ]
Zhang, Xiangping [2 ]
Zhang, Suojiang [2 ]
Zhou, Kebin [1 ]
机构
[1] Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China
[2] Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
Biomaterials; Surface properties; Thin films; Polymers; POLYMERIZATION; DERIVATIVES; DISSOLUTION; SOLVENTS; SYSTEMS;
D O I
10.1016/j.matchemphys.2011.02.062
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Dissolution and regeneration of cotton pulp using ionic liquids as solvent was investigated. The physicochemical properties of the regenerated cellulose films have been characterized by scanning electron microscopy. X-ray diffractometer, infrared spectrometric analyzer, differential scanning calorimeter, and thermogravimetric analysis instrument. The rheological properties of cotton pulp dissolved in ionic liquids have been investigated by steady shear and oscillatory shear measurements. The influences of experimental parameters, such as the reaction temperature, additives on the solubility and degree of polymerization (DP) of regenerated cellulose were also studied. The results show that 1-butyl-3-methylimidazolium chloride ([bmim]Cl) was a good solvent to dissolve cotton pulp and the solubility can reach 13 wt% at 90 degrees C, but the DP remarkably decreased from 510 to 180 within 7h. It was found that additive N-methylimidazole can effectively minimize DP loss of the regenerated cellulose, which can attribute to the fact that in the mixture of [bmim]Cl and NMI solution, the beta-1,4-glycosidic bond of the cellulose chains cannot be broken because of the relative low concentration of Cl-. In the steady shear measurement, all the solutions show a shear thinning behavior at high shear rates. In addition, a mechanism of the dissolution of cellulose in [bmim]Cl was proposed. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:220 / 227
页数:8
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