Zinc chloride aqueous solution as a solvent for starch

被引:41
|
作者
Lin, Meiying [1 ]
Shang, Xiaoqin [1 ]
Liu, Peng [1 ]
Xie, Fengwei [2 ]
Chen, Xiaodong [1 ]
Sun, Yongyi [1 ]
Wan, Junyan [1 ]
机构
[1] Guangzhou Univ, Sch Chem & Chem Engn, Guangzhou 510006, Guangdong, Peoples R China
[2] Univ Queensland, Sch Chem Engn, Brisbane, Qld 4072, Australia
基金
中国国家自然科学基金;
关键词
Starch; ZnCl2 aqueous solution; Non-derivatizing solvent; Dissolution; Zinc-starch complex; SOLID-STATE NMR; IONIC LIQUIDS; RHEOLOGICAL PROPERTIES; STRUCTURAL-CHANGES; LIGHT-SCATTERING; CORN STARCHES; RICE STARCH; CELLULOSE; AMYLOSE; ACID;
D O I
10.1016/j.carbpol.2015.09.007
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
It is important to obtain starch-based homogeneous systems for starch modification. Regarding this, an important key point is to find cheap, low-cost and low-toxicity solvents to allow complete dissolution of starch and its easy regeneration. This study reveals that a ZnCl2 aqueous solution is a good non-derivatizing solvent for starch at 50 degrees C, and can completely dissolve starch granules. The possible formation of a "zinc-starch complex" might account for the dissolution; and the degradation of starch, which was caused by the H+ inZnCl(2) aqueous solution, could not contribute to full dissolution. From polarized light microscopic observation combined with the solution turbidity results, it was found that the lowest ZnCl2 concentration for full dissolution was 29.6 wt.% at 50 degrees C, with the dissolving time being 4 h. Using Fourier-transform infrared (FTIR), solid state C-13 nuclear magnetic resonance (NMR), and X-ray diffraction (XRD), it was revealed that ZnCl2 solution had no chemical reaction with starch glucosides, but only weakened starch hydrogen bonding and converted the crystalline regions to amorphous regions. In addition, as shown by intrinsic viscosity and thermogravimetric analysis (TGA), ZnCl2 solution caused degradation of starch macromolecules, which was more serious with a higher concentration of ZnCl2 solution. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:266 / 273
页数:8
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