Influence of Different Inorganic Salts on Crystallization-driven Morphological Transformation of PCL-b-PEO Micelles in Aqueous Solutions

被引:0
作者
Jie-xin Yang
Wei-na He
徐君庭
Bin-yang Du
Zhi-qiang Fan
机构
[1] MOEKeyLaboratoryofMacromolecularSynthesisandFunctionalization,DepartmentofPolymerScienceandEngineering,ZhejiangUniversity
关键词
Block copolymer; Crystallization; Inorganic salt; Micelle;
D O I
暂无
中图分类号
O648.1 [胶体];
学科分类号
070304 ; 081704 ;
摘要
Different inorganic salts, including NaSCN, NaCl, MgCl2 and Na2SO4, were added into the aqueous solution containing poly(ε-caprolactone)-b-poly(ethylene oxide)(PCL-b-PEO) semicrystalline micelles. The effects of inorganic salt on the micellar size and morphology were investigated with TEM and DLS. It is found that addition of NaSCN leads to increase of the micellar size, but the micelles remain to be spherical. By contrast, the other three inorganic salts can induce sphere-to-cylinder or sphere-to-lamella transformations of the PCL-b-PEO semicrystalline micelles. The alteration rate of the micellar size with the time after addition of the inorganic salts decreases in the following order: Na2SO4 > NaCl ≈ MgCl2 > NaSCN. These results were interpreted in terms of the "salting-out" ability of the cations and anions. The anions SO42- and Cl- have a stronger "salting-out" ability, driving the morphological transformations of the micelles and leading to a rapid change in micellar size. By contrast, SCN- has a weaker salting-out" ability. The cations Na+ and Mg2+ may associate with the PEO blocks, leading to a "salting-out" effect as well. However, the "salting-out" ability of cations is weaker than that of SO42- and Cl- anions, and the "salting-out" abilities of Na+ and Mg2+ are similar.
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页码:1128 / 1138
页数:11
相关论文
共 2 条
[1]  
Inorganic-salt-induced morphological transformation of semicrystalline micelles of PCL-b-PEO block copolymer in aqueous solution .2 He,Wei-Na,Xu,Jun-Ting,Du,Bin-Yang,Fan,Zhi-Qiang,Wang,Xiaosong. Macromolecular Chemistry and Physics . 2010
[2]  
Wang,J,Zhu,W,Peng,B,Chen,Y.M. Polymer . 2013