A facile way to prepare crystalline platelets of block copolymers by crystallization-driven self-assembly

被引:76
作者
Wang, Jing [1 ]
Zhu, Wen [1 ]
Peng, Bo [1 ,2 ]
Chen, Yongming [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Chem, Lab Polymer Phys & Chem, Beijing 100190, Peoples R China
[2] Sun Yat Sen Univ, Sch Chem & Chem Engn, Key Lab Polymer Composite & Funct Mat, Minist Educ PR China, Guangzhou 510275, Guangdong, Peoples R China
基金
美国国家科学基金会;
关键词
Block copolymers; Crystallization-driven self-assembly; Polymer platelets; MICELLAR MORPHOLOGIES; DIBLOCK COPOLYMERS; SELECTIVE SOLVENT; SINGLE-CRYSTALS; CORE; MICELLIZATION; TEMPERATURE; NANOTUBES; INTERPLAY;
D O I
10.1016/j.polymer.2013.10.027
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(epsilon-caprolactone)-block-poly[2-(dimethylamino)ethyl methacrylate] (PCL-b-PDMAEMA) block copolymers were applied to fabricate elongated polymer platelets with axial length of 5-20 mu m and thickness of ca. 10 nm by crystallization-driven self-assembly (CDSA). The block copolymer platelets composed of a crystallized PCL layer sandwiched between two PDMAEMA layers were obtained spontaneously by adding methanol, a selective solvent of PDMAEMA, into the block copolymer solution of THF at 25 degrees C. Therefore, this is a facile approach to generate lamellar nanoobjects of block copolymers. Effects of the block copolymer compositions on the morphologies of platelets were investigated. The presence of PDMAEMA segments along the lamellar surfaces was further confirmed by loading gold nanoparticles. Moreover, PEO-b-PCL-b-PDMAEMA triblock terpolymer could form spindle platelets by this approach. The crystalline platelets were characterized by the transmission electron microscopy (TEM), scanning electron microscopy (SEM), atomic force microscopy (AFM), small-angle X-ray scattering (SAXS) and wide-angle X-ray diffraction (WAXD). (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6760 / 6767
页数:8
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