凝胶渗透色谱法
聚合物
材料科学
高分子化学
甲基丙烯酸酯
聚合
动态光散射
傅里叶变换红外光谱
摩尔质量分布
化学工程
差示扫描量热法
链式转移
自由基聚合
纳米颗粒
复合材料
纳米技术
物理
工程类
热力学
作者
Bingyang Liu,Yuqi Zhou,Xinran Zhou,Xiaogong Wang
标识
DOI:10.1002/macp.201700020
摘要
In this study, two methacrylate‐based azo homopolymers are synthesized and used to fabricate photodeformable microspheres through a self‐assembling approach. The methacrylate‐based azo homopolymer with the narrow molecular weight distribution is synthesized by reversible addition fragmentation chain transfer polymerization, while the other with the relatively broad molecular weight distribution is synthesized by conventional radical polymerization. The azo polymers are characterized by proton nuclear magnetic resonance ( 1 H‐NMR), Fourier transform infrared spectroscopy (FT‐IR), differential scanning calorimetry (DSC), thermal gravimetric analysis TGA, gel permeation chromatography GPC, and ultraviolet‐visible spectroscopy (UV–vis) m. The colloidal spheres are obtained by gradually adding deionized water into the solutions of the azo polymers in N , N ‐dimethylformamide. Laser light scattering analysis and transmission electron microscopy observations show that although both azo polymers can form uniform colloidal spheres in the dispersions, the molecular weight and its distribution show significant effects on the colloid formation process and the sizes of the colloidal spheres formed in the process. Upon irradiation with a linearly polarized Ar + laser beam for a period of time, the azo polymer microspheres show the elongated deformation along the polarization direction of the actinic light. image
科研通智能强力驱动
Strongly Powered by AbleSci AI