Glass transition of poly(methyl methacrylate) nanospheres in aqueous dispersion

被引:16
|
作者
Feng, Shuo [1 ]
Chen, Yuenan [1 ]
Mai, Biyun [1 ]
Wei, Wanchu [1 ]
Zheng, Caixia [1 ]
Wu, Qing [1 ,2 ]
Liang, GuoDong [1 ,2 ]
Gao, HaiYang [1 ,2 ]
Zhu, FangMing [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Sch Chem & Chem Engn, Minist Educ, Key Lab Polymer Composite & Funct Mat, Guangzhou 510275, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Sch Chem & Chem Engn, Inst Polymer Sci, DSAPM Lab, Guangzhou 510275, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
THIN POLYMER-FILMS; ULTRATHIN FILMS; SUBSTRATE INTERACTIONS; STRUCTURAL RELAXATION; FREE SURFACES; T-G; TEMPERATURE; DYNAMICS; POLYSTYRENE; CONFINEMENT;
D O I
10.1039/c4cp01849d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Surfactant-free nanospheres and latex nanospheres of poly(methyl methacrylate) (PMMA) with diameter ranging from 20 to 220 nm are prepared by atom transfer radical polymerization (ATRP) in microemulsions and subsequent dialysis against deionized water. The glass transitions of these PMMA nanospheres are characterized using nano differential scanning calorimetry (nano-DSC) in aqueous dispersions. The glass transition temperature (T-g) of the surfactant-free PMMA nanospheres and nonionic PMMA latex nanospheres with diameters below 150 nm is less than that of the PMMA bulk, and T-g decreases with the decrease of the diameter. In contrast, T-g of the anionic PMMA latex nanospheres is size-independent and is near to that of the PMMA bulk. The influence of the environment surrounding the PMMA nanospheres on glass transitions as well as comparisons to our prior studies with polystyrene (PS) nanospheres in aqueous dispersions are discussed.
引用
收藏
页码:15941 / 15947
页数:7
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