Adjustment of Molecular Weight for a Cellulose-graft-poly(ethylene glycol dimethacrylate) Polymer Brush by Atom Transfer Radical Polymerization in an Ionic Liquid

被引:0
|
作者
Zhou, Jian [1 ]
Tang, Erjun [1 ]
Zhao, Lei [1 ]
Han, Ruitao [2 ]
Liu, Shaojie [1 ]
Zhao, Dishun [1 ]
机构
[1] Hebei Univ Sci & Technol, Sch Chem & Pharmaceut Engn, Shijiazhuang 050018, Hebei, Peoples R China
[2] Hebei Univ Sci & Technol, Sch Mat Sci & Engn, Shijiazhuang 050018, Hebei, Peoples R China
来源
JOURNAL OF POLYMER MATERIALS | 2018年 / 35卷 / 02期
基金
中国国家自然科学基金;
关键词
Cellulose; Ionic liquid; ATRP; Controlled molecular weight; Self-assembly; ACTIVATION RATE CONSTANTS; CELLULOSE; ATRP; LIGAND; METHACRYLATE); COPOLYMERS;
D O I
10.32381/JPM.2018.35.02.9
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A cellulose-graft-poly(ethylene glycol dimethacrylate) (cellulose-g-PEGDMA) molecule brush was synthesized by atom transfer radical polymerization in the ionic liquid 1-allyl-3methylimidazolium chloride. The controlled mechanism of the polymer brush size and polydispersity index (PDI, Mw/Mn) were investigated. The grafting copolymers were characterized by FTIR, H-1-NMR and GPC. The results indicate that the reaction time was the main factor to control the length of the cellulose-g-PEGDMA molecule brush. The ligand was the decisive factor in controlling the PDI of the molecule brush. The PDI of PEGDMA was precisely controlled at 1.1-1.4 by using pentamethyldiethylenetriamine(PMDETA) as the ligand. Moreover, the graft molecule brush length could be varied with the change of PMDETA concentration. The Mn of PEGDMA was 75210 and had a narrow PDI of 1.15 when the PMDETA/CuBr ratio was 20:1. In addition, TEM images show that the cellulose-g-PEGDMA copolymer could aggregate and selfassemble into a sphere-like polymeric structure in solution, indicating that the obtained grafting copolymers have potential applications in biomedical materials.
引用
收藏
页码:245 / 256
页数:12
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