甲基丙烯酸酯
聚合物
石英晶体微天平
高分子化学
原子转移自由基聚合
自由基聚合
聚合物刷
聚合
化学
共聚物
化学工程
生物污染
材料科学
有机化学
吸附
膜
生物化学
工程类
作者
Yong Du,Jingqing Gao,Tingting Chen,Chao Zhang,Jian Ji,Zhi‐Kang Xu
出处
期刊:Langmuir
[American Chemical Society]
日期:2017-07-10
卷期号:33 (29): 7298-7304
被引量:17
标识
DOI:10.1021/acs.langmuir.7b01681
摘要
Poly(oligoethylene glycol methacrylate) (POEGMA) and zwitterionic polymer brushes have been widely used for constructing biocompatible or antifouling surfaces, and their oxidative stability is very important to the practical application. Herein, POEGMA, poly(sulfobetaine methacrylate) (PSBMA), poly(2-(methacryloyloxy)ethyl phosphorylcholine) (PMPC), and poly(carboxybetaine methacrylate) (PCBMA) were grafted on quartz crystal microbalance (QCM) chips via surface-initiated atom transfer radical polymerization (SI-ATRP). XPS and MS analyses demonstrate that the mass loss of these polymer brushes in oxidative environment is due to the scission of the polymer-anchoring segments. Molecular simulation further illustrates this mass loss mechanism should be always true for those polymer brushes anchored on different substrates. In situ QCM monitoring indicates that, compared with zwitterionic polymethacrylates, POEGMA brushes show the lowest mass loss rate mainly due to their cross-linked structures. This study sheds light on the contradictory reports about the oxidative stability of POEGMA and zwitterionic polymethacrylate brushes up to now, and highlights the important role of the polymer-anchoring segments playing in the oxidative stability of polymer brushes.
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