嫁接
原子转移自由基聚合
单体
纤维素
聚合物
甲基丙烯酸甲酯
苯乙烯
甲基丙烯酸酯
高分子化学
聚合
化学
溴化物
纳米纤维素
表面改性
化学工程
有机化学
共聚物
物理化学
工程类
作者
Yelin Hou,Zhen Zhang,Simon Harrisson,Gilles Sèbe
标识
DOI:10.1016/j.carbpol.2024.122346
摘要
This work reports on the possibility of using polydopamine (PDA) as a tool to immobilize bromoisobutyryl moieties at the surface of cellulose nanocrystals (CNCs) and initiate Surface Intitiated Atom Transfer Radical Polymerization (SI-ATRP) reactions from these sites. Two different strategies based on i) the stepwise modification of the CNCs with dopamine (DA) and α-bromoisobutyryl bromide (BiBB) (Protocol 1) and ii) the one-step treatment of the CNCs with a mixture of DA and BiBB-modified DA (Protocol 2), were compared. Only the CNC particles treated according to Protocol 1 guaranteed efficient anchoring of the SI-ATRP initiating sites in our experimental conditions (with limited impact on the CNCs crystalline structure), the coated layer being leached out by certain solvents in the case of Protocol 2. The brominated particles displaying the best performances were subsequently tested as potential ATRP macroinitiators, using methyl methacrylate (MMA) and styrene (St) as model monomers. Polymer-grafted particles were successfully obtained, with a grafting density twice as high for Sty as for MMA, demonstrating the validity of this strategy.
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