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Preparation of hydrophobic tannins-inspired polymer materials via low-ppm ATRP methods

机译:通过低ppm ATRP方法制备疏水性单宁鼓发的聚合物材料

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摘要

The novel hydrophobic coating material was received for the first time by a two-step synthetic route. Firstly, the 15-functional brominated macroinitiator was prepared by the esterification methodology. Next step covers synthesis of star-like polymers by poly(n-butyl acrylate) (PBA) arms polymerization via three low-ppm atom transfer radical polymerization (ATRP) approaches including application of copper and silver wire in SARA and ARGET ATRP, respectively, as driving forces in redox cycle of catalyst, and an external stimulus in the form of electric current (seATRP) as the third approach in copper(II) regeneration system. As expected, the electrochemically mediated technique allows synthesis of tannic acid-inspired coating polymers in precisely controlled manner during the entire polymerization process, proved by linear first-order kinetics plot in contrast to above-mentioned methods, low dispersity ( = 1.18) of star-shaped polymers, and high efficiency of initiation (integral(i) = 81%) determined after detaching of polymers side arms. Macromolecules received by all low-ppm ATRP solutions were characterized by preserved chain-end functionality (theoretical dead chain fraction; DCFtheo <1%). Adhesive and hydrophobic properties of received polymer materials were investigated by contact angles (theta) and free surface energy (FSE) calculations. Prepared polymer films besides excellent hydrophobic properties have great potential as a self-healing solution.
机译:通过两步合成途径首次接收新的疏水涂层材料。首先,通过酯化方法制备15个功能性溴化大类蛋白剂。下一步涵盖通过聚(丙烯酸正丁酯)(PBA)臂聚合通过三种低ppm原子转移自由基聚合(ATRP)方法的合成,包括铜和银线在Sara和Arget ATRP中的应用,作为催化剂氧化还原循环的驱动力,以及电流形式的外部刺激(SEATRP)作为铜(II)再生系统的第三种方法。如所预期的,电化学介导的技术允许在整个聚合过程中以精确控制的方式合成单宁酸鼓励的涂层聚合物,并通过线性一阶动力学图,与上述方法相比,低分散性( = 1.18 “星形聚合物”,在聚合物侧臂分离后测定的高效率(积分(I)= 81%)。所有低PPM ATRP溶液接收的大分子都是通过保存的链末端功能(理论死链分数; DCFtheO <1%)的特征。通过接触角(θ)和自由表面能量(FSE)计算来研究接受聚合物材料的粘合剂和疏水性质。除了优异的疏水性质之外,制备的聚合物膜具有良好的潜力作为自我愈合溶液。

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