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Templated Formation of Silver Nanoparticles Using Amphiphilic Poly(epichlorohydrine-g-styrene) Film

机译:两亲性聚(表氯醇-g-苯乙烯)膜的银纳米粒子的模板化形成。

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摘要

This work has demonstrated that a novel amphiphilic poly(epichlorohydrine)-graft-polystyrene (PECH-g-PS) copolymer at 34:66 wt% was synthesized via atom transfer radical polymerization (ATRP) of styrene using PECH as a macroinitiator. The structure of the graft copolymer was characterized by nuclear magnetic resonance (~1H NMR) and FTIR spectroscopy, demonstrating that the "grafting from" method using ATRP was successful. The self-assembled graft copolymer was used as a template film for the in-situ growth of silver nanoparticles from AgCF3SO3 precursor under UV irradiation. The in situ formation of silver nanoparticles with 6-8 nm in average size in the solid state template film was confirmed by transmission electron microscopy (TEM), UV-visible spectroscopy and wide angle X-ray scattering (WAXS). Differential scanning calorimetry (DSC) also displayed the selective incorporation and the in situ formation of silver nanoparticles within the hydrophilic PECH domains, probably due to stronger interaction of the silvers with the ether oxygens of PECH backbone than that with hydrophobic PS side chains.
机译:这项工作表明,通过使用PECH作为大分子引发剂,通过苯乙烯的原子转移自由基聚合(ATRP)合成了34:66 wt%的新型两亲性聚(表氯醇)-接枝聚苯乙烯(PECH-g-PS)共聚物。通过核磁共振(〜1H NMR)和FTIR光谱对接枝共聚物的结构进行了表征,表明使用ATRP的“接枝”方法是成功的。自组装的接枝共聚物用作模板膜,用于在紫外线照射下从AgCF3SO3前体原位生长银纳米颗粒。通过透射电子显微镜(TEM),紫外-可见光谱和广角X射线散射(WAXS)证实了固态模板膜中原位形成平均粒径为6-8nm的银纳米颗粒。差示扫描量热法(DSC)还显示了在亲水性PECH域内银纳米颗粒的选择性掺入和原位形成,这可能是由于银与PECH主链的醚氧的相互作用比与疏水性PS侧链的相互作用更强。

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