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首页> 外文期刊>Nanomaterials >Effect of Structure of Polymers Grafted from Graphene Oxide on the Compatibility of Particles with a Silicone-Based Environment and the Stimuli-Responsive Capabilities of Their Composites
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Effect of Structure of Polymers Grafted from Graphene Oxide on the Compatibility of Particles with a Silicone-Based Environment and the Stimuli-Responsive Capabilities of Their Composites

机译:从石墨烯氧化物接枝的聚合物结构对基于硅氧烷的环境的相容性及其复合材料的刺激响应能力

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This study reports the utilization of controlled radical polymerization as a tool for controlling the stimuli-responsive capabilities of graphene oxide (GO) based hybrid systems. Various polymer brushes with controlled molecular weight and narrow molecular weight distribution were grafted from the GO surface by surface-initiated atom transfer radical polymerization (SI-ATRP). The modification of GO with poly( n -butyl methacrylate) (PBMA), poly(glycidyl methacrylate) (PGMA), poly(trimethylsilyloxyethyl methacrylate) (PHEMATMS) and poly(methyl methacrylate) (PMMA) was confirmed by thermogravimetric analysis (TGA) coupled with online Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). Various grafting densities of GO-based materials were investigated, and conductivity was elucidated using a four-point probe method. Raman shift and XPS were used to confirm the reduction of surface properties of the GO particles during SI-ATRP. The contact angle measurements indicated the changes in the compatibility of GOs with silicone oil, depending on the structure of the grafted polymer chains. The compatibility of the GOs with poly(dimethylsiloxane) was also investigated using steady shear rheology. The tunability of the electrorheological, as well as the photo-actuation capability, was investigated. It was shown that in addition to the modification of conductivity, the dipole moment of the pendant groups of the grafted polymer chains also plays an important role in the electrorheological (ER) performance. The compatibility of the particles with the polymer matrix, and thus proper particles dispersibility, is the most important factor for the photo-actuation efficiency. The plasticizing effect of the GO-polymer hybrid filler also has a crucial impact on the matrix stiffness and thus the ability to reversibly respond to the external light stimulation.
机译:该研究报告了控制自由基聚合作为用于控制基于石墨烯(GO)的混合系统的刺激响应能力的工具。通过表面引发的原子转移自由基聚合从去表面接枝具有受控分子量和窄分子量分布的各种聚合物刷子(Si-ATRP)。通过热重分析证实,通过热重分析证实了使用聚(甲基丙烯酸甲酯)(PBMA),聚(甲基丙烯酸甲硅烷酯),聚(三甲基甲硅烷基甲硅烷乙基甲基丙烯酸甲酯)和聚(甲基丙烯酸甲酯)和聚(甲基丙烯酸甲酯)和聚(甲基丙烯酸甲酯)和聚(甲基丙烯酸甲酯)(PMMA)进行修饰(TGA)耦合在线傅里叶变换红外光谱(FTIR),透射电子显微镜(TEM)和X射线光电子谱(XPS)。研究了去基材料的各种移植密度,使用四点探针方法阐明了电导率。拉曼移位和XPS用于确认在SI-ATRP期间去粒子的表面性质的降低。接触角测量表明,根据接枝聚合物链的结构,GOS用硅油的相容性的变化。还使用稳定的剪切流变学研究了GOS与聚(二甲基硅氧烷)的相容性。研究了电流的可调节,以及光致动力。结果表明,除了导电性的改性之外,接枝聚合物链的垂侧组的偶极力矩也在电力学(ER)性能中起着重要作用。颗粒与聚合物基质的兼容性,因此适当的颗粒分散性,是光致动效率最重要的因素。 Go - 聚合物杂化填料的塑化作用也对基质刚度的关键影响,从而具有可逆地响应外部光刺激的能力。

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