首页> 外文期刊>Macromolecules >Morphology, Molecular Dynamics, and Interfacial Phenomena in Systems Based on Silica Modified by Grafting Polydimethylsiloxane Chains and Physically Adsorbed Polydimethylsiloxane
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Morphology, Molecular Dynamics, and Interfacial Phenomena in Systems Based on Silica Modified by Grafting Polydimethylsiloxane Chains and Physically Adsorbed Polydimethylsiloxane

机译:基于二二甲基硅氧烷链改性二氧化硅的体系形态,分子动力学和界面现象,物理吸附聚二甲基硅氧烷改性

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摘要

This study deals with effects on structure, molecular mobility, and interfacial polymer nanoparticles (NPs), arising from modification of silica NPs by grafting of small polydimethylsiloxane (PDMS) chains, via siloxane bond breaking, in combination with polymer molecular weight, Wm, both below and above the entanglement threshold (Wm,, 8k). According to infrared (IR), upon grafting of PDMS, the coverage of surface silica hydroxyls is almost complete (100%) and uniform for short chains, whereas it is lower,,--60%, for longer chains (non -uniform). The combination of results by nitrogen adsorption desorption and calorimetry (differential scanning calorimetry, DSC) indicates that the nanoparticle surface 4 5 accessibility by the polymer is dynamic, as it changes non -monotonically with the gradual increasing of polymer adsorption. The grafted chains show no mobility (rigid or dead layer) neither by DSC nor by broadband dielectric spectroscopy (BDS), due to the severe fragmentation during the siloxane breaking process. On the contrary, upon physical adsorption of PDMS of Wm 40k (i.e. Wm,e) onto both modified and unmodified NPs, the polymer exhibits both bulk (glass transition, a relaxation) and retarded interfacial dynamics in BDS (am, relaxation). For adsorbed PDMS > 40%, the bulk -like dynamics is governed by entanglements between bulk polymer chains, whereas for PDMS < 40% by polymer particles interactions and the presence of interfacial polymer. Comparing to previous findings in similar nanocomposites, a,, exhibits relatively short relaxation times and a non -cooperative character, both independent from the type of particles grafting. ain, exhibits a large strength, which is, however, reduced for the grafted particles. Adopting here previously applied models, effects were explained in terms of formation of interfacial PDMS loops of large height (origin of large dielectric strength) and eliminated ability for cooperative motions due to interfacial chain entanglemen
机译:该研究涉及通过硅氧烷键分解的小型聚二甲基硅氧烷(PDMS)链,与聚合物分子量,WM,两者兼容在纠缠阈值(WM ,,8K)以下和之上。根据红外(IR),在接枝PDMS时,表面二氧化硅羟基的覆盖率几乎完全(100%)和短链的均匀,而较低的链条(非均匀)较低, - 60%) 。通过氮吸附解吸和量热法(差示扫描量热法,DSC)的组合表明,纳米颗粒表面4 5通过聚合物可访问性是动态的,因为它随着聚合物吸附的逐渐增加而非调向量变化。由于硅氧烷破碎过程中的严重碎裂,接枝链既不显示DSC也没有由DSC或宽带介电光谱(BDS)显示出来的移动性(刚性或死层)。相反,在改性和未改性的NPS上的WM 40K(即 Wm,E)的PDMS的物理吸附时,聚合物在BDS(AM,松弛)中展示散装(玻璃转变,弛豫)和延迟的界面动态。对于吸附的PDMS> 40%,散装式动态由散装聚合物链之间的缠结控制,而PDMS颗粒相互作用和界面聚合物的存在。与以前的纳米复合材料中的先前发现相比,A,例如,表现出相对短的弛豫时间和非涂层性质,无论是独立于饲养的颗粒的类型。 AIN,表现出大的强度,但是对于接枝颗粒而言,这是减少的。在这里采用以前应用的模型,在形成大高度(大介电强度的起源)的界面PDMS回路的形成方面解释了效果,并消除了由于界面链entanglemen引起的合作运动能力

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