首页> 外文期刊>The European physical journal, E. Soft matter >Measuring surface and bulk relaxation in glassy polymers.
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Measuring surface and bulk relaxation in glassy polymers.

机译:测量玻璃状聚合物的表面和体积松弛。

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We present a comprehensive study of gold nanoparticle embedding into polystyrene (PS) surfaces at temperatures ranging from T (g) + 8 K to T (g) - 83 K and times as long as 10(5) minutes. This range in times and temperatures allows the first concurrent observation of and differentiation between surface and bulk behavior in the 20 nm region nearest the free surface of the polymer film. Of particular importance is the temperature region near the bulk glass transition temperature where both surface and bulk processes can be measured. The results indicate that for the case of PS, enhanced surface mobility only exists at temperatures near or below the bulk T (g) value. The surface relaxation times are only weakly temperature dependent and near T (g), the enhanced mobility extends less than 10nm into the bulk of the film. The results suggest that both the concept of a "surface glass transition" and the use of glass transition temperatures to measure local mobility near interfaces may not universally apply to all polymers. The results can also be used to make a quantitative connection to molecular dynamics simulations of polymer films and surfaces.
机译:我们目前对金纳米颗粒嵌入T(g)+ 8 K到T(g)-83 K的温度范围内长达10(5)分钟的金纳米颗粒进行全面研究。该时间和温度范围允许首次同时观察并区分最接近聚合物膜自由表面的20 nm区域中的表面行为和本体行为。尤其重要的是靠近大块玻璃化转变温度的温度区域,在该区域可以测量表面过程和大块过程。结果表明,对于PS,增强的表面迁移率仅存在于接近或低于体温T(g)值的温度下。表面弛豫时间仅对温度有微弱的影响,并且接近T(g),增强的迁移率延伸到整个薄膜中小于10nm。结果表明,“表面玻璃化转变”的概念和使用玻璃化转变温度来测量界面附近的局部迁移率都可能无法普遍适用于所有聚合物。结果还可以用于定量连接聚合物薄膜和表面的分子动力学模拟。

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