纳米薄膜中的聚合物玻璃化转变

L. R. Arriaga, F. Monroy, D. Langevin
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引用次数: 16

摘要

薄聚合物层的玻璃化转变温度Tg一般不同于块体值。在极薄的薄膜中,当节段运动受到限制体相的存在的影响时,预计Tg会发生很大的变化,厚度只有几纳米。然而,大多数现有的实验数据对应于较厚的膜。为了填补这一空白,我们研究了超薄聚合物薄膜(Langmuir层沉积在水中)。这些薄膜在低温下处于玻璃态,具有有限剪切模量,在玻璃化转变后消失得很好。正如预期的那样,检测到显著的Tg还原,聚合物越疏水,还原幅度越大。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The polymer glass transition in nanometric films
The glass transition temperature Tg of thin polymer layers in general differs from the bulk value. Large changes in Tg are expected to occur with extremely thin films, of thicknesses of a few nm, when segmental motions are affected by the presence of limiting bulk phases. However, most existing experimental data correspond to thicker films. In order to fill the gap, we have studied ultrathin polymer films (Langmuir layers deposited on water). These films are in the glass state at low temperature, with a finite shear modulus that vanishes well above the glass transition. As expected, significant Tg reductions are detected, the more hydrophobic the polymer, the larger the reduction.
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