玻璃化转变
含氟聚合物
材料科学
无定形固体
原子力显微镜
等温过程
分析化学(期刊)
基质(水族馆)
大气温度范围
复合材料
聚合物
热力学
纳米技术
化学
结晶学
有机化学
海洋学
物理
地质学
作者
Amer A. El Banna,Gregory B. McKenna
摘要
Abstract Ultra‐stable amorphous fluoropolymers glasses were created using vacuum pyrolysis deposition (VPD). Glass films with thickness ranging from 90 to 160 nm were grown at a substrate temperature of 0.86 T g , where T g is the glass transition temperature of the virgin polymer and is in units of K. Atomic force microscope (AFM) dilatometry measurements were conducted to investigate density behavior of the ultra‐stable glasses. Thickness measurements were made in stepwise fashion over a range of temperatures from ambient to above the T g . Results show that the intersections of the line for the equilibrium liquid and those for the rejuvenated and stable glasses identifying the fictive temperature T f result in T f, rejuvenated = 347.3 K and T f, stable = 269.5 K, that is, nearly 80 K below the T g of the rejuvenated material and well below the notional Kauzmann temperature as estimated from the Vogel‐Fultcher‐Tammann (VFT) analysis of the cooling rate dependence of the calorimetric glass transition temperature reported previously. The results corroborate the published calorimetric results on the same ultra‐stable fluoropolymer glasses that witnessed T f reductions of up to 62.6 K below the T g of the rejuvenated system. In addition, to demonstrate the versatility of the AFM dilatometry methodology for the thin film response, isothermal de‐aging experiments were carried out to illustrate the devitrification kinetics. We also carried out one of the Kovacs’ signature key experiments, the asymmetry of approach, to further illustrate the method.
科研通智能强力驱动
Strongly Powered by AbleSci AI