玻璃化转变
材料科学
聚苯乙烯
聚合物
纳米颗粒
复合材料
纳米复合材料
复合数
组态熵
转变温度
热力学
纳米技术
超导电性
量子力学
物理
作者
V. I. Roldughin,О. А. Серенко,E. V. Getmanova,Natalia A. Novozhilova,Galina G. Nikifirova,Mikhail I. Buzin,С. Н. Чвалун,А. N. Ozerin,Aziz M. Muzafarov
摘要
Changes in the glass transition temperatures of composites based on polystyrene and nanosized macromolecular nanostructures (molecular silicasols, dendrimers) are reported. Silicasols are nanosized particles consisting of a silica core and an ethyl phenyl shell; dendrimers are formed using a carbosilane core with ethyl phenyl end groups. It has been observed that the glass transition temperatures of the composites ( T gc ) may be either above or below the glass transition temperature of polystyrene, depending on the size of the filler particles. A theoretical model based on the relation between the glass transition temperature and the configurational entropy of the composite, which satisfactorily describes the experimental dependence, was developed. It is found that the effect of the size of the hybrid nanoparticles on T gc was determined using two factors. First, the presence of an organic layer on the surface of nanoparticles increases the number of degrees of freedom and the entropy of the system, thereby reducing T gc . Second, the particles present in the polymer reduce the number of configuration states of macromolecules, which reduces the disorientation entropy. This effect leads to an increase T gc . The competition between these two main factors determines the sign of the glass transition temperature deviation. The size of the particles and their organic surface layer play the key roles in the thermodynamic properties of the composites. POLYM. COMPOS., 37:1978–1990, 2016. © 2015 Society of Plastics Engineers
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