Open AccessВзаимосвязь между молекулярной динамикой полистирола и его модификаций и параметрами терагерцового поглощения в ИК спектрах
Author(s) -
Валерий Александрович Рыжов
Publication year - 2021
Publication title -
optika i spektroskopiâ
Language(s) - English
Resource type - Journals
eISSN - 2782-6694
pISSN - 0030-4034
DOI - 10.21883/os.2021.03.50655.264-20
Subject(s) - intermolecular force , polystyrene , monomer , polymer , libration (molecule) , relaxation (psychology) , absorption (acoustics) , chemistry , absorption spectroscopy , absorption band , substituent , macromolecule , spectral line , chemical physics , materials science , molecule , crystallography , stereochemistry , organic chemistry , physics , psychology , social psychology , biochemistry , geometry , point (geometry) , mathematics , quantum mechanics , astronomy , optics , composite material
The IR spectra of polystyrene (PS) and its modifications obtained by replacing hydrogen atoms in the benzene ring with methyl groups and / or chlorine and bromine atoms have been measured and analyzed. All these spectra have an anomalously wide asymmetric absorption band with a maximum in the terahertz range from 40 to 80 cm – 1, depending on the nature of the substituent. It can be attributed to absorption associated with libration (rotational vibrations) of phenolic rings of monomer units, i.e., to absorption by the Poly mechanism. The relationship between the spectral parameters of this absorption and the molecular characteristics of the studied polymers makes it possible to directly analyze the role of the molecular structure and intermolecular forces in the dynamics of their macromolecules. It was found that the heights of potential barriers to libration of monomeric units of PS and its modifications, estimated from the analysis of Poly absorption, are close to the activation energies of low-temperature delta-relaxation in these glassy polymers. Comparison of the barriers to libration of monomeric units of macromolecules of PS and its modifications with the activation barriers of local segmental mobility in the same PS confirms that the beta process as an elementary act of segmental dynamics is caused by correlated librational movement of the chain section, which is statistically independent of neighboring regions. In this sense, the universal delta process is a high-frequency precursor of the beta process in polymers like PS.