4.7 Article

Temperature dependence of vibrational motions of thin polystyrene films by infrared reflection-absorption spectroscopy: A single measurement tool for monitoring of glass transition and temperature history

Journal

POLYMER TESTING
Volume 101, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.polymertesting.2021.107305

Keywords

Infrared reflection-absorption spectroscopy; Polarization; Glass transition temperature; Polystyrene; Thin film

Funding

  1. Czech Science Foundation [19-23513S]
  2. Operational Program Research and Development for Innovations
  3. European Regional Development Fund (ERDF)
  4. national budget of the Czech Republic [CZ.1.05/2.1.00/19.0409]
  5. Ministry of Education, Youth and Sports of the Czech Republic - DKRVO [RP/CPS/2020/006]

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The study investigated the temperature-dependent changes of polystyrene thin films using polarization-modulated infrared reflection-absorption spectroscopy, revealing specific changes in individual spectral regions and their relation to the processing and thermal history of the thin film. The different behaviors of spectral regions were rationalized by considering the contribution of vibrational free volume to the total free volume of the system, influenced by the nature of functional groups.
A method for monitoring of vibrational response and temperature region of glass transition by a single analysis is introduced with the use of an otherwise well-known spectroscopic method. The temperature-dependent changes of polystyrene (PS) thin films were investigated by polarization-modulated infrared reflection-absorption spectroscopy. The study revealed that changes in individual spectral regions with the temperature increase are specific and provide the relation to the processing and thermal history of the thin film. Temperature responses of infrared spectral region areas; an abrupt change of C-ar-H stretching, a step-like change of C-ar-H out-of-plane bending, a linear decrease of C-H stretching and C-H bending area, granted information on the temperature domain represented by local molecular motion change (beta-transition) of PS. The different behavior of spectral regions is rationalized by consideration of vibrational free volume contribution to the total free volume of the system that is certainly influenced by functional groups nature, such as their size, geometry and involvement of non-bonding interaction.

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