# Correlating the Segmental Relaxation Time of Polystyrene

**Authors:** C. A. Hieber

PMC · DOI: 10.3390/polym16152154 · Polymers · 2024-07-29

## TL;DR

This paper shows how the relaxation time of polystyrene changes with temperature using a combination of exponential and VFTH models.

## Contribution

A new composite correlation for the segmental relaxation time of polystyrene is developed without adjustable parameters.

## Key findings

- The equilibrium relaxation time shows exponential temperature dependence below 100 °C.
- A crossover temperature of 99.22 °C was identified where τeq = 92.15 s.
- The composite model accurately describes relaxation time data around the glass transition.

## Abstract

A previous related paper dealing with the density relaxation of polystyrene (PS) has shown that the equilibrium relaxation time (τeq) has a purely exponential temperature dependence (ETD) below ≈100 °C. Such an ETD is now also confirmed based upon available dielectric spectra data for PS. By combining the ETD behavior of τeq (or aT) at low temperatures with a VFTH behavior at higher temperatures (based mainly on available recoverable shear compliance data), a composite correlation for τeq (or aT) is developed, which is continuous with continuous slope at a crossover temperature that is found to be 99.22 °C, where τeq = 92.15 s. This composite representation is shown to describe (without any adjustable parameters) available independent data for the segmental relaxation time over a finite range both above and below Tcrossover (i.e., the glass transition temperature).

## Linked entities

- **Chemicals:** PS (PubChem CID 7408258)

## Full-text entities

- **Chemicals:** PS (MESH:D011137)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11314254/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC11314254/full.md

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Source: https://tomesphere.com/paper/PMC11314254