Effects of annealing above Tg on the physical aging of quenched PLLA studied by modulated temperature FTIR. Issue 3 (25th November 2018)

• Record Type: Journal Article
• Authors: Di Lisio, Valerio; Sturabotti, Elisa; Francolini, Iolanda; Piozzi, Antonella; Martinelli, Andrea
• Is Part Of: Journal of polymer science. Volume 57:Issue 3(2019)
• Page Start: 174
• Page End: 181
• Publication Date: 2018-11-25
• Subjects: annealing -- amorphous -- FT‐IR -- FTIR spectroscopy -- glass transition -- modulated temperature -- physical aging -- poly(l‐lactide) -- rejuvenation -- thermal properties; 547
• DOI: 10.1002/polb.24769
• Languages: English
• ISSNs: 0887-6266

Abstract

ABSTRACT: The effect of the annealing few degrees above the glass transition temperature ( T da = 62 °C) on the physical aging ( T pa = 51 °C) of amorphous quenched poly(l ‐lactide) is investigated by an implementation of variable temperature Fourier transform infrared (FTIR). By using a temperature program composed of a linear heating ramp superimposed to a temperature modulation (modulated temperature FTIR), the reversing and nonreversing intensity variation of selected bands, related to high‐energy gg and low‐energy gt conformers, is investigated. It is observed that the annealing above T g changes irreversibly the conformation distribution of the liquid polymer. The glasses obtained from annealed and nonannealed liquids behave differently, evolving in the physical aging toward their own liquid state and retaining the memory of their original condition before the vitrification. The recovery through T g of the relaxation occurred in the physical aging depends not only from aging conditions but also by the thermal history of the sample above the T g . © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys.2019, 57, 174–181 Abstract : The reversing and nonreversing variations of amorphous poly(l ‐lactide) conformer relative concentration as a function of temperature are investigated by modulated temperature Fourier transform infrared. It is observed that different thermal histories of the polymer above the glass transition temperature affect the relaxation of the glass during the physical aging.