Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/116800
Title: Poly-3-hydroxybutyrate, a Crystal-Mobile Biodegradable Polyester
Author(s): Anuar, AfiqLook up in the Integrated Authority File of the German National Library
Yu, QiangLook up in the Integrated Authority File of the German National Library
Jariyavidyanont, KataleeLook up in the Integrated Authority File of the German National Library
Petzoldt, AlbrechtLook up in the Integrated Authority File of the German National Library
Androsch, RenéLook up in the Integrated Authority File of the German National Library
Thurn-Albrecht, Thomas
Saalwächter, KayLook up in the Integrated Authority File of the German National Library
Issue Date: 2024
Type: Article
Language: English
Abstract: Poly(3-hydroxybutyrate) (P3HB), a biodegradable thermoplastic with the potential to partially replace oil-based commodities, suffers from embrittlement over storage time. We here investigate possible causes by monitoring aging processes in the sample through changes in mechanical and thermal properties as well as the semicrystalline morphology (crystallinity, lamellar stack dimensions, and its inhomogeneity) over time, using advanced small-angle X-ray scattering analyses for the latter. We find that the slow rise in the shear modulus of the materials is accompanied by secondary crystallization, detected as lamellar thickening and an increase in the melting point. These morphology changes may be due to the chain mobility in the crystallites. This is a feature of “crystal-mobile” polymers that are known to be able to crystallize more fully than their crystal-fixed counterparts. We present the first evidence of the related crystalline αc relaxation in P3HB by dynamic-mechanical analysis (DMA) and investigate the process microscopically by advanced magic-angle spinning solid-state exchange NMR techniques, specifically centerband-only detection of exchange. We show that monomer jumps in the P3HB crystals are comparably slow (i.e., with an average correlation time τc of 0.1 s at 120 °C). Their apparent activation energy (80 to 90 kJ/mol) is found to be independent of the crystallization temperature and in good agreement with the DMA results.
URI: https://opendata.uni-halle.de//handle/1981185920/118759
http://dx.doi.org/10.25673/116800
Open Access: Open access publication
License: (CC BY 4.0) Creative Commons Attribution 4.0(CC BY 4.0) Creative Commons Attribution 4.0
Journal Title: Macromolecules
Publisher: Soc.
Publisher Place: Washington, DC
Volume: 57
Issue: 17
Original Publication: 10.1021/acs.macromol.4c00938
Page Start: 8507
Page End: 8518
Appears in Collections:Open Access Publikationen der MLU

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