Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/46429
Title: Thymine as a Melt-Soluble Nucleating Agent for Poly(3-hydroxybutyrate-co-4-hydroxybutyrate)
Authors: Geeraert, Hannelore
DEN HAESE, Milan 
van den Brande, Niko
Peeters , Eveline
PITET, Louis 
Issue Date: 2025
Publisher: AMER CHEMICAL SOC
Source: Acs Applied Polymer Materials, 7 (13) , p. 8798 -8811
Abstract: Poly(3-hydroxybutyrate-co-4-hydroxybutyrate) (P(3HB-co-4HB)) is a biopolymer with promising biomedical and sustainable material applications, but its slow crystallization complicates processing. In this study, the potential of thymine as a biocompatible nucleating agent was evaluated using polarized optical microscopy (POM), differential scanning calorimetry (DSC), and tensile testing. Poly(3-hydroxybutyrate) (PHB) and P(3HB-co-4HB) with 6, 7, and 9 mol % 4HB were biosynthesized in-house usingCupriavidus sp. USMAA2-4, ensuring high purity necessary for this study. Thymine was found to dissolve in the polymer melt and recrystallize into needle-like crystals upon cooling, thereby creating effective nucleation sites. The addition of 1 wt % thymine consistently enhanced the crystallization rate under both nonisothermal and isothermal conditions, although it did not exceed the polymers' intrinsic self-nucleation potential. Initial tensile testing on heat-pressed films further revealed improved ductility in thymine-nucleated samples. These findings highlight the potential of thymine as a melt-soluble additive for enhancing the crystallization and mechanical performance of P(3HB-co-4HB).
Notes: van den Brande, N (corresponding author), Vrije Univ Brussel, Lab Phys Chem & Polymer Sci FYSC, Res Grp Sustainable Mat Engn SUME, B-1050 Brussels, Belgium.
Niko.Van.den.Brande@vub.be
Keywords: Polyhydroxyalkanoate (PHA);Poly(3-hydroxybutyrate-co-4-hydroxybutyrate);(P(3HB-co-4HB));thymine;biosynthesis;nucleating agent;differential scanning calorimetry (DSC);crystallization
Document URI: http://hdl.handle.net/1942/46429
ISSN: 2637-6105
e-ISSN: 2637-6105
DOI: 10.1021/acsapm.5c01493
ISI #: 001516861700001
Datasets of the publication: 10.5281/zenodo.11119380
Rights: 2025 The Authors. Published by American Chemical Society
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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