Melt and solution processability of poly(butylene succinate‐dilinoleic succinate) copolymers modified with poly(ethylene glycol) using 3D printing and electrospinning

• Published in: Polymers for advanced technologies Vol. 34; no. 11; pp. 3586 - 3602
• Main Authors: Zarei, Moein, Żwir, Marek J., Wiśniewska, Ewa, Michalkiewicz, Beata, El Fray, Miroslawa
• Format: Journal Article
• Language: English
• Published: Bognor Regis Wiley Subscription Services, Inc 01.11.2023
• Subjects: 3-D printers; Chemical synthesis; Copolymers; Crystallites; Crystallization; Filaments; Glass transition temperature; Magnesium; Melting points; Morphology; Polyethylene glycol; Polymer melts; Segments; Three dimensional printing; Water baths
• ISSN: 1042-7147; 1099-1581
• DOI: 10.1002/pat.6159

Abstract Fabrication of complex structures usually requires a combination of different advanced manufacturing techniques at different length scales. In this work, we discuss the structure‐properties relationship of recently developed biodegradable poly(butylene succinate‐dilinoleic succinate) (PBS‐DLS) copolymers modified with hydrophilic poly(ethylene glycol) (PEG) towards their processibility via 3D printing and electrospinning. Notably, filaments suitable for 3D printing with 1.75 mm diameter were fabricated directly from the reactor after the synthesis of copolymers through extruding polymer melt into a water bath thus overcoming the postprocessing. Two series of copolymers containing 60 wt% and 70 wt% of hard PBS content were synthesized using magnesium‐titanium butoxide as heterometallic catalyst. Differential scanning calorimetry indicated biphasic morphology with low‐glass transition temperature and high‐melting point, which were dependent from the PBS hard segments content. Crystallized copolymers exhibited distinct spherulitic morphology, but presence of crystallites has no adverse effect on warping or delamination of subsequent layers during 3D printing. Furthermore, these copolymers demonstrated also easy processability through electrospinning, yielding uniform nanofibers with diameters ranging from 400 to 600 nm. The addition of 5 wt% PEG to copolymers with higher hard segments content (70 wt%) increased the elasticity up to 830% and improved hydrophilicity of the copolymers. Overall, these findings together with the excellent cell viability of new materials highlight their potential for different applications, including the biomedical sector.