Photodegradation versus network densification in UV-cured PolyJet 3D-printed polymers: A structure-mechanics study

PolyJet™ 3D printing of MED610™ photopolymer is increasingly used for dental and prosthetic structures; however, the coupled effects of in-plane printing direction and post-curing temperature on network evolution, photooxidation, and mechanical durability remain insufficiently understood. Herein, MED610 specimens were printed in two horizontal orientations (X and Y) and post-cured at room temperature or 64 °C to establish a chemistry-based structure-property relationship. The Y-oriented specimens exhibited lower roughness and pore-like defects than the X-oriented specimens, leading to improved tensile and flexural performance. The room-temperature post-curing enhanced interlayer bonding and increased flexural stress by approximately 8.5% compared with the untreated Y-oriented sample, while maintaining tensile strength. In contrast, UV post-curing at 64 °C caused substantial deterioration, reducing tensile stress, flexural stress, flexural modulus, wear resistance, and effective network integrity. FTIR and XPS confirmed post-curing-induced surface chemical changes, with the O 1 s/C 1s atomic ratio increasing from 0.13 to 0.21 after 64 °C treatment, indicating enhanced surface oxidation. DMA further revealed that room-temperature post-curing increased Tg and effective crosslink density, whereas 64 °C treatment produced the lowest storage modulus and effective crosslink density. These results support a competition between beneficial network densification/interlayer strengthening at room temperature and UV-assisted photooxidative degradation within the glass-transition region at 64 °C. This work distinguishes itself from previous processing-focused studies by linking PolyJet horizontal orientation and post-curing temperature to molecular-level network evolution, surface oxidation, and wear-mechanical performance, providing guidance for optimising MED610-based dental structures within the tested conditions.

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Journal
Materials Today Chemistry
Published
2026-11-02
DOI
https://doi.org/10.1016/j.mtchem.2026.104142
Primary Topic
Dental materials and restorations
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article
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article

Photodegradation versus network densification in UV-cured PolyJet 3D-printed polymers: A structure-mechanics study

Mojtaba Ahmadi, Weiwei Lei, Minoo Naebe, Milad Laghaei et al.
3 links
Materials Today Chemistry
Dental materials and restorations
article

Photodegradation versus network densification in UV-cured PolyJet 3D-printed polymers: A structure-mechanics study

Mojtaba Ahmadi, Weiwei Lei, Minoo Naebe, Milad Laghaei, Billy J. Murdoch, Omid Zabihi, Alireza Vahid, Qi Chao
article en

Abstract

PolyJet™ 3D printing of MED610™ photopolymer is increasingly used for dental and prosthetic structures; however, the coupled effects of in-plane printing direction and post-curing temperature on network evolution, photooxidation, and mechanical durability remain insufficiently understood. Herein, MED610 specimens were printed in two horizontal orientations (X and Y) and post-cured at room temperature or 64 °C to establish a chemistry-based structure-property relationship. The Y-oriented specimens exhibited lower roughness and pore-like defects than the X-oriented specimens, leading to improved tensile and flexural performance. The room-temperature post-curing enhanced interlayer bonding and increased flexural stress by approximately 8.5% compared with the untreated Y-oriented sample, while maintaining tensile strength. In contrast, UV post-curing at 64 °C caused substantial deterioration, reducing tensile stress, flexural stress, flexural modulus, wear resistance, and effective network integrity. FTIR and XPS confirmed post-curing-induced surface chemical changes, with the O 1 s/C 1s atomic ratio increasing from 0.13 to 0.21 after 64 °C treatment, indicating enhanced surface oxidation. DMA further revealed that room-temperature post-curing increased Tg and effective crosslink density, whereas 64 °C treatment produced the lowest storage modulus and effective crosslink density. These results support a competition between beneficial network densification/interlayer strengthening at room temperature and UV-assisted photooxidative degradation within the glass-transition region at 64 °C. This work distinguishes itself from previous processing-focused studies by linking PolyJet horizontal orientation and post-curing temperature to molecular-level network evolution, surface oxidation, and wear-mechanical performance, providing guidance for optimising MED610-based dental structures within the tested conditions.

Materials Today ChemistryVol. 58
Nanjing Tech University (CN), Deakin University (AU), RMIT University (AU)
Openalex Percentile: Top 12%
Dental materials and restorations
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