Reducing part deformation of isotactic polypropylene specimens fabricated with powder bed fusion technique through controlling crystallization behaviors
Research output: Contribution to journal › Article › Research › peer-review
Standard
In: Journal of polymer science, Vol. 62.2024, No. 13, 24.04.2024, p. 3025-3037.
Research output: Contribution to journal › Article › Research › peer-review
Harvard
APA
Vancouver
Author
Bibtex - Download
}
RIS (suitable for import to EndNote) - Download
TY - JOUR
T1 - Reducing part deformation of isotactic polypropylene specimens fabricated with powder bed fusion technique through controlling crystallization behaviors
AU - Gao, Xia
AU - Guo, Junqiang
AU - Zhang, Daijun
AU - Li, Jing
AU - Su, Yunlan
AU - Arbeiter, Florian
AU - Li, Huayi
N1 - Publisher Copyright: © 2024 Wiley Periodicals LLC.
PY - 2024/4/24
Y1 - 2024/4/24
N2 - Serious shrinkage and warpage are obstacles to the development of ideal isotactic polypropylene (iPP) materials for polymer-based powder bed fusion (PBF) technique. In this work, the variations of the dimensional accuracy of the PBF-printed iPP parts were investigated with various printing parameter and nucleating agent. The iPP parts printed at a scanning speed of 700 mm/s exhibit smaller extents of shrinkage and curling than those at lower speeds, due to a lower degree of crystallinity. Interestingly, iPP blended with the α- or β-nucleating agent demonstrates more serious part deformation with respect to neat iPP. Especially, α-nucleating agent tends to trigger the most severe curling under the investigated printing parameters. Based on X-ray diffraction and differential scanning calorimetry (DSC) results, both neat iPP and α-iPP parts crystallize into α-crystal, while β-iPP parts display the coexistence of β- and α-crystals. And, the difference of the crystallinity is less than 3% in three specimens. This suggests that both crystallinity and crystalline structure are not the main reasons for the shrinkage and warpage in this case. Instead, the severe part deformation of the α-iPP parts is assigned to the narrower sintering window as well as the higher onset crystallization temperature of α-iPP, which hinder relaxation of residual stresses. This work provides insights into the part deformation mechanism for PBF-processed polymer materials.
AB - Serious shrinkage and warpage are obstacles to the development of ideal isotactic polypropylene (iPP) materials for polymer-based powder bed fusion (PBF) technique. In this work, the variations of the dimensional accuracy of the PBF-printed iPP parts were investigated with various printing parameter and nucleating agent. The iPP parts printed at a scanning speed of 700 mm/s exhibit smaller extents of shrinkage and curling than those at lower speeds, due to a lower degree of crystallinity. Interestingly, iPP blended with the α- or β-nucleating agent demonstrates more serious part deformation with respect to neat iPP. Especially, α-nucleating agent tends to trigger the most severe curling under the investigated printing parameters. Based on X-ray diffraction and differential scanning calorimetry (DSC) results, both neat iPP and α-iPP parts crystallize into α-crystal, while β-iPP parts display the coexistence of β- and α-crystals. And, the difference of the crystallinity is less than 3% in three specimens. This suggests that both crystallinity and crystalline structure are not the main reasons for the shrinkage and warpage in this case. Instead, the severe part deformation of the α-iPP parts is assigned to the narrower sintering window as well as the higher onset crystallization temperature of α-iPP, which hinder relaxation of residual stresses. This work provides insights into the part deformation mechanism for PBF-processed polymer materials.
KW - crystallization behavior
KW - isotactic polypropylene
KW - part deformation
KW - powder bed fusion technique
UR - http://www.scopus.com/inward/record.url?scp=85191175212&partnerID=8YFLogxK
U2 - 10.1002/pol.20240121
DO - 10.1002/pol.20240121
M3 - Article
AN - SCOPUS:85191175212
VL - 62.2024
SP - 3025
EP - 3037
JO - Journal of polymer science
JF - Journal of polymer science
SN - 2642-4150
IS - 13
ER -