Study on the Differences in Crystallization Behavior of Poly(lactic acid) (PLA) Induced by Amide-based and Hydrazide-based Nucleating Agents
RESEARCH ARTICLE|Updated:2026-03-10
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Study on the Differences in Crystallization Behavior of Poly(lactic acid) (PLA) Induced by Amide-based and Hydrazide-based Nucleating Agents
Chinese Journal of Polymer ScienceVol. 44, Pages: 1-13(2026)
Affiliations:
Guangdong Provincial Key Laboratory of Functional Soft Condensed Matter, School of Materials and Energy, Guangdong University of Technology, Guangzhou 510006, China
Lin, J. H.; Xiao, W. H.; Wu, J. B.; Wu, J. L.; Xu, R. J.; Lei, C. H. Study on the differences in crystallization behavior of poly(lactic acid) (PLA) induced by amide-based and hydrazide-based nucleating agents. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3575-z
Jiang-Hua Lin, Wen-Hao Xiao, Jing-Bo Wu, et al. Study on the Differences in Crystallization Behavior of Poly(lactic acid) (PLA) Induced by Amide-based and Hydrazide-based Nucleating Agents[J/OL]. Chinese Journal of Polymer Science, 2026, 441-13.
Lin, J. H.; Xiao, W. H.; Wu, J. B.; Wu, J. L.; Xu, R. J.; Lei, C. H. Study on the differences in crystallization behavior of poly(lactic acid) (PLA) induced by amide-based and hydrazide-based nucleating agents. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3575-zDOI:
Jiang-Hua Lin, Wen-Hao Xiao, Jing-Bo Wu, et al. Study on the Differences in Crystallization Behavior of Poly(lactic acid) (PLA) Induced by Amide-based and Hydrazide-based Nucleating Agents[J/OL]. Chinese Journal of Polymer Science, 2026, 441-13. DOI: 10.1007/s10118-026-3575-z.
Study on the Differences in Crystallization Behavior of Poly(lactic acid) (PLA) Induced by Amide-based and Hydrazide-based Nucleating Agents
Although amide- and hydrazide-based nucleating agents have been extensively used to enhance the crystallization performance of poly(lactic acid) (PLA)
structurally similar nucleating agents exhibit significant differences in their crystallization-promoting efficiency
and the underlying mechanism remains unclear. In this study
a series of nucleating agents
including
N
N
-diphenylterephthalamide (DPTA)
N
N
N
-triphenyl-1
3
5-benzenetricarboxamide (TPTA)
N
N
-diphenyl terephthalohydrazide (DBTA)
and
N
N
N
-tribenzoyl-1
3
5-benzenetricarbohydrazide (TBTA)
were designed and synthesized to investigate the differences in their effects on the crystallization performance of PLA. Density functional theory (DFT) and molecular dynamics (MD) simulations showed that DBTA had a smaller electrostatic potential difference (66.2 kcal/mol). During the cooling process
DBTA could stably form more intermolecular hydrogen bonds with PLA and exhibit a higher interaction energy
thus theoretically enabling more efficient promotion of PLA crystallization. Further differential scanning calorimetry (DSC) results revealed that at a 0.5 wt% loading of DBTA
the crystallization peak temperature of the PLA-DBTA composite reached 118.1 °C during cooling
whereas no distinct crystallization peak was observed for pure PLA under identical conditions. The crystallinity of the composite was significantly increased to 58.4% compared to 14.6% of pure PLA. Moreover
under isothermal crystallization at 130 °C
DBTA reduced the half-crystallization time of PLA to 2.9 min
while the half-crystallization time for pure PLA was 27.4 min. Time-resolved Fourier transform infrared spectroscopy (FTIR) results also confirmed that DBTA promoted the formation of gt conformational isomers of PLA during the crystallization process. This study elucidates the mechanism behind the performance differences between structurally similar nucleating agents in regulating PLA crystallization from the perspective of molecular electrostatic potential and hydrogen bonding interactions
providing a theoretical basis for the molecular design of efficient nucleating agents.
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