Crystallization kinetics of chain extended poly(L-lactide)s having different molecular structures
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10.1016/j.matchemphys.2019.122217
Inclou dades d'ús des de 2022
Cita com:
hdl:2117/171482
Tipus de documentArticle
Data publicació2020-01-15
Condicions d'accésAccés obert
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Abstract
Poly(L-lactide)s (PLLAs) with different chain structures were prepared by reactive melt processing and using Joncryl ADR as chain extender. Results of gel permeation chromatography (GPC) revealed that chain extended PLLAs had high molecular weights and two differentiated molecular weight distributions. Linear rheology was sensitive to the obtained molecular structures and revealed as the increase on the amount of chain extender gradually led to a decrease of the loss factor in the whole frequency region and to an increase of melt viscosity and both storage and loss moduli. In addition, the entanglement density increased significantly with addition of chain extender and had a significant influence on crystallization kinetics. Correlation of molecular weight, viscosity and entanglements changed the crystallinity and crystallization kinetics of chain extended PLLAs in both isothermal and non-isothermal crystallizations. Specifically, samples prepared from 1 wt-% of Joncryl (PLLA1R) revealed the highest nucleation and the fastest crystallization rate.
CitacióYousefzade, O. [et al.]. Crystallization kinetics of chain extended poly(L-lactide)s having different molecular structures. "Materials chemistry and physics", 15 Gener 2020, vol. 240, núm. 122217, p. 122217:1-122217:11.
ISSN0254-0584
Versió de l'editorhttps://www.sciencedirect.com/science/article/abs/pii/S0254058419310326
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