4.7 Article

Enhancing Crystallization and Toughness of Wood Flour/Polypropylene Composites via Matrix Crystalline Modification: A Comparative Study of Two β-Nucleating Agents

Journal

POLYMERS
Volume 14, Issue 17, Pages -

Publisher

MDPI
DOI: 10.3390/polym14173561

Keywords

wood filler; polypropylene; composite; nucleating agent; beta-nucleation; crystallization behavior; mechanical properties

Funding

  1. National Natural Science Foundation of China [31901250]

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This research investigated the effect of introducing self-assembling beta-nucleating agents into the polypropylene matrix to improve the toughness of wood flour/polypropylene composites. The results showed that the nucleating agents effectively induced beta-crystal formation, decreased spherulite size, increased crystallization temperature, and accelerated the crystallization process. The addition of the nucleating agents significantly improved the toughness and crystallization of the composites.
Incorporation of short wood fillers such as wood flour (WF) into polypropylene (PP) often results in a marked reduction of toughness, which is one of the main shortcomings for WF/PP composites. This research reports a facile approach to achieve toughening of WF/PP composites via introducing self-assembling beta-nucleating agents into PP matrix. The effect of two kinds of nucleating agents, an aryl amide derivative (TMB5) and a rare earth complex (WBG II), at varying concentrations on the crystallization and mechanical properties of WF/PP composites was comparatively investigated. The results showed that both nucleating agents were highly effective in inducing beta-crystal for WF/PP, with beta-crystal content (k(beta)) value reaching 0.8 at 0.05 wt% nucleating agent concentration. The incorporation of TMB or WBG significantly decreased the spherulite size, increased the crystallization temperature and accelerated the crystallization process of WF/PP. As a result of PP crystalline modification, the toughness of composites was significantly improved. Through introducing 0.3 wt% TMB or WBG, the notched impact strength and strain at break of WF/PP increased by approximately 28% and 40%, respectively. Comparatively, although WF/PP-WBG had slightly higher K-beta value than WF/PP-TMB at the same concentration, WF/PP/TMB exhibited more uniform crystalline morphology with smaller spherulites. Furthermore, the tensile strength and modulus of WF/PP-TMB were higher than WF/PP-WBG. This matrix crystalline modification strategy provides a promising route to prepare wood filler/thermoplastic composites with improved toughness and accelerated crystallization.

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