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通过基体结晶改性提高木粉/聚丙烯复合材料的结晶度和韧性:两种β成核剂的对比研究

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

作者信息

Luo Shupin, Lv Chao, Chang Liang, Guo Wenjing

机构信息

Research Institute of Wood Industry, Chinese Academy of Forestry, No 2 Dongxiaofu, Haidian District, Beijing 100091, China.

出版信息

Polymers (Basel). 2022 Aug 29;14(17):3561. doi: 10.3390/polym14173561.

DOI:10.3390/polym14173561
PMID:36080633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9459986/
Abstract

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 β-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 β-crystal for WF/PP, with β-crystal content (k) 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 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.

摘要

将木粉(WF)等短木填料加入聚丙烯(PP)中,通常会导致韧性显著降低,这是WF/PP复合材料的主要缺点之一。本研究报道了一种简便的方法,通过在PP基体中引入自组装β成核剂来实现WF/PP复合材料的增韧。比较研究了两种成核剂,一种芳基酰胺衍生物(TMB5)和一种稀土配合物(WBG II),在不同浓度下对WF/PP复合材料结晶和力学性能的影响。结果表明,两种成核剂对WF/PP诱导β晶都非常有效,在成核剂浓度为0.05 wt%时,β晶含量(k)值达到0.8。加入TMB或WBG显著减小了球晶尺寸,提高了结晶温度,并加速了WF/PP的结晶过程。由于PP结晶改性,复合材料的韧性显著提高。通过引入0.3 wt%的TMB或WBG,WF/PP的缺口冲击强度和断裂应变分别提高了约28%和40%。相比之下,虽然在相同浓度下WF/PP-WBG的K值略高于WF/PP-TMB,但WF/PP/TMB表现出更均匀的结晶形态,球晶更小。此外,WF/PP-TMB的拉伸强度和模量高于WF/PP-WBG。这种基体结晶改性策略为制备具有改善韧性和加速结晶的木填料/热塑性复合材料提供了一条有前景的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/e7d9ff7fa83d/polymers-14-03561-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/b7ed3be2c6c1/polymers-14-03561-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/477cd2070945/polymers-14-03561-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/fa3231f8ad9f/polymers-14-03561-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/957df9eabc1d/polymers-14-03561-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/ba754360a51b/polymers-14-03561-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/90b0037a9deb/polymers-14-03561-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/d1033a72eca4/polymers-14-03561-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/e7d9ff7fa83d/polymers-14-03561-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/b7ed3be2c6c1/polymers-14-03561-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/477cd2070945/polymers-14-03561-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/fa3231f8ad9f/polymers-14-03561-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/957df9eabc1d/polymers-14-03561-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/ba754360a51b/polymers-14-03561-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/90b0037a9deb/polymers-14-03561-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/d1033a72eca4/polymers-14-03561-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/9459986/e7d9ff7fa83d/polymers-14-03561-g008.jpg

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