Bioinspired surface modification of mussel shells and their application as a biogenic filler in polypropylene composites

被引:1
作者
Xu, Jing [1 ,2 ]
Mucalo, Michael R. [1 ]
Pickering, Kim L. [2 ]
机构
[1] Univ Waikato, Sch Sci, Hamilton, New Zealand
[2] Univ Waikato, Sch Engn, Hamilton, New Zealand
来源
COMPOSITES PART C: OPEN ACCESS | 2024年 / 15卷
关键词
PP composite; Mussel shell; Surface modification; Interfacial adhesion; CALCIUM-CARBONATE POLYMORPHS; MECHANICAL-PROPERTIES; COUPLING AGENT; THERMAL-PROPERTIES; PARTICLE-SIZE; DISPERSION; DENSITY; CACO3; POLYDOPAMINE; ADHESION;
D O I
10.1016/j.jcomc.2024.100520
中图分类号
TB33 [复合材料];
学科分类号
摘要
This study explores the potential of mussel shells (MS) as biogenic fillers in polymer composites. The chemical composition and crystal structures of MS were characterised. To improve MS filler dispersion and adhesion within a polypropylene (PP) matrix, three surface modification methods were evaluated: polydopamine (PDA) coating, maleic anhydride-grafted polypropylene (MAPP) modification, and PDA/MAPP co-modification. The PDA coating, inspired by the adhesive properties of mussel foot proteins, successfully functionalized the MS surface, as confirmed by X-ray photoelectron spectroscopy (XPS). Thermodynamic analysis, based on contact angle measurements, revealed that MAPP and PDA/MAPP modifications reduced surface energies and potential energy differences. These changes enhanced filler dispersion and interfacial bonding by increasing hydrophobicity and reducing agglomeration in the PP matrix. Consequently, PP composites with 20% PDA/MAPPmodified MS fillers exhibited a 2.9% increase in tensile strength and a 7.5% increase in flexural strength compared to neat PP. Scanning electron microscopy (SEM) also showed reduced filler-matrix debonding and fewer voids. The proposed mechanism attributes these macroscopic property enhancements to the ability of the PDA coating to facilitate chemical and hydrogen bonding between MS fillers and MAPP.
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页数:14
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