Using molecular entanglement as a strategy to enhance carbon fiber-epoxy composite interfaces

被引:41
|
作者
Eyckens, Daniel J. [1 ]
Demir, Baris [2 ]
Randall, James D. [1 ]
Gengenbach, Thomas R. [3 ]
Servinis, Linden [1 ]
Walsh, Tiffany R. [1 ]
Henderson, Luke C. [1 ]
机构
[1] Deakin Univ, Inst Frontier Mat, Waurn Ponds, Vic 3216, Australia
[2] Univ Queensland, Ctr Theoret & Computat Mol Sci, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
[3] CSIRO Mfg, Clayton, Vic 3168, Australia
基金
澳大利亚研究理事会;
关键词
SURFACE MODIFICATION; ANODIC-OXIDATION; ADHESION; STRENGTH; MATRIX; FUNCTIONALIZATION; INTERPHASE; CHEMISTRY; NANOTUBE; DESIGN;
D O I
10.1016/j.compscitech.2020.108225
中图分类号
TB33 [复合材料];
学科分类号
摘要
The tethering of an amphiphilic molecule to the surface of carbon fiber resulted in significant (+283%) improvements in interfacial shear strength. Molecular dynamics simulations revealed that lateral association of hydrophobic sections lead to a 'hooked' conformation through which polymer chains become entangled. Further simulations indicated that a small molecule, forced into this conformation via two covalent attachment points to the fiber surface (similar to a 'horseshoe'), would provide similar adhesion improvements and confirm this conformational effect on interfacial phenomena. This prediction was confirmed by the synthesis and grafting of such a molecule to a carbon fiber surface, giving an almost identical improvement in interfacial adhesion (+276%). This work validates the use of molecular dynamics to inform molecular architectural design and demonstrates the translation of molecular conformation and shape at a composite interface from nano-to macroscale.
引用
收藏
页数:8
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