&ITIn situ&IT nanomechanical behavior and self-healing response of polymeric multilayer thin films

被引:9
作者
Humood, Mohammad [1 ]
Polychronopoulou, Kyriaki [1 ,2 ]
Song, Yixuan [1 ]
Grunlan, Jaime C. [1 ]
Polycarpou, Andreas A. [1 ]
机构
[1] Texas A&M Univ, Dept Mech Engn, College Stn, TX 77843 USA
[2] Khalifa Univ, Dept Mech Engn, Abu Dhabi 127788, U Arab Emirates
关键词
Wet nanoindentation; Self-healing; Polymer swelling; High temperature nanoindentation; Thermal crosslinking; MECHANICAL-PROPERTIES; POLYELECTROLYTE MULTILAYERS; AFM NANOINDENTATION; YOUNGS MODULUS; CROSS-LINKING; COATINGS; WATER; HUMIDITY; NANOCOMPOSITE; SURFACE;
D O I
10.1016/j.polymer.2017.10.036
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Self-healing of mechanical damages was triggered in polymeric multilayer films of polyethylenimine/polyacrylic acid (PEI/PAA) by exposure to high humidity conditions such as immersion in deionized (DI) water. In situ wet nanoindentation was carried out to demonstrate the swelling behavior of thin films in high humidity. Once immersed in DI water, the film became softer, where roughness, modulus and hardness were reduced by about 100%. Once the film was dried, its mechanical properties were restored but not its morphology. Heating was found to be required to promote the evaporation of immobilized water molecules, which bonds with the polymer once being immersed in DI water. When heating above glass transition temperature (Tg) was introduced, a formation of new bonding between both PEI and PAA took place leading to the formation of new topographical features similar to the as-deposited film. This reconstruction under high temperature (HT) was accompanied by more than 50% increase in the mechanical properties, which were measured using in situ HT nanoindentation. Multiple stimuli were required to achieve complete self-healing. The molecular mechanisms of these stimuli were determined using X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR). (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:169 / 178
页数:10
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