Mechanical Properties and Wear Resistance of Sulfonated Graphene/Waterborne Polyurethane Composites Prepared by In Situ Method

被引:25
作者
Feng, Jianyan [1 ,2 ]
Wang, Xuechuan [1 ,2 ]
Guo, Peiying [3 ]
Wang, Yujie [1 ,2 ]
Luo, Xiaomin [1 ,2 ]
机构
[1] Shanxi Univ Sci & Technol, Coll Bioresources Chem & Mat Engn, Xian 710021, Shanxi, Peoples R China
[2] Shanxi Univ Sci & Technol, Natl Demonstrat Ctr Expt Light Chem Engn Educ, Xian 710021, Shanxi, Peoples R China
[3] Shanxi Univ Sci & Technol, Sch Arts & Sci, Xian 710021, Shanxi, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
sulfonated grapheme; waterborne polyurethane; in situ method; mechanical resistance properties; wear resistance; GRAPHITE OXIDE; GRAPHENE;
D O I
10.3390/polym10010075
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In order to improve the dispensability of graphene oxide (GO) in waterborne polyurethane (WPU), sulfonated graphene (SGO) with superior dispersity was prepared by modifying graphene oxide with sodium 2-chloroethane sulfonate to introduce hydrophilic sulfonic groups into the structure. SGO/WPU composites were prepared using isophorone diisocyanate (IPDI), polytetramethylene ether glycol (PTMEG 2000), dimethylolpropionic acid (DMPA) and SGO as raw materials. The influence of SGO content on composite properties were investigated. The structure and morphology of SGO and SGO/WPU composites were characterized by infrared spectroscopy, X-ray diffractometry and transmission electron microscopy etc. Their mechanical properties and wear resistance were analyzed as well. The experimental results showed that SGO was successfully grafted onto polyurethane macromolecule by an in situ method and, with the introduction of sulfonic groups, the interfacial compatibility of GO and PU was improved significantly so that SGO evenly dispersed into WPU. The SGO that was grafted onto WPU macromolecules exhibited layered morphology with nanometers in the WPU matrix. With increasing SGO content, the tensile strength and the wear resistance of the film increased, but the addition of more than 0.8 wt % SGO yielded unfavorable results. When the added amount of SGO was 0.8 wt % of WPU, the tensile strength of the composite film was 46.53% higher than that of the blank group, and the wear resistance of the film was remarkably improved, which was due to a strong interaction between the SGO and WPU phases. Thus, the conclusion can be drawn that appropriate amount of SGO addition can enhance the mechanical properties of SGO/WPU composite film.
引用
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页数:12
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