Effect of graphene treated with cyclohexyl diamine by diazonium reaction on cure kinetics, mechanical, thermal, and physical properties of natural rubber/graphene nanocomposite foam

石墨烯 材料科学 纳米复合材料 表面改性 热重分析 拉曼光谱 复合材料 硫化 氧化石墨烯纸 傅里叶变换红外光谱 化学工程 天然橡胶 纳米技术 光学 物理 工程类
作者
Pollawat Charoeythornkhajhornchai,Chavakorn Samthong,Anongnat Somwangthanaroj
出处
期刊:Polymer Composites [Wiley]
卷期号:40 (S2) 被引量:10
标识
DOI:10.1002/pc.25160
摘要

The influence of functionalization of cyclohexyl diamine onto the graphene surface via diazonium reaction on the cure kinetics as well as morphology, mechanical, thermal and physical properties of natural rubber (NR)/graphene nanocomposite foam was investigated. The surface functionalization of graphene was confirmed by Fourier transform infrared spectroscopy, Raman spectroscopy, and thermogravimetric analysis (TGA). Without an addition of blowing agent, the vulcanized NR composites containing cyclohexyl amine‐treated graphene showed not obvious different dispersion of graphene nanoplatelets than those containing untreated graphene as confirmed by transmission electron microscopy micrographs. Although the addition of untreated graphene could accelerate the sulfur vulcanization rate of NR nanocomposite foam due to the high thermal conductivity of graphene particle, and the remaining oxygen functional groups on the surface of graphene, the amines from cyclohexyl diamine on the treated graphene could react with carboxylic and epoxide group on the surface of graphene leading to a reduction of reactive oxygen functional groups on graphene surface and in turn slowed vulcanization rate. The fast vulcanization rate in untreated graphene system led to small bubble size in the NR nanocomposite foams. In contrast, the treated graphene system showed high tensile strength and low thermal expansion coefficient owing to low cell density. Finally, the defect on the graphene surface after functionalization was detected by Raman spectroscopy; this resulted in poor thermal conductivity for the treated graphene composite system. POLYM. COMPOS., 40:E1766–E1776, 2019. © 2018 Society of Plastics Engineers
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