首页> 外文期刊>Journal of Materials Science >Fabrication and characterization of superparamagnetic nanocomposites based on epoxy resin and surface-modified c-Fe_2O_3 by epoxide functionalization
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Fabrication and characterization of superparamagnetic nanocomposites based on epoxy resin and surface-modified c-Fe_2O_3 by epoxide functionalization

机译:基于环氧树脂和表面改性c-Fe_2O_3的超顺磁性纳米复合材料的环氧官能团制备与表征

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In this study, the effect of modified epoxideterminated c-Fe_2O_3 on the magnetic, mechanical, and thermal properties of epoxy nanocomposite was investigated. The c-Fe_2O_3 nanoparticles were prepared via a wet chemical approach, surface modified with 3-glycidoxypropyltrimethoxysilane (GPTMS), and characterized by particle size analyzer, XRD, FT-IR, and TGA techniques. The catalytic effect of c-Fe_2O_3 on the cure reaction temperature of epoxy/triethylenetetramine (TETA) was determined by differential scanning calorimeter (DSC). The glass transition temperature (T_g) of nanocomposite containing 5 wt% modified c-Fe_2O_3 increased slightly (12 ℃), while the initial decomposition temperature (T_(ID)) did not show improvement. Transmission electron microscopy (TEM) showed improvement in dispersion of surfacemodified c-Fe_2O_3 nanoparticles in the resin matrix. The effect of interfacial bonding between modified c-Fe_2O_3 and epoxy resin, via crosslink reactions, on the mechanical properties of nanocomposite such as flexural and tensile strength was studied, and the fractured surface of samples was investigated by scanning electron microscopy (SEM). Comparing with the mechanical properties of neat epoxy resin, tensile, and flexural strength of 10 wt% modified c-Fe_2O_3/epoxy nanocomposite increased 20 and 19 %, respectively, while tensile and flexural strength of 10 wt% unmodified/epoxy nanocomposite decreased slightly. The saturation magnetization (M_s) of 5 wt% modified c-Fe_2O_3/ epoxy nanocomposites with superparamagnetic property was approximately 80 % greater than that of unmodified c-Fe_2O_3/epoxy nanocomposites.
机译:在这项研究中,研究了改性的环氧封端的c-Fe_2O_3对环氧纳米复合材料的磁,机械和热性能的影响。通过湿化学方法制备c-Fe_2O_3纳米颗粒,用3-环氧丙氧基丙基三甲氧基硅烷(GPTMS)表面改性,并通过粒度分析仪,XRD,FT-IR和TGA技术进行表征。用差示扫描量热仪(DSC)测定了c-Fe_2O_3对环氧/三亚乙基四胺(TETA)固化反应温度的催化作用。含有5 wt%的改性c-Fe_2O_3的纳米复合材料的玻璃化转变温度(T_g)略有升高(12℃),而初始分解温度(T_(ID))没有显示出改善。透射电子显微镜(TEM)显示出表面改性的c-Fe_2O_3纳米颗粒在树脂基质中的分散性得到改善。通过交联反应,研究了改性c-Fe_2O_3与环氧树脂的界面键合对纳米复合材料力学性能(如抗弯强度和拉伸强度)的影响,并通过扫描电子显微镜(SEM)研究了样品的断裂表面。与纯环氧树脂的机械性能相比,10 wt%改性c-Fe_2O_3 /环氧纳米复合材料的拉伸强度和挠曲强度分别增加20%和19%,而10 wt%未改性/环氧纳米复合材料的拉伸强度和挠曲强度略有下降。具有超顺磁性的5wt%改性的c-Fe_2O_3 /环氧纳米复合材料的饱和磁化强度(M_s)比未改性的c-Fe_2O_3 /环氧纳米复合材料的饱和磁化强度大约80%。

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