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Epoxy resin nanosuspensions and reinforced nanocomposites from polyaniline stabilized multi-walled carbon nanotubes

机译:聚苯胺稳定的多壁碳纳米管的环氧树脂纳米悬浮液和增强纳米复合材料

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摘要

The high performance multi-walled carbon nanotubes (MWNTs) reinforced epoxy polymer nanocomposites (PNCs) have been synthesized at different MWNT loading levels. The surface functionalization of MWNTs with conductive PANI was achieved by using a facile surface initiated polymerization method with the aid of the oxidations of CNTs and subsequent anilines by hexavalent chromium (Cr(VI)) oxidant. The effects of MWNT loading, surface functionalization and temperature on the rheological behaviors of liquid epoxy resin nanosuspensions and on the physicochemical properties of cured solid PNCs were systematically investigated. The glass transition temperature (T_g) of the cured epoxy PNCs filled with functionalized MWNTs obtained from the dynamic mechanical analysis (DMA) test was increased about 6-25 °C than that of cured pure epoxy. The PNCs reinforced with functionalized MWNTs demonstrated an enhanced tensile strength than either cured pure epoxy or its PNCs filled with the as-received MWNTs. The electrical conductivity of cured epoxy PNCs with functionalized MWNTs was improved by 5.5 orders of magnitude compared with cured pure epoxy. Thermogravimetric analysis (TGA) revealed an enhanced thermo-stability in the cured epoxy PNCs filled with functionalized MWNTs than that of cured pure epoxy and its PNCs filled with the as-received MWNTs. The observed strong interfacial interaction between MWNTs and the epoxy resin matrix was responsible for the enhanced mechanical tensile strength. The nanocomposite formation mechanism is proposed based on the analysis from Fourier transform infrared (FT-IR), thermogravimetric analysis (TGA), Raman and differential scanning calorimetry (DSC) tests.
机译:高性能多壁碳纳米管(MWNTs)增强的环氧聚合物纳米复合材料(PNCs)已在不同的MWNT负载水平下合成。 MWNTs具有导电性PANI的表面功能化是通过使用便捷的表面引发的聚合方法,借助CNT的氧化以及随后的苯胺被六价铬(Cr(VI))氧化剂的氧化而实现的。系统地研究了MWNT的负载量,表面官能化和温度对液态环氧树脂纳米悬浮液的流变行为以及对固化的固体PNC的理化性质的影响。通过动态力学分析(DMA)测试获得的填充有功能化MWNT的固化环氧树脂PNC的玻璃化转变温度(T_g)比固化纯环氧树脂的玻璃化温度提高了约6-25°C。用功能化的MWNT增强的PNC表现出比固化的纯环氧树脂或其填充了MWNT的PNC更高的拉伸强度。与固化的纯环氧树脂相比,具有官能化MWNT的固化的环氧树脂PNC的电导率提高了5.5个数量级。热重分析(TGA)显示,填充有功能化MWNT的固化环氧树脂PNC的热稳定性要高于填充纯MWNT的固化纯环氧树脂及其PNC。所观察到的MWNT与环氧树脂基体之间的强界面相互作用是增强的机械拉伸强度的原因。在傅立叶变换红外光谱(FT-IR),热重分析(TGA),拉曼光谱和差示扫描量热法(DSC)测试分析的基础上,提出了纳米复合材料的形成机理。

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