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Flame-Retardant Electrical Conductive Nanopolymers Based on Bisphenol F Epoxy Resin Reinforced with Nano Polyanilines

机译:纳米聚苯胺增强双酚F环氧树脂的阻燃导电纳米聚合物

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Both fibril and spherical polyaniline (PANI) nanostructures have successfully served as nanofillers for obtaining epoxy resin polymer nano-composites (PNCs). The effects of nanofiller morphology and loading level on the mechanical properties, rheological behaviors, thermal stability, flame retardancy, electrical conductivity, and dielectric properties were systematically studied. The introduction of the PANI nanofillers was found to reduce the heat-release rate and to increase the char residue of epoxy resin. A reduced viscosity was observed in both types of PANI—epoxy resin liquid nanosuspension samples at lower loadings (1.0 wt% for PANI nanospheres; 1.0 and 3.0 wt% for PANI nanofibers), the viscosity was increased with further increases in the PANI loading for both morphologies. The dynamic storage and loss modulii were studied, together with the glass-transition temperature (T_g) being obtained from the peak of tan 5. The critical PANI nanofiller loading for the modulus and T_g was different, i.e., 1.0 wt % for the nanofibers and 5.0 wt % for the nanospheres. The percolation thresholds of the PANI nanostructures were identified with the dynamic mechanical property and electrical conductivity, and, because of the higher aspect ratio, nanofibers reached the percolation threshold at a lower loading (3.0 wt %) than the PANI nanospheres (5.0 wt %). The PANI nanofillers could increase the electrical conductivity, and, at the same loading, the epoxy nanocomposites with the PANI nanofibers showed lower volume resistivity than the nanocomposites with the PANI nanospheres, which were discussed with the contact resistance and percolation threshold. The tensile test indicated an improved tensile strength of the epoxy matrix with the introduction of the PANI nanospheres at a lower loading (1.0 wt%). Compared with pure epoxy, the elasticity modulus was increased for all the PNC samples. Moreover, further studies on the fracture surface revealed an enhanced toughness. Finally, the real permittivity was observed to increase with increasing the PANI loading, and the enhanced permittivity Was analyzed by the interfacial polarization.
机译:原纤维和球形聚苯胺(PANI)纳米结构均已成功地用作获得环氧树脂聚合物纳米复合材料(PNC)的纳米填料。系统研究了纳米填料的形貌和填充量对力学性能,流变行为,热稳定性,阻燃性,电导率和介电性能的影响。发现引入PANI纳米填料可降低热释放速率并增加环氧树脂的炭残留量。两种类型的PANI-环氧树脂液体纳米悬浮液样品在较低的负载量下(PANI纳米球为1.0 wt%; PANI纳米纤维为1.0和3.0 wt%)都观察到粘度降低,随着两种材料的PANI负载进一步增加,粘度增加形态。研究了动态储能和损耗模量,并从tan 5的峰获得了玻璃化转变温度(T_g)。模量和T_g的临界PANI纳米填料负载不同,即,纳米纤维和T_g的1.0 wt%。对于纳米球为5.0重量%。 PANI纳米结构的渗透阈值由动态力学性能和电导率确定,并且由于高纵横比,纳米纤维在比PANI纳米球(5.0 wt%)低的载荷(3.0 wt%)时达到了渗透阈值。 。 PANI纳米填料可以提高电导率,并且在相同的负载下,具有PANI纳米纤维的环氧纳米复合材料的体积电阻率低于具有PANI纳米球的纳米复合材料,这在接触电阻和渗透阈值中进行了讨论。拉伸试验表明,以较低的负载量(1.0 wt%)引入PANI纳米球后,环氧树脂基质的拉伸强度有所提高。与纯环氧树脂相比,所有PNC样品的弹性模量均增加。此外,对断裂表面的进一步研究显示出增强的韧性。最后,观察到实际介电常数随PANI负载的增加而增加,并且通过界面极化分析了增强的介电常数。

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