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Development and characterization of graphite nanoplatelets filled copolymer of benzoxazine and epoxy

机译:苯并嗪和环氧树脂填充共聚物的石墨纳米型纳米型纳米型共聚物的发展与鉴定

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In this study, graphite nanoplatelets (GNPs) were dispersed in a copolymer matrix consisting of bisphenol-A based benzoxazine (BZ) and bi-functional cycloaliphatic epoxy (CER), using two solvent-free techniques: ultrasonication and three-roll mill (3RM). The effects of GNP addition on the tensile performance, storage modulus, glass-transition temperature (T-g), and electrical conductivity were evaluated. A maximum increase of nearly 46% and 20% in tensile modulus and strength, respectively, was found at 1.8 wt% of GNP content dispersed using the ultrasonication technique. In comparison, a superior enhancement with 55% and 37% increase in the tensile modulus and strength could be obtained at a lower GNP content, 0.9 wt%, dispersed via 3RM calendering, respectively. In the electrical conductivity measurement, a percolation threshold was achieved in the range between 0.6 wt% and 0.9 wt% of GNP content using the 3RM technique, which was in agreement with the predicted values. The theoretical stiffness obtained from the simplified Halpin-Tsai model corresponded with the experimental data at low fractions. The incorporation of GNPs into the BZ/CER copolymer resulted in the full recovery of all the performance losses from the addition of CER to BZ. Choosing a proper dispersing technique, the 3RM calendering in this case, could lead to a minimum required GNP content for achieving superior nanocomposite performances.
机译:在该研究中,使用两种无溶剂技术:超声波和三辊磨机(3RM )。评估GNP加法对拉伸性能,储存模量,玻璃化温度(T-G)和电导率的影响。在使用超声波技术分散的1.8wt%的GNP含量下,分别最大增加了近46%和20%的抗拉性模量和强度。相比之下,在较低的GNP含量,0.9wt%,通过3RM压延分散,可以获得具有55%和37%的拉伸模量和强度增加的优异增强。在电导率测量中,使用3RM技术在0.6wt%和0.9wt%的GNP含量的范围内实现渗透阈值,这与预测值一致。从简化的卤素-SAI模型获得的理论刚度与低级分的实验数据相对应。将GNP掺入BZ / CER共聚物中导致从加入CER到BZ的所有性能损失完全恢复。在这种情况下选择适当的分散技术,在这种情况下,3RM压延机会可能导致最低所需的GNP含量以实现优异的纳米复合性能。

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