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Influence of filler/matrix interactions on resin/hardener stoichiometry, molecular dynamics, and particle dispersion of silicon nitride/epoxy nanocomposites

机译:填料/基体相互作用对树脂/固化剂化学计量,分子动力学和氮化硅/环氧树脂纳米复合材料颗粒分散的影响

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摘要

The addition of nanofillers can have a significant influence on the resin stoichiometry of thermosetting polymer systems. Based on differential scanning calorimetry (DSC) results, it is estimated that the inclusion of 2 wt% and 5 wt% of silicon nitride nanofiller displaces the resin/hardener stoichiometry of an epoxy/amine network by 6.5% and 18%, respectively. Dielectric spectroscopy results confirm the above findings, in that the spectra of the nanocomposite samples were found to be equivalent to the spectra of unfilled samples when the above stoichiometric effect was taken into account. Therefore, this study provides clear evidence that the presence of a nanofiller can directly and significantly affect the curing process of an epoxy network. Consequently, this should always be considered when introducing nanofillers into thermosetting matrices. These results indicate the presence of covalent bonding between the nanoparticles and the surrounding polymer and, therefore, provide an opportunity to explore the influence of this bonding on the molecular dynamics of the polymer layer around the particles. However, the obtained DSC and dielectric spectroscopy results suggest that, in the system considered here, either the covalent bonding does not have an appreciable influence on the segmental dynamics of the polymer, as revealed by these techniques, or that the thickness of the affected layer is less than 1 nm and therefore too small to be distinguished from experimental uncertainties.
机译:纳米填料的添加可能对热固性聚合物体系的树脂化学计量有重大影响。根据差示扫描量热法(DSC)结果,估计包含2 wt%和5 wt%的氮化硅纳米填料会分别使环氧树脂/胺网络的树脂/固化剂化学计量取代6.5%和18%。介电谱结果证实了上述发现,因为当考虑到上述化学计量效应时,发现纳米复合材料样品的光谱与未填充样品的光谱相等。因此,这项研究提供了明确的证据,表明纳米填料的存在可以直接且显着影响环氧网络的固化过程。因此,在将纳米填料引入热固性基质中时,应始终考虑这一点。这些结果表明在纳米颗粒和周围的聚合物之间存在共价键,因此,提供了探索这种键合对颗粒周围的聚合物层的分子动力学的影响的机会。然而,获得的DSC和介电谱结果表明,在此处考虑的系统中,共价键对聚合物的链段动力学没有显着影响(如这些技术所揭示),或者受影响层的厚度小于1nm,因此太小而不能与实验不确定性区分开。

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