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首页> 外文期刊>Journal of Composite Materials >Distributed internal strain measurement of the fluid-solid state coefficients of thermal expansion below the glass transition temperature during a composite manufacturing process
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Distributed internal strain measurement of the fluid-solid state coefficients of thermal expansion below the glass transition temperature during a composite manufacturing process

机译:分布式内应变测量在复合制造工艺期间玻璃化转变温度低于玻璃化转变温度的流体固态系数

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摘要

The total distributed strain produced during a vacuum-assisted resin infusion moulding composite manufacture process is measured in real time by using optical fibre sensors embedded in three different layers of a thin 5-harness satin weave flat plate cured with low-viscosity epoxy resin/cycloaliphatic polyamine epoxy resin polymer matrix. We present and discuss the chemical reaction of the epoxy resin polymer matrix adhesive to show that under manufacturing conditions, well below the glass transition point, substrates gradually come into contact with and become covered with epoxy resin polymer matrix strongly bonded to their surfaces. The fluid dynamics of the reaction system under such conditions reduces to a Cauchy equilibrium found in stressed solids, which leads to a strength of materials argument to show that the embedded, distributed optical fibres can accurately measure the motion of the surrounding epoxy resin polymer matrix before the gel point. The same argument is applied to the embedded 5-harness satin carbon fibre weave and leads immediately to an extension of the composite laminate theory for the thermodynamic liquid phase before the glass transition temperature. The predictions of the modified composite laminate theory framework are found to be consistent with experiment.
机译:在真空辅助树脂输注模塑复合制造工艺中产生的分布式菌株是实时测量的,使用嵌入三个不同层的薄5线束缎纹平板固定的光纤传感器实时测量,用低粘度环氧树脂/环脂族多胺环氧树脂聚合物基质。我们展示并讨论环氧树脂聚合物基质粘合剂的化学反应表明,在制造条件下,孔低于玻璃化转变点,基材逐渐与其覆盖物覆盖,并用它们的表面强粘合的环氧树脂聚合物基质覆盖。在这种条件下的反应系统的流体动力学降低到在应激固体中发现的Cauchy平衡,这导致材料参数的强度表明嵌入式分布式光纤可以准确地测量周围环氧树脂聚合物基质的运动之前凝胶点。将相同的参数应用于嵌入式5线束缎碳纤维编织,并立即引入玻璃化转变温度之前的热力学液相的复合层压理论的延伸。发现改进的复合层压材料理论框架的预测与实验一致。

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