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首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Predicting the counter-intuitive stress relaxation behavior of glass forming materials
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Predicting the counter-intuitive stress relaxation behavior of glass forming materials

机译:预测玻璃形成材料的反向直观应力松弛行为

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摘要

The ability to relax a macroscopically applied stress is often associated with molecular mobility, or the possibility for a molecule to move outside the confines of its current position, within the material of which the stress is applied. Here, a viscoelastic constitutive analysis is used to investigate the counterintuitive experimental observation of "mobility decrease with increased deformation through yield" [1] for a glass forming polymer during stress relaxation while under compressive and tensile loading conditions. The behavior of an epoxy thermoset is examined using an extensively validated, thermorheologically simple, material "clock" model, the Simplified Potential Energy Clock (SPEC) model.[2] This methodology allows for a comparison between the linear viscoelastic (LVE) limit and the true non-linear viscoelastic (NLVE) representation and enables exploration of a wide range of conditions that are not practical to investigate experimentally. The model predicts the behavior previously described as "mobility decrease with increased deformation" in the LVE limit and at low strain rates for NLVE. Only when loading rates are sufficient to decrease the material shift factor by multiple orders of magnitude is the anticipated deformation induced mobility or "mobility increase with increased deformation" observed. While the model has not been "trained" for these behaviors, it also predicts that the normalized stress relaxation response is indistinguishable amongst strain levels in the "post-yield" region, as has been experimentally reported. At long time, which has not been examined experimentally, the model predicts that even the normalized relaxation curves that exhibit "mobility increase with increased deformation" "cross back over" and return to the LVE ordering. These findings demonstrate the ability of rheologically simple models to represent the counter-intuitive experimentally measured material response and present predictions at long time scales that could
机译:放松宏观施加的应力的能力通常与分子迁移率相关,或者分子在其当前位置的限制范围内移动的可能性在施加应力的情况下。这里,粘弹性本构体分析用于研究对玻璃形成聚合物在压缩和拉伸负载条件下的玻璃形成聚合物期间对玻璃形成聚合物的逆向实验观察。使用广泛的验证的热管道学简单的材料“时钟”模型来检查环氧热固性的行为,简化的潜在能量钟(规格)模型。[2]该方法允许在线性粘弹性(LVE)限制和真正的非线性粘弹性(NLVE)表示之间进行比较,并且能够探索天际上不实际调查的广泛条件。该模型预测先前描述的行为作为LVE限制中的变形和随着变形的增加变形的移动性降低,并且对于NLVE的低应变速率。只有当加载速率足以减少材料换档因子,才通过多个数量级是预期变形诱导的迁移率或观察到随着变形增加的移动性增加“。虽然该模型尚未“培训”这些行为,但它还预测,正常报道的“产量后”区域中的归一化应力松弛响应难以区分。长时间尚未通过实验检查,模型预测,即使是呈现“流动性增加随着变形增加”的归一化弛豫曲线,也会返回到LVE排序。这些发现表明了流变简单模型代表反向直观的实验测量的材料响应和可能的预测能力

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