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Structure-property relationships of silica/silane formulations in natural rubber, isoprene rubber and styrene-butadiene rubber composites

机译:天然橡胶,异戊二烯橡胶及苯乙烯 - 丁二烯橡胶复合材料中二氧化硅/硅烷制剂的结构 - 性质关系

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摘要

The mechanical performance of natural rubber (NR), synthetic poly-isoprene rubber (IR), and styrene-butadiene rubber (SBR) composites filled with various silica/silane systems is investigated. The results are analyzed by referring to micro-mechanical material parameters, which quantify the morphological and structural properties of the polymer and filler network. These are obtained from fits with the dynamic flocculation model (DFM) describing the strongly nonlinear quasi-static stress-strain response of filler-reinforced elastomers as found from multihysteresis measurements of the investigated compounds. We focus on the reinforcement mechanisms of silica compounds with coupling and covering silane, respectively. The fitted material parameters give hints that the coupling silane provides a strong chemical polymer-filler coupling, which is accompanied by improved strength of filler-filler bonds for all three rubbers types. This may result also from the chemical coupling of short chains bridging adjacent silica particles. It implies larger stress values for the coupling silane and, in the case of NR and IR, a more pronounced "Payne effect" compared to the covering silane. In contrast, for SBR, the coupling silane delivers a lower Payne effect, which is explained by differences in the compatibility between rubber type and silane-grafted silica surface. (c) 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019, 136, 48435.
机译:研究了天然橡胶(NR),合成聚异戊二烯橡胶(IR)和含有各种二氧化硅/硅烷系统的苯乙烯 - 丁二烯橡胶(SBR)复合材料的机械性能。通过参考微机械材料参数来分析结果,这量化了聚合物和填料网络的形态学和结构性能。这些来自具有动态絮凝模型(DFM)的拟合,描述从研究化合物的多神经术测量中发现的填充增强弹性体的强非线性准静态应力响应。我们专注于二氧化硅化合物与偶联和覆盖硅烷的加固机制。拟合材料参数提供耦合硅烷提供强化学聚合物 - 填充耦合的暗示,其伴随着所有三种橡胶类型的填充填料粘合强度的提高。这也可以从桥接相邻二氧化硅颗粒的短链的化学偶联中产生。它意味着偶联硅烷的压力值较大,并且在NR和IR的情况下,与覆盖硅烷相比,更明显的“工资效果”。相反,对于SBR,偶联硅烷提供较低的PAYNE效应,其橡胶型和硅烷接枝二氧化硅表面之间的相容性的差异解释。 (c)2019 Wiley期刊,Inc.J.Phill。聚合物。 SCI。 2019,136,48435。

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