首页> 外文期刊>Rheologica Acta: An International Journal of Rheology >Effect of maleic anhydride content on the rheology and phase behavior of poly(styrene-co-maleic anhydride)/poly(methyl methacrylate) blends
【24h】

Effect of maleic anhydride content on the rheology and phase behavior of poly(styrene-co-maleic anhydride)/poly(methyl methacrylate) blends

机译:马来酸酐含量对聚苯乙烯-顺丁烯二酸酐/聚甲基丙烯酸甲酯混合物的流变学和相行为的影响

获取原文
获取原文并翻译 | 示例
           

摘要

We investigated the thermo- rheological behavior of high glass transition, high molecular weight and small dynamic asymmetry blends of poly(styrene-co-maleic anhydride) (SMA) and poly (methyl methacrylate) (PMMA) with varying amounts of maleic anhydride (MA) content, namely 8 wt%, 14 wt% and 32 wt%, in the SMA component. The phase separation (binodal) temperature of each blend was determined rheologically using a combination of dynamic frequency and temperature sweeps in parallel plate geometry; it was marked by a change in slope of the elastic modulus and the occurrence of a peak in tan 6 in temperature sweeps. Failure of the time-temperature superposition principle and observation of two peaks in the Cole-Cole plots corroborated these findings. The blends displayed lower critical solution temperature (LCST) behavior with the critical temperatures exhibiting a non-monotonic dependence on the MA content. From rheological and thermal measurements it was concluded that SMA/PMMA blends containing 14% MA were more miscible than those containing 8% or 32% MA, a finding attributed to the compositional dependence of the interplay between SMA-SMA and SMA-PMMA interactions in the different samples. MA also influenced the dynamic asymmetry and pretransitional concentration fluctuations. The phase diagrams corresponding to each blend were modeled using a two-parameter temperature dependent interaction parameter, based on the concept of generalized Gibbs free energy of mixing. The fitted values of interaction parameter were in good agreement with values calculated explicitly using the Flory-Huggins theory. [References: 30]
机译:我们研究了高玻璃化转变温度,高分子量和聚(苯乙烯-马来酸酐)(SMA)和聚(甲基丙烯酸甲酯)(PMMA)以及少量马来酸酐(MA)的小的动态不对称共混物的热流变行为。含量,即SMA组分中的8重量%,14重量%和32重量%。使用动态频率和平行板几何形状中的温度扫描的组合,通过流变学方法确定每种共混物的相分离(双曲线)温度;其特征在于弹性模量的斜率变化和温度扫描中tan 6中出现峰值。时间-温度叠加原理的失败以及在Cole-Cole图中观察到两个峰证实了这些发现。共混物显示出较低的临界溶液温度(LCST)行为,并且临界温度对MA含量表现出非单调依赖性。从流变学和热学测量得出的结论是,含有14%MA的SMA / PMMA共混物比含有8%或32%MA的SMA / PMMA共混物更易混溶,这一发现归因于SMA-SMA与SMA-PMMA相互作用之间的相互作用。不同的样本。 MA还影响了动态不对称性和过渡前浓度的波动。基于广义的吉布斯混合自由能的概念,使用取决于温度的两参数相互作用参数对与每种共混物相对应的相图进行建模。相互作用参数的拟合值与使用Flory-Huggins理论明确计算出的值非常吻合。 [参考:30]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号