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首页> 外文期刊>Journal of Applied Polymer Science >Influence of hydrogen bonding interaction on the damping properties of poly( n- butyl methacrylate)/ small molecule hybrids
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Influence of hydrogen bonding interaction on the damping properties of poly( n- butyl methacrylate)/ small molecule hybrids

机译:氢键相互作用对聚甲基丙烯酸正丁酯/小分子杂化物阻尼特性的影响

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The hydrogen bonding interactions between poly(n-butyl methacrylate) and a series of low molecular weight phenols containing two to four hydroxyl groups with different steric effects were investigated by differential scanning calorimetry and Fourier-transform infrared spectroscopy. Results showed that the hydrogen bonding strength between the two components varies greatly according to the steric effects of the phenolic hydroxyl group. As the size of the group beside the hydroxyl increases, the hydrogen bond strength weakens. The glass transition temperature of binary hybrid systems was put into relation with the corresponding hydrogen bonding interaction strength. Strong hydrogen bonding strength increased T-g to higher values than that predicted by the linear additivity rule; by contrast, T-g of hybrid systems with weak hydrogen bonds showed linear changes. All of the samples showed linear variations at low concentrations of small molecules. The damping properties of five systems were analyzed by dynamic mechanical analysis. Either the loss factor or area of tan peak of the five systems increased compared with that of the pure polymer, thereby showing great improvements in the damping properties of the poly(n-butyl methacrylate)/small molecule hybrid material. (c) 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 41954.
机译:通过差示扫描量热法和傅里叶变换红外光谱法研究了聚甲基丙烯酸正丁酯与一系列具有不同空间效应的含两个至四个羟基的低分子量酚之间的氢键相互作用。结果表明,两种组分之间的氢键合强度根据酚羟基的空间效应而变化很大。随着羟基旁基团的大小增加,氢键强度减弱。将二元杂化体系的玻璃化转变温度与相应的氢键相互作用强度联系起来。强大的氢键结合强度将T-g增加到比线性加和法则所预测的更高的值;相反,具有弱氢键的杂化系统的T-g呈线性变化。所有样品在小分子低浓度下均表现出线性变化。通过动态力学分析对五个系统的阻尼特性进行了分析。与纯聚合物相比,这五个系统的损耗因子或tan峰面积均增加,从而显示出聚(甲基丙烯酸正丁酯)/小分子杂化材料的阻尼特性得到了极大的改善。 (c)2015 Wiley Periodicals,Inc. J. Appl。 Polym。科学2015,132,41954。

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