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High-Temperature Viscoelastic Relaxation in All-Cellulose Composites

机译:全纤维素复合材料中的高温粘弹性松弛

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All-cellulose composites were prepared across a range of different crystallinities in order to examine relationships between phase composition and viscoelastic behaviour in the temperature range of 270 ±C to 340 °C corresponding to the a1 mechanical relaxation. Composite films were prepared by partial dissolution of microcrystalline cellulose in a LiCl/N,N-dimethylacetamide (LiCl/DMAc) solvent system using the film casting technique. Dynamic mechanical analysis showed two contributions to α1 relaxation, with tan δ dmaxima at 303±2 °C and at approximately 325 °C. The height of the maximum or shoulder at 303±2 °C decreased with increasing crystallinity, and was therefore assigned to molecular motion associated with chemical decomposition in non-crystalline domains. The maximum at 325 °C was assigned to chemical decomposition in chains associated with the surfaces of crystalline domains. Composites with high crystallinity showed best retention of the dynamic storage modulus when tested at 300 °C.
机译:在一系列不同的晶体中制备全纤维素复合材料,以检查相对于A1机械松弛的270±C至340℃的温度范围内的相组合物和粘弹性行为之间的关系。通过使用薄膜浇铸技术将微晶纤维素中的微晶纤维素部分溶解来制备复合膜。动态力学分析显示出α1弛豫的两种贡献,TANδDmaxima在303±2°C和约325℃下。随着结晶度的增加,303±2℃的最大或肩部的高度降低,因此分配给与非结晶结构域中的化学分解相关的分子运动。 325℃的最大值被分配给与结晶结构域的表面相关的链中的化学分解。具有高结晶度的复合材料显示在300℃下测试时的动态储存模量的最佳保留。

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