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High-Temperature Viscoelastic Relaxation in All-Cellulose Composites

机译:全纤维素复合材料的高温粘弹性松弛

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摘要

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 α_1 relaxation, with tan δ maxima 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:为了检查相组成和粘弹性行为在270°C至340°C温度范围(对应于a1机械松弛)之间的关系,制备了一系列不同结晶度的全纤维素复合材料。使用薄膜流延技术,通过将微晶纤维素部分溶解在LiCl / N,N-二甲基乙酰胺(LiCl / DMAc)溶剂体系中来制备复合薄膜。动态力学分析显示了对α_1弛豫的两个贡献,tanδ最大值在303±2°C和约325°C时。最大值或肩部的高度在303±2°C时随着结晶度的增加而降低,因此被指定为与非晶体域中化学分解相关的分子运动。 325°C时的最大值被分配给与晶畴表面相关的链中的化学分解。在300°C下进行测试时,具有高结晶度的复合材料显示出最佳的动态储能模量保持率。

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