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Crystallization and shear modulus of a forming biopolymer film determined by in situ x-ray diffraction and ultrasound reflection methods

机译:通过原位X射线衍射和超声反射方法确定的生物聚合物薄膜的结晶度和剪切模量

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The structure and the rigidity of a forming biopolymer film were determined using concurrent x-ray diffraction and ultrasonic reflection measurements. Film formation of a xylan solution (de-ionized water, 10 g/l xylan, 4 g/l glycerol) was studied during water evaporation at 24(±2) ℃, 37(±5) %RH. X-ray diffraction (XRD) data showed the crystallization and ultrasonic data the increase of the shear modulus (G) during water evaporation. Xylan crystallized into small xylan dihydrate crystallites, the number of which increased as water evaporated. Crystallization began earlier than the increase in G during film formation. The increase in G also continued after the crystallites were fully formed, indicating still ongoing structural changes in the amorphous parts. The maximum value of G was 0.1-0.5 GPa. XRD measurements performed ex situ showed a crystallinity of 16%-19% (±5%) and a fairly isotropic crystallite orientation in the surface plane of the films.
机译:使用同时进行的X射线衍射和超声反射测量来确定形成的生物聚合物膜的结构和刚度。研究了木聚糖溶液(去离子水,10 g / l木聚糖,4 g / l甘油)在24(±2)℃,37(±5)%RH的水蒸发过程中的成膜情况。 X射线衍射(XRD)数据显示结晶,而超声数据显示水蒸发过程中剪切模量(G)增加。木聚糖结晶为小的木聚糖二水合物微晶,其数量随着水的蒸发而增加。在成膜过程中,结晶开始的时间早于G的增加。在微晶完全形成后,G的增加也继续,表明非晶部分仍在进行结构变化。 G的最大值为0.1-0.5GPa。异地进行的XRD测量显示,薄膜的表面结晶度为16%-19%(±5%),且各向同性的微晶取向。

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