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All-cellulose composites based on microfibrillated cellulose and filter paper via a NaOH-urea solvent system

机译:基于微纤化纤维素和滤纸的全纤维素复合材料,通过NaOH-尿素溶剂系统

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摘要

All-cellulose composites were produced by partial dissolution of two cellulosic sources in a mixture of sodium hydroxide and urea at low temperature. Filter paper (FP) and microfibrillated cellulose (MFC) were used to examine the role of the fiber dimensions of the initial reinforcing network on the final mechanical properties of thin self-reinforced all-cellulose composites. The dissolution time was used to control the extent of the transformation. The initial fiber structure was progressively transformed into a thoroughly consolidated composite material. X-ray diffraction and Fourier-transform infrared spectroscopy were able to show that the initial cellulose I allomorph was replaced with a cellulose II allomorph. FP underwent a fast crystallinity loss and transformation to cellulose II. In contrast, the crystallinity of MFC decreased slowly after dissolution. This result was also correlated with a slower allomorphic transformation. The crystallinity of MFC decreased to a level comparable to that of FP after 40 min and it remained comparatively unaffected at extended dissolution times. Comparison between powder and transmission XRD measurements demonstrated that the cellulose II present in all films after dissolution was strongly textured with its (10) plane lying parallel to the sample surface despite fibrous microstructural features remaining from the initial substrates. The tensile strength and elastic modulus of FP increased significantly (+690 and +528 %, respectively) after only 20 min, while that of MFC remained relatively unaltered as a function of the dissolution time.
机译:通过在低温下将两种纤维素来源部分溶解在氢氧化钠和尿素的混合物中来生产全纤维素复合材料。使用滤纸(FP)和微纤化纤维素(MFC)来检查初始增强网络的纤维尺寸对薄型自增强全纤维素复合材料最终机械性能的作用。溶解时间用于控制转化程度。最初的纤维结构逐渐转变为完全固结的复合材料。 X射线衍射和傅立叶变换红外光谱法能够显示出最初的纤维素I同种异形体被纤维素II同种异形体替代。 FP快速结晶损失并转化为纤维素II。相反,MFC的结晶度在溶解后缓慢降低。该结果也与较慢的同构转化有关。在40分钟后,MFC的结晶度降低至与FP相当的水平,并且在延长的溶解时间下相对不受影响。粉末XRD和透射XRD测量值之间的比较表明,溶解后所有薄膜中存在的纤维素II都具有很强的纹理,其(10)平面平行于样品表面,尽管初始基材上仍保留有纤维微结构特征。 FP的抗张强度和弹性模量仅在20分钟后就显着增加(分别为+690和+528%),而MFC的抗张强度和弹性模量相对于溶解时间却保持相对不变。

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