Fiber and Chemical Sciences Research, USDA FS, Forest Products Laboratory, 1 Gifford Pinchot Drive, Madison, Wisconsin 53726-2398, United States.
Biomacromolecules. 2021 Apr 12;22(4):1357-1373. doi: 10.1021/acs.biomac.0c01389. Epub 2021 Mar 26.
Aggregated states of celluloses remain poorly understood, and therefore, the topic requires careful investigation. In this study, Raman, IR, and X-ray diffraction (XRDs) were used to study cotton microcrystalline cellulose (MCC) and MCC that has been ball-milled to various degrees. Raman and IR spectroscopy methods indicated that when these ball-milled samples were wet with water, most underwent conformational changes at the molecular level. Although formation of cellulose II was observed in longer duration ball-milled samples, the changes primarily gave rise to increased contributions in spectral and diffraction regions typically associated with the contributions of crystalline cellulose I. Moreover, when the wet samples were air-dried at 25 °C, the newly formed cellulose I-like structures partly reverted to the previous form present in the initial dry state. These findings explained for the previously reported XRD and NMR observations, where the addition of water resulted in increased crystallinities of cellulose samples. The implications of these findings to cellulose crystallinity measurements and other situations are discussed.
纤维素的聚集态结构仍不清楚,因此需要仔细研究。在这项研究中,我们使用拉曼、红外和 X 射线衍射(XRD)研究了棉微晶纤维素(MCC)和经过不同程度球磨的 MCC。拉曼和红外光谱方法表明,当这些球磨样品用水润湿时,大多数在分子水平上发生构象变化。尽管在较长时间球磨的样品中观察到纤维素 II 的形成,但这些变化主要导致光谱和衍射区域的贡献增加,通常与结晶纤维素 I 的贡献有关。此外,当湿样品在 25°C 下空气干燥时,新形成的类似纤维素 I 的结构部分恢复到初始干燥状态下存在的先前形式。这些发现解释了先前报道的 XRD 和 NMR 观察结果,其中水的加入导致纤维素样品的结晶度增加。讨论了这些发现对纤维素结晶度测量和其他情况的影响。