Zlenko Dmitry V, Nikolsky Sergey N, Vedenkin Alexander S, Politenkova Galina G, Skoblin Aleksey A, Melnikov Valery P, Michaleva Marya M, Stovbun Sergey V
Faculty of Biology, M.V. Lomonosov Moscow State University, Lenin Hills 1/12, 119192 Moscow, Russia.
N.N. Semenov Institute of Chemical Physics, RAS. Kosygina 4, 119991 Moscow, Russia.
Polymers (Basel). 2019 May 13;11(5):873. doi: 10.3390/polym11050873.
Cellulose hydrogels and films are advantageous materials that are applied in modern industry and medicine. Cellulose hydrogels have a stable scaffold and never form films upon drying, while viscous cellulose hydrosols are liquids that could be used for film production. So, stabilizing either a gel or sol state in cellulose suspensions is a worthwhile challenge, significant for the practical applications. However, there is no theory describing the cellulose fibers' behavior and processes underlying cellulose-gel-scaffold stabilizing. In this work, we provide a phenomenological mechanism explaining the transition between the stable-gel and shapeless-sol states in a cellulose suspension. We suppose that cellulose macromolecules and nanofibrils under strong dispersing treatment (such as sonication) partially untwist and dissociate, and then reassemble in a 3D scaffold having the individual elements twisted in the nodes. The latter leads to an exponential increase in friction forces between the fibers and to the corresponding fastening of the scaffold. We confirm our theory by the data on the circular dichroism of the cellulose suspensions, as well as by the direct scanning electron microscope (SEM) observations and theoretical assessments.
纤维素水凝胶和薄膜是应用于现代工业和医学的优势材料。纤维素水凝胶具有稳定的支架结构,干燥时不会形成薄膜,而粘性纤维素水溶胶是可用于薄膜生产的液体。因此,在纤维素悬浮液中稳定凝胶或溶胶状态是一项值得挑战的任务,对实际应用具有重要意义。然而,目前尚无理论描述纤维素纤维的行为以及纤维素凝胶支架稳定化背后的过程。在这项工作中,我们提供了一种现象学机制,解释了纤维素悬浮液中稳定凝胶态和无定形溶胶态之间的转变。我们假设,在强分散处理(如超声处理)下,纤维素大分子和纳米纤维会部分解捻和解离,然后重新组装成一个三维支架,其单个元素在节点处发生扭曲。后者导致纤维间摩擦力呈指数增加,并使支架相应地固定。我们通过纤维素悬浮液的圆二色性数据、直接扫描电子显微镜(SEM)观察结果以及理论评估来证实我们的理论。