Chemical Engineering and Materials Department, Universidad Complutense de Madrid, Avda. Complutense s/n, 28040, Madrid, Spain.
BioPRIA, Chemical Engineering Department, Monash University, Melbourne, VIC, 3800, Australia.
Carbohydr Polym. 2020 Jan 1;227:115340. doi: 10.1016/j.carbpol.2019.115340. Epub 2019 Sep 19.
The characterization of nanocellulose fibres (NC) length is a difficult and indirect measurement which relies on aspect ratio calculation and fibre diameter analysis. The aspect ratio can be directly calculated from the gel point, a parameter obtained from sedimentation experiments. The gel point has been used with macroscopic fibres and microfibrillated cellulose, that easily sediment by gravity. However, this methodology has not yield consistent results with highly charged nanofibres nor with fibres with sediment layer difficult to observe. In this study, the gel point methodology is modified: 1) dying the fibres with Crystal Violet to enable the visualization of the fibrils sedimentation line without affecting the fibre network; and 2) by optimizing the sedimentation time to ensure complete settling. The two types of fibrils characterized -low and high fibrillated NC (LF-NC, HF-NC)- behave differently due to the slower sedimentation of HF-NC. The time to reach a stable sedimented layer increases with the level of fibre fibrillation, the charge and the decrease of fibre dimension. Reproducible gel point can be measured after 2 days for LF-NC; however, 8 days are required for HF-NC. The modified methodology was validated by quantifying the influence of pH and salt concentration. As expected, low pHs and the addition of CaCl coagulate HF-NC into flocs which increase the ratio: final over initial fibres height (H/H); this decreases significantly the gel point, as a lower amount of HF-NC are required to interconnect all fibres. This modified method is a valuable tool for the accurate dimensional characterisation of highly charged and low diameter cellulose nanofibres.
纳米纤维素纤维(NC)长度的特征化是一项困难且间接的测量,依赖于纵横比计算和纤维直径分析。纵横比可以直接从凝胶点计算得出,凝胶点是从沉降实验中获得的参数。凝胶点已用于宏观纤维和容易通过重力沉降的微纤化纤维素。然而,这种方法在带高电荷的纳米纤维或沉降层难以观察的纤维上没有产生一致的结果。在这项研究中,修改了凝胶点方法:1)用结晶紫对纤维进行染色,以在不影响纤维网络的情况下使纤维的沉降线可视化;2)通过优化沉降时间来确保完全沉降。所表征的两种类型的纤维 - 低和高纤维化 NC(LF-NC,HF-NC) - 由于 HF-NC 的沉降速度较慢而表现出不同的行为。达到稳定沉降层所需的时间随着纤维纤维化程度、电荷和纤维尺寸的减小而增加。LF-NC 可在 2 天后测量到可重复的凝胶点;然而,HF-NC 需要 8 天。该方法通过定量 pH 和盐浓度的影响进行了验证。如预期的那样,低 pH 值和添加 CaCl 会将 HF-NC 凝结成絮体,从而增加最终纤维高度与初始纤维高度之比(H/H);这会显著降低凝胶点,因为需要更少的 HF-NC 来连接所有纤维。这种改进的方法是对高电荷和低直径纤维素纳米纤维进行准确尺寸特征化的有价值的工具。