Chemin Maud, Beaumal Baptiste, Cathala Bernard, Villares Ana
French National Research Institute for Agriculture, Food and Environment (INRAE), UR Biopolymer, Interactions, Assemblies (BIA), F-44316 Nantes, France.
Nanomaterials (Basel). 2020 Jul 15;10(7):1380. doi: 10.3390/nano10071380.
Inspired by plant movements driven by the arrangement of cellulose, we have fabricated nanopapers of nanofibrillated cellulose (NFC) showing actuation under pH changes. Bending was achieved by a concentration gradient of charged groups along the film thickness. Hence, the resulting nanopapers contained higher concentration of charged groups on one side of the film than on the opposite side, so that pH changes resulted in charge-dependent asymmetric deprotonation of the two layers. Electrostatic repulsions separate the nanofibers in the nanopaper, thus facilitating an asymmetric swelling and the subsequent expanding that results in bending. Nanofibrillated cellulose was modified by 2,2,6,6-tetramethylpiperidin-1-yl)oxyl radical (TEMPO) oxidation at two reaction times to get different surface concentrations of carboxylic acid groups. TEMPO-oxidized NFC was further chemically transformed into amine-modified NFC by amidation. The formation of graded nanopapers was accomplished by successive filtration of NFC dispersions with varying charge nature and/or concentration. The extent of bending was controlled by the charge concentration and the nanopaper thickness. The direction of bending was tuned by the layer composition (carboxylic acid or amine groups). In all cases, a steady-state was achieved within less than 25 s. This work opens new routes for the use of cellulosic materials as actuators.
受纤维素排列驱动的植物运动启发,我们制备了纳米纤丝化纤维素(NFC)纳米纸,其在pH值变化时会产生驱动作用。通过沿薄膜厚度的带电基团浓度梯度实现弯曲。因此,所得纳米纸在薄膜的一侧比另一侧含有更高浓度的带电基团,使得pH值变化导致两层的电荷依赖性不对称去质子化。静电排斥使纳米纸中的纳米纤维分离,从而促进不对称溶胀以及随后导致弯曲的膨胀。在两个反应时间通过2,2,6,6-四甲基哌啶-1-氧基自由基(TEMPO)氧化对纳米纤丝化纤维素进行改性,以获得不同表面浓度的羧酸基团。通过酰胺化将TEMPO氧化的NFC进一步化学转化为胺改性的NFC。通过连续过滤具有不同电荷性质和/或浓度的NFC分散体来完成梯度纳米纸的形成。弯曲程度由电荷浓度和纳米纸厚度控制。弯曲方向通过层组成(羧酸或胺基团)进行调节。在所有情况下,均在不到25秒内达到稳态。这项工作为将纤维素材料用作驱动器开辟了新途径。