pH-Responsive Properties of Asymmetric Nanopapers of Nanofibrillated Cellulose

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 contai...

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Main Authors: Maud Chemin, Baptiste Beaumal, Bernard Cathala, Ana Villares
Format: Article
Language:English
Published: MDPI AG 2020-07-01
Series:Nanomaterials
Subjects:
Online Access:https://www.mdpi.com/2079-4991/10/7/1380
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author Maud Chemin
Baptiste Beaumal
Bernard Cathala
Ana Villares
author_facet Maud Chemin
Baptiste Beaumal
Bernard Cathala
Ana Villares
author_sort Maud Chemin
collection DOAJ
description 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-yloxyl 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.
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spelling doaj.art-64adea214d9540b2a9a2f68e5a7a85a22023-11-20T06:50:39ZengMDPI AGNanomaterials2079-49912020-07-01107138010.3390/nano10071380pH-Responsive Properties of Asymmetric Nanopapers of Nanofibrillated CelluloseMaud Chemin0Baptiste Beaumal1Bernard Cathala2Ana Villares3French National Research Institute for Agriculture, Food and Environment (INRAE), UR Biopolymer, Interactions, Assemblies (BIA), F-44316 Nantes, FranceFrench National Research Institute for Agriculture, Food and Environment (INRAE), UR Biopolymer, Interactions, Assemblies (BIA), F-44316 Nantes, FranceFrench National Research Institute for Agriculture, Food and Environment (INRAE), UR Biopolymer, Interactions, Assemblies (BIA), F-44316 Nantes, FranceFrench National Research Institute for Agriculture, Food and Environment (INRAE), UR Biopolymer, Interactions, Assemblies (BIA), F-44316 Nantes, FranceInspired 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-yloxyl 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.https://www.mdpi.com/2079-4991/10/7/1380nanocellulosecellulose nanofiberfilmactuatorbending
spellingShingle Maud Chemin
Baptiste Beaumal
Bernard Cathala
Ana Villares
pH-Responsive Properties of Asymmetric Nanopapers of Nanofibrillated Cellulose
Nanomaterials
nanocellulose
cellulose nanofiber
film
actuator
bending
title pH-Responsive Properties of Asymmetric Nanopapers of Nanofibrillated Cellulose
title_full pH-Responsive Properties of Asymmetric Nanopapers of Nanofibrillated Cellulose
title_fullStr pH-Responsive Properties of Asymmetric Nanopapers of Nanofibrillated Cellulose
title_full_unstemmed pH-Responsive Properties of Asymmetric Nanopapers of Nanofibrillated Cellulose
title_short pH-Responsive Properties of Asymmetric Nanopapers of Nanofibrillated Cellulose
title_sort ph responsive properties of asymmetric nanopapers of nanofibrillated cellulose
topic nanocellulose
cellulose nanofiber
film
actuator
bending
url https://www.mdpi.com/2079-4991/10/7/1380
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AT anavillares phresponsivepropertiesofasymmetricnanopapersofnanofibrillatedcellulose