TY - JOUR
T1 - Enhanced electromechanical performance of bio-based gelatin/glycerin dielectric elastomer by cellulose nanocrystals
AU - Ning, Nanying
AU - Wang, Zhifei
AU - Yao, Yang
AU - Zhang, Liqun
AU - Tian, Ming
N1 - Publisher Copyright:
© 2015 Elsevier Ltd. All rights reserved.
PY - 2015/6/14
Y1 - 2015/6/14
N2 - To meet the growing demand of environmental protection and resource saving, it is imperative to explore bio-based elastomers as next-generation dielectric elastomers (DEs). In this study, we used a bio-based gelatin/glycerin (GG) elastomer as the DE matrix because GG exhibits high dielectric constant (εr). Cellulose nanocrystals (CNCs), extracted from natural cellulose fibers, were used to improve the mechanical strength of GG elastomer. The results showed that CNCs with a large number of hydroxyl groups disrupted the hydrogen bonds between gelatin molecules and formed new stronger hydrogen bonds with gelatin molecules. A good interfacial adhesion between CNCs and GG was formed, and thus a good dispersion of CNCs in GG matrix was obtained, leading to the improved mechanical strength of GG. More interestingly, the εr of GG elastomer was obviously increased by adding 5 wt% of CNCs, ascribed to the increase in the polarizability of gelatin chains caused by the disruption of hydrogen bonds of gelatin. As a result, a 230% increase in the actuated strain at low electric field of GG was obtained by adding 5 wt% of CNCs. Since CNCs, gelatin and glycerol are all bio-based, this study offers a new method to prepare high performance DE for its application in biological and medical fields.
AB - To meet the growing demand of environmental protection and resource saving, it is imperative to explore bio-based elastomers as next-generation dielectric elastomers (DEs). In this study, we used a bio-based gelatin/glycerin (GG) elastomer as the DE matrix because GG exhibits high dielectric constant (εr). Cellulose nanocrystals (CNCs), extracted from natural cellulose fibers, were used to improve the mechanical strength of GG elastomer. The results showed that CNCs with a large number of hydroxyl groups disrupted the hydrogen bonds between gelatin molecules and formed new stronger hydrogen bonds with gelatin molecules. A good interfacial adhesion between CNCs and GG was formed, and thus a good dispersion of CNCs in GG matrix was obtained, leading to the improved mechanical strength of GG. More interestingly, the εr of GG elastomer was obviously increased by adding 5 wt% of CNCs, ascribed to the increase in the polarizability of gelatin chains caused by the disruption of hydrogen bonds of gelatin. As a result, a 230% increase in the actuated strain at low electric field of GG was obtained by adding 5 wt% of CNCs. Since CNCs, gelatin and glycerol are all bio-based, this study offers a new method to prepare high performance DE for its application in biological and medical fields.
KW - Actuated strain
KW - Cellulose nanocrystals (CNCs)
KW - Dielectric elastomers
KW - Gelatin
KW - Hydrogen bond
UR - https://www.scopus.com/pages/publications/84930929727
U2 - 10.1016/j.carbpol.2015.03.083
DO - 10.1016/j.carbpol.2015.03.083
M3 - 文章
C2 - 26076625
AN - SCOPUS:84930929727
SN - 0144-8617
VL - 130
SP - 262
EP - 267
JO - Carbohydrate Polymers
JF - Carbohydrate Polymers
ER -