Controlling the Rate of Water-Induced Switching in Mechanically Dynamic Cellulose Nanocrystal Composites

被引:32
|
作者
Dagnon, Koffi L. [1 ]
Way, Amanda E. [1 ]
Carson, Sidney O. [1 ]
Silva, Jorge [1 ]
Maia, Joao [1 ]
Rowan, Stuart J. [1 ]
机构
[1] Case Western Reserve Univ, Dept Macromol Sci & Engn, Cleveland, OH 44106 USA
基金
美国国家科学基金会;
关键词
TEMPO-MEDIATED OXIDATION; POLYMER NANOCOMPOSITES; RESPONSIVE POLYMERS; STRESS-TRANSFER; WHISKERS; NANOWHISKERS; DISPERSION; POLY(N-ISOPROPYLACRYLAMIDE); POLY(EPSILON-CAPROLACTONE); BIONANOCOMPOSITES;
D O I
10.1021/ma4008187
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Carboxylated cellulose nanocrystals with varying charge densities, ranging from ca. 270 to -1100 mmol/kg, were prepared via partial functionalization of 1100 mmol/kg carboxylated CNCs with different equivalents of propylamine. Incorporation of these differently charged nanofillers into poly(vinyl acetate) produced a series of water-responsive mechanically adaptable nanocomposite materials. Dynamic mechanical analysis and rheological studies of the nanocomposite samples indicated that both the degree of water swelling and the rate of mechanical softening are related to the CNC charge density. Interestingly, however, the mechanical properties of the nanocomposites, either dry or fully swollen, are more-or-less independent of the charge density of the CNC nanofillers. Thus, these results highlight a method to tailor the rate of mechanical switching (or diffusion of water through the nanocomposite material) without significantly impacting its mechanical properties.
引用
收藏
页码:8203 / 8212
页数:10
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