Thermal expansion of self-organized and shear-oriented cellulose nanocrystal films.

Abstract:

:The coefficient of thermal expansion (CTE) of cellulose nanocrystal (CNC) films was characterized using novel experimental techniques complemented by molecular simulations. The characteristic birefringence exhibited by CNC films was utilized to calculate the in-plane CTE of self-organized and shear-oriented self-standing CNC films from room temperature to 100 °C using polarized light image correlation. CNC alignment was estimated via Hermans order parameter (S) from 2D X-ray diffraction measurements. We found that films with no preferential CNC orientation through the thickness (S: ∼ 0.0) exhibited an isotropic CTE (∼25 ppm/K). In contrast, films with aligned CNC orientations (S: ∼0.4 to 0.8) had an anisotropic CTE response: For the highest CNC alignment (S: 0.8), the CTE parallel to CNC alignment was ∼9 ppm/K, while that perpendicular to CNC alignment was ∼158 ppm/K. CNC film thermal expansion was proposed to be due primarily to single crystal expansion and CNC-CNC interfacial motion. The relative contributions of inter- and intracrystal responses to heating were explored using molecular dynamics simulations.

journal_name

Biomacromolecules

journal_title

Biomacromolecules

authors

Diaz JA,Wu X,Martini A,Youngblood JP,Moon RJ

doi

10.1021/bm400794e

subject

Has Abstract

pub_date

2013-08-12 00:00:00

pages

2900-8

issue

8

eissn

1525-7797

issn

1526-4602

journal_volume

14

pub_type

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