Despite the relevance of water interactions, explicit analysis of vapor adsorption on biologically derived surfaces is often difficult. Here, a system was introduced to study the vapor uptake on a native polysaccharide surface; namely, cellulose nanocrystal (CNC) ultrathin films were examined with a quartz crystal microbalance with dissipation monitoring (QCM-D) and spectroscopic ellipsometry (SE). A significant mass uptake of water vapor by the CNC films was detected using the QCM-D upon increasing relative humidity. In addition, thickness changes proportional to changes in relative humidity were detected using SE. Quantitative analysis of the results attained indicated that in preference to being soaked by water at the point of hydration each individual CNC in the film became enveloped by a 1 nm thick layer of adsorbed water vapor, resulting in the detected thickness response.

The demand for industrially produced cellulose nanocrystals (CNCs) has been growing since 2012, when CelluForce Inc. opened its inaugural demonstration plant with a production capacity of 1 tonne per day. Currently, there are 10 industrial CNC producers worldwide, each producing a unique material. Thus, academic researchers and commercial users alike must consider the properties of all available CNCs and carefully select the material which will optimize the performance of their desired application. To support these efforts, this article presents a thorough characterization of four new industrially produced CNCs including sulfated CNCs from NORAM Engineering and Constructors Ltd. (in cooperation with InnoTech Alberta and Alberta-Pacific Forest Industries Inc.) and Melodea Ltd., as well as carboxylated CNCs from Anomera Inc. and Blue Goose Biorefineries Inc. These materials were benchmarked against typical lab-made, sulfated CNCs. While all CNCs were similar in size, shape, crystallinity, and suspension quality, the sulfated CNCs had a higher surface charge density than their carboxylated counterparts, leading to higher colloidal stability. Additionally, significant differences in the rheological profiles of aqueous CNC suspensions, as well as CNC thermal stability and self-assembly behavior, were observed. As such, this article highlights both the subtle and significant differences between five CNC types and acts as a guide for end-users looking to optimize the performance of CNC-based materials.

Pressure sensitive adhesive (PSA) films were prepared from in situ semi‐batch emulsion polymerizations using isobutyl acrylate, n‐butyl acrylate, and methyl methacrylate in the presence of cellulose nanocrystals (CNCs). The CNCs at loadings of up to 1 wt% with respect to monomer resulted in significant and simultaneous improvement in tack, peel strength and shear strength for the PSA films. While most latex properties were unchanged, the CNCs also led to increased latex viscosity. A range of compositions were used to test the limits of the application. Microscopy was used to demonstrate that the CNCs were dispersed throughout the latex but outside of the polymer particles. Comparison to latex/CNC blends showed that the in situ technique provided higher shear strength PSA films. POLYM. COMPOS., 40:1365–1377, 2019. © 2018 Society of Plastics Engineers

Modern technology has enabled the isolation of nanocellulose from plant-based fibers, and the current trend focuses on utilizing nanocellulose in a broad range of sustainable materials applications. Water is generally seen as a detrimental component when in contact with nanocellulose-based materials, just like it is harmful for traditional cellulosic materials such as paper or cardboard. However, water is an integral component in plants, and many applications of nanocellulose already accept the presence of water or make use of it. This review gives a comprehensive account of nanocellulose–water interactions and their repercussions in all key areas of contemporary research: fundamental physical chemistry, chemical modification of nanocellulose, materials applications, and analytical methods to map the water interactions and the effect of water on a nanocellulose matrix.