Aerogel from Sustainably Grown Bacterial Cellulose Pellicles as a Thermally Insulative Film for Building Envelopes.

Improving building energy performance requires the development of new highly insulative materials. An affordable retrofitting solution comprising a thin film could improve the resistance to heat flow in both residential and commercial buildings and reduce overall energy consumption. Here, we propose cellulose aerogel films formed from pellicles produced by the bacteria Gluconacetobacter hansenii as insulation materials. We studied the impact of the density and nanostructure on the aerogels' thermal properties. A thermal conductivity as low as 13 mW/(K·m) was measured for native pellicle-based aerogels that were dried as-is with minimal post-treatment. The use of waste from the beer brewing industry as a solution to grow the pellicle maintained the cellulose yield obtained with standard Hestrin-Schramm media, making our product more affordable and sustainable. In the future, our work can be extended through further diversification of food wastes as the substrate sources, facilitating higher potential production and larger applications.

Rheology of regenerated cellulose suspension and influence of sodium alginate.

Cellulosic colloidal suspensions present unique opportunities for rheological modification of complex fluids. In this work, the rheological behavior of regenerated cellulose (RC) suspensions, including their oscillating shear and time-dependent behavior, as well as yield stress, were studied. The rheological effects of sodium alginate's addition to aqueous RC solutions subject to shear flow were investigated. The results reveal that the RC suspension exhibited "gel-like" behavior and had a shear-thinning property. At increasing RC concentrations, the suspensions' yield stress and the extent of viscosity recovery after plastic deformation had both increased. The viscoelastic suspensions underwent a transition from "solid-like" to "liquid-like" behavior upon sodium alginate's inclusion. Sodium alginate was found to enhance RC suspensions' viscosity recoverability. Furthermore, with increasing concentrations of sodium alginate, the yield stress of RC suspension began to decrease and then vanished, occurring below the 1:1 RC: sodium alginate weight ratio with total solid content fixed at 1 wt%, due to RC's inability to form an extended network RC. This study yields insights into the rheology of RC suspensions and the influence of sodium alginate and supports both their usage as rheological modifies in applications such as coatings, drug delivery systems, and additive manufacturing techniques such as 3D printing.

Plasmonic Metamaterial Gels with Spatially Patterned Orientational Order via 3D Printing.

Optical properties can be programmed on mesoscopic scales by patterning host materials while ordering their nanoparticle inclusions. While liquid crystals are often used to define the ordering of nanoparticles dispersed within them, this approach is typically limited to liquid crystals confined in classic geometries. In this work, the orientational order that liquid crystalline colloidal hosts impose on anisotropic nanoparticle inclusions is combined with an additive manufacturing method that enables engineered, macroscopic three-dimensional (3D) patterns of co-aligned gold nanorods and cellulose nanocrystals. These gels exhibit polarization-dependent plasmonic properties that emerge from the unique interaction between the host medium's anisotropic optical properties defined by orientationally ordered cellulose nanocrystals, from the liquid crystal's gold nanorod inclusions, and from the complexity of spatial patterns accessed with 3D printing. The gels' optical properties that are defined by the interplay of these effects are tuned by controlling the gels' order, which is tuned by adjusting the gels' cellulose nanocrystal concentrations. Lithe optical responsiveness of these composite gels to polarized radiation may enable unique technological applications like polarization-sensitive optical elements.

Regenerated cellulose-dispersed polystyrene composites enabled via Pickering emulsion polymerization.

Cellulose composites are an important class of polymeric composites due to their renewable, biodegradable feedstock, and tend to have exceptional properties due to peculiar increase of the matrix-filler interface. In this work, a new breed of colloids enabled by regenerated cellulose (RC) was used to prepare polystyrene/cellulose composites. Specifically, an oil-in-water Pickering emulsion of styrene stabilized by RC was prepared, followed by polymerization of styrene, allowing us to obtain a uniformly dispersed PS/RC composite. When the RC concentration was above 0.8 wt%, a network of RC spontaneously formed in the composite, as evidenced by rheological testing. Furthermore, the addition of RC to polystyrene improved the composite's thermal stability and tensile mechanical properties while minimally impacting average visible light transmission (with a decrease in average transmission by about 1-5%). Regenerated cellulose is a promising nanofiller for polymeric composites due to its environment friendly and cost effective nature, and could be used for preparation of other novel RC-reinforced composites.