Structural properties of cellulose nanofibril foam depending on wet foaming conditions in Pickering stabilization

Porous cellulose nanofibril (CNF) foam was prepared by stabilizing bubbles with CNF and a surfactant and then drying the stabilized wet foam in a convection oven. The consistency of carboxymethylated CNF (CMCNF) and the addition amount of the surfactant were controlled and the effects of these factors on the CNF wet foam and dry foam properties were investigated. An adequate amount of the surfactant (0.02–0.04 wt%) with CMCNF consistency higher than 0.5 wt% yielded wet foams with excellent stability. When the wet foam was dried at 60 °C in an oven, dry CNF foam with over 97% porosity was generated. The stable wet foams resulted in dry CNF foam with a sphere-like pore structure and low levels of shrinkage during drying. In contrast, unstable wet foams generated dry foam with severe shrinkage and large cavities. The pore size and the porosity of the dried foam were determined by the shape of bubbles in the wet foam and the degree of shrinkage during drying, which, in turn, affected the mechanical strength. In addition, the compressive strength of the oven-dried foam was 83% higher than that of the freeze-dried foam. Therefore, the preparation of a stable wet porous CMCNF foam by controlling the CMCNF consistency and the amount of surfactant was essential for obtaining a porous CMCNF foam with a uniform pore structure and good mechanical strength by oven drying. Graphic abstract

Pickering stabilization of a dynamic intracellular emulsion

Biomolecular condensates are cellular compartments that form by phase separation in the absence of limiting membranes. Studying the P granules of C. elegans, we find that condensate dynamics are regulated by protein clusters that adsorb to the condensate interface. Using in vitro reconstitution, live observations and theory, we demonstrate that localized assembly of P granules is controlled by MEG-3, an intrinsically disordered protein that forms low dynamic assemblies on P granules. Following classic Pickering emulsion theory, MEG-3 clusters lower surface tension and slow down coarsening. During zygote polarization, MEG-3 recruits DYRK/MBK-2 kinase to accelerate localized growth of the P granule emulsion. By tuning condensate-cytoplasm exchange, interfacial clusters regulate the structural integrity of biomolecular condensates, reminiscent of the role of lipid bilayers in membrane-bound organelles.

Polymeric Carbon Nitride Armored Centimeter-Wide Organic Droplets in Water for All-Liquid Heterophase Emission Technology

High potential of emission chemistry has been visualized in many fields, from sensors and imaging to displays. In general, conjugated polymers are the top rankers for such chemistry, despite the fact that they bring solubility problems, high expenses, toxicity and demanding synthesis. Metal-free polymeric semiconductor graphitic carbon nitride (g-CN) has been an attractive candidate for visible light-induced photocatalysis, and its emission properties have been optimized and explored recently. Herein, we present modified g-CN nanoparticles as organodispersible conjugated polymer materials to be utilized in a heterophase emission systems. The injection of a g-CN organic dispersion in aqueous polymer solution not only provides retention of the shape by Pickering stabilization of g-CN, but high intensity emission is also obtained. The heterophase all-liquid emission display can be further modified by the addition of simple conjugated organic molecules to the initial g-CN dispersion, which provides a platform for multicolor emission. We believe that such shape-tailored and stabilized liquid–liquid multicolor emission systems are intriguing for sensing, displays and photonics.