It is well known that addition of a small amount of nanoparticles to liquid crystals may enhance their nonlinear optical properties. To date, in most reports, semiconductor- or metallic-core nanoparticles in LCs have been described. Here, we report on the synthesis of two types of novel nanoparticles based on a cubic siloxane cage (RSiO_3/2)₈, known as polyhedral oligosilsesquioxane (POSS) with the Si–O skeleton surrounded by covalently attached eight groups (R) of azo-benzene mesogenes differing in the length of their aliphatic chains. These dielectric-core nanoparticles substituted with mesogenic groups are well adapted to the calamitic liquid crystal matrix. Azo-benzene units add an important light-driven functionality to the system via their conformational photoisomerisation. We report on the photochromic properties of these new compounds in chloroform. By embedding the nanoparticles in a nematic liquid crystalline matrix, a functional hybrid nanocomposite material has been obtained. Our research was focused on the characterization of the third order nonlinear optical properties in this system linked to photochromism. The experimental results of all-optical switching in an optical Kerr effect configuration are discussed in the framework of light-induced modification of the aliphatic chains containing azo-benzene photoisomerizing moieties and following local director reorientation in nematic liquid crystals. The described properties are useful in the field of real-time holography.

Spent coffee grounds (SCG) have potential as a sustainable bio-filler in poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) composites, offering an environmentally friendly approach to waste utilization. This study investigated the effect of SCG content on the mechanical, thermal, and morphological properties of PHBV biocomposites and compared them with those of composites containing wood flour and hemp fibers. The biocomposites were fabricated via extrusion and injection molding, followed by the characterization of their mechanical performance, thermal behavior, and microstructure. The results indicated that SCG increased the stiffness of PHBV but did not enhance its tensile strength due to the weak interfacial adhesion between the filler and matrix. Unlike other lignocellulosic fillers, SCG requires lower processing temperatures, which is advantageous for thermally sensitive applications. SEM analysis revealed well-dispersed SCG particles at low concentrations, but visible aggregation and interfacial voids at higher loadings. While SCG serves as an effective and cost-efficient filler for improving the stiffness of PHBV, it does not reinforce the material in the conventional sense.

The curing behaviour of the composition of a liquid-crystalline diepoxy monomer (LCEM) with the central triaromatic mesogenic group was studied using differential scanning calorimetry, conventional DSC and temperature-modulated TMDSC and nuclear magnetic resonance ¹H-NMR spectroscopy. The stoichiometric amount of primary aromatic diamine, 4,4′-diaminodiphenylmethane (DDM), was used as a curing agent. TMDSC TOPEM^® allowed the separation of the thermal effects related to reversible processes (e.g. phase transitions) from irreversible processes (cross-linking reaction) and determining that irreversible curing reaction occurs at the same time as reversible transition of the LCEM from crystal to the liquid-crystalline nematic phase. Additionally, ¹H-NMR analysis of the LCEM/DDM mixture preheated to a temperature from the temperature range of complex thermal changes was conducted. The obtained spectrum clearly showed the presence of partially cured products in the investigated samples and additionally proved that during the endothermic phase transition of the LCEM monomer an exothermic cross-linking reaction was occurring.