RESUMEN
Confined water has demonstrated distinct structural and dynamic properties compared to bulk water. Although many studies have explored the water structure within simple geometries using materials such as carbon and silica, studies on gas solubility in confined water and the underlying physics of water structure-solubility remain limited. Recent research has illuminated the concept of "oversolubility", wherein gases display increased solubility within liquids confined in small pores compared to their bulk form. This study focuses on zeolites, naturally abundant materials with versatile applications, to study the hydrogen solubility within confined water through careful experimentation. Our findings underscore the relationship between the pore dimension and gas solubility enhancement within confined water. Hydrogen solubility is closely associated with the rearrangement of water molecules within the porous framework of the zeolite. Our research shows that a 2 nm pore size results in the greatest increase in hydrogen solubility in the water trapped inside the zeolite framework. The double donor-double acceptor (DDAA) bonds play a critical role in hydrogen solubility. Our research provides fundamental insight into the role of the molecular bonding type on hydrogen solubility in water, paving the way for potential applications in hydrogen storage and utilization.
RESUMEN
HYPOTHESIS: When ice accumulates on a surface, it can adversely impact functionality and safety of a platform in infrastructure, transportation, and energy sectors. Despite several attempts to model the ice adhesion strength on ice-shedding materials, none have been able to justify variation in the ice adhesion strength measured by various laboratories on a simple bare substrate. This is primarily due to the fact that the effect of underlying substrate of an ice-shedding material has been entirely neglected. EXPERIMENTS: Here, we establish a comprehensive predictive model for ice adhesion using the shear force method on a multi-layered material. The model considers both shear resistance of the material and shear stress transfer to the underlying substrate. We conducted experiments to validate the model predictions on the effect of coating and substrate properties on the ice adhesion. FINDINGS: The model reveals the importance of the underlying substrate of a coating on ice adhesion. Most importantly, the correlation between the ice adhesion and the coating thickness are entirely different for elastomeric and non-elastomeric materials. This model justifies different measured ice adhesion across various laboratories on the same material and elucidates how one could achieve both low ice adhesion and high mechanical durability. Such predictive model and understanding provides a rich platform to guide the future material innovation with minimal adhesion to the ice.
RESUMEN
The demand for effective and long-term durable antibacterial surfaces has been ever-growing in the past decades. A wide variety of long-lasting antibacterial surfaces developed from release-killing, active-killing, and anti-fouling strategies have demonstrated the desired effectiveness and durability so far. Most of these successful designs were developed from toxic and fossil-based materials, which failed to comply with the green design criteria. Furthermore, the longevity of these surfaces remained an unaddressed challenge. Herein, we present a disruptive paradigm that emphasizes both eco-friendliness and long-lasting antibacterial properties. A bio-based active-killing essential oil, namely carvacrol, and nonfouling carboxybetaine zwitterionic moieties were combined and incorporated into a highly bio-based polyurethane (BPU). The long-lasting active-killing property for this antibacterial BPU coating was enabled through the extended release of the bounded carvacrol via hydrolysis in an aqueous environment and compared to unbound carvacrol by liquid infusion. Also, the release of carvacrol generates zwitterionic moieties to prevent further bacterial attachment at the release site, resulting in a "kill and defend" synergistic antibacterial function in the BPU. The kinetics of the extended-release property were investigated and compared with unbound carvacrol BPU coatings; unbound carvacrol infused into BPU was quickly exhausted after 2 days of immersion in water, while the extended-release surface exhibited a nearly constant release rate of â¼128 ng cm-2 h-1 even after 45 days. The in vitro antibacterial efficiency of the BPUs was quantitatively evaluated using the modified ISO standard for cross-laboratory comparison. As a result, approximately 98.9 and 98.7% of Escherichia coli and Staphylococcus aureus were eliminated from the coating surfaces, and only a negligible variance in the antibacterial efficiency was observed after 5 cycles of test. The feasibility for practical application was also demonstrated by challenging the BPU coatings in everyday settings. This "built-to-last" design theory provided insights for future development of greener antibacterial coatings with long-term performance.