Molecular Changes in Spider Viscid Glue As a Function of Relative Humidity Revealed Using Infrared Spectroscopy.

Spider aggregate glue can absorb moisture from the atmosphere to reduce its viscosity and become tacky. The viscosity at which glue adhesion is maximized is remarkably similar across spider species, even though that viscosity is achieved at very different relative humidity (RH) values matching their diverse habitats. However, the molecular changes in the protein structure and the bonding state of water (both referred to here as molecular structure) with respect to the changes in RH are not known.

Hygroscopic compounds in spider aggregate glue remove interfacial water to maintain adhesion in humid conditions.

Adhesion in humid environments is fundamentally challenging because of the presence of interfacial bound water. Spiders often hunt in wet habitats and overcome this challenge using sticky aggregate glue droplets whose adhesion is resistant to interfacial failure under humid conditions. The mechanism by which spider aggregate glue avoids interfacial failure in humid environments is still unknown.

Ice-like water supports hydration forces and eases sliding friction.

The nature of interfacial water is critical in several natural processes, including the aggregation of lipids into the bilayer, protein folding, lubrication of synovial joints, and underwater gecko adhesion. The nanometer-thin water layer trapped between two surfaces has been identified to have properties that are very different from those of bulk water, but the molecular cause of such discrepancy is often undetermined. Using surface-sensitive sum frequency generation (SFG) spectroscopy, we discover a strongly coordinated water layer confined between two charged surfaces, formed by the adsorption of a cationic surfactant on the hydrophobic surfaces.

Effect of Acid-Base Interactions on Conformation of Adsorbed Polymer Chains.

Sum frequency generation spectroscopy (SFG) and attenuated-total-reflection IR (ATR-IR) were used to investigate polymer adsorption on solid surfaces in CCl (neutral), CHCl (acidic), and acetone (basic) solvents. Fowkes showed that the adsorbed amount of the polymer from acidic and basic solvents is less than that from a neutral solvent ( , , 3-7). Here, we show that besides the differences in adsorbed amount, chains adsorbed from an acidic solvent adopted a flat conformation with a much smaller ratio of segments of loops and tails to trains compared to those adsorbed from a neutral solvent.

Adsorption and viscoelastic analysis of polyelectrolyte-surfactant complexes on charged hydrophilic surfaces.

The aggregation of surfactants around oppositely charged polyelectrolytes brings about a peculiar bulk phase behavior of the complex, known as coacervation, and can control the extent of adsorption of the polyelectrolyte at an aqueous-solid interface. Adsorption kinetics from turbid premixed polyelectrolyte-surfactant mixtures have been difficult to measure using optical techniques such as ellipsometry and reflectometry, thus limiting the correlation between bulk phases and interfacial adsorption. Here, we investigated the adsorption from premixed solutions of a cationic polysaccharide (PQ10) and the anionic surfactant sodium dodecyl sulfate (SDS) on an amphoteric alumina surface using quartz crystal microbalance with dissipation (QCMD).