Slippage of water over hydrophobic surfaces

The interaction and behavior of surfaces orcolloids is of quantitative significance inunderstanding the transport and fate ofcompounds and microorganisms in environmentalsystems. Historically, the DLVO model ofcolloid stability has described theseinteractions. This model finds its basis in aforce (energy) balance that comprisesattractive van der Waals and repulsiveelectrostatic interactions. Recently, the DLVOmodel has been found unable to fully describebiotic and abiotic colloidal behavior inaqueous media. The suspending phase (commonlywater) is often treated as a force (energy)transmitting or propagating medium. It isreasonable to believe that the structure ofwater may participate in a more significantfashion. Moreover, other moieties (sorbed anddissolved) may also have non-DLVO effects. Significant work has been focused on extendingthe precepts of the traditional DLVO model toaccommodate these non-DLVO forces (energies). This paper reviews many of the interactionsthat play a role in environmental systems andare not commonly subsumed by the traditionalDLVO model: e.g., hydrogen bonding and thehydrophobic effect, hydration pressure,non-charge transfer Lewis acid baseinteractions, and steric interactions.

A review of non-DLVO interactions in environmental colloidal systems

Probing polyamide membrane surface charge, zeta potential, wettability, and hydrophilicity with contact angle measurements

Thin-film composite polyamide membranes are state-of-the-art materials for membrane-based water purification and desalination processes, which require both high rejection of contaminants and high water permeabilities. However, these membranes are prone to fouling when processing natural waters and wastewaters, because of the inherent surface physicochemical properties of polyamides. The present work demonstrates the fabrication of forward osmosis polyamide membranes with optimized surface properties via facile and scalable functionalization with fine-tuned nanoparticles. Silica nanoparticles are coated with superhydrophilic ligands possessing functional groups that impart stability to the nanoparticles and bind irreversibly to the native carboxyl moieties on the membrane selective layer. The tightly tethered layer of nanoparticles tailors the surface chemistry of the novel composite membrane without altering the morphology or water/solute permeabilities of the membrane selective layer. Surface characteriz...

N. V. Churaev

Papers

Structure of water in thin layers