29 research outputs found
Trapped non-equilibrium states in aqueous solutions of oppositely charged polyelectrolytes and surfactants: effects of mixing protocol and salt concentration
Fewer referrals to Swedish emergency departments among nursing home patients with dementia, comprehensive cognitive decline and multicomorbidity
Impact of Multi-Interface Surfactant Adsorption on Wettability in Dense Nonaqueous Phase Liquid Systems
Abstract The wettability, and hence the distribution and transport, of dense nonaqueous phase liquid (DNAPL) wastes in the subsurface is strongly affected by surfactants that are present in the wastes. To understand their impact, this work examined the dependence of the contact angle of quartz/tetrachloroethylene (PCE)/water systems containing the anionic surfactant Aerosol OT (AOT) or/and the nonionic surfactant hexaoxyethylene glycol mono-n-dodecyl ether (C12E6) on the surfactants' adsorption at both the PCE/water and silica/water interfaces. Results showed that C12E6 enhanced oil wetness at low pH. However, the system reverted to water-wet upon the addition of AOT, which by itself, did not alter the wettability of the system. To mechanistically explain such behavior, it was proposed that, based on measurements of adsorption onto quartz and calculations of surface excess using an equation-of-state approach, the increased oil-wetness in systems containing C12E6 is due to the entropy-driven attraction between the oxyethylene groups of the adsorbed C12E6 at both the PCE/water and water/silica interfaces. Addition of AOT reduced the adsorbed C12E6 at both interfaces, lowering the attraction between PCE and silica. Thus, a consideration of surfactant adsorption at both interfaces, and the subsequent interaction between the molecules sorbed at both interfaces, is critical to explaining the wettability behavior of waste DNAPLs.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/85122/1/ees_2009_0240.pd
A small-angle X-ray scattering study of complexes formed in mixtures of a cationic polyelectrolyte and an anionic surfactant
Preparation and characterization of W/O/W type double emulsion containing PGPR–lecithin mixture as lipophilic surfactant
Shear response of nanoconfined water on muscovite mica: role of cations
By monitoring the thermal noise of a vertically oriented micromechanical force sensor, we detect the viscoelastic response to shear for water in a subnanometer confinement. Measurements in pure water as well as under acidic and high-ionic-strength conditions relate this response to the effect of surface-adsorbed cations, which, because of their hydration, act as pinning centers restricting the mobility of the confined water molecules
Feeling the squeeze: shear viscoelasticity of nanoconfined water
How water molecules confined in nanometer gaps respond to shear: as a viscoelastic solid, viscous fluid or something in between?
This important question relevanti in biology, geochemistry, mineralogy, colloidal science and engineering continues to be debated with experimental evidence provided for conflicting point of view.
Here we show clear results obtained using innovative technique based on vertically oriented micromechanical force sensors investigating viscoelastic response of water on muscovite mica