1: Magnetic Particles: Preparation, Properties and Applications: M. Ozaki. 2: Maghemite (gamma-Fe2O3): A Versatile Magnetic Colloidal Material C.J. Serna, M.P. Morales. 3: Dynamics of Adsorption and Oxidation of Organic Molecules on Illuminated Titanium Dioxide Particles Immersed in Water M.A. Blesa, R.J. Candal, S.A. Bilmes. 4: Colloidal Aggregation in Two-Dimensions A. Moncho-Jorda, F. Martinez-Lopez, M.A. Cabrerizo-Vilchez, R. Hidalgo Alvarez, M. Quesada-PMerez. 5: Kinetics of Particle and Protein Adsorption Z. Adamczyk.

Surface and Colloid Science

The adsorption data presented in the preceding paper (Part II of this series) have been used to deduce the molecular structures of β-casein, bovine serum albumin (BSA), and lysozyme films at the air-water and oil-water interfaces. The hydrophobic, disordered β-casein molecules are more surface-active than the globular BSA and lysozyme molecules. β-Casein is in an all-train configuration at low surface pressures (π 10−2 wt%) giving films thicker than 100 A. Although the primary layer is irreversibly adsorbed, molecules in subsequent layers are reversibly adsorbed. Lysozyme molecules are denatured at low π values (π < 8 mN m−1), and at higher values essentially native molecules (which are reversibly adsorbed) coexist in the surface film. Much residual native structure remains even in the denatured film because lysozyme is very resistant to denaturation. At the oil-water interface, the adsorbed lysozyme molecules are denatured to a greater extent than those at the air-water interface; native molecules are not stable at this interface. The adsorbed BSA molecules contain residual native structure, but there is no abrupt conformational change in the film at a particular packing density. The structure at the air-water interface is intermediate to those of lysozyme and β-casein. BSA has the same π-A curve as lysozyme at the oil-water interface.

Proteins at liquid interfaces

A mechanism of general anesthesia is suggested and investigated using lattice statistical thermodynamics. Bilayer membranes are characterized by large lateral stresses that vary with depth within the membrane. Incorporation of amphiphilic and other interfacially active solutes into the bilayer is predicted to increase the lateral pressure selectively near the aqueous interfaces, compensated by decreased lateral pressure toward the center of the bilayer. General anesthesia likely involves inhibition of the opening of the ion channel in a postsynaptic ligand-gated membrane protein. If channel opening increases the cross-sectional area of the protein more near the aqueous interface than in the middle of the bilayer, then the anesthetic-induced increase in lateral pressure near the interface will shift the protein conformational equilibrium to favor the closed state, since channel opening will require greater work against this higher pressure. This hypothesis provides a truly mechanistic and thermodynamic understanding of anesthesia, not just correlations of potency with structural or thermodynamic properties. Calculations yield qualitative agreement with anesthetic potency at clinical anesthetic membrane concentrations and predict the alkanol cutoff and anomalously low potencies of strongly hydrophobic molecules with little or no attraction for the aqueous interface, such as perfluorocarbons.

The lateral pressure profile in membranes: a physical mechanism of general anesthesia.

Hydrocarbon production, gas recovery from shale, CO2 storage and water management have a common scientific underpinning: multiphase flow in porous media. This book provides a fundamental description of multiphase flow through porous rock, with emphasis on the understanding of displacement processes at the pore, or micron, scale. Fundamental equations and principal concepts using energy, momentum, and mass balance are developed, and the latest developments in high-resolution three-dimensional imaging and associated modelling are explored. The treatment is pedagogical, developing sound physical principles to predict flow and recovery through complex rock structures, while providing a review of the recent literature. This systematic approach makes it an excellent reference for those who are new to the field. Inspired by recent research, and based on courses taught to thousands of students and professionals from around the world, it provides the scientific background necessary for a quantitative assessment of multiphase subsurface flow processes, and is ideal for hydrology and environmental engineering students, as well as professionals in the hydrocarbon, water and carbon storage industries.

Multiphase Flow in Permeable Media: A Pore-Scale Perspective

A major scientific challenge of the past decade pertaining to the field of soft matter has been to craft 'adaptable' materials, inspired by nature, which can dynamically alter their structure and functionality on demand, in response to triggers produced by environmental changes. Amongst these, 'smart' surfactant wormlike micelles, responsive to external stimuli, are a particularly recent area of development, yet highly promising, given the versatility of the materials but simplicity of the design-relying on small amphiphilic molecules and their spontaneous self-assembly. The switching 'on' and 'off' of the micellar assembly structures has been reported using electrical, optical, thermal or pH triggers and is now envisaged for multiple stimuli. The structural changes, in turn, can induce major variations in the macroscopic characteristics, affecting properties such as viscosity and elasticity and sometimes even leading to a spontaneous and effective 'sol-gel' transition. These original smart materials based on wormlike micelles have been successfully used in the oil industry, and offer a significant potential in a wide range of other technological applications, including biomedicine, cleaning processes, drag reduction, template synthesis, to name but a few. This review will report results in this field published over the last few years, describe the potential and practical applications of stimuli-responsive wormlike micelles and point out future challenges.

Smart wormlike micelles

In conformity with the conclusion obtained previously, the mixed micelle formation of surfactants was treated thermodynamically as the appearance of a macroscopic bulk phase with the aid of the excess thermodynamic quantities similar to those used for the adsorbed film. The composition of surfactant in the mixed micelle and the thermodynamic quantities of micelle formation were found to be evaluated by applying the thermodynamic equations derived. These equations were extended so as to be applicable to any kind of surfactant mixture. It was shown that the critical micelle concentration vs. composition of surfactant curves form a diagram analogous to the phase diagram of binary mixture. Applying the equation to the published data on typical surfactant systems, this thermodynamic approach was proved to be useful to clarify the miscibility of surfactants in the micellar state.

Kinsi Motomura

Papers

Thermodynamic consideration of the mixed micelle of surfactants

Thermodynamic studies on adsorption at interfaces. I. General formulation

Thermodynamic studies on adsorption at interfaces: IV. Dodecylammonium chloride at water/air interface

The critical micelle concentration of sodium dodecyl sulfate-bivalent metal dodecyl sulfate mixtures in aqueous solutions

Phase transition in the adsorbed films at water/air interface