Slow sedimentation and deformability of charged lipid vesicles

The study of vesicles in suspension is important to understand the complicated dynamics exhibited by cells in vivo and in vitro. We developed a computer simulation based on the boundary-integral method to model the three dimensional gravity-driven sedimentation of charged vesicles towards a flat surface. The membrane mechanical behavior was modeled using the Helfrich Hamiltonian and near incompressibility of the membrane was enforced via a model which accounts for the thermal fluctuations of the membrane. The simulations were verified and compared to experimental data obtained using suspended vesicles labelled with a fluorescent probe, which allows visualization using fluorescence microscopy and confers the membrane with a negative surface charge. The electrostatic interaction between the vesicle and the surface was modeled using the linear Derjaguin approximation for a low ionic concentration solution. The sedimentation rate as a function of the distance of the vesicle to the surface was determined both experimentally and from the computer simulations. The gap between the vesicle and the surface, as well as the shape of the vesicle at equilibrium were also studied. It was determined that inclusion of the electrostatic interaction is fundamental to accurately predict the sedimentation rate as the vesicle approaches the surface and the size of the gap at equilibrium, we also observed that the presence of charge in the membrane increases its rigidity

Mass transport and electrochemical properties of La2Mo2O9 as a fast ionic conductor

La2Mo2O9, as a new fast ionic conductor, has been investigated widely due to its high ionic conductivity which is comparable to those of the commercialized materials. However, little work has been reported on the oxygen transport and diffusion in this candidate electrolyte material. The main purpose of this project was to investigate oxide ion diffusion in La2Mo2O9 and also the factors which could affect oxygen transport properties. Oxygen isotope exchange followed by Secondary Ion Mass Spectrometry (SIMS) measurements were employed to obtain oxygen diffusion profiles. A correlation between oxygen ion transport and the electrochemical properties such as ionic conductivity was built upon the Nernst Einstein equation relating the diffusivity to electrical conductivity. In-situ neutron diffraction and AC impedance measurements were designed and conducted to investigate the correlation between crystal structure and oxygen transport in the bulk materials. Other techniques, such as synthesis, microstructure studies, and thermal analysis were also adopted to study the electrochemical properties of La2Mo2O9. The results of the study on the effects of microstructure on oxygen diffusion in La2Mo2O9 revealed that the grain boundary component played a significant role in electrochemical performance, although the grain size seemed to have little influence on oxygen transport. The oxygen isotope exchange in 18O2 was successfully carried out by introducing a silver coating on the sample surface, which solved the main difficulty in applying oxygen isotope exchange on pure ionic conductors. The ionic conductivity obtained from the diffusion coefficients was consistent with the result from AC impedance spectroscopy. The number of mobile oxygen ions was estimated to be 5 per unit cell. There was a difference of oxygen self diffusion coefficient when the isotope exchange was conducted in 18O2 and H2 18O. The activation energy of oxygen diffusion in humidified atmosphere was higher than that measured in dry atmosphere. It indicated that the humidified atmosphere had affected oxygen transport in the material. The studies on hydroxyl incorporation and transport explained the decreased oxygen diffusion coefficients in wet atmosphere and also suggested proton conductivity in La2Mo2O9, which leads to further investigation on applications of La2Mo2O9 as a proton conductor. In-situ neutron diffraction and AC impedance measurement revealed a close relationship between crystal structure and ionic conductivity. The successful application of this technique provides a new method to simultaneously investigate crystal structure and electrical properties in electro-ceramics in the future

Controlling interactions in supported bilayers from weak electrostatic repulsion to high osmotic pressure

Understanding interactions between membranes requires measurements on well-controlled systems close to natural conditions, in which fluctuations play an important role. We have determined, by grazing incidence X-ray scattering, the interaction potential between two lipid bilayers, one adsorbed on a solid surface and the other floating close by. We find that interactions in this highly hydrated model system are two orders of magnitude softer than in previously reported work on multilayer stacks. This is attributed to the weak electrostatic repulsion due to the small fraction of ionized lipids in supported bilayers with a lower number of defects. Our data are consistent with the Poisson-Boltzmann theory, in the regime where repulsion is dominated by the entropy of counter ions. We also have unique access to very weak entropic repulsion potentials, which allowed us to discriminate between the various models proposed in the literature. We further demonstrate that the interaction potential between supported bilayers can be tuned at will by applying osmotic pressure, providing a way to manipulate these model membranes, thus considerably enlarging the range of biological or physical problems that can be addressed.Comment: 14 pages, 8 figure

High electrical conductance enhancement in Au-nanoparticle decorated sparse single-wall carbon nanotube networks

The authors thank the Engineering and Physical Science Research Council for funding through the Imperial College London/Queen Mary Unive

Analysis and three-dimensional modeling of vanadium flow batteries

This study presents 1.) a multi-dimensional model of vanadium Redox Flow Batteries (RFB); 2.) rigorous explanation of porelevel transport resistance, dilute solution assumption, and pumping power; and 3.) analysis of time constants of heat and mass transfer and dimensionless parameter. The model, describing the dynamic system of a RFB, consists of a set of partial differential equations of mass, momentum, species, charges, and energy conservation, in conjunctionwith the electrode's electrochemical reaction kinetics. The governing equations are successfully implemented into three-dimensional numerical simulation of charging, idling, and discharging operations. The model, validated against experimental data, predicts fluid flow, concentration increase/decrease, temperature contours and local reaction rate. The prediction indicates a large variation in local reaction rate across electrodes and the time constants for reactant variation and temperature evolution, which are consistent with theoretical analysis. © 2014 The Electrochemical Society. All rights reserved

Surface charge and hydrodynamic coefficient measurements of {\it Bacillus subtilis} spore by Optical Tweezers

In this work we report on the simultaneous measurement of the hydrodynamic coefficient and the electric charge of single {\it Bacillus subtilis} spores. The latter has great importance in protein binding to spores and in the adhesion of spores onto surfaces. The charge and the hydrodynamic coefficient were measured by an accurate procedure based on the analysis of the motion of single spores confined by an optical trap. The technique has been validated using charged spherical polystyrene beads. The excellent agreement of our results with the expected values demonstrates the quality of our procedure. We measured the charge of spores of {\it B. subtilis} purified from a wild type strain and from two isogenic mutants characterized by an altered spore surface. Our technique is able to discriminate the three spore types used, by their charge and by their hydrodynamic coefficient which is related to the hydrophobic properties of the spore surface.Comment: 21 pages 5 figure

Interfaces and interfacial effects in glass reinforced thermoplastics - Keynote Presentation

Optimization of the fibre-matrix interphase region is critical to achieving the required performance level in thermoplastic matrix composites. Due to its initial location on the fibre surface, the sizing layer is an important component in the formation and properties of the composite interphase. Consequently, any attempt to understand the science of the composite interphase must encompass an understanding of the science of sizing. In this paper the role of sizings from fibre manufacture through to performance of composite parts is reviewed. In particular the role of organosilane coupling agents and how the formation of a polysiloxane interphase is influenced by the surface properties of the fibre is examined. The influence of the sizing film former in terms of its level of interaction with the silane coupling agent is also examined. The importance of residual stresses in thermoplastic composites in the values obtained for the apparent adhesion levels in these systems is highlighted. These residual stresses are shown to play a significant role in determining the level of interfacial strength in thermoplastic composites and in particular in polyolefin matrices. By applying some of the available models for this phenomenon this analysis is extended to explore the effect of the anisotropic fibre microstructure of carbon, aramid and natural fibres on the apparent interfacial strength in thermoplastic composites