Interaction and flocculation of spherical colloids wetted by a surface-induced corona of paranematic order

Particles dispersed in a liquid crystal above the nematic-isotropic phase transition are wetted by a surface-induced corona of paranematic order. Such coronas give rise to pronounced two-particle interactions. In this article, we report details on the analytical and numerical study of these interactions published recently [Phys. Rev. Lett. 86, 3915 (2001)]. We especially demonstrate how for large particle separations the asymptotic form of a Yukawa potential arises. We show that the Yukawa potential is a surprisingly good description for the two-particle interactions down to distances of the order of the nematic coherence length. Based on this fact, we extend earlier studies on a temperature induced flocculation transition in electrostatically stabilized colloidal dispersions [Phys. Rev. E 61, 2831 (2000)]. We employ the Yukawa potential to establish a flocculation diagram for a much larger range of the electrostatic parameters, namely the surface charge density and the Debye screening length. As a new feature, a kinetically stabilized dispersion close to the nematic-isotropic phase transition is found.Comment: Revtex v4.0, 16 pages, 12 Postscript figures. Accepted for publication in Phys. Rev.

Synthoil hydrodynamics. Combined third and fourth quarterly report, December 1, 1975--May 31, 1976

This report deals with two-phase flow (gas and liquid) in a packed bed in the synthoil process reactor and preheater; in particular, nonuniform radial distribution of the liquid phase is studied. In addition, temperature profiles and possible instability of control due to the exothermic reactions are studied with respect to the synthoil reactor. This factor may limit the reactor diameter to about six inches. (LTN

Total internal reflection fluorescence imaging using an upconverting cover slip for multicolour evanescent excitation

Total internal reflection fluorescence microscopy is well known as a means of studying surface-bound structures in cell biology. It is usually measured either by coupling a light source to the sample using a prism or with a special objective where light passing through the periphery of the lens illuminates the contact region beyond the critical angle. In this study we present a new and simple approach to total internal reflection fluorescence microscopy where the sample is mounted on a cover slip prepared from a high-index upconverting glass-ceramic. Excitation of the cover slip with a low-cost near-infrared laser diode generates intense narrow-band visible emission within the cover slip, some of which is totally internally reflected. This emission gives rise to an evanescent wave at the interface and hence can excite surface-bound fluorescent species. Depending on the excitation conditions the cover slip can generate violet, green and red emission and hence can excite a wide range of fluorescent labels. Fluorescence emission from the sample can be detected in spectral regions where the direct emission from the cover slip is very weak. The advantages and limitations of the technique are discussed in comparison with conventional total internal reflection fluorescence microscopy measurements and prospects for novel total internal reflection fluorescence microscopy geometries are considered

Electrokinetic salt removal from porous building materials using ion exchange membranes

The removal of salt from porous building materials under the influence of an applied voltage gradient normally results in high pH gradients due to the formation of protons and hydroxyl ions at the electrodes. The formed acidic and alkaline regions not only lead to disintegration of the porous material, but also affect the salt transport. In this work we use ion exchange membranes between the electrodes and the porous material to prevent the protons and hydroxyl ions from intruding into the material. The porous material used in this study is fired clay brick, which has been saturated with a 4 mol/l sodium chloride solution prior to the desalination treatment. In order to experimentally determine the salt removal, we monitored the sodium ion concentration profiles across the material with nuclear magnetic resonance (NMR). In addition, we present theoretical predictions for the salt removal according to a model based on the Poisson–Nernst–Planck theory for ion transport. From the work reported here, we can conclude that the use of ion exchange membranes to desalinate porous building materials is not useful since it reduces the salt removal rate to such an extent that desalination with poultices, which is driven by diffusion only, is more efficient. The reason behind this is twofold. First, the ion exchange membranes provide a penalty for the ions to leave the material. Second, in the absence of acidic and alkaline regions, the salt concentration at the edges of the porous material will reduce to almost zero, which leads to a locally increased electrical resistance, and thus a reduction of the electrical field in the bulk of the material. Due to this reduction the effect of the applied voltage gradient across the material vanishes, and the salt removal is limited by diffusion.Materials Innovation InstituteMechanical, Maritime and Materials Engineerin

Electrochemistry and capacitive charging of porous electrodes in asymmetric multicomponent electrolytes

We present porous electrode theory for the general situation of electrolytes containing mixtures of mobile ions of arbitrary valencies and diffusion coefficients (mobilities). We focus on electrodes composed of primary particles that are porous themselves. The predominantly bimodal distribution of pores in the electrode consists of the interparticle or macroporosity outside the particles through which the ions are transported (transport pathways), and the intraparticle or micropores inside the particles, where electrostatic double layers (EDLs) are formed. Both types of pores are filled with electrolyte (solvent plus ions). For the micropores we make use of a novel modified-Donnan (mD) approach valid for strongly overlapped double layers. The mD-model extends the standard Donnan approach in two ways: (1) by including a Stern layer in between the electrical charge and the ions in the micropores, and (2) by including a chemical attraction energy for the ions to go from the macropores into the micropores. This is the first paper where the mD-model is used to model ion transport and electrochemical reactions in a porous electrode. Furthermore we investigate the influence of the charge transfer kinetics on the chemical charge in the electrode, i.e., a contribution to the electrode charge of an origin different from that stemming from the Faradaic reaction itself, e.g. originating from carboxylic acid surface groups as found in activated carbon electrodes. We show that the chemical charge depends on the current via a shift in local pH, i.e. “current-induced charge regulation.” We present results of an example calculation where a divalent cation is reduced to a monovalent ion which electro-diffuses out of the electrode.National Science Foundation (U.S.) (NSF Contract No. DMS 0948071)Massachusetts Institute of Technology. Energy Initiative (Seed grant