Validity of the scaling functional approach for polymer interfaces as a variational theory

We discuss the soundness of the scaling functional (SF) approach proposed by Aubouy Guiselin and Raphael (Macromolecules 29, 7261 (1996)) to describe polymeric interfaces. In particular, we demonstrate that this approach is a variational theory. We emphasis the role of SF theory as an important link between ground-state theories suitable to describe adsorbed layers, and "classical" theories for polymer brushes.Comment: 8 pages, 1 figure, to be published in Phys. Rev.

Effective interactions and phase behaviour for a model clay suspension in an electrolyte

Since the early observation of nematic phases of disc-like clay colloids by Langmuir in 1938, the phase behaviour of such systems has resisted theoretical understanding. The main reason is that there is no satisfactory generalization for charged discs of the isotropic DLVO potential describing the effective interactions between a pair of spherical colloids in an electrolyte. In this contribution, we show how to construct such a pair potential, incorporating approximately both the non-linear effects of counter-ion condensation (charge renormalization) and the anisotropy of the charged platelets. The consequences on the phase behaviour of Laponite dispersions (thin discs of 30 nm diameter and 1 nm thickness) are discussed, and investigation into the mesostructure via Monte Carlo simulations are presented.Comment: LaTeX, 12 pages, 11 figure

Effective interactions in the colloidal suspensions from HNC theory

The HNC Ornstein-Zernike integral equations are used to determine the properties of simple models of colloidal solutions where the colloids and ions are immersed in a solvent considered as a dielectric continuum and have a size ratio equal to 80 and a charge ratio varying between 1 and 4000. At an infinite dilution of colloids, the effective interactions between colloids and ions are determined for ionic concentrations ranging from 0.001 to 0.1 mol/l and compared to those derived from the Poisson-Boltzmann theory. At finite concentrations, we discuss on the basis of the HNC results the possibility of an unambiguous definition of the effective interactions between the colloidal molecules.Comment: 26 pages, 15 figure

Exact asymptotic expansions for the cylindrical Poisson-Boltzmann equation

The mathematical theory of integrable Painleve/Toda type systems sheds new light on the behavior of solutions to the Poisson-Boltzmann equation for the potential due to a long rod-like macroion. We investigate here the case of symmetric electrolytes together with that of 1:2 and 2:1 salts. Short and large scale features are analyzed, with a particular emphasis on the low salinity regime. Analytical expansions are derived for several quantities relevant for polyelectrolytes theory, such as the Manning radius. In addition, accurate and practical expressions are worked out for the electrostatic potential, which improve upon previous work and cover the full range of radial distances

Evidence of environmental strains on charge injection in silole based organic light emitting diodes

Using d. functional theory (DFT) computations, the authors demonstrated a substantial skeletal relaxation when the structure of 2,5-bis-[4-anthracene-9-yl-phenyl]-1,1-dimethyl-3,4-diphenyl-silole (BAS) is optimized in the gas-phase comparing with the mol. structure detd. from monocrystal x-ray diffraction. The origin of such a relaxation is explained by a strong environmental strains induced by the presence of anthracene entities. Also, the estn. of the frontier orbital levels showed that this structural relaxation affects mainly the LUMO that is lowered of 190 meV in the gas phase. To check if these theor. findings would be confirmed for thin films of BAS, the authors turned to UV photoemission spectroscopy and/or inverse photoemission spectroscopy and electrooptical measurements. The study of the c.d. or voltage and luminance or voltage characteristics of an ITO/PEDOT/BAS/Au device clearly demonstrated a very unusual temp.-dependent behavior. Using a thermally assisted tunnel transfer model, this behavior likely originated from the variation of the electronic affinity of the silole deriv. with the temp. The thermal agitation relaxes the mol. strains in thin films as it is shown when passing from the cryst. to the gas phase. The relaxation of the intramol. thus induces an increase of the electronic affinity and, as a consequence, the more efficient electron injection in org. light-emitting diodes

Nanofiber-based filters as novel barrier systems for nanomaterial exposure scenarios

In this article our latest advances in the development of efficient barrier systems against micro- and nano-particulate materials are presented. Nanofibrous polyamide 6 (PA6) mats were fabricated by electrospinning onto a nonwoven viscose substrate. The influence of electrospinning parameters including solution concentration, viscosity, and conductivity, were studied for the production of nonwovens with different fiber size distribution ranging from 74 to 261 nm in diameters. Moreover, the formation of nanowebs (30-40 nm) which are widely distributed among fibers was observed. By varying several process parameters, membranes with different thickness of the nanofiber layer and therefore air permeability and nanoparticle filtration efficiency were obtained.The financial support of this work was provided by MICINN (Spanish Ministry of Science and Innovation) and ERDF (European Regional Development Fund) (ref: PSE-420000-2008-003)

Superparamagnetic iron oxide nanoparticle-loaded polyacrylonitrile nanofibers with enhanced arsenate removal performance

Novel nanocomposite sorbents of superparamagnetic iron oxide nanoparticles (SPION) supported onto electrospun polyacrylonitrile nanofibers were synthesized by a simple and scalable method. The influence of both nanofiber size and SPION loading on As(V) adsorption capacity was studied and optimization was conducted. A maximum uptake capacity of 32.5 mmol As(V) per gram SPION in batch mode tests using an extremely low loading of only 2.9 mg of SPION per gram of adsorbent was achieved. This represents a remarkable improvement of 36 times compared with SPION in suspension. The optimal material was tested in continuous flow operation mode, reaching an adsorption capacity of 851.7 mg As(V) per gram of adsorbent at pH 3.8. It is also demonstrated that the new adsorbents can retain high performance when tested under real conditions using polluted wastewater from a lixiviation dump containing a large amount of competing anions (Cl- and F- ) and interfering cations (K+, Na+, Mg2+, and Ca2+). Furthermore, there was no release of nanoparticles observed during the operation and the spent porous material can be compressed, generating a small amount of solid waste that can be easily treated or stored

Arsenate removal with 3-mercaptopropanoic acid-coated superparamagnetic iron oxide nanoparticles

In the present work, superparamagnetic iron oxide nanoparticles (SPION) surface-coated with 3-mercaptopropanoic acid (3-MPA) were prepared and their feasibility for the removal of arsenate from dilute aqueous solutions was demonstrated. The synthesized 3-MPA-coated SPION was characterized using transmission electron microscopy (TEM), thermogravimetric analysis (TGA) and Fourier transform infra-red spectrometry (FTIR). Separation efficiency of the coated nanoparticles and the equilibrium isotherm of arsenate adsorption were investigated. The obtained results reveal the arsenate adsorption to be highly pH-dependent, and the maximum adsorption was attained in less than 60 min. The resulting increase of 3-MPA-coated SPION adsorption capacity to twice the adsorption capacity of SPION alone under the same conditions is attributed to the increase of active adsorption sites. An adsorption reaction is proposed. On the other hand, efficient recovery of arsenate from the loaded nanoparticles was achieved using nitric acid (HNO3) solution, which also provides a concentration over the original arsenate solutio

Inverse lift: a signature of the elasticity of complex fluids?

To understand the mechanics of a complex fluid such as a foam we propose a model experiment (a bidimensional flow around an obstacle) for which an external sollicitation is applied, and a local response is measured, simultaneously. We observe that an asymmetric obstacle (cambered airfoil profile) experiences a downards lift, opposite to the lift usually known (in a different context) in aerodynamics. Correlations of velocity, deformations and pressure fields yield a clear explanation of this inverse lift, involving the elasticity of the foam. We argue that such an inverse lift is likely common to complex fluids with elasticity.Comment: 4 pages, 4 figures, revised version, submitted to PR