Effect of the counter-ion of the basification agent on the pore texture of organic and carbon xerogels

Organic and carbon xerogels were prepared by polycondensation of resorcinol with formaldehyde in water, followed by evaporative drying and, eventually, pyrolysis. The pH of the precursor’s solution was fixed at 6.0 in all cases by adding various hydroxides as basification agent. Three alkali metal hydroxides (LiOH, NaOH and KOH) and three alkaline earth metals hydroxides (Ca(OH)₂, Ba(OH)₂, Sr(OH)₂) were used. It was found that the pore texture of the organic and carbon xerogels is totally independent on the cation size, but depends on the charge and concentration of the counter-cation. Indeed, the pore size of the alkaline earth metal loaded samples is larger than that of the alkali metal-doped xerogels. As a matter of fact, to reach the same initial pH, the concentration in alkali metal hydroxide must be twice that of the alkaline earth metal base. The effect of ions on the pore texture was thus attributed to electrostatic effects on the microphase separation process that occurs prior to gelation.     

Assessment of the 3D localization of metallic nanoparticles in Pd/SiO2 cogelled catalysts by electron tomography

The purpose of this study is to analyze the localization of palladium nanoparticles within their silica support, in two heterogeneous catalysts synthesized by the sol-gel process, with different metal loadings. Electron tomography demonstrates that the palladium particles are localized deep inside the silica skeleton. The use of digital image analysis further shows that the dispersion of palladium is optimal in the sample with the lowest loading. The particles are regularly spaced in the middle of the silica skeleton, with a distance between them comparable to the diameter of the struts of silica.     

Nitrogen adsorption on silica xerogels or the odd look of a t plot

Nitrogen adsorption in some silica xerogels leads to t plots that cannot be interpreted by the occurrence of capillary condensation or by the filling of micropores. Their particular appearance stems from the unique columnar structure of these samples at the nanometer scale, by which the adsorbent surface has a positive curvature. A standard thermodynamic approach allows the phenomenon to be exploited to characterize the samples.     

On the nature of pulsars

The paper contains a relatively non-technical summary of some recent work by the author and Jeremy Butterfield. The goal is to find a way of assigning meaningful truth values to propositions in quantum theory: something that is not possible in the normal, instrumentalist interpretation. The key mathematical tool is presheaf theory where multi-valued, contextual truth values arise naturally. We show how this can be applied to quantum theory, with the ‘contexts’ chosen to be Boolean subalgebras of the set of all projection operators.     

Structure of silica xerogels synthesized with organoalkoxysilane co-reactants hints at multiple phase separation

The microstructure of hybrid silica xerogels synthesized by the base-catalyzed polymerization of tetraethoxysilane (TEOS) in ethanol in the presence of 3-aminopropyltriethoxysilane (AES) and of 3-(2-aminoethylamino)propyltrimethoxysilane (EDAS) as co-reactants, and dried in subcritical conditions, is analyzed. A thorough structural characterization of the samples is performed combining nitrogen adsorption, small-angle X-ray scattering (SAXS), and transmission electron microscopy coupled with digital image analysis. The use of these methods shows that, for both co-reactants, the xerogels are made of macropores supported by filaments, with each filament being formed of smaller structures. The quantitative impact of the additive on each structural level is assessed. The data are compared with a previous time-resolved SAXS study conducted during the formation of the gels (J. Phys. Chem. B 2004, 108, 8983-8991). The results are analyzed in the framework of a double phase separation model.     

Density of States for a specified correlation function and the energy landscape

The degeneracy of two-phase disordered microstructures consistent with a specified correlation function is analyzed by mapping it to a ground-state degeneracy. We determine for the first time the associated density of states via a Monte Carlo algorithm. Our results are explained in terms of the roughness of an energy landscape, defined on a hypercubic configuration space. The use of a Hamming distance in this space enables us to define a roughness metric, which is calculated from the correlation function alone and related quantitatively to the structural degeneracy. This relation is validated for a wide variety of disordered structures.     

Supercooling of the disordered vortex lattice in Bi(2)Sr(2)CaCu(2)O(8+delta)

Time-resolved local induction measurements near the vortex lattice order-disorder transition in optimally doped Bi(2)Sr(2)CaCu(2)O(8+delta) crystals show that the high-field, disordered phase can be quenched to fields as low as half the transition field. Over an important range of fields, the electrodynamical behavior of the vortex system is governed by the coexistence of ordered and disordered vortex phases in the sample. We interpret the results as supercooling of the high-field phase and the possible first-order nature of the order-disorder transition at the "second magnetization peak."