The Mössbauer spectrum of synthetic hureaulite: Fe5 2+(H2O)4(PO4H)2(PO4)2

The crystal structure of synthetic ferrous hureaulite, Fe₅ ²⁺ (H₂O)₄(PO₄H)₂(PO₄)₂, was refined from single-crystal X-ray data. It is monoclinic, space group C2/c, with a=17.487(4), b=9.017(2), c=9.338(2) Å, β=96.27(3)°, V=1463.6(6) Å³, Z=4 and D _calc=3.327 g/cm³. This end member of the hureaulite series was crystallized under distinctly acidic conditions, by a method that gives perfect crystals, large enough for X-ray single crystal studies. The main feature of the hureaulite structure is that it has an equal number of normal (PO₄)³⁺ and acid (PO₄H)²⁺ tetradentate groups. These are centered on Fe²⁺ atoms and share corners with edge-linked octahedra, forming pentamer units. The five Fe²⁺ atoms are distributed on three distinct sites in these units. This can be directly observed in the Mössbauer spectrum at 295 K, which contains three doublets whose relative intensities correspond to the 1:2:2 distributions of crystallographic sites.     

On the adjacencies of triangular meshes based on skeleton-regular partitions

For any 2D triangulation τ, the 1-skeleton mesh of τ is the wireframe mesh defined by the edges of τ, while that for any 3D triangulation τ, the 1-skeleton and the 2-skeleton meshes, respectively, correspond to the wireframe mesh formed by the edges of τ and the “surface” mesh defined by the triangular faces of τ. A skeleton-regular partition of a triangle or a tetrahedra, is a partition that globally applied over each element of a conforming mesh (where the intersection of adjacent elements is a vertex or a common face, or a common edge) produce both a refined conforming mesh and refined and conforming skeleton meshes. Such a partition divides all the edges (and all the faces) of an individual element in the same number of edges (faces). We prove that sequences of meshes constructed by applying a skeleton-regular partition over each element of the preceding mesh have an associated set of difference equations which relate the number of elements, faces, edges and vertices of the nth and (n−1)th meshes. By using these constitutive difference equations we prove that asymptotically the average number of adjacencies over these meshes (number of triangles by node and number of tetrahedra by vertex) is constant when n goes to infinity. We relate these results with the non-degeneracy properties of longest-edge based partitions in 2D and include empirical results which support the conjecture that analogous results hold in 3D.     

Poly(dimethylaminoethylmethacrylate) hydrochloride (PDMAEM-HCl) a well behaving polycation for multilayer formation on planar surfaces

The polycation preparation of poly(dimethylaminoethylmethacrylate) hydrochloride and the multilayer formation in combination with poly(sodium 4-styrenesulphonate) as polyanion studies onto different substrates, as followed by streaming potential measurements, in situ surface plasmon resonance spectroscopy, and multi-wavelength ellipsometry, are reported. Furthermore, we studied the resulting multilayer buildup of dry surfaces by UV-Vis spectroscopy, X-ray photoelectron spectroscopy, and atomic force microscopy measurements. Thereby, the layer built up at the solid/liquid-interface could be followed and quantified at the molecular level.This revised version was published online in April 2005 with corrections to the article category.     

Algorithm for the Semigroup of a Space Curve Singularity

The semigroup of values of irreducible space curve singularities is the set of intersection multiplicities among hypersurfaces and the given curve. It is an invariant of the singularity, and for plane curves it characterizes the equisingularity type considered by Zariski. For space curve singularities the semigroup of values is a numerical semigroup and it can not be computed by means of the exponents of any Puiseux parametrization, as in the plane case. We obtain an algorithm for calculating the semigroup of values of a space curve singularity, which determines the generators of the semigroup and the valuation ideals associated with the semigroup. We give a Maple version of the algorithm.     

A question of passman on the symmetric ring of quotients

We give an example of a domain such that the sequence of iterated symmetric rings of quotients does not stabilize. This answers a question of Passman. The work of the first author has been partially supported by CICYT PB 86-0353-C02-01 and that of the second author by CICYT PB87-0703 and the Institut d’Estudis Catalans.     

Effect of additives and measurement procedure on the electrorheology of hematite/silicone oil suspensions

The effects of measuring procedures and activating additives on the electrorheological (ER) behaviour of hematite/silicone oil suspensions are analysed. The structures built up in the presence of an electric field without shear are stronger than those produced with both electric and shear fields simultaneously applied. Such differences are measurable when the field strength is not high enough to dominate over hydrodynamic interactions. Regarding the effect of additives, the ER response is enhanced by water until a certain maximum amount, beyond which the effect decreases. The increase in water concentration also leads to higher values of the electric current. Similar results are observed when Brij 30 is used. However, this surfactant only raises the yield stress at low fields. Contrary to water, the surfactant forms droplets in solution, instead of adsorbing on the hematite surface. At sufficiently high field strengths, the droplets can coalesce, enclosing the hematite particles and thus reducing the overall ER effect.     

Insights into the Catalytic Activity of Nitridated Fibrous Silica (KCC‐1) Nanocatalysts from 15N and 29Si NMR Spectroscopy Enhanced by Dynamic Nuclear Polarization

Fibrous nanosilica (KCC‐1) oxynitrides are promising solid‐base catalysts. Paradoxically, when their nitrogen content increases, their catalytic activity decreases. This counterintuitive observation is explained here for the first time using ¹⁵N‐solid‐state NMR spectroscopy enhanced by dynamic nuclear polarization.     

Adsorption of the anionic surfactant sodium dodecyl sulfate on a C18 column under micellar and high submicellar conditions in reversed‐phase liquid chromatography

Micellar liquid chromatography makes use of aqueous solutions or aqueous‐organic solutions containing a surfactant, at a concentration above its critical micelle concentration. In the mobile phase, the surfactant monomers aggregate to form micelles, whereas on the surface of the nonpolar alkyl‐bonded stationary phases they are significantly adsorbed. If the mobile phase contains a high concentration of organic solvent, micelles break down, and the amount of surfactant adsorbed on the stationary phase is reduced, giving rise to another chromatographic mode named high submicellar liquid chromatography. The presence of a thinner coating of surfactant enhances the selectivity and peak shape, especially for basic compounds. However, the risk of full desorption of surfactant is the main limitation in the high submicellar mode. This study examines the adsorption of the anionic surfactant sodium dodecyl sulfate under micellar and high submicellar conditions on a C₁₈ column, applying two methods. One of them uses a refractive index detector to obtain direct measurements of the adsorbed amount of sodium dodecyl sulfate, whereas the second method is based on the retention and peak shape for a set of cationic basic compounds that indirectly reveal the presence of adsorbed monomers of surfactant on the stationary phase.