Biomedical subjects

Pedro Bosch

Publications and source records attributed to Pedro Bosch.

6 recordsLinked to original sources

PubMed2006

II. Cesium leaching in CsA and CsX zeolites: use of blocking agents to inhibit the cesium cation mobility.

Cesium-exchanged A and X zeolites were loaded with cesium acetate species and thermally treated in order to inhibit the mobility of exchangeable cesium cations. The proposed procedure seems to block the cavities channels avoiding the releasing of cesium cations under the leaching conditions. The cesium impregnated species did not induce strong structural modifications if they are used in small amounts (0.2 meq/g zeolite), but they promote transformation toward cesium orthosilicate if they are loaded in amounts as high as 2 meq/g zeolite. This orthosilicate retains safely the cesium as it is a component of the lattice.

Journal Article↗

PubMed2006

Immobilization of cobalt in collapsed non-irradiated and gamma-irradiated X zeolites.

Cobalt exchanged X zeolites were gamma irradiated and heated until the zeolite structure collapsed. Heating destroys the zeolite network as found by X-ray-diffraction and 29Si, 27Al MAS NMR spectroscopy. Gamma irradiation treatment diminished the collapsing temperature of zeolite. Cobalt leaching from crystalline and amorphized zeolites was verified by ion exchange with NaCl solution. Results show that cobalt is not released from the amorphous materials. Furthermore adsorption of xenon and 129Xe NMR spectroscopy reveal that cobalt ions are heterogeneously distributed in the non irradiated amorphous materials. Gamma irradiation causes the mobility of cobalt in the amorphous materials resulting then in a more homogeneous distribution. Cobalt is, thus, retained safely in the amorphous materials.

Journal Article↗

PubMed2005

Structural evolution of phosphated alumina during sol-gel synthesis.

Phosphated alumina gels were prepared by the sol-gel method. Gels were aged from 1 to 8 days in air. Gel structure evolution, as time went on, was followed by 27Al magic angle spinning nuclear magnetic resonance, X-ray diffraction, and small-angle X-ray scattering. It is concluded that the aging time is a crucial parameter in the formation of coordinately unsaturated sites of aluminum (AlIV and AlV). The gel network is shown to have a fractal structure.

Journal Article↗

PubMed2005

Passivation of the calcite surface with phenylmalonate and benzylmalonate ions.

We explored the affinity of calcite to adsorbed organic molecules as an approach to the conservation of cultural heritage built of marble and limestone. The utilization of phenylmalonic and benzylmalonic acids provided a hydrophobic adsorptive interface, adequate to prevent processes of aqueous weathering. Samples of marble powder (polycrystalline calcite) were impregnated with solutions of phenylmalonic and benzylmalonic acid at three concentrations (5 x 10(-2), 5 x 10(-3), and 5 x 10(-4) M) and different pH values (6.00, 7.00, and 8.00). The surface charge of the calcite suspensions was determined by potentiometric measurements under equilibrium conditions at room temperature in aqueous solution of the dicarboxylic acids, in order to understand the influence of the electrokinetic potential in the surface association. The adsorbed amounts were determined by calculation of the thermodynamic equilibria of solutions. The presence of the organic interface on the mineral surface was corroborated by Raman spectroscopy and small-angle X-ray scattering (SAXS). The results indicate effective adsorption of both dicarboxylic acids as a function of the concentration and pH, and several other conditions that favors coulombic interaction, an absence of electrophoretic mobility or surface electroneutrality related to the solid surface potentials. The coverage of pores by dicarboxylic adsorbate modified the geometrical pore shape and the pore size distribution, filling all the pores of larger than 80 A diameter, giving as a result a mesoporous structure. This change in the surface morphology by organic adsorbates constitutes a modification in the diffusional processes of the environment on the mineral surface.

Journal Article↗

PubMed2005

Characterization of enamel with variable caries risk.

Small angle X-ray scattering (SAXS), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR) have been used to look at enamel from nine premolars, three each from individuals in low, medium and high risk caries groups. Only SAXS was able to detect consistent differences between any of the groups. In enamel from the high caries risk group, the micropores between the hydroxyapatite crystals were laminar. In enamel from the low caries risk group, the micropores were cylindrical. Other parameters varied between teeth but were not correlated with caries risk.

Adolescent↗

PubMed2004

Passivation of the calcite surface with malonate ion.

Samples of polycrystalline calcite were impregnated with solutions of malonic acid of three concentrations (5 x 10(-2), 5 x 10(-3) , and 5 x 10(-4) M) and different pH values (6.00, 7.00, and 8.00). The impregnation was carried out at room temperature to evaluate the adsorption of malonate ion in the calcite surface to optimize the conditions for possible application on limestone and marble in cultural heritage materials. The affinity of the malonate ion was determined through the potentiometric measurement of the surface charge and the corresponding adsorbed amounts by titration, Raman spectroscopy, and small-angle X-ray scattering (SAXS). The results indicate effective adsorption of the malonate ion on the surface at a pH value close to the point of zero charge (pHpzc approximately 8.20) and changes in some surface morphological properties such as the pore shape and the pore size distribution. The presence of a malonate adsorptive layer on calcite generates an interface interaction potential that may influence the reaction and transport mechanisms within the medium.

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