Nannoplankton and planktonic foraminifera biostratigraphy of the eastern Betics during the Tortonian (SE Spain)

El final del Serravalliense y principio del Tortoniense es un periodo de fuerte actividad tectónica en la Cordillera Bética. Además, existe un debate sobre la existencia de sedimentos de edad Tortoniense inferior al no existir claras atribuciones fósiles en esa edad. Estos sedimentos se asignan a dicha edad por criterios indirectos, tanto estratigráficos como por la ausencia de contenido fósil más antiguo o más reciente. En este trabajo se describe la sección compuesta de Les Moreres-Albatera, que es probablemente una de las secciones más completas de edad Tortoniense en la bibliografía de la Cordillera Bética, pese a tener un importante hiato de cerca de 1 Millón de años ligado a un evento tectónico intra-Tortoniense. La sección presenta dos unidades litológicas calizas a la base (El Castellà) y al techo (Las Ventanas) y dos unidades intermedias margosas, la inferior, llamada Les Moreres, y la superior, Galería de los Suizos se encuentran separadas por el conglomerado de la Raya del Búho. Se han identificado las biozonas de nanofósiles calcáreos CN5b/NN7 a CN9a/NN11a (Okada & Bukry, 1980; Martini, 1971) y de foraminíferos planctónicos de MMi9 a MMi12a (Lourens et al., 2004). La biostratigrafía de los primeros ha permitido identificar un hiato que incluye la parte alta de las biozonas CN7/NN9 hasta la parte baja de CN9a/NN11a (Okada & Bukry, 1980; Martini, 1971). La integración de los datos biostratigráficos con los paleomagnéticos en la sección Albatera permite la calibración del límite de los magnetocrones C4r.1r/C4n.2n.

Time-Precision Flexible Arithmetic Unit

Paper submitted to the XVIII Conference on Design of Circuits and Integrated Systems (DCIS), Ciudad Real, España, 2003.

Parametrizable Architecture for Function Recursive Evaluation

Paper submitted to the XVIII Conference on Design of Circuits and Integrated Systems (DCIS), Ciudad Real, España, 2003.

Successful functionalization of superporous zeolite templated carbon using aminobenzene acids and electrochemical methods

A novel and selective electrochemical functionalization of a highly reactive superporous zeolite templated carbon (ZTC) with two different aminobenzene acids (2-aminobenzoic and 4-aminobenzoic acid) was achieved. The functionalization was done through potentiodynamic treatment in acid media under oxidative conditions, which were optimized to preserve the unique ZTC structure. Interestingly, it was possible to avoid the electrochemical oxidation of the highly reactive ZTC structure by controlling the potential limit of the potentiodynamic experiment in presence of aminobenzene acids. The electrochemical characterization demonstrated the formation of polymer chains along with covalently bonded functionalities to the ZTC surface. The functionalized ZTCs showed several redox processes, producing a capacitance increase in both basic and acid media. The rate performance showed that the capacitance increase is retained at scan rates as high as 100 mV s−1, indicating that there is a fast charge transfer between the polymer chains formed inside the ZTC porosity or the new surface functionalities and the ZTC itself. The success of the proposed approach was also confirmed by using other characterization techniques, which confirmed the presence of different nitrogen groups in the ZTC surface. This promising method could be used to achieve highly selective functionalization of highly porous carbon materials.

Characterization of a zeolite-templated carbon by electrochemical quartz crystal microbalance and in situ Raman spectroscopy

Electrochemical quartz crystal microbalance was used to monitor the mass changes during the electrochemical characterization of a zeolite-templated carbon (ZTC) in 1 M H2SO4 medium. Under electrochemical oxidation conditions, a high anodic current and a net mass increase were recorded, resulting in the increase of the specific capacitance owing to the contribution of the pseudocapacitance, mainly derived from the hydroquinone–quinone redox couple. Under more severe electrochemical conditions, a net mass loss was observed, revealing that electrochemical gasification took place. Surface chemistry, before and after the electrochemical treatments, was analyzed through temperature programmed desorption experiments. Furthermore, in situ Raman spectroscopy was used to further characterize the structural changes produced in ZTC under the electrochemical conditions applied, supporting that high potential values produce the electrochemical oxidation and degradation of the carbon material.