Activated Carbon Fibre Monoliths for Hydrogen Storage

Porous adsorbents are currently investigated for hydrogen storage application. From a practical point of view, in addition to high porosity developments, high material densities are required, in order to confine as much material as possible in a tank device. In this study, we use different measured sample densities (tap, packing, compacted and monolith) for analyzing the hydrogen adsorption behavior of activated carbon fibres (ACFs) and activated carbon nanofibres (ACNFs) which were prepared by KOH and CO2 activations, respectively. Hydrogen adsorption isotherms are measured for all of the adsorbents at room temperature and under high pressures (up to 20 MPa). The obtained results confirm that (i) gravimetric H2 adsorption is directly related to the porosity of the adsorbent, (ii) volumetric H2 adsorption depends on the adsorbent porosity and importantly also on the material density, (iii) the density of the adsorbent can be improved by packing the original adsorbents under mechanical pressure or synthesizing monoliths from them, (iv) both ways (packing under pressure or preparing monoliths) considerably improve the storage capacity of the starting adsorbents, and (v) the preparation of monoliths, in addition to avoid engineering constrains of packing under mechanical pressure, has the advantage of providing high mechanical resistance and easy handling of the adsorbent.

Methane dry reforming over Ni supported on pine sawdust activated carbon: Effects of support surface properties and metal loading

The influence of metal loading and support surface functional groups (SFG) on methane dry reforming (MDR) over Ni catalysts supported on pine-sawdust derived activated carbon were studied. Using pine sawdust as the catalyst support precursor, the smallest variety and lowest concentration of SFG led to best Ni dispersion and highest catalytic activity, which increased with Ni loading up to 3 Ni atoms nm-2. At higher Ni loading, the formation of large metal aggregates was observed, consistent with a lower "apparen" surface area and a decrease in catalytic activity. The H2/CO ratio rose with increasing reaction temperature, indicating that increasingly important side reactions were taking place in addition to MDR.

Palladium and Bimetallic Palladium–Nickel Nanoparticles Supported on Multiwalled Carbon Nanotubes: Application to Carbon–Carbon Bond-Forming Reactions in Water

Palladium and bimetallic Pd–Ni nanoparticles (NPs) protected by polyvinylpyrrolidone were prepared by the reduction-by-solvent method and deposited on multiwalled carbon nanotubes (MWCNTs). The catalytic activity of these NPs to carbon–carbon bond-forming reactions was studied by using 0.1 mol % Pd loading, at 120 °C for 1 h and water as a solvent under ligand-free conditions. The Suzuki–Miyaura reaction took place quantitatively for the cross-coupling of 4-bromoanisole with phenylboronic acid, better than those obtained with potassium phenyltrifluoroborate, with Pd50Ni50/MWCNTs as a catalyst and K2CO3 as a base and TBAB as an additive, with good recyclability during 4 cycles with some Ni leaching. The Hiyama reaction of 4-iodoanisole with trimethoxyphenylsilane, under fluoride-free conditions using 50 % aqueous NaOH solution, was performed with Pd/MWCNTs as a catalyst in 83 % yield with low recyclability. For the Mizoroki-Heck reaction 4-iodoanisole and styrene gave the corresponding 4-methoxystilbene quantitatively with Pd50Ni50/MWCNTs using K2CO3 as a base and TBAB as an additive although the recycle failed. In the case of the Sonogashira-Hagihara reaction, Pd/MWCNTs had to be used as a catalyst and pyrrolidine as a base for the coupling of 4-iodoanisole with phenylacetylene under copper-free conditions. The corresponding 4-methoxytolane was quantitatively obtained allowing the recycling of the catalyst during 3 cycles.

Electrochemical behaviour of activated carbons obtained via hydrothermal carbonization

Activated carbons were prepared by chemical activation of hydrochars, obtained by hydrothermal carbonisation (HTC) using low cost and abundant precursors such as rye straw and cellulose, with KOH. Hydrochars derived from rye straw were chemically activated using different KOH/precursor ratios, in order to assess the effect of this parameter on their electrochemical behaviour. In the case of cellulose, the influence of the hydrothermal carbonisation temperature was studied by fixing the activating agent/cellulose ratio. Furthermore, N-doped activated carbons were synthesised by KOH activation of hydrochars prepared by HTC from a mixture of glucose with melamine or glucosamine. In this way, N-doped activated carbons were prepared in order to evaluate the influence of nitrogen groups on their electrochemical behaviour in acidic medium. The results showed that parameters such as chemical activation or carbonisation temperature clearly affect the capacitance, since these parameters play a key role in the textural properties of activated carbons. Finally, symmetric capacitors based on activated carbon and N-doped activated carbon were tested at 1.3 V in a two-electrode cell configuration and the results revealed that N-groups improved the capacitance at high current density.

Un nuevo enfoque didáctico para la enseñanza de la Nanotecnología en titulaciones superiores y Máster Universitarios de Ciencias: MOOC en Nanotecnología

Habida cuenta del interés del alumnado de Ciencias, tanto a nivel bachillerato como universitario, por la Nanotecnología y tras la organización de dos cursos sobre la misma en la UVRA, el Laboratorio de Nanotecnología Molecular de la UA se embarcó en el proyecto de diseño y construcción del primer MOOC (del inglés Massive On-line Open Course) sobre Nanotecnología en España, contando con el asesoramiento de UniMOOC. El objetivo del curso es obtener una mejor comprensión de la nanotecnología y su conexión con la vida real; un nuevo enfoque didáctico para la enseñanza de la Nanotecnología en titulaciones superiores y Máster Universitarios. El sitio web es la principal guía a través de los recursos y actividades del curso, donde el estudiante dispone de una serie de herramientas gratuitas que descubrirá en las diferentes unidades, como vídeos, tutoriales, applets, etc. En este contexto, hemos creado una Red de investigación en docencia universitaria en colaboración con el Dpto. Lenguajes y Sistemas de la UA y UniMOOC, cuyo objetivo es la actualización de contenidos, actividades y recursos del mismo, su puesta en marcha y difusión, así como el análisis de su posible implantación en titulaciones afines.

Promoter effect of sodium in graphene-supported Ni and Ni–CeO2 catalyst for the low-temperature WGS reaction

The low temperature water–gas shift (WGS) reaction has been studied over Ni–CeO2/Graphene and Ni/Graphene. The catalysts were prepared with 5 wt.% Ni and 20 wt.% CeO2 loadings, by deposition-precipitation employing sodium hydroxide and urea as precipitating agents. The materials were characterized by TEM, powder X-ray diffraction, Raman spectroscopy, H2-temperature-programmed reduction and X-ray photoelectron spectroscopy (XPS). The characterization and the reaction results indicated that the interaction between the active species and the support is higher than with activated carbon, and this hinders the reducibility of ceria and thus the catalytic performance. On the other hand, the presence of residual sodium in samples prepared by precipitation with NaOH facilitated the reduction of ceria. The catalytic activity was highly improved in the presence of sodium, what can be explained on the basis of an associative reaction mechanism which is favored over Ni-O-Na entities.

Evaluación de metodologías didácticas en trabajos de fin de grado en titulaciones de Ciencias Experimentales

Mediante encuestas a estudiantes que se encuentran finalizando el Trabajo de Fin de Grado (TFG) y profesores que dirigen de los seis grados de la facultad de Ciencias (Biología, Ciencias del Mar, Geología, Matemáticas, Óptica y Optometría, Química) de la Universidad de Alicante, se han identificado los puntos de menor fortaleza de los TFGs independientemente para cada grado. A continuación, hemos comparado los resultados entre grados para ver el nivel de similitud entre ellos y la singularidad de cada uno de ellos. A partir de ahí, hemos identificado los posibles factores que configuran cada TFG con el fin de intentar entender su singularidad en cada caso. Esta información es importante para ayudarnos a comprender cómo se podrían fortalecer posibles carencias en TFGs específicos. Con esta información y en base a la experiencia previa, proponemos medidas que permitan favorecer la implementación y desarrollo de los TFGs. Con estas propuestas se espera mejorar la eficiencia de los TFGs y conseguir un mayor nivel de satisfacción y el rendimiento en esta asignatura común en todos los grados.

Análisis de los Trabajos de Fin de Grado desde la visión docente

El Trabajo Fin de Grado (TFG) en los grados de la Facultad de Ciencias, constituye una asignatura con importantes competencias transversales que representa la fase final del plan de estudios, y supone la realización por parte del estudiante de un proyecto, memoria o estudio bajo la supervisión de un tutor o tutora. En este trabajo se realiza un estudio general de los TFGs y la utilización del UA-project, desde la visión del profesorado. Para poder optimizar el desarrollo de los TFGs, en este trabajo se realizó un análisis interno mediante un cuestionario. Para dar mayor amplitud y proyección a la propuesta se han enviado los cuestionarios a profesores de todos los grados de la Facultad de Ciencias: Biología, Ciencias del Mar, Química, Geología, Matemáticas y Óptica y Optometría. Estos cuestionarios reflejan la experiencia docente obtenida en los últimos años en la tutorización de los TFGs, para así poder obtener conclusiones e ideas de mejora para su posterior aplicación.

Adaptación de los TFGs de Ciencias al Espacio Europeo de Educación Superior: valoración del alumnado

Este estudio tiene el objetivo de obtener una percepción desde el punto de vista del alumnado del Trabajo de Fin de Grado (TFG). Para ello, se realizaron encuestas a estudiantes de grado que están finalizando el (TFG) en la facultad de Ciencias (Biología, Ciencias del Mar, Geología, Matemáticas, Óptica y Optometría, y Química) de la Universidad de Alicante. En un principio, se analizaron para cada grado de forma independiente con el propósito de tener una visión global de la percepción de los alumnos para cada grado. A continuación, se contrastaron los resultados obtenidos entre los grados para buscar posibles similitudes entre ellos y entender las singularidades de cada uno. Mediante este estudio podemos conocer la opinión sobre TFG desde el punto de vista del alumnado. Dichos resultados pueden sentar las bases para enriquecer y optimizar el desarrollo de los TFGs con el fin de favorecer su capacidad formativa al ser una asignatura obligatoria común en todos los grados.

Enhanced electro-oxidation resistance of carbon electrodes induced by phosphorus surface groups

The electro-oxidation of carbon materials enormously degrades their performance and limits their wider utilization in multiple electrochemical applications. In this work, the positive influence of phosphorus functionalities on the overall electrochemical stability of carbon materials has been demonstrated under different conditions. We show that the extent and selectivity of electroxidation in P-containing carbons are completely different to those observed in conventional carbons without P. The electro-oxidation of P-containing carbons involves the active participation of phosphorus surface groups, which are gradually transformed at high potentials from less-to more-oxidized species to slow down the introduction of oxygen groups on the carbon surface (oxidation) and the subsequent generation of (C*OOH)-like unstable promoters of electro-gasification. The highest-oxidized P groups (–C–O–P-like species) seem to distribute the gained oxygen to neighboring carbon sites, which finally suffer oxidation and/or gasification. So it is thought that P-groups could act as mediators of carbon oxidation although including various steps and intermediates compared to electroxidation in P-free materials.

Functionalization of carbon nanotubes using aminobenzene acids and electrochemical methods. Electroactivity for the oxygen reduction reaction

Functionalized carbon nanotubes (CNTs) using three aminobenzene acids with different functional groups (carboxylic, sulphonic, phosphonic) in para position have been synthesized through potentiodynamic treatment in acid media under oxidative conditions. A noticeable increase in the capacitance for the functionalized carbon nanotubes mainly due to redox processes points out the formation of an electroactive polymer thin film on the CNTs surface along with covalently bonded functionalities. The CNTs functionalized using aminobenzoic acid rendered the highest capacitance values and surface nitrogen content, while the presence of sulfur and/or phosphorus groups in the aminobenzene structure yielded a lower functionalization degree. The oxygen reduction reaction (ORR) activity of the functionalized samples was similar to that of the parent CNTs, independently of the functional group present in the aminobenzene acid. Interestingly, a heat treatment in N2 atmosphere with a very low O2 concentration (3125 ppm) at 800 °C of the CNTs functionalized with aminobenzoic acid produced a material with high amounts of surface oxygen and nitrogen groups (12 and 4% at., respectively), that seem to modulate the electron-donor properties of the resulting material. The onset potential and limiting current for ORR was enhanced for this material. These are promising results that validates the use of electrochemistry for the synthesis of novel N-doped electrocatalysts for ORR in combination with adequate heat treatments.

Switchable surfactant-assisted carbon nanotube coatings: innovation through pH shift

The inner surface of fused-silica capillaries has been coated with a dense/homogeneous coating of commercial multi-wall carbon nanotubes (MWCNTs) using a stable ink as deposit precursor. Solubilization of the MWCNTs was achieved in water/ethanol/dimethylformamide by the action of a surfactant, which can switch between a neutral or an ionic form depending on the pH of the medium, which thus becomes the driving force for the entire deposition process. Careful control of the experimental conditions has allowed us to selectively deposit CNTs on the inner surface of insulating silica capillaries by a simple, reproducible, and easily adaptable method.

Análisis de la acción tutorial en ingeniería y arquitectura. Gestión eficaz del tiempo

En este trabajo expondremos un análisis exhaustivo de como se ha desarrollado la acción tutorial en la Escuela Politécnica Superior de la Universidad de Alicante en el curso 2014/2015. El marcado carácter de voluntariedad de la acción tutorial en nuestro centro por parte de estudiantes y tutores permite que el trabajo se realice más satisfactoriamente tanto por parte de tutores como por parte de los estudiantes, puesto que han decidido seguir el plan por ello mismos y no como una imposición. Además expondremos nuestras experiencias en el desarrollo del Taller de Gestión Eficaz del Tiempo, taller desarrollado en nuestro centro bajo la tutela de la experta Nuria Alberquilla, que tiene entre otros muchos objetivos el aprendizaje y puesta en práctica de técnicas para realizar una gestión eficaz del tiempo, con un mejor equilibrio entre la vida académica y personal y la identificación de los principales factores externos e internos que influyen en los resultados obtenidos, y cómo mejorarlos.

Study on Electrochemical Capacitance using Templated Carbons

The template carbonization technique enables the production of porous carbons and carbon-based composites with precisely designed, controlled pore structures. The resulting templated carbons are therefore useful to investigate and understand the relation between carbon nanostructure and electrocapacitive properties. In this short review paper, we introduce our works on electrochemical capacitance using zeolite-templated carbons and carbon-coated anodic aluminum oxide.

Design of hybrid asymmetric capacitors in aqueous electrolyte using ZTC and ultraporous activated carbons

The use of two different materials as electrodes allows the construction of asymmetric and hybrid capacitors cells with enhanced energy and power density. This approach is especially well-suited for overcoming the limitations of pseudocapacitive materials that provide a huge capacitance boost, but in a limited potential window. In this work, we introduce the concepts and protocols that are required for a successful design of such systems, which is illustrated by the construction of an asymmetric hybrid cell where a zeolite-templated carbon and an ultraporous activated carbon have been combined.