Vanadium oxide supported on porous clay heterostructure for the partial oxidation of hydrogen sulphide to sulfur

Vanadium oxide supported on porous clay heterostructures (PCH) catalysts have been synthesized, characterized and evaluated in the selective oxidation of H2S to elemental sulfur. The catalysts were characterized by XRD, adsorption-desorption of N-2 at -196 degrees C, diffuse reflectance UV-vis, H-2-TPR, Raman spectroscopy and XPS. The catalysts with higher vanadium content are more active and selective, exhibiting a H2S conversion close to 70% after 360h on stream with a high selectivity toward elemental sulfur and a low formation of undesired SO2. The catalysts with V2O5 crystallites have shown a higher activity and resistance to the deactivation. The analysis of the spent catalyst has revealed the formation of V4O9 crystals during the catalytic test, which has been reported as the active phase in the selective oxidation of the H2S. (C) 2015 Elsevier B.V. All rights reserved.The authors would like to thank the DGICYT in Spain (Projects CTQ2012-37925-C03-01, CTQ2012-37925-C03-03 and FEDER funds, and MAT2010-19837-C06-05) and project of Excellence of Junta de Andalucia (project P12-RNM-1565) for financial support. A. Natoli thanks to SECAT (Spain) for a grant.Soriano Rodríguez, MD.; Cecilia, JA.; Natoli, A.; Jimenez-Jimenez, J.; López Nieto, JM.; Rodriguez Castellon, E. (2015). Vanadium oxide supported on porous clay heterostructure for the partial oxidation of hydrogen sulphide to sulfur. Catalysis Today. 254:36-42. https://doi.org/10.1016/j.cattod.2014.12.022S364225

Fe2O3 supported on hollow micro/mesospheres silica for the catalytic partial oxidation of H2S to sulfur

[EN] A family of Fe-based catalysts supported hollow silica mesospheres has been synthesized and tested in the catalytic partial oxidation of H2S to elemental sulfur at 170.180 degrees C, atmospheric pressure and under 300 min of time-on-stream. The characterization of the synthesized catalysts by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance UV-vis spectra (DRS), H-2-termoprogrammed reduction (H-2-TPR), N-2 adsorption-desorption at -196 degrees C and X-ray photoelectron spectroscopy (XPS) reveals the formation of a catalytic system with high micro- and mesoporosity with high dispersion of the Fe2O3 species. The catalytic results reported high activity in the selective oxidation of H2S, reaching a highest conversion value close to 94% with a selectivity towards elemental sulfur of 98% after 300 min of time on stream (TOS) at 180 degrees C for the HMS-10Fe catalyst. The comparison of Fe-containing HMS (10 wt% of iron loading) with other SiO2-based supports, as a fumed silica (Cab-osil) or a mesoporous silica (SBA-15), presents different H2S conversion values, following the next trend: HMS-10Fe > SBA-10Fe > Cab-10Fe. These results suggest that the use of a support with a narrow pore tend to facilitate the iron dispersion favoring higher conversion rates.The authors wish to acknowledge the financial support provided by the Ministry of Economy and Competitiveness (Spain) (MINECO) CTQ2015-68951-C1-3R y CTQ2015-68951-C3-3R, Junta de Andalucia (Spain) P12-RNM 1565 and FEDER funds. In addition, the authors also thank Fundacao Cearense de Apoio ao Desenvolvimento Cientifico e Tecnologico (FUNCAP) by the Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES) - Processo: PDSE 99999.002602/2014-08.Cecilia, J.; Soriano Rodríguez, MD.; Marques Correia, L.; Rodríguez-Castellón, E.; López Nieto, JM.; Silveira Vieira, R. (2020). Fe2O3 supported on hollow micro/mesospheres silica for the catalytic partial oxidation of H2S to sulfur. Microporous and Mesoporous Materials. 294:1-10. https://doi.org/10.1016/j.micromeso.2019.109875S11029

L'insigne et la médaille de blessés de guerre

[Article sur un lot de médailles des blessés depuis sa création - octobre-novembre-décembre 2003

Core–shell structured Li0.33La0.56TiO3 perovskite as a highly efficient and sulfur-tolerant anode for solid-oxide fuel cells

Solid oxide fuel cells (SOFCs), which directly convert chemical energy into electricity, have several advantages, such as fuel flexibility and low emissions. Unfortunately, the performance and stability of SOFCs with state-of-the-art Ni-based anodes are sensitive to impurities, such as sulfur, which is a common component of practical fuels, including natural gas and renewable biogas. The development of sulfur-tolerant anode materials is important for successfully operating SOFCs with sulfur-containing practical fuels. In this study, a core–shell architecture was fabricated from solution infiltration and was evaluated as a sulfur-tolerant anode for SOFCs. For the first time, we used a lithium conductive material, Li0.33La0.56TiO3 (LLTO, perovskite oxide), as the shell for anodic reactions. The resulting cell delivered higher electrochemical activities than similar cells, with widely used sulfur-tolerant perovskite anodes. In addition, the cell with the core–shell structured anode demonstrated favorable stability over 70 hours' operation when using 1000 ppm H2S–H2 fuel at 800 °C. In contrast, the cell with an anode composed of nanoparticles failed after only 5.5 hours under the same operation conditions. This study offers a new strategy for developing highly sulfur tolerant and efficient anodes for SOFCs