Au-Cu/SBA(Ti) based catalysts for photocatalytic applications

Comunicación a congresoIn this work, it has been synthesized several Au and Au-Cu alloy photocatalysts supported on two different mesoporous supports: a non-commercial SBA-15 and a post-synthesis TiO2 modified SBA-15 (TiSBA-15), with which a high dispersion of TiO2 species have been achieved maintaining the SBA-15 structure. In addition, it has also been obtained highly dispersed Au nanoparticles confined in SBA-15 pore channels, as can be observed in Figure 1. The photocatalysts have been preliminary tested in the preferential CO oxidation in a H2-rich stream (CO-PROX) at room temperature and atmospheric pressure under simulated solar light irradiation. In spite of the very low gold and copper loading (1.5 wt% and 0.5wt% respectively), the catalysts resulted active and selective in the low temperature photo-CO-PROX.Universidad de Málaga, Campus de Excelencia Internacional Andalucía Tec

Role of Mo in catalysts based on noble metals in hydrodeoxygenation reactions

The use of bio-energy as a renewable alternative to fossil fuels is nowadays attracting more and more attention. The bio-fuel from biomass seems to be a potential energy substitute for fossil fuels since it is a renewable resource that could contribute to sustainable development and global environmental preservation and it appears to have significant economic potential1. The problem is its high oxygen content, which gives undesirable properties for combustion. To remove oxygen, catalytic hydrodeoxygenation (HDO) reactions are carried out. Monometallic Mo/Si, Pt/Si as well as bimetallic PtMo/Si catalysts were prepared and evaluated in the hydrodeoxygenation (HDO)reaction of dibenzofurane (DBF) as a model molecule in biomass derived bio-oil.Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech

Sustainable organic dyes from winemaking lees for photoelectrochemical dye-sensitized solar cells

During the last two decades, Dye Sensitized Solar Cells (DSSCs) have received a great deal of attention as a promising, low-cost alternative to conventional silicon photovoltaic devices. Natural dye molecules can be used as a sensitizer for their low cost, good light absorbance, easy preparation process, and biodegradability. In this study, dyes were obtained from wine lees, the last by-product of winemaking process, supplied by a venetian winery (Italy). Polyphenols, like tannins and anthocyanins, which were extracted from winemaking lees, were adsorbed on a nanostructured ordered mesoporous titanium dioxide, previously treated at different temperatures (400-600 ffiC). Both dyes and titania semiconductor samples were studied with different techniques. The tests were carried out on prototypes to evaluate the cell power and the photocurrent generated under simulated solar light irradiation. The obtained solar energy conversion efficiencies are comparable to those that were reported in literature by using organic dyes extracted from vegetables, fruits, and plants. It is significant that these dyes are largely available and cost effective, since recovered from a waste otherwise to be disposed of, opening up a perspective of feasibility for inexpensive and environmentally friendly dye solar cells to generate green electricity and transforming agri-food waste into a resource

Nanoestructuras de ceria-titania para fotodegradar azul de metileno con luz solar simulada

En los últimos años la protección ambiental y el uso de fuentes de energía renovables son dos objetivos principales en la investigación química. La energía solar se puede aprovechar para la degradación fotocatalítica de moléculas orgánicas contaminantes, hormonas o medicamentos, tanto en el aire, en el agua, como en las superficies, porque la luz solar es capaz de descomponerlas [1]. A pesar de la gran cantidad de aplicaciones fotocatalíticas de la titania (TiO2), fotocatalizador no tóxico, de bajo costo y muy prometedor [2], hay algunos factores críticos que limitan su fotoactividad. El principal es el valor de su salto de energía, que limita su uso como fotocatalizador en la región UV del espectro. Con el objetivo principal de extender su uso a la región visible del espectro, en literatura se ha propuesto el depósito de metales nobles en su superficie, modificaciones superficiales, así como el dopaje con iones de metales de transición o elementos de tierras raras. En este sentido, el uso de ceria (CeO2) ha atraído una gran atención debido a propiedades como su biocompatibilidad, inercia química así como su actividad en reacciones de oxidación, relacionada con la formación vacantes de oxígeno en su superficie [3]. Se ha comprobado que el sistema oxídico mixto CeO2-TiO2 es más fotoactivo que la titania pura debido a la disminución del salto de energía y a la mejora en la movilidad de los excitones. Este trabajo tiene como objetivo desarrollar fotocatalizadores basados en nanoestructuras de titania que sean activas en el visible, dopando la matriz de titania con cerio. Principalmente se pretende evaluar tanto el papel del cerio como la morfología del nanomaterial en la respuesta fotocatalítica bajo luz UV y solar.Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech

NiO diluted in high surface area TiO2 as efficient catalysts for the oxidative dehydrogenation of ethane

[EN] Catalysts consisting of NiO diluted in high surface area TiO2 can be as efficient in the oxidative dehydrogenation of ethane as the most selective NiO-promoted catalysts reported previously in the literature. By selecting the titania matrix and the NiO loading, yields to ethylene over 40% have been obtained. In the present article, three different titanium oxides (TiO2) have been employed as supports or diluters of nickel oxide and have been tested in the oxidative dehydrogenation of ethane to ethylene. All TiO2 used present anatase as the main crystalline phase and different surface areas of 11,55 and 85 m(2) g(-1). It has been observed that by selecting an appropriate nickel loading and the titanium oxide extremely high selectivity towards ethylene can be obtained. Thus, nickel oxide supported on TiO2 with high surface areas (i.e. 55 and 85 m(2) g(-1)) have resulted to give the best catalytic performance although the optimal nickel loading is different for each case. The optimal catalyst has been obtained for NiO-loadings up to 5-10 theoretical monolayers regardless of the TiO2 employed. Free TiO2 is inactive whereas unsupported NiO is active and unselective (forming mainly carbon dioxide) and, therefore, unmodified NiO particles have to be avoided in order to obtain the optimal catalytic performance. The use of low surface area titania (11 m(2) g(-1)) have led to the lowest selectivity to olefin due to the presence of an excess of free NiO particles. (C) 2017 Elsevier B.V. All rights reserved.The authors would like to acknowledge the DGICYT in Spain CTQ2012-37925-C03-2, CTQ2015-68951-C3-1-R, CTQ2015-68951-C3-3-R and SEV-2012-0267 Projects for financial support. D.D. also thanks Severo Ochoa Excellence fellowship (SVP-2014-068669). We also thank the University of Valencia (UV-INV-AE-16-484416 project) and SCSIE-UV for assistanceSanchis, R.; Delgado-Muñoz, D.; Agouram, S.; Soriano Rodríguez, MD.; Vázquez, MI.; Rodriguez-Castellon, E.; Solsona, B.... (2017). NiO diluted in high surface area TiO2 as efficient catalysts for the oxidative dehydrogenation of ethane. Applied Catalysis A General. 536:18-26. https://doi.org/10.1016/j.apcata.2017.02.012S182653

Porous clays heterostructures as supports of iron oxide for environmental catalysis

[EN] Porous Clays Heterostructures (PCH) from natural pillared clays (bentonite with a high proportion of montmorillonite) have been used as supports of iron oxide for two reactions of environmental interest: i) the elimination of toluene (a representative compound of one of the most toxic subsets of volatile organic compounds, aromatics) by total oxidation and ii) the selective oxidation of H2S to elemental sulfur. For both reactions these catalysts have resulted to be remarkably more efficient than similar catalysts prepared using conventional silica as a support. Thus, in the total oxidation of toluene it has been observed that the catalytic activity obtained using siliceous PCH is two orders of magnitude higher than that with conventional silica. The catalytic activity has shown to be dependant of the capacity of the support for dispersing iron oxide in a way that the higher the dispersion of iron oxide on the surface of the support, the higher is the activity. In the case of the selective oxidation of H2S to S both higher catalytic activity and higher selectivity to S have been observed using siliceous porous clays heterostructures than using conventional silica. Highly dispersed FeOx species have been shown as highly selective towards elemental sulfur whereas more aggregated FeOx species favour the formation of sulphur oxides decreasing the selectivity to S. Analyses of the surface by XPS have shown the predominance of sulfate species in the catalysts presenting low selectivity to elemental sulfur.The authors would like to acknowledge the DGICYT in Spain (CTQ2015-68951-C3-1-R, CTQ2015-68951-C3-3-R, CTQ2012-37925-C03-2, CTQ2012-37925-C03-3 and CTQ2012-37984-C02-01) and FEDER for financial support. We also thank the University of Valencia for funding (UV-INV-AE-16-484416) and SCSIE-UV for assistance.Sanchis Martinez, R.; Cecilia, J.; Soriano Rodríguez, MD.; Vazquez, I.; Dejoz, A.; López Nieto, JM.; Rodriguez-Castellon, E.... (2008). Porous clays heterostructures as supports of iron oxide for environmental catalysis. Chemical Engineering Journal. 334:1159-1168. https://doi.org/10.1016/j.cej.2017.11.060S1159116833

M/TiO2 (M = Fe, Co, Ni, Cu, Zn) catalysts for photocatalytic hydrogen production under UV and visible light irradiation

In order to improve the photocatalytic response of TiO2 to UV and visible light for hydrogen photoproduction, low cost M/TiO2 semiconductor catalysts were prepared by the impregnation method of five different first row transition metals (M = Fe, Co, Ni, Cu or Zn) on a commercial titania support. The maximum hydrogen production efficiency was achieved for the Cu/TiO2 photocatalyst, with ∼5000 and ∼220 μmol h−1 g−1 H2 production rates for UV and visible irradiation, respectively. Ni/TiO2 and Co/TiO2 also showed a significant photocatalytic activity when UV light was used. The best performing catalyst, Cu/TiO2, was characterized by TEM and XPS measurements. The data showed that Cu was highly dispersed over the TiO2 support and the copper species existed as both reduced Cu0/Cu+ and oxidized Cu2+ on TiO2. Besides, during the hydrogen production reaction, the reduced Cu was partially oxidized to Cu2+ by the transfer of photogenerated holes under UV or visible light irradiation. With UV and visible lamps, the H2 production rates were higher than those obtained with non-impregnated TiO2 by factors of 16 and 3, respectively. These results demonstrated that a Cu/TiO2 photocatalyst could be considered a promising low-cost alternative to the well-known Pt/TiO2 system for hydrogen production, making the Cu-based catalyst an ideal cost-effective candidate for this reactionThe authors would like to thank Ministerio de Economía y Competitividad of Spain (CTQ2015-68951-C3-3-R and MAT2016-80933-R), Ministerio de Ciencia, Innovación y Universidades of Spain (Project RTI2018-099668-B-C22) and FEDER fund

Comparative study of CuO supported on CeO2, Ce0.8Zr0.2O2 and Ce0.8Al0.2O2 based catalysts in the CO-PROX reaction

CuO supported on CeO2, Ce0.8Zr0.2O2 and Ce0.8Al0.2O2 based catalysts (6%wt Cu) were synthesized and tested in the preferential oxidation of CO in a H2-rich stream (CO-PROX). Nanocrystalline supports, CeO2 and solid solutions of modified CeO2 with zirconium and aluminum were prepared by a freeze-drying method. CuO was supported by incipient wetness impregnation and calcination at 400 C. All catalysts exhibit high activity in the CO-PROX reaction and selectivity to CO2 at low reaction temperature, being the catalyst supported on CeO2 the more active and stable. The influence of the presence of CO2 and H2O was also studied

Effectiveness of rotavirus vaccination in Spain

With the aim of determining rotavirus vaccine effectiveness (RVVE) in Spain, from Oct-2008/Jun-2009, 467 consecutive children below 2 years old with acute gastroenteritis (AGE) were recruited using a pediatric research network (ReGALIP-www.regalip.org) that includes primary, emergency and hospital care settings. Of 467 enrolled children, 32.3% were rotavirus positive and 35.0% had received at least one dose of any rotavirus vaccine. RRVE to prevent any episode of rotavirus AGE was 91.5% (95% CI: 83.7%-95.6%). RVVE to prevent hospitalization by rotavirus AGE was 95.6% (85.6-98.6%). No differences in RVVE were found regarding the vaccine used. Rotavirus vaccines have showed an outstanding effectiveness in Spain

The DECam Local Volume Exploration Survey Data Release 2

We present the second public data release (DR2) from the DECam Local Volume Exploration survey (DELVE). DELVE DR2 combines new DECam observations with archival DECam data from the Dark Energy Survey, the DECam Legacy Survey, and other DECam community programs. DELVE DR2 consists of similar to 160,000 exposures that cover >21,000 deg(2) of the high-Galactic-latitude ( divide b divide > 10 degrees) sky in four broadband optical/near-infrared filters (g, r, i, z). DELVE DR2 provides point-source and automatic aperture photometry for similar to 2.5 billion astronomical sources with a median 5 sigma point-source depth of g = 24.3, r = 23.9, i = 23.5, and z = 22.8 mag. A region of similar to 17,000 deg(2) has been imaged in all four filters, providing four-band photometric measurements for similar to 618 million astronomical sources. DELVE DR2 covers more than 4 times the area of the previous DELVE data release and contains roughly 5 times as many astronomical objects. DELVE DR2 is publicly available via the NOIRLab Astro Data Lab science platform