Scientific Papers in SCI
2019
2019
Fotocatálisis Heterogénea: Aplicaciones
Photodegradation of 2,4-dichlorophenoxyacetic acid over TiO2(B)/anatase nanobelts and Au-TiO2(B)/anatase nanobelts
Chenchana, A.; Nemamcha, A.; Moumeni, H.; Doña Rodríguez, J.M.; Araña, J.; Navío, J.A.; González Díaz, O.; Pulido Melián, E.Applied Surface Science, 467-468 (2019) 1076-1087
In this work, novel TiO2-based nanobelts with various phases were synthesized: biphasic TiO2(B)/anatase, pure TiO2(B) and pure anatase. These catalysts were obtained via hydrothermal reaction using two nanoparticulated TiO2 photocatalysts as precursors: Aeroxide TiO2 P25 (P25) and TiO2 synthesized via a sol-gel process (SG). In addition, the surface of the photocatalysts was modified with gold using a photodeposition method. A characterization study of the different photocatalysts was performed with X-ray diffraction analysis (XRD), UV–Vis diffuse reflectance spectra (DRS), scanning electron microscopy (SEM), X-ray photoelectron spectrum analysis (XPS) and Brunauer-Emmett-Teller measurements (BET). The photocatalytic reaction of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) was investigated under UVA irradiation. A toxicity analysis was performed with the marine bioluminescent bacteria Vibrio fischeri. The highest 2,4-D removal efficiency of 99.2% was obtained with the biphasic Au-TiO2(TiO2(B)/anatase) nanobelts with anatase as predominant phase. Toxicity was mainly due to the intermediate 2,4-dichlorophenol (2,4-DCP) which was eliminated in 4 h. The TiO2 nanobelt phase structure is shown to have a significant effect on photocatalytic activity.
February, 2019 | DOI: 10.1016/j.apsusc.2018.10.175
Nanotecnología en Superficies y Plasma
Study of the Interface of the Early Stages of Growth under Quasi-Equilibrium Conditions of ZnO on Graphene/Cu and Graphite
Morales, C; Black, A; Urbanos, FJ; Granados, D; Mendez, J; del Campo, A; Yubero, F; Soriano, LAdvanced Materials Interfaces, 6 (2019) art. 1801689
The study of the early stages of growth of ZnO on graphene supported on Cu and on highly oriented pyrolytic graphite by means of reactive thermal evaporation of metallic Zn at room temperature is presented. This growth method allows to go in depth in the study of the fundamental interaction between ZnO and graphene at the interface in quasi-equilibrium conditions. Quantitative, chemical, and morphological analysis is performed using photoemission spectroscopy, atomic force, and scanning microscopies as experimental characterization techniques and factor analysis and inelastic peak shape analysis as modeling techniques. The growth of ZnO on a highly oriented pyrolytic graphite substrate is also studied using the same growth method for comparison. The results show that, in spite that the first atomic layer of both substrates is identical, the growth kinetics and morphology of the deposits are completely different. A model for the kinetics of the growth of ZnO on both substrates is proposed.
February, 2019 | DOI: 10.1002/admi.201801689
Reactividad de Sólidos
Mechanochemical combustion synthesis of vanadium carbide (VC), niobium carbide (NbC) and tantalum carbide (TaC) nanoparticles
Jalaly, M; Gotor, FJ; Sayagues, MJInternational Journal of Refractory Metals & Hard Materials, 79 (2019) 177-184
The nanoparticles of vanadium, niobium, and tantalum carbides were synthesized by a mechanically induced magnesiothermic combustion in the separate Mg/V2O5/C, Mg/Nb2O5/C, and Mg/Ta2O5/C systems. Initial materials in these systems ignited after short milling times of 10, 10, and 23 min, respectively. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), energy-dispersive X-ray spectroscopy (EDS), high-resolution transmission electron microscopy (HRTEM) and elemental mapping techniques were employed to characterize the combustion products. In this process, magnesium reduces initial oxides to generate elemental V/Nb/Ta to react with carbon, forming the carbide phases.
February, 2019 | DOI: 10.1016/j.ijrmhm.2018.12.011
Reactividad de Sólidos
Multicycle CO2 capture activity and fluidizability of Al-based synthesized CaO sorbents
Azimi, B; Tahmasebpoor, M; Sanchez-Jimenez, PE; Perejon, A; Valverde, JMChemical Engineering Journal, 358 (2019) 679-690
CaO-based materials have been identified as promising sorbents for highly efficient pre-combustion and post-combustion CO2 capture in fluidized beds operated at high temperatures by means of the Calcium Looping (CaL) process. However, Ca-based sorbents suffer from a decline of the capture capacity over multiple sorption/desorption cycles, mainly due to sintering, and from a markedly heterogeneous fluidization behavior due to the strength of interparticle attractive forces as compared to particle weight. The present study is focused on the development of novel synthetic CaO/Al2O3 sorbents for CO2capture with enhanced CaL performance and fluidizability by dry mixing with flow conditioner nanopowders. The influence of initial precursors on the sorbents multicycle activity at realistic CaL conditions has been investigated. The formation of a stable Ca9Al6O18 mixed-phase during the preparation of the sorbents promotes the multicycle capture capacity. The type of Ca and Al precursors, either soluble or insoluble, can significantly affect the dispersion of this stabilizer (Ca9Al6O18) in the sorbent matrix and, consequently, may affect the carbonation activity of the materials. The sorbent prepared from soluble aluminum nitrate and calcium nitrate precursors by sol-gel method exhibits a very stable multicycle capture capacity with a capture capacity around 0.2 g of CO2/g of sorbent after 21 cycles keeping a 72% of its initial capture capacity. The fluidizability of this promising sorbent was also investigated as affected by the addition of three different flow conditioners. Fluidization experiments confirmed the positive effect of using hydrophilic alumina and hydrophobic silica nanoparticles on improving the fluidizability of the synthesized sorbents.
February, 2019 | DOI: 10.1016/j.cej.2018.10.061
Fotocatálisis Heterogénea: Aplicaciones
Catalytic Efficiency of Cu-Supported Pyrophyllite in Heterogeneous Catalytic Oxidation of Phenol
El Gaidoumi, A.; Doña-Rodríguez, J.M.; Pulido Melián, E.; González-Díaz, O.M.; Navío, J.A.; El Bali, B.; Kherbeche, A.Arabian Journal for Science and Engineering, (2019) 1-13
The copper-impregnated pyrophyllite (Cu/RC) was prepared and used as catalyst in catalytic wet peroxide oxidation (CWPO) of phenol. The catalyst was prepared by impregnation of copper (2.5 wt%) into pyrophyllite-type clay and characterized by X-ray diffraction, X-ray fluorescence, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, and transmission electron microscopy. The optimum operation conditions for CWPO of phenol over Cu/RC were determined by investigating the effects of pH, temperature, catalyst amount, and hydrogen peroxide concentration. Stability of the Cu/RC catalyst and toxicity of treated solution were studied, by measuring the copper concentration leached out from the catalyst and the inhibition of Vibrio fischeri bacteria bioluminescence, respectively. The probable degradation mechanism of phenol over Cu/RC was considered by HPLC analysis. The obtained results showed that Cu/RC achieved highest activity (total phenol degradation and 80% TOC reduction) and detoxification with remarkable low copper leaching concentration (0.006 mg\,L−1)mg\,L−1) at optimized conditions (pH == 3, T=50∘T=50∘C, 2 g\,L−1g\,L−1 catalyst amount, 50 mg L−1L−1phenol concentration and 7.45 mmol\,L−1mmol\,L−1 hydrogen peroxide concentration during 4 h). Meanwhile, few intermediates with low concentration were observed by the HPLC analysis for the CWPO of phenol. The Cu/RC catalyst showed a good activity after five successive runs (88% of degradation and 73% mineralization) at optimized conditions.
February, 2019 | DOI: 10.1007/s13369-019-03757-2
Química de Superficies y Catálisis
Immobilization of Stabilized Gold Nanoparticles on Various Ceria-Based Oxides: Influence of the Protecting Agent on the Glucose Oxidation Reaction
Chenouf, M; Megias-Sayago, C; Ammari, F; Ivanova, S; Centeno, MA; Odriozola, JACatalysts, 9 (2019) 125
The influence of the protecting agent's nature on gold particle size and dispersion was studied in this work over a series of gold-based catalysts. CO and glucose oxidation were chosen as catalytic reactions to determine the catalyst's structure-activity relationship. The nature of the support appeared to be the predominant factor for the increase in activity, as the oxygen mobility was decisive for the CO oxidation in the same way that the Lewis acidity was decisive for the glucose oxidation. For the same catalyst composition, the use of montmorillonite as the stabilizing agent resulted in better catalytic performance.
February, 2019 | DOI: 10.3390/catal9020125
Reactividad de Sólidos
Insight into the BiFeO3 flash sintering process by in-situ energy dispersive X-ray diffraction (ED-XRD)
Perez-Maqueda, LA; Gil-Gonzalez, E; Wassel, MA; Jha, SK; Perejon, A; Charalambous, H; Okasinski, J; Sanchez-Jimenez, PE; Tsakalakos, TCeramics International, 45 (2019) 2828-2834
The sintering mechanism of BiFeO3 has been investigated in-situ by energy dispersive X-ray diffraction (ED-XRD) using a high-energy white collimated X-ray beam from the Advanced Photon Source (Argonne National Laboratories). Such radiation is very penetrating thereby allowing measurements of the sample even when placed inside the flash sintering set up. Additionally, the fast ED-XRD measurements permit monitoring the flash sintering process by providing information about phase composition and sample temperature in real time. Moreover, profile scans, obtained by moving the stage vertically while recording the ED-XRD spectra, permit investigating the homogeneity of the flash for the entire length of the sample. All experiments have been complemented by ex-situ studies. It has been concluded that flash sintering of BiFeO3 is a homogeneous process without any directionality effects. Furthermore, flash sintering takes place at quite low temperatures (below the Tc ≈ 830 °C), which may be related to the high quality of the samples, as pure, highly insulating ceramics without evidence of secondary phases with a homogenous nanostructured grain size distribution are obtained by this technique. Moreover, it is also evidenced that the rapid heating of the sample does not seem to justify, at least by itself, the densification process. Therefore, it appears that the electric current should play a role in the enhanced mobility during the sintering process.
February, 2019 | DOI: 10.1016/j.ceramint.2018.07.293
Nanotecnología en Superficies y Plasma
Environmentally Tight TiO2-SiO2 Porous 1D-Photonic Structures
Garcia-Valenzuela, A; Lopez-Santos, C; Rico, V; Alvarez, R; Palmero, A; Gonzalez-Elipe, ARAdvanced Materials Interfaces, 6 (2019) art. 1801212
Although thin film porosity is the basis of many optical sensors, it can be deleterious for a stable optical behavior of passive optical elements due to the condensation of water and other vapors in their pores. This paper proposes a new strategy for the magnetron sputtering (MS) fabrication of environmentally tight SiO2-TiO2 porous multilayers. Thin films of these two oxides deposited in an oblique angle configuration (MS-OAD) present a nanocolumnar and highly porous nanostructure and, as a consequence, experience significant changes in their optical properties when exposed to water vapor. Similarly, the optical properties of Bragg reflectors and Bragg microcavities made of the stacking of porous and compact SiO2 and TiO2 thin films experience reversible changes when these 1D-photonic structures are exposed to water pressure. A key finding of this work is that a very thin capping layer of SiO2 deposited on the surface of porous SiO2 films in the stack, at the interlayer between the two oxides, efficiently seals the pores making the photonic structures environmentally tight. This capping layer approach is a useful strategy to incorporate porosity as an additional parameter to design the optical behavior of planar photonic structures while preserving optical and environmental stability.
February, 2019 | DOI: 10.1002/admi.201801212
Amber, beads and social interaction in the Late Prehistory of the Iberian Peninsula: an update
Odriozola, CP; Sousa, AC; Mataloto, R; Boaventura, R; Andrade, M; Garcia, RV; Garrido-Cordero, JA; Rodriguez, E; Martinez-Blanes, JM; Aviles, MA; Daura, J; Sanz, M; Riquelme, JAArchaeological and Anthropological Sciences, 11 (2019) 567-595
The identification of archaeological amber has been used in Iberian prehistory to evidence long-distance exchanges and engage Iberia in networks that connect western Europe with central and northern Europe, the emergence of social complexity, and the consolidation of trade networks. However, until now, no comprehensive analytical study of the Iberian amber has been produced to support any of the interpretive models currently in use. This paper approaches the analysis of Iberian Peninsula amber artefacts by considering their provenance (based on FTIR characterization), chronology, and spatial relationship with other exotica. Our work increases the number of analyzed artefacts to 156 (24%), out of the c. 647 currently known for the Iberian Peninsula. Based on these new data and a review of Murillo-Barroso and Martinon-Torres (2012), this overview outlines amber consumption patterns from the 6th to 2nd millennia BCE and demonstrates long-distance amber exchange connecting Iberia with the Mediterranean region from the Neolithic period onwards.
February, 2019 | DOI: 10.1007/s12520-017-0549-7
Reactividad de Sólidos
Production of Ag-ZnO powders by hot mechanochemical processing
Guzman, D; Aguilar, C; Rojas, P; Criado, JM; Dianez, MJ; Espinoza, R; Guzman, A; Martinez, CTransactions of nonferrous metals society of China, 29 (2019) 365-373
Ag-CdO composites are still one of the most commonly used electrical contact materials in low-voltage applications owing to their excellent electrical and mechanical properties. Nevertheless, considering the restriction on using Cd due to its toxicity, it is necessary to find alternative materials that can replace these composites. In this study, the synthesis of Ag-ZnO alloys from Ag-Zn solid solutions was investigated by hot mechanochemical processing. The hot mechanochemical processing was conducted in a modified attritor mill at 138 degrees C under flowing O-2 at 1200 cm(3)/min for 3.0 h. The microstructure and phase evolution were investigated using X-ray diffractometry, field emission gun scanning electron microscopy and transmission electron microscopy. The results suggest that it is possible to complete the oxidation of Ag-Zn solid solution by hot mechanochemical processing at a low temperature and short time. This novel synthesis route can produce Ag-ZnO composites with a homogeneous distribution of nanoscale ZnO precipitates, which is impossible to achieve using the conventional material processing methods. Considering the fact that the fundamental approach to improving electric contact material performance resides in obtaining uniform dispersion of the second-phase in the Ag matrix, this new processing route could open the possibility for Ag-ZnO composites to replace non-environmentally friendly Ag-CdO.
February, 2019 | DOI: 10.1016/S1003-6326(19)64946-0
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