UTN- FRC -Producción Académica de Investigación y Desarrollo - Artículos
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Item Reservorio nanoscópico de hidrógeno a partir de biorresiduos de casacara de naranjas.(Universidad Tecnológica Nacional., 2022) Juárez , Juliana María; Ledesma , Brenda Cecilia; Anunziata , Oscar Alfredo; Gómez Costas , Marcos Bruno; Beltramone, Andrea Raquel; Beltramone, Andrea Raquel; Anunziata , Oscar Alfredo; Ledesma , Brenda CeciliaEste trabajo aborda el enfoque de valorización de biorresiduos para el desarrollo de un novedoso nanomaterial carbonoso para ser utilizado en la adsorción de hidrógeno como una alternativa en el uso de hidrógeno verde. En esta investigación, los carbones activados se sintetizaron a partir de cáscara de naranja utilizando diferentes condiciones de síntesis. Con los carbones activados obtenidos con la mejor estructura y textura se estudió la adsorción de hidrógeno y los efectos en la meso/microporosidad de estos. La activación del carbón se realizó mediante un proceso químico con ácido fosfórico como agente activador, variando la concentración de ácido, la relación sustrato / agente activador y el tiempo de contacto entre ellos. El mejor material se obtuvo utilizando tiempo de carbonización de 1 h, temperatura de carbonización de 470oC, concentración de ácido fosfórico de 50% en peso y con área BET de 1402 m2 / g. Dicho material mejoró significativamente el comportamiento de almacenamiento de H2 en comparación con el carbón nanoestructurado del tipo CMK-3 (3,1% en peso a -196,15 oC y 10 bar). El material sintetizado es prometedor en la absorción de hidrógeno por fuerzas de enlace débiles (fisisorción).Item Vanadium oxide supported on mesoporous SBA-15 modified with AI and Ga as a highly active catalyst in the ODS of DBT.(Universidad Tecnológica Nacional., 2017) Rivoira , Lorena Paola; Martínez , María Laura; Anunziata , Oscar Alfredo; Beltramone, Andrea Raquel; Beltramone, Andrea Raquel; Anunziata , Oscar Alfredo; Martínez , María LauraVanadium oxides supported on mesoporous SBA-15 catalysts with different vanadium loadings were studied in the oxidative desulfurization (ODS) of dibenzothiophene as a model sulfur compound. The catalytic activity was improved when SBA-15 framework was modified by adding Al and Ga. Structural and textural characterization of the catalysts were performed by means of XRD, N2 adsorption, UVeVis eDRS, XPS, NMR, TEM, Raman, TPR and Py-FTIR. UVeViseDRS and Raman demonstrated that highly dispersed vanadium VO—3 species are responsible for the high activity in the sulfur removal. The Ga modified support with an intermediate V/Si ratio of 1/30 was the most active catalyst for ODS of DBT, using hydrogen peroxide as oxidant and acetonitrile as solvent. 100% of DBT elimination was attained at a short time in mild conditions. Gallium and aluminum incorporation into the support modified suc cessfully the nature of the SBA-15 surface by generating Bronsted and Lewis acidity. The interaction between the acid sites with the active vanadium sites improved the activity of the catalysts. The high dispersion depended on the vanadium loading and on the nature of the support. The more acidic support allowed better dispersion of the vanadium species due to stronger interaction metal-support. The reusability of the catalysts indicates that vanadium oxide supported on mesoporous SBA-15 modified with Ga and Al are potential catalysts for the ODS of dibenzothiophene.Item Hidrogenación e hidrodesulfurización de compuestos poliaromáticos utilizando Pt-Pd/AI203.(Universidad Tecnológica Nacional., 2016) Balangero , Gerardo Simón; Falcón , Horacio; Beltramone, Andrea Raquel; Beltramone, Andrea RaquelSe estudió la hidrogenación de compuestos poliaromáticos como tetralin y fenantreno en presencia de dibenzotiofeno y 4,6-dimetildibenzotiofeno utilizando un catalizador bimetálico Pt-Pd soportado sobre alúmina. El catalizador fue caracterizado por TEM, SEM y BET. Se obtuvo un catalizador con partículas metálicas bien dispersas y de muy pequeño tamaño. Los resultados fueron comparados con un catalizador comercial NiMo/Al2O3. Las reacciones se llevaron a cabo en un reactor de flujo continuo a 345°C y 500 psi (35 atm) variando los tiempos de contacto. Los resultados preliminares muestran que el catalizador desarrollado es más activo que el catalizador comercial. Se observó que los compuestos con mayor número de anillos aromáticos inhiben la velocidad de compuestos con menor número de anillos. Este efecto puede ser explicado en términos de una competitiva adsorción. Se realizó un test de desactivación y se observó que el catalizador no pierde su actividad luego de 20 horas de reacción.Item Vanadium oxide supported on mesoporous SBA-15 modified with AI and Ga as a highly active catalyst in the ODS of DBT.(Universidad Tecnológica Nacional., 2017) Rivoira , Lorena Paola; Martínez , María Laura; Anunziata , Oscar Alfredo; Beltramone, Andrea Raquel; Anunziata , Oscar Alfredo; Martínez , María LauraVanadium pentoxide supported on mesoporous SBA-15 catalysts with different vanadium loadings were studied in the oxidative desulfurization (ODS) of dibenzothiophene as a model sulfur compound. The catalytic activity was improved when SBA-15 framework was modified with Al and Ga as heteroatom substituting Si. Structural and textural characterization of the catalysts were performed by means of XRD, N2 adsorption, UV–Vis–DRS, XPS, NMR, TEM, Raman, TPR and Py-FTIR. UV–Vis– DRS and Raman demonstrated that highly dispersed vanadium pentoxide crystallites are responsible for the high activity in the sulfur removal. The high dispersion depends on the vanadium loading and on the nature of the support. The more acidic support allowed better dispersion of the vanadium species. The Ga modified support with an intermediate V/Si ratio of 1/30 was the most active catalyst for ODS of DBT, using hydrogen peroxide (H2O2) as oxidant and acetonitrile as solvent. 100% of DBT elimination was attained at a short time in mild conditions. Gallium and aluminum incorporation into the support modified successfully the nature of the SBA-15 surface by generating Bronsted and Lewis acidity. The interaction between the acid sites with the active vanadium sites improved the activity of the catalysts. The reusability of the catalysts indicates that vanadium oxide supported on mesoporous SBA-15 modified with Ga and Al are potential catalysts for the ODS of dibenzothiophene.Item Preparation of carbon nanotubes with hybrids nanostructure materials.(Universidad Tecnológica Nacional., 2017) Martínez , María Laura; Juárez , Juliana María; Gómez Costa, Marcos Bruno; Beltramone, Andrea Raquel; Juárez , Juliana MaríaCarbon nanotubes (CNT's) are allotropes carbon, like diamond, graphite and fullerenes. There are different types of CNT's, depending on the type of the graphite layers, it can be single wall carbon nanotubes (SWCNT's) and multi wall carbon nanotubes (MWCNT's). These nanomaterials show good physical properties such as their density, strength and thermal conductivity. The controllable synthesis of materials with the desired structure and dimensionality is of great significance in material science. In this work, the hierarchical carbon nanotubes (CNTs) were synthesized via a simple chemical conversion route by using Carbon Substrate/Fe3O4-SBA-15 hybrid (all in one). The synthesis of Carbon Substrate/Fe3O4-SBA-15 hybrid was carried out using Fe3O4- SBA-15 as a hard template and sucrose as carbon precursor. Sucrose was dissolved in a solution of H2SO4 in water and to this solution, Fe3O4-SBA-15 was added. The resulting mixture was dried at 373 K and then heated at 433 K for 6 h. A second impregnation was performed in order to ensure the filling of the template pores with the carbon precursor. To obtain the carbon nanotubes, the sample was placed in muffle at 1173 K under nitrogen flow (20mL/min) for 30 min. In order to remove the silica, the material was placed in an HF solution. The CNTs was filtered, washed and dried at 323 K. In the present work, we report the synthesis and characterization of CNTs materials of hybrid material. The material was characterized by X-ray diffraction (XRD) and the morphologies and structural features of the prepared materials were observed from the SEM and TEM images.Item Aniline adsorption and polymerization over gallium modified mesoporous material.(Universidad Tecnológica Nacional., 2018) Martínez , María Laura; Rivoira , Lorena Paola; Beltramone, Andrea Raquel; Anunziata, Oscar Alfredo; Anunziata, Oscar Alfredo; Rivoira , Lorena PaolaIn this work we study aniline polymerization over a mesoporous Ga-SBA-3 synthesized in our laboratory. In order to modify the intrinsic acidity of the mesoporous material gallium was incorporated into the structure by post synthesis wet impregnation method using gallium nitrate. Structural and textural characterization of the materials was performed by X-ray diffraction (XRD), ICP and EDX analysis, N2 adsorption-desorption and BET area analysis, FTIR and scanning electron microscopy (SEM). The catalytic material presented a ratio Si/Ga=32. Aniline is a weak organic base and an amphiprotic compound, so it can accept or donate protons. The polyaniline (PANI) exists in diverse ways presenting different chemical and physical properties. The protonated polyaniline feature the conductivity of a semiconductor material, over 100 S/cm. Toward achieve aniline adsorption, the solid gallium silicate was exposed to aniline vapours. The aniline adsorption was studied by infrared spectroscopy and the results obtained were evaluated so as to been able to polymerize it over the mesoporous material generating a unique polyaniline-host composite with new properties. Those polyaniline/hosts composites obtained by a polymerization in-situ technique were characterized by infrared spectroscopy (FTIR) and X-ray diffraction (XRD) analysis. Comparing to previous results FTIR analysis of the polyaniline/Ga SBA-3 composite (PANI/Ga-SBA-3) showed characteristics bands attributed to the quinoidal stretching (N=Q=N) and C-C stretching of the benzene ring. The low angle XRD analysis showed that the mesoporous structure was maintained in spite of the gallium incorporation. The absence of PANI peaks and G2O3 in the wide angle XRD pattern confirms that the polyaniline is adsorbed over the gallium silicate mesoporous surface and the gallium is well dispersed over the support.Item SINTESIS DIRECTA DE CMK-3 MODIFICADA CON TI, COMO SOPORTE DE IR APLICADO A REACCIONES DE HIDRODENITROGENACION.(Universidad Tecnológica Nacional., 2018) Ledesma , Brenda Cecilia; Juárez , Juliana María; Beltramone, Andrea Raquel; Juárez , Juliana MaríaEn el presente trabajo se sintetizó Ti-CMK-3 mediante un nuevo método de síntesis, en el cual se evita la utilización de un molde, con el fin de reducir el tiempo, el consumo de energía y por ende el costo. La caracterización estructural y superficial del catalizador se realizó mediante adsorción de N2, XRD, UV-Vis DRS, espectroscopía Raman y TEM. Los resultados de la caracterización indicaron que las propiedades texturales y estructurales del material sintetizado son comparables con las propiedades del material preparado por el método tradicional. El catalizador Ir-Ti-CMK-3 obtenido fue activo y selectivo para la reacción de hidrodenitrogenación (HDN) del indol. La principal ventaja del presente estudio es la reducción de tiempo y costo de la síntesis, simultáneamente con la aplicabilidad en las reacciones de Hidrotratamiento (HDT)Item Experimental desing optimization of the tetralin hydrogenation over Ir-Pt-SBA-15.(Univesidsad Tecnológica Nacional., 2015) Vallés , Verónica Alejandra; Ledesma , Brenda Cecilia; Rivoira , Lorena Paola; Cussa , jorgelina; Anunziata , Oscar Alfredo; Beltramone, Andrea Raquel; Anunziata , Oscar Alfredo; Cussa , jorgelina; Rivoira , Lorena Paola; Ledesma , Brenda CeciliaExperiment design-response surface methodology (RSM) is used in this work to model and optimize two responses in the hydrogenation of tetralin to decalin using bimetallic Ir–Pt-SBA-15 catalyst. In this study, we analyze the influence of the nature of the catalyst (metal molar fraction and metal loading), the catalyst/substrate ratio and the temperature of the reaction as factors for the design. The responses analyzed were conversion at 3 h and at 5 h of reaction time. The response surfaces were obtained with the Box– Behnken design, finding the best combination between the reaction parameters that allowed optimizing the process. By applying the statistic methodology, the higher levels of the two objective functions were obtained employing the catalyst with 1 wt.% of iridium and 0.7–0.8 wt.% of platinum; the optimal ratio between mass of catalyst and mole of tetralin was 17–19 g/mol and temperature between 200 and 220 ◦CItem Vanadium and titanium oxide supported on mesoporous CMK-3 as new catalysts for oxidative desulfurization.(Univesidsad Tecnológica Nacional., 2016) Rivoira , Lorena Paola; Juárez , Juliana María; Falcón , Horacio; Gómez Costa , Marcos Bruno; Anunziata , Oscar Alfredo; Beltramone, Andrea Raquel; Anunziata , Oscar Alfredo; Juárez , Juliana MaríaVanadium supported-CMK-3 catalysts with vanadium loading of 1–7 wt.% were studied in the oxidative desulfurization (ODS) of dibenzothiophene as a model sulfur compound. The activity was compared with titanium supported-CMK-3. Structural and textural characterization of the catalysts was performed by means of N2 adsorption, XRD, UV–vis–DRS, Raman spectroscopy, XPS, TEM and TPR. The dispersion and the nature of the vanadium species depend on the V loading, so does the catalyst activity. Vanadium supported-CMK-3 with 7 wt.% of vanadium loading was the most active catalyst for ODS of DBT using hydrogen peroxide (H2O2) as oxidant and acetonitrile as solvent. 100% of DBT elimination was attained at short time in mild conditions. Carbon ordered mesoporous CMK-3 with high surface area and high pore volume promotes a very good anchorage of metallic oxides in the carbons framework reaching high active sites distribution and more stable nanoclusters. The reusability of the catalyst indicates that V-CMK-3 is a potential catalyst for the ODS of dibenzothiopheneItem Sulfur elimination by oxidative desulfurization with titanium-modified SBA-16.(Univesidsad Tecnológica Nacional., 2015) Rivoira , Lorena Paola; Vallés , Verónica Alejandra; Ledesma , Brenda Cecilia; Ponte , María Virginia; Martínez , María Laura; Anunziata , Oscar Alfredo; Beltramone, Andrea Raquel; Anunziata , Oscar Alfredo; Martínez , María Laura; Ponte , María Virginia; Ledesma , Brenda Cecilia; Vallés , Verónica AlejandraTiO2-modified mesoporous SBA-16 and titanium-substituted mesoporous SBA-16 were developed and tested in the oxidative desulfurization (ODS) of dibenzothiophene prevailing in liquid fuel. Pure TiO2 was used as reference. The titania-based catalysts were characterized by chemical analysis, XRD, EDX and TEM. The titanium state as tetrahedral (in Ti-SBA-16 sample) or octahedral (in TiO2/SBA-16 sample) coordination surrounding in the silicate matrix was determined by XPS, UV–vis DRS, FTIR, Raman and XANES. We assessed the impact exerted on performance of different reaction variables, including (nature and amount of the active catalytic species, phase system, molar ratio of oxidant H2O2 and DBT, reaction temperature, nature of the substrate and reuse of catalysts). In addition, we carried out a kinetic study and the activation energy was determined. We achieved 90% of S removal from a 0.2 wt.% dibenzothiophene solution at 60 ◦C in less than 1 h of reaction. The best catalytic results are obtained with high exposed surface of nanometric TiO2 species of TiO2/SBA-16 sample. The activated catalyst is very active in ODS reaction and can be reused four times with no loss in activity.