Desarrollo, Producción e Innovación en la Investigación científica
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Item Synthesis of SBA-1, SBA-3 and SBA-7 mesoporous materials. Study of the effect of time and temperature.(Universidad Tecnológica Nacional., 2016) Martínez , María Laura; Ponte , María Virginia; Falcón , Horacio; Beltramone , Andrea Raquel; Anunziata , Oscar Alfredo; Anunziata , Oscar Alfredo; Beltramone , Andrea Raquel; Ponte , María VirginiaIn recent years, physicists, chemists and engineers have focused their research on the design of new functional materials. In the synthesis and control of materials in nanometer dimensions, the aim is currently directed towards the development of systems and devices that take advantage of chemical properties and physical principles, where their causes lie in the nanometer scale. Although there are numerous investigations about the synthesis of mesoporous materials from inorganic silicon salt, for example the synthesis of SBA-3. Ting et al [1] studied the synthesis of SBA-1; they obtained mesoporous SBA-1 with cubic structures, with a high porous system, by utilizing agents’ routers short chain structure such as the dodecyltrimethyl ammonium chloride. Recent research also showed that the formation of mesophases is affected by the presence of the counter ions and templates or surfactants can adopt a mesophase or other phases. So, Che et al. [2] found a phase shift 2D-hexagonal cubes from P6mm to Pm3n. We have published results for synthesis of SBA-3 with silica gel as silica source; we have found that the formation of mesophase is function of NaOH concentration in the dissolutions of silica gel. The influence of reaction temperature, time and NaOH concentration was investigated. During studies for the best synthesis conditions for synthesis of SBA-3, we also obtained SBA-1 and SBA-7 mesoporous materials.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 Óxidos de vanadio y titanio soportados sobre CMK-3 como un nuevo catalizador para la desulfuración oxidativa de DBT.(Universidad Tecnológica Nacional., 2016) Beltramone , Andrea Raquel; Anunziata , Oscar Alfredo; Gómez Costa , Marcos Bruno; Falcón , Horacio; Juárez , Juliana Maria; Rivoira , Lorena Paola; Rivoira , Lorena Paola; Juárez , Juliana Maria; Anunziata , Oscar AlfredoEn el presente trabajo se estudiaron catalizadores de vanadio soportados sobre el carbón mesoporosos CMK 3 con diferentes contenidos de Vanadio (1-7 % p/p) en la desulfurización oxidativa de dibenzotiofeno (DBT) como modelo de compuestos sulfurados. La actividad catalítica se comparó con catalizadores de Titanio soportados en CMK-3. Las propiedades estructurales y texturales de los catalizadores se analizaron mediante estudios de adsorción de N2, XRD, UV-Vis-DRS y TEM. Tanto la dispersión como la actividad catalítica dependen fuertemente del contenido de vanadio. La muestra que contiene el 7% p/p de Vanadio es el catalizador con mejor actividad catalítica para la reacción de ODS de DBT utilizando peróxido de hidrógeno ((H2O2) como oxidante y acetonitrilo como solvente. El 100% de la eliminación de DBT se alcanzó a corto plazo en condiciones suaves. El carbon mesoporoso CMK-3 con una alta área superficial y gran volumen de poros promueve el anclaje del metal en la red de carbono, lo que permite alcanzar una alta distribución de sitios activos y nanoclusters más estables. La reutilización del catalizador indica que V-CMK-3 es un catalizador potencial para los ODS de dibenzotiofeno.Item Probing the Catalytic Activity of Sulfate-Derived Pristine and Post-Teatred Porous TiO2(101) Anatase Mesocrystals by the Oxidative Desulfurization of Dibenzothiophenes.(Universidad Tecnológica Nacional., 2017) Rivoira , Lorena Paola; Martínez , María Laura; Falcón , Horacio; Beltramone , Andrea Raquel; Campos , Martín José; Fierro , José; Tartaj , Pedro; Martínez , María LauraMesocrystals (basically nanostructures showing alignment of nanocrystals well beyond crystal size) are attracting considerable attention for modeling and optimiza tion of functionalities. However, for surface-driven applications (heterogeneous catalysis), only those mesocrystals with excellent textural properties are expected to fulfill their potential. This is especially true for oxidative desulfuration of dibenzothiophenes (hard to desulfurize organosulfur com pounds found in fossil fuels). Here, we probe the catalytic activity of anatases for the oxidative desulfuration of dibenzothiophenes under atmospheric pressure and mild temperatures. Specifically, for this study, we have taken advantage of the high stability of the (101) anatase surface to obtain a variety of uniform colloidal mesocrystals (approximately 50 nm) with adequate orientational order and good textural properties (pores around 3−4 nm and surface areas around 200 m2 /g). Ultimately, this stability has allowed us to compare the catalytic activity of anatases that expose a high number of aligned single crystal-like surfaces while differing in controllable surface characteristics. Thus, we have established that the type of tetrahedral coordination observed in these anatase mesocrystals is not essential for oxidative desulfuration and that both elimination of sulfates and good textural properties significantly improve the catalytic activity. Furthermore, the most active mesocrystals have been used to model the catalytic reaction in three-(oil− solvent−catalyst) and two-phase (solvent−catalyst) systems. Thus, we have been able to observe that the transfer of DBT from the oil to the solvent phase partially limits the oxidative process and to estimate an apparent activation energy for the oxidative desulfuration reaction of approximately 40 kJ/mol in the two-phase system to avoid mass transfer limitations. Our results clearly establish that (101) anatase mesocrystals with excellent textural properties show adequate stability to withstand several post treatments without losing their initial mesocrystalline character and therefore could serve as models for catalytic processes different from the one studied hereItem Pt-Pd-F/AI₂O₃ Catalyst applied in the HDT process.(Universidad Tecnológica Nacional., 2015) Balangero, Gerardo Simón; Falcón , Horacio; Beltramone , Andrea RaquelThe inhibiting effect of basic and non-basic nitrogen compounds on the hydrogenation of polyaromatic compounds and on the hydrodesulphurization (HDS) of dibenzothiophene (DBT) and 4,6-dimethyl dibenzothiophene (4,6DMDBT), has been investigated on Pt-Pd-F/Al2O3 and compared with a commercial NiMo hydrotreating catalyst. Langmuir-Hinshelwood type rate equations were used to describe the reaction kinetics accurately with physically meaningful and well identified parameter values. Model parameters were tuned by fitting experimental data obtained in a continuous flow reactor at 345°C, 1000 psi pressure and different contact times. Pt-Pd-F/Al2O3 was more active than NiMo catalyst and conversion remained constant during 24 h of TOS. The model was able to correctly interpret all the experimental data. Parameter estimation results showed that phenanthrene and naphthalene inhibited the tetralin hydrogenation rate, whereas naphthalene and tetralin had no appreciable effect on the rate of phenanthrene conversion. This inhibition could be explained by the competitive adsorption and was described in the kinetic model by adsorption terms obtained from the multicomponent experiments. The inhibiting effect of different nitrogen compounds on the polyaromatic hydrogenation was determined. The following nitrogen compounds were investigated in this study: quinoline, 1,2,3,4-tetrahydroquinoline, indole, and indoline. The degree of inhibition was expressed in terms of an apparent adsorption constant derived from the kinetics.The inhibiting effect on the HDS of DBT and 4,6 DBT followed the same trendItem INIHIBITION BY NITROGEN COMPOUNDS IN THE SIMULTANEOUS HYDROGENATION OF POLYAROMATIC COMPOUNDS OVER Pt-Pd-F/AI₂O₃ CATALYST.(Universidad Tecnológica Nacional., 2015) Balangero , Gerardo Simón; Falcón , Horacio; Beltramone , Andrea RaquelThe inhibiting effect of basic and non-basic nitrogen compounds on the hydrogenation of polyaromatic compounds and on the hydrodesulphurization (HDS) of dibenzothiophene (DBT) and 4,6-dimethyl dibenzothiophene (4,6DMDBT), has been investigated on Pt-Pd-F/Al2O3 and compared with a commercial NiMo hydrotreating catalyst. Langmuir-Hinshelwood type rate equations were used to describe the reaction kinetics accurately with physically meaningful and well identified parameter values. Model parameters were tuned by fitting experimental data obtained in a continuous flow reactor at 345°C, 1000 psi pressure and different contact times. Pt-Pd-F/Al2O3 was more active than NiMo catalyst and conversion remained constant during 24 h of TOS. The model was able to correctly interpret all the experimental data. Parameter estimation results showed that phenanthrene and naphthalene inhibited the tetralin hydrogenation rate, whereas naphthalene and tetralin had no appreciable effect on the rate of phenanthrene conversion. This inhibition could be explained by the competitive adsorption and was described in the kinetic model by adsorption terms obtained from the multicomponent experiments. The inhibiting effect of different nitrogen compounds on the polyaromatic hydrogenation was determined. The following nitrogen compounds were investigated in this study: quinoline, 1,2,3,4-tetrahydroquinoline, indole, and indoline. The degree of inhibition was expressed in terms of an apparent adsorption constant derived from the kinetics.The inhibiting effect on the HDS of DBT and 4,6 DBT followed the same trend.Item Probing the Catalytic Activity of Sulfate-Derived Pristine and Post-Teatred Porous TiO2(101) Anatase Mesocrystals by the Oxidative Desulfurization of Dibenzothiophenes.(Univesidsad Tecnológica Nacional., 2017) Rivoira , Lorena Paola; Martínez , María Laura; Falcón , Horacio; Beltramone , Andrea Raquel; Campos , Martín; Fierro, José; Tartaj, Pedro; Martínez , María LauraMesocrystals (basically nanostructures showing alignment of nanocrystals well beyond crystal size) are attracting considerable attention for modeling and optimiza- (heterogeneous catalysis), only those mesocrystals with excellent textural properties are expected to fulfill their potential. This is especially true for oxidative desulfuration of dibenzothiophenes (hard to desulfurize organosulfur com pounds found in fossil fuels). Here, we probe the catalytic activity of anatases for the oxidative desulfuration of dibenzothiophenes under atmospheric pressure and mild temperatures. Specifically, for this study, we have taken advantage of the high stability of the (101) anatase surface to obtain (pores around 3−4 nm and surface areas around 200 m2 /g). Ultimately, this stability has allowed us to compare the catalytic activity of anatasesthat expose a high number of aligned single crystal-like surfaces while differing in controllable surface essential for oxidative desulfuration and that both elimination of sulfates and good textural properties significantly improve the catalytic activity. Furthermore, the most active mesocrystals have been used to model the catalytic reaction in three-(oil− the oil to the solvent phase partially limits the oxidative process and to estimate an apparent activation energy for the oxidative establish that (101) anatase mesocrystals with excellent textural propertiesshow adequate stability to withstand several post treatments without losing their initial mesocrystalline character and therefore could serve as modelsfor catalytic processes different from the one studied here.Item 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 Pt-Pd-F/AI203catalyst applied in the HDT process.(Univesidsad Tecnológica Nacional., 2015) Balangero, Gerardo Simón; Falcón , Horacio; Beltramone , Andrea RaquelThe inhibiting effect of basic and non-basic nitrogen compounds on the hydrogenation of polyaromatic compounds and on the hydrodesulphurization (HDS) of dibenzothiophene (DBT) and 4,6-dimethyl dibenzothiophene (4,6DMDBT), has been investigated on Pt-Pd-F/Al2O3 and compared with a commercial NiMo hydrotreating catalyst. Langmuir-Hinshelwood type rate equations were used to describe the reaction kinetics accurately with physically meaningful and well identified parameter values. Model parameters were tuned by fitting experimental data obtained in a continuous flow reactor at 345°C, 1000 psi pressure and different contact times. Pt-Pd-F/Al2O3 was more active than NiMo catalyst and conversion remained constant during 24 h of TOS. The model was able to correctly interpret all the experimental data. Parameter estimation results showed that phenanthrene and naphthalene inhibited the tetralin hydrogenation rate, whereas naphthalene and tetralin had no appreciable effect on the rate of phenanthrene conversion. This inhibition could be explained by the competitive adsorption and was described in the kinetic model by adsorption terms obtained from the multicomponent experiments. The inhibiting effect of different nitrogen compounds on the polyaromatic hydrogenation was determined. The following nitrogen compounds were investigated in this study: quinoline, 1,2,3,4-tetrahydroquinoline, indole, and indoline. The degree of inhibition was expressed in terms of an apparent adsorption constant derived from the kinetics.The inhibiting effect on the HDS of DBT and 4,6 DBT followed the same trend