Caracterización superficial de pigmentos sobre artefactos paleolíticos de la zona de los Montes Albanos (Roma, Italia) por microscopía óptica y espectroscopía raman

Preliminary results of the characterization of red pigmentations on paleolithic artefacts from the southern area of Montes Albanos (Rome, Italy) are presented. The set of materials consists of three decorated rounded pebblestones and a cortical flint blade typologically attributable to the Upper Paleolithic (Final Epigravetense, 14,000-12,000 cal BP). The findings were observed with optical microscope Nikon SMZ 1000/800 with magnifications of 1x to 6.3x. In two pebblestones, one decorated with parallel engravings, residues of ocher were detected in association with traces of use. In the third one, stained red dye was observed to form geometric patterns. Finally, reddish pigmentations were located on the cortical dorsal surface of a flint blade. To characterize chemically the coloring agent detected, macro-microscopically, Raman spectroscopy was used, a technique that allowed the study of the nature of the residues and the detection of additional organic materials whose presence must be related to post-depositional contaminations produced by the manipulation or/and surface exposure of artifacts

High Temperature Stability of Onion-Like Carbon vs Highly Oriented Pyrolytic Graphite

Abstract The thermodynamic stability of onion-like carbon (OLC) nanostructures with respect to highly oriented pyrolytic graphite (HOPG) was determined in the interval 765–1030 K by the electromotive force (emf) measurements of solid electrolyte galvanic cell: (Low) Pt|Cr3C2,CrF2,OLC|CaF2s.c.|Cr3C2,CrF2,HOPG|Pt (High). The free energy change of transformation HOPG = OLC was found positive below 920.6 K crossing the zero value at this temperature. Its trend with temperature was well described by a 3rd degree polynomial. The unexpected too high values of LDrHT LT P ~DcPðTÞ jointly to the HR-TEM, STEM and EELS evidences that showed OLC completely embedded in rigid cages made of a Cr3C2/CrF2 matrix, suggested that carbon in the electrodes experienced different internal pressures. This was confirmed by the evaluation under constant volume of dP dT by the a k ratio for OLC (0.5 MPa K21) and HOPG (8 Pa K21) where a and k are the isobaric thermal expansion and isothermal compressibility coefficients, respectively. The temperature dependency of the pressure was derived and utilized to calculate the enthalpy and entropy changes as function of temperature and pressure. The highest value of the internal pressure experienced by OLC was calculated to be about 7 GPa at the highest temperature. At 920.6 K, DrH and DrS values are 95.8 kJ mol21 and 104.1 JK21 mol21, respectively. The surface contributions to the energetic of the system were evaluated and they were found negligible compared with the bulk terms. As a consequence of the high internal pressure, the values of the enthalpy and entropy changes were mainly attributed to the formation of carbon defects in OLC considered as multishell fullerenes. The change of the carbon defect fraction is reported as a function of temperature

Synthesis of dimethyl carbonate by transesterification of propylene carbonate with methanol on ceo2-la2o3 oxides prepared by the soft template method

In this study, CeO2, La2O3, and CeO2-La2O3 mixed oxide catalysts with different Ce/La molar ratios were prepared by the soft template method and characterized by different techniques, including inductively coupled plasma atomic emission spectrometry, X-ray diffraction, N2 physisorption, thermogravimetric analysis, and Raman and Fourier transform infrared spectroscopies. NH3 and CO2 adsorption microcalorimetry was also used for assessing the acid and base surface properties, respectively. The behavior of the oxides as catalysts for the dimethyl carbonate synthesis by the transesterification of propylene carbonate with methanol, at 160 °C under autogenic pressure, was studied in a stainless-steel batch reactor. The activity of the catalysts was found to increase with an increase in the basic sites density. The formation of dimethyl carbonate was favored on medium-strength and weak basic sites, while it underwent decomposition on the strong ones. Several parasitic reactions occurred during the transformation of propylene carbonate, depending on the basic and acidic features of the catalysts. A reaction pathway has been proposed on the basis of the components identified in the reaction mixture

Aplicación de la fase (NH4)6MnMo9O32 como catalizador de oxidesulfurización

Los iso/heteropolianiones conteniendo molibdeno y tungsteno son una clase importante de compuestos que poseen propiedades particulares como alta reactividad y versatilidad estructural

MCM-41 supported co-based bimetallic catalysts for aqueous phase transformation of glucose to biochemicals

The transformation of glucose into valuable biochemicals was carried out on different MCM-41-supported metallic and bimetallic (Co, Co-Fe, Co-Mn, Co-Mo) catalysts and under different reaction conditions (150 °C, 3 h; 200 °C, 0.5 h; 250 °C, 0.5 h). All catalysts were characterized using N2 physisorption, Temperature Programmed Reduction (TPR), Raman, X-ray Diffraction (XRD) and Temperature Programmed Desorption (TPD) techniques. According to the N2-physisorption results, a high surface area and mesoporous structure of the support were appropriate for metal dispersion, reactant diffusion and the formation of bioproducts. Reaction conditions, bimetals synergetic effects and the amount and strength of catalyst acid sites were the key factors affecting the catalytic activity and biochemical selectivity. Sever reaction conditions including high temperature and high catalyst acidity led to the formation mainly of solid humins. The NH3-TPD results demonstrated the alteration of acidity in different bimetallic catalysts. The 10Fe10CoSiO2 catalyst (MCM-41 supported 10 wt. þ, 10 wt. %Co) possessing weak acid sites displayed the best catalytic activity with the highest carbon balance and desired product selectivity in mild reaction condition. Valuable biochemicals such as fructose, levulinic acid, ethanol and hydroxyacetone were formed over this catalyst

MCM-41 Supported Co-based Bimetallic Catalysts for Aqueous Phase Transformation of Glucose in Biochemicals

The transformation of glucose into valuable biochemicals was carried out on different MCM-41-supported metallic and bimetallic (Co, Co-Fe, Co-Mn, Co-Mo) catalysts and under different reaction conditions (150 °C, 3 h; 200 °C, 0.5 h; 250 °C, 0.5 h). All catalysts were characterized using N2 physisorption, Temperature Programmed Reduction (TPR), Raman, X-ray Diffraction (XRD) and Temperature Programmed Desorption (TPD) techniques. According to the N2-physisorption results, a high surface area and mesoporous structure of the support were appropriate for metal dispersion, reactant diffusion and the formation of bioproducts. Reaction conditions, bimetals synergetic effects and the amount and strength of catalyst acid sites were the key factors affecting the catalytic activity and biochemical selectivity. Sever reaction conditions including high temperature and high catalyst acidity led to the formation mainly of solid humins. The NH3-TPD results demonstrated the alteration of acidity in different bimetallic catalysts. The 10Fe10CoSiO2 catalyst (MCM-41 supported 10 wt.þ, 10 wt.%Co) possessing weak acid sites displayed the best catalytic activity with the highest carbon balance and desired product selectivity in mild reaction condition. Valuable biochemicals such as fructose, levulinic acid, ethanol and hydroxyacetone were formed over this catalyst

Remediación de aguas empleando catalizadores con vistas al desarrollo de un sistema integrado para la potabilización de aguas contaminadas con oxoaniones

Se estudió la eliminación de los oxoaniones NO3-, NO2- y BrO3- en muestras de agua sintética y real, empleando catalizadores en polvo y estructurados usando PdCu como fase activa soportados sobre materiales con características redox a base de CeO2  pura o modificada con 10%p/p ZrO2 (10ZrCe) y H2 como agente reductor. Se determinó por las técnicas de caracterización DRX, Raman, FTIR y TPR que los soportes CeO2 y 10ZrCe poseen vacancias de oxígeno siendo mayores en el soporte modificado con ZrO2 por la presencia de iones Zr4+ en la red de CeO2

Remediación de aguas empleando catalizadores con vistas al desarrollo de un sistema integrado para la potabilización de aguas contaminadas con oxoaniones

Centro de Investigación y Desarrollo en Ciencias Aplicada

Remediación de aguas empleando catalizadores con vistas al desarrollo de un sistema integrado para la potabilización de aguas contaminadas con oxoaniones

Centro de Investigación y Desarrollo en Ciencias Aplicada

Remediación de aguas empleando catalizadores con vistas al desarrollo de un sistema integrado para la potabilización de aguas contaminadas con oxoaniones

Centro de Investigación y Desarrollo en Ciencias Aplicada