Au/CeO2 Photocatalyst for the Selective Oxidation of Aromatic Alcohols in Water under UV, Visible and Solar Irradiation

Au nanoparticles supported on CeO2 have been prepared and investigated as photocatalysts for the photocatalytic selective oxidation of benzyl alcohol and 4-methoxybenzyl alcohol to the correspondent benzaldehydes, in aqueous suspensions and room conditions under UV, visible and natural solar light irradiation. Au nanoparticles have been supported by impregnation (1 and 3 wt.%) on two types of CeO2 (i.e., a commercial one and a home prepared oxide obtained in the presence of NaOH as precipitation agent). The Au impregnated samples showed strong visible radiation absorption at 565–570 nm associated to localized surface plasmon resonance (LSPR). The bare CeO2 samples are activated by UV light and resulted virtually inactive under visible irradiation, whereas the presence of Au improved both the conversion of the alcohols and the selectivity of the reaction towards the aldehyde, giving rise to good results, particularly under visible and natural solar light irradiation. The activity of the materials increased by increasing the Au content

Investigation of Co3O4 and LaCoO3 interaction by performing N2O decomposition tests under Co3O4-CoO transition temperature

The research presented in this paper addresses the question: How does the addition of a small amount of LaCoO3 impact the activity of a Co3O4 catalyst? By testing such a catalyst in N2O decomposition under conditions at which the thermal decomposition of Co3O4 to CoO is possible, one gains unique insight into how the two phases interact. The activity of such a catalyst increases in the entire studied temperature range, unlike the activity of the undoped cobalt catalyst which is lower at 850 °C than at 800 °C due to the reduction of Co3O4 to CoO. XRD measurements showed that CoO was also the main cobalt oxide present in the Co3.5La catalyst after operating at 850 °C, as did the XPS measurements, but there was no drop of activity associated with this change. The influence of NO, O2 and H2O on the activity of the new catalyst, Co3.5La, was determined. Lack of positive effect of NO, a known oxygen scavenger, on the activity was noticed at all temperatures, showing that the effect of LaCoO3 is probably due to increased oxygen desorption. Temperature programed oxidation (TPO) tests showed that the beneficial effects of the presence of LaCoO3 on the activity of cobalt oxide at 850 °C were probably caused by enhanced diffusion of O2− anions through the entire catalyst, which facilitates desorption of oxygen molecules from the surface

Synergistic effect in Ag/Fe-MnO2 catalysts for ethanol oxidation

Here we report the synergistic effect of OMS-2 catalysts tested in ethanol oxidation, and the effects produced by both the addition of an Fe modifier in the catalyst preparation stage, and the introduction of Ag on its surface by the impregnation method. To analyze the action of each component, the Fe-modified, Ag-containing OMS-2 catalysts with different Mn/Fe ratios were prepared. Combined XPS and XRF elemental analysis confirms the states and distribution of the Ag- and Fe-containing species between the surface and bulk of the OMS-2 catalysts, which form highly dispersed Ag species on the surface of 0.05Fe–OMS-2, and are also incorporated into the OMS-2 crystalline lattice. The cooperative action of Ag and Fe modifiers improves both reoxidation ability (TPO results) and the amount of adsorbed oxygen species on the catalyst surface. The introduction of Ag to the OMS-2 and 0.05 Fe–OMS-2 surface allows a high level of activity (T80 = 150–155 °C) and selectivity (SAc80 = 93%) towards the acetaldehyde formation

Application of potassium ion deposition in determining the impact of support reducibility on catalytic activity of au/ceria-zirconia catalysts in CO oxidation, NO oxidation, and C3H8 combustion

The purpose of the study was to show how a controlled, subtle change of the reducibility of the support by deposition of potassium ions impacts the activity of gold catalysts. Since the activity of supported gold catalysts in carbon monoxide oxidation is known to strongly depend on the reducibility of the support, this reaction was chosen as the model reaction. The results of tests conducted in a simple system in which the only reagents were CO and O2 showed good agreement with the CO activity trend in tests performed in a complex stream of reagents, which also contained CH4, C2H6, C3H8, NO, and water vapor. The results of the X-ray Diffraction (XRD) studies revealed that the support has the composition Ce0.85Zr0.15O2, that its lattice constant is the same for all samples, and that gold is mostly present in the metallic phase. The reducibility of the systems was established based on Temperature Programmed Reduction (TPR) and in situ XRD measurements in H2 atmosphere. The results show that the low temperature reduction peak, which is due to the presence of gold, is shifted to a higher value by the presence of 0.3 at% potassium ions on the surface. Moreover, the increase of the potassium loading leads to a more pronounced shift. The T50 of CO oxidation in the simple model stream was found to exhibit an excellent linear correlation with the maximum temperature of the low temperature reduction peak of Au catalysts. This means that stabilizing oxygen with a known amount of potassium ions can be numerically used to estimate the T50 in CO oxidation. The results in the complex stream also showed a similar dependence of CO conversion on reducibility, though there was no substantial difference in the activity of the catalysts in other reactions regardless of the potassium loading. These studies have shown that the influence of potassium varies depending on the reaction, which highlights differences in the impact of reducibility and importance of other factors in these reactions

Hectorite/Phenanthroline-Based Nanomaterial as Fluorescent Sensor for Zn Ion Detection: A Theoretical and Experimental Study

The development of fluorescent materials that can act as sensors for the determination of metal ions in biological fluids is important since they show, among others, high sensitivity and specificity. However, most of the molecules that are used for these purposes possess a very low solubility in aqueous media, and, thus, it is necessary to adopt some derivation strategies. Clay minerals, for example, hectorite, as natural materials, are biocompatible and available in large amounts at a very low cost that have been extensively used as carrier systems for the delivery of different hydrophobic species. In the present work, we report the synthesis and characterization of a hectorite/phenanthroline nanomaterial as a potential fluorescent sensor for Zn ion detection in water. The interaction of phenanthroline with the Ht interlaminar space was thoroughly investigated, via both theoretical and experimental studies (i.e., thermogravimetry, FT-IR, UV-vis and fluorescence spectroscopies and XRD measurements), while its morphology was imaged by scanning electron microscopy. Afterwards, the possibility to use it as sensor for the detection of Zn2+ ions, in comparison to other metal ions, was investigated through fluorescent measurements, and the stability of the solid Ht/Phe/Zn complex was assessed by different experimental and theoretical measurements

Supporting Information Hectorite/phenanthroline based nanomaterial as fluorescent sensor for Zn ions detection: a theoretical and experimental study

Figure S1. Change in fluorescence spectra of phenanthroline upon addition of different metal ionsPeer reviewe

New Frontiers in Gold Catalyzed Reactions

For many years, gold has been regarded as a poor catalyst due to its chemical inertness towards reactive molecules such as oxygen and hydrogen. The interest in using gold in catalysis has increased during the last 20 years, since Haruta reported the surprisingly high activity in CO oxidation at low temperature for small (3–5 nm) gold particles supported on various oxides. [...