Structure control of silica-supported mono and bimetallic Au–Pt catalysts via mercapto capping synthesis

Cataloged from PDF version of article.SiO2-supported monometallic and bimetallic platinum-gold catalysts are prepared by deposition of metal nanoparticles stabilized by mercaptopropyltriethoxysilane (MPTES) after different aging time of the solution containing metal ions and MPTES. The materials are tested in the hydrodesulfurization (HDS) reaction of thiophene and compared with corresponding catalysts prepared by the conventional deposition-precipitation (DP) method. The monometallic Pt and the bimetallic Au-Pt prepared by DP have comparable activity. With respect to the platinum catalyst prepared by DP, the corresponding platinum catalyst prepared by MPTES particle stabilization exhibits a substantial enhancement of the activity regardless the solution aging time. On the contrary, the MPTES-assisted Au-Pt catalysts have different activities, depending on the solution aging time, with the most active being the one obtained with the 5-day-aged solution. In accord with XRD, XPS, and FTIR, the aging time of the solution, through the different interaction of Pt or Au precursors with the mercapto groups, has a crucial effect on the structure and on the surface of the catalysts. The observed differences in the catalytic activity are related to the structural and compositional changes of the bimetallic particles. (C) 2012 Elsevier Inc. All rights reserved

Lower Body Kinematics Do Not Differ Between Flat Ground and Mound Baseball Throwing

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The Effect of Seated Posture on Thoracolumbar Fascia, thus Influencing Balance

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Upper Body Kinetics has No Difference for Mound and Flat Ground Throwing

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In situ FT-IR investigation of the reduction of NO with CO over Au/CeO2-Al2O3 catalyst in the presence and absence of H-2

Cataloged from PDF version of article.he NO + CO + H-2 reaction over CeO2, Au/CeO2 (3 wt% Au), Au/CeO2-Al2O3 (2.9 wt% Au, 20 wt% Al2O3) and CeO2-Al2O3 mixed support prepared by co-precipitation has been Studied by FT-IR spectroscopy at elevated temperatures. Formation of NCO species has been detected on all of the samples. The presence of metallic gold is not necessary for the generation of the isocyanates on ceria and the mixed ceria-alumina support. The NCO species are produced by a process involving the dissociation of NO on the oxygen vacancies of the support, followed by the reaction between N atoms lying oil the surface and CO molecules. Gold plays an important role in the modification of ceria leading to Ce3+ and oxygen vacancies formation, and causes significant lowering of the reduction temperature of CeO2 and CeO2-Al2O3 enhancing the reducibility of ceria surface layers. The role of H-2 is to keep the surface reduced during the course of the reaction. The onset temperature, at which the interaction between the surface isocyanates and No begins, is low (100 degrees C). This explains the high activity of the Au/CeO2-Al2O3 catalyst with 100% selectivity in the reduction of NO by CO at low temperature (200 degrees C) and in the presence of H-2 (C) 2008 Elsevier B.V. All rights reserve

Fischer–Tropsch Synthesis Over Zr-Promoted Co/γ-Al2O3 Catalysts

Two Zr-modified alumina supports were synthetized containing the same amount of Zr but a different distribution of this modifier over the alumina surface. These supports, together with the unmodified alumina carrier, were used to prepare three cobalt-based catalysts which were characterized and tested under relevant Fischer–Tropsch conditions. The three catalysts presented very similar porosity and cobalt dispersion. The addition of Zr nor its distribution enhanced the catalyst reducibility. The catalyst activity was superior when using a carrier consisting of large ZrO2 islands over the alumina surface. The use of a carrier with a homogeneous Zr distribution had however, a detrimental effect. Moreover, a faster initial deactivation rate was observed for the Zr-promoted catalysts, fact that may explain this contradictory effect of Zr on activity. Finally, the addition of Zr showed a clear enhancement of the selectivity to long chain hydrocarbons and ethylene, especially when Zr was well dispersed

Highly stable defective TiO2-x with tuned exposed facets induced by fluorine: Impact of surface and bulk properties on selective UV/visible alcohol photo-oxidation

Titanium dioxide samples were prepared in the presence of different amounts of fluorine via hydrothermal method. It has been found that the presence of fluoride influenced the physico-chemical properties of TiO2 in various ways as polymorphic form stability, surface hydroxylation, generation of hydroxyl radicals under irradiation and formation of Ti3+ centers and oxygen vacancies. The generation rate of [rad]OH radicals was investigated by the photoluminescence technique in the presence of terephthalic acid. X-ray diffractometry indicated that fluorine stabilized the anatase TiO2. X-Ray photoelectron spectroscopy (XPS) revealed the presence of fluorine on the surface and the shift of the valence band edge towards less negative potentials, electron paramagnetic resonance (EPR) confirmed the formation of Ti3+ in the bulk of the photocatalysts, UV–vis spectra showed the extension of the TiO2 photo-response in the visible light region. 2-Propanol degradation and 4-methoxybenzyl alcohol partial oxidation were studied as probe reactions by using the home prepared powders as photocatalysts. Surprisingly, the photocatalytic activity resulted to be mainly affected by [rad]OH radicals formation ability under irradiation, rather than by the presence of {0 0 1} facets, although it cannot be excluded that the latter could influence the ability to form radicals under irradiation

EU-Rotate_N – a decision support system – to predict environmental and economic consequences of the management of nitrogen fertiliser in crop rotations

A model has been developed which assesses the economic and environmental performance of crop rotations, in both conventional and organic cropping, for over 70 arable and horticultural crops, and a wide range of growing conditions in Europe. The model, though originally based on the N_ABLE model, has been completely rewritten and contains new routines to simulate root development, the mineralisation and release of nitrogen (N) from soil organic matter and crop residues, and water dynamics in soil. New routines have been added to estimate the effects of sub-optimal rates of N and spacing on the marketable outputs and gross margins. The model provides a mechanism for generating scenarios to represent a range of differing crop and fertiliser management strategies which can be used to evaluate their effects on yield, gross margin and losses of nitrogen through leaching. Such testing has revealed that nitrogen management can be improved and that there is potential to increase gross margins whilst reducing nitrogen losses