Search results for "element"
showing 10 items of 13601 documents
In-situ characterisation of organosilane films formation on aluminium alloys by electrochemical quartz crystal microbalance and in-situ ellipsometry
2005
Abstract Organosilane pre-treatments have been studied intensively during the last years in order to replace hexavalent chromium conversion treatments. The aim of this study is to follow in-situ the formation of this organosilane layer in solution. Two in-situ techniques, spectroscopic ellipsometry and electrochemical quartz crystal microbalance, were used to investigate the mechanism and the kinetics of this protective film formation. In-situ measurements highlight that the organosilane film observed after the drying process is not formed into the solution, but during the emersion and drying step. Hence, it has been possible to characterise the presence of a very thin organosilane layer in…
The determination of mineral acidity excess in solutions containing Ga(III), Al(III), Bi(III)
2002
Abstract A new procedure is proposed to carry out volumetric determinations of the strong acid content of a solution in the presence of inorganic cations such as Ga 3+ , Al 3+ , Bi 3+ which, showing in aqueous solution an acidic behaviour, introduce non negligible interferences in these determinations. Before the acid–base titration, an equivalent amount of a ligand, such as dihydrogen ethylendiamino tetraacetate is added, in order to strongly complex the cation masking it toward the successive addition of a strong base. Interferences are thus removed, and the volumetric determination of the strong acid excess plus the hydrogen ions set free from the ligand, as a consequence of the complex …
Microheterogeneous electrocatalytic chiral recognition at monoclinic vanadium-doped zirconias: enantioselective detection of glucose.
2007
Synthetic tetragonal and monoclinic vanadium-doped zirconias (t- and m-VxZr1-xO2, 0.005x0.150) exert an effective catalytic effect toward the electrochemical oxidation of glucose in aqueous alkaline media. The catalytic effect of monoclinic specimens attached to carbon and fluorine-doped tin oxide electrodes exhibits a remarkable enantioselectivity, so that catalytic currents for the oxidation of L-glucose at +0.92 V vs AgCl/Ag are considerably larger than those obtained for the oxidation of D-glucose. This enantioselectivity can be associated with the existence of a noncentrosymmetric coordination of vanadium centers in the monoclinic crystalline form of zirconia. From the electrochemical …
Selective recognition of fluoride anion in water by a copper(II) center embedded in a hydrophobic cavity
2014
The ability of a water-soluble pentacationic calix[6]arene-based CuII complex to bind anions in water has been explored. Quite remarkably, the complex exhibits strong and selective fluoride binding in the pH range of 6–7. The binding constant at pH 5.9 was evaluated to be 85 000 M−1, which is one of the highest values ever reported for a fluoride probe in water and at this pH. The complex also binds chloride ions, but 1000 times less efficiently. The combination of the calix[6]arene hydrophobic cavity with the CuII complex, presenting its labile site in the endo position, is the reason for the selective recognition process. The single crystal X-ray structure of the organo-soluble parent com…
Water-Soluble Palladium Nanoparticles: Click Synthesis and Applications as a Recyclable Catalyst in Suzuki Cross-Couplings in Aqueous Media
2010
A new PEG-tagged material, which was prepared by a threefold copper-catalyzed [3+2] cycloaddition (click chemistry), was found to act as an efficient stabilizer for palladium nanoparticles. The newly formed material proved to be active as a recyclable catalyst in Suzuki coupling; the presence of polyether chains allowed for the catalytic runs to be conducted in aqueous media.
Cobalt Metal-Organic Framework Based on Layered Double Nanosheets for Enhanced Electrocatalytic Water Oxidation in Neutral Media
2020
A new cobalt metal-organic framework (2D-Co-MOF) based on well-defined layered double cores that are strongly connected by intermolecular bonds has been developed. Its 3D structure is held together by π-π stacking interactions between the labile pyridine ligands of the nanosheets. In aqueous solution, the axial pyridine ligands are exchanged by water molecules, producing a delamination of the material, where the individual double nanosheets preserve their structure. The original 3D layered structure can be restored by a solvothermal process with pyridine, so that the material shows a "memory effect"during the delamination-pillarization process. Electrochemical activation of a 2D-Co-MOF@Nafi…
Effect of Anions and Oxygen on the Kinetics of the Anodic Dissolution of Nickel
2006
An electrochemical impedance spectroscopy study on electrochemical dissolution and active/passive transition of polycrystalline nickel in acid media has been performed in sulfate and nitrate aqueous solutions. Oxygen favors the nickel electrodissolution in a nitrate aqueous acid medium, but the dissolution decreases in the sulfate medium due to nickel passivation. The anion and oxygen effect is analyzed from a model where Ni(I) species are stabilized on the Ni metal surface and all anions present in the solution compete in the neutralization of Ni(I) and Ni(II) and in the solubilization of Ni(II).
Conductimetric study of struvite crystallization in water as a function of pH
2017
Abstract The main objective of this work was to investigate the best pH for phosphorus removal from synthetic aqueous solutions using chemical precipitation of struvite, at constant temperature. The experimental approach, developed in the present study, consisted to precipitate struvite in synthetic wastewater containing PO 4 3− , NH 4 + and Mg 2+ ions in an equal molar ratio, using a stirred tank with continuous monitoring by conductimetry, at 25 °C. Different laboratory experiments were used to evaluate the effects of pH in the range of 8.5 till 11.8, on size, shape, and purity of the precipitated crystals. Struvite crystals were characterized by Infrared spectroscopy (FTIR), scanning ele…
Dioxygen reduction by cobalt(II) octaethylporphyrin at liquid|liquid interfaces.
2010
Oxygen reduction catalyzed by cobalt(II) (2,3,7,8,12,13,17,18-octaethylporphyrin) [Co(OEP)] at soft interfaces is studied by voltammetry and biphasic reactions. When Co(OEP) is present in a solution of 1,2-dichloroethane in contact with an aqueous acidic solution, oxygen is reduced if the interface is positively polarized (water phase versus organic phase). This reduction reaction is facilitated when an additional electron donor, here ferrocene, is present in excess in the organic phase.
Catalytic reduction of nitrates and nitrites in water solution on pumice-supported Pd–Cu catalysts
2000
Abstract Two series of pumice-supported palladium and palladium–copper catalysts, prepared by impregnation with different palladium and copper precursors, were tested for the hydrogenation of aqueous nitrate and nitrite solutions. Measurements were performed in a stirred tank reactor, operating in batch conditions, in buffered water solution at atmospheric pressure and at 293 K. The activities of the catalysts were calculated in terms of nitrate and/or nitrite removal. With the monometallic Pd/pumice, the reduction of nitrite is highly selective; only 0.2% of the initial nitrite content is converted to ammonium ions. The activity in terms of turn over frequency (TOF) is higher as compared t…