Search results for "HYDROGEN"
showing 10 items of 4254 documents
Quantitative XPS analysis of leached layers on optical glasses
1993
The corrosion of optical glasses often reduces the utility of uncoated glasses as well as the adhesion of resistive coatings deposited onto corroded glasses. Photoelectron spectroscopy (XPS) was applied to study glass surfaces with respect to their surface corrosion. In particular, leaching by the influence of polish slurries, pure water, air and even residual gases inside a vacuum device was studied in detail. Pure quartz glass and different sodium and barium silicate glasses were broken in ultrahigh vacuum (4 × 10−10 mbar) for the determination of sensitivity factors of the different XPS signals. It was found that a quantitative determination of the surface composition of corroded and lea…
Proton Transfer versus Hydrogen Bonding: The Reduction of Ubiquinone Q2Incorporated in a Self-Assembled Monolayer in Unbuffered Aqueous Solution
2014
The electrochemical reduction of ubiquinone Q2 (UQ2) in unbuffered aqueous media was investigated over a pH range of 2 to 11, and the results were compared to those obtained in our previous work in buffered solutions. The short isoprene chains of UQ2 were incorporated in a self-assembled monolayer. Analysis of the mechanism and a study in D2O solutions allowed us to demonstrate the important role of hydrogen bonding in the stabilization of the reduced species, also in water. If the concentration of H+ is low relative to that of the quinone, the electrochemical reaction does not proceed through proton-coupled electron transfer, as it does in buffered medium or at low pH values (pH<4.4). We p…
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 …
Structural and Vibrational Study of a New Mixed Dipotassium Hydrogenselenate Dihydrogenphosphate K2(HSeO4)1.5 (H2PO4)0.5.
2006
Abstract Ongoing studies of the KHSeO4–KH2PO4 system, aimed at developing novel proton conducting solids, resulted in the new compound K2(HSeO4)1.5(H2PO4)0.5 (dipotassium hydrogenselenate dihydrogenphosphate). The crystals have been prepared by slow evaporation of an aqueous solution at room temperature. The structural properties of the crystals were characterized by X-ray single analysis (performed at room temperature), which revealed that K2(HSeO4)1.5(H2PO4)0.5 (KHSeP) crystallizes in space group P 1 ¯ with lattice parameters: a = 7.417(3) A, b = 7.668(2) A, c = 7.744(5) A, α = 71.59(3)°, β = 87.71(4)° and γ = 86.04(6)°. The compound has a unit cell volume 416.8(3) A3 and two formula unit…
The influence of ultrasound on the RuI3-catalyzed oxidation of phenol: Catalyst study and experimental design
2009
Abstract The influence of ultrasound at 24 kHz on the heterogeneous aqueous oxidation of phenol over RuI3 with hydrogen peroxide (H2O2) was studied isothermally at 298 K. Effect of ultrasound irradiation on catalytic properties and performance of RuI3 has been studied in details by means of scanning electron microscopy (SEM), X-ray powder diffraction (XRD), dispersion analyzer and a surface analyzer. Turn over frequency of the catalyst was also calculated. In this work, experimental design methodology was applied to optimize the degradation of phenol in aqueous solution, while minimizing an excessive consumption of chemical reagents. The independent variables considered were the catalyst lo…
Conformational investigations of bis(α-aminoalkyl)phosphinic acids and studies of the stability of their complexes with Cu(II)
2008
Abstract Conformational investigations of a group of bis(α-aminoalkyl)phosphinic acids were performed by use of NMR spectroscopy and theoretical calculations. In the case of one of the studied compounds, substituted with aminobenzyl and amino(p-chlorobenzyl) moieties, a pH-dependent equilibrium between conformers, stabilized by intermolecular hydrogen bonds was observed. Potentiometric studies proved that these molecules formed stable complexes with copper(II) ions, where stoichiometry was 1:1 and 1:2 depending on pH of their aqueous solution.
Ti(iv)-amino triphenolate complexes as effective catalysts for sulfoxidation
2010
C 3 -symmetric Ti (IV) amino triphenolate complexes efficiently catalyze, without previous activation and in excellent yields, the oxidation of sulfides at room temperature, using both CHP and the more environment friendly aqueous hydrogen peroxide as terminal oxidants, with catalyst loadings down to 0.01%. The Ti(IV) catalysts and the intermediate Ti(IV)-peroxo complexes have been characterized in solution by 1H NMR and ESI-MS techniques and via density functional studies.
N-Alkyl Ammonium Resorcinarene Chloride Receptors for Guest Binding in Aqueous Environment
2016
Host systems with guest binding ability in water and/or biological fluids are a current challenge in supramolecular host–guest chemistry. Here we present the first syntheses of water-soluble N-ethanol ammonium resorcinarene chlorides (NARCls) with terminal hydroxyl groups at the upper rim. The NARCls possess deep cavities and are shown to bind a variety of guest molecules such as linear and cyclic alkanes, linear halogenated alkanes, and aromatic fluorophores (naphthalene, p-(phenylazo)phenol) in water through hydrophobic interactions, as well as 1,4-dioxane (a water soluble guest) via hydrogen bonds. The receptors are monomeric in aqueous media and form 1:1 host–guest complexes with bindin…
Reaction pathways of glucose oxidation by ozone under acidic conditions.
2009
The ozonation of d-glucose-1-(13)C, 2-(13)C, and 6-(13)C was carried out at pH 2.5 in a semi-batch reactor at room temperature. The products present in the liquid phase were analyzed by GC-MS, HPAEC-PAD, and (13)C NMR spectroscopy. Common oxidation products of glucose have also been submitted to identical ozonation conditions. For the first time, a pentaric acid was identified and its formation quantitatively correlated to the loss of C-6 of glucose in the form of carbon dioxide. Potential mechanisms for the formation of this pentaric acid are discussed. The well-accepted pathway involving the anomeric position in glucose, gluconic acid, arabinose, and carbon dioxide is reinvestigated. The …
Molecular and Functional Characterisation of Hemocyanin of the Giant African Millipede Archispirostreptus gigas
2013
SummaryIn contrast to other terrestrial arthropods where gaseous O2 that fuels aerobic metabolism diffuses to the tissues in tracheal tubes, and most other metazoans where O2 is transported to tissues by circulating respiratory proteins, the myriapods (millipedes and centipedes) strikingly have tracheal systems as well as circulating hemocyanin (Hc). In order to elucidate the evolutionary origin and biological significance of millipede Hc we report the molecular structure (subunit composition and amino acid sequence) of multimeric (36-mer) Hc from the forest-floor dwelling giant African millipede Archispirostreptus gigas and its allosteric oxygen binding properties under various physico-che…