Search results for "Oxide"
showing 10 items of 6424 documents
Electrochemical reduction of graphene oxide films in aqueous and organic solutions
2013
Abstract Electrochemical reduction of graphene oxide (GO) films cast on tin oxide glass substrates were carried out in aqueous solutions and in propylene carbonate and acetonitrile. Cyclic voltammetric measurements indicate successful reduction of GO films. The reduction process begins in aqueous solutions at less negative potentials than in organic solutions. Additionally the pH value of the aqueous solutions influences the reduction potential. According to spectroscopic analysis the reduction process of the GO film can be controlled by the choice of reduction potential and electrolyte medium. The potential window in this work was made broader by increasing pH or by using organic electroly…
Expanding the atrane route: Generalized surfactant-free synthesis of mesoporous nanoparticulated xerogels
2008
Abstract A diversity of silica-based and non-silica nanoparticulated mesoporous xerogels have been synthesized from aqueous solution using a surfactant-free strategy, and starting from molecular atrane complexes as precursors. This approach constitutes an extension of the “atrane route” previously described for the surfactant-assisted synthesis of mesoporous materials, and allows us to unify the multiplicity of protocols described for the preparation of conventional xerogels. In fact, we have used exactly the same preparative conditions for obtaining all the compositions reported here. The xerogels synthesized in this way include pure silica (UVM-11), aluminosilicates and titanosilicates (M…
Solid-State Electrochemical Method for Determining Core and Shell Size in Pd@PdO Nanoparticles
2010
Electrochemical characterization of palladium nanoparticles surrounded by a palladium oxide shell (Pd@PdO) is described from a combination of voltammetry plus electrochemical quartz crystal microbalance experiments at nanoparticle deposits on graphite electrodes in contact with aqueous H2SO4 and NaOH solutions. A method for determining the metal core size and oxide shell thickness of the Pd@PdO nanoparticles, based on a combination of conventional voltammetry of nanoparticles in DMSO solution and voltammetry of nanoparticle deposits in contact with 0.10 M aqueous NaOH solution, is described.
Original Supercritical Water Device for Continuous Production of Nanopowders
2011
Well-crystallized ZnO, ZrO2, TiO2, CeO2, Y2O3 and La2O3 nanoparticles are synthesized under supercritical water conditions (T > 647 K and P > 22.1 MPa) using a home-made continuous process. At room temperature, metallic salts with or without aqueous hydroxide solution (KOH or NaOH) are pressurized to 25–30 MPa. Then, the reactant(s) is/are rapidly heated to 673–773 K by mixing with the supercritical water in a patented reactor. Residence time is in the range from 2 to 8 s. XRD, TEM and surface area analyses highlight the production of pure and well-crystallized nanoparticles with a uniform size distribution.
Micellization and Micellar Structure of a Poly(ethylene oxide)/Poly(propylene oxide)/Poly(ethylene oxide) Triblock Copolymer in Water Solution, As St…
1997
The micellization of the triblock copolymer Pluronic P85 (poly(oxyethylene)27/poly(oxypropylene)39/poly(oxyethylene)27) in aqueous solution was followed vs temperature and addition of aliphatic alcohols, using the spin probe technique. Different types of probes properly chosen (spin-labeled (SL) poly(oxyethylene(4))nonylphenol, SL-Pluronic L62, TEMPO-laurate, TEMPO-hexanoate, CAT 4, CAT 8, CAT 11, CAT 16, and 5-, 7-, 10-, and 12-doxylstearic acids) provided information about the micellar structure (polarity, viscosity, and order degree) at different radial locations. Micellization was found to be low at room temperature, even for 10% aqueous solutions, but strongly increasing with temperatu…
Functionalization of Crosslinked Vesicles by Co-Self-Assembly of a Gelable Diblock Copolymer and Mercaptosilane
2008
Herein, a convenient and general method to simultaneously fix and functionalize polymeric vesicles with sulphydryl groups by the co-self-assembly of poly(ethylene oxide)-block-poly[3-(triethoxysilyl)propyl methacrylate] (PEO-b-PTESPMA) and 3-mercaptopropyltrialkoxysilane in an aqueous solution is reported. The presence of sulphydryl groups across the vesicle membrane has been confirmed by using an energy-filtered technique during TEM analysis and by capturing Au nanoparticles.
Double-Shell Vesicles, Strings of Vesicles and Filaments Found in Crosslinked Micellar Solutions of Poly(1,2-butadiene)-block-poly(ethylene oxide) Di…
2001
Micellar structures of amphiphilic poly(1,2-butadiene)-block-poly(ethylene oxide) diblock copolymers have been crosslinked in aqueous solution by γ-irradiation. By transmission electron microscopy (TEM) of neganively stained specimen it is shown that the precominant structures present are sopolymer sesicles (which appear to be double latered. These fived vesules are stable with respect to their share and can be transferred from water into a good solvent for blue filbeks, such as tetrahydrofuran, this demonstrating the effectiveness of the crosslinking. In addition to the resicles a small number of flexible cylindrichl/filimented structures sequentially fused vesicles/strings of vesicles and…
Electrochemical conversion of pressurized CO2 at simple silver-based cathodes in undivided cells: study of the effect of pressure and other operative…
2020
Abstract Electrochemical reduction of pressurized CO2 is proposed as an interesting approach to overcome the main hurdle of the CO2 electrochemical conversion in aqueous solution, its low solubility (ca. 0.033 M), and to achieve good faradaic efficiency in CO using simple sheet silver cathodes and undivided cells, thus lowering the overall costs of the process. The effect on the process of CO2 pressure (1–30 bar), current density, nature of the supporting electrolyte and other operative conditions, such as the surface of the cathode or the mixing rate, was studied to enhance the production of CO. It was shown that pressurized conditions allow to improve drastically the current efficiency o…
Structural Characterization of Zirconia Nanoparticles Prepared by Microwave-Hydrothermal Synthesis
2009
Nanocrystalline zirconia powders have been prepared by microwave-hydrothermal synthesis starting from aqueous solution of ZrOCl2·8H2O. Results of investigations on the aqueous suspension stability of the washed zirconia nanopowders by dynamic light scattering showed that the suspension, constituted by superaggregates of nanoparticles (131 ± 10 nm), was stable up to 15 days. Nanopowders were investigated by means of transmission electron microscopy and small angle x-ray scattering measurements which proved that the zirconia nanopowder is constituted by small primary nanoparticles of ca. 8 nm that agglomerate forming bigger aggregates of 50 ± 1 nm.
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 …