Electrical Transport and Magnetic Properties of Metal/Metal Oxide/Metal Junctions Based on Anodized Metal Oxides

In this paper we present magnetoelectric properties of metal/metal-oxide/metal junctions. We use Ti and Fe as metallic layers separated by the porous metal-oxides of iron or titanium formed with the anodization method. This allowed to prepare double junctions with at least one ferromagnetic layer. Here we show magnetoresistance and current-voltage characteristics of the junctions together with their magnetic characteristics. We found positive or negative magnetoresistance depending on junction composition. We discuss also the nature of differential resistance calculated from I-V characteristics. Our findings show that the strongest influence on observed behaviour has a top metallic layer and the interface between this layer and anodized oxide where strong interatomic diffusion is expected.

Ultrasound-Assisted Synthesis of Nanostructured Oxide Materials

This chapter is focused on the use of high intensity ultrasound for the preparation of nanostructured materials with an emphasis on recent prominent examples of the production of dense or porous metal oxides through sonochemical and ultrasonic spray pyrolysis routes. Sonochemistry enables the synthesis of oxides that are often unachievable by traditional methods or affords known materials with shape, size, and nano/microstructure control under fast reaction conditions. The fundamental principles of acoustic cavitation, as well as the main ultrasonic parameters affecting the cavitation phenomenon, are first summarized. Next, the applications of ultrasound in the synthesis of nanostructured oxide materials following both preparation methods are reviewed. Particular focus is given to the ultrasound-assisted synthesis of metal oxide nanoparticles for energy applications.

Catalyst Performance Studies on the Guerbet Reaction in a Continuous Flow Reactor Using Mono- and Bi-Metallic Cu-Ni Porous Metal Oxides

Higher alcohols like 1-butanol are considered important biofuels with superior properties compared to the more readily available bio-ethanol. An attractive route to prepare 1-butanol from ethanol is the Guerbet reaction. We here report the use of hydrotalcite-derived mono- (Cu-PMO or Ni-PMO) and bi-metallic (CuNi-PMO) porous metal oxide catalysts for the Guerbet coupling of ethanol to 1-butanol in a continuous flow reactor (320 °C, 0.1 MPa, LHSV = 15 mL g−1 h−1) at extended times on stream (~160 h). Two distinct regimes with different product distributions were observed for the Cu-PMO and CuNi-PMO catalyst with time on stream. At the start of the run, the initial conversion of ethanol dropped from about 85% to less than 20% after 60 h and acetaldehyde was the main product (regime 1). At prolonged times on stream (60–160 h), fairly constant low conversions of ethanol (14%) were observed and 1-butanol was the main product (regime 2). Performance of the monometallic Cu-PMO catalyst in terms of 1-butanol yield and stability was lower compared to the bi-metallic CuNi-PMO. Detailed catalyst characterization studies (XRD, H2-TPR, sorption of acrylic acid, TGA, TEM, HAADF-STEM, and EDS mapping) on both fresh and spent CuNi-PMO taken at various times on stream was performed to determine the changes in catalyst morphology and composition during a run, and particularly to obtain information on changes in catalyst structure operating in regime 1 or 2. The change in chemoselectivity is in line with an increase in basicity of the catalyst at extended runtimes.

Supercritical methanol depolymerization and hydrodeoxygenation of pyrolytic lignin over reduced copper porous metal oxides

Supercritical methanol depolymerization and hydrodeoxygenation (SCM-DHDO) is a process to produce fuel from biomass with supercritical methanol and CuMgAlOx catalyst.

Supercritical methanol depolymerization and hydrodeoxygenation of lignin and biomass over reduced copper porous metal oxides

Supercritical methanol upgrading with a CuMgAlOx catalyst is effective at depolymerizing and hydrodeoxygenating lignin into monomers and oligomers.