ABSTRACT
In the paper, the mechanism of the process of the Rh(III) ions adsorption on activated carbon ORGANOSORB 10-AA was investigated. It was shown, that the process is reversible, i.e., stripping of Rh(III) ions from activated carbon to the solution is also possible. This opens the possibility of industrial recovery of Rh (III) ions from highly dilute aqueous solutions. The activation energies for the forward and backward reaction were determined These are equal to c.a. 7 and 0 kJ/mol. respectively. Unfortunately, the efficiency of this process was low. Obtained maximum load of Rh(III) was equal to 1.13 mg per 1 g of activated carbon.
ABSTRACT
In this paper, a novel method for the synthesis of Pt nanoparticles (PtNPs) using a microwave autoclave reactor is proposed. For benchmarking, the obtained results are compared with the traditional, batch method. A novel process window is proposed, which is the application of high-temperature and high-pressure. The main finding is that this only brings advantage, when the ionic strength of the system is enough low. It is explained, that at high pressure and high temperature, water behaves like only a slightly polar solvent, approaching a subcritical state. This reduces the electrostatic stabilization of the particles. Moreover, a change in the Pt particle shape is observed under high pressure and temperature conditions, suggesting that additional physical-chemical processes are involved.
ABSTRACT
The objective of this work was to test vanadium isopolyoxoanions as potential corrosion inhibitors of the intermetallic phase Al2Cu in sulfuric acid solutions at pH = 1.3 and 2.5. The intermetallic was melted in an electric arc furnace. Its phase composition was confirmed using X-ray diffraction, light microscopy, and differential scanning calorimetry. Then Al2Cu corrosion kinetics was studied. Chemical composition of the solution after corrosion was determined using inductively coupled plasma-optical emission spectroscopy. The surface of corroded specimens was analyzed using scanning electron microscopy and X-ray photoelectron spectroscopy. Subsequent electrochemical studies involved determination of open-circuit potential, electrochemical impedance spectra, and polarization curves. It was found that the Al2Cu phase corrodes selectively and vanadium isopolyoxoanions increase this process both at pH = 1.3 and 2.5 with two exceptions. Corrosion inhibition was observed for 100 and 200 mM of Na3VO4 at pH 1.3, with inhibition efficiency 78% and 62% respectively, due to precipitation of V2O5.
ABSTRACT
The objective of this work was to establish the influence of sodium molybdate on the corrosion kinetics of 7075 aluminium alloy in orthophosphoric acid aqueous solution. Corrosion rate was decreased from 75.98 to 3.24 g per m2 per day. The mechanism of corrosion inhibition was studied using scanning electron microscopy, X-ray photoelectron spectroscopy, UV-Vis spectrophotometry and electrochemical impedance spectroscopy. It was revealed that heteropolyoxomolybdate species act as the corrosion inhibitor. They adsorb onto the surface and inhibit an anodic process. Their influence on a cathodic process is much weaker. Phosphomolybdenum blue species do not inhibit corrosion process and their formation is undesirable.
ABSTRACT
In the presented work the photoelectrochemical properties of SbSI along with the electronic structure (i.e. conduction and valence band edge potentials as well as conductivity type) of sonochemically obtained nanowires are discussed for the first time. The spectroscopic investigations indicate interesting optical properties, including surface isotope effect and excitonic emission. The photoelectrochemical investigation of SbSI revealed the occurrence of the photoelectrochemical photocurrent switching effect. It may be defined as a change in photocurrent direction (generated at the illuminated semiconducting electrode immersed in electrolyte) due to an appropriate polarization of the electrode versus the reference electrode. It is often observed for semiconductors as a result of the reduction of molecular oxygen dissolved in the electrolyte. However, in the case of SbSI, the photocurrent switching was recorded regardless of the presence of molecular oxygen in the electrolyte, probably due to the reduction of triiodide species formed at anodic polarization of the SbSI electrode, in an iodide-containing electrolyte. The switching potential (i.e. the potential where anodic-to-cathodic photocurrent transition occurs) equals to ca. 0.4 V versus standard hydrogen electrode, which is close to the formal potential of the I(-)/I3(-) redox couple. Therefore, this semiconducting material is of potential interest for the construction of new photovoltaic systems, novel optoelectronic switches and logic devices.
ABSTRACT
BixLa1-xVO4 solid solutions were obtained in the form of fine powder via a microwave-assisted hydrothermal route. The presence of a solid solution in the studied system was confirmed using X-ray diffraction (XRD) and optical spectroscopy techniques. Pure BiVO4 and LaVO4 were obtained in the monoclinic form, whereas solid solutions in the tetragonal, zircon-type structure. The optical band gap dependence on the composition of the solid solution is parabolic, thus there is a possibility to tune this parameter in a wide concentration range, from 2.4 to 4.0 eV. An absorption coefficient maximum is also concentration-dependent, possibly, due to the structural disorder of the samples. Solid solutions with Bi(3+) concentration between 11.94 and 32.57 at.% exhibit intense, green luminescence. This indicates the presence of Bi-originated electronic states within the band gap. The value of the conduction band edge potential, measured by both electrochemical impedance spectroscopy and work function measurements, is concentration-independent. Moreover, solid solutions exhibit a photoelectrochemical photocurrent switching effect, thus they may be promising materials for molecular electronics and as dioxygen activators.
