Search results for "Oxidation state"
showing 10 items of 91 documents
Mössbauer Study of Lanthanum–Strontium Ferromanganite Oxides
2004
The La0.88Sr0.2Mn(1−y)Fey0(3±δ, i (LSMF with y = 0, 0.2, 0.5, 0.8, 1) compounds are prospective cathode materials for advanced solid oxide fuel cells (SOFC) application operating at 700° C. Usual analysis methods like thermogravimetric analysis or redox titration enable to determine the average oxidation state of both manganese and iron cations. The comparative role of iron and manganese in B-site was evaluated by 57Fe Mossbauer spectroscopy. Spectra revealed that the complete substitution of iron for manganese induces the formation of Fe5+ for the compound with y = 1. However, no tetravalent iron cation was observed in air for the LSMF compounds with y = 0.2, 0.5 and 0.8. This means that o…
Niobium implantation effects in BaTiO3 and SrTiO3
1992
Abstract Single crystals of BaTiO3 and SrTiO3 have been implanted at room temperature with 150 keV Nb+ ions to doses ranging from 1014 to 1017 ions cm2. The structure and the oxidation state of the damaged layer have been investigated by Rutherford backscattering-ion channeling and electron spectroscopy, respectively. SrTiO3 is rendered amorphous at relatively low doses of 2 × 1015 ions cm−2, but the damage is efficiently annealed at 450°C for 1 2 h. For both materials, the oxidation state of niobium varies from + 5 to + 2 along the depth. Moreover, a considerable chemical shift (2.3 eV) is observed for barium in BaTiO3.
The significance of the order of impregnation on the activity of vanadia promoted palladium-alumina catalysts for propane total oxidation
2011
The increased activity of alumina-supported palladium catalysts promoted with vanadium oxide has been investigated. Three different vanadium promoted Pd/Al2O3 catalysts with the same composition but synthesized employing sequential and co-impregnation were tested for the total oxidation of propane. The order of impregnation was critical to produce high activity catalysts. Vanadium and palladium co-impregnation on the Al2O3 support led to the most active catalyst, whereas the step-wise impregnated catalysts show a catalytic performance similar to or slightly better than unpromoted palladium catalysts. The high activity of the co-impregnated catalysts is related to the particle size and oxida…
Synthesis and properties of new phosphorus-functionalized bithiophene materials
2003
The synthesis and reactivity of the novel dithieno[3,2-b:2',3'-d]-phosphole system and its potential use in polymeric sensory materials was investigated. Due to the nucleophilic nature of the phosphorus atom, these materials were found to be easily tunable. Classical reactions at the phosphorus center were performed to modify the electronic structure of the system and the corresponding changes were detected by UV/Vis and fluorescence spectroscopy. Depending on the oxidation state of the central phosphorus atom or its substitution pattern, the dithieno[3,2-b:2',3'-d]-phospholes show varying wavelengths for absorption and emission allowing to distinguish between different compounds by means o…
Clarification of the oxidation state of cobalt corroles inheterogeneous and homogeneous catalytic reduction of dioxygen
2008
Co(III) corroles were investigated as efficient catalysts for the reduction of dioxygen in the presence of perchloric acid in both heterogeneous and homogeneous systems. The investigated compounds are (5,10,15-tris(pentafluorophenyl)corrole)cobalt (TPFCor)Co, (10-pentafluorophenyl-5,15-dimesitylcorrole)cobalt (F 5PhMes 2Cor)Co, and (5,10,15-trismesitylcorrole)cobalt (Mes 3Cor)Co, all of which contain bulky substituents at the three meso positions of the corrole macrocycle. Cyclic voltammetry and rotating ring-disk electrode voltammetry were used to examine the catalytic activity of the compounds when adsorbed on the surface of a graphite electrode in the presence of 1.0 M perchloric acid, a…
Stoichiometric and kinetic study of the 99Tc-DMSA complex obtained with stannous excess: A possible model for the physico-chemical behaviour of the r…
1982
A stoichiometric and kinetic study was made of the 99mTc-DMSA complex obtained in the presence of large amounts of Sn2+. It is demonstrated that the Tc oxidation state is 3+. It is established that the complex degrades to another one if there is an Sn2+ deficiency. These results were confirmed by spectroscopic and spectrophotometric methods.
Ab initio modelling of oxygen vacancies and protonic defects in La1−xSrxFeO3−δ perovskite solid solutions
2016
Using hybrid density functionals, detailed ab initio calculations were performed for oxygen vacancies and protons in La1−xSrxFeO3−δ perovskite solid solutions which may serve as a cathode material in protonic ceramic fuel cells. The atomic and electronic structures of different configurations of defects and the role of Fe oxidation state are analyzed in detail. The energetics of the reduction and hydration reactions are investigated. The hydration energy is found to be significantly smaller than for Ba(Zr1−xYx)O3−x/2 electrolyte materials, and the role of basicity as one decisive factor is discussed.
A New Procedure for the Lightning Experiment: Mn2O7 and Ethanol
2010
Formation of Mn2O7 and its reaction with ethanol is commonly referred to as “underwater lightnings”. Classic procedures are reviewed, along with their weak points, and physical and chemical properties of dimanganese heptaoxide are shown. A new improved approach is finally presented, safer and easier, and suited for lecturehall activities.
Electrochemical characterization of praseodymia doped zircon. Catalytic effect on the electrochemical reduction of molecular oxygen in polar organic …
2011
The voltammetry of microparticles and scanning electrochemical microscopy methodologies are applied to characterize praseodymium centers in praseodymia-doped zircon (PrxZr(1−y)Si(1−z)O4; y + z = x; 0.02 < x < 0.10) specimens prepared via sol–gel synthetic routes. In contact with aqueous electrolytes, two overlapping Pr-centered cathodic processes, attributable to the Pr (IV) to Pr (III) reduction of Pr centers in different sites are obtained. In water-containing, air-saturated acetone and DMSO solutions as solvent, PrxZr(1−y)Si(1−z)O4 materials produce a significant catalytic effect on the electrochemical reduction of peroxide radical anion electrochemically generated. These electrochemical…
Interface charge density matching as driving force for new mesostructured oxovanadium phosphates with hexagonal structure, [CTA]xVOPO4·zH2O
1999
Hexagonal mesostructured mixed-valence oxovanadium phosphates [CTA]xVOPO4·zH2O, in short ICMUV-2, have been synthesized through a S+I- cooperative mechanism using cationic surfactant (cetyltrimethylammonium, CTAB) rodlike micelles as a template. On the lines of the hypothesis that the driving force leading to the formation of mesostructured solids is the charge density matching at the interface between the supramolecular−organic and supramolecular−inorganic moieties, the self-assembling process between CTA+ micelles and VOPO4q- planar anions can be thought of as consequence of the adequate adjustment of the metal mean oxidation state. X-ray powder diffraction and TEM techniques show that th…