Synthesis and properties of platinum metal oxides of the type MxPt3O4

1982 ◽  
Vol 21 (9) ◽  
pp. 3372-3382 ◽  
Author(s):  
R. D. Shannon ◽  
T. E. Gier ◽  
P. F. Carcia ◽  
P. E. Bierstedt ◽  
R. B. Flippen ◽  
...  
Keyword(s):  
1994 ◽  
Vol 353 ◽  
Author(s):  
Masayosi Uno ◽  
Youji Kadotani ◽  
Chie Miyake ◽  
Misato Horie

AbstractThe reducing reactions of platinum metal oxides and the formation of the complex oxides were studied to estimate the process at high temperatures. Heat treatment of Re207 with TiN causes reduction up to the sublimation point of Re207 and exhibits the highest value of the recovery among the reducing agents used in the present study. Reducing reactions of the platinum metal oxides with the reducing agents lower the melting temperature. The simplified complex oxides contain the complex oxides of the representative elements of FP and the metallic elements of the reducing agents, which contribute to a decrease of melting temperature, neodymium zirconium oxides and neodymium barium oxide which may transform to the other phases during heating. Uranium may dissolve in the phases in which uranium is identified by EPMA but cannot detected by X-ray diffraction.


2020 ◽  
Vol 14 (4) ◽  
pp. 1479-1488
Author(s):  
Lemeyonouin Aliou Guillaume Pohan ◽  
Ollo Kambiré ◽  
Mohamed Berté ◽  
Lassiné Ouattara

Pt, IrO2, RuO2, Pt-IrO2 and Pt-RuO2 electrodes have been shown to be effective in their application in various fields. However, it is necessary to study their long-term stability. So, our objective is to prepare them and study their lifetime using intensiostatic measurement. Then they were prepared at 400 °C on titanium plates used as a substrate. Physical measurements (scanning electron microscopy) of these anodes revealed that their surface are rough and porous structures. Lifetime study was carried out in H2SO4 9 N and under a current density of 410 mA /cm2. The long-term stability of Pt improved when coupled to IrO2 in contrast to RuO2. From this study, the performance of the electrode was found to increase in the order: RuO2 < Pt-RuO2 < Pt < Pt-IrO2 < IrO2. For RuO2 and IrO2 pure electrodes, the deactivation would be due to the dissolution of precursors deposited on the titanium. For the Pt pure electrode, deactivation would be due to the detachment of platinum coating. The deactivation of the Pt-IrO2 and Pt-RuO2 electrode would be due, on the one hand to the platinum detachment from IrO2 or RuO2 and on the other hand to the metal oxides (IrO2 or RuO2) dissolution.Keywords: Electrodes, platinum, metal oxides, lifetime.


2018 ◽  
Vol 2018 ◽  
pp. 1-6 ◽  
Author(s):  
Sebastian Chalupczok ◽  
Peter Kurzweil ◽  
Helmut Hartmann

The voltammetric response of platinum metal oxides is discussed with respect to novel pH sensors combining both miniaturization and stability. For practical applications in solutions of any kind, for example, in tap water and in domestic sewage, various interferences must be considered, such as chloride and reducing agents. This work clarifies the voltammetric behavior of RuO2 electrodes in solutions of different pH values and ionic strengths.


1982 ◽  
Vol 13 (50) ◽  
Author(s):  
R. D. SHANNON ◽  
T. E. GIER ◽  
P. F. CARCIA ◽  
P. E. BIERSTEDT ◽  
R. B. FLIPPEN ◽  
...  
Keyword(s):  

Author(s):  
R. Ai ◽  
H.-J. Fan ◽  
L. D. Marks

It has been known for a long time that electron irradiation induces damage in maximal valence transition metal oxides such as TiO2, V2O5, and WO3, of which transition metal ions have an empty d-shell. This type of damage is excited by electronic transition and can be explained by the Knoteck-Feibelman mechanism (K-F mechanism). Although the K-F mechanism predicts that no damage should occur in transition metal oxides of which the transition metal ions have a partially filled d-shell, namely submaximal valence transition metal oxides, our recent study on ReO3 shows that submaximal valence transition metal oxides undergo damage during electron irradiation.ReO3 has a nearly cubic structure and contains a single unit in its cell: a = 3.73 Å, and α = 89°34'. TEM specimens were prepared by depositing dry powders onto a holey carbon film supported on a copper grid. Specimens were examined in Hitachi H-9000 and UHV H-9000 electron microscopes both operated at 300 keV accelerating voltage. The electron beam flux was maintained at about 10 A/cm2 during the observation.


Author(s):  
Michel Fialin ◽  
Guy Rémond

Oxygen-bearing minerals are generally strong insulators (e.g. silicates), or if not (e.g. transition metal oxides), they are included within a rock matrix which electrically isolates them from the sample holder contacts. In this respect, a thin carbon layer (150 Å in our laboratory) is evaporated on the sections in order to restore the conductivity. For silicates, overestimated oxygen concentrations are usually noted when transition metal oxides are used as standards. These trends corroborate the results of Bastin and Heijligers on MgO, Al2O3 and SiO2. According to our experiments, these errors are independent of the accelerating voltage used (fig.l).Owing to the low density of preexisting defects within the Al2O3 single-crystal, no significant charge buildup occurs under irradiation at low accelerating voltage (< 10keV). As a consequence, neither beam instabilities, due to electrical discharges within the excited volume, nor losses of energy for beam electrons before striking the sample, due to the presence of the electrostatic charge-induced potential, are noted : measurements from both coated and uncoated samples give comparable results which demonstrates that the carbon coating is not the cause of the observed errors.


1977 ◽  
Vol 38 (C1) ◽  
pp. C1-333-C1-336 ◽  
Author(s):  
P. CAVALLOTTI ◽  
R. ROBERTI ◽  
G. CAIRONI ◽  
G. ASTI

2014 ◽  
Vol 59 (4) ◽  
pp. 401-404
Author(s):  
G.S. Dragan ◽  
◽  
K.V. Kolesnikov ◽  
V.M. Ulianytskyi ◽  
◽  
...  

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