Effects of Potential Range and Sweep Rate on Dissolution of Platinum under Potential Cycling in 0.5 M H2SO4 Solution

2019 ◽  
Vol 16 (24) ◽  
pp. 117-123 ◽  
Author(s):  
Yuu Sugawara ◽  
Amar P. Yadav ◽  
Atsushi Nishikata ◽  
Tooru Tsuru

1988 ◽  
Vol 66 (9) ◽  
pp. 2259-2267 ◽  
Author(s):  
Sara Alfonsina Dora Aldabe De Bilmes ◽  
María Cristina Giordano ◽  
Alejandro Jorge Arvia

The voltammetric stabilization of electrofaceted (100)-type Pt electrodes prepared from polycrystalline Pt by fast repetitive triangular potential cycling are followed by conventional voltammetry in the H-electroadsorption/electrodesorption potential range in either 1 M H2SO4 (0 to 35 °C) or 0.5 M HClO4 (−2 to 35 °C). The influence of CO adsorption on the stabilized voltammetric profile is also considered. Depending on the potential cycling used in conventional voltammetry, two well-defined stabilized profiles at 0.1 V/s in the H-electroadsorption/electrodesorption range can be obtained, namely, that corresponding to the H-adsorption stabilized electrofaceted (100)-type Pt, and that related to the O-adsorption stabilized electrofaceted (100)-type Pt.The changes in the conventional voltammetric profiles can be interpreted in terms of surface modifications basically associated with either adsorption or electroadsorption processes. The influence of the anion (electrolyte composition) prevailing in solution is accounted for in terms of a competitive adsorption between anions and H-adatoms. The influence of temperature in the range covered by this work is smaller than that of the structure of the solution at the electrode/solution interface.


1999 ◽  
Vol 1 (3) ◽  
pp. 143-145 ◽  
Author(s):  
K. Hansongnern ◽  
P. Chooto ◽  
P. Amornpitoksuk

Violanthrone is an anthraquinone vat dye, which is resistant to photochemical damage. Most previous work has concentrated on its chemiluminescence properties. In this report, electrogenerated chemiluminescence (ECL) of violanthrone has been investigated in dimethyl sulfoxide with 0.1M of tetraethylammonium bromide as electrolyte. Violanthrone luminesces in the potential range between 0.0V and-4:0V. At the sweep rate 1000 mV/s, the intensity of the violanthrone ECL is about 2% of that of tris(2,2′-bipyridine) ruthenium(II) ion under the same conditions. It was found that bromine was also produced during the ex- periment, leading to the conclusion that the luminescence arises from the reaction between radical anion of violanthrone and molecular bromine. The mechanism is discussed in detail.


2010 ◽  
Vol 75 (10) ◽  
pp. 1413-1420 ◽  
Author(s):  
Vladimir Panic ◽  
Aleksandar Dekanski ◽  
Vesna Miskovic-Stankovic ◽  
Slobodan Milonjic ◽  
Branislav Nikolic

The electrochemical characteristics of Ti0.6Ir0.4O2/Ti and Ti0.6Ru0.4O2/Ti anodes prepared by the sol-gel procedure from the corresponding oxide sols, obtained by force hydrolysis of the corresponding metal chlorides, were compared. The voltammetric properties in H2SO4 solution indicate that Ti0.6Ir0.4O2/Ti has more pronounced pseudocapacitive characteristics, caused by proton-assisted, solid state surface redox transitions of the oxide. At potentials negative to 0.0 VSCE, this electrode is of poor conductivity and activity, while the voltammetric behavior of the Ti0.6Ru0.4O2/Ti electrode is governed by proton injection/ejection into the oxide structure. The Ti0.6Ir0.4O2/Ti electrode had a higher electrocatalytical activity for oxygen evolution, while the investigated anodes were of similar activity for chlorine evolution. The potential dependence of the impedance characteristics showed that the Ti0.6Ru0.4O2/Ti electrode behaved like a capacitor over a wider potential range than the Ti0.6Ir0.4O2/Ti electrode, with fully-developed pseudocapacitive properties at potentials positive to 0.60 VSCE. However, the impedance characteristics of the Ti0.6Ir0.4O2/Ti electrode changed with increasing potential from resistor-like to capacitor-like behavior.


2005 ◽  
Vol 475-479 ◽  
pp. 3355-3358 ◽  
Author(s):  
Yong Wang Kang ◽  
Chun Gen Zhou ◽  
Sheng Kai Gong ◽  
Hui Bin Xu

Al-Cu-Fe-Cr quasicrystalline coating was deposited on a substrate of stainless steel by low-pressure plasma spraying (LPPS) method. The corrosion behavior of such coating was studied by polarization in 1mol/l H2SO4 and 0.1mol/l NaOH solutions at room temperature. The polarization curve shows that LPPS Al-Cu-Fe-Cr quasicrystalline coating can turn to passive state both in 1mol/l H2SO4 solution and in 0.1mol/l NaOH solution. The corrosion resistance of the coating is poorer than that of bulk quasicrystal in 0.1mol/l NaOH solution. Moreover, in strong acid solution LPPS Al-Cu-Fe-Cr quasicrystalline coating has more corrosion resistance than 1Cr18Ni9Ti in some potential range ranging from -200mVSCE to -35mVSCE, but in strong alkaline solution the corrosion resistance of the coating is poorer than 1Cr18Ni9Ti.


2003 ◽  
Vol 47 (5) ◽  
pp. 51-56 ◽  
Author(s):  
M.S. Gião ◽  
M.I. Montenegro ◽  
M.J. Vieira

The effect of experimental conditions on cyclic voltammetry experiments on platinum electrodes covered with biofilms formed by Pseudomonas fluorescens for 2 hours was investigated. Results show that recycling the potential stabilizes the shape of the cyclic voltammogram after 135 cycles, but the observation of the electrodes by epifluorescence microscopy showed that cells are still adhered to the platinum surface. Some experimental conditions were changed during the electrochemical measurements - sweep rate, pH of the buffer and applied potential range. Some of these parameters had a strong impact on the bacteria that are adhered to the surface, increasing the death and removal in some circumstances.


2006 ◽  
Vol 932 ◽  
Author(s):  
Iva G. Betova ◽  
Martin S. Bojinov ◽  
Jussi Heinonen ◽  
Petri Kinnunen ◽  
Christina Lilja ◽  
...  

ABSTRACTStress corrosion cracking is a potential failure mechanism of the copper canister proposed to be the main corrosion barrier in the Scandinavian design of the final nuclear waste disposal vault. The main target in SCC-oriented research is to determine the limiting values for the critical concentration of harmful species, the potential range in which these species cause SCC and the threshold stress level required for SCC. The present paper attempts to redefine the criteria for SCC susceptibility of copper in acetate solutions through analysis of potentiodynamic curves using both rotating disc and thin plate electrodes insulated on one side. A potential range in which the current densities at a slow sweep rate are lower than those at a fast sweep rate exists for Cu in 0.001 M - 0.1 M acetate. However, the values of the current densities within this range are significantly smaller than those postulated for active anodic dissolution, implying dissolution mediated by a surface film. New criteria for the SCC susceptibility of pure copper in acetate solutions have been formulated through Stern-Geary analysis of the polarisation curves. Several electrochemical characteristics, such as the current density at the positive crossover potential, the ratio between the corrosion current densities determined from the slow and fast sweeps, as well as the anodic current density in a fast sweep show a clear jump for concentrations between 0.01 M and 0.05 M. This, however, cannot yet be considered as an indication of SCC susceptibility at higher acetate concentrations, as evidenced by complementary SSRT tests.


2020 ◽  
Vol 10 (2) ◽  
pp. 138-145
Author(s):  
Sanaa El Aggadi ◽  
Nidae Loudiyi ◽  
Aicha Chadil ◽  
Zoubida El Abbassi ◽  
Abderrahim El Hourch

Electrochemical polymerization of aniline was carried on platinum (Pt) wire electrode in sulfuric acid (H2SO4) solution by cyclic voltammetry using a conventional three-electrode cell at room temperature (20°C). The effects on the electrodeposition of the monomer concentration, anodic potential and potential scan rate are discussed. The conductive layer of emeraldine base polyaniline (Pani) was prepared in this work by repeating potential cycling between -0.24 and 0.9 V/SCE at 50 mV/s in 1 M H2SO4 solution containing 0.1 M aniline monomer.


TAPPI Journal ◽  
2016 ◽  
Vol 15 (7) ◽  
pp. 467-477
Author(s):  
PASI NIEMELAINEN ◽  
MARTTI PULLIAINEN ◽  
JARMO KAHALA ◽  
SAMPO LUUKKAINEN

Black liquor high solids (about 80%) concentrators have often been found to suffer from aggressive corrosion. In particular, the first and second effect bodies are susceptible to corrosion attacks resulting in tube leaks and wall thinning, which limit the availability and lifetime of evaporator lines. Corrosion dynamics and construction materials have been studied extensively within the pulp and paper industry to understand the corrosion process. However, it has been challenging to identify root causes for corrosion, which has limited proactive measures to minimize corrosion damage. Corrosion of the first phase concentrator was studied by defining the potential regions for passive area, stress corrosion cracking, pitting corrosion, and general corrosion. This was achieved by using a technique called polarization scan that reveals ranges for the passive area in which the equipment is naturally protected against corrosion. The open circuit potential, also known as corrosion potential, and linear polarization resistance of the metal were monitored online, which allowed for definition of corrosion risks for stainless steel 304L and duplex stainless steels 2205 and SAF 2906. An online temperature measurement added insight to the analysis. A process diagnostics tool was used to identify root causes of the corrosion attacks. Many of the root causes were related to process conditions triggering corrosion. Once the metal surface was activated, it was difficult to repassivate the metal naturally unless a sufficient potential range was reached.


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