scholarly journals Modification of the Corrosion Properties of a Model Fe-8Ni-18Cr Steel Resulting from Plastic Deformation and Evaluated by Impedance Spectroscopy

2012 ◽  
Vol 2012 ◽  
pp. 1-6
Author(s):  
Pierre-Yves Girardin ◽  
Adrien Frigerio ◽  
Patrice Berthod
Keyword(s):  
Plastic Deformation ◽  
Impedance Spectroscopy ◽  
Corrosion Behaviour ◽  
Charge Transfer Resistance ◽  
Compression Tests ◽  
Corrosion Properties ◽  
Transfer Resistance ◽  
Minor Elements ◽  
Cylindrical Parts

A model {minor elements}-free Fe-8Ni-18Cr alloy (wt%) was elaborated by foundry, then cut in several cylindrical parts which were subjected to compression tests leading to different plastic deformation rates. The axis surface of the obtained samples were characterized in corrosion by impedance spectroscopy in an acid sulphuric solution. The obtained EIS results were plotted in the complex plan of Nyquist and the diagrams were all semicircular but with an average radius decreasing when the deformation rate increased. The plastic deformation obviously induced a decrease in charge transfer resistance, revealing a detrimental effect of the corrosion behaviour as the most often reported in studies involving stationary methods of electrochemical characterization of corrosion. It was also found that the capacitance tends to increase with the rate of plastic deformation by compression.

Corrosion of Ni-Al and Ni-Al-Al2O3 Plasma Sprayed Coatings in 0.01 M H2SO4 and 3.5% NaCl Solutions

2013 ◽  
Vol 199 ◽  
pp. 390-395
Author(s):  
Robert Starosta
Keyword(s):  
Impedance Spectroscopy ◽  
Current Density ◽  
Corrosion Current Density ◽  
Corrosion Potential ◽  
Composite Coatings ◽  
Corrosion Current ◽  
Charge Transfer Resistance ◽  
Al Alloy ◽  
Corrosion Properties ◽  
Transfer Resistance

In the paper researches results of corrosion properties of Ni-Al alloy and Ni-Al-Al2O3 composite coatings were presented. Coatings were obtained by plasma torch. The studies in 0.01 M H2SO4 and 3.5 NaCl environments were realized. Measurements were made following methods: polarization and impedance spectroscopy. Rated coatings are more resistant to the 3.5% NaCl environment than the 0.01 M H2SO4. Corrosion current density for alloy coatings in artificial seawater was 19 μΑ/cm2 and 28 μA/cm2 environment acidic. Impedance spectroscopy studies showed that the alloy and composite coatings are characterized by greater charge transfer resistance in sodium chloride solution than in sulfuric acid solution. The value of corrosion potential in an environment of 3.5% NaCl is about 300 mV lower than 0.01 M H2SO4. Composite coatings Ni-Al-Al2O3 were characterized by a higher corrosion current densities and increased resistance than Ni-Al coatings in 0.01 M H2SO4 solution. It is related to the porosity of composite coatings. It was found little effect of oxide phase participation on corrosion current density and corrosion potential in 3.5% NaCl environment.

scholarly journals Corrosion and Electrochemical Impedance Spectroscopy of Thin TiALN and TiCN PVD Coatings for Protection of Ballast Water Screen Filters

2021 ◽  
Vol 58 (2) ◽  
pp. 64-78
Author(s):  
R. Kalnina ◽  
V. Priednieks ◽  
K. Lukins ◽  
A. Gasparjans ◽  
A. Rijkure
Keyword(s):  
Stainless Steel ◽  
Electrochemical Impedance Spectroscopy ◽  
Impedance Spectroscopy ◽  
Surface Passivation ◽  
Electrochemical Impedance ◽  
Protective Coatings ◽  
Corrosion Behaviour ◽  
Charge Transfer Resistance ◽  
Transfer Resistance ◽  
Ticn Coating

Abstract The electrochemical impedance spectroscopy (EIS) and corrosion behaviour of physical vapour deposited (PVD) TiAlN and TiCN coatings of 50 µm mesh shaped AISI 316 stainless steel were estimated under simulated marine conditions (3.5 wt. % NaCl solution). The coatings were prepared by creating adhesive Cr-CrN interlayer with the thickness of about 0.3 µm. The obtained thicknesses of produced coatings were measured to be in a range between 2 and 3.5 µm. The presence of protective coatings leads to corrosion potential (Ecorr ) shifting to more positive values as compared to the bare stainless steel. This effect indicates higher protection efficiency of coated steel under marine conditions. The protective behaviour of produced coating leads to the decreased corrosion current density (jcorr ) by indicating up to 40-fold higher polarization resistance as compared to resistance of the naturally formed oxide layer over the stainless steel. The Nyquist and Bode plots were obtained with the help of EIS measurements by applying alternating potential amplitude of 10 mV on observed Ecorr . The obtained plots were fitted by appropriate equivalent circuits to calculate pore resistance, charge transfer resistance and capacitance. The present study reveals that pore resistance was the highest in the case of TiCN coating (Rpore =3.22 kΩ·cm2). The increase in duration of the immersion up to 24 h leads to change in the capacitive behaviour of the coatings caused by the penetration of the aqueous solution into pore system of TiCN coating with low wettability and surface passivation of reactive TiAlN coating. The presence of defects was confirmed by examining the obtained samples with the help of the scanning electron microscope.

scholarly journals Deciphering the Disaggregation Mechanism of Amyloid Beta Aggregate by 4-(2-Hydroxyethyl)-1-Piperazinepropanesulfonic Acid Using Electrochemical Impedance Spectroscopy

Sensors ◽  
2021 ◽  
Vol 21 (3) ◽  
pp. 788
Author(s):  
Hien T. Ngoc Le ◽  
Sungbo Cho
Keyword(s):  
Electrochemical Impedance Spectroscopy ◽  
Impedance Spectroscopy ◽  
Electrochemical Impedance ◽  
Specific Binding ◽  
Amyloid Β ◽  
Electrochemical Measurement ◽  
Charge Transfer Resistance ◽  
Chemical Agent ◽  
Transfer Resistance ◽  
K Value

Aggregation of amyloid-β (aβ) peptides into toxic oligomers, fibrils, and plaques is central in the molecular pathogenesis of Alzheimer’s disease (AD) and is the primary focus of AD diagnostics. Disaggregation or elimination of toxic aβ aggregates in patients is important for delaying the progression of neurodegenerative disorders in AD. Recently, 4-(2-hydroxyethyl)-1-piperazinepropanesulfonic acid (EPPS) was introduced as a chemical agent that binds with toxic aβ aggregates and transforms them into monomers to reduce the negative effects of aβ aggregates in the brain. However, the mechanism of aβ disaggregation by EPPS has not yet been completely clarified. In this study, an electrochemical impedimetric immunosensor for aβ diagnostics was developed by immobilizing a specific anti-amyloid-β (aβ) antibody onto a self-assembled monolayer functionalized with a new interdigitated chain-shaped electrode (anti-aβ/SAM/ICE). To investigate the ability of EPPS in recognizing AD by extricating aβ aggregation, commercially available aβ aggregates (aβagg) were used. Electrochemical impedance spectroscopy was used to probe the changes in charge transfer resistance (Rct) of the immunosensor after the specific binding of biosensor with aβagg. The subsequent incubation of the aβagg complex with a specific concentration of EPPS at different time intervals divulged AD progression. The decline in the Rct of the immunosensor started at 10 min of EPPS incubation and continued to decrease gradually from 20 min, indicating that the accumulation of aβagg on the surface of the anti-aβ/SAM/ICE sensor has been extricated. Here, the kinetic disaggregation rate k value of aβagg was found to be 0.038. This innovative study using electrochemical measurement to investigate the mechanism of aβagg disaggregation by EPPS could provide a new perspective in monitoring the disaggregation periods of aβagg from oligomeric to monomeric form, and then support for the prediction and handling AD symptoms at different stages after treatment by a drug, EPPS.

scholarly journals INFLUENCE OF A PREFABRICATED-CROWN ROLLING PROCESS ON THE CORROSION BEHAVIOUR OF AZ31 MAGNESIUM ALLOY

2021 ◽  
Vol 55 (4) ◽  
Author(s):  
Zhiquan Huang ◽  
Jinchao Zou ◽  
Junpeng Wang ◽  
Yanjie Pei ◽  
Renyao Huang ◽  
...  
Keyword(s):  
Magnesium Alloy ◽  
Corrosion Behavior ◽  
Electrochemical Impedance ◽  
Corrosion Behaviour ◽  
Plate Thickness ◽  
Az31 Alloy ◽  
Rolling Process ◽  
Charge Transfer Resistance ◽  
Az31 Magnesium Alloy ◽  
Transfer Resistance

The present study aims to investigate the effect of a prefabricated-crown rolling process on the corrosion characteristic of the AZ31 magnesium alloy. Specimens made of the AZ31 alloy were rolled under various crown conditions, and their microstructure evolution and corrosion behavior were analyzed. The corrosion behavior was studied using potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). The results showed that the corrosion-current density of the AZ31 alloy with a side pressure of 37.5 % of the plate thickness of the precast convexity decreased from 3.79 × 10–6 A/cm2 to 1.80 × 10–6 A/cm2, and the difference between the edge and the middle of the AZ31 alloy was shortened from 2.05 × 10–6 A/cm2 to 1.14 × 10–6 A/cm2. The charge-transfer resistance also increased from 507.1 Ω·cm2 to 581.2 Ω·cm2. The improvement in the corrosion resistance is a result of the more stable corrosion products and microstructure refinement formed after the prefabricated-crown rolling process.

scholarly journals Investigation of Temperature and Aging Effects in Nanostructured Dye Solar Cells Studied by Electrochemical Impedance Spectroscopy

2009 ◽  
Vol 2009 ◽  
pp. 1-15 ◽  
Author(s):  
Minna Toivola ◽  
Janne Halme ◽  
Lauri Peltokorpi ◽  
Peter Lund
Keyword(s):  
Solar Cells ◽  
Electrochemical Impedance Spectroscopy ◽  
Impedance Spectroscopy ◽  
Electrochemical Impedance ◽  
Charge Transfer Resistance ◽  
Aging Effects ◽  
Transfer Resistance ◽  
Deterioration Rate ◽  
Dye Solar Cells ◽  
Effects Of Aging

Effects of aging and cyclically varying temperature on the electrical parameters of dye solar cells were analyzed with electrochemical impedance spectroscopy. Photoelectrode total resistance increased as a function of time due to increasing electron transport resistance in theTiO2film. On the other hand, photoelectrode recombination resistance was generally larger, electron lifetimes in theTiO2were film longer, and charge transfer resistance on the counter electrode was smaller after the temperature treatments than before them. These effects correlated with the slower deterioration rate of the temperature-treated cells, in comparison to the reference cells.

scholarly journals Electrochemical, Structural and Morphological Characterization of Hydrothermally Fabricated Binary Palladium Alloys PdCo and PdNi

Metals ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 796
Author(s):  
Edson Meyer ◽  
Raymond Taziwa ◽  
Dorcas Mutukwa ◽  
Nyengerai Zingwe
Keyword(s):  
Solar Cells ◽  
Charge Transfer ◽  
Binary Alloys ◽  
Dye Sensitized Solar Cells ◽  
Charge Transfer Resistance ◽  
Palladium Alloys ◽  
Transfer Resistance ◽  
Dye Sensitized ◽  
Sensitized Solar Cells

This article details the development and characterization of binary palladium alloys synthesized via a hydrothermal process. Palladium alloys, being good redox catalysts, could potentially replace platinum in many applications such as in dye sensitized solar cells, capacitors and vehicular catalytic converters where platinum is vital for maximum productivity. A good replacement should be cheap, readily available and be able to offer comparable catalytic activity to that of platinum. As such we hereby attempt to hydrothermally fabricate and characterize binary palladium alloys PdNi and PdCo that could be ideal replacements for platinum. XRD analysis of the as-synthesized binary alloys revealed the existence of only palladium peaks at 2θ values of 40.1°, 46.7°, 68.1°, 82.1° and 86.6°, indicative of the successful formation of the binary alloys. SEM micrographs revealed that both alloys consisted of spherical particles with PdCo agglomerating to an extent, whereas PdNi was widely distributed, thus it could enhance electrolyte adsorption during catalytic reduction reactions. Cyclic voltammetry analysis at 50 mV∙s−1 revealed that PdNi is more electrocatalytically active with a reduction current density of 41 mA∙cm−2 compared to 18 mA∙cm−2 for PdCo. Lower charge transfer resistance from electrochemical impedance spectroscopy confirmed the superior catalytic ability of PdNi. The two palladium alloys also produced maximum specific capacitances of 68 and 27 F∙g−1 for PdNi and PdCo respectively. Analysis of the sample stability yielded coulombic efficiency retention of 98.7 and 97% for PdNi and PdCo respectively after 1000 cycles. Results obtained have shown that the palladium alloys with their low charge transfer resistance could be ideal replacements for platinum in dye sensitized solar cells. Modest specific capacitance for PdNi illustrates its potential as an electrode catalyst in capacitors.

scholarly journals Yeast Propagation Control: Low Frequency Electrochemical Impedance Spectroscopy as an Alternative for Cell Counting Chambers in Brewery Applications

Chemosensors ◽  
2020 ◽  
Vol 8 (2) ◽  
pp. 27
Author(s):  
Georg Christoph Brunauer ◽  
Oliver Spadiut ◽  
Alfred Gruber ◽  
Christoph Slouka
Keyword(s):  
Electrochemical Impedance Spectroscopy ◽  
Impedance Spectroscopy ◽  
Pathogen Detection ◽  
Electrochemical Impedance ◽  
Low Frequency ◽  
Charge Transfer Resistance ◽  
Cell Counting ◽  
Delayed Response ◽  
Transfer Resistance ◽  
Cell Counts

Electrochemical impedance spectroscopy is a powerful tool in life science for cell and pathogen detection, as well as for cell counting. The measurement principles and techniques using impedance spectroscopy are highly diverse. Differences can be found in used frequency range (β or α regime), analyzed quantities, like charge transfer resistance, dielectric permittivity of double layer capacitance and in off- or online usage. In recent contributions, applications of low-frequency impedance spectroscopy in the α regime were tested for determination of cell counts and metabolic burden in Escherichia coli and Saccharomyces cerevisiae. The established easy to use methods showed reasonable potential in the lab scale, especially for S. cerevisiae. However, until now, measurements for cell counts in food science are generally based on Thoma cell counting chambers. These microscopic cell counting methods decelerate an easy and quick prediction of yeast viability, as they are labor intensive and result in a time delayed response signal. In this contribution we tested our developed method using low frequency impedance spectroscopy locally at an industrial brewery propagation site and compared results to classic cell counting procedures.

scholarly journals Electrochemical Impedance Spectroscopy on the Performance Degradation of LiFePO4/Graphite Lithium-Ion Battery Due to Charge-Discharge Cycling under Different C-Rates

Energies ◽  
2019 ◽  
Vol 12 (23) ◽  
pp. 4507 ◽  
Author(s):  
Yusuke Abe ◽  
Natsuki Hori ◽  
Seiji Kumagai
Keyword(s):  
Charge Transfer ◽  
Electrochemical Impedance Spectroscopy ◽  
Impedance Spectroscopy ◽  
Electrochemical Impedance ◽  
Specific Capacity ◽  
Lithium Ion ◽  
Performance Degradation ◽  
Charge Transfer Resistance ◽  
Transfer Resistance ◽  
Charge Discharge

Lithium-ion batteries (LIBs) using a LiFePO4 cathode and graphite anode were assembled in coin cell form and subjected to 1000 charge-discharge cycles at 1, 2, and 5 C at 25 °C. The performance degradation of the LIB cells under different C-rates was analyzed by electrochemical impedance spectroscopy (EIS) and scanning electron microscopy. The most severe degradation occurred at 2 C while degradation was mitigated at the highest C-rate of 5 C. EIS data of the equivalent circuit model provided information on the changes in the internal resistance. The charge-transfer resistance within all the cells increased after the cycle test, with the cell cycled at 2 C presenting the greatest increment in the charge-transfer resistance. Agglomerates were observed on the graphite anodes of the cells cycled at 2 and 5 C; these were more abundantly produced in the former cell. The lower degradation of the cell cycled at 5 C was attributed to the lowered capacity utilization of the anode. The larger cell voltage drop caused by the increased C-rate reduced the electrode potential variation allocated to the net electrochemical reactions, contributing to the charge-discharge specific capacity of the cells.

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