Academic literature on the topic 'Cathodic polarisation'

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Journal articles on the topic "Cathodic polarisation"

1

Arjmand, Farzin, and Annemie Adriaens. "Effect of cathodic polarisation on the corrosion behaviour of 316L stainless steel under static and dynamic conditions." Corrosion Reviews 33, no. 5 (2015): 249–61. http://dx.doi.org/10.1515/corrrev-2015-0023.

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AbstractThe role of cathodic polarisation on the corrosion of 316L stainless steel was investigated under static and dynamic conditions. The results reveal that the applied flow regime during the cathodic polarisation process has a direct effect on the corrosion behaviour of steel. The cathodic polarisation of steel under static conditions increases the oxygen reduction rate and shifts the corrosion potential towards nobler potentials. Under dynamic conditions, depending on the regime of the applied fluid flow during cathodic and anodic polarisation, the oxygen reduction rate can increase, causing the corrosion potential of the cathodically polarised steel to shift towards more positive direction. On the contrary, the oxygen reduction rate can decrease and the corrosion potential of the cathodically polarised steel shifts towards more negative potentials.
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2

Leach, J. S. Llewelyn, B. R. Pearson, and A. Rahmat. "Cathodic Polarisation in Aqueous Solutions." Key Engineering Materials 20-28 (January 1991): 563–69. http://dx.doi.org/10.4028/www.scientific.net/kem.20-28.563.

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3

Shubina Helbert, Varvara, Andrei Nazarov, Flavien Vucko, Nicolas Larché, and Dominique Thierry. "Effect of Cathodic Polarisation Switch-Off on the Passivity and Stability to Crevice Corrosion of AISI 304L Stainless Steel." Materials 14, no. 11 (2021): 2921. http://dx.doi.org/10.3390/ma14112921.

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The effects of cathodic polarisation switch-off on the passivation of AISI 304L stainless steel in air and its crevice corrosion susceptibility in 3.5 wt.% NaCl aqueous electrolyte were investigated. Scanning Kelvin probe (SKP) data showed that the oxide film is significantly destabilised and the rate of steel passivation in air is slowed down. Thermal desorption analysis (TDA) highlighted that hydrogen absorption is proportional to the applied cathodic current density. A special crevice corrosion set-up was designed to realise simultaneous reproducible monitoring of potential and galvanic current to study the impact of prior cathodic polarisation on crevice corrosion onset.
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4

Cox, B., Yin-Mei Wong, and C. W. F. Quon. "Cathodic polarisation of corroding Zircaloy-4." Journal of Nuclear Materials 223, no. 3 (1995): 321–26. http://dx.doi.org/10.1016/0022-3115(95)00045-3.

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5

Rathod, Nikita, Peter Slater, George Sergi, Gamini Seveviratne, and David Simpson. "A fresh look at depolarisation criteria for cathodic protection of steel reinforcement in concrete." MATEC Web of Conferences 289 (2019): 03011. http://dx.doi.org/10.1051/matecconf/201928903011.

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Criteria for the successful application of cathodic protection (CP) for steel reinforced concrete have been fixed for decades and form part of ISO EN12696. The most used criterion is the achievement of 100 mV depolarization over a period not exceeding 24 hours after discontinuation of the applied current. Although more empirical than theoretically based, the criterion has served the CP industry well. It does, however, exclude any systems that may not always achieve that level of depolarization but have been shown to offer adequate protection, and so there is a need to explore ways of assessing depolarisation data more effectively. On a fundamental level, non-linear polarisation, as described by the Butler Volmer equation, relates corrosion rate to polarisation for a given applied current density and shows that at low current densities, estimated corrosion rates can be shown to be still insignificant at less than 100 mV polarisations. This paper explores the use of non-linear polarisation as an additional supportive criterion based on the measured 24-hour depolarisation level for a known applied current density and tests its applicability in the laboratory and in the field. It speculates that a reducing apparent corrosion current density trend in combination with a depolarised potential moving in a more noble direction is likely to be a suitable alternative criterion, where 100 mV depolarisation is not achieved.
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6

Simonet, Jacques. "The Platinised Platinum Interface Under Cathodic Polarisation." Platinum Metals Review 50, no. 4 (2006): 180–93. http://dx.doi.org/10.1595/147106706x152703.

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7

Fanigliulo, A., and B. Bozzini. "Damage to gold surfaces induced by cathodic polarisation." Corrosion Engineering, Science and Technology 38, no. 3 (2003): 228–34. http://dx.doi.org/10.1179/147842203770226979.

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8

Balčiūnaitė, Aldona, Kush K. Upadhyay, Kristina Radinović, Diogo M. F. Santos, M. F. Montemor та Biljana Šljukić. "Steps towards highly-efficient water splitting and oxygen reduction using nanostructured β-Ni(OH)2". RSC Advances 12, № 16 (2022): 10020–28. http://dx.doi.org/10.1039/d2ra00914e.

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β-Ni(OH)2 nanoplatelets produced via a hydrothermal method exhibit good performance as trifunctional electrocatalysts for the ORR, OER, and HER in alkaline media along with excellent stability under cathodic/anodic polarisation conditions.
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9

Mjwana, Phumlani, Philippe Refait, Babatunde A. Obadele, Marc Jeannin, and Peter Olubambi. "Electrochemical Study of Calcareous Deposit Formation in Simulated Soil Solution under Cathodic Protection." Key Engineering Materials 821 (September 2019): 307–12. http://dx.doi.org/10.4028/www.scientific.net/kem.821.307.

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Cathodic protection induces the formation of a calcareous layer has been shown to improve metal protection against corrosion by reducing the oxygen diffusion on the metal surface. The present study focuses on the electrochemical scaling induced by the application of cathodic polarisation. A combination of non-invasive in-situ electrochemical techniques and electrochemical impedance spectroscopy was used. Metal/electrolyte interface behaviour was studied using voltammetry to determine the controlling anodic and cathodic reactions. One-week long experiments were conducted. Applied potential –1.2 VSCE was shown to enable the formation of CaCO3 allotropes calcite and aragonite, and brucite due to increased interfacial pH which resulted in the formation of hydrogen at the electrode surface. Time constants from bode plots for applied potential –1.2 VSCE also illustrated the inhomogeneity of the calcareous layer. Modelling of polarisation curves illustrated a “passivation” phenomenon which resulted from formation of hydroxyl cations. This was further validated by bode plots with the added information on the diffusion reaction process. High frequency behaviour showed a steady increase in the electrolyte resistance which may be attributed to the formation of the calcareous layer. Evidence of the initial Mg-gel porous layer, which precedes the formation of brucite, was found.
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10

Cheruvathur, Sini Varghese, Joby Thomas Kakkassery, Vinod Raphael Palayoor, Binsi M. Paulson, and Ragi Kooliyat. "Electrochemically Synthesized Poly(2-Aminobenzenesulphonic Acid) – An Efficient Protection for Carbon Steel Corrosion." Oriental Journal of Chemistry 35, no. 2 (2019): 678–83. http://dx.doi.org/10.13005/ojc/350223.

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The corrosion protection efficacy of electrochemically synthesized poly(2-aminobenzenesulphonic acid) (P2ABSA) on carbon steel in 1.0 M HCl was investigated by electrochemical impedance spectroscopy, Tafel polarisation, scanning electron microscopy (SEM) and FT-IR spectral studies. The polymeric coating was prepared on the steel surface using cyclic voltammetry. Investigations established that P2ABSA effectively prevent the metal dissolution in HCl medium. Polarisation studies revealed that this polymer hinder both anodic and cathodic process of corrosion appreciably. The structures of the chemically and electrochemically synthesised polymers were compared using IR spectroscopy. Morphology of the steel surface confirmed the intact response of P2ABSA on steel surface treated with HCl.
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