A Mechanical–Electrochemical Approach for the Determination of Precursor Sites for Pitting Corrosion at the Microscale

2006 ◽  
Vol 153 (9) ◽  
pp. B352 ◽  
Author(s):  
Vincent Vignal ◽  
Nicolas Mary ◽  
Roland Oltra ◽  
Jéro^me Peultier
2021 ◽  
Vol 2021 ◽  
pp. 1-14
Author(s):  
Chin Boon Ching ◽  
Jaafar Abdullah ◽  
Nor Azah Yusof

Palm oil is one of the major oils and fats produced in the world today. The quality of palm oil is crucial to be investigated, and one of the quality indices is free fatty acid (FFA) content. Therefore, in this study, an electrochemical approach for the determination of FFA has been explored as an alternative to replace the conventional method (titration method). The electrochemical method was developed based on electrochemically reduced graphene oxide (rGO) coupled with gold nanoparticles (AuNPs) deposited onto a screen-printed carbon electrode (SPCE) via drop-casting technique. The voltammetric behaviour of 2-methyl-1,4-naphthoquinone (VK3) in the presence of palmitic acid at the modified electrode was investigated in an acetonitrile/water mixture containing lithium perchlorate (LiClO4). The electrochemical detection of palmitic acid was based on the voltammetric reduction of VK3 to form the corresponding hydroquinone which is proportional to the concentration of palmitic acid. Under optimum conditions, the developed method showed a good linear relationship towards palmitic acid in the concentration ranging from 0.192 mM to 0.833 mM with the detection limit of 0.015 mM. The exploration of the developed system is expected to achieve high sensitivity and excellent selectivity towards the determination of FFA content in palm oil.


CORROSION ◽  
10.5006/3562 ◽  
2020 ◽  
Vol 76 (8) ◽  
pp. 786-795
Author(s):  
Abraham A. Becerra Araneda ◽  
Mariano A. Kappes ◽  
Martín A. Rodríguez ◽  
Ricardo M. Carranza

Low potential pitting corrosion (LPPC) of Alloys 690 and 800 (UNS N06690 and N08800) was studied in neutral solutions, containing chloride ions from 0.1 M to 1 M and thiosulfate ions from 5 × 10−5 M to 10−3 M. LPPC occurred close to the corrosion potential (–0.25 VAg/AgCl) by a synergic effect of the chloride and thiosulfate ions. The threshold concentrations of aggressive species for LPPC occurrence were identified by potentiostatic tests with mechanical scratching of the surface, which yielded more conservative estimations compared to other electrochemical tests. The ranges of potential and concentration of chloride and thiosulfate where LPPC occurred and where it merged with the conventional chloride pitting were determined. The lowest threshold concentrations were measured in Alloy 800, with a lower Cr content than Alloy 690. Thermally-aged Alloys 800 and 690 had lower resistance to LPPC than the corresponding solution-annealed material. In 1 M chloride-based solutions, for aged Alloy 800, LPPC occurred at a thiosulfate concentration as low as 5 × 10−5 M; in 10−3 M thiosulfate-based solutions, the chloride threshold was 0.1 M. For thermally-aged alloys, pits propagated intergranulary in some experiments. In solutions with chloride and thiosulfate concentrations close to the threshold required for pitting, repassivation of LPPC was observed after a sustained period of pit growth, originally initiated by scratching the surface. Such a repassivation has not been reported before in the literature in chloride and thiosulfate solutions. Two possible explanations were presented for this phenomenon.


CORROSION ◽  
1978 ◽  
Vol 34 (12) ◽  
pp. 437-442 ◽  
Author(s):  
H. -J. RAETZER-SCHEIBE

Abstract The characteristic pitting potentials of Ti and Ti6AI4V were determined by measurement of potentiodynamic current-potential curves in solutions of 1N NaCl, 1N Nal, and 1N NaBr. Under the same conditions current-time curves were measured for various potentials after generation of a new metallic surface. By means of these curves, one can study the repassivation behavior of materials. The comparison between the potential of pit repassivation and the repassivation/nonrepassivation potential shows a relatively good correlation. The determination of the critical repassivation potentials enables us to predict the pitting corrosion behavior.


Author(s):  
A. Baniya ◽  
S. Thapa ◽  
E. Borquist ◽  
D. Bailey ◽  
D. Wood ◽  
...  

Hydrogen sulfide (H2S) is rapidly emerging as a biologically significant signaling molecule. In recent studies, sulfide level in blood or plasma has been reported to be in the concentration between 10 and 300 μM suggesting it acts in various diseases. This work reports progress on a new Lab-on-a-Chip (LOC) device for these applications. The uniquely designed, hand-held device uses advanced liberation chemistry that releases H2S from liquid sample and an electrochemical approach to detect sulfide concentration from the aqueous solution. The device itself consists of three distinct layers of Polydimethylsiloxane (PDMS) structures and a three electrode system for direct and rapid H2S concentration measurement. In this work specifically, the oxidation of sulfide at the gold (Au) and platinum (Pt.) electrodes has been examined. This is the first known application of electrochemical H2S sensing in an LOC application. The analytical utility and performance of the device has been assessed through direct detection using chronoamperometry (CA) scan and cyclic voltammetry (CV). An electrocatalytic sulfide oxidation signal has been recorded for sulfide concentration range vs, Ag/AgCl at different pH buffers at the trapping chamber. The calibration curve in the range 1 μM to 1 M was obtained using this electrode setup. The detection limit was found to be 0.1 μM. This device shows promise for providing fast and inexpensive determination of H2S concentration in aqueous samples.


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