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This work demonstrates an approach using solid state electrochemical cells to study the long-term oxidation of materials at 800 °C. The capability of zirconia-based cells to control the oxygen partial pressure was first evaluated using an empty chamber. For most voltages applied to the pump cell, the steady state sensor voltage matches the pump voltage, leakage rates are low, and response times are short, allowing precise and prompt control over the chamber atmosphere. The technique was validated by measuring the oxidation of niobium and nickel. Niobium was oxidized at pump voltages ranging from 0 mV to +500 mV; decreasing the oxygen partial pressure around the specimen reduces the oxidation rate. Comparing the integrated oxidation rate with the weighed mass gain showed good agreement. Measured oxidation rates for nickel were of order 1μg h−1, illustrating the sensitivity of this technique. For higher oxidation rates, a depression in oxygen partial pressure was observed around the specimen. Improved control over the oxidation potential was achieved by using a sensor cell to dynamically tune the pump voltage. Rates for both metals are compared to literature reports using other techniques.
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A Turn-Off Fluorescent Sensor for Metal Ions Quantifies Corrosion in an Organic Solvent
We demonstrate that the corrosion of AISI 1045 medium carbon steel and pure aluminum can be quantified by the turn-off fluorescent sensor Phen Green-SK (PGSK) in ethanol-based solutions. We first evaluate the dependence of the chelation enhanced quenching of PGSK on iron and aluminum ion concentrations. Subsequently, we apply PGSK to examine the anodic dissolution of metal corrosion. The observed time-dependent PGSK-quenching quantifies the corrosion rates of two metals over 24 h of immersion in ethanol-based solutions. The PGSK-based quantification of corrosion is compared to scanning electron microscopy and electrochemical techniques, including open circuit potential and Tafel extrapolation. The corrosion rates calculated from PGSK-quenching and Tafel extrapolation are in agreement, and both indicate a decrease in corrosion rates over 24 h. Our work shows PGSK can efficiently sense and quantify anodic corrosion reactions at metal interfaces, especially in organic solvents or other non-aqueous environments where the application of electrochemical techniques can be limited by the poor conductivity of the surrounding medium.
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- Award ID(s):
- 2142821
- PAR ID:
- 10506100
- Publisher / Repository:
- The Electrochemical Society
- Date Published:
- Journal Name:
- Journal of The Electrochemical Society
- Volume:
- 171
- Issue:
- 5
- ISSN:
- 0013-4651
- Format(s):
- Medium: X Size: Article No. 051502
- Size(s):
- Article No. 051502
- Sponsoring Org:
- National Science Foundation
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