Ohio University
Thermodynamics and Kinetics of Carbon Dioxide Corrosion of Mild Steel at Elevated Temperatures
Abstract
dc:description<p>CO<sub>2</sub> corrosion of mild steel in the oil and gas industry has been widely investigated. Nevertheless, research on high temperature CO<sub>2</sub> corrosion has been rarely conducted, and its mechanisms remain unclear. Therefore, it is important to complete an in-depth study of CO<sub>2</sub> corrosion of mild steel at high temperature. The entire scope of this Ph.D. research is to investigate and model CO<sub>2</sub> corrosion of mild steel over a range of 25-250¿¿C. The research is divided into four main sections: chemical thermodynamics, electrochemical thermodynamics, electrochemical kinetics, and the proposal of mechanisms of CO<sub>2</sub> corrosion. </p><p>In the chemical thermodynamics segment, water chemistry components of CO<sub>2</sub> systems were studied. In the absence of Fe2+, pH increased with temperature in both predicted and experimental results. With addition of Fe2+, pH did not change with temperature due to FeCO<sub>3</sub> precipitation.</p><p>Pourbaix diagrams for the Fe-CO<sub>2</sub>-H<sub>2</sub>O systems were constructed using thermodynamic theory and data, subsequently validated with observed CO<sub>2</sub> corrosion phenomena. In the range of 80-150¿¿C, FeCO<sub>3</sub> and Fe<sub>2</sub>(OH)<sub>2</sub>CO<sub>3</sub> formed on the steel surface, for experiments lasting 4 days. At 200-250¿¿C, the corrosion product was exclusively Fe3O4. Kinetic studies conducted at 120¿¿C show full transformation from plate-like Fe<sub>2</sub>(OH)<sub>2</sub>CO<sub>3</sub> to oblong prismatic FeCO<sub>3</sub> crystals over time. In relation to pressure effects, FeCO<sub>3</sub> is the more favored corrosion product than Fe<sub>3</sub>O<sub>4</sub> at high pCO<sub>2</sub>. With surface pH consideration, the generated Pourbaix diagrams were validated by experimental results.</p><p>The corrosion kinetic experiments at elevated temperatures were further investigated including the effects of pH and flow. It was concluded that corrosion rates did not monotonously decrease with temperatures due to formation of corrosion products. Corrosion rates at pH 4.0 were higher than those at pH 6.0, independent of temperature. The main corrosion product was FeCO<sub>3</sub> with Fe<sub>3</sub>O<sub>4</sub> present at temperatures above 150¿¿C. No flow sensitivity was observed due to the formation of corrosion products.</p><p>Mechanisms of CO<sub>2</sub> corrosion at temperatures of 25-250¿¿C were proposed based on the current CO<sub>2</sub> corrosion model with an addition of Fe<sub>3</sub>O<sub>4</sub> formation. The thermodynamics and kinetics of Fe<sub>3</sub>O<sub>4</sub> formation were identified. As soon as thermodynamic conditions for Fe<sub>3</sub>O<sub>4</sub> are achieved, it forms and protects the steel.</p>
Degree
thesis:*- Name thesis:degree_name
- Doctor of Philosophy (PhD)
- Level thesis:degree_level
- doctoral
- Discipline thesis:degree_discipline
- Chemical Engineering (Engineering and Technology)
- Grantor dc:publisher
- Ohio University
- Year dc:date
- 2012
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Tanupabrungsun, Tanaporn
- Contributors dc:contributor
-
- Nesic, Srdjan
Subjects
dc:subject × 8Rights
dc:rights- Statement dc:rights
-
- unrestricted
- This thesis or dissertation is protected by copyright: all rights reserved. It may not be copied or redistributed beyond the terms of applicable copyright laws.
- Language dc:language
- English
Identifiers
dc:identifier.*- Repository record dc:identifier
- http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1355328679
- OAI identifier oai:identifier
- oai:etd.ohiolink.edu:ohiou1355328679