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51316-7375-Premature Failure of Access Fittings Installed on High Pressure Effluent Water Lines Due to Microbiologically Induced Corrosion

Product Number: 51316-7375-SG
ISBN: 7375 2016 CP
Author: Saba Navabzadeh Esmaeely
Publication Date: 2016
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The two dominant cationic species in reservoir brine are sodium (Na+) and calcium (Ca2+). Because calcite (CaCO3) and siderite (FeCO3) are isostructural Ca2+ incorporates readily into the hexagonal FeCO3 lattice and vice versa. In aqueous carbon dioxide (CO2) solutions where both Ca2+ and ferrous iron (Fe2+) are present (such as downhole gas reservoirs or deep saline aquifers after CO2 injection) mixed metal carbonates with the formula FexCayCO3 (x+y=1) can form. This inhomogeneity may lead to localized corrosion. During carbon steel corrosion experiments conducted in electrolytes containing high Ca2+ concentrations inhomogeneous corrosion product layers with the composition FexCayCO3 (x+y=1) were indeed observed along with non-uniform corrosion. Determining relative molar fractions of Ca2+ and Fe2+ in FexCayCO3 is paramount to predicting the relative properties and stability of such mixed metal carbonates. Using Bragg’s Law and equations to relate inter-planar spacings to unit cell parameters X-ray diffraction (XRD) data yielded values for the molar fraction of Ca2+ in FexCayCO3. Procedures in the current study were designed to develop a range of specific corrosion product layers on mild steel samples. The compositional analysis of these surface layers was used to develop a relationship with the observed corrosion mechanisms. Experiments were conducted at constant Cl- concentration with and without 10000 ppm Ca2+ in stagnant conditions for two different flow conditions. In stagnant conditions. localized corrosion was associated with the presence of Ca2+ and the inhomogeneity of the corrosion product layer. The corrosion attack became uniform when flow was introduced.
The two dominant cationic species in reservoir brine are sodium (Na+) and calcium (Ca2+). Because calcite (CaCO3) and siderite (FeCO3) are isostructural Ca2+ incorporates readily into the hexagonal FeCO3 lattice and vice versa. In aqueous carbon dioxide (CO2) solutions where both Ca2+ and ferrous iron (Fe2+) are present (such as downhole gas reservoirs or deep saline aquifers after CO2 injection) mixed metal carbonates with the formula FexCayCO3 (x+y=1) can form. This inhomogeneity may lead to localized corrosion. During carbon steel corrosion experiments conducted in electrolytes containing high Ca2+ concentrations inhomogeneous corrosion product layers with the composition FexCayCO3 (x+y=1) were indeed observed along with non-uniform corrosion. Determining relative molar fractions of Ca2+ and Fe2+ in FexCayCO3 is paramount to predicting the relative properties and stability of such mixed metal carbonates. Using Bragg’s Law and equations to relate inter-planar spacings to unit cell parameters X-ray diffraction (XRD) data yielded values for the molar fraction of Ca2+ in FexCayCO3. Procedures in the current study were designed to develop a range of specific corrosion product layers on mild steel samples. The compositional analysis of these surface layers was used to develop a relationship with the observed corrosion mechanisms. Experiments were conducted at constant Cl- concentration with and without 10000 ppm Ca2+ in stagnant conditions for two different flow conditions. In stagnant conditions. localized corrosion was associated with the presence of Ca2+ and the inhomogeneity of the corrosion product layer. The corrosion attack became uniform when flow was introduced.
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