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Communication : The galvanic effect on the under-deposit corrosion of titanium in chloride solutions Liu, Y.; Asselin, Edouard
Abstract
Solid deposits are commonly present during industrial operations. The corrosion behavior of solid-covered Ti-2 in a solid-covered/uncovered galvanic cell was studied here. Corrosion is maximized at a specific deposit thickness: not too thin and not too thick. It initiated when the deposit layer thickness was 4 cm, and became more severe as the thickness increased to 6 cm. However, a further increase in the thickness resulted in significant mass transfer resistance in the corrosion process and did not result in exacerbated corrosion. Under-deposit corrosion of titanium in a neutral chloride solution manifested the autocatalytic characteristics of occluded cell corrosion.
Item Metadata
Title |
Communication : The galvanic effect on the under-deposit corrosion of titanium in chloride solutions
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Creator | |
Publisher |
The Electrochemical Society
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Date Issued |
2021-07-21
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Description |
Solid deposits are commonly present during industrial operations. The corrosion
behavior of solid-covered Ti-2 in a solid-covered/uncovered galvanic cell was studied here.
Corrosion is maximized at a specific deposit thickness: not too thin and not too thick. It
initiated when the deposit layer thickness was 4 cm, and became more severe as the thickness
increased to 6 cm. However, a further increase in the thickness resulted in significant mass
transfer resistance in the corrosion process and did not result in exacerbated corrosion.
Under-deposit corrosion of titanium in a neutral chloride solution manifested the
autocatalytic characteristics of occluded cell corrosion.
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Genre | |
Type | |
Language |
eng
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Date Available |
2021-07-28
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Provider |
Vancouver : University of British Columbia Library
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Rights |
Attribution-NonCommercial-NoDerivatives 4.0 International
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DOI |
10.14288/1.0400923
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URI | |
Affiliation | |
Citation |
Y. Liu and E. Asselin 2021 J. Electrochem. Soc. 168 071512
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Publisher DOI |
10.1149/1945-7111/ac1399
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Peer Review Status |
Reviewed
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Scholarly Level |
Faculty
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Copyright Holder |
Publishers
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Rights URI | |
Aggregated Source Repository |
DSpace
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Item Citations and Data
Rights
Attribution-NonCommercial-NoDerivatives 4.0 International