1973
DOI: 10.1007/bf02666196
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An electrochemical model for hot-salt stress-corrosion of titanium alloys

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1973
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Cited by 19 publications
(16 citation statements)
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“…This would account for the chlorine 535 identification in the blue spot layer and is consistent with previous studies that state chloride ions would be expected to extend down the crack [33]. It is hence believed that the blue spot layer is formed via reaction 3 and is associated with the deposition and consequent rupture of the TiO 2 reaction product near the mouth of the crack.…”
supporting
confidence: 88%
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“…This would account for the chlorine 535 identification in the blue spot layer and is consistent with previous studies that state chloride ions would be expected to extend down the crack [33]. It is hence believed that the blue spot layer is formed via reaction 3 and is associated with the deposition and consequent rupture of the TiO 2 reaction product near the mouth of the crack.…”
supporting
confidence: 88%
“…The deposited TiO 2 splits and condenses onto the crack walls near the mouth, allowing further hydrolysis of titanium chlorides and a looping process between reactions 2 and 3 to proceed. The proposed mechanism considers water, via gaseous HCl, to be the source of hydrogen in this HSSCC mechanism, a hypothesis which is supported by many from the 1960s and 70s [6,33]. Chloride is therefore the means by which 485 hydrogen from water molecules is transported into the crack tip.…”
mentioning
confidence: 97%
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“…On breaking this passive layer, un-oxidised titanium beneath the patch may react with the HCl, producing titanium-alloy chlorides and atomic hydrogen that can "charge" the parent [2,11,34,35,39,42]. Thermodynamic analyses indicate that HCl preferentially attacks aluminium and tin in the alloy [39,43,44], generating more hydrogen than from attack of the titanium alone [39].…”
Section: Discussion -Mechanism and Chemistrymentioning
confidence: 99%