1990
DOI: 10.1016/0010-938x(90)90112-i
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Aluminum pitting in chloride solutions: morphology and pit growth kinetics

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Cited by 98 publications
(39 citation statements)
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“…29 Others dealt with aluminum pitting, the critical chemistry requirement in that case, 30 and the distinction between pits and tunnels. 31 A persistent theme was the initiation of crevice corrosion, which according to most authors occurs by a slow process of passive dissolution, gradually building up the necessary chemistry, 32,33 but according to others, is due to pitting that would be metastable if it were to occur on a free surface, but is stabilized by the crevice (higher 'x' in Galvele's model). 34 .…”
Section: Related Advancesmentioning
confidence: 99%
“…29 Others dealt with aluminum pitting, the critical chemistry requirement in that case, 30 and the distinction between pits and tunnels. 31 A persistent theme was the initiation of crevice corrosion, which according to most authors occurs by a slow process of passive dissolution, gradually building up the necessary chemistry, 32,33 but according to others, is due to pitting that would be metastable if it were to occur on a free surface, but is stabilized by the crevice (higher 'x' in Galvele's model). 34 .…”
Section: Related Advancesmentioning
confidence: 99%
“…9a and b, in 2 M NaCl solution, pure Al and Al-Bi-Pb alloy undergo the crystallographic corrosion which is a typical corrosion behavior of aluminum alloys in chloride solutions. [42][43][44] The presence of some geometric facets can be explained by the fact that the corrosion occurs probably along the well-dened crystallographic directions of {100} facets. 45 Whereas, Al-Bi-Pb-Ga alloy exhibits a crack structure, which may be ascribed to the …”
mentioning
confidence: 99%
“…This turning point did not emerge in several other solutions. According to the classical pitting corrosion mechanism, the small size of Cl À can penetrate the surface of magnesium alloy at some weak spots, such as casting defects, etc., then forming localized corrosion pits [19][20][21]. The polarization currents (i corr ) for AZ61 in urea solution and water were comparable, while corrosion potential (E corr ) in the urea solution was located at around À1.44 V, which was significantly more positive than that in pure water (Table 3).…”
Section: Potentiodynamic Polarization Measurementsmentioning
confidence: 99%