1997
DOI: 10.1016/s0010-938x(97)00029-2
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The behaviour of cadmium monocrystals and polycrystals in acid chloride solution

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Cited by 6 publications
(6 citation statements)
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“…In support of this, previous studies on similarly oriented Cd monocrystals in acidic 0.1 M NaCl ͑pH 1.3͒ showed the anodic dissolution behavior to be independent of surface orientation. 17 Similar anodic Tafel behavior was exhibited by the ͑0001͒, ͑12 ¯10͒, and ͑101 ¯0͒ surface orientations. 17 Furthermore, anodic polarization studies conducted up to 200 A m 2 in the acidic solution produced roughened surfaces with symmetry effects unique to each orientation, 17 as observed in the later stages of pitting in the present study.…”
Section: C370mentioning
confidence: 64%
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“…In support of this, previous studies on similarly oriented Cd monocrystals in acidic 0.1 M NaCl ͑pH 1.3͒ showed the anodic dissolution behavior to be independent of surface orientation. 17 Similar anodic Tafel behavior was exhibited by the ͑0001͒, ͑12 ¯10͒, and ͑101 ¯0͒ surface orientations. 17 Furthermore, anodic polarization studies conducted up to 200 A m 2 in the acidic solution produced roughened surfaces with symmetry effects unique to each orientation, 17 as observed in the later stages of pitting in the present study.…”
Section: C370mentioning
confidence: 64%
“…The observed b a was similar to a value of 27 Ϯ 2 mV reported previously for anodic behavior of Cd monocrystals in acidic ͑pH 1.3͒ 0.1 M NaCl solutions. 17 Increasing the potential in the passive region eventually caused a large increase in anodic current indicative of sustained film breakdown and pitting. The potential at which the sustained breakdown occurred, usually termed the pitting potential E pit , was not reproducible.…”
Section: C368mentioning
confidence: 99%
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“…It is known that transport effects may control the b value of other metals during oxidation to the +2 state, as shown by recent studies on the oxidation of Cd to CdClt in acidic chloride solutions. 26 Limiting current behavior.-The initiation of L behavior in 1 M H2S04 occurred at potentials below E20 and nearer to ECUSO4.5H20 (+0.323 V5 in Table III), as shown by positive deviations from Tafel behavior in Fig. 3 and 4.…”
Section: Resultsmentioning
confidence: 92%
“…The only oxidation state considered was Cd II because a stable Cd I state has not been reported in aqueous solutions or any oxide/hydroxide (9). It is possible an intermediate adsorbed Cd I state exists on the Cd surface prior to a second electron transfer step leading to aqueous Cd II species (10)(11)(12).…”
Section: Introductionmentioning
confidence: 99%