1993
DOI: 10.1007/bf00234818
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Current efficiency during anodic dissolution of iron to ferrate(vi) in concentrated alkali hydroxide solutions

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Cited by 62 publications
(36 citation statements)
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“…This positive influence of temperature was already observed by Pick [11] and other authors [117,118]. Bouzek et al [49][50][51][52][53] studied different iron anode materials and concluded that pure iron had the strongest tendency to form a compact and stable surface layer. A higher temperature, 30-50 • C depending on the electrolysis conditions, is necessary to overcome this problem.…”
Section: Temperaturesupporting
confidence: 60%
See 1 more Smart Citation
“…This positive influence of temperature was already observed by Pick [11] and other authors [117,118]. Bouzek et al [49][50][51][52][53] studied different iron anode materials and concluded that pure iron had the strongest tendency to form a compact and stable surface layer. A higher temperature, 30-50 • C depending on the electrolysis conditions, is necessary to overcome this problem.…”
Section: Temperaturesupporting
confidence: 60%
“…There has been a marked increase in new applications of ferrate(VI) , in particular the utilization of ferrate in organic synthesis [22][23][24][25][26], corrosion protection [27] and environmental improvement [28][29][30][31][32]. More recent research on ferrate(VI) also has involved the development of new characterization techniques that allow deeper insight into the reaction mechanisms and properties of ferrate(VI) [45][46][47][48][49][50][51][52][53][54].…”
Section: Introductionmentioning
confidence: 99%
“…Other researches involving electrolytes such as NaOH, KOH and LiOH revealed that NaOH provided the best condition for ferrate(VI) production (19). Bouzek et al also reported that the optimal concentration in case of using NaOH as electrolyte was 14 molar (31)(32)(33).…”
Section: Ferrate(vi) Production By Electrochemical Methodsmentioning
confidence: 98%
“…The electrolytes in both compartments were 0.3 mol/L NaOH solution, and their volume was 100 mL. The anode was activated by cathodic polarization for 30 min at a constant current of 1.0 A before the start of electro-synthesis [26]. Cell temperature was controlled within 711C by ice-water cooling bath.…”
Section: Methodsmentioning
confidence: 99%