dc.contributor.author |
Panias, D |
en |
dc.contributor.author |
Taxiarchou, M |
en |
dc.contributor.author |
Douni, I |
en |
dc.contributor.author |
Paspaliaris, I |
en |
dc.contributor.author |
Kontopoulos, A |
en |
dc.date.accessioned |
2014-03-01T01:12:26Z |
|
dc.date.available |
2014-03-01T01:12:26Z |
|
dc.date.issued |
1996 |
en |
dc.identifier.issn |
0008-4433 |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/12101 |
|
dc.subject |
Iron |
en |
dc.subject |
Iron Oxide |
en |
dc.subject |
Organic Acid |
en |
dc.subject |
Oxalic Acid |
en |
dc.subject |
Thermodynamics |
en |
dc.subject.classification |
Metallurgy & Metallurgical Engineering |
en |
dc.subject.other |
Agents |
en |
dc.subject.other |
Chemical reactions |
en |
dc.subject.other |
Dissolution |
en |
dc.subject.other |
Free energy |
en |
dc.subject.other |
Ions |
en |
dc.subject.other |
Organic acids |
en |
dc.subject.other |
pH |
en |
dc.subject.other |
Solutions |
en |
dc.subject.other |
Solvents |
en |
dc.subject.other |
Thermodynamics |
en |
dc.subject.other |
Non reductive dissolution |
en |
dc.subject.other |
Oxalic acid |
en |
dc.subject.other |
Reductive dissolution |
en |
dc.subject.other |
Solvent reagents |
en |
dc.subject.other |
Iron oxides |
en |
dc.title |
Thermodynamic analysis of the reactions of iron oxides: Dissolution in oxalic acid |
en |
heal.type |
journalArticle |
en |
heal.identifier.primary |
10.1016/S0008-4433(96)00018-3 |
en |
heal.identifier.secondary |
http://dx.doi.org/10.1016/S0008-4433(96)00018-3 |
en |
heal.language |
English |
en |
heal.publicationDate |
1996 |
en |
heal.abstract |
The mechanism of dissolution of pure iron oxides by means of organic acids comprises two different chemical pathways: (a) non-reductive dissolution and (b) reductive dissolution. In this paper, the thermodynamic analysis of these pathways for the iron oxides-oxalic acid system is presented. In low acid solutions (pH higher than 3) the only thermodynamically stable complex ions of bivalent and trivalent iron are [Fe2+(C2O4)(2)](2-) and [Fe3+(C2O4)(3)](3-). Uncomplexed Fe2+ ion can be identified only in high acid solutions, while uncomplexed Fe3+ ion is not likely to build-up in oxalic acid solutions. In the pH range 1-2 the [Fe3+(C2O4)(2)](-) and [Fe3+C2O4](+) ions are stable, while at pH less than 1, the [Fe3+HC2O4](2+) is the only ion existing. Copyright (C) 1996 Canadian Institute of Mining and Metallurgy. Published by Elsevier Science Ltd. |
en |
heal.publisher |
PERGAMON-ELSEVIER SCIENCE LTD |
en |
heal.journalName |
Canadian Metallurgical Quarterly |
en |
dc.identifier.doi |
10.1016/S0008-4433(96)00018-3 |
en |
dc.identifier.isi |
ISI:A1996WC39600006 |
en |
dc.identifier.volume |
35 |
en |
dc.identifier.issue |
4 |
en |
dc.identifier.spage |
363 |
en |
dc.identifier.epage |
373 |
en |