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Thermodynamic properties of scorodite and parascorodite (FeAsO4 center dot 2H(2)O), kankite (FeAsO4 center dot 3.5H(2)O), and FeAsO4

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F12%3A00107089" target="_blank" >RIV/00216224:14310/12:00107089 - isvavai.cz</a>

  • Alternative codes found

    RIV/67985831:_____/12:00377319 RIV/00216208:11310/12:10126479

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S0304386X12000291" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0304386X12000291</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.hydromet.2012.02.002" target="_blank" >10.1016/j.hydromet.2012.02.002</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Thermodynamic properties of scorodite and parascorodite (FeAsO4 center dot 2H(2)O), kankite (FeAsO4 center dot 3.5H(2)O), and FeAsO4

  • Original language description

    Iron arsenates, either well or poorly crystalline, are the usual phases of choice for arsenic immobilization in waste forms of variable origin. Among these phases. scorodite (FeAsO4 center dot 2H(2)O) is used very often because of its favorable properties. The thermodynamic properties of this phase, necessary for the prediction of its dissolution or precipitation, have been usually constrained by solubility experiments. Here, we measured the thermodynamic properties of scorodite, its polymorph parascorodite, the mineral kafikite (FeAsO4 center dot 35H(2)O), and the anhydrous FeAsO4 by a combination of calorimetric techniques, thus avoiding the inherent uncertainties of the solubility experiments. The enthalpies of formation from elements at standard temperature and pressure for scorodite, parascorodite, kankite, and FeAsO4 are -1508.9 +/- 2.9, -1506.6 +/- 2.9, -1940.2 +/- 2.8, and -899.0 +/- 3.0 kJ.mol(-1), respectively. The measured standard entropies for scorodite and kafikite are 188.0 +/- 2.1 and 247.6 +/- 2.8J.mol(-1). K-1, respectively; entropies of FeAsO4 and parascorodite were estimated. The resulting Gibbs free energies of formation for scorodite, parascorodite, karikite, and FeAsO4 are -1284.8 +/- 2.9, -1282.5, -1629.6 +/- 2.9. and -786.7 kJ.mol(-1), respectively. The solubility product for scorodite of -25.83 +/- 0.52 is in an excellent agreement with a previously selected best value of -25.83 +/- 0.07 from Langmuir et al. (2006). As expected, scorodite is stable under a wide range of conditions applicable to terrestrial surface environments. The anhydrous FeAsO4, parascorodite, and kankite are either metastable or stable under restricted conditions which are unlikely for the terrestrial surface environments. Using the thermodynamic data for scorodite and for a suite of ferric oxides, we can predict the aqueous As concentrations in systems in which scorodite dissolves and ferric oxides precipitate. These models show that the As concentration can vary widely as function of the nature, chemical composition, and crystallinity of these ferric oxides.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    20501 - Materials engineering

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2012

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Hydrometallurgy

  • ISSN

    0304-386X

  • e-ISSN

    1879-1158

  • Volume of the periodical

    117

  • Issue of the periodical within the volume

    APR

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    10

  • Pages from-to

    47-56

  • UT code for WoS article

    000303486500007

  • EID of the result in the Scopus database

    2-s2.0-84859426036