Thermodynamics of vivianite-group arsenates M 3 (AsO 4 ) 2 ⋅ 8H 2 O ( M is Ni, Co, Mg, Zn, Cu) and chemical variability in the natural arsenates of this group
In this work, we investigated the M3(AsO4)2⋅ 8H2O end members annabergite (M is Ni), erythrite (M is Co), and hörnesite (M is Mg) and their solid solutions. Acid-solution calorimetry and relaxation calorimetry were used to determine the solubility products (log Ksp) for annabergite (−33.7), erythrit...
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Veröffentlicht in: | European journal of mineralogy (Stuttgart) 2024-01, Vol.36 (1), p.31-54 |
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Sprache: | eng |
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Zusammenfassung: | In this work, we investigated the M3(AsO4)2⋅ 8H2O end members annabergite (M is Ni), erythrite (M is Co), and hörnesite (M is Mg) and their solid solutions. Acid-solution calorimetry and relaxation calorimetry were used to determine the solubility products (log Ksp) for annabergite (−33.7), erythrite (−32.1), and hörnesite (−22.3). Solubility products for other end members of this group were extracted from the literature and critically evaluated. The enthalpies of mixing are complex, related to subsystems M(1)3(AsO4)2⋅ 8H2O–M(1)M(2)2(AsO4)2⋅ 8H2O and M(1)M(2)2(AsO4)2⋅ 8H2O–M(2)3(AsO4)2⋅ 8H2O. They are small and positive for the annabergite–erythrite solid solution and small and negative for the annabergite–hörnesite solid solution. Autocorrelation analysis of Fourier-transform infrared (FTIR) spectra shows correlation of strain decrease in the structure with the negative enthalpies of mixing in the annabergite–hörnesite solid solution. A set of more than 600 electron microprobe analyses of the M3(AsO4)2⋅ 8H2O minerals documents the variability and complexity in this group. Most common compositions are those dominated by Ni, Co, or Ni–Co. The analytical results were used to calculate the maximal configurational entropies which could be a factor that compensates for the small enthalpies of mixing in the annabergite–erythrite solid solution. The data presented here can be used to model sites polluted with metals and arsenic and to enhance our understanding of complex solid solutions. |
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ISSN: | 1617-4011 1617-4011 |
DOI: | 10.5194/ejm-36-31-2024 |