TY - JOUR
T1 - Crystallization and characterization of a new magnesium sulfate hydrate MgSO4 11H2O
AU - Genceli, F. Elif
AU - Lutz, Martin
AU - Spek, Anthony L.
AU - Witkamp, Geert Jan
PY - 2007/12
Y1 - 2007/12
N2 - The MgSO4 crystal hydrate formed below approximately 0 °C was proven to be the undecahydrate, MgSO4; · 11H2O (meridianiite) instead of the reported dodecahydrate MgSO4 ·12H2O. The crystals were grown from solution by eutectic freeze and by cooling crystallization. The crystal structure analysis and the molecular arrangement of these crystals were determined using single crystal X-ray diffraction (XRD). Reflections were measured at a temperature of 110(2) K. The structure is triclinic with space group Pl̄ (No. 2). The crystal is a colorless block with the following parameters F.W. = 318.55, 0.54 × 0.24 × 0.18 mm3, a = 6.72548(7) Å, b = 6.77937(14) Å, c = 17.2898(5) Å, α = 88.255(1)°, β= 89.478(2)°, γ = 62.598(1)°, V = 699.54(3) Å3, Z = 2, Dcalc = 1.512 g/cm3, μ = 0.343 mm-1. Raman spectroscopy was used for characterizing MgSO4 · 11H2O and for comparing the vibrational spectra with the MgSO4 · 7H 2O salt. Between the two salts, there are significant differences mainly in the type of interactions of water with sulfate groups in the lattice, in view of the different O-H stretching vibrations, as well as sulfate, O - H - O (sulfate) and O - Mg - O bands vibrational modes. Thermogravimetric analysis confirmed the stochiometry of the MgSO4 · 11H2O salt. Additionally, the Miller indices of the major faces of MgSO4 · 11H2O crystals were defined.
AB - The MgSO4 crystal hydrate formed below approximately 0 °C was proven to be the undecahydrate, MgSO4; · 11H2O (meridianiite) instead of the reported dodecahydrate MgSO4 ·12H2O. The crystals were grown from solution by eutectic freeze and by cooling crystallization. The crystal structure analysis and the molecular arrangement of these crystals were determined using single crystal X-ray diffraction (XRD). Reflections were measured at a temperature of 110(2) K. The structure is triclinic with space group Pl̄ (No. 2). The crystal is a colorless block with the following parameters F.W. = 318.55, 0.54 × 0.24 × 0.18 mm3, a = 6.72548(7) Å, b = 6.77937(14) Å, c = 17.2898(5) Å, α = 88.255(1)°, β= 89.478(2)°, γ = 62.598(1)°, V = 699.54(3) Å3, Z = 2, Dcalc = 1.512 g/cm3, μ = 0.343 mm-1. Raman spectroscopy was used for characterizing MgSO4 · 11H2O and for comparing the vibrational spectra with the MgSO4 · 7H 2O salt. Between the two salts, there are significant differences mainly in the type of interactions of water with sulfate groups in the lattice, in view of the different O-H stretching vibrations, as well as sulfate, O - H - O (sulfate) and O - Mg - O bands vibrational modes. Thermogravimetric analysis confirmed the stochiometry of the MgSO4 · 11H2O salt. Additionally, the Miller indices of the major faces of MgSO4 · 11H2O crystals were defined.
UR - http://www.scopus.com/inward/record.url?scp=37549021032&partnerID=8YFLogxK
U2 - 10.1021/cg060794e
DO - 10.1021/cg060794e
M3 - Article
AN - SCOPUS:37549021032
SN - 1528-7483
VL - 7
SP - 2460
EP - 2466
JO - Crystal Growth and Design
JF - Crystal Growth and Design
IS - 12
ER -