TY - JOUR
T1 - Crystal chemistry and temperature behavior of the natural hydrous borate colemanite, a mineral commodity of boron
AU - Lotti, Paolo
AU - Gatta, G. Diego
AU - Demitri, Nicola
AU - Guastella, Giorgio
AU - Rizzato, Silvia
AU - Magrini, Fabrizio
AU - Ortenzi, Marco Aldo
AU - Comboni, Davide
AU - Guastoni, Alessandro
AU - Fernandez-Diaz, Maria Teresa
N1 - Publisher Copyright:
© 2017, Springer-Verlag GmbH Germany.
PY - 2018/5/1
Y1 - 2018/5/1
N2 - Colemanite, CaB3O4(OH)3⋅H2O, is the most common hydrous Ca-borate, as well as a major mineral commodity of boron. In this study, we report a thorough chemical analysis and the low-temperature behavior of a natural sample of colemanite by means of a multi-methodological approach. From the chemical point of view, the investigated sample resulted to be relatively pure, its composition being very close to the ideal one, with only a minor substitution of Sr2+ for Ca2+. At about 270.5 K, a displacive phase transition from the centrosymmetric P21/a to the acentric P21 space group occurs. On the basis of in situ single-crystal synchrotron X-ray (down to 104 K) and neutron diffraction (at 20 K) data, the hydrogen-bonding configuration of both the polymorphs and the structural modifications at the atomic scale at varying temperatures are described. The asymmetric distribution of ionic charges along the [010] axis, allowed by the loss of the inversion center, is likely responsible for the reported ferroelectric behavior of colemanite below the phase transition temperature.
AB - Colemanite, CaB3O4(OH)3⋅H2O, is the most common hydrous Ca-borate, as well as a major mineral commodity of boron. In this study, we report a thorough chemical analysis and the low-temperature behavior of a natural sample of colemanite by means of a multi-methodological approach. From the chemical point of view, the investigated sample resulted to be relatively pure, its composition being very close to the ideal one, with only a minor substitution of Sr2+ for Ca2+. At about 270.5 K, a displacive phase transition from the centrosymmetric P21/a to the acentric P21 space group occurs. On the basis of in situ single-crystal synchrotron X-ray (down to 104 K) and neutron diffraction (at 20 K) data, the hydrogen-bonding configuration of both the polymorphs and the structural modifications at the atomic scale at varying temperatures are described. The asymmetric distribution of ionic charges along the [010] axis, allowed by the loss of the inversion center, is likely responsible for the reported ferroelectric behavior of colemanite below the phase transition temperature.
KW - Borates
KW - Colemanite
KW - Ferroelectric behavior
KW - Low temperature
KW - Neutron diffraction
KW - Phase transition
KW - Synchrotron
UR - http://www.scopus.com/inward/record.url?scp=85033705716&partnerID=8YFLogxK
U2 - 10.1007/s00269-017-0929-7
DO - 10.1007/s00269-017-0929-7
M3 - Article
AN - SCOPUS:85033705716
SN - 0342-1791
VL - 45
SP - 405
EP - 422
JO - Physics and Chemistry of Minerals
JF - Physics and Chemistry of Minerals
IS - 5
ER -