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.

Crystal chemistry and temperature behavior of the natural hydrous borate colemanite, a mineral commodity of boron / P. Lotti, G.D. Gatta, N. Demitri, G. Guastella, S. Rizzato, M.A. Ortenzi, F. Magrini, D. Comboni, A. Guastoni, M.T. Fernandez-Diaz. - In: PHYSICS AND CHEMISTRY OF MINERALS. - ISSN 0342-1791. - 45:5(2018 May), pp. 405-422.

Crystal chemistry and temperature behavior of the natural hydrous borate colemanite, a mineral commodity of boron

P. Lotti
Primo
;
G.D. Gatta
Secondo
;
S. Rizzato;M.A. Ortenzi;F. Magrini;D. Comboni;
2018

Abstract

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.
borates; colemanite; ferroelectric behavior; low temperature; neutron diffraction; phase transition; synchrotron; materials science (all); geochemistry and petrology
Settore GEO/09 - Georisorse Miner.Appl.Mineral.-Petrogr.per l'amb.e i Beni Cul
Settore CHIM/03 - Chimica Generale e Inorganica
Settore CHIM/04 - Chimica Industriale
mag-2018
14-nov-2017
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/557129
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