The crystal structure of sarmientite, Fe3+2(AsO4)(SO4)(OH)·5H2O, solved ab initio from laboratory powder diffraction data

COLOMBO, FERNANDO; RIUS, JORDI; VALLCORBA, ORIOL; PANNUNZIO MINER, ELISA VICTORIA

MINERALOGICAL MAGAZINE

MINERALOGICAL SOC

Lugar: Middlesex; Año: 2014

0026-461X

The crystal structure of sarmientite, Fe3+ 2 (AsO4)(SO4)(OH)·5H2O, from the type locality (Santa Elena mine, San Juan Province, Argentina), was solved and refined from in-house powder diffraction data (CuKα1,2 radiation). It is monoclinic, space group P2/n, with unit cell dimensions a = 6.5298(1), b = 18.5228(4), c = 9.6344(3) Å, beta = 97.444(2)º, V = 1155.5(5) Å3, and Z = 4.The structure model was derived from cluster-based Patterson-function direct methods and refined by means of the Rietveld method to Rwp = 0.0733 (chi2 = 2.20). The structure consists of pairs of octahedral-tetrahedral (Fe-As) chains at (y, z) = (0,0) and (½,½) running along a. There are two symmetry-independent octahedral Fe sites: The Fe1 octahedra share two corners with the neighboring arsenate groups. Both individual chains are related by a symmetry center and joined by two symmetry-related Fe2 octahedra. Each Fe2 octahedron shares three corners with double-chain polyhedra (O3, O4 with arsenate groups; the O8 hydroxyl group with the Fe1 octahedron) and one corner (O11) with the monodentate sulfate group. The coordination of the Fe2 octahedron is completed by two H2O molecules (O9 and O10). There is also a complex network of H bonds that connects polyhedra within and among chains. Raman and infrared spectra show that (SO4)2- tetrahedra are strongly distorted.