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Combined neutron powder and X-ray single-crystal diffraction refinement of the atomic structure and hydrogen bonding of goslarite (ZnSO4·7H2O)

Published online by Cambridge University Press:  05 July 2018

J. L. Anderson ,
R. C. Peterson  and
I. P. Swainson
J. L. Anderson*
Affiliation:
Department of Geological Sciences and Geological Engineering, Queen's University, Kingston, Ontario, Canada K7L 3N6
R. C. Peterson
Affiliation:
Department of Geological Sciences and Geological Engineering, Queen's University, Kingston, Ontario, Canada K7L 3N6
I. P. Swainson
Affiliation:
Neutron Program for Materials Research, National Research Laboratory, Chalk River, Ontario, Canada K0J 1J0
*
*E-mail: [email protected]
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Abstract

The atomic structure of synthetic, deuterated goslarite (ZnSO4·7D2O), a = 11.8176(6) Å, b = 12.0755(7) Å, c = 6.8270(4)Å, space group P212121, Z = 4, has been refined in a combined neutron powder diffraction and X-ray single-crystal data refinement to wRp 1.92%, Rp 1.45% and R(F2) 12.66% for the neutron powder data contribution and R(F2) 8.72% for the X-ray single-crystal data contribution. Both data sets were necessary to achieve the best overall fit agreement in the Rietveld refinement and reasonable geometry within structural units. The results of this study confirm that the H-bonding scheme for goslarite is the same as that of the other epsomite group minerals. Small but significant variations of the Zn–O bond lengths can be attributed to details of the H bonds to the O atoms of the Zn octahedra. This investigation of the atomic structure and hydrogen bonding of goslarite is groundwork for future studies into phase relationships and the mechanisms of hydration and dehydration in the ZnSO4–H2O system.

Keywords

goslaritehydrogen bondingmine wastesulphate mineralscrystal structureneutron diffraction
Type
Research Article
Information
Mineralogical Magazine , Volume 69 , Issue 3 , June 2005 , pp. 259 - 271
Copyright
Copyright © The Mineralogical Society of Great Britain and Ireland 2005

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