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Licensed Unlicensed Requires Authentication Published by De Gruyter March 28, 2015

The role of water in the structures of synthetic hallimondite, Pb2[(UO2)(AsO4)2](H2O)n and synthetic parsonsite, Pb2[(UO2)(PO4)2](H2O)n, 0 ≤ n ≤ 0.5

  • Andrew J. Locock EMAIL logo , Peter C. Burns and Theodore M. Flynn
From the journal American Mineralogist


The crystal structures of synthetic hallimondite and synthetic parsonsite have been refined by fullmatrix least-squares techniques to agreement indices (hallimondite, parsonsite) wR2 of 5.5, and 7.6% for all data, and R1 of 2.7 and 3.4%, calculated for 3391 and 3181 unique observed reflections (|Fo| ≥ 4σF), respectively. Hallimondite is triclinic, space group P1̅, Z = 2, a = 7.1153(8), b = 10.4780(12), c = 6.8571(8) Å, α = 101.178(3)°, β = 95.711(3)°, γ = 86.651(3)°, V = 498.64(3) Å3, and is isostructural with parsonsite, triclinic, space group P1 . , Z = 2, a = 6.8432(5), b = 10.4105(7), c = 6.6718(4) Å, α = 101.418(1)°, β = 98.347(2)°, γ = 86.264(2)°, V = 460.64(5) Å3. In both structures, hexavalent uranium occurs as a uranyl pentagonal bipyramid. The uranyl polyhedra share an edge, forming dimers that are linked by edge- and vertex-sharing with arsenate or phosphate tetrahedra to form chains along [001]. Two symmetrically distinct Pb positions connect the chains. In hallimondite, a partially occupied oxygen atom is located in the cavity between the uranyl arsenate chains and Pb positions, and is attributed to an H2O group. The crystal of synthetic parsonsite investigated does not have appreciable electron density at this position, but its structural cavity is large enough to contain H2O. The presence of H2O in synthetic hallimondite, and its absence in synthetic parsonsite, are supported by the results of FTIR spectroscopy. In conjunction with thermogravimetric results from the literature, we suggest that the formula of parsonsite should be considered Pb2[(UO2)(PO4)2](H2O)n, and hallimondite, Pb2[(UO2)(AsO4)2](H2O)n, with 0 ≤ n ≤ 0.5 in each case.

Received: 2004-5-10
Accepted: 2004-7-23
Published Online: 2015-3-28
Published in Print: 2005-1-1

© 2015 by Walter de Gruyter Berlin/Boston

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