JOESMITHITE, A PLUMBOUS AMPHIBOLE REVISITED AND COMMENTS ON BOND VALENCES

Citation
Pb. Moore et al., JOESMITHITE, A PLUMBOUS AMPHIBOLE REVISITED AND COMMENTS ON BOND VALENCES, Mineralogy and petrology, 48(2-4), 1993, pp. 97-113
Citations number
23
Categorie Soggetti
Mineralogy,Geology
Journal title
ISSN journal
09300708
Volume
48
Issue
2-4
Year of publication
1993
Pages
97 - 113
Database
ISI
SICI code
0930-0708(1993)48:2-4<97:JAPARA>2.0.ZU;2-E
Abstract
Joesmithite is a complex clinoamphibole which contains at least 14 com ponents in its formula. Its ideal formula would be PbCa2Mg3Fe23+(Si6Be 2O22)(OH)2. It is monoclinic holosymmetric, an ordered derivative of t he C2/m clinoamphiboles, a = 9.915(2), b = 17.951(4), c = 5.243(1)angs trom, beta = 105.95(2)degrees, Z = 2, space group P2/a, D(obs) = 3.83( 1), D(cal) = 3.91 g cm-3. R = 0.056 for 2299 independent F0. The cells of joesmithite and pargasitic amphibole were compared according to di fferences, DELTA, in their structure cells. The same procedure was app lied to the margarosanite, PbCa2Si3O9 and walstromite, BaCa2Si3O9 pair s. In both pairs, the anion positions differed by 0.2 angstrom at most , but the Pb/A, Pb/Ba differences ranged from 0.4 to 0.6 angstrom. The lone pair Pb2+ cation responds according to the bond valence sums of its coordinating anions compared with its closed core counterpart. It appears that when the bond valence sums for the coordinating anions ar e different, Pb2+ moves toward the most underbonded anion. If the anio n bond valence sums are equal for all vertices of the coordinating pol yhedron (as in wulfenite, Pb2+Mo6+O4), then Pb2+ does not shift.