Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/85961
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Type: Journal article
Title: Sb⁵⁺ and Sb³⁺ substitution in segnitite: a new sink for As and Sb in the environment and implications for acid mine drainage
Other Titles: Sb(5+) and Sb(3+) substitution in segnitite: a new sink for As and Sb in the environment and implications for acid mine drainage
Author: Mills, S.
Etschmann, B.
Kampf, A.
Poirier, G.
Newville, M.
Citation: American Mineralogist: an international journal of earth and planetary materials, 2014; 99(7):1355-1359
Publisher: Mineralogical Society of America
Issue Date: 2014
ISSN: 0003-004X
1945-3027
Statement of
Responsibility: 
Stuart J. Mills, Barbara Etschmann, Anthony R. Kampf, Glenn Poirier and Matthew Newville
Abstract: A sample of Sb-rich segnitite from the Black Pine mine, Montana, U.S.A., has been studied by microprobe analyses, single-crystal X-ray diffraction, and μ-EXAFS and XANES spectroscopy. Linear combination fitting of the spectroscopic data provided Sb5+:Sb3+ = 85(2):15(2), where Sb5+ is in octahedral coordination substituting for Fe3+ and Sb3+ is in tetrahedral coordination substituting for As5+. Based upon this Sb5+:Sb3+ ratio, the microprobe analyses yielded the empirical formula Pb1.02 H1.02(Fe3+2.36Sb5+0.41Cu2+0.27)∑3.04(As5+1.78Sb3+0.07S6+0.02)∑1.88O8(OH)6.00. The crystal structure refinement and bond valence analysis are consistent with these cation site assignments. The formation of Sb-rich segnitite opens new possibilities for Sb sinks within the supergene zone. Segnitite may, in fact, be an ideal host for the sequestering of several toxic elements for pH < 2. At higher pH values, As is more likely to be incorporated into schwertmannite and ferrihydrite.
Keywords: μ-EXAFS; XANES; crystal structure; segnitite; antimony; valency; alunite supergroup; oxidized zone
Rights: © 2014 Mineralogical Society of America
DOI: 10.2138/am.2014.4834
Published version: http://dx.doi.org/10.2138/am.2014.4834
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