Quick
Search: 
 
advanced search
 GSW Home    GeoRef Home    My GSW Alerts    Contact GSW    About GSW    Journals List    Help 
American Mineralogist RIMG advertisement
JOURNAL HOME HELP CONTACT PUBLISHER SUBSCRIBE ARCHIVE SEARCH TABLE OF CONTENTS

American Mineralogist; October 1997; v. 82; no. 9-10; p. 900-912
This Article
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Order Hardcopy of Full Text via AGI/GeoRef
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Rinker, M. J.
Right arrow Articles by Pratt, A. R.
Right arrow Search for Related Content
GeoRef
Right arrow GeoRef Citation

Marcasite oxidation in low-temperature acidic (pH 3.0) solutions; mechanism and rate laws

M. J. Rinker, H. W. Nesbitt, and A. R. Pratt

University of Western Ontario, Department of Earth Sciences, London, ON, Canada

Marcasite surfaces were analyzed using X-ray photoelectron spectroscopy (XPS) and auger electron spectroscopy (AES). XPS data of a pristine marcasite surface are used as a template to examine the characteristics of a marcasite surface after exposure to vigorous cleaning procedures and after reaction in oxygenated and mildly acidic (pH 3.0) solution. Minor changes are observed to the Fe(2p (sub 3/2) ) spectrum after cleaning the surface with concentrated HCl. A new species is observed at approximately 709 eV, representing 10-15% of the total Fe spectrum. Chloride was detected by XPS broadscans and OH (super -) was observed in the O(1s) spectrum. The new Fe species at 709 eV may be associated with either OH (super -) or Cl (super -) . XPS sulfur spectrum of the surface exposed to oxygenated, HCl solution (pH = 3.0) indicates that polysulfide increases at the expense of disulfide. The Fe species observed at 709 eV is also present and represents 10-15% total Fe. XPS broadscan analyses indicate trace amounts of chloride. Oxide O (super 2-) is absent from the O(1s) spectrum but OH (super -) is present. AES depth profiles reveal no compositionally distinct zones after reaction. Leach rates for the aqueous oxidation of marcasite were determined at 25 degrees C in O-saturated chloride solution at pH 3.0. Two rate experiments were performed on crushed and sieved size fractions of marcasite: one sample was vigorously cleaned to investigate fundamental aspects of marcasite leaching and the other was untreated to simulate conditions found in natural environments. The oxidative leach rate of Fe(aq) from pristine marcasite is 4.25X10 (super -5) mmol/(m 2 .s). Analyses of aqueous S speciation reveal fluctuations in S content of oxidation state lower than SO (super 2-) 4 . The XPS results suggest that the fluctuation may result from periodic release of polysulfide to solution, after accumulation on the reactive marcasite surface.

This record provided courtesy of AGI/GeoRef.




This article has been cited by other articles:


Home page
American MineralogistHome page
R.A. Jones and H. W. Nesbitt
XPS evidence for Fe and As oxidation states and electronic states in loellingite (FeAs2)
American Mineralogist, November 1, 2002; 87(11-12): 1692 - 1698.
[Abstract] [Full Text] [PDF]




JOURNAL HOME HELP CONTACT PUBLISHER SUBSCRIBE ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2009 by Mineralogical Society of America