SSSAJ Journal of Natural Resources and Life Sciences Education
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Published in Soil Sci Soc Am J 51:1131-1136 (1987)
© 1987 Soil Science Society of America
677 S. Segoe Rd., Madison, WI 53711 USA
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bloom, P. R.
Right arrow Articles by Erich, M. S.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Bloom, P. R.
Right arrow Articles by Erich, M. S.
Agricola
Right arrow Articles by Bloom, P. R.
Right arrow Articles by Erich, M. S.

Effect of Solution Composition on the Rate and Mechanism of Gibbsite Dissolution in Acid Solutions1

P. R. Bloom and M. S. Erich2

ABSTRACT

The rate of dissolution of gibbsite was measured as a function of H+ concentration and anion concentration. The anions examined were nitrate, sulfate, and phosphate and the pH range used was 1.5 to 4.0. Rates of gibbsite dissolution were low and comparable to reported dissolution rates for feldspars. In the presence of nitrate and sulfate the dissolution reaction was first-order with respect to H+ below pH 2.5. In phosphate there was no dependence of the rate on H+. Above pH 3.5 in nitrate the reaction order with respect to H+ approached zero. The order of the reaction with respect to anion concentration was about 0.6, 0.4, and 0.9 for nitrate, sulfate, and phosphate, respectively. The rate dependence of gibbsite dissolution on H+ and anion concentration suggested that the mechanism of dissolution, as well as the rate, is a function of solution composition. In solutions containing ions not specifically adsorbed (e.g., NO-3 and SO2-4), proton attack of the surface is the rate-determining step. In solutions containing phosphate, anion attack predominated, and the rate of the reaction is not dependent on pH.


NOTES

1 Contribution from the Minnesota Agric. Exp. Stn., Dep. of Soil Science, Univ. of Minnesota, St. Paul, MN 55108, Scientific Journal Series, Paper no. 15 146.

2 Associate Professor, Dep. of Soil Science, Univ. of Minnesota, St. Paul, MN 55108, and Assistant Professor, Dep. of Plant and Soil Sciences, Univ. of Maine, Orono, ME 04469.

Received for publication June 26, 1986.


This article has been cited by other articles:


Home page
Soil Sci.Home page
M. Hamer, R. C. Graham, C. Amrhein, and K. N. Bozhilov
Dissolution of Ripidolite (Mg, Fe-Chlorite) in Organic and Inorganic Acid Solutions
Soil Sci. Soc. Am. J., March 1, 2003; 67(2): 654 - 661.
[Abstract] [Full Text] [PDF]


Home page
J. Environ. Qual.Home page
T.-T. Lim, J.-H. Tay, and C.-I. Teh
Contamination Time Effect on Lead and Cadmium Fractionation in a Tropical Coastal Clay
J. Environ. Qual., May 1, 2002; 31(3): 806 - 812.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
The SCI Journals Agronomy Journal Crop Science
Journal of Natural Resources
and Life Sciences Education
Vadose Zone Journal
Journal of Plant Registrations Journal of
Environmental Quality
The Plant Genome
Copyright © 1987 by the Soil Science Society of America.