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 50:1406-1411 (1986)
© 1986 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 Schulthess, C. P.
Right arrow Articles by Sparks, D. L.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Schulthess, C. P.
Right arrow Articles by Sparks, D. L.
Agricola
Right arrow Articles by Schulthess, C. P.
Right arrow Articles by Sparks, D. L.

Backtitration Technique for Proton Isotherm Modeling of Oxide Surfaces1

C. P. Schulthess and D. L. Sparks2

ABSTRACT

Batch potentiometric titration analyses were made on a {gamma}-Al2O3 colloidal suspension and interpreted in terms of the electroneutrality principle. Three titration methods involving a singular reference curve were compared. The first reference used was theoretical, the latter two were representative supernatant curves: an electrolyte solution, and an aliquot of the zero point of titration (ZPT) supernatant. All three methods resulted in similar charge isotherms and a zero point of charge (ZPC) = 8.60. A fourth titration method was developed involving each supernatant of the batch titration sample to act as a unique reference. This latter method is a backtitration technique which accounts for all sources that also consume H+ ions, leaving the difference to be the adsorbed proton concentration only. The NaClO4 electrolyte solution used is postulated to be adsorbed with competitive cation and anion exchange mechanisms with a point of zero salt effect (PZSE) = 7.50.


NOTES

1 Published with the approval of the Director of the Delaware Agric. Exp. Stn. as Miscellaneous Paper no. 1121 Contribution no. 199 of the Dep. of Plant Science, Univ. of Delaware, Newark, DE 19717-1303.

2 University Graduate Research Assistant and Associate Professor of Soil Chemistry, respectively.

Received for publication November 8, 1985.


This article has been cited by other articles:


Home page
Soil Sci.Home page
C.P. Schulthess and Z. Hu
Impact of Chloride Anions on Proton and Selenium Adsorption by an Aluminum Oxide
Soil Sci. Soc. Am. J., May 1, 2001; 65(3): 710 - 718.
[Abstract] [Full Text] [PDF]


Home page
Soil Sci.Home page
N. U. Yamaguchi, A. C. Scheinost, and D. L. Sparks
Surface-Induced Nickel Hydroxide Precipitation in the Presence of Citrate and Salicylate
Soil Sci. Soc. Am. J., May 1, 2001; 65(3): 729 - 736.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
L. M. He and B. M. Tebo
Surface Charge Properties of and Cu(II) Adsorption by Spores of the Marine Bacillus sp. Strain SG-1
Appl. Envir. Microbiol., March 1, 1998; 64(3): 1123 - 1129.
[Abstract] [Full Text]




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 © 1986 by the Soil Science Society of America.