Quick
Search: 
 
advanced search
 GSW Home    GeoRef Home    My GSW Alerts    Contact GSW    About GSW    Journals List    Help 
Clays and Clay Minerals Email Content Delivery
JOURNAL HOME HELP CONTACT PUBLISHER SUBSCRIBE ARCHIVE SEARCH TABLE OF CONTENTS

Clays and Clay Minerals; June 2008; v. 56; no. 3; p. 338-343; DOI: 10.1346/CCMN.2008.0560304
© 2008 Clay Minerals Society
This Article
Right arrow Figures Only
Right arrow Full Text
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 Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
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 Kaufhold, S.
Right arrow Articles by Houben, G.
Right arrow Search for Related Content
GeoRef
Right arrow GeoRef Citation

THE pH OF AQUEOUS BENTONITE SUSPENSIONS

Stephan Kaufhold1,*, Reiner Dohrmann1,2, Dietrich Koch3 and Georg Houben1

1 BGR Bundesanstalt für Geowissenschaften und Rohstoffe, Stilleweg 2, D-30655 Hannover, Germany
2 LBEG Landesamt für Bergbau, Energie und Geologie, Stilleweg 2, D-30655 Hannover, Germany
3 S&B Industrial Minerals, Schmielenfeldstrasse 72, D-45770 Marl, Germany

* E-mail address of corresponding author: s.kaufhold{at}bgr.de

The pH of aqueous bentonite suspensions is known to be influenced by carbonates present even in minor amounts. On the other hand, at high solid:liquid ratios (at standard pH measurement conditions: 2% w/w suspension), the type of exchangeable cation in the smectite is also known to determine pH (particularly Na+ or Ca2+). By cation-exchange tests we proved that exchanging the Ca2+ for Na+ results in an increase in the pH. However, this increase in pH was only found if excess salts were removed from the system (by washing or dialysis, respectively). The effect of the type of exchangeable cation can, at least partially, be explained by hydrolysis of Ca2+. On the other hand, a pronounced alkalinity of Na bentonites is observed which can, at least partially, be attributed to the hydrolysis of montmorillonite (Na+ is exchanged for H+ of water). The increase in the volume of the Stern layer, caused by increasing the degree of delamination, is also suggested to play a role. H+ and Na+ are concentrated in the Stern layer. Hence, increasing the Stern layer volume decreases the amount of H+ and Na+ in solution and thus increases pH. Unfortunately, both processes, montmorillonite hydrolysis and delamination, depend on the ionic strength. Distinguishing the processes quantitatively, therefore, is an analytical challenge, and impossible based on the data presented here.

To model the pore-water chemistry of clays and clay stones, all of the above-mentioned processes have to be considered. It is possible that other reactions, not identified in the present work, contribute toward the pH values of aqueous bentonite suspensions.

Key Words: Bentonite pH • Carbonate Content • Clay-water Interaction




This article has been cited by other articles:


Home page
Clays and Clay MineralsHome page
R. Dohrmann and S. Kaufhold
THREE NEW, QUICK CEC METHODS FOR DETERMINING THE AMOUNTS OF EXCHANGEABLE CALCIUM CATIONS IN CALCAREOUS CLAYS
Clays and Clay Minerals, June 1, 2009; 57(3): 338 - 352.
[Abstract] [Full Text] [PDF]


Home page
Clays and Clay MineralsHome page
S. Kaufhold and R. Dohrmann
COMPARISON OF THE TRADITIONAL ENSLIN-NEFF METHOD AND THE MODIFIED DIENG METHOD FOR MEASURING WATER-UPTAKE CAPACITY
Clays and Clay Minerals, December 1, 2008; 56(6): 686 - 692.
[Abstract] [Full Text] [PDF]




JOURNAL HOME HELP CONTACT PUBLISHER SUBSCRIBE ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2009 by Clay Minerals Society