|
|
|
|||||||||||||||||
| JOURNAL HOME | HELP | CONTACT PUBLISHER | SUBSCRIBE | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Research Paper |
1 Bureau de Recherches Géologiques et Minières (BRGM), Environnement & Procédés, 3, avenue Claude Guillemin, BP 6009, 45060 Orléans Cedex 2, 2 Unité de Science du sol, INRA dOrléans, Avenue de la pomme de pin, BP 20619, 45166 Olivet Cedex, 3 Laboratoire Environnement et Minéralurgie, UMR 7569 INPL & CNRS, ENSG - BP 40 - 54501 Vand
uvre-les-Nancy Cedex, and 4 Laboratoire de Chimie de lEau et de lEnvironnement, 40, Avenue du Recteur Pineau, 86022 Poitiers Cedex, France
* E-mail: a.saada{at}brgm.fr
(Received 18 March 2002; revised 5 May 2003)
The mechanisms governing the adsorption of a commercial humic acid (HA) on a kaolinitic clay were determined. The amount of HA fixed increased with the ionic strength of the medium and the presence of divalent ions (Ca2+). The effect of Ca2+ is due to its ability to establish (1) intramolecular bridges causing condensation of the HA, and (2) intermolecular bridges between the clay and the HA. A stable clay-humic complex containing only the fraction of HA that withstands washing with water was prepared and characterized by high-resolution Ar adsorption volumetry. The overall results show that (1) HA interacts strongly with the basal surfaces of the clay, (2) Ca serves to establish Ca2+ bridges between HA and clay, and (3) HA and clay interact via at least two distinct adsorption mechanisms.
KEYWORDS: kaolinite, natural organic matter, sorption, calcium
| JOURNAL HOME | HELP | CONTACT PUBLISHER | SUBSCRIBE | ARCHIVE | SEARCH | TABLE OF CONTENTS |