Details
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | 2746-2752 |
| Seitenumfang | 7 |
| Fachzeitschrift | Applied geochemistry |
| Jahrgang | 23 |
| Ausgabenummer | 9 |
| Frühes Online-Datum | 8 Juli 2008 |
| Publikationsstatus | Veröffentlicht - Sept. 2008 |
Abstract
The selectivity of organoclays for different anions is not well understood. It is of particular importance when potentially hazardous anions from nuclear waste matrixes or contaminated ground water are in competition with each other, or with other naturally occurring anions. This study focuses on the adsorption of I-, ReO4-, NO3-, Br-, SO42 -- and SeO32 - to hexadecylpyridinium-, hexadecyltrimethylammonium-, and benzethonium-modified bentonites (MX-80) and the understanding of the selectivity of the process. Adsorption experiments were carried out using the batch technique. Anion concentrations were determined by ion chromatography of the solution and X-ray fluorescence analysis of the organoclays. Anion adsorption to the studied organobentonites is mainly due to anion exchange with Cl-. The results showed a clear selectivity of the organoclays, with the affinity sequence being ReO4- > I- >NO3- > Br- > Cl- >SO42 - - >SeO32 - . This sequence corresponds to the sequence of increasing hydration energies of the anions, thus indicating that the observed selectivity of the organobentonites could be due to the process of minimisation of energy of the system.
ASJC Scopus Sachgebiete
- Umweltwissenschaften (insg.)
- Umweltchemie
- Umweltwissenschaften (insg.)
- Umweltverschmutzung
- Erdkunde und Planetologie (insg.)
- Geochemie und Petrologie
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in: Applied geochemistry, Jahrgang 23, Nr. 9, 09.2008, S. 2746-2752.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - Anion selectivity of organobentonites
AU - Behnsen, Julia
AU - Riebe, Beate
PY - 2008/9
Y1 - 2008/9
N2 - The selectivity of organoclays for different anions is not well understood. It is of particular importance when potentially hazardous anions from nuclear waste matrixes or contaminated ground water are in competition with each other, or with other naturally occurring anions. This study focuses on the adsorption of I-, ReO4-, NO3-, Br-, SO42 -- and SeO32 - to hexadecylpyridinium-, hexadecyltrimethylammonium-, and benzethonium-modified bentonites (MX-80) and the understanding of the selectivity of the process. Adsorption experiments were carried out using the batch technique. Anion concentrations were determined by ion chromatography of the solution and X-ray fluorescence analysis of the organoclays. Anion adsorption to the studied organobentonites is mainly due to anion exchange with Cl-. The results showed a clear selectivity of the organoclays, with the affinity sequence being ReO4- > I- >NO3- > Br- > Cl- >SO42 - - >SeO32 - . This sequence corresponds to the sequence of increasing hydration energies of the anions, thus indicating that the observed selectivity of the organobentonites could be due to the process of minimisation of energy of the system.
AB - The selectivity of organoclays for different anions is not well understood. It is of particular importance when potentially hazardous anions from nuclear waste matrixes or contaminated ground water are in competition with each other, or with other naturally occurring anions. This study focuses on the adsorption of I-, ReO4-, NO3-, Br-, SO42 -- and SeO32 - to hexadecylpyridinium-, hexadecyltrimethylammonium-, and benzethonium-modified bentonites (MX-80) and the understanding of the selectivity of the process. Adsorption experiments were carried out using the batch technique. Anion concentrations were determined by ion chromatography of the solution and X-ray fluorescence analysis of the organoclays. Anion adsorption to the studied organobentonites is mainly due to anion exchange with Cl-. The results showed a clear selectivity of the organoclays, with the affinity sequence being ReO4- > I- >NO3- > Br- > Cl- >SO42 - - >SeO32 - . This sequence corresponds to the sequence of increasing hydration energies of the anions, thus indicating that the observed selectivity of the organobentonites could be due to the process of minimisation of energy of the system.
UR - http://www.scopus.com/inward/record.url?scp=50249157469&partnerID=8YFLogxK
U2 - 10.1016/j.apgeochem.2008.06.019
DO - 10.1016/j.apgeochem.2008.06.019
M3 - Article
AN - SCOPUS:50249157469
VL - 23
SP - 2746
EP - 2752
JO - Applied geochemistry
JF - Applied geochemistry
SN - 0883-2927
IS - 9
ER -