Details
Originalsprache | Englisch |
---|---|
Seiten (von - bis) | 125-133 |
Seitenumfang | 9 |
Fachzeitschrift | Applied clay science |
Jahrgang | 67-68 |
Publikationsstatus | Veröffentlicht - Okt. 2012 |
Abstract
The binding of anions at interlayer sites of organo-clay minerals is supposed to be stronger and more specific than on the external surfaces. In this study the Cr(VI) adsorption properties of two hydrous phyllosilicates, a montmorillonite and a vermiculite modified with Hexadecylpyridinium (HDPy), Hexadecyltrimethylammonium (HDTMA) and Benzethonium (BE) were investigated at pH 3-9. Structural features were determined by X-ray diffraction. The surface charge of the organo-clays at different pH was analyzed by polyelectrolyte titration in the cell of a particle charge detector. The effect of competing anions Cl-, NO3- and SO42- on Cr(VI) adsorption was determined. The interlayer space structures of the organo-vermiculites were paraffin-type, whereas it was pseudotrimolecular for the organo-montmorillonites. Besides organic cations also considerable amounts of inorganic cations were present in the interlayer space. As a consequence of organic cation treatment the surface charge of the clays shifted from negative to positive values up to 269mmolckg-1; it was highly affected by the specific surface area, layer charge and pH. Depending on the kind of organic cation, organo-vermiculites and -bentonites showed comparable adsorption capacity for Cr(VI), which was at pH 4.5 0.38 and 0.30molkg-1 for HDPy- and HDTMA-vermiculites, respectively and 0.37 and 0.26molkg-1 for the corresponding bentonites. For all organo-clays the adsorbed amount of Cr(VI) decreased with increasing pH. The effect of competing anions, Cl-, NO3- and SO42- on Cr(VI) adsorption appeared to be small. For organo-vermiculites a higher portion of anion adsorption sites was located in the interlayer space. In context with the high share of adsorption sites in the interlayer space it is suggested that both organo-vermiculites and organo-bentonites are promising adsorbents of Cr(VI) in water purification methods.
ASJC Scopus Sachgebiete
- Erdkunde und Planetologie (insg.)
- Geologie
- Erdkunde und Planetologie (insg.)
- Geochemie und Petrologie
Zitieren
- Standard
- Harvard
- Apa
- Vancouver
- BibTex
- RIS
in: Applied clay science, Jahrgang 67-68, 10.2012, S. 125-133.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - Organic cation exchanged montmorillonite and vermiculite as adsorbents for Cr(VI)
T2 - Effect of layer charge on adsorption properties
AU - Dultz, Stefan
AU - An, Jong Hyok
AU - Riebe, Beate
N1 - Funding information: The work was supported by the Federal Ministry for Economic Affairs and Employment (BMWA) under contract number 02E9481 and the Gottlieb Daimler- and Karl Benz-Foundation through their fellowship program (J.-H. An).
PY - 2012/10
Y1 - 2012/10
N2 - The binding of anions at interlayer sites of organo-clay minerals is supposed to be stronger and more specific than on the external surfaces. In this study the Cr(VI) adsorption properties of two hydrous phyllosilicates, a montmorillonite and a vermiculite modified with Hexadecylpyridinium (HDPy), Hexadecyltrimethylammonium (HDTMA) and Benzethonium (BE) were investigated at pH 3-9. Structural features were determined by X-ray diffraction. The surface charge of the organo-clays at different pH was analyzed by polyelectrolyte titration in the cell of a particle charge detector. The effect of competing anions Cl-, NO3- and SO42- on Cr(VI) adsorption was determined. The interlayer space structures of the organo-vermiculites were paraffin-type, whereas it was pseudotrimolecular for the organo-montmorillonites. Besides organic cations also considerable amounts of inorganic cations were present in the interlayer space. As a consequence of organic cation treatment the surface charge of the clays shifted from negative to positive values up to 269mmolckg-1; it was highly affected by the specific surface area, layer charge and pH. Depending on the kind of organic cation, organo-vermiculites and -bentonites showed comparable adsorption capacity for Cr(VI), which was at pH 4.5 0.38 and 0.30molkg-1 for HDPy- and HDTMA-vermiculites, respectively and 0.37 and 0.26molkg-1 for the corresponding bentonites. For all organo-clays the adsorbed amount of Cr(VI) decreased with increasing pH. The effect of competing anions, Cl-, NO3- and SO42- on Cr(VI) adsorption appeared to be small. For organo-vermiculites a higher portion of anion adsorption sites was located in the interlayer space. In context with the high share of adsorption sites in the interlayer space it is suggested that both organo-vermiculites and organo-bentonites are promising adsorbents of Cr(VI) in water purification methods.
AB - The binding of anions at interlayer sites of organo-clay minerals is supposed to be stronger and more specific than on the external surfaces. In this study the Cr(VI) adsorption properties of two hydrous phyllosilicates, a montmorillonite and a vermiculite modified with Hexadecylpyridinium (HDPy), Hexadecyltrimethylammonium (HDTMA) and Benzethonium (BE) were investigated at pH 3-9. Structural features were determined by X-ray diffraction. The surface charge of the organo-clays at different pH was analyzed by polyelectrolyte titration in the cell of a particle charge detector. The effect of competing anions Cl-, NO3- and SO42- on Cr(VI) adsorption was determined. The interlayer space structures of the organo-vermiculites were paraffin-type, whereas it was pseudotrimolecular for the organo-montmorillonites. Besides organic cations also considerable amounts of inorganic cations were present in the interlayer space. As a consequence of organic cation treatment the surface charge of the clays shifted from negative to positive values up to 269mmolckg-1; it was highly affected by the specific surface area, layer charge and pH. Depending on the kind of organic cation, organo-vermiculites and -bentonites showed comparable adsorption capacity for Cr(VI), which was at pH 4.5 0.38 and 0.30molkg-1 for HDPy- and HDTMA-vermiculites, respectively and 0.37 and 0.26molkg-1 for the corresponding bentonites. For all organo-clays the adsorbed amount of Cr(VI) decreased with increasing pH. The effect of competing anions, Cl-, NO3- and SO42- on Cr(VI) adsorption appeared to be small. For organo-vermiculites a higher portion of anion adsorption sites was located in the interlayer space. In context with the high share of adsorption sites in the interlayer space it is suggested that both organo-vermiculites and organo-bentonites are promising adsorbents of Cr(VI) in water purification methods.
KW - Anion exchange
KW - Cr(VI)
KW - Layer charge
KW - Organo-clay minerals
KW - Selectivity
UR - http://www.scopus.com/inward/record.url?scp=84869163876&partnerID=8YFLogxK
U2 - 10.1016/j.clay.2012.05.004
DO - 10.1016/j.clay.2012.05.004
M3 - Article
AN - SCOPUS:84869163876
VL - 67-68
SP - 125
EP - 133
JO - Applied clay science
JF - Applied clay science
SN - 0169-1317
ER -