Details
| Original language | English |
|---|---|
| Pages (from-to) | 188-200 |
| Number of pages | 13 |
| Journal | Journal of Colloid and Interface Science |
| Volume | 478 |
| Publication status | Published - 15 Sept 2016 |
Abstract
Hypothesis: Interface properties of organoclay particles can be related directly to type of organic cation, and density and arrangement of organic coating at clay surfaces. Experiments: This study provides detailed nanoscale insights on surface structure of hexadecyltrimethylammonium/hexadecylpyridinium-montmorillonite (HDTMA+/HDPy+-M) organoclays by combining several experimental methods (e.g. transmission electron microscopy, TEM, and X-ray photoelectron spectroscopy, XPS) with molecular simulations. Findings: TEM showed a relation between the thickness of the organic coating and the amount of organic cation loading. Furthermore, coating thickness varied for the same sample indicating a heterogeneous surface of clay particles. The changes in elemental composition determined by XPS were correlated with the thickness of the organic coating. High resolution XPS showed changes in binding energies of CN bonds, which were attributed to varying local environment of head groups of organic cations. Classical molecular dynamics (MD) simulations showed a successive transformation of the organic cation coating of the montmorillonite surface from thin disordered monolayers at low up to disordered bilayer or quasi paraffin-type arrangements at high surfactant coverages. For organoclays with low cation loading no significant difference was observed between HDTMA+ and HDPy+. However, at high cation loading, surface packing density was higher for HDTMA+ than for HDPy+.
Keywords
- Alkylammonium organoclays, MD simulation, TEM, XPS
ASJC Scopus subject areas
- Materials Science(all)
- Electronic, Optical and Magnetic Materials
- Materials Science(all)
- Biomaterials
- Materials Science(all)
- Surfaces, Coatings and Films
- Chemical Engineering(all)
- Colloid and Surface Chemistry
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In: Journal of Colloid and Interface Science, Vol. 478, 15.09.2016, p. 188-200.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - External surface structure of organoclays analyzed by transmission electron microscopy and X-ray photoelectron spectroscopy in combination with molecular dynamics simulations
AU - Schampera, B.
AU - Tunega, D.
AU - Šolc, R.
AU - Woche, S. K.
AU - Mikutta, R.
AU - Wirth, R.
AU - Dultz, S.
AU - Guggenberger, G.
N1 - Funding information: We thank A. Schreiber from the Geo Forschungs Zentrum (GFZ) for preparation of TEM samples. This study was supported within the frame of the D-A-CH bilateral collaboration by the Deutsche Forschungsgemeinschaft (DFG, Germany) under contract number SCHA 1732/1-1 and the Fonds zur Förderung der wissenschaftlichen Forschung ( FWF , Austria) under contract number I880-N21 . The computational results presented have been achieved using the Vienna Scientific Cluster (VSC).
PY - 2016/9/15
Y1 - 2016/9/15
N2 - Hypothesis: Interface properties of organoclay particles can be related directly to type of organic cation, and density and arrangement of organic coating at clay surfaces. Experiments: This study provides detailed nanoscale insights on surface structure of hexadecyltrimethylammonium/hexadecylpyridinium-montmorillonite (HDTMA+/HDPy+-M) organoclays by combining several experimental methods (e.g. transmission electron microscopy, TEM, and X-ray photoelectron spectroscopy, XPS) with molecular simulations. Findings: TEM showed a relation between the thickness of the organic coating and the amount of organic cation loading. Furthermore, coating thickness varied for the same sample indicating a heterogeneous surface of clay particles. The changes in elemental composition determined by XPS were correlated with the thickness of the organic coating. High resolution XPS showed changes in binding energies of CN bonds, which were attributed to varying local environment of head groups of organic cations. Classical molecular dynamics (MD) simulations showed a successive transformation of the organic cation coating of the montmorillonite surface from thin disordered monolayers at low up to disordered bilayer or quasi paraffin-type arrangements at high surfactant coverages. For organoclays with low cation loading no significant difference was observed between HDTMA+ and HDPy+. However, at high cation loading, surface packing density was higher for HDTMA+ than for HDPy+.
AB - Hypothesis: Interface properties of organoclay particles can be related directly to type of organic cation, and density and arrangement of organic coating at clay surfaces. Experiments: This study provides detailed nanoscale insights on surface structure of hexadecyltrimethylammonium/hexadecylpyridinium-montmorillonite (HDTMA+/HDPy+-M) organoclays by combining several experimental methods (e.g. transmission electron microscopy, TEM, and X-ray photoelectron spectroscopy, XPS) with molecular simulations. Findings: TEM showed a relation between the thickness of the organic coating and the amount of organic cation loading. Furthermore, coating thickness varied for the same sample indicating a heterogeneous surface of clay particles. The changes in elemental composition determined by XPS were correlated with the thickness of the organic coating. High resolution XPS showed changes in binding energies of CN bonds, which were attributed to varying local environment of head groups of organic cations. Classical molecular dynamics (MD) simulations showed a successive transformation of the organic cation coating of the montmorillonite surface from thin disordered monolayers at low up to disordered bilayer or quasi paraffin-type arrangements at high surfactant coverages. For organoclays with low cation loading no significant difference was observed between HDTMA+ and HDPy+. However, at high cation loading, surface packing density was higher for HDTMA+ than for HDPy+.
KW - Alkylammonium organoclays
KW - MD simulation
KW - TEM
KW - XPS
UR - http://www.scopus.com/inward/record.url?scp=84973444264&partnerID=8YFLogxK
U2 - 10.1016/j.jcis.2016.06.008
DO - 10.1016/j.jcis.2016.06.008
M3 - Article
AN - SCOPUS:84973444264
VL - 478
SP - 188
EP - 200
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
SN - 0021-9797
ER -