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@ARTICLE{Tombacz:36028,
author = {Tombacz, E. and Libor, Z. and Illes, E. and Majzik, A. and
Klumpp, E.},
title = {{T}he role of reactive surface sites and complexation by
humic acids in the interaction of clay mineral and iron
oxide particles},
journal = {Organic geochemistry},
volume = {35},
issn = {0146-6380},
address = {Amsterdam [u.a.]},
publisher = {Elsevier Science},
reportid = {PreJuSER-36028},
pages = {257 - 267},
year = {2004},
note = {Record converted from VDB: 12.11.2012},
abstract = {Aggregation and dispersion of mineral particles
spontaneously take place under changing environmental
conditions in natural systems. The structure of particle
network in soils, the retardation or release of colloidal
particles, and their mobility and transport are inherently
influenced by natural organic matter bound to the mineral
matrix. Since the surface properties of clay mineral and
metal oxide particles, and the electrified mineral-water
interfaces play a major role in formation, structure and
strength of aggregates, any surface modification, especially
by polyanionic organic complexants such as humic substances,
has a significant affect on particle interaction in a
mineral assemblage. The permanently and/or conditionally
charged clay minerals (montmorillonite and kaolinite) and
iron oxides (hematite and magnetite), as known major mineral
components in natural waters, were selected for studying
their surface charge characteristics and pH dependent
interactions. We discuss how the surface charge correlates
with particle aggregation through some characteristic
examples for homo and heterocoagulation of similar and
dissimilar mineral particles under acidic condition (at pH
similar to4) in the dilute and concentrated systems studied
by means of light scattering and theology, respectively. The
adsorption of a brown coal derived humic acid, and its
influence on the surface charge character and particle
aggregation of clay and iron oxide particles were also
studied in dilute and concentrated suspensions. Humic acids
can be bound to the most reactive surface sites of clay and
oxide particles, i.e. to Al-OH mainly at the edges of clay
lamellae, and to Fe-OH on iron oxides, in surface
complexation reaction, therefore their role in particle
aggregation is specific. Relations between surface
complexation, surface charge modification, and particle
aggregation in pure and mixed montmorillonite-iron oxide
systems are explained. (C) 2003 Elsevier Ltd. All rights
reserved.},
keywords = {J (WoSType)},
cin = {ICG-IV},
ddc = {540},
cid = {I:(DE-Juel1)VDB50},
pnm = {Chemie und Dynamik der Geo-Biosphäre},
pid = {G:(DE-Juel1)FUEK257},
shelfmark = {Geochemistry $\&$ Geophysics},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000220523800004},
doi = {10.1016/j.orggeochem.2003.11.002},
url = {https://juser.fz-juelich.de/record/36028},
}