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@PHDTHESIS{Khalaf:33181,
author = {Khalaf, Moustafa},
title = {{E}ffect of the fractionation and immobilization on the
sorption properties of humic acid},
volume = {4046},
issn = {0944-2952},
school = {Techn. Hochsch. Aachen},
type = {Dr. (FH)},
address = {Jülich},
publisher = {Forschungszentrum Jülich GmbH Zentralbibliothek, Verlag},
reportid = {PreJuSER-33181, Juel-4046},
series = {Berichte des Forschungszentrums Jülich},
pages = {114 p.},
year = {2003},
note = {Record converted from VDB: 12.11.2012; Aachen, Techn.
Hochsch., Diss., 2003},
abstract = {Humic substances modify the surface of inorganic soil
constituents changing the nature and amount of adsorption
sites for contaminants and also influencing the
particle-particle interactions and thus the mobility and
transport behavior of the soil particles. The aim of this
PhD work was to investigate the effects of the interactions
between two important soil components, aluminum oxide and
humic acid, on the sorption behavior of 2,4-dichlorophenol
under laboratory conditions selected to model the soil
systems. Humic acid is very heterogeneous in terms of
physical and chemical properties. To reduce the chemical
heterogeneity of the extracted humic acid (from the A$_{p}$
horizon of the Orthic Luvisol, Merzenhausen, Germany), a
fractionation scheme using the ultrafiltration technique was
used to obtain eight size fractions of the humic acid. The
extracted humic acid and its fractions were characterized by
potentiometric acid-base titration, elemental analysis and
different spectroscopic methods (NMR, UV-VIS and FT-IR
spectroscopy). Clear chemical differences between the humic
acid size fractions were observed. Smaller size fractions of
the soil humic acid contained more chargeable functional
groups and larger percentage of aromatic carbon than the
larger size fractions. Conversely, the percentage of
aliphatic carbon increased with increasing apparent
molecular weight. Moreover, the solid-state $^{19}$F-NMR was
used to study the sorptive uptake of hexafluorobenzene by
the humic acid and its fractions. It was found that humic
acid molecules have different chemical environments into
which organic pollutant such as hexafluorobenzene can sorb.
Small humic acid molecules have at least three sorption
sites (“rigid”, “soft” and other new domains) that
are more clearly defined and homogeneous than the sorption
domains found in larger humic acid molecules. The effect of
the pH and the electrolyte concentration on the adsorption
of the humic acid onto alumina surfaces as well as on the
colloidal stability of these systems were studied. To better
understand the binding mechanisms these results were also
compared to those of polyacrylic acid. The adsorption of
humic acid or polyacrylic acid to alumina varied with pH and
electrolyte concentration, suggesting that the conformation
of the humic acid or polyacrylic acid in solution
significantly determines their structures on the mineral
surface. At low pH (< point of zero charge (PZC) of
alumina), increasing amounts of humic acid or polyacrylic
acid are adsorbed on the alumina surface with increasing
concentrations of solutes, resulting in a charge reversal
from positive to negative net total particle charge whilst
at high pH (> PZC), the electrophoretic mobility was shifted
to more negative values. The colloidal stability of the
alumina dispersions containing increasing amounts of the
added humic acid and polyacrylic acid, respectively, was
monitored using the dynamic light scattering technique. The
maximum aggregate size was observed around the zero
electrophoretic mobility, indicating the importance of the
charge neutralization mechanism. By comparing the adsorption
of the humic acid fractions on alumina surfaces, it was
found that the adsorbed amount increases with increasing
humic acid molecular size. Furthermore, an increase in the
rise of the adsorption isotherm in the plateau regions by
increasing the humic acid fraction size was also observed
which indicates a higher contribution of the hydrophobic
interactions due to the increase in the aliphatic carbon and
the decrease in the chargeable groups. The sorption results
of 2,4-dichlorophenol on the immobilized humic acid at
different pH and salt concentrations revealed that the value
of the sorption coefficient decreases as the ionic strength
decreases or the pH value increases which gives direct
evidence for the importance of the conformation of the
immobilized HA. These sorption isotherms can be described as
a linear isotherm, which indicates that the sorption of
2,4-dichlorophenol is predominantly a partitioning process
between the aqueous phase and the immobilized humic acid.},
cin = {ICG-IV},
cid = {I:(DE-Juel1)VDB50},
pnm = {Chemie und Dynamik der Geo-Biosphäre},
pid = {G:(DE-Juel1)FUEK257},
typ = {PUB:(DE-HGF)11 / PUB:(DE-HGF)3},
url = {https://juser.fz-juelich.de/record/33181},
}