• Journal of Korean Society of Environmental Engineers
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• v.27 no.1
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• pp.11-16
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• 2005

Humic substances(HS) from raw and process waters at a conventional water treatment plant were isolated and extracted by physicochemical fractionation methods to investigate their characteristics. They are characterized for their functionality, chemical composition, and spectroscopic characteristics using FT-IR(Fourier transform infrared) and $^1H-NMR$(proton nuclear magnetic resonance) spectroscopy. Humic fraction gradually decreased from 47.2% to 26.4%(from 0.97 to 0.54 mgC/L) through conventional water treatment processes. Concentration of phenolic groups in the HS fraction gradually decreased from 60.5% to 21.8%(from 12.2 to $6.0\;{\mu}M/L$ as phenolic-OH) through water treatment. In the case of carboxylic groups, the concentration increased from 39.5% to 46.9%(from 7.9 to $10.6\;{\mu}M/L$ as COOH) by pre-chlorination, but gradually decreased to 34.2%($9.4\;{\mu}M/L$ as COOH) through sedimentation and sand filtration. From the results of the FT-IR and $^1H-NMR$ spectra of HS, the content of carboxylic groups increased and ratio of aliphatic protons to aromatic protons($P_{Al}/P_{Ar}$) also increased through water treatment, which indicated the increase of aliphatic compounds.

• Journal of Korean Society of Environmental Engineers
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• v.22 no.3
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• pp.453-461
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• 2000

Aquatic humic substance (AHS) was extracted from Soyang lake water using XAD-8 resin. and its concentration distribution in the lake from May to October. 1997 was determined. Ozonation characteristics of the AHS were studied as factors of pH, carbonate ion concentration. and the biodegradability and structural changes of the AHS were also investigated after ozonaticn. DOC distribution in Soyang Lake water was 1~3 mg/L. and the concentrations of AHS ranged between 0.2~0.8 mg/L. which was corresponding to 20~30% of DOC. AHS was composed of around 20% of HA and 80% of FA. The optimum pH value for AHS ozonation was in range of pH 7~9. When carbonate ions were added for AHS ozonation as a ladical scavenger. it was found that DOC removals were decreased. and the absorbance decreases were increased slightly. Biodegradability of the ozonized AHS was 50% higher than that of unozonated AHS. $^{13}C-NMR$ analysis showed that the aromatic compounds of AHS, after ozonation, were decreased from 49% to 17%. and the aliphatic and carboxylic compounds were increased from 34% to 51% and from 17% to 32%. respectively.

• Journal of Korea Water Resources Association
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• v.50 no.11
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• pp.715-723
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• 2017

Extracellular Polymeric Substances (EPS) in the water environment assemble fine, colloidal particles, such as clays, microorganisms and biomass, in large flocs, which are eventually subject to sedimentation and deposition and determine water/sediment quality and quantity. This study hence aimed to investigate the way that water and colloidal chemistry affects EPS-mediated flocculation of colloidal particles, using a jar-test experiment. Especially, ionic strength, divalent cation and humic substances concentrations were selected as experimental variables in the jar-test experiments, to elucidate their effects on EPS-mediated flocculation. A higher ionic strength increased flocculation capability, reducing electrostatic repulsion between EPS-attached colloidal particles and enhancing particle aggregation. 0.1 M NaCl ionic strength had higher flocculation capability, with 3 times larger floc size and 2.5 times lower suspended solid concentration, than 0.001 M NaCl. Divalent cations, such as $Ca^{2+}$, built divalent cationic bridges between colloidal particles and EPS (i.e., $colloid-Ca^{2+}-EPS$ or $EPS-Ca^{2+}-EPS$) and hence made colloidal particles to build into large, settelable flocs. A small $Ca^{2+}$ concentration enhanced flocculation capability, reducing suspended solid concentration 20 times lower than the initial dosed concentration. However, humic substances, adsorbed on colloidal particles, reduced flocculation, because they blocked EPS adsorption on colloidal particles and increased negative charges and electrostatic repulsion of colloidal particles. Suspended solid concentration in the tests with humic substances remained as high as the initial dosed concentration, indicating stabilization rather than flocculation. Findings about EPS-mediated flocculation in this research will be used for better understanding the fate and transport of colloidal particles in the water environment and for developing the best management practices for water/sediment quality.