• Journal of Korean Society on Water Environment
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• v.38 no.2
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• pp.63-71
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• 2022

This study aimed to maximize the potential of fluorescence 3D excitation-emission matrix (EEM) for predicting the trihalomethane formation potential (THMFP) of DOM with various sources. Fluorescence spectroscopy is a useful tool for characterizing dissolved organic matter (DOM). In this study, differential spectroscopy was applied to EEM for the prediction of THMFP, in which the difference between the EEM before and after chlorination was taken into account to obtain the differential EEM (DEEM). For characterization of the original EEM or the DEEM, the maximum intensities of several different fluorescence regions in EEM, fluorescence EEM regional integration (FRI), and humification index (HIX) were calculated and used for the surrogates for THMFP prediction. After chlorination, the fluorescence intensity decreased by 77% to 93%. In leaf-derived and effluent DOM, there was a significant decrease in the protein-like peak, while a more pronounced decrease was observed in the humic-like peak of river DOM. In general, leaf-derived and effluent DOM exhibited a relatively lower THMFP than the river DOM. Our results were consistent with the high correlations between humic-like fluorescence and THMFP previously reported. In this study, HIX (r= 0.815, p<0.001), FRI region V (r=0.727, p<0.001), humic-like peak (r= 0.827, p<0.001) from DEEM presented very high correlations with THMF P. When the humic-like peak intensity was converted to a logarithmic scale, a higher correlation was obtained (r= 0.928, p<0.001). This finding suggests that the humic-like peak in DEEM can serve as a universal predictor for THM formation of DOM with various origins.

• Environmental Engineering Research
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• v.7 no.2
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• pp.93-101
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• 2002

The seasonal patterns of dissolved organic matter (DOM) in Lake Kasumigaura, a shallow, eutrophic lake, and serveral DOM sources in its catchment area were investigated. DOM was fractionated using three resin adsorbents into classes: aquatic humic substances (AHS=humic acid+fulvic acid), hydrophobic neutrals (HoN), hydrophilic acids (HiA), bases (BaS) and hydrophilic neutrals (HiN). The DOM produced significantly different fraction distributions depending on the origin of sample. AHS and HiA prevailed over AHS in the lake while AHS and HiA existed at almost the same concentration levels in the rivers. AHS seems to be a more dominant component in rever water than lake water. The dominance of organic acids was also observed in the DOM sources: forest stream (FS), plowed field percolate (PFP), domestic sewage (DS) and sewage treatment plant effluent (STPE).

• Membrane Journal
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• v.18 no.1
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• pp.65-74
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• 2008

NOM and fine particles are the main target materials in water treatment using membranes. Particularly, humic substances extracted from soils are frequently used in many fundamental studies representing natural organic matter in raw water for drinking water treatment. In this study, ultrafiltration (UF) of artificial humic water and natural river water was conducted and the characteristics of removal efficiency and permeability were compared. In the UF of river water, the transmembrane pressure increased in the same pattern with that of 5 mg/L humic water. For the removal of organic matter and fine particles, however, two types of feed water had shown different trends. Kaolin particles and humic acids added to artificial water were better removed, while colloids and organics in natural water were relatively poorly removed. From the $UV_{254}$ and GPC analyses, it seemed that the hydrophobicity and size of humic substances contributed to the greater removal of organic matter. The UF membrane applied for humic water also showed a higher flux recovery by caustic chemical cleaning than that for river water.

• Journal of Applied Biological Chemistry
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• v.51 no.1
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• pp.36-44
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• 2008

Organic forms of arsenic (As) were determined through fractionation procedure of soil organic matter (SOM) in soil, sediments and mine tailing samples from the Myungbong, Dongil, and Okdong mining areas of southern Korea. An alkaline extraction method was applied to soil samples followed by the fractionation procedures of SOM by the DAX-8 and XAD-4 resin adsorption method. Major fraction of organic As species (42% to 98%) was found in acid-soluble fraction, whereas minor fraction (0.1 % to 67.8%) was present in the humic-associated As. In acid-soluble fractions, the transphillic- and hydrophilic-associated As were dominant in addition to As binding with humic and fulvic SOM. Arsenic binding was the strongest between pH 6 to 8 and reduced to about 70% at both low and high pH regions. The amount of both transphillic and hydrophillic associated As was less changed than humic and fulvic-associated As, in both low and high pH regions. This apparently indicates that As has stronger affinity towards hydrophillic rather than hydrophobic organics. From the experimental observation of As-binding SOM in natural soil, the ligand exchange model may be a feasible explanation of transphillic and hydrophillic affinity of As.

• Journal of Industrial Technology
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• v.31 no.B
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• pp.127-132
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• 2011

Humic substances is accounted for for the largest proportion in natural organic matter(NOM) and NOM is widely distributed in varying concentration in all aquatic and soil. They can affect water quality adversely in several ways by contributing undesirable color, complexing with metal and yielding metal concentrations exceeding normal solubility. Ozonation is one of the efficient treatments for degradation of humic substances which cause some problems in water treatment. Especially, the combination of ozone and granular activated carbon was applied to degradation humic acid in aquatic system. The aim of this work to test the available of acid-treated granular activated carbon as catalyst in the ozonation of humic acid.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 1998.11a
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• pp.236-239
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• 1998

This research was performed to check the transport characteristics of heavy metals in contaminated soil, that is, the influence of humic acid and phosphate on transport characteristics of heavy metals was studied. From the results of column mode experiments about heavy metal behavior, the order time to reach breakthrough and equilibrium was soil ＋ humic acid( 20g ) > soil ＋ humic acid ( 5 g ) > soil without Humic acid addition > soil+humic acid( 50g ). It is because the dissolved organic carbon content increased as the soil organic matter content increased. As the phosphate increased, so did the time to reach breakthrough and equilibrium. The order of time was soil + phosphate( 50 mg ) > soil + phosphate( 20 mg ) > soil . phosphate( 10 mg ) > soil without phosphate addition. It is because the phosphate ion worked as alkalinity donor and the calcium ion co-injected worked as the accelerator of coprecipitation of heavy metals.

• Journal of Korean Society of Environmental Engineers
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• v.22 no.7
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• pp.1253-1261
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• 2000

Natural organic matter (NOM) which occurs ubiquitously in both surface and ground waters, consists of both humic (i.e., humic and fulvic acids) and nonhumic components. NOM in general as well as certain constituents are problematic in water treatment. From a regulatory perspective, concerns focus upon the role of NOM constituents as disinfection byproduct (DBP) precursors. The fractionation of NOM through water treatment processes can provide insight into treatment process selection and applicability. Problematic NOM fractions can be targeted for removal or transformation. Significant source-related differences in NOM were observed among various source waters. This study found that bulk Dissolved Organic Carbon (DOC) concentration was hardly removed by oxidation process. Oxidation transformed high Molecular Weight (MW) hydrophobic fraction into low MW hydrophilic fraction. Ozone reduced s-pecific Ultraviolet Absorbance (SUVA) value more than chlorine. High MW hydrophobic fraction was effectively removed by coagulation process. About 50% of Trihalomethane Formation Potential (THMFP) was removed by coagulation process.

• Applied Biological Chemistry
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• v.40 no.2
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• pp.128-133
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• 1997

This study was conducted to evaluate the adsorption, desorption, leaching and degradation pattern of fungicide fluazinam in the soil environment under the laboratory conditions. The mode of isothermal adsorption of fluazinam in soil was coincident with the Freundlich equation. The adsorption amount of fluazinam was much higher on soils containing organic matter than on soils oxidized with hydrogen peroxide. The presence of organic matter, humic acid or fulvic acid, increased the adsorption amount of fluazinam on soils. The Freundlich constant K was much higher in soil added with humic acid than in soil added with fulvic acid. The desorption ratio of fluazinam adsorbed to soil was increased by removal of organic matter. In leaching experiment using soil column, the fluazinam applied on the soil surface was not moved down to the bottom of soil and was not detected in leachate water. The degradation of fluazinam was faster in Soil I with rich organic matter than Soil II with poor organic matter, in non-sterilized soil than sterilized soil, and in flooded soil than unflooded soil.

• Journal of environmental and Sanitary engineering
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• v.13 no.2
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• pp.156-164
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• 1998

This study was performed to select media for the development of biological activated carbon process. Using activated carbon made by Norit, Calgon, Samchully Co., removal efficiency of humic acid by the isothermal adsorption test and biodegradation of organic matters by microbes attached to BAC and observation and counting of microbes attached to BAC were examined. The removal efficiency of humic acid with dose of activated carbon was influenced by initial concentration. Compared with other activated carbon, Norit was found to be most effective in view of adsorption capacity, biodegradation of organic matter, and attachment characteristics of microorganism. In conclusion, Norit which has high adsorption capacity and good biodegradation of organic matter was recommended for selecting media in BAC process.

• Journal of Korean Society on Water Environment
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• v.37 no.5
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• pp.344-354
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• 2021

Optical methods such as UV and fluorescence spectrophotometers can be applied not only in the qualitative analysis of dissolved organic matter (DOM), but also in real-time quantitative DOM monitoring for wastewater and natural water. In this study, we measure the UV₂₅₄ and fluorescence excitation emission spectra for a sewage treatment plant influent and effluent, and river water before and after sewage effluent flows into the river to examine the composition and origin of DOM. In addition, a correlation analysis between quantified DOM characteristics and dissolved organic carbon (DOC) was conducted. Based on the fluorescence excitation emission spectra analysis, it was confirmed that the protein-type tryptophan-like DOM was the dominant substance in the influent, and that the organic matter exhibited relatively more humic properties after biological treatment. However, DOM in river water showed the fluorescence characteristics of terrestrial humic-like and algal tyrosine-like (protein-like) organic matter. In addition, a correlation analysis was conducted between the DOC and optical indices such as UV₂₅₄, the fluorescence intensity of protein-like and humic-like organic matter, then DOC prediction models were suggested for wastewater and river monitoring during non-rainfall and rainfall events. This study provides basic information that can improve the understanding of the contribution of DOC concentration by DOM components, and can be used for organic carbon concentration management in wastewater and natural water.