• Korean Journal of Soil Science and Fertilizer
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• v.18 no.4
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• pp.352-358
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• 1985

Loss of cationic zeolites saturated with different ions, sodium, potasium, ammonium, magnesium and calcium ions, and changes of hydraulic conductivity were investigated in labortory. The 0.5 to 1mm sands and the zeolite particles passed 0.1mm sieve were used in the column tests. The amount of zeolite particle loss was in order of Na- > K- > $NH_4-$ saturated zeolites, and little loss was observed from Mg and Ca saturated zeolites. The loss of zeolite particles was mainly due to dispersion in solution, which was prominant when 0.01N dilute mono ionic solution and distilled water were percolated. The results also showed that the changes in hydraulic conductivity were greater in the columns where the loss of dispersed zeolite particles was higher.

• Journal of Industrial and Engineering Chemistry
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• v.67
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• pp.301-311
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• 2018

In this study, the ion-gelation method was applied to fabricate novel Fe-carbon-bentonite-alginate beads ($Fe^0$/C-BABs). $Fe^0$/C-BABs could effectively control Fe release during persulfate (PS) activation in N-acetyl-p-aminophenol (APAP) oxidation. A novel two-stage approach that combined $Fe^0$/C-BABs and an oyster-shell-filled bed (OSFB) column was developed to address the low pH and high Fe concentration of the effluent of the traditional PS process. The application of the $Fe^0$/C-BABs and OSFB column regulated pH levels and Fe release during the advanced oxidation of APAP. The characteristics of $Fe^0$/C-BABs were also investigated through scanning electron microscopy, energy dispersive spectrometry, and Fourier transform infrared spectroscopy. The long-term operation performance of $Fe^0$/C-BABs in a continuous fixed-bed reactor under simultaneous PS and APAP feeding was also evaluated. The effects of initial PS concentration, pH, fixed-bed weight, in-flow rate, and dissolved oxygen (DO) were investigated. Under selected conditions, 86.3% efficiency was achieved during the first stage of APAP degradation (effluent pH of 3.05, Fe contents: $106.25mgL^{-1}$). Water quality improved after the effluent was passed through the OSFB column (effluent pH of 6.32, Fe contents: $21.43mgL^{-1}$). Moreover, this study analyzed the free radicals and intermediates produced during APAP degradation to identify the possible routes of APAP degradation.

• Proceedings of the Korea Society of Environmental Biology Conference
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• 2004.05a
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• pp.27-27
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• 2004

We studied algal growth-related water quality of the Sangsa lake which is the drinking water reservoir for the south-eastern region of Jeonnam province. Peridinium cinctum and several diatomic algal species frequently caused water bloom throughout the lake from early spring to late autumn. With the heaviest predominance of Peridinium cintum in May 2003, COD was 22.7 mg/l in the surface layer. Highly turbid surface water of 15 NTU was also caused by Perdinium bloom. Cyanobacterial growth was effectively prohibited by dominant growth of Peridinium in the Sangsa lake, otherwise confronted with cyanobacterial bloom. Dense algal layer was confined in the upper several meters of the water column above the thermocline, which gives relatively algae-free water in deeper layer suitable for drinking source water supply. Upon collapse of thermocline, water quality of the surface layer was improved while deeper layer was deteriorated. This paper deals with some details of water quality changes with algal growth in the Sangsa lake past two years.

• Korean Journal of Environmental Agriculture
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• v.6 no.2
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• pp.46-52
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• 1987

This study of adsorption and column percolation was conducted to examine the utilization of natural zeolite for the removal of heavy metals from waste water to compare with that of absorption activated carbon. The adsorption of heavy metals by natural zeolite was conformed to the Freundlich isotherm (1/n values: $0.12{\sim}0.45$, K values: $18.77{\sim}59.48$) and natural zeolite was turned out to be an effective adsorbent of heavy metals. At the same particle size and percolation velocity, zeolite adsorbed a greater amount of heavy metals was adsorbed on natural zeolite than activated carbon. The smaller the particle size, the more heavy metals that were adsorbed. It was postulated that the most effective size as an adsorbent of heavy metals from waste water ranged from 0.5 to 2.0mm. The slower the percolation velocity that of the heavy metal solution in column, the more heavy metals were adsorbed. Natural zeolite in a single solution adsorbed more heavy metals than that in mixed solution, and the order of the adsorption amount on natural zeolite was Cu>Zn>Cd.

• The Korean Journal of Pesticide Science
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• v.17 no.3
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• pp.168-177
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• 2013

This experiment was carried out to estimate leaching potential of thirteen endocrine disruptor-suspected pesticides in upland soils using soil columns (5 cm I.D. ${\times}$ 35 cm H.) packed with soil A (sandy loam) and soil B (loam). When 12.6 mL of water, average precipitation in Cheongju area during the period from June to August, 2001-2010, was percolated through soil column packed with soil A every day for 21 days, no pesticides were detected from leachate, with the exception of metribuzin which was detected with negligible. Also, when 2 L of water was percolated consecutively five times through soil columns packed with soil A and B, irrespective of soil types, cypermethrin, endosulfan, fenvalerate, parathion and trifluralin, which were very low water solubilities and high soil $K_{oc}s$, were not detected from leachate and were distributed mostly in the depth of 0-5 cm, representing that water solubility and soil $K_{oc}$ are major contributing factors to their leaching behavior. Despite high average leaching rates in carbaryl and methomyl, actual possibilities of ground water contamination in the agricultural environment by them would be very low, considering that the negligible amount of pesticide was percolated through a lysimeter with an undisturbed soil core simulating the field conditions, while most of pesticide was percolated through a soil column with the disturbed soil profile.

• The Sea:JOURNAL OF THE KOREAN SOCIETY OF OCEANOGRAPHY
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• v.5 no.4
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• pp.295-304
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• 2000

Vertical measurement of CTDT at about 30 min intervals and spatial surface temperature, salinity, and concentration of suspended particulate matters were conducted to elucidate the character of water column and the dispersal pattern in a floating ice-dominated fjord, Marian Cove, West Antarctica. Marian Cove showed two distinct water layers in terms of turbidity; 1) cold, fresh, and turbid surface plume in the upper 2 m,2) warm, saline, and relatively clean Maxwell Bay inflow between 15-45 m in water depth. Thermal melting of Maxwell Bay inflow and tidewater glacier/floating ices developed the surface mixed layer and the activity of floating ices cause Maxwell Bay inflow to be unstable. Due to the unstable water column, the development of Maxwell Bay inflow and subsequent surface plume are not influenced by tidal frequency. Coastal current generated by strong northwesterly wind may extend warm, saline, and turbid surface plume into the central part of the cove along the northern coast via the western coast of Weaver Peninsula. Terrigenous sediments of meltwaters from the glaciated ice cliffs near the corner of tidewater glacier and some coasts enter into the cove and their dispersion depends upon the hydrographic regimes (tide, wind, wave etc.). At the period of spring tide, the strong wind stress with the northwesterly wind direction reserve suspended sediment-fed surface plume and so allow the possibility of deposition of terrigenous sediments within the basin of cove.

• Journal of Korean Society of Water and Wastewater
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• v.20 no.5
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• pp.727-736
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• 2006

Granular activated carbon (GAC) has been identified as a best available technology (BAT) by the United States Environmental Protection Agency (USEPA) for removal disinfection by-product (DBP) precursors, such as dissolved organic carbon (DOC) and dissolved organic nitrogen (DON). Rapid small-scale column test (RSSCT) were used to investigate four types of carbon (F400, Norit1240, Norit40S, and Aquasorb1500) for their affinity to absorb natural organic matter (NOM). DOC, $UV_{254}$, and Total dissolved nitrogen (TON) concentrations were measured in the column effluent to track GAC breakthrough. DOC and $UV_{254}$ breakthrough occurred at around 3500 bed volumes (BVs) of operation for all GACs investigated. The $UV_{254}$ breakthrough curves showed 33% to 48% at 8000 BVs, when the DOC was 48% to 65%. All GACs showed greater removal in DOC than $UV_{254}$. The NORIT1240 GAC was determined to have the highest adsorption capacity for DOC and $UV_{254}$. The removal of nitrate (NOTN) had not broken through over BVs. The initial TON breakthrough curves were started around 50%, when the DOC breakthrough was only 10 % at 500 BVs. The curves were gradually increased after 3500 BVs and approximately 69% through 81% of TON breakthrough occurred at 8000 BVs. All of the GACs were able to remove TON, in the case of this investigation the majority of the TON was present as DON. Because nitrate nitrogen was seldom removed and ammonium nitrogen ($NH_3-N$) was not detected in the effluent from RSSCTs even though raw water. The carbon usage rate of DOC was from 2 to 6 times less than that of TON. The NORIT1240 GAC demonstrated the best performance in terms of DOC removal, while the F400 GAC was best in terms of TON removal. Excitation emission matrix(EEM) analysis was used to show that GAC adsorption successfully removed most of Humic-like DOC and Fulvic-like DOCs. However, soluble microbial product(SMP)-like DOC in the absence of raw water were detected in the NORIT40S and Aquasorb1500 GAC. The authors assumed that this results is due probably to the part of GAC in the RSSCT which was converted into biological activated carbon(BAC). To compare with organics removal by GAC according to preloading, the virgin GACs had readily accessible sites that were adsorbed DOC more rapidly than preloaded GACs, but the TDN removal had not showed differences between those GACs.

• Journal of the Korean Chemical Society
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• v.37 no.12
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• pp.1035-1046
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• 1993

Some iron(III)porphyrin complexes were prepared, and identified by the spectroscopic methods. Elution behavior of iron(III)porphyrin complexes was investigated by reversed-phase HPLC. The optimum conditions for the separation of iron(III)porphyrin complexes were examined with respect to flow rate and mobile phase strength. These complexes were successfully separated on NOVA-PAK $C_{18}$ column using methanol / water(95/5) for $[T_pCF_3PP)Fe(R)]$ and methanol / water (98/2) for $[(P)Fe(C_6F_5)]$ as a mobile phase. It was found that these complexes were largely eluted in an acceptable range of capacity factor value ($0{\leq}logk'{\leq}1$). The dependence of the capacity factor (k') on the volume fraction of water in the binary mobile phase as well as the dependence of k' on the liquid-liquid extraction distribution ratio$(D_c)$ in methanol-water / n-pentadecane extraction system showed a good linearity. It means that the retention of iron(III)porphyrin complexes on NOVA-PAK $C_{18}$ column is largely due to the solvophobic effect. Also, there was a good linear dependence of the capacity factor(k') on the column temperature and enthalpy calculated by van't Hoff plot. From these results, it was confirmed that the retention mechanism of iron(III)porphyrin complexes in reversed-phase liquid chromatography was invariant under the condition of various temperature, and the solvophobic binding process exhibited isoequilibrium behavior.

• Proceedings of the Korean Nuclear Society Conference
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• 2004.10a
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• pp.543-544
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• 2004

• Proceedings of the KSEEG Conference
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• 2001.04a
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• pp.387-389
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• 2001