• Journal of the Mineralogical Society of Korea
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• v.27 no.1
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• pp.41-51
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• 2014

The four natural zeolites collected in Pohang and Gyeongju area, Kyungsangbuk-do, Korea, were characterized by XRD, XRF, DTA, TGA, and CEC analysis. The primary species of these zeolite are heulandite, modenite, illite, and illite in Kuryongpo (Ku), Pohang (Po), Yangbuk-A (Ya-A), and Yangbuk-B (Ya-B) samples. The XRF analysis showed that the four zeolites contain Si, Al, Na, K, Mg, Ca, and Fe. Cation exchange capacity of Kuryongpo (Ku) zeolite was the highest compared to other zeolites. The adsorption capacities of Cs and Sr in the four natural zeolites were compared at $25^{\circ}C$. On the basis of adsorption data Langmuir and Freundlich adsorption isotherm model were confirmed. The equilibrium process was descried well by Langmuir isotherm model. This study shows that Ya-A zeolite is the most efficient for the $Cs^+$ and $Sr^{2+}$ ion adsorption compared to the other natural zeolites.

• Advances in environmental research
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• v.2 no.3
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• pp.167-177
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• 2013

We investigated that removal of aqueous U(VI) by nano-sized Zero Valent Iron (nZVI) and Fe(II) bearing minerals (controls) in this study. Iron particles showed different U(VI) removal efficiencies (Mackinawite: 99%, green rust: 95%, nZVI: 91%, magnetite: 87%, pyrite: 59%) due to their different PZC (Point of Zero Charge) values and surface areas. In addition, noticeable amount of surface Fe(II) (181 ${\mu}M$) was released from nZVI suspension in 6 h and it increased to 384 ${\mu}M$ in the presence of U(VI) due to ion-exchange of U(VI) with Fe(II) on nZVI surface. Analysis of Laser-Induced Breakdown Detection (LIBD) showed that breakdown probabilities in both filtrates by 20 and 200 nm sizes was almost 24% in nZVI suspension with U(VI), while 1% of the probabilities were observed in nZVI suspension without U(VI). It indicated that Fe(II) colloids in the range under 20 nm were generated during the interaction of U(VI) and nZVI. Our results suggest that Fe(II) colloids generated via ion-exchange process should be carefully concerned during long-term remediation site contaminated by U(VI) because U could be transported to remote area through the adsorption on Fe(II) colloids.

• Particle and aerosol research
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• v.5 no.1
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• pp.1-7
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• 2009

Fe- and V-doped titanium dioxide nanoparticles consisting of spherical primary nanoparticles were synthesized from a mixed liquid precursor by using the flame spray pyrolysis. The effects of dopant concentration on the powder properties such as morphology, crystal structure, and light adsorption were analyzed by TEM, XRD, and UV-Vis spectrophotometer, respectively. As the V/Ti molar ratio increased, pure anatase particles were synthesized. On the contrary, rutile phase particles were synthesized as the Fe/Ti ratio increased. Photocatalytic property of as-prepared $TiO_2:Fe,V$ nanoparticles was investigated by measuring the removal efficiency for volatile organic compounds (VOCs) under the irradiation of visible light. After 2 hrs under visible light, the removal efficiencies of benzene, p-xylene, ethylbenzene, and toluene were reached to 21.9%, 21.4%, 19.8% and 17.6% respectively.

• Journal of Korean Society of Water and Wastewater
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• v.20 no.4
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• pp.559-571
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• 2006

The overall objective of this research was to find out the interrelation of coagulant and organic matter during rapid mixing process and to identify the change of organic matter by mixing condition and to evaluate the effect of coagulation pH. During the coagulation, substantial changes in dissolved organics must be occurred by coagulation due to the simultaneous formation of microflocs and NOM precipitates. Increase in the organic removal efficiency should be mainly caused by the removal of microflocs formed during coagulant injection. That is, during the mixing period, substantial amount of dissolved organics were transformed into microflocs due to the simultaneous formation of microflocs and NOM precipitates. The results also showed that 40 to 80% of dissolved organic matter was converted into particulate material after rapid mixing process of coagulation. During the rapid mixing period, for purewater, formation of dissolved Al(III) (monomer and polymer) constant by rapid mixing condition, but for raw water, the species of Al hydrolysis showed different result. During the rapid mixing period, for high coagulant dose, Al-ferron reaction increases rapidly. At A/D(Adsorption and Destabilization) and sweep condition, both $Al(OH)_3(s)$ and dissolved Al(III) (monomer and polymer) exist, concurrent reactions by both mechanism appear to cause simultaneous precipitation.

• Journal of the Korean Ceramic Society
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• v.55 no.5
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• pp.473-479
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• 2018

Highly toxic gases such as hydrogen sulfide ($H_2S$), carbon dioxide ($CO_2$), and ammonia ($NH_3$) are generated by both nature and human activities and affect human health. In this research, activated carbon combined with $Ca(OH)_2$ and $CaCO_3$ (AC-CO and AC-CC, respectively) were fabricated and applied in absorbing toxic gases from air pollutants. Activated charcoal powder was compressed in the form of pellets and used in the designated conditions. The optimum operating conditions and material properties, such as adsorption capacity, effect of weight ratio of the mixture, and hardness, have been investigated after combining with the calcium derivative. The good performance exhibited in this study suggests that this material is expected to be an effective and economically viable adsorbent for $NH_3$, $CO_2$, and $H_2S$ removal from the air system.

• Journal of Soil and Groundwater Environment
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• v.25 no.4
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• pp.28-34
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• 2020

Nitrate released from chemical fertilizer, animal wastes, and synthetic detergents can cause methemoglobinemia to infants, thus the standard in drinking water is set to 10 mg/L as World Health Organization recommended. In this study, zero-valent iron-modified rice straw biochar was used to reduce and remove nitrate in the aqueous phase. The rice straw biochar was prepared by pyrolyzing the biomass at 700℃ for 3 hours, and the biochar was modified using 1 M Fe(III), and the Fe(III) on the biochar was reduced to zero-valent iron using sodium borohydride. The modified biochar removed nitrate effectively, which removed more than 91% of nitrate. For the synthetic groundwater, the nitrate removal was lowered to 82% due to the presence of other anions.

• Journal of Wetlands Research
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• v.17 no.1
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• pp.38-44
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• 2015

In Korea, most rainfall events occur during summer which then leads to an increasing concern regarding high influx of non-point source pollutants since the pollutant loadings from these non-point sources are very significant. In particular, the first flush of roof-harvested rainfall is said to contain the most highest concentration of nutrients and heavy metals. Accordingly, it is important to develope the possible water quality management options in treating the contaminants and considering reclaimed water reuse. The rain garden could be one of suitable alternatives in addressing this issue. In this study, the development of an effective adsorption media and its application to a lab-scale rain garden was tested to evaluate the removal rate of various nutrient and organic matter (TN, TP, CODcr), and heavy metals (Cu, Cd, Pb). Results showed that carbonized peatmoss produced at higher temperature have better adsorption capacity as compared to the one produced at a lower temperature. When the carbonized peatmoss was applied as rain garden media, the highest removal of TN, TP, and CODcr was observed compared to no carbonized peatmoss applied rain garden. Therefore, this study showed that the carbonized peatmoss would be effectively applied to the rain garden for removing nutrients and heavy metals from roof-harvested rainwater.

• Journal of Korean Society of Water and Wastewater
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• v.19 no.4
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• pp.455-461
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• 2005

This study was designed to investigate the fundamental aspects of a possible recovery of phosphorus strategy from wastewater by using the zirconium mesoporous structured materials as a new type of ion exchangers. Zirconium mesoporous structure material was synthesized by hydro-thermal synthesis. The synthesized zirconium mesoporous structure was examined by X-ray diffraction (XRD) and Transmission electron micrograph (TEM). From the results of XRD and TEM, it was found out that hexagonal mesoporous structure, pore size was about $47{\AA}$, was synthesized. Experimental results showed that the complex of zirconium sulfate tetrahydrate and surfactant micelles had very high ability for capture of phosphorus. The amount of phosphate ions exchanged into the solid was as great as 3.4mmol/g-ZS. And the ion exchange reaction was occurred between $PO_4{^{3-}}$ and $SO_4{^{2-}}$ and also between $PO_4{^{3-}}$ and $OH^-$. Therefore, it is possible to get the higher removal efficiency than other ion exchange media and adsorbent.

• Journal of Korean Society of Water and Wastewater
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• v.24 no.1
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• pp.15-24
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• 2010

Coagulation can be used for pretreatment of NF membrane filtration. Foulants such as organic matter and particulate can be removed effectively with the process while high flux recovery is maintained. Recently various types of polyaluminium coagulants including polyaluminium chloride(PAC) are commercially available for water treatment. This study examines effects of polymeric Al and hydrolysis products of PAC on nanofiltration membrane performance. Dominant hydrolysis products were polymeric Al, $Al(OH)_3$, and ${Al(OH)_4}^{-1}$ at acidic, neutral, and alkaline pH conditions, respectively. Under acidic pH condition, flux decline was increased with increasing PAC concentrations, possibly due to polymeric Al adsorption on membrane pore and/or surfaces. For neutral and alkaline pH conditions, little flux decline was observed with increasing PAC concentrations except the highest ${Al(OH)_4}^{-1}$ concentration, with which rapid flux decline was shown. Removal of ionic matters was also varied with pH conditions in this study. Especially, conductivity removal was substantially low and $Ca^{2+}$ concentration in the permeate was quite high at neutral pH condition.

• Journal of Korean Society of Environmental Engineers
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• v.32 no.2
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• pp.201-208
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• 2010

The $SO_2$ and $NO_x$ removal with an activated coke catalyst was conducted by a two-stage reaction which first $SO_2$ was oxidized to $H_2SO_4$ and then $NO_x$ was reduced to $N_2$. But if unreacted sulfur dioxide entered in the second stage, the $NO_x$ reduction was hindered by the reaction with ammonia. In this study, experimental investigations by using lab-scale column apparatus on the product and the reactivity of $SO_2$ with ammonia over coke catalyst which was activated with sulfuric acid was carried out through ultimate analysis DTA, TGA and SEM of catalyst before and after the reaction. Also, the effect of reaction emperature on the reactivity of $SO_2$ with ammonia was determined by means of breakthrough curves with time. The obtained results from this study were summarized as following; Activated cokes were decreased carbon component and increased oxygen and sulfur components in comparison with original cokes. The products over coke catalyst were faced fine crystal of $(NH_4)_2SO_4$, which results in the pressure loss of reacting system. The order of general reactivity in terms of the reaction temperature after breakthrough for $SO_2$ was found to be $150^{\circ}C$ > $200^{\circ}C$ > $100^{\circ}C$. This was related to adsorption amounts of ammonia on the activated cokes.