• Journal of Soil and Groundwater Environment
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• v.19 no.6
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• pp.72-79
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• 2014

Cavitation generated by ultrasonic irradiation can enhance the diffusional transport of organic contaminants from soil surfaces or pores. Therefore, ultrasound soil washing can be an alternative of traditional soil washing process. In this study, soil was artificially contaminated with n-tetradecane, n-hexadecane and phenanthrene. A plate type ultrasonic reactor at 25 kHz frequency and 1000W power was used for laboratory soil washing experiments. Ultrasonic soil washing efficiency was compared with those of traditional soil washing using mechanical mixing. Various operational parameter such as soil/liquid ratio, irradiation time, particle size, and soil organic matter content was tested to find out the optimum condition. It was found that ultrasonic soil washing demonstrates better performance than mechanical soil washing. Optimum soil:liquid ratio for ultrasonic soil washing was 1 : 5. Desorption of organic contaminants from soils by ultrasonic irradiation was relatively fast and reached equilibrium within 10 minute. However, decrease in the soil particle sizes by ultrasonic irradiation results in re-adsorption of contaminants to soil phase. It was also observed that soil particle size distribution and soil organic matter content have significant effects on the efficiency of ultrasonic soil washing.

• Korean Journal of Soil Science and Fertilizer
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• v.31 no.4
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• pp.414-419
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• 1998

The contribution of soil organic matter on the soil surface charge characteristic of paddy and upland soils weathered from granite or limestone was evaluated. The surface charge characteristics of the soils with and without soil organic matter by pre-treatment with hydrogen peroxide was determined at pH 3.5~9.0 range using the ion adsorption method. Regardless of soil organic matter removal, the soil surface negative charge increased linearly by the increase of pH with high statistical significance at all kinds of soils. Here, the differential increasement of soil surface negative charge by pH inclease, dCEC/dpH, was proposed as the parameter of pH dependency of the soil surface charge. The dCEC/dpH of soils with organic matter was in the range of 0.91~4.59, while it was dramatically decreased to the range 0.16~1.91 by the removal of organic matter. The soil surface charge derived from soil organic matter ranged from 15% to 82% to the total amount of surface charge. The magnitude of surface charge carried by 1% of soil organic matter showed considerable differences between soils from 0.22 to $5.03cmol^+\;kg^{-1}$. The effect of soil organic matte on the dCEC/dpH was higher in paddy soils with high oxalic acid extractable Fe than upland soils.

• Journal of Environmental Science International
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• v.23 no.9
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• pp.1627-1634
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• 2014

Odor control technology include absorption, adsorption, incineration and biological treatments. But, most of processes have some problems such as secondary organic acids discharge at the final odor treatment facility. In order to solve the problems for effective treatment of organic acids in odor, it is necessary to develop a new type advanced odor control technology. Some of the technology are plasma only process and plasma hybrid process as key process of the advanced technology. In this study, odor removal performance was compared DBD(Dielectric Barrier Discharge)plasma process with PCHP(plasma catalysis hybrid process) by gaseous ammonia, formaldehyde and acetic acid. Plasma only process by acetic acid obtained higher treatment efficiency above 90%, and PCHP reached its efficiency up to 96%. Acetic acid is relatively easy pollutant to control its concentration other than sulfur and nitrogen odor compounds, because it has tendency to react with water quickly. To test of the performance of DBD plasma process by applied voltage, the tests were conducted to find the dependence of experimental conditions of the applied voltage at 13 kV and 15 kV separately. With an applied voltage at 15 kV, the treatment efficiency was achieved to more higher than 13 kV from 83% to 99% on ammonia, formaldehyde and acetic acid. It seems to the odor treatment efficiency depends on the applied voltage, temperature, humidity and chemical bonding of odors.

• Applied Chemistry for Engineering
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• v.2 no.1
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• pp.77-85
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• 1991

A series of samples having different $SiO_2/Al_2O_3$ ratio were prepared by treating hydrogen mordenites with boiling hydrochloric acid and with hydrofluoric acid. The acidities of these samples were measured by TPD of $NH_3$ and by pyridine adsorption using IR, and the catalytic activities and selectivities of isomerization were measured for the reaction of ortho-xylene. For the samples treated by boiling hydrochloric acid, the acidities decreased with the increasing $SiO_2/Al_2O_3$ ratio caused by the extraction of framework aluminum. The sample having the $SiO_2/Al_2O_3$ ratio or 22 showed better activity than the others. For the samples treated by hydrofluoric acid, the content of chemically binding fluorine increased with the increasing contact time of hydrofluoric acid solution. The catalytic activities decreased with the hydrofluoric acid treatment due to the decreased acid sites resulted from the extraction of aluminum and silicon as well as the hydroxyl group replacement by the fluoride ion. The slightly increasing catalytic activities, however, came from the newly created acid sites, due to the removal of surface silicon, having enhanced by the inductive effect of binding fluorin with further acid treatment.

• Korean Journal of Materials Research
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• v.24 no.5
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• pp.243-248
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• 2014

Silicon-carbon composite was prepared by the magnesiothermic reduction of mesoporous silica and subsequent impregnation with a carbon precursor. This was applied for use as an anode material for high-performance lithium-ion batteries. Well-ordered mesoporous silica(SBA-15) was employed as a starting material for the mesoporous silicon, and sucrose was used as a carbon source. It was found that complete removal of by-products ($Mg_2Si$ and $Mg_2SiO_4$) formed by side reactions of silica and magnesium during the magnesiothermic reduction, was a crucial factor for successful formation of mesoporous silicon. Successful formation of the silicon-carbon composite was well confirmed by appropriate characterization tools (e.g., $N_2$ adsorption-desorption, small-angle X-ray scattering, X-ray diffraction, and thermogravimetric analyses). A lithium-ion battery was fabricated using the prepared silicon-carbon composite as the anode, and lithium foil as the counter-electrode. Electrochemical analysis revealed that the silicon-carbon composite showed better cycling stability than graphite, when used as the anode in the lithium-ion battery. This improvement could be due to the fact that carbon efficiently suppressed the change in volume of the silicon material caused by the charge-discharge cycle. This indicates that silicon-carbon composite, prepared via the magnesiothermic reduction and impregnation methods, could be an efficient anode material for lithium ion batteries.

• Applied Chemistry for Engineering
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• v.16 no.2
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• pp.200-205
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• 2005

We have prepared the porous carrier that has high capacity for immobilization of microorganisms and adsorption capacity for cation using fly ash in the previous work. In this study, we investigated the characteristics of piggery wastewater treatment in comparison with commercial carrier and conventional activated sludge process by continuous-flow fixed biofilm process in laboratory scale at the same experimental conditions to develop the biofilm process using porous fly ash carrier for wastewater treatment. As a result, the prepared fly ash carrier showed that removal efficiency of COD, TN and $NH_4{^+}-N$ items were 80%, 77% and 65%, respectively, which were higher efficiency than the commercial carrier and conventional activated sludge process. And the result of measurement for immobilized microorganisms after treatment showed higher capacity than the commercial carrier, and it was confirmed by SEM observation on fly ash carrier that the colony of microorganisms was stably formed.

• Polymer(Korea)
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• v.25 no.3
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• pp.311-317
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• 2001

In this study, we synthesized bead-type GMA-DVB copolymer using glycidylmethacrylate (GMA) with high reactivity and hydrophilicity. Macrorecticular anion exchanger containing the trimethylammonium group were then prepared by amination with trimethylammonium chloride. We observed that the size of $NO_3^-$ is smaller than that of $SO_4^{2-}$ which disturb $NO_3^-$ removal in most of coexistent anions in ground water. Thus we investigated selective affinity for $NO_3^-$ and properties of individual ion exchangers with various DVB content. For each resins, we confirmed formation of copolymer by FT-IR spectrometer and investigated ion exchange capacity, swelling ratio, the amination yield and the effect with degree of crosslinking on adsorbability for nitrate. When amount of DVB is 4 wt%, amination yield, ion exchange capacity and swelling ratio was 384.3%, 3.25 meq/g and 77.1%, respectively. In these result, it can found that synthetic optimal condition is 4 wt% DVB content for monomer.

• Korean Chemical Engineering Research
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• v.49 no.6
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• pp.739-744
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• 2011

Activated carbon SCR(CSCR) catalyst that is used to remove $NO_x$ in exhaust gas including boron discharged from the production process of liquid crystal display(LCD) shows deactivation when boron is deposited to block the pores within the catalyst or to cover its active sites. The spent carbon catalyst is regenerated by washing with various surfactants, drying and calcination. For comparison of the physical and chemical properties before and after the regeneration with the variables, type of surfactants and calcination condition, element analysis by ICP, $N_{2}$ adsorption were conducted. $DeNO_{x}$ in SCR with $NH_3$ was carried out in a fixed bed reactor at $120^{\circ}C$. The activated carbon catalyst regenerated through washing with a non-ionic surfactant in $H_{2}O$ at $90^{\circ}C$ and calcination under $N_{2}$ gas at $550^{\circ}C$ shows similar level of surface area and $NO_x$ removal efficiency with those of fresh catalyst.

• Analytical Science and Technology
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• v.24 no.4
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• pp.275-281
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• 2011

$AlPO_4$-type material was synthesized by a reaction of $Al(OH)_3$ and H3PO4 with organic templates from wastewater of detergent manufacturer. The surface of material was coated with carboxylate groups by the reaction of succinic anhydride with surface amino groups which were formed by treatment of the material with APTMS. Powder XRD patterns showed the characteristic patterns of $AlPO_4$. Morphology of the material was examined using a SEM and the functional groups were investigated by FT-IR analysis. The surface charge of a aqueous suspension was analyzed: $AlPO_4-NH_2$ has positively charged surface while $AlPO_4$-COOH has negatively charged one. They were used for the removal of toxic metals from aqueous solution. The lead ions were adsorbed on the surface by the formation of complexes with carboxylate of surface and $K_d$ was 91.1 mL/g. In conclusion, the $AlPO_4$-COOH might be applicable in the removal of toxic metal ions from aqueous system.

• Clean Technology
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• v.19 no.2
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• pp.121-127
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• 2013

The objective of this study is optimization of extrusion process for preparation of pellet-type adsorbents employed with alum sludge. Effects of water content and methyl cellulose as a binder on the possibility of extrusion and physical properties of pellet-type adsorbents were investigated. The physical characteristics of the pellet-type adsorbents were studied using nitrogen adsorption and compression strength. With a ratio of water to sludge, 63/100, the adsorbent was well extruded with a cylindrical form and the compressive strength was the highest. With increasing methyl cellulose content, the compressive strength of pellet-type adsorbent could be improved, but the specific surface area decreased. The breakthrough time of the hydrogen sulfide could be increased significantly through calcination and the breakthrough capacity reached to 1,700 mg/g, which seems to be due to increase of surface area during calcination.