• Journal of Korean Society of Water and Wastewater
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• v.22 no.5
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• pp.523-529
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• 2008

Algal blooms in a local eutrophic lake often produces the musty and earthy taste & odor problems. Since the odor causing compounds(OCCs) including geosmin and 2-MIB have their own volatility, the OCCs can be removed from water by air stripping methods. Removal of TON(threshold odor number) as an index for OCCs could be fitted well with the first order equations($R^2=0.9$ above), where the air stripping coefficient of TON, k was in the range between 0.0055 and 0.0097 according to the aeration time. k within 30min aeration tests was 0.0097, while it was 0.0055 where the aeration time extended to 150min. With 15 mg/L of PAC, removal of TON was not simulated with 1st order equation within 30min aeration. Within 30min aeration, OCCs rather than geosmin and/or 2-MIB could be removed easily by air stripping or PAC adsorption, while OCCs such as geosmin and/or 2-MIB could be removed slowly by air stripping after 30min aeration. Geosmin and 2-MIB were not readily removed by air stripping(k of them were 0.0018~0.0047 and 0.0018~0.0034, respectively at different air flow rates). Geosmin could be removed by air stripping a little better than 2-MIB.

• Korean Journal of Soil Science and Fertilizer
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• v.20 no.2
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• pp.153-159
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• 1987

Adsorption and desorption characteristics of $^{42}K$ and $^{45}Ca$ were studied by making use of the natural zeolite, bentonite, and vermiculite. The work included that the fittness tests for the Freundlich and the Langmuir adsorption isotherms and desorption of the radionuclides from adsorbents by extracting with $NH^+_4$ ($1N-NH_4OAc$). The adsorption by the radionuclides are fitted well with both of the adsorption equations. The Langmuir adsorption maximum of $^{42}K$ is higher than that of $^{45}Ca$ by the zeolite and bentonite except vermiculite, and the values of $^{42}K$ decrease in the order of Zeolite (Zt)>Bentonite (Bt)>Vemiculite (Vt). As for $^{45}Ca$, the maximum adsorption values decrease in the order of Bt>Vt>Zt. The ionic radii of K and Ca seem to be closely related with fixation in the cavity of the zeolite that adsorb more $^{42}K$ than $^{45}Ca$. The smaller ionic size of Ca seems to be resulted in the lower adsorption of $^{45}Ca$ by the zeolite because Ca could leave easily from the cavity. Ionic size of K, however, seems to be similar with size of the cavity. $^{45}Ca$ adsorption by the bentonite, on the other hand, show higher adsorption than $^{42}K$. The higher charge density of the divalent cations than those of the monovalent cations seems to be the main consideration. For the retention strength of the adsorbed $^{42}K$ and $^{45}Ca$ by the adsorbents, a comparison is made by use of the Langmuir constant(k). The results indicated that the constant values for K are smaller than those of Ca in all the adsorbents. It seems that the smaller values of the constant, the weaker retention strength. For $^{42}K$, the percentage of desorption decrease in the order of Zt>Bt>Vt, but in the case of $^{45}Ca$, it decreases in the order of Vt>Zt>Bt. The results show that the weaker binding strength as represented by small value of the Langmuir constant, the higher percentage of the removal except fixing preferably $K^+$ by the vemiculite. In conclusion, the zeolite could adsorb much more $^{42}K$ and remove it more than others. For $^{45}Ca$, the bentonite could adsorb more and desorb less than others.

• Journal of Environmental Health Sciences
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• v.36 no.2
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• pp.136-140
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• 2010

The integrated gasification combined cycle (IGCC) is one of the most promising proposed processes for advanced electric power generation that is likely to replace conventional coal combustion. This emerging technology will not only improve considerably the thermal efficiency but also reduce or eliminate the environmentally adverse effects normally associated with coal combustion. The IGCC process gasifies coal under reducing conditions with essentially all the sulfur existing in the form of hydrogen sulfide ($H_2S$) in the product fuel gas. The need to remove $H_2S$ from coal derived fuel gases is a significant concern which stems from stringent government regulations and also, from a technical point of view and a need to protect turbines from corrosion. The waste seashells were used for the removal of hydrogen sulfide from a hot gas stream. The sulphidation of waste seashells with $H_2S$ was studied in a thermogravimetric analyzer at temperature between $600^{\circ}C$ and $800^{\circ}C$. The desulfurization performance of the waste seashell sorbents was experimentally tested in a fixed bed reactor system. Sulfidation experiments performed under reaction conditions similar to those at the exit of a coal gasifier showed that preparation procedure and technique, the type and the amount of seashell, and the size of the seashell affects the $H_2S$ removal capacity of the sorbents. The pore structure of fresh and sulfided seashell sorbents was analyzed using mercury porosimetry, nitrogen adsorption, and scanning electronmicroscopy.

• Proceedings of the Korean Vacuum Society Conference
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• 2010.02a
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• pp.348-348
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• 2010

Behaviors of $TiO_2$-based photocatalysts with different surface structures on the removal of gas-phase toluene with and without UV irradiation are reported. P-25(Degussa) $TiO_2$ powder dispersed in distilled water by sonication was deposited on the transparent glasses and then dried. Some of the samples were further annealed in oven for 1 hr. These samples obtained before and after annealing were characterized by Brunauer- Emmett-Teller (BET), Transmission Electron Microscope (TEM), X-ray Photoelectron Spectroscopy (XPS) and Fourier Transform Infrared (FT-IR) spectrometry, respectively. Based on BET and TEM data, no significant structural change upon annealing could be identified. However, the sample without annealing showed a significantly higher ability for removing toluene both in the presence and absence of the UV light. XPS and FT-IR results clearly revealed that the population of the OH groups on the surface of $TiO_2$ was higher for the sample without annealing, indicating that the OH groups can enhance the adsorption capacity and photocatalytic activity of $TiO_2$ for the removal of the gas-phase toluene.

• Journal of the Korean Applied Science and Technology
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• v.31 no.3
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• pp.466-471
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• 2014

It is important to develop the smart ventilation system in order to minimize a building energy consumption using ventilation. In this study, We evaluated the efficiency of the smart ventilation system being developed at the nursery. To evaluate the energy savings and carbon dioxide removal efficiency, two kinds of experimental conditions were compared. First, air conditioner and Smart HVAC system were operated. Second, air conditioner was operating and external air was put into the inside by rate of air circulation. It was more effective when working with air conditioning and ventilation system at the same time. If the Smart HVAC system is applied in a multi-use facility, indoor air quality will be comfortable and the social cost will be reduced.

• Journal of Korean Society of Environmental Engineers
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• v.36 no.3
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• pp.206-213
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• 2014

Nutrients such as phosphorus and nitrogen have been widely known as important source of algal appearance in eutrophic water. In order to prevent lake eutrophication, it is required to remove these nutrients not only presented in the lake water, but also released from the sediment. In order to solve this problem this study, the trivalent lanthanum ions and ammonia Nitrogen ($NH_4{^+}-N$) for the adsorption capacity of a zeolite support as it combines the lake water has dissolved in the nutrient removal, as well as deposits in the eluted in the continuously adsorbing the complex to develop and study was to inhibit the growth of algae. In experimental results, lanthanum complexes when the adsorption characteristics were evaluated $PO_4{^{3-}}-P$ and the $NH_4{^+}-N$ removal was confirmed that has an excellent ability, when it applied lake water the time of Chl-a and the turbidity decreased. In this study, these results suggest that the lanthanum complexes produced inhibitory effects on algae in the lake water is determined to excellent. Further, when applied to a complex of lanthanum in lake water to a standard 48 hours Acute Toxicity Method of toxicity were measured, and the results for the toxic effect was not observed.

• Economic and Environmental Geology
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• v.42 no.5
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• pp.435-444
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• 2009

In situ stabilization of heavy metals through adsorption onto indigenous bacterial biofilm developed on soil particles was investigated. Biofilms were developed in soil columns by supply of various carbon sources such as acetate, lactate and glucose. During development of biofilms, acetate, lactate, and glucose solutions were flew out from the soil columns with volume ratios of 98.5%, 97.3%, and 94.7%, respectively, when compared with soil column supplied with deionized water. Decrease in effluent amounts through the soil columns amended with carbon sources over time indicated the formation of biofilms resulting in decrease of soil porosity. Solutions of Cd, Cr(VI), Cu, Pb, and Zn were injected into the biofilms supported on soil particles in the columns, and the dissolved heavy metals in effluents were determined. Concentrations of dissolved Cd, Cr(VI), Cu, and Zn in the effluents through biofilm columns were lower than those of control column supplied with deionized water. The result was likely due to enhanced adsorption of the metals onto biofilms. Efficiency of metal removal by biofilms depended on the type of carbon sources supplied. The enhanced removal of dissolved heavy metals by bacterial biofilms in this study may be effectively applied to technical development of in situ stabilization of heavy metals in natural soil formation contaminated with heavy metals.

• Korean Journal of Environmental Agriculture
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• v.29 no.2
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• pp.152-158
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• 2010

Biosorption is considered to be an alternative method to replace the present adsorbent systems for the treatment of metal contaminated wastewater. In this study, by-product which was abandoned from brewing factory was used to remove metal component in aqueous solution. The experimental results showed that the range of the removal efficiency is 60~91% and adsorption equilibrium was reached in about 3 hr. FT-IR and stereo microscope has been used to observe the surface conditions and changes in functional groups by calcination. At the end of elution, the amount of nitrogen and phosphorus in water was increased 11 and 7 times compare raw sample to calcinated samples. The Langmuir isotherm adequately described the adsorption of waste materials and the maximum adsorption capacity was 28.17 mg/g for Cd. The overall results suggested that waste material might can be used for biosorption of Cd.

• Clean Technology
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• v.6 no.1
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• pp.27-38
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• 2000

A physicochemical process called Ultra Rapid Coagulation(URC) can dramatically remove organics, metals, and phosphates in wastewater by adding weighted coagulation additive(WCA) and recycling sludge into the coagulation basin to increase the growth rate and adsorption ability of floc. Also this process can improve floc settling rate than conventional coagulation process and reduce the pollutants loaded into the receiving water for securing water source. It was evaluated that WCA and sludge added have effects on the removal efficiency and estimated the possibilities of reusing the effluent from this process.

• Proceedings of the Korean Radioactive Waste Society Conference
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• 2004.06a
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• pp.32-42
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• 2004

Recently, plasma surface-cleaning or surface-etching techniques have been focused in respect of the decontamination of spent or used nuclear parts and equipment. In this study the removal rate of metallic cobalt surface is experimentally investigated via its surface etching rate with a $CF_4-o_2$mixed gas plasma. Experimental results reveal that a mixed etchant gas with about 80% $CF_4$-20% $O_2$ (molar) gives the highest reaction rate and the rate reaches 0.06 ${\mu}m$/min at $380^{\circ}C$ and ion-assisted etching dramatically enhances the surface reaction rate. With a negative 300 V DC bias voltage applied to the substrate, the surface reaction initiation temperature lowers and the rate increases about 20 times at $350^{\circ}C$ and up to 0.43 ${\mu}m$/min at $380^{\circ}C$, respectively. Surface morphology analysis confirms the etching rate measurements. Auger spectrum analysis clearly shows the adsorption of fluorine atoms on the reacted surface. From the current experimental findings and the results discussed in previous studies, mechanistic understanding of the surface reaction, fluorination and/or fluoro-carbonylation reaction, is provided.