• Korean Chemical Engineering Research
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• v.45 no.3
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• pp.258-263
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• 2007

Ammonia water was investigated as a new absorbent of the chemical absorption process for the removal of $CO_2$ in flue gas. The suitable range of ammonia water concentration and $CO_2$ loading ($mol\;CO_2/mol\;NH_3$) were decided in the point of view of $CO_2$ absorption capacity and $NH_4HCO_3$ precipitation. The absorption capacity of $CO_2$ and the precipitation of $NH_4HCO_3$ in liquid phase were calculated by the Pitzer model for electrolyte solution. The $CO_2$ absorption capacity of the ammonia water over $5\;molNH_3/kgH_2O$ was higher than that of conventional amine absorbent. The $CO_2$ loadings where precipitation occurred were decided at various absorbent concentrations. Theses values were higher than 0.5 in the concentration range of $5-14\;molNH_3/kgH_2O$ at 293, 313 K. The absorber for the removal of $CO_2$ in flue gas could be operated without $NH_4HCO_3$ precipitation by using high concentration of ammonia water below these $CO_2$ loading values. The optimum temperature of the ammonia water absorbent for removal of $CO_2$ in flue gas was 297-312 K depending on the concentration of ammonia water.

• Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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• v.8 no.2
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• pp.115-122
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• 2010

In this study, the removal of Cs and Tc from a simulated fission products (FP) solution which were co-dissolved with U during the oxidative-dissolution of spent fuel in a mixed carbonate solution of $(Na_2CO_3-NaHCO_3)-H_2O_2$ was investigated by using a selective precipitation method. As Cs and Tc might cause an unstable behavior due to the high decay heat emission of Cs as well as the fast migration of Tc when disposed of underground, it is one of the important issues to removal them in views of the increase of disposal safety. The precipitation of Cs and Re (as a surrogate for Tc) was examined by introducing sodium tetraphenylborate (NaTPB) and tetraphenylphosponium chloride (TPPCl), respectively. Precipitation of Cs by NaTPB and that of Re by TPPCl were completed within 5 minutes. Their precipitation rates were not influenced so much by the temperature and stirring speed even if they were increased by up to $50^{\circ}C$ and 1,000 rpm. However, the pH of the solution was found to have a great influence on the precipitation with NaTPB and TPPCl. Since Mo tends to co-precipitate with Re at a lower pH, especially, it was effective that a selective precipitation of Re by TPPCl was carried out at pH of above 9 without co-precipitation of Mo and Re. Over 99% of Cs was precipitated when the ratio of [NaTPB]/[Cs]>1 and more than 99% of Re, likewise, was precipitated when the ratio of [TPPCl]/[Re]>1.

• Nuclear Engineering and Technology
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• v.50 no.6
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• pp.886-889
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• 2018

This article presented two-staged chemical precipitation for radioactive wastewater decontamination by using chemical agents. The total amount of radioactive wastewater was $35m^3$, and main radionuclides were Cs-137, Cs-134, and Co-60. Initial radioactivity concentration of the liquid waste was 2264, 17, and 9 Bq/L for Cs-137, Cs-134 and Co-60, respectively. Potassium ferrocyanide, nickel nitrate, and ferrum nitrate were selected as chemical agents at high pH levels 8-10 according to the laboratory jar tests. After the process, radioactivity was precipitated as sludge at the bottom of the tank and decontaminated clean liquid was evaluated depending on discharge limits. By this precipitation method decontamination factors were determined as 66.5, 8.6, and 9 for Cs-137, Cs-134, and Co-60, respectively. By using the potassium ferrocyanide, about 98% of the Cs-137 was removed at pH 9. At the bottom of the tank, radioactive sludge amount from both stages was totally $0.98m^3$. It was transferred by sludge pumps to cementation unit for solidification. By chemical processing, 97.2% of volume reduction was achieved. The potassium ferrocyanide in two-staged precipitation method could be used successfully in large-scale applications for removal of Cs-137, Cs-134, and Co-60.

• Atmosphere
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• v.22 no.2
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• pp.279-285
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• 2012

The weighing precipitation gauge with auto-empting capability was developed in the R&D project organized by the Research Agency for Climate Science (RACS) and supported by the Korea Meteorological Administration (KMA). This project was initiated in line with the KMA's plan executed since 2010 to introduce the weighing precipitation gauges partly into of their Automatic Weather Station (AWS) network in order to upgrade the quality of precipitation data. The innovative feature of this research is that the auto-empting in weighing precipitation gauge is realized by abrupt rotation of receiving container. The prototype was tested in compliance with the relevant standards of KMA. The results of performance test on rainfall measurement in laboratory verified that the accuracies for 20 mm and 100 mm reference rainfall amount were 0.1 mm and 0.4 mm, respectively in both conditions of auto-empting and no-empting. During the rotation of container for auto-empting, the data was extrapolated smoothly by applying the same precipitation intensity of the previous 10 sec. Consequently, it was found that the auto-empting precipitation gauge developed in this research is quite enough to be used for the operational purpose of accurate measurement with 0.1 mm resolution, regardless of the precipitation intensity.

• Journal of Ecology and Environment
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• v.41 no.6
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• pp.165-172
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• 2017

Background: This study investigated the temporal variation in soil $CO_2$ efflux and its relationship with soil temperature and precipitation in the Quercus glauca and Abies koreana forests in Jeju Island, South Korea, from August 2010 to December 2012. Q. glauca and A. koreana forests are typical vegetation of warm-temperate evergreen forest zone and sub-alpine coniferous forest zone, respectively, in Jeju island. Results: The mean soil $CO_2$ efflux of Q. glauca forest was $0.7g\;CO_2\;m^{-2}\;h^{-1}$ at $14.3^{\circ}C$ and that of A. koreana forest was $0.4g\;CO_2\;m^{-2}\;h^{-1}$ at $6.8^{\circ}C$. The cumulative annual soil $CO_2$ efflux of Q. glauca and A. koreana forests was 54.2 and $34.2t\;CO_2\;ha^{-1}$, respectively. Total accumulated soil carbon efflux in Q. glauca and A. koreana forests was 29.5 and $18.7t\;C\;ha^{-1}$ for 2 years, respectively. The relationship between soil $CO_2$ efflux and soil temperate at 10 cm depth was highly significant in the Q. glauca ($r^2=0.853$) and A. koreana forests ($r^2=0.842$). Soil temperature was the main controlling factor over $CO_2$ efflux during most of the study period. Also, precipitation may affect soil $CO_2$ efflux that appeared to be an important factor controlling the efflux rate. Conclusions: Soil $CO_2$ efflux was affected by soil temperature as the dominant control and moisture as the limiting factor. The difference of soil $CO_2$ efflux between of Q. glauca and A. koreana forests was induced by soil temperature to altitude and regional precipitation.

• Journal of Korea Water Resources Association
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• v.39 no.8 s.169
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• pp.669-676
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• 2006

Hydrological factors, especially the spatial distribution of interpretation on precipitation is often topic of interest in studying of water resource. The popular methods such as Thiessen method, inverse distance method, and isohyetal method are limited in calculating the spatial continuity and geographical characteristics. This study was intended to overcome those limitations with improved method that will yield higher accuracy. The monthly and yearly precipitation data were produced and compared with the observed daily precipitation to find correlation between them. They were then used as secondary variables in Co-kriging method, and the result was compared with the outcome of existing methods like inverse distance method and kriging method. The comparison of the data showed that the daily precipitation had high correlation with corresponding year's average monthly amounts of precipitation and the observed average monthly amounts of precipitation. Then the result from the application of these data for a Co-kriging method confirmed increased accuracy in the modeling of spatial distribution of precipitation, thus indirectly reducing inconsistency of the spatial distribution of hydrological factors other than precipitation.

• Journal of Powder Materials
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• v.28 no.6
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• pp.497-501
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• 2021

Cobalt (Co) is mainly used to prepare cathode materials for lithium-ion batteries (LIBs) and binder metals for WC-Co hard metals. Developing an effective method for recovering Co from WC-Co waste sludge is of immense significance. In this study, Co is extracted from waste cemented carbide soft scrap via mechanochemical milling. The leaching ratio of Co reaches approximately 93%, and the leached solution, from which impurities except nickel are removed by pH titration, exhibits a purity of approximately 97%. The titrated aqueous Co salts are precipitated using oxalic acid and hydroxide precipitation, and the effects of the precipitating agent (oxalic acid and hydroxide) on the cobalt microstructure are investigated. It is confirmed that the type of Co compound and the crystal growth direction change according to the precipitation method, both of which affect the microstructure of the cobalt powders. This novel mechanochemical process is of significant importance for the recovery of Co from waste WC-Co hard metal. The recycled Co can be applied as a cemented carbide binder or a cathode material for lithium secondary batteries.

• Journal of Korean Society for Atmospheric Environment
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• v.18 no.E2
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• pp.97-106
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• 2002

The purpose of this study was to quantitatively estimate the washout removal efficiencies of criteria air pollutants such as SO$_2$, TSP, PM10, CO, NO$_2$, and O$_3$corresponding to the amounts and durations of precipitation. The removal patters by washout were studied with air pollutants data and the corresponding precipitation data in Seoul, Korea during the periods of 1990 to 1999. In addition, washout patterns were classified into four seasons and four time Bones, i.e., night, morning, afternoon, and evening. In this study, natures of air pollutants by sequential precipitation were also intensively studied by examining the linear relationships between removal efficiencies and the amounts and durations of precipitation for each pollutant. The results of this study showed that SO$_2$, TSP, and O$_3$were rapidly removed by initial precipitation; however, NO$_2$was slowly removed 2-hour after precipitation. Both CO and PM10 were weakly removed by washout and their removal patters showed to be irregular.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.10 no.4
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• pp.852-856
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• 2009

Poly(ethyleneglycol methacrylate-co-benzyl methacrylate) (P(PEGMA-co-BMA)) microgel was prepared by precipitation copolymerization of PEGMA and benzyl methacrylate in poly(acrylic acid)/ethanol solution. The microgels with various sizes were obtained by changing the concentration of poly(acrylic acid), monomer and nature of solvents. The particle size of P(PECMA-co-BMA) microgels was decreased with increasing the concentration of poly(acrylic acid) and increased with that of monomer. By increasing solubility parameter of solvents, the particle size was inecreased. The size of P(PEGMA-co-BMA) microgels was controlled by experimental conditions from $0.1{\mu}m$ to $0.35{\mu}m$.

• Journal of the Korean Electrochemical Society
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• v.14 no.2
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• pp.98-103
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• 2011

[ $Li[Ni_{0.8}Co_{0.15}Al_{0.05}]O_2$ ]cathode material for lithium secondary battery is obtained using co-precipitation method. To determine the optimal metal solution concentration value, the CSTR coprecipitation was carried out at various concentration values(1-2 mol/L). The surface morphology of coated samples was characterization by SEM(scanning electron microscope) and XRD (X-Ray Diffraction)analyses. Impedance analysis and cyclic voltammogram presented that internal resistance of the cell was dependent upon the concentration of metal solution. such data is very helpful in determining the optimal content of metal solution concentration to enhancing electrochemical property by adjusting powder size distribution and crystal structure.