• Journal of Environmental Science International
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• v.8 no.4
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• pp.485-490
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• 1999

We will calculate concentration of air pollutants using ISCST3, FDM and AERMOD of models recommended in U. S. EPA which are able to predict concentration of short term for point source, complex like industrial complex, power plant and burn-up institution. Before executing model, as analyzing computational result of many cases according to selecting of input data, we will increasing predictable ability of model in limit range of model. Especially, we analyzed three cases-case of considering various emission rate according to time scale and not, case considering effect of atmospheric pollution materials removed by physical process. In our study, after comparing and analyzing results of three model, we choose the atmospheric dispersion model reflected well the characteristic of the area. And we will investigate how large the complex pollutant sources such as industrial complex contribute to atmospheric environment and air quality of the surrounding the area as predicting and estimating chosen model.

• Journal of Korean Society for Atmospheric Environment
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• v.10 no.3
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• pp.170-174
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• 1994

Atmospheric lead concentrations in Seoul were monitored for ten years from January 1984 to June 1993 using X-ray fluorescence Spectrometer. 342 aerosol samples were collected using high volume samplers at two sites : one at Chungang University campus from 1984 to 1988 and the other at Yonsei University campus from 1989 to 1993. Lead concentration increased steadily from about 300ng/㎥ to the maximum of about 600ng/㎥ in 1988 and then decreased, and this is similar to the pattern of Korean leaded gasoline sales implying that Korean automobile emission is the main source. However, the emission from nation's coal combustion appeared to be substantial as welt, and this emmision is the major cause for the secondary feature strong seasonal variability. Lead concentration varied systematically from season to season, low in summer and high in winter. The region's characteristic climate, frequent and heavy precipitations in summer and dry in winter is considered to be another cause for the seasonal variability.

• Journal of Korean Society for Atmospheric Environment
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• v.20 no.6
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• pp.729-738
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• 2004

Seasonal variation of major inorganic ions in the greater Seoul area was estimated using a photochemical box model and a gas/aerosol equilibrium model with emphasis on semi -volatile nitrate. Pollutant emission was determined by season by comparing the predicted concentration with the measurement one obtained for a year from the late 1996. The results showed that particulate nitrate was the highest in summer but about 40% of total nitrate was present in the gas phase. This was due to volatilization at high temperature since ammonia was sufficient to neutralize all nitrate regardless of season. As relative humidity in summer was higher than the deliquescence point, particulate ion concentration with water was two times higher than that in other season. So called ‘NOx disbenefit’ indicating increase in particulate ion concentration with decrease in NOx emission was evident especially in winter.

• Journal of the Korean Institute of Electrical and Electronic Material Engineers
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• v.14 no.11
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• pp.922-927
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• 2001

Single-layer green ELs was fabricated with using molecularly-dispersed Bu-PBD into poly-N-vinylcarbazole(PVK) which has low operating voltage and high quantum efficiency. A EL cell structure of glass substrate/indium-tin-oxide/PVK:Bu-PBD:C6(∼ 100nm)/Ca(20nm)/Al(20nm) was employed with variable doping concentration. The keys to obtain high quantum efficiency was excellent film forming capability of molecularly dispersed into PVK and appropriate combination of cathode for avoiding exciplex. We obtained the turn-on voltage of 4.2V and quantum efficiency of 0.52% at 0.lmol% of C6 concentration which has been improved about a factor of 50 in comparison with the undoped cell. The PL peak wavelengths wouldn\`t be turned by changing the concentration of the C6 dopant. Green EL emission peak and FWHM were 520nm and 70nm respectively. PL emission peak was obtained at 495nm.

• Journal of Environmental Health Sciences
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• v.30 no.5 s.81
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• pp.378-387
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• 2004

This study was carried to investigate the emission characteristics of mercury from domestic and industrial MSW (municipal solid waste) incinerator stacks. The mercury concentration levels of flue gas from 32 MSW incinerators stacks selected were above the criteria level ($5{\mu}g/S\;m^3$). MSWI facilities exceeding the criteria levels in Korea are due to the poor units comparison of combustion chamber(CC)-cyclone(CY)-stack. So, the mercury from MSW incinerators stack were suspected to contaminate the natural system unless the MSW incinerators were properly controlled. Mean-while, the relationship between mercury concentration and temperature of flue gas in MSW incinerator stacks were examined at two temperature ranges (Group A : $29.85{\sim}327.63^{\circ}C$, Group B : $446.9{\sim}848.15^{\circ}C$). The mercury concentration in flue gas with high temperature range was higher than that of flue gas with low temperature rage. This mean that the temperature of flue gas plays an important role in mercury control in MSW incinerator. The emission characteristics oi mercury was also evaluated by using the correlation matrix between the mercury and NOx, $PM_{10}$, moisture (MO.) at both low temperature and high temperature flue gas ranges. The mercury concentration was mainly affected by NOx, $PM_{10}$. moisture (MO.) at low temperature range, while the mercury concentration at high temperature flue gas was mainly affected by NOx, moisture (MO.). From these results, it was suggested that the temperature of cooling system and the air pollution control device should be properly regulated in order to control mercury of flue gas in MSWI incinerator.

• Journal of the Korean Institute of Electrical and Electronic Material Engineers
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• v.30 no.11
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• pp.710-716
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• 2017

New white-light-emitting $SrSnO_3:Dy^{3+}$ phosphors were prepared using different concentrations of $Dy^{3+}$ ions via a solid-state reaction. The phase structure, luminescence, and morphological properties of the synthesized phosphors were investigated using X-ray diffraction analysis, fluorescence spectrophotometry, and scanning electron microscopy, respectively. All the synthesized phosphors crystallized in an orthorhombic phase with a major (020) diffraction peak, irrespective of the concentration of $Dy^{3+}$ ions. The excitation spectra were composed of a broad band centered at 298 nm, ascribed to the $O^2-Dy^{3+}$ charge transfer band and five weak bands in the range of 350~500 nm. The emission spectra of $SrSnO_3:Dy^{3+}$ phosphors consisted of three bands centered at 485, 577, and 665 nm, corresponding to the $^4F_{9/2}{\rightarrow}^6H_{15/2}$, $^4F_{9/2}{\rightarrow}^6H_{13/2}$, and $^4F_{9/2}{\rightarrow}^6H_{11/2}$ transitions of $Dy^{3+}$, respectively. As the $Dy^{3+}$ concentration increased from 1 to 15 mol%, the intensities of all the emission bands gradually increased, reached maxima at 15 mol% of $Dy^{3+}$ ions, and then decreased rapidly at 20 mol% due to concentration quenching. The critical distance between neighboring $Dy^{3+}$ ions for concentration quenching was calculated to be $9.4{\AA}$. The optimal white light emission by the $SrSnO_3:Dy^{3+}$ phosphors was obtained when the $Dy^{3+}$ concentration was 15 mol%.

• Journal of the Korean Vacuum Society
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• v.20 no.6
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• pp.430-435
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• 2011

$Y_{1-x}PO_4:{Eu_x}^{3+}$ red phosphors were synthesized with changing the concentration of $Eu^{3+}$ ion by using a solid-state reaction method. The crystal structures of all the red phosphors were found to be a tetragonal system composed of (200) diffraction peak centered at $25.88^{\circ}$, and the morphology of grains approached the spherical form with homeogenous size distribution as the concentration of $Eu^{3+}$ ion increased. As for the photoluminescence properties, all of the ceramic phosphors, irrespective of $Eu^{3+}$ ion concentration, showed the red-orange and the red emission peaked at 593.0 and 619.2 nm respectively. As the concentration of $Eu^{3+}$ ion increased, the excitation spectrum moved into a longer wavelength with the increase of emission intensity. The maximum excitation and the emission spectrum were observed at 0.15 mol of $Eu^{3+}$ ion.

• Korean Journal of Materials Research
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• v.29 no.6
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• pp.356-362
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• 2019

$BaSiO_3:RE^{3+}$ (RE = Sm or Eu) phosphor powders with different concentrations of activator ions are synthesized using the solid-state reaction method. The effects of the concentration of activator ions on the structural, photoluminescent, and morphological properties of the barium silicate phosphors are investigated. X-ray diffraction data reveals that the crystal structure of all the phosphors, regardless of the type and the concentration of the activator ions, is an orthorhombic system with a main (111) diffraction peak. The grain particles agglomerate together to form larger clusters with increasing concentrations of activator ions. The emission spectra of the $Sm^{3+}$-doped $BaSiO_3$ phosphors under excitation at 406 nm consist of an intense orange band at 604 nm and three weak bands centered at 567, 651, and 711 nm, respectively. As the concentration of $Sm^{3+}$ increases from 1 to 5 mol%, the intensities of all the emission bands gradually increase, reach maxima at 5 mol% of $Sm^{3+}$ ions, and then decrease significantly with further increases in the $Sm^{3+}$ concentration due to the concentration quenching phenomenon. For the $Eu^{3+}$-doped $BaSiO_3$ phosphors, a strong red emission band at 621 nm and several weak bands are observed. The optimal orange and red light emissions of the $BaSiO_3$ phosphors are obtained when the concentrations of $Sm^{3+}$ and $Eu^{3+}$ ions are 5 mol% and 15 mol%, respectively.

• Journal of Environmental Science International
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• v.32 no.7
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• pp.503-520
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• 2023

In this study, numerical simulations using community multiscale air quality (CMAQ) were conducted to analyze the change in ozone (O₃) concentration due to the reduction in nitrogen oxides (NO_x)andvolatile organic compounds (VOCs) emissions in Busan. When the NO_x and, VOCs emissions were reduced by 40% and, 31%, respectively, the average O₃ concentration increased by 4.24 ppb, with the highest O₃ change observed in the central region (4.59 ppb). This was attributed to the decrease in O₃ titration by nitric oxide (NO) due to the reduction of NO_x emissions in Busan, which is classified as a VOCs-limited area. The distribution of O₃ concentration changes was closely related to NO_x emissions per area, and inland emissions were highly correlated with daily maximum concentrations and 8-h average O₃ concentrations. Contrastingly, the effect of emission reduction depended on the wind direction. This suggests that the emission reduction effects may vary depending on the environmental conditions. Further research is needed to comprehensively analyze the emission reduction effects in Busan.

• Korean Chemical Engineering Research
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• v.54 no.2
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• pp.187-199
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• 2016

In this study CALPUFF modeling was performed to predict a contribution of a separate single point pollutant source as well as of total point pollutant sources of major synthetic fiber manufacturers in Gumi national industrial complex to atmospheric trimethylamine concentration of the same area. In addition, a contribution of the separate single point pollution source to the atmospheric trimethylamine concentration of the same area was estimated relatively to the total point pollutant sources. As a result of the CALPUFF modeling, the maximum atmospheric concentration of trimethylamine in Gumi national industrial complex was appeared upon improving T company emission facility frequently in complex 3 in winter (January) and spring (April) while frequently in complex 1 in summer (July) and autumn (October). Besides, the predicted range of the maximum atmospheric concentration of trimethylamine in complex 1 was improved upon improving its emission facility. However, even though in complex 3 the upper bound of the predicted maximum atmospheric concentrations of trimethylamine was increased upon improving T company emission facility, the predicted value of their second upper bound below the upper bound was very similar to the upper bound of measured atmospheric trimethylamine concentrations in Gumi prior to improving its emission facility. Thus, the effect of improving T company emission facility was estimated huge in complex 1 while it was trivial in complex 3. These maximum concentrations of trimethylamine predicted to estimate the expected contribution of total point pollutant sources by CALPUFF modeling showed the similar values to those measured in the region of Gumi. Therefore, the expected contribution of total point pollutant sources to atmospheric trimethylamine concentration in the area of Gumi was validated.