• Journal of Korean Society for Atmospheric Environment
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• v.26 no.4
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• pp.412-419
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• 2010

Concurrent Multi Path-Differential Optical Absorption Spectroscopy (CMP-DOAS) is a novel active optical system to measure simultaneously ambient trace gases (such as $NO_2$, $SO_2$, $O_3$, and HCHO) present on several light paths. The CMP-DOAS system consists of a 2D CCD camera, spectrometer, receiving telescopes, and artificial light sources. The system receives spectra, which have been transported through several paths. It also covers wavelength ranges of which trace gases of interest share at the same time. This study presents the instrumental setup of a CMP-DOAS in detail. A field campaign for a comparative measurement was carried out at an urban site in Gwangju for a month on January 2009. $NO_2$ mixing ratios measured by the CMP-DOAS system and in-situ $NO_2$ analyzers were in good agreement by 83%. It demonstrates the high capacities of the CMP-DOAS technique to cover atmospheric trace gases dispersed across wide light paths.

• Journal of Korean Society for Atmospheric Environment
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• v.20 no.2
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• pp.161-174
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• 2004

Aerosol formation and growth by water vapor reactions were investigated in a 2.5 -㎥ indoor smog chamber filled with the unfiltered ambient air. The relative humidity of test ambient air was elevated at 59～64% or 84～88% by adding water vapor. The aerosol number size distribution and the concentrations of $O_3$, NO, NO$_2$, and SO$_2$ were measured during the experiments. The $O_3$ and NO$_2$ gases were well reacted with the water vapor at high relative humidity of 84～88%, and the reaction rates of these gases seemed to be decreased at low relative humidity of 59～64%. The formation and condensational growth phenomena of ambient aerosols by water vapor reactions were observed in a Teflon bag, depending strongly on the initial particle size distribution. The water vapor reactions might be affected by the contents of oxidants produced by photochemical reactions under sunlight.

• Journal of Environmental Science International
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• v.11 no.8
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• pp.773-781
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• 2002

The natural carbon cycle has been perturbed since the mid-19th century by anthropogenic CO$_2$emissions from fossil fuel combustion and deforestation due to population growth and industrialization. The current study simulated the global carbon cycle for the past 42 years using an eight-box carbon cycle model. The results showed that since the terrestrial biospheric carbon sink was roughly offset by the deforestation source, the fossil fuel emission source was partitioned between the atmospheric and oceanic sinks. However, the partitioning ratio between the atmosphere and the ocean exhibited a change, that is, the carbon accumulation rate was faster in the atmosphere than in the ocean, due to a decrease in the so-called ocean buffering capacity. It was found that the ocean buffering capacity to take up excess CO$_2$decreased by 50% in terms of the buffer factor over the past 42 years. Accordingly, these results indicate that if the current CO$_2$emission trend continues, the future rate of increase in the atmospheric CO$_2$concentration will accelerate.

• Journal of Korean Society for Atmospheric Environment
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• v.17 no.E4
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• pp.157-162
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• 2001

Jet Bubbling Reactors(JBRs) were operated for the removal of SO$_{x}$ in flue gases produced from many electric power plants. However, many JBR flue gas desulfurization (FGD) facility faced a decrease of SO$_{x}$ removal efficiency and an increase of scale problems with continuous operations. We increased alkalinity of the SO$_{2}$ absorbing medium by adding the dibasic acids (DBAs) to solve these problems more effectively. The SO$_{2}$ removal efficiency, the purity of CaCO$_{3}$ and COD of the wastewater was measured to identify the addition effects of DBAs (150, 200, 250, and 400 ppm) for 2hr in a day into the JBR attached to the large-scale power plants (400 MW$\times$3). Addition of the DBAs resulted in the improvement of the SO$_{2}$ removal efficiency from 2 to 5% and the purity of the gypsum from 1 to 2%; these improvement were due to the alkalinity increase of the absorbing medium and the reduction of a proportion of un-reacted CaCO$_{3}$, respectively. Also, the scale problems formed by un-reacted CaCO$_{3}$ inside the reaction zone of the JBR were substantially reduced. Even though the effluent COD of the wastewater slightly increased from 10~15 to 18~36 mg/l and the erosion problems in the injection pump and duct occurred, this method of increasing SO$_{2}$ removal efficiency by adding the DBAs could be considered as a profitable approach.ach.

• Journal of Korean Society for Atmospheric Environment
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• v.27 no.2
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• pp.168-180
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• 2011

The variation of the physicochemical properties of atmospheric aerosols in coexistence of the heavy Asian Dust and Haze observed from $15^{th}$ to $17^{th}$ March 2009 in Seoul was scrutinized through the mass and ion concentration observations and synoptic weather analysis. Although the ratio of PM1.0/PM10 was constant at 0.3 (which is typical during Asian Dust period in Korea) during the measurement period, both PM10 and PM1.0 mass concentrations were 3~6 times and 2~4 times higher than that of clear days, respectively. Water-soluble ion components accounted for 30~50% of PM10 and 50~70% of PM1.0 mass concentration. One of the secondary pollutants, $NO_3^-$ was found to be associated with $Ca^{2+}$ and $Na^+$ in coarse mode indicating that the aerosol derived from natural source was affected by anthropogenic pollutants. While the acidity of the aerosols increased in fine mode when the stagnation of weather patterns was the strongest (March $16^{th}$), the alkalinity increased in coarse mode when new air masses arrived with a southwestern wind after ending a period of stagnation (March $17^{th}$). In the selected case, SOR (Sulfur Oxidation Ratio, $nSO_4^{2-}/[nSO_4^{2-}+nSO_2]$) and NOR (Nitrogen Oxidation Ratio, $nNO_3^-/[nNO_3^-+nNO_2]$) values of ion components were higher than the general values during Asian Dust period. These results imply that dust aerosols could be mixed with pollutants transported from China even in heavy Asian Dust cases in Korea.

• Journal of Korean Society for Atmospheric Environment
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• v.31 no.1
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• pp.15-27
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• 2015

The collection of fine particulate matter samples was made at Gosan site of Jeju Island, one of the background sites of Korea, during a year of 2013, and their water-soluble ionic species were analyzed in order to examine the chemical compositions and pollution characteristics. The concentrations of $nss-SO_4{^{2-}}$, $NH_4{^{+}}$, $NO_3{^{-}}$, and $K^+$ had occupied 66.0% of water-soluble ionic species in $PM_{10}$, especially 94.3% in $PM_{2.5}$ fine mode, however the $nss-Ca^{2+}$ and $Na^+$ showed high concentrations in $PM_{10-2.5}$ coarse mode. $NO_3{^-}/nss-SO_4{^{2-}}$ concentration ratios in $PM_{10}$ and $PM_{10-2.5}$ were 0.30 and 0.13, showing less significant effect from automobile and local pollution sources. The sulfate and nitrate compounds were presumed to be long-range transported to Gosan area by the relatively high SOR and NOR values. The trajectory cluster analysis showed the higher concentrations of the major secondary pollutants ($nss-SO_4{^{2-}}$, $NO_3{^{-}}$, $NH_4{^{+}}$) and $nss-Ca^{2+}$ when the air masses had moved from China continent and Korean peninsula into Gosan area.

• Journal of Korean Society for Atmospheric Environment
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• v.22 no.4
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• pp.477-486
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• 2006

Dry deposition fluxes for $SO_2$, particulate sulfate, nitrate, ammonium and $HNO_3$ were estimated in urban area for the time period January$\sim$ October 2005. Fluxes were generated using atmospheric concentration data collected both in Acid Deposition and Air Quality Monitoring Networks, and deposition velocities computed by combining land-use data with meteorological information. The resulting annually averaged $SO_2$, $NO_3$, and aerosol deposition velocities were found to be 0.4 cm/s, 4.3 cm/s and 0.1 cm/s, respectively, and thus deposition rates were 4.4 mg/$m^2$. day for $SO_2$, and 5.4 mg/$m^2$ . day for $NHO_3$, and particulate sulfate, ammonium and nitrate recorded 1.0 mg/$m^2$ . day, 0.4 mg/$m^2$ . day and 0.4 mg/$m^2$ day, respectively. Maximum for in seasonal variation of monthly averaged deposition velocities occurred in summer in contrast to $HNO_3$ showing peak in spring. There was no significant variation for aerosol. The dry to total (wet and dry) deposition contributed about 40% for sulfur and 28% for nitrogen species in this study.

• Journal of Korean Society for Atmospheric Environment
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• v.21 no.1
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• pp.73-81
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• 2005

It is widely accepted that, at present, the SO$_2$ emissions in China are not increasing thanks to the rigorous Chinese government policies. However, with the development of western China, it is possible that the SO$_2$ emission amounts might increase in regional scale. In this study, changes of sulfur deposition pattern and unprotected ecosystem in east Asia due to the sulfur emission pattern changes in China are studied by using the RAINS-Asia model. Five scenarios have been postulated to understand the effects on east Asia, especially, on Korea and Japan. It is found that the increase of SO$_2$ emission in western China might increase the total emission in whole China. And the amount of sulfur deposition from western China on east Asia would be higher than those from eastern China. The deposition amount of sulfur species on Asia is 3.2 Mt when SO$_2$ are emitted from western China only while 2.6 Mt from eastern China only. Generally, Korea and Japan are influenced more by emissions from eastern China than western China. However, if the SO$_2$ emissions from western China increase by 100% while those decrease by 10% in eastern China compared to the base case, the deposition amount of sulfur species on Korea and Japan would be higher than the base case. The fraction of unprotected ecosystem in Korea and Japan for the base case are 50 and 5%. However, if the emissions from western China increase by 100% while those decrease by 10% in eastern China, the fraction of unprotected ecosystem in Korea and Japan would be 52 and 6%.

• The Journal of Korea Institute of Information, Electronics, and Communication Technology
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• v.14 no.4
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• pp.328-337
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• 2021

Air pollution, which is a class 1 carcinogen, such as asbestos and benzene, is the cause of various diseases. The spread of ultra-air pollution is one of the important causes of the spread of the corona virus. This paper analyzes and predicts fine dust and ultra-air pollution from 2015 to 2019 based on weather data such as average temperature, precipitation, and average wind speed in Seoul and atmospheric environment data such as SO2, NO2, and O3. Linear regression, SVM, and ensemble models among machine learning models were compared and analyzed to predict fine dust by grasping and analyzing the status of air pollution and ultra-air pollution by season and month. In addition, important features(attributes) that affect the generation of fine dust and ultra-air pollution are identified. The highest ultra-air pollution was found in March, and the lowest ultra-air pollution was observed from August to September. In the case of meteorological data, the data that has the most influence on ultra-air pollution is average temperature, and in the case of meteorological data and atmospheric environment data, NO2 has the greatest effect on ultra-air pollution generation.

• Journal of Korean Society for Atmospheric Environment
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• v.14 no.1
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• pp.11-23
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• 1998

The purpose of this study was to survey chemical distribution of inorganic elements and ions in the submicron particles, to characterize qualitatively emitting sources by factor analysis, and finally to reveal existing patterns in terms of chemical compounds by a stepwise multiple regression analysis. Total of 141 samples were collected by a cascade impactor from 1989 to1996. Fifteen chemical species (Al, Ba, Cd, K, Pb, Cu, Fe, Ni, $Cl^-, NO_3^-, SO_4^{2-}, K^+, Mg^{2+}, Ca^{2+}, and Na^+$) were characterized by AAS and IC. The study showed that average seasonal levels of submicron particulate matters $(d_p<0.43 \mum)$ were 18.7 $\mug/m^3$ in spring, 15.5 $\mug/m^3$ in summer, 15.7 $\mug/m^3$ in fall, and 24.5 $\mug/m^3$ in winter, respectively. All of the anion concentrations in the particle were highest in the winter season. By applying a factor analysis, 5 source patterns were qualitatively obtained, such as sulfate related source, nitrate related source, oil burning source, calcium related source, and coal combustion source. Finally, when applying a stepwise multiple regression analysis, the results clearly showed that $Na^+ and Ca^{2+}, K^+ and Ca^{2+}, NO_3^-$ and relative humidity, $Cl^-$ and ambient temperature, $Ca^{2+} and Cl^-, Mg^{2+} and SO_4^{2-}, Na^+ and NO_3^-, and Ca^{2+} and NO_3^-$, respectively, are negatively contributed to each other. As a result of those statistical analysis, we could suggest that some chemical compounds in the submicron particles such as$NaNO_3, MgSO_4, Ca(NO_3)_2, and CaCl_2$ may not exist on the filter as final composing products; however, other compounds may possibly exist in the form of $Mg(NO_3)_2, CaSO_4, Na_2SO_4, K_2SO_4, MgCl_2, NaCl, and KCl$. Thus, it must be necessary to identify differences between the results of above statistical analysis and of the real world by laboratory experiments.