• Bulletin of the Korean Chemical Society
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• 제33권11호
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• pp.3651-3656
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• 2012

The size-segregated atmospheric aerosols have been collected at 1100 m site of Mt. Halla in Jeju, a background area in Korea, using 8-stage cascade impact air sampler during Asian dust and non-Asian dust storm periods. Their ionic and elemental species were analyzed, in order to examine the pollution characteristics and composition change between Asian dust and non-Asian dust periods. The major ionic species such as nss-$SO_4{^{2-}}$, $NH_4{^+}$, and $K^+$ were predominantly distributed in the fine particles (below $2.1{\mu}m$ diameter), and besides the $NO_3{^-}$ was distributed more in coarse particle fraction than fine particle. On the other hand, the typical soil and marine species i.e., nss-$Ca^{2+}$, $Na^+$, $Cl^-$, and $Mg^{2+}$, were mostly existed in the coarse particles (over $2.1{\mu}m$ diameter). As well in the elemental analysis of aerosols, the major soil-originated Al, Fe, Ca, and others showed prominently high concentrations in the coarse particle fraction, whereas the anthropogenic S and Pb were relatively high in the fine particle fraction. From the comparison of aerosol compositions between Asian dust and non-Asian dust periods, the concentrations of the soil-originated species such as nss-$Ca^{2+}$, Al, Ca, Fe, Ti, Mn, Ba, Sr have increased as 2.7-4.2 times during the Asian dust periods. Meanwhile the concentrations of nss-$SO_4{^{2-}}$ and $NO_3{^-}$ have increased as 1.4 and 2.0 times, and on the contrary $NH_4{^+}$ concentrations have a little bit decreased during the Asian dust periods. Especially the concentrations of both soil-originated ionic and elemental species increased noticeably in the coarse particle mode during the dust storm periods.

• Ocean and Polar Research
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• 제44권4호
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• pp.297-310
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• 2022

To understand the chemical composition of aerosols in the Cheju-Korea Straits and their contribution to the ocean by deposition, aerosol samples were collected on board R/V Eardo from November 1997 to May 1999. The average concentrations of Al, NO₃^-, non-sea-salt (nss)-SO₄^2-, and NH₄⁺ in aerosols were 2.19, 5.59, 6.16 and 2.08 ㎍ m^-3, respectively. The Al concentration in the high yellow dust period was about 100 times higher than that in the non-yellow dust period. The concentration ratio of NO₃^-/nss-SO₄^2- ranged between 0.47 and 1.5, indicating that the aerosols in the Cheju-Korea Straits are under the effects of NO_x and SO_x emitted from China, Korea and Japan. The equivalent concentration ratio of [NH₄⁺]/[nss-SO₄^2-+ NO₃^-] with the average of 0.58±0.29 indicates that nss-SO₄^2- and NO₃^- are not neutralized by NH₄⁺. A high activity concentration of ²¹⁰Pb with 1.13-1.23 mBq m^-3 was observed during the high yellow dust period, indicating that ²¹⁰Pb is easily adsorbed in the yellow dust originating from the continent of Asia. The distribution of ⁷Be and NH₄⁺ concentrations showed a strong negative linear correlation during the low yellow dust period, April 1998. The total mineral dust flux in the Cheju-Korea Straits was estimated to be 1.21×10⁶ tons yr^-1, accounting for about 12% of the annual sediment discharge via the Nakdong River. The combined annual deposition of NH₄⁺ and NO₃^- was 0.103 mole N m^-2 yr^-1 was estimated to support 4% of the annual primary productivity in the East China Sea.

• 한국입자에어로졸학회지
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• 제19권4호
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• pp.129-144
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• 2023

The PM_1.0 and PM_2.5 samples were collected synchronously using a single channel particulate sampler equipped with PM_1.0 and PM_2.5 cyclones, respectively, and seasonal mass concentration and chemical composition of PM_1.0 and PM_2.5 were quantified in Seoul and Gwangju in 2021-2022. The mass concentrations of PM_1.0 and PM_2.5 were 17±11 and 22±14 ㎍/m³ in Seoul, and 16±9 and 19±12 ㎍/m³ in Gwangju, respectively. The average ratios of PM_1.0/PM_2.5 were 83±16% in Seoul and 83±7% in Gwangju. The chemical compositions of PM_1.0 and PM_2.5 were similar at both sites with OC component being the most dominant, and NO₃^- increasing from summer to winter, while, the difference of chemical distribution at the two sites was most distinct in the autumn. Gwangju showed a higher proportion of OC and a lower proportion of NO₃^- compared to Seoul during the autumn. Both sites appear to reflect their urban characteristics, with Gwangju also reflecting the impact of biomass combustion as a part of rural activities.

• 한국대기환경학회지
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• 제34권3호
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• pp.430-446
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• 2018

To improve understanding of the sources and chemical properties of particulate pollutants on the Korean Peninsula, An Aerodyne High Resolution Time of Flight Aerosol Mass Spectrometer (HR-ToF-AMS) measured non-refractory fine particle ($NR-PM_1$) from 2013 to 2015 at Baengnyeong Island and Seoul metropolitan area (SMA), Korea. The chemical composition of $NR-PM_1$ in Baengnyeong island was dominated by organics and sulfate in the range of 36~38% for 3 years, and the organics were the dominant species in the range of 44~55% of $NR-PM_1$ in Seoul metropolitan area. The sulfate was found to be more than 85% of the anthropogenic origin in the both areas of Baengnyeong and SMA. Ratio of gas to particle partition of sulfate and nitrate were observed in both areas as more than 0.6 and 0.8, respectively, representing potential for formation of additional particulate sulfate and nitrate. The high-resolution spectra of organic aerosol (OA) were separated by three factors which were Primary OA(POA), Semi-Volatility Oxygenated Organic Aerosol (SV-OOA), and Low-Volatility OOA(LV-OOA) using positive matrix factorization (PMF) analysis. The fraction of oxygenated OA (SOA, ${\fallingdotseq}OOA$=SV-OOA+LV-OOA) was bigger than the fraction of POA in $NR-PM_1$. The POA fraction of OA in Seoul is higher than it of Baengnyeong Island, because Seoul has a relatively large number of primary pollutants, such as gasoline or diesel vehicle, factories, energy facilities. Potential source contribution function (PSCF) analysis revealed that transport from eastern China, an industrial area with high emissions, was associated with high particulate sulfate and organic concentrations at the Baengnyeong and SMA sites. PSCF also presents that the ship emissions on the Yellow Sea was associated with high particulate sulfate concentrations at the measurement sites.

• 대한원격탐사학회지
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• 제37권3호
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• pp.543-557
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• 2021

에어로솔은 입자의 크기와 조성 및 관측센서에 따라 상이한 분광특성을 보이기 때문에, 다양한 센서의 에어로솔 산출물에 대한 비교분석이 반드시 필요하다. 그러나, 우리나라에서 다종위성의 공식적인 AOD (Aerosol Optical Depth) 산출물을 대상으로 수년간의 자료를 수집하여 정확도 비교평가를 수행한 사례는 아직 보고된 바가 없다. 이에, 본 연구에서는 2015년 1월부터 2019년 12월까지 MODIS (Moderate Resolution Imaging Spectroradiometer), VIIRS (Visible Infrared Imaging Radiometer Suite), Himawari-8, Sentinel-3 AOD 산출물과 AERONET (Aerosol Robotic Network) 지상 태양광도계 자료의 비교분석을 통하여 위성 AOD의 성능을 평가하고, 계절적 및 지리적 차이에 따른 정확도 특성을 분석하였다. 오랜 기간 축적되어온 산출 기술에 MAIAC (Multiangle Implementation of Atmospheric Correction) 알고리듬을 추가하여 최적화된 MODIS 산출물이 가장 높은 정확도를 나타냈고(CC=0.836), VIIRS와 Himawari-8이 그보다 약간 낮은 정도의 성능을 보였으며, Sentinel-3는 비교적 최근에 발사되어 알고리듬 최적화가 아직 덜 이루어진 관계로 정확도가 낮게 나타났다. MODIS, VIIRS, Himawari-8 AOD 산출물은 계절에 따라, 그리고 도시/비도시에 따라 별다른 정확도 차이를 보이지는 않았지만, 일부 해안지역에서는 혼합화소 문제로 인하여 약간 정확도가 떨어지는 경우도 존재했다. AOD는 위성영상 대기보정의 핵심 인자이기 때문에, 본 연구의 AOD 비교평가는 향후 국토위성, 농림위성 등의 대기보정 연구에도 중요한 참고자료가 될 것으로 사료된다.

• 분석과학
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• 제23권4호
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• pp.371-382
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• 2010

제주도 고산지역에서 TSP (total suspended particulate), PM2.5 (particulate matter, below $2.5\;{\mu}m$ particle size) 대기에어로졸을 채취, 분석하여 에어로졸의 조성과 오염 특성을 조사하였다. 고산지역 대기에어로졸에서 nss(non-sea salt)-$SO_4^{2-}$과 $NH_4^+$은 다른 국내 청정지역 및 도시지역에 비해 높은 조성비를보이고 $NO_3^-$는 상대적으로 낮은 조성비를 나타내었다. 에어로졸 성분의 입경별 분포를 비교해 본 결과, 인위적 기원의 nss-$SO_4^{2-}$, $NO3_^-$, $NH_4^+$ 성분들은 대체적으로 미세입자에, 토양기원의 nss-$Ca^{2+}$과 해염기원의 $Na^+$, $Cl^-$, $Mg^{2+}$은 상대적으로 조대입자에 많이 분포하고 있는 것으로 확인되었다. 계절별로는 봄철에 nss-$Ca^{2+}$, Al, Fe, Ca, $NO_3^-$ 성분의 농도가 크게 상승하고, nss-$SO_4^{2-}$은 여름과 봄철에 높은 농도를 나타내었다. 인자분석 결과, 에어로졸은 대체적으로 인위적 발생원의 영향을 많이 받고, 다음으로 해양 및 토양 영향을 많이 받았다. 또한 역궤적 분석법으로 에어로졸 성분의 유입경로를 조사해 본 결과, nss-$SO_4^{2-}$, $NO_3^-$, Pb, nss-$Ca^{2+}$ 성분들은 대체적으로 기류가 중국대륙으로부터 제주지역으로 이동할 때 훨씬 더 높은 농도를 나타낸 반면, 북태평양에서 제주지역으로 이동할 때 상대적으로 낮은 농도를 나타내었다.

• 한국군사과학기술학회지
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• 제18권3호
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• pp.335-342
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• 2015

Laboratory facilities for biology are designed as biosafety level 1, biosafety level 2, biosafety level 3, and biosafety level 4. Biosafety level designations are based on a composite of the design features, construction, containment facilities, equipment, practice and operation procedures required for working with agents from the various risk groups. Generally, biosafety level 3 means the facility that is appropriate for the experiments using pathogens which can cause serious diseases by aerosol transmission. The biosafety level assigned for the specific work to be done is driven by professional judgement based on a risk assessment, rather than by automatic assignment according to the particular risk group designation of the pathogenic agents to be used. In this paper, we introduced the biosafety level 3 facility operated in ADD(Agency for defense development). It contains the overview of facility, microbiological experiment, animal experiment, decontamination and waste disposal. Biosafety level 3 laboratory in ADD has served the vital role in the research of biological agents and antidote development.

• Bulletin of the Korean Chemical Society
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• 제27권10호
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• pp.1572-1576
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• 2006

A dimeric precursor, $[Cu(dmae)(OCOCH_3)(H_2O)]_2$ for the CVD of copper metal films, (dmaeH = N,N-dimethylaminoethanol) was synthesized by the reaction of copper(II) acetate monohydrate ($Cu(OCOCH_3)_2{\cdot}H_2O$) and dmaeH in toluene. The product was characterized by m.p. determination, elemental analysis and X-ray crystallography. Molecular structure of $[Cu(dmae)(OCOCH_3)(H_2O)]_2$ shows that a dimeric unit $[Cu(dmae)(OCOCH_3)(H_2O)]_2$ is linked to another through hydrogen bond and it undergoes facile decomposition at 300 C to deposit granular copper metal film under nitrogen atmosphere. The decomposition temperature, thermal behaviour, kinetic parameters, evolved gas pattern of the complex, morphology, and the composition of the film were also investigated.

• 대한기계학회:학술대회논문집
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• 대한기계학회 2007년도 춘계학술대회A
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• pp.126-129
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• 2007

The particle formation using pyrolysis has many advantages over other particle manufacturing techniques. The particles by pyrolysis have relatively uniform size and chemical composition. Also, we can easily produce high purity particles. Thus, we studied the formation of silicon particles by pyrolysis of 50% $SiH_4$ gas diluted in Ar gas. A pyrolysis furnace was used for the thermal decomposition of $SiH_4$ gas at $800^{\circ}C$ and atmospheric pressure. The aerosol flow from furnace is separated into two ways. The one is to the Scanning Mobility Particle Sizer (SMPS) for particle size distribution measurement and the other is to the particle deposition system. The produced silicon particles are deposited on the wafer in the deposition chamber. SEM measurement was used to compare the particle size distribution results from the SMPS. Depending on the experimental conditions, particles of high concentration in the $30\sim80$ nm size range were generated.

• Asian Journal of Atmospheric Environment
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• 제4권2호
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• pp.72-79
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• 2010

In this study, the ionic composition of volcanogenically derived particles and their temporal and spatial distributions have been investigated to evaluate the impact of the volcanic eruption on the local ecosystem and residents. To this end, an intensive field study was conducted to measure the size-segregated particulate matters at the east part of Sakurajima in Japan. Fractionated sampling of particles into > $PM_{10}$, $PM_{10-2.5}$, and $PM_{2.5}$ was made by a multi nozzle cascade impactor (MCI). The concentration of various ions present in the size-resolved particles was determined by Ion chromatography. The time dependent 3-dimensional Volcanic Ash Forecast Transport And Dispersion (VAFTAD) model developed by the NOAA Air Resources Laboratory (ARL) indicated that the sampling site of this work was affected by the volcanic aerosol particles plume. The temporal distributions of sulfate and $PM_{2.5}$ during the field campaign were significantly variable with important contributions to particle mass concentration. The chlorine loss, suspected to be caused by acidic components of volcanic gases, occurred predominantly in fine particles smaller than $10\;{\mu}m$.