• 한국지리정보학회지
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• 제4권1호
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• pp.18-26
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• 2001

본 연구에서는 Landsat TM을 이용하여 연안해역의 수질을 모니터링하기 위해 현장에서 조사된 수중광학 측정자료를 Landsat TM 밴드에 적용하여 Landsat TM 밴드비율 알고리듬을 구성하였다. 수중광학 측정장치인 PRR(profiling reflectance radiometer)을 이용하여 획득된 수중 광 반사도를 Landsat TM 밴드 폭으로 보정한 후 현장에서 실측된 피그먼트와 통계적으로 분석하여 관계식을 도출하였다. 수중 광 반사도를 TM 밴드 1과 밴드 2 의 비율에 의한 알고리듬으로 구성하여 $Y=3.8352{\times}(R(band\;1)/R(band\;2))^{-2.1978}$ ($R^2$=0.7069)과 같은 관계식을 도출하였고, 밴드 1과 밴드 3의 비율에 의한 반사도와 피그먼트의 관계는 $Y=23.288{\times}(R(band\;1)/R(band\;3))^{-1.5243}$ ($R^2$=0.8062) 이다. 수면 위로 올라오는 광량과 TM의 레이디언스 값을 각각 구하여 대기효과 중의 Rayleigh 산란과 Mie 산란에 의한 대기중의 잡음비율을 파악하였으며, 연안해역의 조사지점에서 80% 이상의 대기잡음이 있음을 제시하였다. 본 연구에서 도출된 수중 광 알고리듬을 Landsat TM에서 수신된 영상신호에 적용하여 시화호와 연안해역의 수질을 정량적으로 분석하기 위해서는 수중 구성 성분들의 수중 광학 특성을 고려한 수중 알고리듬의 보정과 대기중의 잡음을 효율적으로 제거할 수 있는 대기보정기법의 적용이 요구된다.

• 한국대기환경학회지
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• 제23권5호
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• pp.515-525
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• 2007

In this study, various techniques for measurement and analysis of PAHs in the ambient air were verified in order to select a more reliable method. Sampling and analysis of PAHs were done by the EPA TO-13a method. QA/QC of the measurement was conducted to minimize errors in sampling and analyzing processes. The linearity of calibration curve of the PAH standards was good ($R^2{\geq}0.99$). Audit accuracy was evaluated using 5 internal standards of PAHs ($Naphthalene-d_8,\;Acenaphthene-d_{10},\;Phenanthrene-d_{10},\;Chrysene-d_{12},\;Perylene-d_{12}$). Relative standard deviations of the internal standard of the PAHs were ranged from 6.22% for $acenaphthene-d_{10}$ to 8.11% for $chrysene-d_{12}$. To evaluate the surrogate recoveries, two field surrogate standards of PAHs ($fluoranthene-d_{10},\;benzo(a)pyrene-d_{12}$) and two extract surrogate standards of the PAHs ($fluorene-d_{10},\;pyrene-d_{12}$) were spiked into all samples before field sampling and sample extraction, respectively. Recoveries of field the surrogate standards ranged from $80.4{\pm}12.2%$ for $fluoranthene-d_{10}$ to $66.2{\pm}12.8%$ for $benzo(a)pyrene-d_{12}$. Extraction recoveries of the surrogate standards ranged from $70.4{\pm}10.2%$ for $fluorene-d_{10}$ to $77.6{\pm}10.8%$ for $pyrene-d_{10}$. The detection limit of benzo(a)pyrene among 16 PAHs standards for quantitation was 20 pg.

• 암석학회지
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• 제21권4호
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• pp.415-429
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• 2012

화산가스의 측정법은 크게 원격 측정법과 직접 채취법이 있다. 원격 측정법에서 COSPEC는 $SO_2$를, Li-COR는 $CO_2$를, FT-IR는 다양한 화산가스를 측정한다. 하지만 주변 수계의 영향으로 백두산의 화산가스 농도가 낮아 원격 측정법에 의한 화산가스의 분석은 불가능하다. 대신 직접 채취법은 화산체에서 분출하는 화산가스를 직접 채취해 분석하는 방법으로 화산가스의 농도가 낮은 백두산에 적용할 수 있다. 직접 채취법은 포집방법에 따라서 진공병법과 관류병법이 있으며, 포집용액에 따라 Giggenbach method, $NH_4OH$ method, acid condensate method로 나뉜다. 직접 채취법에 의해 얻은 시료는 전처리 과정을 거친 후 포집용액과 화산가스의 종류에 따라서 GC, IC, HPLC, 적정법, TOC-IC, ICP-MS 등을 이용해 분석한다. 최근 들어 백두산이 가까운 장래에 다시 분출할 것이라는 징후가 속속 보고되고 있다. 하지만, 현재 우리나라는 화산가스의 채취 및 분석법이 확립되지 않은 실정이다. 따라서 본 연구에서는 지금까지 보고된 다양한 화산가스의 측정법을 검토하고, 이들 중 백두산 화산가스의 측정에 활용 가능한 기법을 상술했다.

• Journal of Korean Society for Atmospheric Environment
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• 제18권E2호
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• pp.57-68
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• 2002

Atmospheric dry deposition fluxes and size segregated concentrations of particulate metal elements were measured at four sites in Kunpo, a small city in the Seoul metropolitan area in Korea. At each site, aerosol samples were collected by dry deposition plates, a cascade impactor, and a coarse panicle rotary impactor during four sampling periods. At all sites, the average fluxes of metals measured during daytime were higher than nighttime fluxes due to higher wind speeds and higher ambient concentrations during daytime. The average fluxes of crustal elements (Al, Ca) were 1∼2 orders of magnitude higher than anthropogenic elements (As, Cd, Cu, Mn, Ni, Pb, and Zn). The daytime fluxes of Al and Ca were between 90 and 12000 $\mu\textrm{g}$ m$\^$-2/ day$\^$-1/, and the nighttime fluxes of Al and Ca were between 20 and 2200 $\mu\textrm{g}$ m$\^$-2/ day$\^$-1/. The daytime fluxes of Pb, a typical anthropogenic element, were between 20 and 160$\mu\textrm{g}$ m$\^$-2/ day$\^$-1/, and the nighttime fluxes of Pb were between ND and 100$\mu\textrm{g}$ m$\^$-2/ day$\^$-1/. Also the ambient metal concentrations during daytime were higher than nighttime. Based on a dust emission estimation study in Kunpo, it was found that dust emissions during daytime are higher than nighttime. The concentrations of crustal elements were higher than anthropogenic elements. The distributions of heavy metals were mainly in small particles (D$\_$p/ 9㎛). The fraction of crustal elements in the large particles (D$\_$p/> 9㎛) were higher than anthropogenic elements.

• 한국대기환경학회지
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• 제15권4호
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• pp.485-493
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• 1999

This paper presents the results of the first interlaboratory comparison of ambient particles measurement conducted by 5 laboratories under the framework of Korean Society for Atmospheric Environment(KOSAE) on the May of 1998 in Seoul. Collection of particles less than 10$mu extrm{m}$(PM10) was carried out by two different types of PM10 sampler, and their concentration reported by three laboratories ranged from 36.2~56.05$\mu\textrm{g}$/㎥. Analyses of chemical composition of particles collected by each lab were performed by the destructive and nondestructive instrumental methods. Statistical analysis of the measurement results could not be carried out because a comprehensive QA/QC had not been applied before experiment. The importance of QA/QC as well as the performance of QA/QC for the measurement of PM10 was discussed in detail.

• 한국대기환경학회지
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• 제19권6호
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• pp.647-661
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• 2003

For continuous monitoring of atmospheric visibility in the city of Kwanaju, Korea, a transmissometer system consisting of a transmitter and a receiver was installed at a distance of 1.91 km across the downtown Kwanaju. At the transmitter site an integrating nephelometer and an aethalometer were also installed to measure the scattering and absorption coefficients of the atmosphere, respectively. At the receiver site. an URG PM$_{2.5}$ cyclone sampler and an URG-VAPS (Versatile Air Pollutant Sampler) with three filter packs and two denuders were used to collect both PM$_{2.5}$ and PM$_{10}$ samples at a 2-hour or 12-hour sampling interval for aerosol chemical analysis. Sulfate, organic mass by carbon (OMC), nitrate, elemental carbon (EC) components of fine aerosol were the major contributors to visibility impairment. Diurnal variation of visibility during best-case days showed rapid improvement in the morning hours, while it was delayed until afternoon during the worst-case days. Aerosol mass concentration of each aerosol component for the worst-case was calculated to be 11.2 times larger than the best-case for (NH$_4$)$_2$SO$_4$(NHSO), 19.0 times for NH$_4$NO$_3$ (NHNO), 2.2 times for OMC, respectively. Also result shows that elemental carbon and fine soil (FS) were 3.7 and 2.2 times more than those of best-case. respectively- Sum of total contributions of wet NHSO and NHNO to light extinction was calculated to be 301 Mm$^{-1}$ for the worst-case. However, sum of contributions by dry NHSO and NHNO was calculated to be 123 Mm$^{-1}$ for the best case. Mass extinction efficiencies of fine and coarse particles were calculated to be 5.8$\pm$0.3 $m^2$/g and 1.8$\pm$0.1 $m^2$/g, respectively.ely.

• 한국대기환경학회지
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• 제23권4호
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• pp.405-419
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• 2007

A series of tracer experiments for the evaluation of atmospheric dispersion was performed over the urban area of Seoul using two inert, non-deposition perfluorocarbon (PMCH and m-PDCH) gases during three years campaign on 2002, 2003 and 2005. 30 sampling sites for collecting these tracers were located along two arcs of 2.5 and 5 kilometers downwind from the release point. About ten measurements which each lasted for 2 hours or 4 hours were made over the two consecutive days during each campaign. CALPUFF and MM5 meteorological model were applied to evaluate the urban dispersion in detail. Size of Modeling domain was $27\;km{\times}23\;km$ and the fine nest in the modeling domain had a grid size of 0.5 km. The results showed that CALPUFF dispersion model had a tendency to estimate tracer concentrations about $2{\sim}5$ times less than those of ambient samples under many conditions. These consistent inaccuracy in urban dispersion was attributed to inherent inaccuracy and lack of details in terrain data at urban area.

• 한국대기환경학회지
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• 제19권5호
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• pp.529-540
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• 2003

A closed chamber system was used for measuring $N_2$0 fluxes from an agriculturally managed upland soil in Kunsan during the growing season from May to July 2002. It is known that soil is one dominant source of atmospheric $N_2$O, contributing to about 57% (9 Tg y $^{-1}$ ) of the total annual global emission. Hence, its increasing emissions and concentrations are largely associated with agricultural activities. In order to elucidate characteristics of soil nitrogen emissions from intensively managed agricultural soils and to understand the roles of soil parameters (soil moisture, soil pH, soil temperature, and soil nitrogen) in the gas emission, $N_2$O soil emissions were measured at every hour during the experimental period (21 days). Soil $N_2$O fluxes were calculated based on changes of $N_2$O concentrations measured inside a closed chamber at every hour. The analysis of $N_2$O was made by using a Gas Chromatography (equipped with Electron Capture Detector). Soil parameters at sampling plots were also analyzed. Monthly averaged $N_2$O fluxes during May, June, and July were 0.14, 0.05, and 0.13 mg-$N_2$O m$^{-2}$ h$^{-1}$ , respectively. Soil temperature and soil pH did not significantly vary over the experimental period; soil temperatures ranged from 12∼$25^{\circ}C$, and soil pH ranged 4.56∼4.75. However, soil moisture varied significantly from 32% to 56% in WFPS. Relationships between soil parameters and $N_2$O fluxes exhibited positive linear relationships. Strong positive correlation ($R^2$ = 0.57, P< 0.0001) was found between $N_2$O flux and sil moisture. It suggests that soil moisture has affected strongly soil $N_2$O emissions during the experimental periods, while other parameters have remained relatively at constant levels. $N_2$O flux from agricultural soils was significant and should be taken account for the national emission inventory.

• 한국입자에어로졸학회지
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• 제9권3호
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• pp.187-197
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• 2013

To understand the characteristics of organic aerosol(OA) at the background atmosphere of Korea, an observation of atmospheric PM10 was conducted at a Global Atmospheric Watch(GAW) station operated by the Korean Meteorological Administration at Anmyon Island during 2010. Various organic compounds were analyzed from 26 samples by using a gas chromatography-mass spectrometer. Water soluble organic carbon(WSOC) was also analyzed by using a total organic carbon(TOC) analyzer. Among 6 classes with 68 target compounds detected, the classes of n-alkanoic and alkenoic acids ($326.67{\pm}75.40ngm^{-3}$) and dicarboxylic acids ($323.74{\pm}361.89ngm^{-3}$) were found to be major compound classes in the atmosphere of Anmyon Island. Compared to the previous results reported for 2005 spring samples at Gosan site, the concentrations of organic compounds at Anmyon Island were 3-10 times higher than Gosan site due to the difference of location and sampling period. The concentrations of organic compounds were varied with the atmospheric conditions. Significant increase of the concentrations of dicarboxylic and carboxylic acids in the smog episode indicated that secondary oxidation of organic compounds was major factor to increase OA concentration during smog episode in the Anmyon Island. It was found that the compositions of the OA measured at Anmyon Island were dependent on the air parcel trajectories.

• 한국환경보건학회지
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• 제31권5호
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• pp.387-397
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• 2005

In oder to understand the deposition possibility of water-soluble inorganic ions in the atmospheric fine particulates for the human respiratory tract, the mass size distribution of ion species was measured using an Anderson sampler in the Iksan during fall, 2004. Samples were analyzed for major water-soluble ions using Dionex DX-100 ion chromatograph. The size distribution of water-soluble inorganic ions in the atmospheric particulates appeared bimodal distribution, which were divided around $1-2{\mu}m$ into two groups. Mass site distribution of total ion in the coarse mode was found to be almost similar level during the sampling period, but fluctuations of mass size distribution in the fine mode were observed. Considering the mass size distribution of total ion concentrations for the respiratory deposition region, it was found that about 77.1% of total tons could be deposited in the alveolar region, and which dominated the daily variation of total ion concentrations. The concentration of total ions, which could be deposited in both the head region and the tracheobronchial region, was $3.95{\mu}g/m^3$, whereas that in the alveolar rerion was $13.28{\mu}g/m^3$. Dominant ions which could be deposited in the alveolar region were ${NO_3}{^-},\;{SO_4}^{2-}\;and\;{NH_4{^+}$, accounting for about 40%, 27% and 22% of the total ions, respectively. Although $K^+$ was approximately 3% of total ions, it was shown that most of this could be deposited in the alveolar region due to its high fraction of small size distribution originated from anthropogenic source of biomass burning. The presence of these ions in the fine mode may be of public health significance as they are very biologically harmful to health and have a high probability of being deposited in human lung tissue.