• 한국대기환경학회지
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• 제8권3호
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• pp.191-197
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• 1992

In order to investigate the chemical components of acid precipitation at Kangwha near the Yellow Sea and Seoul in Korea, the precipitation samples were collected by wetonly precipitation sampler from February 1991 to January 1992, and pH, electric conductivity(E. C.) and major water-soluble ionic components were analyzed. Strong negative linear correlations were observed between the rainfall amount and the sum of major ionic components in $\mu eq/\ell$ at two sites. The sum of major ionic components also correlated negatively with rain intensity. The analytical results of precipitation samples at two sites were compared each other. Average values of volume-weighted pH were found to be 5.21 at Kangwha and 5.09 at Seoul. The cationic abundance($\mu eq/\ell$) in rainwater showed the general trend $NH_4^+ > Na^+ > Ca^{2+} > Mg^{2-+} > H^+ > K^+$ at Kangwah and $NH_4^+ > Ca^{2+} > Na^+ > H^+ > Mg^{2+} > K^+$ at Seoul. The anionic abundance showed the general trend $SO_4^{2-} > Cl^- > NO_3^-$ at Kangwha and $SO_4^{2-} > NO_3^- > Cl^-$ at Seoul. The concentrations of seasalt such as $Na^+ and Cl^-$ were higher at Kangwha than Seoul. The concentrations of $nss-SO_4^{2-}, nss-Cl^- and NO_3^-$ which are acid composition were higher at Seoul(96.3 $\mu eq/\ell$) than Kangwha(69.0 $\mu eq/\ell$). The contribution of seasalt to the composition of precipitation were higher at Kangwha(34.1%) than Seoul(15.7%). Ammonia and calcium species in rainwater at Kangwha and Seoul are interpreted to have 91% of neutralizing capacity of the original sulfuric and nitric acids. Provided that the precipitation acidity originates primarily from sulfate and nitrate, sulfate was found to contribute about 73-75% of the free precipitation acidity.

• 한국대기환경학회지
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• 제27권3호
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• pp.291-302
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• 2011

[ $PM_{10}$ ]measurements were made at two coastal sites, i.e., Taean and Gangneung, for summer to examine the characterization of water-soluble organic carbon (WSOC) and inorganic ionic species, and to investigate their difference between the sites. The fractions of three major inorganic water-soluble components ($NO_3^-$, $SO_4^{2-}$, and $NH_4^+$) at Taean and Gangneung sites were 30.6% (16.2~62.0%) and 25.6% (13.0~52.5%) of the $PM_{10}$, respectively. $SO_4^{2-}$ is the most dominant species of water-soluble ions at both sites, accounting for up to 20.5% (9.1~44.9%) and 16.3% (5.5~34.2%) of their respective PM10 mass concentrations. Using the paired T-test, $PM_{10}$ (p<0.01), $NO_3^-$ (p<0.05), $SO_4^{2-}$ (p<0.01), $NH_4^+$ (p<0.001), and WSOC (p<0.05) concentrations exhibited strong fluctuations on a daily basis between Taean and Gangneung sites. Relationship between the concentrations of $SO_x$ ($SO_4^{2-}+SO_2$) and CO indicates that the slopes of $SO_x$ /CO were 0.007 and 0.019 in the Taean and Gangneung sites, respectively. The smaller $SO_x$/CO slope in the Taean site could be related to the aged air with wet scavenging of $SO_x$ during transport. The correlation between the concentrations of CO and WSOC suggests that WSOC observed in the Gangneung ($R^2$=0.82) be transported from combustion-related sources, while the WSOC at the Taean site could be formed through atmospheric processing of primary volatile organic species during transport.

• 한국입자에어로졸학회지
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• 제17권3호
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• pp.43-54
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• 2021

Size distributions of atmospheric particulate matter (PM) and its water-soluble organic and inorganic components were measured between January and February 2021 at an urban site in Gwangju in order to identify the major factors that determine their size distributions. Their size distributions during the study period were mainly divided into two groups. In the first group, PM, NO₃^-, SO₄^2-, NH₄⁺ and water-soluble organic carbon (WSOC) exhibited bi-modal size distributions with a dominant condensation mode at a particle size of 0.32 ㎛. This group was dominated by local production of secondary water-soluble components under atmospheric stagnation and low relative humidity (RH) conditions, rather than long-range transportation of aerosol particles from China. On the other hand, in the second group, they showed tri-modal size distributions with a very pronounced droplet mode at a diameter of 1.0 ㎛. These size distributions were attributable to the local generation and accumulation of secondary aerosol particles under atmospheric conditions such as atmospheric stagnation and high RH, and an increase in the influx of atmospheric aerosol particles by long-distance transportation abroad. Contributions of droplet mode NO₃^-, SO₄^2-, NH₄⁺ and WSOC to fine particles in the second group were significantly higher than those in the first group period. However, their condensation mode contributions were about two-fold higher in the first group than in the second group. The significant difference in the size distribution of the accumulation mode of the WSOC and secondary ionic components between the two groups was due to the influx of aerosol particles with a long residence time by long-distance transport from China and local weather conditions (e.g., RH).

• 한국환경보건학회지
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• 제24권3호
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• pp.114-123
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• 1998

Particulate matters(less than 10 $\mu$m, PM10) at Kanghwa and Yangyang, which are located in the western and the eastern coastal regions in Korea, were measured in using low volume air sampler from December 1995 to November 1996, and their characteristics were investigated from the view point of background level.(and in order to characterize the particulate matters.) The particulate matters were analyzed for major water soluble ionic components(SO$_{4}^{2-}$, NO$_{3}^{-}$, Cl$^{-}$, Na$^{+}$, NH$_{4}^{+}$, K$^{+}$, Mg$^{2+}$ and Ca$^{2+}$) by ion chromatography. Mass concentrations of particulate matters were $48.77 \pm 22.45 \mug/m^{3}$ at Kanghwa and $54.04 \pm 32.98 \mug/m^{3}$ at Yangyang and SO$_{4}^{2-}$, NO$_{3}^{-}$ and NH$_{4}^{+}$ contributed largely to water soluble ionic components. nss(non sea salt)-SO$_{4}^{2-}$, contributed more than 95 percentage to SO$_{4}^{2-}$ and nss-K$^{+}$ and nss-Ca$^{2+}$ also contributed high percentages to K$^{+}$ and Ca$^{2+}$. It was supposed that most SO$_{4}^{2-}$, was originated from anthropogenic sources, and K$^{+}$ and Ca$^{+}$ were mainty originated from soil. The results of factor analysis suggested possibility of interpreting the correlation between air pollutants and regional characteristics.

• 한국환경과학회지
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• 제7권5호
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• pp.707-716
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• 1998

The chemical characteristics of precipitation was investigated in Pusan area. Samples were collected from January to November in 1996 at 4 sites, and analyzed pH, major soluble ionic components(C $l^{[-10]}$ , N $O_3$$^{[-10]}$ , S $O_4$$^{2-}$, N $a^{+}$, $K^{+}$, N $H_4$$^{+}$, $Mg^{2+}$, $Ca^{2+}$). The order of anion and cation concentrations for the initial precipitation were C $l^{[-10]}$ ＞ S $O_4$$^{2-}$ ＞ N $O_3$$^{[-10]}$ , and $Ca^{2+}$ ＞ N $a^{+}$ ＞ N $H_4$$^{+}$ ＞ $Mg^{2+}$ ＞ $K^{+}$, respectively. At coastal sites(P1 and P2) C $l^{[-10]}$ and N $a^{+}$ of maritime sources (seasalt) were high, but at inland sites(P3 and P4) nss-C $a^{2+}$ and nss-S $O_4$$^{2-}$ were high. Calcium ion for the initial precipitation showed high value of enrichement factor(EF) relative to seawater composition. The contribution of seasalt to the composition of precipitation was higher at bite P1 (53.5%) than those of the other sites. Throughout the year the concentrations of major ions for the initial precipitation were low in the heavy rain season. The mean pH for the initial precipitation was 5.4 and showed the negative relationship with the precipitaion amount. The S $O_4$$^{2-}$ and N $O_3$$^{[-10]}$ do not play an important role in rain acidification due to the high(97%) neutralizing effect of amonia and calcium species.and calcium species.

• Korean Chemical Engineering Research
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• 제48권1호
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• pp.20-26
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• 2010

수용성 유기 및 무기성분은 대기 에어로졸 입자의 중요한 구성성분들이며 간접적으로 기후에 영향을 미치는 구름응결핵으로 작용한다. 유기 및 원소탄소(organic and elemental carbon, OC 및 EC) 및 수용성 유기탄소(water soluble OC, WSOC) 및 이온성분농도를 조사하기 위하여 광주지역에서 24시간 기준의 미세입자($PM_{2.5}$)를 측정하였다. 측정기간 중 $PM_{2.5}$ 수용성 분율의 주요성분인 WSOC, $NO_3^-$, $SO_4^{2-}$ 및 $NH_4^+$의 평균농도는 각각 2.11, 5.73, 3.51 및 $3.31{\mu}g/m^3$ 이었으며, $PM_{2.5}$ 농도의 12.0(2.9~23.9%), 21.0(12.9~37.6%), 11.6(2.5~25.9%), 및 11.7%(3.8~18.6%)를 차지하였다. 총 수용성 성분(유기+무기) 중 WSOC 화합물이 차지하는 분율은 평균 17.6%(5.4~35.9%)이었다. EC 추적자 기법을 이용해 평가한 2차 OC 및 WSOC 농도는 각각 평균적으로 0.78 및 $0.34{\mu}g/m^3$이었으며, 전체 OC 및 WSOC 중의 평균 17.9%(범위: 0~44.4%) 및 평균 11.2%(범위: 0~51.4%)를 차지하였다. 광주지역 겨울철에 측정한 $SO_4^{2-}$ 입자는 국지적인 기상산화반응보다는 장거리 이동 또는 수용액 변환과정에 의한 영향, 구름 내 변환과정 등이 황산염 입자 생성에 중요하게 작용했을 것으로 판단한다.

• Journal of Korean Society for Atmospheric Environment
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• 제19권E4호
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• pp.177-186
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• 2003

The total of 1,454 aerosol samples were collected by high volume tape sampler at the Gosan Site in Jeju Island from 1992 to 1999, and the major water-soluble ionic components were chemically analyzed. The mean concentrations of nss-S $O_4$$^{2-}$, N $H_4$$^{＋}$, and N $O_3$$^{[-10]}$ showed high values, which were 6.73, 1.45, and 1.45 ${\mu}{\textrm}{m}$/㎥, respectively, while $Ca^{2+}$ and $K^{+}$ concentrations were low with the values of 0.49 and 0.42 $\mu\textrm{g}$/㎥. The concentrations of most components increased in spring but decreased in summer, especially with the remarkable increase of $Ca^{2+}$ and N $O_3$$^{[-10]}$ concentrations in spring. The seasonal comparison of nss-S $O_4$$^{2-}$ concentrations showed higher values with the order of spring > fall 〉 winter〉 summer, but spring 〉 winter〉 fall 〉 summer for N $O_3$$^{[-10]}$ Meanwhile, the concentration levels of N $a^{+}$ and C $l^{[-10]}$ increased more in winter season. According to the investigation of wind direction effect, the concentrations of most aerosol ionic components showed higher values consistently at the westerly and northerly wind conditions. Based on the factor analysis, the atmospheric aerosols in the Gosan Site are considered to be largely affected by marine sources, followed by anthropogenic and soil sources.urces..

• Asian Journal of Atmospheric Environment
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• 제11권2호
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• pp.79-95
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• 2017

A number of field studies have provided evidence that biomass burning is one of the major global sources of atmospheric particles. In this study, we have collected $PM_{2.5}$ emitted from biomass burning combusted at open burning and laboratory chamber situations. The open burning experiment was conducted with the cooperation of 9 farmers in Chiba Prefecture, Japan, while the chamber experiment was designed to evaluate the characteristics of chemical components among 14 different plant species. The analyzed categories were $PM_{2.5}$ mass concentration, organic carbon (OC), elemental carbon (EC), ionic components ($Na^+$, ${NH_4}^+$, $Ca^{2+}$, $Mg^{2+}$, $K^+$, $Cl^-$, ${NO_3}^-$ and ${SO_4}^{2-}$), water-soluble organic carbon (WSOC), water-insoluble inorganic carbon (WIOC), char-EC and soot-EC. OC was the dominant chemical component, accounting for the major fraction of primary $PM_{2.5}$ derived from biomass burning, followed by EC. Ionic components contributed a small portion of $PM_{2.5}$, as well as that of $K^+$. In some cases, $K^+$ is used as biomass burning tracer; however, the observations obtained in this study suggest that $K^+$ may not always be suitable as a tracer for biomass burning emissions. Also, the results of all the samples tested indicate relatively low values of char-EC compared to soot-EC. From our results, careful consideration should be given to the usage of $K^+$ and char-EC as indicators of biomass burning. The calculated ratios of WSOC/OC and WIOC/OC were 55.7% and 44.3% on average for all samples, which showed no large difference between them. The organic materials to OC ratio, which is often used for chemical mass closure model, was roughly estimated by two independent methods, resulting in a factor of 1.7 for biomass burning emissions.

• 한국환경과학회지
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• 제23권5호
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• pp.743-753
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• 2014

The number concentrations and the water soluble ionic concentrations of $PM_{2.5}$ have measured at Gosan site in Jeju, Korea, from March 2010 to December 2010, to clarify their characteristics. $PM_{2.5}$ number concentrations vary from 22.57 to $975.65particles/cm^3$ with an average value of $240.41particles/cm^3$, which have been recorded evidently high in spring season as compared with those in other season. And the concentrations in small size ranges are greatly higher than those in large size ranges, so the number concentration in the size range $0.25{\sim}0.45{\mu}m$ has more than 94% of the total number concentration of $PM_{2.5}$. The major ionic components in $PM_{2.5}$ are $SO{_4}^{2-}$, $NH_4{^+}$ and $NO_3{^-}$, which are mainly originated from anthropogenic sources, on the other hand, the concentrations of $Cl^-$, $K^+$, $Ca^{2+}$ and $Mg^{2+}$ are recorded relatively lower levels. The concentrations of the major ionic components are very high in spring season, but the concentration levels of the other components are recorded significantly high in winter season. On the other hand, in summer season, the lowest concentration levels are observed for overall components as well as the sum of them. The concentration ratios of nss-$SO{_4}^{2-}/SO{_4}^{2-}$ and nss-$Ca^{2+}/Ca^{2+}$ are 98.1% and 88.9%. And the concentration ratio of $SO{_4}^{2-}/NO_3{^-}$(3.64) is greatly higher than the value in urban area due to no large $NO_x$ emission sources in the measurement. In addition, the correlation and the factor analysis for the number and the ionic concentrations of $PM_{2.5}$ are performed to identify their sources. From the Pearson correlation analysis and the factor analysis, it can be suggested that the smaller parts(< $0.5{\mu}m$) of $PM_{2.5}$ is contributed by anthropogenic sources, but the sources of the remaining larger parts of $PM_{2.5}$ are not able to be specified sources in this study.

• 한국환경보건학회지
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• 제20권4호
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• pp.1-9
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• 1994

In order to investigate the regional level of air pollutants at Kangwha island situated on the western coast in Korea, the suspended particulate matter samples were collected by using the low volume air sampler on ten interval from March 1992 to February 1993 and the mass concentration of suspended particulate matter (SPM) and the chemical composition of water-soluble major ionic components in SPM samples were measured. During the sampling period, the average concentration of SPM under diameter 10 $\mu$m was found to be 48 $\mu$g/m$^3$ (+ 12). The seasonal concentration of SPM was showed in order of spring>fall>winter>summer. It was considered that higher concentration on spring than other season was affected by the long-range transport of Yellow sand particulate from China continent and lower concentration on summer by the washout and rainout effect of large rainfall. The content of water-soluble component in SPM samples was founded to be about 31% (14.69 $\mu$g/m$^3$) and 65% was unknown or unanalyzed. The content of cationic component showed in order of NH$_4^+$ (44.6%)>Na$^+$ (21.2%)>K$^+$ (14.7%)>Ca$^{2+}$ (13.6%)>Mg$^{2+}$ (5.9 %) and the content of anionic component SO$_4^{2-}$ (62.5%)>NO$_3^-$ (22.3%)>Cl$^-$ (15.2%), respectively. This fact indicates that ammonium and sulfate ion of water-soluble component in SPM sample were dominant in this region. From the chemical composition of water-soluble component, the most of Na$^+$, Mg$^{2+}$ and Cl$^-$ were originated from seawater source but K$^+$, Ca$^{2+}$ and SO$_4^{2-}$ were originated from other non-marine source. The contribution of seasalt to the composition of precipitation was 23%.