• Title/Summary/Keyword: TSP sampler

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Measurements at Kosan, Cheju Island during the Summer, 1994: (I) Aerosol Ion Composition (제주도 고산에서의 1994년 여름 측정: (I) 입자 이온 조성)

  • 김용표;김성주;진현철;백남준;이종훈;김진영;심상규;강창희;허철구
    • Journal of Korean Society for Atmospheric Environment
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    • v.12 no.3
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    • pp.297-305
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    • 1996
  • Aerosol measurements were carried out at Kosan, Cheju Island, Korea for the period from July 20 to August 10, 1994. Total suspended particles were collected by high volume samplers and PM 2.5 particles with gaseous volatile species were collected by a filter pack sampler and their ionic composition are analyzed. The average mass concentration of PM 2.5 particles was comparable to that of PM 3 particles collected during March, 1994 at the same site but the average non sea-salt sulfate concentration was higher that that of PM 3 particles, implying the fraction of anthropogenic air apllutants during this period is higher than that during March, 1994. During the measurement period, two distincitive patterns were observed, high concentrations of mass and water soluble ions were observed between July 20 and August 1 while those during after August 2 were low. Back trajectory analysis results show that air masses arriving at Kosan during the earlier period were mainly from Korea and Japan while those during the later period were from the North Pacific Ocean. It is suggested that the particle ion concentrations during the later period are marine background concentrations at Kosan during the summertime.

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Residence Times and Chemical Composition of Atmospheric Aerosols I. Concentration of Major Ions and Heavy Metals in Pusan (대기 에어로졸의 체류시간과 화학조성 I. 부산지역에서 주요이온과 중금속의 농도)

  • Yang, Han-Sub;Jeon, Eun-Ju;Kim, Young-Il;Ok, Gon
    • Journal of Environmental Science International
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    • v.8 no.1
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    • pp.51-59
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    • 1999
  • Chemical composition of atmospheric aerosols was measured at 4 sites in Pusan. All the samples were collected with a high volume air sampler from January to October 1996, to analyze major ions and heavy metals. Dominant ions of aerosols were S $O_4$$^{2-}$ in anion and N $a^{+}$ in cation. Sulfate, nitrate and ammonium ions in aerosols showed high enrichment factor to soil and seawater composition. The concentrations of heavy metals in aerosols was lowest at the site PI near the coast. The lowest concentrations of major ions and heavy metals mainly appeared in August, probably due to scavenging by frequent rains. Especially, the concentrations of total suspended particulate matter(TSP) and heavy metals in aerosols showed good correlations in Pusan. Based on crustal Al, enrichment factors for some metals(Zn, Cu, Pb, Cd) in aerosols were significantly greater than unity, and the order was Cd > Pb > Zn > Cu. This evidence suggests that Cd and Pb are derived predominantly from non-crustal sources.s.

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The Analyses of Causes of Visibility Impairment in Pusan (부산지역 시정악화의 원인 분석)

  • Kim Yoo-Keun;Moon Yun-Seob;Bae Joo-Hyun;Kwak Jin
    • Journal of Environmental Science International
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    • v.8 no.6
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    • pp.639-643
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    • 1999
  • After analyzing the correlation between air pollution and visibility, TSP and $NO_2$ is responsible for poor visibility in Pusan. After analyzing the correlation between meteorological factors and visibility, general pattern of humidity has clear negative correlation. The variation of wind speed has a positive correlation. In order to investigate the cause of poor visibility in Pusan area, the Andersen sampler and PM-2.5 are used to collect and analyze aerosol. This study was carried out to monitor the visibility using Forward scattering meter and to find out the characteristics and the cause of good visibility case and poor visibility case by measuring and analyzing a variety of parameters, such as particle size distributions, chemical compositions, and meteorological conditions in Pusan. According to the analysis of intensive sampling, $NO_3^-,NH_4^+$ ion concentration increased together with the mass concentration around $0.5\~2.5{\mu}m$ approximately during the case of poor visibility. $NH_4NO_3,\;NH_4Cl,\;and\;NaCl$ were thought to be the major components of fine particles.

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Residence Times and Chemical Composition of Atmospheric Aerosols II. Residence Times of Aerosols in Pusan (대기 에어로졸의 체류시간과 화학조성 II. 부산지역 에어로졸의 체류시간)

  • Yang, Han-Seob;Jun, Eun-Joo;Kim, Young-Ill;Ok, Gon
    • Journal of Environmental Science International
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    • v.8 no.2
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    • pp.171-176
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    • 1999
  • To estimate the residence times of aerosols in air, the activities of $^{210}Pb$ and $^{210}Po$ in aerosols were measured at 4 sites in Pusan. All aerosol samples were collected by a high volume air sampler from January to October 1996. The activities $^{210}Pb$ and $^{210}Po$ in Pusan were varied from 11.77 to 67.57 dpm/1000$m^3$ and from 2.63 to 15.91 dpm/1000$m^3$, respectively. The mean activities were 34.62 dpm/1000$m^3$ for $^{210}Pb$ and 8.24 dpm/1000$m^3$ for $^{210}Po$. The highest values of the activities of $^{210}Pb$ and $^{210}Po$ were appeared at P3 site and the lowest values at P4 site. During the sampling period, the trends of the activities of $^{210}Po$ and $^{210}Pb$ were similar to total suspended particulate matter(TSP) concentrations. The mean residence times of atmospheric aerosols calculated from $^{210}Po$/$^{210}Pb$ activity ratio was about 60~80 days in Pusan. The longest residence time of atmospheric aerosols was in January because of the lack of rainout and washout, but the shortest residence time was in August, largely due to scavenging effect by frequent rains. The activities of $^{210}Po$ and $^{210}Pb$ in atmospheric aerosols were different in time and space, which seems that the distribution of $^{210}Po$ and $^{210}Pb$ activities and scavenging processes in air may be controlled by the local and meteorological conditions.

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Single-particle Characterization of Aerosol Particles Collected Nearby a Lead Smelter in China

  • Jung, Hae-Jin;Song, Young-Chul;Liu, Xiande;Li, Yuwu;Ro, Chul-Un
    • Asian Journal of Atmospheric Environment
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    • v.6 no.2
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    • pp.83-95
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    • 2012
  • China has been a top producer and exporter of refined lead products in the world since the year 2000. After the phasing-out of leaded gasoline in the late 1990s, non-ferrous metallurgy and coal combustion have been identified as potential major sources of aerosol lead in China. This paper presents the single particle analytical results of ambient aerosol particles collected near a lead smelter using a scanning electron microscopy- energy dispersive x-ray spectroscopy (SEM-EDX). Aerosol particle samples were collected over a 24-hour period, starting from 8 pm on 31 May 2002, using a high volume TSP sampler. For this near source sample, 73 particles among 377 particles analyzed (accounting for 19.4%) were lead-containing particles mixed with other species (S, Cl, K, Ca, and/or C), which probably appeared to be from a nearby lead smelter. Lead-containing particles of less than $2{\mu}m$ size in the near source sample were most frequently encountered with the relative abundances of 42%. SEM-EDX analysis of individual standard particles, such as PbO, PbS, $PbSO_4$, $PbCl_2$, and $PbCO_3$, was also performed to assist in the clear identification of lead-containing aerosol particles. Lead-containing particles were frequently associated with arsenic and zinc, indicating that the smelter had emitted those species during the non-ferrous metallurgical process. The frequently encountered particles following the lead-containing particles were mineral dust particles, such as aluminosilicates (denoted as AlSi), $SiO_2$, and $CaCO_3$. Nitrate- and sulfate-containing particles were encountered frequently in $2-4{\mu}m$ size range, and existed mostly in the forms of $Ca(NO_3,SO_4)/C$, $(Mg,Ca)SO_4/C$, and $AlSi+(NO_3,SO_4)$. Particles containing metals (e.g., Fe, Cu, and As) in this near source sample had relative abundances of approximately 10%. Although the airborne particles collected near the lead smelter contained elevated levels of lead, other types of particles, such as $CaCO_3$-containing, carbonaceous, metal-containing, nitrates, sulfates, and fly-ash particles, showed the unique signatures of samples influenced by emissions from the lead smelter.