• Title/Summary/Keyword: ionic components

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Size Distribution Characteristics of Water-soluble Ionic Components in Airborne Particulate Matter in Busan (부산 도심지역 대기중 입자상물질의 크기분포에 따른 수용성 이온성분의 특성)

  • Park, Gee-hyeong;Lee, Byeong-kyu
    • Journal of Korean Society for Atmospheric Environment
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    • v.31 no.3
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    • pp.287-301
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    • 2015
  • This study was conducted to investigate size distribution characteristics of water-soluble ionic components in the airborne particulate matter (PM) collected from an urban area in Busan using a MOUDI cascade impactor from March to October 2010. The inorganic constituents in the fine particles (${\leq}1.8{\mu}m$) predominantly consisted of sulfate, nitrate, ammonium, and potassium. Sulfate and ammonium concentrations showed a high correlation and similar equivalent concentrations in the fine modes including $0.18{\sim}0.32{\mu}m$, $0.32{\sim}0.56{\mu}m$, and $0.56{\sim}1.0{\mu}m$. This indicates that the main chemical component in the fine particles would be forms of ammonium sulfate such as $(NH_4)_3H(SO_4)_2$, $(NH_4)_2SO_4$, and $(NH_4)HSO_4$. Back trajectory analysis showed that relatively higher concentrations of ammonium, nitrate, and sulfate in the fine mode, compared to the coarse mode, are caused both by domestic sources and long-range transports originated from China continent. High concentration episodes of PM both in the fine mode and the coarse mode were attributed both by anthropogenic sources, such as ship emissions and traffic emissions, and by natural sources such as seawater (sea salt), respectively.

A Study on the Development of Standard Method of Total Deposition Sampling in Air Pollutants - Spatial Distribution of Total Deposition by the Filtration-Sampling Method - (대기오염 총침착물의 채취방법 표준화 개발에 관한 연구 -여과식 채취방법을 통한 총침착물의 공간분포 특성-)

  • 박정호;조인철;김찬훈;서정민
    • Journal of Environmental Science International
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    • v.11 no.6
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    • pp.489-496
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    • 2002
  • The purpose of this study was to investigate spatial distributions of total deposition. A total number 79 samples were collected at 17 sampling sites from September 1999 to January 2000. Total (=wet+dry) atmospheric depositions were collected by filtered deposition sampler at sampling site (the Western Part of Kyongsangnam Province). In addition, the deposition of soluble and insoluble fraction was also investigated to find a suitable simplified collection method for a long-term monitoring of total deposition. The total depositions were measured soluble amount(mm/month), insoluble amount(kg/km$^2$/month), pH, conductivity(E.C.) and eight ionic components. The spatial distribution of deposition flux was to estimated by using a kringing analysis. The 17 sites mean fluxes of water soluble ionic components; SO$_4$$\^$2-/, Cl$\^$-/, NO$_3$$\^$-/, Na$\^$+/, NH$_4$$\^$+/, K$\^$+/, Mg$\^$2+/, Ca$\^$2+/ were 100.7∼315.6kg/km$^2$/month, 30.1∼234.3kg/km$^2$/month, 64.4∼ 139.4kg/km$^2$/month, 7.5∼68.3kg/km$^2$/month, 10.7∼48.7kg/km$^2$/month, 5.6∼27.9kg/km$^2$/month, 4.5∼17.5kg/km$^2$/month, 27.6∼81.7kg/km$^2$/month, respectively.

Chemical Compositions of Primary PM2.5 Derived from Biomass Burning Emissions

  • Ichikawa, Yujiro;Naito, Suekazu
    • Asian Journal of Atmospheric Environment
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    • v.11 no.2
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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.

A Review : Underwater Applications of Ionic Polymer -Metal Composites (이온성 고분자-금속 복합체의 수중 응용)

  • 허석;제이슨파켓;김광진
    • Journal of Institute of Control, Robotics and Systems
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    • v.10 no.11
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    • pp.981-990
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    • 2004
  • Specialized propulsors for naval applications have numerous opportunities in terms of research, design and fabrication of an appropriate propulsor. One of the most important components of any propulsor is the actuator that provides the mode of locomotion. Ionomeric electro-active polymer may offer an attractive solution for locomotion of small propulsors. A common ionomeric electro-active polymer, ionic Polymer-Metal Composites (IPHCs) give large true bending deformations under low driving voltages, operate in aqueous environments, are capable of transduction and are relatively well understood. IPMC fabrication and operation are presented to further elucidate the use of the material for a propulsor. Various materials, including IPMCs, are investigated and a simplified propulsor model is explored.

Seasonal Variation of PM2.5 Components Observed in an Industrial Area of Chiba Prefecture, Japan

  • Ichikawa, Yujiro;Naito, Suekazu;Ishii, Katsumi;Oohashi, Hideaki
    • Asian Journal of Atmospheric Environment
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    • v.9 no.1
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    • pp.66-77
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    • 2015
  • In order to survey the seasonal variation of the chemical composition of particulate matter of $2.5{\mu}m$ or less ($PM_{2.5}$), $PM_{2.5}$ was sampled from 8 February 2013 to 31 March 2014 in an industrial area of Chiba Prefecture, Japan. Chemical measurements of the sample included: ionic components ($Na^+$, $NH_4{^+}$, $Ca^{2+}$, $Mg^{2+}$, $K^+$, $Cl^-$, $NO_3{^-}$ and $SO_4{^{2-}}$), carbonaceous components - organic carbon (OC) and elemental carbon (EC), and water-soluble organic carbon (WSOC). Also, secondary organic carbon (SOC) was measured based using the EC tracer method, and char-EC and soot-EC were calculated from the analytical results. The data obtained were interpreted in terms of temporal variation. Of the overall mean value of $PM_{2.5}$ mass concentration obtained during the study period, ionic components, OC and EC accounted for 45.3%, 19.7%, and 8.0%, respectively. $NO_3{^-}$ showed a unique seasonal distribution pattern due to a dependence on temperature and absolute humidity. It was estimated that an approximate temperature of $14^{\circ}C$, and absolute humidity of $7g/m^3$ were critical for the reversible reaction of $NH_4NO_3(p){\leftrightharpoons}NH_3(g)+HNO_3(g)$. The amount of OC and EC contributing to the monthly $PM_{2.5}$ mass concentration was higher in autumn and winter compared to spring and summer. This result could be attributed to the impact of burning biomass, since WSOC and the ratio of char-EC/soot-EC showed a similar pattern during the corresponding period. From the comparison of monthly WSOC/OC values, a maximum ratio of 83% was obtained in August (summer). The WSOC and estimated SOC levels derived from the EC tracer method correlated (R=0.77) in summer. The high occurrence of WSOC during summer was mainly due to the formation of SOC by photochemical reactions. Through long-term observation of $PM_{2.5}$ chemical components, we established that the degree to which the above-mentioned factors influence $PM_{2.5}$ composition, fluctuates with seasonal changes.

Comparison of the Number Concentration and the Chemical Composition of the Atmospheric PM2.5 in Jeju Area

  • Kang, Chang-Hee;Hu, Chul-Goo
    • Journal of Environmental Science International
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    • v.23 no.5
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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.

Viscosity and Wettability of Hyaluronic Acid according to Antimicrobial Supplementation, Ionic Strength, and pH

  • Kho, Hong-Seop;Chang, Ji-Youn;Kim, Yoon-Young;Park, Moon-Soo
    • Journal of Oral Medicine and Pain
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    • v.39 no.3
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    • pp.90-95
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    • 2014
  • Purpose: To investigate viscosity and wettability of hyaluronic acid (HA) solutions according to supplementation of lysozyme and/or peroxidase, and different ionic strength and pH conditions. Methods: Solutions containing HA were prepared using distilled deionized water (DDW) and simulated salivary buffer (SSB) in different conditions. Different concentrations of hen egg-white lysozyme and bovine lactoperoxidase was added into HA solutions. HA solutions with antimicrobials in different ionic strength and pH conditions were prepared. Viscosity was measured using cone-and-plate digital viscometer at six different shear rates and wettability on acrylic resin and Co-Cr alloy was determined by contact angle. Results: The viscosity values of HA dissolved in DDW were decreased in order of HA, HA containing lysozyme, HA containing peroxidase, and HA containing lysozyme and peroxidase. The viscosity values for HA in DDW were decreased as the concentration of lysozyme and/or peroxidase increased. However, the viscosity values for HA in SSB showed no significant changes according to the concentration of lysozyme and/or peroxidase. The viscosity values of HA solutions were inversely proportional to ionic strength and pH. The contact angle of HA solutions showed no significant differences according to tested surface materials, addition of lysozyme and/or peroxidase, and different ionic strength and pH conditions. Contact angles on acrylic resin by HA solutions in all tested conditions were much higher than those by human saliva. Conclusions: The rheological properties of HA supplemented with lysozyme and/or peroxidase in different ionic strength and pH conditions were objectively confirmed, indicating the possibility of HA with lysozyme and/or peroxidase as main components in the development of effective saliva substitutes.

Characterization of Chemical Properties of Precipitation at Busan, Korea, 2009 (2009년 부산지역 강수의 화학적 특성)

  • Jung, Woon-Seon;Park, Sung-Hwa;Kang, Deok-Du;Lee, Dong-In;Kim, Dongchul
    • Journal of Environmental Science International
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    • v.23 no.1
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    • pp.69-79
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    • 2014
  • The seasonal variation of pH and ion components in precipitation were investigated from January to December 2009 at Busan, Korea. The precipitation was acidic with a volume-weighted mean pH concentration of 5.32, which ranged from 3.79 to 8.66. The volume-weighted mean conductivity showed 86.77 ${\mu}S/cm$ and indicated higher concentration about 96.69 ${\mu}S/cm$ in summer. The volume-weighted mean equivalent concentration of components followed the order: $K^+$ > $Ca^{2+}$ > $nss-Ca^{2+}$ > $NH_4^+$ > $Mg^{2+}$ > $Na^+$ > $Li^+$ in cations and $Cl^-$ > $SO_4^{2-}$ > $nss-SO_4^{2-}$ > $NO_3^-$ > $NO^{2-}$ > $F^-$ > $Br^-$ in anions. Particularly, concentration of $K^+$ and $Cl^-$ showed 56 and 78 % in cations and anions. The higher concentration in $K^+$, $Na^+$, $Mg^{2+}$ and $Cl^-$ were shown in Busan city as compared to the other cities. The neutralization factors have been found to have higher value for potassium ion in winter compared with different seasons, indicating significant neutralization of acidic components over the region by potassium. Therefore, the precipitation characteristics at Busan had both continental and coastal as consequence of pH, conductivity and ionic analyses.