• 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.

• Journal of Korean Society for Atmospheric Environment
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• v.2 no.2
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• pp.66-74
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• 1986

Rain samples were collected at 10 sites in the Seoul area during the period of August through November, 1985. THe concentrations of the major cations $(H^+, Ca^{++}, MG^{++}, Na^+, K^+, NH_4^+)$ and the major anions $(SO_4^=, NO_3^-, Cl^-)$ were measured to characterize the main sources of chemical ions in rainwater. Correlating concentrations of ions to pH, calculated coefficients ranged from 0.1485 to 0/4296. Sulfate shows the largest coefficient indicating that sulfate is more closely associated with hydrogen ion than other ions. This may suggest that sulfuric acid contributes more to the acidity of rainwater in Seoul. It appears that the major chemicals measured in rainwater are from the anthropogenic sources of air pollution. Predominant chemicals are acidic at the Guro-, the Sinseol-, the Yangnam-, and the Ssangmun-dong with sulfate being the most predominant. IT also indicates that alkaline substances resulting from soil and dust have a significant effect on pH values of rainwater by neutralizing actions. According to Granat-model analysis, it is estimated that the relative contributions to the rainwater acidity in Seoul are 84% from sulfuric acid, 8% from nitric acid and 8% from hydrochloric acid.

• Journal of environmental and Sanitary engineering
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• v.15 no.2
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• pp.1-9
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• 2000

This research employed a senescence-accelerated mouse(SAM) to explore the possibility that differences exits among the major antioxidants, superoxid dismutase(SOD), in terms of ability to protect such animal treated with Cu, Fe and Mn. To assess the antioxidants function of metal ions on SAM-R/1 and SAM-P/8 were administered with Cu, Fe and Mn orally. The effect of metal ions on SAM towards reversing oxygen sensitivity was determined as a bioassays of SOD in the mouse liver. The data show that the SOD activity was induced by each metal ions in both SAM-R/1 and SAM-P/8. It suggested that induced SOD by each metal ions may protect against oxidative mediated stress. Finally, overall data lead to the possibility of metal ions as an antioxidants or each metal ions act producer of oxygen radicals in the liver of SAM-R/1 and SAM-P/8.

• The Korean Journal of Ecology
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• v.21 no.3
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• pp.195-201
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• 1998

This study was carried out to investigate characteristic of ions in rainwater by throughfall, stemflow and rainfall at air polluted area(Kure city industrial city) and non-air polluted area (Higashihiroshima city non industrial city). pH of rainwater in air polluted area were all low as compared with those in non-air polluted area. EC of rainwater in ir polluted area were high in throughfall and stemflow, but there was no difference between both areas in rainfall. The concentration of major ions in rainwater were generally high at air polluted area, especially of $Mg^{2+}$, $Ca^{2+}$, $Cl^{-}$ and $SO_4^{2-}$ in stemflow. But there was little difference in $NH_4^{+}$, and there was also cases had a high concentration in non-air polluted area. By comparison with forest type, in stemflow concentration of ions in coniferous forest were higher than those in broad-leaved, but in throughfall they were higher in mixed forest rather than coniferous forest. There was no correlation between the amount of rainwater and pH, and also EC. $NO_4^{-}$ and $SO_{4}^{2-}$ had high correlations between major ions besides $Na^{+}$ and $NH_{4}^{+}$ in air poluted area.

• Applied Science and Convergence Technology
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• v.24 no.5
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• pp.190-195
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• 2015

Here, we demonstrated a $Pb^{2+}$ detecting aptasensor using $Pb^{2+}$-sensitive DNAzyme-conjugated gold nanorods (GNRs). Fluorescent DNA substrates that were initially quenched by GNRs, are released in response to $Pb^{2+}$ ions to give a substantial fluorescence signal. The GNR-tethered DNAzyme is reusable at least three times with a LOD of 50 nM.

• Journal of Environmental Health Sciences
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• v.31 no.5 s.86
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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.

• Bulletin of the Korean Chemical Society
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• v.33 no.2
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• pp.505-510
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• 2012

Cobalt oxide nanostructure materials have been prepared by adding several concentrations of spectator Ni ions in solution, and analyzed by electron microscopy, X-day diffraction, calorimetry/thermogravimetric analysis, UV-vis absorption, Raman, and X-ray photoelectron spectroscopy. The electron microscopy results show that the morphology of the nanostructures is dramatically altered by changing the concentration of spectator ions. The bulk XRD patterns of $350^{\circ}C$-annealed samples indicate that the structure of the cobalt oxide is all of cubic Fd-3m $Co_3O_4$, and show that the major XRD peaks shift slightly with the concentration of Ni ions. In Raman spectroscopy, we can confirm the XRD data through a more obvious change in peak position, broadness, and intensity. For the un-sputtered samples in the XPS measurement process, the XPS peaks of Co 2p and O 1s for the samples prepared without Ni ions exhibit higher binding energies than those for the sample prepared with Ni ions. Upon $Ar^+$ ion sputtering, we found $Co_3O_4$ reduces to CoO, on the basis of XPS data. Our study could be further applied to controlling morphology and surface oxidation state.

• Bulletin of the Korean Space Science Society
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• 2011.04a
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• pp.27.3-27.3
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• 2011

The plasmasphere is filled with the ions and electron transported mostly from the mid-latitude ionosphere. In the topside ionosphere where the $O^+$ ions are still major ions, the $O^+$ ions are in chemical equilibrium with the $H^+$ ions and exchange their charges with each other's parent atoms with similar rates in both reactions. During the day, the newly produced $H^+$ ions flow upward to fill the plasmasphere while they flow downward and contribute to the maintenance of the ionospheric density at night under the geomagnetically quiet condition. The ionosphere and plasmasphere are coupled by these plasma fluxes and therefore strongly affect each other. In order to study these coupling we utilized the plasma density measurements from JASON satellite. This satellite measures vertical total electron content (TEC) from the ground to the satellite orbit (about 1336 km) and slant TEC from the satellite orbit to much higher GPS satellites by using the on-board dual-frequency altimeter and GPS receiver, respectively. The former measurement can represent the ionospheric TEC while the latter can represent the plasmaspheric TEC in the equatorial region. We compared these data with different seasons, solar activities and local times, and the results will be presented.

• Journal of Environmental Health Sciences
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• v.18 no.2
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• pp.106-116
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• 1992

In order to examine the influences of diluent, DVB, and ligand content, in the adsorption velocities and capacities of chelating resins to heaw metal ions, the chelating resins containing the PO$_3$H, amide, and PO$_3$H+amide were prepared from AN-STR-DVB copolymer. The adsorption capacities of chelating resins were measured by ICP-AES. The major results of the studies are as follows: The optimized compositions of the chelating resins having the highest adsorptivity for the heavy metal ions were found to be DVB=7 wt%, toluene= 100 vol%. The adsorption rate of the chelating resins to the heaw metal ions was PO$_3$H > PO$_3$H+Amide > Amide in order.

• Bulletin of the Korean Chemical Society
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• v.20 no.5
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• pp.587-591
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• 1999

A molecular dynamics simulation study on the structure and dynamics of Na+ ions in non-rigid dehydrated Na12-A zeolite framework at 298.15 K was conducted using the same method reported in previous studies on rigid and non-rigid Na12-A zeolite frameworks. The agreement between the experimental and calculated results for the zeolite-A framework atoms of structural parameters for non-rigid dehydrated Na12-A zeolite is generally quite good, and for the adsorbed Na+ions the agreement is acceptable. The calculated bond lengths are generally in good agreement with the experimental results and other theoretical data. The calculated IR spectrum by Fourier transform of the total dipole moment autocorrelation function shows two major peaks around 2700 cm-1 and 7000 cm-1. The former appeared in the calculated IR spectra of non-rigid zeolite-A framework only system and the latter remains unexplained except, perhaps, indicating a new formation of a vibrational mode of the framework due to the adsorption of Na+ ions. The peaks above 6200-6800 cm-1 in non-rigid dehydrated Nal2-A zeolite are much larger than those in non-rigid dehydrated H12-A zeolite.