• Resources Recycling
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• v.11 no.1
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• pp.19-25
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• 2002

For $ZnSO_4$-$Na_2$$SO_4$-$H_2$ $SO_4$-$NaOH-H_2$O system, pH of solutions with different electrolyte concentrations was measured at $25^{\circ}C$ and ionic equilibria were analyzed by using K-value method. Activity of water and activity coefficients of solutes were calculated by Pitzer equation. The equilibrium concentration and activity coefficients of solutes were calculated from initial experimental conditions. At high ionic strength of 4m, the pH values calculated were in good agreement with those measured. In the experimental ranges of ionic strength of solution from 3.5 to 4.3 m, the mean activity coefcient of $ZnSO_4$calculated agreed well with those obtained from literature.

• 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.

• Journal of Korean Society for Atmospheric Environment
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• v.24 no.6
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• pp.682-692
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• 2008

Fine particles ($PM_{2.5}$) were collected and analyzed from November 2005 through August 2007 in Chuncheon, Korea to investigate the characteristics of $PM_{2.5}$ and its ionic constituents. The average $PM_{2.5}$ concentration during the study period was $39{\mu}g/m^3$, which is almost two times higher than the annual US NAAQS $PM_{2.5}$ standard of $15{\mu}g/m^3$. $PM_{2.5}$ concentrations were higher in spring and winter than in summer and fall. During spring, Asian Dust events dramatically enhanced $PM_{2.5}$ concentrations, and long-range transport of $PM_{2.5}$ emitted in industrial area of China often occurred during winter based on trajectory analysis. Contribution of $PM_{2.5}$ to $PM_{10}$ concentrations ranged from $72{\mu}g/m^3$ during Asian Dust events to $457{\mu}g/m^3$, indicating that a large portion of $PM_{2.5{\sim}10}$ was transported from China during Asian Dust events. Among the major ionic constituents ${SO_4}^{2-}$ showed the highest concentration, followed by ${NH_4}^+$, ${NO_3}^-$ and ${NO_2}^-$. Chuncheon appeared to be ${NH_4}^+$ rich environment, indicating that $(NH_4)_{2}SO_4$ and ${NH_4}{NO_3}$ were the predominant forms of ${NO_3}^-$ and ${SO_4}^2$ in $PM_{2.5}$. Haze has frequently occurred in Chuncheon since So-Yang dam was constructed in 1973. Haze events were observed on 23 days during sampling period, and the average $PM_{2.5}$ concentration was approximately 1.6 times higher during haze events than during non-haze events. This result suggests that haze enhances the secondary aerosol formation because the aerosol spontaneously absorbs water to form a saturated salt solution, deriving a significant increase in the mass of the particle.

• Analytical Science and Technology
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• v.24 no.1
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• pp.24-37
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• 2011

The ionic compositions of atmospheric aerosols were investigated and characterized in coastal and mountainous sites of Jeju Island, which were Gosan and Mt. Halla-1100 sites respectively. It was found that the concentrations of nss-$SO_4^{2-}$ (non-sea salt sulfate) and $NH_4^+$ at two measurement sites were almost similar and they showed high concentrations in June at the same time. The concentration of soil-originated nss-$Ca^{2+}$ (non-sea salt calcium) was generally associated with that of anthropogenic $NO_3^-$ and its concentration was increased during spring season. From the comparison of time-series variation and regression analysis of ionic species between two measurement sites, TSP (total suspended particulate) in Gosan site was directly influenced by sea salt particles and the concentration levels of nss-$SO_4^{2-}$, $NH_4^+$, nss-$Ca^{2+}$, $K^+$, and $NO_3^-$ were mainly related with long-range transported air pollutants rather than local pollution sources.

• KSBB Journal
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• v.5 no.4
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• pp.411-414
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• 1990

The extraction behavior of an alkaline protease using reversed micelles was investgated. The reversed micellar solution consisted of AOT in isooctane. It was found that distribution of arkaline protease into the organic phase increased at lower pH, lower ionic strength, and higher AOT concentration. When the real fermentation broth was extracted of alkaline protease, an activity yield of 20% and a purification factor of 2.0 were obtained.

• Journal of Environmental Science International
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• v.26 no.6
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• pp.767-778
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• 2017

This research investigates the characteristics of metallic and ionic elements in $PM_{10}$ and $PM_{2.5}$ on haze day and non-haze day in Busan. $PM_{10}$ concentration on haze day and non-haze day were 85.75 and $33.52{\mu}g/m^3$, respectively, and $PM_{2.5}$ on haze day and non-haze day were 68.24 and $23.86{\mu}g/m^3$, respectively. Contribution rate of total inorganic water-soluble ion to $PM_{10}$ mass on haze day and non haze day were 58.2% and 61.5%, respectively, and contribution rate of total water-soluble ion to $PM_{2.5}$ mass on haze day and non haze day were 58.7% and 64.7%, respectively. Also, contribution rate of secondary ion to $PM_{10}$ mass on haze day and non haze day were 52.1% and 47.5%, respectively, and contribution rate of secondary ion to $PM_{2.5}$ mass on haze day and non haze day were 54.4% and 53.6%, respectively. AC (anion equivalents)/CE (cation equivalents) ratio of $PM_{10}$ mass on haze day and non haze day were 1.09 and 1.0, respectively, and AC/CE ratios of $PM_{2.5}$ mass on haze day and non haze day were 1.12 and 1.04, respectively. Also, SOR (Sulfur Oxidation Ratio) of $PM_{10}$ mass on haze day and non haze day were 0.32 and 0.17, respectively, and SOR of $PM_{2.5}$ on haze day and non haze day were 0.30 and 0.15, respectively. Lastly, NOR (Nitrogen Oxidation Ratio) of $PM_{10}$ on haze day and non haze day were 0.17 and 0.08, respectively, and NOR of $PM_{2.5}$ on haze day and non haze day were 0.13 and 0.06, respectively.

• Journal of Environmental Health Sciences
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• v.30 no.5 s.81
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• pp.455-468
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• 2004

The purpose of this paper is to understand the time series and origin of a chemical component and to compare the difference during yellow sand episodes for analysis $PM_{10}$ chemical components in the region of west in Korean Peninsula, 1999-2001. An annual mean concentration of $PM_{10}$ is $29.1\;{\mu}g/m^3$. A monthly mean and standard deviation of $PM_{10}$ concentration are very high in spring but there is no remarkably seasonal variation. Also, water soluble ionic component of $PM_{10}$ be influenced by double more total anion than total cation, be included $NO_{3}^-\;and\;SO_{4}^{2-}$ for the source of acidity and $NH_{4}^+$ to neutralize. Tracer metals of $PM_{10}$ slowly increases caused by emitted for soil and ocean (Fe, Al, Ca, Mg, Na) and Zn, Pb, Cu, Mn for anthropogenic source. According to method of enrichment factor (E.F) and statistics, assuming that the origin of metal component in $PM_{10}$ most of element in the Earth's crust e.g. Mg, Ca, Fe originates soil and Cu, Zn, Cd, Pb derives from anthropogenic sources. The ionic component for $Na^{+}\;Cl^-,\;Mg^{2+}\;and\;Ca^{2+}$ and Mg, Al, Ca, Fe originated by soil component largely increase during yellow sand period and then tracer metal component as Pb, Cd, Zn decrease. According to factor analysis, the first group is ionic component ($Na^+,\;Mg^{2+},\;Ca^{2+}$) and metal component (Na, Fe, Mn and Ni) be influenced by soil. The second group, Mg, Cr also be influenced by soil particle.

• Journal of Korean Society for Atmospheric Environment
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• v.23 no.5
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• pp.612-624
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• 2007

The real-time monitoring of radon ($^{222}Rn$) concentrations has been carried out to evaluate its ambient background concentration levels in Gosan site, Jeju Island between January 2001 and December 2004. In addition, the atmospheric TSP aerosols have been sampled, and their ionic and metallic components were analyzed to understand the characteristics of air pollution. The mean concentration of radon was $3,121{\pm}1,627\;mBq/m^3$, and the seasonal mean concentrations for spring, summer, fall and winter seasons were 2,898, 2,398, 3,571 and $3,646\;mBq/m^3$, respectively, The hourly concentrations have shown the highest value at 7 a.m. and the lowest value at 2 p.m. From the backward trajectory analyses, the radon concentrations have increased, when the air parcels were moved from the Chinese continent to Jeju area. On the other hand, they have decreased, when the air parcels from the North Pacific Ocean. In the analytical results of ionic species and metal elements of TSP aerosols, the concentrations of $nss-{SO_4}^{2-}$ and S were higher in June and March. Meanwhile, the concentrations of other anthropogenic species as well as soil components were mostly higher in March and April. On the basis of factor analysis, the TSP aerosols at Gosan area were largely influenced by soil sources, followed by anthropogenic sources and marine sources. From the result of backward trajectory analyses, the concentrations of $nss-{SO_4}^{2-},\;{NO_3}^-$, Al and Ca were mostly higher, when the air parcels moved from Chinese continent to Jeju area. On the other hand, their concentrations were lower, when the air parcels drifted from the North Pacific Ocean.

• Korean Chemical Engineering Research
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• v.54 no.1
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• pp.36-43
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• 2016

Hydrosilylation reactions of 2.4.6.8-tetrahydro-2.4.6.8-tetramethylcyclotetrasiloxane with allyl butyrate catalyzed by Karstedt's, $H_2PtCl_6$ and Pt/C catalyst were studied and 2.4.6.8-tetra (propyl butyrate)-2.4.6.8-tetramethylcyclotetrasiloxane was obtained. The reaction order, activation energies and rate constants were determined. Ringopening polymerization of 2.4.6.8-tetra (propyl butyrate)-2.4.6.8-tetramethylcyclotetrasiloxane in the presence of $CaF_2$, LiF, KF and anhydrous potassium hydroxide in $60-70^{\circ}C$ temperature range was carried out and methylsiloxane oligomers with regular arrangement of propyl butyrate pendant groups were obtained. The synthesized products were studied by FTIR and NMR spectroscopy. The polysiloxanes were characterized by wide-angle X-ray, gel-permeation chromatography and DSC analyses. Via sol-gel processes of oligomers doped with lithium trifluoromethylsulfonate or lithium bis (trifluoromethylsulfonyl)imide, solid polymer electrolyte membranes were obtained. The dependences of ionic conductivity of obtained polyelectrolytes on temperature and salt concentration were investigated, and it was shown that electric conductivity of the polymer electrolyte membranes at room temperature changed in the range $3.5{\times}10^{-4}{\sim}6.4{\times}10^{-7}S/cm$.

• Bulletin of the Korean Chemical Society
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• v.33 no.9
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• pp.2949-2954
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• 2012

Nano ZnO with an average size of 8 nm was prepared by thermal decomposition of zinc oxalate at $450^{\circ}C$. A series of based composite polymer electrolyte PEO-$LiClO_4$ and nano ZnO as a filler have been synthesized using solution cast technique, with varying the filler ratio systematically. XRD, DSC and FTIR studies have been conducted to investigate the structure and interaction of different groups in the composite polymer electrolyte. Effect of nano ZnO ceramic filler concentration on the structure of composites and their electrical properties (DC-conductivity, AC-conductivity, dielectric constant, dielectric loss and impedance) at different frequencies and temperatures was studied. Melting temperature ($T_m$) of PEO decreased with the addition of both $LiClO_4$ salt and nano ZnO filler due to increasing the amorphous state of polymer. All composite samples showed an ionic conductivity. The maximum room temperature ionic conductivity is found for $(ZnO)_{0.5}(PEO)_{12}(LiClO_4)$ composite sample. All the results are correlated and discussed.