• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 1998.06a
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• pp.43-49
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• 1998

Retardation effect of heavy metals in soils caused by adsorption onto the surfaces of solids particles is well known phenomena. The adsorption of metal ions has been recognized more strong in clay mineral and organic matter contents rather than sands and gravels. In this study, we investigated the retardation effect in two sandy soils by conducting batch and column tests. The column tests were conducted to obtain the relationship between concentration and time known as breakthrough curve (BTC). We applied pulse type injection of ZnCl$_2$solution on the inlet boundary and monitored the effluent concentration at the exit boundary under steady state condition using EC-meter and ICP-AES. Batch test consisted of an equilibrium procedure for fine fractions collected from two sandy soils for various initial ZnCl$_2$concentrations, and analysis of Zn ions in equilibrated solution using ICP-AES. The results of column test showed that i) the peak concentration of Zn analyzed by ICP was far less than that detected by EC-meter for both soils and ii) travel times for peak concentration were more less identical for two different monitoring techniques. The first result can be explained by ion exchange between Zn and other cations initially present in the soil particles since ICP analysis showed a significant amount of Ca, Mg ions in the effluent. From the second result, we found that retardation effect was not present in these soils due to strong cation exchange capacity of Zn ion over other cations since we did not apply a solution containing more adsorptive cations such as Al. The result of batch test also showed high distribution coefficients (K$_{d}$) for two soils supporting the dominant ion exchange phenomena. Based on the retardation factor obtained from the Kd, we predicted the BTC using CDE model and compared with the BTC of Zn concentration obtained from ICP The predicted BTC, however, disagreed with the monitored in terms of travel time and magnitude of the peak concentrations. The only way to describe the prominent decrease of Zn ion was to introduce decay or sink coefficient in the CDE model to account for irreversible decrease of Zn ions in liquid phase.e.

• Journal of Environmental Science International
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• v.24 no.5
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• pp.615-622
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• 2015

East Asia is characterized by anthropogenic emissions resulting from the large population and fast economic growth of this region. Since the prevailing wind is westerly and northwesterly, emissions from Ul-jin can be expected to contribute to acidic deposition increase in downwind direction. Aerosols collected at the near coast site, Uljin geun, gyungbook and were analyzed for $NH_4{^+}$, $Mg^{2+}$, $Na^+$, $Ca^{2+}$, $Cl^-$, $SO_4{^{2-}}$, and $NO_3{^-}$ from Aug. 2012 to Feb. 2013. The seasonal averaged aerosol concentration showed the highest potassium and calcium ion in winter and the highest ammonium ion due to a meadow and high solar intensity in summer. Sodium and chloride ion showed the same ratio all seasons and sulfate and nitrate species showed the maximum value in winter Chemical components of aerosols collected at the near coast site, Uljin geun, gyungbook were lower by 16 to 73% than those collected at other similar environment site such as kanghwa, yangyang. Comparing air quality data at the near coast site, Uljin geun, gyungbook, There was found that Uljin coast site is less influenced by the sea salts(potassium, magnesium, calcium) and nss-$SO_4{^{2-}}$ percentage is 3~13% higher than similar condition site.

• Journal of Korean Society on Water Environment
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• v.23 no.3
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• pp.371-376
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• 2007

The features of precipitating reaction of fluorine have been examined under several aquatic conditions by employing calcium ion as a precipitant. Based on MINTEQ program, fluorine was found to exist in the forms of $H_2F_2$ and HF in strong acidic environment and change into $F^-$ with increasing pH. In the experimental condition, the precipitating reaction of fluorine progressed rapidly within a few minutes after the reaction started and reached its equilibrium in 10 minutes. As the addition of precipitant was increased, removal of fluorine by the formation of precipitate was promoted and its was also enhanced by the rise of pH. The precipitating reaction of fluorine was impeded when its initial concentration was low and X-ray analysis showed that the crystalline structure of precipitate was mainly $CaF_2$ with partly NaF. Coexisting phosphate in solution influenced the fluorine removal by impeding the precipitate formation and similar effect was found when metallic ion such as $Zn^{2+}$ was present with fluorine.

• Journal of Environmental Science International
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• v.9 no.5
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• pp.437-441
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• 2000

A study on the removal of Pb ion from Pb-contaminated soil was carried out using ex-site extraction process. Tartaric acid (TA) and iminodiacetic acid sodium salt(IDA) as a washing agent were evaluated as a function of concentration reaction time mixing ratio of washing agent and recycling of washing agent. TA showed a better extraction performance than IDA. The optimum washing condition of TA and IDA were in the ratio of 1:15 and 1:20 between soil and acid solution during 1 hr reaction. The total concentrations of Pb ion by TA and IDA at three repeated extraction were 368.8 ppm and 267.5 ppm respectively. The recovery of Pb ion from washing solution was achieved by adding calcium hydroxide and sodium sulfide form the precipitation of lead hydroxide and lead sulfide and optimum amounts of sodium sulfide and calcium hydroxide were 7 g/$\ell$ for the TA washing solution and 4 g/$\ell$, 5g/$\ell$ for the IDA washing solution respectively. The efficiency of recycle for TA and IDA washing solution were 78.8% , 95.1%, and 89.2%, 96.6% at third extractions under $Na_2S$ and $Ca(OH)_2$, respectively.

• Journal of Korean Society for Atmospheric Environment
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• v.12 no.4
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• pp.399-406
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• 1996

Acidic fog is catastrophic to aviation and potentially affect materials, vegetation, crops and public health. This paper was carried out to investigate the chemical features of fog sample at Mt. Sobaek (mean sea level : 1, 340m) from June to August 1995. Each sample was analyzed for pH, electrical conductivity and major ions (anion : $Cl^N)_3^-, SO_4^{2-}, cation : Na^+, NH_4^+, K^+, Mg^{2+}, Ca^{2+}$) by ion chromatography. The quality analysis of fog sample data was performed based on ion balance and electrical conductivity method. The wind directions are subdivided into the northerly and southerly wind according to the wind direction data at the Sobaek-san meteorological observation station. Statistical analyses were performed on the complete set of results in order to obtain a description of fog sample. All the statistical treatment was carried out using the SPSS/PC + software package. The major ion concentration of fog samples was higher for the northwesterly wind cases than sourtheasterly wind cases. The pH of fog sample varied between 2.95 and 6.08. The average pH and electrical conductivity of total sample (n=210) were 4.39 and 113.0 $\mu$S/cm, respectively. It may be noted that in nearly all the cases, the dominant major ions in the fog sample at Mt. Sobaek were $SO_4^{2-}, NO_3^-, H^+ and NH_4^+$.

• The Korean Journal of Physiology and Pharmacology
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• v.8 no.1
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• pp.33-41
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• 2004

We developed a cardiac cell model to explain the phenomenon of mechano-electric feedback (MEF), based on the experimental data with rat atrial myocytes. It incorporated the activity of ion channels, pumps, exchangers, and changes of intracellular ion concentration. Changes in membrane excitability and $Ca^{2+}$ transients could then be calculated. In the model, the major ion channels responsible for the stretch-induced changes in electrical activity were the stretch-activated channels (SACs). The relationship between the extent of stretch and activation of SACs was formulated based on the experimental findings. Then, the effects of mechanical stretch on the electrical activity were reproduced. The shape of the action potential (AP) was significantly changed by stretch in the model simulation. The duration was decreased at initial fast phase of repolarization (AP duration at 20% repolarization level from 3.7 to 2.5 ms) and increased at late slow phase of repolarization (AP duration at 90% repolarization level from 62 to 178 ms). The resting potential was depolarized from -75 to -61 mV. This mathematical model of SACs may quantitatively predict changes in cardiomyocytes by mechanical stretch.

• Analytical Science and Technology
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• v.11 no.5
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• pp.409-412
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• 1998

The analytical method to determine europium(III) ion in aqueous solution by fluorescence spectroscopy based upon the conformational change of calmodulin in the presence of the analyte has been studied. The fiber optic chemical sensor used in this study was constructed by entrapping a fluorescein-labeled calmodulin solution, EGTA, buffer solution at the common end of a bifurcated fiber optic bundle by means of a dialysis membrane. The calibration curve to determine europium(III) ion was obtained when concentration of calmodulin, concentration of EGTA, Tris-HCl buffer solution, pH, excitation wavelength and fluorescence wavelength were $5.0{\times}10^{-5}M$, 0.50 mM, 5.0 mM, 7.0, 495 nm and 520 nm, respectively. The detection limit was $1.0{\times}10^{-11}M$ and the working range of the calibration curve for the sensor was $1.0{\times}10^{-11}M{\sim}1.0{\times}10^{-9}M$. The response time was 15 minutes. For the determination of europium(III) ion by the present method, $Na^+$ and $K^+$ ions did not interfere but $Ca^{2+}$ ion seriously interfered.

• Journal of the Korean Ceramic Society
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• v.33 no.11
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• pp.1276-1284
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• 1996

Ultrafine calcim carbonate powders with the size of 0.05~0.1 ${\mu}{\textrm}{m}$ and the calcite phase were prepared by the nozzle spouting method which was conducted by spouting calcium hydroxide slurry in reactor filled with CO2 gas. Well dispersed ultra-fine particles were synthesized in condition of high Ca(OH)2 concentration of the slurry ( 0.5wt%) synthesized calcium carbonate powder was shown the large particle size with agglo-meration.

• Journal of Microbiology and Biotechnology
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• v.15 no.3
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• pp.497-501
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• 2005

This study deals with the removal of mercury species using a packed-bed column with spherical aminated chitosan material. These adsorbents revealed a high adsorption capacity for mercury species. Experiments with feed solutions of 10 ppm Hg dissolved in distilled water showed an excellent removal with a sharp increase of the filter effluent concentration after a total throughput of 900 bed volumes of feed water. Up to $95\%$ desorption was reached by using 3 bed volumes of 0.01 N EDTA solution. EDTA could be recovered by means of sulfuric acid with about $75\%$ efficiency. Almost the same results were obtained in repeated sorption and desorption experiments at identical conditions. The experiments demonstrated that the sorbents possessed practically no sorption capacity for alkaline earth ions ($Ca^{2+}\;and\;Mg^{2+}$). Their influence on the sorption of mercury was negligible. In experiments with spiked tap water of the Karlsruhe Research Centre and a feed mercury concentration of 0.01 mg/l, the breakthrough of Hg was observed only after a total throughput of about 6,000 bed volumes of feed water.

• Bulletin of the Korean Chemical Society
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• v.24 no.9
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• pp.1245-1250
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• 2003

Pseudo-first-order rate constants ($k_{obs}$) have been measured spectrophotometrically for the reactions of 4-nitrophenyl benzoate with a series of pyridines in $H_2O$ containing 20 mol % DMSO. The plots of kobs vs pyridine concentration are linear up to ca. 0.1 M pyridines, indicating that the effect of self-association of pyridines with their conjugate acids are insignificant in this concentration range. The Bronsted-type plot has been obtained to be linear with a ${\beta}_{nuc}$ value 1.11, suggesting that the pyridinolyses proceed through a rate-determining breakdown of the zwiterionic addition intermediate. The pyridines studied have shown higher reactivity than isobasic primary and secondary amines toward the substrate. 1-Benzoyl-4-dimethylaminopyridinium ion, a possible intermediate, has not been detected since the rate of its hydrolysis in the reaction condition is comparable with or even faster than its formation.