• Korean Journal of Ecology and Environment
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• v.46 no.3
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• pp.388-394
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• 2013

Growth, inorganic solutes and glycine betaine accumulation in spinach beet (Beta vulgaris var. cicla L.) were studied under different salt conditions. Plants of fortythree days old were assessed by growing for a further 10 and 20 days at four NaCl concentrations (0, 100, 200, 300 & 400 mM). The dry weight of leaves was maximal in plants which were grown at 100 to 200 mM NaCl treatments and after 10d it was decreased slightly at salt treatments of more than 300 mM NaCl. Under the salt conditions, leaves of B. vulgaris contained high inorganic ions to maintain low water potential, but low water soluble carbohydrate contents. Total ionic content and osmolality increased with increasing salt concentration. Salt stress led to a preferential accumulation of glycine betaine in leaves of B. vulgaris, especially for the 200 mM NaCl treatment. These findings suggest that a high degree of NaCl tolerance of B. vulgaris resulted from the accumulation of glycine betaine, which is known to have osmoprotectant properties in the cytoplasm.

• Journal of Soil and Groundwater Environment
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• v.15 no.6
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• pp.99-106
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• 2010

We investigated springs in Seoul in 2009 to know the change of water quality according to storage method of spring water, the concentration of chemical compounds and their correlation. Even spring water that originally satisfied national standard for drinking water could be exceeded national standard for drinking water by storage method such as storage bottle, temperature and period; especially used PET bottles could affect the increase of total colony counts. Therefore, spring water is desirable to be consumed on the spot, or to be stored in sterilized bottles in refrigerator rather than room temperature at home, and also to be consumed shortly not exceeding 24 hours. Total colony counts, coliform, yersinia, $F^-$, $Cl^-$, $NO_3^--N$, hardness, total Solids, pH, color and Al were exceeded national standard for drinking water at some springs. The result of correlation analysis shows that hardness and total solids, which are caused by several ionic compounds, had relatively high correlations with other chemical compounds.

• Journal of Sensor Science and Technology
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• v.7 no.2
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• pp.111-116
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• 1998

The simple solid electrolyte carbon dioxide sensor with heaters were fabricated by using Li ionic conductor. Two Au electrodes were used for the reference and sensing electrode respectively. Two types of gas sensors, type ( I ) and type (II), were fabricated. Type ( I ) sensor was fabricated by the method of melting and crystallizing alkali metal carbonate at the temperature of $420{\sim}500^{\circ}C$. The sensing membrane of type (II) sensor was formed by the printing method on sensing electrode after metal carbonate was mixed with binder. The response characteristics of sensors fabricated for the carbon dioxide were investigated for a range of $CO_{2}$ concentration from 950 ppm to 9,950 ppm at operating temperature $420^{\circ}C$. Type ( I ) sensor and type (II) sensor showed the sensitivity of 62 mV/decade and 65 mV/decade respectively. The emf/decade of type (II) sensor tested at $420^{\circ}C$ almost followed the theoretical value of Nernst's equation and showed stable response characteristics with the fast response time of $15{\sim}20$ sec. Also type (II) sensor showed excellent stability and reproduction properties for 60 days.

• Korean Journal of Environmental Agriculture
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• v.26 no.2
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• pp.116-123
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• 2007

This experiment was conducted to investigate the distribution and burden characteristics of heavy metals in the rainwater sampled at Suwon area, in the middle part of Korea, from April 2002 to October 2003. The relationship between concentration of heavy metal and other chemical properties in the rainwater was also evaluated. Chemical properties in the rainwater were various differences with raining periods and years. It appeared that a weighted average pH of rainwater was ranged from 4.7 to 5.5. Heavy metal concentrations in the rainwater were ranked as Zn>Pb>Cu>Ni>Cr>As>Cd. As compared with heavy metal concentrations of rainwater in 2002, Cd, Cu and As were higher than other element in 2003. There were positive correlation between major ionic components, such as Ca, Mg, and K, and heavy metal concentrations of rainwater, and As, CU, Cu, Zn and Ni were relatively higher relationship than Pb and Cr in respective to correlation coefficient. For heavy metal distribution of rainwater, the order of average enrichment factors was Cd>Pb>AS>Cu>Zn>Ni>Cr, and these were relatively higher than the natural component such as Fe, Mg and Ca. The monthly enrichment factors were relatively high in the spring (from April to May) at Suwon. The monthly amount of heavy metal precipitation was high in the rainy season from June to August because of great influence of rainfall.

• Land and Housing Review
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• v.4 no.1
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• pp.119-124
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• 2013

Generally, the characteristic of nanofiltration membranes were catagorized into charged membrane, sieve effect, interaction between membarnes and target solutes. This study aims to investigate the effect item of heavy metal separation with view of charge nanofiltration membranes. The experiments of nanofiltration were conducted by nanofiltration set-up with operational pressure of 0.24 MPa at $25^{\circ}C$ by using synthetic wastewater containing 0.1mg/L of Cr, Fe, Cu, Zn, As, Sn, Pb. Nanofiltration membranes rejected heavy metals much better than chloride, sulfate and TOC, of which concentration in synthetic wastewater was higher than that of heavy metals. To consider rejection characteristics of various metals by nanofiltration membranes, separation coefficient, which is the molar conductivity ratio of the metal permeation rate to the chloride ion or TOC permeation rate, was introduced. In spite of different materials and different nominal salt rejection of nanofiltration membrane used, the separation coefficients of metals were nearly the same. These phenomena were observed in the relationship between the molar conductivity and the separation coefficient for heavy metals.

• Journal of Korean Society of Environmental Engineers
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• v.27 no.2
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• pp.158-162
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• 2005

The objective of this study was to assess the assimilable organic carbon (AOC) in processing water, a measurement of biostability, at several stages of a full-scale nanofiltration (NF) water treatment plant. The NF membrane plant investigated was a $45,400\;m^3$/day (12 mgd) water softening facility at Plantation City in southern Florida, which utilized an organic rich groundwater (dissolved organic carbon (DOC) = 17.6 mg/L) originated from a surficial aquifer. The average AOC concentration of raw feed water was estimated at 158 g/L acetate-C. After pretreatment(acid and antiscalant addition), AOC levels increased by 12.7%, suggesting that pretreatment chemicals used to control scaling may deteriorate feed water biostability. The results also demonstrated that nanofiltration was capable of effectively removing 63.4% of AOC and 94.8% of DOC from the raw water. AOC rejection in stage 1 (${\approx}\;68%$) was slightly higher than that of stage 2 (${\approx}\;58%$) indicating that AOC was removed less at the solution environment (i.e. low pH, high ionic strength and high hardness), which was often created in the $2^{nd}$ stage of full-scale membrane plants due to pretreatment (acid addition) and high recovery operation.

• Journal of the Korean Applied Science and Technology
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• v.37 no.3
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• pp.438-447
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• 2020

The critical micelle concentration (CMC) values of the mixed surfactant systems and the solubilization conatant (K_s) values of 4-ethylaniline in those solutions were measured and analyzed by the UV-Vis method. As a result, the mixed surfactant systems of TTAB/LSB and TTAB/TX-100 did not deviate significantly from ideal mixed micellization. However, the mixed systems of SDS/LSB and SDS/TX-100 showed great negative deviations from ideal mixed model. These differences showed that the intensity of the interaction between two components in the mixed micelle was different for each mixed system and that these differences greatly influenced the solubilization of 4-ethylaniline by a mixed surfactant system. Among pure surfactants, an anionic surfactant such as SDS showed a greater K_s value than other ionic surfactants, and the K_s value by each surfactant system decreased in the order of SDS≫TTAB≧LSB>TX-100. In addition, the K_s values of all the mixed surfactant systems were higher than those of the pure surfactants constituting the mixed systems.

• Journal of the Korean Chemical Society
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• v.14 no.1
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• pp.65-74
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• 1970

Formation of the complexes of alkaline earths with citrate ions in aqueous, acetone-water and ethanol-water solutions was studied at room temperature by the equilibrium exchange technique. This technique involved the measurements of distribution of radioactivity between cation exchange resin and solution phase after the radioactive metal ions were equilibriated with the cation exchange resin in the presence of citrate ions ($Cit^{3-}$) of varying concentrations. The pH of the solutions was controlled to 7.2-7.5, and the ionic strength of the solutions was kept at 0.10-0.12. The present study revealed that both barium and strontium ions formed the one to one citrate complexes, $[M Cit]^-$ in all solvent systems examined. It was also observed that calcium ions formed the one to one citrate complex in aqueous solution. In acetone-water and ethanol-water solutions, however, calcium ions were observed to form both one to one and one to two complexes, $[Ca Cit]^-$ and $[Ca\;Cit_2]^{4-}$. The results of the present study indicated also that relative stabilities of the complexes increased in the order; $Ba^{++}\;<\;Sr^{++}\;<\;Ca^{++}$, and in the order of increasing concentration of the organic components in the mixed solvent systems.

• Journal of the Korean Geotechnical Society
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• v.21 no.5
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• pp.231-241
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• 2005

Laboratory experiments were performed to examine the effects of water content and to see if permittivity had sufficient sensitivity to identify subsurface contamination. Both real and imaginary permittivities of unsaturated sand were strongly governed by the volumetric water content. Especially, a linear relationship between real permittivity and volumetric water content was derived at high frequencies (MHz ranges). Heavy metals in pore fluid result in significant increases in the effective imaginary permittivity, due to ionic conduction, but decreases in the real permittivity arises due to the decreased orientational polarization of water molecules caused by hydration of ions. Clear increase in the effective imaginary permittivity with heavy metal concentration was found to be valuable in the application of electrical methods for detecting heavy metals in the subsurface. However, because the permittivity is primarily dependent on the volumetric water content of soil, pre-evaluation on the volumetric water content is required.

• Journal of agricultural medicine and community health
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• v.36 no.4
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• pp.218-226
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• 2011

Objectives: Paraquat (PQ) is a widely used ionic pesticide that is fatal when ingested accidentally or for suicidal purposes. It is thought that chronic exposure of PQ is related with the development of Parkinson's disease, but epidemiological studies have not yet confirmed that theory. This study attempted to estimate the possibility of environmental PQ exposure through soil and water. Materials and Methods: We analyzed the amount of decomposed PQ solution in wet soil after exposure to ultraviolet light. An artificial rainfall condition was simulated over soil sprayed with PQ to measure the amount of eluted PQ. In addition, PQ was diluted in water from three differently rated rivers and the changes in PQ concentration were measured after ultraviolet exposure over one month. High performance liquid chromatography/ultra violet detection was used to analyze the concentrations of PQ. Results: In the method we used, the recovery rate of PQ showed a precision rate less than 5%, an accuracy greater than 88%, and the calibration equation was y=5538.8x-440.01($R^2$=0.9985). There were no significant differences in the concentrations of PQ obtained from the three specimens over a 1-week period. From the PQ-sprayed soil, the artificial rainfall conditions showed no PQ elution over a 1-month period, and there was no significant differences in PQ concentrations according to ultraviolet exposure among the three samples. Conclusions: PQ remains well adsorbed naturally in soil. However, it may still exist in an integrated state for a long time in the hydrosphere, so the possibility of PQ exposure through drinking water cannot be disqualified.