• Analytical Science and Technology
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• v.24 no.5
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• pp.378-386
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• 2011

The goal of this study is to understand the influence of temperature on phosphorus release rate from soil into water. As the temperature increases, $PO_4$-P reaches equilibrium more quickly and the equilibrium concentration increases, and thus the $PO_4$-P concentration increases, and pH decreases. The $PO_4$-P concentration affects pH. $PO_4$-P released from turbidity is not adsorbed onto the turbidity. $PO_4$-P was independent on the turbidity and yet $PO_4$-P was steadily increasing. However, $PO_4$-P was dependent upon the turbidity concentration as the turbidity releases $PO_4$-P. The total phosphorous (T-P) and turbidity were directly linked because T-P changed with the turbidity. T-P includes the $PO_4$-P content of water and the phosphorus content of the turbidity. As the temperature decreases, density of water increases, and the precipitation of turbidity decreases, resulting in an increases in T-P concentration. As the temperature increases, the T-P concentration decreases, but the PO4-P release rate from turbidity increases. At the same time, even at different temperatures, the T-P concentrations of the samples were about the same. When the lake gets deepened, the water temperature decreases, hence, the phosphorus release rate from soil into water was decreased. This mechanism is of great interest because phosphorus is released from soil sediment into the lake water.

• Journal of the Korean Society for Marine Environment & Energy
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• v.11 no.3
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• pp.113-123
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• 2008

We have analyzed a long term data of marine environments, red tide information and meteorology acquired by NFRDI and KMA, in order to understand the characteristics of marine environments in the Narodo coastal waters which is known to be the first outbreak region of Cochlodinium polykrikoides blooms. During the period of from 1992 to 2007, Cochlodinium polykrikoides blooms have first occurred more often in August. However, the outbreak time of the blooms tended to be earlier annually, and in addition, the surface salinity also had a tendency to increase. Consequently, it suggested that there might be a relationship between the transition of the outbreak time of the blooms and salinity. On the other hand, insolation was relatively rich but precipitation was relatively scarce in Gohung Province, compared to Yeosu or Tongyeong, when Cochlodinium polykrikoides blooms first occur in Narodo coastal waters. Average water temperature and salinity in August in Narodo coastal waters were all higher than those in Gamak and Jinhae bays, suggesting that Narodo coastal waters are a region of relatively high water temperature and high salinity. Also, concentrations of nutrients and chlorophyll- a were significantly low than those in Jinhae Bay, which is known to be a eutrophicated region, while the overall water quality seemed to be similar to Gamak Bay. The results of PCA(Principal Component Analysis) proved that insolation and water temperature are the most important factors for the outbreak of Cochlodinium polykrikoides blooms in Narodo coastal waters while concentrations of COD and dissolved oxygen are secondly important. Furthermore, typhoons also appeared to be one of most important factors for the outbreak of Cochlodinium polykrikoides blooms.

• Clean Technology
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• v.17 no.2
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• pp.166-174
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• 2011

The xAl-yCe oxide catalysts with different mol ratios of Al/(Al+Ce) were prepared by a co-precipitation method and Pt supported on xAl-yCe oxide catalysts were synthesized by an incipient wetness impregnation method. The catalysts were characterized by X-ray Diffraction (XRD), $N_2$ sorption, and $H_2$/CO-temperature programmed reduction ($H_2$/CO-TPR) to correlate with catalytic activities in co oxidation. Among the catalysts studied here, Pt/1Al-9Ce oxide catalyst showed the highest activity in dry and wet reaction conditions and the catalytic activity showed a typical volcano-shape curve with respect to Al/(Al+Ce) mol ratio. When the presence of 5% water vapor in the feed, the temperature of $T_{50%}$ was shifted ca. $30^{\circ}C$ to lower temperature region than that in dry condition. From CO-TPR, the desorption peak of $CO_2$ on Pt/1Al-9Ce oxide catalyst showed the highest value and well correlated the catalytic performance. It indicates that the Pt/1Al-9Ce oxide catalyst has a large amount of active sites which can be adsorbed by co and easy to supplies the needed oxygen. In addition, the amount of pentacoordinated $Al^{3+}$ sites obtained through $^{27}Al$ NMR analysis is well correlated the catalytic performance.

• Economic and Environmental Geology
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• v.34 no.1
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• pp.71-88
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• 2001

The Geochemica] and isotope studies on the $CO_2$-rich water from the Shinchon area were carried out. The Shinchon $CO_2$-rich water belongs to Ca(Na)-$HCO_3$ type showing very high $P_{CO_{2}}$ ( $10^{-0.35}$ ~ $10^{0.29}$ atm) and TDS (835-3,144 mg/L). The results of geochemical and isotope analysis indicate that $CO_2$ gas is originated from the deep seated source such as mantle or magmatic gases. The $CO_2$-rich water was evolved by interaction with deep-seated granite and major water-rock interaction was dissolution of p]agioclase resulting high Na content of $CO_2$-rich water. Precipitation and dissolution of secondary calcite might be accompanied with the dissolution of plagioclase maintaining Na/Ca ratio. High contents of K and $SO_4$ indicate that the geochemical characteristics of $CO_2$-rich water were partially affected by interaction with upper sedimentary rock during uprising to surface. N03 and tritium contents suggest that the $CO_2$-rich water was mixed with low $CO_2$ groundwater at some locations. The oxygen-hydrogen isotopes show that all water samples were derived from meteoric waters and the $CO_2$-rich water was isotopically re-equilibrated with lighter $CO_2$ gas. Although some carbon isotope data show isotopically heavy values, carbon isotope data indicate that the $CO_2$ gas was possib]y derived by deep source.

• Economic and Environmental Geology
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• v.32 no.5
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• pp.469-483
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• 1999

Two different types of deep groundwaters occur together in the Jungwon area: $CO_2$-rich water and alkali water. Each water shows distrinct hydrogeochemical and environmental isotopic characteristics. The $CO_2$-rich waters are characterized by lower pH(6.0~6.4), higher Eh (25~85mV) and higher TDS content (up to 3,300 mg/l), whereas the alkali type waters have higher pH (9.1~9.5), lower Eh (-136~-128mV) and lower TDS content (168~254 mg/l). The CO2-rich waters ($Pco_2$=up to 1atm) were probably evolved by the local supply of deep $CO_2$ during the deep circulation, resulting in enhanced dissolution of surrounding rocks to yield high concentrations of $Ca^{2+}, Na^+, Mg^{2+}, K^+\; and \;HCO_3\;^-$ under low pH conditions. On the other hand, the alkali type waters ($Pco_2$=about 10-4.6 atm) were evolved through lesser degrees of simple wate/rock (granite) interaction under the limited suppy of $CO_2$. The alkali waters are relatively enriched in F- (up to 14mg/l), whereas the F- concentration of$CO_2$-rich water is lower (2.2~4.8 mg/l) due to the buffering by precipitation of fluorite. The oxygen-hydrogen isotopes and tritium data indicate that compared to shaltion ($\delta$18O=-9.5~-7.8$\textperthousand$),two different types fo deep groudwaters (<1.0TU)were both derived from pre-thermonuclear (more than 40 years old) meteoric waters with lighter O-H isotopic composition ($\delta$18O=-9.5~-7.8$\textperthousand$) and have evolved through prolonged water/rock interaction. The $CO_2$-rich waters also show some degrees of isotopic re-equilibration with $CO_2$ gas. The $\delta^{34}S$ values of dissolved sulfates (+24.2~+27.6$\textperthousand$) in the $CO_2$-rich waters suggest the reduction of sulfate by organic activity at depths. The carbon isotope data show that dissolved carbon in the $CO_2$-rich waters were possibly derived either from dissolution of calcite or from deep $CO_2$ gas. However, strontium isotope data indicate Ca in the $CO_2$-rich waters were derived mainly from plagioclase in granite, not from hydrothermal calcites.

• Applied Chemistry for Engineering
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• v.5 no.3
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• pp.395-405
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• 1994

The various functional groups, such as hydroxyl(-OH), carboxyl(-COOH) and quinonic oxygen(OC<) on the carbon black(abbreviated to CB) surface were activated with n-butyl lithium solution in n-hexane and then acrylate and methacrylate monomers were graft polymerized onto these activated anionic sites and CB-grafted polymers were obtained. To separate homopolymers from reaction mixture, non-solvent precipitation method or centrifugal separating method were applied. Subsequently, conversion, grafting ratio and efficiency were determined at various reaction temperatures and times. In case of acrylates, the grafting ratio showed 20~30% but methacrylates showed 150~200%. Also the anion polymerizations between CB and monomers were nearly reached to equilibrium state within one or two hours under each reaction temperatures but conversion and grafting ratio were increased a little with reaction temperature increase. In colloidal dispersion stability test, before heat-drying, the all CB-grafted polymers showed good dispersed stability in good solvents for acrylic and methacrylic homopolymers. Futhermore, CB-polymethacrylates were found to show excellent collidal properties for good solvents of methacrylic homopolymer even after heat-drying. Identification of the grafted polyacrylates and polymethacrylates onto the CB surface was performed by FT-IR spectroscopy. In addition, electric resistance values of CB-grafted polymers were measured by Four-probe method, and the increase of the grafting ratio showed the increase of the surface resistance.

• Journal of Advanced Marine Engineering and Technology
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• v.39 no.7
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• pp.779-785
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• 2015

Cathodic protection is recognized as the most cost-effective and technically appropriate corrosion prevention method for the submerged zone of offshore structures, ships, and deep-sea facilities. When cathodic protection is applied, the cathodic currents cause dissolved oxygen reduction, generating hydroxyl ions near the polarized surface that increase the interfacial pH and result in enhanced carbonate ion concentration and precipitation of an inorganic layer whose principal component is calcium carbonate. Depending on the potential, magnesium hydroxide can also precipitate. This mixed deposit is generally called "calcareous deposit." This layer functions as a barrier against the corrosive environment, leading to a decrease in current demand. Hence, the importance of calcareous deposits for the effective, efficient operation of marine cathodic protection systems is recognized by engineers and scientists concerned with cathodic protection in submerged marine environments. Calcareous deposit formation on a marine structure depends on the potential, current, pH, temperature, pressure, sea-water chemistry, flow, and time; deposit quality is significantly influenced by these factors. This study determines how calcareous deposits form in sea water, and assesses the interrelationship of formation conditions (such as the sea water temperature and surface condition of steel), deposited structure, and properties and the effectiveness of the cathodic protection.

• KOREAN JOURNAL OF PACKAGING SCIENCE & TECHNOLOGY
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• v.5 no.2
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• pp.9-16
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• 1999

Edible films were prepared from proteins extracted from soybean curd residue by alkaline extraction and isoelectric precipitation. Effects of film forming solution pH and plasticizers on mechanical and barrier properties of edible films were studied. films were formed within pH $7{\sim}11$ with tensile strength (TS) of $2.9{\sim}3.3$ MPa. Films produced under pH 10 had the highest TS and Elongation (E) (3.3 MPa and 60.1%) but no significant difference was observed among water vapor permeabilities (WVP) of film. Glycerol, sorbitol and its mixture (1:1, w/w) were added as plasticizers. The concentration and mixing ratio of plasticizers also affected the TS, E and WVP of films. TS of films decreased from 15.0 MPa to 2.9 MPa as plasticizer concentration increased from 0.4 to 0.8 g plasticizer/g protein. At a plasticizer concentration, the highest TS was observed when sorbitol was used whereas the highest E was measured when mixture of glycerol and sorbitol was used as plasticizer WVP of films increased as the plasticizer concentration increased. Films plasticized with glycerol showed the highest WVP among the films with the same plasticizer concentrations. Edible films prepared from soybean curd residue protein showed very low oxygen permeabilities ($29.5{\sim}61.1aL{\cdot}m/m^2{\cdot}s{\cdot}Pa$) and oil resistance at all plasticizer concentration level tested.

• Economic and Environmental Geology
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• v.25 no.3
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• pp.233-243
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• 1992

Ore mineralization of the Hwanghak copper deposit in the Ogsan area occurred in three stages of quartz (stage I and II) and calcite (stage III) veining along fissures in Early Cretaceous sedimentary rocks. Ore minerals are pyrite, pyrrhotite, chalcopyrite (dominant), sphalerite, hematite, galena, and Ag-, Pb-, and Bi-sulfosalts. These were deposited during the first stage at temperatures between $370^{\circ}C$ and < $200^{\circ}C$ from fluids with salinities between 0.5 and 7.6 equiv. wt. % NaCl. There is evidence of boiling and this suggests pressures of less than 180 bars during the first stage. Equilibrium thermodynamic interpretation accompanying with mineral paragenesis and fluid inclusion data indicates that copper precipitation in the hydrothermal system occurred due to cooling and changing in chemical conditions ($fs_2$, $fo_2$, pH). Gradual temperature decrease from $350^{\circ}$ to $250^{\circ}C$ of ore fluids by boiling and mixing with less-evolved meteoric waters mainly led to copper deposition through destabilization of copper chloride complexes. Sulfur isotope values of sulfide minerals decrease systematically with paragenetic time from calculated ${\delta}^{34}S_{H_2S}$ values of 8.2 to 4.7‰. These values, together with the observed change from sulfide-only to sulfide-hematite assemblages and fluid inclusion data, suggest progressively more oxidizing conditions, with a corresponding increase of the $sulfate/H_2S$ ratio of hydrothermal fluids. Measured and calculated hydrogen and oxygen isotope valutls of ore-forming fluids suggest meteoric water dominance, approaching unexchanged meteoric water values.

• Journal of Aquaculture
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• v.16 no.1
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• pp.15-23
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• 2003

We have investigated water quality of the coastal saline groundwaters utilized for fish farms in Jeju Island. The water quality investigation included the spatial observations for 75 fish farms during March-May, 1994 and the hi-monthly observations for both coastal saline groundwaters and seawaters at four fish farms from August 1994 to December 1995. Water temperature of the saline groundwaters ranged from 16 to 18$^{\circ}C$ over the study period. Salinity of the saline groundwaters varied between 20.60 ppt and 34.02 ppt, slightly lower than that of the coastal seawaters(26.47~34.53 ppt). This salinity variation must be associated with local precipitation conditions in Jeju Island. The oxygen saturation for most saline groundwater samples was lower than 80%, ranging from 24.7 to 89.8%. The COD and pH values for the saline groundwaters were similar to those for the coastal seawaters. The concentrations of DIP for the saline groundwaters varied between 0.021 mg/L and 0.121 mg/ L, and seasonal variation of DIP in the saline groundwater ranged from 0.014 to 0.077 mg/L, which were higher than that of the coastal seawaters(0.000~0.015 mg/L). Nitrate in the saline groundwaters accounted for more than 90% of the DIM. The maximum concentrations of ammonia, nitrite, nitrate and DIN in the saline groundwaters were 0.085, 0.012, 2.294 and 2.309 mg/L, respectively. These concentrations of the saline groundwaters were considerably lower than those affected culture organisms. Overall, the saline groundwaters utilized for fish farms in Jeju Island appear to maintain good waterquality for fish farms.