• Economic and Environmental Geology
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• v.24 no.2
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• pp.83-96
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• 1991

Haenam pyrophyllite deposit occurred in the rhyolitic tuff of late Cretaceous age is located in the northern part of Haenam-gun, Jeonranam-do. The ore of the Haenam deposit is predominantly composed of pyrophyllite and illite accompanying such clay minerals as kaolinite, chlorite, and smectite. Pyrophyllite ore at the center of altered mass is often associated with kaolin minerals and high temperature minerals such as corundum, andalusite, and diaspore. On the basis of mineral assemblage the Haenam deposit can be devided into three alteration zones from the center to the margin of the deposit; the pyrophyllite zone, kaolinite zone, and illite zone. All alteration zones are associated with appreciable amounts of chalcedonic quartz. Those mineral assemblages indicate that hydrothermal solution which produced the Haenam deposit is strongly acidic solution with high silica and hydrogen activity and low $SO_4{^{2-}}$ activity. Discriminant analysis shows that $Na_2O$, $K_2O$, and $Al_2O$, of major elements are discriminant elements which classify alteration zones, while in case of trace elements Cr, Ni, and Sr turned out to be discriminant elements in this deposit. According to the mineral assemblage and illite geothermometry, pyrophyllite ore is considered to have been formed at about $240-290^{\circ}C$. K-Ar isotopic age for illite from this deposit indicates that it was formed at much the same age of later stage volcanics in the area, suggesting that the hydrothermal alteration of these deposits is associated with later volcanism of the area.

• Korean Journal of Materials Research
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• v.15 no.1
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• pp.31-36
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• 2005

It is well known that PCB (Printed Circuit Board) is a complex mixture of various metals mixed with various types of plastics and ceramics. In this study, high temperature pyre-metallurgical process was investigated to extract valuable metallic components from the PCB scrap. For this purpose, PCB scrap was shredded and oxidized to remove plastic materials, and then, quantitative analyses were made. After the oxidation of the PCB scrap, $30.6wt\%SiO_2,\;19.3wt\%Al_2O_3\;and\;14wt{\%}CaO$ were analyzed as major oxides, and thereafter, a typical composition of $32wt\%SiO_2-20wt\%Al_2O_3-38wt{\%}CaO-10wt\%MgO$ was chosen as a basic slag system for the separation of metallic components. Moreover a size effect of crushed PCB scrap was also investigated. During experiments a high frequency induction furnace was used to melt and separate metallic components. As a result, it was found that the size of oxidized PCB scrap was needed to be less 0.9 m to make a homogeneous liquid slag and to recycle metallic components over $95\%$.

• Journal of Soil and Groundwater Environment
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• v.23 no.2
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• pp.23-29
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• 2018

This study explored secondary effects of the residual hydrofluoric acid (HF) after a hypothetical acid spill accident by investigating the long-term dissolution of minerals and leaching of pre-existing arsenic (As) from two soil samples (i.e., KBS and KBM) through batch and column experiments. An increase in the HF concentration in both soil samples resulted in a dramatic increase in the release of major cations, especially Si. However, the amounts of mineral dissolved were dependent on the soil type and mineral characteristics. Compared to the KBM soil, relatively more Ca, Mg and Si were dissolved from the KBS soil. The column experiment showed that the long-term dissolution rates of the minerals are closely associated with the acid buffering capacity of the two soils. The KBM soil had relatively higher effluent pH values compared to the KBS soil. Also, more As was leached from the KBM soil, with a more amorphous hydrous oxide-bound As fraction. These results suggest that the potential of heavy metal leaching by the residual acid after an acid spill will be influenced by heavy metal speciation and mineral structure in the affected soil.

• Economic and Environmental Geology
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• v.27 no.2
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• pp.131-145
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• 1994

The Daehung and Pyeongan talc mines are located in the Yoogoo area, Chungcheongnam-Do. These deposits occur as the complex vein type in the ultramafic rocks which intruded Precambrian gneiss. The talc ore formed from sepentinitt: originated from ultramafic rocks but some of those from hornblende gneiss. The talcification processes were considered here on the basis of the mineral assemblages, paragenesis, and geochemistry. It appears that there are five processes in talcification ; serpentine$\rightarrow$talc, phlogopite$\rightarrow$chlorite$\rightarrow$talc, phlogopite$\rightarrow$talc, hornblende$\rightarrow$chlorite$\rightarrow$talc, and hornblende$\rightarrow$talc. Among them, the most dominant alteration path is serpentine to talc in these deposits. EPMA data suggest that there might be interstratified minerals were in between parent mineral and talc such as serpentine and talc, and phlogopite and talc. It can be found that tremolite exists in between the inner and outer most part of talcified serpentinite blocks coated with phlogopite. Some of tremolites has been altered to talc. The quartz veins and carbonate minerals were found in the talc ore zone. It indicates that the hydrothermal solution played an important role in talcification. The hydrothermal alteration occured after sepentinization. Ore zones can be divided into two zones; talc-serpentine zone preserving a pseudormorph of olivine (mesh texture) and talc-phlogopite zone showing talcification from phlogopite directly or through chlorite. It can be concluded that the formation of major talc ore body was due to talcification of serpentinite and phlogopite by hydrothermal solution. A nature of hydrothermal solution was relatively pure water at the beginning of serpentinization, and was getting richer in silica composition. There was a large amount influx of K and AI with hydrothermal solution in the later stage, and increased $P_{CO_{2}}$ also. It suggests that phlogopite formed in later stages as a secondary mineral. So, the major part of the talc ore body was formed from one parents rocks, serpentinite originated from ultramafic rocks, by hydrothermal solutions at several times.

• Journal of Life Science
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• v.22 no.2
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• pp.226-231
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• 2012

The effect of cordycepin-enriched Cordyceps militaris JLM 0636 ($CM{\alpha}$) and Cordyceps militaris (CM) on fibrinolytic activity was investigated. The bioactive compounds and nutritional materials such as polyphenolic compounds, flavonoids, glutathione, minerals, and fatty acids were also measured. Concentrations of polyphenol compounds, flavonoids, and glutathione were higher in $CM{\alpha}$ than that in CM. The major minerals of both materials were K, Ca, Mg, and Na. The major fatty acids of both materials were linolenic acid, linoleic acid, oleic acid, and palmitic acid. Fibrinolytic activity was higher in $CM{\alpha}$ than that in CM. These results may provide the basic data to understand the fibrinolytic activity and bioactive compounds of $CM{\alpha}$.

• Economic and Environmental Geology
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• v.10 no.1
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• pp.1-18
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• 1977

Chongyang tungsten ore deposits, one of the most important tungsten mines in South Korea, me open space filling hydrothermal vein deposits embedded in Precambrian biotite gneiss and, Cretaceous (?) granite porphyry. Some wolframite-bearing quartz veins are closely associated with -quartz porphyries which strike about $N15^{\circ}-25^{\circ}W$ and dip $800^{\circ}SE$ to vertical. Mineralization took place in near vertical vein systems of 5 to 2000 meter long in the biotite gneiss and granite porphyry stock during early Cretaceous and Tertiary (?) period. The hydrothermal mineral paragensis has indicated that there were two major stages: vein and vug stages. The principal vein mineral is wolframite in a gangue of quartz with small amount of fluorite, pyrite, beryl and carbonate minerals. Present in minor amounts are molybdenite, bithmuthinite, native bismuth, arsenopyrite, galena, chalcopyrite, pyrrhotite, sphalerite and scheelite. Fluid inclusion study from the minerls at Chongyang mine reveals that vein stage fluids attained a temperature range of $200^{\circ}C-355^{\circ}C$ and vug stage $160^{\circ}C-350^{\circ}C$. The filling temperatures show the higher range of $200^{\circ}-355^{\circ}C$ in quartz and $280^{\circ}C-348^{\circ}C$ in beryls, whereas the lower emperature range of $283^{\circ}C-295^{\circ}C$ in rhodochrosite and $160^{\circ}-253^{\circ}C$ in fluorites. These temperatures are in reasonably good agreement with mineral paragnesis in this ore deposits. Volfamite minerals were analysed for major components. $WO_3$, MnO and FeO by wet chemical method. Chemical analysis indicates that they contain 70.56-71.54% $WO_3$, 8.52-10.01% MnO and 10.00-11.58% FeO. MnO/FeO ratios of wolframites shows the range of 0.78-0.94 which maybe indicates a comparatively high temperature type of hydrothermal deposits.

• Journal of the Korean earth science society
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• v.23 no.1
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• pp.97-104
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• 2002

Mulgeum, Yangseong, Maeri and Kimhae iron ore deposits in Gyeongnam Province are hydrothermal skarn type magnetite ore deposits in propylitized andesitic rock near the contact with Cretaceous Masanite. Symmetrical zoned skarns are commonly developed around the magnetite veins. The skarn zones away from the vein are quartz-garnet skarn, epidote skarn and epidote-orthoclase skarn. Oxygen isotope analyses of coexisting minerals from andesitic rock, Masanite and major skarn zones, and of magnetite, hematite and quartz were conducted to provide the information on the formation temperature, the origin and the evolution of the hydrothermal solution forming the iron ore deposits. Becoming more distant from the ore vein, temperatures of skarn zones represent the decreasing tendency, but most ${\delta}^{18}O$ and ${\delta}^{18}O_{H2O}$ values of skarn minerals represent no variation trend, and also the values are relatively low. Judging from all the isotopic data from the ore deposits, the major source of hydrothermal solution altering the skarn zones and precipitating the ore bodies was magmatic water derived from the deep seated Masanite. This high temperature hydrothermal solution rising through the fissures of propylitized andesitic rock was mixed with some meteoric water, and occurred the extensive isotopic exchange with the propylitized andesitic rock, and formed the skarns. During these processes, the temperature and ${\delta}^{18}O_{H2O}$ value of hydrothermal solution were lowered gradually. At the main stage of iron ore precipitation, because all the alteration was already finished, the new rising hydrothermal solution formed only the magnetite ore without oxygen isotopic exchange with the wall rock.

• Atmosphere
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• v.25 no.4
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• pp.601-610
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• 2015

This study measured the emissivity spectra of 5 major rock-forming minerals using a Fourier Transform Infrared (FT-IR) spectrometer in the spectral region of $650{\sim}1400cm^{-1}$. The mineral samples are quartz, albite, bytownite, anorthite, and sandstone. We compared emissivity spectra measured in this study with spectra provided by Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) and Arizona State University (ASU). The spectral features of emissivity such as Reststrahlen Band (RB) and Christiansen Feature (CF) locations were compared. Results showed that both CF and RB locations of emissivity spectra measured in this study were similar to those from ASTER and ASU. In the case of quartz, the RB was occurred in the region of $700{\sim}850cm^{-1}$ and $1050{\sim}1250cm^{-1}$. The spectral position of emissivity peak was in good agreement with the location of ASTER and ASU. For plagioclase (albite, bytownite, and anorthite), the spectral location of CF was shifted toward larger wavenumber and the emissivity value was increased in the region of $870{\sim}1200cm^{-1}$ with Ca percentage. The CF of anorthite and bytownite was occurred at $1245.79cm^{-1}$, and that of albite was occurred at $1283.79cm^{-1}$. We also confirmed that emissivity feature of sandstone includes both emissivity features of quartz and calcite. However, there were some differences in the magnitude of emissivity and locations of RB and CF. These were due to the differences in measurement methods, and differences in particle size and temperature of samples.

• Food Science and Preservation
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• v.15 no.1
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• pp.79-83
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• 2008

This work measured the approximate levels of chemical components in the fleshpeel of unripe peaches picked at different times. The unripe samples were divided into two groups. Group I was picked on April 20 and Group II on May 2. Both samples were analyzed for organic acids, free sugars, Brix values, acidity, amino acids, and minerals. The major organic acid contents in Group I and Group II samples were oxalic acid> citric acid> malic acid> tartaric acid. The order of major free sugarin Group I and Group II samples were arabinose> sucrose in flesh and arabinose> glucose> sucrose in peel. The order of amino acid levels in all samples was aspartic acid> proline> glutamic acid> serine> leucine> lysine. The Brix values, acidity levels, and pH values of all samples were in the ranges of $7.6-9.8^{\circ}Brix$, 0.50-0.55 % and 4.13-4.17, respectively. The order of mineral content in all samples was K> Ca> Mg> Na.

• Journal of Soil and Groundwater Environment
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• v.16 no.1
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• pp.19-31
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• 2011

This study had been carried out to investigate spatial and temporal variations of the concentrations of trace metals for contaminated surface water in creek affected by leachate from the tailings impoundment of the Yeonhwa II mine for about 2 years. It was also to ascertain the metal removal efficiency for potentially deleterious metals by the artificial and natural attenuation processes such as retention ponds and hydrologic mixing of uncontaminated tributaries. The concentrations of As, Pb, Cd, and Cu for leachate in the rainy season were not detected. On the other hand, the concentrations of Zn, Fe, Mn, Al, and $SO_4^{2-}$ in the rainy season for leachate were 2-66 times higher than those in the dry season, due to the oxidation of the sulfide minerals and the dissolution of the secondary minerals. The concentrations of Zn and Cd for leachate and surface water of the upper creek in the rainy season exceeded the criteria of River Water Quality and Drinking Water Quality but in the dry season, those of analyzed all the metals (As, Pb, Cd, Cu, Zn, Cd, Fe, Mn, and Al) for surface water sampled at the study area were below the criteria of River Water Quality and Drinking Water Quality. In regard of the attenuation efficiency for the concentrations of metals, Fe, Mn, Al, Zn, Cd, As, and Cu were removed highly at retention ponds, while the removal efficiency for major cations and sulfate ($SO_4^{2-}$) were related to mixing of the uncontaminated tributaries. Therefore, the major attenuation processes of the metal and sulfate contents in creek affected by leachate from a tailing dump were precipitation (accompanied by metal co-precipitation and sorption), water dilution, and neutralization.