• Proceedings of the Mineralogical Society of Korea Conference
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• 2001.06a
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• pp.75-75
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• 2001

We report Sr, Nd and Pb isotope data of clinopyroxene separates from ultramafic xenoliths and their host basaltic rocks in Jeju Island, Baekryeong Island, Boeun and Ganseong, Korea. The isotopic data of the xenoliths and host basalts are distinctly different from those of Korean basement rocks. Except for two xenoliths from Ganseong, all samples in this study have isotopic ratios within the combined range of MORB-OIB data. All basaltic rocks have Nd-Sr-Pb isotope compositions different from those of xenoliths, indicating that the host basaltic magma did not derive from the lithospheric mantle where the xenoliths originated. The range of isotopic composition of xenoliths is much greater than that observed in host basalts, which reflects small-scale heterogeneity of the lithospheric mantle. The greater isotopic heterogeneity of the lithospheric mantle probably reflects its long-term stability. The spinel peridotite xenolith data of Jeju Island, Baekryeong Island and Boeun display mixing hyperbolas between DMM and EM II end members. Since Jeju basalts have EM II-like isotopic signature, the mixing relationship shown by the isotopic data of the Jeju xenoliths can be interpreted as the result of infiltration of metasomatic fluid or melt derived from basaltic magma into DMM-like lithospheric mantle. In contrast to other xenolith sites, the Ganseong xenoliths are dominantly clinopyroxene megacryst and pyroxenite. Clinopyroxene megacrysts have different isotopic ratios from their host basalt, reflecting its exotic origin. Two Ganseong xenoliths (wherlite and clinopyroxenite) have much enriched Sr and Nd isotopic ratios and Nd model ages of 2.5-2.9 Ga, and plot in an array away from the MORB-OIB field. The mantle xenoliths from Korean Peninsula have similar $\^$87/Sr/$\^$86/Sr,$\^$143/Nd/$\^$144/Nd and $\^$207/Pb/$\^$204/Pb ratios to, but higher $\^$208/Pb/$\^$204/Pb ratios than, those from eastern China, indicating that Korean xenoliths are derived from the lithospheric mantle with higher Th/U ratio compared with Chinese ones. The isotopic data of xenolith-bearing basalts of Baekryeong Island and Ganseong, along with Ulreung and Dok Islands, show a mixing trend betlveen DMM and EM I in Sr-Nd-Pb isotopic correlation diagrams, which is also observed in tile northeastern Chinese basalts. However, the Jeju volcanic rocks show an EM II signature that is observed in southeastern Chinese basalts. The isotopic variations in volcanic rocks from the northern and southern portions of the East Asia reflect a large-scale isotopic heterogeneity in their source mantle.

• Economic and Environmental Geology
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• v.19 no.spc
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• pp.193-206
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• 1986

A number of auriferous veins occur in the Precambrian metamorphic terrain from Chungju to Mugeug district. These gold (-silver) deposits consist mainly of the fissure-filling quartz veins intruding the Precambrian gneiss or schist and Jurassic or Cretaceous granite. These gold (-silver) deposits can be 'divided into two mineralization epochs, (a) gold-rich veins related to Daebo igneous activity, and (b) gold-silver veins related to Bulgugsa igneous activity. These two groups of ore deposits with different generation can be characterized by the mode of occurrence of ore vein and the ore mineral associations. The auriferous quartz veins of Taechang and Boryeon mines associated with late Jurassic igneous activity are massive in character, and show the simple mineral assemblages and low Ag/Au ratio in the ores, representing a single mineralization system. The ore minerals are predominantly quartz containing minor or trace amonts of pyrrhotite, sphalerite, galena, pyrite, chalcopyrite and electrum. Electrum is closely associated with pyrrhotite and has chemical compositions from 61.4 to 78.5 atomic % Au. Fluid inclusion data suggest that ore minerals were deposited at temperatures between 238 and $390^{\circ}C$ from $CO_2$-rich fluids. The gold and/or silver-bearing quartz veins of Geumwang mine related to middle Cretaceous igneous activity are characterized by the multistage history, diverse mineral assemblages with high Ag/Au ratio in the ores. The ores of Geumwang mine have two contrasting mineral assemblages (1) pyrite+galena+sphalerite+arsenopyrite+electrum+argentite, representing the higher gold mineralization, and (2) pyrite+chalcopyrite+ galena +sphalerite+ arsenopyrite+silver sulfosalts+ electrum+ native silver+argentite, representing the higher silver mineralization. Electrum is closely associated with pyrite and has chemical compositions from 11.2 to 49.9 atomic % Au. The depositional environment during the higher gold mineralization can be estimated as the range of both temperature and sulfur fugacity, T= $200{\sim}300^{\circ}C$, log f ($S_2$) = $10^{-10}{\sim}10^{-15}$. The higher silver mineralization may be interpreted to have formed a range of falling temperature ($150{\sim}200^{\circ}C$) and low sulfur fugacity($10^{-10}{\sim}10^{-15}$). These temperature data are consistent with homogenization temperatures of fluId inclusions in quartz. Thus, the gold veins related to the Daebo igneous activity may be formed by the environment of higher temperature and pressure than the gold-silver veins associated with the Bulgugsa igneous activity.

• Economic and Environmental Geology
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• v.21 no.4
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• pp.367-380
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• 1988

Most of the gold (-silver) vein deposits at Yeongdong District are mainly distributed in the precambrian metamorphic rocks. Based on the Ag/Au total production and ore grade ratios, the chemical composition of electrum and the associated sulfides, the gold(-silver) deposits at Yeongdong District may be classified into 4 classes: pyrrhotite - type gold deposits( I), pyrite - type gold deposits (IT A; massive vein), pyrite - type gold deposits (II B; nonmassive vein) and argentite - type gold - silver deposits(III). The chemical study on electrum(including native gold) revealed that Au content (2.8 to 92.4 atomic%) of electrums varies very widely for different classes of deposits. The Au content of electrum associated with pyrrhotite (Class I), ranging from 47.1 to 92.4 atomic% Au, is clearly higher than that associated with pyrite (Classes IIA, IIB and III). In contrast, classes I, II, and III deposits do not show clear differences in Au content of electrum. In general, pyrrhotite - type gold deposits(I) are characterized by features such as simply massive vein morphology, low values in the Ag/Au total production and ore grade ratios, the absence or rarity of silver - bearing minerals except electrum, and distinctively simple mineralogy. Although the geological and mineralogical features and vein morphology of pyrite - type gold deposits(IIA)are very similar to those of pyrrhotite - type gold deposits (I), Class II A deposits reveal significant differences in the associated iron sulfide (i. e. pyrite) with electrum and Au content of electrum. The Ag/Au total production and ore grade ratios from Class II A deposits are relatively slightly higher than those from Class I deposits. Pyrite - type gold deposits(II B) and argentite - type gold - silver deposits (III) have many common features; complex vein morphology, medium to high values in the Ag/Au total production and ore grade ratios and the associated iron sulfide (i. e. pyrite). In contrast to Class II B deposits, Class III deposits have significantly high Ag/Au total production and ore grade ratios. It indicates distinct difference in the abundance of silver minerals (i. e. native silver and argentite). The fluid inclusion analyses and mineralogical data of electrum tarnish method indicate that the gold mineralization of Classes I and II A deposits was deposited at temperatures between $230^{\circ}$ and $370^{\circ}C$, whereas the gold (-silver) mineralization of Classes ITB and ill formed from the temperature range of $150^{\circ}-290^{\circ}C$. Therefore, Classes I and IT A deposits have been formed at higher temperature condition and/or deeper positions than Classes IIB and III.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2004.04a
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• pp.473-476
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• 2004

In this study, hydrochemical studies of thermal waters in the Bugok and Magumsan areas showing geothermal anomalies were carried, and the applicability of ion seothermometers and multiple mineral equilibrium approach was examined to estimate their potential deep reservoir temperatures. Typical thermal waters of the two areas are clearly grouped into two major types, according to water chemistry: Na-Cl type (group A) and Na-SO4 type (group D). Compared to group A, group B and C waters show some modifications in chemistry. Group E waters show the modified chemistry from group D. Geothermal waters from the two areas showed some different chemical characteristics. The thermal waters of group A and B in Magumsan area are typically neutral to alkaline (pH=6.7 to 8.1) and Cl-rich (up to 446.1 mg/L), while the waters of group D and E in Bugok area are alkaline (pH=7.6 to 10.0) and SO$_4$-rich (up to 188.0 mg/L). The group A (Na-Cl type) and group D (Na-SO$_4$ type) waters correspond to mature or partially immature water, whereas the other types are immature water. The genesis of geothermal waters are considered as follows: group A and B waters were formed by seawater infiltration into reservoir rocks along faults and fracture zones and possibly affected by fossil connate waters in lithologic units through which deep hot waters circulate; on the other hand, group D and E waters were formed by the oxidation of sulfide minerals (mainly pyrite) in surrounding sedimentary rocks and/or hydrothermal veins occurring along restricted fracture channels and were possibly affected by the input and subsequent oxidation of S-bearing gases (e.g. H2S) from deep thermal reservoir (probably, cooling pluton). The application of quartz, Na-K, K-Mg geothermometers to the chemistry of representative group A and D waters yielded a reasonable temperature estimate (99-147$^{\circ}C$ and 90-142$^{\circ}C$) for deep geothermal reservoir. Aqueous liquid-rich fluid inclusions in fracture calcites obtained from drillcores in Bugok area have an average homogenization temperature of 128$^{\circ}C$, which corresponds to the results from ion geothermometers. The multiple mineral equilibrium approach yielded a similar temperature estimate (105-135$^{\circ}C$ and 100-14$0^{\circ}C$). We consider that deep reservoir temperatures of thermal waters in the Magumsan and Bugok areas can be estimated by the chemistry of typical Na-Cl and Na-SO$_4$ type waters and possibly approach 105-135$^{\circ}C$ and 100-14$0^{\circ}C$.

• Journal of the Korea Academia-Industrial cooperation Society
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• v.18 no.1
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• pp.545-552
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• 2017

Ground subsidence can result in the formation of sinkholes, potholes, settlement of structures, and road subsidence. Road subsidence is described as the sudden collapse of the road surface into subsurface cavities caused by the loss of bearing capacity in the ground, such as the dissolution of limestone by fluid flow in the surface causing the formation of voids leading to subsidence at the surface. Road subsidence occurs about 665 times annually, and this incidence has been increasing until 2013. Damaged underground facilities, management negligence, and lowering of the ground water table have been the causes of road subsidence in Seoul. Seoul metropolitan government announced special management counter plans to relieve the anxieties and make the roads safe for passing. Construction sites, such as excavation works, need to be managed properly because they have strong potential to induce road subsidence. The aim of this study was to identify the main causes of road subsidence and suggest management plans. First, life cycle cost analysis revealed the daytime construction to be more appropriate than nighttime. In addition, by analyzing the limitations of using sand as a backfill material, it is proposed to use a flowable backfill material instead of sand. Finally, to reduce the blind spots, which is a problem in surveying the road pavement conditions of local governments, the road to be managed is divided into several zones, and a specialized agency is selected for each zone and a method of surveying the blind spots through collaboration is suggested.

• Geophysics and Geophysical Exploration
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• v.10 no.1
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• pp.37-43
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• 2007

The MH21 Research Consortium has conducted a high-resolution 3D seismic survey and a seafloor geochemical survey, to explore methane hydrate reservoirs in the eastern Nankai Trough, offshore Japan. Excellent geological information about shallow formations was obtained from the high-resolution 3D seismic survey, which was designed to image the shallow formations where methane hydrates exist. The information is useful in constructing a geological and geochemical model, and especially to understand the complex geology of seafloor, including geochemical manifestations and the structure of migration conduits for methane gas or methane-bearing fluid. By comparing methane seep sites observed by submersibles with seismic sections, some significant relationships between methane hydrate reservoirs, free gas accumulations below the seafloor, and seafloor manifestations are recognised. Bathymetric charts and seafloor reflection amplitude maps, constructed from seismic reflections from the seafloor, are also useful in understanding the relationships over a vast area. A new geochemical seafloor survey targeted by these maps is required. The relationships between methane hydrate reservoirs and seafloor manifestations are becoming clearer from interpretation of high-resolution 3D seismic data. The MH21 Research Consortium will continue to conduct seafloor geochemical surveys based on the geological and geochemical model constructed from high-resolution 3D seismic data analysis. In this paper, we introduce a basis for exploration of methane hydrate reservoirs in Japan by fusion of 3D seismic exploration and seafloor geochemical surveys.

• Economic and Environmental Geology
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• v.30 no.2
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• pp.81-87
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• 1997

Chonnam and Kyongsang clay alteration areas are distributed in volcanic fields of the Yuchon Group in late Cretaceous period. The host rock of the Chonnam alteration area is generally acidic and that of the Kyongsang alteration area is acidic to dominantly intermediate volcanics. The important difference of two alteration areas is source of fluid; the Chonnam alteration area is characterized by dominantly meteoric water and the Kyongsang alteration area is characterized by dominantly magmatic water. Accordingly, the high temperature minerals such as pyrophyllite and andalusite, and boron bearing minerals such as dumortierite and tourmaline are common in the Kyongsang alteration area. In contrast to this, the lower temperature minerals such as kaolin and alunite are common in the Chonnam alteration area. The mineralogical difference of two alteration areas were depended on the difference of the formation temperature of clay deposits. The other important geochemical difference is the chemistry of hydrothermal solution such as pH. The alteration of "acid-sulfate type" with alteration mineral assemblage of alunite-kaolin-quartz is dominant in the Chonnam alteration area, which was caused by the attack of strong acid and acid solution. In contrast to this, the that of "quartz-sericite type" with the mineral assemblage of sericite-quartz is dominant in the Kyongsang alteration area, which was caused by the attack of neutral or weak acid solution. Also, the Kyongsang and Chonnam alteration areas show the difference in structural setting; the Chonnam alteration area is commonly associated with silicic domes and the Kyongsang alteration area is commonly associated with calderas.

• Journal of the Mineralogical Society of Korea
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• v.17 no.2
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• pp.135-145
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• 2004

A zeolitic bentonite, which exhibits whitish appearance and contains considerable amounts (nearly 〉 5%) of zeolites, frequently occurs as thin beds less than 1 m in Yeongil area. The bentonites are mostly found in closely association with zeolite beds in the Nuldaeri Tuff and Coal-bearing formations of the Janggi Croup. A discordant occurrence of the bentonite against the bedding plane is also locally found. Montmorillonite, the major mineral constituent of the bentonite, is mostly associated with clinoptilolite as a zeolite. However, instead of clinoptilolite, mordenite is sometimes included in the case of more silicic bentonite, and heulandite in the less silicic one. It is characteristic that the mordenite is accompanied by lots of opal-CT in the silicic bentonite. SEM observations characteristically indicate that these authigenic phases, especially the montmorillonite and zeolite, nearly coexist as mixtures not forming a fine-scale zoning. The zeolitic bentonite seems to be formed in the comparatively silicic pore fluid at the alkaline condition accompanying pH fluctuation Compared to the zeolite-free normal bentonite, the zeolitic types exhibit somewhat higher REE abundance. These chemical characteristics, together with modes of occurrences and authigenic mineral associations, may suggest that the zeolitic bentonite is not merely diagenetic products and a possible hydrothermal alteration could not be excluded in the bentonite genesis.

• Economic and Environmental Geology
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• v.26 no.1
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• pp.41-54
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• 1993

The Ulsan Fe-W deposit, which can be classified as a calcareous skarn deposit, is represented by ore pipe consisting principally of magnetite and lesser amounts of scheelite with minor sulphides, sulphosaits, arsenides, sulpharsenides, etc. At Ulsan mine, metasomatic processes of skarn growth may be divided broadly into two stages based on the paragenetic sequence of calc-silicate minerals and their chemical composition; early and late skarn stages. Early stage has started with the formation of highly calcic assemblages of wollastonite, diopsidic clinopyroxene and nearly pure grossular, which are followed by the formation of clinopyroxenes with salite to ferrosalite composition and grandite garnets with intermediate composition. Based on these calc-silicate assemblages, the temperatures of early skarn formations have been in the ranges of $550^{\circ}$ to $450^{\circ}$. The calc-silicate assemblages formed during the earlier half period of late skarn stage show the enrichment of notable iron and slight manganese, and the depletion of magnesium; clinopyroxenes are hedenbergitic, and grandite garnets are andraditic. The formation temperatures during this skarn stage are inferred to have been in the range of $430^{\circ}$ to $470^{\circ}C$ at low $X_{CO_2}$ by data from fluid inclusions of late andraditic garnets. The later half period of late skarn stage is characterized by the hydrous alteration of pre-existing minerals and the formation of hydrous silicates. The main iron-tungsten mineralization representing prominent deposition of magnetite immediately followed by minor scheelite impregnation has taken place at the middle of early skarn stage, while complex polymetallic mineralization has proceeded during and after the late skarn stage. Various metals and semimetals of Fe, Ni, Co, Cu, Zn, As, Mo, Ag, In, Sn, Sb, Te, Pb and Bi have been in various states such as native metal, sulphides, arsenides, sulphosaits, sulpharsenides and tellurides.

• Journal of Energy Engineering
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• v.26 no.3
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• pp.131-136
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• 2017

Automobile engine oil is the most important lubricant for operating as the engine is started. Recently, manufacturers of the automotive industry and lubricants are considerably improving the quality of oil with additive to extend change cycle period. Most customers are recommended genuine oil among different types from shop expert. Through this report we suggest another reference point for consumer to pick highly efficient lubricant. This report is investigated oil compounds to compare with 6 different automotive considering actual running condition for 7 months. we conducted experiment from physical and chemical perspectives. In the field, through various experiments oil compounds between mineral oil and synthetic oil are largely distinguished in oxidation, viscosity, fluid and TBN. These are influenced by engine part wear as piston, bearing etc. Comparing various investigation with different oil the performance of synthetic oil is shown better condition in flash point, oxidation stability and also found less in change pollutant iron, Al compounds. Additives of oil show clear difference Ca level in detergent-dispersant both mineral oil and synthetic oil. And Zn in extreme pressure additives and P in Lubricity improver make no difference to both.