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RISS 인기검색어
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- 저자 : Seon yu Choi(崔善奎) (검색결과 2 건)
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Gold-Silver Mineralization of the Geojae Area
최선규,지세정,윤성택,고용권,유재신,Choi, Seon-Gyu,Chi, Se-Jung,Yun, Seong-Taek,Koh, Yong-Kwon,Yu, Jae-Shin The Korean Society of Economic and Environmental G 1989 자원환경지질 Vol.22 No.4
경남거제지역 금(金)-은광상(銀鑛床)들은 후기 백악기 안산암류와 화강섬록암(83 m.y.)내의 열극을 충진한 함금(含金)-은(銀) 열수맥상(熱水脈狀) 광체로 구성된다. 열수광화작용(熱水鑛化作用)은 구조운동에 의하여 시기적으로 3회에 걸쳐 진행되었다. 초기 제$370^{\circ}C$의 고온에서 후기 $200^{\circ}C$에 이르는 제 I, II 광화기(鑛化期)에서는 각기 상이한 열수계(熱水系)에 의하여 석영, 유화물이 침전하였으며, $320^{\circ}C$를 전후로 하여 광화류체(鑛化流體)의 비담(沸膽)현상이 일어났다. 제 I, II 광화작용(鑛化作用)시의 압력은 <100기압이고, 심도는 500~1,250m였다. 금(金)-은(銀)의 주광화시기(主鑛化時期)인 광화(鑛化) I 기(期)의 공생광물에 대한 유체포유물(流體包有物) 및 광물열수학적(鑛物熱水學的) 연구에 의하면, 황철석, 섬아연석, 황동석은 $290^{\circ}C$ 이상의 고온에서 비담작용(沸膽作用)과 동시에 정출하였고, 사면동석, 에렉트렘, 스튜자이트는 금(金)-유황종(硫黃種)의 농도가 $10^{-3}{\sim}10^{-4}$molal, 상당염농도(相當鹽濃度)가 2~6wt.% NaCl인 광화유체(鑛化流體)로부터 $220{\sim}260^{\circ}C$, 유황 및 산소분압이 각각 $10^{-11.8}{\sim}10^{-14}$, $10^{-35}{\sim}10^{-36}$ atm인 물리 화학적 환경하에서 침전하였다. 균질화(均質化) 온도와 염농도(相當鹽濃度)와의 관계는 천수류입(天水流入)에 의한 광화류체(鑛化流體)의 냉각(冷却) 및 희석(稀釋)작용이 광석광물 침전의 주된 메키니즘이었음을 지시해 주며, 유체내(流體內) 환원(還元) 유황종(硫黃種)($H_2S$)의 감소에 따른 금류화복합체(金硫化複合體)($Au(HS)_2$) 의 파괴로 금(金)의 침전이 유도되었으리라 사료된다. 유황 및 탄소, 산소 안정동위원소(安定同位元素) 연구(硏究)결과, 광화류체내(鑛化流體內)의 유황 및 탄소는 심부화성(深部火成)기원이었고, 방해석의 산소 안정동위원소(安定同位元素)값으로부터 열수계(熱水系)에서 천수(天水)가 지배적인 역할을 하였으리라 사료된다. The electrum-silver-sulfide mineralization of the Geojae island area was deposited in three stages (I, II, and carbonate) of quartz and calcite veins that crosscut Late Cretaceous volcanic rocks and granodiorite(83 m.y.). Stages I and II were terminated by the onset of fractunng and breCCIation events. Fluid inclusion data suggest that the gold-sulfide-bearing stages I and II each evolved from an initial high temperature( near $370^{\circ}C$) to a later low temperature(near $200^{\circ}C$). Each of those stages represented a separate mineralizing system which cooled prior to the onset of the next stage. The relationship between homogenization temperature and salinity in stages I and II suggests a complex history of boiling, cooling and dilution. Evidence of boiling indicates a pressure of < 100 bars, corresponding to a depth of 500 to 1,250m assummg hthostatlc and hydrostatic pressure regimes, respectively. Fluid inclusion and mineralogical evidence suggest that the electrum-silver mineralization was deposited at a temperature of $220-260^{\circ}C$ from ore fluids with salinities between 1.9 and 8.1 equivalent wt.% NaCl. Total sulfur concentration is estimated to be $10^{-3}$ to $10^{-4}$ molal. The estimated $fs_2$ and $fo_2$ range from $10^{-11.8}$ to $10^{-14}$ atm and $10^{-35}$ to $10^{-36}$ atm, respectively. The chemical conditions indicate that the dominant sulfur species in the ore forming fluids was a reduced form($H_2S$). Rapid cooling and dilution of ore-forming fluids by mixing with less-evolved meteoric waters led to gold-silver deposition through the breakdown of the bisulfide complex($Au(HS)_2$) as the activity of $H_2S$ decreased.
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Seon yu Choi(崔善奎),Jae Ill Chung(鄭在一),Naoya Imai(今井直哉) 대한자원환경지질학회 1986 자원환경지질 Vol.19 No.3
蔚山의 철ㆍ중석 스카른광상에서 산출되는 硫砒鐵石은 그의 産出狀態ㆍ鑛物共生關係ㆍ化學組成을 근거로 세 가지 유형으로 구분된다. 硫砒鐵石 I 은 多金屬鑛化作用 초기에 정출된 것으로 주로 스카른대 내에서 산점상으로 분포하며, Ni-Fe-Co계 유화물과 밀접한 공생관계를 보여준다. 硫砒鐵石 I 의 화학조성은 Ni, Co의 함량이 현저하게 높고 As/S(原子比)>1으로 過剩의 비소를 함유한다. 硫砒鐵石 II는 Cu 또는 As 광석중에서 산출되며, 비독사석 휘창연석 비스무스 황동석 섬아연석과 밀접한 공생관계를 보여준다. 硫砒鐵石 II의 화학조성은 Ni, Co의 함량이 극히 미량이며, As/S>1으로 과잉(過剩)의 비소를 함유한다. 硫砒鐵石 III은 최후기 열수광맥 형성시기에 정출되었으며, 황철석 방연석 섬아연석 자류철석과 밀접한 共生關係를 보여준다. 硫砒鐵石 III의 化學組成은 As/S≦1로 過剩의 S를 함유한다. 硫砒鐵石 I 은 Ni, Co의 함유량이 1%이상이므로 地質溫度計로 사용할 수 없지만, 硫砒鐵石 II 는 비스무스-휘창연석의 共生關係를 보여 주고 있으므로, 이를 Kretschmar and Scott (1976)에 의한 1/T-f(S₂)도에 적용시켜보면 硫砒鐵石 II의 정출환경은 T=460~470℃, log f(S₂)=-7.4~7.0이고, 硫砒鐵石 III의 정출환경은 T=320~440℃, log f(S₂)=-9.0~7.0으로 추정된다. Arsenopyrite in arsenic and polymetallic ores from calcic Fe-W skarn deposit of the Ulsan mine, Republic of Korea, has been investigated by means of electron microprobe analysis and X-ray diffractometry. As a result, it is revealed that the Ulsan arsenopyrite may be classified into the following three species with different generation on the basis of its mode of occurrence, chronological order during polymetallic mineralization and chemical composition; arsenopyrites I, II and III. 1) Arsenopyrite I-(Ni, Co)-bearing species belonging to the oldest generation, which has crystallized together with (Ni, Co)-arsenides and -sulpharsenides in the early stage of polymetallic mineralization. In rare cases, it contains a negligible amount of antimony. It occurs usually as discrete grains with irregular outline, showing rarely subhedral form, and is diffused in skarn zone. The maximum contents of nickel and cobalt are 10.04 Ni and 2.45 Co (in weight percent). Occasionally, it shows compositional zoning with narrow rim of lower (Ni+Co) content. 2) Arsenopyrite II-arsenian species, in which (Ni+Co) content is almost negligible, may occur widely in arsenic ores, and its crystallization has followed that of arsenopyrite I. It usually shows subhedral to euhedral form and is closely associated with löllingite, bismuth, bismuthinite, chalcopyrite, sphalerite, bismuthian tennantite, etc. It is worthy of note that arsenopyrite II occasionally contains particles consisting of both bismuth and bismuthinite. 3) Arsenopyrite III-(Ni, Co)-free, S-excess and As-deficient species is close to the stoichiometric composition, FeAsS. It occurs in late hydrothermal veins, which cut clearly the Fe-W ore pipe and the surrounding skarn zone. It shows euhedral to subhedral form, being extremely coarse-grained, and is closely associated with pyrite, “primary” monoclinic pyrrhotite, galena, sphalerite, etc. Among three species of the Ulsan arsenopyrite, arsenopyrite I does not serve as a geothermometer, because (Ni+Co) content always exceeds 1 weight percent. In spite of the absence of Fe-S minerals as sulphur-buffer assemblage, the presence of Bi(l)-Bi₂S₃ sulphur-buffer enables arsenopyrite II to apply successfully to the estimation of either temperature and sulphur fugacity, the results are, T=460~470℃, and log f(S₂)=-7.4~7.0. With reference to arsenopyrite III, only arsenopyrite coexisting with pyrite and “primary” monoclinic pyrrhotite may serve to restrict the range of both temperature and sulphur fugacity, T=320~440℃, log f(S₂)=-9.0~7.0. These temperature data are consistent with those obtained by fluid inclusion geothermometry on late grandite garnet somewhat earlier than arsenopyrite II. At the beginning of this paper, the geological environments of the ore formation at Ulsan are considered from regional and local geologic settings, and physicochemical conditions are suspected, in particular the formation pressure (lithostatic pressure) is assumed to be 0.5kb (50MPa). The present study on arsenopyrite geothermometry, however, does not bring about any contradictions against the above premises. Thus, the following genetical view on the Ulsan ore deposit previously advocated by two of the present authors (Choi and Imai) becomes more evident; the ore deposit was formed at shallow depth and relatively high-temperature with steep geothermal gradient-xenothermal conditions.
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