• Title/Summary/Keyword: 일라이트-스멕타이트

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감포와 연일 지역 벤토나이트 내 일라이트-스멕타이트 혼합층광물의 팽창성 및 X-선 부합성산란영역크기에 관한 연구

  • 강일모;문희수;유장한
    • Proceedings of the KSEEG Conference
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    • 2003.04a
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    • pp.325-329
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    • 2003
  • 일반적으로 스멕타이트는 온도, 시간, 공극수 내 K 함량 등이 증가하면서 일라이트화 작용을 통하여 일라이트-스멕타이트 혼합층광물(I-S)로 전이된다. 따라서, 벤토나이트(주로 스멕타이트질 광물로 구성된 화산쇄설물의 변질산물)는 지질환경에 따라 스멕타이트 또는 다양한 혼합층비를 갖는 I-S를 함유하게 된다. 이러한 벤토나이트 내 스멕타이트와 일라이트의 혼합층비는 팽창성(expandability)으로 정량화할 수 있다. (중략)

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Mineralogy of Illite/smectite Mixed-Layer Clays from the Beaufort-Mackenzie Basin, Arctic Canada (카나다 보포트-맥켄지 분지의 일라이트/스멕타이트 혼합층 점토광물 연구)

  • Ko, Jaehong;Hesse, R.
    • Economic and Environmental Geology
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    • v.28 no.4
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    • pp.327-335
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    • 1995
  • Illite/smectite (I/S) in the Beaufort-Mackenzie Basin, Arctic Canada has been scrutinized on the basis of mineralogical analysis of 215 core and drill-cutting samples from 22 exploratory wells onshore and offshore. I/S in the Beaufort-Mackenzie Basin includes the following four types: random, a mixture of random and ordered, R1-ordered, and R>1-ordered I/S. A mixture of random and ordered I/S occurs in the transitional interval between random and R>1-ordered I/S, and may represent a metastable state in the ordering reaction. A widespread occurrence of the mixture in natural environments suggests that the ordering reaction may be a slow process that results in co-existence of reactants and products. K-saturation experiments show that layer charges of expandable layers in I/S are variable. High-charge expandable layers transform into illite-like layers upon simple K-saturation. K-saturation alters the composition and/or the degree of ordering in I/S, suggesting that illitization in nature can be transformational.

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Mineral Temperatures of the Sedimentary Basins for Petroleum Resources Exploration, Korea (국내 석유자원탐사 퇴적분자의 광물온도)

  • Son, Byeong-Kook
    • Journal of the Mineralogical Society of Korea
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    • v.24 no.3
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    • pp.165-178
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    • 2011
  • The potential of petroleum generation was investigated by clay mineralogical changes of illite-smectite on the sedimentary basins: Tertiary Pohang basin and Cretaceouls Gyeongsang basin on land, and offshore basins east and west of Korea. Only disordered illite-smectite mixed layer minerals occur in the Pohang sediment, where petroleum generation cannot be expected due to low temperatures below $100^{\circ}C$. By contrast, the Gyeongsang basin is characterized by the occurrence of illite and high temperatures above $200^{\circ}C$ which are obtained by illite crystallinity. The high temperatures indicate that the Gyeongsang sediment ha, already passed through the oil generation stage. The change of disordered illite-smectite to R-l ordered illite-smectite is shown in the sediment of the East Sea continental shelf area at a depth of 2,500 m. Therefore, the oil generation can be expected in the sediments below the depth of 2,500 m. The sequential change of disordered illite-smectie to R=3 ordered illite-smectite through R=l ordered illite-smectite occurs in the sediments of West Sea continental shelf area with burial depth which shows the favorable condition for oil and gas generation. The temperatures of sediments measured by illite-smectite indicate that hydrocarbon potential is very low in the onland basins but high in the continental shelf areas.

Burial Diagenesis of Smectite in the Tertiary Marine Basin, Japan (일본 제3기 해성 퇴적분지에서의 스멕타이트 매몰 속성작용)

  • Son, Byeong-Kook
    • Journal of the Mineralogical Society of Korea
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    • v.19 no.4 s.50
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    • pp.221-229
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    • 2006
  • Mineralogical and chemical examinations were performed on interstratified illite-smectite (I-S) minerals that occur in the mudstones from a petroleum exploration well in the Tertiary marine basin, Japan. X-ray diffraction analysis shows that component layers of illite in the interstratified I-S increase with increasing burial depth while those of smectie decrease. In addition, the randomly (R=0) interstratified illite-smectite is changed into Rp1 ordered I-S at a depth of about 4,000 m, which corresponds to the result of organic analysis and indicates a burial temperature of about $100^{\circ}C$. However, the present geothermal gradient shows that the conversion of the random I-S to R=0 ordered I-S is likely to occur at 3,000 m. This discrepancy may be interpreted by the reverse fault at 2,500 m which resulted in a deeper burial of sediments up to 1,000 m. Chemical analysis also shows the compositional variation in I-S with increasing depth: a decrease in Si and an increases in Al and K, indicating that the substitution of Al for Si in tetrahedral sheets is compensated by the addition of K to interlayers. K may be derived from K-feldspar and micas, which is present in the mudstones.

Review of Microbially Mediated Smectite-illite Reaction (생지화학적 스멕타이트-일라이트 반응에 관한 고찰)

  • Kim, Jin-Wook
    • Economic and Environmental Geology
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    • v.42 no.5
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    • pp.395-401
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    • 2009
  • The smectite-illite (SI) reaction is a ubiquitous process in siliciclastic sedimentary environments. For the last 4 decades the importance of smectite to illite (S-I) reaction was described in research papers and reports, as the degree of the (S-I) reaction, termed "smectite illitization", is linked to the exploration of hydrocarbons, and geochemical/petrophysical indicators. The S-I transformation has been thought that the reaction, explained either by layer-by-layer mechanism in the solid state or dissolution/reprecipitation process, was entirely abiotic and to require burial, heat, and time to proceed, however few studies have taken into account the bacterial activity. Recent laboratory studies showed evidence suggesting that the structural ferric iron (Fe(III)) in clay minerals can be reduced by microbial activity and the role of microorganisms is to link organic matter oxidation to metal reduction, resulting in the S-I transformation. In abiotic systems, elevated temperatures are typically used in laboratory experiments to accelerate the smectite to illite reaction in order to compensate for a long geological time in nature. However, in biotic systems, bacteria may catalyze the reaction and elevated temperature or prolonged time may not be necessary. Despite the important role of microbe in S-I reaction, factors that control the reaction mechanism are not clearly addressed yet. This paper, therefore, overviews the current status of microbially mediated smectite-to-illite reaction studies and characterization techniques.

Minerals in the Core Sediments from the KONOD-1 Area;Northeastern Equatorial Pacific (북동 태평양 적도대 KONOD-1지역 코아 퇴적물 중의 광물에 대한 연구)

  • 한상준;정갑식
    • 한국해양학회지
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    • v.22 no.3
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    • pp.119-129
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    • 1987
  • Sediments in the cores from the KONOD-1 area consist mainly of authigenic smectite and clinoptilolite, and terrigenous minerals of illite, chlorite, kaolinite, quartz, and plagioclase. The authigenic minerals become dominant over the terrigenous minerals with increasing depth. Clinoptilolite occurs at the deeper core depth because its formation is slower than that of smectite. The vertical distribution of minerals indicates that the eolian influence, probably in the late Oligocene, diluted the abundance if smectite in near-surface sediments. This vertical distribution pattern may also have been affected by progressive dissolution of authigenic minerals in the near surface sediments.

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Major, Trace and Rare Earth Element Geochemistry, and Oxygen-Isotope Systematics of Illite/smectite in the Reindeer D-27 Well, Beaufort-Mackenzie Basin, Arctic Canada (카나다 보포트-맥켄지 분지의 일라이트/스멕타이트의 원소 지화학 및 산소동위원소 연구)

  • Ko, J.;Hesse, R.;Longstaffe, F.J.
    • Economic and Environmental Geology
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    • v.28 no.4
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    • pp.351-367
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    • 1995
  • The elemental geochemistry and oxygen isotopes of illite/smectite (I/S) have been studied in relationship to the mineralogical trend in the Reindeer D-27 well, Beaufort-Mackenzie Basin. The increase in concentrations of $K_2O$, Rb and rare earth elements (REE), the decrease in concentrations of tetrahedral elements such as Mg, Ti, Sc, Zn and Zr, and the increase in concentrations of tetrahedral elements such as Be and V can be related to I/S compositions that vary systematically with depth. Layer formulae of S- and I-layers are estimated as $[Al_{1.57}Fe_{.19}Mg_{.31}Ti_{.07}][Si_{3.84}Al_{.16}]O_{10}(OH)_2$ and $[Al_{1.84}Mg_{.16}][Si_{3.33}Al_{.67}]O_{10}(OH)_2$, respectively. The mobilization of REE appears to occur during illitization. The increase in concentrations of REE, especially La and Ce, with depth is probably linked to incorporation of ions with high valency (e.g. $V^{5+}$) in tetrahedral sites. The excess valency due to V is partly counter-balanced by ions with low valency (e.g. $Be^{2+}$) and, in turn, the local valency deficiency caused by $Be^{2+}$ could be compensated by high-charge interlayer cations such as REE (+3). ${\delta}^{18}O$ values of I/S range from 2.91 to 15.72‰ (SMOW), and increase with depth, contrasting to trends observed in the Gulf Coast and elsewhere. The increase in ${\delta}^{18}O$ of I/S results from the rapid increase in ${\delta}^{18}O$ of pore water that overcomes the decrease in temperature-dependent fractionation values with increasing burial depth (${\delta}^{18}O_{pore\;water}>-d{\Delta}/_{I/S-water};\;d{\delta}^{18}O_{I/S}>0$). Calculated ${\delta}^{18}O$ values of pore water in equilibrium with I/S suggest that the original water was probably meteoric water. The stratification of pore water is postulated from the presence of an isotopically light interval, about 450m thick. The depth range of the isotopically light zone overlaps, but does not coincide with the interval of lowered I-content and $K_2O$ concentrations, suggesting that oxygens may have been exchanged independently of mineralogical and geochemical reactions.

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