• Title/Summary/Keyword: pristane

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Petroleum Geochemistry of Organic Matter from the core samples in the Tertiary Pohang Basin (포항 분지 제3기층 시추코아 유기물의 석유 지화학적 특성)

  • Lee Youngjoo;Kwak Young Hoon;Yun Hye Su;Cheong Tae Jin;Oh Jae Ho;Kim Hagju;Kang Moohee
    • The Korean Journal of Petroleum Geology
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    • v.5 no.1_2 s.6
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    • pp.48-58
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    • 1997
  • Core samples from the B, E, F, H wells in the Tertiary Pohang Basin were analysed for total organic carbon (TOC) content and subject to Rock-Eval pyrolysis in order to assess petroleum geochemical characteristics of organic matter. Following geochemical screening, we selected samples from each well for the study of bitumen and kerogens such as optical observation, infra-red spectroscopy and biomarker analyses. Sediments of the Tertiary Yonil Group contain total organic carbon ranging from $0.55{\%} to 3.74{\%}$ with S1+S2 values higher than 2mgHC/g Rock in B, E and F wells, which indicates fair hydrocarbon generation potential. Most organic matter in the B, E, F wells is compared to type II based on the Rock-Eval pyrolysis, infra-red spectroscopy and optical observation. However, organic matter in the H well is compared to type III because the well is located at the margin of the basin where the preservation of terrestrial material is dominant. Geochemical analyses show that organic matter in the Yonil Group is thermally immature although thermal maturity slightly increases with depth. Maturity levels of the extracted kerogens are similar to those of bulk samples ($Tmax<435^{\circ}C$. Petroleum geochemical charateristics of the sediments in the Tertairy Yonil Group is fair in terms of the organic richness and hydrocarbon genetic potential, but organic matter is thermally immature due to the shallow burial depth. Optical observation of the kerogens and biomarker analysis show that organic matter in the Yonil Group is both marine and terrestrial origin, although it was deposited in marine environment. Pristane/phytane ratio suggests rather anoxic depositional environment. Transitional characteristics of organic matter indicate that the marine Yonil Group was deposited near the terrestrial environments. Input of terrestrial organic matter is more prevalent in the samples recovered from the lowermost horizon in the wells due to the terrestrial environment at the time of basin formation.

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Geochemical characteristics of organic matter in the Tertiary sediments from the JDZ Blocks, offshore Korea (대륙붕 한일공동광구에 분포하는 제 3기 시추 시료 유기물의 지화학적 특성)

  • Lee Youngjoo;Yun Hyesu;Cheong Taejin;Kwak Younghoon;Oh Jaeho
    • The Korean Journal of Petroleum Geology
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    • v.6 no.1_2 s.7
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    • pp.25-36
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    • 1998
  • Organic geochemical analyses were carried out in order to characterize organic matter (OM) in the sediments recovered from Korea/japan Joint Development Zone (JDZ V-1, V-3, VII-1 and VII-2) which is located in the northern end of the East China Sea Shelf Basin. Late Miocene sediments from the JDZ V-1 and V-3 wells generally contain less than $0.5\%$ of total organic carbon (TOC). However, early Miocene and Oligocene sediments show TOC values of $0.6-0.8\%$. Middle to late Miocene sediments are rich in TOC up to $20\%$ from JDZ VII-1 and JDZ VII-2 wells. The reason for this rich TOC might be attributed to the presence of coaly shales. Kerogens in the Tertiary sediments from the JDZ series wells are mainly composed of terrestrially derived woody organic matter. Elemental analyses indicate that OM from these wells can be compared to type III. Low hydrocarbon potential and hydrogen index reflect the type of OM. According to the biomarker analyses, the input of the terrestrial OM is prevalent. Oxidizing condition is also indicated by Pristane/Phytane ratio. Samples from the JDZ V-1 and V-3 wells obtain maturities equivalent to the oil generation zone around total depth, and organic matter below 3600 m from JDZ VII-1 and VII-2 wells reached dry gas generation stage. Oligocene sediments below 3500 m in the JDZ VII-1 and JDZ VII-2 wells may have generated limited amount of hydrocarbons, showing a progressive decrease in hydrogen index with depth, due to thermal degradation with increased burial. Gas shows and finely disseminated gilsonite may indicate the generation and migration of the hydrocarbons.

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Identification of Major Crude Oils Imported into Korea using Molecular and Stable Carbon Isotopic Compositions (분자지표 및 탄소안정동위원소 조성비를 이용한 국내 수입 주요 원유의 식별)

  • Kim, Eun-Sic;An, Jun-Geon;Kim, Gi-Beum;Shim, Won-Joon;Joo, Chang-Kyu;Kim, Moon-Koo
    • Journal of the Korean Society for Marine Environment & Energy
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    • v.15 no.3
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    • pp.247-256
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    • 2012
  • Stable carbon isotope ratio of oil components are known to be unaffected by weathering processes and thus has been widely used to determine the origin of spilled oil. In this study, molecular index and composition of stable carbon isotope in 15 crude oils and petroleum product were analyzed and used as oil fingerprints to determine the discriminating power of each fingerprinting method among target crude oils. Through the fingerprints of alkane distribution only Bintulu and B-C(1%) were distinguishable from other crude oils. The pristane/phytane ratio can classify the crude oils into three groups but differentiation of crude oils within a group was impossible using the ratio. The crude oils of A.L., A.S.L., Foroozan and B-C(1%) were differentiated from the other oils using PAH source recognition indexes of C2D/C2P and C3D/C3P. The usage of 4-mD/1-mD and 2/3-mD/1-mD ratio was able to distinguish A.S.L., Bintulu and Oman from the other crude oils. However the PAH source recognition ratios in the other crude oils were similar and thus they were impractical to be used for source identification among the target crude oils. Stable carbon isotope ratios of alkanes were able to uniquely specify each crude oil in the plot of ${\delta}^{13}C_{C21}$ and ${\delta}^{13}C_{C25}$ except A.L., A.M., Qatar-Marine, B-C(1%). The oil fingerprinting method using stable carbon isotope ratios of individual alkane compounds showed more discriminating power among the target crude oils than the conventional source recognition indexes of PAHs or alkanes.