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The effect of organic matter type and organic carbon content on Rock-Eval hydrogen index in oil shales and source rocks
Institution:1. State Key Laboratory of Continental Dynamics, Department of Geology, Northwest University, Xi''an 710069, China;2. PetroChina Turpan-Hami Oilfield Company, Xinjiang 839009, China;3. MLR Key Laboratory of Genesis and Exploration of Magmatic Ore Deposits, Xi''an Center of Geological Survey, China Geological Survey, Xi''an 710054, China;4. State Key Laboratory of Petroleum Resource and Prospecting, College of Geosciences, China University of Petroleum, Beijing 102200, China;5. College of Earth Science, University of Chinese Academy of Sciences, Beijing 100049, China;1. Institute of Geology and Geochemistry of Petroleum and Coal, Energy and Mineral Resources (EMR), RWTH Aachen University, Lochnerstr. 4-20, Aachen 52064, Germany;2. MaP – Microstructure and Pores GmbH, Junkerstrasse 93, Aachen 52064, Germany;3. Nagra - National Cooperative for the Disposal of Radioactive Waste, Hardstr. 73, Wettingen 5430, Switzerland;4. AixMinerals, Sophienstr. 1, Aachen 52070, Germany
Abstract:The amount of “gas-prone” kerogen (woody, fungal and “inert”) and the organic carbon content (TOC) are the two predominant factors affecting the hydrogen index (HI) in the 226 samples of lacustrine and marine oil shales and source rocks studied. HI decreases as a function of the amount of “gas-prone” kerogen and increases as a function of TOC. In addition, the type of amorphous kerogen influences the hydrogen index, and this can be roughly estimated from the fluorescence intensity of the amorphous kerogen. Nearly eighty percent of the variation in HI in these samples can be accounted for by the percentage of “gas-prone” kerogen, the TOC content, and the fluorescence of the amorphous kerogen in a multiple regression analysis.Hydrogen index increases as a function of TOC up to about 10% TOC (the relationship can be approximated by a quadratic equation) and then levels off. A possible explanation for this is that the capability of a rock to generate and expel hydrocarbons during pyrolysis increases with TOC. When the retention capacity of the rock matrix is saturated (at about 10% TOC) further increases in TOC have no effect on HI. It is also possible that the quality (i.e. oil-proneness) of the amorphous kerogen is poorer in low TOC samples than in high TOC samples.The samples came from the following oil shales and source rocks: Rundle (Queensland Eocene-Miocene), Mae Sot (northwestern Thailand, Eocene-Pliocene), River River (northwestern Colorado, Eocene), Toolebuc (western Queensland, Late Albian), the “Posidonienschiefer” (southwestern Germany, Toarcian), an Argentinian lacustrine deposit (Eocene-Miocene), the Kimmeridgian sections from four North Sea wells (blocks 21, 30, and 210), Monterey Shale (California, Miocene), and sections from six wells from the Alaskan Tertiary (North Slope, North Aleutian Shelf, Navarin Basin, Norton Sound). Most samples appear to be thermally immature (T.A.I. less than 1.8; Ro less than 0.6%) so they should be considered only potential source rocks.The lacustrine oil shales have a higher conversion ratio (yeild/TOC or S1 + S2/TOC) than do the marine oil shales in samples with only amorphous and algal kerogen. These, in turn, have a higher conversion ratio than the marine source rocks. These differences are roughly reflected in the fluorescence intensity of the amorphous kerogen. Free hydrocarbons are higher in the marine source rocks than in the marine oil shales, and are lowest in the lacustrine oil shales.
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