Chemical characterization of insoluble macromolecules (Kerogen) from marine and lacustrine sediments –Molecular distribution of aliphatic dicarboxylic acids in alkaline KMnO<sub>4</sub> oxidation products–

  • MORINAGA Shigeo
    Department of Chemistry, Faculty of Science, Tokyo Metropolitan University (Present address) Department of Materials Science and Technology, Faculty of Engineering, Toin University of Yokohama
  • ISHIWATARI Ryoshi
    Department of Chemistry, Faculty of Science, Tokyo Metropolitan University
  • MACHIHARA Tsutomu
    Department of Chemistry, Faculty of Science, Tokyo Metropolitan University (Present address) Technology Research Center, Japan National Oil Corporation

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Other Title
  • 海洋および湖沼堆積物中の不溶性有機物(ケロジェン)のキャラクタリゼーション –アルカリKMnO<sub>4</sub>酸化分解生成物の脂肪族ジカルボン酸の分子分布–
  • 海洋および湖沼堆積物中の不溶性有機物(ケロジェン)のキャラクタリゼーション--アルカリKMnO4酸化分解生成物の脂肪族ジカルボン酸の分子分布
  • カイヨウ オヨビ コショウ タイセキブツチュウ ノ フヨウセイ ユウキブツ ケ

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Abstract

Insoluble macromolecules (kerogen) were isolated from 7 marine and 10 lacustrine sediment samples and subjected to alkaline KMnO4 oxidation, followed by analysis of organic acids in the oxidation products. The major compounds consist of aliphatic C4-C15α, ω-dicarboxylic acids, n-C7-C28 monocarboxylic acids and benzene mono-to-polycarboxylic acids. The α, ω-dicarboxylic acids from lacustrine kerogens have a maximum at C8 or C9. Whereas those from marine ones show a shoulder in this carbon range, have a maximum at C4 and decrease with increasing carbon number. This difference in the relative abundance of C4 and C8, C9 α, ω-dicarboxylic acids may be due to different precursory materials in the different environments. This result is in accordance with our previous findindg, suggesting strongly that a portion of the chemical structures of kerogens from marine and lake environments is generally different from each other. A mathematical expression was proposed to visualize the feature of molecular distribution of α, ω- dicarboxylic acids from kerogens. In addition, it is shown by both alkaline CuO oxidation and KMnO4 experiments that polymerized structure of polyhydroxy acids can be one of the precursors for α, ω-dicarboxylic acids from kerogens.

Journal

  • Chikyukagaku

    Chikyukagaku 30 (1), 35-45, 1996-04-15

    The Geochemical Society of Japan

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