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Distribution of acyclic isoprenoids in fractions from stepwise oxidation of Green River kerogen

Journal Article · · Energy Sources (New York); (USA)
 [1];  [2]
  1. Dept. of Chemistry, Alexandria Univ., Alexandria (EG)
  2. Univ. of Southern California, School of Engineering, Los Angeles, CA (US)

A study on the distribution of isoprenoid structures in the five fractions obtained by mild Na{sub 2}Cr{sub 2}O{sub 7}/AcOH stepwise oxidation of Green River kerogen is presented. Gas chromatography-mass spectrometry analysis of the fractions resulted in the identification of a homologous series of isoprenoid acids ranging from C{sub 14}-C{sub 21} with C{sub 16} as the largest and C{sub 18} entirely absent, as well as the two isoprenoidal ketones; 6,10-dimethyl-2-undecanone and 6,10,14-trimethyl-2-pentadecanone. A semi-quantitative analysis of these components was performed using an INCOS 2300 data system. On the basis of the results obtained, it is suggested that isoprenoid structures do not constitute more than 4% of the kerogen matrix. The results also substantiate previous assumptions that the phytol side chain of chlorophyll is the most likely pregenitor to the chain isoprenoids found in the Green River kerogen.

OSTI ID:
7262991
Journal Information:
Energy Sources (New York); (USA), Journal Name: Energy Sources (New York); (USA) Vol. 10:4; ISSN 0090-8312; ISSN EGYSA
Country of Publication:
United States
Language:
English