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Kerogens products

All quantities in mg product/g kerogen. Production rates as mg product/g kerogen/hour. [Pg.579]

Two proposed mechanisms were tested a single-step mechanism kerogen - products and a two-step mechanism kerogen bitumen products. [Pg.274]

Solvent soluble fraction of crude, isolated phenol kerogen product. [Pg.405]

Kerogen Decomposition. The thermal decomposition of oil shale, ie, pyrolysis or retorting, yields Hquid, gaseous, and soHd products. The amounts of oil, gas, and coke which ultimately are formed depend on the heating rate of the oil shale and the temperature—time history of the Hberated oil. There is Htde effect of shale richness on these relative product yields under fixed pyrolysis conditions, as is shown in Table 5 (10). [Pg.346]

Synthetic fuels derived from shale or coal will have to supplement domestic suppHes from petroleum someday, and aircraft gas turbine fuels producible from these sources have been assessed. Shale-derived fuels can meet current specifications if steps are taken to reduce the nitrogen levels. However, extracting kerogen from shale rock and denitrogenating the jet fuel are energy-intensive steps compared with petroleum refining it has been estimated that shale jet fuel could be produced at about 70% thermal efficiency compared with 95% efficiency for petroleum (25). Such a difference represents much higher cost for a shale product. [Pg.417]

Recently, researchers have detected 2,5-dimethylfuran and 2-methylfuran and normal alkanes in kerogen of the 2.7 x 109 year old Belingwe, Rhodesia stromatolites, by the method of pyrolysis/ GC/MS [26]. They concluded that although furans could probably be derived from many compounds, their probable origin is in bacterial and algal sugars, and that the alkanes are either products of decarboxylation of fatty acids or unaltered constituents of ancient organisms. [Pg.394]

Kerogens isolated from the Fig Tree cherts produced very complex mixtures of pyrolysis products, dominated by a series of methyl branched alkenes with each member of the series having 3 carbon atoms more than the previous member. At each carbon number a highly complex mixture of branched alkanes and alkenes plus various substituted aromatic compounds was found. The highly branched structures may have actually incorporated isoprenoids originally present in the Precambrian microorganisms (Philp Van DeMent, 1983)6>. [Pg.44]

We should caution that the above concept of the genetic relationship between kerogens and asphaltenes differs from the more historic view that asphaltenes are condensation and/or alteration products of hydrocarbons and resins. Certainly, in some petroleum processing treatments and probably at higher maturation levels in nature, various reactions do form new products with asphaltene solubility characteristics. These new condensation products may be regarded as altered asphaltenes and intermediates in the coke or pyrobitumen formation process (62-64)- Contamination of original asphaltenes by subsequently formed or altered products, of course, will result in a less definitive correlation between an asphaltene and its source kerogen. [Pg.22]


See other pages where Kerogens products is mentioned: [Pg.5]    [Pg.406]    [Pg.5]    [Pg.406]    [Pg.12]    [Pg.195]    [Pg.347]    [Pg.354]    [Pg.354]    [Pg.158]    [Pg.161]    [Pg.917]    [Pg.24]    [Pg.98]    [Pg.113]    [Pg.204]    [Pg.77]    [Pg.78]    [Pg.79]    [Pg.471]    [Pg.6]    [Pg.183]    [Pg.184]    [Pg.290]    [Pg.28]    [Pg.33]    [Pg.195]    [Pg.20]    [Pg.64]    [Pg.345]    [Pg.1243]    [Pg.61]    [Pg.192]    [Pg.287]    [Pg.523]    [Pg.3]    [Pg.39]    [Pg.71]    [Pg.29]    [Pg.30]    [Pg.129]    [Pg.151]    [Pg.253]    [Pg.385]   


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Kerogen

Kerogens

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