Abstract
Thermal evaluation of potential source rocks (PSR) include measurements of CO2 evolved (>400°C) designated as IO (Oxygen Index). For whole rock analysis this index frequently exceeds the value derived from organically bonded oxygen. The surplus of CO2 stems mainly from the reaction of carbonates with active acidic volatiles released from the associated clays. The magnitude of this effect is specific for every clay mineral, but for any particular mineral assemblage it correlates directly with the clay/carbonate ratio. The largest discrepancy between IO values and organically bonded oxygen occurs when O.M. is low (ca. 0.5-1%), clays dominate and sufficient carbonates are present to react. Clay minerals and kerogen probably do not react, as such. However, the active volatiles released upon heating attack even before depolymerization. The liquid monomers produced then can react with both clay minerals and their volatiles. These interactions could result in changes of the IH factor (Hydrogen Index), as well as the distribution of products.
| Original language | English |
|---|---|
| Pages (from-to) | 25 |
| Number of pages | 1 |
| Journal | American Chemical Society, Division of Petroleum Chemistry, Preprints |
| Volume | 34 |
| Issue number | 1 |
| State | Published - Mar 1989 |
| Event | Symposium on Comparative Studies of Various Oil Shales - Dallas, TX, USA Duration: 9 Apr 1989 → 14 Apr 1989 |
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