Register      Login
The APPEA Journal The APPEA Journal Society
Journal of Australian Energy Producers
RESEARCH ARTICLE

APPLICATIONS OF AROMATIC HYDROCARBONS: THE LIQUID REACTION ENVIRONMENT IN SOURCE ROCKS—A FUNDAMENTAL STAGE IN OIL FORMATION

B.G.K. van Aarssen, R. Alexander and R.I. Kagi

The APPEA Journal 41(1) 549 - 558
Published: 2001

Abstract

The ratio of two trimethylnaphthalenes in sediment extracts can be used to indicate the establishment of a liquid reaction environment in the source rock. The abundance of 1,3,6-TMN relative to 1,3,7-TMN (denoted here as 136/137) is near constant in crude oils. In sediments however, there is a much larger variation. This difference is attributed to the presence of two different reaction environments in the source rock: a liquid organic phase which is the direct precursor of crude oils, and the kerogen / rock matrix onto which compounds are adsorbed. In the liquid reaction environment, methylated naphthalenes undergo many reactions, leading to a near constant value for 136/137. On the other hand, when they are adsorbed onto kerogen or minerals, different reactions prevail and an excess of 1,3,6-TMN is formed. When measured in sediment extracts, the closer 136/137 is to the value typical for oils, the better the liquid reaction environments established in the source rock. This concept was used to study the behaviour of 136/ 137 with depth in 10 sedimentary sequences from the North West Shelf. The results showed that sediments from several wells were capable of establishing a liquid reaction environment, a necessary step in the formation of oil. Results from other wells indicated that little or no liquid reaction environment could be established, suggesting that these sediments were unlikely to be capable of oil formation. The 136/137 parameter is a convenient indicator for determining the extent to which the liquid reaction environment has been established in the source rock and may be useful in determining oil generation potential.

https://doi.org/10.1071/AJ00027

© CSIRO 2001

Committee on Publication Ethics


Export Citation

View Dimensions