Kinetics of thermal decomposition of crude oils: Insights from principal component analysis and products characterization

Abstract

Energy demand is souring, and fossil fuel reserves are dwindling, making heavy oil resources more attractive. In this study, thermogravimetric and Py-GC/MS analyses were conducted on Iranian crude oil samples to compare high and low API (American Petroleum Institute) crude oils. A kinetic study based on mass loss of crude oil was performed using three model-free methods and distributed activation energy model (DAEM). To do that, TG analysis carried out, the temperature was increased from room temperature to 1000 °C with heating rates of 10, 20, and 30 °C min−1. Activation energy (Ea) and pre-exponential factor (A0) were estimated from Friedman, Kissinger–Akahira–Sunose (KAS), and Ozawa-Flynn–Wall (OFW) methods for oil sample. The Ea and A0 for heavy crude oil (Koroosh) pyrolysis varied between 59.85 and 193.83 kJ mol−1 and 1.34 × 105 to 4.36 × 1011 s−1, respectively. For light crude oil sample Lavan, the Ea and A0 ranged between 35.93 to 62.89 kJ mol−1 and 337.41–722.65 s−1, respectively. Pearson's correlation analysis found that the activation energy barrier increases as the reaction progresses and the temperature rises. This makes it harder to form the activated complex, which is a key step in the reaction. Principal component analysis supported these findings. Saturated and aromatic hydrocarbons were liberated at mild temperature while the resins and asphaltenes consecutively released in favorable condition for developing sustainable heavy oil recovery systems. Py/GC–MS analysis shows the evolution of saturated hydrocarbon in Koroosh-oil and aromatic hydrocarbons in Lavan-oil and demonstrates their suitability for fuel applications.