Role of the interlayer space of montmorillonite in hydrocarbon generation: An experimental study based on high temperature–pressure pyrolysis

Abstract

The interlayer clay–organic complex is an important clay–organic association in sedimentary environments. However, the effects of organic matter storage in the interlayer space of clay minerals on the thermal degradation of organics and the generation of hydrocarbons have not been investigated. In this study, montmorillonite (Mt) and 12-amoniolauric acid (ALA) were used to prepare an interlayer Mt–ALA complex and a Mt–ALA complex in which Mt and ALA were simply mixed. Pyrolysis experiments on the ALA and Mt–ALA complexes were conducted in a confined gold capsule system at a fixed temperature and pressure of 350°C and 36MPa, respectively. X-ray diffraction, elemental analysis and Fourier transform infrared spectroscopy were used to characterize the Mt–ALA complexes, and automatically controlled gas chromatography along with a pyrolysis furnace was used to detect the volatile components released during pyrolysis. In the absence of Mt, the pyrolysis of ALA yielded only a small amount of C1–5 hydrocarbons and CO2. The amounts of C1–5 hydrocarbons released from the pyrolysis of the interlayer Mt–ALA complex and the mixed Mt–ALA complex are approximately 43 and 5 times greater than the amounts released from ALA alone, respectively. The Brønsted acid sites in the interlayer space of Mt, which arise from the interlayer dissociated water, significantly promote the cracking of hydrocarbons through a carbocation mechanism, the isomerization of normal hydrocarbons and alkene–alkane conversion through hydrogenation, resulting in high i-alkane/n-alkane and alkene/alkane ratios in the pyrolysis products. The Lewis acid sites of Mt are primarily involved in the decarboxylation of ALA during pyrolysis and are responsible for CO2 generation.