Abstract
Due to the high costs and associated high CO2 emissions of thermal methods, this study focuses on upgrading heavy oil and enhancing oil recovery within reservoir temperature ranges. In this research, a novel, low-cost, and environmentally friendly multi-metal catalyst has been used, which is actually extracted from electronic waste (E-waste). At optimal conditions, which include 80 °C, 12 h of retention time, and 0.2 % v/v of the multi-metal catalyst, this catalyst effectively reduced the viscosity of heavy oil from 687 to 580 mPa.s. To analyze heavy oil before and after the process, Fourier transform infrared spectroscopy (FTIR) was conducted. FTIR spectra indicates that the multi-metal catalyst has reduced the amount of aromatic compounds, shortened hydrocarbon chains, and decreased double and triple bonds. Micromodel tests were conducted by multi-metal catalyst flooding at optimal temperature and retention time obtained from static experiments. Heavy oil recovery through multi-metal catalyst flooding reached 38 %, which is a 10.5 % increase compared to deionized water flooding. The contact angle of the rock was measured after contact with the multi-metal catalyst. The multi-metal catalyst reduced the contact angle by 55 °, changing the wettability of carbonate rock from oil-wet to water-wet. The absorption test indicates that the multi-metal catalyst dissolves certain metals in the rock, most likely due to the high pH of the catalyst. As a result, the permeability of the rock may increase due to the dissolution of the rock metals.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.