TY - JOUR
T1 - Effect of Organic Acids on CO2 Trapping in Carbonate Geological Formations
T2 - Pore-Scale Observations Using NMR
AU - Baban, Auby
AU - Ali, Mujahid
AU - Arif, Muhammad
AU - Keshavarz, Alireza
AU - Amin, Robert
AU - Iglauer, Stefan
N1 - Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023/2/16
Y1 - 2023/2/16
N2 - Stearic acid is an example of a carboxylic compound naturally present in geological formations (deep saline aquifers and depleted hydrocarbon reservoirs), which renders the rock hydrophobic (CO2-wet) over a geological time scale. Such hydrophobic surfaces are detrimental to residual CO2 trapping. There is, however, a lack of comprehensive dataset about how traces of these organic molecules affect the rock′s CO2 wettability and residual CO2 trapping. We, thus, used in situ NMR T1-T2 2D images to visualize fluid configurations in the pore network and used T1/T2 ratios to assess the microscopic wettability of the rock to pore space fluids subsequent to each process step. The T2 relaxation time was measured to demonstrate displacement processes and evaluate the trapping behavior at the pore scale, which is closely correlated to reservoir-scale flow functions. The trapping in the CO2-wet sample (14%) was significantly lower than that of the analogous water-wet sample (18%). This reduction in CO2 trapping is due to surface macroscopic flow layers acting as conduits allowing slow desaturation of CO2. Importantly, in the CO2-wet sample, trapping predominately occurred in meso- and micropores, whereas trapping in the analogous water-wet rock primarily occurred in macropores. This work thus provides a comprehensive dataset on the impact of organic acids on residual trapping at the pore scale, which ultimately helps to advance industrial-scale implementation of CGS and EOR project schemes in carbonate reservoirs.
AB - Stearic acid is an example of a carboxylic compound naturally present in geological formations (deep saline aquifers and depleted hydrocarbon reservoirs), which renders the rock hydrophobic (CO2-wet) over a geological time scale. Such hydrophobic surfaces are detrimental to residual CO2 trapping. There is, however, a lack of comprehensive dataset about how traces of these organic molecules affect the rock′s CO2 wettability and residual CO2 trapping. We, thus, used in situ NMR T1-T2 2D images to visualize fluid configurations in the pore network and used T1/T2 ratios to assess the microscopic wettability of the rock to pore space fluids subsequent to each process step. The T2 relaxation time was measured to demonstrate displacement processes and evaluate the trapping behavior at the pore scale, which is closely correlated to reservoir-scale flow functions. The trapping in the CO2-wet sample (14%) was significantly lower than that of the analogous water-wet sample (18%). This reduction in CO2 trapping is due to surface macroscopic flow layers acting as conduits allowing slow desaturation of CO2. Importantly, in the CO2-wet sample, trapping predominately occurred in meso- and micropores, whereas trapping in the analogous water-wet rock primarily occurred in macropores. This work thus provides a comprehensive dataset on the impact of organic acids on residual trapping at the pore scale, which ultimately helps to advance industrial-scale implementation of CGS and EOR project schemes in carbonate reservoirs.
UR - http://www.scopus.com/inward/record.url?scp=85147528412&partnerID=8YFLogxK
U2 - 10.1021/acs.energyfuels.2c04186
DO - 10.1021/acs.energyfuels.2c04186
M3 - Article
AN - SCOPUS:85147528412
SN - 0887-0624
VL - 37
SP - 2983
EP - 2992
JO - Energy and Fuels
JF - Energy and Fuels
IS - 4
ER -