Polymer-Assisted-Water-Alternating-Gas for Improving the CO2 Flow Properties in Porous Media

Abstract

Abstract CO2 flow in porous media is vital for both enhanced oil recovery and underground carbon storage. For improving CO2 mobility control and thus improved reservoir sweep efficiency, Water-Alternating-Gas (WAG) injection has often been applied. The effectiveness of WAG diminishes, however, due to the presence of micro-scale reservoir heterogeneity which results in an early breakthrough of gas. We propose Polymer-assisted WAG (PA-WAG) as an alternative method to reduce gas mobility, while also reducing the mobility of the aqueous phase, and consequently improving the performance of WAG. In this method, high molecular weight water-soluble polymers are added to the water slug. The goal of this work was to investigate the feasibility of PA-WAG and study the transport processes in porous media. An ATBS-based polymer (SAV 10 XV) was chosen as polymer and CO2 at immiscible conditions as gas. The objective of the experiments was to compare the performance of CO2, WAG, and PA-WAG injection schemes by conducting a series of X-ray computed tomography (CT)-aided core-flood experiments in Bentheimer cores. Core-flood results clearly demonstrated the beneficial effects of PA-WAG over WAG and continuous CO2 injection. Continuous injection of CO2 led to the recovery factor (RF) of only 39.0 ± 0.5% of the original oil in place (OOIP). In-situ visualization of CO2 displacement showed strong gravity segregation and viscous fingering because of the contrast in the viscosities and densities of CO2 and oil. The injection of WAG almost doubled the oil recovery (i.e., RF=76.0 ± 0.5%); however, the water and gas breakthroughs still occurred in the early stage of the injection (0.22 PV for water and 0.27 PV for CO2). The addition of the polymer to the aqueous phase delayed both the water and CO2 breakthrough (0.51 PV for water and 0.35 PV for CO2). This resulted in an additional 10% in the recovery factor. Using a single injection method, polymer adsorption was found to be 79.0 ± 0.5 μg polymer/g rock. The polymer adsorption can reduce the micro-scale permeability and as a result, mitigates the gas channeling. This in turn leads to the delay in CO2 breakthrough during PA-WAG injection as was evident from in-situ visualization. This experimental study demonstrated a positive response of PA-WAG compared to WAG and paves the way for its implementation in field applications.