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

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.