H53H-1765
One-Dimensional Reactive Transport Modeling of CO2 Storage Systems – Change in Cap Rock Porosity Triggered by Pressure and Temperature Dependent CO2-Water-Rock Interactions

Friday, 18 December 2015
Poster Hall (Moscone South)
Christina Hemme and Wolfgang van Berk, Clausthal University of Technology, Clausthal-Zellerfeld, Germany
Abstract:
In carbon capture and storage (CCS) systems supercritical CO2 is injected into a reservoir and dissolves in the reservoir brine. Subsequently, CO2(aq) diffuses into the cap rock to regions of lower total pressure and temperature and triggers CO2-water-rock interactions that are coupled with mass transport and result in precipitation and/or dissolution of minerals along the CO2 migration path. Such hydrogeochemical interactions change porosities and are responsible for the improvement or deterioration of the long term integrity of the system.

This study presents a semi-generic hydrogeochemical model based on chemical equilibrium thermodynamics, data from several CO2 storage systems, and plausible assumptions regarding non-available data. One-dimensional reactive transport modeling is performed by using the U.S.G.S. PHREEQC code (3.1.4-8929; phreeqc.dat database) to identify and quantify the loss or gain of total porosity affected by hydrogeochemical reactions driven by diffusive mass transport exposed to pressure and temperature gradients. A fine spatial and temporal discretization, the use of non-reactive tracers, and a broad variety of modeling scenarios enable the calculation of the relevant timescale for simulations of long-term storage of CO2 and the consideration of the pressure dependent mass action law constants along the CO2 migration path.

Modeling results show that the relevant timescale for simulations of long-term storage of CO2 is in the range of 106 years, and that pressure/temperature conditions, heterogeneities (veins and fractures) and the mineralogical composition of the cap rock have the strongest influence on the increase in cap rock porosity (maximum increase from initial 5 % to 7.5 %). Critical parameter combinations – total pressure effects are crucial – could put long-term integrity at risks. Nevertheless, a wide range of conditions and parameter combinations for safe CO2 storage is identified by other modeling scenarios.