Abstract

Water weakening is a phenomenon that is observed in high porosity chalk formations. The rock interacts with ions in injected water and additional deformation occurs. This important effect needs to be taken into account when modelling the water flooding of these reservoirs. The models used on field scale are simple and only model the effect as a change in water saturation. In this paper, we argue that the water weakening effect can to a large extend be understood as a combination of changes in water activity, surface charge and chemical dissolution. We apply the de Waal model to analyse compaction experiments, and to extract the additional deformation induced by the chemical interaction between the injected water and the rock. The chemical changes are studied on a field scale using potential flow models. On a field scale, we show that the dissolution/precipitation mechanisms studied in the lab will propagate at a much lower speed and mainly affect compaction near the well region and close to the temperature front. Changes in surface charge travel much faster in the reservoir and might be an important contributor to the observed water weakening effect. We also discuss how mineralogical variations impacts compaction.

Highlights

  • Many of the chalk formations in the North Sea contains large volumes of oil

  • Compaction is a significant driver for oil expulsion, and, as an example, for the Valhall field in the North Sea, the compaction is estimated to contribute to 50% of the total recovery [2]

  • We argue that the water weakening effect is more related to changes in the water chemistry than changes in the water saturation, meaning that it is the changes in the concentration of specific ions that induce enhanced compaction, the ratio between oil and water

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Summary

Introduction

Many of the chalk formations in the North Sea contains large volumes of oil. In some areas, the porosity is higher than 45% [1,2]. The plastic bulk modulus is defined as the ratio of the change in axial stress to the change in volumetric strain in the phase after the core has reached the yield point (the slope of the dashed line in Figure 1a divided by 3). The physical explanation for the macroscopic time-dependent creep stationary contact time is that the contact area between the surfaces increases as the static contact time of rocks is according to de Waal, that the average lifetime of contact points affects the real contact increasesarea [9].which determines the sliding friction. Jorgensen [13] pointed out thatWaal, water adsorption from the air affectedofthe time points dependence of microhardness in nonmetallic materials They found up to a 10% decrease in affects the real contact area whichobserved determines the sliding friction. They found that the de Waal friction factor for the Valhall field was more or less constant over the stress range of interest, which reduced the number of tests required to estimate compaction at field depletion rates

Water Activity Weakens Chalk in Loading Phase
Water Surface Chemistry Affects Chalk Deformation and Creep
Loading
Core Deformation Related to Mineral Alteration
The chalk cores with carbonate content
Line indicates changes in flooding rate from 1from
Fluid–Rock Interactions in Reservoirs
Mapping
Discussion
Findings
The Future and Final Remarks
Full Text
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