A positive temperature coefficient is the term which has been used to indicate that an increase in solubility occurs as the temperature is raised, whereas a negative coefficient indicates a decrease in solubility with rise in temperature.

Effect of Temperature

We study the gas flow processes in ultra-tight porous media in which the matrix pore network is composed of nanometre- to micrometre-size pores. We formulate a pressure-dependent permeability function, referred to as the apparent permeability function (APF), assuming that Knudsen diffusion and slip flow (the Klinkenberg effect) are the main contributors to the overall flow in porous media. The APF predicts that in nanometre-size pores, gas permeability values are as much as 10 times greater than results obtained by continuum hydrodynamics predictions, and with increasing pore size (i.e. of the order of the micrometre), gas permeability converges to continuum hydrodynamics values. In addition, the APF predicts that an increase in the fractal dimension of the pore surface leads to a decrease in Knudsen diffusion. Using the homogenization method, a rigorous analysis is performed to examine whether the APF is preserved throughout the process of upscaling from local scale to large scale. We use the well-known pulse-decay experiment to estimate the main parameter of the APF, which is Darcy permeability. Our newly derived late-transient analytical solution and the late-transient numerical solution consistently match the pressure decay data and yield approximately the same estimated value for Darcy permeability at the typical core-sample initial pressure range and pressure difference. Other parameters of the APF may be determined from independent laboratory experiments; however, a pulse-decay experiment can be used to estimate the unknown parameters of the APF if multiple tests are performed and/or the parameters are strictly constrained by upper and lower bounds.

Gas flow in ultra-tight shale strata

Critical review of low-salinity waterflooding

The low-salinity effect (LSE) in carbonate rock has been less explored in comparison to sandstone rock. Laboratory experiments have shown that brine composition and (somewhat reduced) salinity can have a positive impact on oil recovery in carbonates. However, the mechanism leading to improved oil recovery in carbonate rock is not well understood. Several studies showed that a positive low-salinity flooding (LSF) effect might be associated with dissolution of rock; however, because of equilibration, dissolution may not contribute at reservoir scale, which would make LSF for carbonate rock less attractive for field applications. This raises now the question whether calcite dissolution is the primary mechanism of the LSF effect. In this paper, we aim to first demonstrate the positive response of carbonate rock to low salinity and then to gain insight into the underlying mechanism(s) specific to carbonate rock. We followed a similar methodology as in sandstone rock [Mahani, H.; Berg, S.; Ilic, D.; Bartels, W....

Insights into the Mechanism of Wettability Alteration by Low-Salinity Flooding (LSF) in Carbonates

Review of the litterature available outside the petroleum industry concerning wettability. This litterature discusses surface forces and their effects on wettability, including van der Waal and electrostatic forces. Hydrogen bonding and ion/water interactions, are also discussed. Advancing and receding contact angles for oil/water/mineral systems in terms of these surface forces are described.

Wettability : fundamentals and surface forces

Electrokinetics of Carbonate/Brine Interface in Low-Salinity Waterflooding: Effect of Brine Salinity, Composition, Rock Type, and pH on ζ-Potential and a Surface-Complexation Model

Literature review of low salinity waterflooding from a length and time scale perspective

Low-salinity waterflooding (LSF) is one of the least-understood enhanced-oil-recovery (EOR)/improved-oil-recovery (IOR) methods, and proper understanding of the mechanism(s) leading to oil recovery in this process is needed. However, the intrinsic complexity of the process makes fundamental understanding of the underlying mechanism(s) and the interpretation of laboratory experiments difficult. Therefore, we use a model system for sandstone rock of reduced complexity that consists of clay minerals (Na-montmorillonite) deposited on a glass substrate and covered with crude-oil droplets and in which different effects can be separated to increase our fundamental understanding. We focus particularly on the kinetics of oil detachment when exposed to lowsalinity (LS) brine. The system is equilibrated first under high-salinity (HS) brine and then exposed to brines of varying (lower) salinity while the shape of the oil droplets is continuously monitored at high resolution, allowing for a detailed analysis of the contact angle and the contact area as a function of time. It is observed that the contact angle and contact area of oil with the substrate reach a stable equilibrium at HS brine and show a clear response to the LS brine toward less-oil-wetting conditions and ultimately detachment from the clay substrate. This behavior is characterized by the motion of the three-phase (oil/water/solid) contact line that is initially pinned by clay particles at HS conditions, and pinning decreases upon exposure to LS brine. This leads to a decrease in contact area and contact angle that indicates wettability alteration toward a more-waterwet state. When the contact angle reaches a critical value at approximately 40 to 50 , oil starts to detach from the clay. During detachment, most of the oil is released, but in some cases a small amount of oil residue is left behind on the clay substrate. Our results for different salinity levels indicate that the kinetics of this wettability change correlates with a simple buoyancyover adhesion-force balance and has a time constant of hours to days (i.e., it takes longer than commonly assumed). The unexpectedly long time constant, longer than expected by diffusion alone, is compatible with an electrokinetic ion-transport model (Nernst-Planck equation) in the thin water film between oil and clay. Alternatively, one could explain the observations only by more-specific [nonDerjaguin–Landau–Verwey–Overbeek (DLVO) type] interactions between oil and clay such as cation-bridging, direct chemical bonds, or acid/base effects that tend to pin the contact line. The findings provide new insights into the (sub) pore-scale mechanism of LSF, and one can use them as the basis for upscaling to, for example, pore-network scale and higher scales (e.g., core scale) to assess the impact of the slow kinetics on the time scale of an LSF response on macroscopic scales.

Kinetics of Low-Salinity-Flooding Effect

It has been proposed that increased oil recovery in carbonates by modification of ionic composition or altering salinity occurs mainly at a temperature exceeding 70–80 °C. The argument was that elevated temperatures enhance adsorption of the potential determining ions which then modifies wettability to a less-oil-wetting state. According to this rationale, it becomes questionable if diluted brines or brines without these ions can be still applicable. Therefore, the aim of this paper is to investigate if the wettability alteration truly depends on temperature and if so how the trend with temperature can be explained. We followed a combined experimental and theoretical modeling approach. The effect of brine composition and temperature on carbonate wettability was probed by monitoring contact angle change of sessile oil droplets upon switching from high salinity to lower salinity brines. IFT measurements as a function of salinity and temperature along with extensive ζ-potential measurements as a function of ...

Hassan Mahani

Papers

Insights into the Mechanism of Wettability Alteration by Low-Salinity Flooding (LSF) in Carbonates

Electrokinetics of Carbonate/Brine Interface in Low-Salinity Waterflooding: Effect of Brine Salinity, Composition, Rock Type, and pH on ζ-Potential and a Surface-Complexation Model

Literature review of low salinity waterflooding from a length and time scale perspective

Kinetics of Low-Salinity-Flooding Effect

Insights into the Impact of Temperature on the Wettability Alteration by Low Salinity in Carbonate Rocks