Similarities and Differences of Low Salinity Polymer and Low Salinity LPS (Linked Polymer Solutions) for Enhanced Oil Recovery

Linked polymer solution (LPS) is nano-size particles made of hydrolyzed polyacrylamide (HPAM) cross-linked with aluminum citrate. The propagation of LPS has been compared to non-cross-linked polymers at low brine salinity condition. The possible differences in properties and potentials for oil recovery have been investigated using water-wet and intermediate-wet cores. The target oil for polymer flooding (PF) is assumed to be the portion of the reservoir that has been bypassed by water during waterflooding and not the residual oil saturation in flooded zones. Our recent studies have shown that a positive synergy can be obtained by combining low salinity and PF. It has been claimed in the literature that cross-linking polymer such as colloidal dispersion gels (colloidal dispersion gels (CDG), micron-size aggregates) or LPS (nano-size particles) would extend the application of polymers to also include change in residual oil saturation. The results of this study indicated higher pressure buildup when low salinity LPS was propagated through brine saturated cores compared to low salinity polymer solution. The pressure buildup was even stronger for high salinity LPS injection. In two phase flow experiments, both polymer and LPS under low salinity condition, showed approximately similar propagation and oil recovery potential when injected into water-wet and intermediate-wet cores.     

Salinity Selection for a Low Salinity Water-Low Salinity Surfactant Process

A laboratory selection of salinity for a low salinity water-low salinity surfactant (LS-LSS) process is presented in this paper with systematical investigation on surfactant phase behavior, interfacial tension (IFT), and dynamic retention in porous media with IOS2024 and isoamyl alcohol (IAA) as surfactant system. The results show that 0.4 wt% IOS2024 with 1 wt% IAA can provide ultra-low IFT of 10^?3 mN/m at around 3000–4000 mg/L total dissolved solids, but at that salinity range the surfactant retention is very high. The search for an optimum surfactant formulation has to consider solution properties and retention in addition to the low IFT. The salinity for a LS-LSS process should thus not be focused on either optimal salinity or ultra-low IFT, but instead the best choice could be a compromise between the properties in question. The three-phase region, where ultra-low IFT are found, is also associated with high retention values. However, we show that as salinity is increased from a two-phase region with oil solubilized in a water continuous microemulsion, there is a region close to the three-phase boundary which has potential. This region does not give ultra-low, but fairly low (10^?2 mN/m in this case) interfacial tensions, and also significantly lower retention.      

Cisplatin Adducts on a GGG Sequence within a DNA Duplex Studied by NMR Spectroscopy and Molecular Dynamics Simulations

The antitumor drug cisplatin (cis‐[PtCl₂(NH₃)₂]) reacts with cellular DNA to form GG intrastrand adducts between adjacent guanines as predominant lesions. GGG sites have been shown to be hotspots of platination. To study the structural perturbation induced by binding of cisplatin to two adjacent guanines of a GGG trinucleotide, we examined here the decanucleotide duplex d[(G₁C₂C₃ G₆T₇‐ C₈G₉C₁₀) ? d(G₁₁C₁₂G₁₃A₁₄C₁₅C₁₆C₁₇G₁₈‐ G₁₉C₂₀)] ( dsCG*G*G ) intrastrand cross‐linked at the G* guanines by cis‐{Pt(NH₃)₂}²⁺ using NMR spectroscopy and molecular dynamics (MD) simulations. The NMR spectra of dsCG*G*G were found to be similar to those of previously characterized DNA duplexes cross‐linked by cisplatin at a pyG*G*X site (py=pyrimidine; X=C, T, A). This similarity of NMR spectra indicates that the base at the 3′‐side of the G*G*–Pt cross‐link does not affect the structure to a large extent. An unprecedented reversible isomerization between the duplex dsCG*G*G (bearing a –Pt chelate) and duplex dsGG*G*T (bearing a –Pt chelate) was observed, which yielded a 40:60 equilibrium between the two intrastrand GG–Pt cross‐links. No formation of interstrand cross‐links was observed. NMR spectroscopic data of dsCG*G*G indicated that the deoxyribose of the 5′‐G* adopts an N‐type conformation, and the cytidines C₃, C₁₅, and C₁₆ have average phase angles intermediate between S and N. The NMR spectroscopic chemical shifts of dsGG*G*T showed some fundamental differences to those of pyG*G*–platinum adducts but were in agreement with the NMR spectra reported previously for the DNA duplexes cross‐linked at an AG*G*C sequence by cisplatin or oxaliplatin. The presence of a purine instead of a pyrimidine at the 5′‐side of the G*G* cross‐link seems therefore to affect the structure of the XG* step significantly.     

Connectivity in Vuggy Carbonates, New Experimental Methods and Applications

The length and spatial distribution of the touching-vugs channels affect the degree of permeability variations and is the main contributor to heterogeneity in vuggy carbonates. Hence, this article focuses on vug connectivity characterization and its impact on fluid flow. A whole core sample was scanned by X-ray computed tomography (CT). Image segmentation was used to obtain a binarized three-dimensional (3D) model of the vuggy pore space. Analysis of the binarized 3D model is used to calculate the correlation function and correlation length for the vuggy pore space. Connectivity analysis of the binarized 3D model shows that 79% of the vugs connected network spanning along the sample. The remaining 21% vug porosity exists in a large number of isolated vugs. The correlation length for the connected vug network is found to be larger than for vugs in general. NMR T ₂ measurements at increasing capillary pressure is tested on the vuggy material and used to investigate the amount of connected- and isolated vugs. The results verify the large fraction of connected vugs. Application of NMR T ₂ measurements in combination with capillary pressure experiments can also reveal matrix properties that play an important role in recovery processes. The transition between non-Fickian and Fickian regimes for tracer/solute transport is studied by laboratory experiments performed at various sample lengths, from cm to m scale. For the largest sample measured in our experiments show that effluent concentration curve conform to the CDE solution, suggesting that the Fickian regime has been established.     

Changes in partial molar volume and isentropic partial molar compressibility of self-association of purine and caffeine in aqueous solution at 1–1600 bar

Ultrasound measurements of purine and caffeine in aqueous solution as function of pressure are reported at 25°C and used to calculate the changes in their partial molar volumes and partial molar compressibilities due to self-association. The effect of pressure is to increase the association. The volume changes are negative for the self-association process, becoming less negative with increasing pressure. This is caused by the monomer in the associated state. The partial molar volume of the monomer in the associated state increases with pressure, contrary to what is expected for nonelectrolytes in water. Hydration of the associated monomer must be a key to this increase. The result suggest that dipole-induced dipole interactions is a possible mechanism for the association process and not hydrophobic interactions. The change in the partial molar compressibility of the association is positive, decreasing with increasing pressure.     

Foam Generation,Propagation and Stability in Porous Medium

Transport in Porous Media - There have been several foam field applications in recent years. Foam treatments targeting gas mobility control in injectors as well as gas blocking in production wells...     

Partition Coefficients and Interfacial Activity for Polar Components in Oil/Water Model Systems

Partition coefficients, surface tension, and interfacial tension for some polar organic components dissolved in oil/water model systems have been investigated. The systems consist of isooctane modeling the oil phase and of water solutions of NaCl and CaCl2 modeling the water phase. The organic compounds examined were 1-naphtoic acid, 5-indanol, and quinoline, all well-defined molecules known to be representative of polar components in crude oil. The dependence on pH, salinity, and ionic strength in the water phase was investigated. The surface tension and interfacial tension were also examined as a function of component concentration. The results show a connection between the distribution of the polar components and the interfacial tension. Correspondence between the partition coefficient and the pKa value for the components is also reported. For 1-naphtoic acid none of the two ionization forms of the molecule are found to be surface active in aqueous solution. For 5-indanol both forms are surface active, and for quinoline only the nonionic form of the molecule is found to be surface active. The results indicate that the aqueous phase is the one that governs the interfacial tension. Increasing salinity increases the concentration of the component in the oil phase and decreases the interfacial tension between the oil phase and the aqueous phase. The results are explained due to the "salting-out" effect and to changes in the electrostatics for the various systems. Copyright 1999 Academic Press.     

Network Modeling of EOR Processes: A Combined Invasion Percolation and Dynamic Model for Mobilization of Trapped Oil

A novel concept for modeling pore-scale phenomena included in several enhanced oil recovery (EOR) methods is presented. The approach combines a quasi-static invasion percolation model with a single-phase dynamic transport model in order to integrate mechanistic chemical oil mobilization methods. A framework is proposed that incorporates mobilization of capillary trapped oil. We show how double displacement of reservoir fluids can contribute to mobilize oil that are capillary trapped after waterflooding. In particular, we elaborate how the physics of colloidal dispersion gels (CDG) or linked polymer solutions (LPS) is implemented. The linked polymer solutions consist of low concentration partially hydrolyzed polyacrylamide polymer crosslinked with aluminum citrate. Laboratory core floods have shown demonstrated increased oil recovery by injection of linked polymer solution systems. LPS consist of roughly spherical particles with sizes in the nanometer range (50–150 nm). The LPS process involve mechanisms such as change in rheological properties effect, adsorption and entrapment processes that can lead to a microscopic diversion and mobilization of waterflood trapped oil. The purpose is to model the physical processes occurring on pore scale during injection of linked polymer solutions. A sensitivity study has also been performed on trapped oil saturation with respect to wettability status to analyze the efficiency of LPS on different wettability conditions. The network modeling results suggest that weakly wet reservoirs are more suitable candidates for performing linked polymer solution injection.     

Foam–oil interactions analyzed by static foam tests

There have been many foam field applications in the North Sea area in the recent years. One of the key questions of foam stability is the tolerance to presence of oil in the reservoir. In order to understand the influence of oil saturation on foam, more fundamental experimental studies have been performed. The static foam properties have been investigated by variation in surfactant concentration, amount of added oil, and variation in polarity of the oil phase. An alpha-olefin sulfonate surfactant is used in all experiments. The foam generation ability is connected with surfactant concentration. Foam is also formed with the AOS surfactant even below the critical micelle concentration. For the ionic strength area investigated, foam height for AOS solutions does not change, but foam tests with decane and crude oil are stabilized with lower ionic strength. The foam stability in the presence of alkane-type oils is related to the molecular weight of the oil molecule. The foam generation and stability is possibly connected to the surfactant ability to solubilize oil molecules. Alkanes that solubilize in the micelles seem to destabilize the foam. In crude oil systems more complex relations seem to be active. Alkanes with molecular weight higher than decane are too large to be solubilized in the micelles. The molecules will therefore have less ability to be transported out of the foam and oil seems to stabilize the foam. We have used a multivariate analysis to identify the most important factors influencing foam stability in the presence of oil.     

Fluid flow properties for different classes of intermediate wettability as studied by network modelling

Most clastic reservoirs display an intermediate type of wettability. Intermediate wettability covers several local wetting configurations like fractional wet and mixed-wet where the oil-wet sites could either be in the large or smaller pores. Clastic reservoirs show a large variation in fluid flow properties. A classical invasion–percolation network simulator is used to investigate properties of different intermediate wet situations. Variation in wetting properties like contact angles, process dependent contact angles, contact angle distribution, and fraction of oil wet sites are investigated. The fluid flow properties analysed in particular are residual oil saturation and normalized endpoint relative permeability. Results from network modelling have been compared to reservoir core analysis data. The network models applied are at the capillary limit, while the core flood results are clearly viscous influenced. Even though network modelling does not cover all the physics involved in fluid displacement processes, results show that data from simulations are sufficient to present trends in fluid flow properties which are comparable to experimental data.