Atomic Force Microscopy Study of Wettability Alteration by Surfactants

SPE Journal ◽  
2008 ◽  
Vol 13 (02) ◽  
pp. 137-145 ◽  
Author(s):  
Kamlesh Kumar ◽  
Eric K. Dao ◽  
Kishore K. Mohanty

Summary Waterflooding recovers little oil from fractured carbonate reservoirs, if they are oil-wet or mixed-wet. Surfactant-aided gravity drainage has the potential to achieve significant oil recovery by wettability alteration and interfacial tension (IFT) reduction. The goal of this work is to investigate the mechanisms of wettability alteration by crude oil components and surfactants. Contact angles are measured on mineral plates treated with crude oils, crude oil components, and surfactants. Mineral surfaces are also studied by atomic force microscopy (AFM). Surfactant solution imbibition into parallel plates filled with a crude oil is investigated. Wettability of the plates is studied before and after imbibition. Results show that wettability is controlled by the adsorption of asphaltenes. Anionic surfactants can remove these adsorbed components from the mineral surface and induce preferential water wettability. Anionic surfactants studied can imbibe water into initially oil-wet parallel-plate assemblies faster than the cationic surfactant studied. Introduction Waterflooding is an effective method to improve oil recovery from reservoirs. For fractured reservoirs, waterflooding is effective only when water imbibes into the matrix spontaneously. If the matrix is oil-wet, the injected water displaces the oil only from the fractures. Water does not imbibe into the oil-wet matrix because of negative capillary pressure, resulting in very low oil recovery. Thus there is a need of tertiary or enhanced oil recovery techniques like surfactant flooding (Bragg et al. 1982; Kalpakci et al. 1990; Krumrine et al. 1982a; Krumrine et al. 1982b; Falls et al. 1992) to maximize production from such reservoirs. These techniques were developed in 1960s through 1980s for sandstone reservoirs, but were not widely applied because of low oil prices. Austad et al. (Austad and Milter 1997; Standnes and Austad 2000a; Standnes and Austad 2000b; Standnes and Austad 2003c) have recently demonstrated that surfactant flooding in chalk cores can change the wettability from oil-wet to water-wet conditions, thus leading to higher oil recovery (~70 % as compared to 5% when using pure brine). In 2003 (Standnes and Austad 2003a; Standnes and Austad 2003b; Strand et al. 2003), they identified cheap commercial cationic surfactants, C10NH2 and bioderivatives from the coconut palm termed Arquad and Dodigen (priced at US$ 3 per kg). These surfactants could recover 50 to 90% of oil in laboratory experiments. However, the cost involved is still high because of the required high concentration (~1 wt%) and thus there is a need to evaluate other surfactants. The advantage of using cationic surfactants for carbonates is that they have the same charge as the carbonate surfaces and thus have low adsorption. Nonionic surfactants and anionic surfactants have been tested by Chen et al. (2001) in both laboratory experiments and field pilots. Computed tomography scans revealed that surfactant imbibition was caused by countercurrent flow in the beginning and gravity-driven flow during the later stages. The basic idea behind these techniques is to alter wettability (from oil-wet to water-wet) and lower interfacial tension. Hirasaki and Zhang (2004) have studied different ethoxy and propoxy sulfates to achieve very low interfacial tension and alter wettability from oil-wet to intermediate-wet in laboratory experiments. The presence of Na2CO3 reduces the adsorption of anionic surfactant by lowering the zeta potential of calcite surfaces, and thus dilute anionic surfactant/alkali solution flooding seems to be very promising in recovering oil from oil-wet fractured carbonate reservoirs. It is very important to understand the mechanism of wettability alteration to design effective surfactant treatments and identify the components of oil responsible for making a surface oil-wet. It is postulated that oil is often produced in source rocks and then migrates into originally water-wet reservoirs. Some of the ionic/polar components of crude oil, mostly asphaltenes and resins, collect at the water/oil interface (Freer et al. 2003) and adsorb onto the mineral surface, thus rendering the surface oil-wet. In this work, we try to understand the nature of the adsorbed components by AFM. Recently, AFM has been used extensively to get the force-distance measurements between a tip and a surface. These force measurements can be used to calculate the surface energies using the Johnson-Kendall-Roberts (JKR), the Derjaguin-Muller-Toporov (DMT), and like theories (van der Vegte and Hadziioannou 1997; Schneider et al. 2003). AFM is also used extensively for imaging surfaces. It can be used in the contact mode for hard surfaces and in the tapping mode for soft surfaces. It can be used to image dry surfaces or wet surfaces; tapping mode in water is a relatively new technique. AFM images have been used to confirm the deposition of oil components on mineral surfaces (Buckley and Lord 2003; Toulhoat et al. 1994). In this work, crude-oil-treated mica surface is probed using atomic force microscopy before and after surfactant treatment to study the effects of surfactant. AFM measurements are correlated with contact-angle measurements. We also study surfactant solution imbibition into an initially oil-wet parallel plate assembly to relate wettability to oil recovery. Our experimental methodology is described in the next section, the results are discussed in the following section, and the conclusions are summarized in the last section.

2011 ◽  
Vol 25 (1) ◽  
pp. 183-188 ◽  
Author(s):  
Omolbanin Seiedi ◽  
Marziyeh Rahbar ◽  
Moein Nabipour ◽  
Mohammad A. Emadi ◽  
Mohammad H. Ghatee ◽  
...  

SPE Journal ◽  
2016 ◽  
Vol 21 (03) ◽  
pp. 0720-0729 ◽  
Author(s):  
T.. Hassenkam ◽  
M. P. Andersson ◽  
E.. Hilner ◽  
J.. Matthiesen ◽  
S.. Dobberschütz ◽  
...  

Summary Core tests demonstrated that decreasing the salinity of injection water can increase oil recovery. Optimizing injection-water salinity, however, would offer a clear economic advantage for several reasons. Too-low salinity risks swelling of the clays that would lead to permanent reservoir damage, but evidence of effectiveness with moderate-salinity solutions would make it less difficult to dispose of produced water. The goal is to define boundary conditions so injection-water salinity is high enough to prevent reservoir damage and low enough to induce the low-salinity (LS) effect, while keeping costs and operational requirements at a minimum. Traditional core-plug testing for optimizing conditions has some limitations. Each test requires a fresh sample; core-testing requires sophisticated and expensive equipment; and reliable core-test data require several months because cores must be cleaned, restored, and aged before the tests can begin. It is also difficult to compare data from one core with results from another because no two cores are identical, making it difficult to distinguish between effects resulting from different conditions and effects resulting from different cores. Gathering statistics is limited by the time required for each test and the fact that core material is in short supply. Thus, our aim was to explore the possibility of a less-expensive, faster alternative by probing the fundamental chemical mechanisms behind the LS effect. We developed a method that uses atomic-force microscopy (AFM) to investigate the relationship between the wettability of pore surfaces and water salinity. We functionalize AFM tips with organic molecules and use them to represent tiny oil droplets of nonpolar molecules, and we use sand grains removed from core plugs to represent the pore walls in sandstone. We bring our “oil”-wet tip close to the sand-grain surface and measure the work of adhesion between the tip and the surface. Repeated probing of the surface with the tip produces data that one can convert to maps of adhesion, and we can estimate contact angle. Adhesion work is proportional to wettability and is directly correlated with the salinity of the fluid in contact with the tip and the particle surface. From our measurements, the threshold values for the onset of the LS response are 5,000 to 8,000 ppm, which benchmark remarkably well with observations from core-plug tests. From a mechanistic perspective, the correlation between salinity and adhesion provides evidence for the role of electrical-double-layer (EDL) expansion in the LS response; expansion of the double layer decreases oil wettability. Because AFM experiments can be performed relatively quickly on very little material, they give the possibility of testing salinity response on many samples throughout a reservoir and for gathering statistics. Our approach provides a range of data that one can use to screen conditions to maximize the value of the core-plug testing and to provide extra data that would be too time consuming or too expensive to gather with traditional methods alone. Thus, AFM force mapping is an excellent complement to traditional core-plug testing.


Fuel ◽  
2015 ◽  
Vol 139 ◽  
pp. 328-336 ◽  
Author(s):  
Heloisa P. Dias ◽  
Pedro V. Dixini ◽  
Luiz C.P. Almeida ◽  
Gabriela Vanini ◽  
Eustáquio V.R. Castro ◽  
...  

2021 ◽  
Vol 11 (4) ◽  
pp. 1925-1941
Author(s):  
M. Sadegh Rajabi ◽  
Rasoul Moradi ◽  
Masoud Mehrizadeh

AbstractThe wettability preference of carbonate reservoirs is neutral-wet or oil-wet as the prevailing of hydrocarbon reserves that affects approximately half of the total production of hydrocarbons of the world. Therefore, due to surface wettability of carbonate rocks the notable fraction of oil is held inside their pores in comparison with sandstones. Since shifting the wettability preference toward water-wet system is of great interest, numerous components were used for this purpose. In this experimental research, the wettability alteration of dolomite surface by interacting with a novel nano-surfactant–alkaline fluid has been investigated in order to diminish its adhesion to crude oil droplets. The solutions were prepared by homogenous mixing of nanosilica particles with cetyl trimethyl ammonium bromide and sodium carbonate, respectively, as a cationic surfactant and alkaline agent. The maximum wettability alteration from oil-wet to water system was obtained by employing a mixture of nanoparticles in association with surfactant–alkaline. Then, the fluids were employed in core-surface from detached and attached forms to compare their interfacial effects on saturated thin sections by crude oil and to measure the wettability. In addition, the interfacial tension (IFT) between solutions and crude oil was investigated and the maximum IFT reduction was obtained from nano-surfactant. Finally, all chemical solutions were flooded to the dolomite plugs separately after water flooding in order to evaluate the maximum oil recovery factor acquired by nano-surfactant.


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