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Rocks, surfaces

Oil reservoirs are layers of porous sandstone or carbonate rock, usually sedimentary. Impermeable rock layers, usually shales, and faults trap the oil in the reservoir. The oil exists in microscopic pores in rock. Various gases and water also occupy rock pores and are often in contact with the oil. These pores are intercoimected with a compHcated network of microscopic flow channels. The weight of ovedaying rock layers places these duids under pressure. When a well penetrates the rock formation, this pressure drives the duids into the wellbore. The dow channel size, wettabiUty of dow channel rock surfaces, oil viscosity, and other properties of the cmde oil determine the rate of this primary oil production. [Pg.188]

Wettabihty is defined as the tendency of one fluid to spread on or adhere to a soHd surface (rock) in the presence of other immiscible fluids (5). As many as 50% of all sandstone reservoirs and 80% of all carbonate reservoirs are oil-wet (10). Strongly water-wet reservoirs are quite rare (11). Rock wettabihty can affect fluid injection rates, flow patterns of fluids within the reservoir, and oil displacement efficiency (11). Rock wettabihty can strongly affect its relative permeabihty to water and oil (5,12). When rock is water-wet, water occupies most of the small flow channels and is in contact with most of the rock surfaces as a film. Cmde oil does the same in oil-wet rock. Alteration of rock wettabihty by adsorption of polar materials, such as surfactants and corrosion inhibitors, or by the deposition of polar cmde oil components (13), can strongly alter the behavior of the rock (12). [Pg.188]

Microbes adsorb and grow on reservoir rock surfaces fed by injected nutrients (271) and may have appHcation in plugging thief zones near injection... [Pg.194]

Effect on Oxide—Water Interfaces. The adsorption (qv) of ions at clay mineral and rock surfaces is an important step in natural and industrial processes. SiUcates are adsorbed on oxides to a far greater extent than would be predicted from their concentrations (66). This adsorption maximum at a given pH value is independent of ionic strength, and maximum adsorption occurs at a pH value near the piC of orthosiUcate. The pH values of maximum adsorption of weak acid anions and the piC values of their conjugate acids are correlated. This indicates that the presence of both the acid and its conjugate base is required for adsorption. The adsorption of sihcate species is far greater at lower pH than simple acid—base equihbria would predict. [Pg.7]

The invasion of particles can be eliminated either by using solids-free systems or by formation of a competent filter cake on the rock surface. If the components forming the filter cake are correctly chosen and blended, they will form a very effective downhole filter element. This ensures that colloidal sized clays or polymeric materials are retained within the filter cake and do not enter the formation. Further protection is provided by ensuring that a thin filter cake is formed due to low dynamic and static filtrate losses. Thus, the cake may be easily removed when the well is brought into production. Additionally, the filter cake can be soluble in acid or oil. [Pg.703]

Loss of surfactant due to adsorption onto the rock surface can also be minimized by blending the AOS with DPOS. This is shown in Fig. 28 which is a plot of the amount of surfactant adsorbed onto montmorillonite clay vs. the percentage of AOS in the blend. Clearly, when there is more than about 30% DPOS in the blend, total adsorption of surfactant is suppressed. [Pg.428]

Sandstone rock surfaces are normally highly water-wet. These surfaces can be altered by treatment with solutions of chemical surfactants or by asphaltenes. Increasing the pH of the chemical treating solution decreases the water wettability of the sandstone surface and, in some cases, makes the surface medium oil-wet [1644]. Thus the chemical treatment of sandstone cores can increase the oil production when flooded with carbon dioxide. [Pg.213]

D. H. Smith and J. R. Combeiiati. Chemical alteration of the rock surfaces by asphaltenes or surfactants, and its effect on oil recovery by CO2 flooding. In Proceedings Volume. Annu AICHE Mtg (Chicago, IL, 11/11-11/16), 1990. [Pg.462]

Atoms adsorbed on host rock surfaces. This pool is assumed to readily exchange... [Pg.321]

After completion of the drilling operation, steel casing is lowered down the well bore and into the drilling fluid. A spacer fluid is then pumped down the well bore to remove the drilling fluid and prevent contact of the drilling mud with the cement slurry. Efficient displacement of the drilling mud also promotes bonding of the cement slurry to rock surfaces. [Pg.13]

Injecting epoxy, furan, or furan-formaldehyde resins into poorly consolidated formations to consolidate them was a common sand control practice for thin highly productive formations (44-46). Organic solvents (46) and silane coupling agents (47) are used to promote adhesion of the resin to the rock surface. Excess resin is flushed deeper into the formation to minimize resin hardening in the flow channels since this would reduce formation permeability. [Pg.16]

Adsorption of corrosion inhibitors or cationic surfactants can reduce sandstone formation permeability. Alcohols can be used to remove corrosion inhibitors from rock surfaces. Oil-soluble corrosion inhibitors may be dissolved by organic solvents such as xylene or toluene containing a mutual solvent, most often ethylene glycol monobutyl ether, EGMBE (167). Aqueous fluids containing 5-10% EGMBE can be used to dissolve cationic surfactants. [Pg.26]

In a strongly oil-wet rock, water will tend to invade the larger pores as oil is found in the smaller pores or as a film on rock surfaces. Because the water preferentially flows through the larger pores, flow channels to the producing well develop and water only slowly invades the smaller flow channels. This results in a higher produced water oil ratio and a lower oil production rate than in the water-wet case. [Pg.27]

Compared to partially hydrolyzed polyacrylamide, xanthan gum is more expensive, more susceptible to bacterial degradation, and less stable at elevated temperatures (1). However, xanthan gum is more soluble in saline waters, particularly those containing divalent metal ions generally adsorbs less on rock surfaces and is substantially more resistant to shear degradation (1,34). The extensional viscosity of the semi-rigid xanthan molecule is less that that of the flexible polyacrylamide (263). [Pg.35]

The sessile drop method has several drawbacks. Several days elapse between each displacement, and total test times exceeding one month are not uncommon. It can be difficult to determine that the interface has actually advanced across the face of the crystal. Displacement frequency and distance are variable and dependent upon the operator. Tests are conducted on pure mineral surfaces, usually quartz, which does not adequately model the heterogeneous rock surfaces in reservoirs. There is a need for a simple technique that gives reproducible data and can be used to characterize various mineral surfaces. The dynamic Wilhelmy plate technique has such a potential. This paper discusses the dynamic Wilhelmy plate apparatus used to study wetting properties of liquid/liquid/solid systems important to the oil industry. [Pg.560]

TFSA molecules have been extensively and successfully used as steam additives in cyclic steam operations(27-32). Recently, results of a TFSA-waterflood which was conducted in West Texas were reported(33). The purpose of the work described in this paper was to further evaluate the feasibility of recovering incremental oil in a mature waterflood by injection of surfactants which change the wettability of reservoir rock surfaces. In this paper, we present the results of laboratory studies with Thin Film Spreading Agents and the results of a carefully conducted TFSA-waterflood pilot in the Torrance Field located in the Los Angeles Basin of California. [Pg.578]

RECOVERY MECHANISMS. Being surface active, TFSAs lower oil-water inter facial tension, but not by the three orders of magnitude needed to increase the capillary number sufficiently to recover a substantial amount of incremental oil. Instead, TFSAs enhance the recovery of oil by changing the wettability of reservoir rock surfaces from oil-wet and intermediate wettability to strongly water-wet, and by coalescing emulsions in the near-wellbore region of the production wells. [Pg.582]

Changing the wettability of reservoir rock surfaces from oil-wet to water-wet, increases the permeability of the formation to oil, decreases the permeability to water, decreases mobility ratio, increases sweep efficiency, increases the flowing fraction of oil at every saturation, and increases oil recovery at the economic limit of the waterflood. [Pg.593]

Thin Film Spreading Agents are synthetic surfactants which change the wettability of reservoir rock surfaces from oil-wet and intermediate wettability to water-wet. [Pg.593]

Another hypothesis on homochirality involves interaction of biomolecules with minerals, either at rock surfaces or at the sea bottom thus, adsorption processes of biomolecules at chiral mineral surfaces have been studied. Klabunovskii and Thiemann (2000) used a large selection of analytical data, provided by other authors, to study whether natural, optically active quartz could have played a role in the emergence of optical activity on the primeval Earth. Some researchers consider it possible that enantioselective adsorption by one of the quartz species (L or D) could have led to the homochirality of biomolecules. Asymmetric adsorption at enantiomor-phic quartz crystals has been detected L-quartz preferentially adsorbs L-alanine. Asymmetrical hydrogenation using d- or L-quartz as active catalysts is also possible. However, if the information in a large number of publications is averaged out, as Klabunovskii and Thiemann could show, there is no clear preference in nature for one of the two enantiomorphic quartz structures. It is possible that rhomobohedral... [Pg.251]

Air temperatures in arid zones are generally high and show significant daily variations. Because of the absence of a protective vegetative cover and a specific thermal absorption and desorption effects due to surface or rock colors or slope aspect, air temperatures of 35-45°C may reach peaks up to 50-60°C or more on rock surfaces. [Pg.25]

Abrasion and erosion. The dust-loaded wind has an erosive action and contributes to a physical disintegration of rock surfaces or to a polishing of the components of the desert pavement, giving them a characteristic patina desert varnish) and shape (ventifacts). [Pg.30]

Rock salt semiconductors, 22 141 dating, 21 317-318 selenium occurrence in, 22 78 Rock surface chemistry, in volumetric sweep efficiency, 18 621 Rock varnish, photocatalytic origin of, 19 100-101... [Pg.809]


See other pages where Rocks, surfaces is mentioned: [Pg.121]    [Pg.191]    [Pg.192]    [Pg.708]    [Pg.334]    [Pg.398]    [Pg.202]    [Pg.319]    [Pg.320]    [Pg.331]    [Pg.343]    [Pg.13]    [Pg.21]    [Pg.481]    [Pg.503]    [Pg.574]    [Pg.576]    [Pg.577]    [Pg.577]    [Pg.578]    [Pg.584]    [Pg.15]    [Pg.106]    [Pg.268]   
See also in sourсe #XX -- [ Pg.7 ]




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Adsorption rock surface effect

Change rock surface wettability

Changing the wettability of reservoir rock surfaces

Components, rocks, soil surfaces

Interface of rock/soil-aqueous solutions surfaces

Nanometer Rocks on Smooth Surfaces

Oxide rock-salt-type surface

Polymer rock surface effect

Rock surface, altered wettability

Rock-salt-type surface

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