Page 80 - Standard Handbook Petroleum Natural Gas Engineering VOLUME2
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68    Reservoir Engineering

                   sealed to prevent leakage and the entrance of oxygen. In a second method, the
                   cores are wrapped in Saran or polyethylene film and aluminum foil, and then
                   coated with wax or strippable plastic. Cores obtained by either of these methods
                   are referred to as preserved, native-state, or fresh cores, and are preferred for
                   many  laboratory tests.
                     For  certain laboratory tests,  it  may  be possible to  clean reservoir cores with
                   solvents and  resaturate with  reservoir fluids to  restore the original wetting con-
                   ditions. Details of  preparing such restored-state or extracted cores are discussed
                   subsequently in the section “Coring and Core Analysis.’’ The concept of the method
                   is to clean the core thoroughly until it is water-wet,  saturate with  reservoir brine,
                   flush with  crude oil, and age for over  1,000 hours at reservoir temperature.
                     Regardless of the method of core handling employed, the rock samples used
                   in the laboratory should have a surface state as close as possible to that present
                   in the reservoir. If preserved cores are used, it is essential they be stored under
                   air-free conditions because exposure to air for as little as 6-8  hours can cause
                   water evaporation and other changes in core properties. If  extracted cores are
                   used, drying of the cores can be very critical when hydratable minerals, capable
                   of  breaking down at low  temperatures are present. Contamination from  core
                   holders that  contain certain types of  rubber  sleeves can be prevented by  using
                   an inner liner of  tubular polyethylene film. Because of  the instability of  many
                   oilfield waters, it is usually desirable to prepare synthetic brines to prevent core
                   plugging caused by  deposition of  insolubles.
                     When possible, tests should be made under reservoir conditions of temperature
                   and pressure using live  reservoir  oil.  This is an improvement over room  con-
                   dition techniques where tests are made at atmospheric conditions with refined
                   laboratory oils. Use of  the live crude exposes the rock  to compounds present
                   in  the  oil that  might influence wettability, and  establishes an  environment as
                   close as possible to reservoir conditions. Cores evaluated at atmospheric con-
                   ditions may  be more  oil-wet than  similar tests at reservoir conditions because
                   of the decreased solubility of wettability-altering compounds at lower temperatures
                   and  pressures  [107,123].  In  a  recent  contact  angle  study  [93]  with  calcium
                   carbonate crystals and a crude oil containing 27.3% resins and 2.2% asphaltenes,
                   a complete reversal from a predominantly oil-wet system at lower temperatures
                   to  a predominantly water-wet system at higher temperatures was  found. While
                   pressure  alone  had  little  effect  on  the  wettability of  the  system, the  study
                   speculated that  the addition of  gas-in-solution with  increasing pressure should
                   favor a more water-wet situation than would be indicated from laboratory tests
                   at atmospheric conditions. Even when all precautions have been taken, there is
                   no absolute assurance that reservoir wettability has been duplicated.

                   Capillary Pressure
                     Curvature at  an  interface between wetting and nonwetting phases causes a
                   pressure difference that is called capillary pressure. This pressure can be viewed
                   as a force per unit area that results from the interaction of surface forces and
                    the geometry of  the system.
                      Based on early work in the nineteenth century of  Laplace, Young, and Plateau
                    (e.g., Reference 94),  a general expression for capillary pressure, Pc, as a function
                    of  interfacial tension,  0, and curvature of  the interface is  [19]:
                      P, =.($+$)                                                  (5-74)
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