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Summary. Nettability is a major factor controlling the location, flow, +d .@stributiOn Of fl~d? @ a
reservoir. The wettabdity of a core will affect almost all types of core analyses, including capillary pressure,
refative permeability, waterflood behavior, electrical properties, and simulated tertiary recovery. The most
accurate resuks are obtained when natiye- ‘or restored-state cOr~ Me ~ with native cmde Oil~d brine at
reservoir temperattrre and pressure. Such conditions provide cores that have the same wettab~ky as the
reservoir. ~. .’
The wettabih@’ of, ori&lly water-yet reservoir rock can be altered by the adsorption of polar com~ounds
and/or the deposition of organic materiaf ‘that was originally in tie crude oil. The degree of alteration is deter-
mined by the interaction of the oil constituents, the mineral su~ace,. and tie brine chefi$~. The PrO:~ures
for obtaining native-irate,” clesned, and rsstored-state cores are diSCUSSe4ss we~ aS the eff@s Of cOnng,
preservation, and experimental conditions on nettability. Also reviewed are methods for artificially controlling
the wetmbflity during laboratory experiments.
htrodirotion
This paper is the first of a series of literature surveys demonstmted by allowing water to imbibe into the core.
covering the effects”of nettability on core analysis. 1-3 The water will displace the oil from the rock ,surface, ~-
Changes in nettability have been shown to affect capil- dicating that the,rock sui’face “prefers’? to be in contact
Iq pressure, relative permeability, waterflood behavior, with water rather than oil. Simjkwly, a cow samra!ed with
dispersion of tracers, simulated terdaiy recovery, imedn- water is oil-wet if oil will imbibe into the core and dis-
cible water saturation (IWS), residual 01 saturation place water from the rock surfuce. Depending on the spe-
(ROS), and electilcal properties. 4-26 For core analysis citic interactions of rock, oil, and Mne, the wwab@
to predict the behavior of a reservoir accurately, the net- of a system can range from itrongly water-wet to str022g-
tability of a core must be the same as tbe nettability of Iy oil-wet. When the rock his no strong preference for
the undisturbed reservoir rock. A serious”problem occurs either oif or water, the system is said to be of neufml (or
because many aspects of core handling can drastically af- intermediate) wettabfi~. Besides strong and neutkd net-
fect nettability. tability, a third ~pe is fracdonsl nettability, where differ-
ent areas of the core have different wibing preferences. 27
Water-Wet, Oil-Wet, and Neutrafly Wet. Wettabfity The wettabfity of the rocklfluid system is impoitant
is defined as “the tendency of one fluid to spread on or because it is a major factor controlling the location, flow,
adhere to a solid surface in the presence of other irmnis- snd distribution of fluids in a reservoir. .Jn general, one
cible fluids. ” 7 In a rock/oif/brine system, it is a meas- of the flizids in a porous medium of uniform wettabilky
ure of the preference that tie rock has for either the oil that contis at least two immiscible fluids will be the wet-
or water. When the rock is water-wet, there is a tenden- ting fluid. When the system is iu equilibrium, the wet-
cy for water to occupy the smsll pores and to contact the ting fluid will completely OCCUPY the smsllest pores and
majority of the rock surface. Siarly, in an oil-wet sys- be in contact with a majoriv of the rock s~face (ass~-
tem, the rock is preferentially in contact with the oil; the ing, of course, that the saturation of the weting fluid is
location of the two fluids is reversed from the water-wet sufficiently high). The nonwetting fluid will occupy tie
case, and oil will occupy the small pores and con~ct tie centers of the larger pores and form globules that extend
majority of the rock surface. It is importunt to note, how- over several pores.
ever, that the teim wettabWy is used for the wetting In the remainder of this survey; the terms wetdizg snd
preference of the rockand does not necessarily refer to nonwetting fluid wilf be used in addkion to water-ivet and
the fluid that is in contact with tie rock at any given time. oil-wet. This will help us to draw conclusions about a SYS-
For example, consider a clean sandstone core that is tern with the oppositi wetibility. The behavior of oif in
saturated with a refined ofl. Even though the rock sur- a water-wet system is very similar to tle behavior of water
face is coated with oil, the sandstone core is still preferen- in an oil-wet one: For exmuple, it is generally assumed
tially water-wet. Thk wetting preference can be that for a system with a strong wetting prefererice, the
coP&h!1986society.+Pe!role.mEngineers tietting-phase relative permeab~ky is only a function of
lm’ral of Petmlc.mTechnology,October19S6’ 1125’
ABLE 1—DISTRIBUTION OF RESERVOIR WETTABILITIES BASED ON CONTACT ANGLE34
Contact
Angle Silicate Carbonate Total
(degrees) Resewoirs Reservoirs Reservoirs “
Water-wet o to 75 13 2. 15
Intermediate wet 75 to 105
Oil-wet 105to 180 1: A 3;
Total 30 25 55
its own saturation-i. e., it shows no, hysteresis. 7,12,28 fected the wettsbflity behavior in the contsct-migle tests.
Owens and Arch&28 measured the gas/oil drainage per- As ,iiscussed later, this probably causes amoverestima-
mea.bflily, where the oif was the strongly wetting fluid, ticm of the oil-wetness. Therefore, the large percentage
and compared it with the water/ofi imbibition relative por- of reservoirs found to’be ol-wet is less significant than
‘meahii@, where the water was tie strongly wetting fluid. the general indications that not all reservoirs are water-
The water-imbibkioi reIative permeability (strongly wet and that the r&ervoir wettabilky varies widely.
water-wet system) was a continuation of the oil-drainage Contact-sngJe measurements made by Clilingm snd
relative permeability (strongly oif-wet system), demon- Yen35 suggest that most carbonate reservoirs ramge fiorn
strating the amdogy between systems of opposite wetta- neutrally to oif-wet. They measured the we~bdity of 161
bilities. limestone, dolomitic liiestone, calcitic dolomite, arid
Historically, afl petroleum reservoirs were believed to dolomite cores. The cores tested included (1) 90 cores
be strongly water-wet. This was based on tyo mjor fac~. from Asrnari limestones and dolomites from tie Mid$e
Fust, almost all”clean sedentary rocks are strongly EasG (2) 15 dolotite cores from west Texas; (3)3 cores
water-wet. Second, sandstone reservoirs were deposited of Madison liiestone from Wyoming; (4) 4 cirbonate
in aqueous erivironments into which oil later migrated. cores from Mexican oil fields; (5)”4carbonate cores from
It was assumed that the comate water woufd prevent the the Rengiu’oil field in the People’s Republic of China;’
oil from touching the rock surfaces. In 1934, Nuttingzg (6) 16 csrbonate cores from Albe~ (7) 19 chalk cores
realized that some producing reservoirs were, in fact, ac- from tie North.,SeT (8) 5 samples from India+ amd (9)
@ally strongly oil-wet. He found that the quaitz surfaces 5 samples from Soviet oil fields in the Urals-Volga region.
of the Tensleep sandstone in Wyoming had adsorbed Table2 shows the distribution of wettsbfities with 80%
heavy hydrocmbons in layers about 0.7pm tldck (about of the reservoirs either oil-wet or strongly oil-wet. Some.
1,000 molecules) so fdy that they could not be removed of the strongly oil-wet reservoirs were oil-wet bew+se
by gasoline or vzrious solvents.”When $e hydrocarbon of a bitumen coating. Note that the range of contact an-
film was removed by ,fuing the core, the film could be gles considered to be neutrslly wet is smaller thari the
restored by soaking the cores in crude oil overnight. range given in Table 1. This demonstrates the variation
Examples of other reservoirs that are genertiy recog- , from paper to paper of the cutoff angles between ?Je
nized as sirongly oil-wet are the Bradford sands.of the different wetting statea.
Bmdford pool,, Pennsylvania, 30-32 and the Ordovicisrr As discussed iu more detiril later, reservoir rock can
ssmds of the Okkiborns City field. 33 More recentfy, change from its &iginal, strongly water-wet condition by
Treiber et aL % used the water advancing contact angle adsorption of polar compounds and/or the de ositjon of
to eiamine the wettabdity of 55 oil reservoirs. fn this orgsnic matter originally in the crude oil. 7,3P 6-42 Some
procedure, deoxygenated synthetic fofmation brine and crude oils make a rock oil-wet by depositing a thick or-
dead anaerobic crudes were tested on quartz and calcite ganic film on the mineral surfaces. Ofher crude oils con-
c~stafs at rescrvom temperamre. COnta~. angles (mea.+. ti pOlar compounds that cm be adsorbed to make the
ured through the water) fromOto750 [0 to 1.3 rad] were rock more oif+vet. Some of these compounds are srrffi-
dipmed water:we~ from .75 to 105° [1.3 t6 1.83 rad], ciently water soluble to pass throu~ the aqueous phase
intermediate wet; and from 105 to 180° [1.83 to 3:14 red], to the rock.
oil-wet. As summarized in Table 1, 37 of the reservoirs
tested were classified as oil-wet, 3 were of intemnetilate Fractiormf Wettabilfty. The retilzation that rock wetta-
wegabtity, and 15 were water-w.et. Most of the oil-wet bflity can be akercd by adsorbable crude oil components
reservoirs were mildly oil-wet, with a contact angfe be- lexito tie idea that heterogeneous forma of wettabiity exist
tieen 120 and 140° [2:1 and 2.4 rad]. Of the carbonate in reservoir rock. Generally, the intend surface of re.ser’-
resemoirs included, 8 % were water-wet, 8 % were inter- voir rock is composed of many minerals with different
mediate, and S4% were oil-wet. Most of the carbonate surface chemistry and adsorption properties, which may
. . reservoim were from the west Texas area, however, so lead to variations in nettability. Fractional nettability
there is a geographical bias in the data. slso called heterogeneous, spotted, or fhlmation
Treiber et al. cautioned that these tindlngs could not wettabifky-was proposed by Brown and Fatt27. aud
be considered representative of a trufy random samplhzg others. 43* fn fkactioml wegsbdity, crude oif compo-
of petroleum reservoirs. The sainples were bkmed because nents are strongly adsorbed in certain areas of the rock,
(1) all were operations for the sarnb company, (2) most so a portion of the rock is strongly oil-wet, whie the rest
were being considered for some type of flooding, and (3) @strongly water-wet. Note tit this is cqncepty+fly differ-
some of the reservoirs had demonstrated unusual be- ent from intermediate wettsbtity, which assumes that all
havior. A fourth consideration is how much the use of portioim of the rock surfsce have a slight but equal prefer-
degassed fluids rather than the real formation fluids af- ence to being wetted by water or oil.
1126 lomnalof PetmlaunTechmlo8y,@to&r 1986
hfi@ Wettibifity. Salatfrie147 introduced the term
ririxed wettabilby for a special type of fractional netta-
bility iri which the oil-wet surfaces form continuous paths
I TABLE 2–DiStribUtiOn OF dARBONATE
RESERVOIR WETTABILITIES35 I
through tie larger porca. 48-50The smafler pores remain ‘contact
water-wet and contsin no oil. The fact that sll of the oil Angle Percent of
(degreas) Reservoirs
— .
in a miixed-wettabflity core is located in the lager oif-
Water-wet O to 80 a
tvet pores causes a.smdlbut finite oil permeabtlty to ?x- Intermediate wet .80 to 100
ist down to very low oil sahrrdtiom. T@ in mm pertits oil-wet 100to 160 :
the drainage of oil during a waterflood to continue until Strongly oil-wet 160 to 180 15
verj low oil saturations are reached. Note that the main
distirrction betywen mixed md fractional wettsbtity is that
@.elatter, implies neither specitic locations for the oil-wet be used. only for such measurements as, porosity and air
surfaces nor continuous oil-wet paths. permeability where the wettab~lty will not affect the
SalatMet visualizes the generation of mixed nettability results.
ih,,tie following manner, When od yufially invaded an The third type of core is the restored-state core, in which
ciiiginilly water-wet reservoir, it displaced waler from the the mtive nettability is restored by a three-step process.
larger pores, while the smaller pores remained water-fi!kd The core. is cleaned and then satrmtcd with brine, fol-
becairse 6f capillary forces. A mixed-tiettabihty condl-: lowed by crude oil. F,@ally, @e core is aged at reservoir
tion occuried if the oif deposited a layer of oil-wet or- temperature for about 1,000 hours. The methods used to
ganic, material ody on those rock surfaces tliat were in obtain the.three different types of cnres will be discussed
direct contsct with the oil but not on Me brine-covered in more detail later.
surfaces. Oil-wet “deposits would not be formed in the
small water-ffled. pores, snowing them to remain water-
Factors Affecting the Original
wet. The question that Salatliel did not address was how
the oil first came into direct contact with the rock. As the Reservoir Wenabiiity
oil moyes into the larger pores, a tfdn layer of interstitial The &igiaal strong wa~r-wetness of most, rcservoi ~n-
water remains on @pore walls, preventing the oil from erals csn be altered by the adsorption of polar compounds.
contacting the rock. Under certain conditions, however, and/or the deposition of qr tic matter that was origi-
@e waterfdrn separating the crude and the mineml sur- $
nally in the crude oil. 7,20,3,32,36+155-63 ‘fhe surface-
face cm mpture. Hall et al. 51 sad Melrose52 recently active agents io the oil aze generally believed to be p+w
developed a theoretical model for the stability of these com ounds that contsin oxygen, nitrogen, andlor SU1-..
thiri water films that shows fiat the water ftis become ,@r. ! 6,37,40,41,SS,56,W68 These compounds con@in both
thiier and thinner as more oil enters the rock. The water a polar and i hydrocmbon end. The polar end adsorbs
fim is $tabflized by electrostatic forces arising from the on the rock surface, exposing the hydrocsrbqz end and
eIectficaf double layers at the oillwater and wateif rock making the s+face more oil-wet. Experiments haveshown
interfaces. 51’54As tie water “fifmthickness is further re- fhat some.of these aaturaf surfacfants are sut%cientfysolu-
duced, a critical tlickness is reached where the water films ble iizwater to adsorb onto tic rock surface aftcrpassing
in the larger pores become unstable. The films rupture through a thin layer of water. 42,60S69-71
and are dkplaced, aflowing oil to contact ~e rock. In addition to the oif composition, the degree to.which
the wettabllity is aftcred by fhese surfactants is also deter-
minqi by the pressure, tcmpermmc, mineml surface, and
Native-State, Cleaned, and ReStored-State Coraa.
brine chemistry, including ionic composition and PH. The
Cores in three different stitei .of ,presepatioh are used
in core anafysis: native .Xaie,cleaned, and restored state. effects of pressure and temperature will be discussed Mcr
The best results for mrrftiphase-type flow mialyses are ob- @the section on experimental conditions. The importance
of the mineral surface is shown by the contact-angle @eas-
klincd with mtive-ststi cmes, where alterations to the wet-
tabfity of the un@rrbed reservoir rock are minimized. ‘. orementa +cbssed esrlier, ‘,3s in which a large majority
Ii thk set of paper~ the term “native-state” is used for of tie carbonate reservoirs tested were. oil-wet, while
Many.of the sandstone reservoirs were water-wet: Seveml
niry core that was obtained and stored by methods that
preserve the Nettability of the reservoir. No distinction researchers have found that some polar compounds af-
fect the wettabilky of sandstone and carbmaitc surfaces
is made between cores taken with oil- or water-baked in ~lfferent ~ays, 37,+42,6672-76 The. chemistiy of the
fluids, as long as the native wektabflity is maintained. Be
aware, however, that some papers dktin=gish on tie ba- brine can also alter the. wettabtity. Mrdtivafent cations
sis of drilliig fluid (e.g., see Treiber et al. 34), In these sometimes enhance the adsorption of surfactants on the
finer~ ~“rface. %77-s3 ‘fhe brine pH is also impOrt8nt
papers, “native-state” refers only to cores taken with a
suit8bIe ofl-fjjhte.t~e rhill:mg,mud, which nrtintains the in determination of the nettability and other interfacisf
original connate water saturation. ‘:Fresh:state” refers properties of the cmdelbrinelrock system. 6Z26,~In afka-
Iine floodmE, for example, allmhne chemicals can react
to a core with unaltered wettabtity that was taken with
with some c-fides to pr~duce surfactqts that sfter wett?-
a water-base d@ling mud that cbntsins no compounds that b~lty, 6,26
can alter core tiettabdity. Here, the term native-state is !.
used for both cases.
The second type of ‘core is the cleaned core, where an Surface-Active Compormda in Crude Oil. ~ie the
attempt is made to remove all the fluids and adsorbed or-. surface-acfive components of crude tie found in a wide
ganic msterid by flowing solvents through the cores. ~ge ofWrolem fractions, 41 they are more prevalent
Cleared cores are ususlly strongly water-wet and should m gze heavier fractions of cmde, such as re$ina and
\
Journalof PetroleumTechnology,October19S6 1:127
—
,,
aaphaftenes. These surfactants are believed to be polar Several researchers 57,5s analyzed wetkbiliw-afterirw
compounds that contain oxygen, nit@gen, and/or suffer. compounds extracted from cor~. Jennings58 r~moved ~
The oxygen compounds, which are usually acidic, include portion of the nettability-altering cornpotirids by extract-
the phenols and a bwge number of different carboxylic tig a non-water-wet core with tolnene,, followed by a cfdo-
acids. 67$5,86Seifert mid Howellsw showed that the car- rofordmethanol mixiure. An imblbitioiz test showed tbst
boxylic acids are titerfaciilfy active at alkaline PH. The some of the wettabil@-idtering compounds had been re-
sulfor compounds include the sulfides and tilophenes, moved during the s~ond extraction because the core was
with smaller amounts of other compormda, such as mer- more water-wet. The material ‘remo+ed dtiring the sec-
~ap~s ~d polysulfides. 87,88The nitrogen compo~da ond extraction contained porphytis ~d bigh-moledor-
are generaUy either basic or neutral and include csrba- weight pamffinic and aromatic” cbmpoiihds.
xoles, tides, pyridenes, quinoliies, and porphy- Denekaa et al, 41 used a d~tiflntion pro;exs to separate
~~. 40.s7-90me pVhYtis camf&m imerfadly active cmde oifs into fractions of different molecular weight.
metal/porphyrin complexes with a number of dii%erentm> A clean, dry core wax saturated with the crude oil frac-
tds, including nickel, vanadium, iron, coppr, “tic, titani- tion to be tested, then aged for 24 hotii:. An imbibition
um, calcium, aud mirgnesinm. 9*-95 test based on the relative rate of imbibkion waa nsed to
Because the .9zrfactarrts in cnrde oil are composed of determine the wettxbility Alteration..1“.1 The originxl
a lsrge number of very complex chemicals that represent crqde oil and the heaviest residue left a,fterdistillation had
onfy a small fraction of the,crude, identi@g which com- the greatest effect on the nettability; they were the only
pounds are im ortam in aftering the wettabtity has not fluids that nzadetbe rock oil-wet.’fhia fiplies that a con-
beeipossible ‘6 h addkion, attempts to correlate bulk siderable portion of the surfact+ds, in the crude oiI had
crude propert;ei with the abflity of the crude to ~ter wet- a large molecular weight. Many of the lower-molecular-’,
tabiliw have been unauccessf+ McGhee et al. 62 satn- weight fractions, however, also debreaaed the water-
rated Berek cores with brink, od flooded them to IWS with nettability, demonstrating that the surfactants in crude
different cnides, then incubated them at 140”F [60”C] have a broad range of molecufa.r weights. Cuiecg6 ob-
for 1,0+30hours to allow the wet@bfity to reach equilib- tained similar results. Note that Denekas et al. and Cuiec
rium. .The U.S. BWearr of Mines (USBIvf)wettsbllily in- botlr used@ cores and that idso~tiob of the w&ttnbility-
dex ‘wasthen meaaured and compared with bulk propwties .ikering cOnzpoundswoufd probably have been iltered if
of the crude. They found no correlation between the the cores contained brine during tie aging “process..
USBM index and interfaci.d tension (IFT), organic acid A number of roaearchera have examined the i@rfacinUy
content, percerit nitrogen, or percent suIfnr of the cnrde. active materiak that are cOncentrat&dat the Oil/water in-
oCuiec96 measured the Arnott nettability index of terface. Generalfy, these materi~s can iilso be adsorb@
restored-stnte cor6s and found no correlation between ivet- on tie rock surface to sfter wettsblli~. 3.7,8~g9-*mBar-
tabilky and amonnta of acids, basea, aromatics, resins, tell and Nlederhauser 103managed @ sepirate these, ma-
nitrogen, or srdfur. In all cases, when the restored-state terials from ~e crude oil dqd f6und that they, formed a
cores were water-wet, the crndes bad low sapha.ftenesnd hxfd, black. noncrys@fline substxnce tit was sapI@tic
anffur contents., However, other low-asphaftene”xnd low- in nature.
mdtirr c@des rendered cores neutrally or oil-wet. . .
Experiments that determined the general mtnre of the Adsorption Through Water F~s. Experiments hove
surfactxnts xnd the crude oil fractions in which they are shown tfiat nataml surfactants. ii cimde.are often suffl-
concentrated without attempting “~ determine exactly cienify soluble in water to a&sorb onto the rock surface ,-
which compounds cause wet@bifity alteration have been &r passing tbrougb “a thin ld~er. of water. 42,60>69-71
more success~. Jolwnsen and Danningw,9s found that Meaauremerits comparing aaphd~ene a+orption in cores
asphzdtenea were responsible for changing some cmde- with and without water show tlwt m many. caaes a water
oiWwater/glass systems from water-wet to oil-wet. The film wiUreduce but not completely ir@it =pk+lterfe”nd-
system ,was oil-wet when the cmde was used but wat&r- sowtion. 6M9,70 Be&use the wa~ei .qzd asphaltenes wM
wet when the deasphalted crude was used; The addkion coadsorb, however, the wat4.r film may alter tie detailed
of a very small amount (0.25%) of the whole crude to adsorption mechanism. 70,1w Lyutin @d Burdynm found
Ozedeasphalted crnderestored the oif-wettingness of the that the asphalt&e adsorption f$orn A&h ,crude in an yn-
system. Donafdsbn aud Crocker55 ‘and Donafdson56 consolidated sandpack wai about 80% of the dry y~ue
measured wepabilky alte@ion caused by the polar coin- at a water saturation of 107. PV, decreasing to 40 % when
poaada extracted from aeveml different mincmf oifa. First, the water sapration was incrth+ed to 30% PV. Berezin
the nettability of a series of uizcontanzinated Berea plugs et al. 69 exmzzizzedthe adsorption of .&phalten&s&d ;ex-
was mcasnred”with brine agd a refied mineral oiL The ins from crude onto cleaned sandstone cores. With Tui-
average USBM wettabilky iizdex was 0.81, or strongly mazy crude, a water,satnration of about 17% reduced the
water-wit. After cleanirig, the USBM nettability index adaoz’ption by about a factor. of three. With two other
of the plugs was measured with brine and a 5 % mixture crndes, a water saturation of about 20% completely. in-
of the extracted polar organic componnda in the retined hibited the adsorption. Such complete inhibition by tie,
mineral oil., The phtgs were significantly leas water-wet, water fifm woidd be expected in reservoirs that remain
with USBM wettabtity indices ranging from 0.45 (water- water-wet, with no significant ,adsorption:from the cmde.
wet) to -0.W (xretitmlfy.wet), demonstrating that polar Reisberg ad Doscherbs aged clean glaas slides in
compmmda in cnide can alter the wettabtity. Note that c~de ofi.floating above brine and observed the forma-
there was appsfentfy no aging time with the polar cOm- tion of oif-wet fti. The formation i.nd s~bility of the
ponnds in the plugs, so equilibrium wettxbifities may be oif-wet fti on the slide was observed by lowering .!-be
more strongly oil-wet. slide into the brine and observing whether the brine dis-
/.,’
112s Joumalof PetroleumTechnology,October1986 ‘
“placed alf of the cmde ofl from the slide. They first aged oxygen compounds gave higher airgles on dolumite.tbsn
a clean glass slide in crude mrdfound that a film, d6posited quartz, up to 145° [2.5 rad] for. octanoic acid
over several days, made the slide moderately oil-wet. [CH3(CH2)6COOHJ and up to 165° [2.9 rad] foc law-
They modified the experiment by immersing the slide in ic acid [CH3 (CH2),0 COOH]. Note, however, that tbe
water before aging it in crude. Surprisingly, the oil-wet uxygen-containing acidic compounds appesr to react
fti formed much more rapidly. when a NaCl solution gradualfy with the dolomite, so the contacf angles ae un-
was used instead of water, the slide also became oil-wet, stable and the sy$em gadu?dly becomes more water-wet.
but it was necessary to age the slide for a longer period Cram if.ail noted that none of the relatively simple com-
of time. pounds they tested could create a stcble, oil-wet yu’face.
There fure, they cuncluded that the compounds respomi-.
Sandston& mrd Carbonate Surfaces. The types of min- blefor wettabihty alteration in crude were higher-weight
eral surfaces irr a reservoti are also im ortarrt in deter- polar compounds and other po+ons of the asphaltenes
mi@rg wettabfity. Both Treiber et cd. E and ClriHngai and resins.
ad Yen35 found that carbonate reservoirs are wpi@y. In the inure complex crudeibrinelrock systems, the nrin-
more oil-wet than sandstone ones. Two other sets of ex- er# surface will not necessarily have a preference for
periments show that the mineral surface interacts with the compounds of the opposite acidhy. The simple systems
cmde oil imposition to detefine wettabWy. The first dkcussed here tested each surfactcrd individpaUy and re-
set e~nes the adsorption onto silica and cm’bonatesur- moved the effects of brine chemismy. @ tke section on
faces of relatively simple polar crrmpoundy the second brine chemistry, it will be shown thnt multivalent cations
set exnmines the adsorption of crirde. cnn promote the adsorption of surfactants with the same
Simple Pokr Compounds. Whsin the effects of brine acidigi as the surfcqe. fir addition, “the adsorption of auy
chemistry are removed, silica tends to adsorb simple or- single surfactant in the crude might’ be enhanced or
gtic bases, wh~e the carbonates tend to adsorb simple depressed by the adsorpion of other compounds.’
~rgaic tilds. 37,Q83 This occurs because silica normallY Adsor@on From Crude. A nnmber of researchers
has a negatively charged, weakly acidic surface in water found differences in the adsorption of crude oil cum-
nenr neutral pH, while the carbonates have positively punerits onto dry sandstone and carbonate sur-
charged, weakly bssie surfaces. 37,@,83,105 faces. 41,72-74,l@,110Denekss et al. 41 sepmated out the
These surfaces will preferentially adsorb compounds acidic and basic orgaric compounds from crude arrd test-
of the opposite polarity (acidity) by m acidbase reaction. ed them in initially clean, dry cores by tie method de-
Wettabili~ of silica will be more strongly affected by the scribed earlier. They found that the wettabfity of
organic bases, whfie the carbonates will be more strong- snndstone was altered by both the acidic and basic com-
ly affected by the organic acids. This was found to be the pounds, while the Iiiestone was more sensitive to the ba-
CW+in experiments on the adsorption and nettability al- sic nitrogenous orgmric compounds.
te~tion of refntively simple polar ,compormds oir sand- Several experimenters have compared the adsorption
stone and carbonates. The compounds were dksolved in of asphnbenes from crude onto initially clean, dry sazrd-
a nonpolm oil, and the contact angkeof the oillwatcrhnin- packs composed of either quartz or disaggregared” core
eral system was measured on mr initially km, strongly material that contained both quartz and carbonate. 72,110
water-wet aystal surface. &xreraHy, adsorption mrd wet- They found that adsorption was greater in disaggregate
tabifity nkemtion occurred with basic compounds on the core material. Tumasyan and Babclyan 110.measured the
acidic silici surfaces and acidic compounds on the basic adsorption, of asphaltenes from Kyarovdag cmde onto
ccrbomte surfaces. Acidic compounds had very little ef- quartz and cleaned, disaggregate Kynrovdag core m~-
fect. on sifica, and basic com ounds had litde effect on terial @atconticd 10.4 % carbonate. The adsorption wnc
fieCabonat=. fo~l~Note,
37A42,66.7S.7’J. however, that about 8x 10’4 mg/cm2 for qumtz nnd about 18x 10’4
most of the ,adsorbed compounds chmrged the wettabfiV mglcmz for the core material, mr iacrease of more than
only from strongly to mildly water-wet, rather than to a factor of two: Abdurashitoi ef al. 72 meaarzzedthe ad-
oil-wet. sorption of asphnfte”nesonto sida-sized fractions of pure
The acidic compounds that adsorbed and nftered the quartz samds and sends containing both quartz and car-
wettab~l~ of the carbonates in preference to silica in- bonate. They found that the adsorption on the qunrtz sands
cluded naphtherric acid 37.109mrd a number of carbox$; was as much as an order of magnimde lower Own the ad-
ic acids (RCOOH), including capryfic (octanoic , sorption on the sands containing both minerals. These re-”
psfmitic (.hexadecarroic), 42 stearic (@adecanoic), 102,10s srrks are very qualitative, however, because the speCXc
and oleic (cis-9-octadecnnoic) acids. 42 Basic compounds surface arei of the quartz packs was lower dum the area
that adsorbed on the acidic silica surfaces included iso- of the mixed mineral smrdpacks, which afso reduces the
qrdno~ne37and octadccykmzine [CH3(CH~17NH~. 1ffi,108 ~onnt of adsorption.
@mz40 and Morrow ei al. 66 exded dze adsorption
and wettabilhy alteration on quartz “imddolomite of a num- Brine Chemistry. The salhrity nrzdpH of brine ae very
ber of relatively low-molecukw-weight compounds found imw-t in determining wettabiilg because they strongly
in crude oils. Basic nitrogen compounds gave advancing affect the surface charge on the rock surface and fluid in-
contact angles up to 66” [1.15 rad] (water-wet), with terfaces, which in turn can affect the adsorption of .srrr-
higher angles for qrrnrtz than dolumite. Sulfur compounds factants. ‘o,‘m Positively charged, cationic srrrfactanta
tested provided arzgfes of 40” [0.7 rad] or less with wifl be attracted to negatively chnrged surfaces, while
rto systematic dlffercrrces between the two surfaces, The negatively charged, anionic surfactcnts will be attracted
contact angles either were stable or decreased with time to positively charged sin-faces. The surface charge of Q.
(i.e., the system became more water-wet). The acidic ica and ccfcite in water is positive at low pH, but nega-
--
a solution of the organosilane through it, snowing a suffi- ~onmt, Newcombe et d. 136 stated that contact an~es
cient time for the reaction to occur, and then flushing the sa large aa 154” [2.7 rad] could be obtained for aK1casur-
unreacfed compound from the core. Some control of the faces mated with different conqamations of methylsilOx-
change in we,ttabifi~ can be achieved by variation in the ane polymer, but these contact angles tended to decrease
concentration of organosilsne in the solution. For a com- towsrd 90” [1.6 rid] as they aged. Memwat $?ral. l@
plete description of the method, see Ref. 134. tmatcd silica surfaces with various concentrations of four
In addition tu unifoqnly treating cores, organocldorosi- different organochlorosilanes and obtnincd contact angles
kmca are used to prepare fractionally wetted sand- ffom 75 to 160” [1.3 to 2.8 rad] with water and xylene
Packs, 43,46.50,140-142 Sand gtins txeated with 6rgm30- on the treated surfaces. Depcndmg on the specific treat-
chlorosilmies sre mixed witkuntrcated; water-wet sands. ment, they found that the contact angle could gradually
‘The fraction of oil-wet surface is aasumed to be the sb.me increase or decrcaae aa the system aged. Because&e wet-
as the fraction of orgnndcblorosilane-treated sand. One tabtity of cores treated with organosikmes can range from
problem, however, is that some of the organocblorosi- mildly water-wet to strongly oil-wet depending on the Spe:
lane is known to be transferred to the water-wet sand cific treatment, the Amott or USBM method shoufd be
grains, likely changing their wettabtity.43 Auother used to determine the wettabllity of the treated core.
method of obtaining fractioml nettability is to form ‘tie Quilon@ treatments are mother method that has been
porous medium from water-wet (gkMs)beads and oil-wet used to alter the wettabiIity of sandstofie cores. Tiffii hnd
(tcflon) beads. 146 Yellig 149treated Berea cores with Quiion-C@ to render
Moh~~ ad s~tcr 143have reqedfy publiahcd a tech- them uniformly oil-wet. Workers at tie Petroleum Recov-
nique to generate mixed-nettability cores so that the large ery Inst. have used Quilon-S@, i related com-
pores have continuous’ water-ivet surfacca, leaving the ~md, 15~153 me won compounds consist of a chrome
smalf pores ofi-wet. Note that in these cores, the netta- complex containing a hydrophobic fatty acid group in an
bility is reversed from Salatbiel’s47 mixed-wettability isopropyl alcohol solution. When @iiori is injected into
cores. Cleaned cores are first treated witi orgagosikmes tie core, the molecules bmd to the surface, expose the
to render them uniformly oil-wet. The treated cores are fatty acid group, and render the rock surface oil-wet. 1X
saturated with oil, flooded with heptadecane to dkplace Note that wettabtity of the treated core probably v~ies,
the oil, and then flooded with brine to ROS. Because the depending on concentration, tfcatment time, etc., so it
core is oil-wet, the large pores are fdlcd with brine, but should be meaaured with the USBM or Amott metbnds.
the small ones are fdled with oil. Brine and heptadecane In many crises, the treated core is probably OIIIYneutral-
IMY then be injected simu&aneously to alter the fraction ly to mildly oil-wet.
of pores ffled with oil or water. After the desired satura- These trcatmerita have been used on sandatone core with
tion is reached, the core is fust placed in a cold water the chemical binding to the s~Ica surfaces. Orgsno-.
bath (50”F [1O”C])to freeze the heptsdecane, then an 11.5 chlorosikme treatments, which adsorb on silica surfaces
pH sodium hydroxide solution is injected to diapfimc the by reacting with the hydro+yl grou$a, are generally not
brine. Mohanty and Sslter state that the alkaline solution effective on carbonate surfacea. 1 5,1% A number of
removes the orgnnosilane coating from the lnrger, brine- ~Wche~~ 109.155-157bWe used m hthenic acids to
tilled pores, leaving them strongly water-wet, while the render carbomtc cores more ofl-wet. ?7 The naphtle~c
frozen heptadecane prevents auy change in nettability in acids react with the calcium carbonate to form cslcium
tie small oiLffled, oil-wet pores. Folly, t+e alksdine so- naphthenates, which are ofi-tiening. 109 Note that
lutiori is displaced with brine, arid all of the fluids are re- naphthenic acida will not nlter the wettabtity of saudatone.
moved, leaving a mixed-wet@ ility core. After this s~faces. ‘w
treatment, the cores imbibed both oil and water, indicat- Sharma and Wuuderlich15s altered the nettability of
ing that areas of the. core were both water- and oil-wet. Berea pIugs by saturating’ them with au asphaltic crude:
Unfortunately, Moh&y and Salter did not test the cores Drv Dlum were vacuum-saturated with isrhaltic cmde oil,
: by oil flooding them to determine whether they had a very th&’fl~shed with pentane, which ten& to precipita~
low water.saturation after tie injection of “manyPV’s of asphakenca onto the pore walls. 67 The pentane was”re-
oil. This would have verified the formation of continu- moved in a vacuum, kwiug behind a layer of asphaltenes.
ous water-wet paths through the large pores, which would Tim plugs probably had mixed wettnb~ky after Ecatmenc
be analogous to oil-wet paths in Sala~el’i cores. boti,oil snd water would imbibe spontaneously. 3 An ad-
One problem with orgamochlorosilane treatments is that vsutage of thk method is that it uses com@mda found
the nettability of the tmatcd core varirs depending on such natnrslly in the resetioir and ,pight be a more realktic
variables as the orgtiocidorosil~e used, the concentra- ticatrnent than the other trcahnenta discussed above. Note,
tion, the treatment iiine, the time elapsed since the sur- however, that it is necessary to verify tiat the crude is
face was treated, and the pH of the brine. 147 No compatible with the pentie because some cmdes will plug
dependable treatment has been reported for acgeving a the core when pentane is injeded.
given: core wettahilhy. Note that many organosilane-
treated cores ze only neutrally to mildly oil-wet, instead Artificial Coma. Several rcaearchera have used artificial
of strongly ofl-wet. Coley et al. 134used General Elec- cores and pure fluida to control wettab~hy. The uniform
tric Co. s~lcone fluid No. 99 in concentrations ranging composition of tie core and the absence of surfactimts
from ‘0.002sto 2.0% and were nhle to vmythe contact combine to give a constant; uniform, and reproducible
angle, in. glass capillaries only from 95 to 115° [1.7 to nettability. The most popular material for the artificial
2 fad]. RathnieO et al. 137found that cores treated with core baa been polytetiafluoroethylene (teflon). Stegemeier
dmethyldichlorosikme would still slowly imbibe water, fid Jess&n159used porous packa of tcflon particles. More
indicating that the cores were at most neutrslly wet. In recent experiments hsve used consolidated teflon
1’
NATIVE-STATE CORE
liner can be DESeNed if the ends are capped’and sealed. approaches one as the water-wetness increases. Siniiiar:
A number-of experiments have dem&strated that ex- ly~ the displacement-by-oil ratio is zero for neutrally and
posure to air and drying cao alter the nettability of core. water-wetcores aod approaches one as the oil-wetness
As discussed earlier, Treiber et al. w measured the. net- increases. The cores became more oil-wet as they were
tability of 50 reservoirs usfig deoxygemted synthetic for- either exposed to the air for longer periods of time, o!
mation brine and anaerobic crude. In some cases, the at higher temperatures. Similar tests on an initially weakly
contact angle showed that the reservoir was water-wet. water-wet core showed elmost no change. On the other
For some of those cnrdes, exposure to oxygen changed hand, Mungan 115used the imbibition method to meas-
the wettabili~ to ofi-wet. Bartell mrd Niederhauser103 ure the wettabilhy of native-state cores. In contrast to tie
stodied interracially active materials in crude, which con- experiments discussed above, cores preserved in deaer-
centrate and form solid fflms at the oil/water interface. ated water were oil-wet, but becsore water-wet when ex-
These materiils can also be adsorbed on the rock surface, posed to ti for 1 week. Chfingar and Yen35 have also
rendering it oil-wet. Crodes and brines were obteined and reported that some cores became more water-wet on ex-
stored without exposure to oxygen. Most of these crudes posure to sir, indicating that it is bnpossible to predict
showed very little interfaciel activity. On exposure to air, how the wetfsbtity will be altered by tie oxidation of tie
the cmdes developed moderate-to-strong fdrn-fomning cmde.
tendencies, while the oil/water IFT was lowered by as Mungao 180recnmmendsflushing native-state core with
much as 50 %, indicating that surfactants were formed by five erode oil before sny flow studies are startsd. After
oxidatiori of the crude... native-state cores .havc been prepared, they are usually
Richadson et al. 1s2 stored core’ from a mixed- nm at reservoir conditions with crude oil and brine.
wettability reservoir47 using four different methods. Ox- Probably the greatest, uncontrollable problem with
idation snd drying of the core tiere prevented with the nstive-state core is the alteration of nettability as the core
first two methods: (1) core wrapped in foil and scaled in is brought m the surface., When the pressure is lowered
paraffh and (2) core stored in evacuated (deoxygenated) to atmospheric, light ends are lost from the erode, chang-
formation water. The other methods were (3) core stored ing its properties. In addition, heavy components cm come
in aerated formation water and (4) core stored in cloth out of solution and deposit on the rock, making it more
core bags. The cores were oilflooded with kerosene to oil-wet. 137 The decrease in temperature wilf also
IWS and then waterflooded. The average ROS for the decrease the solubili~ of some wettebfli~-altering com-
samples protected from oxidation and drying (Methods pounds. Pressure coring prevents tie loss of light .erids.
1 and2) was about 13%; forthesamples submergedin However, the cores are frozen before removal, so
aerated water, about 24%; and for the samples storedin wetta.bflity-altering compounds ‘W deposit. Unfortunate-
core bags, about 25%. ly, there is no experimental work avsilableon wettabfli-
Bobciket al. 175used the imbibition method to compare ty alteration as the core is brought to the surface. ..
the nettability of native-state cores at the wellsite, cores
allowed to weather, and cores stored by the two recom- .’
mended metiods discnssed above. The nettability of the Cleaned Core
cores stored by either of the two recommended methods The second type of core used in core aoalyais is the
was the same as the nettability measured at the wellsite, cleaned core. Cr&ig7 recommends that cleaned core be
while most of the weathered cores became more oil-wet. used for multiphase flow measurements only when the
Am0tt177 used bismethtid”t ocompari”th ewettabihy reservoir is known to be strongly water-wet because errors
of native-state cores with similar cores that were exposed iq the core am.lysis will be introduced otiimvise. There
tooxygen ayd~owed to partially dry, asshownin Ta- are two main reasons to clean wre. The first is to remove
ble 3. The native-stste cores were strongly water-wet, with all liquids “fromthe core so that. porosity, permeability,
a dkplacement-by -water ratio of 0.97. In the Amott test, and fluid saturations can be measured. Core cleaning for
the displacement-by-water ratio is the ratio of the oil these roudoe core measurements will not be considered
volume displaced by spontaneous imbibition to the total in this paper. The second reason for cleaning is to obtain
oil volume displaced by .botb imbibition and forced dis- a strongly water-wet core, generally as a first step in
placement. Itiszero forneuqally mdofl-wetcO~~s aod restoring the wettabfity of a contaminated core.
J&mal of Petroleum .Tecbnology, October 1986 1135
In obtaining a cleaned core, an attempt is made to re- tenes 130JW and some of the weakly polar compcmmi.s,lW
move all of the fluids and adsorbed material, leaving a wbile”tbe more,spongly ’polar methanol (ethanol) qcmoves
clean rock surface. Gant aid Anderson 129 discuss the the strongly adsorbed polar compounds that are often
me’ibcdsused,tu clean core. One common method is reflux responsible for altering wettabilky. In addition to
extraction (l)ean-Stark or Soxhfet) with a solvent such as toluenelmethanol and tolueneletbonol, successful clean-
toluene, sometimes followed by extraction with cfdoro- ing has ako been reported with cbforoforndace-
form or methanol. Alternatively, a flow-through system tone 1wZ120. 1= and cfdorofordmetfranol, 1s4 as well as
where the solvents are injected under pressure is some- a number of different series of solvents. ‘,65
times used. 57,&,65lf the cleaning procedure is success- CuieCand his coworkers made the most extensive study
ful, the core is left strongly water-wet. Cuiec”$5 mid of core cleaning for nettability restoration. In a recent
others 57,1w discussed the chemicalreactions involved in paper, Cuiec et az. 130statkd that their core cleaning al-
the cleanin process. ways begins with a toluene flush to remove hydrocarbons
Cui&ca,& compared me efficiency of different solvents and asphaltenes. A number of solvents are then.tested to
in flow-through core cleaning. Initially water-wet outcrop determine the most effective, including (1) a series of non-
sandstone and limestone cores were saturated with differ- polar solvents, e.g., cyclohexane or heptane; (2) acidic
ent cntdes (sometimes the cores also contained brine), then solvents, e.g., cblorofonn, ethanol, or metbanoh (3) ba-
aged. The aged cores ivere ncyrmfly neutr~- to oil-wet, sic solvent’i, e.g., dioxane or pyridine; ond (4) mixtures
as determined. by the Amott wettabflity test. The cores of solvents, e.g., methanollacetoneltoluene. When none
were then cletied with dlffererit solvents, and the Amott of these procedures are effective, other tests are performed
test was used to determine cleauing efficiency. Cuiec by combining the above procedural, using otler solvents,
found that he could clean both sandstone and liiestone ad incremfig the Circdatiog time.’
cores by flowing the f?ll@ig seven solvents through the Tohtene is generally not a very effective solvent, but
core: pdarte, hexane, heptane, cyclobexane, beuzene, it can”alter the nettability of some core. Jennings 186
pyridine, and ethanol. Chloroform, tohtene, and methanol cleaned sever,d cores by toluene extraction and found that
used singly were not very effective. Cuiec also looked the wettabilities and relative penn.eabilities were not
at several dtiercnt acidic and basic solvents used individu- changed. He stoted that this indicated that toluene-
ally and found that the acidic solvents tended to be more extmcted core retoined the reservoir wettabi!ity and coufd
effective in cleaning sandstone, whiie the basic solvents be used for relative p+mneabtity rneosurements, However,
were better in cleaning Iimcstone. This difference was at- this generally is not the case. Aftbough it is less et%cient
tributed to the acidic nature of the sandstone surface and than other solvents, we have found that toluene extrac-
the basic mture of the limestone surface. For examplei tion can alter the wettabili@ and relative penneabtitics
because sandstone (silica) has a weakly acidic surface, of native-state core. fn some cases, neutmlly wet or tidly
it tends to adsorb bases from tie crude oif. When a oil-wet mtive-state core becomes strongly water-wet ti-
stronger acid flows through the sys@m, it will gradually ter extraction witi toluene. The relative permeability
react with and strip off the adsorbed bases, Ieaviug a clean cume~ ~~o ~E,fi. AMOU177 ako found that toluene ex-
silica surface. traction can clean some cores, while it had Wt3e effect
G@ and Anderson 129 surveyed most of the core- for other ones, such as the strongly oil-wet Bradford cores.
cleouing experiments in “the literature. They found that Therefore, because tolueneextraction will alter the wet-
the best choice of solvents depends heavily on the cmde tabilky and relative permeability of many. native-state
~d the mineral surfaces becavse they help determine the cores, m%uremcnts shouId be tie on mtive-state cores
amount and @pe of nettability-altering compounds ad- before toluene extinction.
sorbed. Solvents that give good results with some cores One problem with a cleaned core is that it is sometimes
and cmdes often faif in other cases. For example, Grist difficult, if not impossible, to remove all of the adsorbed
et al. 1s4 and Holbrook and Beruard45 both found that material. If this occurs, the wetta.bfity of tie cleaned core
they could clean core to a strongly water-wet state using wifl be left in some indefinite staie, causing variations in
a cliloroformfmerhanol mixture, while Jennings5s repOrt- core analyses. Grist et al. lW cleaned cores by three cu-
ed. fiat thk was unsuccessful. For cleaning for routine rently used methods and then examined how ROS and end-
core analysis, API 1s5 reports that cbfom form is excel- point effective permeabilities vtied after a waterflood.
lent for many midcontinent .ct’udes,wh~e toluene is us6- ROS was very similar for W methods. However, the end-
ful for asphaltic cntd:s.. point effectiye water permeability varied by more than
hi many cases, it appears that any single solvencis rela- a factor of three betwtin different cleaning methods. Their
tively ineffective in core cleaning and that much better explanation for this behavior was that some methods were
results can be obtained wiih a mixtttfe or series of able to extract more of the adsorbd. components, leav-
solvents. 129 The followhg solvents have, been rCpOfi- ing.the rock more water-wet. In the more water-wet cores,
ed for specflc binbinations of crude and core to give the rwidti oil had a greater tendency to form trapped
pcor resufts when used alone: chloroform, ‘,65 ben- droplets, blocking pore throats and lowering water per-
zene, 5S,1M,120~=bon di~~fide, lU,120 ~~mol, @ ~d meabtity. The least effective of the three cleaniug me~ods
toluene.5@.@.65 .1~.120,1T.l~,1s6 was overnight reflux extinction with toluene. More ef-
Many of the researchers cited above have found that fective was reflux extraction with toluene followed by 2
toluene used alone is one of the least effective solvents. days of extraction with a mixture of cbloroforin oud
However, when combined with other solvents, such as methanol. Finally, tie most efficient method was reflux
methanol (CHs OH) 184 or ethanol (CH3 CH zOH), 61 extraction with tcduene followed by 3 weeks of extrac-
toluene is often ve~ effective. The toluene is effective tion with chloroform and methanol. In the last stage of
in removing the hydrocarbons, including asphal- cleaning, methanol was used alone.
to prevent the deposition of au oil-wet fiim, leaving them meland and Lamondo 192 found little difference in con-
water-wet. Onthe other hand, ifaclcan core is saturated tact angles measured using stock-tank vs. live cmde at
only with oil, tbe entire core, includlu gtbesmallpores, the reservoir temperature (190”F 88”C]) and pressure
will become uniforndy oil-wet, whlchis the wrong wet- (3,800 psi [26.2 MPa]). Mtmgan 10 i measured a water-
tability. Anaddhionalp roblemw ithsaturadngt iec ore advancing contact angle ,of $7” [1.5 rad] using live reser-
solely with oil istbat the effects of brine chemistry are voir crude and synthetic formation brine at resemok tem-
ignored. As discussed previously, the wettabtity of the perikurc (138”F [59”C]) and pressure (1,200, psi [g.3
core depends on the ionic composition and pH of the brine. MPa]). The water-advwcing contact angle was almost
Finally, Clementz10?.120,121$howedtbat flowing cntde identical, 85” [1.48 rad], using degassed crude and brine
oiltbrougha dry core camcause tbeformition of very at ambient pressure and reservoir temperamre.
stable oil-wet, claylorganic complexes. Thepresenceof Because refined oifs are much easier to work with tlum
an initial water film on the clay surfaces haa been shown cmde, it is a common laboratory practice to flush native-
to reduce but not completely inhibit the adsorption of the or restored-state cores with refined oil before testing.
nettability-akering materkds. @@.70 The effects of brine However, there is a possibilky that this idters the netta-
OtI wearability make it necesssry to saturate the core with bility. Craig7 poshdated that it would be possible, once
brine, then oil, during the nettability restoration process. the original wettabtity was restored, to use refined nzin-
eml oil in place of crude oil in laboratory tests without
Experimental Conditions adversely affecting the wetk+bility. Test times are shor!
compared with the time it takes to achieve adsorption equi-
Once a mtive or restored-state core is obtained, core anal-
librium and obtain native wettsbtity (about 1,000 hours).
yses can be performed. These tests can be mn with either
Craig hypothesized that the desorption of wettability-
crude or refined oil at ambient or reservok’ temperature
Mbzencing materials would require a correspondingly
and pressure. Because wettabfity effects are being ig-
long period of time. If this is correct, @e orig@l wetta-
‘Personalc.mm””lcati.nwl,hD..J.Wendel,Pe!r.aleum
TestingSeMceS,Smta btity wotdd be unchanged if laboratory tests using refined
Fe SPringS,CA,No”.19S0. oil and brine were conducted quickly enough.