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Rheology
F μ∗V
o =
A L
o μ (viscosity) = constant of proportionality
o F/A = shear stress
o V/L (velocity gradient) = shear rate
8V
o γ= for pipe flow
D
o γ=12 V /( D 1−D2)
Viscosity is the representation of a fluid’s internal resistance to flow, defined as the
ratio of shear stress to shear rate.
τ shear stress
μ= =
γ shear rate
Dyne × sec
μ= 2
=poise
cm
o Only laminar flow can be described analytically, turbulent flow must be
described empirically
Rotational Viscometers
o Hard to build viscometer with two parallel plates; instead use an outer
sleeve rotating around an inner bob
o Fluid exerts torque on inner bob, which is measured with a torsional spring.
Torque can be related to shear stress
o All fluid characterization measurements must be taken in laminar flow
300∗θ
o μ= ; at N=300, μ= θ
N
o γ=1.7N; where N is RPM of viscometer
Fluid Types
o Newtonian Fluids- shear stress directly proportional to shear rate (i.e.
water, gases, high gravity oil)
o Non-Newtonian Fluid- no direct proportionality between shear stress and
shear rate
o Pseudoplastic- viscosity reduces with increasing shear rates
o Dilatant- viscosity increases with increasing shear rates
o Thixotropic- viscosity decreases with time sheared, mud “thins” over time
with shearing and “gels” when static (usually not modeled)
o Rheopectic- viscosity increases with time sheared
Rheological Models
o Want a high YP/PV ratio. Means the fluid has good shear thinning
properties.
o Effective Viscosity- Viscosity of Non-Newtonian at particular shear rate.
o Apparent Viscosity- Viscosity reading at Θ600 divided by 2 (API). It is a
reflection of the plastic viscosity and yield point combined. An increase in
either or both will cause a rise in apparent viscosity (and probably in funnel
viscosity
o n=3.32× log
( )
θ600
θ300
or n=log
τ1
γ2
γ1
510∗θ600 θN
o K= or K= (lbf/100 ft2)
511
n
( 1.703 × N )n
log
( θ2−YP
)
( )
θ1−YP θ600 −YP
o n= or n=3.32× log
( )
γ2 θ300 −YP
log
γ1
o YP= in practice is taken as the dial reading at RPM
Drilling Hydraulics
[ ]
2
n
1.0678 1
Bx = 2
x
[ 1.0672− 2
]
n n
1.0678
Combined Shear Rate Correction Factor
G=Ba /B x
o Shear Rate at Wall
γ w =(1.6∗G∗V )/d hyd
o Shear Stress at Wall
Pipe , τ w =1.066∗ () 4 n
3
n
∗τ y +k∗γ w
o Calculate Reynolds Number
ρV2
N ReG=
19.36 τ w
o Critical Reynolds Number
N CRe =3470−1370 n
o Laminar Friction Factor
f lam=16/ N ReG
o Turbulent Friction Factor
16 N ReG
f trans= 2
N CRe
o Turbulent Friction Factor
a
f turb=
N bReG
log ( n ) +3.93
a=
50
1.75−log ( n )
b=
7
o Frictional Pressure Loss
2
1.076∗ρ∗V p∗f ∗L
Pipe , P= 5
10 d i
1.076∗ρ∗V 2a∗f∗L
Annulus , P=
105 d hyd
Hole Cleaning
o Solid particle in hole is acted on by four factors
Gravity
Viscous drag
Impact
Buoyancy
o Slip Velocity
h ( ρc − ρ ) .5
V S =2.19( )
ρ
The primary objective of the drilling engineer must be to maintain hole stability,
because a gauge hole can be cleaned with a low viscosity mud, in which case progress
will be rapid and problems will be few. If the hole enlarges, as it inevitably will in many
formations, viscosity and gel strengths will have to be increased in order to clean the
hole, but the higher viscosities and gel structures will decrease penetration rates and
cause high swabbing and surge pressures, gas cutting, etc. The conflicting rheological
requirements will be minimized by using a shear-thinning mud, which sets to a
gel, which is sufficient to suspend cuttings when circulation is stopped, but which
breaks up quickly to a thin fluid when disturbed. Such a mud will have a high yield
point/plastic viscosity ratio, and a low flow-behavior index, n. Techniques for
controlling the rheological requirements in the field are beyond the scope of this
chapter, but it may be said that high YP/PV ratios are best obtained by lowering the
plastic viscosity rather than by increasing the yield point, As a general rule,
therefore, maintain the lowest possible plastic viscosity by mechanical removal of
drilled solids at the surface, and keep the yield point no higher than required to
provide adequate carrying capacity. The yield point is controlled by adding or
maintaining thinners when drilling colloidal clays and by adding bentonite when
drilling other formations.
The clay in its dry state has platelets stacked in face-to-face association, like a deck of cards.
This is Aggregation. When the dry clay is placed into fresh water with no agitation, the
packets adsorb water, hydrate, and swell. Upon agitation, the swollen packets disintegrate
into individual plates or smaller packets of plates. This is Dispersion. As long as agitation
continues, dispersion will be retained and further dispersion can occur. When agitation is
stopped, clay platelets will be mutually attracted in edge-to-edge or edge-to-face
association. This forces a structure similar to a house of cards, termed Flocculation. If an
anionic chemical thinner (deflocculant) is added, such as polyphosphate, lignosulfonate or
lignite, etc., it neutralizes the positive edge charges on clay platelets and the flocculated
state is now Deflocculated. When this deflocculated clay slurry encounters strong ionic
contamination (NaCl, CaSO4, Ca(OH)2 , etc.), the deflocculant chemical is often overpowered
- leading again to flocculation and even to a sort of aggregation where water is lost from the
clay surfaces.