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Step 1. Calculate maximum allowable bottom hole pressure (formation fracture pressure), pfr
p fr = g f D (1)
Where
gf : fracture gradient, psi/ft
D : formation vertical depth, ft
pfr : maximum allowable bottom hole pressure
Where
hp : perforated interval, ft (use pay zone thickness for open hole completion)
k : average permeability, md
pR : reservoir pressure, psi
re : drainage radius, ft
rw : wellbore radius, in.
’
rw : effective wellbore radius, in.
s : skin factor
µ : acid viscosity, cp
The injection rate (qi) to avoid fracturing must clearly be lower than qm (qi<qm). As a practical matter, a
rate 10 percent lower is suggested.
qi = 0.9qm (4)
Preflush is an important feature of sandstone acid treatment. The main purpose of the preflush are to
remove those formation materials which will react to a significant extent with HCl, to displace those
+ ++
formation waters containing ions (Na , Ca , etc) which will tend to precipitate with HF, and to cool the
formation thereby permitting deeper acid penetration.
7.5 or 15 wt% HCl is used frequently as preflush. If corrosion is a substantial problem, preflushing with
formic acid is acceptable. Because of incomplete reactions, higher molecular weight organic acids are
not recommended.
V pf = VC / X (5)
Χ = βa ( ρa / ρr ) (7)
M wr Csr
β100 = (9)
M wa Csa
Where
Csa : stoichiometric coefficient of mineral, Csa=1 for HCl reaction with limestone and dolomite
Csr : stoichiometric coefficient of acid, Csr=2 for Limestone+HCl; and Csr=4 for dolomite+HCl
fC : wt% of acid soluble minerals
Mwa : molecular weight of acid (Table 1)
Mwr : molecular weight of mineral (Table 1)
NPe : Peclet Number
rC : radius of zone containing acid soluble mineral, in
VC : volume of carbonates in formation, gal
Vpf : preflush volume, gal
wHCl : HCl acid concentration, wt%
X : Volumetric dissolving power of acid
βa : gravimetric dissolving power of “a” wt% acid (mass of rock dissolved per unit mass of
“a” wt% acid reacted).
β100 : gravimetric dissolving power of 100 wt% acid (mass of rock dissolved per unit mass
of 100 wt% acid reacted).
ρa : acid density, g/cc (Table 2)
ρr : rock density, g/cc, ρr=2.71 g/cc for limestone and ρr=2.87 g/cc for dolomite
φ : porosity
Mineral β100 5% 10 % 15 % 30 %
A = 336.9 Fq i (11)
1 1.0032 22 1.1083
2 1.0082 24 1.1187
4 1.0181 26 1.1290
6 1.0279 28 1.1392
8 1.0376 30 1.1493
10 1.0474 32 1.15.93
12 1.0574 34 1.1691
14 1.0675 36 1.1789
16 1.0776 38 1.1885
18 1.0878 40 1.1980
20 1.0980
1 + Bf (t )
F = 7.094 ρ a (12)
B
d tiU
B= (13)
33.6
1 1 d ce + d te − d ci − d ti d ci − d te
= + + (14)
U h 600 8.304
0.8
(q ρ )
h = 4778.8 1i .8 a 0.4 (15)
dt, µ
log f (t ) = 0.31333 log Y − 0.06(log Y ) 2 + 0.006666(log Y ) 3 (16)
t
Y= (17)
2.609d ce2
where
A : function defined by Eq. 11, ft
B : function defined by Eq. 13
dce : casing OD, in.
dci : casing ID, in.
dte : tubing OD, in.
dti : tubing ID, in.
2
F : function defined by Eq. 12, hr/ft
f(t) : transient heat-conduction time function defined by Eq. 16
gT : geothermal gradient, °F/ft
2
h : film coefficient of heat transfer, Btu/hr-ft -°F
Tes : earth’s surface temperature, °F
Tas : temperature of acid at surface, °F
2
U : overall heat transfer coefficient, Btu/hr-ft -°F
t : injection time, hr
Y : function defined by Eq. 17
ρa : acid density, g/cc (Table 2)
3h pη rs + rw
Va = (18)
wHF rs − rw + 6
η = 140 + C1 + C 2 x + C 3 y + C 4 x 2 + C 5 xy + C 6 y 2 + C 7 x 3 + C8 x 2 y
x = rs − rw − 4 (20)
y = log(q i / h p ) (21)
Where :
C1–C20 : constants of Eq. 19 (Table 3)
rs : radius of damaged zone, in.
x : function defined by Eq.17
y : function defined by Eq.18
z : function defined by Eq.19
η : specific mud acid volume, gal/ft
Compare tp with initial guess t. Repeat Steps 4 through 6 taking t=tp as necessary until the calculated
injection time does not significantly change.
psi = p p + p fr + p f − ph (25)
0.2369q 2p ρ a
pp = q p = qi / n (26)
d p4α 2
ph = 0.052 ρ a D (27)
where