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-Rajeev Upadhyay
Permeability
Henry Darcy (1856) conducted an experiment in order to study fluid
flow behaviour through a bed of packed sand particles. He observed
that the volumetric flow rate of water through the packed bed is a
function of:
1. Dimension of porous medium
2. The difference in hydraulic head
ℎ1 −ℎ2
𝑞 = 𝐾𝐴 , where 𝐾 is the hydraulic conductivity
𝐿
Darcy's only variation in this experiment was to change the type of sand
pack, which had the effect of altering the value of the constant K;
otherwise, all the experiments were carried out with water and
therefore, the effects of fluid density and viscosity on the flow law were
not investigated.
Darcy’s law is found to be valid for other fluids when the above
equation is modified to include viscosity and density of the fluid:
𝐾𝜌𝐴 ℎ1 − ℎ2
𝑞=
𝜇 𝐿
Permeability
The permeability is the measure of the ease with which a fluid can flow through a rock.
𝑘𝐴∆𝑃
𝑞=
𝜇𝐿 q
P1 P2
A = Area of rock sample , m2
L = Length of rock sample , m
∆𝑃 = Pressure differential across the sample, Pa
𝜇 = fluid viscosity , Pa.sec
q = flow rate , m3/sec
k = Permeability , m2
Unit of Permeability
Permeability has the dimension of m2, but it is commonly expressed in Darcy (D) or millidarcy (mD)
Parameter SI System Darcy System Field
In darcy system,
Length m cm ft
Mass kg g lb q cc/sec = q * 10-6 m3/sec
Time sec sec hr A cm2 = A * 10-4 m2
∆𝑃 atm = ∆𝑃 * 101325 Pa
Rate m3/sec cc/sec Stb/d (liq), 𝜇 cp = 𝜇 * 10-3 Pa.sec
Mscfd(gas) L cm = L*10-2 m
Pressure Pascal atm psia
Suppose 1 Darcy = x m2
Viscosity Pa.sec cp cp
K Darcy = K*x m2
Permeability m2 Darcy mD
𝑘𝑥𝐴 ∗ 10−4 ∆𝑃 ∗ 101325
𝑘𝐴∆𝑃 q ∗ 10−6 =
𝜇 ∗ 10−3 ∗ 𝐿 ∗ 10−2
𝑞=
𝜇𝐿
𝑘𝐴∆𝑃
𝑞 = 1.01325 ∗ 1012 𝑥
𝑥 = 0.987 ∗ 10−12 𝜇𝐿
i.e., 1 Darcy = 0.987 ∗ 10−12 𝑚2 ~10−12 𝑚2
Linear Fluid Flow Through Porous Media
Permeability is defined by the Darcy
P2 P1
Equation :
𝑘𝐴 𝜕𝑃
𝑞=−
𝜇 𝜕𝐿
𝐿 𝑃2
𝑘𝐴
𝑞 න 𝜕𝐿 = − න 𝜕𝑃
𝜇
0 𝑃1
𝑘𝐴
𝑞= ∆𝑃
𝜇𝐿
Linear Fluid Flow Through Porous Media
𝑘𝐴
𝑞= ∆𝑃 P2
𝜇𝐿 P1
q Cross-
sectional
𝑘𝐴
𝑞= ∆𝑃 (In SI unit) L area = A
𝜇𝐿
Conversion into field units:
1.84 ∗ 10−06 𝑞 5.615∗0.0283168 𝑚3
q stb/d = q ∗
0.987 ∗ 10−15 ∗ 0.093𝐴 ∗ 6894.76∆𝑃 24∗3600 𝑠𝑒𝑐
− 06
= In field units =1.84 ∗ 10 𝑞 𝑚3/𝑠𝑒𝑐
𝜇 ∗ 10 ∗ 0.3048𝐿
−3
k mD = 0.987 ∗ 10−15 𝑚2
𝑘𝐴 ∆𝑃 𝑝𝑠𝑖𝑎 = 6894.76∆𝑃 𝑃𝑎
𝑞 = 1.127 ∗ 10−03 ∆𝑃 In field units 𝜇 cp = 𝜇 ∗ 10−3 Pa.sec
𝜇𝐿
A ft2 = 0.093A m2
L ft = 0.3048L m
Linear Fluid Flow Through Porous Media
𝜌
ɸ1 = 𝑃1 − ∆𝑍
144 1
42
ɸ1 = 2000 − 87.15 = 1974.58 𝑝𝑠𝑖
144
𝑘𝐴(ɸ2 − ɸ1 )
𝑞 = 1.127 ∗ 10−3
𝜇𝐿
𝑃𝑉
𝑛=
𝑧𝑅𝑇
𝑛𝑧𝑠𝑐 𝑅𝑇𝑠𝑐
𝑉𝑠𝑐 =
𝑃𝑠𝑐
𝑃𝑉 𝑃𝑠𝑐 𝑉𝑠𝑐
=
𝑧𝑇 𝑇𝑠𝑐
the above relation can be expressed in terms of the reservoir condition flow rate q, in bbl/day, and
surface condition flow rate Qsc, in scf/day, as:
𝑃(5.615𝑞) 𝑃𝑠𝑐 𝑄𝑠𝑐
=
𝑧𝑇 𝑇𝑠𝑐
Linear flow of compressible fluids
𝑃(5.615𝑞) 𝑃𝑠𝑐 𝑄𝑠𝑐
=
𝑧𝑇 𝑇𝑠𝑐
𝑃𝑠𝑐 𝑧𝑇 𝑄𝑠𝑐
𝑞=
𝑇𝑠𝑐 𝑃 5.615
𝑘𝐴 𝜕𝑃
𝑞 = −1.127 ∗ 10−3
𝜇 𝜕𝐿
𝑃𝑠𝑐 𝑧𝑇 𝑄𝑠𝑐 −3
𝑘𝐴 𝜕𝑃
= −1.127 ∗ 10
𝑇𝑠𝑐 𝑃 5.615 𝜇 𝜕𝐿
𝐿 𝑃2
𝑄𝑠𝑐 𝑃𝑠𝑐 𝑇 𝑃
න 𝜕𝐿 = − න 𝜕𝑃
0.006328𝑘𝑇𝑠𝑐 𝐴 𝜇𝑧
0 𝑃1
Linear flow of compressible fluids
For pressure less than 2000 psi, the property 𝜇𝑍 is nearly constant,
Setting 𝑃𝑠𝑐 = 14. 7 psi and 𝑇𝑠𝑐 = 520oR in the above expression
gives:
0.111924𝑘𝐴(𝑃12 −𝑃22 )
𝑄𝑠𝑐 =
𝑇𝐿𝜇𝑧
Radial flow of incompressible fluids
In a radial flow system, all fluids move toward the producing
well from all directions.
−3
𝑘𝐴 𝜕𝑃
𝑞 = 1.127 ∗ 10
𝜇 𝜕𝑟
𝑘𝐴 𝜕𝑃
𝐵𝑜 𝑄𝑜 = 1.127 ∗ 10−3
𝜇 𝜕𝑟
𝐵𝑜 𝑄𝑜 𝑘 𝜕𝑃
= 1.127 ∗ 10−3
2𝜋𝑟ℎ 𝜇 𝜕𝑟
Radial flow of incompressible fluids
𝐵𝑜 𝑄𝑜 𝑘 𝜕𝑃
= 1.127 ∗ 10−3
2𝜋𝑟ℎ 𝜇 𝜕𝑟
𝑟𝑒 𝑃𝑒
𝐵𝑜 𝑄𝑜 𝜕𝑟 −3
𝑘
න = 1.127 ∗ 10 න 𝜕𝑃
2𝜋ℎ 𝑟 𝜇
𝑟𝑤 𝑃𝑤𝑓
0.00708𝑘ℎ(𝑃𝑒 − 𝑃𝑤𝑓 )
𝑄𝑜 =
𝑟
𝜇𝐵𝑜 ln 𝑟𝑒
𝑤
Example
An oil well in a field is producing
at a stabilized rate of 600 STB/day at a stabilized
bottom-hole flowing pressure of 1800 psi. Analysis of the
pressure buildup test data indicates that the pay zone is
characterized by a permeability of 120 md and a uniform
thickness of 25 ft. The well drains an area of
approximately 40 acres. The following additional data is
available
rw = 0. 25 ft, A = 40 acres
Bo = 1. 25 bbl/STB, μo = 2. 5 cp
Calculate the pressure profile (distribution)
0.00708𝑘ℎ(𝑃𝑟 − 𝑃𝑤𝑓 )
𝑄𝑜 =
𝑟
𝜇𝐵𝑜 ln 𝑟
𝑤
𝑟
𝑄𝑜 𝜇𝐵𝑜 ln 𝑟
𝑤
𝑃𝑟 = 𝑃𝑤𝑓 +
0.00708𝑘ℎ
𝑟
600 ∗ 2.5 ∗ 1.25 ln
𝑃𝑟 = 𝑃𝑤𝑓 + 0.25 = 1800 + 88.28 ln 𝑟
0.00708 ∗ 120 ∗ 25 0.25
Radial flow of slightly compressible fluids
𝑘𝐴 𝜕𝑃
𝑞𝑟𝑒𝑓 1 + 𝑐(𝑃𝑟𝑒𝑓 − 𝑃) = 1.127 ∗ 10−3
𝜇 𝜕𝐿
𝑞𝑟𝑒𝑓 1 + 𝑐(𝑃𝑟𝑒𝑓 − 𝑃) −3
𝑘 𝜕𝑃
= 1.127 ∗ 10
2𝜋𝑟ℎ 𝜇 𝜕𝐿
0.00708𝑘ℎ
𝑄𝑜 = 𝑙𝑛 1 + 𝑐(𝑃𝑒 − 𝑃𝑤𝑓 )
𝑟𝑒
𝜇𝐵𝑜 𝑐 ln 𝑟
𝑤
Radial flow of compressible fluids
𝑘𝐴 𝜕𝑃 𝑃
𝑞 = 1.127 ∗ 10−3 𝑇𝑄𝑠𝑐 𝑟 2𝑃
𝜇 𝜕𝑟 ln = 0.703 න 𝜕𝑃
𝑘ℎ 𝑟𝑤 𝜇𝑧
𝑃𝑤𝑓
𝑃𝑠𝑐 𝑧𝑇 𝑄𝑠𝑐
𝑞= Where, 𝑄𝑠𝑐 is in scf/d 𝑃 𝑃𝑤𝑓
𝑇𝑠𝑐 𝑃 5.615 𝑇𝑄𝑠𝑐 𝑟 2𝑃 2𝑃
ln = 0.703 න 𝜕𝑃 − න 𝜕𝑃
𝑘ℎ 𝑟𝑤 𝜇𝑧 𝜇𝑧
𝑃𝑠𝑐 𝑧𝑇 𝑄𝑠𝑐 𝑘𝐴 𝜕𝑃 0 0
= 1.127 ∗ 10−3
𝑇𝑠𝑐 𝑃 5.615 𝜇 𝜕𝑟 𝑃 2𝑃
𝑃𝑠𝑐 𝑧𝑇 𝑄𝑠𝑐 −3
𝑘 ∗ 2𝜋𝑟ℎ 𝜕𝑃 The integral 0 𝜕𝑃 is called the
= 1.127 ∗ 10 𝜇𝑧
𝑇𝑠𝑐 𝑃 5.615 𝜇 𝜕𝑟 “real-gas pseudopressure” and it is usually
represented by m(p).
Assuming that Tsc = 520oR and psc = 14.7 psia
𝑃
𝑇𝑄𝑠𝑐 𝜕𝑟 2𝑃 2𝑃
= 0.703 𝜕𝑃 𝑚 𝑃 =න 𝜕𝑃
𝑘ℎ 𝑟 𝜇𝑧 𝜇𝑧
0
𝑟 𝑃
𝑇𝑄𝑠𝑐 𝜕𝑟 2𝑃 𝑇𝑄𝑠𝑐 𝑟
න = 0.703 න 𝜕𝑃 ln = 0.703 𝑚 𝑃 − 𝑚 𝑃𝑤𝑓
𝑘ℎ 𝑟 𝜇𝑧 𝑘ℎ 𝑟𝑤
𝑟𝑤 𝑃𝑤𝑓
Radial flow of compressible fluids
𝑇𝑄𝑠𝑐 𝑟
ln = 0.703 𝑚 𝑃 − 𝑚 𝑃𝑤𝑓
𝑘ℎ 𝑟𝑤 The equation can be rearranged as
𝑘ℎ 𝑚 𝑃 − 𝑚 𝑃𝑤𝑓 𝑃𝑒
𝑄𝑠𝑐 = 𝑘ℎ 2𝑃
𝑟
1.422𝑇ln 𝑟 𝑄𝑠𝑐 = න 𝜕𝑃
𝑤
𝑟𝑒 𝜇𝑍
1422𝑇ln 𝑃𝑤𝑓
When 𝑟 = 𝑟𝑒 , 𝑚 𝑃 = 𝑚 𝑃𝑒 𝑟𝑤
𝑘ℎ 2 𝑃
𝑄𝑠𝑐 = න 𝑃 𝜕𝑃 𝜇𝑍
1422𝑇ln
𝑟𝑒 𝜇𝑍
(𝑝𝑠𝑖/𝑐𝑝)
𝑟𝑤 𝑃𝑤𝑓
2
𝑘ℎ 𝑃𝑒2 − 𝑃𝑤𝑓
𝑄𝑠𝑐 = 2000 3000
𝑟𝑒
1422𝜇𝑍𝑇ln 𝑃 (𝑝𝑠𝑖)
𝑟𝑤
How to evaluate m(P) function
Gas properties can be estimated using standard correlations of 𝜇 and 𝑍 at reservoir temperature.
P (psia) μ (cp) Z
14.7 0.011841 0.998703
100 0.012021 0.991328
200 0.012232 0.983011
300 0.012445 0.975048
400 0.012659 0.967439
500 0.012874 0.960185
600 0.01309 0.953285
700 0.013308 0.94674
800 0.013526 0.940549
900 0.013746 0.934712
1000
1100
0.013967
0.014188
0.92923
0.924102
Create a table of P, 𝜇 and 𝑍. At any
1200 0.014412 0.919329 pressure, the values of 𝜇 and 𝑍 can be
1300 0.014636 0.91491
1400 0.014861 0.910845
estimated using standard correlations.
1500 0.015087 0.907135
1600 0.015315 0.903779
1700 0.015544 0.900778
1800 0.015773 0.898131
1900 0.016004 0.895838
2000 0.016236 0.8939
2100 0.01647 0.892316
2200 0.016704 0.891087
2300 0.016939 0.890212
2400 0.017176 0.889691
How to evaluate m(P) function
Gas properties can be estimated using standard correlations of 𝜇 and 𝑍 at reservoir temperature.
2𝑃
P (psia) μ (cp) Z
𝜇𝑍
14.7 0.011841 0.998703 2486.123
100 0.012021 0.991328 16783.09
200 0.012232 0.983011 33266.27
300 0.012445 0.975048 49445.91
400 0.012659 0.967439 65323.13
500 0.012874 0.960185 80896.84
600 0.01309 0.953285 96165.4
700 0.013308 0.94674 111118
800 0.013526 0.940549 125767.7
900 0.013746 0.934712 140093.6
1000 0.013967 0.92923 154100.4 2𝑃
1100 0.014188 0.924102 167796 At each pressure, can be evaluated
𝜇𝑍
1200 0.014412 0.919329 181140.7
1300 0.014636 0.91491 194165.7
1400 0.014861 0.910845 206854.8
1500 0.015087 0.907135 219203
1600 0.015315 0.903779 231190.9
1700 0.015544 0.900778 242827.8
1800 0.015773 0.898131 254125.7
1900 0.016004 0.895838 265048.6
2000 0.016236 0.8939 275608.1
2100 0.01647 0.892316 285783.4
2200 0.016704 0.891087 295605.2
2300 0.016939 0.890212 305053.9
2400 0.017176 0.889691 314108.7
How to evaluate m(P) function
Gas properties can be estimated using standard correlations of 𝜇 and 𝑍 at reservoir temperature.
2𝑃
P (psia) μ (cp) Z ΔP
𝜇𝑍
14.7 0.011841 0.998703 2486.123 0
100 0.012021 0.991328 16783.09 85.3
200 0.012232 0.983011 33266.27 100
300 0.012445 0.975048 49445.91 100
400 0.012659 0.967439 65323.13 100
500 0.012874 0.960185 80896.84 100
600 0.01309 0.953285 96165.4 100
700 0.013308 0.94674 111118 100
800 0.013526 0.940549 125767.7 100
900 0.013746 0.934712 140093.6 100
1000
1100
0.013967
0.014188
0.92923
0.924102
154100.4
167796
100
100
∆𝑃 is the incremental pressure at each
1200 0.014412 0.919329 181140.7 100 pressure step.
1300 0.014636 0.91491 194165.7 100
1400 0.014861 0.910845 206854.8 100
1500 0.015087 0.907135 219203 100
1600 0.015315 0.903779 231190.9 100
1700 0.015544 0.900778 242827.8 100
1800 0.015773 0.898131 254125.7 100
1900 0.016004 0.895838 265048.6 100
2000 0.016236 0.8939 275608.1 100
2100 0.01647 0.892316 285783.4 100
2200 0.016704 0.891087 295605.2 100
2300 0.016939 0.890212 305053.9 100
2400 0.017176 0.889691 314108.7 100
How to evaluate m(P) function
Gas properties can be estimated using standard correlations of 𝜇 and 𝑍 at reservoir temperature.
𝟐𝑷 𝟐𝑷
P (psia) μ (cp) Z ΔP
𝝁𝒁 𝝁𝒁
14.7 0.011841 0.998703 2486.123 0 1243.061
100 0.012021 0.991328 16783.09 85.3 9634.608
200 0.012232 0.983011 33266.27 100 25024.68
300 0.012445 0.975048 49445.91 100 41356.09
400 0.012659 0.967439 65323.13 100 57384.52
500 0.012874 0.960185 80896.84 100 73109.99
600 0.01309 0.953285 96165.4 100 88531.12
700 0.013308 0.94674 111118 100 103641.7
800 0.013526 0.940549 125767.7 100 118442.9
𝟐𝑷 ഥ
𝟐𝑷
900
1000
0.013746
0.013967
0.934712
0.92923
140093.6 100 132930.7 Average of , i.e., can be
154100.4 100 147097 𝝁𝒁 𝝁𝒁
1100 0.014188 0.924102
1200 0.014412 0.919329
167796
181140.7
100
100
160948.2
174468.3
estimated between two consecutive
1300 0.014636 0.91491 194165.7 100 187653.2 pressure steps.
1400 0.014861 0.910845 206854.8 100 200510.2
1500 0.015087 0.907135 219203 100 213028.9
1600 0.015315 0.903779 231190.9 100 225196.9
1700 0.015544 0.900778 242827.8 100 237009.3
1800 0.015773 0.898131 254125.7 100 248476.7
1900 0.016004 0.895838 265048.6 100 259587.1
2000 0.016236 0.8939 275608.1 100 270328.4
2100 0.01647 0.892316 285783.4 100 280695.8
2200 0.016704 0.891087 295605.2 100 290694.3
2300 0.016939 0.890212 305053.9 100 300329.6
2400 0.017176 0.889691 314108.7 100 309581.3
How to evaluate m(P) function
Gas properties can be estimated using standard correlations of 𝜇 and 𝑍 at reservoir temperature.
𝟐𝑷
𝟐𝑷 𝟐𝑷 ∗
P (psia) μ (cp) Z ΔP 𝝁𝒁 ΔP
𝝁𝒁 𝝁𝒁
14.7 0.011841 0.998703 2486.123 0 1243.061 0
100 0.012021 0.991328 16783.09 85.3 9634.608 821832.1
200 0.012232 0.983011 33266.27 100 25024.68 2502468
300 0.012445 0.975048 49445.91 100 41356.09 4135609
400 0.012659 0.967439 65323.13 100 57384.52 5738452
500 0.012874 0.960185 80896.84 100 73109.99 7310999
600 0.01309 0.953285 96165.4 100 88531.12 8853112
700 0.013308 0.94674 111118 100 103641.7 10364171
800 0.013526 0.940549 125767.7 100 118442.9 11844287
900 0.013746 0.934712 140093.6 100 132930.7 13293067 ഥ
𝟐𝑷
1000 0.013967 0.92923 154100.4 100 147097 14709699 Estimate ∗ ΔP
𝝁𝒁
1100 0.014188 0.924102 167796 100 160948.2 16094818
1200 0.014412 0.919329 181140.7 100 174468.3 17446834
1300 0.014636 0.91491 194165.7 100 187653.2 18765321
1400 0.014861 0.910845 206854.8 100 200510.2 20051024
1500 0.015087 0.907135 219203 100 213028.9 21302887
1600 0.015315 0.903779 231190.9 100 225196.9 22519694
1700 0.015544 0.900778 242827.8 100 237009.3 23700934
1800 0.015773 0.898131 254125.7 100 248476.7 24847671
1900 0.016004 0.895838 265048.6 100 259587.1 25958715
2000 0.016236 0.8939 275608.1 100 270328.4 27032838
2100 0.01647 0.892316 285783.4 100 280695.8 28069576
2200 0.016704 0.891087 295605.2 100 290694.3 29069431
2300 0.016939 0.890212 305053.9 100 300329.6 30032957
2400 0.017176 0.889691 314108.7 100 309581.3 30958133
How to evaluate m(P) function
Gas properties can be estimated using standard correlations of 𝜇 and 𝑍 at reservoir temperature.
𝟐𝑷 𝟐𝑷
𝟐𝑷 𝟐𝑷 ∗
P (psia) μ (cp) Z ΔP 𝝁𝒁 ΔP 𝒎 𝑷 = ∗
𝝁𝒁 𝝁𝒁 𝝁𝒁 ΔP
14.7 0.011841 0.998703 2486.123 0 1243.061 0 0
100 0.012021 0.991328 16783.09 85.3 9634.608 821832.1 821832.1
200 0.012232 0.983011 33266.27 100 25024.68 2502468 3324300
300 0.012445 0.975048 49445.91 100 41356.09 4135609 7459909
400 0.012659 0.967439 65323.13 100 57384.52 5738452 13198361
500 0.012874 0.960185 80896.84 100 73109.99 7310999 20509360
600 0.01309 0.953285 96165.4 100 88531.12 8853112 29362472
700 0.013308 0.94674 111118 100 103641.7 10364171 39726644
800 0.013526 0.940549 125767.7 100 118442.9 11844287 51570931 𝒎 𝑷
900 0.013746 0.934712 140093.6 100 132930.7 13293067 64863997
1000 0.013967 0.92923 154100.4 100 147097 14709699 79573696
𝟐𝑷
= ∗
1100
1200
0.014188
0.014412
0.924102
0.919329
167796
181140.7
100
100
160948.2
174468.3
16094818
17446834
95668513
1.13E+08
𝝁𝒁 ΔP
1300 0.014636 0.91491 194165.7 100 187653.2 18765321 1.32E+08
1400 0.014861 0.910845 206854.8 100 200510.2 20051024 1.52E+08
1500 0.015087 0.907135 219203 100 213028.9 21302887 1.73E+08
1600 0.015315 0.903779 231190.9 100 225196.9 22519694 1.96E+08
1700 0.015544 0.900778 242827.8 100 237009.3 23700934 2.19E+08
1800 0.015773 0.898131 254125.7 100 248476.7 24847671 2.44E+08
1900 0.016004 0.895838 265048.6 100 259587.1 25958715 2.7E+08
2000 0.016236 0.8939 275608.1 100 270328.4 27032838 2.97E+08
2100 0.01647 0.892316 285783.4 100 280695.8 28069576 3.25E+08
2200 0.016704 0.891087 295605.2 100 290694.3 29069431 3.54E+08
2300 0.016939 0.890212 305053.9 100 300329.6 30032957 3.84E+08
2400 0.017176 0.889691 314108.7 100 309581.3 30958133 4.15E+08
How to evaluate m(P) function
Gas properties can be estimated using standard correlations of 𝜇 and 𝑍 at reservoir temperature.
𝟐𝑷
𝟐𝑷 m(P)
𝟐𝑷vs P ∗ 𝟐𝑷
P (psia) μ (cp) 4.5E+08
Z ΔP 𝝁𝒁 ΔP 𝒎 𝑷 = ∗
𝝁𝒁 𝝁𝒁 𝝁𝒁 ΔP
14.7 4.0E+08
0.011841 0.998703 2486.123 0 1243.061 0 0
100 0.012021 0.991328 16783.09 85.3 9634.608 821832.1 821832.1
200 0.012232 0.983011
3.5E+08 33266.27 100 25024.68 2502468 3324300
300 0.012445 0.975048 49445.91 100 41356.09 4135609 7459909
400 0.012659 0.967439 65323.13 100 57384.52 5738452 13198361
500
3.0E+08
0.012874 0.960185 80896.84 100 73109.99 7310999 20509360
600 0.01309 0.953285 96165.4 100 88531.12 8853112 29362472
2.5E+08
m(P)