Compressor Performance
Compressor Performance
COMPRESSOR
PERFORMANCE CHARACTERISTICS
Note: The source of the technical material in this volume is the Professional
Engineering Development Program (PEDP) of Engineering Services.
Warning: The material contained in this document was developed for Saudi
Aramco and is intended for the exclusive use of Saudi Aramco’s employees.
Any material contained in this document which is not already in the public
domain may not be copied, reproduced, sold, given, or disclosed to third
parties, or otherwise used in whole, or in part, without the written permission
of the Vice President, Engineering Services, Saudi Aramco.
Section Page
INFORMATION ............................................................................................................... 3
INTRODUCTION............................................................................................................. 3
DETERMINING DYNAMIC COMPRESSOR PERFORMANCE CHARACTERISTICS ... 4
Thermodynamics of Compression ........................................................................ 4
Isothermal Process............................................................................................... 8
Isentropic Process ................................................................................................ 8
Polytropic Process.............................................................................................. 12
Compressibility ................................................................................................... 15
DETERMINING POSITIVE-DISPLACEMENT COMPRESSOR PERFORMANCE
CHARACTERISTICS .................................................................................................... 58
WORK AIDS.................................................................................................................. 62
WORK AID 1A: CALCULATION PROCEDURES AND CHARTS FOR
DETERMINING DYNAMIC COMPRESSOR PERFORMANCE
CHARACTERISTICS.......................................................................... 62
WORK AID 1B: CHARTS FOR DETERMINING COMPRESSOR
PERFORMANCE CHARACTERISTICS............................................. 65
WORK AID 2: CALCULATION PROCEDURES FOR DETERMINING POSITIVE-
DISPLACEMENT COMPRESSOR PERFORMANCE
CHARACTERISTICS.......................................................................... 69
GLOSSARY .................................................................................................................. 71
LIST OF FIGURES
LIST OF TABLES
INFORMATION
INTRODUCTION
Compressor performance characteristics can be described as
the operating characteristics that define the ratings of a
compressor. An understanding of compressor performance
characteristics is important when determining compressor
requirements for a system and when evaluating compressor
operation. This module describes compressor performance
characteristics and the methods of determining the compressor
performance characteristics for dynamic and positive-
displacement compressors.
Thermodynamics of Compression
No gas exactly conforms to the Ideal Gas Law, which show the
relationship between the volume, the absolute pressure, and the
absolute temperature of an ideal gas. Most gases, however,
conform to these laws with sufficient accuracy to yield sound
engineering answers relevant to engineering problems. To
understand and to calculate the thermodynamics of
compression, the Mechanical Engineer uses the following
fundamental laws:
• Boyle’s Law
• Charles’ Law
• Dalton’s Law
• Avogadros’ Law
Where: V = Volume
P = Pressure
V2 T2
= when pressure is constant
V1 T1
Where: V = Volume
T = Temperature
Avogadros’ Law states that all gases have the same number of
moles in the same volume and at the same pressure and
temperature. This relationship can be stated through the
following equation:
PV
= Constant
T
Where: P = Pressure
V = Volume
T = Temperature
RT
υ =
P
or
P
ρ =
RT
Where: υ = Specific volume (ft3/lbm)
ρ = Density (lbm/ ft3)
P1V1 P2 V2
=
T1 T2
Where: V = Volume
P = Pressure
T = Temperature
R
CP − C V =
J
• Isothermal Process
• Isentropic Process
• Polytropic Process
Isothermal Process
The isothermal compression process is compression that takes
place at a constant temperature. Because large amounts of
heat transfer area must be supplied to keep the temperature
constant, isothermal compression is not common in the actual
operation of machinery.
Where: P = Pressure
V = Volume
Isentropic Process
The isentropic compression process follows a path of constant
entropy. In the isentropic process, heat is neither added to nor
removed from the gas during compression. The fact that heat is
neither added nor removed does not mean that the temperature
is constant. Because of the work of compression that is
performed on the gas, temperature increases as the pressure
increases. In compressor theory, the terms “isentropic”
(constant entropy) and “adiabatic” (no heat transfer) are
interchangeably used. This interchangeability is valid for the
context in which the terms are used. The actual definition of an
isentropic process is an adiabatic, reversible process.
PV k = Constant
Where: P = Pressure
V = Volume
k = Isentropic exponent
k Pr
k −1 / k
= V1P1 − 1
k − 1 P1
or
Workisen:
(k −1/k )
k Pf
= RTi − 1
k − 1 Pi
As listed above, for all gases, the gas constant (R) is equal to
the universal gas constant (Runiv) divided by the gas molecular
weight (MW), or 1545.32/MW. By definition, the air has a
uniform molecular weight of 28.966; therefore, the specific
gravity (sg) of any gas, relative to air, of molecular weight MW is
equal to MW/28.966. The gas constant (R) for any gas can now
be defined as 1545.32/MW, or 53.34/sg.
ft − lbf
Foot pound force per pound mass
lbm
Isentropic Work
η=
Actual Work
RTi
Hiso = ln(P2 /P1 )
MW
Ti = Initial temperature in °R
ln = Log to base e
Polytropic Process
Polytropic compression is the compression path that closely
follows the compression path in a real centrifugal compressor.
Centrifugal compression is not an ideal thermodynamic process.
The inefficiency of the compression process results in excess
heat input to the process gas, which causes the temperature to
increase faster than it would in isentropic compression.
Because of the temperature increase, the volume at the end of
polytropic compression is larger than the volume at the end of
isentropic compression.
PV n = Constant
Where: P = Pressure
V = Volume
n = Polytropic exponent
n −1 k −1 1
= ×
n k ηp
n
ηp = n − 1
k
k −1
T
Ln 2
n −1 T
= 1
n P
Ln 2
P1
P (k −1/k )
X = 2 − 1
P1
Once the temperature rise factor (X) has been calculated, the
line that corresponds to the temperature rise factor (X) is used
to convert the known efficiency to unknown efficiency. The
point on the unknown efficiency axis that corresponds to the
intersection of the known efficiency and the temperature rise
factor (X) is the unknown efficiency. This point is called
equivalent efficiency.
Compressibility
The relationship of specific volume to pressure and temperature
for an ideal gas can be defined by the equation (P)(υ) = (R)(T).
However, most gases that are encountered in industrial
compression do not exactly obey the Ideal Gas Law equation.
Deviation from the Ideal Gas Law is referred to as
“compressibility.” Compressibility is specifically defined as the
degree to which any given gas varies from the Ideal Gas Law.
T
Tr =
Tc
P
Pr =
Pc
Pc = 617.4 psia
Tc = 666.2°R
T = T + 460°R
= 140 + 460
= 600°R
T
Tr =
Tc
600
=
666.2
= 0.9006
P
Pr =
Pc
300
=
617.4
= 0.4859
Cp and Cp/Cr
at 14.7 psia and
60°F
Critical Constants
Mol. Wt. Pressure Temp. °R Mcp Mcp Mcp
Tc
Compound Formula M Cp Cp/Cr psia Pc at 60°F at at
100°F 200°F
Acetylene C2H2 26.036 0.3966 1.238 905.0 557.4 10.33 10.69 11.53
Air N+O2 28.966 0.2470 1.395 547.0 238.7 6.96 6.96 6.99
Ammonia NH3 17.032 0.5232 1.310 1,657.0 731.4 8.91 8.57 9.02
Benzene C6H6 78.108 0.2404 1.118 714.0 1,013.0 18.78 20.47 24.46
1,2-Butadiene C4H6 54.088 (0.3458) (1.120) 653.0 799.0 18.70
1,3-Butadiene C4H6 54.088 (0.3412) 1.120 628.0 766.0 18.45
N-Butane C4H10 58.120 0.3970 1.094 550.7 765.6 23.07 24.51 26.16
Isobutane C4H10 58.120 0.3872 1.097 529.1 734.9 22.50 23.96 27.62
N-Butene C4H6 56.104 0.3703 1.105 583.0 755.6 20.77 22.09 25.18
Isobutene C4H6 56.104 0.3701 1.106 579.8 752.5 20.76
Butylene C4H6 56.104 0.3703 1.105 583.0 755.6 20.78 21.94 24.86
Carbon dioxide CO2 44.010 0.1991 1.300 1,073.0 548.0 8.76 9.00 9.35
Carbon CO 28.010 0.2484 1.403 510.0 242.0 6.96 6.96 6.98
monoxide
Chlorine Cl2 70.914 0.1149 1.366 1,120.0 751.0 8.15
Ethane C2H4 30.068 0.4097 1.193 708.3 550.1 12.32 12.96 14.68
Ethyl alcohol C2H5OH 46.069 0.3070 1.130 927.0 629.6 14.14
Ethylene C2H4 28.052 0.3622 1.243 742.1 509.8 10.16 10.68 12.08
N-Hexane C6H14 86.172 0.3984 (1.062) 439.7 914.5 34.33 36.23 41.08
Helium He 4.003 1.2480 1.6598 480.0 510.0 5.00
Hydrogen H2 2.016 3.408 1.408 188.0 60.2 6.87 6.90 6.95
Hydrogen H2S 34.076 0.254 1.323 1,306 672.7 8.66 8.18 8.36
sulfide
Methane CH4 16.042 0.5271 1.311 673.1 343.5 8.46 8.65 9.30
Methyl alcohol CH3OH 32.042 0.2700 1.203 1,157.0 924.0 8.65
Nitrogen N2 28.016 0.2482 1.402 492.0 227.2 6.95 6.96 6.963
N-Octane C8H18 114.224 0.3998 (1.046) 362.1 1,025.2 45.67
Oxygen O2 32.00 0.2188 1.401 730 278.2 7.00 7.03 7.120
Cp and Cp/Cr
at 14.7 psia and
60°F Critical Constants
Mol. Wt. Pressure Temp. °R Mcp Mcp Mcp
Compound Formula Cp Cp/Cr
M psia Pc Tc at 60°F at 100°F at 200°F
N-Pentane C5H12 72.146 0.3972 1.074 489.5 845.9 28.66 30.30 34.41
Isopentane C5H12 72.146 0.3880 1.075 483.0 830.0 27.99 29.90 34.44
Propane C3H8 44.094 0.3885 1.136 617.4 666.2 17.13 18.21 20.90
Propylene C3H6 42.078 0.3541 1.154 667 657.4 14.90 15.77 17.88
Sulfur dioxide SO2 64.060 0.1470 1.246 1.142 775.0 9.42
Toluene C7H8 92.134 0.2599 1.091 611 1,069.5 23.95
Water H2O 18.016 0.4446 1.335 3,206 1,165.4 8.01 8.03 8.12
Hydrogen HCl 36.465 0.1939 1.410 1,199.2 584.5 7.07
chloride
Z 2 − Z1
Zavg =
2
Isentropic:
(k −1/k )
k Pf
Headisen = ZavgRTi − 1
k − 1 Pi
(k −1/k )
1545.32Z avgTi k Pf
= − 1
MW k − 1 Pi
Polytropic:
(n −1/n )
n Pf
Headpoly = ZavgR /Ti − 1
n − 1 Pi
(n −1/n )
1545.32Z avg Ti n Pf
= − 1
MW n − 1 Pi
• Critical pressure , PC
• Critical temperature, TC
• Compressibility factor, Z
Of the above properties, MW, CP, CV, PC, and TC are calculated
by addition of the products of the individual mol fraction of each
of the constituents of the gas mixture multiplied by the specific
properties of the individual gas. An application of the individual
mol fraction calculations is shown in Table 2, which presents the
computation of the physical characteristics of a typical sales
gas/fuel gas mixture. The composition is known on the
volumetric basis.
Methane 0.922 16.04 14.78 8.65 7.975 673.1 620.6 343.5 316.7
Ethane 0.048 30.07 1.44 12.96 0.622 708.3 34.0 550.1 26.4
Propane 0.019 44.09 0.84 18.21 0.346 617.4 11.7 666.2 12.7
i-Butane 0.004 58.12 0.23 23.96 0.096 529.1 2.1 734.9 2.9
N-butane 0.006 58.12 0.35 24.51 0.147 550.7 3.3 765.6 4.6
i-pentane 0.001 72.15 0.07 29.90 0.030 483.0 0.5 830.0 0.8
MW = ∑(Xi )(MWi )
∑ = Sum
Runiv
R=
MW
Runiv
R=
∑(Xi )(MWi )
∑(Mi )(c pi )
k=
∑(Mi )(c pi ) − 1.986
∑(Mi )(c pi )
k=
∑(Mi )(c pi ) − 8.32
P = ∑(Xi )(Pi )
T = ∑(Xi )(Ti )
υmix = Σ(Xi)(υi)
Tc mix = ∑( X i )(Tci )
T
Tr =
Tcmix
P
Pr =
Pcmix
mv
ωs =
ma
Pv V Pv
mv R vT R v R a Pv
ωs = = = =
m a Pa V Pa R v Pa
R aT Ra
or
RaPv
ωs =
R v (P − Pv )
T = Absolute temperature
Pv V
mv R v T Pv
φ= = =
P
mg g V Pg
R vT
T = Absolute temperature
The weight flow of dry air at the inlet can be calculated by the
following equation:
QP1 × 144
Weight Flow of Dry Air (W) =
RaT
62,000 × 14.7 × 144
=
53.3 × 520
= 4735 lbm/min
The volume flow rate of air and water vapor at the inlet
conditions can be calculated by the following equation:
WRTi
Qi =
Pa × 144
4735 × 53.3 × 520
=
14.56 × 144
=62,593cfm
Temperature, °F
%RH 35 40 50 60 70 80 90 100 110 120
5 .0019 .0024 .0035 .0050 .0071 .0099 .0136 .0186 .0250 .0332
10 .0039 .0047 .0069 .0100 .0142 .0198 .0273 .0372 .0501 .0668
15 .0058 .0071 .0104 .0150 .0213 .0298 .0411 .0561 .0755 .1007
20 .0078 .0095 .0139 .0200 .0284 .0398 .0549 .0750 .1012 .1351
25 .0098 .0119 .0174 .0251 .0356 .0498 .0689 .0940 .1270 .1699
30 .0117 .0143 .0209 .0301 .0427 .0599 .0828 .1132 .1531 .2051
35 .0137 .0166 .0244 .0351 .0499 .0700 .0969 .1325 .1794 .2407
40 .0156 .0190 .0279 .0402 .0571 .0801 .1110 .1519 .2060 .2768
45 .0176 .0214 .0314 .0453 .0644 .0903 .1251 .1715 .2328 .3133
50 .0195 .0238 .0349 .0503 .0716 .1005 .1394 .1912 .2598 .3502
55 .0215 .0262 .0384 .0554 .0789 .1107 .1537 .2110 .2871 .3876
60 .0235 .0286 .0419 .0605 .0861 .1210 .1681 .2310 .3146 .4254
65 .0254 .0310 .0454 .0656 .0934 .1313 .1825 .2511 .3424 .4637
70 .0274 .0334 .0490 0.707 .1007 .1417 .1970 .2713 .3705 .5025
75 .0294 .0358 .0525 .0758 .1081 .1521 .2116 .2917 .3988 .5418
80 .0313 .0382 .0560 .0810 .1154 .1625 .2263 .3122 .4273 .5816
85 .0333 .0406 .0596 .0861 .1228 .1730 .2410 .3328 .4562 .6219
90 .0353 .0430 .0631 .0913 .1302 .1835 .2559 .3536 .4853 .6627
95 .0372 .0454 .0666 .0964 .1376 .1940 .2707 .3745 .5147 .7041
100 .0392 .0478 .0702 .1016 .1450 .2046 .2857 .3956 .5443 .7460
Table 4. Water Content of Saturated Air in Gallons per 1000 ft3 at Various
Temperatures and Pressures with 100% Relative Humidity
Temperature, °F
0 .0392 .0479 .0702 .1016 .1450 .2046 .2857 .3956 .5443 .7460
10 .0233 .0283 .0416 .0600 .0854 .1200 .1667 .2290 .3119 .4217
20 .0165 .0201 .0295 .0426 .0605 .0849 .1176 .1612 .2186 .2939
30 .0128 .0156 .0229 .0330 .0469 .0657 .0909 .1213 .1682 .2256
40 .0165 .0128 .0187 .0269 .0383 .0536 .0741 .1012 .1367 .1830
50 .0089 .0108 .0158 .0228 .0323 .0452 .0625 .0853 .1152 .1540
60 .0077 .0093 .0137 .0197 .0280 .0391 .0540 .0737 .0995 .1329
70 .0068 .0082 .0121 .0174 .0246 .0345 .0476 .0649 .087 .1169
80 .0060 .0074 .0108 .0155 .0220 .0308 .0425 .0580 .078 .1043
90 .0055 .0067 .0098 .0140 .0199 .0279 .0385 .0524 .0706 .0942
100 .0050 .0061 .0089 .0128 .0182 .0254 .0351 .0478 .0644 .0858
110 .0046 .0056 .0082 .0118 .0167 .0234 .0323 .0439 .0592 .0789
120 .0043 .0052 .0076 .0109 .0155 .0216 .0298 .0407 .0548 .0729
130 .0040 .0048 .0071 .0102 .0144 .0201 .0278 .0378 .0509 .0678
140 .0037 .0045 .0066 .0095 .0135 .0188 .0260 .0354 .0476 .0634
150 .0035 .0042 .0062 .0089 .0126 .0177 .0244 .0332 .0447 .0595
160 .0033 .0040 .0058 .0084 .0119 .0167 .0230 .0313 .0421 .0561
170 .0031 .0038 .0055 .0080 .0113 .0158 .0217 .0296 .0398 .0530
180 .0029 .0036 .0052 .0075 .0107 .0149 .0206 .0281 .0378 .0503
190 .0028 .0034 .0050 .0072 .0102 .0142 .0196 .0267 .0359 .0478
200 .0027 .0032 .0048 .0068 .0097 .0136 .0187 .0254 .0342 .0455
Volumetric Flow
Where:
T1 = Inlet temperature, °R
°R = °F + 460
ACFM = W x V
Z1 RT1
V=
144P1
R univ 1545.32
R = Gas constant from =
MW Molecular Weight
Joules
R = 8.3143 and 144 is replaced
gm mol °R
with 18.129
Mollier Diagrams
H is = h 2is − h1
hi = Inlet enthalpy
h 2is − h1
ηis =
h 2 − h1
h2 = Discharge enthalpy
The specific volume for point 1 (v1) is estimated from the two
adjacent constant volume lines. For this example, v1 is
approximately 8.25 cubic feet per pound.
• Performance Curves
• Performance Characteristics
Performance Curves
• Increased thrust
• Variable pressure
• Variable flow
• Variable speed
Vrel
M=
Vsonic
Kg(1545)T
Vsonic =
MW
T = Temperature in °R
Using the equations for Vsonic and the Mach number, high
molecular weight gases result in low Vsonic values and the Mach
number will quickly approach 1. Figure 10 shows a graphical
representation of the effect of molecular weight on compressor
head versus flow curves.
The general laws for speed characteristics (fan laws) are the
same for centrifugal compressors as for centrifugal fans and
centrifugal pumps. The three basic fan laws are as follows:
N2
Equation 1: Q2 = Q1
N1
2
N
Equation 2: H2 = H1 2
N1
3
N
Equation 3: bhp 2 = bhp1 2
N1
The fan laws can be used for estimation purposes; however, the
accuracy of the calculated results decreases with increasing
speed ratio. Because the change in energy in a fan is
significantly lower than in a compressor, the fan laws are more
accurate for fans than for compressors. Other factors that
contribute to the inaccuracies of the fan laws include the
following:
The first fan law states that speed is proportional to flow rate.
The required new speed can be found as follows:
N
Q 2 = Q1 2
N1
Q2 N 2
=
Q1 N1
Q2
N1 = N 2
Q1
11,000
10,000 8000 = 8800rpm
2
ft lbf 8800
H 2 = 30,000
lbm 8000
H 2 = 30,000[1.21]
ft lbf
H 2 = 36,300
lbm
3
N
bhp 2 = bhp1 2
N1
3
8800
bhp 2 = 2200
8000
bhp 2 = 2200[1.331]
bhp 2 = 2928
• Isentropic Process
• Clearance Volume
• Isentropic Process
The specific heat at constant pressure (Cp) and the specific heat
at constant volume (Cυ) are affected by the variation in
temperatures commonly occurring in reciprocating compressors.
The temperature does not vary as much in centrifugal
compressors. These variations typically will increase the
specific heat constant.
Since points “B” and “D” are at some position during the
cycle, the cycle is made up of a suction stroke (“C” to “A”)
and a discharge stroke (“A” to “C”).
Clearance Volume
clearance volume,in 3
C= ×(100)
piston displacement,in 3
P1V1 = P2 V2
V1 = Inlet volume
P2 = Discharge pressure
V2 = Discharge volume
WORK AIDS
T1 = ( )+( )=( ) °R
T2 = ( )+( )=( ) °R
At the inlet:
P ( ) = ( )
P1 = =
Pt (
)
T ( )
T1 = = = ( )
Tt ( )
Z1 = ( )( Figure 14 and Figure 15)
At the discharge:
Pr =
P
=
( )=( )
Pc ( )
Tr =
T
=
( )=( )
Tc ( )
Zavg =
( )+ ( )=( )
2
Calculate (n-1)/n
(n − 1) / n
T2 P2
=
T1 P1
(n − 1) / n
( ) ( )
=
( ) ( )
(n − 1) 1n( )
= =( )
n 1n( )
Calculate Hp
n P ( n − 1/ n )
H P = Z avg RT1 2 − 1
n − 1 P1
) (
( )
( ) ( )
=( ) ( ) − 1
( ) ( ) (
)
ft − lbf
=( )
lbm
k −1
(( ) −( )/( ))
P ( )
k
X = − 1 =
2
− 1 = ( )
P1 ( )
η=( )
Critical Constants
Critical Constants
= 3.14 ( )2 ( )
2
d
Volume = h
2
where h = piston stroke
=( )2 ( )
Clearance Volume
C= × 100
Piston Displaceme nt
( )
=
( ) × 100
=( )%
GLOSSARY