equations.doc
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College of Engineering and Computer ScienceMechanical Engineering Department
Mechanical Engineering 370Thermodynamics
Spring 2003 Ticket: 57010 Instructor: Larry Caretto
Summary of Important Equations in Thermodynamics
Basic notation and definition of terms
Fundamental dimensions o mass! lengt"! time! temperature! and amount o su#stance $mol% are
denoted! respecti&ely as '! L! T( ! and in t"e a##re&iations #elo)( For e*ample! t"e
dimensions o pressure are 'L+1T+2( T"ermodynamic properties are said to #e e*tensi&e i t"eydepend on t"e si,e o t"e system( -olume and mass are e*amples o intensi&e properties.intensi&e properties! suc" as temperature and pressure! do not depend on t"e si,e o t"e system(T"e ratio o t)o e*tensi&e properties is an intensi&e property( T"e ratio o an e*tensi&e property!suc" as &olume! to t"e mass o t"e system! is called t"e speciic property. e(g(! t"e ratio o&olume to mass is called t"e speciic &olume(
' molecular )eig"t $'/%
m mass $'%
M
mn = num#er o moles $%
nergy or general e*tensi&e property
m
Ee= Speciic molar energy $energy per unit mass% or general e*tensi&e property per
unit mass
eMn
Ee
== Speciic energy $energy per unit mole% or general e*tensi&e property per unit mole
pressure $'L+1T+2%
- &olume $L3%. )e also "a&e t"e speciic &olume or &olume per unit mass! & $L 3'+1%
and t"e &olume per unit mole v $L3+1%
T temperature $%
density $'L+3%. 1/&(
* uality
su#scripts and & denote saturated liuid and stauarated &apor! respecti&ely
4 t"ermodynamic internal energy $'L2T+2%. )e also "a&e t"e internal energy per unit
mass! u $L2T+2%! and t"e internal energy per unit mole! u $'L2T+2+1%
4 6 - t"ermodynamic ent"alpy $'L2T+2%. )e also "a&e t"e ent"alpy per unit mass! " u
6 & $dimensions: L2T+2% and t"e internal energy per unit mole h $'L2T+2+1%
S entropy $'L2T+2+1%. )e also "a&e t"e entropy per unit mass! s$L2T+2+1% and t"e
internal energy per unit mole s $'L2T+2+1+1%
)ork $'L2T+2%
8 "eat transer $'L2T+2%
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uW : t"e useul )ork rate or mec"anical po)er $'L2T+3%
m : t"e mass lo) rate $'T+1%
2
2V
: t"e kinetic energy per unit mass $L2T+2%
g,: t"e potential energy per unit mass $L2T+2%
tot: t"e total energy m$u 62
2V
6 g,% $'L2T+2%
Q : t"e "eat transer rate $'L2T+3%
: t"e rate o c"ange o energy or t"e control &olume( $'L2T+3%
Mass and energy balance equations
T"e euations #elo) use t"e standard t"ermodynamic sign con&ention or "eat and )ork( eatadded to a system is positi&e and "eat re?ected rom a system is negati&e( T"e oppositecon&ention "olds or )ork( ork done #y a system is positi&e. )ork done on $added to% a systemis negati&e( In terms o t"e in! out! 8in! and 8outterms used in t"e te*t )e can make t"eollo)ing statements(
8 8in+ 8out out+ in
T"ese euations may #e su#stituted or any o t"e "eat! 8! or )ork! terms #elo)(
elation o mass lo) to &elocity! speciic &olume and area:v
AVAVm
==
@eneral irst la):
+++
++=
inlet
i
2
i
ii
outlet
i
2
i
iiu
cv gz2
Vhmgz
2
VhmWQ
dt
dE
'ass #alance euation: =outlet
i
inlet
icv mm
dt
dm
Steady+lo) assumptions: 0 and 0
Steady+lo) irst la):
+++
++=
inlet
i
2
i
ii
outlet
i
2
i
iiu gz2
Vhmgz
2
VhmQW
'ass #alance or steady lo)s: =outlet
i
inlet
i mm
Steady+lo) irst la) )it" negligi#le A B : +=inlet
ii
outlet
iiu hmhmQW
Second law of thermodynamics and entropy
9asic deinition o entropy:T
PdVdUdS
+=
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@eneral second la):T
WL
T
Qsmsm
dt
dS cvcv
inlet
ii
outlet
iicv
+=+
Second la) ineuality:T
Qsmsm
dt
dS cv
inlet
ii
outlet
iicv
+
dia#atic steady+lo)! second la) ineuality: 0smsminlet
iioutlet
ii
Ideal-gas equations
1( T"e gas constant
R is t"e uni&ersal gas constant )it" dimensions o energy di&ided #y $moles times
temperature%! andM
RR= is t"e engineering gas constant )it" dimensions o energy di&ided
#y $mass times temperature%( T"e energy dimensions are sometimes e*pressed as energy
units $e(g(! D%( o)e&er! or +&+T calculations! t"e energy dimensions are e*pressed inpressure units times &olume units $e(g(! kaEm3( Some &alues o t"e uni&ersal gas constant ares"o)n #elo)(
Rlbmol
ftpsi!"#$%#0
Rlbmol
lbft"&%#&'&
()mol
m)P"#'%*
()mol
)+"#'%*R
"f
"
=
=
=
=
2( +-+T calculations )it" mass or moles( T"e e*ample in t"e irst euation is air $ 0(2;7kD/kg+A%( 9ot" e*amples are or an ideal gas t"at occupies a &olume o 1 m3at a pressure o100 ka and a temperature o 25 C 2;(15 A(
m 1(1
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c( elations"ips or internal energy and ent"alpy
du c&dT d" cpdT u2G u1 2
#
T
T
vdTc "2G "1
2
#
T
T
PdTc
For constant "eat capacity: u2G u1 c&$T2G T1% and "2G "1 c$T2G T1%
From ideal gas ta#les: u2G u1 uo$T2% G u
o$T1% and "2G "1 "o$T2% G "
o$T1%
=( ntropy c"anges
a( constant "eat capacity
s2+ s1 cpln + ln c&ln + ln
#( &aria#le "eat capacity #y integration
s2+ s1 + ln 6 ln
c( &aria#le "eat capacity #y ideal gas ta#les
s2+ s1 so$T2% + s
o$T1% + ln
5( nd states o an isentropic process or an ideal gas )it"
a( constant "eat capacity $k cp/c&%
T2 T1
/k T2 T1 2 1
k
#( &aria#le "eat capacity using t"e air ta#les
c( &aria#le "eat capacity using general ideal gas ta#les
so$T2% so$T1% + ln
d( &aria#le "eat capacity #y integration o cp$T% or c&$T% euation
ln or ln
Cycles and efficiencies
In an engine cycle a certain amount o "eat! H8H! is added to t"e cyclic de&ice at a "ig"
temperature and a certain amount o )ork HH is perormed byt"e de&ice( T"e dierence
#et)een H8H and HH is H8LH! t"e "eat re?ected rom t"e de&ice at a lo) temperature(
In a rerigeration cycle a certain amount o "eat! H8LH! is added to t"e cyclic de&ice at a lo)
temperature and a certain amount o )ork HH is perormed ont"e de&ice( T"e sum o H8LH and H
H is H8H! t"e "eat re?ected rom t"e de&ice at a "ig" temperature(
For #ot" de&ices: H8H HH 6 H8LH
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ngine cycle eiciency:1Q1
1W1
=
erigeration cycle coeicient o perormance:W
Q/P
L=
T"e isentropic eiciency! s! compares t"e actual )ork! H)aH! to t"e ideal )ork t"at )ould #e done
in an isentropic $re&ersi#le adia#atic% process! H)sH( 9ot" t"e actual and t"e isentropic process
"a&e t"e same initial states and t"e same inal pressure(
For a )ork output de&ice:131
131
s
s=
For a )ork input de&ice:131
131
s
s=
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