0% found this document useful (0 votes)
62 views

Thermodynamics 2 (IITian Notes - Kota)

1) The Carnot cycle is an ideal thermodynamic cycle that describes the maximum theoretical efficiency that a heat engine can achieve during conversion between heat and work. 2) It consists of four stages: two isothermal processes and two adiabatic processes, occurring between two different temperature reservoirs. 3) The efficiency of a Carnot cycle depends only on the temperatures of the hot and cold reservoirs, and represents the highest possible efficiency a heat engine operating between those temperatures can achieve.

Uploaded by

hola chola
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
0% found this document useful (0 votes)
62 views

Thermodynamics 2 (IITian Notes - Kota)

1) The Carnot cycle is an ideal thermodynamic cycle that describes the maximum theoretical efficiency that a heat engine can achieve during conversion between heat and work. 2) It consists of four stages: two isothermal processes and two adiabatic processes, occurring between two different temperature reservoirs. 3) The efficiency of a Carnot cycle depends only on the temperatures of the hot and cold reservoirs, and represents the highest possible efficiency a heat engine operating between those temperatures can achieve.

Uploaded by

hola chola
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
You are on page 1/ 41

Limitation of 1st Law:-

No comment about the direction


of Brows,
No comment about extent of Bro cess .

Spontaneous Process:- Sj take


place it own under
a
process
condition then it called
given , spontaneous .

of fast
> be slow
may
→ Condition affect spontaneity of process
left H2O
>
H2O
so @,
② at I atm ,
10°C spontaneous

⑥ at I atm ,
-

Lok Non spontaneous

at
④ at labs ,
ok Eguib .

#f All natural process are


spontaneous .

Second law of thermodynamics:-


AH = the

Ft
Qc =
-

Ve

w = -

ve

② Ht Re Iwl

3=14
② It
Re
To
M = It LA

Qt
Carnot cycle:-

Ideal Gras AB Isothermal Expansion


Bc Adiabatic Expansion
CD = Isothermal Compression
DA =
Adiabatic Compression
Th

TH TF
AB 00=0
mm

4 W Eve) = tve
?
-
= -

Ck
tht
=hRThhnfB
TE #
→ CD GU =o
-

f W
Cure ) ve
-
=
= -
= -

418
-_nRTcIn⇐c ) = ve
-

hR# In #-)
Z = It

CEA)
WRT# In

"' ""
I

¥=⇐I

-

BC Th VB
=
Talk -

¥
-

-
-

f- I f- I -

④ .
BI Th VA = To ×
YD
c)
In
Urfa =
- In

z
-

-
I -

Eth)
Carnot cycle:-

Ideal Gras AB Isothermal Expansion


Bc Adiabatic Expansion
CD = Isothermal Compression
DA =
Adiabatic Compression
Th

TH FF
AB 00=0
mm

4 W Eve) = tve
?
-
= -

Ck
tht
=hRThhnfB
TE #
→ CD GU =o
-

I W
Cure ) ve
-
=
= -
= -

4$
-_nRTcIn⇐c ) = ve
-

# Elm #-)
Z = It

NAT# In

"' "'
I

¥=⇐I

-

BC Th VB
=
Talk -

¥
-

-
-

f- I f- I -

④ .
DI Th VA = Tc ×
YD
c)
In
Urfa =
- In

z
-

-
I -

Eth)
lwlrev > I WI Ion

' > ' ten


wtf I. him him
>
⇐I
I ' t
>
-

ion

' t
Ith
l - =

new

s*⇐
¥÷ >
¥
-

¥tT÷ to

Igorot 8¥ to Eo

EE to

10¥) to Clausius
inequality
Entropy
For reversible process §(E)=o = DJ

ds=
ds -

(E) ion X
ds
=CE↳ S=f(disorder)
disorder 5

Si SL Sz Sy
S > Sz > Ss >
, Sy

# S is a state function as well as

extensive
property of system .

rev @ Si Drew
-

.
'

'
"
=

@ 2) ion
i -

l
'
-

-
-
.
-
z
.

ion
-
-
epi
① Solid L liq C Gas
entropy

Gas
Gas (

T
, Y T, Va

Va > Y
③ a

a
S

T
④ Diamond ( Graphite

⑤ Ice water

⑥ Rxni
a a

No Gas S
of
moles

Cacus → Cao tcozq ,


: OS tire
ef a ,
-_

→ OS
Nags t3Hzg 2MHz re
i
=
-

,
,

Pas g ,
→ PU , tacy , : OS -
-
tire
9)

It 2HIq ,
>
Itza ,
t
Iza ,
Oser o

05=0 X

⑦ LI HL ) H

Hz 2h
EE HL C H2

EI Nz Etty

H m - same Atoms
IT ST
Atoms same
mga Sf
-

Atoms * Same MT ST
above is hot
# but
true
always

\
Calculation of entropy change for system:-
① for ideal Gas

µd)aw
DS = = =
dutpdv
aw
T

T2 Vu
ds =

nfu
TI
+
nr¥
VI
*

) )
as = main thru
, ,

VI. =

TF Epa,
'

os =
Ncp
tuff ) ,
t HR In
(Az )
⑨ Isothermal Rrocess T=Co①
as
nRtn⇐)=hRhs¥ )
=

③ Isobaric P=Co①
as Mcp In
,⇐)
=

k-contf.os-ncvh.CI)
② Iso choric Rroass
⑨ Adiabatic Process : .

① Reversible 8=0 = Trev


Fuente
ds
GE)aw=o nah
)thRh⇐ )
-
-
- -

iso entropic
process s=Co@
① Irreversible 0--0=9 ing

OS =
= o
X
im

OS = her
buff ,
t n Rh
,
)
OS = tve

✓ OS =
-
ve

OS - tve

OS -
-
tire

as =
a

whiff) ,

§%✓
In
Zxzrx
=

=3 Rh 3

1-
⇐) n
>
itch )
i
¥¥ ⇐I 4 #D . .
- -

X


A fit
ITH
m = I -

f
p
t
Dt¥⇐a
Tithe
"
- E! ,

⑥si "=C¥ , ⇐ ¥.TT#I


I =
on
Carnot cycle:-

Ideal Gras AB Isothermal Expansion


Bc Adiabatic Expansion
CD = Isothermal Compression
DA =
Adiabatic Compression
Th

TH FF
AB 00=0
mm

4 W Eve) = tve
?
-
= -

Ck
tht
=hRThhnfB
TE #
→ CD GU =o
-

I W
Cure ) ve
-
=
= -
= -

4$
-_nRTcIn⇐c ) = ve
-

# Elm #-)
Z = It

NAT# In

"' "'
I

¥=⇐I

-

BC Th VB
=
Talk -

¥
-

-
-

f- I f- I -

④ .
DI Th VA = Tc ×
YD
c)
In
Urfa =
- In

z
-

-
I -

Eth)
lwlrev > I WI Ion

' > ' ten


wtf I. him him
>
⇐I
I ' t
>
-

ion

' t
Ith
l - =

new

s*⇐
¥÷ >
¥
-

¥tT÷ to

Igorot 8¥ to Eo

EE to

10¥) to Clausius
inequality
Entropy
For reversible process §(E)=o = DJ

ds=
ds -

(E) ion X
ds
=CE↳ S=f(disorder)
disorder 5

Si SL Sz Sy
S > Sz > Ss >
, Sy

# S is a state function as well as

extensive
property of system .

rev @ Si Drew
-

.
'

'
"
=

@ 2) ion
i -

l
'
-

-
-
.
-
z
.

ion
-
-
epi
① Solid L liq C Gas
entropy

Gas
Gas (

T
, Y T, Va

Va > Y
③ a

a
S

T
④ Diamond ( Graphite

⑤ Ice water

⑥ Rxni
a a

No Gas S
of
moles

Cacus → Cao tcozq ,


: OS tire
ef a ,
-_

→ OS
Nags t3Hzg 2MHz re
i
=
-

,
,

Pas g ,
→ PU , tacy , : OS -
-
tire
9)

It 2HIq ,
>
Itza ,
t
Iza ,
Oser o

05=0 X

⑦ LI HL ) H

Hz 2h
EE HL C H2

EI Nz Etty

H m - same Atoms
IT ST
Atoms same
mga Sf
-

Atoms * Same MT ST
above is hot
# but
true
always

\
Calculation of entropy change for system:-
① for ideal Gas

µd)aw
DS = = =
dutpdv
aw
T

T2 Vu
ds =

nfu
TI
+
nr¥
VI
*

) )
as = main thru
, ,

VI. =

TF Epa,
'

os =
Ncp
tuff ) ,
t HR In
(Az )
⑨ Isothermal Rrocess T=Co①
as
nRtn⇐)=hRhs¥ )
=

③ Isobaric P=Co①
as Mcp In
,⇐)
=

k-contf.os-ncvh.CI)
② Iso choric Rroass
⑨ Adiabatic Process : .

① Reversible 8=0 = Trev


Fuente
ds
GE)aw=o nah
)thRh⇐ )
-
-
- -

iso entropic
process s=Co@
① Irreversible 0--0=9 ing

OS =
= o
X
im

OS = her
buff ,
t n Rh
,
)
OS = tve

✓ OS =
-
ve

OS - tve

OS -
-
tire

as =
a

whiff) ,

§%✓
In
Zxzrx
=

=3 Rh 3

1-
⇐) n
>
itch )
i
¥¥ ⇐I 4 #D . .
- -

X


A fit
ITH
m = I -

f
p
t
Dt¥⇐a
Tithe
"
- E! ,

⑥si "=C¥ , ⇐ ¥.TT#I


I =
on
} oSum

9g osuniv 70 Spontaneous
osuniv =o Reversible for at
-

Epnib)
osuniv CO Non spontaneous

9
Ismet 9swm= -9=8
e-
rev
, ,

82 Ch
thou -_8z=%

9sys+=
-

I
osswm -_

fyre
where F-
Temp of Sun .
Bubi l mole
of an ideal Gas in expanded from
2 lit to 4 lit at zoo k under isothermal
condition Calculate US Oswin
.
syst , , ostomy .


9J process is reversible

at

9J Process is irreversible .

Sol ① ossyn - = n Rtm


⇐u ) ,
=
Rtn 2

Rhee
OSF -_ o = US
syst tossup Oswin = -

00=0 9= W
④ ossyst Rtn
-

= 2 ,

05*30

sure
=
-

I =⇐) =

-Pextfv

4y+ RCI= k¥4 ¥,


-

=
-

= -

Ix Rft -

E)
=

R2
-
② Entropy change For real Gas

⑤ at cont v ⑧ at Constant P

Ev = du =3 Udt 9p=dH = n
Cpd T

dS=t¥=h§d÷ deff -

hfp.fi
,f oS=hCphnf¥µ)
OS = n cuh

③ for Solid / liquid


Coit
Incompressible V -
-

¢=dd' U = hardt =3 Cmd T

ds =

nfcindt hCmhf =

buff )
ds =
ncm
,


④ Phase Transition

① Reversible phase transition


' am

1¥ G
⑥ Vaporization look

H2O →
Hog at lahm look
=TBp
@ , , ,

Normal B. P
8=0 Huap
osvap =
ottvap
T
Bp

⑥ Melting on fusion : .

H2O g
→ H2O at latm Ok
Tmp
, @,
-_
,

Normal melting pt
f. = OH
fusion

OS OH
fusion =
fusion

T
hip
② Irreversible Phase transition :

EF thos , s H2O @ ,
og
calm ,
-3°C I aim
,
27°C
N
us
,
053
052
Hice , nun (32%1)
"
3
H2O
Lahm Oc t

ok
,

Latin
,

th ottfusion
NC In
227,3-0
-

05=05, toss t
05g
=

273

H2O → H2O
et @ , as
,

lahm 127°C
lahm , 27°C ,

0531
a

051

052
-i

H2O @ ,
> H2O Cq ,

1ohm look
Lahm ,
look ,

05=05 ,
t OSL t 053

} ottzygp-tncph.C)I
n
=
nice , In t
-
3rd law of Thermodynamics:-

Entropy of perfect crystalline substance is zero at 0k

Temp .

¥7 KE is zero

No disorder in perfect Crystal .

OS =
Sq Scs , =
Scg ,
A
,
-

> Age , at 1am

Ok TK

OS
, toss
×
052 054
053 AG ,
Acs ) > A @) - Aa ) >

Tpp TBP
Tmp Tmp

Sq ,
= OS , t 052 toss to Sy t
TBP
05g
Tmp

=nfq tn.9tffpsiontnfc.IT
OK
T
Tmp

notice
+
nfI
Tbp
Q
Sp

gg-ncmhtf-zsxioxurzxenmq.gs#cm
Q

O
Rev .
oSt=o
=
ossysttoswy
Osborn = -

85 Jfk -

hah

= -

l -

5×85 The


2x R In 2 = ZRINL 2×8314×0-603
syst
= =

=/ I 52

¥
-

OS =
-
-

3 -
41 x ( ooo
hour =

II
310 =
-

Q

3rd law of Thermodynamics:-

Entropy of perfect crystalline substance is zero at 0k

Temp .

¥7 KE is zero

No disorder in perfect Crystal .

OS =
Sq Scs , =
Scg ,
A
,
-

> Age , at 1am

Ok Tk

OS
, toss
×
052 054
053 AG ,
Acs ) > A @) - Aa ) >

Tpp TBP
Tmp Tmp

Sq ,
= OS , t 052 toss to Sy t
TBP
05g
Tmp

=nfq tn.9tffpsiontnfc.LI
OK
T
Tmp

notice
+
nfI
Tbp
F


'
E
Ose →
G) °Ss→e
or
I -
G or

osvap → fusion

Sn D


see
B

A
1- →
Entropy change of rxn:

att t b B → CC told

Sao Soo SE Soo atcoutt.rs

per mole

05am =
@ sit DSB ] -

Casaotbsb ]

IFE when p= Cont T ⇐ IT → T2


Genet

osi-ositocpnxnh.CI ) ,

oCp= Cp ( Rroducts
Mxn
-
Reactants)
.

# When F- Cont P =p, s Pz

osi =

ositongrlnfpfz ) FYI Diff in

St Coyt
of
-

X Real Gas
*
Gas ( Rroduct -

Reactants
T Vs S diagram:-
ds
-_⇐↳= EE
A B
g fur = T DS -

"
%
= Area
T
T
Area under Tvs s
graph will

s→ give magnitude of Trev

> # "
I:c:* 's:c:&; "

i.
q¥¥¥¥÷ <
.

?
Area -
-
her -_ tve

C)
s →
Area -_ Trev = -

re

00=0 8 = -
W
rev
rev

Carnot 's
cycle of TVs S
diagram : .

A
t't
B
chttlc = Trev -_
CTH -

Tc ) (S2 Si ) -

sourer TH >
'

- = .
-


TH =
Thx ( S2 Si) -

TT
v
n

Ta

4H¥
c

N
- - -

If
D = I
Sinn
= -

te
'
i
,
i t ,

Si SL

J
'
00=0 D= -
w

w = -
( TH Tc
-

) ( S2 -

Si )
Gibb’s function:- → State function
Extensive
Rropertyy
G =
H -

T S .

→ thermodynamic function

for calculation
of
spontaneity .

OG = o
(H -

IS ] * Absolute value can not be


OG = OH -

OCT S ) .
determined .

at cont T

OG = OH -

T -
OS
at cont P .
4=0 It

or = f -

T OS -

OG = -
T
L Itt
-

OS
) =
- T
.

( ossurrtossyst)
OG = - T .

@ Sun ) ,
at cont T, P

Spontaneous Rrocess
oG=
osuniitve

9J
ve
-

ve OG
② tve
- -

Tf
=

osun
-

Non spontaneous process


.

06=0

Gf at Equi b ( or rev ) =oSunir=o
at cont Tip

# OG OH T.us OG
Equi b
=
at
-
-

-
o

Ist Ind T = =
To =
Eguib
Temp .

OH OS OG

-
re tve
Always -
ve
Always spontaneous
+ ve - ve eve Always Non -

Spontaneous
OG tve
9J T > To
-_
-
Ve - ve

TL To OG =
-
ve

oG=
YT > To ve
-

+ve * ve

TL To oG=tre

Calculation
T# of 0Grxn
① att t b B s CC t DD

OGICA ) OGE @ ) OGIE ) OGEED ) per mole

OG :* =
06°F ( Rroducts - Reactants)
# OGI elements in their natural , most stable form an

taken as zero


.

OGIE OH
n
-
T.

05am

at Tet, OG ? = olti -
T
,
.
Osi

T -
Tz OGI =
?
OGE = Oki -

Tz .
OSE

T
✓ o HE = o Hi to Cram TD
✓ osso si ocpaxs.tn
= o t

,
)

# 9J oCps× ,
Chot given) or
change in
temp is small

then 0 Hi = OHi

OSE =
osi

OGE = ol ti -

Tz .
o
si
and
# Sign of OH
,
as OG

¥ PUS ¢,
s
Reza ,
t
Uzi , :oH-
OG = OH -

T -
OS OS -_ the

¥fFe 9J T> To 0G= -

re

TL To OG -_ the

CI Ccs , oH=
{ 02cg
ve
t s
Coq , i
-

OS -_ tve
OG = OH -

TOS
- - = -
ve
-
ve -
ve

:
eg
- Lacosse ,
→ Goes , t 029 , : OH -

-
tire

or -_ OH -
T OS. OS = the
- -

the -
ve

T> To oGr= -
ve

TL To oG=tve
Q

O 20

n
OS =

Saw -

Sou =
Szow= = O -

813
The
.mu

@ Pt bxlo
°
O -
4 = Ax -

0.92 =a x @ Pt bxzo ④
-

°
[ Rgoclucts Reactants)
own S
168.351mg
=
-

= -

Q
TO
reversible osvap =
ottvap
TBP
30×1000
TBP =
hook

=

Q 0
palm

O
H2O @,
→ H2O at -101
#
OH =
-

ve 0Gr= OH -

T-

OS
--

OS =
-
ve - ve tire

0G_
Q


O
OG = OH - T . OS
- -

+ve -

ve

T > To OG = ve
-

To =

00¥ =
17%002 =
10004
( ) = du t d @v) -

des )

from Ist Law du = 9 tw

DG =
@LtwJtpdVtVdP-T.dS-S.d T
w = W t w
pv Non -

pv
for reversible process
[email protected]
DG
.cl/s)It-Cp./dV)tWnonpvtP.d/VtV-dP-T.d/S-S.dTdGr=WNon-pvtV.tdP
=
CT
-

S
.dT*
① at cont T
,
P DG = W
Non pv -
for Mv Rrocess
Wixon d G V. DP S DT
② Of
=0
Dv = -
.
-

Isothermal Rrocess
P
:

Trout &pd)p=v
Case -1 Solid ( liquid
✓ = Cont
x
Pz

Vfd
.

dor -

-
P dG=V( Pz -

R)
P,

Case -2 Ideal Gas


Ven RT
k

Pu p

dG=fnpRdp dG=nRtIn@p ) ,

Pi
Isobaric Rrocess :
-

f- Cont doe -

5. DT

(F) p= s
-

'


Relation between.DOGG and Equib constant oG=hRThr(¥ ) ,

PA PB Pc PD
& Po
at
- Cantt, P

Po Po Po
.fm
understand
@ a
-
Gao
)=RthP⇐)

*
o

pool bar

=
otto -
T oso
.
RT Otto T
In Kp oso
- -

= .

blip
OLI
-
=

. t

Otto , 0150 = Cont

9J OHI -

ve

tano -_
-
It 05 = tire
o R
-
-7 - -
-

bur
-

) off
1-
'
TT
N_de:① A e-
B c → D

tf -

C
A
-

GT
b
qui
G
AM
-

,
B -

D-

Mxn coordinate

Mxn coordinate

Gmin Equi b Pt

Rxn that direction where


② move in increase
in Total
entropy
take place ,
till it become max .
it
A > B

at
Epub P I
4
Lep =

Php =Iy
oG°= Im 't
-

Rthnkp =
-

RT Int = RT


2140cg , t Elza , → 21406cg ,
060=-8×298 In 108
lip = 40-72 108
=
= -
8×298×8×-2303
(10-92×40-2) 1000
= -43.924J

H2O @ , s H2O @ ) OG -_
VCR Pi )
-

lobar 20bar =
18×(20-10) HOT
bar lit
( mob Huo
-

= 18 Tn E 18M
=
If J/mohe

path
tf R=Rxf L
-
-

= 10×032=4 oats
OS =
Ncp In
IT ,
+
a R In
Az
Iz Rtn 2 t
Rahul =5zRhn2 2rem 2
= -

=
RzIn2

You might also like