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State Equations The Thermodynamics of State An Isentropic ..., Summaries of Thermodynamics

where R is a gas constant for a particular gas (as given in C&B Tables A-1 and A-2). An Isentropic Process for an Ideal Gas. Given: • constant specific heats ...

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State Equations
Reading Problems
6-4 6-12
The Thermodynamics of State
IDEAL GAS
The defining equation for a ideal gas is
Pv
T=constant =R
Knowing that v=V/m
PV
Tm =constant =R
where Ris a gas constant for a particular gas (as given in C&B Tables A-1 and A-2).
An Isentropic Process for an Ideal Gas
Given:
constant specific heats over a wide range of temperature
ds =0
du =c
v
dT c
v
=∂u
∂T
V
dh =c
p
dT c
p
=∂h
∂T
P
1
pf3
pf4
pf5
pf8
pf9
pfa

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State Equations

Reading Problems

The Thermodynamics of State

IDEAL GAS

The defining equation for a ideal gas is

P v

T

= constant = R

Knowing that v = V /m

P V

T m

= constant = R

where R is a gas constant for a particular gas (as given in C&B Tables A-1 and A-2).

An Isentropic Process for an Ideal Gas

Given:

  • constant specific heats over a wide range of temperature
  • ds = 0
  • du = cvdT ≡ cv =

(

∂u

∂T

)

V

  • dh = c p

dT ≡ c p

(

∂h

∂T

)

P

Gibb’s equation can be written as

T ds = du + P dv = cvdT + P dv = 0 (1)

where ds = 0 because we have assumed an isentropic process.

The definition of enthalpy is

h = u + P v

Taking the derivative yields

dh = du + P dv

︸ ︷︷ ︸

≡T ds

+vdP

dh = T ds + vdP ⇒ T ds = 0 = dh − vdP

c p

dT − vdP = 0 (2)

Equating Eqs. (1) and (2) through the dT term gives

dP

P

c p

c v

dv

v

Integrating (3) from its initial state to a final state

P

1

v

k

1

= P

2

v

k

2

= constant = P v

k

where

k =

cp

cv

The product of P · v

k remains constant for an ideal gas when:

  • specific heats are constant
  • Procedure: - given T 1

, P

1

and P 2

for an isentropic process

- determine Pr 1 at T 1 from Table A- - calculate Pr 2 , where

(

P

2

P

1

)

s=const

P

r 2

P

r 1

- read T 2

from Table A-17 for the calculated value of P r 2

  • use a similar procedure if volume is known instead of pressure, where

(

v 2

v 1

)

s=const

v r 2

v r 1

In Summary

For an ideal gas with constant cp and cv

P v = RT

u 2

− u 1

= c v

(T

2

− T

1

h 2

− h 1

= c p

(T

2

− T

1

There are 3 forms of a change in entropy as a function of T & v, T & P , and P & v.

s 2

− s 1

= c v

ln

T

2

T

1

  • R ln

v 2

v 1

= c p

ln

T

2

T

1

− R ln

P

2

P

1

= c p

ln

v 2

v 1

  • c v

ln

P 2

P

1

R = c p

− c v

A General Formulation

Steady State, Steady Flow in a Flow Channel of Arbitrary Cross-section with Work and Heat

Transfer

d

E =

E

f inal

E

initial

E

x+dx

E

x

where

E = m˙(e + P v)

= m˙(u +

(v

∗ )

2

  • gz + P v)

From the 1st law

rate of energy

storage

rate of

work

rate of

heat transf er

net rate of energy

leaving the system

dE CV

dt

= d

W − d

Q − d

E (1)

Special Cases

Reversible, SS-SF Process

Reversible implies ⇒

P

S

  • frictionless process
  • heat transfer is allowed but must be across ∆T → 0
  • which means T T ER

≈ T

CV

= T

Equation 4 becomes

d

W

m ˙

= −T ds + du + d(P v)

︸ ︷︷ ︸

=du + P dv

︸ ︷︷ ︸

=T ds

  • vdP ︸ ︷︷ ︸

+d

(

(v

)

2

)

  • d(gz) (5)

Therefore

d

W

m ˙

= vdP + d

(

(v

)

2

)

  • d(gz) (6)

Integrating Eq. (6) between the inlet and the outlet

W

m ˙

∫ out

in

vdP +

(v

∗ )

2

out

in ︸ ︷︷ ︸

∆KE

  • gz

out

in ︸ ︷︷ ︸

∆P E

but ∆KE and ∆P E are usually negligible.

If ∆KE + ∆P E = 0

W

m ˙

∫ out

in

vdP (8)

Equation can be used for a reversible, SS-SF flow in a liquid or a gas.

If we keep in mind

ρ liq

ρ gas

⇒ v liq

<< v gas

i.e. water @ 25

◦ C ρ = 997 kg/m

3 and air @ 25

◦ C ρ = 1. 18 kg/m

3

Therefore

W

m ˙

liq

W

m ˙

gas

For example: the work required to operate a pump is much less that that required to operate a

compressor.

Incompressible Substance

This is a special case of Eq. (8) where v = constant = v in

− v out

From Equation (8)

W

m ˙

= v in

(P

out

− P

in

The work term represents the minimum work required to pump a liquid from P in

to P out

with

negligible ∆KE and ∆P E.

Incompressible Substance and d

W = 0

From Eq. (6)

vdP + d

(

(v

∗ )

2

)

  • d(gz) = 0 (10)

Therefore

d

(

P

ρ

)

  • d

(

(v

∗ )

2

)

  • d(gz) = 0

W

m ˙

(

k

k − 1

)

(P v) in

(

P

out

P

in

) (k−1)/k

 = c p

(T

out

− T

in

The right side of Eq. (14) is based on the fact that ∆KE + ∆P E = 0 and dh = du + dP v

and du = 0. Which leads to h =

vdP.

Note: for the same inlet state and pressure ratio

W

m ˙

rev.,isothermal

W

m ˙

rev.,adiabatic