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Basics of Fluid Mechanics, 2014a

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2.1. BASIC DEFINITIONS 51<br />

Utilizing equation (2.28) and subsisting into equation (2.30) and dividing by dT yields<br />

C p − C v = R (2.31)<br />

This relationship is valid only for ideal/perfect gases.<br />

The ratio <strong>of</strong> the specific heats can be expressed in several forms as<br />

C v to Spesific Heats Ratio<br />

C v =<br />

R<br />

k − 1<br />

(2.32)<br />

C p to Spesific Heats Ratio<br />

C p =<br />

kR<br />

(2.33)<br />

k − 1<br />

The specific heat ratio, k value ranges from unity to about 1.667. These values depend<br />

on the molecular degrees <strong>of</strong> freedom (more explanation can be obtained in Van Wylen<br />

“F. <strong>of</strong> Classical thermodynamics.” The values <strong>of</strong> several gases can be approximated as<br />

ideal gas and are provided in Table (2.1).<br />

The entropy for ideal gas can be simplified as the following<br />

∫ 2<br />

( dh<br />

s 2 − s 1 =<br />

T − dP )<br />

(2.34)<br />

ρT<br />

Using the identities developed so far one can find that<br />

s 2 − s 1 =<br />

∫ 2<br />

1<br />

1<br />

C p<br />

dT<br />

T − ∫ 2<br />

Or using specific heat ratio equation (2.35) transformed into<br />

1<br />

RdP<br />

P = C p ln T 2<br />

T 1<br />

− R ln P 2<br />

P 1<br />

(2.35)<br />

s 2 − s 1<br />

R<br />

= k<br />

k − 1 ln T 2<br />

T 1<br />

− ln P 2<br />

P 1<br />

(2.36)<br />

For isentropic process, Δs =0, the following is obtained<br />

ln T ( ) k−1<br />

2 P2 k<br />

=ln<br />

T 1 P 1<br />

(2.37)<br />

There are several famous identities that results from equation (2.37) as<br />

Ideal Gas Isontropic Relationships<br />

( ) k−1 ( )<br />

T 2 P2<br />

k<br />

k−1 V1<br />

= =<br />

T 1 P 1 V 2<br />

(2.38)

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