Lecture 11
Lecture 11
Lecture 11
The first law cannot be proven mathematically, but no process in nature is known
to have violated the first law, and this should be taken as sufficient proof.
1
Energy balance for a constant-pressure
expansion or compression process
General analysis for a closed system For a constant-pressure expansion
undergoing a quasi-equilibrium or compression process:
constant-pressure process. Q is to the
system and W is from the system.
2
3
Unrestrained Expansion
of Water
4
SPECIFIC HEATS
Specific heat at constant volume, cv: The
energy required to raise the temperature of
the unit mass of a substance by one degree
as the volume is maintained constant.
Specific heat at constant pressure, cp: The
energy required to raise the temperature of
the unit mass of a substance by one degree
as the pressure is maintained constant.
Constant-volume
and
constant-pressur
e specific heats
cv and cp
(values are for
helium gas). 5
True or False?
cp is always greater than cv
Joule showed
Internal energy and
using this For ideal gases,
enthalpy change of
experimental u, h, cv, and cp
an ideal gas
apparatus that vary with
u=u(T) temperature only.
7
• At low pressures, all real gases approach • u and h data for a number of
ideal-gas behavior, and therefore their gases have been tabulated.
specific heats depend on temperature only. • These tables are obtained by
• The specific heats of real gases at low choosing an arbitrary reference
pressures are called ideal-gas specific point and performing the
heats, or zero-pressure specific heats, and integrations by treating state 1
are often denoted cp0 and cv0. as the reference state.
Ideal-gas
constant-pressur
e specific heats
for some gases
(see Table A–2c Table A-17. In the preparation
for cp equations). of ideal-gas tables, 0 K is
chosen as the reference
temperature.
8
Internal energy and enthalpy change
when specific heat is taken constant
at an average value
(kJ/kg)
9
Three ways of calculating Δu and Δh
1. By using the tabulated u and h data
(Table A-17). This is the easiest and
most accurate way when tables are
readily available.
2. By using the cv or cp relations (Table
A-2c) as a function of temperature
and performing the integrations. This
is very inconvenient for hand
calculations but quite desirable for
computerized calculations. The results
obtained are very accurate.
3. By using average specific heats. This
is very simple and certainly very
convenient when property tables are Three ways of calculating
not available. The results obtained are Δu.
reasonably accurate if the
temperature interval is not very large.
10
Specific Heat Relations of Ideal Gases
The relationship between cp, cv and R
Specific
heat ratio
12
Heating of a Gas by a Resistance Heater
13
Heating of a Gas at Constant Pressure
14