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CHEMICAL PROCESS
PRINCIPLES II
Chapter 7
Energy Balance Concept & Nonreactive Energy Balance
(Mostly Water Species)
Chapter 8
Nonreactive Energy Balance
Chapter 9
Reactive Energy Balance
Chapter 7: Introduction to Energy Balance
Forms of energy
Transfer of energy
Energy Balances on Closed System
Energy Balances on Open System
Reference States and State Properties
Steam Table
Energy Balance Procedure
Forms of Energy
1
E k mu 2
1
E k mu
2
2
Potential Energy Equation (Ep)
Closed system
no mass is transferred across the system boundaries while the
process is taking place
Energy balance
Final System Energy – Initial System Energy
= Net Energy Transferred to the System
When applying energy balance equation to a given process, the following point must be
aware;
1. The internal energy of a system depends almost entirely on the chemical
composition, state of aggregation (solid, liquid, or gas), and temperature of the
system materials. If no temperature changes, phase changes, or chemical reactions
occur in a closed system and if pressure changes are less than a few atmospheres,
then ∆U ≈ 0.
2. If a system is not accelerating, then ∆Ek = 0. If a system is not rising or falling, then
∆Ep = 0.
3. If a system and its surroundings are at the same temperature or the system is
perfectly insulated, then Q = 0. The process is then termed adiabatic.
In open system, mass is transferred across the system boundaries while the
process is taking place.
Therefore work must be done on open system to push mass in and work is done
on the surrounding by mass that emerges from the systems.
Both work terms must be include in the energy balance for open system
The net work done by an open system
and
W W s W fl W fl W out W in PoutVout PinVin
- shaft work
W s - rate of work done by the process fluid on a moving part within
the system such as a pump rotor.
- flow work
W fl - rate of work done by the fluid at the system outlet minus rate of
work done by the fluid at the system inlet.
Energy Balances on Open System
Hˆ Uˆ PVˆ
H m Hˆ
output
j j m Hˆ
input
j j
stream stream
2 2
m ju j m ju j
E k
output 2
input 2
stream stream
E p m
output
j gz j m
input
j gz j
stream stream
Example 7.4-2
500 kg/h of steam drives a turbine. The steam enters the turbine at 44 atm and 450C at a
linear velocity of 60 m/s and leaves at a point 5 m below the turbine inlet at atmospheric
pressure and a velocity of 360 m/s. The turbine delivers shaft work at rate of 70 kW and
the heat loss from the turbine is estimated to be 104 kcal/h. Calculate the specific
enthalpy change associated with the process.
Reference States and State Properties
It is not possible to know the absolute value of Û and Ĥ for a process material, but we can
determine the change in ΔÛ and change in ΔĤ corresponding to a specific change of state
(temperature, pressure, phase).
A convenient way to tabulate ΔÛ and ΔĤ is to choose a temperature, pressure and state of
aggregation (i.e. phase) as a reference state.
Since Ĥ cannot be known absolute, for convenience we may assign a value Ĥo=0 to be
reference state. Then ΔĤ1= Ĥ1-0; ΔĤ2= Ĥ2-0 and so on.
Some enthalpy tables give the reference states on which the listed values of Ĥ are based
and others do not.
However, we do not have to know the reference state to calculate ΔĤ for the transition
from one state to another state since the value are based on the same reference in the
table.
Ĥ and Û can be said as state properties
Property whose change of value in any process depend only on it initial and final states
and do not depend on the path take to reach the state.
Example 7.5-1
Steam Table
Superheated
Vapor
Liquid
Example 7.5-3
Energy Balance Tips
Closed System:
Q U
Open System:
Q H
Example 7.6-3