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Where:
η𝐸 = Energy efficiency; 𝐸𝑚 = Produce power; 𝐸𝑇 = Produced
thermal energy; 𝐸𝑐 = Consumed energy in the process (by
fuel
𝐸𝑚
combustion); ψ = Power and thermal energy ratio, i.e. ψ =
.
𝐸𝑇
The power and heat ratio do not change much when
stationary plants are considered because it’s defined by the
structure of the process and its demands, but changes a lot
when ship’s plant is considered.
Transformation energy equivalent factor 𝐹𝐾,𝐸 in a
cogeneration process is determined by expression:
𝐸
𝐸𝑐 − η 𝑇 1 1 1
𝐹𝐾.𝐸 = 𝐺𝑇
= − = 3.2
𝐸𝑚 η𝑡,𝑘 ψη𝐺𝑃 η𝑡,ε𝑘𝑣
The fuel consumption reduction in a combined system
when compared with the process of separate production is
given with expression:
∆𝐸𝐶 = 𝐸𝐶(𝑠𝑒𝑝) − 𝐸𝐶(𝑐𝑜𝑚𝑏) 3.3
Considering the thermal efficiency of the electricity
production and the steam generator’s efficiency, using the
expressions for the factor 𝐹𝐾,𝐸 expression (3.3) becomes:
1
∆𝐸𝐶 = 𝐸𝐸 − 𝐹𝐾,𝐸 3.4
η𝑡
Almost every field of industry, marine industry included,
has the need for different ‘shapes’ of energy and, when fuel
cost increase is considered, the constant need for process
improvement is understandable.
Cogeneration is well developed approach to increase the
efficiency of fuel chemical energy transformation. Although
the electric energy production coefficient is reduced, the
total energy transformation coefficient is increased.
A trigeneration plants could give further efficiency
increase, resulting in total efficiency of up to 75%. An
implementation of such equipment on board ship should
be a matter of additional research.
An on-board plant is specific when control mechanisms of
ship building are in question. Namely, ships are built
according to the classification societies’ regulation. Its role
is to accept the tendencies in the energy transformation
processes.
Nevertheless, for most ships and most ship owners, diesel
engine still remain the best solution, both in respect to
reliability and in fuel consumption and cost saving. Yet, for
some types of ships systems combining steam and gas
turbines could hold their place in the market.
The basic design considerations and requirements for
HVAC systems designs for marine applications are similar
to those for shore-based installations, except that marine
installations must cope with more demanding criteria and
parameters, some of which are:
- Space available is less for HVAC systems equipment,
ducting and components.
- Ships are mobile thus solar loads can affect compartments
with weather boundary above the waterline.
- In less than a day, a ship can undergo extreme weather
conditions variations.
- HVAC systems installation must be resistant to the
corrosive effects of seawater and salty air.
- An HVAC system must be capable of adequately and
efficiently operating under rough weather conditions of ship
movement
- Design of a marine HVAC system must be capable of
continuous operation with a high degree of reliability
(ships while at sea has little or no availability to supply of
spare parts and thus must carry its own spare parts and
tools).
- A marine HVAC system design and installation concept
must be such as to minimize structure borne and airborne
noise generated by the HVAC system components since the
enclosed area in a ship are generally small and also the
structure of ships offers very little sound dampening.
- The design of marine HVAC system must be watertight as
to prevent water access into the ship during rough weather
conditions.
- Smoke control and fire safety of shipboard systems are
critical due to limited firefighting and egress capabilities.
- In addition to performing its design functions, ships must
also have its own accommodations, storage areas,
generating and propulsion equipment, laundry areas, fuel
supply etc.
Thus the ship HVAC system must be capable of satisfactory
performance under these multitude of internal
compartments conditions, load variations, and functional
requirements.
In addition to the above listed criteria, HVAC systems
designed for special ships such as naval ships must also be
capable of meeting the underlisted requirements:
- They must be designed to withstand shock and vibration
requirements that are based on battle conditions and ship
movement considerations.
- The available space for HVAC systems are even less for a
naval ship because of the complexity of the systems on the
naval ship, and the numerous compartment functions.
- HVAC systems on naval ship must be designed and arranged to
minimize weight as weight is normally very crucial on a naval
ship design.
- The performance and reliability of naval HVAC systems are
critical since these systems serve functions vital to the ship’s
intended purpose and mission (in war time, a naval ship can be
at sea for a long period of time).
- The HVAC design must be capable of coping with the large heat
loads and the variations in heat loads from the various
compartments that large amount of equipment which produces
these high heat load.
- AnHVAC system must be designed to use standardized
equipment and components and as much as practicable,
standardized construction details and methods, to allow for
the expeditious replacement of parts in an emergency or
wartime situation.
- Etc.
Heating is the process of raising the ambient temperature
by adding heat to the air, to achieve higher air temperature.
Heating is achieved by various means on board ships:
- reheaters are used in a central station air-conditioning
system with the cooling functions turned off;
- preheaters and reheaters are used in supply air ventilation
systems; and
- convection or radiant heating is used in spaces not
equipped with either an air-conditioning or supply air
ventilation system.
The air for ventilation and air conditioning plants are
required to provide an acceptable climate for the crew to
live and work, sufficient air for machinery use and to
maintain temperature and humidity at acceptable levels for
the cargo.
All these must be achieved regardless of the conditions
prevailing external to the ship.
Ventilation is the movement of air from the outside or
weather into the ship, or from inside the ship to outside.
This is generally achieved by a combination of supply fans,
exhaust fans, and ductwork.
The type of ventilation system adopted in any given system
varies according to the nature of the space and its
ventilation.
Special requirements exist for auxiliary machinery spaces
where mechanical supply ventilation is provided at a
specified rate of change depending on the size and
specific function of the space.
Inadequate or poor-quality air supplies can seriously
damage most cargos. Fairly simple systems of cargo
ventilation can prevent such damage.
Certain cargos are carried in non-insulated holds as a
result, they are exposed to all climatic changes which may
cause condensation on the hull or cargo. Ventilation of the
hold is therefore necessary.
Refrigerated and frozen cargos are carried in insulated
holds but because of the living, gas producing nature of the
cargo, they also require ventilation.
The purpose of ventilation in non-insulated holds is to
remove excess heat and humidity and to remove gases
produced in the ripening of some fruits and vegetable
cargos.
Natural and mechanical ventilation are used for this
purpose.
Natural ventilation is accompanied by inlet and outlet pipes
and trunking to each cargo space.
Most modern ships use mechanical ventilation. Mechanical
ventilation operates in two distinct systems – the opened
and closed.
The opened system uses axial flow fans fitted in the inlet
and outlet trunks. The closed system recirculates air and a
controlled amount of fresh air can be admitted.
Tanker pump room requires ventilation to carry away
poisonous cargo fumes resulting from leaking glands or
pipe joints.
Mechanical exhaustion of air is achieved by the use of axial
flow fans and trunking.
The trunking draws air from the pump room flow and
emergency intakes at a height of 2.15m from the working
platform. These emergency intakes must be fitted with
dampers which can be opened or closed from the weather
deck or the working platform.
Ventilation of cargo tanks prevents over pressure or partial
pressure conditions which could occur during loading and
unloading of cargo. Temperature fluctuation during a
voyage could have a similar effect.
Vapor pipelines from the cargo hatch are led to
pressure/vacuum relief valves which are usually mounted
on a stand pipe some height above the deck.
Individual vent lines are fitted for each tank, for large
tankers a common venting line is led up a mast or Sampson
post on smaller vessel.
Air conditioning is the process of treating air to
simultaneously control its temperature, humidity, motion
and purity of the atmosphere of a given space or group of
spaces (zone).
Thus, the important factors that are involved in a complete
air conditioning installation are;
i. Temperature control
ii. Humidity control
iii. Air movement and circulation and
iv. Air filtering, cleaning and purification.
Complete air conditioning provides simultaneous control of
these factors for both summer and winter.
Winter conditioning relates to increasing temperature and
humidity whilst summer conditioning relates to decreasing
temperature and increasing humidity.
Air conditioning systems are intended to provide a
controlled environment that is satisfactory for personnel,
equipment, processes etc.
In both naval and commercial ships there are compelling
reasons for the requirement for cooling interior shipboard
spaces by air conditioning.
Some of the reasons common to both naval and
commercial ships are comfort and health.
The basic elements of air conditioning systems (of
whatever form) are;
- Fans for moving air.
- Filters for cleaning air, either fresh, recirculated or both.
- Refrigerating plant connected to heat exchange surface,
such as finned coils or chilled water spray.
- Means for warming the air, such as hot water or steam
heated coils or electrical elements.
- Means for humidification; and or dehumidification.
- Control system to regulate automatically the amount of
cooling or warming.
The air conditioning systems may be divided into two main
classes;
a. The central unit type in which the air is distributed to a
group of spaces through ducting.
- It has the advantage of saving space, economy in pipework
and minimal possibility of refrigerant leaking since the
circuit is sealed in the factory.
b. The self-contained unit types installed in the space it is to
serve.
- The central unit is the most widely applied in one or other
of alternative systems characterized by the means
provided to meet the varying requirements of each of the
spaces being conditioned.
The systems in general use are as follows;
i. Zone control system.
ii. Double duct systems.
iii. Reheat system.
Psychometry is the science that deals with air and water-
vapor mixture.
Psychometric data may be presented in both chart and
tabular form.
The psychometric chart shown below is used in designing
air-conditioning systems because it is easier to use than
tables.
The properties shown on the psychometric chart are
defined as follows;
This chart is used for finding the relative humidity of air
which has been measured using a 'wet and dry bulb'
thermometer.
This is a pair of thermometers, one of which has its bulb
wrapped in a damp cloth.
The drier the air, the greater the evaporation of water off
the cloth and therefore the lower the reading on the 'wet
bulb' thermometer
Dry-bulb temperature – the temperature recorded by a
common thermometer, measured in °C. On the chart, these
are vertical lines from the scale at the bottom.
Wet-bulb temperature – the temperature recorded by a
common thermometer with a moistened wick placed
around the bulb and a stream of air passed over the wick,
measured in °C. On the psychometric chart, these are
sloping lines starting at the saturation line on the left of the
chart and running obliquely down to the right.
Dew-point temperature – the temperature at which
condensation of moisture begins when the air is cooled. It is the
saturation temperature corresponding to the vapor pressure
and relative humidity and is expressed in °C. On the chart, this
temperature is read on the saturation curve on the left side of
the chart. At saturation, the dew-point temperature, dry-bulb
temperature and wet-bulb temperature are the same.
Relative humidity – the ratio of the actual water-vapor
pressure of the air to the saturated water-vapor pressure of the
air at the same temperature, expressed as a percent. On the
psychometric chart these are curved lines from the top right to
the bottom left of the chart.
Specific humidity – on the chart the specific humidity is
indicated on horizontal lines with the scale on the right side
of the chart.
Enthalpy – a thermal property that indicates the quantity of
heat in the air above an arbitrary datum expressed in KJ/Kg
of dry air. The enthalpy values given on the psychometric
chart are for saturated air and are sufficiently accurate for
most air-conditioning calculations. In the psychometric
chart, the enthalpy values are on the left side on a scale
corresponding to the wet-bulb temperature.
Enthalpy deviation – this is caused by the air not being in
the saturated state. An enthalpy correction is applied where
extreme accuracy is required, however, it is neglected for
most air-conditioning estimates.
Specific volume – on the psychometric chart it is shown on
the slopping lines from upper left to lower right.
Sensible-heat factor – the ratio of sensible heat to total
heat. On the chart the scale is on the right-hand side.
All units are expressed in terms of “per kg of dry air”
because the various properties of the moist air changes
during an air-conditioning cycle, and only the weight of dry
air remains constant.
It can be seen that cooling a superheated vapor at constant
pressure will bring it to the saturated vapor line, or Dew
point.
It can also be seen that cooling at constant temperature
raises the partial pressure until the dew point is reached.
Therefore, from the equation below for determining the
relative humidity,
%RH = m/mg x 100 = p/pg x 100
= Pdew/pg point x 100 4.1
Where: g = saturation condition
This means dry air contains the maximum moisture content
(% R.H.) at the saturation conditions.
Refrigeration is a process of cooling by the transfer of heat
from the item or space being refrigerated to a colder
medium, the refrigerant.
Heat is a form of energy and is indestructible so if heat is
removed from a space or substance to cool it to a
temperature below that of its surroundings, the heat
removed must be discarded to some substance at a higher
temperature where it is of no consequence.
This is achieved by using a mechanical refrigeration
process in which a refrigerant is used to alternately absorb
heat from the space or object to be cooled and reject the
Refrigeration thus depends on thermodynamics, heat
transfer and fluid flow for its practical achievement.
On naval ships, refrigeration is installed primarily for the
preservation of food required for the crew.
In commercial ships however, the applications are vaster
and ranges from preserving food for humans to extending
the useful life of perishables such as fresh fruits,
vegetables, flowers, meats, confectionery, chemicals,
The withdrawal of heat to achieve the desired degree of
refrigeration requires the use of any one of several
refrigerating processes.
Each of these depends upon the use of a substance called
the refrigerant, which can readily be converted from a
liquid into a vapor (evaporation), and also from a vapor into
a liquid (condensation), within a reasonable narrow range
of pressures.
Both refrigeration and air conditioning are measured in
tons of refrigeration.
A ton of refrigeration is the cooling effect of one ton of ice
at 0°C that melts in 24hrs – the rating of the refrigeration
machine.
The two major refrigeration systems in commercial use are
the absorption system and the vapor compression system.
Most marine refrigerating plants are of the vapor
compression type.
Vapor compression system
- The basic principles of the vapor compression system are
as follows:
1. A fluid requires and absorbs large quantities of heat when
it changes state from a liquid to a vapor.
2. The temperature at which a fluid evaporates or condenses
depends on the pressure existing at the interface between
the vapor and the liquid. The pressure-temperature
relationship of commonly used refrigerants is shown in the
table below
3. A vapor or gas can be liquified by compression and
cooling by a process known as liquification. The property
which makes the vapor compression system an economic
proposition is that any vapor or gas can be liquified and
recycled by suitably compressing it to a sufficiently high
pressure and then cooling it. If this were not the case, no
refrigerant other than air or water could be used
economically, and neither air nor water is ideal.
The vapor compression cycle takes place in a closed
system and are completed in one cycle comprising a
compressor,
- a condenser,
- a liquid receiver,
- an evaporator, and
- a flow control or expansion valve , interconnected by
discharge, liquid and suction lines.
The flow diagram is shown in Fig. 4.8
The vapor at low temperature and pressure (state 2) enters
the compressor where it is compressed isentropically and
subsequently, its temperature and pressure increase
considerably (state 3)
This vapor after leaving the compressor enters the
condenser where it is condensed into high pressure liquid
(state 4) and is collected in a receiver tank.
From receiver tank, it passes through the expansion valve
where it is throttled down to a lower pressure and has a
lower temperature (state 1)
After finding its way through the expansion valve, it finally
passes on to evaporator where it extracts heat from the
surroundings or circulating fluid being refrigerated and
vaporizes to low pressure vapor (state 2).
The cycle described above and shown in Fig. 4.8, can more
easily be depicted on a pressure-enthalpy (P-H) or Molier
diagram as shown in Fig. 4.9 below.
The Carnot cycle is a theoretical model that is useful for
understanding of a refrigeration cycle.
In some applications the Carnot refrigeration cycle is
known as the reverse Carnot cycle
The reversed Carnot cycle with vapor as refrigerant can be
used as practical cycle with minor modifications.
The isothermal processes of heat rejection and absorption
accompany condensation and evaporation are nearly
perfect processes and easily achieved in practice
The isentropic compression and expansion processes
however have certain limitations which are:
- a. Dry versus wet compression because wet compression
may damage the compressor since liquid cannot be
compressed easily.
- B. Throttling versus isentropic expansion, because the
expansion required a turbine and the work of the turbine is
so small therefore throttling is preferable.
- In plants with large amount of refrigeration charge
(refrigerant) a reservoir is installed in the liquid line. A
drier is also installed in the liquid line in Freon system.
The representation of the saturation vapor
compression refrigeration cycle on the P‐H and T‐S
diagram are as follow:
Line A to B represents the change from high to low
pressure, or expansion process (from 11.92 bar to 1.32
bar).
Line B to 𝐵1 represents the amount of liquid flashed off in
the expansion valve cooling the remaining liquid.
Line B to C represents the evaporation process at constant
saturation temperature and pressure in the evaporator (-
35°C and 1.32 bar). At point C the refrigerant is a dry
saturated vapor.
Line C to 𝐶 1 represents the superheat absorbed by the dry
saturated vapor (from -35°C to -25°C).
Line 𝐶 1 to D represents the compression process.
Line D to E represents the superheat given up by the vapor
in the condenser (from 90°C to 30°C). at point E the
refrigerant is a dry saturated vapor.
Line E to F represents the condensation process at constant
saturation temperature and pressure (30°C and 11.92 bar).
At point F the refrigerant is a saturated liquid.
Line F to A represents the sub cooling of the condensed
liquid (from 30°C to 20°C).
Refrigerating effect is the amount of heat absorbed by each
unit of refrigerant as it flows through the evaporator and is
equal to the difference between the enthalpy of the vapor
leaving the evaporator and the enthalpy of the liquid at the
flow control.
Thus, for the system shown in Fig. 4.9, refrigerating effect
is;
𝑞𝐸 = (ℎ𝐶 1 - ℎ𝐴 ) KJ/Kg 4.1
= 398.3 – 230.3 KJ/Kg = 168.3 KJ/Kg
The rate at which the system will absorb heat from the
refrigerated space or substance is known as the refrigerating
capacity, and is expressed as;
Refrigerating capacity, 𝑄𝐸 = m x 𝑞𝐸 KJ/s 4.3
Where: m = mass flow of refrigerant through the evaporator
(Kg/s)
For the system shown in Fig. 4.9 to achieve a specified
refrigerating capacity, the required mass flow rate is;
𝑄𝐸 𝐾𝐽/𝑠 150
m= = = 0.94Kg/s 4.4
𝑞𝐸 𝐾𝐽/𝐾𝑔 160
The compressor capacity is its ability to remove the vapor
from the evaporator at the same rate at which it is formed.
If the capacity is too small the excess vapor will accumulate
in the evaporator, causing the pressure and saturation
temperature to rise. Consequently, if too large, it will
remove the vapor from the evaporator too rapidly, causing
the pressure and saturation temperature to fall.
To maintain a specified operating condition, a compressor
must have a swept volume equal to the volume of the vapor
formed in the evaporator per unit time (𝑚3 /ℎ).
V = m x v 𝑚3 /h 4.5
For the system shown in Fig. 4.9, v = 0.18𝑚3 /𝑘𝑔 (at -25°C
and 1.32 bar)
i.e. V = 0.94 x 0.18 x 3600 = 609 𝑚3 /h
The energy input from the compressor motor to raise the
pressure of the vapor to the required condensing
temperature is known as the heat of compression, and is
equal to the difference between the enthalpy of the vapor
at the compressor outlet and inlet.
Thus, for the system shown in Fig. 4.9, heat of compression
is;
𝑊𝐶 = ℎ𝐷 − ℎ𝐶 1 = 470 – 398.3 KJ/Kg = 71.7 KJ/Kg 4.6
The rate of heat transfer from the refrigerant in the
condenser to the cooling medium is known as the
condenser duty, and is expressed as;
𝑄𝐶 = 𝑚 𝑥 𝑞𝐶 KJ/s KW 4.7
Where: 𝑞𝐶 , the total heat of rejection, is equal to the
refrigerating effect plus the heat of compression. Thus, for
the system shown in Fig. 4.9,
𝑄𝐶 = 𝑚 𝑞𝐸 + 𝑊𝐶 KW 4.8
= 0.94(470 – 230.3) = 225.3KW
The ratio of refrigerating effect (heat absorbed by the
refrigerant while passing through the evaporator) to the
heat of compression (the work input required to compress
the refrigerant in the compressor) is known as the
coefficient of performance (C.O.P.)
𝑅𝑛 ℎ𝐶1 −ℎ𝐴
C.O.P = = 4.9
𝑊𝐶 ℎ 𝐷 − ℎ 𝐶1
168.0
= = 2.34
71.7
The thermodynamic processes are as follows:
1 ‐ 2: Isentropic compression 𝑆1 = 𝑆2
2 ‐ 3: De super heating and condensation at P=constant
3‐4: Throttling (h=constant)
4 ‐ 1: Evaporation at P =constant
Further calculations:
Q condenser (𝑄𝑐 ) = m (ℎ2 – ℎ3 ) 4.10
Q evaporator (𝑄𝑒 ) = m (ℎ1 – ℎ4 ) 4.11
W compressor 𝑊𝑐 = m (ℎ2 – ℎ1 ) 4.12
ℎ4 = ℎ3 Throttling processes
The mass flow rate m (kg/s) can be calculated as:
m =Refrigeration capacity (kW) / Refrigeration effect
(kJ/kg)
𝑄𝑒
= 4.13
ℎ1 − ℎ 4
The coefficient of performance is obtained as
𝑄𝑒
C.O.P. = 4.14
𝑊
ℎ1 − ℎ 4
= 4.15
ℎ1 − ℎ 2
Piston displacement of the compressor can be given by:
Vp = π (D2 /4) L N / 60
𝑚𝑉
= 4.16
η𝑣
Where: ηv is the volumetric efficiency
v is the specific volume at point 1 (m3 /kg)
L and D is the stroke and diameter of the piston
N is the revolution per minute rpm
The values of enthalpies can be obtained either
from Charts or tables.
If tables are used then: ℎ1 = ℎ𝑔
the evaporator temperature (the low temperature)
ℎ3 = ℎ𝑓 at the condenser temperature (the high temperature)
ℎ4 = ℎ3 : Throttling process
ℎ2 = ℎ𝑔 at condenser temperature + cp (T2 – T condenser)
𝑇2 can be found from:
𝑆1 = 𝑆2 = 𝑆𝑔 at condenser temperature + 𝐶𝑝 Ln (𝑇2 / T
condenser)
Example 1
Consider a refrigerator which operates on the ideal
refrigeration cycle. The evaporator temperature is -20°C and
the condenser temperature is 40°C. the refrigerant is R-134a
and its flow rate in the cycle is 0.2Kg/s. Calculate the
following;
Compressor work rate (W)
Condenser heat rate (𝑄𝑛 )
Evaporator heat rate (𝑄𝐿 )
COP and
COP based on the Carnot cycle
Solution:
Based on the input data given above, we take the thermodynamic
data in terms of enthalpy, pressure and temperature from the
thermodynamic tables of R-134a and list them in the following
table, along with the cycle T-S diagram
For the compressor work;
W = 𝑚(ℎ
ሶ 2 − ℎ1 ) = 0.2(431.24 – 386.08) = 9.0KW
Condenser heat rate;
ሶ 2 − ℎ3 ) = 0.2(431.24 – 256.54) = 34.9KW
𝑄𝑛 = 𝑚(ℎ
Evaporator heat rate (e.g. refrigeration load)
ሶ 1 − ℎ4 ) = 0.2(386.08 – 256.54) = 25.9KW
𝑄𝐿 = 𝑚(ℎ
𝑄𝐿 25.9
COP = = =2.87
𝑊 9.0
The COP based on the Carnot cycle;
𝑇𝐿 (273.15 −20) 253.15
𝐶𝑂𝑃𝐶𝑎𝑟𝑛𝑜𝑡 = = =
𝑇𝐻 − 𝑇𝐿 40+273.15 −(273.15−20) 313.15 −253.15
= 4.22
As seen from the calculation, the COP from energy balance
equations is 32% less than the COP calculated based on the
Carnot cycle which is theoretically the maximum COP that can
be reached.
At present some effort has been devoted to the utilization of
the vast waste energy from diesel engines used onboard
ships for refrigeration.
There are several types of refrigeration technology being
used for marine application including
- compression refrigeration,
- sorption and
- injection refrigeration systems.
Both absorption and adsorption refrigeration systems are
sorption refrigeration technologies
Compression and injection refrigeration need extra
energy to drive the compressor and injectors which lead to
increase in fuel consumption of ships.
A sorption refrigeration system is driven by thermal energy
and needs little electricity and can utilize the waste heat of
the engine and improve the energy conservation efficiency
thus, fuel can be saved considerably.
The absorption refrigeration system comprises of
condenser, expansion valve, evaporator, absorber, pump
and generator.
1. Condenser: Just as in the condenser of the vapor
compression cycle, the refrigerant enters the condenser at
high pressure and temperature and gets condensed. The
condenser is of water-cooled type.
2. Expansion valve or restriction: When the refrigerant
passes through the expansion valve, its pressure and
temperature reduce suddenly. The refrigerant (ammonia in
this case) then enters the evaporator.
3. Evaporator: The refrigerant at very low pressure and
temperature enters the evaporator and produces the cooling
effect. In the vapor absorption cycle, this refrigerant flows to the
absorber that acts as the suction part of the refrigeration cycle.
4. Absorber: The absorber is a sort of vessel that consists of the
weak solution of the refrigerant (ammonia) and absorbent
(water). When ammonia from the evaporator enters the absorber,
it is absorbed by the absorbent due to which the pressure inside
the absorber reduces further leading to more flow of the
refrigerant from the evaporator to the absorber. At high
temperature water absorbs lesser ammonia, hence it is cooled by
external coolant to increase its ammonia absorption capacity.
The refrigerant leaving the evaporator enter the absorber,
where it is absorbed by the absorbent. Pump helps the
strong solution of refrigerant-absorber enter the generator.
The refrigerant then enters the condenser while the
remaining weak solution enters back to the absorber and
the cycle is repeated.
When the refrigerant entering the absorber is absorbed by
the absorbent its volume decreases, thus the compression
of the refrigerant occurs. The absorber thus acts as the
suction part of the compressor. The heat of absorption is
also released in the absorber, which is removed by
external coolant.
5. Pump: When the absorbent absorbs the refrigerant
strong solution of refrigerant-absorbent (ammonia-water) is
formed. This solution is pumped by the pump at high
pressure to the generator. Thus, pump increases the
pressure of the solution to about 10bar.
6. Generator: The refrigerant-ammonia solution in the
generator is heated by external heat source (steam from
exhaust system, jacket water, turbocharger cooling system
or any other suitable source) which increases the
temperature of the solution. The refrigerant in the solution
gets vaporized and leaves the solution at high pressure. The
high pressure and high temperature refrigerant then enter
the condenser, where it is cooled by the coolant, and it then
enters the expansion valve and then finally into the
evaporator where it produces the cooling effect.
This refrigerant is then again absorbed by the weak
solution in the absorber.
The pressure of the refrigerant is increased in the
generator; hence it is considered to be equivalent to the
compression part of the compressor.
The most commonly used refrigerant-absorbent pairs in
commercial systems are:
1. Water-Lithium Bromide (H2O-LiBr) system for above 0o C
applications such as air conditioning. Here water is the
refrigerant and lithium bromide are the absorbent.
2. Ammonia-Water (NH3-H2O) system for refrigeration
applications with ammonia as refrigerant and water as
absorbent.
Efforts are being made to develop other refrigerant-
absorbent systems using both natural and synthetic
refrigerants to overcome some of the limitations of (H2O-
LiBr) and (N𝐻3 -𝐻2 O) systems.
The cycle uses water as the refrigerant and a solution of
lithium bromide in water is used as the absorbent.
In the absorber, the lithium bromide absorbs the water
refrigerant, creating a solution of water and lithium
bromide. This solution is pumped by the pump to the
generator where it is heated.
The water refrigerant gets vaporized and moves to the
condenser where it is cooled while the lithium bromide
flows back to the absorber where it further absorbs water
coming from the evaporator.
This refrigeration system using water-lithium bromide are
extensively used in large capacity air conditioning systems.
Since water is used as refrigerant, using these systems it is
not possible to provide refrigeration at sub-zero
temperatures. Hence it is used only in applications
requiring refrigeration at temperatures above 0°𝐶.
Analysis of this system is easy as the vapor generated in
the generator is almost pure refrigerant (water), unlike
ammonia-water system where both ammonia and water
vapor are generated in the generator.
1. Lithiumbromide has great affinity for water vapor,
however, when the water-lithium bromide solution is formed,
they are not completely soluble with each other under all
the operating conditions of the absorption refrigeration
system. Because of this, the designer must take care that
such conditions would not be created where crystallization
and precipitation of the lithium bromide would occur.
2. The water used as the refrigerant in the absorption
refrigeration system means the operating pressures in the
condenser and the evaporator must be very low. Even the
difference of pressure between the condenser and the
evaporator must be very low. This can be achieved even
without installing the expansion valve in the system, since
the drop in pressure occurs due to friction in the
refrigeration piping and in the spray nozzles.
3. Thecapacity of any absorption refrigeration system
depends on the ability of the absorbent to absorb the
refrigerant, which in turn depends on the concentration of
the absorbent. To increase the capacity of the system, the
concentration of the absorbent should be increased, which
would enable absorption of more refrigerant. Some of the
most common methods used to change the concentration of
the absorbent are: controlling the flow of the steam or hot
water to the generator, controlling the flow of water used for
condensing in the condenser, and re-concentrating the
absorbent leaving the generator and entering the absorber.
There are no moving parts except for the two small
centrifugal pumps.
Step less capacity control down to 0% capacity which is not
possible with reciprocating machines and centrifugal
No feon used
No recharging cost of refrigerant
Low working pressure
Low COP.
High heat rejection factor, thus requires higher cooling
tower and pump capacities.
Corrosive nature of lithium bromide corrodes the heat
exchanger.
The process of a continuously operating absorption system
is characterized by the points 1 to 6.
- Point 1 to 3: The strong solution leaves the generator and
enters the absorber via the heat exchanger. The position of
point 3 is determined by the evaporator pressure (or the
evaporation temperature TE)
- Point 3 to 4: The solution absorbs the water vapor corning
from the evaporator. The absorber temperature TA defines
point 4 and gives the concentration of the weak solution, 𝑋𝑤𝑠 .
- Point 4 to 6: The weak solution is transported from the
absorber to the generator via the heat exchanger. The
location of point 6 depends on the given temperature TG
and thus on the condenser pressure
- Point 6 to 1: Boiling of the solution in the generator. The
generator temperature TG defines point 1 and determines
the concentration of the strong solution, 𝑋𝑠𝑠 .
- Point 6 to 8: Water vapor goes from generator to condenser
and is condensed.
- Point 8 to 9: Water liquid flows from condenser to
evaporator
- Point 9 to 4: Evaporation and absorption of water vapor by
the solution
Referring to figure 4.14, two mass flow balances over the
generator give the following equations.
Total mass flow balance:
𝑀𝑤𝑠 = 𝑀𝑠𝑠 + 𝑀𝑤 4.17
LiBr balance;
𝑀𝑤𝑠 𝑋𝑤𝑠 = 𝑀𝑠𝑠 𝑋𝑠𝑠 4.18
Where: 𝑀𝑠𝑠 , 𝑀𝑤𝑠 and 𝑀𝑤 are the mass flow of the strong
solution, weak solution, and water refrigerant,𝑋𝑠𝑠 and 𝑋𝑤𝑠 ,
are the concentrations of LiBr in the strong and weak
solutions.
The concentration is defined as the ratio of the mass
fraction of LiBr in a solution to the total mass of LiBr and
water contained in the solution are expressed as:
𝑀𝑎𝑠𝑠 𝐿𝑖𝐵𝑟
X= 4.19
𝑀𝑎𝑠𝑠 𝐿𝑖𝐵𝑟+𝑀𝑎𝑠𝑠 𝐻2 𝑂
But;
𝑀𝑤𝑠 𝑋𝑠𝑠
= 4.20
𝑀𝑤 𝑋𝑠𝑠 − 𝑋𝑤𝑠
𝑀𝑠𝑠 𝑋𝑤𝑠
and = 4.21
𝑀𝑤 𝑋𝑠𝑠 − 𝑋𝑤𝑠
Using the notation of figure 4.14, the steady state flow
energy equation will be applied to each component
assuming equilibrium states and uniform temperature
1. Generator: The rate of heat transfer to the solution is;
𝑄𝐺ሶ = 𝑀7 ℎ7 + 𝑀1 ℎ1 - 𝑀6 ℎ6 4.22
But
𝑀1 = 𝑀2 = 𝑀3 = 𝑀𝑠𝑠
𝑀4 = 𝑀5 = 𝑀6 = 𝑀𝑤𝑠
𝑀7 = 𝑀8 = 𝑀9 = 𝑀10 = 𝑀𝑤
Or
𝑄𝐺ሶ = 𝑀𝑤 ℎ7 + 𝑀𝑠𝑠 ℎ1 - 𝑀𝑤𝑠 ℎ6 4.23
Where:
ℎ1 = enthalpy of saturated strong solution at 𝑇1 and 𝑋𝑠𝑠
ℎ6 = enthalpy of weak solution at 𝑇6 and 𝑋𝑤𝑠
ℎ7 = enthalpy of saturated water vapor at 𝑇7
Generator temperature = 𝑇1 = 𝑇7 = 𝑇𝐺
2. Condenser: The rate of heat transfer from the condenser
is;
ሶ − ℎ )
𝑄 ሶ = 𝑀 (ℎ 4.24
𝐶 𝑤 7 8
ℎ8 = enthalpy of saturated water liquid at 𝑇8
Condenser temperature = 𝑇8 = 𝑇𝐶
3. Water pressure restrictor:
ℎ9 = ℎ8
ℎ9 = enthalpy of water liquid at 𝑇9
4. Evaporator: The rate of heat transfer to the evaporator i.e.
the refrigerating capacity is;
𝑄𝐸ሶ = 𝑀𝑤 (ℎ10ሶ − ℎ9 ) 4.25
= 𝑀𝑤 (ℎ10ሶ − ℎ8 ) 4.26
ℎ10 = enthalpy of water vapor at 𝑇10
Evaporator temperature =𝑇10 = 𝑇𝐸
5. Solution pressure restrictor:
ℎ3 = ℎ2
ℎ2 = enthalpy of solution at 𝑇2 𝑎𝑛𝑑 𝑋𝑠𝑠
ℎ3 = enthalpy of solution at 𝑇3 𝑎𝑛𝑑 𝑋𝑠𝑠
6. Absorber: the rate of heat transfer from the absorber is:
𝑄𝐴ሶ = 𝑀3 ℎ3 + 𝑀10 ℎ10 - 𝑀4 ℎ4 4.27
= 𝑀𝑠𝑠 ℎ2 + 𝑀𝑤 ℎ10 - 𝑀𝑤𝑠 ℎ4 4.28
ℎ4 = enthalpy of saturated weak solution at 𝑇4 𝑎𝑛𝑑 𝑋𝑤𝑠
ℎ10 = enthalpy of saturated weak vapor at 𝑇𝐸
Absorber temperature = 𝑇4 = 𝑇𝐴
7. Heat exchanger: Assuming that heat losses to the
surroundings are negligible, the rate of heat transfer
between the strong and weak solutions is;
𝑄𝐻𝑋ሶ = 𝑀𝑠𝑠 ℎ1 − ℎ2 = 𝑀𝑤𝑠 (ℎ6 − ℎ5 ) 4.29
8. Solution pump: The power input to the pump is;
𝑊𝑝ሶ = 𝑀𝑤𝑠 (ℎ5 − ℎ4 ) 4.30
ℎ5 = enthalpy of weak solution at 𝑇5 𝑎𝑛𝑑 𝑋𝑤𝑠
The difference between ℎ4 𝑎𝑛𝑑 ℎ5 is not distinguished on
the charts of specific enthalpy of LiBr – water solutions as
the temperature is approximately the same.
The coefficient of operation of the cycle is;
𝑄ሶ 𝐸 𝑀𝑤 ( ℎ10 − ℎ8 )
COP = = 4.31
𝑄ሶ 𝐺 𝑀𝑤 ℎ7 + 𝑀𝑠𝑠 ℎ1 − 𝑀𝑤𝑠 ℎ6
The second law efficiency of the cycle, given by the
equation below,
−𝑄ሶ 𝐸 (1− 𝑇𝑜ൗ𝑇 )
η= 𝑟
4.32
𝑄ሶ 𝐺 1− 𝑇𝑜ൗ𝑇 + 𝑄ሶ 𝐶 1− 𝑇𝑜
ൗ𝑇𝑐𝑓,1 + 𝑄ሶ 𝐴 (1− 𝑇𝑜
ൗ𝑇𝑐𝑓,2 )
𝐻
where:
(𝑇𝐶𝐻𝑤 + 𝑇𝑐𝐻𝑤,𝑒 )
𝑇𝑟 = average temperature of chilled water =
2
4.33
(𝑇𝐻𝑤1 + 𝑇𝐻𝑤,𝑒 )
𝑇𝐻 = average temperature of hot water =
2
4.34
(𝑇𝑐𝑤1 + 𝑇𝑐𝑤1,𝑒 )
𝑇𝑐𝑓,1 = average temperature of cooling water =
2
4.35
(𝑇𝑐𝑤2 + 𝑇𝑐𝑤2,𝑒 )
𝑇𝑐𝑓,2 = average temperature of cooling water =
2
4.36
𝑇𝑜 = ambient temperature
The values of COP increase in general with increasing
evaporator and generator temperatures then at a certain
value of generator temperature it starts to decrease.
The performance of aqueous LiBr cooling cycles using the
coefficient of performance
- COP increases to a maximum for higher generator
temperatures and then either decreases slightly or becomes
insensitive to generator temperature
- While in case of the Absorber, the COP deceases with
increase in adiabatic temperature of the absorber.
Fig 4.15 shows the schematic of an ammonia-water
absorption refrigeration system.
Compared to water-lithium bromide systems, this system
uses three additional components: a rectification column, a
dephlegmator and a sub- cooling heat exchanger (Heat
Exchanger-I).
The function of rectification column and dephlegmator is to
reduce the concentration of water vapor at the exit of the
generator. Without these the vapor leaving the generator
may consist of five to ten percent of water.
However, with rectification column and dephlegmator, the
concentration of water is reduced to less than one percent.
The sub-cooling heat exchanger, which is normally of
counter-flow type is used to increase the refrigeration
effect and to ensure liquid entry into the refrigerant
expansion valve.
Mass and energy balance equations for all the components
are the same as those of water-lithium bromide systems,
However, the thermal energy input to the generator will be
different due to the heat transfer at the dephlegmator.
Taking a control volume that includes the entire rectifying
column (generator + rectification column + dephlegmator)
as shown in Fig. 4.15, we can write the energy equation as;
𝑄𝑔 − 𝑄𝑑 = 𝑀10 ℎ10 + 𝑀6 ℎ6 − 𝑀4 ℎ4 4.36
Writing the mass flow rates of strong (point 4) and weak
(point 6) solutions in terms of refrigerant flow rate and mass
fractions, we can write the above equation as;
𝑄𝑔 − 𝑄𝑑 = M [(ℎ10 − ℎ4 ) + 𝝀(ℎ6 − ℎ4 )] 4.37
A vapor absorption refrigeration system based on ammonia-
water (Fig.4.15) has refrigeration capacity of 100TR. The
various state properties of the system shown below are
given in the table. Taking the heat rejection rate in the reflux
condenser (𝑄𝑑 ) as 88KW. Find (a)the mass flow rates of
solution through the evaporator, strong solution and weak
solution; (b) enthalpy values not specified in the table and
(c) heat transfer rates at condenser, absorber, generator and
solution pump work (d) system COP.
a). mass flow rate through evaporator, 𝑀1 is given by;
𝑄𝑒 𝑄𝑒 3.517 𝑥 100
𝑀1 = = = = 0.313Kg/s
ℎ14 − ℎ13 ℎ14 − ℎ12 1442.3−318.7
Circulation ratio, 𝛌 is given by;
𝑀𝑤𝑠 𝜁10 − 𝜁7
𝛌= = = 5.345
𝑀1 𝜁7 − 𝜁8
Therefore, mass flow rate of weak solution;
𝑀𝑤𝑠 = 𝑀1 𝑥 𝛌 = 1.673Kg/s
Mass flow rate for strong solution;
𝑀𝑠𝑠 = 𝑀1 𝑥 (1 + λ) = 1.986Kg/s
b). state points 1,7,8, and 13;
From energy balance across Heat Exchanger – 1
(ℎ11 − ℎ12 ) = (ℎ1 − ℎ14 )
ℎ1 = ℎ14 + (ℎ11 − ℎ12 ) = 1467.9KJ/Kg
From energy balance across solution heat exchanger;
𝑀𝑠𝑠 (ℎ4 − ℎ3 ) = 𝑀𝑤𝑠 (ℎ6 - ℎ7 )
ℎ7 = 1.43KJ/Kg
Since expansion through expansion valves is isenthalpic;
ℎ8 = ℎ7 = 1.43KJ/Kg
ℎ12 = ℎ13 = 318.7𝐾𝐽/𝐾𝑔
c). From energy balance;
Heat transfer rate at condenser;
𝑄𝑐 = 𝑀10 ℎ10 − ℎ11 = 365.5𝐾𝑊
Heat transfer rate at absorber;
𝑄𝑎 = 𝑀1 ℎ1 + 𝑀8 ℎ8 − 𝑀2 ℎ2 = 577.4KW
Heat transfer rate at the generator;
𝑄𝑔 = 𝑀10 ℎ10 + 𝑀6 ℎ6 + 𝑄𝑑 − 𝑀4 ℎ4 = 676.5𝐾𝑊
Power input to pump;
𝑊𝑝 = 𝑀2 ℎ3 − ℎ2 = 2.78𝐾𝑊
System COP is given by;
𝑄𝑒 351.7
COP = = = 0.518
𝑄𝑔 + 𝑊𝑝 676.5−2.78
Primary refrigerants are working fluids used in vapor
compression systems. Primary refrigerants should;
a. be non-flammable, non-explosive, and non-toxic and it
should not contaminate foods or damage the environment in
the event of leakage.
b. be non-corrosive, and not react with lubricants, moisture,
and materials used in plant construction.
c. have moderate pressure
d. have a high COP value, i.e. low compressor per input
power unit of refrigerating capacity.
e. have a moderate temperature after compression. A low
discharge temperature reduces the risk of oil decomposition
and overheating of the compressor.
f. be low in cost and readily available.
Secondary refrigerants are used as a heat transfer medium,
with a change of temperature but no change of state.
The secondary refrigerants mostly used in marine plants
are brine and trichloroethylene.
Brine is normally used for temperature down to -34°C,
below which it is extremely viscous resulting in
unacceptable pumping losses.
Trichloroethylene is used for temperature down to -73°C. In
its gaseous state, it is both toxic and heavier than air, has a
maximum permissible concentration in air of 200ppm.
Trichloroethylene acts as a solvent to most synthetic
rubbers and jointing materials. It is non-flammable and
non-toxic.
The liquid is both heavier than, and immiscible with water,
so any water in the system will freeze at temperatures
below 0°C.
Marine refrigerants used on board ships are as follows;
- R11 is used in marine air conditioning, especially for cruise
ships, and for cleaning out marine refrigeration machinery.
- R12 is used for marine air conditioning and food stores in
ships, and has universal use in refrigerated containers.
- R22 used for marine air conditioning and food stores in
new ships, and in most central cargo refrigeration plant,
fishing boat refrigerated storage and freezing plant, and
liquid gas re-liquefication plant.
- R502 are rarely used but when used for low temperature
refrigeration.
- Ammonia (R717) is used for large freezing and low temperature
storage installations on board fish factory vessels, and has very
occasional use in central cargo refrigeration plant.
- Refrigerants are identified by international numerical code
which is prefixed by ‘R’ because of their complex chemical
formulae.
- R11, R12 and R502 are fully halogenated chlorofluorocarbons
(CFC) refrigerants, and R22 is a hydrofluorocarbon (HCFC)
refrigerant.
Examine the performance of engineering devices in relation to the
second law of thermodynamics
Define exergy, which is the maximum useful work that can be
obtained from a system at a given state in a specific environment
Define reversible work, which is the maximum useful work that can
be obtained as a system undergoes a process between two specified
states
Define the exergy destruction, which is the wasted work potential
during a process as a result of irreversibilities
Define the second law efficiency
Develop the exergy balance relation
Apply the exergy balance to closed systems and control volumes.
Thermal power plants (steam power plants, gas turbine
power plants, nuclear power plants, internal combustion
engines etc.) are widely utilized throughout the world for
electricity generation.
In the past, energy-related engineering systems were
designed, and their performance evaluated primarily by
using the energy balance deduced from first law of
thermodynamics which deals with the quantity of energy
and asserts that energy cannot be created or destroyed.
The law was also used to evaluate through energetic
performance criteria the performance of thermal power
plants including electrical power and thermal efficiency.
In recent years the second law analysis, also known as
exergy analysis, has drawn the interest of energy engineers
and scientist. The exergetic performance based on the
second law of thermodynamics has found as useful method
in the design, evaluation, optimization and improvement of
thermal power plants.
The exergetic performance analysis does not only
determine magnitudes, location and causes of
irreversibilities in the plants, but also provides more
meaningful assessment of plant individual components
efficiency.
These points of the exergetic performance analysis are the
basic differences from energetic performance analysis.
Therefore, it can be said that performing exergetic and
energetic analyses together can give a complete depiction
of system characteristics.
Such a comprehensive analysis will be a more convenient
approach for the performance evaluation and
determination of the steps towards improvement.
Exergy is a thermodynamic concept which enables us to
articulate what is consumed by all working systems,
whether they are man-made systems such as thermo-
chemical engines and electricity-driven heat pumps or
biological systems such as microbes, plants, and animals
including the human body.
Exergy is the amount of work obtained when a piece of
matter is brought to a state of thermodynamic equilibrium
with the common components of its surroundings by means
of a reversible process.
Exergy analysis provides an effective technique for
designing, evaluating, and optimizing the performance of a
thermal system. Exergy analysis represents the third step in
the plant system analysis, following the mass and the
energy balances.
The aim of the exergy analysis is to identify the
magnitudes and the locations of exergy losses, in order to
improve the existing systems, processes or components, or
to develop new processes or systems.
Exergy losses include the exergy flowing to the
surroundings, whereas exergy destruction indicates the
loss of exergy within the system boundary due to
irreversibility.
Let us assume a building environmental control system
such as lighting, heating, or cooling systems. Energy and
matter are supplied into the system so that it works.
The inputs are exactly the same as the outputs under
steady-state conditions. This is due to the law of energy and
mass conservation.
If it is so, why do we not reuse the energy and matter as
output directly?
If we could have used the wasted energy and matter, most
of the so-called energy and environmental problems would
have been already solved.
The most general answer to the above question would be
that the energy and matter as input are different from those
as output – i.e. the energy and matter as output have
something that a system in question must discard.
To make the answer clearer, we use the concepts of exergy
and entropy, which can express the difference in energy
and matter between input and output explicitly.
Exergy and entropy, both of which are thermodynamic
concepts, “exergy” is the concept to articulate “what is
consumed” and “entropy” is “what is disposed of”. Stating
in the other way, “exergy” is the concept, which quantifies
the potential of energy and matter to disperse in the course
of their diffusion into their environment and “entropy” is the
concept which quantifies the state of dispersion, to what
extent the energy and matter in question are dispersed.
As shown in the building envelope system in Fig. 5.1 we
assume a steady-state condition that the right-hand side of
the system is warmer than the left-hand side - the particles
in the warmer side of the building envelope vibrate rather
strongly; i.e., the energy flowing into the building envelope
accompanies a certain amount of exergy.
The vibration disperses in the course of energy transfer;
that is, a part of the exergy is consumed as the exergy
flows. Thus, the energy flowing out the building envelope is
accompanied with a smaller amount of exergy.
As a result of the dispersion of vibration, the state of
dispersion as a whole within the system increases. This is
the generation of entropy, the law of entropy increase,
which is parallel to the law of energy and mass
conservation. The amount of increased entropy is
proportional to that of consumed exergy and the
proportional constant is the ambient temperature in the
Kelvin scale as will be described later.
Since the steady-state condition is being assumed, the
distribution of the temperature inside the building
envelope is unchanged. This implies that the amount of
entropy contained by the whole of the building envelope
system is constant.
The entropy of a substance, which is a function of
temperature and pressure, remains unchanged unless the
temperature and the pressure of the substance increases or
decreases.
As described above, a certain amount of entropy is
generated due to exergy consumption within the building
envelope system. This generated entropy must be
discarded into the surrounding (outdoors), from the
building envelope system, otherwise it contradicts the
assumption of the steady-state condition and the
characteristics of the entropy as a function of temperature
and pressure.
It is important to recognize that the energy flowing out the
building envelope is accompanied with not only a
decreased amount of exergy but also an increased amount
of entropy. Disposing of the generated entropy from the
system makes room for feeding on exergy and consuming
it again.
The process described above is called the exergy-entropy
process.
Table 5.1 shows the four fundamental steps of exergy-
entropy process. Any working systems (heating and
cooling systems inclusive) perform these four steps in
series and cyclically.
Energy is the concept to be conserved so that the energy
flowing in must be equal to the sum of the energy stored
within the system and the energy flowing out from the
system. This energy balance can be expressed as follows.
𝐸𝑖𝑛 = 𝐸𝑠𝑡 + 𝐸𝑜𝑢𝑡 5.1
Assuming steady-state condition here, there is no energy
storage and hence equ. 5.1 becomes:
𝐸𝑖𝑛 = 𝐸𝑜𝑢𝑡 5.2
Setting up the entropy equation from equs (5.1) and (5.2)
above. Entropy flows into the system as heat flows in and
some amount of entropy is generated inevitably within the
system in the course of heat transmission. The sum of the
entropy input and the entropy generated must be in part
stored or in part flows out of the system. Therefore, the
entropy balance equation can be expressed in the
following form.
𝑆𝑖𝑛 + 𝑆𝑔𝑒𝑛 = 𝑆𝑠𝑡 + 𝑆𝑜𝑢𝑡 5.3
Also assuming the steady-state condition, there is no
entropy storage as well as no energy storage. Therefore,
equ (5.3) becomes:
𝑆𝑖𝑛 + 𝑆𝑔𝑒𝑛 = 𝑆𝑜𝑢𝑡 5.4
The fact that the outgoing entropy from the system includes
the entropy generated within the system suggests that the
system disposes of the generated entropy with the entropy
output.
Combining the energy and entropy balance equations
brings about the exergy balance equation. Entropy (or
entropy rate) has a dimension of J/K (or W/K) and energy
(or energy rate) has a dimension of J (or W). Therefore, we
need a kind of trick to combine the two equations i.e. the
dispersed energy level of the resource surrounded by the
environmental space is the product of the entropy
contained by the resource and its environmental
temperature in the Kelvin scale. The same expression
applies to the waste discarded by the system.
Therefore, the entropy balance equation can be rewritten
as follows:
(𝑆𝑖𝑛 ) × 𝑇𝑒 + (𝑆𝑔𝑒𝑛 ) × 𝑇𝑒 = (𝑆𝑜𝑢𝑡 ) × 𝑇𝑒 5.5
Where 𝑇𝑒 = Environmental temperature.
The product of entropy and environmental temperature is
called “anergy”, which implies dispersed energy. Using the
term “anergy”, anergy balance equation (equ. 5.5) can be
expressed in the following form:
𝐴𝑖𝑛 + 𝐴𝑔𝑒𝑛 = 𝐴𝑜𝑢𝑡 5.6
Provided that “anergy” is a portion of energy that is already
dispersed, then the other portion is not yet dispersed
(exergy).
Energy therefore consists of two parts: the dispersed part
and the part, which can disperse.
Now let us take the difference of the energy balance
equation (5.2) and anergy balance equation (5.6). This
operation brings about;
[(𝐸𝑖𝑛 ) – (𝐴𝑖𝑛 )] - (𝐴𝑔𝑒𝑛 ) = [(𝐸𝑜𝑢𝑡 ) – (𝐴𝑜𝑢𝑡 )] 5.7
“Anergy generated” is such energy that originally had an
ability to disperse and that has just dispersed. We can state
this in the other way; that anergy generation is equivalent to
exergy consumption. Using the term “exergy”, equation
(5.7) is reduced to:
𝐵𝑖𝑛 - 𝐵𝑐𝑜𝑛 = 𝐵𝑜𝑢𝑡 5.8
This is the exergy balance equation for a system under
steady-state condition such as the building envelope
system shown in Fig. 5.1.
Exergy consumed, which is equivalent to anergy
generated, is the product of entropy generated and the
environmental temperature.
𝐵𝑐𝑜𝑛 = 𝑇𝑒 x 𝑆𝑔𝑒𝑛 5.9
Exergy consumed is exactly proportional to the entropy
generated with the proportional constant of environmental
temperature.
One of the main uses of the exergy concept in an exergy
balance is the analysis of thermal systems.
The exergy balance is a statement of the law of degradation
of energy. Degradation of energy is due to the
irreversibilities of all real processes.
Because open system analysis is much more relevant to the
analysis of thermal plants or chemical systems than closed
system analysis, the exergy balance of an open steady state
system, is shown in Fig. 5.5. The exergy balance is stated
around a control region delimited by specific boundaries.
𝐸ሶ 𝑖 + 𝐸ሶ 𝑄 = 𝐸ሶ 𝑜 + 𝑊ሶ 𝑠ℎ + 𝐼 ሶ 5.10
Where:
𝐸ሶ 𝑖 = σ𝑖 𝑀ሶ 𝑖 𝑒𝑖 5.11
𝐸ሶ 𝑜 = σ𝑜 𝑀ሶ 𝑜 𝑒𝑜 5.12
𝑇0
ሶ ሶ
𝐸 = σ𝑖 𝑄𝑟 1 −
𝑄
5.13
𝑇1
The expression for specific exergy is written as;
𝐶02
e = (h - ℎ0 ) - 𝑇0 (S - 𝑆0 ) + 𝑒𝑐ℎ + + g𝑍0 5.14
2
The exergy flow to the control region is always greater than
that from the control region. The difference between the
two, the rate of loss of exergy, is called the irreversibility
rate. The irreversibility rate is calculated from the Gouy-
Stodola relation, which states that the irreversibility rate of
a process is the product of the entropy generation rate for
all systems participating in the process and the
temperature of the environment
ሶ
𝑄𝑟
ሶ
ሶ𝐼 = 𝑇0 𝑆𝑔𝑒𝑛 ሶ ሶ
= 𝑇0 σ0 𝑀0 𝑆0 − σ𝑖 𝑀𝑖 𝑆𝑖 − σ𝑟 5.15
𝑇𝑟
The various exergy terms, which go into the exergy
balance, are presented in Appendix C.