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HEAT EXCHANGERS (MD-029)
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REV 1: Heat Exchangers (MD-029) Page 2 of 93
REVISI0N HISTORY Revision Number Date Comments
Rev: 0 19-08-2004
Rev. 1 03-11-2004
Comments Received from ODA and Trainers
Signed off by Douglas Milne 06-11-04
ISSUE 1
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TOPICS COVERED INCLUDE
Serpentine
Fin Fan Coolers
Co- Current and Counter Current Flow
Shell and tube heat exchangers ( Fixed head, floating head, hairpin
tube)
Hairpin as a condenser
Plate exchangers
Finned tube
Maintenance of heat exchangers
Heat Exchange media
Specific Heat capacity
Thermal Stability
Lagging properties
Hazards associated with heat exchangers
Parameters for measurement during operation
Heater Treaters and fired heaters
Refrigeration and Chilling Units
Reboilers
Video Cassette: Heat Exchangers (Tech 027)
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CONTENTS
HEAT EXCHANGERS (MD-029)
1. INTRODUCTION
2. MAJOR PARTS OF A HEAT EXCHANGER
2.1. MAJOR PARTS OF A TUBE & SHELL HEAT EXCHANGERS
2.1.1. SHELL
2.1.2. TUBES
2.1.3. TUBE SHEETS
2.1.4. CHANNEL
2.1.5. BAFFLES
2.2. FLOATING HEAD HEAT EXCHANGER
3. DESCRIBE THE FUNCTION & OPERATION OF HEAT EXCHANGERS
3.1. FUNCTION OF SHELL & TUBE HEAT EXCHANGERS
3.1.1. REBOILERS
3.1.2. CONDENSERS
3.1.3. HEATERS
3.1.4. COOLERS
3.2. PLATE TYPE HEAT EXCHANGERS
3.3. PARALLEL PLATE HEAT EXCHANGER
3.3.1. HEAT TRANSFER FACTORS IN PLATE HEAT EXCHANGERS
3.3.2. ADVANTAGES OF PLATE HEAT EXCHANGERS
3.3.3. DISADVANTAGES OF PLATE HEAT EXCHANGERS
3.4. USES OF PLATE HEAT EXCHANGERS
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3.5. OPERATION OF HEAT EXCHANGERS
4. GLOSSARY
5. AIR COOLERS
5.1. INTRODUCTION
6. FIN-FAN COOLER
6.1. MAJOR PARTS OF A FIN-FAN COOLER
6.1.1. HOUSING
6.1.2. FINNED TUBES
6.1.3. FAN ASSEMBLY
6.2. OPERATION OF A FIN-FAN COOLER
7. GLOSSARY
8. FIRED HEATERS
8.1. INTRODUCTION
9. FIRED HEATERS & THEIR MAJOR PARTS , FUNCTION & OPERATION
9.1. MAJOR PARTS OF A HORIZONTAL COIL FIRED HEATER
9.1.1. HOUSING
9.1.2. FIREBOX
9.1.3. TUBES
9.1.4. CONVECTION TUBES
9.1.5. SHOCK TUBES
9.1.6. RADIENT TUBES
9.1.7. BURNERS
9.1.8. FUEL GAS BURNER
9.1.9. FUEL OIL BURNER
9.1.10. STACK
9.2. MAJOR PARTS OF A VERTICAL COIL FIRED HEATER
9.2.1. HOUSING
9.2.2. BURNERS
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9.2.3. TUBES
9.2.4. RADIATING CONE
9.2.5. BAFFLE SLEEVE
9.2.6. STACK
9.3. FIRED HEATER OPERATION
9.4. PRODUCT FLOW
9.5. COMBUSTION CONTROL
9.6. DRAFT
9.7. COKING
10. OPERATION OF A STEAM BOILER
10.1. DEAERATING
10.2. CHEMICAL DOSING
10.3. WATER TUBE BOILER OPERATION
11. GLOSSARY
12. REFRIGERATION
12.1. INTRODUCTION
12.2. USES OF REFRIGERATION
12.2.1. BASIC PRINCIPLES USED IN REFRIGERATION
12.2.2. ADIABATIC CHANGE
12.2.3. ISOTHERMAL CHANGE
12.2.4. THE JOULE-THOMSON EFFECT
12.3. SUMMARY
13. VAPOUR COMPRESSION
13.1. INTRODUCTION
13.2. THE VAPOUR COMPRESSION REFRIGERATION CYCLE
13.2.1. COMPRESSION
13.2.2. CONDENSATION
13.2.3. EXPANSION
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13.2.4. EVAPORATION
13.2.5. RE-CIRCULATION
13.3. SUMMARY
14. REFRIGERANTS
14.1. INTRODUCTION
14.2. PRIMARY REFRIGERANTS
14.2.1. LOW BOILING POINT
14.2.2. LOW FREEZING POINT
14.2.3. HIGH LATENT HEAT
14.2.4. HIGH CRITICAL TEMPERATURE
14.2.5. LOW CRITICAL PRESSURE
14.2.6. NON – CORROSIVE
14.2.7. NON - TOXIC, NON – FLAMMABLE
14.2.8. NON - REACTIVE WITH AND EASILY SEPARATED FROM OIL
14.3. COMMON PRIMARY REFRIGERANTS
14.3.1. AMMONIA
14.3.2. CHLORO-METHANE (METHYL CHLORIDE)
14.3.3. SULPHUR DIOXIDE
14.3.4. PROPANE
14.3.5. HALOCARBON REFRIGERANTS (OFTEN CALLED CFCS)
14.4. SECONDARY REFRIGERANTS
14.4.1. VERY LOW FREEZING POINT
14.4.2. LOW VISCOSITY
14.4.3. CHEAPNESS
14.5. COMMON SECONDARY REFRIGERANTS
14.5.1. BY THE ADDITION OF A SOLUTE TO WATER
14.5.2. BY THE ADDITION OF A LIQUID TO WATER
14.6. SUMMARY
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15. SAFE & EFFICIENT OPERATION
15.1. INTRODUCTION
15.2. REFRIGERATOR PERFORMANCE
15.2.1. REFRIGERATION CAPACITY
15.2.2. REFRIGERATION EFFECT
15.2.3. COEFFICIENT OF PERFORMANCE (C.O.P.)
15.3. HAZARDS ASSOCIATED WITH REFRIGERATION SYSTEMS
15.3.1. THE NATURE OF THE REFRIGERANT MATERIALS
15.3.2. LOW TEMPERATURES
15.3.3. MECHANICAL NOISE
15.4. SUMMARY
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HEAT EXCHANGERS (MD-029)
1. INTRODUCTION
Many hydrocarbon processes require changers in fluid temperatures. This
means we must transfer heat to or from the fluids. In the last two modules,
you have learned about equipment used to directly heat and cool fluids.
Boilers and fired heaters burn fuel to provide the energy needed to heat
fluids. Fin-fan coolers and cooling towers use air to remove heat from fluids
in a process.
We can also use one fluid to heat or cool another fluid, if there is a large
difference in their temperatures. Steam can be used to heat process fluids.
Air or seawater can be used to cool hot process fluids.
A heat exchanger is the device used to transfer heat between fluids. Heat
exchangers are common in hydrocarbon process plants. In part 1 of this
module, we will discuss the parts of the shell and tube heat exchanger. In
part 2, we will discuss the fraction and operation of heat exchangers used in
process operations.
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2. MAJOR PARTS OF A HEAT EXCHANGER
Heat exchangers use a shell and tube arrangement to transfer heat between
fluids. One fluid is passed through the shell, or housing, or the exchanger. A
second fluid is passed through a tube bundle inside the shell. The two fluids
do not mix because they are physically separated. Heat is transferred from
one fluid to the other by conduction through the tube walls.
Figure 1 – Floating Head Heat Exchanger
This figure shows the major parts of a heat exchanger. Refer to this diagram
for the discussion that follows.
2.1. MAJOR PARTS OF A TUBE & SHELL HEAT EXCHANGERS
There are many designs of shell and tube heat exchangers. We will discuss
the most common type called the floating head heat exchanger. Figure 1
shows the parts of a typical floating head heat exchanger.
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2.1.1. SHELL
The shell is the metal housing of the exchanger. In the shell, fluid flows
around the tubes.
Heat is conducted from shell to tube, or from tube to shell, depending upon
the temperature of the fluids flowing through them. The flow of heat is always
from the hotter fluid to the colder fluid.
The inlet and outlet pipes for the shell body are called shellside nozzles. Inlet
and outer pipes for the tubs are called tubside nozzles.
2.1.2. TUBES
The series of small tubes in a heat exchanger is called a tube bundle. The
tubes are positioned inside the shell of the exchanger. There are normally
several, closely packed tubes of a fairly small diameter.
Many small tubes provide a larger surface area then a single large tube. For
example fifteen 1” tubes occupy the same space as one 6 “ tube. However,
fifteen 1” tubes provide 2 ½ times the surface area of the single 6” tube. More
heat can be transferred through the larger surface area of the many small
tubes in a tube bundle.
2.1.3. TUBE SHEETS
Tubes are held together and supported at each end by a plate called a tube
sheet. The tubes and the tube sheets from a solid unit that fastened inside
the shell. Figure 2 shows a tube bundle with a tube sheet on each end.
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Figure 2 – Tube Sheets
Fluid enters and exits the tube bundle through the tube sheets.
2.1.4. CHANNEL
The channel is an inlet and /or outlet chamber for the tubes. The channel is
covered at one end, and connected to a tube sheet at the other end. The
tubeside inlet nozzles direct fluid into the channel. From the channel, fluid is
forced into the tube bundle, through the tube sheet. As fluid exits the tube
sheet, it flows into the outlet channel and through the tubeside outlet nozzle.
2.1.5. BAFFLES
Baffles are metal plates used to change the direction or fluid flow.
Figure 3 – Baffles
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Baffles direct the flow of shellside fluid around the tubes in the tube bundle,
increasing contact between the fluid and the tube surfaces.
Segmental Baffles
Baffles are used to slow down and direct the flow of shellside fluid around the
tubes. The baffles ensure longer contact time between the shellside fluid and
the tubes, allowing more heat exchange.
Figure 4 – Impingement Baffle
The impingement baffle is used at the shellside inlet nozzle to protect the tube
bundle from the force of the fluid entering the shell.
Impingement Baffle
A special baffle, called an impingement baffle, is normally used at the
shellside inlet of the exchanger. An impingement baffle is shown in figure 4.
At high inlet flow, the pressurised fluid entering the shell will erode the tubes.
To reduce erosion, an impingement baffle is used between the inlet nozzle
and the tubes. The impingement baffle absorbs most of the force of the
incoming fluid without restricting flow.
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Channel Baffle
Another special baffle is sometimes used in the channel of the exchanger.
This baffle divides the channel into two separate chambers, separating the
tubeside inlet section from the outlet section. Channel baffles are used in
double-pass heat exchangers.
Figure 5 – Heat Exchanger Flow-Through
In a double-pass arrangement, a channel baffle separates the tubeside inlet
fluid from the outlet fluid.
Figure 5 (a) shows a single-pass flow arrangement. Fluid enters one end of
the tube bundle and leaves at the other end. This is the simplest pattern.
Figure 5 (b) shows a double-pass flow arrangement. By placing a baffle in
the exchanger channel, tubeside fluid enters only half of the tubes. The fluid
must go to the end of the tube bundle, then return through the other half of
the tubes. This arrangement exposes the tubeside fluid to the shellside fluid
two times.
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2.2. FLOATING HEAD HEAT EXCHANGER
Figure 6 shows a cutaway drawing of the floating head heat exchanger.
In the floating head heat exchanger, the tube sheet on one end of the tube
bundle is not attached to the shell. It is free to move, or float, back and forth
inside the shell. This allows the tube bundle to expand and contact when
subjected to hot fluids. With one end of the tube bundle free to float, the
tubes will not bend from thermal expansion.
Figure 6 – Floating head Heat Exchanger
The floating heat exchanger is a double pass exchanger. One end of the
tube bundle is free to move, to allow for thermal expansion.
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3. DESCRIBE THE FUNCTION & OPERATION OF HEAT EXCHANGERS
A heat exchanger is a device used to transfer heat from a hot fluid to a cold
fluid.
Three factors determine the amount of heat transfer in an exchanger:
The initial temperature difference between the two fluids –
The greater the difference in temperature in temperatures, the
more heat exchanged.
The length of contact time between the two fluids – The
greater the time of contact, the greater the change in outlet
temperatures.
The exposed surface area in the exchanger – The greater the
surface are of contact between the fluids, the more heat
exchanged.
3.1. FUNCTION OF SHELL & TUBE HEAT EXCHANGERS
Shell and tube heat exchangers have many uses in hydrocarbon processing.
The name of a heat exchanger is usually a guide to its use.
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3.1.1. REBOILERS
A shell and tube boiler is a heat exchanger used to reheat liquids. Figure 7
shows a typical reboiler.
Figure 7 – Reboiler
Superheated steam flows through the tube side of the exchanger, heating the
liquid flowing through the shell.
The purpose of the boiler is to reheat liquid bottoms product from a distillation
column. Super-heated steam is admitted to the tube side of the exchanger.
The liquid bottoms product from the column flows through the shell side.
Liquid that is vaporized in the reboiler goes out at the top of the shell. The
remaining liquid flows over vertical plate, called a weir, and out of the bottom
of the reboiler shell.
The reboiler in figure 7 is called a kettle reboiler because of the large area
inside the shell above the tube bundle. The large area provides space for
vapours to collect.
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3.1.2. CONDENSERS
A shell and tube condenser is a heat exchanger in which hot vapours are
cooled and condensed.
Figure 8 – Condenser
Condensers cool gases to change them into liquids. Cool ware flowing
through the tube side of the exchanger cools hot gas in the shell, causing the
gas to condense.
Shell and tube condensers are sometimes used with oil or NGL fractionation
columns, to cool overhead gases. The overhead gas enters the shell of the
condenser tube bundle. The cold water flowing through the tubes absorbs
the heat in the gas. This allows most of the gas to condense and leave the
shell liquid.
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3.1.3. HEATERS
A shell and tube heater is a heat exchanger used to increase the temperature
of a cold feedstock.
Figure 9 – Heater
Heaters are used to heat cold feedstock. Hot fluid from a process flows
through the shell side of the exchanger, warming the cooler feedstock flowing
through the tubes.
The heater in figure 9 accomplishes two functions. Cold feedstock is heated
and hot product is cooled. This is an example of using one hydrocarbon
product to change the temperature of another hydrocarbon product. Hot
bottoms product from a fractionation column can be used to heat feedstock
going into the column. In exchange, the cold feedstock cools the bottoms
product.
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3.1.4. COOLERS
A shell and tube cooler is a heat exchanger used to cool a product.
Figure 10 – Cooler
Coolers are used only to cool a product. Cold water flows through the tube
side of the exchanger, cooling hot liquids flowing through the shell.
The cooler in figure 10 is similar to the heater in figure 9. In the heater, both
products benefit from a heat exchange. In the cooler, the only purpose is to
cool the product. Water is commonly used as the cooling agent in coolers.
Once the cooling agent has served its purpose, it is often recirculated through
a cooling tower for reuse in the cooler.
3.2. PLATE TYPE HEAT EXCHANGERS
A number of special types of heat exchanger have been developed to give
improved heat transfer under conditions where shell and tube types are
unsatisfactory. One of these is the plate heat exchanger.
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3.3. PARALLEL PLATE HEAT EXCHANGER
The plate heat exchanger consists of a pack of separate parallel plates. The
middle sections of these plates are corrugated and each plate has two holes
or flow orifices. Figure 11 illustrates the types of plate used.
Seal Spacer Seal
Corrugations
Figure 11 - Plate Heat Exchanger
Alternate plates have the flow orifices as shown in the figure.
The plates are standard and an exchanger may be made up of two hundred
or more of these standard units. Each plate is fitted with two seals (or
gaskets) and a spacer. The fittings are also standard.
One of the seals is shaped so that it fits around the centre corrugated section
and one of the orifices. The other is circular and surrounds the remaining
orifice.
Figure 12 illustrates how these seals (or gaskets) are positioned on the
plates.
Seals are made of rubber or a similar material and usually fit into grooves on
the surface of each plate.
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The plates are arranged alternately as illustrated in Figure 12 and positioned
between end covers. The whole assembly is held together by clamping bolts
so that the seals between each plate are compressed and leak proof.
Figure 12
The plates are arranged so that there are two separate paths through the
exchanger between alternate plates. The size of these paths (i.e. the space
between each of the plates) is established by the thickness of the seals. It is
usually less than 6 mm.
Figure 13 shows how the two fluids flow through these two separate paths
within the exchanger.
Figure 13 - Plate Arrangement
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Note that only four plates are shown - an actual plate exchanger may have
200 or more. Also the end covers, through which the fluids are introduced into
the unit, are not shown.
The cold fluid: bypasses plate D and flows down the space between plates
D and C. It then bypasses plate B and flows up the space between plates B
and A. The whole process continues with other plates to the left of plate A,
which are not shown.
The hot fluid: bypasses plate A and flows down the space between plates B
and C. It then bypasses plate C and flows up through the space between
plates D and E (not shown). The whole process continues with other plates to
the right of plate D.
Note how the position of the plates, holes and seals produces the two
separate paths through which the two fluids flow.
Heat transfer from one fluid to the other is by conduction through the
corrugated walls of each plate. These plates can be made very much thinner
than the tubes of a shell and tube heat exchanger. Accordingly, heat transfer
rates are much higher.
3.3.1. HEAT TRANSFER FACTORS IN PLATE HEAT EXCHANGERS
The factors that contribute to the high heat transfer rates in plate heat
exchangers are as follows:
the thin walls separating the two fluids allow for rapid heat
transfer by conduction
the corrugations on the plates give increased surface area
over which heat transfer can take place
narrow pathways, corrugations and constant changes of
direction produce a high degree of turbulence (even at low
flow rates) which improves heat transfer by convection within
each fluid.
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The high heat transfer rates enable this type of heat exchanger to be used
effectively in situations where the temperature difference between the two
fluids is small.
3.3.2. ADVANTAGES OF PLATE HEAT EXCHANGERS
These are:
high heat exchange rates are possible
the plates are independent units which can be removed,
added to or rearranged for different duties
any plate can be replaced rapidly without removing the others
both sides of each plate are fully accessible for inspection and
cleaning.
Plate heat exchangers tend to have lower capital costs than shell and tube
types because the heat transfer surface can be made from sheet metal, which
is less expensive than tube manufacture. This is of particular benefit if
expensive materials of construction such as stainless steel are necessary.
3.3.3. DISADVANTAGES OF PLATE HEAT EXCHANGERS
These are:
the seals are a weak point - failure will result in a leak of one
or other of the fluids
the working temperatures and pressures are limited by quality
and durability of the seals (safe operating conditions are
normally below 250°C and 20 bar).
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3.4. USES OF PLATE HEAT EXCHANGERS
Since they can be readily taken apart for cleaning and inspection, plate heat
exchangers are used in the food and beverage industries. Their use in the
chemical industry depends on the relative cost for the particular application
compared with a conventional shell and tube heat exchanger.
Note that the plate heat exchanger described is only one of the many designs
available. However, all are based on the principles discussed in this lesson.
3.5. OPERATION OF HEAT EXCHANGERS
We will use a typical plant process to show how heat exchangers maintain
desired temperature levels of process fluids. Figure 14 is a simplified
diagram of a process that removes light natural gases from raw light naphtha.
Figure 14 – Processing Light Naphtha
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Seven different heat exchangers are used to regulate the temperatures of
fluids at different points in the process.
The heat exchangers in the diagram are identified by the numbers 1 to 7 and
by their names. Four different types of heat exchangers are used in this
process. Notice that each type of heat exchanger has a different symbol.
Figure 15 shows the four symbols.
Figure 15 – Heat Exchanger Symbols
The circle is each symbol represents the shell of the exchanger. The jagged
line through the symbol representing the tube bundle.
We will start at the reboiler for the deethanizer and see how each heat
exchanger affects the process.
Circles and identify the reboilers. Both reboilers perform the same
function. They reheat the bottom products from the columns. The purpose of
reheating is to vaporize any natural gases trapped in the liquid naphtha.
In the columns, ethane, propane, butane, pentane, and some of the light
naphtha vapours rise to the top of the columns. The hot gases leave the
columns and go into condensers and . The gases are cooled in the
condensers and changed back into liquids. The liquid, along with any gas
that will not condense, is collected in reflux drums. The liquid in the reflux
drums is fed back into the columns to cool the top of the columns. The
uncondensed gas flows out of the flux drum to the fuel gas system.
The bottoms product leaves the columns and goes into heaters and .
The heat from the bottoms product is used to warm the feedstock into the
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columns. The bottoms product from the deethanizer becomes the feedstock
for the debutaniser column.
The bottoms product from the debutaniser column, which gave up some of its
heat in a heater , goes into a cooler . Colder water is used in the cooler
to further reduce the temperature of the light naphtha, before it goes for
further processing.
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4. GLOSSARY
Bottoms Product: The liquid product, which leaves the bottom of
a column or vessel, after separation of lighter
gases.
Condensation: The changing of a vapour to a liquid by cooling.
Conduction: The transfer of heat energy between objects by
direct contact.
Erode: To wear away.
Overhead Production: The vapour separated from a liquid product,
which leaves the top of a column or vessel.
Thermal Expansion: The expansion or increase in size of solids and
liquids when they are heated.
Baffle: A baffle that changers the direction of the flow
of a liquid, as in a heat exchanger.
Impingement: The collision of a liquid or gas with a baffle at
high velocity.
Shell: The internal compartment of a heat exchanger
formed by the exchanger housing.
Tube Bundle: A set of parallel tubes fixed to one or two tube
sheets.
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5. AIR COOLERS
5.1. INTRODUCTION
Temperature Control Is Very Important In Gas And Oil Processing. As you
learned in the last module, fired heaters and boilers provide a source of heat
for raising temperatures of process fluids. In this module you will learn about
two equipment items which are used to lower the temperature of process
fluids.
Fin-fan coolers are covered in part 1 of the module. Fin-fans are used in
almost all process operations to cool process fluids, lubricating oil, and
refrigerants.
Part 2 of the module covers cooling towers. Cooling towers are commonly
used to cool hot water for reuse in heat exchangers.
You will learn how both of these devices use ambient air to cool hot fluids,
using the principles of evaporation and heat exchange. When you are
assigned to a plant you will be responsible for operation of this equipment and
for keeping it in good working order.
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6. FIN-FAN COOLER
Fin fan coolers are used in gas and oil processing plants to cool hot liquids.
They are also used to cool and condense pressurized gases.
Figure 16 – Fin-Fan Coolers
Fin-Fan coolers are used to cool hot process fluids. Some processes require
several fin-fan coolers to lower the temperature of fluids to the desired level.
The fin-fan cooler consists of two main assemblies, the finned tubes and the
fan assembly.
The cooling of a hot gas or liquid takes place inside the finned tubes. Figure
17 shows a section of a finned tube.
Figure 17 – Finned Tube
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Fins expand the surface area of the tube, improving heat transfer.
Fins are thin metal pieces attached to a tube. They expose more surface to
the air for cooling.
Liquid heats the walls of the finned tubes. Air blows across the tube fins and
carries some of the heat away. This cools the liquid in the tubes. You can
see in figure 18 that finned tubes have more surface area exposed to the air.
The fins allow more heat transfer.
Figure 18 – Air Cooling
Finned tubes provide a large surface area, allowing greater heat transfer.
6.1. MAJOR PARTS OF A FIN-FAN COOLER
In a fin-fan cooler the fan assembly blows air over the finned tube assembly,
cooling the fluid in the tubes. Figure 19 shows how these assemblies are
connected together in a typical fin-fan cooler. The following section describes
the major parts of the cooler. Refer to figure 19 to help identify each part as
you read its description.
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Figure 19 – Fin-Fan Cooler
6.1.1. HOUSING
The housing is made of heavy sheet metal. It forms an enclosure over the
finned tubes. The enclosure ensures that all the air rises through the fan. Air
is drawn in from below the cooler and is blown out of the top of the housing.
Most fin-fan coolers are located high above the ground, so that hot air close
to the ground is not drawn into the cooler.
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6.1.2. FINNED TUBES
Hot liquid gas enters the fin-fan cooler through a large diameter pipe called an
inlet header. Many finned tubes connect to the header. Each finned tube
receives some of the hot liquid or gas. The finned tubes carry the hot fluid
across the cooler. The cooled fluid is collected in an outlet header on the
opposite side of the cooler. Air blowing across the finned tubes cools the
fluid.
6.1.3. FAN ASSEMBLY
The fan assembly is a type of rotating equipment a motor and gear box turns
the fan shaft to rotate the blades. Figure 20 shows the main parts of the fan
assembly and their location in the cooler.
Figure 20 – Fin-fan Cooler
This is an example of an induced draft fan, since the assembly draws air up
through the cooler. Refer to this figure as you read the description of each
major component.
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Fan
The fan circulates air through the cooler. The moving air picks up the heat
from the finned tubes. Fan are designed to produce either forces or induced
draft. A forced draft fan pushes air through a cooler. An induced draft
fan pulls air through a cooler.
Most fin-fan coolers use induced draft. The fin-fan cooler in figure 21 uses an
induced draft fan
The fan blades may have either a fixed or variable pitch angle. Pitch angle
refers to the angle that the blade is turned above or below the horizontal
plane. At an increased pitch angle, the blades will draw more air through the
cooler. At a lower pitch angle, the blades will draw a smaller volume of air.
The pitch angle of the blades can be changed manually or automatically. The
pitch angle is changed to maintain a desired temperature of fluid at the outlet
header.
Figure 21 – Fin-Fan Cooler Fan Blade Pitch
Pitch is the angle above or below the horizontal plane. Increased pitch will
draw more air through the fan, increasing the cooling effect.
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Fan Ring
The fan ring is a metal ring that fits around the top of the cooler housing. The
fan blades rotate inside the ring. The fan ring prevents air from leaking past
the fan. The ends of the fan blades are positioned very close to the fan ring.
Fan Mount
The fan mount is attached to the frame of the fin-fan unit, as shown in figure
21 the shaft of the fan goes through the fan mount. The fan mount serves
two purposes:
To support the weight of the fan
To house bearing that allow the shaft to rotate freely and
prevent it from moving from side to side
Seal Disc
The seal disc is a round piece of metal shaped like a plate. It is attached to
the fan, above the centre, or hub, of the fan. It prevents air leaking past the
hub of the fan blades.
Vibration Switch
A vibration switch is used to stop the fan motor automatically if the fan begins
to vibrate through gearing failure etc. The tips of the fan blades are very
close to the fan ring. If the fan begins to vibrate, the tips of the blades will hit
the fan ring. This will damage both the fan ring and the fan blades. The
vibration switch is usually mounted under the mount, as shown in figure 21.
Fan Motor
An AC electric motor is used to drive the fan. A start/stop switch is located
near the motor. Another start/stop switch may be located in the plant control
room.
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Gearbox
The gearbox is used to reduce the speed of the fan so that it rotates more
slowly than the motor. The gears also change the direction of drive from
horizontal to vertical. The gearbox is filled with oil, to provide lubrication for
the rotating gear assemblies.
6.2. OPERATION OF A FIN-FAN COOLER
Fin-fan coolers maintain the desired process operating temperature during
the daily ambient temperature changes.
Variable pitch fan blades adjust to process conditions by changing the angle
of the blades. The pitch angle increases or decreases the amount of air
passing over the finned tubes.
Fixed pitch blades must be started and stopped to change the airflow over the
tubes. The more air, which passes over the tubes, the greater the cooling
effect on the process fluid.
Operators normally start and stop fin-fans locally (not by remote control). By
starting the equipment in the field, the operator can check the coolers visually
(by eye) and audibly (by ear) to make sure they are operating correctly.
Because of the fin-fan design, sand and dust can collect between the fins on
the tubes. The sand acts as an insulator, reducing the heat transfer from the
process to the surrounding air. To remove this sand build up, fin-fan coolers
must be washed down regularly. They are washed when they isolated.
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7. GLOSSARY
Ambient: Of the surrounding atmosphere. Ambient
temperature is the temperature of the
surroundings.
Evaporation: The change of a liquid into vapor at
temperatures below the liquids boiling point.
Humidity: Water vapor in the air. In the summer, the
humidity in Ras Tanura is very high.
Drift: Tiny droplets of water that are blown away by
the air.
Header: A large diameter pipe to which a number of a
smaller pipes are joined.
Heat Exchanger: A device used to transfer heat from one fluid to
another, normally through a shell and tube
arrangement.
Hub: The centre of the fan, where the blades are
connected to the shaft.
Louver: A fin, or bar, on the side of a cooling tower
which opens and closed to adjust air flow.
Makeup Water: Fresh water added to replace water lost by
evaporation and drift.
Pitch: The angle of a fan blade above or below the
horizontal plane.
Sump: A reservoir serving as a drain or receptacle for
liquids. Also called a water basin.
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8. FIRED HEATERS
8.1. INTRODUCTION
Heat is required for crude oil refining and processing. Most process operation
plants need a source of heat to process hydrocarbons or run utilities. In this
module, you will learn about fired heaters and boilers, the two main heat
sources used in oil gas processing. As a plant operator, you will be
responsible for operating this equipment.
In part 1 of this module, we will discuss the fired heaters used in process
operations. Fired heaters are found in most refinery units. They are
commonly called fired heaters, fire pipe stills, or simply heaters. Fired
heaters are used to heat liquid hydrocarbon feedstock as the first step in
fractional distillation.
In part 2 of the module, we will discuss steam boilers. A steam boiler is a
fired heater. It produces steam by raising the temperature of water above its
boiling point. Steam is used to drive steam turbine engines and as a source
of heat in some hydrocarbon process.
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9. FIRED HEATERS & THEIR MAJOR PARTS , FUNCTION & OPERATION
Process operations uses two types of fired heaters to heat hydrocarbons.
The two types are vertical coil fired heaters and horizontal coil fired heaters.
The main difference between the fired heaters is the positions of the heating
coils. The major parts of each type of fired heater are basically the same.
Figure 22 – Fired heaters
The fired heater consists of a combustion chamber surrounded by a coil of
tubes. In a vertical coil fired heater the tubes run vertically up and down the
fired heater. Tubes are positioned horizontally in a horizontal coil.
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9.1. MAJOR PARTS OF A HORIZONTAL COIL FIRED HEATER
9.1.1. HOUSING
The fired heater housing is a large rectangular steel box. The housing
contains the heating coils and the burners. The housing is sometimes called
the setting.
9.1.2. FIREBOX
The firebox is the area inside the housing where the fuel is burned. The
inside walls and floor of the firebox are lined with a special heat-resistance
material called the refectory lining. This lining is usually made of special heat-
resistance bricks. The purpose of the refractory lining is to reflect heat from
the burners back to the radiant tubes.
Figure 23 – Horizontal Coil Fired Heater Parts
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The drawing shows the need of the fired heater cut away. The individual
tubes are connected to form one continuous coil through the fired heater.
9.1.3. TUBES
The tubes in a fired heater are connected together to form a continuous coil.
The tube coil carries the fluid to be heated through the fired heater. There are
three types of tubes in the coil. Each type of tube is heated in a different way.
9.1.4. CONVECTION TUBES
Convection tubes are located in the upper section of the fired heater. These
tubes absorb heat from the flue gas flowing upward from the burners. The
flue gas passes between the convection tubes on its way to the stack.
9.1.5. SHOCK TUBES
Shock tubes are located between the radiant section and the convection
section. They are called shock tubes because they receive the most heat.
They absorb both radiant heat and convection heat.
9.1.6. RADIENT TUBES
Radiant tubes are located along the walls of the firebox in the lower section of
the fired heater. Fluid flowing through the radiant tubes absorbs heat radiated
directly from the burners and heat reflected from the refractory lining.
9.1.7. BURNERS
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The burners mix the fuel with oxygen in the air. This ensures smooth and
continuous burning. The burners may burn fuel oil. The fuel and air mixture
is ignited just in front of the burner.
9.1.8. FUEL GAS BURNER
A fuel gas burner is designed to mix the gas evenly with the air. Figure 24 is
a cross section drawing of a fuel gas burner. The figure shows how the air is
mixed with fuel gas to produce the best combustion. As fuel gas flows to the
burner, it sucks air in through the primary port. Additional air enters through
the secondary port, mixing with the fuel gas near the flame.
Figure 24 – Fuel Gas Burner
Air enters the burner through the primary port and secondary port and mixes
with the fuel gas.
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9.1.9. FUEL OIL BURNER
One type of fuel oil burner uses steam to heat and atomise the fuel oil (break
it into a fine mist) to make it burn more completely. Figure 25 shows this
operation. Air is mixed with the fuel mist around the tip of the burner.
Figure 25 – Fuel Oil burner
Steam is used to heat and atomise the fuel oil, improving combustion.
9.1.10. STACK
The stack is a vertical duct that rises from the top of the fired heater. It allows
exhaust from the firebox to escape safely, high into the atmosphere.
The stack damper is located in the stack. The damper is very similar to the
butterfly valve you studied in an earlier module. The damper is used to
control the draft (air flow) in the fired heater.
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Figure 26 – Stack Damper
The damper in the exhaust stack adjusts the flow of air, or draft, through the
fired heater.
9.2. MAJOR PARTS OF A VERTICAL COIL FIRED HEATER
9.2.1. HOUSING
The housing is a vertical cylinder. It is lines with a refractory material that
reflects heat back onto the radiant tubes. The vertical coil fired heater
occupies less ground space than the horizontal coil fired heater with the same
capacity.
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Figure 27 – Vertical Coil Fired heater
A vertical coil fired heater occupies less ground space than a horizontal coil
fired heater with the same capacity.
9.2.2. BURNERS
The fired heater may be fired by fuel gas or fuel oil, using the same types of
burners found in the horizontal coil fired heater.
9.2.3. TUBES
Radiant tubes are arranged around the walls of the fired heater. They receive
radiant heat directly from the burners. Additional heat is reflected from the
burners. Additional heat is reflected from the refractory lining. The tubes
extend up into the convection section, where flue gases are concentrated on
their way to the stack.
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9.2.4. RADIATING CONE
A radiating cone is located near the top of the fired heater. The radiating
cone prevents the heat of the burners from passing straight up into the fired
heater stack. The radiating cone reflects the heat outward toward the walls of
the fired heater, where the tubes are located. The cone functions to
concentrate the heat in the fired heater housing.
9.2.5. BAFFLE SLEEVE
A baffle sleeve is connected to the radiating cone. It creates a narrow
passage through the convection section. The baffle sleeve forces all of the
flue gas to pass close to the tubes in the convection section. In this way, the
tubes are able to absorb most of the heat passes through the convection
section.
9.2.6. STACK
The stack is a vertical duct that carries flue gases high into the atmosphere.
The stack also creates a natural draft in the fired heater.
9.3. FIRED HEATER OPERATION
Before beginning this section, you will see a slide tape program on fired
heaters. The program will show some examples of refinery fired heaters, and
explain how they work.
Figure 28 illustrates a typical horizontal coil fired heater. We will use this
example to explain the principle of operation of fired heaters. Vertical coil
fired heaters operate in a similar way.
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Figure 28 – Crude Oil Heater Fired Heater
Crude oil flows back and forth through the tube coil, from the convection
tubes, through the shock tubes and radiant tubes.
9.4. PRODUCT FLOW
The fired heater in figure 28 heats crude oil before it enters a distillation
column.
The crude oil enters near the top of the fired heater. It first passes through
the convection tubes, which absorb heat from the flue gases rising through
the fired heater. The heated oil then passes through the shock tubes, where
more heat is absorbed by convection and radiation. Finally, the hot oil passes
through the radiant tubes. The hot oil leaves the fired heater near the bottom
of the firebox.
9.5. COMBUSTION CONTROL
To maintain fired heater temperatures, an instrument loop automatically
controls the fuel gas flow. This loop increases or decreases fuel flow as
necessary to meet the temperature requirements set for the fired heater.
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Changes in load (the amount of crude oil to be heated) will also affect the
temperature. The instrument loop will adjust the fuel flow to maintain the set
temperature whenever the load changes.
Enough oxygen must be present to allow all the fuel coming from the burner
to burn. This called complete combustion. Air is the source of oxygen for the
fired heater. To produce complete combustion, a balance between air and
fuel must be maintained at all times. Complete combustion occurs when the
flue gas contains 3% oxygen.
The flow of fuel to the fired heater is automatically controlled. The airflow in
most process operations fired heaters, however, is controlled by dampers.
The dampers are locally adjusted by the operators to ensure the correct
balance of air and gas.
The correct damper adjustment is important to ensure proper combustion.
Too much air causes the heat to be carried through the fired heater too
quickly. This heat is lost up the stack, wasting valuable fuel gas.
Too little air will prevent the fuel from burning fully, causing smoke to form in
the fired heater. This smoke prevents good radiant heat transfer and also
puts a black deposit, called soot, on the convection and shock tubes. Soot
acts as insulation and reduces heat transfer.
9.6. DRAFT
Draft refers to the flow of gases through a fired heater. As the gases in the
fired heater are heated, they rise rapidly through the stack. The rising gases
create a partial vacuum in the fired heater in the fired heater, sucking outside
air into the firebox. In the process of combustion, this air is changed to
heated flue gas. This heated gas will rise rapidly into the stack, causing more
cool air to enter the firebox. The action becomes continuous, and constant
flow through the fired heater and up the stack is established.
Natural daft is produced by stacks alone. In a natural draft system, the rising
flue gas creates a low enough pressure to draw in the fresh air needed for
combustion.
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In large systems, however, it is often necessary to use fans above the
convection section of a fired heater to provide enough draft. These fans are
called induced-draft fans.
Figure 29 – Fired heater Draft Systems
Different systems are used in fired heaters to provide the draft needed for
complete combustion. The type of system used depends on the design and
capacity of the fired heater.
Fans can also be mounted around the burners to push air into the combustion
chamber. These fans are called forced draft fans.
A common system on large fired heaters and boilers is the combustion of
forced draft and induced draft fans. This is called a balanced draft system.
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9.7. COKING
Coking is the carbon layer found inside the fired heater tubes when the flame
touches the exterior of the tubes. A flame touching the outside of the tube is
called flame impingement. Flame impingement will overheat the tube. The
high temperature breaks down the hydrocarbons flowing through the tube,
creating solid coke. A coke layer inside the fired heater tubes reduces the
conduction of heat to the oil. It can also create an obstruction in the tubes,
which will reduce flow.
Flame impingement can prevented by proper control of the flame in the
firebox.
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10. OPERATION OF A STEAM BOILER
We will discuss the operation of a water tube steam boiler. The operating
principles o the two types of boilers are generally the same.
10.1. DEAERATING
Dissolved oxygen and carbon dioxide in boiler feedwater can cause pitting
and scaling in the boiler and boiler tubes. A deaerator is used to drive these
dissolved gases out of the boiler feedwater. The steam removes most of the
oxygen and carbon dioxide from the feedwater.
10.2. CHEMICAL DOSING
Chemicals are added to boiler feedwater and to the boiler system to reduce
damage due to unwanted impurities.
Sulfite is a chemical that is injected into the feedwater to remove traces of
oxygen. Oxygen causes corrosion.
Acidity also causes corrosion. Caustic is a chemical that is injected into
feedwater to reduce acidity. Boiler water has a tendency to become acidic.
Caustic balances the PH of the water by neutralizing the acid. PH is an index
of the acidity or alkalinity of water.
Phosphate is a chemical that is injected into the mud drum to keep impurities
suspended in the water. This helps prevent the formation of scale.
10.3. WATER TUBE BOILER OPERATION
Feedwater that has been deaerated and chemically dosed enters the
economiser.
Hot gases rising from the combustion chamber heat the water in the
economizer by convection.
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Warm feedwater enters the steam drum. Here the feedwater picks up more
heat from the water already in the steam drum.
Feedwater flows through the combustion chamber in a tube called
downcomer. The feedwater picks up more heat by radiation.
Hot feedwater flows into the mud drum. The water temperature is very close
to the boiling point. It is almost steam. Impurities in the water cannot turn
into steam, so they remain behind in the mud drum.
Hot water flows out of the mud drum in a tube called a riser. The water in the
riser is immediately exposed to the radiant heat of the burner. The water
turns to steam.
Steam flows upward through the riser into the steam drum.
The steam in the steam drum flows through a tube into the superheater. The
superheater is a small diameter tube coil, which is located above the burner
flame.
In the superheater, the steam temperature is increased to 700F, vaporizing
all water droplets in the steam. Steam pressure increases to 625 psig. At the
temperature and pressure, it is impossible for water to exist in its liquid form.
The super heated dry steam leaves the boiler for use in the plant.
Figure 30 – Operation of a Water Tube Boiler
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This figure 30 shows the operation of a typical water tube boiler. Refer to the
graphic as you read the description of boiler operation.
The temperature controls for a boiler are similar to those for fired heaters.
The correct balance between fuel and air must always be maintained. An
incorrect balance of fuel and air in boilers causes the same problems as in
fired heaters. It is the operator’s responsibility to check the conditions in the
combustion chamber to ensure a correct balance between fuel gas and air.
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11. GLOSSARY
Condensate: Liquid obtained from vapour. For example,
water obtained from steam
Corrosion: Usually, the eating of a metal by an acid
Intermittent: Periodic. Something that happens from time to
time
Saturated: Full of moisture. Thoroughly wet.
Caustic: An alkaline chemical agent used to neutralize
acidic boiler feedwater.
Chemical Dosing: Injecting chemicals into feedwater flow to
remove impurities
Blowdown: To drain liquid under pressure to reduce the
level of impurities in feedwater
Deaerator: A device in the system generation system that
removes oxygen and other undesired gases
from the feedwater
Draft: A slight pressure difference that produced the
flow of air through the fired heater
Firebox: The open area around fired heater burners
Flue: A channel for conveying hot gas or smoke to
the atmosphere.
Natural Draft: The flow of colder air from outside the fired
heater through the combustion chamber to the
hotter air in the stack. This flow pulls the air
through the combustion chamber and up
through the stack, with out the use of fans.
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12. REFRIGERATION
12.1. INTRODUCTION
Refrigeration is the process of lowering the temperature of a substance to
below that of its surroundings. The chemical industry is a major user of
refrigeration facilities. Often, refrigeration is carried out at a central point and
the low temperature produced is then transferred to different areas of the
plant via coolants within a ring main. It is often classified as one of the
services available to the plant.
This first lesson looks at some of the more common uses and also
investigates the basic principles used to produce the low temperatures
required.
12.2. USES OF REFRIGERATION
Refrigeration is the process of lowering the temperature of a substance to
below that of the ambient surroundings. Refrigeration of materials is carried
out for the following reasons, which are in effect, its main uses:
a) To reduce the rate of reaction
b) To store flammable material
c) To condense and store the vapour of low boiling point liquids
d) Air conditioning
e) Freeze drying
These main uses are now considered in more detail.
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To Reduce the Rate of Reaction
Some chemical reactions take place so rapidly that they can only be kept
under control if the reactants are cooled to a low temperature before and
during the reaction process. This is because the reaction rate is slowed by
reducing the temperature.
An example is the decomposition of food. In this case, the rate of
decomposition (reaction with air caused by bacteria) is usually slow.
However, the rate can be slowed even further, by reducing the temperature.
For example, consider meat. If it is left in the kitchen at 20°C, it will probably
go bad in a day or two. If kept in a domestic refrigerator, which lowers the
temperature to about 5°C, meat will probably be useable for about a week. If
placed in a deep freeze at -25°C, it will be useable for at least six months.
There are many similar examples to be found in the chemical industry e.g.
storage of drugs. Refrigeration can also be used for materials whose reaction
rate is very much faster. For example, if strong acid is to be added to strong
alkali, the heat produced by the fast reaction may cause boiling and splashing
of the liquids, thus giving rise to a safety hazard. If, however, both are cooled
to a low temperature and kept cool during the reaction, the reaction is slower
and less likely to create a hazard.
To Store Flammable Materials
Some liquids are flammable. A measure of their flammability (ease of
catching fire) is known as the flash point. This is the lowest temperature at
which the material gives off a vapour that will ignite when exposed to a flame.
There is a second higher temperature known as the auto-ignition
temperature. This is the lowest temperature at which the material will
spontaneously ignite without any external source of ignition.
Liquids that have flash points below the normal ambient temperature are
likely to explode if a spark is present. This may mean they need to be cooled
to a temperature below ambient to store them safely below their flash point.
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To Condense and Store the Vapour of Low Boiling Point Liquids
Normal butane has a boiling point of -0·5°C and is a gas at normal
atmospheric temperatures. As a gas, it occupies a volume over 1,000 times
more than that of the same mass of liquid butane. Storage space for butane
will be smaller if it is converted to a liquid by lowering its temperature to below
-0·5°C using refrigeration.
An illustration of this (in reverse) is that in cold countries, on cold winter days,
butane cylinders cannot be used if left outside because the low temperatures
prevent the liquid butane from turning into gas. In winter, propane cylinders
should be used as the liquid propane boils at -42°C under atmospheric
conditions and will boil even on very cold winter days!
Another way of condensing the butane is to increase the pressure, which in
turn increases its boiling point. A pressure of 5 bar (500 kPa) gives butane a
boiling point of 42°C. This method is utilised to produce the liquid butane used
to fill the storage cylinders. However, some gases at normal atmospheric
temperatures will not condense, no matter what pressure is applied to them.
They will condense, however, if cooled to a specific temperature. This
temperature is known as the critical temperature for the gas concerned.
Critical temperature is defined as: the temperature above which a gas will not
liquefy, irrespective of the pressure applied. Even at the critical temperature,
large amounts of pressure may be needed to liquefy the gas.
Associated with the critical temperature is critical pressure, which is defined
as: the pressure required to change a gas to a liquid at the critical
temperature.
Some typical critical temperatures and pressures are given in the table below.
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Gas Critical Pressure
(mPa)
Critical Temperature
(oC)
Nitrogen 3.4 - 147
Oxygen 5.0 - 118
Methance 4.6 - 83
Ethane 4.9 32
Propane 4.25 96
Table 1
In order to condense the first three gases in the above table, they must be
cooled to very low temperatures as well as being pressurised (5 mPa is
approximately 700 p.s.i.). This process of cooling below critical temperature
and compressing to condense gases is known as liquefaction and the
process is used to produce liquid air. This, in turn, is used to obtain liquid
oxygen and liquid nitrogen. The process is also used to produce Liquified
Natural Gas (LNG).
Air Conditioning
In very hot weather we feel uncomfortable because of the heat and the
amount of water in the atmosphere (humidity). To prevent this in a working
environment where uncomfortable conditions may increase the risk of
accidents and reduce the efficiency of the workers, air conditioning is used.
Basically, this consists of a refrigeration system that cools the air and
removes some of the water vapour by condensation. This reduces the
temperature and lowers the humidity of the air, making conditions more
comfortable.
Freeze Drying
The normal method used to dry materials is to heat them to evaporate the
moisture. This cannot be used if the material is sensitive to heat, as the
process of drying may harm it. To overcome this difficulty, freeze drying is
used.
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The material to be dried is pre-frozen to around -25°C and is then placed
inside a chamber. The temperature is slowly increased and the ice sublimes
(turns directly from a solid to a gas) causing drying of the material
12.2.1. BASIC PRINCIPLES USED IN REFRIGERATION
When petrol or other volatile (low boiling point) material is accidentally
splashed over the hands, there is a cooling effect as the material evaporates.
This is because the change of state occurring (from liquid to gas) requires
heat (latent heat) which the liquid takes from its surroundings (in this case the
hands). Water has the same effect, which is less noticeable because the rate
of evaporation is slower.
12.2.2. ADIABATIC CHANGE
If a volatile liquid is placed in a highly insulated vessel so that heat can
neither enter nor leave the system, evaporation of the liquid causes cooling of
the liquid itself. The sensible heat removed from the liquid is now latent heat
in the gas. This change of state is an example of an adiabatic change - known
as adiabatic evaporation.
An adiabatic change is a process that occurs without heat entering or leaving
a system. In general, an adiabatic change involves a fall or rise in
temperature of the system.
12.2.3. ISOTHERMAL CHANGE
A true adiabatic change is very difficult to achieve in practice. When heat is
added to the evaporating liquid to keep the temperature constant, the process
is called isothermal.
An isothermal change is a change that occurs at constant temperature by the
change taking heat in from, or giving heat out to, the surroundings.
Once again, a true isothermal change is difficult to achieve in practice.
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Boiling pure water at exactly 100°C at atmospheric pressure by adding heat is
an example of an isothermal process. Adiabatic and isothermal processes are
shown in diagrammatic form in Figure 31.
Figure 31
In theory, low temperatures can be achieved by using the adiabatic
evaporation principle. As the liquid cools however, the rate of evaporation will
slow and less cooling will take place. Eventually a low temperature limit is
reached where no evaporation occurs.
The lower the boiling point of the material, the lower is the temperature
produced by its evaporation. Remember, petrol (which starts to boil at 40°C)
has a greater cooling effect on the hands than water (boiling point 100°C).
This is because, in general, the lower the boiling point, the more evaporation
will occur at a given temperature.
A lowering of the pressure above the liquid will cause higher rates of
evaporation at a given temperature due to the lower resistance present above
the liquid.
The evaporation of a volatile liquid is one of the principles used in
refrigeration. The sensible heat removed from the liquid is converted to latent
heat in the gas.
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Adiabatic and Isothermal Compression
If a gas is compressed within a highly insulated vessel so that heat cannot
enter or leave the vessel, the temperature of the gas rises. This is called
adiabatic compression.
If the heat of compression is removed to produce a pressurised gas at the
same temperature as the original un-pressurised gas, this is called isothermal
compression.
Adiabatic and Isothermal Expansion
If the pressure on the gas is now reduced without any addition of heat from
the surroundings, the temperature will fall. This is called adiabatic expansion.
This is because the energy required to expand the gas must come from within
the gas itself since energy can neither be created nor destroyed. Therefore
the temperature of the gas is reduced as energy is provided for expansion.
If heat is supplied from outside the system in order to keep the temperature
constant, this is called isothermal expansion.
12.2.4. THE JOULE-THOMSON EFFECT
Consider what may happen if a gas, which has a low condensing point at
atmospheric pressure, is compressed to a higher pressure but kept at the
same temperature, i.e. is subjected to isothermal compression.
Pressure affects the boiling point of a liquid; the higher the pressure, then the
higher is the boiling point. This is, in effect, the same as saying that an
increase in pressure on a gas will raise the temperature at which the gas will
condense and form a liquid. So, if a gas is subjected to isothermal
compression, it may condense and form a pressurised liquid.
However, this will be the case only if the constant temperature chosen is
below the critical temperature of the gas. The cooling system must remove
the latent heat present in the gas as well as any heat of compression to
condense the gas. Thus large amounts of heat are removed from the system
to keep the temperature constant.
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If the pressure on the liquid is now reduced, the liquid will boil. For this to
happen, latent heat has to be supplied. If the process is carried out so that
heat cannot be taken from the surroundings (adiabatic change), then the
latent heat can only be supplied by the liquid itself losing sensible heat.
The liquid left will therefore cool down until a temperature is reached at which
the liquid is below its boiling point for the new pressure. This cooling caused
by the adiabatic expansion of a gas or liquid is called the Joule-Thomson
effect. This process of compressing a gas, cooling to its original temperature
to form a liquid and then allowing the pressure on the liquid to drop causing
the liquid to vaporise and cool forms the basis of the main type of refrigeration
system used by industry – the Vapour Compression System. This is the
subject of the next lesson.
12.3. SUMMARY
Refrigeration is a service supplied to many chemical plants. The principle
uses of refrigeration are:
to reduce the rate of reaction
to store flammable liquids
to dry-heat sensitive materials
to condense and store vapour from low boiling point liquids for
air conditioning
A gas can only be turned into a liquid by the application of pressure if it is at a
temperature below its critical temperature. The process of cooling a gas to
below its critical temperature and compressing to form a liquid is called
liquefaction.
An adiabatic change is one where heat is neither added to, nor removed from
the surroundings by the change. An isothermal change is one where heat is
added or removed by the surroundings to keep the temperature constant.
The Joule-Thomson effect is the cooling caused by the adiabatic expansion of
a gas or liquid. This principle is used in creating the low temperatures used in
refrigeration.
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13. VAPOUR COMPRESSION
13.1. INTRODUCTION
Although the size of refrigeration plant may vary for different applications, the
basic principle of operation remains unaltered. The principle used in most
refrigeration systems is the Joule-Thomson effect. This lesson considers how
this principle is used industrially in the vapour compression refrigeration cycle
to achieve low temperatures and cooling.
13.2. THE VAPOUR COMPRESSION REFRIGERATION CYCLE
The purpose of a refrigeration system is to maintain a material at a
temperature below that of the surroundings. If this is achieved, then heat will
flow from the warmer surroundings to the colder material. If the material has
to be kept at the low temperature, then the heat flowing from the surroundings
must be continually removed.
As energy cannot be destroyed, this heat will build up somewhere in the
system. It must be removed - but to where? The readily available place is
back to the surroundings, but this appears to be impossible. How can the
same material take heat from the surroundings i.e. it must be colder and then
give heat back to the same surroundings, unless it is hotter. This, however,
does occur!
The principles used in the vapour compression refrigeration system are:
a) As a gas is compressed, its temperature rises. If the gas is cooled to
remove the heat of compression, then the gas may now be at its
condensation point (an increase in pressure causes the condensing or
boiling point to rise). If the latent heat is now removed, the gas will
condense and form a liquid.
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b) If a liquid is expanded adiabatically, it will boil. This causes the liquid to
cool as it loses some of its sensible heat, which is used to provide the
latent heat energy required for the change to gas.
The vapour compression refrigeration system combines these principles to
produce a situation where heat can be both added and removed from the
same temperature surroundings.
The vapour compression system requires:
a compression stage to compress the gas
a cooler (condenser) to remove the heat of compression and
latent heat (condensing the gas)
an expansion device to reduce the pressure causing boiling of
the liquid
a heat exchanger where the cold liquid produced is used to
cool down a second material (the material to be cooled).
The gas formed in the expansion system is then recycled to the compression
stage where the process is repeated. The gas/liquid that is recycled in this
system is known as the primary refrigerant.
The vapour compression refrigeration system is illustrated in Figure 32. Refer
to this diagram as each stage is now studied in more detail.
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Figure 32
The vapour compression refrigeration cycle can be broken down into the
following five stages, which are studied in turn. The number of each stage is
included on Figure 32.
1. Compression
2. Condensation
3. Expansion
4. Evaporation
5. Re-circulation
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13.2.1. COMPRESSION
A compressor is used to pressurise the primary refrigerant gas to a pressure
such that, on cooling the gas back down to atmospheric temperatures
(compressing a gas raises its temperature), it will condense and form a liquid.
The pressure required will depend on how much the condensing point of the
gas is affected by pressure (an increase in pressure raises the condensing
point of a gas). The compressor used generally operates on one of two main
principles:
a) Reciprocating Motion
This consists of a piston inside a cylinder that is moved backwards
and forwards by a driver, sucking gas in on the backstroke and
forcing it out on the forward stroke.
The driver may be outside the main compressor housing (the open
type, reciprocating compressor) or the motor and compressor are
connected by a common shaft and totally enclosed in the same
housing (the hermetic type, reciprocating compressor). The latter type
eliminates leaks but is more difficult to service.
Both types will require lubrication of the piston to reduce friction and to
help seal the piston within the cylinder. This can lead to oil
contamination of the refrigerant, which is undesirable as it reduces the
efficiency of the refrigerant. If oil contamination is likely to occur, then
an oil separation stage is included. This consists of a device that uses
centrifugal force to throw the heavier oil particles to the outside of a
vessel from where they can be removed. Another method is by the
impingement of oil droplets onto baffles so that the droplets form into
large drops, which sink to the bottom of the vessel from where they
are removed.
If a totally oil-free system is required (e.g. if the oil reacts with the
refrigerant chosen) then a diaphragm pump is often used. This type
may also be used if the refrigerant chosen is extremely corrosive.
Usually, reciprocating compressors are used on very low temperature
duties because of their ability to produce high pressures on the
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delivery side and high vacuum on the suction side. However, they are
less likely to be used on very large installations as they cannot handle
large amounts of material unless they themselves are extremely large.
This would make them very expensive due to the high cost of the
precision engineering required.
b) Centrifugal Action
These are multistage centrifugal fans where the high speed created by
the impeller is converted into pressure energy. These have the
advantages of low cost (no precision engineering), they can handle
large quantities of gas and do not require lubrication of parts in contact
with the refrigerant. However, they have a tendency to leak refrigerant
unless the shaft seal is well maintained. Also, they cannot produce the
large suction pressures possible with a reciprocating compressor.
Rotary compressors are rarely used in refrigeration systems. This is
due to the need for lubrication between the moving parts (e.g. the
gears) in contact with the refrigerant and other operating conditions
beyond the scope of this course.
13.2.2. CONDENSATION
The hot compressed gas from the compressor needs to be cooled to remove
the heat of compression. Also, the latent heat needs to be removed at the
condensing point to enable the gas to turn into liquid at the higher pressure.
In small-scale refrigeration systems such as domestic refrigerators, the
condenser consists of a pipe designed to give the maximum heat transfer
surface exposed to the air surrounding it. Using air as the coolant is cheap as
the air costs nothing and does not need to be supplied from an external
source. The condenser on the back of domestic refrigerators can be easily
identified. The major problems with this system are that:
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1. Air is a poor conductor of heat, has a low specific heat capacity and as
it is a gas, has a relatively low density. It cannot therefore, remove
very much heat per kilogram (1 kg of air is about 700 litres in volume).
2. The air in contact with the condenser will heat up and cease to cause
cooling. Movement of the hot air away from the pipe relies on natural
convection currents. These cause the hot air to rise pulling cold air in
behind it. The convection currents can be hindered by placing the
refrigerator underneath a work surface without proper venting at the
top (to allow the hot air out) and the bottom and sides (to allow the
cold air in).
In this situation, the efficiency of the condenser is reduced and the gas
passing back to the compressor becomes hotter and hotter.
Then, the compressor has to develop higher pressures than normal, which
can lead to premature failure of the refrigerator. The modern built-in kitchen
has reduced the 'life' of refrigerators from an average of over 20 years in 1969
to 14�5 years in 1988.
On larger industrial systems, where natural convection currents are not very
effective, a fan may be used to force air over the condenser surfaces. The
design of the condenser can now become more compact, i.e. the pipes and
the fins are tightly packed (like a car radiator) as the pressure developed by
the fan can push the air through smaller spaces.
On very large systems, air-cooling is replaced by water-cooling. Water is a
better conductor and has a higher specific heat capacity than air and will
cause larger amounts of cooling. This means that for a specific duty, the
water-cooled exchanger is much smaller and less expensive. Also, the
provision of water to a process becomes progressively cheaper the more that
is supplied.
One water-cooled condenser design consists of water cascading over the
outside of the pipes containing the hot gas (a cheap system of low efficiency).
Another uses a counter-current shell and tube heat exchanger where the hot
gas is passed into the shell and water passes through the tubes (a more
expensive and effective system). See Heat Exchange, Module 3 for revision
of this type of vessel.
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The cooled liquid at high pressure leaving the condenser then passes to a
storage vessel (the receiver) ready for the next stage.
13.2.3. EXPANSION
The cold pressurised liquid then passes through an expansion (or 'let-down')
valve. The expansion valve is a pressure reducer that automatically controls
the low pressure at a set value. In addition, it can be thermostatically
controlled so that it only allows liquid to pass through if the temperature in the
refrigerator system is above that required.
The expansion valve allows the liquid to pass from the high-pressure region
to a low pressure region. The reduction in pressure causes the liquid
refrigerant to boil. The latent heat required by the liquid to turn into a gas is
provided by the liquid itself, which therefore cools until a temperature is
reached where it stops boiling (the boiling point of the liquid at the controlled
low pressure). The cooled liquid then passes to an evaporator whilst the gas
formed passes to the suction of the compressor.
13.2.4. EVAPORATION
The evaporator takes the cooled liquid from the expansion valve and adds
heat to cause further boiling of the primary refrigerant. The design of this
varies according to the size and duty of the refrigeration system. In the
domestic refrigerator, the evaporator is the metal icebox at the top, which
absorbs heat from the rest of the contents of the fridge, thereby cooling them.
In a deep freeze, the evaporator forms one or more internal sides of the
freezer.
Note that the icebox and some sides of fridges and freezers are hollow and
contain the primary refrigerant. This is why sharp tools should not be used to
remove ice built-up.
In industry the evaporator may be simply a pipe or coil containing a fluid to be
cooled inside a vessel containing the primary refrigerant or may be a more
complex shell and tube design of heat exchanger.
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The heat required by the evaporator is provided either by the surroundings or
by a process fluid known as the secondary refrigerant which, in turn, cools
down.
The heat taken in by the evaporator causes the primary refrigerant liquid to
boil by providing the latent heat required. The temperature remains at the low
value since the liquid is at its boiling point and cannot be heated above this
without the pressure increasing (the pressure is controlled by the expansion
valve!) or until all the liquid has boiled away. Thus the evaporator gives a
controlled low temperature. The net effect is that sensible heat is taken from
the surroundings or secondary refrigerant and is given to the primary
refrigerant as latent heat.
13.2.5. RE-CIRCULATION
The cold gas produced in the evaporator mixes with that from the expansion
valve and passes to the inlet of the compressor where the whole process is
repeated. Thus the primary refrigerant is recycled. Since the main duty of the
refrigeration system is to create cooling in the expansion/evaporator section,
the cold gas is kept as cold as possible as it passes to the compressor.
As it is at a temperature below that of its surroundings, the pipe-work is
usually lagged to prevent loss of the cold by the addition of heat from a part of
the surroundings that does not require cooling. It is also usual to lag all parts
of the expansion/evaporator section that are exposed to higher temperature
material that does not require cooling. For example, a domestic fridge has
lagging in the sides, top and bottom to keep the whole of the fridge from
gaining heat from the kitchen, but the icebox is not lagged allowing the 'cold'
to spread from the box through to all internal parts of the fridge.
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Figure 32
Note
The icebox in a domestic fridge is cold enough to freeze water but the main
part of the fridge will not. This is because the icebox is the coldest part due to
the evaporation taking place there, whilst this 'cold' has to spread through the
rest of the fridge. Compare this to a fire, which is the hottest part of a heating
system. The greater the distance from the fire, the lower the air temperature
becomes).
With the domestic refrigerator, the circulating LP vapour (5) is compressed (1)
and then condensed in an air-cooled finned condenser (2). The liquid formed
passes to a receiver from where it is forced through the piping to an
expansion valve (3) where the pressure is reduced. This causes evaporation
of the liquid in the icebox (4), creating low temperatures (-6°C).
This low temperature spreads throughout the rest of the fridge but due to
leaks of heat into the system, the temperature in the rest of the fridge is
above that of the icebox. The temperature within the fridge is controlled by an
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adjustable thermostat, which switches the compressor on (if temperature
above set point) and off (if temperature below set point).
In the industrial refrigerator, the hot compressed gas is cooled and
condensed in a water condenser. The liquid then passes via a reservoir to the
expansion valve, which reduces the pressure. The evaporating liquid creates
cooling of a brine solution (the secondary refrigerant) surrounding the
evaporator.
This cooled brine solution is then pumped through a system of pipes within
the vessel to be cooled. This helps to spread the cold from a single point (the
evaporator) throughout the whole of the vessel to be cooled. (This can be
compared to a fire in one room trying to heat up a whole house compared to a
central heating boiler in one room with pipes and radiators in other rooms.) In
this case the low temperature in the vessel is controlled by both the
temperature in the evaporator and the rate of circulation of the brine.
13.3. SUMMARY
The vapour compression refrigeration system consists of five stages:
a primary refrigerant gas is compressed by a compressor
(usually of the reciprocating or centrifugal type). Any oil
contamination of the primary refrigerant must be removed at
this stage
cooling the pressurised gas to ambient temperature and
condensing: it into a liquid in a heat exchanger (either a
finned air cooled type or a water cooled, shell and tube heat
exchanger)
reducing the pressure on the liquid by passing it through an
expansion valve (a pressure reducing valve which may be
thermostatically controlled) causing cooling of the liquid
evaporating the liquid to form a gas in an evaporator by
adding heat from the atmosphere or from a secondary
refrigerant
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re-cycling the gas back to the compressor using a system of
lagged pipework
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14. REFRIGERANTS
14.1. INTRODUCTION
In the vapour compression refrigeration cycle, the refrigerant is the fluid
medium that transfers heat from one part of the circuit to another. The choice
of refrigerant is based on the required duty. In this lesson, refrigerants are
classified, the 'desirable properties' of refrigerants are described and the
characteristics of several common refrigerants are listed.
14.2. PRIMARY REFRIGERANTS
In the vapour compression cycle a gas is compressed, cooled and condensed
to a liquid. This is then expanded to reduce the pressure (causing the liquid to
boil and cool) producing a gas, which is recycled back to the compressor. The
gas/liquid circulating in the vapour compression refrigeration cycle is known
as the primary refrigerant.
The desirable properties of primary refrigerants are:
a) low boiling point
b) low freezing point
c) high latent heat
d) high critical temperature
e) low critical pressure
f) non - corrosive
g) non - toxic, non - flammable
h) non - reactive with and easily separated from oil.
The primary refrigerant should also be cheap.
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14.2.1. LOW BOILING POINT
The primary refrigerant has to be a gas at normal atmospheric temperature
and pressure. If not, the system will have to operate (on the recycle side) at a
pressure below atmospheric to evaporate the liquid and form a gas. This
could lead to air leaking into the system. Any moisture within the air will
freeze at the expansion valve, causing blockage of the evaporator. To prevent
this, in most refrigeration systems, the primary refrigerant usually has a
boiling point within the range -100°C to + 10°C (typically -30°C to - 40°C).
14.2.2. LOW FREEZING POINT
The freezing point of the material must be well below that of its boiling point
so that any cooling that occurs as the liquid is evaporated does not cause the
remaining liquid to freeze.
A frozen refrigerant will block the piping system, reduce the efficiency of the
compression system and will eventually damage the compressor.
14.2.3. HIGH LATENT HEAT
Latent heat is the heat required to change the state of a material. The liquid
refrigerant should require a large amount of heat to cause it to change its
state from liquid to gas i.e. a high specific latent heat of vaporisation.
If it possesses a high latent heat, it will remove a lot of sensible heat from
itself or the surroundings, giving large amounts of cooling per kilogram of
liquid evaporated. This will mean that the amount of refrigerant circulating in
the compression cycle can be kept small, thus keeping costs down.
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14.2.4. HIGH CRITICAL TEMPERATURE
Critical temperature is the temperature above which a gas will not form a
liquid on compression. In the vapour compression system, a gas is
compressed to form a liquid. Its critical temperature must therefore be above
normal operating temperatures within the system.
14.2.5. LOW CRITICAL PRESSURE
Critical pressure is the pressure required to turn a gas into a liquid at its
critical temperature. This should be low so that the pressures required to
convert the gas to a liquid in the vapour compression system are low. The
compressor used will then only require a small amount of energy to produce
the low compression pressure, saving on running costs. Also, because of
lower pressures, the strength of the construction needed to contain the
refrigerant can be lower.
14.2.6. NON – CORROSIVE
If the chosen refrigerant is corrosive, the materials of construction would need
to be capable of withstanding the corrosion. Corrosion resistant materials
(e.g. stainless steel) are usually of higher cost than 'normal' materials such as
mild steel. Also, if corrosion did occur, refrigerant that could be hazardous to
personnel and other equipment might leak.
14.2.7. NON - TOXIC, NON – FLAMMABLE
The vapour compression system operates under pressure throughout most of
the system, therefore any leaks will lead to refrigerant gas escaping into the
surroundings. If the gas is toxic or flammable, then a loss of containment
could be very hazardous.
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14.2.8. NON - REACTIVE WITH AND EASILY SEPARATED FROM OIL
The compressor used in the vapour compression system may need
lubricating and the oil used may come into contact with the refrigerant. If it
does, it should not react as this will affect the properties of the refrigerant and
lead to lower efficiency. The oil should also be easily removed from the
refrigerant for the same reasons.
So far, no single substance has been found which ideally fits all these
properties and it is therefore necessary to compromise in order to select the
best refrigerant for each particular duty required. It may be that after
considering the above points, several refrigerants will be suitable.
The last point to consider is the price of the alternatives. Far too often, cost is
put at the top of a list of priorities!
14.3. COMMON PRIMARY REFRIGERANTS
14.3.1. AMMONIA
Ammonia is a colourless, toxic gas with a characteristically pungent smell.
It is a good refrigerant in many ways, with fairly low boiling and freezing points
and it is cheap. It also gives a large amount of refrigeration for a given
compressor size, which keeps costs down. It is non - flammable, but
explosions have occurred when the gas has come into contact with welding
torches.
Against these advantages, however, must be set the fact that it is highly toxic
and irritant, and absorbs water readily. When it has absorbed water it is
severely corrosive to copper alloys.
It is generally used in large-scale industrial refrigeration plants, such as cold
storage plants and breweries. Leak testing for ammonia gas is by means of
hydrochloric acid, which forms a dense white smoke of ammonium chloride in
the presence of ammonia.
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14.3.2. CHLORO-METHANE (METHYL CHLORIDE)
Chloromethane is a colourless gas with a faintly sweetish odour. It has a
relatively low operating pressure, high latent heat capacity and boils at -24°C.
If chloromethane absorbs water, it becomes very corrosive to aluminium,
magnesium and zinc alloys. Better refrigerants are now available and chloro-
methane is little used. Leak testing is done with a special alcohol burning
torch whose flame exhibits a colour change when chloro-methane is present.
14.3.3. SULPHUR DIOXIDE
Sulphur dioxide is a colorless gas with a pungent smell and is highly toxic. It
is non-explosive and non-flammable, but when mixed with water, forms
sulphurous acid which is highly corrosive to metals. It has good latent heat
capacity and is capable of achieving low refrigeration temperatures.
The toxicity and corrosive properties of sulphur dioxide have led to its
replacement by more modern refrigerants. Leak tracing can be done using an
ammonia swab, which will give white fumes in the presence of sulphur
dioxide.
14.3.4. PROPANE
Propane is a highly flammable gas whose boiling point is - 42°C. It is a good
refrigerant in many ways, its main disadvantage being its high flammability.
So, it should not be used if there is the possibility of escaped refrigerant
coming into contact with a naked flame.
14.3.5. HALOCARBON REFRIGERANTS (OFTEN CALLED CFCS)
The defects of the refrigerants generally available led to much research in the
late 1930s aimed at producing a more satisfactory material. Many substances
were investigated and in the 1940s a range of refrigerants were developed
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based mainly on two hydrocarbon chemicals, ethane and methane. These are
the principal refrigerants in use today, usually under trade names such as
'Arcton' and 'Freon'.
Typical refrigerants in this group are dichlorodifluoromethane and
trichlorotrifluoroethane.
The name 'halocarbon' is derived from the fact that these refrigerants are
chemical combinations of halogens (the group of elements containing chlorine
and fluorine) with hydrocarbons.
All these refrigerants are non-flammable, have low toxicity and are non -
irritant at normal temperatures. They have good latent heat capacities and a
wide range of physical and thermodynamic properties which enable them to
be 'tailored' to meet the requirements of most refrigerator systems.
Leak detection is usually carried out using an electronic leak detector.
Although the halocarbon refrigerants are not health hazards at normal
temperatures, at high temperatures, such as those encountered in welding or
in a fire on the plant, they can break down chemically, forming very irritating
and toxic compounds.
Modern research has shown that halocarbons (or CFCs) affect the ozone
layer, which protects the earth from the harmful ultraviolet radiation emitted by
the sun and contribute to global warming. ‘Environmentally friendly’
substances are gradually replacing halocarbons, which are used in air
conditioning as well as refrigeration systems. Typically, these hydrocarbon-
based substances have an atmospheric lifetime of less than 1 year
(compared to the atmospheric life-time of 130 years for CFCs).
In industrial applications, refrigerants are not known by their actual chemical
name but are given a numerical designation. Some of these numerical
designations together with the corresponding chemical name are given in the
table in the Appendix (for information purposes only).
In the vapour compression system the evaporation of the primary refrigerant
creates cooling. In the domestic refrigerator this occurs in the icebox which
then cools down the rest of the fridge. However, the rest of the fridge is never
as cold as the icebox.
Heat is transferred by conduction, convection and radiation. In a cool fridge,
radiation will not occur. The fridge has mainly air inside, which is a poor
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conductor of heat, so conduction will be low. This will mean that the air will
cool down very slowly. For convection there must be a temperature difference
to cause hot air to rise and colder air to fall. Thus the 'cold' will not easily
transfer from the icebox to the rest of the fridge.
In industrial systems, the 'fridge' is much larger so the cold needs to be
forcibly spread throughout the space if it is to be made cold. To do this, a
second refrigerant is used to take the cold from the evaporator and spread it
through the fridge. This refrigerant is known as the secondary refrigerant.
14.4. SECONDARY REFRIGERANTS
These are materials that are circulated through the evaporator, cooled and
then passed to other parts of the plant to spread the cold. In the process of
cooling the other parts, the secondary refrigerants are heated. The heated
material is then recycled back to the evaporator to be re-cooled. This process
was illustrated in the previous lesson which showed an industrial cold storage
system.
Note: primary and secondary refrigerants never come into direct contact with
each other; they are always separated by a heat exchange surface.
Secondary refrigerants, like primary refrigerants, should possess certain
properties:
a) very low freezing point
b) low viscosity, i.e. easily pumped
c) cheapness
d) non-toxic
e) non-flammable
f) non-corrosive.
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14.4.1. VERY LOW FREEZING POINT
The secondary refrigerant passes through the evaporator, which is the
coldest part of the vapour compression system. It must not freeze as it would
block the piping system and not spread the cold. Boiling point is not so
important except that it should be above normal working temperatures to
maintain the refrigerant as a liquid. In other words, it should not easily boil or
evaporate at working temperatures.
14.4.2. LOW VISCOSITY
The refrigerant should have a low viscosity so that it is easily pumped through
the piping system. As temperature decreases, viscosity increases. This
means that the liquid will become more viscous during its passage through
the evaporator. The change of viscosity with temperature must be taken into
account when choosing the refrigerant.
14.4.3. CHEAPNESS
Large amounts of the secondary refrigerant are required to spread the cold
around the plant system. If the material is expensive, it would involve a high
cost. However, as before, the cost should only be a factor when the
properties mentioned earlier are met.
Water meets most of the above properties (especially cost) with one
exception i.e. it is unsuitable because it freezes at low temperatures. Most
secondary refrigerants however, are based on water with additives to reduce
the possibility of freezing.
A secondary refrigerant must also be non – toxic, non – flammable and non –
corrosive for the same reasons as primary refrigerants.
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14.5. COMMON SECONDARY REFRIGERANTS
Secondary refrigerants can be formed:
14.5.1. BY THE ADDITION OF A SOLUTE TO WATER
Common salt (sodium chloride) when dissolved in water will lower its freezing
point. This is why roads are salted when the temperature is likely to fall below
freezing point (0°C). The stronger the solution made by adding salt, the lower
the temperature at which the water will freeze. A typical solution strength
used is 25% which freezes at around -20°C. This solution is often called
brine.
The major problem with salt solution is that it is very corrosive especially to
steel (e.g. it causes cars to rust). Other problems are:
the stronger the solution, the more difficult it is to pump
the maximum strength possible (saturated solution) limits the
lowest temperature to about -25°C.
Calcium chloride solution, which acts in a similar way to sodium chloride, can
be used instead. Although less corrosive, it is more expensive.
14.5.2. BY THE ADDITION OF A LIQUID TO WATER
Methanol and ethylene glycol have low freezing points (methanol -98°C and
ethylene glycol -16°C). When added to water, the mixture produced has a
lower freezing point than water alone. These are commonly used in car
radiators in winter to stop the cooling system from freezing and are known as
antifreeze. The strength of the mixture will once again determine the freezing
point.
Methanol is relatively cheap, but at normal temperatures its rate of
evaporation is high and the strength of the mixture will therefore change with
time giving less protection from low temperatures. Glycol is more expensive
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and more corrosive but will not evaporate. Even though ethylene glycol has a
higher freezing point than methanol, when mixed with water it has a greater
effect on depressing the freezing point. A 50% mixture of ethylene
glycol/water freezes at -49°C whilst a 50% methanol/water mixture freezes at
a higher temperature.
In both these cases, a corrosion inhibitor is usually added to the mixtures to
reduce the amount of corrosion. Also, it is important that any loss of liquid is
replaced using the correct strength solution and not simply topped up with
water. Regular checks of refrigerant strength should also be carried out to
ensure that it gives the necessary protection.
Other secondary refrigerants used in industry, together with some of their
important properties, are:
air - cheap, does not freeze but has a low capacity for
removing heat and is a poor conductor
carbon dioxide - can be converted into a solid (dry ice) and
used to give portable 'cold' transfer
oils - these have low freezing points and are non-corrosive
but tend to be very viscous
process fluid - sometimes it is the process fluid that is cooled
by the refrigeration system so its properties cannot be listed
14.6. SUMMARY
Primary refrigerants are the materials circulating in the vapour compression
refrigeration cycle, which produce the cooling effect as they change from
liquid to gas.
They must possess certain properties, the most important of which is that
they must easily change from a liquid to a gas.
The most commonly used primary refrigerants in modern industrial systems
are the halocarbons (Freons and Arctons).
Secondary refrigerants are materials used to spread the cold to different parts
of the refrigeration system.
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These must possess certain properties, the most important of which is that
they must not freeze.
Typical secondary refrigerants are water mixed with substances that depress
its freezing point, eg. salt, antifreeze.
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15. SAFE & EFFICIENT OPERATION
15.1. INTRODUCTION
In the previous chapter, it was seen that there are many refrigerants, some of
which have hazardous properties. It is important therefore, that a refrigeration
system is run in a safe manner. Also, as with all processes, refrigeration
systems must be run efficiently to keep costs at a reasonable level.
In this chapter, some of the factors that affect the safe and efficient operation
of refrigeration systems are considered.
15.2. REFRIGERATOR PERFORMANCE
The system shown in Figure 33 is of a vapour compression refrigerator. When
operating at a steady state, the total energy within this system will be constant
(energy can neither be created nor destroyed, only changed from one form to
another).
Figure 33
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Electrical energy is supplied to the electric motor that drives the compressor.
Heat energy enters the system from the secondary refrigerant or process
fluid, which cools down (the main reason for refrigeration). It may also enter
from the surroundings. Heat energy is removed by the cooling water that is
supplied to the condenser.
Any measure of a refrigerator’s performance must include how much cooling
it achieves. It should also include how much energy is put into the system to
produce the cooling.
There are three commonly used methods of measuring the performance of a
refrigerator in industry. These are:
a) Refrigeration Capacity
b) Refrigeration Effect
c) Coefficient of Performance
15.2.1. REFRIGERATION CAPACITY
This is simply the amount of heat removed from the secondary refrigerant (the
amount of cooling) per second. It is expressed in kilowatts (kW).
Refrigeration Capacity is not a measure of efficiency but simply a measure of
the refrigerator's capacity to create cooling. It will depend to a great extent on
the size of the refrigerator system, i.e. the bigger the system, the more
cooling it is likely to produce.
15.2.2. REFRIGERATION EFFECT
This is the quantity of heat that each kilogram of primary refrigerant removes
as it passes through the evaporator. It is expressed as kilojoules per kilogram
(kJ kg -1).
Again, this is not a measure of efficiency but a measure of how good the
primary refrigerant is at removing heat. It will depend to a large extent on the
specific latent heat of evaporation of the refrigerant.
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15.2.3. COEFFICIENT OF PERFORMANCE (C.O.P.)
This compares the Refrigeration Effect (the cooling produced) with the
electrical energy (the driving force for refrigeration) put into the system per
kilogram of refrigerant compressed, i.e.
Refrigeration Effect
C.O.P. = Energy Input (per kg)
C.O.P. has no units because they cancel out. The higher its value, the better
is the refrigeration system. It can have a value greater than 1, i.e. a greater
amount of heat energy can be removed from the secondary refrigerant than
the amount of energy supplied to the compressor. It compares the cooling
produced with the power input (both of these are in effect energy inputs to the
system) and so is not a measure of efficiency. Heat energy is removed from
the system by the cooling/condenser, which must be included in efficiency
measurements.
C.O.P. does, however, enable direct comparisons of performance of both
refrigerants (since refrigeration effect measures this) and refrigeration
systems (since power input is included) to be made. It is therefore, the most
common way of expressing the performance of a refrigeration system.
The main factors that affect the value of the C.O.P. are:
choice of primary refrigerant
correct expansion valve setting
moisture control
use of insulation
control of heat exchangers
Choice of Primary Refrigerant
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In an earlier lesson, some of the many different primary refrigerants and their
properties were studied. It is important, therefore, that the correct refrigerant
is chosen for a particular duty.
For example, if a very low temperature is required (say -25°C), then the
refrigerant should have a slightly lower boiling point (say -35°C) so that the
condensing and evaporating pressures can be kept close together. This will
avoid large compression costs. Also, if the refrigerant has a high specific
latent heat of evaporation, it will produce more cooling per kilogram than one
with a low latent heat value.
Correct Expansion Valve Setting
The expansion valve setting controls the pressure and flow of primary
refrigerant to the evaporator. If the pressure is too high, then the liquid may
not evaporate at the required rate, leading to insufficient cooling. If the
pressure is too low, excessive evaporation may occur leading to very low
temperatures. These may cause the secondary refrigerant to freeze and block
the system. Also, the low temperature and pressure gaseous primary
refrigerant produced will require a large input of energy at the compressor to
pressurize it back to a liquid.
If the flow rate is wrong, then too much liquid may enter the evaporator and
cause flooding so that evaporation does not occur. Alternatively, too little
liquid may enter, starving the evaporator and giving little cooling.
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Moisture Control
If moisture is present within the primary refrigerant it may freeze at the
temperatures produced by the refrigerator. The ice formed may block pipes
and lead to non-circulation of refrigerant.
This will obviously reduce the efficiency of the system as the circulation of
refrigerant creates the cooling.
Also, if the air on the outside of plant equipment is humid, this may freeze on
the equipment. The presence of ice means that the cooling effect produced
by the refrigerator is being wasted on ice production. The ice may also act as
an insulation layer on surfaces where insulation is not required. This can be
illustrated with reference to a domestic fridge. Insulation is provided in the
sides, door, top and bottom of the fridge to prevent the ingress of heat from
the surroundings. Inside the fridge, the icebox (evaporator) cools the rest of
the fridge.
Notice how ice builds up on the icebox more quickly if the door is opened
often rather than when it is kept closed.
This is due to the air (and any moisture it contains) within the fridge being
replaced every time it is opened. The moisture in the air freezes on the
icebox. This build-up of ice prevents the cold from spreading out by acting as
an insulation layer. The ice should be removed at regular intervals to maintain
the efficient operation of the fridge.
Most modern fridges do this automatically to maintain the good performance
expected from modern devices. If not automatically defrosted, the ice should
be removed by manual defrosting but do not use a sharp instrument!
The reason is that the icebox is the evaporator. It is hollow and contains the
primary refrigerant. A sharp instrument may penetrate the evaporator and
cause leakage of the primary refrigerant.
From the earlier discussion, it is obvious that the presence of moisture within
the system should be kept to a minimum. This can be done by:
operating at a positive pressure throughout the system so that
any leakage is from the system to the surroundings
allowing air to contact cooled surfaces as little as possible.
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Use of Insulation
For effective cooling it is important that any heat removed by the system
should come from the secondary refrigerant. This means that all piping
systems and equipment where cold surfaces may be exposed to warmer
surroundings should be insulated to prevent heat gain from the surroundings.
Control of Heat Exchangers
There are two heat exchangers in the vapour compression system, both of
which will affect the value of the coefficient of performance.
Heat is removed from the compressed primary refrigerant in the condenser to
cool and condense it. This is the only place where heat is removed from the
vapour compression system. It is important that the heat is removed in an
effective way, ensuring that all gaseous refrigerant is condensed and cooled
to the required temperature. If not, then energy is wasted in compressing gas
that is not condensed.
Also the evaporator has less liquid to evaporate thus reducing the
refrigeration effect.
The cooling water system should, therefore, have a flow indicator/controller
(to ensure the correct amount of water is flowing). Temperature indicators on
inlet and outlet water flows will enable the operator to see if the cooling water
is at the correct temperature and if it is performing its duty. A similar control
system would be required if the condenser were air-cooled.
The second heat exchanger is the evaporator. Its purpose is to remove heat
from the secondary refrigerant to evaporate the primary refrigerant. Once
again the operation of this will affect the value of the C.O.P.
For example, if too little secondary refrigerant is passed into the evaporator,
then the temperature of the secondary refrigerant will become closer to that of
the primary refrigerant. The closer the temperature difference becomes, the
lower is the amount of heat transferred. It is important that a control system is
used on the evaporator heat exchanger to ensure efficient operation and a
high value of the coefficient of performance.
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15.3. HAZARDS ASSOCIATED WITH REFRIGERATION SYSTEMS
The three main hazards associated with vapour compression refrigeration
systems are:
the nature of the refrigerant materials
low temperatures
mechanical noise
15.3.1. THE NATURE OF THE REFRIGERANT MATERIALS
Refrigerants are classed into three basic Groups 1, 2, 3, depending on their
health and safety characteristics. These groups are:
Refrigerants in Group 1 are non-flammable and may be used
in systems where the total charge in the refrigerator would
cause no undue hazard if accidentally released into a space
occupied by humans.
Refrigerants in Group 2 have toxicity as a major
characteristic. If a typical refrigerator charge accidentally
leaked into a space occupied by humans, the concentration
would be toxic. A few of the refrigerants in this group are
flammable and when these are used, additional restrictions
are imposed by the authorities.
Refrigerants in Group 3 are generally non-toxic, but are more
flammable and explosive than the materials in Group 2. They
are particularly suited to some specialist requirements but
special restrictions are imposed when they are used.
There is a large volume of regulations and instructions associated with the
various types of refrigerants and reference should always be made to them
when compiling operator instructions. It is also good policy to consult the
manufacturer of the refrigerant for advice on any hazards caused by the
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material. It is obvious that, if the refrigerants are in any way hazardous, the
correct choice of construction materials must be made.
15.3.2. LOW TEMPERATURES
Physical contact with very cold metal surfaces can produce painful injuries,
which are very similar to burns caused by heat. Accordingly, these injuries are
often called 'freeze' or 'cold burns'. Every effort should be made to fit and
maintain lagging on pipes and other equipment that carry the primary and
secondary refrigerants through areas where operators are likely to come into
contact with them.
This will prevent direct contact between the cold surfaces and the operator.
Furthermore, the lagging will also increase the efficiency of the refrigeration
system. If an operator is to enter the cooled space e.g. a cold store, then he
should be provided with and wear protective clothing (especially insulated
gloves).
15.3.3. MECHANICAL NOISE
The vapour compression system uses a compressor to compress the primary
refrigerant. Most compressors (especially reciprocating types) are extremely
noisy (well above the danger level in some cases). To reduce this hazard,
large or numerous compressors should be housed in a soundproof building. If
entry to the building is required, ear protection in the form of plugs and/or
muffs, must be worn.
15.4. SUMMARY
The performance of a refrigerator can be expressed in the following terms:
Refrigeration Capacity
Refrigeration Effect
Coefficient of Performance
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Many factors will affect the performance of the refrigeration system including
correct choice of refrigerant
correct expansion valve setting
moisture control
use of insulation
control of heat exchangers
The hazards associated with vapour compression refrigeration systems are:
hazardous refrigerant materials
low temperatures
mechanical noise