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2022 CELCHB2 Prac Manual
2022 CELCHB2 Prac Manual
2022 CELCHB2 Prac Manual
CHEMICAL ENGINEERING
LABORATORY B2
CELCHB2
PRACTICAL MANUAL
2022
Table of Contents
1
1. Preliminary Note____________________________________________________________
2. General Instructions__________________________________________________________
3. Laboratory Safety____________________________________________________________
4. Guidelines for Technical Report Writing__________________________________________
5. Lab Assignments___________________________________________________________13
5.1 Refrigeration_________________________________________________________________
Laboratory Assignment Report Format and Marking Rubric___________________________16
5.2 Single Stage Compression_______________________________________________________
Laboratory Report Format and Marking Rubric (Air compression)______________________26
5.3 Steam Plant__________________________________________________________________
Experiment 1: Separating and Throttling Calorimeter___________________________27
Experiment 2: Separating Calorimeter and Throttle_____________________________32
Laboratory Assignment Report Format and Marking Rubric___________________________34
6. Lab Practicals______________________________________________________________35
6.1 Gas Absorption_______________________________________________________________
Laboratory Report Format and Marking Rubric (NEW RUBRIC)_______________________42
6.2 Fluid dynamics_______________________________________________________________
Laboratory Report Format and Marking Rubric (Fluid dynamics)_______________________52
6.3 Cooling Tower________________________________________________________________
Laboratory Report Format and Marking Rubri (cooling tower )_________________________58
Course Information and Laboratory Schedule_______________________________________61
1. Preliminary Note
You MUST arrive for your Practical on time. Please ensure that you study the Lab
rooster carefully.
2
Before entering the lab, please make sure that you have read and understood the
Laboratory Safety rules.
Please do not place your bags in the walkway. There are designated areas in the lab
where you must place your bags.
All Practicals will be conducted according to the Lab rooster. Please follow the
schedule as per Lab rooster.
If you have missed a Practical, please provide a doctor’s note or valid reason
(according to UJ’s policy) to the respective Laboratory Assistant, so that you could be
given an opportunity to perform the Practical.
Any misbehavior in the lab will mean that you will be asked to leave the lab with
immediate effect, and you will get zero for the practical.
You are to listen to your Laboratory Assistant at ALL times. Failure to do so will
mean expulsion from the lab.
If you do not submit your lab report to your Laboratory Assistant within 2 weeks/10
working days of each practical, 5 % will be deducted for each day of late submission.
You will obtain zero for the practical if this exceeds 5 days. Please submit your lab
report on/before the deadline.
Lab assignments need to be submitted within 5 working days. Late submissions will
be considered invalid, and you will obtain a zero mark that assignment
2. General Instructions
A. Clothing requirements
Closed shoes.
Long sleeves (not loose fitting).
3
Unless it is hot, long pants to be worn.
No dangling items of clothing or jewelry.
Always do a visual check on the area in which you are working. Look for a fault that
stands out.
Is there any water on the floor? Wipe before you start.
Are your shoes slipping on the floor? Make sure you walk carefully.
Are you working with dangerous chemicals? If so, make sure that you are provided
with the necessary safety gear (gloves, respirators for volatile gases and safety
goggles for corrosive substances and other volatile substances).
If you are working with flammable substances, ask the Laboratory Assistant where
the nearest fire extinguisher can be located.
Be aware of the other practical in progress in the laboratory. If there is an accident anywhere
in the lab it will affect you and your peers.
Think of what emergencies you could encounter while using this piece of equipment.
What could go wrong? Then decide on the quickest and safest way of dealing with it.
Keep that in the back of your mind just in case.
You need to obtain a good idea of what needs to be done and what the aim of the
practical is before you start.
Do not touch the equipment until the Laboratory Assistant has explained to you on
how to use it.
Do not fiddle with any equipment settings unless you are instructed to do so.
Make sure that you know if any part of the equipment is going to be hot. Do not touch
it with your bare hands!
Report any breaks or damage done to the equipment to the Laboratory Assistant. PLEASE do
not hide the damage. It may result in someone from another group being severely injured.
3. Laboratory Safety
Safe laboratory practices attempt to limit the exposure of chemical hazards to the laboratory
user. In devising procedures, the user should be aware of what is a safe exposure, and proper
handling techniques. The following criteria are used to determine and implement control
measures to reduce exposures to hazardous chemicals.
Exposure Monitoring
Exposure monitoring is conducted upon request if there is reason to believe that exposure
levels for a particular substance may routinely exceed either the action level or the
permissible exposure limit set forth by Occupational Safety and Health Act 85 of 1993
(OSHA).
Control Measures
5
Engineering controls are the primary means of control for exposure to hazardous chemicals.
Local ventilation, including fume hoods, ducted bio-safety cabinets, glove boxes, vented
storage cabinets, and vented canopies are the most common types of engineering controls.
Protective equipment, including gloves, face shields, safety glasses, safety goggles, lab coats
and aprons, are used when engineering controls are not sufficient to adequately control
exposure. Specifically, this equipment is used to prevent exposure to the skin or eyes.
Personal protective equipment is carefully selected to ensure that it is compatible with the
chemicals used. Information about selection of appropriate protective equipment is available
from the laboratory supervisor
Administrative Controls
Reproductive toxin includes any chemical that may affect the reproductive
capabilities including chromosomal damage (mutations) and effects on fetuses
(teratogenesis).
High acute toxicity includes any chemical that falls within any of the following
categories:
A chemical with a median lethal dose (LD 50) of 50 mg or less per kg of body weight when
administered orally to certain test populations. A chemical with an LD 50 of 200 mg or less per
kg of body weight when administered by continuous contact for 24 hours (or less if death
occurs within 24 hours) to certain test populations. A chemical with a median lethal
6
concentration (LC50) in air of 200 parts per million (ppm) by volume or less of gas or vapor,
or 2mg/l or less of mist, fume, or dust, when administered to certain test populations by
continuous inhalation for one hour, provided such concentration and/or condition are likely to
be encountered by humans when the chemical is used in any reasonably foreseeable manner.
A hazardous substances list is filed in the lab and is available for perusal on request.
Personal protective equipment (PPE) is special gear used to protect the wearer from specific
hazards of a hazardous substance. It is a last resort protection system, to be used when
substitution or engineering controls are not feasible. PPE does not reduce or eliminate the
hazard, protects only the wearer, and does not protect anyone else.
PPE includes gloves, respiratory protection, eye protection, and protective clothing. The need
for PPE is dependent upon the type of operations and the nature and quantity of the materials
in use, and must be assessed on a case-by-case basis. Workers who rely on PPE must
understand the functioning, proper use, and limitations of the PPE used.
Eye protection
Safety glasses
7
Safety glasses look much like normal glasses but have lenses that are impact resistant and
frames that are far stronger than standard street-wear glasses. Safety glasses must have side
shields and should be worn whenever there is the possibility of objects striking the eye, such
as particles, glass, or metal shards.
Chemical Splash Goggles should be worn when there is potential for splash from a hazardous
material. Like safety glasses, goggles are impact resistant. Chemical splash goggles should
have indirect ventilation so hazardous substances cannot drain into the eye area.
When the possibility of chemical contamination exists, protective clothing that resists
physical and chemical hazards should be worn over street clothes. Lab coats are appropriate
for minor chemical splashes and spills, while plastic or rubber aprons are best for protection
from corrosive or irritating liquids. Disposable outer garments (Tyvek suits) may be useful
when cleaning and decontamination of reusable clothing is difficult. Loose clothing (such as
overlarge lab coats or ties), skimpy clothing (such as shorts), torn clothing and unrestrained
hair may pose a hazard in the laboratory.
Shoes should be worn at all times in buildings where chemicals are stored or used. Perforated
shoes, sandals or cloth sneakers should not be worn in laboratories or where mechanical work
is conducted. Such shoes offer no barrier between the laboratory worker and chemicals or
broken glass.
Chemical resistant overshoes or boots may be used to avoid possible exposure to corrosive
chemical or large quantities of solvents or water that might penetrate normal footwear
8
Gloves
Not only can many chemicals cause skin irritation or burns, but also absorption through the
skin can be a significant route of exposure to certain chemicals. Dimethyl sulphoxide
(DMSO), nitrobenzene, and many solvents are examples of chemicals that can be readily
absorbed through the skin into the bloodstream, where the chemical may cause harmful
effects. Protective gloves should be worn when handling hazardous materials, chemicals of
unknown toxicity, corrosive materials, rough or sharp-edged objects, and very hot or very
cold materials. When handling chemicals in a laboratory, disposable latex, vinyl or nitrile
examination gloves are usually appropriate for most circumstances.
Technical writing generally is written reports, grants, proposals, and other similar papers.
Aside from writing ethically, the main goal of technical writing is to convey information
precisely and clearly.
Simply put, being ethical in writing implies not making up data, not making up sources,
not taking credit for what’s not yours, and citing your sources accurately. Misleading
information in a technical report can lead to incorrect conclusions.
9
4.2 Why do Chemical Engineers need to write technical reports?
Chemical Engineers need to be good, clear technical writers in order to communicate better.
The first two misconceptions tend to go together with some sort of reciprocal justification,
and we simply contradict them. The third is mistaken impression gained from wide exposure
to Techlish.
Engineers are not poor writers naturally. They may learn to be poor writers, or may not gain
good writing skills. Writing well comes from practice. Reports and papers are one of the
main methods for scientist and engineers to report their research to each other. And, contrary
to popular belief, proper grammar is extremely important in technical writing. The rules for
proper non-technical and technical writing are the same.
The first principle of readable writing: Express important actions as verbs, and the characters
associated with those actions as the subjects of those verbs.
The second principle of readable writing: Keep subjects as short as possible so that sentences
move quickly from short, specific subject to an action verb.
The third principle of readable writing: Sentences should begin with old information and end
with new information. As chemical engineers we need to be sure to make ethical decisions in
the work place.
This section describes a general format for lab reports that one can adapt as needed.
10
Lab reports are the most frequent kind of document written in engineering and can count for
as much as 25% of a course and yet so little time is devoted to write good reports.
Regardless of the variations, however, the goal of lab reports remains the same. A good lab
report does more than present data; it demonstrates the writer’s comprehension of the
concepts behind the data. Merely recording the expected and observed results is not
sufficient; you should also identify how and why differences occurred, explain how they
affected your experiment, and shows your understanding of the principles the experiment was
designed to examine. Bear in mind that a format, however helpful, cannot replace clear
thinking and organized writing. You still need to organize your ideas carefully and express
them coherently.
11
The title page needs to contain the name of the Institution, name of the Department, name of
the experiment, student name, student number, Group number, Date of submission. The title
should be straightforward, informative, and less than ten words.
For example: To develop the drying curve characteristics of sand and pulp.
Synopsis (Abstract)
Synopsis summarizes five essential aspects of the report: the purpose of the experiment,
method or procedure, key findings (results), significant point of discussion and major
conclusions. The synopsis often also includes a brief reference to theory or methodology. The
information should clearly enable readers to decide whether they need to read your whole
report. The synopsis should be one/two paragraphs of 100-250 words.
For example: The experiment examined the effect of flow rate on the performance of a
double-pass shell and tube heat exchanger. This was conducted by a counter current flow
arrangement. Both fluid and temperatures at the inlet and the outlet of the heat exchanger
were obtained. The fluid flow parameter and Nusselt Number was characterized. The ratios
of convective and conductive heat transfer rates were compared. Higher Nusselt Numbers
were obtained with increasing Reynolds Number for the same fluid. This shows that the heat
exchanger performance was enhanced with higher Reynolds Number. This is an agreement
with the Diltus-Boelter – Correlation.
Declaration
Declaration declares that the report was done by you and the work is not a copy of someone
else’s work (see ethical).
Acknowledgement
Acknowledgement list all assistance received during the practical and writing of the report.
Table of Contents
12
Table of Contents it is a complete list of numbered headings and subheadings, together with
the respective page numbers.
Introduction
The Introduction is more narrowly focused than the synopsis. It states the objective of the
experiment and provides the reader with background and theory to the experiment.
For example: Heat exchangers are important equipment found in process industries. The two
mechanisms are conduction and convection by which heat is exchanged in this equipment.
The heat load being transferred per unit time is high when the convection heat transfer co-
efficient is high
Experimental Procedure
Experimental Procedure describes the process in chronological order. Using clear paragraph
structure, explain all steps in the order they actually happened, not as they were supposed to
happen. All you are trying to convey is a mental picture of what you did. Remember that your
audience should be able to repeat your description if they wish to do so. A diagram of the
apparatus used may be helpful but should not replace a good verbal description.
Results are usually dominated by calculations, tables and figures (graphs). Graphs need to be
clear, easily read, and well labeled (e.g. Fig.1: Moisture Content vs. Time).
In most cases, providing a sample calculation is sufficient in the report. Leave the remainder
in an appendix. Likewise, your raw data can be placed in an Appendix. Refer to Appendices
as necessary, pointing out trends and identifying special features.
Discussions are the most important part of your report, because here, you show that you
understand the experiment beyond the simple level of completing it. Explain. Analyse.
13
Interpret. Some people like to think of this as the “subjective” part of the report. This part of
the lab focuses on a question of understanding “What is the significance or meaning of the
results?” To answer this question, use both aspects of discussion:
Conclusions
Conclusions can be very short in most undergraduate laboratories. Simply state what you
know now for sure, as the result of the lab:
For example: Heat transfer in heat exchangers is enhanced with higher fluid flow rates.
Recommendations
References
14
For example:
Felder and Rousseau: Elementary principles of chemical Engineering, 5th Edition Chapter
14; page 125-140
Harriett, P., McCabe, W. L., & Smith, J. C. (2005) Unit Operations of Chemical Engineering
(Seventh Edition) Singapore: McGraw-Hill
Pilusa TJ; DMS Quality Control Systems; DeBeers CHQ Diamond Processing 2003; Chapter
2;page 12-22
Appendices
Appendices typically include such elements as raw data, sample calculations, graphs or tables
that have been included in the report itself. Each kind of item should be contained in a
separate appendix. Make sure that you refer to each appendix at least once in your report.
For example:
15
5.Refrigeration
The purpose of this experiment is to study the thermodynamic relationship that expansion of
a refrigerant has on the work done on a compressor and the Coefficient of Performance
(COPref)
Objectives
Investigate the thermodynamics of refrigerant R134-a (tetrafluoro ethane) with
varying expansions stages.
Develop a conclusive theory on how expansion is related to the work done by the
compressor.
Determine the COPref of the refrigeration cycle for the different expansion stages
Apparatus
The system consists of an evaporator, condenser, compressor, throttle valve (1-12), capillary
tubes of varying expansion lengths and manometers. Thermo couples are placed at various
positions to monitor the temperature at different points. The unit is working in two modes,
namely domestic and commercial.
Experimental Procedure
Set Up Refrigerator Unit
1. Set the unit to domestic mode.
2. Switch the unit to refrigerator mode.
16
3. Set both the evaporator and the condenser fans to setting 1.
4. Switch the thermometers on
Expansion through 1m capillary tube
5. Close valves 4, 2, 1 and 7. All the other valves should be left open.
6. Press the reset button to reset the pressure gauges (at the top of the pressure gauges).
7. Switch on the MAIN SWITCH by turning the key on the unit.
cosφ
8. Record the Ampere reading and the power factor ( ) at the beginning of the
refrigeration cycle (Observation table given below)
9. Also record the temperatures at the beginning of the cycle.
10. Wait for unit to reach the point of balance and record all the temperatures, power
factor and the Ampere reading.
11. Safely switch off the refrigeration unit.
Expansion through 2m capillary tube
12. Close valves 4, 1, 3, 7. All the other valves should be left open
13. Repeat steps 6 to 11.
Expansion through 3m capillarity tube.
14. Close valves 4, 2, 3, 7. All the other valves should be left open
15. Repeat steps 6 to 11.
Results
Draw the schematic diagram of the refrigeration cycle.
Plot the P-H diagram for the 1m expansion stage.
Calculate the actual work done by the compressor at the point balance for the different
expansion stages.
Calculate the efficiency of the compressor for each expansion stage.
Calculate the mass flow rate of the refrigerant for each expansion stage.
Calculate the COPref for each expansion stage.
Draw a histogram of the COPref versus expansion stage.
High
Capillary Power factor Low Pressure
Voltage (V) Amps (I) Pressure
Length (Cos) (kPa)
(kPa)
1m
2m
3m
17
T1 (oc) T2 (oc) T3 (oc) T4 (oc)
Capillarity Work Done
Temp In for Temp Out for Temp In for Temp Out for COPref
length (W) kW/kg
Evaporator Evaporator Compressor Compressor
1m
2m
3m
Data Sheet for R134-a (N.B. not all properties are found in this figure)
Discussion
Comment on the work done for each expansion stage
Comment on the efficiency of the compressor for the different expansion stages.
Comment on the COPref for the different expansion stages.
References
M.J. Moran and H.N. Shapiro, Fundamentals of Engineering Thermodynamics, John Wiley
& Sons, Third Edition, 1988, chapter 11, pg479
18
Smith, Van Ness, Abbott, Chemical Engineering Thermodynamics, McGraw-Hill Chemical
Engineering Series, Sixth Edition, 2001, Chapter 9, pg 309
Mark Allocation
Typed laboratory assignment reports must be prepared, and will be assessed, using the topics
presented below.
(3)
Enthalpies 5-6/6 4-3/6 2-1/6 0/6
19
representation on the P-
H diagram for all 3
expansion stages (6)
Schematic diagram of
the refrigeration cycle 3/3 2/3 1/3 0/3
(3)
P-H plot for 1M
3/3 2/3 1/3 0/3
capillary (3)
Actual work done by
compressor for the 3 5-6/6 4-3/6 2-1/6 0/6
Determination of
3/3 2/3 1/3 0/3
COPref (3)
5-6/6 3-4/6 1-2/6 0/6
All the All the All the
All the
observations observations observations
observations
Tabulated but Tabulated but Tabulated and
Observations/ Findings Tabulated and
implied data not implied data not implied data do
(6) implied data
accurately determined. not represent
accurately
determined. experimental
determined.
data.
20
The purpose of this study is to expose the student to the technical operation of a single stage
compression unit and theoretical
Objectives
1. To study the compressor characteristics i.e., volumetric efficiency, isothermal
efficiency, brake horsepower and pressure ration.
2. To investigate the effect of compressor outlet pressure on the afore mentioned
parameters.
Theoretical Background
Introduction
There are two generic principles for the compression of air (or gas): positive displacement
compression and dynamic compression. Positive displacement compressors include, for
example, reciprocating (piston compressors, orbital compressors, and other different types of
rotary compressors namely, screw, tooth, and vane.
In positive displacement compressors, the air is drawn into one or more compression
chambers, which are then closed from inlet. Gradually the volume of each chamber
decreases, and the air is compressed internally. When the pressure has reached the designed
built-in pressure ration, a port or valve is opened, and the air is discharged into the outlet
system due to continued reduction of the compression chamber’s volume.
In dynamic compression, air is drawn between blades on a rapidly rotating compression
impellor and accelerates to a high velocity. The gas is then discharged through a diffuser
where kinetic energy is transformed into static pressure. Most dynamic compressors are turbo
compressors with an axial or radial flow pattern. All are designed for large volume rates.
In a reciprocating compressor, compression takes place as a result of the back-and-forth
travel, or stroke of a piston in a cylinder equipped with inlet and discharge valves. The cycle
is usually described by a Pressure-Volume (PV) diagram.
21
Changes in state for gas can be followed from one to another in a PV diagram. For real life
cases, three axes for the variables p, V and T are required. With a change in state, we are
moved along a 3-dimensional curve on the surface in a p, V and T space. However, to
simplify, we usually consider the projection of the curve in one of the three planes. This is
usually the p/V plane. Five different changes in state can be considered:
- Isochoric process (constant volume)
- Isobaric process (constant pressure)
- Isothermal process (constant temperature)
- Isentropic process (without heat exchange with surroundings)
- Polytropic process (complete heat exchange with the surroundings)
We will consider only Isothermal, Isentropic and Polytropic process.
Isothermal Process
If a gas in a cylinder is compressed isothermally, a quantity of heat equal to the applied work
must be gradually removed. This is unpractical as such a slow process cannot occur
Q=mRT . ln
( )
P2
P1 ( )
=P 1 V 1 ln
V2
V1
Isentropic Process
An isentropic process exists if a gas is compressed in a fully-insulated cylinder without any
heat exchange with the surroundings. It may also exist if a gas is expanded through a nozzle
so quickly that no heat exchange with the surroundings has time to occur.
22
( ) ( )
k k
P2 V 1 T2 k−1
= =
P1 V 2 T1
The isothermal process involves full heat exchange with the surroundings and the isotropic
process involves no heat exchange whatsoever. In reality, all processes occur somewhere in
between these extreme, the polytropic process. The relation for such a process is:
n
P V =constant =k
In actual practice, the compression process is neither isothermal nor Isentropic but a
combination of both processes. This third is called polytropic process.
Figure 4. PV diagram for ideal process (A) and real process (B)
23
These relations show that more work is required for isentropic compression than for
isothermal compression.
Compression work with isothermal compression:
W =P1 V 1 ln
( )
P2
P1
Wcycle = Work done in the compression process + Work done in the expansion process
[( ) ] [( ) ]
n−1 m−1
n P2 n m P3 m
W cycle = P1 V 1 −1 − P4V 4 −1
n−1 P1 m−1 P4
Since P1 = P4 and P2 = P3, and the expansion work is very small in comparison with the
compression work. Thus, it can be assumed that m = n causing only small discrepancy in
using the above equation.
25
[( ) ]
n−1
n P2 n
W cycle = P1 ( V 1−V 4 ) −1
n−1 P1
The difference between the two work equatons lies in the term V 4 which volume depends on
the pressure P1 and temperature T1 respectively.
Performance Index
Electrical power (EP)
EP is the electrical power supplied to the motor to drive an air compressor
EP=E × I ×φ
The electrical power may also be driectly measured by a Watt meter
Brake power (BP) or Shaft power
This is the power that the motor supplies to the compressor
2 πn N . m
BP=Torque × ω=Fr =W
60 s
Air mass flow rate (ṁ = qm)
The air mass flow rate of the compressor outlet from the air receiver, it can be calculated
from the flow rate through the orifice and differential pressure of the manometers in the same
manner as above. If the pressure in the air receiver is constant, both flow rates (in and out of
the compressor) will be equal. In normal practice, the mass flow through the inlet box is
basically used.
Isentropic Power (W)
This is the theoretical power from the theory of isentropic compression process, (Reversible
adiabatic process).
[( ) ] [( ) ]
k−1 k−1
P2 k P3 k
W =qm C p T 1 −1 +q m C p T 2 −1
P1 P2
W Total =P1 V 1 ln ( )
P2
P1
+ P 3 V 3 ln ( )
P3
P2
¿ P1 V 1 ( ln P3−ln P 1)
P3
¿ P1 V 1 ln
P1
Where, P = Pressure, N/m2 and V = Volume per unit time, m3/sec
26
Isentropic efficiency, (Isen.eff%)
W
Isen . eff %=100
BP
Isothermal efficiency (Iso.eff%)
W total
Iso . eff %=100
BP
System efficiency (Sys.Eff%)
W total
Sys . eff %=100
BP
Volumetric Efficiency (Vol.eff%)
Flow Capacity ×100 qv
Vol .eff %= =
First stage displacement Swept volume
× speed
Cycle
Equipment Description
Experimental Procedure
1. Level the table by turning the adjusting screw and observing the level inclined
manometer at horizontal position
2. Close the air receiver discharge valve and the drain valve
3. Turn on ELCB and CB at the right side of the control box
4. Adjust the compressor speed to 400 rpm
27
5. Press the Start button at the inverter
6. The motor will run and the compressor outlet pressure gauge start to increase
7. Record the data as given in the Table below at pressures 1 bar, 2 bar, 3 bar and 4 bar.
Repeat steps 1 to 7 but now adjusting the compressor speed to 700 rpm
After each set of experiments, open the drain valve to release the compressed air
Results
Arm length = 120 mm
Air box diameter = 210 mm
Orifice diameter = 15 mm
Patm = 1.013 x 105 N/m2
28
Expansibility factor ε for orifice plates in atmospheric air
Calculations
Your calculations are a comparison between the motor speeds at a specific pressure of your
choosing.
Cylinder displacement
Air delivery
Isentropic power
Isothermal power
Isentropic efficiency
Isothermal efficiency
Volumetric efficiency.
Discussions
Pressure – Volume relationship (use a diagram)
The effect of pressure on the temperature of the gas
29
Comment on the behaviour of the gas (ideal/ non-ideal?) Explain.
Comment on the compressor’s efficiency.
NB: Your results should include graphs drawn from recorded data and calculations
References
J. M. Smith, 2001, Introduction to Chemical Engineering Thermodynamics, McGraw-Hill,
Boston.
Mark Allocation
Content Mark allocated Mark Obtained
Introduction 5
Experimental Procedure 4
Results/Calculations 30
Observations/Findings 6
Conclusions 5
Total 50
Objective:
The objective of this experiment is to determine the dryness fraction of wet steam.
APPARATUS:
Steam bench
a) Steam generator
b) Separating and throttling calorimeter
c) Measuring Beaker
32
33
Separating Throttling
Calorimeter Calorimeter
Thermometer
Manometer
Condenser
Cooling Water
In
Condensate
M2
THEORY:
The separating calorimeter is a vessel used initially to separate some of the moisture from the
steam, to ensure superheat conditions after throttling. The steam is made to change direction
suddenly; the moisture droplets, being heavier than the vapor, drop out of suspension and are
collected at the bottom of the vessel.The throttling calorimeter is a vessel with a needle valve
fitted on the inlet side. The steam is throttled through the needle valve and exhausted to the
condenser. Suppose M kg of wet steam with a dryness fraction of x (state A) enters the
separating calorimeter. The vapour part will have a mass of xM kg and the liquid part will
have a mass of (1-x)M kg. In the separating calorimeter part of the liquid, say M 1 kg will be
separated from the wet steam. Hence the dryness fraction of the wet steam will increase to x1
(state B) which will pass through the throttling process valve. After the throttling process the
steam in the throttling calorimeter will be in superheated state (state C).
34
T
P1
A B
T1 ● ● P2
●
T2 C
Q – W = h C - hB
Since throttling takes place over a very small distance, the heat transfer is negligible, i.e.,
Q = 0. Then the steady flow energy equation for the throttling process becomes,
hC = hB
hC = hf1 + x1 hfg1
If the pressure of the steam before throttling, the pressure and temperature of the steam after
throttling, are known the value of x1 can be calculated using steam tables.
Mx1 2
Therefore, X = M +M 1 2
35
Where, M2 is the mass of condensate.
PROCEDURE:
1. Start the boiler and supply steam to the separating and throttling calorimeter unit.
2. Start the cooling water flow through the condenser.
3. Open steam valve and allow the steam to flow through the calorimeters to warm
through the steam.
4. Open the throttle valve and adjust to give a pressure at exhaust of about 5cm Hg
measured on the manometer.
5. Drain the separating calorimeter.
6. Start the test and take readings at 2-3 minutes intervals.
7. When a reasonable quantity of condensate is collected measure the quantity of
separated water and the quantity of condensate.
TABLE OF OBSERVATIONS
Reading # 1 2 3 Average.
Steam pressure in main P1 (bars)
Steam pressure after throttling P2 (bars)
Temperature of main T1 (oC)
Temperature after throttling T2 (oC)
Quantity of Separated water m1 (kg)
Quantity of condensate m2 (kg)
36
Atmospheric pressure Pa (bars)
Objective:
37
Apparatus
Combined separating and throttling calorimeter fitted with digital thermometer, pressure
gauge, mercury manometer, sight gradated glass and measuring beaker.
PROCEDURE:
38
1. Start the boiler and supply steam to the separating and throttling calorimeter unit.
2. Start the cooling water flow through the condenser.
3. Open steam valve and allow the steam to flow through the calorimeters to warm
through the steam.
4. Open the throttle valve and adjust to give a pressure at exhaust of about 5cm Hg
measured on the manometer.
5. Drain the separating calorimeter.
6. Start the test and take readings at 2-3 minutes intervals.
7. When a reasonable quantity of condensate is collected measure the quantity of
separated water and the quantity of condensate.
Results
Tabulate results as follows:
Readings Units Reading1 Reading2 Final values
Steam pressure in main P1 bar P1av=
Steam temperature in main t1 ⁰C t1av =
Water collected in m ml mf = m2 - m1=
Steam pressure after
separator P3 bar P3av =
Steam temperature after
throttling t3 ⁰C t3av =
Steam condensed after
throttling M ml Mf = M2 – M1 =
Barometer
throttling reading Patm mmHg
Analysis of results
Dryness fraction of the steam leaving the
separator/entering the throttling calorimeter
Apparent dryness fraction of steam in main
pipe
True dryness fraction of the steam in the
main
Typed laboratory assignment reports must be prepared, and will be assessed, using the topics
presented below.
Results Indicates clearly Indicates the Does not Indicate The Analysis of
the formulas formulas but the formulas and data does not
(Mathematical
used and step-by- does not follow a does not follow a work at all as
manipulation) (30) step procedure of step-by-step step-by-step required.
40
procedure of procedure of
calculating one
calculating one calculating one
set of tabulated
set of tabulated set of tabulated
results
results results
condensate, m1 and m2
Data Analysis 5 (5)
5/5 4/5 3/5 1/5
Calculating x1
Data Analysis 6 (5)
5/5 4/5 3/5 1/5
Calculating x2
Data Analysis 7 (5)
5/5 4/5 3/5 1/5
Calculating actual x
Data Analysis 8 (3)
3/3 2/3 1/3 0/3
Graph
Data Analysis 9 (3) 3/3 2/3 1/3 0/3
41
TOTAL POINTS out of 50
6. Lab Practicals
Objectives
Determine the CO2 composition in the various streams around the column
Evaluate the columns absorption efficiency
Discuss the effect of varied liquid flow rates on pressure drop
Discuss the effect of varied liquid flow rates on the absorbed CO 2 composition
in the liquid outlet stream, hence on mass transfer.
Theory/ Background
The liquid –gas solutions are systems of two components (e.g liquid solvent and gaseous
solute) for studying the absorption process, you must know the solubility of the gas to be
absorbed in liquid which is to be used as the absorber.
To evaluate absorption, you must know the solubility of the gas to absorbed in the liquid
which is to be used as the absorber and its variations as function of the temperature and
pressure in which the process is to be carried out. In practice, you must know the gas liquid
42
equilibrium curve, connecting the solute gas equilibriums to each temperature, divided into
the gaseous and liquid phase.
For diluted solutions and ideal gases, the activity of the gas to be absorbed in gaseous phase
can be considered equal to its partial pressure, which means that at a given temperature, the
molar fraction of a gas dissolved into a liquid is proportional to its partial pressure (henry’s
law)
Pa = HXa (see given values for CO2 in literature)
The value of the constant (H from Henry) depends on the temperature, the nature of the
solvent and the nature of the absorbed gas.
Ficks law:
If we consider two different phases (gas-liquid) in mutual contact, containing a soluble gas
component in both phases but distributed in different concentrations this component passes
from one phase to the other to reach an equilibrium of concentrations.
To perform this passage, the gas to be absorbed meets two resistances, the first in spreading
the higher concentration from the phase center to the inter phase zone, the second is the one it
meets when passing from the inter phase zone to the core of the second phase.
Inter-phase
G L
Applications of gas absorption
Gas absorption is a unit operation in which one or more soluble components of a gas mixture
are dissolved in a liquid. Gas absorption is a key method in the controlling of industrial air
pollution and generally aims at the separation of acidic impurities from mixed gas streams.
43
Impurities include carbon dioxide, Hydrogen sulfide, and organic sulphur compounds the
most important being C02. For both air pollution control and recovery of process gases,
packed towers are one of the most common mass transfer devices in current use.
Description
1) Schematic Diagram:
2) Material balance:
G2 Y2 L2 X2
G L
y
Y X
L1X1
44
G1 Y1 L1X1
(For dilute systems, the solute content is small relative to the non-soluble inerts and non-
volatile liquid. Thus, we can assume: L1=L2=L and G1=G2=G
45
Apparatus:
Packing material: Provides a large area of contact between the liquid and the solute
containing gas entering the bottom of the absorber.
Mixer: The gases are mixed using a specially designed mixing tube located after the flow
meters and prior to entering the bottom of the tower.
Gas supply: CO2 and air are available from cylinders equipped with regulators. The flow
rates are maintained at desired levels using flow control valves.
Liquid supply: Water is pumped from a sump tank to the top of the column. It flows
downward through the column and can be returned to the sump tank or diverted to the drain.
Measurements:
Temperature transmitter - temperature can be read from the control panel
Differential pressure gauge -Gives the pressure drop across each of the two sections of the
column
1. Start – up Procedure
46
Connect valve V8 to the compressed air supply at 1.5 bar by means of the pressure reducer on
the unit
Connect the cylinder of the gas (CO2) to be absorbed to valve V9 at 2 bar by means of the
pressure reducer on the unit
Shut off valves V2, V3, V4, V5, V6, V7 and V10
Select the loop no 1 of the controller (by key Loop)
Turn the loop no 1 in manual mode (by key M/A/C , red led on)
Select on display, by means of key Ind , the Out and decrease it to zero by means of the
up/down scroll (valve FV1 closed)
Turn the loop no 2 of the controller in manual mode (by key Loop, red led on)
Select on display, by means of key Ind , the Out and decrease it to zero by means of the
up/down scroll (valve FV2 closed)
Open valves V1, V8, V9
Select loop no 3 (by key Loop)
Select on display, by means of key Ind , the indication Out and set the flowrate of the pump
at 30% output (80 l/hr) by means of the up/down scroll
RUN 1
Wait for 10mins and record the differential pressure (mmH2O) across the packed column
Turn the pump G1 to position 0; and close valves 8 and 9.
47
Drain all the water from the bottom of the column through valve 10; and close the valve
thereafter
Use a pipet to take about 100 ml (for each titration run) of the sample and pipet into the 250
ml conical flasks
Titrate with a standard solution of 0.100 mol/dm3 (0.1M) sodium hydroxide solution and
0.100 mol/dm3 hydrochloric acid (HCl) standard solution
Use phenolphthalein as indicator for the titration
Determine the concentration of the carbonic acid solution /carbonate solution at the end point
RUN 2
RUN 3
RUN 4
4. Materials
Stop watch
250 ml Conical flask x2
Phenolphthalein bottle with dropper
100 ml pipet x2
2 x 50 ml burette with stand
1000 ml Volumetric flask
Mass balance
Sodium hydroxide pellets; hydrochloric acid (32%) and de-ionised water
Sampling bucket/1 l beaker
funnels
Results
49
Determine the C02 mole fraction in the incoming gaseous mixture for each run.
Determine the C02 mole composition in the liquid outlet stream, by titration for
each run (Perform a mass balance around the column)
Plot the operating line and equilibrium line for each run and interpret diagram.
Plot gas mass flow rate versus pressure drop and discuss the relationship
References
J.M Coulson & J.F Richardson, Particle Technology & Separation Processes (2002) , Vol 2,
5th Ed, Elsevier Butterworth Heinemann.
McCabe, W. L. and J. C. Smith, Unit Operations of Chemical Engineering,4th Edition,
McGraw Hill Book Company, New York, NY, 1985.
Mark Allocation
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Used the recommended
Title page used is
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not acceptable
Title page. some elements
are missing.
51
1-4
Data Analysis 5 (2)
Equilibrium line - 2/2 1/2 0/2
equation
Data Analysis 6 (2)
Graphs for run 1-4
- 2/2 1/2 0/2
(operating line and
equilibrium line)
Data Analysis 7 (3)
Column’s absorption 3/3 2/3 1/3 0/3
vs pressure drop)
In-text In-text
Detailed in-text referencing done referencing not in
In-text references No in-text
referencing (Discussion correctly and havard format but
not sufficient reference
sufficiently in references are
and Introduction)
Harvard format. sufficient
Conclusions and Conclusions and Some core Most salient There is little or
52
and salient points Conclusions and and
Recommendation
are highlighted. Recommendation Recommendation.
2. Theoretical background
2.1. Fluid dynamics terms
53
2.1.1. Pressure drops
When crossing a straight pipeline, a bend, a valve, etc…, the flow of liquid always meets with a
mutual friction between the particles of the fluid and between these particles and the walls of the
vessel, of the valves, of elbows, etc…
This leads to a continuous and local reduction of the energy of the fluid and the energy the fluid will
receive to cover the distance between two far spots of circuit.
For instance, this phenomenon can easily be detected through two pressure gauges installed in a
pipeline of constant section at a distance from each other.
Reading these pressure gauges will lead to realize that P1 > P2; this means that there is a pressure
drop due to friction between the particle of the fluid and between these and the wall.
Generally, the problem consists in assessing one of these three quantities:
Flow rate
Diameter of the pipeline
Pressure drops
∆ P=10
−5 f × ρ × L ×V 2
2D
=10
−5 f × L
D
1
( 2
× ρ ×V ¿
2 ) (1)
Where
P = pressure drop (in bar)
L = length of pipeline (in meter)
D = diameter of the pipeline (in meter)
V = means velocity of fluid (in m/s)
F = dimensionless friction factor
Ρ = density of fluid (in kg/m3)
This equation shows that the pressure drop of a liquid flowing in a straight pipeline depends on the
following factors:
Length of the pipeline
Diameter of the pipeline
Velocity of the fluid
Density of the fluid
Friction factor
But the most important element for assessing the valves of the friction factor (f) and the pressure drop
in the type of flow:
54
Laminar flow
Transition flow
Turbulent flow
Laminar flow occurs at low velocities in narrow and smooth pipes. It is characterized by rectilinear
and parallel motion.
The flow cylinder in direct contact with the wall of the pipeline adheres to this wall and its velocity is
zero.
After exceeding a certain limit value of mean velocity of the flow depending on the characteristics of
the liquid and on the diameter of the pipeline, the regular rectilinear motion is replaced by an irregular
and whirling movement where the separate liquid particles run at velocities varying in time and in
section. And this is the turbulent flow.
A quantitative differentiation between these flows can be given by the ratio between maximum
velocity and mean velocity; this equal to 2 for the laminar flow and 1.16 and 1.23 for turbulent flow.
But the type of flow and the value of the fluid resistance corresponding to a certain velocity must be
determined with reference to the considered liquid and pipeline; therefore Osborne Reynolds has
introduced characteristic dimensionless number, called Reynolds number and is given by:
ρ× V × D V × D
ℜ= = (2)
μ v
Where
ρ = density of fluid (in kg/m3)
V = mean velocity of this length of pipeline (m/s)
D = inner diameter of pipeline (in m)
V = kinematic viscosity (in m2/s)
µ = dynamic viscosity (in Ns/m2)
It is known from experience that a certain critical value of Reynolds number, considered as element of
separation between the two possible types of flow, will correspond to a certain type of section.
Comparing this value will determine if the flow is laminar or turbulent. The Moody diagram explains
how the factor depends on Reynolds number.
55
56
Observing this diagram will lead to the conclusion that only f depends on Re in laminar flow
according to the following formula:
16
f= (3)
ℜ
Replacing the formula (2) and (3) in equation (1) will lead to:
−5 32 × L ×V
∆ P=10 ¿ (4)
D2
The drag coefficient K depends on the ratio R/D between bend radius and inner diameter of the pipe
as well as on the bending angle of the same pipe.
3. Apparatus to be used
57
58
3.1. Procedure
Automatic control
Select the set point with pushbutton SP-W
Set the value of the set point with pushbutton ▲▼
Adjust, if necessary, the value of the gain and integral time controller
Bleed the circuit of all the air
Open the vale V3
Close the angle valve V16
Bleed the circuit of the all air
Open the valve V4
Close the valve V3
Bleed the circuit of all the air
Open valve V5
Close valve V4
Bleed the circuit of all the air
Open the valve V6
Fill the tank D1
Close the valve V5
Bleed the circuit of all the air
Open valve V7
Close valve V6
Bleed the circuit of all the air
Open valve V8
Close valve V7
Bleed the circuit of all the air
Open valve V10
Close valve V8
Bleed the circuit of all the air
Open valve V14
Close valve V10
Bleed the circuit of all the air
After bleeding the hydraulic circuit of all the air, carry out the following operations:
Open the by-pass valve V46 to prevent Hg from flowing out
Select element Calibrated orifice plate by opening its respective valve V6 and closing all the
other valves
Open the valves V20, V21, V44 and V45 until the measuring circuit is bled of all air
59
Close V44 and V45
Open V22 and V23
Close V46
Set the flow rate at 10 m3/h by adjusting valve FV1
Fix the flow rate and read the pressure drop measured before and after the calibrated orifice
on the differential pressure guage
Vary the flow rate of liquid by adjusting the pneumatic valve and detect pressure drop
Open valve V46
Select the venture tube
Open V7 and close V6
Open V20, V21, V44 and V45 until measuring circuit is bled of all the air
Close V44 and V45
Open V24 and V25
Close V46
Set the flow rate at 10 m3/h by adjusting valve FV1
Fix the flow rate and read the pressure drop measured before and after the calibrated orifice
on the differential pressure gauge
Vary the flow rate of liquid by adjusting the pneumatic valve and detect pressure drop
Open valve V46
Carry out the same operations on the other elements of the plant
Test with tracer (laminar flow)
Open the valve V10
Close the valve of the last element used
Close the valve V10
Stop the pump G1
Open the valve V9
Remove the plug of the tank D2
Pour some red ink watered down
Close the plug of the tank D2
Open valve V9 partially
Adjust the valve V1 to obtain a regular flow of the tracer
4. Procedure
Fitting Flow rate (m3/hr) Pressure differential Discharge
(bar) coefficient/Friction
factor
Tube of stainless steel
DN 15
Tube of glass DN 15
Calibrated orifice
plate
Venturi tube
5. Reference
Wilkes, James O. Fluid mechanics for chemical engineers, 2 nd ed., with microfluidics and
CFD
Streeter, V.L., ed., Handbook of fluid dynamics. New York: McGraw-Hill, 1961.
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Title Page (2) recommended title page but
not acceptable
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are missing.
61
10/10 6-8/10 2-4/10 0/10
62
Batch control 2 (3)
Feedback control 3/3 2/3 1/3 0/3
system at 50◦C
Batch control 3 (3)
Feedback control 3/3 2/3 1/3 0/3
system at 40◦C
On/Off control 4 (4)
3-4/4 2/4 1/4 0/4
Graph Temp vs Time
On/Off control 5 (3)
Feedback control 3/3 2/3 1/3 0/3
Time
16-20/20 10-15/20 5-9/20 0/20
Salient points are Some core Salient points are No connection
highlighted and elements are not missing. between the
thoroughly thoroughly theoretical theoretical
discussed. discussed but background and background and
insightful accurate the practical the practical.
Discussion (20) discussion Core element
connection
between between missing.
theoretical theoretical
background and background and
the practical the practical
In-text In-text
Detailed in-text referencing done referencing not in
In-text references No in-text
referencing (Discussion correctly and havard format but
not sufficient reference
sufficiently in references are
and Introduction)
Harvard format. sufficient
Conclusions and Some core Most salient
There is little or
Recommendation elements are not points are missing
Conclusions and no conclusions
is done correctly elaborated in the in the conclusions
Recommendation (10) and salient points Conclusions and and
and
Recommendation
are highlighted. Recommendation Recommendation.
63
cited properly and cited but not
cited, but has not cited or is
in Harvard formatted
errors. cited incorrectly.
format. correctly.
64
6.3 Cooling Tower
Objective:
Apparatus:
65
Experimental Procedure:
Before the start of the experiment familiarize yourself with the equipment.
Make sure the equipment is completely switch off prior start of the experiment
Wet the wick of both wet-bulb temperature probes (t2 and t4) with tap water.
Fill the load tank above the minimum water level.
Fill the make-up tank with tap water (approx.1.2 L) use a measuring cylinder.
Switch the equipment on with zero heat load (0 kW).
Adjust the water flow rate to 30g/s.
Make sure the damper on the fan is close.
Let the equipment run for at least 10 minutes to wet the packing and to stabilize the
equipment.
Switch the equipment off again and increase the heat load to 0.5 kW.
Fill the make-up tank again with tap water (see the mark on the tank).
Use a measuring cylinder to measure how much of the tap water you have added.
Switch the equipment on and make sure the orifice differential over the packing is
about 16 mm H2O by adjusting the damper setting on the fan.
Keep the operating conditions constant for the entire operation.
Record the make – up rate after 10 min.
Record the temperatures (t1 – t6) after 30 min.
Increase the heat load to 1 kW and keep operating conditions the same.
Record the temperatures (t1 – t6) after 30 min.
Increase the heat load to 1.5 kW and keep operating conditions the same.
Record the temperatures (t1 – t6) after 30 min
Safely switch off the Apparatus.
Experimental Data
66
Operating Time(min) 30 30 30
T1 (air inlet dry-bulb temperature)
T2 (air inlet wet-bulb temperature)
T3 (air outlet dry bulb temperature)
T4 (air outlet wet bulb temperature)
T5 (water inlet temperature to tower)
T6 (water outlet temperature from the
tower)
Orifice differential mm H2O 16 16 16
Heat Load kW 0.5 1. 1.5
Water flow rate (g/s) 40 40 40
Table C.1: Experimental data table
67
Theory/Background
The Bench top Cooling Tower is designed to provide an understanding of the construction,
design and operational characteristics of an evaporative cooling system. It is an example of
an “open system” through which two streams flow (water and air) with a mass transfer from
the one to the other. The configuration is similar to a full-size forced draught cooling tower.
The Water Cooling Tower in the Chemical Engineering laboratory is illustrated in Fig. C.1. It
is completely self-contained and includes both the simulated heating load and the circulating
pump. It has much the same configuration as a full size force draught cooling tower, has the
same characteristics and stabilizes quickly. In this unit a fan is placed at the base of the tower
to drive air upwards through the packing. Natural buoyancy assists the fan and helps dissipate
the humid air from the top of the tower. A float valve is provided to allow accurate
measurement of 'make-up'. When the cooled water falls to the load tank it is reheated before
circulation.
The difference between the exit- water temperature and the entering air wet-bulb temperature
is called the “wet-bulb temperature approach”.
Water loss due to evaporation, entrainment or “blow down” can be calculated by performing
a mass balance around the cooling tower.
Heat been removed from the hot water can be calculated by performing a energy balance
around the system and also using the available Psychrometric chart for air-water at
atmospheric pressure.
m a=0.0137
√ x
va
× A …………………………………………………………….[1]
Where:
.
ma = mass flow rate of air, kg/s.
68
v a = specific volume of air leaving top of column, (m3/kg)
When mass and energy balances are considered, there should be proper assumptions made
and bases stated that satisfy the current situation of the system. Credit will be earned for
proper statement, assumptions and organized work.
69
Results
Discussions
References
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70
2/2 1/2 0/2
Used the
Used the recommended
Title page used is
Title Page (2) recommended title page but
not acceptable
Title page. some elements
are missing.
Results (20) Indicates clearly Indicates the Does not Indicate The Analysis of
the formulas used formulas but does the formulas and data does not
and step-by-step not follow a step- does not follow a work at all as
procedure of by-step procedure step-by-step required.
calculating one of calculating one procedure of
71
calculating one
set of tabulated set of tabulated
set of tabulated
results results
results
In-text In-text
Detailed in-text referencing done referencing not in
In-text references No in-text
referencing (Discussion correctly and havard format but
not sufficient reference
sufficiently in references are
and Introduction)
Harvard format. sufficient
Conclusions and Conclusions and Some core Most salient There is little or
72
are highlighted. Recommendation Recommendation. n
73
CHEMICAL ENGINEERING LABORATORY
Course Information and Laboratory Schedule
OBJECTIVES
GROUP PRACTICALS/ASSIGNMENTS
A student will be designated by the group as the group leader for one experiment and others
assigned different roles within the team. These roles are expected to be rotational in
subsequent experiments.
See the Lab rooster on notice board in front of Lab G403 and Chemical Engineering
Departmental notice board (4th floor)
74
PARTICIPATION IN LABORATORY
It is expected from Students to come prepared to the Laboratories (e.g. Must be in possession
of his/her own Laboratory Manual, PPE, have an idea of what is expected during the
experiment). Students must have adequate background of the subject matter before
conducting the experiments. Each member of the group is expected to be thoroughly familiar
with the practical as well as the theoretical aspects of the experiments. Each group member
will be judged individually and the grade will be assigned accordingly.
Group leaders are expected to direct the experiment and coordinate data collection. The
leader should plan a division of tasks, know what data is to be acquired and devise an
experimental plan. The other Students are expected to be knowledgeable and provide
technical assistance to the group leader. Students will be judged by the Laboratory Assistants
on their active participation in the laboratory according to their role. Students will be quizzed
by Laboratory Assistants in the Laboratory (ad hoc basis). The quiz questions will cover both
theoretical and practical aspects of the experiments. Responses to questions as well as active
participation in the Laboratory will both contribute to the participation grade.
FORMAL REPORT (refer to the Guidelines for Technical Report Writing Manual)
Students will also be assessed based on their verbal presentation skills. All Students will be
expected to submit a group report (will be announced during the lab session) for the Fluid
Dynamics or Liquid Diffusion Experiment and make an oral presentation (not more than 10
slides) thereafter. It is highly recommended for Students to prepare their presentation on
Microsoft Power Point.
A timetable will be put out for the Presentations on a weekly basis (see notice board). It is
preferred that all the Presentations will take place on Fridays after the submission of the
report (see notice board for any other day/schedule).
Reports are due a maximum of two weeks/10 working days after the experiment; 5% will be
deducted for each day’s delay. The formal report should be no more than 15 typed pages in
length excluding Appendices (pending on the type of experiment).
75
Reports are due a maximum of two weeks/10 working days after the experiment; 5% will be
deducted for each day’s delay. The formal report should be no more than 15 typed pages in
length excluding Appendices (pending on the type of experiment).
LAB ASSIGNMENTS
Lab Assignments are due a maximum of 5 working days after the experiment. No late
submissions are accepted. The assignment should be no more than 10 typed pages in
length (pending on the type of experiment). The format will be explained during the Practical
session.
GRADING SCHEME
Please keep in mind that the course module is a continuous assessment module, basically the
student need to write all lab tests and submit all Lab reports and assignments to pass the
module. A pass mark of 50 % must be obtained to pass the module.
76
Total 100%
Breakdown of Lab
assignments:
Assessment type Lab Assignment Weight
GROUP REPORT
Pre - practical questionnaire – 5% (a pre - practical test will be written before the
practical).
Group Report – 60 % (The mark obtained for the lab report will be assigned to each Student
in that particular Group).
TOTAL – 100%
Students will be examined on the following criteria during the presentations:
77
90% Contribution
Technical Content Presentation Skills
Intro & Results Conclusio Slide Communication Time
Methodology
Aim Interpretation n Quality Skills Penalty
10 10 20 20 10 10 10
10% Contribution
Question Handling per each student in a group of four
1 2 3 4
10 10 10 10
ASSESSMENT OF THE REPORTS
Students can consult with the Laboratory Assistant five days after submission of the report
(See Consultation Time Table of the Laboratory Assistant).
All the Students have five days to consult after the marks have been published on the notice
board. No marks will be changed after these prescribed five days.
It is therefore expected that Students must submit their Reports on time (BEFORE 12
0’CLOCK ON DAY OF DUE DATE), if fail to abide to this rule 5% will be deducted for
each day of late submission.
PLAGIARISM
78
Please Note:
The above mentioned are STRICTLY not allowed. Any student who fails to abide by these
rules will obtain 0% and will be given a final written warning. Please read the UJ Policy
regarding plagiarism.
It is impossible to carry out the experiments in a useful and intelligent manner without
adequate knowledge of the principles of the particular subject matter. It is strongly
recommended that Students make a conscious effort to learn the underlying theory of the
experiment being carried out.
PROCEDURE
Before starting an experiment, a student must become thoroughly familiar with the equipment
provided in the laboratory and its safety protocol. The following procedure must then be
followed.
ANALYSIS
With the experimental data collected in the Laboratory it should be possible to make a
reasonably complete assessment of the performance characteristics of the experimental
apparatus. Detailed steps to be followed will obviously vary from one experiment to another.
LABORATORY SAFETY
All Students must abide by the laboratory safety rules. Lab coats and safety glasses must be
supplied by each Student. Please note that contact lenses should not be worn in the laboratory
– wear glasses instead. Details are provided in the Safety Protocol Manual
80
81