Industrial training report - Dangote sugar refinery
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Transcript of Industrial training report - Dangote sugar refinery
CHAPTER ONE
INTRODUCTION
1.1 BACKGROUND INFORMATION
In the earlier stage of Science and Technology
education in Nigeria, students were graduating from
their respective institution without any technical
knowledge or work experience. It was in this view
that students undergoing Science and Technology
courses where mandated for students in different
institution in the view of widening their horizons so
as to enable them have technical knowledge or working
experience before graduation.
The student industrial work experience scheme (SIWES)
is the acceptable skill training program, which forms
part of the approved minimum academic standard in the
various degree programs for all the Nigerian
universities. It is an effort to bridge the gap
between theory and practice of engineering and
technology, sciences, agriculture, medical,
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management and other professional educational
programs in Nigerian tertiary institutions. It is
aimed at exposal to machines and equipments,
professional work areas and workers in industries and
other organizations. The minimum duration of the
program is directed by the industrial training fund
(I.T.F) and the National universities commission
(N.U.C). The scheme is a tripartite program involving
the students, universities and industries (employers
of labour). It is founded by the federal government
of Nigerian and jointly coordinated by I.T.F and
N.U.C.
1.2 BRIEF HISTORY OF THE SIWES UNIT
The Industrial Training Fund (ITF) established
Student Industrial Work Experience Scheme (SIWES) in
1973 to solve the problems of lack of adequate
practical skills preparatory for employment in the
industries by Nigeria graduates of tertiary
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institutions. The scheme was designed to expose
students to industry based skills necessary for
smooth transition from the classroom to the world of
work and enable them develop occupational
competencies so that they can readily contribute the
quota to national economic and technological
development after graduation. It offers students of
tertiary institutions the opportunity of being
exposed familiarized and exposed to the needed
experience in real time job demands.
1.3 OBJECTIVES OF SIWES
Specifically the objectives of the student’s
industrial work experience scheme are to:
i. Provide an avenue for students in Nigerian
universities to acquire industrial skills and
experience in their course of study.
ii. Prepare students for the work situation they
are likely to meet after graduation.
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iii.Expose students to work methods and techniques
in handling equipments and machinery that may
not be available in their universities.
iv. Make the transition from the university to the
labour world easier and thus enhance students’
contacts for later job placement.
v. Provide students with an opportunity to apply
their theoretical knowledge in real work
situation, thereby bridging the gap between
universities and actual practices.
vi. Enlist and strengthen employers’ involvement
in the entire educational processes of
preparing university graduates for employments
in the industries.
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CHAPTER TWO
2.1 BRIEF HISTORY OF DANGOTE SUGAR REFINERY
The Dangote Sugar Refinery is a subsidiary of Dangote
Group located in Lagos State, at Nigeria’s largest
port, The Apapa Wharf. The company commenced business
in March 2000 and the sugar refining plant was
commissioned in 2001, with an initial capacity of
600,000MT p.a. The company imports raw sugar from
Brazil and refine it into white granulated sugar
5
which is divided into two types; FORTIFIED and NON –
FORTIFIED sugar.
The fortified white sugar contains Retinol (vitamin A)
while the non-fortified white sugars are for industrial
use and it is not fortified with retinol. Dangote
Sugar Refinery PLC is in the business of refining
white sugar using new technology of ION EXCHANGE
RESIN (I.E.R).
The Dangote Sugar Refinery has excellent facilities
designed and installed by TATE and Lyle for
production of refined sugar. TATE and TYLE is the
largest sugar refinery in Europe and its refining
technology is regarded as one of the best in the
world.
The company’s operation comprises two key business
areas; refining of raw sugar imported from Brazil and
marketing and distribution for direct consumption and
industrial needs. In compliance with the National
Agency For Food Drug Administration And Control
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(NAFDAC) policy, which makes the fortification of
staple foods mandatory in Nigeria, Dangote Sugar
Refinery PLC produces and packages fortified refined
white sugar in 1kg, 500grams, 250grams and 50kg bags
for direct consumption under the brand name ‘DANGOTE
SUGAR’ as well as the unfortified white sugar for
industrial use and sells its product across Nigeria.
Interestingly, ‘D.S.R’ is one of the very few sugar
refined in the world that produces RETINOL fortified
white sugar at its Apapa factory under strict NAFDAC
policy.
2.2 OBJECTIVE OF DANGOTE SUGAR REFINERY
Touch the lives of people by providing their
basic needs.
To become a global, integrated, low cost sugar
producer focused on maximizing long term
shareholder returns while establishing a leading
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Safety is an act of being safe in the line of duty.
It ensures that all staffs must observe and adhere to
all protocols, precautions and procedures in order to
avoid accidents and injuries. Safety entails in using
what is known as P.P.E that is ‘personal protective
equipments’ which includes:
Wearing of Hand-gloves to avoid chemicals eating
up the fingers etc, then eye goggles to avoid
spillage of chemical or light rays.
Safety boots to avoid metals or nails
perforating through your soft shoes.
Nose mask to avoid inhaling the chemicals.
Helmet to prevent any metal drop or accidental
hit on the head.
Laboratory coat to prevent spillage of chemicals
on the body.
Hair net to avoid contamination of the sugar.
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The basic precaution is the use of our hand
sanitizers to get rid of germs and to prevent the
dangerous disease called EBOLA. There is always a
penalty for staffs that are reported for lack of
P.P.E. and if an accident is reported also, the first
question is if the P.P.E is on or not on use.
PICTORIAL VIEW OF DANGOTE RAW SUGAR
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PRE- MELTING STAGE
MELTING STAGE
CLARIFICATION STAGE
DECOLORIZATION STAGE
EVAPORATION STAGE
CRYSTALLIZATION STAGE
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CENTRIFUGATION STAGE
DRYING STAGE
BLENDING/ROTEX STAGE
FORTIFICATION STAGE
BAGGING STAGE
PRE-MELTING STAGE
This stage is the first unit in Dangote Sugar
Refinery and is also known as the VERY HIGH POLARITY
[V.H.P] STAGE. The pay loaders conveys the raw sugar
into the oban pan which have a hole underneath that
allows sugar to drop on the belt drag out conveyor,
then it drags the sugar down to the elevator and
inside the drag out there is a magnet which magnets
any metal found in the raw sugar before it goes to
the elevator. The elevator, which have a bucket
inside now transfers the raw sugar to the silo [V.H.P
sugar hoppers], then the screw drag out conveyor
drags the sugar to the pre melting tank which have a
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sever that sieves all the unwanted particles from the
raw sugar. Inside the boiling tank there is a rod
stirrer that spins around to dissolve the sugar once
it gets to the tank to avoid clots/lumps of sugar.
The water used in boiling the sugar is called sweet
water after boiling the slurry pump will open and
transfers the liquor to the next stage. Expected Brix
here is 66-67.
MELTING STAGE
This stage detects and corrects the carryovers done
in the first stage. If the brix is too high or too
low this stage will report to the first stage and
they will make amendment. They use steam to control
the brix, the higher the steam the lower the brix and
vice versa. There is Lin catchers here that further
detects the carryover dirt from the first stage and
then trap them. At this stage it is assumed that the
16
sugar has been completely dissolved before it goes to
the next stage.
N.B: At every stage there is an expected range of
brix. Expected brix here is 62-64.
TALOCLARIFICATION STAGE
17
This is where the Dangote Sugar Refining unit place
more emphasis in removing the impurities present in
the melted liquor, this stage is an essential part of
the raw sugar processing. Taloclarification is the
removal of color and turbidity from melted liquor
through the process of flocculation, floatation and
separation techniques. The main objective here is
removal of 90percent of turbidity and 40percent of
color then the main parameters we check here is the
brix, temperature, and the pH. When we have a low
brix it creates high turbidity of the liquor and when
it’s too low it creates filtration problem. The
expected brix in taloclarification is 62-63.Also when
we obtain a high temperature it tends to increase the
expected color of the liquor while low temperature
will result to incomplete reaction of the liquor.
Expected temperature here is 80-84. PH of the liquor
is very important here, when the pH is low the sugar
will be very wet and will not dry well because it is
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acidic, and also it will cause inversion of sugar
that is the splitting of sucrose to glucose and
fructose. It will be inform of dust and the expected
grain size will be lost. But when the pH is high it
causes high color formation. Expected pH here is 6.9-
7.2.
NOTE; When we discover a high pH and high temperature
in the liquor solution we recycle it back to the
melting stage for curing.
4 chemicals are added here in talo-clarification
namely;
Phosphoric acid which is colorless and odorless. It
serves as a neutralizing agent.
Hydrated lime; it helps in the decolorization of
the liquor.
Talofloc; this is the main decolorizing agent that
further breaks down the particles into smaller
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particles and they come together with the aid of
stirrer in the reaction tank.
Taloflote[flocculants]; this makes the aggregated
particles in the liquor solution to float on the
liquor thus enable proper separation of the scum
from the clarified liquor .flocculants are
advantageously use in the sugar clarification cause
it helps to float the scum present in the liquor
solution.
SCUM
This is a layer of dirt formed on the surface of a
liquid, or the firmly layer of an impure matter that
rises to the surface of the liquor solution.
HEAT EXCHANGER: This is a device in taloclarification
process that increases the temperature of the liquor
solution to the expected temperature [80-84] so that
a complete reaction can take place as the liquor gets
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to the reaction tank. Shell and tubes heat exchanger
is used such that the liquor will run through the
heated tubes and the steam flows through the shell so
that heat can be exchanged between the two fluids. In
Dangote Sugar Refinery we have about 144 tubes in one
heat exchanger.
DECOLORIZATION STAGE
This stage makes use of ion exchange resin and resin
is the chemical that mainly extracts all the
colorants from the liquor solution. By definition;
ion exchange resin or ion exchange polymer is an
insoluble matrix normally in form of small [0.5-1mm
diameter] beads, usually white or yellow in color.
The beads are typically porous, providing a high
surface area. The trapping of ions occurs with
concomitant releasing of other ions thus the process
is called ion exchange. Resins are widely used in
different separation, purification and
decontamination processes.
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We have two types of resin commonly use in ion
exchange process. Namely; the cation resin and anion
resin.
Cat ion resin are those resins that attract the
positively charge ions in a solution. Anion resins
are those resins that attract the negatively charged
ions in a solution, and that is the one we make use
of in Dangote Sugar Refinery because the liquor is
cationic in nature. The resin inside the batteries is
what carries out the decolorization process because
it attracts all the cationic ions and colorants to
itself and an improved state of liquor will be
obtained. In this stage we are focusing on bringing
down the turbidity of the liquor sample by 30-40 with
the help of our pressure filters. One pressure filter
pan in Dangote Sugar Refinery contains about 36filter
beds and the membrane is about 46micron meter in
space that can hardly allow any form of impurity to
penetrate. Normally once the pressure filters absorb
22
much impurity it will automatically stop functioning
until the beds are changed. The liquor gotten from
the pressure filters are named polished filter liquor
because it is now free from any form of impurity and
thus ready for crystallization.
EVAPORATION STAGE
Evaporator is a device in Dangote Sugar Refinery that
is used to brix up the liquor solution by eliminating
excess water from the liquor solution thereby
providing a fine liquor very thick example pap. The
expected brix in this stage is about 70-80.from this
stage we get our massecuite which is the mixture of
syrup and the sucrose then it goes to the next stage
which is crystallization stage
CRYSTALLIZATION STAGE
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Crystallization is done under vacuums in Dangote
Sugar Refinery to avoid color formation, to reduce
the rate of steam consumption, to avoid excess loss
of sucrose, to lower the evaporative equipment and to
reduce the operative temperature. Slurry is added in
this stage for crystal formation and the slurry
timing determine a good grain size of the sugar. One
vacuum pan contains about 600-750bags of sugar per
yield batch. In this stage liquor boils at about 1;
30minutes per strike before it goes on to the next
stage called centrifugal stage
PREPARATION OF SLURY
Take 1.620kg of sieved sugar [600micron or 0.6mm]
with 3.6 liters of Isopropyl alcohol. Put into the
slurry machine and switch the machine on for 24hours
then slurry is formed.
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CENTRIFUGAL STAGE
This is the stage were separation of sugar crystals
from the mother syrup takes place using a batch
centrifuge. Batch centrifuges consist of a metal
basket1220mm in diameter, the holes of which are
smaller moving towards the centre. A thin perforated
copper plate called a mesh or cloth with 0.5mm
diameter holes is placed on the side. The basket is
mounted on a vertical shaft through a bearing which
connects to an overhead drive motor. There will be
between 20-26batches or cycles per hour, each cycle
starts by charging the basket with massecuite as it
rotates at 250rpm. An evenly distributed full charge
of massecuite would be 203mm thick and weigh 1250kgs.
The basket accelerates to 1500rpm for a present
period then decelerates to 50rpm at which speed the
spun sugar is removed by a ploughing mechanism. The
unit is then ready for the next cycle. During the
25
cycle, a wash is applied to centrifugal machine to
remove residual syrup adhering to the crystals. From
the centrifuge the sugar is then conveyed to the next
stage which the sugar dries
DRYER
Sugar leaves the centrifuges containing between ½ and
11/2 moisture. The majority of water is driven off in
the driers. There are three driers in Dangote Sugar
Refinery each capable of drying 30 tones of sugar per
hour. The driers are horizontal cylindrical vessels
approximately 2.7m in diameter by 12m long [9 feet in
diameter by 40 feet long]. The driers are of co-
current design, that is the air and the sugar both
travels through the driers in the same direction.
Both hot air and cold air are applied to the drier
for drying and subsequent cooling of the product. The
hot air enters the drier through a vent inside the
vessel and passes through a bed of sugar. The air
26
then travels down the air space inside the drier. As
the drier drum is rotating at 10rpm, sugar is carried
up to a height and then falls to the bottom forming a
curtain down the length of the drier. The hot air
passes through the curtain of sugar. Typical hot air
temperatures are 50 to 60’c. Air at ambient
temperature is applied to the drier to cool the
sugar.
BLENDING STAGE
This is a unit in Dangote Sugar Refinery were the
grain sizes of the sugar sent from driers are
determined before going to the fortification section.
They make use of a Rotex machine which have a screen
mesh opening of 0.067mm.it sieves the sugar and send
the lumps to be recycled.
FORTIFICATION STAGE
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Fortified sugar is made by adding the vitamin A
premix to the sugar either in the centrifuge at the
end of centrifugation, over the belt conveyor that
leads the sugar to the drying turbines or after
drying when the sugar is moving down to the packing
chutes. A reliable mechanism is used to ensure that
homogeneity of the vitamin A content in sugar is
maintained. Premix contains sugar, retinyl palmitate,
vegetable oil, and an antidioxidant. The premix is a
free flowing product that is light yellow in color,
slightly oily to touch, and smells like retinol.
Premix that is stored for more than 2months or that
is badly prepared or inadequately stored can develop
an unpleasant rancid smell indicating that the oil
has been oxidized. The premix is prepared inside the
v-shaped blender and the range at which we add it is
1kg of vitamin into 1000kg of sugar. The cremix
(coconut oil) we use in dangote sugar refinery is
28
imported from Malaysia.
BAGGING SECTION
The sugar leaves the driers and is conveyed to silo,
which is capable of storing a maximum of 80 tones of
sugar each. From the silo the sugar passes over
magnets to further check if there is trace of any
metal object, then is sieved again to remove coarse
lumps of sugar, and finally bagged in 50kilo bags.
Then the belt conveyor carries it down to where the
trucks are packed.
THE TYPES OF SUGAR WE GET IN THE REFINERY.
HIGH GRADE SUGARS
- R1 == This is the very first sugar and is very
white.
- R2 == This is the second run off sugar and is
not as white as R1
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- R3 == This is called run off 3 sugar not as
white as R2 but closer
- R4 == This is run off 4 sugar more or less
like a brown sugar
LOW GRADE SUGAR
A- SUGAR= This is gotten from the R4 sugar and is
brownish in color just like the raw sugar.
NOTE: From A Sugar we get our molasses which some
industries order to make their chocolate, malt,
biscuit and other foods.
30
CHAPTER FOUR
QUALITY ASSURANCE DEPARTMENT
ANALYSIS CARRIED OUT IN THE LABORATORY
pH determination; collect your samples and
cool to room temperature then using your glass
beaker take some samples out and immerse the
probe of the electrode inside the sample and
take the reading on the display of the meter.
Calibration of pH meter; this is a process
whereby the pH meters are standardized or made
31
ready for efficient measurement via buffer
solutions. (i.e. 7,4,10 etc) to forestall
deviations and/or correct errors.
Types of buffer for
calibration of the pH:
1). Buffer 4 solution: This is used to calibrate
the pH meter based on the acidity level or range.
2). Buffer 7 solution: This is used to calibrate
the pH meter based on the neutral range.
3). Buffer 10 solution: This is used to calibrate
the pH meter based on the alkalinity range.
32
Pictorial View Of the p.H meter.
DETERMINATION OF COLOR AND TURBIDITY IN SUGAR
SAMPLES
EQUIPMENTS USED: spectrophotometer
- spectrophotometer cells
33
- brixometer
- vacuum filtration apparatus, capable of
supporting 0.45um filter pads
- vacuum filtration flasks 250ml or 500ml capacity
- vacuum pump
- filter pads 0.45um
- beakers
- shakers/stirrers
- analytical balance
- distilled water
PROCEDURE:
Weigh 50g of sugar sample into your conical
flask, dilute with 50g of distilled water
making it 100g.
Using your orbital shaker, dissolve properly
until no trace of sugar grains
Check the brix on the brixometer
machine.
34
Using the vacuum pump filter the sample
through a membrane filter of pore
size/diameter 50mm respectively into a clean
dry conical flask
Using the talameter machine, determine
absorbance of filtered solution with 10cell
lens
Take your readings and calculate the
results.
Formula: IU= A/BC, where A is the absorbance
B is the cell length
C is the brix factor
IU is ICUMSA, unit for measuring colour
ICUMSA stands for international commission for
uniform method of sugar analysis.
35
Determine absorbance of unfiltered solution
and calculate the turbidity using
AU= (Aunf --Afil) *f/b where Aunf is unfiltered
absorbance
A fil
is filtered absorbance
f
is the brix factor from turbidity table
b
is the cell length and AU is absorbance unit, unit
for measuring turbidity.
DETERMINATION OF VITAMIN PRESENT IN THE SUGAR.
SAMPLE; BAGGING LINES.
Equipments; Orbital Shaker, Weighing balance, Text
tubes, Text tube rack, Glass beaker, Distilled water
and Spatula.
Procedure:
36
Using ratio 1:1, weigh your sample and
dissolve with distilled water
Place on the orbital shaker and switch it on
to further dissolve the solution evenly
Using your text tube rack, pour small quantity
of the dissolved sample
Add 5ml of chromogenic reagent and take your
reading immediately you see color change. If
no color change it means vitamin is absent.
37
Orbital Shaker
ANALYSIS ON A- SUGAR SAMPLE
EQUIPMENT: metal beaker, hot plate stirrer,
brixometer, distilled water, weighing balance and
spatula.
38
Procedure:
Place your metal beaker on the weighing
balance and tare
Measure 30g of sample and dilute with 70g of
distilled water
Put magnetic stirrer into the sample and place
on the hot plate stirrer and dissolve
Check your brix using the brixometer machine
Filter straight using the vacuum pump
Check the absorbance using the talameter
machine with 1cm cell lens
Take your readings and calculate your result.
Formula; filtered absorbance/cell length/brix
factor
ANALYSIS ON MOLASSES ALSO KNOWN AS RECOVERY
The molasses include; A molasses, B molasses, C
molasses and final molasses.
39
Procedure; using your metal beaker weigh ratio 1:1 of
sample and distilled water
- add your magnetic stirrer and place on the hot
plate then dissolve
- allow to cool to room temperature and check your
brix
- using your 50mil flask place on the weighing
balance and tare then measure out 13gram of
diluted sample
- add octapol to it and fill the flask up to the
mark with distilled water
- filter straight using the acetate filter paper
then take the filtrate
- using the saccharimeter machine place the sample
and check the polarity
- Then calculate your readings using the formula:
4 multiply by the polarity/2 multiply by brix
factor then multiply by 100/1.
40
Vacuum Pump
ANALYSIS ON SCUM
- Using your 50ml flask place on the weighing
balance and tare
- Measure 26g of sample add octapol and dilute
with distilled water up to the mark
- Filter using the acetate filter paper and
collect the filtrate
41
- Using the saccharimeter machine place the sample
on it and take your readings
- From the polarity we determine if the impurity
is high or not.
DETERMINATION OF THE SUGAR SIZES (MA/CV)
- Arrange preweighed sieves of varying apertures
sizes, 850u, 600u, 500u, 425u, 300u, 212u and
base pan in descending order recording the
weights.
- Weigh in 100g of the refined sugar sample into
the first sieve and cover
- place on the mechanical shaker, shake for
15minutes
- Reweigh and record the final weight and take
the readings
- With the result the sugar analyst will determine
if the grain sizes are okay or if is too dusty.
42
SPECIAL LABOURATORY ANALYSIS ON LOW POUR FUEL OIL
(LPFO)
A). FLASH POINT
This is the temperature at which the vapor of the
fuel wills a flame. This analysis is carried out to
check the burning ability of automated gas oil
(A.G.O) and the burning ability is the temperature
explosion of the product.
PROCEDURE:
-Fill the sample chamber to the mark with the sample
- Ignite the gas source
- Switch on the tester
- Insert the thermometer
- Stir the sample with the stirrer checking the
temperature at intervals
43
- Note and record the exact temperature at which the
vapor of the sample flashes
- Then you switch off the tester.
REDUCING SUGAR ANALYSIS (INVERT SUGAR)
Inverted or invert sugar syrup is a mixture of
glucose and fructose, it is obtained by splitting
sucrose into two components. Compared with its
precursor, sucrose, inverted sugar is sweeter and its
product tends to retain moisture and is less prone to
crystallization. Sucrose is a disaccharide which
means that it is a molecule derived from two simple
sugars (monosaccharide). In the case of sucrose,
these monosaccharide building blocks are fructose and
glucose. The splitting of sucrose is a hydrolysis
reaction and hydrolysis is a chemical reaction in
which a molecule breaks down by the addition of
water.
44
The essence of carrying out this analysis is to stop
inversion of sugar from taking place in the sugar
refinery because once inversion of sugar takes place
we term to have a very low yield of the sugar. Things
that could stop inversion of sugar from taking place
may include regulation of the temperature to the
expected range and pH.
PREPARATION OF SOME REAGENTS USED:
A). EDTA solution: prepare a solution containing
0.930g per liter of the disoldium salt of
ethylenediaminetetra-acetic acid (EDTA) as required
and discard after use. Alternatively dilute 50ml of
o.o1mol\L EDTA solution to 200ml as required.
B).MUREXIDE INDICATOR: Prepare by grinding with
pestle mortal 0.5g of the murexide which is in powder
form and store in a dessicator over silica gel
because humid conditions tend to cause caking. A
solution of an indicator is not stable.
45
PROCEDURE:
- Weigh accurately 5g of sugar into a text tube
- Dissolve in 5ml of distilled water by shaking
without warming
- Add exactly 2ml of alkaline copper solution
- Thoroughly mix the tube and immerse in a boiling
water bath for 5minutes
- Cool immediately in a cold bath
- Transfer the tube contents and washings to a
white conical flask
- Add approximately 0.1g of the indicator by means
of a small spatula or flattened glass rod
- Titrate the solution with the EDTA solution
while stirring with a glass rod
NOTE: EDTA should be added from the burette to the
conical flask continuously through the titration
procedure and maintain the stirring of the solution
46
at all times. As the end point is approached the rate
of addition of EDTA can be slowed to 2-3drops per
second but should never be stopped, until the end
point is reached. The reason for this is that the
color formed can disappear due to oxidation, meaning
that if the titration is stopped an incorrect
estimation of the end point may be made, after
restarting the titration. The colour change during
the titration is gradual, the solution starts from
green, will turn to grey and finally purple. These
changes are gradual, but the end point can be
considered to be reached when the first full purple
colour (i.e. ., when the body of he whole solution is
purple) has been reached.
On stopping the titration, there should be no concern
if the colour starts disappearing. This is due to
oxidation and no more EDTA should be added, every
sample should be analyzed in duplicate to ensure
47
accurate estimation of reducing sugars. The reducing
sugar content is obtained from the table.
MOISTURE ANALYZER
This is one important aspect in final stage of
granulated white sugar before the bagging stage in
order to avoid caking of sugar because we cannot bag
a wet sugar. The normal sugar
Moisture value should not exceed 0.04.
OPERATING INSTRUCTIONS:
- Switch on the moisture analyzer
- Open the sample chamber and place an unused
sample pan on the support
- When “g” appears, press enter key to tare the
sample pan.
- Weigh approximately 10g of your sample
- Close the sample chamber
- When “g” appear again, press the enter key to
start the analysis
48
- The machine will make a sound and indicate end
then you take your readings.
LIQUOR ANALYSIS
1). BRIX
- Pace the liquor in the sample compartment of the
meter
- Take direct reading from the brixometer as
displayed on the screen
2). pH
- Cool the liquor in a cold water bath
- Insert the pH probe into the liquor
sample
- Take the reading displayed on the screen
when the meter beeps
3). COLOR/TURBIDITY
- Take the original brix of the liquor
- Weigh 30g of melt and 50g for other liquors
49
- Add distilled water to make to a weight
equivalent to the original brix and mix well
with your spatula
- Filter the sample solution under vacuum through
a membrane filter of pore size 0.45um/50mm
respectively into a clean dry conical flask
- Turn on the talameter, set the wavelength at
420nm and zero with distilled water using your
cell lens
- Determine absorbance of filtered and unfiltered
solution
- Take your readings and calculate its colour and
turbidity.
MICROBIOLOGY DEPARTMENT
This is another department in Quality Assurance that
sees to the progress of dangote sugar refinery.
Equipments used in carrying out analysis
in microbiology laboratory:
50
Autoclave: This is a machine used to sterilize
our prepared agar under heat and pressure at a
temperature of 121%C.
Incubator: This is a machine where we incubate
or culture our plates.
Laminar flow cabinet: This is a hood where we
carry out analysis because is said to be free
from microorganisms.
Lumitester: This is a machine used to carry out
swab test.
Ultra violet light: This helps in sterilizing
the environment before an analysis is carried
out.
Air conditioner: This machine prevents the
growth of microorganisms because some microbes
grow at a higher temperature so with the help of
air conditioner we regulate their temperature.
Colony counter: This is a machine used in
counting our incubated plates.
51
Refrigerator: This is a place where we store our
Petri dishes, Agar, Sterilized swab sticks,
Spatula etc.
Microscope: This machine is used to view
organisms that can not be seen with naked eyes.
Magnetic stirrer/hotplate: This is a machine
used to dissolve a substance.
Analytical weigh balance and Top weigh balance:
This is machine used to take measurement of
samples.
Thermometer: This is an instrument used to
measure the temperature of products.
Hot air oven: An instrument used in drying our
equipments examples; conical flask, spatula,
glass Petri dishes, sampling bottles, pipettes,
etc.
Analysis carried out in microbiology
laboratory:
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Raw sugar analysis
Refined sugar analysis
In process liquors
Water analysis
Sanitation
Environmental hygiene monitoring (swab test)
Miscellaneous.
Determination of temperature of all the equipments
used in the microbiology labouratory. All the
equipment has a standard temperature for example:
Incubator 25*C
Big incubator 35*C
Refrigerator 4*C
Thermometer 100*C
Air conditioner 18*C
Hot air oven 50*C
NOTE: This analysis is done every
Monday before carrying out analysis of that
week.
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Procedure:
Using ethanol and cotton wool clean your
thermometer very well to sterilize it.
Insert or place the thermometer on the
equipment
Allow to stand for 5minutes
Take your readings in that equipment before
bringing it out so that the temperature in
the environment will not affect your
readings.
Using your Hot plate machine, boil water
until bubbles appear
Insert the thermometer in the hot water,
once the red mark reach 100* then is ready
Allow to cool and store in the
refrigerator.
Water Analysis
SAMPLES: Boreholes
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Aqua - plant A, B, C
Treated water tank
Refinery taps
Canteen/kitchen taps
Control: negative and atmospheric
Frequency: Weekly
SAMPLING:
Samplings are carried out using sterilized 25ml
capacity universal sampling bottle with caps. Clean
disposable hand gloves and nose masks should be worn
during sampling. Samples are collected aseptically
from representative points within the refinery.
METHOD:
Clean and disinfect the working area with
ethanol before commencing the analysis.
Prepare and sterilize your agar medium in the
Autoclave at 121^C for 15minutes
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Aseptically expose two poured plates of plate
count agar (PCA) and potato dextrose agar (PDA)
on work surface area to serve as atmospheric
control.
Pipette 1ml of water sample into sterile marked
plates with dates for PCA and MCA
Cool sterilized agar (medium) to about (45-47)*C
in a water bath, then pour about 20ml each of
molten prepared agar of PCA and MCA into marked
plates.
Tilt/mix plate by rotating gently to avoid
spilling of content, pour about 20ml of same
molten prepared agars of PCA and MCA into
another sterile labeled plates without water
samples. These represent the negative control
and if any growth is found in this control, it
invalidates the result of the analysis done.
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Allow plate to solidify then invert and incubate
plate. PCA plate and MCA plate are incubated at
30*C for 48hrs.
Count colonies and record.
NOTE; Results are reported in colony forming unit
(CFU) per ml.
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CHAPTER FIVE
WATER TREATMENT DEPARTMENT
Water treatment is, collectively, the industrial
scale processes that make water more acceptable for
end-use, which may be drinking, industry, or
medicine.
In Dangote sugar refinery, we have 3 divisions of
Aqua plants in water treatment department and each
comprises of 3 different sections.
The reaction tank chamber
The sedimentation chamber
The filtration chamber.
REACTION TANK CHAMBER:
Here the chemical added is known as the caustic soda
(NaOH). The essence of adding this chemical is to
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boost the pH of the water from 6.5 to 7.0 normally
the source of the water we used in the Dangote sugar
refinery is from boreholes and there are about 7
boreholes in the refinery and the pH of the different
boreholes are very acidic and thus not good for human
consumption and industrial use. We therefore add this
chemical to increase it to be neutral.
Another chemical that is being added in this stage is
known as sodium Aluminates (Alum). This serves as a
catalyst and catalyst are chemical reaction that
changes the state of a substance. So the sodium
Aluminate’s removes the charges of the microorganisms
found in water thereby rendering them immobile and
thus coagulate together to form clogs, and this will
then make their density to be very heavy than water
and they will sediment at the bottom of the chamber.
Coagulation removes dirt and other particles
suspended in water. Alum and other chemicals are
added to water to form tiny sticky particles called
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“floc” which attracts the dirt particles. The
combined dirt and the alum {floc} become heavy enough
to sink to the bottom during sedimentation.
SEDIMENTATION CHAMBER:
As the water and the floc particles progress through
the treatment process, they move into the
sedimentation basins where the water moves slowly and
the heavy particles (floc) settle to the bottom and
the clear water moves to filtration.
In this chamber, chlorine is added to the tank
to further perform the following functions:
Render the microorganisms present in water
inactive but doesn’t kill them.
It helps to clarify the water and thus making it
colourless.
FILTRATION CHAMBER
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The water flows through a filter designed to remove
particles in the water, some made of layers of sand,
gravel, and charcoal that help remove even smaller
particles. Filtration collects the suspended
impurities in water and enhances the effectiveness of
disinfection. The filters are routinely cleaned by
backwashing.
Sand, stones, and gravels of various sizes are
used to make beddings example:
0.5-0.8mm
1-2mm
2-6mm
6-14mm
14-20mm
They are arranged in layers to aid proper filtration
of water as it flows from the sedimentation chamber.
Only filtrate is allowed to pass through the
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filtration chamber and then enters into the sand
filters with the aid of filter pumps with pipes.
DISINFECTION
Water is disinfected before it enters the
distribution system to ensure that any disease
causing bacteria, viruses, and parasites are
destroyed. Chlorine is used because it is a very
effective disinfectant, and residual concentrations
can be maintained to guard against possible
biological contamination in the water distribution
system.
STORAGE: Water is placed in a closed tank or
reservoir in order for disinfection to take place.
The water then flows through pipes to all round the
refinery where it is needed.
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CHAPTER SIX
CONCLUSION
My Industrial training in Dangote Sugar Refinery at
Apapa whorf in Lagos State was indeed a remarkable
one. I was able to put into practice all I was taught
in school and also learnt more. I was able to acquire
all the necessary skills and by God’s grace today am
proud to say that I can cope in any industry I find
myself after graduation because Dangote Sugar
Refinery Industry is one of the best Industries in
the whole world wide. Thanks to Student Industry Work
Experience Scheme (SIWES) for organizing the program
and Federal University of Technology Owerri (FUTO)
for granting me the opportunity to participate in the
program.
Finally, the aim of the training was achieved as
necessary training has been acquired.
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RECOMMENDATION
Organizations should try as much as possible to
encourage students participate in this training
exercise by making Job placement easy after
graduation. Research has shown that industrial
training is important for student to acquire
practical experience of the theoretical skills.
In every organizations student should be appreciated
and supervisors should be pleased to correct them.
However, student should take this program very
serious because the merits are more than the
demerits.
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Organizations should Endeavour to pay students well
during this training and make provision of staff bus
for the students who comes from a far distance.
GLOSSARY OF SOME TERMS USED IN SUGAR REFINING
BRIX : Percentage by weight of sugar present in
a solution
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CAKE: The solid waste material from a filter
press or pressure filter
COLOUR: Complex molecules of impurity
CRYSTALLISATION: Production of sugar crystals
from a solution
EVAPORATION : Increase in the concentration of
a sugar solution by removing water through
boiling.
FILTRATION: Removal of suspended solids from a
liquid.
FINE LIQUOR: Liquor after the final
purification.
LIQUOR: Solution of sugar before
crystallization.
MASSECUITE: Mixture of crystals and its mother
syrup boiled in a vacuum pan, often shortened as
*masse*.
MOLASSES: Sugar from the last boiling in the
recovery process.
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pH: Measurement of how acidic or alkaline a
solution is. A neutral solution is 7 pH.
RAW SUGAR: The product of a raw sugar factory. A
raw sugar has between 96 and 95% sucrose. The
rest is impurity.
RESIN: This is a man-made compound used to
remove colour and impurities from liquor.
SYRUP: Sugar solution that contain high amount
of impurities.
VACUUM PAN: Vessel for crystallization of sugar.
APPENDICES
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