Professional Documents
Culture Documents
PRODUCTION OF CEMENT
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Acknowledgment
By the grace of Allah almighty I get a chance to do internship in Thatta cement
plant and I have learnt a lot during this internship. I am writing maximum
knowledge that I gained during this period.
I would like to thank the management staff at Thatta cement especially with their
help I gained a lot of information regarding the cement industry and also to gave
me an opportunity to learn and understand the working of organization as an
internee. They gave me chance to improve my industrial skills that will surely help
me in the practical field.
Below given are the table of contents and data which I collected during my stay at
this plant. With my limited knowledge I have tried to cover all the portions of the
plant which I have visited during my internship.
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Contents
Acknowledgment.......................................................................................................2
1 History Of Portland Cement....................................................................................6
1.1 Introduction Of Thatta Cement Company Limited..........................................6
1.1.1 Location:....................................................................................................7
1.1.2 Initiatives:..................................................................................................7
1.1.3 Valued Customers:....................................................................................7
1.1.4 Our Products:............................................................................................8
1.1.5 Advantages:...............................................................................................9
2. Cement Production Process.................................................................................10
2.1 Quarry And Raw Material..............................................................................10
2.1.1 Drilling.....................................................................................................10
2.1.2 Blasting:...................................................................................................10
2.1.3 Raw materials..........................................................................................10
2.2 Limestone/Clay Crusher.................................................................................11
2.3 Storage Yard...................................................................................................11
2.4 Raw Mill Area.................................................................................................12
2.4.1 Raw Mill..................................................................................................12
2.4.2 Cyclone....................................................................................................13
2.4.3 Bucket elevator.......................................................................................13
2.4.4 CF Silo......................................................................................................13
2.5 Preheater.......................................................................................................14
2.6 Burning in a kiln.............................................................................................15
2.6.1 The burning process................................................................................15
2.7 Clinker Cooler.................................................................................................17
2.8 Electrostatic Precipitator (ESP)......................................................................18
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2.9 Clinker Storage...............................................................................................18
2.10 Coal Mill.......................................................................................................18
2.11 Finish Mill and Slag Mill...........................................................................18
2.12 Packing Plant:...............................................................................................19
2.13 Reactions Occurring.....................................................................................20
2.14 Gases Produced and NEQS...........................................................................20
2.14.1 Sox:........................................................................................................20
2.14.2 NOx:.......................................................................................................20
2.14.3 CO:.........................................................................................................20
3 Laboratory.............................................................................................................21
3.1 Soundness Test:.............................................................................................21
3.2 Setting Time:..................................................................................................21
3.2.1 Initial Setting Time:.................................................................................21
3.2.2 Final Setting Time:...................................................................................22
3.3 Expansion Test:..............................................................................................22
3.4 Compressive Strength Test:...........................................................................22
3.5 XRF Spectrometry Test:..................................................................................23
3.5.1 About X-ray fluorescence spectroscopy:................................................24
3.6 Blaine Test:.....................................................................................................24
3.7 Oli Well Cement.............................................................................................25
4 Instrumentation Devices.......................................................................................26
4.1 Temperature Sensors:....................................................................................26
4.1.1 Thermocouples:......................................................................................26
4.1.2 Resistive Temperature Devices:..............................................................26
4.1.3 Infrared Sensors:.....................................................................................27
4.2 Vibration Sensors:..........................................................................................27
4.3 Pressure Transmitters:...................................................................................28
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4.3.1 Absolute Pressure Transmitter:..............................................................28
4.3.2 Gauge Pressure Transmitter:..................................................................29
4.3.3 Differential Pressure Transmitter:..........................................................29
4.4 Flue Gas Analysis:...........................................................................................29
4.5 Protection Devices.........................................................................................30
4.5.1 Relay:.......................................................................................................30
4.5.2 Magnetic Contactors:..............................................................................30
4.5.3 Circuit Breakers:......................................................................................30
5 Power Plant...........................................................................................................31
Motors..................................................................................................................31
6 Auto Shop..............................................................................................................32
7 Civil Department...................................................................................................33
8 Water Supply System............................................................................................34
9 Suggestions...........................................................................................................35
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1 History Of Portland Cement
The use of concrete dates back to the Roman Empire. The Castle de San Angelo
was built in Rome in 138 A.D. The stone facing was stripped away hundreds of
years ago, exposing concrete that is still in good condition. In North America, it is
believed that the mission priests in charge of construction learned the secret of
making natural cement from the Native Americans of Mexico. The widespread
knowledge and use of natural hydraulic cement was demonstrated by a diversion
dam in San Diego, California. Some believe this was the first concrete structure in
America, built in about 1769.
In 1824, Joseph Aspdin, a British stone mason, obtained a patent for a cement he
produced in his kitchen. The inventor heated a mixture of finely ground limestone
and clay in his kitchen and ground the mixture into a powder creating a hydraulic
cement – one that hardens with the addition of water. Aspdin named the product
portland cement because it resembled a stone quarried on the Isle of Portland off
the British Coast. With this invention, Aspdin laid the foundation for today's
portland cement industry. The first large use of this modern-day portland cement,
and its first engineering use, was in a tunnel under the Thames River in 1828. The
first recorded shipment of portland cement to the US was in 1868. The first
portland cement manufactured in the US was produced at a plant in Coplay,
Pennsylvania in 1871.
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1.1.4 Our Products:
Ordinary Portland Cement:
Thatta OPC is unique in its Low Alkali content feature with a total content of
alkalies below 0.4 percent. Thatta OPC has an advantage that it can be used in
concrete made with aggregates that contain a form of silica which reacts with
alkalies if present in high proportion to cause an expansion which disrupts
concrete. Another special feature of the Thatta OPC is that it has low contents of
Tricalcium Aluminate. This helps to control the effect of spontaneous over-heating
in large masses of concrete and resistance to sulfate attack.
Thatta OPC prevents chemical attack and corrosion on RCC. Its low heat of
hydration makes it suitable for mass concreting. Its high early strength makes it
ideal for use in load bearing structures. Thatta OPC has a higher Blaine value and
fineness which facilitates denser concrete. Thatta OPC can be used in concrete
mortars and grouts. Thatta OPC is a technically advanced and cost effective
solution for construction above or below ground.
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2.1 Quarry And Raw Material
Quarry is the place from where Raw Material is extracted. Drilling and Blasting is
done to extract the material. There are two types of quarry:
2.1.1 Drilling
Drilling is done in the quarry with the help of drilling machine, Crawler Drill
Machine that works on air compressor.
The horizontal distance (Space) between two holes is 8 feet.
Vertical distance (Burden) is approx. 2 feet.
The Diameter of the hole is 75 mm.
The depth of the hole is 15 to 25 feet.
Drilling takes place after every two days period.
2.1.2 Blasting:
The powder explosive is blasted under a controlled process to get the rocks in the
form of pieces of different small sizes. This extracted material is loaded on
dumper trucks and conveyed to the crusher. The explosives used are ammonium
nitrate, nitro glycrine explosives which are provided by Biafo Industry Limited.
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c) Additives (<1%): Iron Ore, Bauxite & Silica:
Iron ore is not extracted from quarry unit but it is bought from contractors. This is
added in very small quantity to strengthen the cement.
d) Gypsum (5%):
Gypsum is retarding agent and is used to increase setting time (to slow down
hardening process).
To deal with the magnetic particles, iron separator is used which is a magnet and
thus separates the ferric material out there. There are also a separate clay
hopper but mostly we used the same hopper.
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2.4 Raw Mill Area
The raw mill feed area consists of 3 feed hoppers:
The capacity of first hoppers is 800 tons while the other two hoppers have a
capacity of 600 tons. The feed from each pile is conveyed to the hoppers through
conveyor belts in relevant hoppers. Each hopper has four load cells.
Load Cells are sensing devices from which the feed in required proportions is
transferred by the belt conveyor to the Raw Mill. A lot of dust is produced during
the conveying of material, to avoid this problem Bag Filters are installed.
Raw mill contains a huge rotating disk, ball mill with the dimensions of
10.6m length and a diameter of 3.2m.
The grinding media in the ball mill is balls made of alloy.
There are three sections in the ball mill:
1: Drying 2: Crushing 3: Grinding
The total numbers of ball are 72, 35 in the 1 st section and 37 in the 2nd
section.
Ball mill moves with the help of motor with an rpm of 16.6 and ball move
on it.
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Material on the rotating disk moves away toward the rollers due to
centrifugal force and thus grinded. Raw mill has a mechanism of hot gases
passing through it which takes very fine particles to the cyclones through
air separator and the coarse particles back to the raw mill by breaking their
kinetic energy. the temperature is up to 70-80 oC.
2.4.2 Cyclone
These are funnel type structures. Strong vacuum is created in them through dig
tubes suspended in their centres. Air with the grinded particles from the mill is
allow to come at very high velocity and move in circular manner due to the
designed shape of inlet. By this kinetic energy of material particles are broken
down and they are collected through rotary locks.
2.4.4 CF Silo
The fine particles from the conditioning tower and electrostatic precipitator and
the powdered feed from the raw mill are conveyed to the bucket elevator. The
bucket elevator picks this feed and takes it to the top of the CF silo and then
throws it in. For burning 458 tonnes/hr is taken from the silo. In it flow of
material is counter current. CF silo have extract points. Air slides are also present
here. Here pressurized air is present at the bottom.
Specifications of a CF Silo:
Length = 54 m
Diameter = 22.4 m
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2.5 Preheater
Multistage preheaters and pre-calciners make use of the waste heat from the kiln
and clinker cooler to pre-heat and pre-process the kiln feed, and thereby allow for
considerable energy savings. Whenever economically feasible a wet process kiln
can be converted to a state-of-the art dry process production facility that includes
either a multi-stage preheater, or a multi-stage pre-heater and a pre-calciner.
Such transformations are usually feasible for new plants and major upgrades. Kiln
systems with five cyclone preheater stages and precalciner are considered
standard technology for ordinary new plants. Typical efficiency values that can be
obtained with the use of multi-stage preheaters and precalcination is provided in
the table below:
The feed is stored in silo after grinding in Raw mill, is transported to kiln feed bin
via bucket elevator and then transported to the impact flow machine to control
the amount of feed. Then feed is transported to the distributor just about
Preheater Cyclone 2N-2S and it will distribute the feed and send to Preheater
Cyclone 1N-1S. Preheater Cyclone 1N-1S will send the feed to 3N-3S and 3S-3N
will send into 5N-5S. Eventually, 5N-5S will sent the feed into kiln hose. The
Preheater 4 gets feed from 2N-2S and hot gases from 5N-5S.
Hot Gases from kiln and calciner will enter 5N-5S and from that cyclone the
exhaust gases will enter 3N-3S. From 3S-3N hot gases will enter 2N-2S and
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eventually it will enter into 1N-1S. From 1N-1S, exhaust gases will sent to the Bag
filter.
To heat the kiln, a mixture of fuel and air is injected into the kiln and burned at
the bottom end. The hot gases travel up the kiln to the top, through a dust
collector, and out a smokestack. A variety of fuels can be used, including
pulverized coal or coke, natural gas, lignite, and fuel oil. These fuels create
varying types and amounts of ash, which tend to have compositions similar to
some of the aluminosilicate ingredients in the raw mix. Since the ash combines
with the raw mix inside the kiln, this must be taken into account in order to
correctly predict the cement compassion. There is also an increasing trend to use
waste products as part of the fuel, for example old tires. In the best-case
scenario, this saves money on fuel, reduces CO2 emissions, and provides a safe
method of disposal.
The raw mix enters at the upper end of the kiln and slowly works its way
downward to the hottest area at the bottom, undergoing several different
reactions as the temperature increases. It is important that the mix move slowly
enough to allow each reaction to be completed at the appropriate temperature.
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Because the initial reactions are endothermic (energy absorbing), it is difficult to
heat the mix up to a higher temperature until a given reaction is complete. The
general reaction zones are as follows:
2.6.1.1 Dehydration zone (up to ~ 450˚C): This is simply the evaporation and
removal of the free water. Even in the “dry process” there is some adsorbed
moisture in the raw mix. Although the temperatures required to do this are not
high, this requires significant time and energy. In the wet process, the
dehydration zone would require up to half the length of the kiln, while the dry
process requires a somewhat shorter distance.
2.6.1.2 Calcination zone (450˚C – 900˚C): The term calcination refers to the
process of decomposing a solid material so that one of its constituents is driven
off as a gas. At about 600˚C the bound water is driven out of the clays, and by
900˚C the calcium carbonate is decomposed, releasing carbon dioxide. By the end
of the calcination zone, the mix consists of oxides of the four main elements
which are ready to undergo further reaction into cement minerals. Because
calcination does not involve melting, the mix is still a free-flowing powder at this
point.
2.6.1.3 Solid-state reaction zone (900˚ - 1300˚C): This zone slightly overlaps, and
is sometimes included with, the calcination zone. As the temperature continues
to increase above ~ 900˚C there is still no melting, but solid-state reactions begin
to occur. CaO and reactive silica combine to form small crystals of C2S (dicalcium
silicate), one of the four main cement minerals. In addition, intermediate calcium
aluminates and calcium ferrite compounds form. These play an important role in
the clinkering process as fluxing agents, in that they melt at a relatively low
temperature of ~ 1300˚C, allowing a significant increase in the rate of reaction.
Without these fluxing agents, the formation of the calcium silicate cement
minerals would be slow and difficult. In fact, the formation of fluxing agents is the
primary reason that portland (calcium silicate) cements contain aluminum and
iron at all. The final aluminum- and iron-containing cement minerals (C3A and
C4AF) in a portland cement contribute little to the final properties. As the mix
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passes through solid-state reaction zone it becomes “sticky” due to the tendency
for adjacent particles to fuse together.
2.6.1.4 Clinkering zone (1300˚C – 1550˚C): This is the hottest zone where the
formation of the most important cement mineral, C3S (alite), occurs. The zone
begins as soon as the intermediate calcium aluminate and ferrite phases melt.
The presence of the melt phase causes the mix to agglomerate into relatively
large nodules about the size of marbles consisting of many small solid particles
bound together by a thin layer of liquid. Inside the liquid phase, C3S forms by
reaction between C2S crystals and CaO. Crystals of solid C3S grow within the
liquid, while crystals of belite formed earlier decrease in number but grow in size.
The clinkering process is complete when all of silica is in the C3S and C2S crystals
and the amount of free lime (CaO) is reduced to a minimal level (<1%).
2.6.1.5 Cooling zone: As the clinker moves past the bottom of the kiln the
temperature drops rapidly and the liquid phase solidifies, forming the other two
cement minerals C3A (aluminate) and C4AF (ferrite). In addition, alkalis (primarily
K) and sulfate dissolved in the liquid combine to form K2SO4 and Na2SO4. The
nodules formed in the clinkering zone are now hard, and the resulting product is
called cement clinker. The rate of cooling from the maximum temperature down
to about 1100˚C is important, with rapid cooling giving a more reactive cement.
This occurs because in this temperature range the C3S can decompose back into
C2S and CaO, among other reasons. It is thus typical to blow air or spray water
onto the clinker to cool it more rapidly as it exits the kiln.
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2.8 Electrostatic Precipitator (ESP)
It removes air and dust by electrodes. Small hammer present it drop the dust to
hopper. Its mechanism based on crona effect. Very high voltages produced in EP .
The gases coming from rotary furnace after cooling enter ESP and then evaded to
atmosphere. Now these gases have temperature 300_360 Celsius and used in
waste heat recovery plant. The efficiency of ESP is 99.9%.
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Clinker is stored in clinker silo then it is transported to the hopper via conveyer
belt and bucket belt. Others hoppers are also there that contain gypsum, slag and
limestone. A mixed and proportional feed is sent to raw and slag mill from the
hoppers and grinded.
The grinded feed is stored in the SRC, HSRC and OPC silo for storages that is
transported via conveyer belt and bucket belt.
There are 3 cement storage silos in which crushed cement is stored up till
packing. To convey the cement to the other 2 silos air slides are used. Now these
air slides take the cement to the packing plant.
2.14.1 Sox:
As imported coal is used from Indonesia and it have 0.5% sulphur so Sox produced
is negligible. NEQS National Environment Quality Standard states that 1700
mg/Nm3 Sox can be present in one cubic and the analyzer detect that 80 mg/Nm3
is being produced on this plant.
2.14.2 NOx:
For NOx calciner provide reducing effect and reduces NOx. NEQS NOx standard is
1200mg/Nm3.
2.14.3 CO:
According to NEQS the quantity of CO can be 800mg/Nm3.
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3 Laboratory
There are several physical tests that are done in Laboratories for the qualitative
analysis of cement of different types.
Expansion test
Setting time
Residue On 90 µ %
Compressive Strength
Blaine Test
Bomb Calorimeter test
XRF Spectrometry Test
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above bottom of the paste experiment is stopped and time lapse between the
addition of water and end if the experiment is noted as initial setting time.
3.2.2 Final Setting Time: The square needle is replaced with annular collar.
Experiment is continued by allowing this needle to freely move after gently
touching the surface of the paste. Time lapse between the addition of water and
the mark of needle but not of annular ring is found on the paste. This time is
noted as final setting time.
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12000 ± 400 vibration per minute. A hopper is secured at the top and the
remaining mortar is filled. The mould is vibrated for two minutes and hopper
removed. The top is finished with a knife or with a trowel and levelled. After 24 ±
1 hour mould is removed and cube is placed under clean water for curing.
After specified period cubes are tested in compression testing machine, keeping
the specimen on its level edges. Average of three cubes is reported as crushing
strength. The compressive strength at the end of 3 days is 23 MPa and that at the
end of 7 days is 33 MPa and at the end of 28 days is 43 MPa.
Residue on 90 µ %
We need to determine the fineness of cement by dry sieving as per IS: 4031 (Part
1) – 1996.The principle of this is that we determine the proportion of cement
whose grain size is larger than specified mesh size.
The apparatus used are 90µm IS Sieve, Balance capable of weighing 10g to the
nearest 10mg.
Procedure to determine fineness of cement
Weigh approximately 10g of cement to the nearest 0.01g and place it on the
Alpine jet sieve. Agitate the sieve by swirling, planetary and through suction, until
no more fine material passes through it. Weigh the residue and express its mass
as a percentage R1, of the quantity first placed on the sieve to the nearest 0.1
percent. Gently brush all the fine material off the base of the sieve. Repeat the
whole procedure using a fresh 10g sample to obtain R2. Then calculate R as the
mean of R1 and R2 as a percentage, expressed to the nearest 0.1 percent. When
the results differ by more than 1 percent absolute, carry out a third sieving and
calculate the mean of the three values.
Reporting of Results
Report the value of R, to the nearest 0.1 percent, as the residue on the 90µm
sieve.
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of Horzog press which works on the principle of hydraulic press after this our
sample is ready to be tested in the XRF
XRF is an analytical technique that can be used to determine the chemical
composition of a wide variety of sample types including solids, liquids, slurries and
loose powders. XRF is also used to determine the thickness and composition of
layers and coatings. It can analyse elements from beryllium (Be) to uranium (U) in
concentration ranges from 100 wt% to sub-ppm levels.
XRF is a robust technique, combining high precision and accuracy with
straightforward, fast sample preparation. It can be readily automated for use in
high-throughput industrial environments, plus XRF provides both qualitative and
quantitative types of information on a sample. Easy combination of this ‘what?’
and ‘how much?’ information also makes rapid screening (semi-quantitative)
analysis possible.
3.5.1 About X-ray fluorescence spectroscopy:
XRF is an atomic emission method, similar in this respect to optical emission
spectroscopy (OES), ICP and neutron activation analysis (gamma spectroscopy).
Such methods measure the wavelength and intensity of ‘light’ (X-rays in this case)
emitted by energized atoms in the sample. In XRF, irradiation by a primary X-ray
beam from an X-ray tube, causes emission of fluorescent X-rays with discrete
energies characteristic of the elements present in the sample.
The technology used for the separation (dispersion), identification and intensity
measurement of a sample’s X-ray fluorescence spectrum gives rise to two main
types of spectrometer: wavelength dispersive (WDXRF) and energy dispersive
(EDXRF) systems.
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4 Instrumentation Devices
There are several instruments and used in cement industry are given below.
Temperature Sensors
Pressure Transmitters
Vibration Sensors
Actuators
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4.1.3 Infrared Sensors:
Infrared sensors are noncontacting sensors. As an example, if you hold up a
typical infrared sensor to the front of your desk without contact, the sensor will
tell you the temperature of the desk by virtue of its radiation - probably 68°F at
normal room temperature.
In a noncontacting measurement of ice water, it will measure slightly under 0°C
because of evaporation, which slightly lowers the expected temperature reading.
At the pre-heater, ball mill and raw mill – O2 content is checked to monitor
the change in false air, due to air ingress.
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Combustion in ball mill and raw mill – O2, CO, CO2 measured to check
effective and complete combustion.
The testo solution for the above cement applications is a testo 350 with O2, CO,
and a CO2 IR sensor . It is recommended to use a Peltier Chiller, and a fresh air
valve. This will help long term measurements, and also take care of moisture that
may be present in stack gas.
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5 Power Plant
For continuous and smooth operations of the plant uninterrupted power supply is
very crucial. The power is supplied to the huge machinery with the help of
Motors
Motors of the following power are being used mainly.
Name Power (kW)
Limestone Crusher
Kiln
Raw Mill
Finish Mill
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6 Auto Shop
The purpose of auto shop is to provide the services to production and mechanical
department. The list of services is given below.
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7 Civil Department
The main function of civil department is to check all the maintenance work done
on the plant site as well as on the colonies site. On the plant site, there main focus
is on the Kiln, Preheater, Burner, and Cooler. As they have to apply insulation
boards, insulation wool and chemical insulation boards in order to make the
processes taking place safely.
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8 Water Supply System
TCCL gets its water from KB (Kalari Baghar) feeder, Indus river.
Water is transported through a paved channel into two ponds which has a
capacity of 1 crore and 1.3 crore respectively.
The distance of paved channel is 1000m and the distance between pond
area and site reservoir is 3347 meters.
The diameter of the pipe is 6 inches.
The paved channel has a width of 2 feet and a height of 3 feet.
Three pumps are installed at pond area that pumps water to the site
reservoirs with the rate of 600 gal/min.
The capacity of site reservoirs is 24 lakhs gallons each.
There is a bed filter with the capacity of 3.2 gallons.
Two pumps are installed at site reservoirs that supply water to industry,
officer colony, worker colony, and for gardening for drinking and industrial
purpose.
Water is cleaned by chlorination method on weekly basis.
Water Supply Water consumption
Industrial Use 50000-60000 gal/day
Grid Station 5m3/hr per engine
Worker, officer Colony 250000gal/day
Gardening 24000gal/day
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9 Suggestions
Data regarding to internship should be provided at first day, so that
internee go through the process taking place.
There should be a common room in which people could be able to give
suggestions freely.
Internet should be provided for research purpose.
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