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VOCATIONALTRAINING REPORT
ON
AT
PREPARED BY:-
VIJAY JETHWA (140280105021)
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PREFACE
Practical knowledge means the visualization of the knowledge, which we read in our books. For
this, we perform experiments and get observations. Practical knowledge is very important in
every field. One must be familiar with the problems related to that field so that he may solve
them and become a successful person.
After achieving the proper goal in life, an engineer has to enter in professional life. According to
this life, he has to serve an industry, may be public or private sector or self-own. For the efficient
work in the field, he must be well aware of the practical knowledge as well as theoretical
knowledge. To be a good engineer, one must be aware of the industrial environment and must
know about management, working in the industry, labor problems etc. so he can tackle them
successfully in future.
Due to all the above reasons and to bridge the gap between theory and practical, our engineering
curriculum provides a practical training of 30 days.
During this period, a student works in the industry and gets all type of experience and knowledge
about the working and maintenance of various types of machinery.
Vijay Jethwa,
140280105021 (7thSem),
Chemical Department,
L.D.College of Engineering
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ACKNOWLEDGEMENT
The internship opportunity I had with GNFC (BHARUCH) was a great chance for learning and
professional development. Therefore, I consider myself as a very lucky individual as I was
provided with an opportunity to be a part of it. I am also grateful for having a chance to meet so
many wonderful people and professionals who led me though this internship period.
I perceive as this opportunity as a big milestone in my career development. I will strive to use
gained skills and knowledge in the best possible way, and I will continue to work on their
improvement, in order to attain desired career objectives. Hope to continue cooperation with all
of you in the future.
In this journey, A group of people we might call them INDUSTRY EXPERTS have helped me
so as a sincere student I would like to thank all the people that helped me.
First of all a big thank you to,
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ENVIRONMENTAL POLICY
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INDEX
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3.4 Interlock System 38
4 Utilities 39
5 Material Safety 40
5.1 Carbon Dioxide 40
5.2 Ammonia Synthesis Gas 42
6 Safety 44
6.1 Personal Protective Equipment 44
6.2 Toxicity of Chemicals & Catalyst 45
7 Conclusion 46
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1. INTODUCTION
GNFC at Glance
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1.1. Vision
Ammonia
4,45,000 MTPA,
Technology: From M/s Linde AG, Germany, GE Energy, USA, BASF, Germany,
HaldorTopsoe, Denmark
Methanol
The Counties largest capacity. 1,85,000 MTPA available for sale.
Technology: From ICI, UK, Product conforms of highest purity grade of US Federal AA.
Acetic Acid
The Countries largest capacity. 1,15,000 MTPA available for sale.
Technology: From M/s B.P.Chemicals, UK. The only manufacture in the country to
employ Methanol route.
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Formic Acid
The Countries largest capacity. 20,000 MTPa available for sale.
Technology: From Kemira OY, Finland.
Methyl Formate
3,000 MTPa available for sale.
Technology: From Kemira OY, Finland.
Aniline
The Countries largest single stream capacity. 40,000 MTPA available for sale.
Technology: M/s Du Pont, USA.
Toluene Di-Isocyanate
The only producer in South East Aisa. 67,000 MTPA available for sale.
Technology: M/s Du Pont, USA.
Nitrobenzene
2,000 MTPA available for sale.
Technology: M/s Chemtur Engineering AB, Sweden.
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1.4. Production Highlights
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1.6. Hall of Fame:
Set up the world's largest single stream, fuel oil based Ammonia - Urea plant
All fertilizers under the brand name of Narmada, along with extensive support activities,
have been well accepted by the country's farmer community.
India's largest producer of Formic Acid, Acetic acid, Methanol and premium quality
Ethyl Acetate.
India's only manufacturer of Glacial Acetic Acid through the cutting-edge Methanol
route.
India's largest single stream plant of Aniline.
The only manufacturer of Toluene Di-Isocyanate in South East Asia.
Record capacity utilizations in all plants, defying the vintage through ingeniously
innovative maintenance measures.
Development of the first indigenous, eco-friendly technology for H2S removal,
CATSOL, a much awarded product of the Company's R&D labs.
Set up 21 MW wind turbo generators.
Cogeneration power and stream unit with capacity of 33 MW power and 61 MT / HR
steam Commissioned.
Ammonia synthesis gas generation plant for LSHS to natural gas conversion has been
commissioned.
Ethyl Acetate plant for 50,000 MTA a capacity has been commissioned.
Facilities for Neem coated urea have been established.
Neem project: GNFC has undertaken a solo economic Neem project for manufacturing its
sown requirement of Neem oil for coating urea and for selling, also to make Organic
Neem cake fertilizer with main objective of women empowerment and uplifting of poor
rural population.
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2. PROCESS DESCRIPTION
2.1. Introduction
This document contains information on chemical reactions, catalysts and an overview of
the process in each of the main sections:
Desulphurization
Reforming
CO Conversion
CO2 Removal
Pressure Swing Adsorption
Compression
Process Condensate Stripping
Incoming Lines
Natural Gas Feed
DM Water for BFW Preparation Unit
HP Superheated Steam
Cooling Water Supply
Nitrogen
Refrigerant Ammonia Supply
Start Up and Emergency H2
Outgoing Lines
Ammonia Synthesis Gas Product
CO2 Product
Refrigerant NH3 Return
Cooling Water Return
Stripping Condensate to BFW Preparation
Turbine Condensate to BFW Preparation
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Production
Consumption
The process steps necessary for production of synthesis gas and CO2 from the above
mentioned raw materials.
The hydrocarbon feed is desulphurized to ppb level in the desulphurization section.
The desulphurized hydrocarbon feed is reformed with steam into process gas. The gas
contains mainly hydrogen, carbon monoxide, carbon dioxide and steam.
In the gas purification section, the CO is first converted into CO2. Then the CO2 is
recovered from the process gas in the CO2 removal section. The CO and CO2 residues in
the gas outlet of the CO2 removal unit are removed in the PSA section.
The purified hydrogen gas is mixed with nitrogen to form synthesis gas which is then
compressed. After that the gas is sent to the existing ammonia loop.
The CO2 product is compressed, dried and chilled before it is sent to the battery limit.
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Process Block Diagram
2.2.1. Desulphurization
Gas contains HS and organic sulphur compounds.
First, organic sulphur compound converted into HS in hydrogenator and HS absorption
takes place in sulphur absorbers.
After these process, content of sulphur is less than 0.1 volume ppm.
Desulphurisation Section
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Hydrogenation
RSH + H2 RH + H2S
R1SSR2 + 3H2 R1H + R2H + 2H2S
R1SR2 + 2H2 R1H + R2H + H2S
(CH)4S + 4H2 C4H10 + H2S
COS + H2 CO + H2S
where R is hydrocarbon radical.
The hydrogenation catalyst must not get into contact with hydrocarbons without the
presence of hydrogen. The result would be poor conversion of the organic sulphur
compounds causing an increased sulphur slip to the reforming section.
The catalyst is oxidized at delivery and resumes its activity when sulphided. In the
sulphided state the catalyst is pyrophoric and it must be not exposed to air at temperatures
above 70oC.
If oxygen is present in the feed gas, an exothermic reaction takes place in the reactor.
2H2 + O2 2H2O
H2S Absorption
The hydrogenated natural gas is fed to the SulphurAbsorbers . The two sulphur absorbers,
located in series, are identical. acts as a guard in case of sulphur is taken out of service for
catalyst replacement. Both reactors contain a layer of desulphurization catalyst.
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In addition to this layer, also contains a bottom layer of sulphur guard catalyst, to secure a
very low slip of sulphur to reforming and shift section catalyst. The normal operating
temperature is approximately 365oC.
The zinc oxide reacts with the hydrogen sulphide and carbonyl sulphide in the following
equilibrium reactions:
The catalyst does not react with oxygen or hydrogen at any practical temperature. Zinc
sulphide is not pyrophoric and no special care during unloading is required. Steam
operations should not be carried out in:
The zinc oxide would hydrate and it would then be impossible to regenerate the ZnO
material in the reactor. The sulphur content in the natural gas leaving the final
desulphurisation is reduced to less than 0.1 ppm by weight.
The gas from the desulphurization section is mixed with steam and sent to the reforming
section where hydrocarbons are reacted over nickel catalysts with steam in two steps. At
first, in the adiabatic prereformer and then in the tubular reformer. The steam reforming
of hydrocarbons can be described by the following reactions:
1) CnHm + nH2O nCO + (n+ )2 Heat
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Adiabatic Prereforming
The steam reforming of the hydrocarbon feed takes place in two stages, an adiabatic
prereformer and a direct fired tubular reformer.
The hydrocarbon feed coming from the desulphurization unit is mixed with steam. The
steam/carbon ratio is 2.9.
The reaction mixture is preheated to 520oC and is taken to the Prereformer, where all
higher hydrocarbons are completely converted to methane, hydrogen, carbon monoxide,
and carbon dioxide over a highly active reforming catalyst, in an overall endothermic
reaction sequence.
The outlet stream from, now free of all higher hydrocarbons, shall be heated further to a
627oC, before being sent to the Tubular Reformer,. A sketch of Prereformer, given in
figure
Adiabatic Prereforming
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Tubular Reforming
The prereformed gas from the Prereformer, is preheated and sent to the Tubular
Reformer, in which most of the methane reforming takes places, decomposing the
methane into hydrogen, carbon monoxide, and carbon dioxide over a nickel catalyst. The
reaction is strongly endothermic and the heat of reaction is supplied by indirect firing.
The tubular reformer is constructed as a simplex furnace containing a number of
vertically mounted, high alloy Cr-Ni steel tubes filled with catalyst. The tubes are
mounted in a single row along the centre line of the chamber. The process gas is flowing
downwards with the gas being distributed to the top of the tubes from a header through
"hairpins" at a temperature of about 627oC. The gas leaves the bottom of the tubes and
enters a refractory lined collector.
The tubes are heated by a number of burners located in each side wall of the furnace
chamber and arranged in horizontal rows at several elevations to provide easy control of
the uniform temperature profile along the length of the catalyst tubes.
In this manner, the optimal utilization of the expensive high alloy tubes is obtained. Flue
gas flow is upwards with outlet near the top of the radiant chamber. The flue gas
temperature is about 1050oC.
The fuel for the reformer furnace is mainly off-gas from the PSA unit, and the CO2
removal section with a balance of natural gas.
The Combustion Air Blower, supplies combustion air to the burners, which has been
preheated to 261C in the flue gas waste heat recovery section. To ensure a complete
combustion of the fuel gas, the burners must operate with excess air.
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Tubular Reforming
The Flue Gas from the Tubular Reformer Furnace passes via the flue gas duct to the flue
gas heat recovery section, in which the sensible heat of the flue gas is utilized for the
following duties:
At Outlet, the flue gas temperature is reduced to approximate 140oC. A Flue Gas blower
takes the flue gas to the stack.
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2.2.4. CO Shift Conversion
The carbon monoxide in the process gas leaving the reforming section is converted into
carbon dioxide and hydrogen according to the shift reaction:
CO + H2O CO2 + H2+ Heat
The shift reaction equilibrium is moved towards higher conversion of CO by lower
temperature and more water vapour, however, the reaction rate increases with higher
temperature. The optimum temperature for the shift reaction depends upon catalyst and
composition of gas.
The CO conversion takes place in the two shift converters: High Temperature Shift
Converter, and Low Temperature Shift Converter, with process gas cooling after each
converter. The process gas leaves the reforming section at about 850oC. It is cooled to
about 360oC in the Waste Heat Boiler , and sent to the CO conversion.
After reforming, about 13% CO is present in the gas (dry basis). In the High Temperature
Shift Converter, the CO content is reduced to approximately 2-3 vol%, and the
temperature increases from 360oC to 423oC. The gas is then cooled to 205oC and passed
on to the Low Temperature Shift Converter, in which the CO content is reduced to
approximately 0.25vol%, while the temperature increases to 227oC.
Shift Conversion
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High Temperature Shift Converter
The High Temperature Shift Converter contains a Cu-promoted high temperature shift
catalyst type, which features high activity and high mechanical strength. The catalyst is to
be installed in its highest oxidized state.
Reduction is carried out in process gas containing hydrogen during start-up of the
reforming section. The activated catalyst can operate continuously in the range of 320oC-
480oC.
Fresh catalyst should be operated at a gas inlet temperature of about 360oC. Later, as the
catalyst ages the optimum inlet temperature will increase, but as long as the outlet
temperature has not reached 460oC, the catalyst activity will only decrease slowly. The
activity of the catalyst increases with increasing temperature, but the life of the catalyst is
shortened.
Chlorine and inorganic salts are poisons to the catalyst. The content of chlorine in the
process gas should be well below 1 ppm. However, the reforming and low temperature
shift catalysts are much more sensitive to these contaminants; therefore they are always
removed to a level well below the tolerance limit of the catalyst.
Heating in condensing steam will not harm the catalyst in any way. The hot catalyst
should not, however, be exposed to liquid water, since this might cause disintegration of
the catalyst.
The Low Temperature Shift Converter is loaded with low temperature shift catalyst type,
which is characterized by high activity, high strength, and high tolerance towards sulphur
poisoning.
The catalyst is activated at 150oC-200oC in circulating nitrogen containing 0.2-2%
hydrogen. During the reduction process, the copper oxide reacts with hydrogen to form
free copper.
The catalyst can be operated within a temperature range of 170oC-250oC. Fresh catalyst
should be operated at a gas inlet temperature of about 205oC. The activity of the catalyst
increases with increasing temperature, but the life of the catalyst is shortened.
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2.2.5. CO2 Removal
The CO2 removal system is based on the two-stage activated MDEA process. The solvent
used for CO2 absorption is aMDEA. The main process system consists of a two-stage
CO2 absorber, a CO2 stripper and two flash vessels.
The CO2 is recovered from the gas by absorption in the aMDEA solution containing 40
wt% aMDEA. The aMDEA solution contains an activator, which increases the mass
transfer rate of CO2 from the gas phase to the liquid phase. The rest of the solution is
water. The overall reactions occurring during the CO2 absorption process are described
by the following equations:
Process Description
The gas leaving the CO conversion unit contains a considerable amount of recoverable
heat. Owing to the content of steam, this heat is present mainly as latent heat. It is
recovered in a BFW Preheater, in the Stripper Reboiler, and in the DMW Preheater.
For removal of the carbon dioxide, the activated aMDEA process is used. Main
equipment in the aMDEA process is the CO2 Absorber, and the CO2 Stripper.
The extracted CO2 will be delivered from the unit cooled to 43oC and at a pressure of
0.50 bar g. CO2 is removed from the process gas by counter-current absorption in two
stages. In the lower part of the CO2 Absorber, flash-regenerated solution is used for bulk
CO2 removal.
In the upper part of the absorber, regenerated solution is used for scrubbing. The flash
regeneration of the rich solution is performed in two stages. In the HP Flash Drum, a
large part of the dissolved inert components is expelled at a pressure of 7.8 bar g.
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The flashed gas is sent as fuel to the Tubular Reformer. The flashed solution from the
bottom of the LP Flash Drum is divided and the major part of the solution is transferred
to the lower part of the absorber.
Only a minor part of the lashed solution is fed to the CO2 Stripper, where CO2 is stripped
out with steam to obtain a low residual CO2 loading. The lean solvent from the bottom of
the stripper is pumped to the top of the CO2 Absorber.
In this way, a nearly complete removal of CO2 with only 0.05 vol% CO2 (on dry basis)
left in the treated gas is obtained with very low heat consumption.
CO2 Removal
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2.2.6. PSA Unit
After removal of CO2, the process gas contains about 92% H2 (on dry basis). A Pressure
Swing Adsorption (PSA) unit is installed in order to purify the process gas to 99.9% H2.
The basic principle of pressure swing adsorption is to adsorb the impurities contained in
the hydrogen stream at high pressure, while the hydrogen passes through the adsorbent
and then releases the impurities again at low pressure and in this way regenerates the
adsorbent. The UOP POLYBED PSA unit uses Pressure Swing Adsorption (PSA).
Impurities are adsorbed at high pressure and then desorbed at low pressure. Each
adsorber goes through the same cycle of adsorption and regeneration without change in
temperature, except for the heat of adsorption and desorption.
In the main mode of operation, there are always 3 adsorbers in adsorption, while the
others are in depressurisation, regeneration or repressurisation.
Process Description
During adsorption, feed gas enters the bottom of the adsorber, while pure hydrogen
leaves from the top. At the end of adsorption, the adsorber is loaded with impurities,
concentrated at the bottom.
The remaining hydrogen concentrated at the top is first removed by co-current
depressurisation and used to repressurise (equalize) and purge other adsorbers.
Subsequently, the adsorbers are counter-currently depressurised (from top to bottom) in
the dump step.
Following the dump step the adsorbers are purged with the high purity stream provided in
step B (providing purge). In steps C and D the gas leaving the adsorbers at the bottom is
sent to surge drum to obtain a steady and homogeneous off-gas flow.
Before going back into the adsorption step, the adsorber has to be repressurised with gas
provided in step B (equalization) and a slipstream of the feed gas.
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2.2.7. Compression
Nitrogen Compression
Nitrogen gas which is coming from air separation unit is compressed in N2 Compressor
up to 23.1 bar g. The hydrogen gas is mixed with compressed nitrogen, to give a
hydrogen/nitrogen ratio of approximately 3 to 1 in the product gas, which is used as
make-up gas to the ammonia synthesis loop.
CO2 Compression
Carbon dioxide from the aMDEA CO2 removal section is compressed in the
CO2Compressor, to 4.8 bar g.
Compressed CO2 is cooled to 9 C in 1st CO2 product chiller and then sent to CO2 dryer.
CO2 Dryer
CO2 dryer, CO2 gas saturated at 4 bar g and at 9C, is dehydrated to an outlet moisture
content of 100 ppm. CO2 dryer operates on the principle of Thermal Swing Adsorption.
It operates in a cycles of adsorption and regeneration. For detailed description of drying
process, refer vendor document - Process Description / Sequence Operation.
The dried CO2 is chilled to -15C with ammonia in 2nd CO2product chiller, before being
delivered to the urea plant.
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2.2.8. Condensate Stripper Section
Process condensate, which is separated from the synthesis gas produced in the front end,
is purified in the Process Condensate Stripper.
Small amounts of methanol are formed in the Low Temperature Shift Converter.
Together with the carbon dioxide in the raw synthesis gas, these compounds enter the
process condensate according to the following equilibrium reactions:
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2.2.9. Steam System
The major part of the waste heat available is utilized for production of High Pressure
steam in waste heat boliers. This High Pressure steam is Superheated in Steam
Superheater (Flue Gas Duct).
Superheated High Pressure Steam is used to run the Synthesis Gas and CO2 Compressors.
The Medium Pressure Steam is let down to Low Pressure Steam, which is used for
deareation of Boiler Feed Water.
Steam System
Process gas venting through various PSVs and vent valves are sent to flare for burning
obnoxious gases before venting to safe location in to atmosphere. Flare system comprises
of flare network, flare stack which is equipped with low flare tip with flame stabilizers
and pilot burners which maintains constant source of ignition.
Natural gas is used as a source of ignition. The Ignition system provided for the Flare is
FD (forced draft) Flame Front Generator type to lit Pilot burners sequentially. Molecular
Seal is located just below the Flare tip.
The seal has been designed to prevent air ingress into the flare riser thus preventing the
formation of an explosion mixture in the system.
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2.2.11. Effluent Collection & Treatment
The liquid effluents generated from the ammonia syngas plant are as listed below:
Oily Water
Amine Blowdown to Amine Treatment System
Effluent from Condensate Polishing Unit to Reverse Osmosis System
Cooling Tower Blowdown and Backwash Effluent from Side Stream Filter
Boiler Blowdown
Condensate from flare system
Water released during catalyst reduction
Process condensate during start up
Cooling water system caters to the cooling water requirement of various process units
and utilities. Cooling water from the cooling tower sump is pumped to various users by
the cooling water pumps (P 60901 A/B/C).
Cooling water is supplied at a pressure of 3.5 bar g and 33C temperature. Cooling water
return from various consumers at 43C is returned back to the cooling tower where it is
cooled to 33C. Cooling water system comprises of the following:
Cooling Tower including fans
Side stream filter
Cooling water pumps
Chemical (corrosion inhibitor/biocide) dosing system is provided for cooling water
system to prevent corrosion and fouling in the circulating system. Chemicals/biocide are
dosed directly into the cooling tower sump.
Side stream filtration unit will be provided on the cooling water circuit wherein a small
stream of circulating cooling water will be circulated through a filter to remove the
suspended impurities from the water.
The effluent generated from the backwash of the side stream filter will be routed to the
Cooling tower blowdown pit and pump to B/L for further processing by GNFC.
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General Terms Used in Cooling Water Systems:
Hold up capacity of the system: It is an amount of water contained in basin and sump of
cooling tower + water contained in piping and equipment.
Blow down: Since pure water is evaporated out of the System, the dissolved and the
Suspended solids are concentrated in the circulating water. Beyond certain limit, these
Solids will cause massive scale and corrosion. In order to balance this, a certain amount
of Water is removed from the System by blow down.
Make up Water: This is the water, which is to be added to replace the water lost by
evaporation, blow downdrift and leakages
Drift: Some water droplets escape along with the evaporation. A usual drift loss in
conventional Cooling towers is in the range of about 0.05 - 1% of the recirculation rate
System Losses: Circulating water is lost in the plant through pumps, valves or leakages
through flanges, etc.
Cycle of Concentration: Due to evaporation of water in Cooling tower the impurities get
concentrated in recirculating Water. Number of times the impurities get concentrated in
recirculating water is known as Cycle of Concentration (C.O.C.).
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2.3. Key Notes
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3. IMPORTANT UNITS
Compressor
Lube Oil System
DSC
Important Controls in ASGP
Interlock System
The Compressors are designed to achieve different operating conditions. The 2BCL508
(LP) Syn Gas Compressor is a two-phase machine wherein 8 impellers are arranged in
series and 2BCL407/A (HP) Compressor is a two-phase machine wherein 7 impellers are
arranged in series.
This 2BCL508 (LP)Compressor has a suction nozzle of 14 handling a flow of 7324
m3/h at a pressure of 19.41 bar g and delivering the gas at 44.76 bar g through a
discharge nozzle of 10.
The 2BCL407/A (HP) Compressor has a 1st suction nozzle of 10 handling a flow of
2367 m3/h at a pressure of 44.27 bar g and delivering the gas at 76.2 bar g through a
discharge nozzle of 6.
The compressors are being driven by a Steam turbine connected to each other by flexible
couplings.The Compressors runs at a maximum continuous speed (MCS) of 9421 rpm.
A L.S. of Compressor
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3.1.1. Casing
The casing of the compressors is barrel shaped, closed at the ends by two vertical flanges
(casing heads).
The suction and discharge nozzles are welded to the casing. Four paws projecting from
the horizontal centerline and laid on special pillars support the casing.
The transverse alignment of the machine is ensured with the help of two guide keys and
centering plate. The guide keys are welded to the casing along longitudinal axis whereas
the corresponding guides are welded to the base plate. This arrangement permits thermal
expansions without changing the machine alignment.
3.1.2. Diaphragms
The diaphragms make up the separating wall between each compression stage.
Each diaphragm constitutes a diffuser, which converts the kinetic energy of the gas at the
outlet of the impeller into pressure and the return channel, which leads the gas to the
suction of the next impeller.
3.1.3. Rotor
It consists of a shaft on which impellers and spacers are assembled. The spacers are
shrunk on the shaft and they axially position the impellers as well as protect the shaft
sections between the impellers from contacting the gas.
The impeller is the part of the centrifugal compressor that adds energy to the gas.
The impellers are of enclosed, backward- bladed type and are shrunk and keyed on to the
shaft.
The centrifugal compressor rotor is subjected to an axial thrust towards the suction end
due to the differential pressure acting on the hubs and shrouds of the impellers.
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In these types of compressors, the axial thrust is partially balanced by the balance drum
fitted between the discharge sides of the two stages.
Balance Drum
3.1.5.Journal bearings
The journal bearings are of the tilting pad type with forced lubrication. Oil under pressure
enters the bearings radially, goes through holes to lubricate pads and blocks. After
picking up the heat, the hot oil is axially discharged.
The thrust bearing is designed to support the residual axial thrust acting on the rotor that
is partially balanced by the balance drum.
The bearing is double acting tilting pad type, and is installed at both sides of the thrust
collar at the compressor shaft end.
It is provided with an oil control ring to minimize the power loss due to churning of the
oil in the bearing cavity under high speed operation.
The internal seals, used between rotating and stationary parts of the compressor to reduce
gas leakage between areas of different pressure, are labyrinth type. The labyrinth seal
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consists of a ring the periphery of which is shaped on a series of fins having small
clearance with the rotor.
These rings are manufactured in 2 halves of a soft alloy, resistant to corrosion to avoid
damage to the rotor in the event of an accidental contact. The upper halves of the rings
are fastened to relevant diaphragm. The lower halves of the rings can be easily removed
by rotating them in their grooved seat in the diaphragms.
The positions of the rotor which face the labyrinths seals are: the impeller disk, the shaft
sleeves between the impellers and the balance drum. The same type of seals is located at
the shaft end to limits the gas leakage out of the compressor.
The Dry Gas seals are located between rotating and stationary parts of the compressor to
reduce gas leakage from the ends. These are usually of tandem type (i.e., two
pneumatically balanced single seals) with an intermediate labyrinth seal. These seals are
supplimented by a barrier seal which separates the bearing chamber and seal zone.
The Dry Gas seals are of uni-directional and bi-directional type. The uni-directional seals
have a geometry on the sealing face that is specific to the direction of rotation, Whereas
the bi-directional seals have a sealing geometry that is independent of the direction of
rotation.
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3.2. Lube Oil System
The lubrication and seal oil system for a machine must provide the rotating equipment
with, 1) the necessary amount of, 2) the correct fluid, at 3) the correct pressure, at 4) the
correct time. The proper amount of fluid is needed to remove bearing and seal losses and
control the temperature of these components to reduce wear and maintain proper
clearances.
The correct fluid is that for which the rotating equipment is designed to run and that
which the oil console is designed to deliver at the required flow, pressure, temperature,
and cleanliness.
The use of other than the design lubricant supplied at the design conditions may cause or
contribute to problems, such as premature wear, rotor instability or vibration, or poor
system response.
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3.2.3. Coolers
The oil is cooled by a TWIN OIL COOLER (E-60731 A/B) (one as stand-by to the
other). During normal operation, the oil flow is directed to only one of the coolers,
leaving the other as a standby.
3.2.4. Filters
The oil reaches the 5- duplex oil filters (S-60731 A/B) (2x100%). Each filter provides a
continuous filtration of the total oil supplied by the oil system.
Only One filter at a time is put to service so that the cleaning, inspection and maintenance
of the second filter can be performed without interrupting oil flow or shutting down the
machines.To equalize the oil pressure and facilitate the changeover operation, a bypass
valve connects the two filters.
The pressure drop in the filter units is measured by means of a differential pressure
indicator (PDG-7142). To annunciate a high differential pressure across filter, a
Differential pressure transmitter, PDT 7141 is connected to an alarm in DCS. When the
differential pressure exceeds 1.5 kg/cm2, take the filter for cleaning by switching the oil
flow to the standby filter.
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3.3.1. DCS Elements
Local Control Unit:: This unit can handle 8 to 16 individual PID loops.
Data Acquisition Unit:: Digital (discrete) and analog I/O can be handle.
Batch Sequencing Unit:: This unit controls a timing counters, arbitrary function generators,
and internal logic.
Local Display: This
is device provides analog display stations, and video display for readout.
Bulk Memory Unit: This unit is used to store and recall process data.
Computer:: This unit is programmed by a customer or third party to
General Purpose Computer
perform optimization, advanc
advance control, expert system, etc
Display:: This unit typically contain several consoles for operator
Central Operator Display
communication with the system, and multiple video color graphics display units
Data Highway: A serial digital data transmission link connecting all other components in
the system. It allow for redundant data highway to reduce the risk of data loss
Local area Network (LAN)
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3.4. Interlock System
Last signal alarm system with and without secondary trip effect
Any last alarm will be indicated by flashing light and the horn will sound. By pressing the alarm
acknowledge key the horn will be silenced and the flashing light will change to steady on light.
After the cause of the alarm is corrected, the alarm light turns off completely.
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4. UTILITIES
Cooling water
Supply
Temperature 33oc
Pressure 3.5 bar g.
Return
Temperature 43oC
Pressure 2.5 bar g.
Instrument Air
Temperature Ambient
Pressure 6 bar g.
Electric Power
Inert Gas System (N2)
Refrigerant Ammonia
H2 for Emergency and Startup
Methanol for Emergency
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5. MATERIAL SAFETY
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5.1.3. Physical and Chemical Properties
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5.2. Ammonia Synthesis Gas
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collar, tie, belt or waistband. As this product rapidly becomes a gas when released, refer
to the inhalation section.
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6. SAFETY
The safety procedures described in this chapter are those which specifically apply to
potential hazards within battery limit.
It is assumed that safety practices with general application or with specific application to
other processes outside battery limit is described elsewhere. The general safety practices
referred to above should include:
Traffic safety
Fire-fighting
First aid
Work permit procedures
Vessel entry procedures
Sampling procedures
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6.2. Toxicity of Chemicals and Catalysts
Toxic gases
The toxic gas normally present within the battery limits of the plant is carbon monoxide,
which is an extremely insidious gas. Ammonia vapour is also toxic but its odour gives
ample warning before hazardous conditions exist. Safety Information Sheets for carbon
monoxide and ammonia are included as appendices to this chapter.
Hydrazine
Catalysts
The catalysts in the various reactors contain nickel and other metal salts which in the
form of dust can be poisonous and irritating if brought into contact with skin, eyes or
mucous membranes.
When the plant is running, catalysts are inaccessible: thus there is no hazard involved.
However, when loading or unloading catalysts, it is vital for the personnel doing the work
to be dressed in adequate protective clothing, including dust masks, eye goggles and
gloves.
Safety data sheets for the individual catalysts used in the plant, including toxicological
information for individual components, are included as an appendix to this chapter.
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7. CONCLUSION
Here, I learn about the various different Application & Equipment of the process that
were theoretically learned during our college curriculum. In Ammonium Synthesis Gas
Generation Plant, I learned about the new Natural Gas based Process along with the old
LSCO Gasification based Process. I also saw the Mammoth Reformer, Tall Absorbers
and Huge Compressors.
Learned, What type of problems can occur in the operating plant.
Came to know about the safety precautions taken by the industrialists while operating a
plant.
I am sure that knowledge for my experience during this industrial training will help me in
future to the get a better and quicker understanding of Plants, Process, Techniques and
Working Principle of various Equipments.
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