HPCL Report
HPCL Report
HPCL
CERTIFICATE
This is to certify that Mr.Chinthapalli Prem Sai Reddy , bearing Admission number 21131A0810 in
Chemical Engineering Bonafide a student, Gayatri Vidya Parishad College of Engineering (Autonomous)
Visakhapatnam has undergone industrial internship in M/s. HINDUSTAN PETROLEUM
CORPORATION Ltd., Visakh Refinery During the period of training he involved in all activities carried
out in Over all process on crude distillation unit (CDU-IV). He acquired good knowledge about CDU-IV.
During the period of training his conduct is found to be
ACKNOWLEDGEMENT
The satisfaction that accompanies the successful completion of any task would be
incomplete without mentioning the people who made it possible and whose constant guidance and
encouragement grown all the efforts with success. This acknowledgement transcends the reality of
formality when we like to express deep gratitude and respect to all those people behind the screen who
guided, inspired and helped us for the completion of the report.
We are thankful to the Human Resource (HR) Department especially to Mr. RAVI KUMAR,
Mr. K. NITHISH BHARADWAJ and Mentor Mr.Y.V.TARAK for his concern in giving the opportunity
toperdue industrial training and for providing guidance.
The encomium goes to the Dr. B.SREENIVASULU M.Tech, Ph.D(A.U), Head of Chemical
Engineering
On conclusion, we will remember our experiences in this industrial training and put of presenting
the training experience to prove our ability and work for pride of the organization in all respects
wherever we get an opportunity.
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INDEX
1. INTRODUCTION TO HPCL.
2. INTRODUCTION TO CDU-IV.
2.1 Pre treatment of crude oil
2.2 Description of the crude oil and demulsifier
2.3 Mechanisms and devices of process of dehydration-desalination
2.4 The salts in crude oil
6. PROCESS CHEMISTRY
---Range of hydrocarbons in typical crude---
7.BRIEF PROCESS DESCRIPTION
7.1 CRUDE DISTILLATION UNIT
7.2 NAPHTHA STABILISER
7.3 VACUUM DISTILLATION UNIT
7.4 TEMPETED WATER SYSTEM
7.5 STEAM GENERATION SECTION
7.6 HOT WELL OFF GAS SYSTEM
PROCESS UNITS:
processing)(DISMANTELD) CDU-
II: 3.6MMTPA
CDU-III:
4.16MMTPA
CDU- IV:
9.0MMTPA
REVAMP:1.2MMTP
A FCCU-II:
0.97MMTPA
VIS-BRTEAKING UNIT:
UNIT: 225,000TPA
520,000TPA
SR-LPG: 288KTPA
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2. INTRODUCTION TO CDU-IV:
The Crude and Vacuum Distillation Unit-IV is to be commissioned as one of the units under the VISAKH Refinery
Modernization Project (VRMP) to enhance the crude refining capacity to 15.0 MMTPA.
CDU-IV has a design capacity to process 9.0 MMTPA of crude oil. The design feed stock for the unit is 86.7% Basra
and 13.3% Doba under Case-1 and 92.5% Arab Heavy and 7.5% Dar Blend under Case-2. The unit is designed to
process 1127 tons per hour of crude oil feedstock.
CDU-IV is designed to produce Liquefied Petroleum Gas (LPG), Straight Run Naphtha, Kerosene Oil (Kero/ATF),
Diesel (LGO and HGO) and Reduced Crude Oil (RCO).
The VDU is designed to process RCO from CDU and to produce Vacuum Diesel, Light Vacuum Gas Oil
(LVGO), Heavy Vacuum Gas Oil (HVGO), and Vacuum Residue (VR). CDU / VDU are designed to operate in
conjunction and independent operation of either of these units is not considered
. The CDU also comprises the Naphtha Stabilizer section. The crude oil is pumped from the off-site storage tanks
to the Crude Distillation Unit. The various stages of operation are as follows:
iii) Preheating the desalted crude in process heat exchangers (Preheat Train-II)
v) Fractionation in Crude Column vi) Separation of Naphtha and LPG in Naphtha Stabilizer
vii) Products steam stripping (Swing Naphtha, Kero/ATF, LGO and HGO) and routing to designated Product
tanks or treatment facilities
x) Routing of products (VD, LVGO, HVGO, Slop, and Vacuum Residue) to designated tanks/units.
• stream type;
• temperature regime
. In the separators, they usually separate gas is usually from the oil in two or three steps under slight pressure or
dilution. The separators of the first stage simultaneously play the role of buffer reservoirs and are usually located on
the deposit. The separators of the second and third stages are mostly on the territory of central collection and
distribution points (the sites of pre-treatment and pumping of oil) [7, 17]. The vertical separators are more productive
in comparison with horizontal ones, but also the vertical separators have a higher price. They are suitable for
enterprises with high production capacities, as well as if the emulsion contains many solid particles [18]. The
horizontal separators are the best option for processing small volumes of material, as well as liquids with a high
content of dissolved gas. They are in the greatest demand, as they are quite productive and affordable. To achieve
maximum efficiency when using horizontal oil and gas separators, the oil is mixed in the separation process; the
temperature is increased, and the pressure is reduced. To increase the depth and improve the quality of separation in
Russia, introducing hot drainage water before separation with a threephase separator is often used. Thus, they use
heat, which increases the selection of gas, intensifies the process of demulsification of oil, improves the quality of
spilled formation water, reduces investments, energy costs of processes, and significantly improves the conditions of
Environmental protection. The three-phase separator can split oil, gas, and water at once. However, separators have
limits. Even with a three-stage separation, complete separation of gas from oil is not achieved [8]. Besides, it should
be noted that, despite the improvement in oil and gas separation techniques and technologies, field separators remain
cumbersome and expensive devices
and constantly collide with each other [21]. But these collisions of Na+ and OH ions, H+ and Cl ions do not lead to
the formation of compounds, since NaOH is a strong base, and HCl is a strong acid. Since weak electrolytes are not
formed when sodium chloride is dissolved in water, sodium chloride is not hydrolyzed. The concentration of H+ ions
is equal to the concentration of OH ions, so the color of the indicators does not change [13, 20]. All chemical
compounds based on chlorine hydrolyze, except for NaCl, hydrolyze at high temperature to hydrogen chloride:
CaCl2 þ 2H2O ! Ca OH ð Þ2 þ 2HCl (1) MgCl2 þ 2H2O ! Mg OH ð Þ2 þ 2HCl (2) Any remaining salts are
neutralized by the injection of sodium hydroxide which reacts with the calcium and magnesium chloride to produce
sodium chloride because NaCl does not hydrolyze to the corrosive hydrogen chloride.
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3. CRUDE DISTILLATION UNIT
3.1 INTRODUCTION:
A crude distillation unit (CDU) is a key component in the refining of crude oil into various petroleum
products. The primary purpose of the CDU is to separate the crude oil into different fractions based
on their boiling points. This process is also known as atmospheric distillation because it is typically
carried out at atmospheric pressure.
Feedstock:
The feedstock for the CDU is crude oil, which is a complex mixture of hydrocarbons. Crude oil
is obtained from oil wells and contains a wide range of components with different boiling points.
Process Overview:
The crude oil is first heated in a furnace to a temperature where it enters the atmospheric
distillation column as a vapor. The column consists of a series of trays or packing
material.
Fractionation:
Inside the distillation column, the crude oil is separated into fractions based on boiling points.
The lighter components with lower boiling points rise to the top of the column, while
the heavier components with higher boiling points sink to the bottom.
Product Streams:
The fractions obtained from the CDU include gases (such as methane and propane), naphtha,
kerosene, diesel, and heavier components like atmospheric gas oil and residues. Each fraction
has specific uses in the production of various refined products.Heat exchangers are employed to
cool down the vaporized fractions, causing them to condense into liquid form. This allows for
the
separation and collection of different products.
Side Strippers and Pumparound Systems:
Side strippers and pumparound systems are used to enhance separation by further distilling
specific fractions. These systems help optimize the production of desired products.
Bottoms Product:
The heaviest fraction, often referred to as atmospheric residue, is the bottom product of the
distillation column. This residue may undergo further processing in a vacuum distillation unit to
extract additional valuable products.
Utilities:
The CDU relies on various utilities such as steam and cooling water to maintain
optimal operating conditions.
Control Systems:
Advanced control systems are employed to ensure efficient and safe operation of the CDU.
These systems regulate temperatures, pressures, and flow rates throughout the unit.
Integration with Refinery Units:
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The output streams from the CDU are sent to various downstream units for further processing, such as
• Multiple evaporations
• Gradual evaporation
• by technological application;
• by an internal device (plates) ensuring contact between the steam and theliquid;
2. Stabilized Naphtha to
a. Stabilized Naphtha storage tanks
b. Export Naphtha storage tanks
c. Naphtha Hydrotreater Unit (NHT)
3. Swing Naphtha to
a. NHT Unit
b. DHT/DHDS Unit
c. Offsite Naphtha Storage
d. Export Naphtha storage tanks
e. Sour Diesel storage
4. Kerosene/ATF to
a. Existing MEROX Unit when on ATF regulation
b. DHDS Unit c. Sour Diesel Storage
d. Residue Upgradation Facility (RUF)
e. DHT unit
f. Kero storage
5. LGO to
a. DHDS Unit through Coalescer
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6. HGO to
a. DHDS Unit through Coalescer
b. Sour diesel storage tanks
c. DHT unit
1. Vac. Diesel to
a. DHDS Unit
b. Sour Diesel storage
c. DHT unit
2. LVGO, HVGO to
a. FCHCU
b. VGO storage
3. Slop-Distillate to
a. Vacuum Heater (as recycle stream) along with RCO
b. RUF, along with VR product
4. VR to
a. Cold VR + Slop to Storage
b. Hot VR + Slop to RUF
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PRODUCT PURPOSE
LPG Mainlyuse d for cooking
Motor spirit/Petrol purpose Use for indigenous
Superior Kerosene oil vehicles Domestic purpose
(SKO) Heavy Diesel oil Used as fuel for heavy vehicles
(HDO) Propylene Raw materials for
Naphtha petrochemicals Industrial Power
Jute Batching Oil (JBO) Generation Used as Jute
Light Diesel Oil (LDO) machines lubrication Used as
Fuel OIL (FO) fuel for ships
Low Sulphur Heavy Stock Used as Industrial fuel for heaters
(LSHS) Bitumen/Asphalt Used for power generation in
Sulphur industries Used for laying roads
Industrial usage
Mineral Turpentine oil Used in paint
(MTO) Aviation turbine industry Used as fuel
fuel (ATF) for planes
5. PROCESS PRINCIPLE
5.1 PRINCIPLE
If solution of two components with different boiling points is allowed to flash in a vessel, the liquid
and vapour portions separate and after sufficient time attain equilibrium. The vapors will be richer in
lighter components and the liquid residue therefore leaner. Suppose the vapours are condensed and
flashed again, the resulting vapours will be richer in the lighter components. By repeating the
procedure, we will reach a stage when vapours will be full of the lighter components (ideally).
Similarly, by repeatedly heating and flashing the liquid portion, we will eventually end up with a
liquid which is hundred per cent the heavier component. The same principle is used in a distillation
column with an integration of the above process and each step where the heavier component in the
vapours is condensed and the lighter component in the liquid is vaporized known as an equilibrium
stage. The total number of theoretical stages will be decided by the extent of separation relative
volatility of the components involved.
In a typical distillation operation, the feed is introduced into a vertical cascade of stages. Vapour
rising in the section above the feed (called enriching / rectifying section) is washed with liquid to
remove the less volatile components. The wash liquid is provided by condensing the vapour from the
top (rich in more volatile component) called reflux; a portion of the condensate is removed as
distillate. In the section below the feed (called stripping section), the liquid is stripped of the volatile
component by vapours rising from bottom. The vapours are generated by supplying the necessary
energy at the bottom through a reboiler or furnace. The liquid rich in less volatile component is
removed from the
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bottom.
5.2 Multicomponent distillation:
Through a binary system is ideal to design and operate, many of the separations encountered in
the industry are not so; they involve more than two components. The principles of binary
solutions are generally applicable to such distillations but nevertheless some special consideration
and techniques are needed more volatile components are designated as light and the less volatile,
heavy. Suppose
a solution has to be separated by distillation, the majority component among the bottom product
components compared to the other lighter components is called the light key component.
Similarly, the one among the distillate components which is present in considerable amount when
compared to the other heavier components is the heavy key component. With this key component
as the basis,
now the problem of multi-component distillation is treated in much the same way as binary
distillation. The difficulty of separation, as measured by the number of trays for a given reflux ratio, is
fixed by the key component concentrations in the products. It is, therefore, important to establish the
key components in a multi-component distillation.
The distillations involved in petroleum industry are further complicated by aspects like withdrawal
of side streams (apart from top and bottom products), circulating refluxes, stripping steam, etc.
Here, the separation is achieved not directly on the basis of components but by boiling ranges. Each
product comprises multiple components and its end use requirements specify certain properties such
as boiling range, flash point, specific gravity, viscosity, etc., rather than component purity. The
design of such systems is very complex and cannot be accomplished by totally theoretical methods;
pilot plant
studies coupled with past experience generally yield satisfactory results. Many software packagesavailable
in the present day market to evaluate the performance of the existing columns and also
to design new columns.
5.3 DISTILLATION TOWERS:
Fractionating towers and related equipment are mechanical devices for repeatedly establishing
equilibrium between ascending vapour and descending liquid and repeated separation of the two
phases. Hence, a means of attaining a large interface for contact and affecting a complete
separation of the two phases must be incorporated in any successful design. The choice of
contacting device in a column depends on
• Operating pressure and pressure drop.
• Turn-down ratio
• Nature of the solution (foaming tendency, presence of solids, etc.)
• Number of side streams
The most generally used in the industry are tray towers in which the liquid and vapour are
contacted in steps or trays or plates.
Types of trays:
• Trays with down-comers (Bubble -cap, Sieve, Valve)
• Trays without down-comers (Dual flow, baffle)
• Multi down-comer trays
• Collection or chimney trays
In tray towers, the liquid from the stage above flows across each tray and through a down-comer to
the tray below. The gas passes upward through opening in the tray, then bubbles through the liquid,
disengages and passes on to the next tray above. The depth of liquid on the tray required for gas
contacting is maintained by an overflow weir. Each tray of the column is a stage. The number of
equilibrium stages (theoretical trays) determines the number of actual trays. Tray spacing is usually
decided on the basis of adequate insurance against flooding & entrainment and on expediency in
construction, maintenance & cost. It varies from 300 - 900 mm depending on the diameter and
service of the tower. Column diameter or cross-sectional area is determined on the basis of
gas/liquid volumes to be handled. Packed columns are preferred to tray towers under the following
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circumstances:
• for columns of less than 2 ft. diameter
• for acids and other corrosive materials
• for foaming liquids
• for thermally sensitive liquids which require low liquid hold-up
• for lower pressure drop or for vacuum operation
• for greater mass transfer efficiency
The design of packed towers involves the determination of HETP (Height Equivalent to Theoretical
Plate). Packings can be either random or structured. The various types of packings available are,
Generation Type of packing
First Raschig, Lessing, Cross Partion Rings, Berl saddles
Second Pall Rings, Hypak, Intalox Metal Tower packing(IMTP), Cascade Mini
Rings (CMR), Nutter rings
Third Gempak, Mellapak, Intalox ( structured )
Care should be exercised to distribute feed and reflux streams uniformly throughout the cross-
section of the packing to avoid channeling. The withdrawals will be from collector or chimney trays.
6. PROCESS CHEMISTRY:
Crude oil is one of the two major fossil fuels on earth, the other being coal. It is the major and a cost-
effective energy source today; though efforts are on to discover other means. Crude oils vary widely
in appearance and consistency from country to country and from field to field. However, all crude
oils consist essentially of hydrocarbons.
Hydrocarbons:
Organic compounds of carbon and hydrogen are known collectively by the name hydrocarbons. As
carbon has a valency of four and hydrogen is monovalent, it can normally be expected that carbon
should form only one tetra-hydride by combining with four atoms of hydrogen. Such a compound
known as methane or CH4 does exist, but as carbon can also combine with itself and can also leave
some of its valencies unsatisfied by getting involved in unsaturated bonds or linkages, the number of
hydrocarbons is truly myriad.
Saturated and Unsaturated Hydrocarbon Compounds:
In any compound made up of carbon and hydrogen the carbon atoms behave as though they had
four arms and the hydrogen atoms behave as though each had only one arm. Each arm of the
carbon atom must always be occupied, that is, it must be holding something, either a hydrogen
atom or
another carbon atom. When all the carbon arms or bonds are used to hold other atoms, the compound
is said to be “saturated”. Similarly, a compound which does not have all the carbon arms or bonds
taken up by other atoms is said to be “unsaturated”. There are millions of different ways in which
carbon and hydrogen atoms can be connected together to form hydrocarbon molecules. To help
describe these in a systematic way, Science has classified hydrocarbons into various families
depending on their molecular structure. In petroleum chemistry, hydrocarbons are classified
primarily into four groups
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Type of Hydrocarbon Group
1. Paraffinic Family:
The first family of hydrocarbons is Paraffins. They are saturated hydrocarbons with the general
formula CnH2n+2.
In the normal butane, the chain is straight where as in the iso-butane, the chain is branched, although
both compounds have the same number of carbon and hydrogen atoms. For heavier hydrocarbons
there can be more isomers.
Properties of Paraffins:
1) Good natural stability. However, high reactivity in presence of oxygen or under
the influence of heat.
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Naphthenic Family:
Naphthenic hydrocarbons have fewer hydrogen atoms per molecule than paraffins. This is because
they have a closed or ring structure. Naphthene molecules with one ring have the general formula
CnH2n. They are also known as cyclo-paraffins. While rings can be small (3, 4 carbon atoms) or
large (above 6) many naphthene’s in petroleum have 5 or 6 membered rings.
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Properties of Naphthene’s:
1) Naphthene’s in motor oils form soft fluffy carbon deposits
2) Viscosity is affected more by temperature change. Viscosity index is lower for
naphthenic lubricants for paraffinic ones.
3) Naphthenic lubricants have low pour points.
4) Naphthene’s in gasoline improve its octane rating e.g. n-heptane has 0 octane and
methyl cyclo-hexane, 78 octane number.
Olefin Family:
Olefinic are unsaturated hydrocarbons with the general formula CnH2n. While olefins as such are not
normally found in natural crude oil, they are produced by cracking reactions. The simplest member
of this family is ethylene. Like paraffins, the higher members of the olefinic family can exist in
straight chain (normal) or branch (iso) structure. The location of the double bond can vary, leading to
different isomeric compounds.
Properties of Olefins:
1) Olefins are highly reactive. Thus, their presence in gasoline or lubricating oils leads
to interaction with oxygen to form sludge, gum and varnish.
2) In gasoline the presence of some olefins does improve octane rating (anti –knock
properties).
However, anti-oxidants will have to be added to suppress oxidation tendencies.
Aromatic Family:
Aromatics are unsaturated ring type hydrocarbons of a special chemical category. In these structures,
alternating double and single bonds having a property known as resonance confer some stability and
other special characteristics.
Aromatic streams from a refinery normally contain benzene or its derivatives, condensed aromatic
hydrocarbons like naphthalene or their derivatives.
Properties of Aromatics:
1) In view of the property of electronic resonance, benzene hydrocarbons are quite stable.
2) High octane values render aromatics excellent blended components.
3) Have high solvency power. They make good commercial solvents.
4) They are poor viscosity index components in lubricating oils.
5) Aromatics in kerosene produce smoky flames (low smoke point
Crude Oil:
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Various systems of classification have been attempted since the early production of crude oil from
the last century. Based on the nature of hydrocarbons present in Crude Oils, they are Abroadly
classified into
Paraffin Based Crude Oils:
These consist mainly of paraffinic hydrocarbons and little / no Asphaltenes matter. They usually give
good yields of paraffinic wax, high grade SKO and high-grade lubricating oils.
Asphaltene Based Crude Oils:
They contain little / no paraffin wax but Asphaltene material is usually present in large proportions.
They consist of mostly Naphthene’s. Lube Oils of these crude oils are more sensitive to temperature.
These crude oils give high quality Gasoline.
Mixed Base Crude Oils:
These crude oils exhibit considerable overlapping of the both types described above. A majority of
the crude oils are of this type.
Recent classifications are based on their API gravity (calculated from specific gravity) and sulphur
content. Generally, the higher the API gravity (or lighter the crude) the more distillate products it
contains and the higher is its value.
Sulphur is a significant factor in the crude cost as it is an impurity. The sulphur content in the
petroleum products is restricted by product specifications. High sulphur crudes also have to be
processed after all, but the investment and operational costs are high. Sulphur in crude occurs in
different forms like free Sulphur, Hydrogen Sulphide, Mercaptans, etc.
Nitrogen is also present in crude oils in very minute quantities in the form of Indoles, Pyridines,
Quinolines, etc. Nitrogen compounds create problems while processing and to the stability of the
products. Catalyst deactivation or poisoning, gum formation are some of the offshoots of Nitrogen.
Pour point is also important factor to the extent of handling the crude oil. Crude oils with high pour
point require special handling facilities such as heat tracing and tank heating coils. Sometimes pour
depressing additives are also used. Pour point is an indication of-wax content in crude oil.
Piping provision for addition of wash water using water injection pump at crude charge pump
discharge is also available.
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B. Desalter:
A 2-stage electrostatic Crude Desalter is provided for removal of salt and water from the crude to
desired level. The desalter is designed to handle feed salt content of 57 PTB and feed BS&W of 2.0
vol. % (max). The principle of desalting operation requires mixing of preheated wash water in a
mixing valve with the crude under controlled conditions and to extract impurities. The water/crude
mixture is then resolved by coalescence in a high voltageelectrical field and subsequently separated
in the desalter. Sufficient pressure is maintained at the desalter to ensure no vaporization. This is
achieved by the pressure control valve located at the discharge of the Crude charge pump.
Sufficient quantity of water is mixed with the crude upstream of desalter to dissolve the salts present
in the crude. The desalting water is preheated in Desalter water/brine exchanger and Desalter
water/Kero exchanger before mixing with the crude in order to maintain crude temperature. Strong
electric field is applied in the desalter to break the oil water emulsion and achieve desired phase
separation.
The salt rich water phase (brine) from desalter is sent to the effluent treatment plant. The oil phase
(treated crude) obtained from desalter top is sent for further processing under its own pressure.
The first and second stage desalter vessels are connected in series. The crude enters the firststage and
desalted crude leaves from the second stage. The desalting water flows in a counter current fashion to
the crude flow. The fresh water enters the second stage, and the brine solution leaves from the first
stage desalter. Piping provision exists for maintenance bypass of any one stage to enable unit
operation with only one stage in operation for short duration.
Typically, stripped sour water from Sour Water Stripper Unit shall be used for desalting. Provision to
use service water/DM water is also made. The Desalting Water is pumped from the Desalting Water
Drum operating at 0.5 kg/cm²g pressure through 2nd stage desalting water pump. Desalting water is
pumped under flow control to the Desalter Water/brineexchanger and Desalter water/Kero
exchanger. The water is heated to a temperature of 135°C before it is mixed with crude entering the
2nd stage Crude Desalter. Good mixing of crude and water is achieved through mixing valves
provided at desalter inlet.
The water from 2nd stage Crude Desalter is pumped by 1st stage desalting water pumps under level
control of second stage. This water is mixed with the crude entering 1st stage desalter in a mixing
valve. Hot brine from 1st stage crude desalter is cooled in Desalting Water/Brine Exchanger and
subsequently cooled to 40°C in Brine Cooler before it is sent under interface level control of desalter
to the Effluent Treatment Plant under its own pressure.
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Demulsifier injection is done at the inlet of Desalter using. Provision for Demulsifier injection in
crude pump suction is also available.
A special provision for swing case of operation of pre-heat exchangers is provided based on the
required desalting temperature corresponding to different types of crude to be processed in the unit.
flashing. Crude from parallel trains of Pre-heat train-II is combined and routed to crude heaters,
temperature of crude from pre-heat train-II is 313°C (case 1) and 319.5°C (case 2).
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D. Crude Heaters:
The preheated crude is divided equally between two identical heaters by crude throughput controller.
This crude throughput controller sends soft signal to ratio controller for controlling flow to each pass.
The amount of crude oil that flows through the coils is regulated by means of the Pass Total Flow
Controller and the furnace Pass Balancing Control adjusts the flow rate to each pass, to equalize the
outlet temperature. The estimated coil outlet temperature of each heater for Basra + Doba crude case
is 376.4°C and for Arab Heavy + Dar Blend is 382.5 °C. Each Crude Heater is a six-pass vertical
tube box-multicellular type heater.
Crude Heaters are designed with combination firing burners i.e., for full firing of either fuel gas or
fuel oil or both. Provision for firing of Hot Well-Off gases from Vacuum Column overhead system
and vent gases from SR LPG unit has been provided in Crude Heaters.
Individual heater pass flow controllers are reset by flow controller on inlet heater stream.
Coil outlets of each heater join common heater outlet manifolds and single transfer line is routed to
Crude Distillation Column.
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Sour water separated in reflux drum is routed to the Sour Water Stripper Unit by sour water pumps
after preheating the wash water (Sour water/ Wash water) in followed by further cooling by cooling
water in under inter phase level control. The uncondensed vapours from the Reflux Drum are fully
condensed in Overhead Naphtha Air Cooler and Overhead Naphtha Trim Cooler. The hydrocarbon
liquid (unstabilized naphtha) and recycle water are separated in Overhead Naphtha Drum.
The Unstabilized naphtha consisting of all the fuel gas, LPG and Naphtha components is pumped
under level-cascaded flow control by Stabilizer Feed Pumps to Naphtha Stabilizer Column after
preheating in the Stabilizer Feed/ Bottom exchanger and Stabilizer Feed/ Swing
Naphtha Product Exchanger. Separated sour water is routed to the Sour Water Stripper unit by
Overhead Naphtha Drum Sour Water Pumps.
Crude column top pressure is maintained by split-range pressure control with Fuel gas blanket on
Overhead Naphtha Drum.
To avoid severe local corrosion by strong acids, wash water is injected to overhead vapours at the
inlet of the Crude / Crude Column OVHD Exchanger. The wash water is added to the overhead
vapours to force the water dew point of vapours at the inlet of overhead exchangers. All the salts
(primarily chlorides of calcium, magnesium and sodium) present in overhead vapours are dissolved
in wash water and are purged out of the system through sour water purge stream to Sour Water
Stripper unit. Additionally, Filming Amine and Neutralising Amine are also injected in the Crude
Column overhead line in order to protect the overhead line and the Column top dome. Provision for
injecting Wash water at inlet of AFC is available to remove salt deposits on the bundle, this shall be
used if pressure drop across AFC increases. Filming amine and Neutralizing amine are also injected
in crude column reflux line to protect the column top. During start-up, unstabilized naphtha shall be
taken from DHT unit using start up line provided in Overhead Naphtha drum.
stripper reboiler Light ends in Heavy Naphtha are knocked off by reboiler so as to achieve the
desired Swing Naphtha product flash point. Swing Naphtha stripper reboiler duty is controlled
regulating the
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opposite acting control valves of Kero product flow. Light hydrocarbon vapours from the side
stripper are routed back to crude column below tray #
51. The bottom product of Swing naphtha Stripper is pumped by Swing naphtha Product
pump to Stab feed / Swing Nap product exchanger followed by SR Swing Naphtha Air
cooler. Swing Naphtha is routed to NHT unit at 87°C. Provision is also kept to route Swing
naphtha to Diesel pool at 40°C. Swing naphtha Product Trim Cooler is also provided in the
rundown line to route the Cold Swing Naphtha at 40°C to offsite storage or Export Naphtha
storage tanks. Provision for routing Swing Naphtha to Existing DHDS unit or New DHT unit
at 87°C is available.
H. Kerosene Section:
Kerosene is drawn from tray # 36 (through chimney tray #3) of Crude Column. The Kero drawflows
to the Kero Stripper under Stripper level control. Kero stripper is a reboiled stripper using HGO CR
as reboiling medium. The Kero Stripper has horizontal thermosiphon reboiler. Light ends in Kero
product are knocked off by the reboiler so as to achieve the desired Kero product flash point. Kero
Stripper Reboiler duty is controlled regulating the opposite acting control valves of HGO CR flow.
The light Hydrocarbon vapours leaving the Kero stripper are returned to the Crude column below
tray # 39.
Kero Product is pumped by Kero Product Pumps to Swing Nap Stripper reboiler, Crude/Kero Pdt
Exch-1, Crude/Kero Pdt Exchanger-II, followed by Desalter water/Kero Exchanger. The Kero
Product is further cooled in Air cooler. The Kero product is cooled in Kero Product Air Cooler-II and
Kero Product Trim Cooler to 40 °C and is routed as a feed to Existing Merox. Provision is also kept
to route Kero at 40 °C to Sour Diesel storage / Kero storage.
Piping arrangement is provided to route Kero Product from upstream/downstream of Air Coolers to
RUF unit or from upstream of Air Cooler to DHT / DHDS unit.
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Provision for LGO Product cooling in LGO Product Air cooler and LGO Product Trim Coolers to 40
°C is provided. Cold LGO product from is routed to Sour Diesel Storage.
Kero CR:
Kero CR is drawn from tray # 36 along with Kero draw to Kero Stripper and is pumped by Kero CR
pump. The heat available in Kero CR is removed in Crude/Kero CR exchanger’s and routed to the
Crude Column on tray # 38 under flow
control.
LGO CR:
LGO CR is drawn from tray # 25 along with LGO draw to LGO Stripper and is pumped by LGO CR
Pump. The heat available in LGO CR is removed in Crude/LGO CR exchanger-I, Crude/LGO CR
exchanger-II and Crude/LGO CR exchanger-III before being routed to Crude Column on tray # 27
under flow control
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HGO CR:
HGO CR is drawn from tray # 16 along with HGO draw to stripper and is pumped by HGO CR
Pump. The HGO CR stream exchanges heat with crude in crude preheat exchanger Crude/HGO CR
exchanger and then HGO CR is used as a hot medium in the Kero reboiler before being routed back to
the Crude Column on tray # 18 under flow control.
to route Kero product to storage at 40 °C. Depending on the demand of Kero Product in DHTunit and
Merox unit, the balance product is routed to storage.
Provision for manually bypassing the cascade control and run individual flow control loop (FT/FIC)
on Kero Product rundown lines is considered in case any of the FT/FIC malfunction.
Unstabilized naphtha consisting of fuel gas, LPG and Naphtha components is pumped under level-
cascaded flow control by Stabilizer Feed Pumps to Naphtha Stabilizer after preheating in the
Stabilizer Feed/Bottom Exchanger and Stabilizer Feed I Swing Naphtha Product Exchanger.
Stabilizer column has 48 trays with feed normally entering the 25th tray. Stabilizer Reboiler isheated
by LGO Product. Stabilizer Tray # 3 temperature is controlled by controlling the LGO Product flow
in the Stabilizer Reboiler, with opposite acting control valves.
The overhead products are condensed in the Stabilizer Overhead Condenser before routing to
Stabilizer Reflux Drum. Any water present in the overheads is separated in Stabilizer Reflux Drum
and sent to Sour Water Stripper Unit through a common sour water line under level control of Boot.
The LPG from Stabilizer Reflux Drum is pumped under level-cascaded flow by LPG product pump
to LPG Treater Unit. Stabilizer reflux is pumped by Stabilizer Reflux Pumps.
The desired composition of stabilised naphtha & LPG can be obtained either by controlling the
reboiling rate or by controlling the condensing rate. Reboiling rate is controlled by tray # 3
temperature regulating the hot medium (LGO Product). Condensing rate is controlled by Tray # 46
temperature cascaded with reflux flow. Only one of the temperature controllers shall be employed at
a time.
Stabilizer column pressure is controlled through hot vapour bypass control scheme wherein part of
overhead vapour bypasses the overhead condenser and provides enough vapour to Stabilizer Reflux
Drum to maintain control. In case of any accumulation of non-condensable, excess pressure is
relieved to fuel gas header via control valve which is routed to DHT FGATU.
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During normal operation, there will not be any release to fuel gas header and 100% vapours will
condense down, however, in case of any upsets, the same shall be taken care by the overhead vapour
line control valve.
Stabilised Naphtha product from Stabilizer Column bottom is pumped by Stabilised Naphthaproduct
pumps and cooled in feed/bottom exchanger before being routed to Naphtha Hydrotreater unit as hot
feed. Stabilised Naphtha is further cooled in the exchanger to 40°C before routing to offsite storage /
Export Naphtha storage tank / Slip stream for Filming Amine in Filming amine Drum for dilution as
per requirement.
During start-up, Naphtha Stabilizer is bypassed and unstabilized naphtha is routed to slop header.
To avoid build-up of corrosive salts in the naphtha stabilizer, filming amine and neutralizing amine
dosing provision is available at the column top and column reflux (only filming amine).
During start-up, Naphtha Stabilizer is bypassed and unstabilized naphtha is routed to slop header.
To avoid build-up of corrosive salts in the naphtha stabilizer, filming amine and neutralizing amine
dosing provision is available at the column top and column reflux (only filming amine).
A. Vacuum Heater:
Hot RCO from Crude column bottom is pumped by RCO pumps to vacuum heater where RCO is
heated and partially vaporised. RCO enters the Vacuum heater at temperature of 367.1°C (for case 1)
& 373.2°C (for case 2).
Vacuum Heater is an eight-pass twin cell cabin type heater. Total RCO flow is equally distributed
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among eight passes by flow controllers located on each pass. The amount of RCOthat flows through
the coils is regulated by means of the Pass Total Flow Controller and the furnace Pass Balancing
Control adjusts the flow rate to each pass, to equalize the outlet temperature. Individual pass flow
controllers are reset by the total flow controller cascaded with Crude column Level controller.
Vacuum Heater is designed with combination firing burners i.e. for full firing of Fuel Oil or Fuel Gas
or both. The Fuel Gas or Fuel Oil supply to the Heater is controlled by the Vacuum Heater outlet
manifold temperature. The atomizing steam is supplied under differential pressure control with
respect to fuel oil pressure.
MP steam (coil steam) is injected in the coils at appropriate locations to start vaporisation bylowering
the partial pressure of hydrocarbons. Coil steam also helps in maintaining requisitevelocities in
heater passes and to prevent coking owing to high coil outlet temperatures. Thetarget coil outlet
temperature of Vacuum Heater for Basra + Doba and Arab Heavy + Dar blend Crude is 425°C.
Each coil outlet of Vacuum Heater joins the transfer line and the combined product is routed to the
Flash Zone of Vacuum Column.
above flash zone ensures optimal vapour liquid separation. The Vacuum Column Flash zone pressure
is maintained at 39 mmHga and temperature of about 410°C.
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C. Stripping section:
Stripping section is provided with six valve type trays. The heavy hydrocarbons are stripped on valve
trays by means of superheated LP stripping steam. During start-up, LP steam from LP steam header
shall be used and during normal operation or after vacuum heater stabilization, superheated LP steam
from vacuum heater shall be used. Subsequently the residue is quenched to a temperature of 350°C
by the vacuum residue Quench to prevent after cracking in the bottom compartment of the column.
Quench at 250°C is recycled back to the column bottom under flow control cascaded with column
bottom stream temperaturecontroller to maintain the required temperature.
The vaporised portion entering the flash zone of the column along with the stripped light ends from
the bottoms, rise up the column and is fractionated into 4 side stream products in 5 packed sections.
Demister pads are provided at the top of the column to minimize carryover of hydrocarbons to the
ejector section.
The various side streams from Vacuum Column are Vacuum Diesel (VD), LVGO, HVGO and Slop
Distillate. Vacuum Residue (VR) + Quench is drawn from the bottom of the column. Vacuum
Column
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Overhead Circuit:
Overhead vapours from Vacuum column goes to the vacuum system to maintain a pressure of about
28 mmHga at the Vacuum Column top. The vacuum system is designed with a two- stage ejector and
Liquid ring vacuum pump package. The two stage steam jet ejectors operating during normal
operation are 1st Stage Ejectors and 2nd Stage Ejectors. The vacuum system also includes ejector 1st
stage Inter condenser, Ejector 2nd stage after condenser & LRVP package. MP steam is used as
motive steam to the Ejectors. To avoid build-up of corrosive salts in the Vacuum column, filming
amine and neutralizing amine dosing provision is available at column top. There are two number of
neutralizing amine dosing points at the vacuum column overhead line. One is- used for dosing
neutralizing amine during normal operation and the other is normally blinded, which shall be used
only during shutdown for decontamination of overhead line by using KMnO4 dosing.
Vacuum Column overhead vapours are drawn by 1st stage ejectors. The hydrocarbon and water
vapours from first stage ejectors are partially condensed in the Ejector first stage Inter condenser and
the liquid from Inter condenser flows to the Hot well. The vapours from Inter-condenser are fed to
the 2nd stage Ejector. The HC + Water vapours from 2nd stage ejector are condensed in the ejector
2nd stage After condenser the HC + Water vapour fromafter condenser is sent to LRVP package and
the liquid is sent to Hot well. A spillback line to the 1st stage ejector inlet from the 1st stage outlet is
provided to maintain the Column top pressure. Vent gases from Hot well are sent to the Hot well
Catch Pot from where vent gas issent for Amine Treatment before being routed to the Crude Heaters
burners. Flame arrestorsare provided on the line to the burners to prevent flame flash back.
Sour water from Hot well is pumped by hot well sour water pumps. Sour water ex-Hot well flows
under interphase level-cascaded flow control for further treatment in sour water stripper unit.
Slop oil from Hot well is pumped by Hot well Slop Oil Pumps under level-cascaded flow control
through a Coalescer to LGO product rundown line as a hot feed to existing DHT
/DHDS unit or Sour diesel storage. Alternatively, this stream can be routed to light slop header.
Vacuum Diesel from Bed # 1 collector tray is drawn and pumped by Vacuum Diesel Product +CR +
IR Pump and is divided into 2 streams, namely, Vacuum Diesel IR, Vacuum Diesel CR + Product.
Vacuum Diesel IR is returned under flow control to the Vacuum Column above Bed # 2 through
gravity distributor. The product + CR stream is routed through Vacuum diesel Product + CR Air
cooler. Cold Vacuum Diesel Product rundown and part CR stream is further cooled in the Vacuum
Diesel Product Trim Cooler to a temperature of 40°C before the product is routed to Sour diesel
storage. Vacuum diesel product hot rundown line is available through Air Coolers to DHDS / DHT
unit.
The temperature control of CR stream at 50 °C is achieved by Temperature control split range control
valves, one on Vacuum Diesel CR line at the outlet of Exchangers and the otheron Vacuum Diesel
CR line bypassing.
The temperature-controlled Vacuum Diesel CR stream is routed back to Vacuum column above bed
#1 under flow control cascaded with Column top temperature control.
The vacuum diesel bed (# 1) is also a heat transfer section where the heat transfer duty is provided by
Vacuum Diesel CR.
E. Light LVGO:
Light LVGO from Bed #2 collector tray is pumped by Light LVGO pump under tray level control
and is merged with LVGO CR before entering the top of bed #3. This combined stream passes
through LVGO CR filters before entering vacuum column, to remove any foreign particles.
LVGO product, after exchanging heat with Crude in Crude/LVGO Product Exchangers is combined
with hot HVGO product and the combined VGO is routed as Hot VGO to FCHCU unit.
In case of cold rundown operation, LVGO is cooled in Tempered water coolers then combined with
cooled HVGO and routed to storage under flow control. The LVGO rundown temperature is
controlled at 80 °C by a temperature controller which manipulates opposite acting control valves on
tempered water side.
mixed with Vacuum Residue stream after Vacuum Residue stream exchanges heat with Crude in
preheat train exchangers and third stream as recycle to vacuum heater inlet.
Over flash is the reflux on to the tray above the flash zone to knockout the entrained crude oil and
wash it down into the bottom of the column. The Over flash removes heavier components in the
vapor flowing upward from the flash zone by condensation and by coalescing entrained liquid
droplets. This lowers the heavy vacuum gasoil (HVGO) end point by removing heavier components
that belong in the vacuum residue. This also serves to reduce other contaminants such as organic
metals, carbon, and asphaltenes. Over flash flowis controlled through, and required quantity is 74915
kg/hr (for case 2) & 77422 kg/hr (for case 2).
Combined stream of Vacuum Residue + Slop after exchanging heat in MP Steam generator and LP
Steam Generator and VR+Slop / BFW preheaters and TW coolers is sent as hot feed to RUF.
The slop bed #5 is immediately above Flash Zone and serves as a wash zone to prevent entrainment
of Vacuum Residue into HVGO. This bed consists of two portions - the bottom layer is grid packing
and the top layer is structured packing. Vapours rising from Flash Zone are condensed by HVGO IR
and collected as slop in bed # 5 collector tray. This liquid providesthe required washing in this
section. Also, fractionation between HVGO & Slop takes place inthis bed.
For proper operation of wash bed, sufficient wetting all over the wash bed is of utmost importance. If
the liquid load of the bed becomes too low, part of the packing will run dry resulting in hot spots and
local coke formation. Further, more entrainment will no longer be removed and the fractionation in
the bed will be adversely affected. Wash oil rate which determines the wetting rate on the top &
bottom of the wash bed is governed by HVGO product yield. HVGO yield can be lowered to increase
the wetting rate and improve the HVGO product quality.
The slop drum is provided with minimum hold up to take care of the surge required for the slop
distillate pump. It is advised to keep the level in the slop drum at minimum possible. This is required
to avoid excessive residence time of the slop drum liquid and the possibility of cracking/coking.
Cooling of high pour point products like Vacuum Residue and VGO is done by tempered water to
prevent exchanger congealing and to reduce exchanger maintenance. A recirculating tempered water
circuit is provided in the unit for this purpose. Tempered water at 60°C is pumped from Tempered
Water Drum by Tempered Water Pumps to LVGO Product/TW Cooler, HVGO Product/TW Cooler-
I, HVGO Product/TW Cooler-II, VR+Slop / TW Water Coolers I and II. The heated tempered water
at 80°C is then returned to Tempered Water Drum after cooling to 60°C in Tempered Water Air
Cooler. Temperature at the
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downstream of Air cooler is maintained at 60°C by a temperature controller which manipulates the
fan pitch to control the temperature (50% of fan are variable pitch type). Intermittent make up of
Boiler feed water (DM water is not to be used) compensates for theevaporation and other losses from
the system. Pressure of the Tempered Water Drum is controlled by Nitrogen blanketing.
When VR + Slop products, HVGO product are required to be routed as cold feed to storage, excess
heat available in the streams will be removed in a set of MP & LP steam generators, BFW preheater
and tempered water coolers.
Horizontal thermosyphon exchangers connected to MP Steam drum constitute the MP steam
generation section.
The LP Steam Generation section comprises the following:
1. Horizontal thermosyphon exchangers connected to LP Steam Drum
2. Horizontal thermosyphon exchangers connected to LP Steam Drum II
Steam Drums are operated at higher pressure than the maximum header pressure of MP& LP steam.
MP and LP steam drums pressure is controlled by a pressure control valve located on the steam outlet
line of each drum. The MP and LP Steam generated in the steam drums are at saturated conditions at
the respective pressure of the two drums and attain some superheat before it joins the steam header
because of reduction in pressure by the pressurecontrol valve.
Make-up BFW is preheated by VR+Slop runs downstream in VR+Slop/BFW preheaters I and
II. Make up preheated BFW from is fed to MP Steam Drum while BFW from is fed to the LP Steam
Drum. Make up BFW to is direct. The make-up BFW to each Steam Drum is controlledby the steam
flow from that Drum cascaded with the level of the respective steam drum.
Provision for bypassing steam drums has also been made in this unit for IBR inspection. In case of
MP steam out of service during IBR inspection, exchanger’s will be isolated and VR + slop will be
routed through the bypass of these exchangers. No cold rundown of VR+slop to storage tanks will be
possible in this scenario. When LP Steam Drum is out of service for IBR inspection, exchangers will
remain out of service. In this case additional exchanger of single shell in series will be required in
addition to tempered water cooler for to meet hot rundown case of operation for VR+Slop. No cold
rundown of VR+ slop to storage tanks is possible in this scenario.
When LP Steam Drum is out of service for IBR inspection, exchanger will remain out of service.
Exchanger will need to be taken in line to cool and route VR Product to Bitumen Tanks (if the need
for this routing arises).
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For both the modes of operation, it will be possible to route HVGO at hot rundown temperature
similar to design cases as well as cold rundown of HVGO, if required.
Blowdown from MP steam drum is flashed in a LP flash drum floating with LP steam header. The
flashed condensate from this LP Flash Drum and blowdown from LP Steam Drum is sent to Steam
Blowdown Drum after exchanging heat with BCW in Exchanger where it is quenched with service
water before draining it to IETP.
Hot well Off-gases from the Hot well catch pot of the Vacuum section of CDU/VDU is routed to the
Hot well Off-gas treatment section containing Amine Absorber column. Amine Absorber column is a
two packed bed column.
Lean amine from VRMP/DHT ARU is routed to the Amine Absorber column on flow control,
where it strips H2S in the Off-gases entering the column from the Hot well catch pot. H2S
concentration in Off-gas at Absorber inlet is 21.29 - 21.52 WT % which is reduced to 0.09 WT
% in Sweet Off-gas at Amine Absorber outlet. Most of the H2S absorption occurs in first bed (bottom
bed) of the amine column and remaining H2S is absorbed in the second bed (top bed) of the column.
H2S stripped Off-gases exit the column from top and is routed to CDU heaters through Off-Gas
Knock-out Drum as a fuel source. Any carry over or any condensed off gases in the Sweet Off-gas
from the Amine Absorber column are separated in Off-Gas Knock-out Drum before being routed to
Crude heaters. Rich amine exits the column from bottom and is routed back to VRMP/DHT ARU for
amine regeneration. In case amine is not available in Amine Absorber, Caustic scrubber provided will
strip off H2S from the Off-gases before being vented to atmosphere. Venting to atmosphere is done
only during start-up operation or any other upset scenario. The Amine Absorber column is also
provided with skimming facility to skim off any hydrocarbon accumulated on the surface of amine in
the column. As the lean amine in the column becomes richer in H2S it converts into rich amine which
is finally pumped out of the system by Rich Amine Pumps on level control to VRMP/DHT Amine
Regeneration Unit.
Temperature differential control is provided in between Lean amine and Hot well sour gas in order to prevent
any condensation of the sour off gas entering the Amine Absorber column.Typically, Lean amine temperature
should be minimum 5 degree above Hot well off gas temperature entering into the Amine absorber column.
During start- up, LP Steam is used forheating the lean amine in Lean Amine/Tempered Water Exchanger with
temperature control. During normal operation, Temperature control will provide the set point to Flow control
on tempered water line to control the lean amine temperature. Set point to located on tempered water return line
is adjusted based on set point of flow control to balance the flow rate in tempered water circuit. Selector switch
is provided to switch between start-up and normal operation mode.
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HPCL
8. STRAIGHT RUN LPG TREATING SECTION
Introduction:
Amine treated LPG enters the caustic pre-wash column in bottom bed,
having
structured packings. Before entering pre-wash column, LPG
passes through LPG amine
Settler filters to arrest carryover of foreign materials back to column.
Bottom bed of pre-wash column is intially filled with 12% caustic.
This section
functions in semi-continuos mode. In this arrangement LPG
stream passes continuously
through a pool of caustic solution. Once the caustic concentration
reaches 2% i. e,
spent caustic it is transferred from column bottom to degassing vessel.
LPG from this section goes to top bed of pre-wash column which
operates in
continuos mode.) LPG contacts counter-currently with caustic coming
from seperators,
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HPCL
through filters to arrest carryover of foreign materials back to column.
Rich caustic from top bed of pre-wash column is sent to Caustic
Regenerator system
through caustic heater.From top of this column LPG goes throughLPG
filters to
remove solids larger than 100microns.Then LPG enters the caustic wash
column
where it again contacts with rengenerated caustic solution. The treated
LPG passes
through a coalescer pad located in caustic seperator and then it is
cooled in LPG cooler
Using cooling water upto 40°C.The treated LPG is filtered in filter
to arrest caustic
carry over and LPG product is finally sent to storage outside battery limit.
Fresh 18% caustic from B/L is fed into 18% caustic tank. A small
amount of 18% caustic
Is required for continuous make up in caustic wash section and rest of
18% caustic is required
For preparing 12% caustic solution by addition of DM water.
12% caustic solution is directly
Prepared in 12% caustic tank by mixing of 18% caustic and DM water
using jet educator.
12% caustic is used for unit start up and also for intermediate
batch requirement of Prewash
Column.
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HPCL
9. MAJOR EQUIPMENT IN CDU
9.1 DESALTER
Crude oil desalter is a device used in petroleum refineries to remove in organic salts, water and
sediment from the incoming petroleum crude oil feed stock before it is refined. This article
focuses on the use of electrostatic desalters to produce a dehydrated, desalted crude oil with
allow sediment content. Almost al refineries now use electro static desalters. However, there
may stil be a few refineries employing the older, less efficient method that utilizes chemicals
and settling tanks.
Removal of the salts, water and sediment is necessary to avoid excessive fouling of equipment
as wel as corrosion from the generation of hydrochloric acid (HCl) by the hydrolysis of the
chloride salts present in the incoming crude oil, in particular magnesium chloride (MgCl2) and
calcium chloride (CaCl2). Any salts that are not removed represent a source of metals that can
"poison expensive catalysts used in various petroleum refinery processes.
The amount of water, salts and sediment in the crude oil as received at petroleum refineries
Varies widely with the source of the crude oil, the prior processing of the crude oil at the
source sites and with the mode of transporting the crude oil from its source to the refineries.
The salts present in petroleum crude oils are mainly chloride with following approximate
breakdown:
15 weight percent Magnesium chloride (MgCl2) 10 weight percent Calcium chloride (CaCl2)
These diment present in petroleum crude oils include clay, rust, iron sulfide (FeS), asphaltenes
and various other water-insoluble particles.
Such oil field processing typically involves washing the oil with water to remove salts, some
heating, use of demulsifying chemicals and simple settling vessels and tanks. In some cases,
the oil field processing includes electro static desalting as well. In general, the oil field
processing
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HPCL
facilities strive to remove enough water, sediment and salts so that the transported crude oil
contains less that 1 to 2% by volume of sediment and water (BS&W) and less than 10to20
pounds of salts per 1000 barrels (PTB) of clean, water- free crude oil (which is equivalent to a
salt content of 34 to 68 ppm by weight).
Never the less, the crude oils as received at petroleum refineries have a salt content that
ranges from a PTB of 10 to 300 (34to1,020 ppm by weight), based on spot samples of many
different crude oils as delivered to refineries.
At that point, wash water is injected and mixed in to the continuous flow of crude oil and there
resulting oil-water emulsion then continuously enters the electrostatic desalter. The rate of
wash water required is about 4 to10% by volume of the crude oil rate. The optimum wash
water rate varies with the API gravity of the crude oil and with the desalter temperature.
The oil water emulsion that enters from the bottom of the desalter through the feed line Is a
thorough mixture of two non-
Miscible liquids consisting of a continuous phase (the crude oil) and a dispersed phase (water
in the form of very small droplets with dimensions ranging from1to10 micrometres).
Asphaltenes and finely divided sediment solids are adsorbed on the oil- water interface and
stabilize the emulsion. Thus the degree of difficulty involved in coalescing the droplets into
large globules which can be settled and removed is related to the presence of asphaltenes,
sediments and other water- insoluble contaminants.
In other words, the electrostatic field results in each droplet having a positive charge on one side
and a negative charge on the other which cause the droplets to coalesce because of the attractive
force generated by the opposite charges on neighboring droplets. The resulting larger water
droplets (globules), along with water- Insoluble solids, then settle to the bottom of the desalter.
The settled water is continuously with drawn from the desalter from a point some what above
the desalter bottom (see Figure2) and is referred to as a brine because it contains the inorganic
salts that originaly entered the desalter with the water in the crude oil. The settled sediment at
the bottom of desalter is with drawn as a sludge at intermitent intervals as needed to prevent
solids from entering the settled water withdrawal outlet. Cross-sectional end- view diagram of a
horizontal, cylindrical crude oil desalter.
The purpose of desalting is to remove these undesirable impurities, especially salts and water,
from the crude oil prior to distillation.
9.2 FURNACE
A furnace is an equipment to melt metals for casting or heat materials for change
of shape
(rolling, forging etc) or change of properties (heat treatment).
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HPCL
9.2.1 Types and Classification of Different Furnaces
Based on the method of generating heat, furnaces are broadly classified into two types namely
combustion type (using fuels) and electric type. In case of combustion type furnace, depending
upon the kind of combustion, it can be broadly classified as oil fired, coal fired or gas fired.
• Based on the mode of charging of material furnaces can be classified as
(i) Intermittent or Batch type furnace or Periodical furnace and
(ii) Continuous furnace.
• Based on mode of waste heat recovery as recuperative and regenerative furnaces.
• Liberation of sufficient heat within the furnace to heat the stock and overcome all
heat losses.
• Transfer of available part of that heat from the furnace gases to the surface of the
heating stock.
• Equalisation of the temperature within the stock.
• Reduction of heat losses from the furnace to the minimum possible extent.
Amongst of all type of exchangers, shell and tube exchangers are most commonly used heat exchange
equipment. The common types of shell and tube exchangers are:
Fixed tube-sheet exchanger (non-removable tube bundle): The simplest and cheapest type of shell
and tube exchanger is with fixed tube sheet design. In this type of exchangers the tube sheet is welded to
the shell and no relative movement between the shell and tube bundle is possible
Removable tube bundle: Tube bundle may be removed for ease of cleaning and replacement.
Removable tube bundle exchangers further can be categorized in floating head and U-tube exchanger.
A PROJECT REPORT ON
Shell Typical Advantages
HPCL Limitations
and TEMA
Tube code
Exchangers
Fixed tube BEM, Provides maximum Shell side / out side of the tubes are
sheet AEM, heat transfer area for a inaccessible for mechanical
NEN given shell and tube cleaning.
diameter.
No provision to allow for differential thermal
Provides for single and expansion developed between the tube and
multiple tube passes to the shell side. This can be taken care by
assure proper velocity. providing expansion joint on the shell side.
U-tube BEU, AEU U-tube design allows for Because of U-bend some tubes are omitted
differential thermal at the centre of the tube bundle.
expansion between the
shell and the tube bundle Because of U-bend, tubes can be cleaned
as well as for individual only by chemical methods.
tubes.
Due to U-tube nesting, individual tube
Both the tube bundle and is difficult to replace.
the shell side can be
inspected and cleaned No single tube pass or true
mechanically. countercurrent flow is possible.
9.4 Condenser
The change from liquid phase to vapor phase is called vaporization and the reverse phase
transfer is condensation. The change from liquid to vapor or vapor to liquid occurs at one
temperature (called saturation or equilibrium temperature) for a pure fluid compound at a given
pressure. The industrial practice of vaporization and condensation occurs at almost constant
pressure; therefore the phase change occurs isothermally.
Condensation occurs by two different physical mechanisms i.e. drop-wise condensation and
film condensation.
The nature of the condensation depends upon whether the condensate (liquid formed from
vapor) wets or does not wet the solid surface. If the condensate wets the surface and flows on
the surface in the form of a film, it is called film condensation. When the condensate does not
wet the solid surface and the condensate is accumulated in the form of droplets, is drop-wise
condensation. Heat transfer coefficient is about 4 to 8 times higher for drop wise
condensation. The condensate forms a liquid film on the baresurface in case of film
condensation. The heat transfer coefficient is lower for film condensation due to the resistance
of this liquid film.
Dropwise condensation occurs usually on new, clean and polished surfaces. The heat exchanger
used for condensation is called condenser. In industrial condensers, film condensation normally
occurs.
Upflow vertical condenser: In case of upflow condenser, the vapor enters at the bottom
and flows upwards inside the tubes. The condensate drains down the tubes by gravity
only.
ii. Horizontal condenser: The condensation may occur inside or outside the horizontal tubes
(Figure 1.8). Condensation in the tube-side is common in aircooled condensers.
The main disadvantage of this type of condenser is that the liquid tends to build up
in the tubes. Therefore the effective heat transfer coefficient is reduced
significantly.
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Figure 1.7. Downflow vertical condenser with condensation inside tube [5].
Figure 1.8. Horizontal condenser with condensation outside horizontal tubes [5].
Vertical cut-segmental baffles are generally used in condensers for side-to-side vapor flow and
not for top to bottom. An opening at the bottom of the baffles is provided to allow draining of
condensate.
Reboilers
Figure 1.10. Thermosyphon reboiler [5]. (a) Horizontal thermosyphon reboiler. (b) Vertical thermosyphon
reboiler
ii. Forced circulation reboiler: The liquid is fed by means of a pump. Forced
circulation reboilers with vertical or horizontal tubes boiling may be designed. Forced
circulation reboilers are similar to vertical thermosiphon reboilers, except the pump is
used for the circulation of the liquid and the hot liquid flows inside column. To
calculate the heat transfer coefficient it is generally assumed that, heat is transferred
only by forced convection. The usual method of shell and tube exchanger design can
be used. Advantage: suitable for viscous and highly fouling fluids.
Disadvantage: high pumping and maintenance cost; pump is required to circulate the
boiling liquid through the tubes and back into the column.
iii. Kettle reboiler: The tube bundle is immerged in a pool of liquid at the base of the
column in an oversize shell (Figure 1.11). Kettle reboiler is also called a
“submerged bundle reboiler”. The height of the tube bundle is usually 40-60% of
the shell ID. The submergence of the tube bundle is assured by an overflow weir at
height of typically 5-15 cm from the upper surface of topmost tubes.
Advantage: suitable for vacuum operation and high vaporization rate up to about 80%
of the feed.
Limitations: low heat transfer rate than other types as there is no liquid circulation (low
velocity); not appropriate for fouling fluids; kettle reboiler is not suitable for heat
sensitive materials as it has higher residence time.
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9.5 VALVES
A valve is a mechanical device that controls the flow of fluid and pressure within a system or
process. A valve controls system or process fluid flow and pressure by performing any of the
following functions:
The disk of a gate valve is completely removed from the flow stream when the valve is fully open.
This characteristic offers virtually no resistance to flow when the valve is open. Hence, there is little
pressure drop across an open gate valve.
Globe Valves
A globe valve is a linear motion valve used
to stop, start, and regulate fluid flow. A Z-
body globe valve is illustrated in Figure 9.
Most ball valve actuators are of the quick-acting type, which require a 90° turn of the valve
handle to operate the valve. Other ball valve actuators are planetary gear-operated. This type of
gearing allows the use of a relatively small handwheel and operating force to operate a fairly
large valve.
Plug Valves
A plug valve is a rotational motion valve used to stop or start fluid flow. The name is derived
from the shape of the disk, which resembles a plug. A plug valve is shown in Figure 13. The
simplest form of a plug valve is the petcock. The body of a plug valve is machined to receive
the tapered or cylindrical plug. The disk is a solid plug with a bored passage at a right angle to
the longitudinal axis of the plug.
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In the open position, the passage in the plug lines up with the inlet and outlet ports of the
valve body. When the plug is turned 90° from the open position, the solid part of the plug
blocks the ports and stops fluid flow.
Diaphragm Valves
A diaphragm valve is a linear motion valve that is used to start, regulate, and stop fluid flow.
The name is derived from its flexible disk, which mates with a seat located in the open area at
the top of the valve body to form a seal. A diaphragm valve is illustrated in Figure 14.
Diaphragm valves are, in effect, simple "pinch clamp" valves. A resilient, flexible diaphragm is
connected to a compressor by a stud molded into the diaphragm. The compressor is moved up
and down by the valve stem. Hence, the diaphragm lifts when the compressor is raised. As the
compressor is lowered, the diaphragm is pressed against the contoured bottom in the straight
through valve.
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Reducing Valves
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Reducing valves automatically reduce supply pressure to a preselected pressure as long as the
supply pressure is at least as high as the selected pressure. As illustrated in Figure 16, the
principal parts of the reducing valve are the main valve; an upward-seating valve that has a
piston on top of its valve stem, an upward-seating auxiliary (or controlling) valve, a controlling
diaphragm, and an adjusting spring and screw.
Reducing valve operation is controlled by high pressure at the valve inlet and the adjusting screw on top
of the valve assembly.
Pinch Valves
The relatively inexpensive pinch valve, illustrated
in Figure 18, is the simplest in any valve design. It
is simply an industrial version of the pinch cock
used in the laboratory to control the flow of fluids
through rubber tubing.
Butterfly Valves
A butterfly valve, illustrated in Figure 19, is a rotary motion valve
that is used to stop, regulate, and start fluid flow. Butterfly valves are
easily and quickly operated because a 90o rotation of the handle
moves the disk from a fully closed to fully opened position. Larger
butterfly valves are actuated by handwheels connected to the stem
through gears that provide mechanical advantage at the expense of
speed.
Needle Valves
A needle valve, as shown in Figure 20, is used to make relatively fine
adjustments in the amount of fluid flow.
A swing check valve is normally recommended for use in systems employing gate valves because of the
low pressure drop across the valve. Swing check valves are available in either Y-pattern or straight body
design.
A relief valve, illustrated in Figure 28, gradually opens as the inlet pressure increases above the
setpoint. A relief valve opens only as necessary to relieve the over-pressure condition. A safety valve,
illustrated in Figure 29, rapidly pops fully open as soon as the pressure setting is reached. A safety
valve will stay fully open until the pressure drops below a reset pressure. The reset pressure is lower
than the actuating pressure setpoint. The difference between the actuating pressure setpoint and the
pressure at which the safety valve resets is called blowdown.
Blowdown is expressed as a percentage of the actuating pressure setpoint.
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Relief valves are typically used for incompressible fluids such as water or oil. Safety valves are
typically used for compressible fluids such as steam or other gases. Safety valves can often be
distinguished by the presence of an external lever at the top of the valve body, which is used as an
operational check.
9.6.1 PRINCIPLE :
Steam Jet Ejectors offer a reliable & economical means for producing vacuum. In
Steam Jet Ejector, pressure energy of motive fluid is converted into velocity
energy. The velocity energy entrains the suction fluid. This entrained mixture of
motive fluid & suction fluid are discharged via convergent/divergent diffuser
where its velocity energy is reconverted into pressure energy. This action makes
the discharge pressure higher then suction pressure thus a Steam Jet Ejector behaves like a compressor.
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9.6.2 The ejector performance is affected by either high/low supply steam pressure to the
ejector or by high condensate level in the ejector. In such cases, put the starting air ejector in
service immediately along with the running main air ejector to prevent a decrease in
vacuum.
Because part of the operating liquid also flows out of the pump along with the discharged gases, it has to
replenished by fresh liquid. The continuous flow of the operating liquid also takes away part of the heat
of compression from the gases handled thereby cooling the pump. The liquid must not contain solid
materials, e.g. sand, otherwise the casing will be subject to heavy wear or the impeller will jam. The
three methods/schemes to replenish operating liquid are: once-through system (no recovery), partial
recovery system and total recovery system.
In this method, the operating liquid discharged along with gases is separated from the gases in a
separator and allowed to flow into a drain. The lost quantity of operating liquid is replenished by fresh
operating liquid (full quantity) from an external source. This is a popular method and is used where
there is an abundant supply of fresh liquid and its conservation or contamination is not a concern. It is
recommended that the operating liquid should be supplied to the pump with a pressure, approximately
0.5 to 1 bar (7.25 and 14.5 psi) above the inlet pressure of the gases. The flow rate of the operating
liquid depends on the pump capacity and the operating vacuum.
This method is used where it is desired to minimize the use of fresh operating liquid. In this method,
the operating liquid enters and leaves the pump like the once-through system. However, part of the
discharged liquid is recycled from the discharge separator and the balance is continuously supplied
from an external source. The temperature of the mixed liquid supplied to the pump will be higher than
the temperature of the fresh make-up liquid. Its final temperature will depend upon the amount of the
recycled liquid. It is important to remember that with higher operating liquid temperature, the pump
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performance (capacity) will decrease with the possibility of operating the pump in the cavitation area.
Hence, fresh make-up of the operating liquid should be introduced in a sufficient quantity to maintain
the proper temperature of the operating liquid that is essential for good performance.
Comparing with other mechanical vacuum pumps, the liquid ring vacuum pump has many advantages.
There is no need to lubricate the pump cavity because there is no metal to metal contact. Their
operation and maintaining is easier. As the gases in the pump cavity are compressed under almost the
same temperature, the liquid ring vacuum pump can pump the gases that are flammable/explosive.
Tray Columns utilize a pressure and temperature differential to separate the products. For most
tray columns, the weir holds a liquid level of each tray. Liquid enters from the downcomer of
the tray above. The vapor must overcome this liquid head to move up the column. On the tray
the vapor and liquid are contacted becomes bubble or froth where the mass transfer takes place
and then above the tray they are separated where froth flows over the outlet weir and vapor with
the light volatile compound is disengaged.
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Tray column performs well in high liquid and vapor loading. Tray have higher pressure drop
than packed, and It also have high resistance to corrosion.
1. Bubble captray
The oldest widely used equilibrium-stage plate is the bubble cap tray. A bubble cap tray is
perforated flat plate which has a riser (chimney) over the holes covered with a cap. They are
usually equipped with slots to allow the passage of vapor to be mixed with the liquid flowing
across the tray forming bubble where the mass transfer takes place. Each tray is provided with
one or more downcomers which the liquid flowing across the tray is conducted to the tray
below. A liquid head is maintained on the tray by a dam placed on outlet side of the tray near the
downcomer, it is called the outlet weir. Bubble cap tray is able to operate at low vapor and liquid
rates (less than 2 gpm per foot of average flow width) because liquid and foam is trapped on the
tray to a depth at least equal to the weir height.
Bubble cap trays work well in high turndown applications because the orifices in the bubble
caps are in the form of risers whose top opening is elevated significantly above the tray deck.
The size of the cap tends to create hydraulic gradient across the deck and a high vapor side
pressure drop. The cost of the bubble cap tray is far the highest.
The bubble cap tray can be used where very low vapor rates have to be handled or adequate
residence time is necessary for separation
2. Sieve tray
Sieve tray is perforated plate with holes punched into the plate and usually has holes 3/16 in to
I in diameter. The standard size is 0.5 inch with the perforation punched downward, Vapor
comes out from the holes to give a multi orifice effect. The vapor velocity keeps the liquid
from flowing do through the holes (weeping). The number and size of the perforations control
the vapor flow through the tray deck to contact the liquid.
The punching direction affects the dry pressure drop, a smaller hole diameter result in lower
pressure drop for the same open area. This due to the ratio of the hole diameter to the tray
thickness. The number and hole size are based on vapor flow up the tower. The liquid flow is
transported down the tower by down-comers, a dam and overflow device on the side of the plate.
A sieve tray has higher entrainment than valve tray at the same vapor velocity. This is due to
the spray of liquid directed upwards to the next tray. For efficient operation, the hole velocity
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must be sufficient to balance the head of liquid on the tray deck and thus prevent liquid from
passing through the perforations to the tray. Sieve tray can be used in almost all services.
Sieve deck tray has a minimum capacity approximately 70%. Their capacity and efficiency
are atleast as high as that of other standard trays used commercially. Sieve trays may be used
in moderately fouling services, provided that large holes (3/4 in to 1 in) are used. Sieve trays
are simple and easy to fabricate and therefore relatively inexpensive.
The sieve tray can be used in the distillation of highly viscous or self-polymerized mixtures such
as the separation of vinyl acetate from a polyvinyl acetate.
3. Dual flowtray
Dual flow tray is a sieve tray without downcomer. Vapors move up to the tray move through
the hole, while the liquid travels down in the same hole that can result in mal-distribution and
low efficiency.
Dual flow trays are designed with enough open area on the tray deck to eliminate stagnation
and promote back missing that makes it suited to handle highly fouling services, slurries and
corrosive services. Dual flow trays are well suited also for the fractionation of polymerizable
compounds and give more bubbling area, therefore have a greater capacity than other tray
types.
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Dual flow tray is also the least expensive to make and easiest to install and maintain. Dual
flow tray performs best in the operating region of 60-85% of flood and increases the efficiency
with vapor rate. The challenge of dual flow instability is developed it propagates down the
column.
The top of a column will move in a typical storm as much as 6 inches. This movement will
cause the hydraulic load to migrate in the column. If the hydraulic flow instability is developed
it propagated the column.
Valve tray
Valve tray uses valve (movable dise) which almost closes off completely at low vapor rate,
thus minimize tray open area. When lifted, as vapor rate increases, the open area increases for
vapor flow between the valve dise and tray dise.
Valves can be round or rectangular, with or without caging structured. Most types of valves,
the opening may be varied by the flow, so that the trays can operate over a wide range of flow
rates with high separation efficiency and large flexibility.
Because of their flexibility and price 9slightly more expensive that sieve tray), valve trays are
tending to replace bubble-cap trays.
Valve tray has maximum capacity approximately 60%. The dry pressure drop of valve tray is
lower than bubble cap, because the valve does not need a chimney for the vapor and it
depends on weight valve.
The valve tray can used in condition where vapor rate change unpredictability over a given
section of tower. A tower utilized in blocked operation at varying rate and feed compositions, a
fluctuation in feed rate, and servicing of auxiliary equipment operating the entire unit.
1. Structured packings
Structure Packed column is crimped layers or corrugated sheets which is stacked in the
column. Each layer is oriented at 70° to 90° to the layer below. Structured packed offers 30%
capacities higher than random packed for equal efficiency up to 50% higher at the same
capacity.
Structured packings are typically constructed as blocks of alternating layers of thin corrugated
sheet, gauze, or mesh, which can be fabricated from a wide range of metal alloys or nonmetals
such as plastics, ceramic and graphite. This structure spreads the vapor and liquids evenly
over the cross-section of the tower.
In general, structured packings create lower pressure drops and achieve better separation
efficiencies with shorter bed heights than random packings, but they are also generally more
expensive than random packings and are more time-consuming to install.
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The base material for structured packing is generally a thin (0.1-0.2 mm) metal sheet, Lower
surface area packings have deeper crimping and therefore may require a thicker material for
structural purposes. Since structured packing materials are very thin and have a large amount
of surface area, there is essentially no corrosion allowance. Thus, material of construction is a
very important consideration. Wire gauze packings fabricated from woven metal cloth are used
for very-high-efficiency applications at low liquid loadings such as those at deep vacuum
(although high-surface-area sheet-metal packings with high-quality liquid distributors are also
successfully used in deep vacuum services).
Random packings
Random packings come in a wide range of geometries: cylindrical rings, saddles, spheres,
and various other shapes. Traditional shapes such as Raschig Rings (cylinders) and Intalox
saddles have mostly been replaced by more modern designs such as Pall Rings, Nutter
Rings, IMTP packings, and proprietary designs. Suppliers continue to develop novel shapes
Random packings are usually characterized by their nominal size or diameter, although
different packings of equivalent size may provide very different performance in terms of
capacity and separation efficiency (modern packings typically offer significant performance
advantages over the traditional designs). In small towers with any random packing design, a
minimum tower-to- packing diameter ratio of 8:1 to 10:1 is recommended to minimize loss of
separation efficiency due to voids in the packed bed and wall effects.
Random packings are made from material of various thicknesses, so the maximum allowable
bed depth for each packing needs to be considered carefully. This is especially true with plastic
packings, which may experience some degree of crushing at the bottom of the bed that worsens
at elevated temperatures due to plastic softening. Bed heights as tall as 12 m have been
successfully operated, although these tall towers use larger packing. Even if a packing's
mechanical strength can withstand a high bed depth, in order to maintain effective liquid
distribution, a height of no more than 10-14 theoretical stages is recommended for a single bed
without liquid redistribution.
Random packing has been used for fractionation, absorption and stripping operations in gas,
refinery and chemical plants for many years and the benefits are well established. Furthermore,
ease of replacement and storage make random packing the ideal choice for
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• “Turbine” is a general term for any device that extracts mechanical energy from a fluid –
generally converting it to rotating energy of a turbine wheel.
• For liquids, we usually call them “hydraulic turbines” or “hydroturbines”.
• For gases, we usually call them “wind turbines”, “gas turbines”, or “steam turbines”, depending
on the type of gas being used.
• Just as with pumps, there are two basic types of turbine:
o Positive displacement turbines – fluid is forced into a closed volume, and then the fluid
is pushed out.
o Dynamic turbines – no closed volume is involved; instead, rotating blades called
runner blades or buckets extract energy from the fluid.
• In general, positive-displacement turbines are used for flow measurement, rather than for
production of power, whereas dynamic turbines are used for both power generation and
flow measurement.
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9.9.1 TYPES OF TURBINES
Positive-Displacement Turbines:
• The nutating disc flowmeter, commonly used to measure the volume of water supplied to a house,
is an example of a positive-displacement turbine.
Nutating disk
• Other geometries are also used for positive-displacement turbines; e.g., a flowmeter that uses
a double helical three-lobe impeller design, as discussed in Chapter 8:
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Dynamic Turbines:
• Dynamic turbines do not have closed volumes. Instead, spinning blades called runners or buckets
transfer kinetic energy and extract momentum from the fluid.
• Dynamic turbines are used for both flow measurement and power production. For example,
turbine flowmeters for air and water are discussed in Chapter 8.
There are two main types of dynamic turbines: impulse turbines and reaction turbines.
• Impulse turbines: Fluid is sent through a nozzle that then impinges on the rotating blades,
called buckets. Compared to reaction turbines, impulse turbines require higher head, and work
with a lower volume flow rate.
• The most common example is the Pelton wheel turbine.
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CLASSIFICATION OF PUMPS
9.10 Introduction
Pumps are used to transfer and distribute liquids in various industries. Pumps convert mechanical
energy into hydraulic energy. Electrical energy is generally used to operate the various types of pumps.
Pumps have two main purposes.
Ø Transfer of liquid from one place to another place (e.g. water from an underground into a
water storage tank).
Ø Circulate liquid around a system (e.g. cooling water or lubricants through machines and
equipment).
Classification
There exist a wide variety of pumps that are designed for various specific applications. However, most
of them can be broadly classified into two categories as mentioned below. i. positive displacement
ii. dynamic pressure pumps
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The term positive displacement pump is quite descriptive, because such pumps are designed to displace
a more or less fixed volume of fluid during each cycle of operation. The volumetric flow rate is
determined by the displacement per cycle of the moving member (either rotating or reciprocating) times
the cycle rate (e.g. rpm). The flow capacity is thus fixed by the design, size, and operating speed of the
pump. The pressure (or head) that the pump develops depends upon the flow resistance of the system in
which the pump is installed and is limited only by the size of the driving motor and the strength of the
parts.
Consequently, the discharge line from the pump should never be closed off without allowing for
recycle around the pump or damage to the pump could result. They can be further classified as:
Pumping takes place by to and fro motion of the piston or diaphragm in the cylinder. It is often used
where relatively small quantity of liquid is to be handled and where delivery pressure is quite large.
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Piston pump: A piston pump is a type of positive displacement pump where the high-pressure seal
reciprocates with the piston. The pump has a piston cylinder arrangement. As the piston, goes away
after the delivery stoke, low pressure is created in the cylinder which opens the suction valve. On
forward stoke, the fluid filled inside the cylinder is compressed which intern opens the delivery valve
for the delivery of liquid.
Diaphragm pump: uses a combination of the reciprocating action of a rubber, thermoplastic or Teflon
diaphragm and suitable non-return check valves to pump a fluid. Sometimes this type of pump is also
called a membrane pump.
Rotary pumps
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In rotary pumps, relative movement between rotating elements and the stationary element of the pump
cause the pumping action. The operation is different from reciprocating pumps, where valves and a
piston are integral to the pump. They also differ from centrifugal pumps, where high velocity is turned
into pressure. Rotary pumps are designed so that a continuous seal is maintained between inlet and outlet
ports by the action and position of the pumping elements and close running clearances of the pump.
Therefore, rotary pumps do not require valve arrangements similar to reciprocating pumps.
Gear pumps: uses the meshing of gears to pump fluid by displacement. They are one of the most
common types of pumps for hydraulic fluid power applications. The rigid design of the gears and houses
allow for very high pressures and the ability to pump highly viscous fluids.
Lobe pump: Lobe pumps are similar to external gear pumps in operation in that fluid flows around
the interior of the casing. As the lobes come out of mesh, they create expanding volume on the inlet
side of the pump. Liquid flows into the cavity and is trapped by the lobes as they rotate. Liquid
travels around the interior of the casing in the pockets between the lobes and the casing. Finally, the
meshing of the lobes forces liquid through the outlet port under pressure.
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Fig. 29.5 Lobe pump
Screw Pump: These pumps are rotary, positive displacement pumps that can have one or more screws
to transfer high or low viscosity fluids along an axis. Although progressive cavity pumps can be
referred to as a single screw pumps, typically screw pumps have two or more intermeshing screws
rotating axially clockwise or counterclockwise. Each screw thread is matched to carry a specific
volume of fluid. Screw pumps provide a specific volume with each cycle and can be dependable in
metering applications.
Vane pump: A rotary vane pump is a positive-displacement pump that consists of vanes mounted to a
rotor that rotates inside of a cavity. In some cases, these vanes can be variable length and/or tensioned
to maintain contact with the walls as the pump rotates.
Rotary plunger pump: The pumping action takes place by rotating rotor and reciprocating plunger. In a
rotary plunger rotary pump, the axes of the plungers are perpendicular to the rotational axis of the rotor or
at an angle of not less than 45° to the axis; the rotor is located eccentrically with respect to the axis of the
case.
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Suction and forced delivery of the liquid occur with the reciprocating motion of the plungers as a
result of centrifugal forces and spring action. Rotary pumps of this type may have as many as 72
plungers arranged in multiple rows, provide a delivery Q ≤ 400 liters/min, and build up a pumping
2
pressure ρ ≤ 100 MN/m .
In dynamic pressure pump, during pumping action, tangential force is imparted which accelerates the
fluid normally by rotation of impeller. Some systems which contain dynamic pump may require
positive displacement pump for priming. They are normally used for moderate to high discharge rate.
The pressure differential range for this type of pumps is in a range of low to moderate. They are
popularly used in a system where low viscosity fluids are used.
They use a rotating impeller to increase the pressure of a fluid. Centrifugal pumps are commonly used to
move liquids through a piping system. The fluid enters the pump impeller along or near to the rotating
axis and is accelerated by the impeller, flowing radially outward into a diffuser or volute chamber
(casing), from where it exits into the downstream piping system. Centrifugal pumps are used for large
discharge through smaller heads. These types of pumps are used for supply of water and handling of
milk in dairy plants.
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Propeller pump
A propeller pump is a high flow, low lift impeller type device featuring a linear flow path. The propeller
pump may be installed in a vertical, horizontal, or angled orientation and typically has its motor situated
above the water level with the impeller below water. These pumps function by drawing water up an
outer casing and out of a discharge outlet via a propeller bladed impeller head.
Flow measurement is vital to many different industries such as oil, power, water and wa ste
treatment. These industries require that they know exactly how much fluid is passing through a
point at any given point. Flowmeters help to determine how much fluid is passing through to
determine how much money should be billed or how much product is being produced. A
flowmeter is an instrument used to measure linear, non-linear, mass or volumetric flow rate of
a liquid or gas.
Most flow meters work by forcing flow through a known confined space and measuring
different properties to determine the flow rate of fluid. Examples of measured properties include
pressure, thermal, magnetic, etc. In the report below, we will provide example for five different
types of flowmeters. Most popular flowmeters include: Coriollis, Differential Pressure,
Magnetic, Positive Displacement and Variable area. The most common type of flowmeter is
differential pressure and is pictured in Figure 3. The piezometers at the entrance and center
measures the incoming pressure used to determine the velocity of the flow.
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9.11 Types of Flowmeters:
There are many different types of flow meters and each performs optimally under different
conditions. The most important part to choosing a flow meter is to have a clear understanding of
the particular applications requirements. Some good questions that can help determine the type
of flow meter needed for different applications are; what type of fluid is being measured, what is
the expected temperature of the fluid, what is the maximum pressure expected at the location,
how accurate must the meter be, will the fluid flow be continuous or sporadic, what range of
flows will the system be under, and what is the size of the pipe the meter will be installed on?
Each of these questions will be very important when decided which flow meter should be used
in different applications.
This section is going to discuss the most common types of flowmeters including;
It will also identify the major advantage and disadvantages of each flow meter when necessary.
Differential pressure flow meters operate by introducing a restriction in the cross sectional area
of a flowing fluid. Restricting the flow area causes a pressure drop across the constriction, this
pressure drop is cause by a change in the fluids velocity. The operating principal is based on the
Bernoulli equation and the continuity equation of fluid flow, combining these equations you
can find the relationship between the flow rate and pressure drop. This theory can be seen
below.
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9.12.1 Pressure Gauges with Bourdon Tube
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Bourdon tubes are oval tubes bent into a circular arc. The pressure which is to be measured acts upon the
interior of the tube so that the tube's oval cross section becomes approximately circular. The edge stress
produced through this deforming effect causes the arc of the Bourdon tube to open. The end of the
Bourdon tube which is not affixed performs a motion, this motion being a measure for the pressure. For
pressure ranges up to 40 bar Bourdon tubes bent into a circulararc over angle of 270 degrees are
commonly used, for higher pressure ranges helical Bourdon tubes having several turns are employed.
Bourdon tubes have a relatively low restoring force. This must be taken into account when using
additional accessories like indicating pointers, limit switches or potentiometric tained. Pressure
gauges with a Bourdon tube can normally only be protected in a limited way against overloading by
supporting the elastic element at a specific pressure limit.
Bourdon tube pressure gauges of accuracy grades between 0.6 and 2.5 are commonly used for
measurements in the range between 0.6 bar to 4000 bar. The influence of temperature changes on the
indication depends chiefly on the temperature coefficient (TEC = change in stiffness caused by change
in temperature) that is specific for the elastic modulus of the Bourdon tube. Depending on the material
used, the accuracy error caused by temperatures differing from the reference temperature will amount
to between 0.3 % and 0.4 % per 10 K.
There exist gauges with a horizontally arranged diaphragm and gauges with a vertically arranged
diaphragm, i.e. where the diaphragm is placed in parallel to the dial. Generally for pressure ranges below
0.6 bar diaphragms having a diameter of 160 mm are used for pressure gauges with horizontal
diaphragm, whereas diaphragms having a diameter of 100 mm are used for higher pressure ranges.
Owing to the annular fixing arrangement of the diaphragm the inaccuracy caused by temperature
changes is significantly greater compared to gauges with a Bourdon tube. Diaphragm pressure gauges
are applied for pressure ranges between 10 mbar up to 25 bar with standard accuracy grades of 1.6 or 2.5,
in exceptional cases also 4.0.
Selection Criteria
against overpressures,
9.12.3Principles of measurement
The pressure gauges described in these Operating
Positive leg
If there is a difference in temperature between the hot junction and cold junction, a small voltage is
created. This voltage is referred to as an EMF (electro-motive force) and can be measured and in
turn used to indicate temperature.
The voltage created by a thermocouple is extremely small and is measured in terms of millivolts
(one millivolt is equal to one thousandth of a volt). In fact, the human body creates a larger
millivolt signal than a thermocouple.
Base metal thermocouples are known as Types E, J, K, T and N and comprise the most commonly
used category of Thermocouple. The conductor materials in base metal thermocouples are made of
common and inexpensive metals such as Nickel, Copper and Iron.
Type E: The Type E thermocouple has a Chromel (Nickel-10% Chromium) positive leg and a
Constantan (Nickel- 45% Copper) negative leg. Type E has a temperature range of -330 to 1600 F,
has the highest EMF Vs temperature values of all the commonly used thermocouples, and can be
used at sub-zero temperatures. Type E thermocouples can be used in oxidizing or inert atmospheres,
and should not be used in sulfurous atmospheres, in a vacuum or in low oxygen environments where
selective oxidation will occur. The color code for TYPE E wire is purple and red.
Type J: The Type J thermocouple has an Iron positive leg and a Constantan negative leg. Type J
thermocouples can be used in vacuum, oxidizing, reducing and inert atmospheres. Due to the
oxidation (rusting) problems associated with the iron leg, care must be used when using this
thermocouple type in oxidizing environments above 1000 F. The temperature range for Type J is
32 to 1400 F and it has a wire color code of white and red.
Type K: The Type K thermocouple has a Chromel positive leg and an Alumel (Nickel- 5%
Aluminum and Silicon) negative leg. Type K is recommended for use in oxidizing and
completely inert
environments. Because it’s oxidation resistance is better than Types E, J, and T they find widest use
at temperatures above 1000 F. Type K, like Type E should not be used in sulfurous atmospheres, in
a vacuum or in low oxygen environments where selective oxidation will occur. The temperature
range for Type K is -330 to 2300 F and it’s wire color code is yellow and red.
Type N: The Type N thermocouple has a Nicrosil (Nickel-14% Chromium- 1.5% Silicon)
positive leg and a Nisil (Nickel- 4.5% Silicon- .1% Magnesium) negative leg. Type N is very
similar to TYPE K but is less susceptible to selective oxidation effects. Type N should not be
used in a vacuum or in reducing atmospheres in an unsheathed condition. The temperature range
is 32- 2300 deg F and its wire color code is orange and red.
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Type T: The Type T thermocouple has a Copper positive leg and a Constantan negative leg.
Type T thermocouples can be used in oxidizing, reducing or inert atmospheres, except the
copper leg restricts their use in air or oxidizing environments to 700 F or below. The
temperature range for Type T is -330 to 700 F and it’s wire color code is blue and red.
Noble Metal Thermocouples are another category of thermocouples and are made of the
expensive precious metals Platinum and Rhodium. There are three types of noble metal
thermocouples:
Type B (Platinum/Platinum-30% Rhodium)
Type R (Platinum/Platinum-13% Rhodium)
Type S (Platinum/Platinum-10% Rhodium)
Types R and S have temperature ranges of 1000 to 2700 F and Type B thermocouples have
a temperature range of 32 to 3100 F.
As can be seen above, the difference between these three thermocouples is the amount of
Rhodium contained in the negative leg. Types R and S can exhibit excessive grain growth in the
platinum when exposed to the higher end of its temperature range. The increased amount of
Rhodium in the Type B thermocouple helps to reduce the grain growth problem allowing for a
slightly increased temperature range.
Noble metal thermocouples are intended for use in oxidizing or inert atmospheres. They must not
be used in reducing atmospheres or in applications containing metallic or nonmetallic vapors.
Noble metal thermocouples are soft and prone to being damaged if mishandled. These
thermocouple assemblies are usually assembled in ceramic insulators and supplied with ceramic
protection tubes. Noble metals should never be supplied in metal protection tubes only. The color
code for Types R and S is black and red, and the color code for Type B is gray and red.
Refractory Metal Thermocouples are the last category of thermocouple that Pyromation
manufactures. These thermocouples are made of the exotic metals Tungsten and Rhenium, which are
expensive, difficult to manufacture, brittle, and must be handled carefully. There are three types of
refractory metal thermocouples:
Type G (Tungsten/Tungsten 26% Rhenium)
Type D (Tungsten 3% Rhenium/Tungsten 26% Rhenium)
Type C (Tungsten 5% Rhenium/Tungsten 26% Rhenium)
(Note: The Type designations listed for the refractory thermocouples are industry
standard designations, not standardized thermocouple types)
All of these types have a temperature range of 32-4200 deg F. Refractory metal thermocouples
are normally used in vacuum furnaces beyond the temperature capabilities of platinum. They are
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seldom used below approximately 2500 F since there are other thermocouple types more suited for
the lower temperatures. Refractory metal thermocouples and their associated refractory metal
protection tubes must not be used in the presence of oxygen at temperatures above 500°F.
The color code for refractory thermocouples are: Type G: White with blue tracer and red
Type D: White with yellow tracer and red
Type C: White with red tracer and red
9.14 Steam traps are automatic valves used in every steam system to remove
condensate, air, and other non-condensable gases while preventing or minimizing the passing of
steam. If condensate is allowed to collect, it reduces the flow capacity of steam lines and the
thermal capacity of heat transfer equipment. In addition, excess condensate can lead to “water
hammer,” with potentially destructive and dangerous results. Air that remains after system startup
reduces steam pressure and temperature and may also reduce the thermal capacity of heat transfer
equipment. Non-condensable gases, such as oxygen and carbon dioxide, cause corrosion. Finally,
steam that passes through the trap provides no heating service. This effectively reduces the heating
capacity of the steam system or increases the amount of steam that must be generated to meet the
heating demand.
The inverted bucket trap is a mechanically actuated model that uses an upside down
linkage, sinks when condensate fills the steam trap; thereby, opening the outlet valve.
The bucket floats when steam enters the trap; thereby, closing the valve.
The ball float type trap operates by sensing the difference in density
between steam and condensate. The float and thermostatic (F&T) trap is a
hybrid. As condensate collects, it lifts a float which opens a valve as much as
required. A built-in thermostatic element purges air and other non-
condensable gases and closes off when steam enters the trap.
Thermodynamic traps can be used on high pressure and superheated steam and
are not affected by water hammer or vibration.
4) Thermodynamic traps are not damaged by freezing and are unlikely to freeze,
if installed with the disc in a vertical plane and discharging freely to atmosphere.
There are two important points to consider regarding this simple element:
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1. Operation of the steam trap takes place at a certain fixed temperature,
which may
not satisfy the requirements of a steam system possibly operating at varying
pressures and temperatures.
2. Because the power exerted by a single bimetal strip is small, a large mass
would have to be used which would be slow to react to temperature changes in
the steam system
There are two important points to consider regarding this simple element:
1. Operation of the steam trap takes place at a certain fixed temperature,
which may
not satisfy the requirements of a steam system possibly operating at varying
pressures and temperatures.
2. Because the power exerted by a single bimetal strip is small, a large mass would
have to be used which would be slow to react to temperature changes in the
steam system
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Forced draft:
The forced draft unit allows an easy access for maintenance to thefans
and to the bundles. Furthermore, the fans remain in the coldambient
air.
HEADER CONSTRUCTION:
D-type Header:
The welded bonnet type header is used in some cases for special services such as:
ammonia, freon and vacuum steam condensers. One advantage of this design is the
full welded construction which provides the perfect sealing required for such
applications.
The cover plate header is used for fluids with high foulingfactors up to 40 bar working pressure
where a frequentmechanical cleaning is necessary. It is used also for verycorrosive process
fluids so as to periodically check thecorrosion allowance. Special cover plate headers
usingwelded gaskets are provided for hydrogen service units inhydrocracking plants.
Demulsifier
Demulsifier chemical is unloaded into Demulsifier Drums. Provision is made for addition of Swing
Naphtha to for dilution. The drum is provided with a mixer which can be used for preparation of desired
concentration levels of the solution. Demulsifier injection is done by Demulsifier Injection Pumps at the
inlet of First Stage and second stage Desalter. Provision of demulsifier injection in Crude Charge Pumps
suction line is also made.
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12% Caustic
18% caustic is transferred from offsite into caustic solution tank. This 18% caustic is diluted with DM water
to make 12% caustic solution. A ratio controller is provided for this purpose. To achieve homogeneous
mixture of 12% caustic concentration a static mixer is provided. 12% caustic is injected using caustic
injection pumps (first stage discharge (H1) is used for injecting caustic at suction and second stage
discharge (H2) along with crude slip stream via vortex mixer for injection to Booster pump suction. A
vortex mixer is provided at thedischarge of Caustic injection pump to mix a small quantity of crude along
with caustic.
Filming Amine
Filming Amine is unloaded into Filming Amine Drum. Provision is made for addition of Stabilised Naphtha
to Filming amine drums for dilution the drum is provided with a mixer which can be used for preparation of
desired concentration levels of the chemical. Filming Amine injection is done using Filming Amine
Injection Pumps -I to Crude Column and Naphtha Stabilizer overhead and Filming Amine Injection Pumps
-II into the overhead line of Vacuum Column.
Neutralising Amine
Neutralising Amine is unloaded into Neutralising Amine Drum. Provision is made for additionof DM water
for dilution. The drum is provided with a mixer which can be used for preparation of desired concentration
levels of the chemical. Neutralising Amine injection is done using Neutralising Amine Injection Pumps-I to
Crude Column and Naphtha Stabilizer overhead and Neutralising Amine Injection Pumps-II into the
overhead line of Vacuum Column.
Provision has been made to use the same system for KMnO4 dosing during turnaround of the CDU-IV Unit.
Anti-foulant
anti-foulant is unloaded into Anti-foulant vessel- I for injection into Crude line at the common discharge of
Crude Charge pump. Injection is done using Anti-foulant injection pumps-I. Anti-foulant vessel- II is used
for injection into VR+Quench line at Common suction of Pump. Injection is done using Anti-foulant
injection pumps II.
It is to be done to know the composition is in its range. Collect 100ml of LPG sample in a
tube and place it in water. Install thermo meter in it and then keep the apparatus in
atmosphere until its volume reaches 5ml. Record the temperature and it should be
between
+2 and -2 then its proportion is in its range. If it exceeds +2 then c5, c6 are in high
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proportion, it its temperature is less than-2 then c1 ,c2 are in high proportion.
PH test:
The pH test is done fo reffluent water, stripped water, wash water. The testing water is
taken in a test tube and 1 or 2 drops of universal indicator is added and colour change will
occur. The respective colour will match on chart of the indicator and the colour has the
value and that is our required value.
Another method is by using pH meter and it will give digital reading. The pH value
from 1-7 is acid,
7-14 is base and 7 is neutral.
Generally the value should be 6.5 and we need to adjust value if it increase or decreases.
This system also called OWS is mainly to collect water contaminated with hydrocarbon oil.
Such streams are generated during equipment draining and flushing during routine operation.
Streams suitable for OWS also generated as a result of floor washing and cleaning or spilled oil
etc. Drained streams received through OWS funnels etc. are routed to ETP through a combined
header All equipments having CBD connections are normally provided with OWS connection
also. No OWS points are provided near the heater for safety reasons. The OWS man holes are
sealed and a vent pipe provided releases any hydrocarbon trapped at a higher elevation. The final
outlet of the OWS is located at the south east corner of the unit. The OWS system is common
for both CDU and VBU units. The effluent generated in the unit reaches ETP for treatment and
oil recovery. Care should be taken that at no time any spark reaches vapour space of OWS
funnels. This may result in explosion immediately there or else where in network wherever
explosive mixture of air and hydrocarbon vapours is present in appropriate concentration for
explosion.
Standing Instruction on OWS system: Presently during wet weather, the collection of
Rainwater was exceptionally high and is more than what ETPs are actually to hold. This is
resulting in overflowing of the Surge ponds and oil break through into Refinery Effluent. In
View of the above, it is Required to ensure that, the entire OWS system is properly maintained
and operated in order, not to get excess/ unwanted influent entry in to oily water sewer system.
The following actions need to be compiled in Process Units.
Ensure that no Fire water usage for House keeping/ Floor washing.
g. Ensure that spent caustic is routed to Merox unit for dumping in Chemical sewer.
The peripheral surface Drain with double valve arrangement to route it either to OWS or to
Storm Sewer System depending upon its oil content. Normaly, surface drain outlets are
kept floating on OWS system. During rains, the outlet is changed over to Storm water
It is used as mothering steam in fire box to halt the fire in case of emergency. MP steam
Pressure (kg/cm2) : 10-12
0
Temperature(c) : 250-280
(kg/cm2): 5-7
0
Temperature (c) : 30-45
Pressure (kg/cm2) : 20
0
Temperature (c) : 120
water:
Pressure(kg/cm2) :3.5-5
0
Temperature(c) :150-170
lines.
Fuel oil
Pressure (kg/cm2) : 9
0
Temperature (c) : 130
about 9800.
Fuel gas
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Pressure (kg/cm2) : 4
0
Temperature (c) : 40
14 .PINCH TECHNOLOGY:
The term “Pinch Technology” was introduced by Linnhoff and Vredeveld to represent a new
set of thermodynamically based methods that guarantee minimum energy levels in design of
heat exchanger networks. Over the last two decades it has emerged as an unconventional
development in process design and energy conservation.
Pinch technology presents a simple methodology for systematically analys- ing chemical
processes and the surrounding utility systems with the help of the First and Second Laws of
Thermodynamics. The First Law of Thermo- dynamics provides the energy equation for
calculating the enthalpy changes
( H) in the streams passing through a heat exchanger. The Second Law deter- mines the direction
of heat flow. That is, heat energy may only flow in the direction of hot to cold. This prohibits
‘temperature crossovers’ of the hot and cold stream profiles through the exchanger unit. In a heat
exchanger unit nei- ther a hot stream can be cooled below cold stream supply
temperature nor a cold stream can be heated to a temperature more than the supply tempera- ture
of hot stream. In practice the hot stream can only be cooled to a tem- perature defined by the
‘temperature approach’ of the heatexchanger. The temperature level at which DTmin is observed
in the process is referred to
as “pinch point” or “pinch condition”. The pinch defines the minimum driving force allowed in
the exchanger unit.
15. INSPECTION TESTS
RADIO GRAPHY TEST:
The radio graphy test isa nondestructive examination (NDE) technique that involves the use of
either x-rays or gamma rays to view the internal structure of a com- potent. In the petrochemical
industry, RT is often used to inspect machinery,
such as pressure vessels and valves, to detect for flaws. RT is also used to inspect weld repairs.
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Compared to other NDE techniques, radiography has several advantages. It is highly
reproducible, can be used on a variety of materials, and the data gathered can be stored for
later analysis. Radiography is an effective tool that requires very
little surface preparation. Moreover, many radiographic systems are portable, which allows for
use in the field and at elevated positions.
Stress relief test is form of post weld heat treatment. In stress relieving we heat a material to a
specific temperature; hold it at this temperature for a specified amount of time in order to reduce
or eliminate residual stresses; and then
cool it at a slow enough rate to prevent these stresses from redeveloping.
It is mainly checked at the point of the welding joints and welded areas with a temperature
which steadily increases by the value of approximately 200°c per hour. It attains the
temperature upto 610°c from where the temperature is brought down uniformly at a rate of
150°c to the normalatmospheric temperature. Here the pipelines are testedto check
howeffectively the pipe can resist or withstand the
temperature of the hot process fluids.
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16. ENVIRONMENTAL POLLUTION CONTROL & FACILITIES
Air emissions from the petroleum industry can be classified as combustion emissions,
process emissions, fugitive emissions, emissions from storage and handling of
petroleum liquids and secondary emissions.
Combustion emissions are produced with the onsite burning of fuels usually for energy
production and transportation purposes. Flaring is a specific source of combustion
emissions in the petroleum industry. It is used to control pressure and remove gas, which
can not be otherwise used. Fugitive emissions (equipment leak emissions) are released
through leaking valves, pumps, or other process devices. Process emissions are
generated in the process units and released from process vents. Storage and handling
emissions are contributed from the storage and manipulation of natural gas and crude
oil, as well as their intermediate and finished derivatives. The water systems of a
production or processing site (tanks, ponds, sewer system drains, etc.) are the main
source of secondary emissions.
Polluted water in the petroleum industry is usually generated in the various production
or processing operations. Leaks of liquids from the production, process, storage
equipment or pipelines to the ground can also contribute to pollution of underground
water.
Solid wastes containing varying amounts of different pollutants are generated from
particular processes or as sludge in storage tanks.
3.1. Pollution from Exploration and Production of Crude oil and Natural Gas.
Production of oil and gas is a major operation of the petroleum industry. Nearly 100
countries are involved in it world wide, and a considerable amount of oil and gas is
produced off shore. In the USA only, there are more than 575 000 crude oil wells, 252
000 gas wells and 724 gas plants.
Major activities in this branch of the petroleum industry include exploration and well
site preparation; drilling; crude oil and gas production, enhanced (secondary) recovery.
Emissions Control:
Emissions from Refinery operations which significantly affect the environment are (i) Sulphur
Dioxide (SO2), (ii) Carbon Monoxide (CO), (iii) Oxides of Nitrogen (NOx), (iv) Suspended
Particulate Matter (SPM), (v) Hydrocarbon (HC), and (vi) Noise.
Low NOx burners have been provided in heaters to reduce NOx emissions.
The refinery flare gases are safely flared in a tall vertical flare stack with proper water seal and
steam dispersion to avoid black smoke. The flare piping network is closed system
interconnecting all the process units.
To facilitate control of fugitive emissions from tanks and pumps, refinery has installed floating
roof tanks for Crude oil tanks and light product storage tanks. All pumps in use are equipped
with mechanical seals and for of LPG and lighter product pumps double mechanical seals are
used.
At the time of equipment purchase itself it will be specified that noise level to be below the
statutory limit with required acoustic enclosures.
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17. FIRE & SAFETY:
Fire and safety is these to practices intended to reduce the destruction caused by fire. Fire safety
measures include those that are intended to prevent ignition of an uncontrolled fire, and those
that are used to limit the development and effects of a fire after it starts.
Fire safety measures include those that are planned during the construction of a building or
implemented in structures that are already standing, and those that are taught to occupants of
the building.
Threats to fire safety are commonly referred to as fire hazards. A fire hazard may include a
situation that increases the likely hood of a fire or may impede escape in the event a fire
occurs.
Limiting anyone or more of the factors of fire tetrahedron can do extinguishment of fire. These
are classified as:
Hydrants:
Hydrants are located keeping in view the fire hazards at different sections of the premises to be
protected and to give most effective service. Atleast one hydrant posts hal be provided for every
30 meters of the perimeter of unit battery limit. The hydrants should be located at a minimum
distance of 15 meters from the periphery of hazardous equipment. Double headed hydrants with
two separate landing valves on 4” stand post should be used.
They are provided for immediate usage of fire water during fire emergency or push the spiled
oil into OWS. They are of 30 meters length as per OISD guide lines and contain a nozzle at the
opened. It should not be used for floor washing but can be used for pushing spiled oil into
nearest storm sewer
/OWS. In this condition, immediately car seal should be put back.
Monitors:
Monitors are located at strategic locations for protection of cluster of columns, heaters, etc.
and where it may not be possible to approach the higher levels. Monitors shall be located to
direct water on the object as wel as to provide water shield to fire men approaching the fire.
The monitors should not be installed less than15 meters from the hazardous equipment and
shal not exceed 45meters from the hazard to be protected.
The butterfly valves of the monitors should be periodically checked for free operation and if
isolation valves are gate valves, it should be greased regularly and medium sized wheel spanner
should be welded near it. Monitor rotation levers should be periodically checked for its function.
Fixed Water Sprinkler System:Fixed water sprinkler system is a fixed pipe tailor made system to
which sprinklers with fusible bulbs are attached. Each sprinkler system includes a controlling
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valve and a device for actuating an alarm for the operation of the system. The system is usually
activated by heat from a fire and discharges water over the fire area automatically.
Foam extinguisher:
These are used to fight A&B type fires. Contents are dry bicarbonate of soda, a foam
stabilizing agent such as soap bark dissolved in water for the inner cylinder. Reaction between
the aluminium sulfate and bicarbonate of soda produces CO2 gas in the form of bubbles and
aluminium hydroxide in the bubble film, which expels the foam upto 40ft.
Flare system is designed to burn at all times from the discharge of pressure relief systems and
gases from depressurizeing of equipments. Any liquid hydrocarbon discharge into the flare
header is separated in the knock out drums and pumped to slop tanks.
The existing flare system is designed for a load of 284716Kg/hr. The existing flare system
consisting of flare stack (32"Diameter&55mheight), flare tip, fluidic seal, flame front
generator, water seal drum, knock out drums, and two blow down pumps.
Instrumentation
The Instrumentation is an art and science of applying measuring device or measuring
and controlling devices to an object or a combination of objects
(a system) for the purpose of determining the identify and /or magnitude of certain varying
Physicalor Chemical quantities and offer for the controlling these quantities with in the
specified limitations.
Different types of measurements techniques are possible to measure a physical variable. But a
proper selection must be made to suit the application. Each technique has its own advantages
and disadvantages.
Al the physical variables have to be indicated to estimate the present process conditions. These
must be recorded for future reference also.
As the process is of large scale, different variable shave to display at the remote locations.
Additional devices are used to do this. The signal transmission is of pneumatic type. So at
transmitter of receiver i/p converters will be used. Pressure regulators had to use to maintain
constant pressure supply to al the instruments.
The controlling actions are done mostly by pneumatic values. Butterfly valves, bal valves,
spring– diaphragm valves and solenoid valves are mostly used in these plant.
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facilitate emergency evacuations are fire alarms, exit signs, and
emergency lights. Some structures need
special emergency exits or fire escapes to ensure the availability
of alternative escape paths.
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