Introduction

Thermal cracking is the oldest and, in a way, the simplest cracking process. It basically aims at the
reduction of molecular size by application of heat without any additional sophistication such as catalyst or
hydrogen. At a temperature level of 450-500 C, the larger hydrocarbon molecules become unstable and
tend to break spontaneously into smaller molecules of all possible sizes and types. By varying the time,
temperature and pressure under which a particular feedstock remains under cracking conditions, the
desired degree of cracking (conversion) can be controlled. Temperature and time (residence time) are
important process variables pressure plays a secondary role.

Obviously, the cracking conditions to be applied and the amount and type of cracked products will depend
largely on the type of feedstock. In practice, the feedstock for thermal cracking is a mixture of complex
heavy hydrocarbon molecules left over from atmospheric and/or vacuum distillation of crude. The nature of
these heavy, high molecular weight fractions is extremely complex and much fundamental research has
been carried out on their behavior under thermal cracking conditions. However, a complete and
satisfactory explanation of these reactions that take place cannot be given, except for relatively simple and
well-defined types of products. For instance, long chain paraffinic hydrocarbon molecules break down into
a number of smaller ones by rupture of a carbon-to-carbon bond (the smaller molecules so formed may
break down further). When this occurs, the number of hydrogen atoms present in the parent molecule is
insufficient to provide the full complement for each carbon atom, so that olefins or "unsaturated"
compounds are formed. The rupturing can take place in many ways, usually a free radical mechanism for
the bond rupture is assumed.

However, paraffinic hydrocarbons are usually only a small part of the heavy petroleum residues, the rest
being cyclic hydrocarbons, either aromatic or naphthenic in character. In these, the rupture takes place in
the paraffinic side-chain and not in the ring. Other side reactions also take place. In particular, the
condensation and polymerisation reactions of olefins and of the aromatics are of considerable practical
importance, since they can lead to undesirable product properties, such as an increase in the sludge or tar
content. Hence, in practice, it is very difficult to assess the crackability of various feedstocks without plant
trials. The final products consist of gas, light hydrocarbons in the gasoline and gasoil range and heavier
products. By selection of the type of unit, feedstock and operating conditions, the yields and quality of the
various products can, within limits be controlled to meet market requirements.

The maximum conversion that can be obtained will be determined by the quality of the bottom product of
the thermal cracker, thermally cracked residue. This stream is normally routed to the fuel oil blending pool.
When the cracking has taken place at a too high severity, the fuel can become 'unstable' upon blending
with diluent streams (see below). Normally, the refinery scheduler will assess what the maximum severity
is that the thermal cracking unit can operate on, without impacting on the stability of the refinery fuel
blending pool.

When thermal cracking was introduced in the refineries some 80 years ago, its main purpose was the
production of gasoline. The units were relatively small (even applying batch processing), were inefficient
and had a very high fuel consumption. However, in the twenties and thirties a tremendous increase in
thermal cracking capacity took place, largely in the version of the famous DUBBS process, invented by
UOP. Nevertheless, thermal cracking lost ground quickly to catalytic cracking (which produces gasoline of
higher octane number) for processing heavy distillates with the onset of the latter process during World
War II. Since then and up to the present day, thermal cracking has mostly been applied for other
purposes : cracking long residue to middle distillates (gasoil), short residue for viscosity reduction
(visbreaking), short residue to produce bitumen, wax to olefins for the manufacture of chemicals, naphtha
to ethylene gas (also for the manufacturing of chemicals), selected feedstocks to coke for use as fuel or for
the manufacture of electrodes.

In modern oil refineries there are three major applications of the thermal cracking process:

VISBREAKING
THERMAL GASOIL PRODUCTION
COKING

Visbreaking
Visbreaking (i.e. viscosity reduction or breaking) is an important application of thermal cracking because it
reduces the viscosity of residue substantially, thereby lessening the diluent requirements and the amount
of fuel oil produced in a refinery. The feed, after appropriate preheat, is sent to a furnace for heating to the
cracking temperature, at about 450-460 degrees C. The cracking takes place to a small extent in the
furnace and largely in a soaker (reaction chamber) just downstream of the furnace. At the soaker outlet,
the temperature is lower than at the furnace outlet (soaker inlet) because the cracking reactions are
endothermic. The products are quenched at the soaker outlet to stop the cracking reaction (to prevent
excessive coke formation). After that, the products enter the fractionator at a temperature level of 300- 400
degrees C and from here onward the processing is similar to any normal distillation process. The products
are separated into gas, gasoline, kero, gasoil and residue. The residue so obtained has a lower viscosity
that the feed (visbreaking), which leads to a lower diluent requirement to make the fuel on specification for
viscosity. The up-flow soaker provides for a prolonged residence time and therefore permits a lower
cracking temperature than if the soaker was not used. This is advantageous as regards cost in furnace and
fuel. Modern soakers are equipped with internals so as to reduce back mixing- effects , thus maximising
the viscosity reduction. Since only one cracking stage is involved, this layout is also named one-stage
cracking. The cracking temperature applied is about 440-450 degree C at a pressure of 5-10 barg in the
soaker. The fractionator can be operated at 2-5 barg, depending on furnace constraints, condenser
constraints and fuel cost.

Thermal Gasoil Production

This is a more elaborate and sophisticated application of thermal cracking as compared with visbreaking.
Its aim is not only to reduce viscosity of the feedstock but also to produce and recover a maximum amount
of gasoil. Altogether, it can mean that the viscosity of residue (excluding gasoil) run down from the unit is
higher than that of the feed.
In the typical lay out is the first part of the unit quite similar to a visbreaking unit. The visbroken residue is
vacuum-flashed to recover heavy distillates, which are then sent back to a thermal cracking stage, together
with heavy distillate recovered from the fractionator, in a second furnace under more severe cracking
conditions ( temperature 500 degrees C; pressure 20-25 barg) . More severe conditions are necessary
because the feedstock has a smaller molecular size and is therefore more difficult to crack than the larger
residue molecules in the first stage. This layout is referred to as tow-stage cracking.

Delayed Coking
This is an even more severe thermal cracking application than the previous one. The goal is to make a
maximum of cracking products - distillates - whereby the heavy residue becomes so impoverished in
hydrogen that it forms coke. The term "delayed" is intended to indicate that the coke formation does not
take place in the furnace (which would lead to a plant shutdown) but in the large coke drums after the
furnace. These drums are filled/emptied batch-wise (once every 24 hours), though all the rest of the plant
operates continuously. A plant usually has two coke drums, which have adequate capacity for one day's
coke production (500-1500 m2). The process conditions in the coke drum are 450-500 degrees C and 20 -
30 bar. Only one coke drum is on-line; the other is off line, being emptied or standing by. Only the vapour
passes from the top of the coke drums to the fractionator, where the products are separated into the
desired fractions. The residue remains in the coke drum to crack further until only the coke is left. Often the
heaviest part of the fractionator products is recycled to feed.

Product Quality
Thermally cracked products - distillates - are not suitable for commercial use as produced in other units;
they require further refinement or treatment in order to improve their quality, particularly sulfur and olefins
content. Formerly, wet treating processes, for example treatment with caustic or an other extraction
medium, were applied to remove or "sweeten" the smelly sulfur products, but nowadays the catalytic
hydrotreating is employed almost without exception, both for gasoline and for gas oil range products. Of
course, the gases too have to be desulphurised before being used as fuel gas within the refinery.
The residual products from thermal cracking are normally not treated any further, except for coke, which
may be calcined if the specifications require it to be treated. The cracked residue is normally disposed of
as refinery or commercial fuel. Here a very important aspect of the process is the stability of the cracked
residues or of the final fuels after blending with suitable diluents. Residue contains asphaltenes,which are
colloidally dispersed uniformly in the oil in a natural way. In the cracking process, the character of the
asphaltenes as well as of the oil changes, and if the cracking is too severe the natural balance of the
colloidal system can be affected to the extent that part of the asphaltenes precipitates in the equipment or
in the storage tanks, forming sludge. If the sludge formation is excessive, i.e. above a certain specified
limit, the product (fuel) is considered to be unstable.

Plant Operations/Decoking
A practical aspect of operation of thermal cracking units is that, in spite of good design and operating
practice, furnaces, and sometimes also other equipment, gradually coke up, so that the unit has to be shut
down and decoked. Furnaces can be decoked by " turbining" (using special rotary tools to remove coke
from inside furnace pipes) or by steam-air decoking process. In the latter case, the coke is burnt off in a
carefully controlled decoking process in which air and steam are passed through the tubes at elevated
temperatures. Air serves to burn coke, where as the steam serves to keep the burning temperatures low so
that they do not exceed the maximum tolerable temperatures.
More recently, a new decoking method using studded 'pigs' propelled with water, is getting more popular.
The plastic pigs have a size slightly smaller than the tube inside diameter and are equipped with metal
studs. When the pigs are pumped through the furnace pipes, they move around in a rotating fashion, thus
scraping the cokes from the inside of the furnace tubes.
Other coked equipment is usually cleaned by hydrojetting techniques. Owing to these unavoidable stops
for decoking, the on-stream time i.e. on stream days per annum, for thermal cracking units is slightly
shorter than for most other oil processes.
Introduction
To recover additional distillates from long residue, distillation at reduced pressure and high temperature
has to be applied. This vacuum distillation process has become an important chain in maximising the
upgrading of crude oil. As distillates, vacuum gas oil, lubricating oils and/or conversion feedstocks are
generally produced. The residue from vacuum distillation - short residue - can be used as feedstock for
further upgrading, as bitumen feedstock or as fuel component. The technology of vacuum distillation has
developed considerably in recent decades. The main objectives have been to maximise the recovery of
valuable distillates and to reduce the energy consumption of the units.

At the place where the heated feed is introduced in the vacuum column - called the flash zone - the
temperature should be high and the pressure as low as possible to obtain maximum distillate yield. The
flash temperature is restricted to about 420 0C, however, in view of the cracking tendency of high-
molecular-weight hydrocarbons. Vacuum is maintained with vacuum ejectors and lately also with liquid ring
pumps. Lowest achievable vacuum in the flash zone is in the order of 10 mbar.

In the older type high vacuum units the required low hydrocarbon partial pressure in the flash zone could
not be achieved without the use of "lifting" steam. The steam acts in a similar manner as the stripping
steam of crude distillation units. This type of units is called "wet" units. One of the latest developments in
vacuum distillation has been the deep vacuum flashers, in which no steam is required. These "dry" units
operate at very low flash zone pressures and low pressure drops over the column internals. For that
reason the conventional reflux sections with fractionation trays have been replaced by low pressure- drop
spray sections. Cooled reflux is sprayed

via a number of specially designed spray nozzles in the column

countercurrent to the up-flowing vapour. This spray of small droplets
comes into close contact with the hot vapour, resulting in good heat and
mass transfer between the liquid and vapour phase.

To achieve low energy consumption, heat from the circulating refluxes and rundown streams is used to
heat up the long residue feed. Surplus heat is used to produce medium and/or low-pressure steam or is
exported to another process unit (via heat integration). The direct fuel consumption of a modern high-
vacuum unit is approximately 1% on intake, depending on the quality of the feed. The steam consumption
of the dry high-vacuum units is significantly lower than that of the "wet" units. They have become net
producers of steam instead of steam consumers.

Three types of high-vacuum units for long residue upgrading have been developed for commercial
application:

FEED PREPARATION UNITS

LUBOIL HIGH- VACUUM UNITS
HIGH - VACUUM UNITS FOR BITUMEN PRODUCTION

Feed Preparation Units

These units make a major contribution to deep conversion upgrading ("cutting deep in the barrel"). They
produce distillate feedstocks for further upgrading in catalytic crackers, hydrocrackers and thermal
crackers. To obtain an optimum waxy distillate quality a wash oil section is installed between feed flash
zone and waxy distillate draw-off. The wash oil produced is used as fuel component or recycled to feed.
The flashed residue (short residue) is cooled by heat exchange against long residue feed. A slipstream of
this cooled short residue is returned to the bottom of the high-vacuum column as quench to minimise
cracking (maintain low bottom temperature).

Luboil High-Vacuum Units

Luboil high vacuum units are specifically designed to produce high-quality distillate fractions for luboil
manufacturing. Special precautions are therefore taken to prevent thermal degradation of the distillates
produced. The units are of the "wet" type. Normally, three sharply fractionated distillates are produced
(spindle oil, light machine oil and medium machine oil). Cutpoints between those fractions are typically
controlled on their viscosity quality. Spindle oil and light machine oil are subsequently steam- stripped in
dedicated strippers. The distillates are further processed to produce lubricating base oil. Short residue is
normally used as feedstock for the solvent de-asphalting process to produce deasphalted oil, an
intermediate for bright stock manufacturing.
High-Vacuum Units for Bitumen Production
Special vacuum flashers have been designed to produce straight-run bitumen and/or feedstocks for
bitumen blowing. In principle, these units are designed on the same basis as the previously discussed feed
preparation units, which may also be used to provide feedstocks for bitumen manufacturing.

BITUMEN BLOWING

Asphaltic bitumen, normally called "bitumen" is obtained by vacuum distillation or vacuum flashing of an
atmospheric residue. This is " straight run" bitumen. An alternative method of bitumen production is by
precipitation from residual fractions by propane or butane- solvent deasphalting.

The bitumen thus obtained has properties which derive from the type of crude oil processed and from the
mode of operation in the vacuum unit or in the solvent deasphalting unit. The grade of the bitumen
depends on the amount of volatile material that remains in the product: the smaller the amount of volatiles,
the harder the residual bitumen.

In most cases, the refinery bitumen production by straight run vacuum distillation does not meet the market
product quality requirements. Authorities and industrial users have formulated a variety of bitumen grades
with often stringent quality specifications, such as narrow ranges for penetration and softening point. These
special grades are manufactured by blowing air through the hot liquid bitumen in a BITUMEN BLOWING
UNIT. What type of reactions take place when a certain bitumen is blown to grade? Bitumen may be
regarded as colloidal system of highly condensed aromatic particles (asphaltenes) suspended in a
continuous oil phase. By blowing, the asphaltenes are partially dehydrogenated (oxidised) and form larger
chains of asphaltenic molecules via polymerisation and condensation mechanism. Blowing will yield a
harder and more brittle bitumen (lower penetration, higher softening point), not by stripping off lighter
components but changing the asphaltenes phase of the bitumen. The bitumen blowing process is not
always successful: a too soft feedstock cannot be blown to an on-specification harder grade.

The blowing process is carried out continuously in a blowing column. The liquid level in the blowing column
is kept constant by means of an internal draw-off pipe. This makes it possible to set the air-to-feed ratio
(and thus the product quality) by controlling both air supply and feed supply rate. The feed to the blowing
unit (at approximately 210 0C), enters the column just below the liquid level and flows downward in the
column and then upward through the draw-off pipe. Air is blown through the molten mass (280-300 0C) via
an air distributor in the bottom of the column. The bitumen and air flow are countercurrent, so that air low in
oxygen meets the fresh feed first. This, together with the mixing effect of the air bubbles jetting through the
molten mass, will minimise the temperature effects of the exothermic oxidation reactions: local overheating
and cracking of bituminous material. The blown bitumen is withdrawn continuously from the surge vessel
under level control and pumped to storage through feed/product heat exchangers.
Introduction
Already in the 30's it was found that when heavy oil fractions are heated over clay type materials, cracking
reactions occur, which lead to significant yields of lighter hydrocarbons. While the search was going on for
suitable cracking catalysts based on natural clays, some companies concentrated their efforts on the
development of synthetic catalyst. This resulted in the synthetic amorphous silica-alumina catalyst, which
was commonly used until 1960, when it was slightly modified by incorporation of some crystalline material
(zeolite catalyst). When the success of the Houdry fixed bed process was announced in the late 1930s, the
companies that had developed the synthetic catalyst decided to try to develop a process using finely
powdered catalyst. Subsequent work finally led to the development of the fluidised bed catalytic cracking
(FCC) process, which has become the most important catalytic cracking process.

Originally, the finely powdered catalyst was obtained by grinding the catalyst material, but nowadays, it is
produced by spray-drying a slurry of silica gel and aluminium hydroxide in a stream of hot flue gases.
Under the right conditions, the catalyst is obtained in the form of small spheres with particles in the range
of 1-50 microns.

When heavy oil fractions are passed in gas phase through a bed of powdered catalyst at a suitable velocity
(0.1-0.7m/s), the catalyst and the gas form a system that behaves like liquid, i.e. it can flow from one
vessel to another under the influence of a hydrostatic pressure. If the gas velocity is too low, the powder
does not fluidise and it behaves like a solid. If velocity is too high, the powder will just be carried away with
the gas. When the catalyst is properly fluidised, it can be continously transported from a reactor vessel,
where the carcking reactions take place and where it is fluidised by the hydrocarbon vapour, to a
regenerator vessel, where it is fluidised by the air and the products of combustion, and then back to the
reactor. In this way the proces is truly continous.

The first FCC unit went on stream in Standard Oil of New Jersey's refinery in Baton Rounge, Louisiana in
May 1942. Since that time, many companies have developed their own FCC process and there are
numerous varieties in unit configuration.

FCC Process Configuration

: Hot feed, together with some steam, is introduced at the bottom of the riser via special distribution
nozzles. Here it meets a stream of hot regenerated catalyst from the regenerator flowing down the inclined
regenerator standpipe. The oil is heated and vaporised by the hot catalyst and the cracking reactions
commence. The vapour, initially formed by vaporisation and successively by cracking, carries the catalyst
up the riser at 10-20 m/s in a dilute phase. At the outlet of the riser the catalyst and hydrocarbons are
quickly separated in a special device. The catalyst (now partly deactivated by deposited coke) and the
vapour then enter the reactor. The vapour passes overhead via cyclone separator for removal of entrained
catalyst before it enters the fractionator and further downstream equipment for product separation. The
catalyst then descends into the stripper where entrained hydrocarbons are removed by injection of steam,
before it flows via the inclined stripper standpipe into the fluidised catalyst bed in the regenerator.
Air is supplied to the regenerator by an air blower and distributed throughout the catalyst bed. The coke
deposited is burnt off and the regenerated catalyst passes down the regenerator standpipe to the bottom of
the riser, where it joins the fresh feed and the cycle recommences.

The flue gas (the combustion products) leaving the regenerator catalyst bed entrains catalyst particles. In
particular, it entrains "fines", a fine dust formed by mechanical rubbing of catalyst particles taking place in
the catalyst bed. Before leaving the regenerator, the flue gas therefore passes through cyclone separators
where the bulk of this entrained catalyst is collected and returned to the catalyst bed.

Normally modern FCC is driven by an expansion turbine to mimimise energy consumption. In this
expansion turbine, the current of flue gas at a pressure of about 2 barg drives a wheel by striking impellers
fitted on this wheel. The power is then transferred to the air blower via a common shaft. This system is
usually referred to as a "power recovery system". To reduce the wear caused by the impact of catalyst
particles on the impellers (erosion), the flue gas must be virtually free of catalyst particles. The flue gas is
therefore passed through a vessel containing a whole battery of small, highly efficient cyclone separators,
where the remaining catalyst fines are collected for disposal.

Before being disposed of via a stack, the flue gas is passed through a waste heat boiler, where its
remaining heat is recovered by steam generation.

In the version of the FCC process described here, the heat released by burning the coke in the regenerator
is just sufficient to supply the heat required for the riser to heat up, vaporise and crack the hydrocarbon
feed. The units where this balance occurs are called " heat balanced" units. Some feeds caused excessive
amounts of coke to be deposited on the catalyst, i.e. much more than is required for burning in the
regenerator and to have a "heat balanced" unit. In such cases, heat must be removed from the
regenerator, e.g. by passing water through coils in the regenerator bed to generate steam. Some feeds
cause so little coke to be deposited on the catalyst that heat has to be supplied to the system. This is done
by preheating the hydrocarbon feed in a furnace before contacting it with the catalyst.

Main Characteristics
A special device in the bottom of the riser to enhance contacting of catalyst and hydrocarbon feed.
The cracking takes place during a short time (2-4 seconds) in a riser ("short-contact time riser") at
high temperatures ( 500-540 0C at riser outlet).
The catalyst used is so active that a special device for quick separation of catalyst and
hydrocarbons at the outlet of the riser is required to avoid undesirable cracking after the mixture
has left the riser. Since, no cracking in thereactor is required, the reactor no longer functions as a
reactor; it merely serves as a holding vessel for cyclones.
The regenerator takes place at 680-720 0C. With the use of special catalysts, all the carbon
monoxide (CO) in the flue gas is combusted to carbon dioxide (CO 2) in the regenerator.
Modern FCC includes a power recovery system for driving the air blower.

Equipment in FCC
Large storage vessels for catalyst (fresh and equilibrium)
Regenerator
Reactor
Main Fractionator
Product Work Up section (several distillation columns in series
Product treating facilities

Feedstock & Yield

Before the introduction of residues, vacumn distillates were used as feedstock to load the Catalytic Cracker
fully. These days, even residues are used to load the cracker. The term used for this type of configuation is
Long Residue Catalytic Cracking Complex. The only modification or addition needed are a residue desalter
and a bigger and more heat resistent reactor.

The yield pattern of an FCC unit is typically as follows:

Product % wt on fresh feed

 C3 & C4 15
Gasoline 40-50
Heavy Gas Oil 10
Coke 5

Conclusion
The FCC Unit can a real margin improver for many refineries. It is able to convert the residues into high
value products like LPG , Butylene, Propylene and Mogas together with Gasoil. The FCC is also a start for
chemical production (poly propylene). Many FCC's have 2 modes: a Mogas mode and a Gasoil mode and
FCC's can be adapted to cater for the 2 modes depending on favourabale economic conditions. The only
disavantage of an FCC is that the products produced need to be treated (sulfur removal) to be on
specification. Normally Residue FCCs act together with Residue Hydroconversion Processes and
Hydrocrackers in order to minimise the product quality give away and get a yield pattern that better
matches the market specifications. Via product blending, expensive treating steps can be avoided and the
units prepare excellent feedstock for eachother: desulfurised residue or hydrowax is excellent FCC feed,
while the FCC cycle oils are excellent Hydrocracker feed.

In the near future, many refiners will phase the challenge how to desulfurise cat cracked gasoline without
destroying its octane value. Catalytic destillation appears to be one of the most promising candidate
processes for that purpose.

HYDROCRACKING

Introduction
The need for gasoline of a higher quality than that obtained by catalytic cracking led to the development of
the hydrocracking process. The history of the process goes back to the later 1920s when a plant for the
commercial hydrogenation of brown coal was commissioned at Leuna in Germany. Tungsten sulphide was
used as a catalyst in this one-stage unit , in which high reaction pressures, 200-300 bar, were applied. The
catalyst displayed a very high hydrogenation activity: the aromatic feedstock, coal and heavy fractions of
oil, containing sulphur, nitrogen and oxygen, was virtually completely converted into paraffins and
isoparaffins. The result of the Leuna plant - loss of octane number from aromatic hydrogenation of
impurities in the feedstock, notably nitrogen compounds, followed by a hydrocracking step. In 1939, ICI
developed the second-stage catalyst for a plant that contributed largely to Britain's supply of aviation
gasoline in the subsequent years.

During World War II, two stage processes were applied on a limited scale in Germany, Britain and USA. In
Britain, feedstock were creosote from coal tar and gas oil from petroleum. In the USA, Standard Oil of New
Jersey operated a plant at Baton Rouge, producing gasoline from a Venezuelan kerosine/light gasoil
fraction. Operating conditions in those units were comparable: approximate reaction temperature 400 0C
and reaction pressures of 200-300 bar.
After the war, commercial hydrocracking was stopped because the process was too expensive.
Hydocracking research, however, continued intensively. By the end of the 1950s, the process had become
economic, for which a number of reasons are identified.

The development of improved catalyst made it possible to operate the process at considerably lower
pressure, about 70-150 bar.

This in turn resulted in a reduction in equipment wall thickness, whereas simultaneously, advances were
made in mechanical engineering, especially in the field of reactor design
and heat transfer. These factors, together with the availability of relatively
low cost hydrogen from steam reforming process, brought hydrocracking
back on the refinery scene. The first units of the second generation were built in USA to meet the demand
for conversion of surplus fuel oil in the gasoline-oriented refineries.

Now, hdyrocracking is well established process from many licensors.

Basis for the Choice of Conversion Route

Refiners are continuously faced with trends towards increased conversion, better product qualities and
more rapidly changing product patterns. Various processes are available that can meet the requirements to
a greater or lesser degree: coking, visbreaking/thermal cracking, catalytic cracking and hydrocracking.

The type of process applied and the complexity of refineries in various parts of the world are determined to
a greater extent by the product distribution required. As a consequence, the relatively importance of the
above process in traditionally fuel-oil dominated refineries such as those in Western Europe will be quite
different from those of gasoline-oriented refineries in, for instance, the USA.

An important aspect of the coking, thermal cracking and catalytic cracking process is that they operate at
low pressures. This gives advantages in the fields of capital, matallurgy and engineering.

A particular feature of the hydrocracking process, as compared with its alternatives, is its flexibility with
respect to product outturn and high quality of its products. In the areas where quantitative imbalance exists
of lighter products, middle distillates and fuel, hydrocracking is a most suitable process for correction.
Moreover, the hydrocracker does not yield any coke or pitch byproduct: the entire feedstock is converted
into the required product range, an important consideration in a situation of limited crude oil availability.
The development of the low-pressure catalytic reforming process, which produces relatively cheap, high
quality hydrogen, has continued substantially to the economic viability of hydrocracking. On the whole,
hydrocracking can handle a wider range of feedstock than catalytic cracking, although the latter process
has seen some recent catalyst developments which narrowed the gap. There are also examples where
hydrocracking is complementary rather than alternative to the other conversion process; an example, cycle
oils, which cannot be recycled to extinction in the catalytic cracker, can be processed in the hydrocracker.

Notwithstanding many extensive comparisons between the various processes, the experince shows the
generalisation with respect to the optimum conversion route still cannot be made.

Process Description
All hydrocracking process are characterised by the fact that in a catalytic operation under relatively high
hydrogen pressure a heavy oil fraction is treated to give products of lower molecular weight.

Hydrocracking covers widely different fuels, ranging from C3/C4 production from naphta, on the other
hand, to luboil manufacture from deasphalted oils, on the other.

Most hydrocrackers use fixed beds of catalyst with downflow of reactants. The H-Oil process developed by
Hydrocarbon Research Corp and Cities Service R & D employs an ebullient bed reactor in which the beds
of particulate catalyst are maintained in an ebullient or fluidised condition in upflowing reactants.

When the processing severity in a hydrocracker is increased, the first reaction occuring leads to saturation
of any olefinic material present in feedstock. Next comes the reaction of desulphurisation, denitrogenation
and de-oxygenation. These reactions constitute treating steps during which in most cases, only limited
cracking takes place. When the severity is increased further, hydrocracking reaction is initiated. They
proceed at various rates, with the formation of intermediate products (eg. saturation of aromatics), which
are subsequently cracked into lighter products.

Process Configuration
When the treating step is combined with the cracking reaction to occur in one reactor, the process is called
a SINGLE-STAGE PROCESS.

SINGLE-STAGE PROCESS: In this simplest of the hydrocracker configuration, the lay out of the reactor
section generally resembles that of hydrotreating unit. This configuration will find application in cases
where only moderate degree of conversion (say 60% or less) is required. It may also be considered if full
conversion, but with a limited reduction in molecular weight, is aimed at. An example is the production of
middle distillates from heavy distillate oils. The catalyst used in a single-stage process comprises a
hydrogenation function in combination with a strong cracking function. The hydogenation function is
provided by sulphided metals such as cobalt, molybdenum and nickel. An acidic support, usually alumina,
attends to the cracking function. Nitrogen compounds and ammonia produced by hydrogenation interfere
with acidic activity of the catalyst. In the cases of high/full conversion is required, the reaction temperatures
and run lenghts of interest in commercial operation can no longer be adhered to. It becomes necessary to
switch to a multi-stage process, in which the cracking reaction mainly takes place in an added reactor. With
regard to the adverse effect of ammonia and nitrogen compounds on catalyst activity, two versions of the
multi stage hydrocracker have been developed: the TWO STAGE HYDROCRACKER and SERIES FLOW
HYDROCRACKER.

In the first type, the undesirable compounds are removed from the unconverted hydrocarbons before the
latter are charged to the cracking reactor. This type is called the TWO STAGE PROCESS. The other
variety is ofen referred to as SERIES FLOW HYDROCRACKER. This type uses a catalyst with an
increased tolerance towards nitrogen, both as ammonia and in organic form.

TWO STAGE CONFIGURATION: Fresh feed is preheated by heat exchange with effluent from the first
reactor. It is combined with part of a not fresh gas/recycle gas mixture and passes through a first reactor
for desulphurisation/denitrogenation step. These reactions, as well as those of hydrocracking, which
occurs to a limited extent in the first reactor, are exothermic. The catalyst inventory is therefore divided
among a number of fixed beds. Reaction temperatures are controlled by introducing part of the recycle gas
as a quench medium between beds. The ensuing liquid is fractionated to remove the product made in the
first reactor. Unconverted, material, with a low nitrogen content and free of ammonia, is taken as a bottom
stream from the fractionation section. After, heat exchange with reactor effluent and mixing with heated
recycle gas, it is sent to the second reactor. Here most of the hydrocracking reactions occur. Strongly
acidic catalyst with a relatively low hydrogenation activity (metal sulphides on, for example, amorphous
silica-alumina) are usually applied. As in the first reactor, the exothermicity of the process is controlled by
using recycle gas as quench medium the catalyst beds. Effluent from the second reactor is cooled and
joins first stage effluent for separation from recycle gas and fractionation. The part of the second reactor
feed that has remained unconverted is recycled to the reactor. Feedstock is thereby totally converted to the
product boiling range.

SERIES FLOW CONFIGURATION: The principal difference is the elimination of first stage cooling and
gas/liquid separation and the interstage ammonia removal step. The effluent from the first stage is mixed
with more recycle gas and routed direct to the inlet of the second reactor. In contrast with the amorphous
catalyst of the two-stage process, the second reactor in series flow generally has a zeolitic catalyst, based
on crystalline silica-alumina. AS in the two stage process, material not converted to the product boiling
range is recycled from the fractionation section.

Conclusion
Both two stage and series flow hydrocracking are flexible process: they may yield, in one mode of
operation, only naphtha and lighter products and, in a different mode, only gasoil and lighter products. In
the naphtha mode, both configurations have comparable yield patterns. In modes for heavier products,
kerosine and gasoil, the two stage process is more selective because product made in the first reactor is
removed from the second reactor feed, In series flow operation this product is partly overcracked into
lighter products in the second reactor.

ISOMERIZATION

The isomerisation process involves the transformation of one molecular structure into another (isomer)
whose component atoms are the same but arranged in a different geometrical structure. Since isomers
may differ greatly in physical and chemical properties, isomerisation offers the possibility of converting less
desirable compounds into isomers with desirable properties, in particular to convert n-paraffins into iso-
paraffins, thereby increasing the octane of the hydrocarbon stream. The main fields of application of
isomerisation are:

ISOMERISATION of normal butane into isobutane

ISOMERISATION of pentanes and hexanes into higher- branched isomers

Since branched isomers have a higher antiknock quality than the corresponding linear paraffins, this form
of isomerisation is important for the production of motor fuels.

In addition to the above applications, isomerisation is applied for the conversion of ortho-xylene and meta-
xylene into para- xylene, used for the manufacturing of polester fibres.

Isomerisation of low molecular weight paraffins has been commercially applied for many years. After
extensive laboratory work had been carried out during the 1930s, World War 2 prompted the development
of the laboratory processes into full- scale commercial units in order to meet the demand for isobutane
necessary for the manufacture of large amounts of alkylate. While the first butane isomerisation unit went
on stream in late 1941, by the end of the war nearly 40 butane isomerisation units were in operation in the
USA and the Caribbean. Two pentane and two light naphtha isomerisation units also came on stream
towards the end of the war to provide an additional source of blending aviation gasoline.
Though butane isomerisation has maintained its importance, present day interest isomerisation is specially
focussed on the upgrading of fractions containing C5 Pentane and C6 Hexane for use as motor gasoline
components. This application has been prompted by the world drive to remove the lead additives gradually
from motor gasoline in order to reduce air pollution. The octane loss caused by the removal or reduction of
lead antiknock additives can be compensated for by isomerisation of pentane/hexane paraffin fraction of
the light gasoline fractions.

Isomerisation technology has also improved substantially due to the hard work of many technologist. In
order to achieve the low temperature necessary to obtain an acceptable yield of isomers, the Catalyst
systems used in the early units were based on aluminium chloride in some form. These catalyst systems,
however, had the drawback of being highly corrosive and difficult to handle. In recent years, catalyst of a
different type have come in use. These are solid catalysts consisting of a support having an acidic carrier
and a hydrogenation function, frequently a noble metal. Modern isomerisation units utilise these dual-
function catalysts and operate in the vapour phase and the presence of hydogen. For these reasons, these
process are called hydro- isomerisation processes.

The first hydro- isomerisation unit was introduced nin 1953 by UOP, followed in 1965 by the first BP one,
while in 1970 the first Shell hydro-isomerisation (HYSOMER) unit was started up. At present the following
hydro-isomerisation processes are commercially available:

UOP BUTAMER for butane isomerisation

UOP PENEX for pentane/hexane isomerisation
BP C4 isomerisation for butane isomerisation
BP C5/C6 isomerisation for pentane/hexane isomerisation
SHELL Hysomer for pentane/hexane isomerisation

All these processes takes place in the vapour phase on a fixed bed catalyst containing platinum on a solid
carrier.

As an example, the Shell Hysomer process will be briefly described. The liquid feedstock is
pentane/hexane from light naphtha. naphtha splitters are widely used to split light naphtha, heavy naphtha
and also LPG. The light naphtha (C5/C6) is combined with the recycle gas/ fresh gas mixture. The
resultant combined reactor feed is routed to a feed/ effluent heat exchanger, where it is heated and
completely vaporised by the effluent of the reactor. The vapourised combined reactor feed is further heated
to the desired reactor inlet temperature in the reactor charge heater. The hot charge enters the Hysomer
reactor at the top and flows downwards through the catalyst bed, where a portion of normal and mono-
branched paraffins is converted into higher branched (high octane) components. Temperature rise from the
heat of reaction release is controlled by a cold quench gas injection into the reactor. Reactor effluent is
cooled and subsequently separated in the product separator into two streams: a liquid product (isomerate)
and a recycle gas stream returning to the reactor via the recycle gas compressor.

The catalyst is a dual function catalyst consisting of platinum on a zeolite basis, highly stable and
regenerable.
Temperatures and pressure vary in a range of 230 - 285 0C and 13-30 bar, C5/C6 content in product
relative to that in feed is 97% or better, and octane upgrading ranges between 8 and 10 points, depending
on feedstock quality. The Hysomer process can be integrated with catalytic reformer, resulting in
substantial equipment savings, or with iso-normal separation processes which allows for a complete
conversion of pentane/hexane mixtures into isoparaffin mixtures. An interesting application in this field is
the total isomerisation process (TIP) in which the isomerisation is completely integrated with a Union
Carbide molecular sieve separation process or the naphtha IsoSiv Process by UOP.

Highlights of TIP

The following are some of the highlights of the TIP process:

A. TIP has been in commercial operation since 1975

B. UOP manufacturers both the zeolite isomerisation catalyst and the IsoSiv Grade Molecular Sieve
adsorbent.
C. UOP's zeolite catalyst will tolerate sulfur and/or water upsets, the effects of which are usually reversible,
either with time or by in situ regeneration (which minimises any down time).
D. The expected life of the catalyst and adsorbent is 10 years or more.
F. The combination of zeolite isomerisation and IsoSiv molecular separation is possible because each
station has similar operating conditions of temperature, pressure and environment. This eliminates the
need for a second compressor, intermediate stabilisation and the costs associated with cooling, purifying
and reheating the recylce normal paraffins.
G. TIP and IsoSiv separation permits maximum flexibility in changing the C5/C6 ratio and iso/normal ratio
of the feed.

Conclusion:

Nowadays many refiners are looking into the isomerisation processes to add potential extra value and
complimentary to the platforming process. Directly both the platforming and isomerisation process work
hand in hand in several ways. C5 paraffins tend to crack away in the platformer, but give high upgrading in
the isomerisation unit. C6 components convert nicely to benzene in the platformer, but nowadays the
specs on aromatics and benzene are tightening, which makes conversion of these components to C6
isomers preferred. Furthermore, benzene is hydrogenated in the isomerisation unit. By adjusting the
cutpoint between the light and heavy naphtha, i.e. the cutpoint between the feed to the isomerisation feed
and the platformer feed, the refiner has the flexibility to control the benzene content of its gasoline pool

Motor gasoline (Mogas) production starts with the distillation of crude oil. One of the products out of that
process is a fraction of low octane gasoline, normally referred to as naphtha, typically boiling in the range
100 - 160 0C. Other gasoline fractions are produced as a result of secondary processes like catalytic
cracking, isomerisation, alkylation and platforming. Petrol is then produced by blending a variety of these
gasoline components of different qualities to meet a series of product specifications.

One very important property of Mogas is the octane number, which influences "knocking" or "pinking"
behaviour in the engine of cars. Traditionally lead compounds have been added to petrol to improve the
octane number. Over the past years, in many countries legislation has been implemented aimed at
reducing the emission of lead from exhausts of motor vechiles and this, calls for other means of raising the
octane number.

The role of a platformer is to pave the way for this by a process which reforms the molecules in low octane
naphtha to produce a high octane gasoline component. This is achieved by employing a catalyst with
platinum as its active compound; hence the name Platformer. For many refinery catalyst applications, a
promoter is used, and in the platforming process, it is a chloride promoter which stimulates the 'acidity' of
the catalyst and thereby the isomerisation reactions. Often, a bimetallic catalyst is used, i.e. in addition to
the platinum, a second metal, for instance Rhenium is present on the catalyst. The main advantage is a
higher stability under reforming conditions. The disadvantage is that the catalyst becomes more sensitive
towards poisons, process upsets and more susceptible to non-optimum regenerations.
Chemistry:

The main reactions of platforming process are as follows:

Dehydrogenation of naphthenes, yielding aromatics and hydrogen

Dehydro-isomerisation of alkyl cyclopentanes to aromatic and hydrogen
Isomerisation of paraffins and aromatics
Dehydrocyclisation of paraffins to aromatics and hydrogen
Hydrocracking of paraffins and naphthenes to ligher, saturated paraffins at the expense of
hydrogen

The process literally re-shapes the molecules of the feed in a reaction in the presence of a platinum
catalyst. Normally it is the hydrocarbon in the C6-C10 parafins that get converted to aromatics.

The above reactions takes place concurrently and to a large extent also sequentially. The majority of these
reactions, involve the conversion of paraffins and naphtenes and

result in an increase in octane number and a nett production of hydrogen. Characteristic of the total effect
of these reactions is the high endothermicity, which requires the
continuous supply of process heat to maintain reaction temperature in the
catalyst beds. That is why the process is typically done in four reactors in series with furnaces in between,
in order to remain sufficiently high reactor temperatures.

The reactions takes place at the surface of the catalyst and are very much dependent, amongst other
factors, on the right combination of interactions between platinum, its modifiers or activators, the halogen
and the catalyst carrier. During operating life of the catalyst, the absolute and relative reaction rates are
influenced negatively by disturbing factors like gradual coke deposition, poisons and deterioration of
physical characteristic of the catalyst (surface area decline).

The process of platforming:

The feedstock of the platformer is drawn from the refinery's distillation units. This is first treated by passing
the feedstock together with hydrogen over a catayst, in a process called 'hydrotreating, to convert the
sulphur and nitrogen compunds to hydrogen sulphide and ammonia, in order to prevent poisoning of the
expensive platformer catalyst. After hydrotreating, ,the reactor effluent moves on through a stabiliser
column to remove the gases formed (hydrogen sulphide, ammonia and fuel gas). In a second column, the
C5 and some of the C6 is removed in a separate fraction called 'tops'. The reason to remove C5/C6 is that
this component will crack in the platformer to produce fuel gas, while C6 gets converted into benzene,
which can only be allowed in limited amount into the mogas because of its toxicity. From the bottom of the
splitter column, the naphtha stream is produced, which is the feed for the Platforming section.

At the heart of the Platformer process are the four reactors, each linked to furnaces to sustain a suffiently
high reaction temperature, about 500 0C at the inlet of the reactors.
Over time, coke will build up on the catalyst surface area, which reduces the catalyst activity. The catalyst
can be easily regenerated however, by burning the coke off with air. After coke burning, the catalyst needs
to be reconditioned by a combined treatment of air and HCl under high temperature. This regeneration
step is called 'oxy-chlorination'. After this step the catalyst is dryed with hot nitrogen and subsequently
brought in its active condition by reducing the surface with hot hydrogen. The refinery will therefore
regulary have to take out one of the reactors to undergo this regeneration process. This type of process is
therefore called semi-regen platforming.

During the regeneration process, the refinery will suffer production loss, which is the reason why UOP
developed a major process enhancement by making the regeneration possible continuously, in a
Continous Catalytic Reformer, CCR. In the CCR unit, the reactors are cleverly stacked, so that the catalyst
can flow under gravity. From the bottom of the reactor stack, the 'spent' catalyst is 'lifted' by nitrogen to the
top of the regenerator stack. In the regenerator, the above mentioned different steps, coke burning,
oxychlorination and drying are done in different sections, segregated via a complex system of valves,
purge-flows and screens. From the bottom of the regenerator stack, catalyst is lifted by hydrogen to the top
of the reactor stack, in a special area called the reduction zone. In the reduction zone, the catalyst passes
a heat exchanger in which it is heated up against hot feed. Under hot conditions it is brought in contact with
hydrogen, which performs a reduction of the catalyst surface, thereby restoring its activity. In such a
continuous regeneration process, a constant catalyst activity can be maintained without unit shutdown for a
typical runlength of 3 - 6 years. After 300 - 400 cycles of reaction/regeneration, the surface area of the
catalyst will have dropped to a level (120 - 130 m2/g) that it becomes more difficult to maintain catalyst
activity and at such a time normally the catalyst will be replaced by a fresh batch. The batch of 'spent'
catalyst is then sent for platinum reclaim to recover the valuable precious metals.

For economic reasons, the design capacities of Platformer units vary from 1000 - 4500 t/d; operating
pressures can vary over a wide range, units with from 3.5 barg up to 30 barg can be found, whereby the
latest generation CCR's are typically at the lower pressure range. A lower pressure enhances the
endothermic reactions, which gives less cracking reactions and thereby a higher liquid yield. However, at a
lower reactor operating pressure, the hydrogen partial pressure will be lower as well, which favours coke
formation. The reason why semi regen platformers will not operate at a too low pressure, otherwise the
cycle length between regenerations becomes to short. A second disadvantage of operating at a lower
pressure is that a larger compressor will be required to boost the pressure of the hydrogen up to the
normal pressure of the hydrogen system (about 20 barg). Typical design reformate octane numbers are in
the 95-104 range. The reactor temperature is in a region of 450-530 0C.

At the outlet of the last reactor the product is still well above 400 0C. It is cooled down against cold feed in
massive heat exchanger, either a so called 'Texas Tower' or a Packinox plate-pack heat exchanger. The
special design of those heat exchangers ensures that minimum heat loss occurs in order to minimise the
fuel consumption of the furnaces. After passing the feed/effluent exchanger, the reaction products are
cooled in air/water coolers and routed to a product separator, where the hydrogen is the main gaseous
product. Part of the hydrogen produced is recycled back (via a compressor) to the feed, in order to
maintain a high enough hydrogen partial pressure in the reactors. The remainder of the gases are
compressed and brought in contact again with the liquid from the product separator. This is step is called
'recontacting' and is done in order to recover as much as possible hydrocarbons from the hydrogen
produced. The reactor product, now in liquid form, goes on to the platformer stabiliser which removes
Liquid Petroleum Gas ( LPG) and other gases to leave a liquid high octane gasoline component called
platformate, ready for blending into the refinery mogas pool. Summarising, the Platformer unit produces
about 85% liquid platformate, 10% hydrogen and 5% LPG.

The Continuous Catalytic Reforming unit or better known as CCR Platformer is licensed by UOP, Universal
Oil Products, based in USA. More recently, other technology vendors have copied the concept, one of the
main competitors for UOP in this field is IFP from France.

Main Equipment in a CCR Platformer:

A CCR typically contains a feed/effluent heat exchanger (Texas Tower or Packinox), 4 furnaces, 4 reactors,
a regenerator, overhead recontacting section, net gas compressor, recycle gas compressor and a stabiliser
column.

The objective of the Hydrotreating prococess is to remove suplur as well as other unwanted compunds,
e.g. unsaturated hydrocarbons, nitrogen from refinery process streams.

Until the end of World War 2, there was little incentive for the oil industry to pay significant attention to
improving product quality by hydrogen treatment. However, soon after the war the production of high
sulphur crudes increased significantly, which gave a more stringent demand on the product blending
 flexibility of refineries, and the marketing specifications for the
products became tighter, largely due to environmental
considerations. Furthermore, the catalyst used in the
Platforming process can only handle sulfur in the very low ppm
level, so hydrotreating of naphtha became a must. The
necessity for hydrotreating of middle distillates
(kerosene/gasoil) originates from pressure to reduce sulfur
emissions into the environment. Overall, this situation resulted
in an increased necessity for high sulphur removal capability in
many refineries.

As catalytic reforming gives hydrogen as a byproduct, it gave

additional momentum to the development of sulphur removal
process by hydrogen treatment. In this treatment, the sulphur
compounds are removed by converting them into hydrogen
sulphide by reaction with hydrogen in the presence of a
catalyst. This results in high liquid product yields, since only
sulphur is removed. Furthermore, the hydrogen sulphide
produced can be easily removed from the product gas stream,
for example by an amine wash. In this way, hydrogen sulphide
is recovered as a higly concentrated stream and can be further
converted into elemental sulphur via the "Claus" process.

Hydrodesulphursiation has been extensively used commercially for treating naphtha as feedstock for
catalytic reformers to meet the very stringent sulphuir specification of less than 1 ppm wt to protect the
platinum catalyst. It has also been widely used for removal of sulphur compounds from kerosine and
gasoils to make them suitable as blending components. In cases where products are from catalytic or
thermal crackers, hydrogen treatment is used to improve product quality specifications like colour, smoke
point, cetane index, etc.

For Hydrotreating, two basic processes are applied, the liquid phase (or trickle flow) process for kerosine
and heavier straight-run and cracked distillates up to vacumn gas oil and the vapour phase process for
light straight-run and cracked fractions.

Both processes use the same basic configuration: the feedstock is mixed with hydrogen-rich make up gas
and recycle gas. The mixture is heated by heat exchange with reactor effluent and by a furnace and enters
a reactor loaded with catalyst. In the reactor, the sulphur amd nitrogen compounds present in the feedstock
are converted into hydrogen sulphide and ammonia respectively. The olefins present are saturated with
hydrogen to become di-olefins and part of the aromatics will be hydrogenated. If all aromatics needs to be
hydrogenated, a higher pressure is needed in the reactor compared to the conventional operating mode.

The reactor operates at temperatures in the range of 300-380 0C and at a pressure of 10-20 bar for naphta
and kero, as compared with 30-50 bar for gasoil, with excess hydrogen supplied. The temperature should
not exceed 380 0C, as above this temperature cracking reactions can occur, which deteriorates the colour
of the final product. The reaction products leave the reactor and, after having been cooled to a low
temperature, typically 40-50 0C, enter a liquid/gas separation stage. The hydrogen-rich gas from the high
pressure separation is recycled to combine with the feedstock, and the low pressure off-gas stream rich in
hydrogen sulphide is sent to a gas-treating unit, where hydrogen sulphide is removed. The clean gas is
then suitable as fuel for the refinery furnaces. The liquid stream is the product from hydotreating. It is
normally sent to a stripping column where H 2S and other undesirable components are removed, and finally,
in cases where steam is used for stripping, the product is sent to a vacumn drier for removal of water.
Some refiners use a salt dryer in stead of a vacuum drier to remove the water.

The catalyst used is normally cobalt, molybdenum and nickel finely distributed on alumina extrudates. It
slowly becomes choked by coke and must be renewed at regular

intervals (typically 2-3 years). It can be regenerated (by burning off the coke) and reused typically once or
twice before the breakdown of the support's porous structure
unacceptably reduces its activity. Catayst regeneration is, nowadays,
mainly carried out ex- situ by specialised firms. Other catalysts have also
been developed for applications where denitrification is the predominant reaction required or where high
stauration of olefins is necessary.
A more recent development is the application of Hydrotreating for pretreatment of feedstcok for the
catalytic cracking process. By utilisation of a suitable hydrogenation-promoting catalyst for conversion of
aromatics and nitrogen in potential feedstocks, and selection of severe operating conditions, hydrogen is
taken up by the aromatic molecules. The increased hydrogen content of the feedstock obtained by this
treatment leads to significant conversion advantages in subsequent catalytic cracking, and higher yield of
light products can be achieved.

Hydrotreatment can also be used for kerosine smoke point improvement (SPI). It closely resembles the
conventional Hydrotreating Process however an aromatic hydrogenation catalyst consisting of noble
metals on a special carrier is used. The reactor operates at pressure range of 50-70 bar and temperatures
of
260-320 0C. To restrict temperature rise due to the highly exothermic aromatics conversion reactions,
quench oil is applied between the catalysts beds. The catalyst used is very sensitive to traces of sulphur
and nitrogen in the feedstock and therefore pretreatment is normally applied in a conventional hydrotreater
before kerosine is introduced into the SPI unit. The main objective of Smoke Point Improvement is
improvement in burning characteristics as the kerosine aromatics are converted to naphthenes.

Hydrotreatment is also used for production of feedstocks for isomersiation unit from pyrolysis gasoline
(pygas) which is one of the byproducts of steam cracking of hydrocarbon fractions such as naphtha and
gasoil.

A hyrotreater and a hydrodesulphuriser are basically the same process but a hydotreater termed is used
for treating kerosene or lighter feedstock, while a hydodesulhuriser mainly refers to gasoil treating. The
hydrotreatment process is used in every major refinery and is therefore also termed as the work horse of
the refinery as it is the hydrotreater unit that ensures several significant product quality specifications. In
most countries the Diesel produced is hydrodesulhurised before its sold. Sulphur specifications are getting
more and more stringent. In Asia, countries such as Thailand, Singapore and Hong Kong already have a
0.05%S specification and large hydrodesulphurisation units are required to meet such specs.

The by-products obtained from HDT/HDS are light ends formed from a small amounts of cracking and
these products are used in the refinery fuelgas pool. The other main by-product is Hydrogen Sulphide
which is oxidized to sulphur and sold to the chemical industry for further processing

In combination with temperature, the pressure level (or rather the partial pressure of hydrogen) generally
determines the types of components that can be removed and also determines the working life of the
catalyst. At higher (partial) pressures, the desulphurisation process is 'easier', however, the unit becomes
more expensive for instance due to larger compressors and heavier reactors. Also, at higher pressure, the
hydrogen consumption of the unit increases, which can be a signficant cost factor for the refinery. The
minimum pressure required typically goes up with the required severity of the unit, i.e. the heavier the
feedstock, or the lower levels of sulphur in product required.

Distillation is the first step in the processing of crude oil and it takes place in a tall steel tower
called a fractionation column. The inside of the column is divided at intervals by horizontal trays.
The column is kept very hot at the bottom (the column is

insulated) but as different hydrocarbons boil at different

temperatures, the temperature gradually reduces towards the top, so
that each tray is a little cooler than the one below.

The crude needs to be heated up before entering the fractionation column and this is done at first
in a series of heat exchangers where heat is taken from other process streams which require
cooling before being sent to rundown. Heat is also exchanged against condensing streams from
the main column. Typically, the crude will be heated up in this way upto a temperature of 200 -
280 0C, before entering a furnace.

As the raw crude oil arriving contains quite a bit of water and salt, it is normally sent for salt
removing first, in a piece of equipment called a desalter. Upstream the desalter, the crude is mixed
with a water stream, typically about 4 - 6% on feed. Intense mixing takes place over a mixing
valve and (optionally) as static mixer. The desalter, a large liquid full vessel, uses an electric field
to separate the crude from the water droplets. It operates best at 120 - 150 0C, hence it is
conveniently placed somewhere in the middle of the preheat train.
Part of the salts contained in the crude oil, particularly magnesium chloride, are hydrolysable at
temperatures above 120 0C. Upon hydrolysis, the chlorides get converted into hydrochloric acid,
which will find its way to the distillation column's overhead where it will corrode the overhead
condensers. A good performing desalter can remove about 90% of the salt in raw crude.

Downstream the desalter, crude is further heated up with heat exchangers, and starts vaporising,
which will increase the system pressure drop. At about 170 -200 0C, the crude will enter a 'pre-
flashvessel', operating at about 2 - 5 barg, where the vapours are separated from the remaining
liquid. Vapours are directly sent to the fractionation column, and by doing so, the hydraulic load
on the remainder of the crude preheat train and furnace is reduced (smaller piping and pumps).

Just upstream the preflash vessel, a small caustic stream is mixed with the crude, in order to
neutralise any hydrochloric acid formed by hydrolysis. The sodium chloride formed will leave the
fractionation column via the bottom residue stream. The dosing rate of caustic is adjusted based
on chloride measurements in the overhead vessel (typically 10 - 20 ppm).

At about 200 - 280 0C the crude enters the furnace where it is heated up further to about 330 -370
0
C. The furnace outlet stream is sent directly to the fractionation column. Here, it is separated into
a number of fractions, each having a particular boiling range.

At 350 0C, and about 1 barg, most of the fractions in the crude oil vapourise and rise up the
column through perforations in the trays, losing heat as they rise. When each fraction reaches the
tray where the temperature is just below its own boiling point, it condenses and changes back into
liquid phase. A continuous liquid phase is flowing by gravity through 'downcomers' from tray to
tray downwards. In this way, the different fractions are gradually separated from each other on the
trays of the fractionation column. The heaviest fractions condense on the lower trays and the
lighter fractions condense on the trays higher up in the column. At different elevations in the
column, with special trays called draw-off trays, fractions can be drawn out on gravity through
pipes, for further processing in the refinery.

At top of the column, vapours leave through a pipe and are routed to an overhead condenser,
typically cooled by air fin-fans. At the outlet of the overhead condensers, at temperature about 40
0
C, a mixture of gas, and liquid naphtha exists, which is falling into an overhead accumulator.
Gases are routed to a compressor for further recovery of LPG (C3/C4), while the liquids
(gasoline) are pumped to a hydrotreater unit for sulfur removal.
A fractionation column needs a flow of condensing liquid downwards in order to provide a
driving force for separation between light and heavy fractions. At the top of the column this liquid
flow is provided by pumping a stream back from the overhead accumulator into the column.
Unfortunately, a lot of the heat provided by the furnace to vaporise hydrocarbons is lost against
ambient air in the overhead fin-fan coolers. A clever way of preventing this heat lost of
condensing hydrocarbons is done via the circulating refluxes of the column. In a circulating
reflux, a hot side draw-off from the column is pumped through a series of heat exchangers
(against crude for instance), where the stream is cooled down. The cool stream is sent back into
the column at a higher elevation, where it is been brought in contact with hotter rising vapours.
This provides an internal condensing mechanism inside the column, in a similar way as the top
reflux does which is sent back from the overhead accumulator. The main objective of a circulating
reflux therefore is to recover heat from condensing vapours. A fractionating column will have
several (typically three) of such refluxes, each providing sufficient liquid flow down the
corresponding section of the column. An additional advantage of having circulating refluxes is
that it will reduce the vapour load when going upwards in the column. This provided the
opportunity to have a smaller column diameter for top sections of the tower. Such a reduction in
diameter is called a 'swage'.

The lightest side draw-off from the fractionating column is a fraction called kerosene, boiling in
the range 160 - 280 0C, which falls down through a pipe into a smaller column called 'side-
stripper'. The purpose of the side stripper is to remove very light hydrocarbons by using steam
injection or an external heater called 'reboiler'. The stripping steam rate, or reboiled duty is
controlled such as to meet the flashpoint specification of the product. Similarly to the atmospheric
column, the side stripper has fractionating trays for providing contact between vapour and liquid.
The vapours produced from the top of the side stripper are routed back via pipe into the
fractionating column.

The second and third (optional) side draw-offs from the main fractionating column are gasoil
fractions, boiling in the range 200 - 400 0C, which are ultimately used for blending the final diesel
product. Similar as with the kerosene product, the gasoil fractions (light and heavy gasoil) are first
sent to a side stripper before being routed to further treating units.

At the bottom of the fractionation column a heavy, brown/black coloured fraction called residue is
drawn off. In order to strip all light hydrocarbons from this fraction properly, the bottom section
of the column is equipped with a set of stripping trays, which are operated by injecting some
stripping steam (1 - 3% on bottom product) into the bottom of the column.
Introduction

Modern optimization techniques have challenged organizations to rethink the way they
conduct

business both internally and externally, i.e. how efficiently and effectively their entire supply
chain is managed. Supply Chain Management (SCM) is one
such business function that has benefited substantially from
optimization software advances and solutions. The primary goal
of SCM is to maximize profit by integrated management of material and transactional flows
within a business and to customer and partner companies.

The petroleum refining industry has effectively embraced the software solutions to optimize
the business supply chain to maximize the profit margins and create order in the chaos of
numerous opportunities and challenges. The supply chain of a typical petroleum refining
company involves a wide spectrum of activities, starting from crude purchase and crude
transportation to refineries, refining operations, product transportation and finally delivering
the product to the end user. The nature of the value chain is such that its economics are
extremely complex and heavily linked (Refer to Fig. 1.0). For example, the process of
selecting the right crude is linked not only to the transportation costs involved in delivering it
to the refinery, but it must take into consideration the refinery configuration, capabilities and
constraints in converting the crude into products, as well as the product volume and price
fluctuations.

Figure 1: Typical Supply chain of Petroleum business

Software solutions based on Linear Programming (LP) technique have emerged as leaders
among various mathematical optimization techniques available to optimize the entire supply
chain from crude evaluation and selection, production planning and product logistic planning.

The objective of this article is to create an appreciation among readers about the application
of Linear Programming (LP) in refinery planning and optimization as a key component of the
business supply chain.

The article includes:

 Petroleum Refinery: Complexity of operations and the need and scope of optimization
Implementation of Linear Programming for refinery planning and optimization
Experiences in implementation and usage of Linear Programming
The bottom line

Refinery planning and optimization is mainly addressed through successive linear

programming software like RPMS (Honeywell Hi-Spec Solutions), PIMS (Aspen Technology),
and GRTMPS (Haverly Systems), while more rigorous non-linear planning models for refinery
planning have been recently developed. The experiences discussed in this article pertain to
RPMS, as the authors have been involved in the development and application of refinery LP
models using RPMS (Refinery and Petrochemical Modeling System). RPMS was developed
more than 35 years ago by Bonner & Moore, which was acquired by Honeywell Hi-Spec
Solutions in 1999. RPMS is used today at more than 100 refineries and petrochemical plants
worldwide for operations planning, crude oil evaluation and selection, inventory management,
future investment analysis and to analyze what if scenarios.

PETROLEUM REFINERY: COMPLEXITY OF OPERATIONS AND THE NEED AND SCOPE

OF OPTIMIZATION

COMPLEXITY OF REFINERY OPERATIONS

Crude selection

Modern petroleum refineries are designed to process a variety of indigenous and imported
crudes. As the crude cost is about 90% of the refinery input cost, the selection of optimum
crude mix is extremely important to achieve higher margins. However, the number of options
for buying the crudes under a fluctuating price scenario and transporting them to refineries
are so enormous that it is very difficult to evaluate all the crudes and decide on the optimum
crude mix for the refinery. Refineries buy crudes both on term contracts with leading
suppliers and also by spot purchases from the market. The optimum selection of term and
spot crudes is extremely difficult when multiple refineries are involved and work in an
integrated scenario.

Crude transportation

Once the crudes are selected and purchased, the focus is to optimize the transportation cost
from the crude suppliers to refineries. The transportation cost can be minimized by
considering the multiple options available for cargo sizes, sea routes, loading and unloading
infrastructure facilities, taxes and duties, etc.

Crude processing

The crudes often land at refinery sites as a mix of various crudes and various options of crude
blending are evaluated before it is processed. The ultimate challenge a refinery faces is
processing the crudes in the best possible manner and maximize the $/bbl (dollars per barrel)
for the crude input. Determining the best possible option is a very difficult task, as modern
day refineries are built with complex processing schemes, having a combination of various
technologies for heavy ends upgrading, product quality improvement, efficient fuel usage and
controlling refinery emissions. The most common configuration includes catalytic cracking,
hydro cracking and thermal cracking to maximize the bottom of the barrel. The other process
technologies like catalytic reforming, hydro treating and sulfur recovery are a must to comply
with stringent environment and product quality regulations (Refer to Fig. 2.0 for a process flow
diagram of a modern refinery).
Figure 2: Process flow diagram of a modern refinery
http://www.uop.com/refining/1010.html

Product demands

The product demands, quality and prices drive the entire crude processing and secondary
unit operations. Multiple streams with multiple blending options to make different grades of a
product further make the task of refinery planning cumbersome and demanding.

Moreover, the future promises to add even more complexity through additional product
specifications, environmental norms, changing feedstock, product prices, mergers and
acquisitions.

NEED AND SCOPE FOR OPTIMIZATION IN REFINERY OPERATIONS

Most refineries are owned by integrated oil companies having a variety of interests, from
exploration and production through refining and marketing to retail sales. Within such an
organization the refinery works under the direction of the Head office. The Head office
negotiates long-term and short-term crude supply contracts while the product Supply and
Distribution department sells products. The refinery itself typically works within the overall
framework of the organization to maximize the corporate profitability. This makes the refining
an extremely complex and dynamic activity. Along with the complexity of refining, there also
exists a great degree of freedom in refinery operations. For example, one of the most
commonly used refinery products is fuel for automobiles, and the customer does not care
about the complexity or simplicity of the refinery, what crudes it purchased, which processing
technology it used, what blending or additive components it used in making the fuel. The
customer is only concerned with the proper running of his vehicle and the value for the money
spent. Therefore, the refiners have got both an enormous complexity and considerable
freedom to satisfy the customer requirement and make profit. This requires the optimization
of multiple objectives in the refinerys business supply chain.

The table below provides a glimpse of the multiple objectives of refinery optimization:

Minimize crude landed cost at refinery

Optimize refinery crude mix
Optimize black oil generation and upgradation, optimize overall product mix and dispatch
Minimize quality giveaway
Optimize fuel consumption, minimize losses
Optimize utilization of the assets
Optimize inventory management
Optimize capacity utilization and shutdown planning
Optimize unit operations maintaining highest standards of safety, catalyst life and activity,
etc.

All of the objectives mentioned above present a refinery with a challenging problem and an
opportunity to maximize the overall profitability.

In a nutshell, the need and scope for optimization is so vast in a refinery that it is essential to
use software tools not only to arrive at the best plan, but also to quickly evaluate the new
optimum with internal or external changes in the business scenario. However, in todays
refinery environment, data acquisition, simulation and optimization tools often reside in silos
in different groups across the refinery. This results in various local and plant-level
optimizations only, not the most profitable refinery-wide optimization. A holistic view via an
integrated model of the refinery is required to give refinery planners the ability to evaluate
opportunities optimally, accurately and quickly.

MEANING OF OPTIMIZATION AND LINEAR PROGRAMMING

Optimization means "the action of finding the best solution within the given constraints and
flexibilities. Linear Programming (LP) is a mathematical technique for finding the maximum
value of some equation subject to stated linear constraints. It is commonly used in refinery
planning to identify with confidence the most profitable refinery-wide operating strategy.

LP has been around since the 1940s and has now reached a very high level of advancement
with the meteoric rise in computing power. The "linear" in LP stands for the algebraic aspect,
i.e. all the constraints and objective functions are linear and satisfy two fundamental
properties: proportionality and additivity. The "programming" in LP actually means "planning"
only. The implementation of LP involves the development of an integrated LP model
representing the refinery operations with all constraints and flexibilities and then solving it to
determine the optimum plan.

The refinery-wide optimization using an LP model has been proven to bring economic gains
far higher than unit-specific simulation models or advance process control techniques.

In short, the LP model is an excellent economic evaluation tool to drive the entire supply
chain toward higher profit.

Some of the key areas for LP applications in the oil industry are:

Grassroots refinery design/configuration

Selection and evaluation of crude oils and raw materials
Long-range and short-term operations planning
Capital investments evaluation for process equipment
Analysis of the profitability of merging and acquisition plans and the creation of ad-hoc
models for joint venture refineries
Evaluation of processing agreements and product exchange contracts
Evaluation of new process technologies
Control of the refinery performance
Product blending control
Down-time planning
Inventory management

IMPLEMENTATION OF LP FOR REFINERY PLANNING AND OPTIMISATION

Refinery planning forms the foundation for the business decisions that have the biggest
impact on refinery profitability.

A refinery typically prepares the following types of plans:

Annual plans for annual budgeting, term crude contracts and maintenance shutdown
planning
Monthly rolling plans for spot crude purchases and conducting refinery operations
inline with product demands
Weekly plans for finding operating strategies for units at the weekly level, i.e. the
refinery knows precisely which crudes it has and must decide which crude cocktails to
run, how long to do so and how it is going to meet any particularly large or difficult
product demands
Strategic plans for future years and expansion projects
Profitability improvement plans for plant -level modifications and revamp projects

The preparation of any of the above types of plans requires a set of standard procedures and
an LP model customized for the refinery configuration.

DEVELOPMENT OF A REFINERY LP MODEL

Development of a refinery planning LP model primarily involves customization of

commercially available LP modeling software to refinery configuration. The table below
provides a list of major suppliers and the LP software.

Supplier LP Software
Honeywell Hi-Spec RPMS Refinery & Petrochemical
Solutions Modeling System
Aspentech PIMS Process Industry Modeling
System
Haverly GRMPTS
Development of a refinery LP model is an arduous task that demands sound, accurate and
complete understanding of the refining process and planning functions. It requires compilation
of enormous plant data and meticulous documentation of the same.

Major steps the in development of a refinery LP model

Some of the major steps involved in the development of a refinery LP model include:

Mapping of the existing planning process and data collection

Development of a future planning process inline with best practices
Finalization of Functional and Design Specifications (FDS) for the refinery LP model
building, software and hardware configuration
Refinery model building as per FDS
Factory acceptance test of refinery model
Tuning of model at site and trial usage for planning and case studies
Site acceptance test of the refinery LP model

The list of steps mentioned is not exhaustive and requires micro-level activity planning. The
role of an LP consultant is very important as he has to balance the needs of the refinery
planner and the intricacies involved in modeling each constraint and options. Initially, it is
better to keep the model simple and understand its behavior. The complexities must be
added gradually, keeping in mind what economic impact they have on refinery profitability.

Description of a refinery LP model

A good LP model is one that closely represents the operational reality of a refinery. A typical
refinery LP model contains the end-to-end configuration of the refinery with a detailed
representation of primary and secondary processing units, blending facilities, power and
utilities. A model contains structural data, or fixed data, which represents the physical reality
concerned, and variable data, which expresses the contingency of the particular problem.
The addition of variable data like costs, prices, raw materials availabilities and products
requests, process units capacities and product quality specifications enables the model to set
up a problem, from which infinite variant cases can be created and run to arrive at the optimal
plan.

Mathematically, an LP model consists of a matrix, while for the users it can be better thought
of as a set of data tables necessary and sufficient for the automatic matrix generation. A
typical refinery model represents an LP matrix with 1,500 rows, 3,500 columns, 1,500
equations, 1,500 constraints and 5,000 variables. The LP software uses different optimizers
like MOPS, XPRESS, OSL, etc. to solve the matrix. RPMS uses the state-of-the-art
XPRESS optimizer software licensed from Dash Associates.

The model can have different time period variants to meet different planning objectives
associated with Annual Planning (1X4 quarter), Quarterly Planning (1X3 months) and Monthly
Planning (1X4 weeks).

Some of the key features of a refinery LP model include:

Objective function in an LP model

A refinery LP model is generally configured with a single objective function of maximizing the
profit as explained below:

To maximize { (Product value) - (Raw Material cost) - (Refinery Variable Costs),

 subject to the various constraints defined in the model including the inventory value
and carrying cost parameters.

Modeling techniques and optimization features

A refinery LP model contains modeling capabilities like Successive Linear Programming

(SLP), Mixed integer programming (MIP), Implicit and Explicit Pooling, Multi-period modeling,
Distributive property recursion, attribute error tracking, rigorous sulfur distribution, etc.
Compared to an approach based on average values, these techniques provide very accurate
estimates of yields and qualities of finished goods, all the while keeping short computation
times.

Additional information can be obtained by referring to standard books on LP to understand

the meaning of the LP terms used above. A good reference book is Operations Research, 7 th
Edition by Hamdy A. Taha, Univ. of Arkansas, and Fayetteville.

The refinery LP models use latest unit modeling techniques like swing cut modeling, delta
vector modeling and mode wise modeling.

The crude and vacuum unit is modeled based on the stream TBP (True Boiling Point ) cut
point scheme. The crude assay manager software like ASSAY2, PASSMAN uses TBP cuts
and the TBP curve of the crude oils from the various crude assay database for generating the
crude wise yields and properties. It is possible to model the single physical crude unit into
several logical units depending refinery specific requirement. For example, a refinery
processing high sulfur (HS) and low sulfur (LS) crudes in blocked out operation can be
modeled with two logical unit one for HS and another for LS crude operation.

The secondary units are modeled using delta-yield vector or mode wise yield vectors. For
example, the catalytic cracker is generally modeled by setting up base yield vectors with yield
controlling delta vectors for Feed UOP K, MeABP and Severity/Conversion. The static input
data for determination of delta vectors can be generated from kinetic models, test runs and
standard correlations. Relevant capacity and quality constraints on the feed and product side
are configured. All possible blending options for unit feed and products are configured. Unit
wise steam, power, fuel consumption and catalyst consumption are also built in. The rigorous
recursion structure for feed and product stream properties is set up. For example, sulfur in
cat cracker streams is recalculated on the basis of feed sulfur changes.

Model Input

Once all the static data is configured, the model is updated with the variable data in model for
solving a particular problem. The common variable data required includes:

Crude oil or any other raw material prices and minimum and maximum
availability

Selling prices and minimum and maximum demands for the different finished
goods

Available process unit capacities

Available Inventory stocks and minimum and maximum storage limits

Quality specifications, etc.

User Interface
LP software commercially available today is highly advanced with features to provide a
maximum user-friendly experience. RPMS has a powerful Graphical User Interface (GUI),
which provides a highly effective and intuitive interface for working with the model. It contains
a model navigation window with graphical objects. The graphical objects contain information
on Charge Yields, Feeds, Products, Results, etc. Data and Report factory is an integrated
application of RPMS for input of static and variable data and generating standard reports in
Excel (Fig. 3.0 provides a glimpse of a GUI for a refinery LP model).

Figure 3: RPMS GUI

Model Output

The LP matrix generator transforms the input data into a great number of equations and
variables. The LP optimization algorithm solves the matrix and calculates which combination
of supply, processing, blending and selling activities gives the highest margin. The LP
reporting system reports this optimal combination of activities, together with the financial
results. The output is generated in the form of different types of text and Excel files. RPMS
has a powerful report factory utility for generating various customized Excel reports. The
reports contain detail output with respect to crudes quantities, product numbers, capacity
utilization, power, utilities and chemical consumption levels. The outputs also provide
valuable information like reduced cost, pi values, DJ values, etc.

For further information on RPMS, explore the RPMS link listed under References.

TRADITIONAL LIMITATIONS AND LATEST ADVANCES IN LP

The LP modeling has changed substantially. The static yield-driven models with fixed stream
properties have now been replaced by variable property-driven models using latest non-linear
distributive recursion techniques. Swing cuts for cut-point optimization have been semi-
automated using implicit pooling techniques. Multi-period and multi-refinery modeling
capabilities have been enhanced. The linkage of crude assay data into the LP assay tables
has been enhanced and automated. Process unit representations have changed from
multiple mode type yield structures to base-delta vector yield representations.

In a nutshell, current LP systems offer embedded process simulation and other non-linear
representation capabilities to provide even more accuracy and realism for refinery LP
representations. The LP technique is far superior when compared to any Excel programs
traditionally used for planning. However, it is worthwhile to keep in mind certain limitations of
LP in order to appreciate the LP solutions:

1. Non-linear nature of refinery processes: The nature of the refining processes is

mainly non-linear whereas linear programming - as the name already suggests -
assumes that a linear combination of the provided options is valid. RPMS uses a
specialized recursion technique called Successive Linear Programming (SLP) for
modeling and solving non-linear problems. For most of these, engineers have
developed "linear blend indices," which transform the measured qualities into index
values, which can be constrained using ordinary linear constraints.

2. Data overload: While developing the model, providing all the possible processing
options is impossible. Increasing the number of variables and constraints increases
the efforts to maintain the database and the difficulty to maintain the required data
consistency. It also reduces the systems transparency, therefore increasing the
chances of big errors in data and logic. RPMS has a powerful interface with Excel and
tools like Fast Data Import, model comparison, etc. to minimize the data errors.

3. LP does not consider the elements of time and storage: It assumes that all
activities occur simultaneously and that all identified components are separately
available for further processing or blending (like there are separate tanks available for
all individual components). A refinery may process HS and LS crudes in a blocked-out
fashion, whereas an LP model mixes HS and LS crudes simultaneously. This limitation
is addressed by reducing the time bucket while making the plan and using multi-period
models. Weekly planning methodology can be used for making plans closer to actual
operations and address scheduling issues.

4. LP exercises no judgment: One point must always be remembered: LP Models are

just as good as the data put in and the assumptions used to create them. Models
should not replace good and sound engineering judgment. The LP requires quality
input data in order to provide workable and practical solutions. Yield and property data
are based on plant measurements and rule-of-thumb calculations or estimations.
Pricing data used is often based on the statistical average of past months or years.
Based on the input data only, the LP model solves the problem and it exercises no
judgment. A small change in one piece of data may result in a completely different
solution, and will ignore all uncertainties and risks to achieve just a minor increase in
profits. This problem has been tackled by sensitivity analysis where many cases can
be run using Model Modifier (MMOD) feature of RPMS and arriving at practical and
implement-able solutions.

EXPERIENCES AND BENEFITS

Building a refinery LP model is not a trivial exercise. It needs clear understanding

of the entire web of refinery operations and the compilation of good quality data. The
model development activity is very time consuming and can take about a year for
developing a good and robust model. The following important points need to be kept
in mind while building the model:
o Make sure that the crude cut strategy represents accurately the qualities (and
 variations) of the cuts that are critical for a site. For example, if there are issues
concerning distillate 95% point or CCR values, characterize your crude cuts
very thinly around the heavy gas oil/atmospheric residue cut (typically in the 330
- 390C range).
o Obtain good representation of unit operating modes and parameters from
process models. As the LP cannot work with non-linear correlations, there is a
need to linearize the non-linear behavior of process units by introducing several
linear "vectors. These vectors can be generated through sound refinery
process models (e.g. KBC Profimatics FCC-SIM for the FCC, REF-SIM for a
reformer, etc.) for different feeds/crudes, operating conditions (severities,
conversion, etc.), etc.
o Ensure that the model has sufficient flexibility to generate feasible solutions in
the first place. It is easier to start with a fairly "loose" model, which can be
subsequently tightened.

Interpretation of LP Output: The task of analyzing the LP output is not a simple

exercise, mainly due to the limitations of the technique and the complexity of its output.
It requires sustained effort in generating and analyzing the various feasible and
optimum solutions and rigorous sensitivity analysis.

Computation Time: Today, we solve substantially more complex LP problems in mere

seconds on our desktop PCs. The running time limitations have lost much of their
relevancy with the availability of desktop PCs with higher computing power. For
example, solving four-period models takes only about two to three minutes on a
Pentium-IV and 256 MB RAM PC.

Benefits of LP in refinery planning

LP works on the principles of pure mathematics and Petroleum Refining is more complex
than the mathematics that describe it. With all the approximations and uncertainty we should
not expect or even desire a true mathematical optimum. LP should be viewed only as a
mathematical optimization technique, or as a convenient method to obtain a feasible and
economic plan for the supply, processing and logistic activities of a petroleum complex,
together with a description of its driving forces and constraints. In day-to-day working, an LP
solution helps in achieving two key practical aspects:

It facilitates in the decision-making process by keeping the focus on profit under any
scenario
It provides the targets and operating strategies for the actual operation

LP does much more than planning for the future. LP refinery models always challenge the
people and their deep-rooted rule-of-thumb approach in the refinery operations. The
implementation of LP models often creates awareness among executives and management
about the profit factor. LP-based planning can provide potential benefits to the tune of 15-20
cents/bbl. One of the major advantages of LP programming is that it acts as a watch dog for
the refinery operations always asking for more, the LP model helps in identifying the
bottlenecks in processing more crude and directs in achieving the benchmark for operation. It
clearly tells the inefficiency of operations in terms of money, and thats where it is very close
to managements heart.

The LP solution has not only enabled arriving at a better plan, but has also provided many
valuable insights for optimizing unit operations, crude mix and product blending. The other
most important benefit realized is it quantifies the impact of a change in a variable on overall
refinery profitability. As a tool, RPMS provides answers to the typical questions that refinery
management asks for faster decision making, including: What is optimum HS-LS crude mix?,
How to maximize distillate yield and minimize the fuel & loss?, What products to be
maximized?, Which units to be run and what capacity levels?, When to plan unit shutdowns?,
etc.

Key to successful implementation of LP in refinery planning

The output from an LP model gives us an optimal plan. In practice, the real benefit comes
from implementation of the strategies and guidelines from the model. Implementing all of the
LP solutions in a refinery is a difficult task. Product pricing and unit constraints often change
weekly, but changing unit operating philosophy and addressing hardware constraints take
time to accomplish. Even after the steps for improving optimal performance have been
identified and implemented, if the pressure to improve is removed, operation tends to return
to the older, more comfortable routine. The LP optimization group must continue to stress the
potential savings while improving the operations until the savings are achieved.

The key to the successful implementation of LP in refinery planning is an integrated approach

that addresses the following issues:

Regular Model updates and maintenance: There is one human tendency of giving
maximum care and attention to the thing which is very valuable or important to him.
The same tendency should be kept alive for LP models, as these models provide the
decision-making power (involving large amounts of money), money-related policies
and future action plans. The models are continuously interacting with inside
constraints and outside changes (price and product demands), making them dynamic
in nature. All of these factors imply that the maintenance of these models should be
carried out as regularly as possible. The type of updates can be a reduction in the
yield of unit, change of catalyst, property change of secondary stream, energy
consumption reduction due to application of energy conservation suggestion, etc.

Integrated application of different software solutions: Refineries use a number of

stand-alone software solutions like Automation Blenders, Online analyzers and
sensors, APC, Scheduling software, Simulation software, RTDBMS for optimization of
operations. There is a strong need to integrate the working of such software to create
the maximum benefit by bringing the operations and blending close to the LP output.

Clear and well documented planning procedures: There are no two opinions on
using LP based software for planning. The real problem of using the LP for economic
decision-making is how to interpret the LP results and how to use it for decision-
making. The planning tool needs to be backed by clear cut and systematic planning
procedures. The entire planning process should be carried out under the overall
supervision and guidance of top management group in an integrated way. The
procedures for the four key functions of plan preparation, plan implementation, plan
monitoring and what-if case studies must be in place and working to enable the
success of LP optimization.

THE BOTTOM LINE

Petroleum refining in the new millennium will continue to be an extremely competitive

business. The application of LP methodology has shown potential margin benefits of 15-20
cents/bbl for the refineries.

The bottom line is that experienced people are the key to success: software and computers,
no matter how powerful and quick, are not the substitutes for understanding and optimizing
the refinery business. However, LP technique has provided an efficient and effective method
to quickly evaluate and quantify the impact of internal and external changes on overall
refinery profitability.

REFERENCES :
1. LP Modeling Past, Present and Future , Michael A. Tucker, Senior Staff Consultant
,KBC Advanced Technologies, Inc., Houston, Texas
2. Notes on LP , Uberne A. Tapia , Manager , Refinery Planning & Optimisation ,
Honeywell Hi Spec Solutions , Houston , Texas
3. Operations Research , 7th Edition , Hamdy A. Taha , Univ. of Arkansas , Fayetteville
4. Decision-making and Modeling in Petroleum Refining , Hans Hartmann, Independent
Consultant
5. Multi Objective Intra-Refinery Optimisation , Ahmed Sirag Khogeer Department of
Chemical Engineering , Colorado State University
6. Honeywell Web site , www.honeywell.com
7. Hartmann, J.C.M.; Distinguish between scheduling and planning models; Hydrocarbon
Processing, Vol. 77 Issue 7, p93-98, Jul 98.
8. RPMS Introduction
http://www.acs.honeywell.com/ichome/Doc/0/O2N58SSJ5BAH3AJ1001B69DOBB/RP
MS.pdf