This document provides an overview of petroleum refining processes. It discusses the three main steps of refining: separation, conversion, and purification. Some key separation processes mentioned include crude distillation, solvent deasphalting, and solvent extraction. Important conversion processes include catalytic reforming, hydrotreating, hydrocracking, catalytic cracking, alkylation, and isomerization. Thermal processes like delayed coking, flexicoking, and visbreaking are also outlined. The document concludes with a more detailed explanation of crude distillation and desalting.
This document provides an overview of petroleum refining processes. It discusses the three main steps of refining: separation, conversion, and purification. Some key separation processes mentioned include crude distillation, solvent deasphalting, and solvent extraction. Important conversion processes include catalytic reforming, hydrotreating, hydrocracking, catalytic cracking, alkylation, and isomerization. Thermal processes like delayed coking, flexicoking, and visbreaking are also outlined. The document concludes with a more detailed explanation of crude distillation and desalting.
Original Description:
Chemistry and Technology of Petroleum (Class 1) for Student
This document provides an overview of petroleum refining processes. It discusses the three main steps of refining: separation, conversion, and purification. Some key separation processes mentioned include crude distillation, solvent deasphalting, and solvent extraction. Important conversion processes include catalytic reforming, hydrotreating, hydrocracking, catalytic cracking, alkylation, and isomerization. Thermal processes like delayed coking, flexicoking, and visbreaking are also outlined. The document concludes with a more detailed explanation of crude distillation and desalting.
This document provides an overview of petroleum refining processes. It discusses the three main steps of refining: separation, conversion, and purification. Some key separation processes mentioned include crude distillation, solvent deasphalting, and solvent extraction. Important conversion processes include catalytic reforming, hydrotreating, hydrocracking, catalytic cracking, alkylation, and isomerization. Thermal processes like delayed coking, flexicoking, and visbreaking are also outlined. The document concludes with a more detailed explanation of crude distillation and desalting.
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CHEMISTRY AND TECHNOLOGY OF
PETROLEUM
By Dr. Dang Saebea
REFINING CHEMISTRY
INTRODUCTION Petroleum refining plays an important role in our lives. Most transportation vehicles are powered by refined products such as gasoline, diesel, aviation turbine kerosene (ATK) and fuel oil.
THE REFINING INDUSTRY IN THREE WAYS
An increased search for fuel products from non-fossil sources such as biodiesel and alcohols from vegetable sources. The development of better methods to process tar sand, coal gasification and synthesis of fuels by new technology. The initiation of long-term plans to look for renewable energy sources.
REFINING MEANS. . . 1. To a pure state, to remove impurities 2. To improve product
Step 1 - Separation The oil is separated into its constituents by distillation, and some of these components (such as the refinery gas) are further separated with chemical reactions and by using solvents.
REFINING IS CARRIED OUT
Step 2 - Conversion o The various hydrocarbons produced are then chemically altered to make them more suitable for their intended purpose. o For example, naphthas are "reformed" from paraffins and naphthenes into aromatics.
REFINING IS CARRIED OUT
Step3 - Purification o The hydrogen sulfide gas which was extracted from the refinery gas in Step 1 is converted to sulfur, which is solid in liquid form to fertiliser manufacturers.
Crude Distillation Crude oils are first desalted and then introduced with steam to an atmospheric distillation column.
The atmospheric residue is then introduced to a vacuum distillation tower operating at about 50 mmHg, where heavier products are obtained. Atmospheric distillation Vacuum distillation
Solvent Deasphalting This is the only physical process where carbon is rejected from heavy petroleum fraction such as vacuum residue. Propane in liquid form (at moderate pressure) is usually to dissolve the whole oil, leaving asphaltene to precipitate. The deasphalted oil (DAO) has low sulphur and metal contents since these are removed with asphaltene. This oil is also called Bright Stock and is used as feedstock for lube oil plant. The DAO can also be sent to cracking units to increase light oil production.
Solvent Extraction In this process, lube oil stock is treated by a solvent, such as phenol and furfural, which can dissolve the aromatic components in one phase (extract) and the rest of the oil in another phase (raffinate).
The solvent is removed from both phases and the raffinate is dewaxed.
Solvent Dewaxing The raffinate is dissolved in a solvent (methyl ethyl ketone, MEK) and the solution is gradually chilled, during which high molecular weight paraffin (wax) is crystallized, and the remaining solution is filtered.
The extracted and dewaxed resulting oil is called lube oil. In some modern refineries removal of aromatics and waxes is carried out by catalytic processes in all hydrogenation process
2.R Chemical Conversion Processes EFINERY-Catalytic PETROCHEMICAL INTEGRATION
Catalytic Reforming In this process a special catalyst (platinum metal supported on silica or silica base alumina) is used to restructure naphtha fraction (C6C10) into aromatics and isoparaffins.
The produced naphtha reformate has a much higher octane number than the feed. This reformate is used in gasoline formulation and as a feedstock for aromatic production (benzenetoluenexylene, BTX).
2.R Chemical Conversion Processes EFINERY-Catalytic PETROCHEMICAL INTEGRATION
Hydrotreating This is one of the major processes for the cleaning of petroleum fractions from impurities such as sulphur, nitrogen, oxy-compounds, chloro-compounds, aromatics, waxes and metals using hydrogen.
The catalyst is selected to suit the degree of hydrotreating and type of impurity. Catalysts, such as cobalt and molybdenum oxides on alumina matrix, are commonly used.
2.R Chemical Conversion Processes EFINERY-Catalytic PETROCHEMICAL INTEGRATION
Catalytic Hydrocracking For higher molecular weight fractions such as atmospheric residues (AR) and vacuum gas oils (VGOs), cracking in the presence of hydrogen is required to get light products.
In this case a dual function catalyst is used. It is composed of a zeolite catalyst for the cracking function and rare earth metals supported on alumina for the hydrogenation function. The main products are kerosene, jet fuel, diesel and fuel oil.
2.R Chemical Conversion Processes EFINERY-Catalytic PETROCHEMICAL INTEGRATION
Catalytic Cracking Fluid catalytic cracking (FCC) is the main player for the production of gasoline. The catalyst in this case is a zeolite base for the cracking function.
The main feed to FCC is VGO and the product is gasoline, but some gas oil and refinery gases are also produced.
2.R Chemical Conversion Processes EFINERY-Catalytic PETROCHEMICAL INTEGRATION
Alkylation Alkylation is the process in which isobutane reacts with olefins such as butylene (C4 ) to produce a gasoline range alkylate.
The catalyst in this case is either sulphuric acid or hydrofluoric acid. The hydrocarbons and acid react in liquid phase. Isobutane and olefins are collected mainly from FCC and delayed coker
2.R Chemical Conversion Processes EFINERY-Catalytic PETROCHEMICAL INTEGRATION
Isomerization Isomerization of light naphtha is the process in which low octane number hydrocarbons (C4, C5, C6) are transformed to a branched product with the same carbon number. This process produces high octane number products.
One main advantage of this process is to separate hexane (C6) before it enters the reformer, thus preventing the formation of benzene which produces carcinogenic products on combustion with gasoline. The main catalyst in this case is a Pt-zeolite base.
3. Thermal Chemical Conversion Processes
Delayed Coking This process is based on the thermal cracking of vacuum residue by carbon rejection forming coke and lighter products such as gases, gasoline and gas oils.
The vacuum residue is heated in a furnace and flashed into large drums where coke is deposited on the walls of these drums, and the rest of the products are separated by distillation.
Flexicoking In this thermal process, most of the coke is gasified into fuel gas using steam and air.
The burning of coke by air will provide the heat required for thermal cracking. The products are gases, gasoline and gas oils with very little coke.
3. Thermal Chemical Conversion Processes
Visbreaking This is a mild thermal cracking process used to break the high viscosity and pour points of vacuum residue to the level which can be used in further downstream processes.
In this case, the residue is either broken in the furnace coil (coil visbreaking) or soaked in a reactor for a few minutes (soaker visbreaker). The products are gases, gasoline, gas oil and the unconverted residue.
The End
CRUDE DISTILLATION
CRUDE DISTILLATION Crude distillation unit (CDU) is at the front-end of the refinery, also known as topping unit, or atmospheric distillation unit. It receives high flow rates hence its size and operating cost are the largest in the refinery. This involves the removal of undesirable components like sulphur, nitrogen and metal compounds, and limiting the aromatic contents.
TYPICAL PRODUCTS FROM THE UNIT ARE:
CRUDE OIL DESALTING
o
The crude oil contains salt in the form of dissolved salt in the tiny droplet of water which forms a water-in oil emulsion. This water cannot be separated by gravity or through mechanical means. It is separated through electrostatic water separation. This process is called desalting.
CRUDE OIL DESALTING
In the electrostatic desalter, the salty water droplets are caused to coalesce and migrate to the aqueous phase by gravity. It involves mixing the crude with dilution water (56 vol%) through a mixing valve.
POOR DESALTING HAS THE FOLLOWING EFFECTS:
1. Salts deposit inside the tubes of furnaces and on the tube bundles of heat exchangers creating fouling, thus reducing the heat transfer efficiency; 2. Corrosion of overhead equipment. 3. The salts carried with the products act as catalyst poisons in catalytic cracking units.
TYPES OF SALTS IN CRUDE OIL
Salts in the crude oil are mostly in the form of dissolved salts in fine water droplets emulsified in the crude oil. The salts can also be present in the form of salts crystals suspended in the crude oil. These are mostly magnesium, calcium and sodium chlorides with sodium chloride being the abundant type.
TYPES OF SALTS IN CRUDE OIL
These chlorides, except for NaCl, hydrolyze at high temperatures to hydrogen chloride: CaCl2 2 H 2O Ca(OH )2 2 HCl MgCl2 2 H 2O Mg (OH )2 2 HCl
Hydrogen chloride dissolves in the overhead system water, producing hydrochloric acid, an extremely corrosive acid
DESALTING PROCESS The process is accomplished through the following steps: 1. Water washing: - Water is mixed with the incoming crude oil through a mixing valve. - The water dissolves salt crystals and the mixing distributes the salts into the water, uniformly producing very tiny droplets. - Demulsifying agents are added at this stage to aide in breaking the emulsion by removing the asphaltenes from the surface of the droplets.
DESALTING PROCESS 2. Heating: - The crude oil temperature should be in the range of 49-54 C (120130 F) since the wateroil separation is affected by the viscosity and density of the oil.
DESALTING PROCESS 3. Coalescence: - The water droplets are so fine in diameter in the range of 1 10 mm that they do not settle by gravity. Coalescence produces larger drops that can be settled by gravity. - This is accomplished through an electrostatic electric field between two electrodes. - The electric field ionizes the water droplets and orients them so that they are attracted to each other. - Agitation is also produced and aides in coalescence.
DESALTING PROCESS 4. Settling: According to Stocks law the settling rate of the water droplets after coalescence is given by k( H 2O Oil )d 2
Settling rate =
oil
where
is the density is the viscosity, d is the droplet diameter k is a constant.
DESCRIPTION OF DESALTER Two electrodes
Simplified flow diagram of an electrostatic desalter
DESCRIPTION OF DESALTER
A primary field of about 600 V/cm This field helps the water droplets settle faster.
Simplified flow diagram of an electrostatic desalter
DESCRIPTION OF DESALTER
A secondary field of about 1000 V/cm The ionization of the water droplets and coalescence takes place here
Simplified flow diagram of an electrostatic desalter
TWO-STAGE DESALTING
- The desalter of this design achieves 90% salt removal. However 99% salt removal is possible with two-stage desalters. -A second stage is also essential since desalter maintenance requires a lengthy amount of time to remove the dirt and sediment which settle at the bottom. -The crude unit can be operated with a one stage desalter while the other is cleaned.
DESALTER OPERATING VARIABLES
For an efficient desalter operation, the following variables are controlled: Desalting temperature: The settling rate depends on the density and viscosity of the crude T density & viscosity settling rate
Desalting temperature can vary between 50 and 150 C Washing water ratio: Adding water to the crude oil helps in salt removal. Wash water rate
Coalescence rate
DESALTER OPERATING VARIABLES
Water level: - Raising the water level reduces the settling time for the water droplets in the crude oil -However, if the water level gets too high and reaches the lower electrode, it shorts out the desalter. - it is always better to keep the level constant for stable operation.
DESALTER OPERATING VARIABLES
Washing water injection point: -Usually the washing water is injected at the mixing valve. - However, if it is feared that salt deposition may occur in the preheat exchangers, part or all of the washing water is injected right after the crude feed pump.
DESALTER OPERATING VARIABLES
Type of washing water: -Process water in addition of fresh water is used for desalting. The water should be relatively soft in order to prevent scaling. - It should be slightly acidic with a pH in the range of 6. It should be free from hydrogen sulphide and ammonia so as to not create more corrosion problems.
ATMOSPHERIC DISTILLATION
330 C
Process flow diagram of an atmospheric distillation unit
COMPONENT OF ATMOSPHERIC DISTILLATION
Rectifying section
Flash zone
Stripping section
Description OF ATMOSPHERIC DISTILLATION
The vapor from pipestill furnace discharge as a foaming stream into distillation tower. The partially vaporized crude is transferred to the flash zone. The vapour goes up the tower to be fractionated into gas oil that is called the overhead product . liquid portion of feed go down to bottom of tower
Description OF STRIPPING SECTION
Steam reboilers may take the form of a steam coil in the bottom of the tower or a separate vessel. The bottom product from the tower enters the rebolier where part is vaporized by heat from steam coil.
The hot vapor is directed back to the bottom of the tower and the nonvolatile leaves the rebolier and passes through a heat exchanger, where its heat is transferred to the feed to the tower.
Description OF STRIPPING SECTION
Steam is also injected into the column -To strip the atmospheric residue of any light hydrocarbon. - To lower the partial pressure of the hydrocarbon vapours in the flash zone. This has the effect of lowering the boiling point of the hydrocarbons and causing more hydrocarbons to boil and go up the column to be eventually condensed and withdrawn as side streams.
Description OF RECTIFYING SECTION
As the hot vapours from the flash zone rise through the trays up the column, they are contacted by the colder reflux down the column. In the overhead condenser, the vapours are condensed and part of the light naphtha is returned to the column as reflux.
Reflux is provided by several pumparound streams along the column.
IMPROVEMENT OF DISTILLATION EFFICIENCY WITH
PUMPAROUND
Vapours Cold liquid condenses Reflux To compensate for the withdrawal of products from the column. The addition to the heat removal from the condenser. The thermal efficiency of the column is improved and the required furnace duty is reduced.
Description OF RECTIFYING SECTION
Liquid collects on each tray to a depth, and the depth controlled by a dam or weir. As the liquid spills over the weir into a channel, which carries the liquid to the tray below.
IMPORTANT OF STRIPPING AND RECTIFYING
SECTION
Stripping section The more volatile component are stripped the descending liquid
from
Rectifying section The concentration of the less volatile component in the vapor is reduced
Straight-Run Naphtha and Gases 125 C 160 C 250 C Crude Oil 300 C
Heavy Naphtha Kerosene Gas Oil The Temperature of tray is progressively cooler from bottom to top
Residuum
THE EFFICIENT OPERATION OF THE DISTILLATION
Tower requires the rising vapors to mix with liquid on each tray. This is usually achieved by installing a bubble caps. The cap forces the vapor to go below the surface of the liquid and to bubble up through it.
LIMITING TEMPERATURE OF ATMOSPHERERIC
DISTILLATION
It is important not to subject the crude oil to temperatures above 350 C because the high molecular weight components in the crude oil will undergo thermal cracking and form petroleum coke .
Formation of coke would result in plugging the tubes in the furnace and the piping from the furnace to the distillation column as well as in the column itself. The constraint imposed by limiting the column inlet crude oil to a temperature of less than 350 C yields a residual oil from the bottom of the atmospheric distillation column.
VACUUM DISTILLATION
To further distill the residual oil from the atmospheric distillation column, the distillation must be performed at absolute pressures as low as 10 to 50 mmHg so as to limit the operating temperature to less than 350C. Vacuum distillation is the reduced temperature requirement at lower pressures. Vacuum distillation increases the relative volatility of the key components.
Vacuum distillation can improve a separation by:
Prevention of product degradation or polymer formation because of reduced pressure leading to lower tower bottoms temperatures. Reduction of product degradation or polymer formation because of reduced mean residence time especially in columns using packing rather than trays. Reduction of capital cost because of reduced the height and diameter.
FRACTIONS OBTAINED BY VACUUM DISTILLATION
Gas Oil used as catalytic cracking stock or, after suitable treatment, light lubricating oil
Atmospheric Residuum
Vacuum Distillation
Light Medium Heavy Lube oil
Residuum, Nonvolatile
used directly as asphalt or converted to asphalt
OPERATION OF CRUDE DISTILLATION UNITS
The factors affect the design and operation of the unit are explored
1. Fractionation The degree of fractionation in a crude unit is determined by the gap or overlap between two adjacent side stream products. Example: The gap or overlap in the boiling point range between kerosene and LGO. Lighter product: kerosene end boiling point Heavier product: LGO initial boiling point
In the ideal case there would be no overlap
However, if we compare the ASTM distillation boiling points, and since ASTM distillation does not give perfect fractionation. Since determining the initial and end point on the laboratory test is not always possible or accurate. The fractionation gap is defined as the difference between the ASTM 5% boiling point of the heavier product and the 95% point of the lighter product.
a gap indicating good fractionation
some of the light product is still in the heavier product
2. Overflash
The partially vaporized crude is transferred to the flash zone. The furnace outlet temperature should be enough to vaporize all products withdrawn above the flash zone plus about 35 vol% of the bottom product. This overflash has the function of providing liquid wash to the vapours going up the column from the flash zone. The overflash improve fractionation on the trays above the flash zone, thereby improving the quality of the HGO and reducing the overlap with the bottom products below the flash zone.
3. Column Pressure The pressure inside the CDU column is controlled by the back pressure of the overhead reflux drum at about 0.20.34 bar gauge (35 psig). The top tray pressure is 0.40.7 bar gauge (610 psig) higher than the reflux drum. The flash zone pressure is usually 0.340.54 bar (58 psi) higher than the top tray.
Pflash zone > PTop tray > Preflux drum
4. Overhead Temperature The overhead temperature must be controlled to be 1417 C higher than the dew point temperature for the water at the column overhead pressure so that no liquid water is condensed in the column.
This is to prevent corrosion due to the hydrogen chloride dissolved in liquid water (hydrochloric acid).
EXAMPLE If the overhead stream contains 8.5 mol% water at a pressure of 34.7 psia (2.36 bars), calculate the overhead temperature for safe operation.
EXAMPLE If the overhead stream contains 8.5 mol% water at a pressure of 34.7 psia (2.36 bars), calculate the overhead temperature for safe operation.
Solution: The saturation temperature of water at the partial pressure of water in the overhead vapour. Water partial pressure = 0.085 x 2.36 =0.2 bars From the steam tables: Saturated steam temperature at 0.2 bars = 61 C Safe overhead operating temperature = 61+17 C
