◆ ATMOSPHERIC RESIDUE VACUUM DISTILLATION


1. PURPOSE AND PRINCIPLE OF THE INSTALLATION

The vacuum distillation installation is designed to separate atmospheric residue into several petroleum cuts. The actual fractionation depends on the composition of the atmospheric residue and the ultimate use different cuts obtained.

There are currently three principal uses:
   - bitumen production
   - production of VGO for upgrading by catalytic caracking or hydrocracking
   - production of base lube oils.

The cuts required for the first two uses can be simultaneously obtained in a single vacuum distillation installation. However the cut for the third use requires its own especially sized unit called an oil vacuum distillation unit. When a production of the gas oil cuts is left in the atmospheric residue after atmospheric fractionation, a vacuum gas oil is obtained at the lightest cut. Examples of cuts corresponding to the two different types of vacuum distillation of atmospheric residue are shown below.

In both cases, fractionation is carried out in a single multiple draw off distillation column, called a vacuum distillation column because it operates at a pressure well below atmospheric pressure. By this operation distillation temperatures can be lowered, thus avoiding thermal degradation of high boiling temperature hydrocarbons. Temperatures can be maintained below 400 °C level which, in this unit, is approximately the limit for hydrocarbon stability.

A section device for residue gases at the top of the column creates a vacuum, the vacuum gasoil and the vacuum distillates are withdrawn as sidestreams and the vacuum residue is obtained at the bottom of the column. Quality control of the products obtained is generally based on the following standard tests:

Heavy gasoil

cloud point

VGO for conversion

color, metal content, Conradson carbon residue

VGO for oils

viscosity, flash point

Residue for bitumen

penetrability

2. EXAMPLE OF A UNIT : OPERATION AND OPERATING CONDITIONS

2.1 Description

A vacuum distillation flow scheme is shown in Figure 5. The installation is integrated in the atmospheric distillation unit and is designed to produce a VGO for conversion (VGO1), and possibly a bitumen vacuum residue from a suitable crude. When the installation is operating under bitumen-producing conditions, specifications for VGO1 (particularly metal content) and for vacuum residue (penetrability) have to be simultaneously met which means obtaining an intermediate cut (VGO2) which is generally used a base fuel. Withdrawing VGO2 as a sidestream is only justified when the specifications for both cuts, VGO1 and vacuum residue, are incompatible.

2.2 Atmospheric Residue Inlet

Atmospheric residue is fed in at the base of the vacuum column and its partial vaporization creates the vapor flux necessary for distillation. As in the atmospheric column, the vapor flow rate corresponds more or less to the flow rate of all the sidestreams withdrawn higher up the column, i.e. heavy gas oil+VGO. This degree of vaporization is obtained by:
   - heat supplied in the vacuum furnace
   - the considerable expansion of the atmospheric residue owing to the very low pressure in the vacuum column.

The residue inlet temperature is generally between 390 °C and 430 °C.

2.3 Vacuum System and Heavy Gas Oil Side-Streaming

Gas oil is condensed at the top of the column by a circulating reflux which is injected cold at the top of the column and acts as a genuine integrated condenser. The small amount of vapors that enter this section are sucked up by the steam ejectors which are arranged in 3 stages separated by intermediary condensers. Any noncondensable material is ejected at a pressure slightly higher than atmospheric pressure and can thus be sent to the unit furnace for incineration. The pressure thus obtained is about 60 mbar at the top of the column, and allowing for pressure drop, this gives a pressure of around 90 mbar pressure in the feed inlet section. Nowadays some units are even working under a 10 mbar pressure at the top of the column.

A total sidestream tray located below this section is used at a temperature of 170 °C to withdrawn the gas oil circulating reflux, the heavy oil sidestream and the internal reflux which is reinjected just below the tray to separate the heavy gas oil and VGO.

2.4 VGO1 and VGO2 Sidestream

The total VGO1 sidestream is withdrawn in the same manner at a temperature of around 300 °C. VGO1 and VGO2 are in this case separated by reinjection of the internal reflux below the sidestream tray. The VGO2 cut sidestream is withdrawn just below the feed inlet section at a temperature of 360 °C.

2.5 Column Bottom Stripping

The purpose of the column bottom section is to steam strip the liquid part of the feed to obtain vacuum residue. Incidentally, by recirculating the cooled vacuum residue the temperature at the bottom of the column can be lowered, thereby avoiding thermal degradation of the hydrocarbons present. Some fractionation columns operate without steam injection and the process is then called dry vacuum distillation.

2.6 Liquid-Vapor Contact

Liquid and vapor are brought into contact by trays and packed beds (pall rings, grid packing, etc.). The latter are increasingly used in this type of column because they combine very effective liquid - vapor contact and minor pressure drops, thereby maintaining low pressure throughout the column. A metal wire mesh can be used to prevent droplets of heavy liquid from being entrained in the flux of ascending vapors.

3. VACUUM DISTILLATION OF LUBE OILS

The simplified flow scheme below shows an oil vacuum distillation unit. The higher quality required for separations chiefly involves:
   - a greater numbers of trays
   - steam strippers for each sidestream on the column.

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◆ CRUDE ASSAY AND PRODUCT YIELDS


1. CRUDE ASSAY AND TBP CURVE

In order to obtain a general data of producing various refining products from a crude oil, an assay analysis will provide general data on the oils. On the preliminary planning stage of a refinery construction, ASTM Distillation test D-86 and D-1160 are used as a Crude Assay, since it is cheaper and easier to run than a comprehensive assay analysis using True Boiling Point(TBP) distillation, ASTM Test Method D-2892. Since a crude distillation is based on TBP curve, it is desirable to have an assay data with TBP test, ASTM D-2892. If the apparatus of TBP test is not available, then the method of converting ASTM distillation curve to TBP curve is available in the API Technical Data Book or in the Edrnister's book, "Applied Hydrocarbon Thermodynamics. However, an error of converting ASTM to TBP might be sometimes more than 15 °F. Crude assay must also include the light end analysis in either volume or weight percent. API gravity and viscosity as well as sulfur distribution curves against liquid volume percent should be given on an assay.

2. PSEUDO COMPONENT BREAKDOWN

Crude oil is made up of an almost infinite number of discrete hydrocarbons, ranging from methane to heavy molecules in the range of carbon number over 70. Hence, component by component breakdown of crude is not feasible and not practical. Pseudo component as a petroleum fraction in the given boiling range is, therefore, defined and driven from a TBP curve. In general, intervals of TBP cut points of each pseudo component are 25 °F for the TBP range from 50 °F to 700 °F, 50 °F for the TBP range from 700 to 900 °F, and 100 °F for the TBP range over 900 °F. Characterization of each pseudo component is then determined by the methods and correlations given by API Technical data Book.

3. DISTILLATE PRODUCT BREAKUP AND ITS YIELD

Distillate products are normally specified by either TBP cut points on crude or by ASTM distillation end points. In case of TBP cut points specified, the expected volume % yield of each distillate product is read directly from the TBP distillation curve. In case of ASTM end points given, the end point is to be converted to TBP cut point by the correlation shown on the figure 4. TBP breakup points for products are widely varied and decided by overall refinery requirements. As an illustration, Table 2 shows the expected product yields taken from Figure 3, Arabian Mixed Crude. First column on this table shows the given TBP cut points and the second column indicates the corresponding accumulative liquid volume percent obtained directly from Figure 3. On the third column, the expected product yield is computed by taking interval cut volume percent. The final design product yield might be slightly differ from these expected yields to meet the product specifications such as ASTM gap or ASTM end point. Further detail will be discussed below under the topic of process control variables. The columns fourth through eleventh are estimated normal boiling point, density, mole weight, and molal flow rate for each product, which are determined by using the empirical correlations described in API technical data book. These properties and flow rate will be used in the following part IIl, the empirical design method.

Table 2 Expected Product Yields and Properties

Figure 3  TBP Curve Arabian Light Crude Oil

Figure 4   Relationship Between ASTM and TBP Initial and Final Boiling Points

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◆ CRUDE OIL DESALTING


1. CRUDE OIL DESALTING

The crude oils delivered to refineries always contain a little water (generally 0.1 to 0.6% volume), mineral salts (20 to 300 grams per ton of crude) and sediments. The mineral salts come from the producing wells or are the result of sea water contamination during transportation. They consist principally of sodium, magnesium and calcium chlorides and they have two main drawbacks:
   - like sediments they clog the crude oil preheating heat exchangers
   - some of them (calcium and magnesium chlorides) undergo hydrolysis at high temperatures, which produces hydrochloric gas(HCl).
      As soon as the latter comes into contact with liquid water it becomes soluble and is converted into hydrochloric acid which is very
      corrosive where metal material is concerned. This type of corrosion affects the sections where steam is likely to condense, i.e. the
      top of corrosion affects the sections where steam is likely to condense, i.e. the top of the atmospheric columns and the condenser.

The desalting operation designed to eliminate the water, mineral salts and sediments contained in crudes is an effective mean of combatting the problems they involve. Desalting is carried out in practically all atmospheric distillation installations. It is integrated in the heat exchanger train in the following 3 stages:

1.1 Crude Oil Washing

Crude oil washing with desalting water to extract the mineral salts, resulting in an emulsion of tiny droplets of salt water in the crude.

1.2 Enlarging the Water Droplets by Electrocoalescence

Enlarging the water droplets by electrocoalescence in an electrostatic field inside a horizontal drum called a desalting drum or desalter

1.3 Water-Crude Separation by Decantation

water-crude separation by decantation in the desalting drum. The desalted crude is less dense and is withdrawn at the top of the drum while the water is withdrawn from the lower part.

 

2. DESALTING OPERATION

An efficient desalting operation requires:
   - a fairly temperature (110 °C to 150 °C), particularly if the crude is rather heavy and viscous, so as to facilitate water-crude decantation.
   - an injection (from 3 to 8% volume per crude) of water depending on how difficult the crude is to desalt.
   - a fairly long crude residence time (20 to 30 minutes) in the desalter, which explains the latter's considerable size. In a unit processes
     1000 m3 of crude per hour the cylindrical desalter will be 50 meters long with a 5 meter diameter.
   - the possible use of a demulsifying agent.

Nevertheless, desalting is never totally effective and the inevitable formation of hydrochloric acid has to be combatted downstream in the unit. This entails two main injection operations:
   - the injection of soda in the heat exchanger train to convert the HCl into stable sodium chloride.
   - the injection of ammonia or another neutralizing agent in the sections where water is likely to condense (top of the atmospheric column
     and condenser system)

The additional treatment are shown Figure 4.

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