ATMOSPHERIC RESIDUE VACUUM DISTILLATION
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◆ 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. | ||||||||
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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.
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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. | ||||||||
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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 As in the atmospheric column, the vapor flow rate corresponds more or less to the flow rate of all the sidestreams withdrawn higher up the column, i.e. heavy gas oil+VGO.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: | ||||||||
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. | ||||||||
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: | ||||||||
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CRUDE ASSAY AND PRODUCT YIELDS
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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 [출처] ◆ CRUDE ASSAY AND PRODUCT YIELDS ◆|작성자 엔지니어 |
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CRUDE OIL DESALTING
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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: |
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. |
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2. DESALTING OPERATION |
An efficient desalting operation requires: |
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 additional treatment are shown Figure 4. |
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[출처] ◆ CRUDE OIL DESALTING ◆|작성자 엔지니어
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