vacuum distillation in petroleum refining

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Vacuum distillation in petroleum refining Petroleum crude oil is a complex mixture of hundreds of different hydrocarbon compounds generally having from 3 to 60 carbon atoms per molecule , although there may be small amounts of hydrocarbons outside that range. [1] [2] [3] The refining of crude oil begins with distilling the incoming crude oil in a so- called atmospheric distillation column operating at pressures slightly above atmospheric pressure. [1] [2] [4] In distilling the crude oil, it is important not to subject the crude oil to temperatures above 370 to 380 °C because the high molecular weight components in the crude oil will undergo thermal cracking and formpetroleum coke at temperatures above that. Formation of coke would result in plugging the tubes in the furnace that heats the feed stream to the crude oil distillation column. Plugging would also occur in 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 more than 370 to 380 °C yields a residual oil from the bottom of the atmospheric distillation column consisting entirely of hydrocarbons that boil above 370 to 380 °C. To further distill the residual oil from the atmospheric distillation column, the distillation must be performed at absolute pressures as low as 10 to 40 mmHg (also referred to as Torr ) so as to limit the operating temperature to less than 370 to 380 °C. Image 1 is a photograph of a large vacuum distillation column in a petroleum refinery and Image 2 is a process diagram of a petroleum refinery vacuum distillation column that depicts the internals of the column. The 10 to 40 mmHg absolute pressure in a vacuum distillation column increases the volume of vapor formed per volume of liquid distilled. The result is that such columns have very large diameters. [5]

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Page 1: Vacuum Distillation in Petroleum Refining

Vacuum distillation in petroleum refiningPetroleum crude oil is a complex mixture of hundreds of different hydrocarbon compounds generally having from 3 to 60 carbon atoms per molecule, although there may be small amounts of hydrocarbons outside that range.[1][2][3] The refining of crude oil begins with distilling the incoming crude oil in a so-called atmospheric distillation column operating at pressures slightly above atmospheric pressure.[1][2][4]

In distilling the crude oil, it is important not to subject the crude oil to temperatures above 370 to 380 °C because the high molecular weightcomponents in the crude oil will undergo thermal cracking and formpetroleum coke at temperatures above that. Formation of coke would result in plugging the tubes in the furnace that heats the feed stream to the crude oil distillation column. Plugging would also occur in the pipingfrom 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 more than 370 to 380 °C yields a residual oil from the bottom of the atmospheric distillation column consisting entirely of hydrocarbons that boil above 370 to 380 °C.

To further distill the residual oil from the atmospheric distillation column, the distillation must be performed at absolute pressures as low as 10 to 40 mmHg (also referred to as Torr) so as to limit the operating temperature to less than 370 to 380 °C.

Image 1 is a photograph of a large vacuum distillation column in a petroleum refinery and Image 2 is a process diagram of a petroleum refinery vacuum distillation column that depicts the internals of the column.

The 10 to 40 mmHg absolute pressure in a vacuum distillation column increases the volume of vapor formed per volume of liquid distilled. The result is that such columns have very large diameters.[5]

Distillation columns such those in Images 1 and 2, may have diameters of 15 meters or more, heights ranging up to about 50 meters, and feed rates ranging up to about 25,400 cubic meters per day (160,000 barrels per day).

The vacuum distillation column internals must provide good vapor-liquid contacting while, at the same time, maintaining a very low pressure increase from the top of the column top to the bottom. Therefore, the vacuum column uses distillation trays only where withdrawing products from the side of the column (referred to as side draws). Most of the column uses packing material for the vapor-liquid contacting because such packing has a lower pressure drop than distillation trays. This packing material can be eitherstructured sheet metal or randomly dumped packing such as Raschig rings .

The absolute pressure of 10 to 40 mmHg in the vacuum column is most often achieved by using multiple stages of steam jet ejectors. [6]

Many industries, other than the petroleum refining industry, use vacuum distillation on a much a smaller scale.

Page 2: Vacuum Distillation in Petroleum Refining

o 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).

Page 3: Vacuum Distillation in Petroleum Refining

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.