Apparatus and process for improved aromatic extraction from gasoline

Information

  • Patent Grant
  • 6303021
  • Patent Number
    6,303,021
  • Date Filed
    Tuesday, December 12, 2000
    24 years ago
  • Date Issued
    Tuesday, October 16, 2001
    23 years ago
Abstract
The improved process and apparatus of the present invention for extracting high purity aromatics from gasoline using a glycol solvent based extraction process decrease liquid-vapor flashing, reduce reflux flow rate, and use heat of enthalpy produces at one point as a source of energy used at another point, decreasing energy consumption while significantly increasing purity and amount of product obtained.
Description




BACKGROUND OF THE INVENTION




1. Field of the Invention




The present invention relates to an improved apparatus and process for extracting high-purity aromatics from gasoline which increases system capacity while reducing energy consumption.




2. Prior Art




Several commercially proven processes and apparatus are available for extracting high-purity aromatics from gasoline, coke oven light oil, and pyrolysis naphtha. Most include a liquid-liquid extractor followed by an extractive distillation column for extracting a high-purity aromatic stream, apparatus for removing solvent from the product streams, and solvent conditioning facilities.




The extraction of benzene and heavier aromatic homologs has been practiced commercially for about a century. Prior to the preparation of high-octane gasoline from crude oil, aromatics were extracted from liquids produced during the coking and gasification of coal. With the advent of platinum reforming (“Platforming”) in the late 1940's, a large source of less expensive aromatics became available in oil refineries.




At about the same time Dow and others were developing commercial plants to produce ethylene glycol for the automotive antifreeze market. One of the heavy byproducts of this process was di-ethylene glycol. Dow found that this material could be used to extract aromatics from gasoline, and developed a process to accomplish this.




Dow made an arrangement for UOP to market the process once it was proved, naming it UDEX in honor of the new partnership promoting the process. This process dominated the extraction field through the 1950's until the Shell Sulfolane process supplanted it in the 1960's.




The early UDEX units used di-ethylene glycol (“DEG”) and diglycol amine (“DGA”) for solvents. The consumption of energy was typically in the range of 1200 to 1500 BTU/pound of extract. In the early 1960's, tri-ethylene glycol replaced most of the DEG/DGA, reducing energy consumption to 1000 to 1200 BTU/pound of extract, and increasing unit capacity by 20 to 30%. In the 1970's, tetra-ethylene glycol replaced most of the tri-ethylene. With this change, the energy consumption dropped to the range of 800 to 1000 BTU/pound of extract and the capacity increased another 10 to 20%. A solvent additive called “Carom” was used in the 1960's to decrease the energy consumption and increase capacity, each changing in the range of 5 to 10%.




The introduction of the Shell Sulfolane process in the 1960's ended the design and construction of most UDEX apparatus. The Shell Sulfolane apparatus usually consumes less than 700 BTU/pound of extract. While this is a strong advantage, the process has two important disadvantages.




First, the Sulfolane process requires four large columns rather than the two required for the UDEX process. This increases capital cost.




Second, the solvent can become corrosive. Reboiler replacement and exotic metallurgy are not uncommon due to this corrosive nature. Entire columns have had to be replaced at times.




Thus, because of the low capital cost and non-corrosive nature of the glycol units, a UDEX apparatus having a low consumption of energy would have substantial application in the aromatics field.




SUMMARY OF THE INVENTION




Accordingly, it is a primary object of the invention to produce an improved process and apparatus for glycol based extraction of aromatics from gasoline and the like commonly referred to as the UDEX process.




Such object, as well as others, is accomplished by the process and apparatus of the present invention which decrease liquid-vapor flashing, reduce reflux flow rate, and use heat of enthalpy produced at one point as a source of energy used at another point, decreasing energy consumption while significantly increasing purity and amount of product obtained.











BRIEF DESCRIPTION OF THE DRAWINGS





FIG. 1

is a schematic diagram of the prior art apparatus, commonly referred to as UDEX, used in the glycol based process of extracting aromatics from gasoline.





FIG. 2

is a schematic diagram showing the apparatus of

FIG. 1

shown in phantom incorporating structure not shown in phantom proposed for addition for carrying out the process of the present invention in an improved manner, increasing yield while at the same time decreasing energy consumption.











DESCRIPTION OF THE PREFERRED EMBODIMENT




Traditional apparatus for carrying out the UDEX process is shown in FIG.


1


. Inasmuch as the apparatus of the present invention adds onto existing apparatus, for the sake of brevity, the description of

FIG. 2

will incorporate a description of the apparatus of FIG.


1


.





FIG. 2

shows the UDEX apparatus of

FIG. 1

in phantom and incorporates added structure to provide the improved apparatus of the present invention commonly referred to by reference numeral


10


. The description will further define process flow as it relates to the apparatus


10


.




A feed stream


11


, normally at ambient temperature, is first heated with raffinate in a suitable heat exchanger


12


and further heated in a suitable heater


13


before being sent to an extractor column


14


.




Raffinate stream


15


exits at the top of the extractor column


14


, is cooled in the heat exchanger


12


and is cooled again in a suitable cooler


16


. The cooled raffinate stream


15


is mixed with a recycled water stream


17


to extract solvent from the raffinated stream


15


, and the combined stream


15


is sent to a separator


18


where the water and solvent separate from the raffinate into what is defined as a heavy phase


85


.




The raffinate, defined as a light hydrocarbon phase


45


, from separator


18


is mixed with a second water stream


19


and sent to a separator


20


. This second mixing of water and raffinate further reduces the solvent concentration in the raffinate which becomes product stream


21


.




Returning to the extractor column


14


, a rich solvent stream


22


is removed at the bottom of the column


14


, heated in a lean/rich heat exchanger


23


, and is typically sent to a flash drum A at the top of a stripper column


24


. While physically part of stripper column


24


, the flash drum A is an isolated unit and operates at a higher pressure than tray portions BC of the stripper column


24


but at a lower pressure than extractor column


14


. As stream


22


encounters the lower pressure in the flash drum A some of the hydrocarbons dissolved in the rich solvent stream


22


flash and exit stripper column


24


as a vapor stream


25


. Because of low volatility of the solvent at the temperature and pressure in the flash drum A, vapor stream


25


contains virtually no solvent.




The solvent, carrying dissolved hydrocarbons therein, exits flash drum A as stream


26


, and enters at an uppermost or top tray B


1


position within the multitiered upper tray portion B of the stripper column


24


. Because pressure in the stripper column tray portions BC is lower than in the flash drum A, another portion of the hydrocarbons dissolved in stream


26


flashes and exits the stripper column


24


as a vapor stream


28


. The liquid portion of stream


26


which has not flashed flows down and across tiered trays B


2


isolated from the top tray B


1


in tray portion B, contacting an upwardly flowing vapor stream


29


to be defined hereinafter. As a result of the vapor-liquid contact between streams


26


and


29


in trays B


2


, the vapor stream


29


strips most of the non-aromatic hydrocarbons out of stream


26


and carries them out of the stripper column


24


.




The vapor streams


28


and


29


flow into vapor stream


25


and the combined stream


125


flows to condenser


32


. Once condensed, the stream


125


flows to a receiver


33


.




Condensed hydrocarbons in the receiver


33


are recycled to the bottom of extractor column


14


as stream


34


. The purpose of stream


34


is to control the purity of the extract


40


. As stream


34


flow rate is increased, a similar increase must be seen in streams


25


,


28


and/or


29


. Whatever portion of the flow increase occurs in streams


25


or


28


provides no improvement in purity. In fact, increasing flow of either stream


25


or


28


often reduces purity, as shown recently in both simulation models and empirical tests. Only the portion of the flow increase produced with stream


29


improves the purity of extract


40


.




The means by which streams


25


,


28


and


29


are generated helps explain why they produce such different results. Streams


25


and


28


are produced by the enthalpy of the rich solvent stream


26


. Stream


29


is produced by stripping of non-aromatic hydrocarbons from stream


26


in trays B


2


of portion B of the stripper column


24


. As the flow rate of stream


29


increases, more of the non-aromatic hydrocarbons are removed.




Inside stripper column


24


, the down-flowing rich solvent stream


26


contacts the up-flowing vapor stream


29


. Such counter-current contact removes the non-aromatic hydrocarbons from the rich solvent stream


26


. Because of a high degree of non-ideality introduced by the presence of solvent in stream


26


, even non-aromatic hydrocarbons with up to 9 carbon atoms become volatile and can be removed from the rich solvent stream


26


. Thus, the tiered trays B


2


of portion B of the stripper column


24


function as an extractive distillation column.




Although not normally needed for most applications, non-aromatic hydrocarbons with


10


or more carbon atoms can also be made as volatile as benzene by increasing concentration of solvent in the down-flowing stream


26


. The condensed hydrocarbon stream


34


recycled to the extractor column


14


thus contains almost all of the non-aromatic hydrocarbons stripped from rich solvent stream


26


, plus a substantial amount of benzene and heavier aromatics.




Moving now to a bottom portion C of the stripper column


24


, an upward-flowing steam vapor stream


30


is generated by a combination of a stripping stream


35


and a vapor stream


49


generated by a reboiler


36


. In the bottom portion C of stripper column


24


, upward-flowing vapor stream


30


strips dissolved aromatic hydrocarbons from the down-flowing rich liquid solvent stream


26


since virtually all of the non-aromatic hydrocarbons were removed in the upper portion B of the stripper column


24


. A first portion of vapor stream


30


is removed as side-cut stream


37


, is sent to a side-cut condenser


38


and flows to a side-cut receiver


39


. The aromatic hydrocarbons are removed from the side-cut receiver


39


as the high purity aromatic extract


40


. Another portion of stream


30


rises through portion B, becoming vapor stream


29


by stripping the non-aromatic hydrocarbons from fluid stream


26


.




Water condensed from the stream


30


by condenser


38


and received in the side-cut receiver


39


is split into three streams. A first stream


41


is recycled to mix with the condensed side-cut stream


37


downstream of side-cut condenser


38


to ensure the removal of solvent strained within stream


37


. A second stream


42


is sent to an accumulator


43


. The third stream


19


is fed into separator


20


for washing the stream


45


.




Since a substantial portion of vapor stream


30


, which splits into side-cut stream


37


and vapor stream


29


, is steam, a portion of vapor stream


29


rising through portion B of the stripper column


24


must also be steam. Therefore, some of the condensed material in receiver


33


will also be water which flows to the accumulator


43


as water stream


44


.




A stream


46


from accumulator


43


flows to a tube and shell vaporizer


47


where a substantial portion of stream


46


is converted to vapor or steam, which generates stripping stream


35


. It should be noted that several variations of this basic design of UDEX apparatus exist with some incorporating water columns and some having the vaporizer


47


on the rich solvent line


22


or


54


.




Portion


48


of the down-flowing stream


26


which reaches a bottom area of tray portion C of stripper column


24


is looped through reboiler


36


and returned as vapor stream


49


. A lean solvent stream


50


, the net bottoms product from stripper column


24


flows to a tube side of the vaporizer


47


. Boiling of water on a shell side of the vaporizer


47


reduces the temperature of the lean solvent stream SO. The lean solvent stream


50


then flows to lean/rich heat exchanger


23


(in a design in which a lean/rich exchanger is included) along line


51


, and returns to the top of extractor column


14


as stream


52


.




In an apparatus


10


where no exchanger


23


is provided, it will be understood that the stream


52


will be identical to stream


51


, and will obviously be hotter than a stream


52


exiting an exchanger


23


.




The down-flowing solvent stream


52


in the extractor column


14


contacts the upward-flowing hydrocarbon streams


11


and


34


. This counter-current flow extracts virtually all of the aromatics and an equilibrium amount of non-aromatics from the upward-flowing stream


34


, generating rich solvent stream


22


.




Using gathered data, a steady state simulation model of the typical UDEX apparatus described above was prepared. Inasmuch as the model was set up to calculate compositions of internal as well as external streams, with multiple runs it became possible to understand what occurs in the flash drum A and at the isolated top tray B


1


of portion B of the stripper column


24


.




Based on the pressure in the flash drum A and in the top tray B


1


of portion B in the stripper column


24


, it is assumed that the vapor-liquid flashes taking place therein reduce vapor loading or stream velocity in the trays B


2


of portion B of the stripper column


24


. In this way, the diameter of the stripper column


24


is most probably reduced.




With the steady state model, it was possible to run a series of calculations in which the amount of vapor flashed in flash drum A to form stream


25


was reduced to zero. With every decrease in the amount of vapor flashed, purity of the extract


40


improved. Since the flow of hydrocarbon stream


34


was held constant, each decrease in the flow of vapor stream


25


from the flash drum A required an equal increase in flow of vapor streams


28


and


29


from stripper column


24


. Thus, it appears that not all reflux materials, vapor streams


25


,


28


and


29


, effect extract


40


purity equally.




The next set of calculations methodically reduced the flow rate of hydrocarbon stream


34


until the purity of the extract


40


was returned to a starting point purity. This showed that the same extract


40


purity could be generated at significantly different flow rates of hydrocarbon stream


34


. Thus, the unexpected result was that the purity of the extract


40


increased when the flow of hydrocarbon stream


34


was reduced in a specific manner.




The next set of simulation model runs involved reducing the amount of vapor flashed at the top tray B


1


of portion B of stripper column


24


. As with the vapor stream


25


produced in the flash drum A, the vapor stream


28


produced at the top tray B


1


of portion B of the stripper column


24


had little effect on the purity of the extract


40


. When the flow rate of the hydrocarbon stream


34


was held constant while the vapor stream


28


produced at the top tray B


1


of portion B was reduced, the purity of the extract flow of


40


increased. Likewise, when the purity of hydrocarbon stream


34


decreased to the starting purity, less flow of stream


34


was required. Again, the surprising result of greater purity of extract


40


with less stream


34


flow was observed.




The vapor streams


25


and


28


produced at the flash drum A and at the top tray B


1


of portion B of the stripper column


24


, respectively, share one common factor: they do not contact a counter-current flow of liquid solvent stream


26


as do the remaining trays B


2


of portion B of the stripper column


24


. Thus, it appears that sequential flashes in the absence of contact with a counter-current flow of liquid solvent do not produce as much purification of extract


40


as does contacting the vapor stream


29


with the counter-current liquid solvent stream


26


.




With existing technology, the normal range for the volumetric ratio of reflux to extract (“R/E”) is 1.1 to 2.5, depending on the composition of the feed and the requirements for purity of the extract.




With the improvements proposed herein in place, this ratio drops to a range of 0.5 to 1.0. The reason for this reduction is that the new technology eliminates the portion of the reflux that does not enhance purity. The reflux generated in the flash drum A and on the top tray B


1


of the stripper column


24


does not improve purity. Only the portion generated in the counter-current trayed section of the stripper column


24


selectively removes impurities.




To eliminate ref lux in the flash drum A and the top tray B


1


in the stripper column


24


, energy must be removed from the rich solvent stream upstream of the flash drum A. This is accomplished with the new solvent cooler.




Most units now run at about 1.1 R/E. This should drop to approximately 0.6 with the proposed improvements, so most units will see a reduction of about 0.5.




By comparison, the vapor stream


29


flow from trays B


2


of portion B of the stripper column


24


for the above models showed that, for constant extract


40


purity, the flow rate of the vapor stream


29


remained constant. A few more runs showed that this flow correlated well with extract


40


purity. Thus, the flow rate of stream


29


was found to determine the purity of the extract


40


.




In addition to purity issues, the simulation model provided another surprise. As the flow of hydrocarbon stream


34


was reduced, the model showed that purity of the raffinate


21


increased. With less aromatics in the raffinate


21


, the recovery of aromatics increased and the flow of extract


40


increased slightly. Therefore, a series of model runs was made to return the raffinate


21


purity to the starting point purity. Since recovery of aromatics is affected by lean solvent stream


52


flow, this flow was reduced.




With the current technology, the normal range for the volumetric ratio of solvent to feed (“S/F”) is 3.0 to 5.0, depending on the composition of the feed.




With the proposed improvements, this will drop to a range of 2.0 to 2.8. The range reflects the difficulty of processing the particular feed.




As an example, for a feed comprising 50% aromatics and a solvent to feed ratio of 4.0, the solvent to extract ratio will be 8.0. This can be used to show how the improvement in the technology holds constant the concentration of hydrocarbons in the rich solvent stream


22


leaving the bottom of the extractor


14


. The hydrocarbons consist of the extract and the reflux. Using E for extract flow, R for ref lux flow and S for solvent flow, the equation for calculating the concentration of hydrocarbons in the rich solvent is:






Hydrocarbons in solvent=(E=R)/(E+R+S)






Dividing each term by E provides an equation that is easier to use:






=(E/E+R/E)/(E/E+R/E+S/E)






Starting with a solvent to feed ratio of 4.0 and 50% aromatics in the feed, the solvent to extract ratio will be 8.0. Likewise, with a reflux to feed ratio of 0.8, the reflux to extract ratio would be 1.6. Using these values, the concentration of hydrocarbons in the solvent is about:






(1.0+1.6)/(1.0+1.6+8.0)=24.5%






With the proposed improvements, the S/E ratio will drop to 5.3 and the R/E will drop to 0.7:






(1.0+0.7)/(1.0/+0.7+5.3)=24.3%






Thus, even with the modifications to the flow scheme, the heat balance and the key ratios, the concentration of the hydrocarbons in the solvent stream


22


at the bottom of the extractor


14


are about the same with both the new and old technologies. As a result, the selectivities will be about the same even though the energy consumption will be substantially reduced.




As the flow of lean solvent stream


52


was reduced, several things happened. First, as expected, the raffinate


21


was found to include more aromatics. Second, the lower flow rates of solvent stream


52


and hydrocarbon stream


34


decreased tray loadings in the extractor column


14


and stripper column


24


. Third, with less solvent stream


52


flow, the flow of stripping stream


35


from the vaporizer


47


to the bottom of portion C of the stripper column


24


could be decreased.




From the standpoint of the flow of energy, the reboiler


36


of stripper column


24


provides the energy, for the process. Most of this energy is removed in the condensers


32


and


38


associated with the stripper column


24


. Since the feed


11


and products


21


and


40


enter and leave the process at the same temperature, the reboiler


36


duty must balance the duties of the two condensers


32


and


38


and of the raffinate cooler


16


. Thus, any change that reduces the duty of condenser


32


and/or condenser


38


must produce an equal change at the reboiler


36


.




Reducing the flow of material to the flash drum A and the top tray B


1


of portion B of the stripper column


24


reduces flow to the condenser


32


. In practice, the energy to vaporize the hydrocarbons in the flash drum A and at the top tray B


1


of portion B of the stripper column


24


actually comes from reboiler


36


and travels to the flash drum A in the enthalpy of the solvent stream


50


,


51


,


52


, and


22


. Thus, as the flow of hydrocarbon stream


34


decreases, the duties of the reboiler


36


and condenser decrease by the same amount.




As the flow of lean solvent stream


52


decreases, the flow of stripping steam in stream


35


can be decreased. With less steam in stream


35


flowing up the stripper column


24


, less will flow to both condensers


32


and


38


. Thus, lower flow of solvent stream


52


also decreases the consumption of energy.




With the current technology, the ratio of stripping steam to solvent flow is in the range of 2 to 5% with the average about 4%. As described above, the solvent flow drops by about one-third. Since the basic job of stripping the hydrocarbons out of the solvent does not change with the new technology, the ratio of stripping steam to lean solvent will not change. Because the flow rate of solvent decreases by one-third, the flow of stripping steam also decreases by one-third.




As seen in the model, upon elimination of flashing of the rich solvent stream


22


, the consumption of energy at the stripper reboiler


36


decreased from over 900 to about 600 BTU/pound of extract


40


. In addition, upon decreasing flow rates of streams


35


and


26


in the stripper column


24


, the tray loading in portions B and C of stripper column


24


dropped by nearly one half of previous valves.




The relative expense for the capacity of the UDEX apparatus


10


is strongly related to apparatus


10


capacity, relative primarily to extractor column


14


size, stripper column


24


size, and the need for the two stripper condensers


32


and


38


and the stripper reboiler


36


.




Thus, modifying the UDEX process flow scheme as empirically determined and set forth above the load on all of the structures except for a top section of the extractor column


14


.




Therefore, with the modified apparatus


10


described hereinbelow, used in the empirical testing, the feed stream


11


flow rate could be doubled after incorporating the above modifications into the improved process.




Turning now to a study of the modified apparatus


10


proposed herein for carrying out the improved process, it was first appreciated that hydrocarbon flashing in flash drum A needed to be eliminated.




To eliminate hydrocarbon flashing in flash drum A, it was determined that energy, in the form of heat, or enthalpy, must be removed from the solvent stream


22


. The enthalpy in the solvent stream


22


was found to be useable in other areas of the apparatus


10


.




The excess energy is in the solvent stream. This excess is removed in a cooler


70


on the solvent stream. While the cooler


70


can be in either the lean solvent or the rich solvent streams, the preferred embodiment is to insert the new cooler in the lean solvent line


52


.




First, direct flow of liquid stream


26


from portion B


2


to portion C of stripper column


24


was eliminated by placement of a suitable barrier


71


therebetween. As is known in the art, the stripper column


24


includes doors, (not shown) commonly referred to as manways, through which a worker can enter the column


24


with appropriate parts to create the barrier


71


by assemblage of the parts inside the column


24


. Those skilled in the art will have full knowledge of use of such manways and erection of the barrier


7


hin the column


24


. It will be understood that a further barrier


79


is also commonly used to stop flow of vapor stream


29


to top tray B


1


from the multitiered trays B


2


located therebeneath in portion B


2


of the stripper column


24


. Then, a shell and tube heat exchange reboiler


60


could draw bottom stream


80


from portion B


2


, at a point just above the side-cut in the stripper column


24


, therethrough, to heat same prior to routing the stream


80


into an upper area of portion C, the stream


80


being heated by transfer of heat thereto from lean solvent stream


50


. Such increased temperature requires less flow of stripping steam in stream


35


, further reducing the consumption of energy since the temperature of the lean solvent stream


50


leaving the bottom of the stripper column


24


is high enough to provide an adequate temperature difference for such heat exchange.




Second, since water stream


85


from the raffinate wash contains a significant amount of soluble non-aromatics, a stream


77


tapped off of stream


85


can be sent to a small hydrocarbon stripping column


74


which can be used to keep these non-aromatics out of the bottom portion C of the stripper column


24


. Contamination of the extract


40


can be eliminated by sending these non-aromatics via line


78


to condenser


32


. Further, the flow of stream


34


can be reduced by reducing energy input from reboiler


36


. Lean solvent stream


50


, even after coursing through reboiler


60


, would still have a temperature to supply energy to a reboiler


75


for the small column


74


. A bottoms stream


76


from the column


74


containing water and solvent, in a preferred embodiment, would flow into the vaporizer


47


.




Third, after coursing through reboiler


75


on the hydrocarbon stripping column


74


, the lean solvent stream


50


would still be hot enough to provide energy to the vaporizer


47


. Process calculations also indicated that the enthalpy of the solvent stream


50


would still be high enough to vaporize some of the hydrocarbons in the solvent stream


52


. Therefore, a cooler


70


, probably in the form of a cooling water exchanger


70


, would be required to cool a substantial portion of the stream


52


prior to its entry into the extractor column


14


, completing the improved apparatus


10


.




Since sub-cooling rich solvent stream


22


upstream of flash drum A would increase reboiler


60


duty, it is proposed to control the flow of lean solvent stream


22


though the cooling water exchanger


70


by creating a secondary route


53


bypassing the cooler


70


. Flow through the secondary route


53


is controlled by a valve


55


which is operated under control of a flow meter


72


electronically coupled thereto and provided for sensing an instantaneous rate of flow of the stream


25


from the flash drum A, with elimination of substantially all flow of the stream


25


being desired.




Substantially complete elimination of flow of stream


25


can be produced by manipulation of the valve


55


in a predetermined manner relative to a desired temperature for the solvent stream


52


, by producing a degree of valve


55


closure sufficient to substantially eliminate flow of stream


25


by increasing the volume of lean solvent stream


52


flowing through the cooler


70


without sub-cooling the stream


52


. Conversely, should it be found that sub-cooling of the stream


52


is taking place, it may be desirable to allow creation of a negligible rate of flow of stream


25


to a predefined upper limit by producing a degree of valve


55


opening to decrease the volume of stream


52


flowing through the cooler


70


, thereby warming the stream


52


prior to its flowing into the extractor column


14


.




With the current technology, there is no issue on removing energy from the solvent entering the flash drum A.




With the proposed improved flow scheme, the amount of energy in the solvent can be optimized. If the temperature is too high (as it is with the current technology), then some of the hydrocarbons in the rich solvent stream


22


vaporize in the flash drum A. This leads to more reflux flow, more solvent flow, more stripping steam flow, lower capacity and higher consumption of energy. If, on the other hand, the temperature of the rich solvent stream


22


is too low, then the stream


22


must be reheated to its bubble point with vapors from the reboiler consuming more energy. At the optimum, the rich solvent stream


22


entering the flash drum will be at its bubble point and the use of energy will be minimized.




To adjust the removal of energy from the solvent so that the stream


22


entering the flash drum A is at its point, it is possible to monitor the flow of vapor from the flash drum A. To accomplish this, the pressure of the drum must be set at the pressure of the top of the stripper column


24


. At this pressure, any vapor generated in the flash drum A represents the degree to which the solvent stream


22


contains too much energy. Therefore, the measurement of the flow of vapor from the flash drum A provides a signal or index that can be used to remove the excess heat from the solvent steam


22


. With a cooler


70


on the solvent and control valves in place as proposed, the flow of vapor from the flash drum A can be used to adjust removal of excess energy from the solvent.




The last set of process calculations performed with the model investigated the water concentration in the lean solvent stream


50


. After modifying the process flow scheme, the best combination of purity and recovery was obtained at about a 5 to 6% concentration of water. Higher concentrations lost recovery faster than gaining purity while lower concentrations produced the opposite effect.




As a side note, solvent additives such as ether glycol, while having significant effects at high water concentrations, were found to have negligible significance at the optimum water concentrations.




Almost all present day UDEX apparatus are believed to have the same process flow scheme, making the proposed modifications substantially universally applicable. Likewise, similar modifications appear applicable for use in other glycol solvent systems.




As described above, the method of the present invention provides a number of advantages, some of which have been described above and others of which are inherent in the invention. Also, modifications may be proposed to the method without departing from the teachings herein. Accordingly, the of the invention is only to be limited as necessitated by the accompanying claims.



Claims
  • 1. An improved process for the recovery of aromatic hydrocarbons from a feed comprising a mixture thereof with non-aromatic hydrocarbon, the process comprising at least the steps of:a) contacting the feed with a lean solvent stream and a recycle stream in an extractor column operated at extraction conditions effective to separate the feed into a raffinate stream comprising non aromatic hydrocarbons and a first rich solvent stream comprising solvent, aromatic hydrocarbons and non aromatic hydrocarbons; b) passing the first rich solvent stream to a flash drum wherein the stream encounters a reduction in pressure causing the stream to separate into two streams comprising a vapor hydrocarbon stream produced by flashing and a second rich solvent stream; c) passing the second rich solvent stream to an isolated top tray of a stripper column wherein the stream encounters a further reduction in pressure causing the stream to separate again into a vapor hydrocarbon stream produced by flashing and a third rich solvent stream; d) passing the third rich solvent stream to a multitiered tray portion of the stripper column, contacting the stream with an upwardly flowing vapor hydrocarbon-steam stream under conditions suitable for stripping and recovering a first flashless vapor stream; e) combining the vapor streams from the flash drum, isolated top tray and multitiered tray portion into a condensed overhead mixed hydrocarbon stream and passing said mixed hydrocarbon vapor stream to said extr8Xcolumn as at least a portion of said recycle stream; f) separating water from the overhead vapor stream and combining the separated water with water from a raffinate wash system and further water streams created by the process and sending the combined water stream to a vaporizer where the steam of the upwardly flowing hydrocarbon-steam stream of the stripper column is generated; g) recovering an aromatic product stream together with a portion of the upwardly flowing steam from said upwardly flowing vapor stream and withdrawing a lean solvent stream from the bottom of the stripping column; and h) returning the lean solvent stream to the extractor column for recirculation; the improvement comprising: creating, a barrier across the multitiered tray portion of the stripper column at a position below-that at which the aromatic product stream is recovered to produce a top tray portion and a bottom tray portion; diverting the lean solvent stream exiting the bottom portion of the stripper column through a heat exchanger; diverting the third hydrocarbon stream from the top tray portion through the heat exchanger to which heat is supplied from the diverted lean solvent stream from the stripper column; and creating a fourth heated hydrocarbon stream which is then fed to the bottom tray portion of the stripper column for continuation through steps d) through h) above, the heating of the fourth hydrocarbon stream generated significantly improving the degree of extraction of the aromatic product.
  • 2. An improved process for the recovery of aromatic hydrocarbons from a feed comprising a mixture thereof with nonaromatic hydrocarbons, the process comprising at least the steps of:a) contacting the feed with a lean solvent stream and a recycle stream in an extractor column operated at extraction conditions effective to separate the feed into a raffinate stream comprising nonaromatic hydrocarbons and a first rich solvent stream comprising solvent, aromatic hydrocarbons and non-aromatic hydrocarbons; b) passing the first rich solvent stream to a flash drum wherein the stream encounters a reduction in pressure causing the stream to separate into two streams comprising a vapor hydrocarbon stream produced by flashing and a second rich solvent stream; c) passing the second rich solvent stream to an isolated top tray of a stripper column wherein the stream encounters a further reduction in pressure causing the stream to separate again into a vapor hydrocarbon stream produced by flashing a third rich solvent stream; d) passing the third rich solvent stream to a multitiered tray portion of the stripper column, contacting the stream with an upwardly flowing vapor hydrocarbon-steam stream under conditions suitable for stripping and recovering a first flashless vapor stream; e) combining the vapor streams from the flash drum, isolated top tray and multitiered tray portion into a condensed overhead mixed hydrocarbon vapor stream and passing said mixed hydrocarbon to said extractor column as at least a portion of said recycle stream; f) separating water from the overhead vapor stream and combining the separated water with water from a raffinate wash system and further water streams created by the process and sending the combined water stream to a vaporizer where the steam of the upwardly flowing hydrocarbon-steam stream of the stripper column is generated; g) recovering an aromatic product stream together with a portion of the upwardly flowing steam from said upwardly flowing vapor stream and withdrawing a lean solvent stream from the bottom of the stripping column, and h) returning the lean solvent stream to the extractor column for recirculation; the improvement comprising: cooling the lean solvent stream to remove sufficient energy from the stream so that the flash drum and the top tray of the stripper column produce no vapor.
  • 3. An improved process for the recovery of aromatic hydrocarbons from a feed comprising a mixture thereof with nonaromatic hydrocarbons, the process comprising at least the steps of:a) contacting the feed with a lean solvent stream and a recycle stream in an extractor column operated at extraction conditions effective to separate the feed into a raffinate stream comprising non-aromatic hydrocarbons and a first rich solvent stream comprising solvent, aromatic hydrocarbons and nonaromatic hydrocarbons; b) passing the first rich solvent stream to a flash drum wherein the stream encounters a reduction in pressure causing the stream to separate into tow streams comprising a vapor hydrocarbon stream produced by flashing and a second rich solvent stream; c) passing the second rich solvent stream to an isolated top tray of a stripper column wherein the stream encounters a further reduction in pressure casing the stream to separate again into a vapor hydrocarbon stream produced by flashing and a third rich solvent stream; d) passing the third rich solvent stream to a multitiered tray portion of the stripper column, contacting the stream with an upwardly flowing vapor hydrocarbon-steam stream under conditions suitable for stripping and recovering a first flashless vapor stream; e) combining the vapor streams from the flash drum, isolated top tray and multitiered tray portion into a condensed overhead mixed hydrocarbon vapor stream and passing said mixed hydrocarbon vapor stream to said extractor column as at least a portion of said recycle stream; f) separating water from the overhead vapor stream and combining the separated water with water from a raffinate wash system and further water streams created by the process and sending the combined water stream to a vaporizer where the steam of the upwardly flowing hydrocarbon-steam stream of the stripper column is generated; g) recovering an aromatic product stream together with a portion of the upwardly flowing steam from said upwardly flowing vapor stream and withdrawing a lean solvent stream from the bottom of the stripping column; and h) returning the lean solvent stream to the extractor the improvement comprising: reducing the flow of reflux to the extractor correspondingly with a reduction in vapor created in the flash drum and the top for recirculation; tray of the stripper by removal of energy from the lean solvent stream flowing therethrough.
  • 4. An improved process for the recovery of aromatic hydrocarbons from a feed comprising a mixture thereof with non-aromatic hydrocarbons, the process comprising at least the steps of:a) contacting the feed with a lean solvent stream and a recycle stream in an extractor column operated at extraction conditions effective to separate the feed into a raffinate stream comprising nonaromatic hydrocarbons and a first rich solvent stream comprising solvent, aromatic hydrocarbons and nonaromatic hydrocarbons; b) passing the first rich solvent stream to a flash drum wherein the stream encounters a reduction in pressure causing the stream to separate into two streams comprising a vapor hydrocarbon stream produced by flashing and a second rich solvent stream; c) passing the second rich solvent stream to an isolated top tray of a stripper column wherein the stream encounters a further reduction in pressure causing the stream to separate again into a vapor hydrocarbon stream produced by flashing a third rich solvent stream; d) passing the third rich solvent stream to a multitiered tray portion of the stripper column, contacting the stream with an upwardly flowing vapor hydrocarbon-steam stream under conditions suitable for stripping and recovering a first flashless vapor stream; e) combining the vapor streams from the flash drum, isolated top tray and multitiered tray portion into a condensed overhead mixed hydrocarbon vapor stream and passing said mixed hydrocarbon vapor stream to said extractor column as at least a portion of said recycle stream; f) separating water from the overhead vapor stream and combining the separated water with water from a raffinate wash system and further water streams created by the process and sending the combined water stream to a vaporizer where the steam of the upwardly flowing hydrocarbon-steam stream of the stripper column is generated; g) recovering an aromatic product stream together with a portion of the upwardly flowing steam from said upwardly flowing vapor stream and withdrawing a lean solvent stream from the bottom of the stripping column; and h) returning the lean solvent stream to the extractor column for recirculation; the improvement comprising: reducing the flow of solvent to the extractor correspondingly with a reduction of flow of reflux produced by removing energy from the stream entering the stripper column.
  • 5. An improved process for the recovery of aromatic hydrocarbons from a feed comprising a mixture thereof with nonaromatic hydrocarbons, the process comprising at least the steps of:a) contacting the feed with a lean solvent stream and a recycle stream in an extractor column operated at extraction conditions effective to separate the feed into a raffinate stream comprising non-aromatic hydrocarbons and a first rich solvent stream comprising solvent, aromatic hydrocarbons and nonaromatic hydrocarbons; b) passing the first rich solvent stream to a flash drum wherein the stream encounters a reduction in pressure causing the stream to separate into two streams comprising a vapor hydrocarbon stream produced by flashing and a second rich solvent stream; c) passing the second rich solvent stream to an isolated top tray of a stripper column wherein the stream encounters a further reduction in pressure causing the stream to separate again into a vapor hydrocarbon stream produced by flashing and a third rich solvent stream; d) passing the third rich solvent stream to a multitiered tray portion of the stripper column, contacting the stream with an upwardly flowing vapor hydrocarbon-steam stream under conditions suitable for stripping and recovering a first flashless vapor stream; e) combining the vapor streams from the flash drum, isolated op tray and multitiered tray portion into a condensed overhead mixed hydrocarbon vapor stream and passing said mixed hydrocarbon vapor stream to said extractor column as at least a portion of said recycle stream; f) separating water from the overhead vapor stream and combining the separated water with water from a raffinate wash system and further water streams created by the process and sending the combined water stream to a vaporizer where the steam of the upwardly flowing hydrocarbon-steam stream of the stripper column is generated; g) recovering an aromatic product stream together with a portion of the upwardly flowing steam from said upwardly flowing vapor stream and withdrawing a lean solvent stream from the bottom of the stripping column; and h) returning the lean solvent stream to the extractor column for recirculation; the improvement comprising: reducing the stripping steam in the stripper column correspondingly with a reduction of flow of the lean solvent stream.
  • 6. An improved process for the recovery of aromatic hydrocarbons from a feed comprising a mixture thereof with nonaromatic hydrocarbons, the process comprising at least the steps of:a) contacting the feed with a lean solvent stream and a recycle stream in an extractor column operated at extraction conditions effective to separate the feed into a raffinate stream comprising non-aromatic hydrocarbons and a first rich solvent stream comprising solvent, aromatic hydrocarbons and non-aromatic hydrocarbons; b) passing the first rich solvent stream to a flash drum wherein the stream encounters a reduction in pressure causing the stream to separate into two streams comprising a vapor hydrocarbon stream produced by flashing and a second rich solvent stream; c) passing the second rich solvent stream to an isolated top tray of a stripper column wherein the stream encounters a further reduction in pressure causing the stream to separate again into a vapor hydrocarbon stream produced by flashing and a third rich solvent stream; d) passing the third rich solvent stream to a multitiered tray portion of the stripper column, contacting the stream with an upwardly flowing vapor hydrocarbon-steam stream under conditions suitable for stripping and recovering a first flashless vapor stream; e) combining the vapor streams from the flash drum, isolated top tray and multitiered tray portion into a condensed overhead mixed hydrocarbon vapor stream and passing said mixed hydrocarbon vapor stream to said extractor column as at least a portion of said recycle stream; f) separating water from the overhead vapor stream and combining the separated water with water from a raffinate wash system and further water streams created by the process sending the combined water stream to a vaporizer where the steam of the upwardly flowing hydrocarbon-steam stream of the stripper column is generated; g) recovering an aromatic product stream together with a portion of the upwardly flowing steam from said upwardly flowing vapor stream and withdrawing a lean solvent stream from the bottom of the stripping column; and h) returning the lean solvent stream to the extractor column for recirculation; the improvement comprising: using a control system that detects flow of vapor from the flash drum and top tray of the stripper column to control removal of energy from the stream entering the stripper column.
  • 7. An improved process for the recovery of aromatic hydrocarbons from a feed comprising a mixture thereof with nonaromatic hydrocarbons, the process comprising at least the steps of:a) contacting the feed with a lean solvent stream and a recycle stream in an extractor column operated at extraction conditions effective to separate the feed into a raffinate stream comprising non-aromatic hydrocarbons and a first rich solvent stream comprising solvent, aromatic hydrocarbons and nonaromatic hydrocarbons; b) passing the first rich solvent stream to a flash drum wherein the stream encounters a reduction in pressure causing the stream to separate into tow streams comprising a vapor hydrocarbon stream produced by flashing and second rich solvent stream; c) passing the second rich solvent stream to an isolated top tray of a stripper column wherein the stream encounters a further reduction in pressure causing the stream to separate again into a vapor hydrocarbon stream produced by flashing and a third rich solvent stream; d) passing the third rich solvent stream to a multitiered tray portion of the stripper column, contacting the stream with an upwardly flowing vapor hydrocarbon-steam stream under conditions suitable for stripping and recovering a first flashless vapor stream; e) combining the vapor streams from the flash drum, isolated top tray and multitiered tray portion into a condensed overhead mixed hydrocarbon vapor stream passing said mixed hydrocarbon vapor stream to said extractor column as at least a portion of said recycle stream; f) separating water from the overhead vapor stream and combining the separated water with water from a raffinate wash system and further water streams created by the process and sending the combined water stream to a vaporizer where the steam of the upwardly flowing hydrocarbon-steam stream of the stripper column is generated; g) recovering an aromatic product stream together with a portion of the upwardly flowing steam from said upwardly flowing vapor stream and withdrawing a lean solvent stream from the bottom of the stripping column; and h) returning the lean solvent stream to the extractor column for recirculation; the improvement comprising: creating a barrier in the stripper column to detour the down-flowing stream to an external heat exchanger, heating the detoured stream with heat from the lean solvent stream in the external heat exchanger, and returning the stream to the stripper column at a point just below the barrier, the barrier being positioned between the point of recover of the aromatic product and the bottom of the column, the heating to the detoured stream decreasing the amount of upward flowing stripping steam required in the stripper column.
  • 8. An improved process for the recovery of aromatic hydrocarbons from a feed comprising a mixture thereof with nonaromatic hydrocarbons, the process comprising at least the steps of:a) contacting the feed with a lean solvent stream and a recycle stream in an extractor column operated at extraction conditions effective to separate the feed into a raffinate stream comprising non-aromatic hydrocarbons and a first rich solvent stream comprising solvent, aromatic hydrocarbons and non-aromatic hydrocarbons; b) passing the first rich solvent stream to a flash drum wherein the stream encounters a reduction in pressure causing the stream to separate into tow streams comprising a vapor hydrocarbon stream produced by flashing and a second rich solvent stream; c) passing the second rich solvent stream to an isolated top tray of a stripper column wherein the stream encounters a further reduction in pressure causing the stream to separate again into a vapor hydrocarbon stream produced by flashing and a third rich solvent stream; d) passing the third rich solvent stream to a multitiered tray portion of the stripper column, contacting the stream with and upwardly flowing vapor hydrocarbon-steam stream under conditions suitable for stripping and recovering a first flashless vapor stream; e) combining the vapor streams from the flash drum, isolated top tray and multitiered tray portion into a condensed overhead mixed hydrocarbon vapor stream and passing said mixed hydrocarbon vapor stream to said extractor column as at least a portion of said recycle stream; f) separating water from the overhead vapor stream and combining the separated water with water from a raffinate wash system and further water streams created by the process and sending the combined water stream to a vaporizer where the steam of the upwardly flowing hydrocarbon-steam stream of the stripper column is generated; g) recovering an aromatic product stream together with a portion of the upwardly flowing steam from said upwardly flowing vapor stream and withdrawing a lean solvent stream from the bottom off the stripping and h) returning the lean solvent stream to the extractor column for recirculation; the improvement comprising: removing the non-aromatic hydrocarbons from the water used in producing the stripping steam and removing further energy from the lean solvent stream.
CROSS REFERENCE TO RELATED APPLICATIONS

This application is a Continuation In Part of U.S. application Ser. No. 09/298,428 filed Apr. 23, 1999 of the same title, now abandoned.

US Referenced Citations (4)
Number Name Date Kind
2933448 Morin et al. Apr 1960
5059306 Kramer Oct 1991
5336840 Forte Aug 1994
5399244 Gentry Mar 1995
Continuation in Parts (1)
Number Date Country
Parent 09/298428 Apr 1999 US
Child 09/735452 US