Low cost selective Octene process : RHT-Octene

Abstract

This invention covers a process for making Octene from mix C4 Feed by a low cost highly selective multistage process. The multi staging of reactors essentially provides lower cost than conventional processes. Two options are provided in FIGS. 1 and 2 as regards to configuration based on the same catalyst but as can be seen that FIG. 1 configuration is low cost option with very high selectivity. The process provides conversion of butene to Octene >95% and product purity >96%. Product can be fractionated and can have a high purity Octene product by removing the trimers/polymers from the octene product. As mentioned due to the nature of the process configuration, one achieves high yield and selectivity with low cost.

Description

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 is a simplified process flow diagram of the process, where the C₄ mix feed is pumped from storage to the operating pressure of about 100 psig stream 1. The Stream 1 goes through a absorber bed item 9, which removes any impurities which will deactivate the catalyst. The stream 2 after heating with the product is fed to the column item 3. The C₄'s are driven over head and are taken as side draw where the n-butene concentration is maximum. The side draws streams 6 is heated to the reactor temperature of 280 to 300 F and pressure of about 400 psig, and are fed to the reactor item 8. The reaction of n-butene to octene is performed at WHSV of 2 to 4 (WHSV of 2 is enough to provide high conversions of over 95%). As two reactors are being used to multistage for high selectivity and yield, hence WHSV of about 4 is good for each reactor. The operating conditions for both the reactors are the same. The reactor effluent stream 7 is fed back to the column so as to fractionate the reactor effluents and octene is taken as bottom product and C₄ inerts, lighter olefins and other unreacted C₄'s are taken as overhead raffinate product. From this unique configuration one expects a conversion of over 95% to octene and also selectivity of about 95%. If higher purity octene product is required the product can be fractionated to remove the trimers/polymers as heavy's drag stream and take the octene product overhead at high purity.

The art also claims that in this process ethylene feed in vapor phase at about 450 psig comes from Battery limit and after cleaning in the absorber bed item 9 it is heated with the product stream 4, and further heated to about 210 to 250 F and is fed to reactors in parallel item 8, and reactor effluent is fed to the fractionator. In this application the fractionator is operated at 150 to 300 psig, and vapor stream is taken as overhead product which can be recycled after recovery. The bottom product is Octene/Octene-1 and is sent to storage. The people in the art will be able to see the merits of the process and see the optimization potential that will be provided in design of the unit.

FIG. 2 is alternate mode of the simple process flow diagram of the above flow scheme and all things are same except the reactor configuration which is bulk catalyst in the column. The feed at the same conditions as to other reactor 380 psig and 260 to 300 F is fed to Debutanizer reactor column item 4, after going through absorber bed item 2, so as to remove the impurities. The feed is heated in the Feed/Product exchanger and is fed to the Debutanizer Reactor column item 4, at about 250 F. on to the Multiple beds of catalyst in the column item 5, is provided so as to improve the selectivity. The technique of vapor bypass by chimney tray or external pipe can be used. The Debutanizer reactor item 4 operates in this case at about 350 to 400 psig. Some of unreacted C4's are taken with the bottom octene product so as to keep the bottom temperature low. The octene separation is done in the Octene column item 9, where octene is taken from bottom stream 5 and the unreacted C4's are recovered overhead item 7, and recycled to the Feed. The Debuanizer Reactor Column Item 4, overhead stream is taken C4 raffinate and is sent to the battery limit, This configuration is not suitable for Ethylene conversion to octene.

DETAILED DESCRIPTION OF THE INVENTION

The major art and know how described here is a disclosure of producing Octene/Octene-1, with the n-butene or ethylene feed as described above and convert it to octene by unique process configuration as described in FIGS. 1 and 2 (for n-butene feed). This provides low cost, highly selective and high conversion process. This highly selective option and conversion over 95% and purity over 95%, which can be further improved by further distillation to remove the drag stream of trimers/polymers.

The art as described in paragraph above, FIG. 1 can be utilized to convert the ethylene to octene/octene-1 in vapor phase operation ass described above, with the same equipment.

The alternate option in FIG. 2 is provided, for Debutanizer Reactor Column configuration, which provides installing bulk catalyst beds in the column and this scheme is good for only n-butene feed conversion to octene.

Based on the configuration and feed compositions following conditions will be required for the Octene process for the FIG. 1 and FIG. 2

FIG. 1:

Stream 1, Inlet Temp(F.)         100 (170 to 200 F. to
                                 Fractionator preferable)
Pressure (psig)                  100 to 120 Stream 1
Fractionator overhead Presssure(psig) 75 to 100
LHSV (hr)−1                      Reactor 2 to 10 (preferably 4
                                 for each reactor)
Reactor Pressure (psig)          370 to 400
Reactor Temperature (F.)         250 to 300
Conversion                       >95% to Octene
Purity Octene                    >95% (can be improved by
                                 removal of trimers by distillation)

FIG. 2

Feed to Debutanizer Reactor      185 to 200 F. (based on the
                                 temperature profile in the column)
Pressure overhead of Debutanizer 300 to 400
Reactor Column (psig)
Pressure Octene Column (psig)    60 to 100

Reaction Chemistry

Claims

1. A Process for producing Octene/Octene-1 Comprising: A) As per art of claim 1, providing an adsorption bed for removal of impurities from the Mixed C4's feed or Ethylene feed which will effect the catalyst life and process economics.B) As per art of claim 1, FIG. 1, the effluent from the adsorption bed is fed to Fractionator after heating with octene product. The Fractionator operates at optimum pressure of 60 100 psig which is optimum for distillation. It provides low energy and low capital cost.C) As per art of claim 1, FIG. 1, the side draws are drawn from the fractionator where maximum amounts of n-butene are present in the fractionator. Each side draw is pumped to the reactor temperature of 350 to 400 psig and heated to 250 to 300 F and is fed to the reactor. The effluent product is essentially Octene, where n-butene has been converted to the order of 85 to 95%. This is fed to the fractionator for separation where Octene is taken as bottom product and C4 raffinate is taken as overhead product.D) As per FIG. 1, this multistage of reactor with separation provide low cost highly selective and high yield process, with high purity. As mentioned this purity can be improved by further distillation if so required.

2. The method of claim 1, A) Where as in the art of this invention unique configuration per FIG. 1, is being used to take the Ethylene feed and convert that to Octene as stated in the description of the FIG. 2 to produce Octene-1.B) As per art of claim 1, the reactor in the FIG. 1 could be up flow or down flow and could be single or two phase for the n-butene Feed case and for Ethylene it will be vapor phase reactor.C) As per art of claim 1, FIG. 1, the multistage reactor system is unique to the process for low cost and high selectivity for Octene/Octene-1 production, from n-butene or Ethylene Feed.

3. The method of claim 3, A) The method of claim 3, where in the art of the invention, it is claimed the technique and configuration of FIG. 2, where the multiple bulk catalyst beds are installed so as to take the feed from adsorber bed after heating is fed to the Debutanizer reactor Column, and the reaction and separation are done alternately, so as to provide low cost system and high selectivity. The FIG. 2 also provides high conversion and yields.B) The method of claim 3, where in the art of invention provides the method to install the bulk catalyst without using cumbersome catalyst packaging. The mixed octene product/C4 mix is taken to Octene column for separation.C) The catalyst is Zeolite, Zeolite/Pt or any other catalyst that is available in the market for this service. The process is not limited to the Zeolite catalyst use.