Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Aromatics transalkylation to ethylbenzene and xylenes

a technology of ethylbenzene and xylene, which is applied in the direction of hydrocarbons, chemistry apparatus and processes, organic chemistry, etc., to achieve the effects of increasing the selectivity of xylenes, promoting methyl-group species transalkylation, and reducing the overall yield of valuable xylenes

Inactive Publication Date: 2005-09-29
BOGDAN PAULA L +2
View PDF16 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0010] Accordingly, one embodiment of the present invention is directed to a process using transalkylation catalysts to covert heavy aromatic compounds of carbon number nine (and heavier carbon numbers), otherwise called C9+ alkylaromatics, with benzene to form carbon number eight aromatics. The catalyst system preserves ethyl-group species on the heavier aromatics that are otherwise de-ethylated over most gas-phase transalkylation catalysts to form undesired ethane gas with benzene or toluene. The catalyst system also promotes methyl-group species transalkylation at conditions of at least partial liquid phase to directly and economically produce valuable xylenes. Such a liquid phase process offers obvious advantages over a gas phase process in capital requirements, such as the elimination of a phase separator vessel and a recycle gas compressor.
[0011] In another embodiment of the present invention, a process for transalkylation of benzene and C9+ alkylaromatics is integrated with a separate transalkylation process. The integrated process increases selectivity to xylenes by addressing the preservation of ethylbenzene in a first transalkylation unit that would otherwise be lost in a second transalkylation unit, which results in a higher overall yield of valuable xylenes from both units. Preferably, the first transalkylation unit is substantially liquid phase, while the second separate transalkylation process is substantially gas phase.
[0012] In yet another embodiment of the present invention, a greater yield of para-xylene or other carbon number eight aromatics may be achieved overall within an integrated aromatics complex using a para-xylene production unit.

Problems solved by technology

Xylenes and benzene are produced from petroleum by reforming naphtha but not in sufficient volume to meet demand, thus conversion of other hydrocarbons is necessary to increase the yield of xylenes and benzene.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Aromatics transalkylation to ethylbenzene and xylenes
  • Aromatics transalkylation to ethylbenzene and xylenes

Examples

Experimental program
Comparison scheme
Effect test

example i

[0032] An increased selectivity to A8s at the expense of light ends has been demonstrated in pilot plant tests and is shown in the following material balance comparison. The prior art, gas-phase transalkylation process, is compared against the present invention, which combines a liquid-phase transalkylation process with a gas-phase process. This comparison shows the benefits of the present invention as increased xylenes and ethylbenzene, and concomitantly decreased benzene and light-end gas (especially ethane). By reducing the production of ethane by de-ethylation in gas-phase reactions within an aromatics complex, the invention provides improved total retention of aromatics relative to prior art transalkylation units used in complexes that produce xylenes.

[0033] With reference to the FIGURE, showing the flow scheme of the present invention, a simulated material balance is shown below. The liquid-phase transalkylation process unit is combined with the gas-phase transalkylation proc...

example ii

[0035] The unexpected transalkylation of methyl groups along with ethyl groups at the expense of light ends has been demonstrated in pilot plant tests with cylindrical down-flow liquid-phase reactors operated at a pressure of about 35 kg / cm2 and is shown in the following results. A stream of A9+ comprising about 75-wt% A9 and about 25 wt-% A10 with an endpoint around 200° C., contacted one of two catalysts comprising a zeolitic aluminosilicate of type Y or type Beta. A pure benzene stream was combined and fed to each catalyst in a different molar ratio with a A9+ stream. These results are summarized in the following table:

CatalystYBetaTemperature (° C.)250250WHSV (hr−1)9.59.5Benzene / Ag+4.31.1(mol / mol)Product Net Wt-%Ethylbenzene4.45.7Toluene5.47.2Xylenes3.34.2Non-Aromatics0.20.3Heavies1.42.5Benzene + A9 + A10 &4.9 (7.8)20.3 (18)(Tri-methylbenzene)conversion

[0036] Thus, the present invention provides a benefit by directly producing more of the desirable xylenes material and indirec...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
temperatureaaaaaaaaaa
temperatureaaaaaaaaaa
molar ratioaaaaaaaaaa
Login to View More

Abstract

The use of transalkylation catalysts to react heavy aromatic compounds of carbon number nine (and heavier carbon numbers) with benzene to form carbon number eight aromatics is disclosed. The catalyst system preserves ethyl-group species on the heavier aromatics that are otherwise de-ethylated over most gas-phase transalkylation catalysts to form undesired ethane gas with benzene or toluene. The catalyst system also promotes methyl-group species transalkylation at selected conditions. Thus, by using the transalkylation system, a greater yield of para-xylene or other carbon number eight aromatics may be achieved overall within an integrated aromatics complex.

Description

CROSS-REFERENCE TO RELATED APPLICATION [0001] This application is a Division of copending application Ser. No. 10 / 461,138 filed Jun. 13, 2003, the contents of which are hereby incorporated by reference in its entirety.FIELD OF THE INVENTION [0002] This invention relates to an improved process for the conversion of aromatic hydrocarbons. More specifically, the present invention concerns a liquid-phase process for transalkylation of benzene with C9+ alkylaromatics to directly obtain xylenes and ethylbenzene that would otherwise be lost via de-alkylation to benzene or toluene in a conventional gas-phase transalkylation process. The invention also increases yields of xylenes when combined with another transalkylation and / or isomerization process. BACKGROUND OF THE INVENTION [0003] The xylene isomers are produced in large volumes from petroleum as feedstocks for a variety of important industrial chemicals. The most important of the xylene isomers is para-xylene, the principal feedstock f...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(United States)
IPC IPC(8): C07C5/22C07C5/27C07C6/12
CPCC07C6/126C07C15/073C07C15/08
Inventor BOGDAN, PAULA L.JAMES, ROBERT B. JR.MAHER, GREGORY F.
Owner BOGDAN PAULA L
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products