Xylene Isomerization Process and Catalyst Therefor

a technology of isomerization process and catalyst, which is applied in the direction of hydrocarbon preparation catalyst, physical/chemical process catalyst, bulk chemical production, etc., can solve the problems of complex process arrangement and high cost, and achieve the effect of convenient determination by electron microscopy

Active Publication Date: 2016-02-11
EXXONMOBIL CHEM PAT INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The process achieves high paraxylene yields with low byproduct formation and reduced catalyst deactivation, even in the presence of impurities like phenol and styrene, while operating without the need for high hydrogen pressure, resulting in a cost-effective and simple process.

Problems solved by technology

Most isomerization technologies also require high hydrogen partial pressure to maintain the catalyst activity, which makes the process arrangement complex and expensive.
The presence of such impurities are believed to be detrimental to numerous downstream processing steps in the conversion of paraxylene to polyester fibers and resins.

Method used

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  • Xylene Isomerization Process and Catalyst Therefor
  • Xylene Isomerization Process and Catalyst Therefor

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0054]Three ZSM-5 crystals listed below in Table 1 were prepared to investigate the effects of silica / alumina ratio and crystal size in a process according to the present invention.

TABLE 1Crystal Sizes,ZSM-5 CrystalsSiO2 / Al2O3 RatiosmicronI250.5II60III25

[0055]The crystals were ion exchanged to proton form and extruded into 1 / 20″ (about 0.127 cm) extrudates with an alumina binder. The weight ratio of crystal to binder was 4. The extrudates were calcined at 538° C. The extrudates were evaluated using a feed of 13.28 wt % para-xylene, 63.72 wt % meta-xylene, 17.94 wt % ortho-xylene, 1.52 wt % ethylbenzene, 1.28 wt % toluene, and 2.25 wt % non-aromatics, and low levels of benzene and nine-carbon aromatic compounds. The tests were performed in a ¼″ (about 0.635 cm) stainless steel reactor with the feed going up flow through the catalyst bed. Test conditions are listed below in Table 2.

TABLE 2Flowrate, WeightCatalystReactorReactorHourly SpaceCrystalsloading, gtemp., ° C.pressure, psigVelo...

example 2

[0057]Two parallel runs were conducted to investigate the effect of feed contaminants phenol and styrene on liquid phase isomerization. Catalyst was 1 / 20″ (about 0.127 cm) catalyst extrudates prepared from Catalyst III. Run #1 used Test Feeds and Run #2 used Reference Feeds (free of styrene and phenol). Typical compositions of the two feeds are 3.6-4.7 wt % paraxylene, 57.9-60.4 wt % metaxylene, 24.8-26.0 wt % orthoxylene, 8.7-9.5 wt % ethylbenzene, 0.15-0.19 wt % toluene, 1.2-2.8 wt % non-aromatics, and low levels of benzene and nine-carbon aromatic compounds. Test Feeds contained 20 ppm styrene and 2 ppm phenol.

[0058]Performance tests were conducted in a ¼″ (0.635 cm) stainless steel reactor with the feed going up flow through a catalyst bed. Test conditions are listed below in Table 3.

TABLE 3ReactorFlowrate, WeightCatalystReactorpressure,Hourly Spaceloading, gtemp., ° C.psigVelocityRun #1 with0.5056235, 2552651.5-2.6Test FeedRun #2 with0.5150235, 2552651.8-2.5Reference Feed

[0059]...

example 3

[0060]The following experiments were run using the preferred catalyst of the invention on various feedstreams (Table 4) at the same conditions, including a temperature of 255° C. and 2.1 hr−1 (WHSV). Experiments were run in a micro-unit; “PX concentration decrease (%)” is paraxylene decrease relative to other C8 aromatic hydrocarbons in the product versus feed, and are extrapolations based on observed trends for six months (run 1 and 2), one week (run 3), and 2 weeks (2 weeks).

TABLE 4RunPhenol, ppmStyrene, ppmPX concentration decrease (%)1000 (i.e. no deactivation)2220032434.344204.7

[0061]Two styrene concentrations studied were 20 and 43.2 wppm. The temperature of testing was 255° C. for both feeds. Catalyst aging data showed that with 43.2 wpm styrene in the feed, the LPI catalyst deactivated at a rate of 4.3% decrease in PX yield per year (Table 1).

[0062]Two phenol concentrations studied were 2 and 4 wppm. Temperatures of testing were 255 and 275° C. for the 2 wppm phenol feed, an...

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Abstract

The invention concerns a xylenes isomerization process for the production of equilibrium or near-equilibrium xylenes from a feedstream comprising phenol and / or styrene.

Description

CROSS REFERENCE TO RELATED APPLICATIONS[0001]This application claims priority to and the benefit of Provisional Application No. 61 / 695,493, filed on Aug. 31, 2012.FIELD OF THE INVENTION[0002]The invention relates to a xylene isomerization process and catalyst therefor.BACKGROUND OF THE INVENTION[0003]An equilibrium mixture of xylenes contains about 24 wt % paraxylene (PX), 56 wt % metaxylene (MX), and 20 wt % orthoxylene (OX). PX is relatively high value as compared with MX and OX, since it is a starting material for polyester fibers and resins. Therefore it is advantageous to isomerize OX and / or MX to PX, such as isomerizing a PX-lean stream (i.e., depleted from equilibrium value) to equilibrium for PX recovery. It is an active area of research.[0004]Typically, xylene streams found in chemical or petrochemical plants also contain ethylbenzene (EB). Conventional isomerization technologies operating at high temperatures (e.g., 400° C.) in vapor phase isomerize the xylenes and dealkyl...

Claims

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Application Information

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Patent Type & AuthorityApplications(United States)
IPC IPC(8): C07C5/27
CPCC07C2529/40C07C5/2737Y02P20/52C07C15/08B01J29/7038
InventorOU, JOHN DI-YILUO, SHIFANG L.JAIN, SURBHI
OwnerEXXONMOBIL CHEM PAT INC