{ "id": "epk42e27ea", "slug": "transalkylation", "title": "Transalkylation", "updated": "2026-10-15", "topic_path": [ { "id": "physical", "label": "Physical world and mathematics", "api_url": "https://www.edgepedia.org/api/v1/topics/physical" }, { "id": "physical.chemistry", "label": "Chemistry", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry" }, { "id": "physical.chemistry.methods", "label": "Chemical principles and methods", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry.methods" }, { "id": "physical.chemistry.methods.chemical-synthesis", "label": "Chemical synthesis", "api_url": "https://www.edgepedia.org/api/v1/topics/physical.chemistry.methods.chemical-synthesis" } ], "geo": [ { "id": "geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis", "label": "Non-geographic · 1946 to 2000: Chemical synthesis", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis", "path": [ { "id": "geo.nongeo", "label": "Non-geographic", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo" }, { "id": "geo.nongeo.t1946", "label": "Non-geographic · 1946 to 2000", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946" }, { "id": "geo.nongeo.t1946.physical", "label": "Physical world and mathematics", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical" }, { "id": "geo.nongeo.t1946.physical.chemistry", "label": "Chemistry", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry" }, { "id": "geo.nongeo.t1946.physical.chemistry.methods", "label": "Chemical principles and methods", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry.methods" }, { "id": "geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis", "label": "Chemical synthesis", "api_url": "https://www.edgepedia.org/api/v1/geo/geo.nongeo.t1946.physical.chemistry.methods.chemical-synthesis" } ] } ], "excerpt": "Transalkylation is a catalytic reaction that transfers an alkyl group from one aromatic molecule to another, used industrially to convert toluene and C9 aromatics into benzene and xylenes.", "snippet": "Transalkylation is a catalytic reaction that transfers an alkyl group from one aromatic molecule to another, used industrially to convert toluene and C9 aromatics into benzene and xylenes.", "node": "physical.chemistry.methods.chemical-synthesis", "markdown": "# Transalkylation\n\nTransalkylation is a catalytic reaction that transfers an alkyl group from one aromatic molecule to another, used in petroleum refining to convert surplus alkylbenzenes, chiefly toluene and C9+ aromatics, into benzene and mixed xylenes.[1](https://cdn.ihs.com/www/pdf/RP25E-toc.pdf) The reaction is run industrially over solid acid zeolite (microporous crystalline mineral used as industrial catalyst) catalysts at 400–450 °C under hydrogen, and it is coupled with disproportionation, in which two molecules of the same alkylbenzene exchange alkyl groups.[2](https://portfolio-pplus.com/TechnologyTypes/Details/116)\n\n| Key fact | Value |\n|---|---|\n| Main products | Mixed xylene (>98 wt% C8) and high-purity benzene (>99.9 wt%)[1](https://cdn.ihs.com/www/pdf/RP25E-toc.pdf) |\n| Product slate | Toluene disproportionation: 41.4 wt% benzene, 56.1 wt% xylene; with 25% trimethylbenzenes in feed: 25.2 wt% benzene, 71.6 wt% xylene[2](https://portfolio-pplus.com/TechnologyTypes/Details/116) |\n| Typical conditions | 400–450 °C, 3 MPa, H2:hydrocarbon 6–10 mol/mol, space velocity about 1.0 h⁻¹[2](https://portfolio-pplus.com/TechnologyTypes/Details/116) |\n| Per-pass conversion | Normally controlled at 40–50 wt%[3](https://doi.org/10.1002/9783527827992.ch16) |\n| Equilibrium limit | Para-xylene is 24% of the equilibrium xylene mixture[4](https://www.aidic.it/cet/17/57/158.pdf) |\n| First commercial unit | Toray Kawasaki plant, summer 1969[5](https://www.jstage.jst.go.jp/article/jpi1959/13/1/13_1_116/_pdf) |\n| Catalysts | Mordenite, Y, Beta, ZSM-5, MCM-22, NU-87, and related zeolites[4](https://www.aidic.it/cet/17/57/158.pdf) • [6](https://pubs.acs.org/doi/abs/10.1021/acscatal.9b00763) • [7](https://www.sciencedirect.com/science/article/abs/pii/S0021951717303664) |\n\n## How it works\n\nTransalkylation moves an alkyl group, usually a methyl group, from one aromatic ring to another over a Brønsted acid site. Two mechanistic pictures describe the chemistry. In one, the alkyl group transfers through dealkylation–alkylation steps with surface alkoxy species as intermediates; in the other, two aromatic rings stay connected through bulkier diaryl intermediates.[6](https://pubs.acs.org/doi/abs/10.1021/acscatal.9b00763) Experimental and theoretical work on toluene transalkylation with 1,2,4-trimethylbenzene identifies diphenylmethane derivatives (2mDPM, 3mDPM, 4mDPM) as the main intermediates and supports a bimolecular, diphenylmethane-mediated mechanism.[7](https://www.sciencedirect.com/science/article/abs/pii/S0021951717303664)\n\nPore architecture decides which pathway dominates. ZSM-5, a medium-pore 10-ring zeolite, is active for ethylbenzene dealkylation but hinders toluene and ethylbenzene disproportionation because the bulky diphenylmethane-type intermediate does not fit, while large-pore Y and mordenite allow it.[8](https://digital.csic.es/bitstream/10261/290381/1/Xylene_isomerization_SHI_postprint.pdf) DFT calculations show that within MWW-type materials (MCM-22, DS-ITQ-2) the diaryl intermediates are better stabilized in the 10-ring channel system than at the external \"cups\", which explains their higher low-temperature activity compared with ZSM-5.[6](https://pubs.acs.org/doi/abs/10.1021/acscatal.9b00763) This surface-mediated behavior distinguishes zeolites from homogeneous Friedel–Crafts systems, where AlCl3 coordination produces a relatively free carbocation in the bulk liquid.[9](https://www.mdpi.com/2624-781X/7/1/20)\n\n## How it is done\n\nIn the industrial flow scheme, feed toluene mixed with C9 aromatics is carried with makeup and recycle hydrogen, heated first in an exchanger and then in a furnace, and passed through a single adiabatic fixed-bed reactor.[5](https://www.jstage.jst.go.jp/article/jpi1959/13/1/13_1_116/_pdf) The effluent goes to a product separator, from which hydrogen-rich gas is recycled with a purge, and a stripper column removes dissolved light gases. Reference operating conditions are 3 MPa, 400–450 °C, an H2:hydrocarbon mole ratio of 6–10, space velocity about 1.0 h⁻¹, and recycle gas with at least 70 mol% hydrogen.[2](https://portfolio-pplus.com/TechnologyTypes/Details/116) A UOP patent describes the applicable window more broadly, 200–480 °C and up to 1500 psig for C7–C15 alkylaromatics, with ring loss of 0.37–1.07 mol% across catalyst examples.[10](https://www.freepatentsonline.com/4300012.html)\n\nHydrogen is present even though the transalkylation reaction itself consumes none; net hydrogen consumption arises from dealkylation and hydrocracking side reactions. The hydrogen also suppresses coke: at lower H2/feed ratios more coke forms on the catalyst, so a ratio above 5 is desirable, while higher severity per pass increases ring loss and lowers overall yield.[5](https://www.jstage.jst.go.jp/article/jpi1959/13/1/13_1_116/_pdf)\n\n## Origin\n\nT. Tsai published a 1999 review in Applied Catalysis A: General surveying the disproportionation and transalkylation of alkylbenzenes over zeolite catalysts.[11](https://doi.org/10.1016/s0926-860x%2898%2900396-2) A UK patent covering isomerization, transalkylation, and disproportionation of alkylbenzenes over an exchanged zeolite tuff at 300–650 °C gives examples that disproportionate toluene to benzene and xylenes at 450 °C and 30 kg/cm² in the presence of hydrogen.[12](https://www.freepatentsonline.com/3541174.html) The first commercial plant was built at Toray's Kawasaki site in summer 1969 and ran on-stream for over a year.[5](https://www.jstage.jst.go.jp/article/jpi1959/13/1/13_1_116/_pdf) A flow scheme places the process inside a naphtha-based aromatics complex, and the first UOP-licensed units started at Braskem in Camaçari, Brazil (1978) and Yochun NCC in Yosu, Korea (1980); more than 70 plants have since been designed with over 130 million t/y of aggregate feed capacity.\n\n## Variants\n\nThe Tatoray catalyst line has progressed through generations: TA-1 (1969) was mordenite alone with no metals; the TA-20 series (2004) added a secondary zeolite and a noble metal for stability; TA-30 (2010) used a nanosize UOP zeolite with a non-noble metal, and TA-32, commercialized in 2014, is an optimized formulation of the TA-30 catalyst designed for low to medium severity feeds; and TA-42 (2019) delivers higher xylene yields than TA-30. ExxonMobil's TransPlus 5 is the third generation of its licensed technology, using a co-extruded dual zeolite catalyst with low precious metal content, higher weight hourly space velocity, and an expanded temperature window; first-generation TransPlus catalysts achieved cycle lengths of 7+ years.[13](https://www.exxonmobilchemical.com/en/catalysts-and-technology-licensing/xylenes-production/heavy-aromatics-alkylation) Catalyst acidity matters as well as topology: over HZSM-5 with SiO2:Al2O3 ratios from 30 to 800, the transalkylation rate falls as the ratio rises.[14](https://onlinelibrary.wiley.com/doi/10.1002/jctb.5040340307)\n\n## Applications\n\nThe main application is upgrading toluene, C9, and C10 aromatics in an aromatics complex, where the Tatoray unit often accounts for more than 50% of the mixed xylenes ultimately converted to para-xylene; only very heavy fractions are rejected to avoid coking, with most C9+ species recycled until converted. Product economics depend on the benzene-to-xylene balance: pure toluene disproportionation gives 41.4 wt% benzene and 56.1 wt% xylene, while a 75:25 toluene–trimethylbenzene feed gives 25.2 wt% benzene and 71.6 wt% xylene, so the C9 content tunes the ratio between roughly 0.8:1 and 1:10.[2](https://portfolio-pplus.com/TechnologyTypes/Details/116) [Laboratory](https://www.edgepedia.org/laboratory) data illustrate the catalyst spread: at 400 °C, 1.0 MPa, H2/HC = 4, and WHSV 5 h⁻¹, zeolite Beta at the lowest Si/Al ratio gave 41 wt% conversion with 61 wt% xylene selectivity, while Y zeolites (Si/Al 6–30) gave about 27 wt% conversion and 43 wt% selectivity.[4](https://www.aidic.it/cet/17/57/158.pdf) Pore geometry can outperform the commercial benchmark: H-NU-87, with intersecting 10- and 12-ring channels, gave a 40% xylene yield versus 23% for H-Y at 673 K and retained 31% versus 17% conversion after 30 h on stream.[7](https://www.sciencedirect.com/science/article/abs/pii/S0021951717303664)\n\n## Limitations and alternatives\n\nThree constraints dominate. First, coke: deactivation proceeds through carbon accumulation on the catalyst, managed with hydrogen co-feed and eventual decoking.[5](https://www.jstage.jst.go.jp/article/jpi1959/13/1/13_1_116/_pdf) Second, ring loss: higher severity raises side reactions such as dealkylation and hydrocracking that destroy aromatic rings and consume hydrogen. Third, thermodynamics: within the xylene product the para isomer equilibrates at 24%, and the 12-ring large-pore zeolites tested show virtually no shape selectivity to shift that distribution.[4](https://www.aidic.it/cet/17/57/158.pdf)\n\nAlternatives serve different balances. The CB&I Detol process converts a toluene-rich stream to high-purity benzene, and UOP isomerization converts meta- and ortho-xylenes toward an equilibrium xylene mixture.[1](https://cdn.ihs.com/www/pdf/RP25E-toc.pdf) A lower-temperature liquid-phase route over sulfated Group IVB oxides operates at 110–250 °C without hydrogen, with higher space velocities raising the para-xylene ratio at the expense of conversion.[15](https://patents.google.com/patent/US6593504)\n\n## References\n\n1. [Aromatics Upgrading Technologies (IHS/PEP Report 25E table of contents)](https://cdn.ihs.com/www/pdf/RP25E-toc.pdf)\n2. [Tech-Type: Aromatics Transalkylation and Disproportionation](https://portfolio-pplus.com/TechnologyTypes/Details/116)\n3. [Honeywell UOP Tatoray Process: Maximizing Feed Utilization for Aromatics Production (book chapter, hosted on aggregator)](https://doi.org/10.1002/9783527827992.ch16)\n4. [Transalkylation of Toluene with 1,2,4-Trimethylbenzene over Large Pore Zeolites with Differing Si/Al Ratios (Chemical Engineering Transactions, 2017)](https://www.aidic.it/cet/17/57/158.pdf)\n5. [TATORAY process paper (Journal of the Japan Petroleum Institute, 1969/1970)](https://www.jstage.jst.go.jp/article/jpi1959/13/1/13_1_116/_pdf)\n6. [Control of the Reaction Mechanism of Alkylaromatics Transalkylation by Means of Molecular Confinement Effects Associated to Zeolite Channel Architecture](https://pubs.acs.org/doi/abs/10.1021/acscatal.9b00763)\n7. [Reaction intermediates and mechanism of the zeolite-catalyzed transalkylation of 1,2,4-trimethylbenzene with toluene (Journal of Catalysis, 2018)](https://www.sciencedirect.com/science/article/abs/pii/S0021951717303664)\n8. [Zeolite: Disproportionation and Transalkylation / Xylene isomerization over zeolites (book chapter postprint)](https://digital.csic.es/bitstream/10261/290381/1/Xylene_isomerization_SHI_postprint.pdf)\n9. [Dual Roles of Coke in Fresh and Modified HY Zeolite Catalyzed Aromatic Alkylation (MDPI)](https://www.mdpi.com/2624-781X/7/1/20)\n10. [US4300012, Process for transalkylation of alkylaromatic hydrocarbons (UOP Inc.)](https://www.freepatentsonline.com/4300012.html)\n11. [Disproportionation and transalkylation of alkylbenzenes over zeolite catalysts (Applied Catalysis A General, 1999)](https://doi.org/10.1016/s0926-860x%2898%2900396-2)\n12. [UK Patent 1,254,462, Toray Industries, catalyst in use for transalkylation of alkyl-benzenes (exchanged zeolite tuff)](https://www.freepatentsonline.com/3541174.html)\n13. [Heavy Aromatic Transalkylation, ExxonMobil TransPlus 5](https://www.exxonmobilchemical.com/en/catalysts-and-technology-licensing/xylenes-production/heavy-aromatics-alkylation)\n14. [Transalkylation of toluene with C9 aromatic hydrocarbons over ZSM5 zeolites (J. Chem. Technol. Biotechnol.)](https://onlinelibrary.wiley.com/doi/10.1002/jctb.5040340307)\n15. [US Patent 6,593,504, Selective aromatics transalkylation (copy on aggregator)](https://patents.google.com/patent/US6593504)\n\n---\n*Topic: Encyclopedia › Physical world and mathematics › Chemistry › Chemical principles and methods › Chemical synthesis*\n\n*Initially written Sep 29, 2026 · Edited: Oct 15, 2026*\n\n*Copyright 2026 EdgeChat AI, a subsidiary of Biostate AI.*\n\nLicense: Edgepedia Community License 1.0, https://www.edgepedia.org/edgepedia/license\n", "same_as": [], "url": "https://www.edgepedia.org/transalkylation", "markdown_url": "https://www.edgepedia.org/transalkylation.md", "license": { "name": "Edgepedia Community License 1.0", "url": "https://www.edgepedia.org/edgepedia/license", "summary": "Free with credit, commercial use included. AI training is open to everyone. For other uses, organizations over USD 100M in revenue or 100M monthly users license separately.", "spdx": "LicenseRef-Edgepedia-Community-1.0" }, "credit": "\"Transalkylation\", Edgepedia (EdgeChat), https://www.edgepedia.org/transalkylation. Edgepedia Community License 1.0.", "credit_md": "\"[Transalkylation](https://www.edgepedia.org/transalkylation)\", Edgepedia (EdgeChat), [https://www.edgepedia.org/transalkylation](https://www.edgepedia.org/transalkylation). [Edgepedia Community License 1.0](https://www.edgepedia.org/edgepedia/license).", "credit_html": "\"Transalkylation\", Edgepedia (EdgeChat), https://www.edgepedia.org/transalkylation. Edgepedia Community License 1.0.", "speakable": "Transalkylation is a catalytic reaction that transfers an alkyl group from one aromatic molecule to another, used industrially to convert toluene and C9 aromatics into benzene and xylenes." }