Uop Lcc

James F Himes

Michael Z Mikulicz

Terry L Marker

Joseph A Kocal

Harold U Hammershaimb

Robert J Cornish

An HF-agent complex, such as HF-pyridine complex where the complexing agent is pyridine, is recovered and recycled from a by-product stream containing ASO, and ASO is rejected from the by-product stream, in an alkylation process using the complex.

Alkylation process with separate rejection of light and heavy acid

An HF-agent complex, such as HF-pyridine complex where the complexing agent is pyridine, is recovered and recycled from a by-product containing stream in an alkylation process using the complex by (a) selectively removing a portion of the HF from the by-product stream to produce an HF-depleted stream having a molar ratio of HF per Lewis base site of the complexing agent of 3:1 to 5:1, (b) separating the resulting HF-depleted stream into a hydrocarbon phase enriched in ASO and an acid phase depleted in ASO and containing a substantial portion of the complex, and (c) recycling the acid phase to the hydrocarbon alkylation step.

Recovery and recycle of HF-amine complex in HF alkylation

A process is disclosed for the production of alkylaromatic hydrocarbons by the HF-catalyzed reaction of an aromatic hydrocarbon with a C.sub.8 -plus acyclic olefin. The production of linear alkylbenzenes is preferred. The HF is regenerated in a regeneration column in which high boiling compounds are removed from the HF fed to the column. The main stream of HF enters an upper intermediate point in the regeneration column. A second portion of the HF is fed to the top of the regeneration column as reflux. This second portion of HF is withdrawn from the reaction zone rather than from the overhead receiver of the HF regeneration column as in the prior art regeneration method.

HF regeneration in aromatic hydrocarbon alkylation process

A process is disclosed for the alkylation of an aromatic hydrocarbon with an olefin-acting alkylating agent. The aromatic hydrocarbon is commingled with a first portion of said alkylating agent in a first alkylation reaction zone at alkylation reaction conditions in contact with a hydrofluoric acid catalyst. The acid phase of the effluent from the first alkylation reaction zone is separated, and the hydrocarbon phase, comprising alkylate and unreacted aromatic hydrocarbon is commingled with a second portion of said alkylating agent at alkylation reaction conditions in a second alkylation reaction zone in contact with a hydrofluoric acid catalyst separately charged thereto, the hydrofluoric acid catalyst being that separated from the effluent of the first alkylation reaction zone. The acid phase is separated from the effluent from the second alkylation reaction zone and recycled to the first alkylation reaction zone, and the alkylate product is recovered from the hydrocarbon phase.

Alkylation process

A process is disclosed for the alkylation of an isoparaffinic hydrocarbon with an olefin-acting alkylating agent. The isoparaffinic hydrocarbon is commingled with a first portion of said alkylating agent in a first alkylation reaction zone at alkylation reaction conditions in contact with a hydrofluoric acid catalyst. The acid phase of the effluent from the first alkylation reaction zone is separated, and the hydrocarbon phase, comprising alkylate and unreacted isoparaffin, is commingled with a second portion of said alkylating agent at alkylation reaction conditions in a second alkylation reaction zone in contact with a hydrofluoric acid catalyst separately charged thereto, the hydrofluoric acid catalyst being that separated from the effluent of the first alkylation reaction zone. The acid phase is separated from the effluent from the second alkylation reaction zone and recycled to the first alkylation reaction zone, and the alkylate product is recovered from the hydrocarbon phase.

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Mt. Prospect, IL, United States of America

James F Himes