Integrated Para-Xylene Production Process

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Solution Overview

Problem

Current methods for producing xylenes from reformate in aromatics complexes are inefficient, as they do not effectively recycle benzene and toluene, leading to reduced xylenes production and catalyst deactivation due to inert C10+ aromatic hydrocarbons.

Innovation Solution

A method and system that includes a dealkylation reactor to convert C9+ aromatic hydrocarbons to C6-C8 hydrocarbons, followed by a transalkylation reactor with separate units for dealkylation and transalkylation reactions, and a p-xylene separation unit, optimizing the production of para-xylene by recycling streams and maintaining specific reaction conditions.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Device complexity

If a single reactor is used for both dealkylation and transalkylation reactions, then device complexity is reduced, but manufacturing precision and reaction optimization are compromised

Engineering Contradiction:
Improvereactor configurationVSAvoidreaction optimization
Core Design Contradiction:
Device complexityVSManufacturing precision

Solution Approach 1:

The process is divided into two separate reactors: a first reactor dedicated to dealkylation reactions and a second reactor dedicated to transalkylation reactions. This segmentation allows each reactor to be optimized for its specific function, with tailored catalysts, temperature profiles, and residence times, thereby resolving the contradiction between device simplicity and reaction optimization precision.

Inventive Principle:
Principle #1Segmentation

2Productivity

If C10+ aromatic hydrocarbons are not removed from the transalkylation reactor, then productivity is maintained, but catalyst activity decreases due to deactivation

Engineering Contradiction:
Improvexylenes productionVSAvoidcatalyst activity
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

Dealkylation reactions are performed in the first reactor before the transalkylation reactions in the second reactor. This preliminary action removes C10+ aromatic hydrocarbons and converts them to C9 aromatics, preventing catalyst deactivation in the transalkylation reactor while maintaining continuous xylenes production through the sequential reaction pathway.

Inventive Principle:
Principle #10Preliminary action

3Device complexity

If benzene and toluene are not recycled in the process, then process complexity is reduced, but xylenes production decreases

Engineering Contradiction:
Improverecycle systemVSAvoidxylenes production
Core Design Contradiction:
Device complexityVSProductivity

Solution Approach 1:

Benzene and toluene streams are recycled back to the transalkylation reactor where they participate in further reactions to produce additional xylenes. This feedback loop maximizes the utilization of aromatic hydrocarbons and increases overall xylenes yield, justifying the added complexity of the recycle system through improved productivity.

Inventive Principle:
Principle #23Feedback

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

This approach increases xylenes production by reducing C10+ aromatic hydrocarbons in the transalkylation reactor, prolonging catalyst activity, and optimizing each unit's performance for specific reactions, resulting in higher yields and improved process efficiency.

Implementation Method 1

a dealkylation reactor to convert C9+ aromatic hydrocarbons to C6-C8 hydrocarbons

Methodology Applied
Scientific EffectDealkylation reaction: Chemical Transport Reactions

Implementation Method 2

a transalkylation reactor with separate units for dealkylation and transalkylation reactions

Methodology Applied
Scientific EffectTransalkylation reaction: Chemical Transport Reactions

Implementation Method 3

converting the m-xylene and o-xylene in the p-xylene depleted stream in the isomerization unit to produce an isomerization effluent

Methodology Applied
Scientific EffectIsomerization reaction: Chemical Transport Reactions

Data Source

PatentUS11618723B2Integrated process for optimum production of para-xylene
Publication Date: 2023.04.04 SAUDI ARABIAN OIL CO
  • US11618723B2 patent drawing
  • US11618723B2 patent drawing
  • US11618723B2 patent drawing

AI summary

A method of producing p-xylene comprising the steps of separating the reformate feed in the reformate splitter to produce a benzene stream, a combined heavy stream, a xylene stream, and a toluene stream, converting the C9+ aromatic hydrocarbons in the presence of a dealkylation catalyst in the dealkylation reactor to produce a dealkylation effluent, separating the dealkylation effluent in the dealkylation splitter to produce a C9 stream and a C10+ stream, reacting the C9 stream, the toluene stream, the benzene stream, and the hydrogen stream in the presence of a transalkylation catalyst in the transalkylation reactor to produce a transalkylation effluent, separating the p-xylenes from the xylene stream in the p-xylene separation unit to produce a p-xylene product and a p-xylene depleted stream, converting the m-xylene and o-xylene in the p-xylene depleted stream in the isomerization unit to produce an isomerization effluent.