Aromatic Hydrocarbon Production via Segmented Zeolite Reactors

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Solution Overview

Problem

Existing methods for producing aromatic hydrocarbons from light aliphatic hydrocarbons face challenges such as low yield and selectivity, catalyst deactivation, and increased energy costs due to inefficient temperature control and feedstock recycling, particularly in processes using pentasil-based zeolite catalysts.

Innovation Solution

The method involves separating gaseous fractions into hydrogen-containing gas and natural gas liquids containing olefins, using these gases to synthesize oxygenates which are then fed back into reactors with pentasil-based zeolite catalysts, maintaining optimized temperatures, and using a catalyst composition with specific zeolite ratios and modifications to enhance aromatic hydrocarbon production and catalyst longevity.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If the mixed feedstock is brought into contact with the catalyst at high temperature to address less reactive feedstock components, then propane and ethane conversion is improved, but the coking rate increases and catalyst life is reduced

Engineering Contradiction:
Improvepropane and ethane conversionVSAvoidcatalyst life
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

The reaction process is divided into two separate reaction zones with different temperature conditions. The first zone operates at higher temperature (450-550°C) to convert less reactive ethane and propane, while the second zone operates at lower temperature (400-500°C) to convert butane and propylene, thereby preventing excessive coking in any single zone and extending catalyst life.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

Different temperature conditions are applied to different sections of the reaction system. The first reaction zone uses higher temperature to address less reactive components, while the second zone uses lower temperature to minimize coking, creating locally optimized conditions for each feedstock component.

Inventive Principle:
Principle #3Local quality

2Reliability

If the mixed feedstock is brought into contact with the catalyst at lower temperature, then coking rate is reduced, but propane and ethane conversion is insufficient

Engineering Contradiction:
Improvecatalyst lifeVSAvoidpropane and ethane conversion
Core Design Contradiction:
ReliabilityVSProductivity

Solution Approach 1:

The reaction system is segmented into two zones with different temperature profiles. The first zone provides higher temperature (450-550°C) necessary for propane and ethane conversion, while the second zone operates at lower temperature (400-500°C) to reduce coking, thus achieving both high conversion and extended catalyst life.

Inventive Principle:
Principle #1Segmentation

3Productivity

If feedstock recycling is implemented to increase conversion, then unconverted feedstock is reused, but energy costs increase and equipment volume increases

Engineering Contradiction:
Improvefeedstock conversion efficiencyVSAvoidenergy costs
Core Design Contradiction:
ProductivityVSUse of energy by stationary object

Solution Approach 1:

The system dynamically adjusts the split of feedstock between the two reaction zones based on composition and conversion requirements, optimizing the use of each feedstock component in real-time without requiring extensive recycling, thereby reducing energy costs while maintaining high conversion efficiency.

Inventive Principle:
Principle #15Dynamics

4Device complexity

If a single reaction zone is used for converting all feedstock components, then the process is simpler, but conversion efficiency of different components cannot be optimized

Engineering Contradiction:
Improveprocess simplicityVSAvoidconversion efficiency
Core Design Contradiction:
Device complexityVSProductivity

Solution Approach 1:

The reaction system is divided into two zones with different temperature conditions optimized for different feedstock components. The first zone (450-550°C) optimizes conversion of ethane and propane, while the second zone (400-500°C) optimizes conversion of butane and propylene, achieving high overall conversion efficiency while maintaining reasonable process complexity.

Inventive Principle:
Principle #1Segmentation

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 the yield and selectivity of aromatic hydrocarbons, particularly alkylbenzenes, while extending catalyst life and reducing energy consumption by maintaining adiabatic conditions and avoiding local catalyst superheating, thus improving the overall efficiency of the process.

Implementation Method 1

the feedstock is fed to two serially connected reactors, a first and second with pentasil-based zeolite catalysts, which differ in the conditions of conversion of aliphatic to aromatic hydrocarbons

Methodology Applied
Scientific EffectCatalysis: Catalysis

Implementation Method 2

maintaining adiabatic conditions and avoiding local catalyst superheating

Methodology Applied
Scientific EffectAdiabatic heating: Adiabatic Heating

Data Source

PatentUS10550331B2Method of producing aromatic hydrocarbon concentrate from light aliphatic hydrocarbons, and installation for implementing same
Publication Date: 2020.02.04 UNIVERSAL FUEL TECHNOLOGIES INC
  • US10550331B2 patent drawing
  • US10550331B2 patent drawing

AI summary

A method and an installation for producing a concentrate of aromatic hydrocarbons from light aliphatic hydrocarbons and from mixtures thereof with oxygenates. Initial raw material is fed into two in-series-connected reaction units, with zeolite catalysts a mixture obtained following the reaction units is separated into a liquid fraction and a gas fraction, and the gas fraction is fed to the inlet of the first and second reaction unit. The method is characterized in that the gas fraction obtained following the reaction units is separated into a hydrogen-containing gas and into a broad fraction of light hydrocarbons, containing olefins, and in that the hydrogen-containing gas is fed into an oxygenate synthesis unit, in that the resultant oxygenates are fed to the inlet of the first and second reaction unit, and in that the broad fraction of light hydrocarbons, containing olefins, is fed to the inlet of the first reaction unit.