Methane Conversion Moving Bed Reactor System

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Solution Overview

Problem

Current processes for converting methane to higher hydrocarbons, such as aromatic compounds, face challenges including high energy input, thermodynamic limitations, coke formation, catalyst coking, and mechanical stress, which affect efficiency and selectivity.

Innovation Solution

A process involving a reactor system with at least two series-connected reaction zones, where methane is converted to higher hydrocarbons using a catalytic particulate material in a moving bed fashion, with heat management and catalyst regeneration to optimize conditions for high selectivity and minimize coke formation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If dehydroaromatization is used to convert methane to aromatic hydrocarbons, then aromatic hydrocarbon production is achieved, but high energy input and thermodynamic limitations occur

Engineering Contradiction:
Improvearomatic hydrocarbon productionVSAvoidenergy input
Core Design Contradiction:
ProductivityVSUse of energy by moving object

Solution Approach 1:

The reaction system is divided into multiple reaction zones with different temperature profiles. The first reaction zone operates at higher temperature (700-900°C) for initial dehydroaromatization, while the second reaction zone operates at lower temperature (500-700°C) for product stabilization, allowing energy-efficient multi-stage conversion

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The catalyst undergoes periodic regeneration cycles where it is alternately exposed to methane feed for product formation and then to air for coke combustion. This periodic operation maintains catalyst activity while managing the thermodynamic constraints of the endothermic reaction

Inventive Principle:
Principle #19Periodic action

2Productivity

If high temperature is used for methane conversion, then conversion efficiency is improved, but coke formation and catalyst coking increase

Engineering Contradiction:
Improvemethane conversion efficiencyVSAvoidcoke formation
Core Design Contradiction:
ProductivityVSObject-generated harmful factors

Solution Approach 1:

The coke that forms on the catalyst at high temperature is converted into a beneficial process feature: during catalyst regeneration, the coke combusts exothermically to produce heat that is used to preheat the methane feed and maintain reaction temperature, turning a harmful byproduct into a useful energy source

Inventive Principle:
Principle #22Blessing in disguise (Convert harm into benefit)

Solution Approach 2:

The system dynamically adjusts operating parameters including temperature, pressure, and space velocity to optimize conversion while minimizing coke. The temperature profile is carefully controlled to stay below thresholds that promote excessive coking while maintaining adequate conversion rates

Inventive Principle:
Principle #35Parameter changes

3Productivity

If catalyst circulation rate is increased to maintain activity, then conversion efficiency is maintained, but mechanical stress on catalyst increases

Engineering Contradiction:
Improveconversion efficiencyVSAvoidcatalyst mechanical stress
Core Design Contradiction:
ProductivityVSStrength

Solution Approach 1:

The catalyst circulation system is designed with dynamic control where the circulation rate is adjusted based on real-time monitoring of catalyst activity and product composition. This allows maintenance of conversion efficiency while minimizing unnecessary catalyst movement and associated mechanical stress

Inventive Principle:
Principle #15Dynamics

4Device complexity

If single reaction zone is used for simplicity, then device complexity is reduced, but heat transfer and selectivity are insufficient

Engineering Contradiction:
Improvereactor system structureVSAvoidselectivity
Core Design Contradiction:
Device complexityVSManufacturing precision

Solution Approach 1:

The reaction system is segmented into multiple zones with distinct temperature and pressure conditions. The first zone favors dehydroaromatization while the second zone optimizes for product stability and minimizes secondary reactions, achieving high selectivity through spatial differentiation of reaction conditions

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 enhances the efficiency of methane conversion to aromatic hydrocarbons by improving heat transfer, hydrocarbon-catalyst contacting, and selectivity while reducing coke formation and catalyst circulation rates, thereby extending catalyst life and reducing mechanical stress.

Implementation Method 1

converting methane to higher hydrocarbon(s) using a catalytic particulate material

Methodology Applied
Scientific EffectCatalysis: Catalysis

Implementation Method 2

improving heat transfer

Methodology Applied
Scientific EffectHeat transfer: Conduction (thermal)

Implementation Method 3

with heat management and catalyst regeneration to optimize conditions

Methodology Applied
Scientific EffectThermal management: Convection

Data Source

PatentUS7888543B2Process for methane conversion
Publication Date: 2011.02.15 EXXONMOBIL CHEMICAL PATENTS INC
  • US7888543B2 patent drawing
  • US7888543B2 patent drawing
  • US7888543B2 patent drawing

AI summary

A process for converting methane to higher hydrocarbon(s) including aromatic hydrocarbon(s) comprises providing a hydrocarbon feedstock containing methane and a catalytic particulate material to a reactor system having at least first and second reaction zones connected in series. Each of the reaction zones is operated under reaction conditions sufficient to convert at least a portion of the methane to said higher hydrocarbon(s) and is maintained in a moving bed fashion, with the bulk of the catalytic particulate material being moved from the first reaction zone to the second reaction zone and with the bulk of the hydrocarbon feedstock being moved from the second reaction zone to the first reaction zone.