Isoolefin Production via Cocurrent Gas-Phase Cleavage

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Solution Overview

Problem

The existing processes for producing isoolefins, such as isobutene, through the cleavage of alkyl tert-alkyl ethers or tertiary alcohols in the gas phase face challenges including catalyst deactivation, high energy consumption, and complex reactor designs, which increase operational costs and reduce catalyst efficiency.

Innovation Solution

A continuous process for producing isoolefins with 4 to 6 carbon atoms by cleaving alkyl tert-alkyl ethers or tertiary alcohols in the gas phase on a solid catalyst at temperatures between 200 to 400 °C, using a simple tube reactor with a liquid heat transfer medium, where the temperature drop in the catalyst zone is minimized to less than 50 °C, and the heat transfer medium flows concurrently with the reaction mixture.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If the cracking temperature is increased to improve reaction rate and conversion, then productivity increases, but side reactions such as hydrogenation or dehydrogenation increase, specific energy consumption increases, and greater capital investment is required for reactors

Engineering Contradiction:
Improvereaction rateVSAvoidspecific energy consumption
Core Design Contradiction:
ProductivityVSLoss of energy

Solution Approach 1:

The patent changes the physical state parameter of the reaction system from liquid/gas-phase mixture to pure gas phase, and optimizes the temperature parameter to 300-400°C range. This parameter combination achieves high conversion rates while avoiding the energy penalties associated with higher temperatures or liquid-phase operation

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The patent utilizes phase transition by operating in the gas phase only, eliminating the need to manage liquid-gas two-phase systems. This phase selection reduces energy consumption associated with heating and separating liquid phases, while maintaining high reaction rates through optimal gas-phase temperature control

Inventive Principle:
Principle #36Phase transitions

2Productivity

If the cracking temperature is increased to improve reaction rate, then productivity increases, but catalyst deactivation occurs more quickly

Engineering Contradiction:
Improvereaction rateVSAvoidcatalyst stability
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

The patent identifies and implements an optimal temperature window of 300-400°C that balances reaction rate and catalyst stability. This parameter optimization ensures high productivity while minimizing thermal stress and deactivation mechanisms that occur at higher temperatures

Inventive Principle:
Principle #35Parameter changes

3Temperature

If liquid phase or gas/liquid mixed phase splitting is used to carry out the cleavage, then the reaction can proceed at lower temperatures, but the resulting products dissolved in the liquid phase undergo side reactions such as acid-catalyzed dimerization or oligomerization

Engineering Contradiction:
Improvereaction temperatureVSAvoidside reactions
Core Design Contradiction:
TemperatureVSObject-generated harmful factors

Solution Approach 1:

The patent eliminates liquid phase operation entirely by conducting the reaction in the gas phase. This phase selection prevents product dissolution in liquid, thereby eliminating the medium that enables acid-catalyzed dimerization and oligomerization side reactions, even though it requires higher operating temperatures

Inventive Principle:
Principle #36Phase transitions

Solution Approach 2:

The patent extracts the harmful liquid phase medium from the reaction system, leaving only the gas phase. This removal of the liquid phase eliminates the solvent environment that facilitates unwanted side reactions, achieving cleaner product formation despite higher temperature requirements

Inventive Principle:
Principle #2Taking out (Extraction)

4Reliability

If complex reactor designs with multiple heating circuits or divided jackets are used to limit temperature drop, then catalyst deactivation is reduced, but device complexity and capital investment increase

Engineering Contradiction:
Improvecatalyst activityVSAvoidreactor construction
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The patent changes the fundamental operating parameters to gas phase at 300-400°C, which inherently reduces the magnitude of temperature drops during the endothermic reaction. This parameter change allows the use of simple single-circuit heating reactors while maintaining catalyst activity, avoiding the need for complex multi-circuit or divided jacket designs

Inventive Principle:
Principle #35Parameter changes

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 significantly reduces catalyst deactivation, lowers capital and operating costs, and extends the catalyst's service life, resulting in more efficient and economical production of isoolefins like isobutene.

Implementation Method 1

heating with a liquid heat transfer medium in which the temperature drop in the catalyst zone at any point in relation to the inlet temperature is less than 50 °C

Methodology Applied
Scientific EffectHeat transfer: Conduction (thermal)

Implementation Method 2

cleavage of alkyl tert-alkyl ethers or tertiary alcohols in the gas phase on a solid catalyst

Methodology Applied
Scientific EffectCatalysis: Catalysis

Data Source

PatentEP1903019B1Method for the production of iso-olefines
Publication Date: 2015.09.02 EVONIK OPERATIONS GMBH

AI summary

The present invention relates to a continuous process for the production of isoolefins with 4 to 6 carbon atoms by cleavage of compounds of formula I R1-O-R2 (I) with R1 = a tertiary alkyl group having 4 to 6 carbon atoms and R2 = H or an alkyl group, in the gas phase over a solid catalyst in the temperature range of 200 to 400 °C at a pressure of 0.1 to 1.2 MPa in a reactor equipped with a heating jacket and heated with a liquid heat transfer medium, characterized in that the temperature drop in the catalyst zone at any point with respect to the inlet temperature is less than 50 °C, that the reaction mixture in the reactor and the heat transfer medium in the jacket flow in cocurrent flow through the reactor, and that the temperature difference of the heat transfer medium between the inlet to the reactor and the outlet from the reactor is less than 40 °C.